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Reporte zur Charge EW 0162

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

500Reporte angezeigt
37Todesfaelle
200Hospitalisiert
35Lebensbedrohlich
39Bleibende Schaeden
MI 83 CA 46 PA 31 TX 27 OH 22 NY 20 VA 18 GA 16 TN 14 FL 14 MN 12 NJ 12

VAERS 2674532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
67,0
Geschlecht
M
Eingang
22.08.2023
Impfdatum
09.04.2021
Beginn
25.01.2022
Tage bis Beginn
291,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure Angiogram pulmonary abnormal Asthenia C-reactive protein increased COVID-19 pneumonia Chest discomfort Cough Laboratory test abnormal

Symptomtext

Pneumonia due to COVID 19.; acute hypoxic respiratory failure. complained of generalzed weakness and non-productive cough with chest tightness. Labs reveal >20 CRP. CTA positive for Right sided PE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2660036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TN
Alter
67,0
Geschlecht
M
Eingang
24.07.2023
Impfdatum
16.04.2021
Beginn
21.11.2022
Tage bis Beginn
584,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Patient Deceased

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Colon Polyps, Anemia, BPD, GERD, Hiatal Hernia, HTN, Neurogenic Bladder, Spina Bifida, S/P Nephrectomy, urinary Meatus Stricture, Shingles, Scoliosis
Andere Medikamente
Unknown
Allergien
Levaquin
Vorherige Impfungen
-

VAERS 2658291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
40,0
Geschlecht
F
Eingang
19.07.2023
Impfdatum
15.04.2021
Beginn
07.04.2023
Tage bis Beginn
722,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure Dyspnoea Hypoxia Respiratory failure

Symptomtext

J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/7/2023 SHORTNESS OF BREATH J96.02 ACUTE HYPERCAPNIC RESPIRATORY FAILURE 4/7/2023 SHORTNESS OF BREATH R09.02 HYPOXIA 4/7/2023 SHORTNESS OF BREATH

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2657733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
CO
Alter
92,0
Geschlecht
F
Eingang
18.07.2023
Impfdatum
14.04.2021
Beginn
08.01.2022
Tage bis Beginn
269,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure Dyspnoea SARS-CoV-2 test positive Suspected COVID-19

Symptomtext

Presented to ED w/SOB; admitted for acute resp failure w/hypoxia & suspect COVID; COVID test +, tx w/ O2, abx & steroids; dc'd home w/ O2.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
4,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2653106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
58,0
Geschlecht
F
Eingang
06.07.2023
Impfdatum
20.04.2021
Beginn
18.01.2022
Tage bis Beginn
273,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure COVID-19 Diabetic ketoacidosis SARS-CoV-2 test positive

Symptomtext

Admitted with DKA, resolved now, also tested positive for COVID-19; had acute respiratory failure with hypoxia and required high-flow oxygen, steroids and abx; received Actemra on 01/19; DC home on RA.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
7,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2648413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
61,0
Geschlecht
F
Eingang
22.06.2023
Impfdatum
17.04.2021
Beginn
29.03.2023
Tage bis Beginn
711,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure

Symptomtext

ACUTE RESPIRATORY FAILURE 3/29/2023 ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/29/2023 ACUTE RESPIRATORY FAILURE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2591904

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
65,0
Geschlecht
F
Eingang
06.03.2023
Impfdatum
20.04.2021
Beginn
01.09.2022
Tage bis Beginn
499,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Arrhythmia COVID-19 COVID-19 pneumonia Death Endotracheal intubation General physical health deterioration Incisional drainage Multiple organ dysfunction syndrome Necrotising fasciitis Renal failure SARS-CoV-2 test positive Septic shock

Symptomtext

3RD DOSE PFIZER COVID VACCINE GIVEN 05/13/2022, FP4554; Pt admitted to hospital from rehab on 9/7/22 with necrotizing fasciitis of left hip and COVID PNA; pt had a positive COVID test; taken to OR multiple times for I & D; condition worsened requiring intubation; multi-organ and renal failure; septic shock; arrhythmias; transitioned to comfort care and pt passed away in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
7,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2566680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
64,0
Geschlecht
F
Eingang
24.01.2023
Impfdatum
20.04.2021
Beginn
01.07.2022
Tage bis Beginn
437,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acute kidney injury COVID-19 Computerised tomogram thorax abnormal Death Endotracheal intubation General physical health deterioration Haemodialysis Hyperkalaemia Pneumonia bacterial Respiratory failure SARS-CoV-2 test positive Tracheostomy Unresponsive to stimuli

Symptomtext

3RD DOSE PFIZER COVID VACCINE GIVEN 10/27/21, LOT #FH8028; pt found unresponsive at home by family; when EMS arrived, pt's O2 saturation was in the 50s;O2 supplementation given; when arrived to hospital, in severe respiratory failure; found to be positive for COVID test; CT of chest showed bacterial pneumonia; started on ABX; eventually required intubation; hyperkalemic; worsening AKI; given dexamethasone; required hemodialysis; eventually extubated but later required intubation with tracheostomy performed; pt's condition deteriorated; family chose withdrawal of care; pt passed away in the hosppital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
27,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
ESRD s/p renal transplant, DM, HTN
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2196262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
72,0
Geschlecht
M
Eingang
15.11.2022
Impfdatum
24.04.2021
Beginn
07.02.2022
Tage bis Beginn
289,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acute kidney injury Acute respiratory failure COVID-19 Chest X-ray abnormal Cough Anticoagulant therapy Death Decreased appetite Diarrhoea Dyspnoea Endotracheal intubation Nausea Pneumonia Pneumonia bacterial Respiratory tract congestion SARS-CoV-2 test positive Positive airway pressure therapy Respiratory disorder

Symptomtext

pt to hosp with c/o SOB, dyspnea, cough, congestion, nausea, vomiting, diarrhea, anorexia; increased O2 needs; placed on BiPAP; positive for COVID; bilateral multifocal pneumonia; given Remdesivir, dexamethasone, ABX, heparin drip; worsening respiratory status requiring intubation; transitioned to DNR/DNI with focus on comfort care; pt passed away in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
17,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
chronic DVT, mild obstructive lung disease, on O2 3 L via NC as baseline, CKD 3B
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2411266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
69,0
Geschlecht
F
Eingang
15.08.2022
Impfdatum
29.04.2021
Beginn
01.10.2021
Tage bis Beginn
155,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Agitation Blood culture positive COVID-19 Death Erythema Gram stain positive Hypervolaemia Hypotension Intensive care International normalised ratio increased Melaena Pain SARS-CoV-2 test positive Shock Swelling

Symptomtext

10/12/21 pt had a positive COVID test; 11/3-12/7/21 pt had a hospitalization for melena; 12/18/21 pt to ED after being transferred from outside hospital (name unknown) due to hypotension, bilateral swelling and redness, concerning for possible cellulitis; INR from outside hospital was 6; started on Levophed; transferred to alternate hospital for further care; admitted to hospital; shock, hypotension, rule out sepsis, likely related to volume overload, pt has not missed HD; outside hospital called and stated blood cultures growing gram positive cocci; started on ABX; pt became progressively agitated and c/o diffuse all over pain; unable to localize; given low dose oxycodone with pain improvement; rapid progression of hypotension; treated with vasopressors; transitioned to comfort care; pt expired in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
16,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
ESRD on HD, CAD status post CABG; Atrial Fibrillation, mitral valve replacement
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2402981

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge EW0162

kritisch
Staat
MI
Alter
56,0
Geschlecht
F
Eingang
05.08.2022
Impfdatum
18.03.2021
Beginn
31.07.2022
Tage bis Beginn
500,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Agitation Asymptomatic COVID-19 Death of relative Mania SARS-CoV-2 test positive

Symptomtext

7/31--presently admitted 57y.o. female known to me as an outpatient who has been struggling ever since her husband and her dog died recently. Patient became very agitated and manic. Was potential danger to herself and was admitted on a locked inpatient psychiatric unit for protection of self. 8/1 Tested positive for COVID on 7/31/2022. Previously tested positive for COVID 2-3 weeks ago on a home test. Currently asymptomatic. It has been more than 10 days since the initial positive. COVID isolation precautions have been discontinued.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death of relative
Hospital-Tage
-
Labordaten
7/31-- SARS-CoV-2 by NAA, detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2388157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
69,0
Geschlecht
M
Eingang
25.07.2022
Impfdatum
30.04.2021
Beginn
09.07.2022
Tage bis Beginn
435,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Agitation Blood culture negative Blood pressure systolic increased COVID-19 Chest X-ray abnormal Coma scale Computerised tomogram head normal Electroencephalogram abnormal Encephalopathy Endotracheal intubation Gastrointestinal tube insertion Hypertension Hypotension Intensive care Mental status changes Muscle rigidity Obstructive airways disorder Oropharyngeal suctioning

Symptomtext

Patient with 2 Pfizer COVID vaccinations who admitted with positive COVID test. Provider D/C note below: "Hospital Course: Patient, a covid positive 70-year-old male with history of traumatic brain injury, epilepsy with two recent 2 hospitalizations followed by Dr. at medical facility taking dilantin and zonisamide, and alcohol use disorder presented to the emergency department in status epilepticus. On arrival patient GCS of 3. He was given 8mg of ativan and a loading dose of fosphenytoin. Patient was intubated and started on propofol drip with concerns of his compromised airway. Stat EEG and neurology consult ordered. CT imaging of the head unremarkable for acute pathology. With initial concerns of sepsis, the patient was started on prophylactic antibiotics and blood cultures were obtained. Stat EEG revealed encephalopathic changes without seizure activity seen. Per Neurology recommended to maintain 100 mg of IV Dilantin q8 hours after his initial fosphenytoin load. They recommended to maintain on Depakote and zonisamide and change propofol to precedex at that time. Norepinephrine was given briefly on 7/9, central line was not needed. In the ICU, patient has had episodes of hypotension along with agitation. On 07/10, became hypertensive tachycardic and tachypneic after nursing provides ETT suction. patient appeared slightly rigid particularly in the upper extremities bilaterally. Bilateral eyes did not show nystagmus and pupils PERRLA. Did not follow commands or show purposeful movement. Neurology was consulted and no stat EEG was done. patient was stabilized by the end of the night. Last precedex and propofol use 7/10. Patient extubated on 07/11. patient has remained relatively hemodynamically stable however has required hypertensive medications for elevated systolic pressures. Failed swallow study 7/12, NG tube was placed. Concerns for aspiration pneumonia on cxr and met SIRS criteria unasyn was started (7/12-). Bcx 7/9- NGTD. Vancomycin and Zosyn D/ced (7/9-7/10). Pt however has had slow improvement in mentation with concerns for subclinical seizures. Neurology wanted an MRI done today (7/14), however was decided to transfer to Neuro-ICU under Dr. for further evaluation."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Coma scale
Hospital-Tage
15,0
Labordaten
COVID detected PCR on 07/09/22.
Aktuelle Erkrankungen
-
Vorgeschichte
Simple partial epilepsy Scoliosis of thoracolumbar spine Cannabis use disorder, mild, abuse Normocytic anemia Mixed hyperlipidemia Traumatic brain injury Hypothyroidism
Andere Medikamente
Aspirin Lipitor Depakote Folic acid Ensure supplemental drinks Levothyroxine Nayzilam Zonegran
Allergien
Gabapentin Bendramine Diphenydramine Hcl (seizures) Keppra
Vorherige Impfungen
-

VAERS 2433361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
64,0
Geschlecht
M
Eingang
21.07.2022
Impfdatum
21.04.2021
Beginn
07.05.2022
Tage bis Beginn
381,0
Dosis
1
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
COVID-19 Death

Symptomtext

Narrative: PATIENT PASSED AWAY DUE TO COVID-19. HE WAS HOSPITALIZED AND HAD RECEIVD A COVID-19 VACCINE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2310274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
GA
Alter
47,0
Geschlecht
M
Eingang
06.06.2022
Impfdatum
08.05.2021
Beginn
06.10.2021
Tage bis Beginn
151,0
Dosis
2
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Amnesia Cerebrovascular accident Laboratory test normal

Symptomtext

I had a Stroke . After all of the testing my arteries were crystal clean and all of the tests could not find a reason other than the covid vaccine . The Vaccine gave me a stroke .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
4,0
Labordaten
10/6/21 ambulance to hospital, was there for about four days for treatement . Partally recovered . Memory is gone , not good .
Aktuelle Erkrankungen
none , healthy
Vorgeschichte
gout
Andere Medikamente
Allopurinol , metformin , rosuvastatin
Allergien
none
Vorherige Impfungen
-

VAERS 2296460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
68,0
Geschlecht
F
Eingang
26.05.2022
Impfdatum
08.04.2021
Beginn
15.09.2021
Tage bis Beginn
160,0
Dosis
2
Route/Site
UN / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute kidney injury Anticoagulant therapy Blood potassium increased COVID-19 COVID-19 pneumonia Carbon dioxide increased Confusional state Death Endotracheal intubation Haemofiltration Intensive care Mental status changes SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Presented with AMS/confusion x2 days; Covid + in ED; Admit ICU 9/15 Covid PNA; tx 9/16 zinc, singulair, merrem, steroids, eliquis, 9/17 vanc,; with High K+ and AKI with admit..not candidate for remdesivir or baricitinib; O2 initially on 6 LPM NC; transitioned to HF O2 within 24 hours; 9/20 pt intubated; 10/2 CRRT started; 10/7 Currently; pt on 1 pressor, 100% FiO2, High CO2 values and unresponsive >24 hours off sedation and paralytics; Discussing comfort measures with family. Patient has been made DNR by family members,and was pronounced dead on 10/15/2021

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
31,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2275697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
67,0
Geschlecht
M
Eingang
13.05.2022
Impfdatum
21.04.2021
Beginn
01.01.2022
Tage bis Beginn
255,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acute kidney injury Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac failure congestive Chronic obstructive pulmonary disease Condition aggravated Confusional state Death Dyspnoea Fatigue Oedema Pneumonia Respiratory failure SARS-CoV-2 test positive Weight increased

Symptomtext

pt to ED with SOB, increased edema, confusion, fatigue and weight gain; COVID test negative; CHF exacerbation, acute renal failure and PNA with hypoxic respiratory failure; another COVID test done on 1/30/22 was positive; O2 supplementation; remdesivir not given due to solitary kidney; dexamethasone given; acute on chronic HRF secondary to COVID pneumonia/COPD; DNR; requesting hospice; comfort care; pt in Transitional Care Center; death certificate and med records sent per VAERS request.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2233701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
78,0
Geschlecht
F
Eingang
14.04.2022
Impfdatum
17.04.2021
Beginn
27.12.2021
Tage bis Beginn
254,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute kidney injury Anaemia macrocytic Anticoagulant therapy Back pain Blood lactic acid increased Blood magnesium decreased COVID-19 COVID-19 pneumonia Chronic kidney disease Clostridium difficile infection Condition aggravated Cough Death Diarrhoea Electrophoresis protein Full blood count abnormal Haemoglobin Hepatic enzyme increased

Symptomtext

Patient with 2 Pfizer COVID vaccines, last dose on 04/17/21 who admitted to the hospital with COVID complications. Provider discharge note below: "Brief Summary of Hospital Stay: Patient is a 79 YO year old female with past medical history of T2DM, CAD s/p NSTEMI and DES (2015), hypertension, hyperlipidemia, and depression. She is presenting to Hospital with complaint of worsening diarrhea and cough x3 days. Of note, she was treated for C diff one month ago. Diarrhea initially worsened and there was associated nausea and vomiting. Only had two loose stools during this hospitalization, then resolved and GI PCR was negative. Cough was new onset 3 days ago and testing revealed she was positive for COVID pneumonia, she was vaccinated. Initial workup also demonstrated AKI on CKD stage IV, elevated lactate, elevated liver enzymes and hepatic steatosis on RUQ US. Blood counts significant for macrocytic anemia likely secondary of anemia of chronic kidney disease, folic acid given. Patient given 2 units of PRBC with inadequate hgb response. Epoetin given 12/28. Of note, SPEP performed demonstrating elevated IgG Kappa. Additionally patient complained of lower extremity cramping and back/pelvic pain. Magnesium was low and replaced. There is history of pelvic fracture, which may be causing some ongoing pain. PT/OT evaluated and receommended that it would be benificial with SNF. However pt refused to go to a such facility and chose home instead. Pt was participating on PT sessions since last November to help with her mobility and we will place PT on discharge. Prescribed Tylenolol, avoid opiates and NSAIDS. Follow up with PCP to address anemia and labs (BMP) as out pt on 1/3/21. Pt currently on 5mg BID eliquis and pt is approaching her 80th Birthday. PCP can discuss about decreasing her eliquis dose appropriate with the dose. " Of note, patient has since died on hospice services on 04/01/22.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
4,0
Labordaten
COVID detected PCR on 12/27/2021
Aktuelle Erkrankungen
-
Vorgeschichte
Hyperlipidemia Macrocytic anemia HTN Diet-controlled type 2 diabetes mellitus (HCC) Overweight (BMI 25.0-29.9) mitral valve regurgitation, moderate to severe B12 deficiency Paroxysmal atrial fibrillation (*) Moderate to severe pulmonary hypertension (*) Mild intermittent asthma Atrial flutter (*) LVH (left ventricular hypertrophy) due to hypertensive disease Recurrent major depressive disorder, in partial remission (*) Osteoarthrosis involving lower leg Osteoporosis GERD Bilateral low back pain without sciatica CAD s/p stent x1 (2016) moderate Tricuspid regurgitation Chronic kidney disease (CKD), stage IV (severe) (*) Recurrent cold sores Chronic fatigue Vertigo Iron deficiency anemia due to chronic blood loss Elevated ferritin level Mediastinal lymphadenopathy Chronic heart failure with preserved ejection fraction (*) Multiple closed fractures of pelvis (*) Closed fracture of left inferior pubic ramus (*) Anemia of chronic disease Hypomagnesemia NSTEMI (non-ST elevation myocardial infarction) (*) Transaminitis Hepatic steatosis Thrombocytopenia (*) Pleural hemorrhage Folic acid deficiency Severe protein-calorie malnutrition (*) Calciphylaxis
Andere Medikamente
Albuterol Breo Ellipta Ativan Antivert Nitrostat (PRN)
Allergien
Aminophyllin: Stevens-Johnson dermatitis from skin contact Iodinated Contrast: Rash Flexeril: Blisters and joints swell Lisinopril: Cough Simvastatin: Myalgia Thimerosal: Blisters
Vorherige Impfungen
-

VAERS 2223340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
65,0
Geschlecht
M
Eingang
08.04.2022
Impfdatum
17.04.2021
Beginn
01.01.2022
Tage bis Beginn
259,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
COVID-19 Cardiac arrest Cardio-respiratory arrest Central venous catheterisation Cough Death Dyspnoea Endotracheal intubation General physical health deterioration Intensive care Wheezing

Symptomtext

pt brought to ED with c/o SOB, cough, and wheezing x 2 days; port surgically placed 6 days ago; found to be positive for COVID; given dexamethasone, remdesivir, ABX, Vitamin C and zinc; pt worsened; coded; intubated; transferred to ICU; made a DNR; went into asystole and expired in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
9,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
DM, HTN, bladder CA
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2220532

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NJ
Alter
58,0
Geschlecht
F
Eingang
07.04.2022
Impfdatum
11.04.2021
Beginn
13.06.2021
Tage bis Beginn
63,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Anticoagulant therapy Blood test Cerebral thrombosis Cerebrovascular accident Hemiparesis Monoplegia Neurologic neglect syndrome Scan

Symptomtext

STROKE, CVA, blood clot in brain;carotid artery-- medication, blood thinners and rehab--left side weakness, neglect; left paralyzed on left side- leg and arm and handL in-patient rehab for 5 weeks; hospitalized 2 weeks before that; consistent therapy to regain ability continues to date-- I have an ongoin bill at hospital that to date, is more than $1000. I dont know how I'll ever pay that.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
-
Labordaten
several scans and blood tests from June 13 through October 2021
Aktuelle Erkrankungen
none
Vorgeschichte
recurring shingles
Andere Medikamente
multivitamin
Allergien
environmental
Vorherige Impfungen
-

VAERS 2218050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TN
Alter
73,0
Geschlecht
F
Eingang
06.04.2022
Impfdatum
27.04.2021
Beginn
01.10.2021
Tage bis Beginn
157,0
Dosis
2
Route/Site
SYR / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Death Inappropriate schedule of product administration

Symptomtext

Information unavailable. Patient died at home. Covid 19 listed as a cause of death on death certificate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2216698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
GA
Alter
54,0
Geschlecht
M
Eingang
05.04.2022
Impfdatum
14.04.2021
Beginn
05.06.2021
Tage bis Beginn
52,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Anticoagulant therapy Blood test Chest X-ray Computerised tomogram Deep vein thrombosis Pulmonary embolism Scan Ultrasound Doppler

Symptomtext

Pulmonary embolism DVT in right leg Treatment: 8 days in hospital, after hospital Eliquis, 5 mg twice per day from June 2021 - January 2022. Scans of legs and lungs every three months, visits with pulmonologist, consultation with vascular surgeon, and currently undergoing examinations with hematologist. At present, no underlying blood condition observed that could have caused clots.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary embolism
Hospital-Tage
8,0
Labordaten
Admitted to hospital on Saturday June 19, 2021. Between 6/19/21 and 6/26/21 when I was discharged I underwent numerous blood tests, CT scans, ultrasounds, and x-rays. Since being discharged, approximately every three months I have had ultrasounds on my leg, numerous blood tests in an attempt to determine the cause of my clots, and several x-rays of my lungs.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multivitamin
Allergien
None
Vorherige Impfungen
-

VAERS 2194590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
58,0
Geschlecht
M
Eingang
23.03.2022
Impfdatum
15.04.2021
Beginn
11.01.2022
Tage bis Beginn
271,0
Dosis
2
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Cardiac arrest Death Dyspnoea Endotracheal intubation Extubation Productive cough Pulseless electrical activity

Symptomtext

very little records received from hospital; pt presents to hospital with SOB and productive cough; intubated during the course of his hospitalization; DNR; pt suffered PEA cardiac arrest; palliatively extubated and pt passed away in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
12,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
ESRD, HIV, HTN, A Fib, seizure disorder, history of CVA
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2171653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
53,0
Geschlecht
F
Eingang
10.03.2022
Impfdatum
07.09.2021
Beginn
11.12.2021
Tage bis Beginn
95,0
Dosis
2
Route/Site
IM / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Amylase increased Blood albumin decreased Blood bicarbonate decreased Blood creatinine increased Blood glucose normal Blood lactate dehydrogenase increased Blood lactic acid Blood urea increased C-reactive protein increased COVID-19 Chest X-ray abnormal Chills Death Diarrhoea Differential white blood cell count Dyspnoea exertional Fall Fibrin D dimer

Symptomtext

Reports indicate patient presented to the hospital for evaluation because of worsening difficulty in breathing with activity. She did test positive for COVID-19 on 12/04. Patient reports at least a greater than 5 day history of nasal congestion, chest congestion associated a cough that is sometimes productive of clear, but sometime discolored phlegm. Symptoms are associated with chills, but no fever. Patient also reports nausea with dry heaving, but no vomiting. Patient reports chronic, but not acute or acute worsening diarrhea.. Reports indicate patient was found to be saturating down at 89% on arrival. On arrival into the hospital, patient was noted to be normotensive with blood pressure 100/54, otherwise afebrile saturating 93% on 2 liters/minutes supplemental by then. Initial temperature was 99?. Further workup in the emergency room does include a CMP that shows a BUN and creatinine of 34 and 2.1 respectively with a glucose of 97. Albumin and total protein 2.2 and 5.8. CRP was elevated at 3.76. Ferritin was 288.7. LDH 285. Procalcitonin 0.13. Troponin was 33.3. D-dimer is 218. Lactic acid 1.3. CBC with differential shows shows a hemoglobin and hematocrit 9.5 and 31.4 respectively with a platelet count of 450 and a white count of 8.08 with 94% represents segmented neutrophils.. COVID-19 testing was positive. Because the patient symptoms, patient did go on to receive a L of normal saline as a bolus, she was given a starter dose of dexamethasone Doxycycline and Rocephin empirically started. Decadron and Remdesivir started per covid Protocol. O2 support continued from ER. Dr spoke with another Dr regarding anti-rejection medications noting amylase, lipase and creatinine levels were increasing with concern of transplant rejections. Dr spoke with another Dr transplant team. There were no beds available for transfer to hospital. They discussed medication adjustments including Tacrolimus and Cellcept adjustments. Patient continued to decline and night of 12/18, "12/18 night shift patient sustained accidental fall night shift with no new injury. Patient also required non-rebreather mask overnight. Chest x-ray bilateral pulmonary infiltrate. Labs revealed white cell count increased to 24. But procalcitonin 0.06 CRP 1.67." Bicarbonate started after drop in bicarb and diarrhea. She had IV fluid adjustments. Breathing continued to decline and REACH call completed. Code status re-addressed and she was adament regarding DNR/DNI status. With continued declined, patient stated she could not continue as such. She endorses knowing she was dying and "was done." She pulled off her Bipap which was quickly replaced with nasal cannula. She subsequently removed nasal cannula. She was transitioned to Comfort Measures. Patient's sister was notified and came to hospital. Patient's son was notified. On December 12/21/2021 at 0526 pt died from complications of Covid 19 Sepsis and Pneumonia.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
10,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
11/17/2016 Encounter for hydration prior to CT scan 5/10/2016 Dermatitis 10/27/2015 Common wart 6/2/2014 GERD (gastroesophageal reflux disease) Date Unknown Arthritis Date Unknown Bowel incontinence Date Unknown CAD (coronary artery disease) Date Unknown Complication of anesthesia Date Unknown Dementia Date Unknown Dialysis patient Date Unknown GERD (gastroesophageal reflux disease) Date Unknown Heart disease, unspecified Date Unknown HTN (hypertension) Date Unknown Hyperlipidemia Date Unknown Ischemic cardiomyopathy 2006-2009 Kidney dialysis Date Unknown MI (myocardial infarction) Date Unknown Neuropathy Date Unknown TIA (transient ischemic attack) Date Unknown Unspecified adverse effect of anesthesia Date Unknown Unspecified disorder of kidney and ureter
Andere Medikamente
apixaban (ELIQUIS) 5 MG TABS tablet Cholecalciferol (VITAMIN D3) 2000 UNIT CAPS docusate sodium (COLACE) 100 MG capsule metoclopramide (REGLAN) 10 MG tablet metoprolol tartrate (LOPRESSOR) 25 MG tablet mycophenolate sodium (MYFORTIC) 1
Allergien
-
Vorherige Impfungen
-

VAERS 2135626

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

kritisch
Staat
CA
Alter
59,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
04.05.2021
Beginn
03.07.2021
Tage bis Beginn
60,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Angiogram Coronary angioplasty Echocardiogram Electrocardiogram Metabolic function test Myocardial infarction

Symptomtext

Myocardial infarction treated with multiple (3) angioplasties to coronary arteries

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
3,0
Labordaten
Metabolic Angiogram Echocardiogram EKG
Aktuelle Erkrankungen
None
Vorgeschichte
Excellent health
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2088511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
61,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
08.04.2021
Beginn
29.01.2022
Tage bis Beginn
296,0
Dosis
2
Route/Site
IM / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute respiratory failure Anaemia COVID-19 COVID-19 pneumonia Cardiac arrest Condition aggravated Death Dyspnoea Endotracheal intubation Gastrointestinal haemorrhage Haemodialysis Haemoglobin decreased Hypotension Intensive care Melaena Oesophagogastroduodenoscopy Osteomyelitis Radioembolisation

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Received Pfizer Vaccines 03/18/21 and 04/08/2021. COVID + at outside facility 1/6/22 and in ED 1/21/22. Presented to ED 1/21/22 with SOB and melena with HGB of 6. Recently admitted to outside facility for osteomyelitis and d/ced on doxycycline and flagyl on 1/18/22. Admitted to ICU for GI bleed and acute hypoxemic respiratory failure due to Covid PNA. Stablized and transferred to floor for 2 days then returned to ICU 2/2 GI bleed post RRT during HD session. Went to IR for embolization and went into cardiac arrest with ROSC after 35 min. Treated with amiodarone. On 1/29/22 developed hypotension and anemia worsened. She had mild improvement in BP and was transferred to the GI lab for emergent EGD and went into another cardiac arrest during intubation. CPR was initiated and later stopped at request of family at bedside. Patient expired on 1/29/22

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
8,0
Labordaten
1/21/22 Covid + :This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
Aktuelle Erkrankungen
bilateral pedal skin ulcers 12/2021
Vorgeschichte
CAD, DM2,grangrene of left foot, macrocytic anemia, ESRD on dialysis, chronic cholecystitis, CHF EF 35%, aortic stenos aortic stenosis post TAVR,
Andere Medikamente
tylenol, tylenol with codeine, carvedilol, vitamin c with rose hip, aspirin, atorvastatin, auryxia, brimonidine, calcitriol, doxazosin, losartan, mirtazapine, pantoprazole
Allergien
Gabapentin, adhesive, nifedipine
Vorherige Impfungen
-

VAERS 2071993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

kritisch
Staat
-
Alter
49,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
16.12.2021
Beginn
23.12.2021
Tage bis Beginn
7,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Acute respiratory failure COVID-19 pneumonia Dyspnoea

Symptomtext

12/23/21: Pt admitted to the hospital due to SOB from covid-19 pneumonia with acute respiratory failure. Pt was started on IV decadron, start pulmicort and combivent. Symptoms were >7 days therefore remdesivir was not started. Pt was given O2 by NC, titrating as needed. 12/24: Pt clinically improved. Discharged without O2. Pt was discharged with dexamethasone 6mg tab - 1 tablet once daily for 5 days and albuterol HFA prn.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2068741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
84,0
Geschlecht
M
Eingang
27.01.2022
Impfdatum
14.04.2021
Beginn
12.01.2022
Tage bis Beginn
273,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia COVID-19 Cough Death Dyspnoea Fluid intake reduced General physical health deterioration Hypophagia Inappropriate schedule of product administration Mental status changes SARS-CoV-2 test positive

Symptomtext

Pfizer COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/17/2021 and 4/14/2021. Presented to ED on 1/5/2022 and diagnosed with COVID-19, received monoclonal antibody treatment on 1/10/2022. Returned to ED 1/12/2022 with complaints of worsening shortness of breath, cough, altered mental status and weakness two weeks in duration. Per EMS SpO2 on room air was 78% and improved to the 90s on 2 L NC. Additionally, patient has not been eating or drinking. Continued to decline and expired on 1/17/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
5,0
Labordaten
Positive COVID-19 on 1/5/2022 and 1/12/2022 using the platform using PCR or equivalent testing technology.
Aktuelle Erkrankungen
-
Vorgeschichte
A-fib, Automatic implantable cardioverter-defibrillator in situ, basal cell carcinoma, CAD s/p stent to RCA, CHF, HFrEF, CKD, GERD, C. diff diarrhea, Heart murmur, hyperlipidemia, hypertension, H/O MI, Lumber compression fracture, Osteoarthritis, osteoporosis, Rheumatoid arthritis.
Andere Medikamente
Acetaminophen, Atorvastatin, Benzonatate, Cholecalciferol, Divalproex, folic acid, methotrexate, metoprolol, omeprazole, prednisone, rivaroxaban, sertraline, furosemide.
Allergien
Midodrine, Codeine
Vorherige Impfungen
-

VAERS 2063078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
64,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
23.11.2021
Beginn
14.01.2022
Tage bis Beginn
52,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute kidney injury Acute left ventricular failure Acute respiratory failure Angiogram abnormal Angiogram pulmonary abnormal Anticoagulant therapy Asthenia Atrial fibrillation Bacteraemia Biopsy adrenal gland Blood bilirubin increased Blood creatinine normal Blood glucose normal Blood pH decreased Blood test Breast cancer female Breast cancer stage I CHA2DS2-VASc-score

Symptomtext

Hospitalized (1.17.22 - present); COVID-19 positive (1.14.22); fully vaccinated (3 doses) ASSESSMENT / PLAN: Patient is a 64 y.o. female with a past medical history of left breast cancer on chemotherapy presented with fatigue found to be in shock, undifferentiated requiring norepinephrine, covid-19 pna, pancytopenia, new onset afib with RVR Brief History and Medical Decision-Making: This is a 64 year old female patient with past medical hx significant for left breast cancer (stage 1A) s/p left partial mastectomy and SLNB performed on 10/4/21. She is currently receiving adjuvant chemotherapy. She recently underwent CT guided left adrenal biopsy which was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, s/p IR embolization of T10, T11 and T12 and pleural drain placement. She was diagnosed with COVID-19 Pneumonia on 1/14/2022, she presented to ED today with feeling of generalized weakness and not feeling well. Noted to be in acute hypoxemic respiratory failure and shock requiring pressors to maintain MAP more than 65. She was also noted to be in acute kidney injury ( suspect pre-renal in etiology). In regards to the shock, the main differential currently is septic shock given neutropenia and findings on CT chest of With increasing left sided pleural effusion that is mostly likely related to recent hemothorax and differential include empyema, She also has nodule opacities in left upper lobe. We will contine broad spectrum Abx ( cefepime and vancomycin) pending blood culture results and consult ID. We will add stress dose steroids. Obtain echo to assess for LV function and presence of pericardial effusion. Consult IR for potential drain placement in the left chest and send diagnostic samples to rule out empyema ( her platelets are low and given recent bleeding, we need to transfuse before any intervention, She might also require thoracic surgery consult). No active signs of bleeding but we will continue to follow serial Hemoglobin, anticipate the drop in hemoglobin is related to chemotherapy given findings of neutropenia and thrombocytopenia. Start Amiodarone given Atrial fibrillation with RVR on presentation. For the COVID-19 pneumonia, we will hold off on remedisivr given AKI and she is currently on stress dose steroids. Check D--dimer and obtain DVT US of both lower extremities. Progress Note from 1.25.22: ASSESSMENT / PLAN: 64-year-old female with past medical history of left breast cancer stage IA, status post left partial mastectomy and sentinel lymph node biopsy on 10/04/2021, currently receiving adjuvant chemo with curative intent, who recently underwent CT-guided left adrenal biopsy was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, status post IR embolization of T10, T11, and T12, with pleural drain placement. Patient also recently diagnosed with COVID on 1/14. Patient presented with generalized weakness and not feeling well. Admitted to intensive care unit with shock, acute hypoxic respiratory failure. 1. Acute hypoxic respiratory failure Multifactorial in setting COVID-19 PCR, left empyema, Staph aureus pneumonia and bacteremia. Had acute tachypneic and hypoxic event on 1/24 requiring increased vent settings and further sedation. Plan: - Wean vent settings as tolerated - Lasix 40 IV qd, goal net negative - goal O2 sat 88% and above 2. Shock - resolved - multifactorial in setting of left empyema, multifocal bilateral pneumonia, Staph aureus pneumonia and bacteremia. Plan: - Off Pressors - Solumedrol taper - 40, 30, 20, 10 per day 3. Left empyema IR placed left chest tube on 01/18. Pleural fluid exudative with pH 6.72, glucose less than 2. IR recommended tPA / dornase. However, initially held off on tPA / dornase given recent hemothorax requiring emoblization and also pancytopenia. CT scan of the chest 1/19 showed improving left-sided empyema, however, with minimal drainage on 1/20. Drainage likely will be limited due to loculated infection. - 1/20: s/p trial tPA / dornase at 1/2 dose (5 mg) x 1 on 1/20. - 1/21: started on tPA / dornase at normal dose, plan for 5 total doses - 1/23: receiving final doses/ CXR appears well improved, no further drainage from chest tube, no signs of bleeding - 1/24: Completed tPA / dornase therapy, no immediate complications, stable and improved left lower consolidation on CXR - 1/25: significant drainage from L chest tube 355cc over last 24 hours 4. Febrile Patient became febrile during the night of 1/24-1/25. This was in the setting of recently starting Precedex and following return from IR procedure. This is likely 2/2 medication effects however superimposed new bacterial infection cannot be ruled out on exam alone. Plan: - Follow-up culturers - Discontinued Precedex - Continue to monitor temperature 5. Multifocal bilateral pneumonia Left lower lobe Staph aureus pneumonia Staph aureus bacteremia 1/18 respiratory cultures positive for MSSA, with left pleural fluid cultures positive for Staph aureus, and blood cultures positive for GPC in clusters. CT chest 1/19 (obtained for re-evaluation of left empyema) showed new multifocal pneumonia in right side, suspected to be a progression of left-sided Staph aureus pneumonia. Plan: - Escalated current abx based on repeat fever with CXR and clinical course concerning for HAP/VAP, continue Zosyn + Vanc for empiric coverage pending cultures and ID recommendations - Obtain sputum culture, if unable patient will need bronchoscopy w/ BAL - Given Staph aureus bacteremia, will need to consider future TEE for rule out infective endocarditis when stabilized - IR successfully removed R portacath evening of 1/24, will need replaced once discharged for continued chemotherapy 6. Acute systolic heart failure / heart failure with reduced ejection fraction 22% New reduced EF 22%, compared to EF 65% in 12/14/2021. Cardiology consulted, and discussed case with Cardiology Oncology, who thinks that overall less likely due to anthracycline therapy, but possible. Patient's new reduced systolic function likely due to stress-induced cardiomyopathy in setting of shock. Plan: - could consider future repeat echo 7. Loose Stools - prolonged illness with tube feeds, unlikely to be infectious at this time, will continue to monitor temperature and for other signs of infection. Plan: - remove rectal tube as soon as possible, high risk for adverse sequela including pressure ulcers - monitor rectal tube output - follow-up C. Diff and enteric pathogens - bowel regiment changed from standing to PRN 8. Atrial fibrillation with RVR - resolved No history of atrial fibrillation, likely 2/2 shock in the setting of stress cardiomyopathy. Converted to sinus rhythm while on amiodarone drip on 1/20, has remained in sinus rhythm since. Plan: - On PO amiodarone 400mg BID, decrease dosing once received entire 10g loading dose - Patient is high risk for thromboembolic event based on CHADS-VASC2 > 3, for that reason we are starting therapeutic heparin drip - Patient also plans on receiving chemotherapy on discharge causing transient thrombocytopenia, this puts her at high risk for bleeding sequela, this issue will have to be addressed on discharge for further anticoagulation planning - plan to resume BB as able now that shock resolved 9. Pancytopenia - stable In the setting of active chemotherapy for breast cancer. On arrival had significant neutropenia, now improved but is on stress dose steroids for shock. Hb and Plt stable. Plan: - transfuse if platelets less than 10 or less than 50 if active bleeding - transfuse if hemoglobin less than 7 10. AKI - resolved Likely prerenal in setting of shock on presentation. Based on chart review, patient has a baseline creatinine of 0.5-0.7. Plan: - patient continues to be at baseline following resuscitation - continue to trend on daily CMP 11. Elevated liver enzymes - resolved RUQ US 1/19 obtained due to gradually rising bilirubin. Negative for biliary obstruction, cholelithiasis, cholecystitis. Showed heterogeneous liver which may be due to hepatic steatosis. Consider dedicated liver screening with patient more stable. 12. Metastatic breast cancer Stage IA, status post left partial mastectomy and sentinel lymph node biopsy on 10/04/2021, currently receiving adjuvant chemo with curative intent, who recently underwent CT-guided left adrenal biopsy was complicated by hemothorax and pseudoaneurysm of left T1 intercostal artery, status post IR embolization of T10, T11, and T12, with pleural drain placement. Plan: - holding chemotherapy pending clinical course - palliative care consult, for supportive care for husband who is patient's sole caregiver and management of chronic conditions

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
8,0
Labordaten
-
Aktuelle Erkrankungen
12.20.21-12.24.21 - hospital admission - Hemothorax on left - HOSPITAL COURSE: Patient is a 64 year old female with PMH significant for invasive ductal breast carcinoma, HTN, rosacea, who presented to the ED following a CT guided adrenal bx due to acute bleeding. After procedure pt c/o pain and shortness of breath, BP was found to be 74/38, pt received fluid bolus and a CT was obtained with findings of hemothorax, Pseudoaneurysm of left T11 intercostal artery with extravasation into left pleural space. Pt was taken to IR and underwent intercostal angios (T 10, 11, and 12) with microcoil embolizations. Left internal mammary angio; left pleural drain placement. Her blood counts where closely monitored throughout hospitalization. She received 1 unit PRBC in ED but did not require any further transfusions. Cardiothoracic team was consulted for evaluation and recommended continuing current conservative managment with drain. The patient did have one episode of near-syncopal episode which resolved after fluid bolus. Her antihypertensive medications where briefly held and all restarted before discharge.
Vorgeschichte
Family history of coronary artery disease Essential hypertension Class 2 obesity due to excess calories without serious comorbidity with body mass index (BMI) of 39.0 to 39.9 in adult Psoriasis Family history of leukemia Pain in joint, multiple sites Family history stroke in brother and father in early 60s Leukocytosis Chronic pain of left knee Rosacea, acne Encounter for consultation Carcinoma of upper-outer quadrant of left breast in female, estrogen receptor positive (HCC) Hemothorax on left
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet atenolol-chlorthalidone (TENORETIC) 100-25 MG per tablet B Complex Vitamins (VITAMIN B COMPLEX) tablet Cholecalciferol 2000 units CAPS diphenhydrAMINE (BENADRYL) 25 MG t
Allergien
Contrast Dye [Ivp Dye, Iodine Containing]Itching TramadolDizziness CephalexinRash Ciprofloxacin CyclobenzaprineRash EtodolacOther, Palpitations Fish Flu Virus VaccineSwelling Lisinopril MacrolidesRash, Swelling Neomycin-bacitracin-polymyxinRash Nickel Nitrofuran DerivativesRash Nitrous Oxide PenicillinsRash Sulfa DrugsRash Taxotere [Docetaxel]Rash
Vorherige Impfungen
-

VAERS 2062995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
51,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
31.03.2021
Beginn
02.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Arthralgia Fatigue Myalgia Myocardial infarction Oxygen saturation decreased

Symptomtext

Athralgia, myalgia, fatigue. heart attack, Low SPO2

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2058029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
63,0
Geschlecht
F
Eingang
23.01.2022
Impfdatum
26.04.2021
Beginn
05.01.2022
Tage bis Beginn
254,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acidosis Altered state of consciousness Angiogram cerebral Angiogram pulmonary abnormal Anticoagulant therapy Atrial fibrillation Blood culture positive Bronchitis chronic COVID-19 Cardiac arrest Cardiac valve vegetation Computerised tomogram abdomen Computerised tomogram head normal Condition aggravated Cough Death Dialysis Echocardiogram abnormal

Symptomtext

Patient is DECEASED; hospitalized (1.11.2022); COVID-19 positive (1.5.22); fully vaccinated (no booster) Admission Date: 1/11/2022 Date of Death: 1/16/22 Time of Death: 4:37 AM Preliminary Cause of Death: Shock DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Atrial fibrillation with RVR [I48.91] Hypervolemia, unspecified hypervolemia type [E87.70] Shock [R57.9] HOSPITAL COURSE: Patient is a 63 y.o. female with a past medical history of ESRD on HD, COPD on 3L at baseline, OSA on BiPAP, tob use disorder, BiFV HF with diastolic dysfunction, T2DM, HTN and obesity who initially presented after missing two days of HD and was admitted with afib with RVR now with worsening lactic acidosis and requiring CRRT. Patient was transferred to ICU service after found to be more altered and the unresponsive even to noxious stimuli. Patient intubated. Vancomycin, flagyl, cefepime started empirically. Nephrology consulted for CRRT and this was started the morning of 1/14. Patient had increasing pressor needs up to 3 pressors. Bedside echo was done by the ICU fellow and showed a largely dilated RV and possible clot present in RV and RA. An official echo was ordered stat and did not show evidence of clot but did see a vegetation on pulmonic valve. PERT was activated in case of need for systemic tPA or thrombectomy was needed. IR recommended CTA of the thorax and head first to assess for clot burden. Cardiology did not see signs of a clot either and recommended further imaging. Heparin was started for possible PE and rising Ddimer. Blood cultures grew E. Coli. Bilateral upper and lower extremity ultrasounds showed no signs of DVT. CTA of head and thorax were done emergently. CT head showed no signs of infarction. CTA thorax showed a small segmental PE in the right lower lobe. IR was contacted and they did not recommend systemic tPA or thrombectomy. General surgery consulted to assess for bowel ischemia, but based on CT A/P findings and physical exam, they did not have any intervention to benefit the patient at that time. Patient improved with increase in Epinephrine infusion. CRRT was started by nephrology and fluid removal was set to 25ml/hr in the afternoon of 1/14. Bedside echo and bubble study was performed and showed no signs of VSD but there was very poor forward flow. Veletri, duonebs were started. Peep was reduced to 5 in order to reduce RV stress. Evening of 1/15 she developed worsening acidosis and increasing pressor requirements eventually being placed on angiotensin II. She had worsening acidosis as well. She did have cardiac arrest in the early morning with ROSC after 2 rounds of compressions. At that point further discussion was had with family who were present at bedside who decided to change code status to DNR. Shortly thereafter she passed away with family around her at bedside. Official TOD 4:37am.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
1.4.22 - primary care - office visit: Assessment and Plan 1. Cough 2. Fatigue, unspecified type 3. Chronic respiratory failure with hypoxia 4. Chronic bronchitis, unspecified chronic bronchitis type Her symptoms are concerning for pneumonia which could be bacterial or viral. With progressively worsening nature, subjective fevers, productive sputum, will treat for bacterial pneumonia. Will also get CXR and blood work. Certainly this could be COVID as well and will test in the clinic today. There was some concern that she had already been tested for COVID at HD, but she denies this since her hospital discharge. She has been vaccinated, though not boosted, and should wait until acute illness resolves then get her booster. She has bad COPD requiring oxygen and OSA as well. She does not have a nebulizer and will send in prescription and refill her duonebs. - Check CBC and CMP - Check CXR for pneumonia - Start azithromycin 500 mg daily for 5 days - Check COVID in the office today - Will send in a nebulizer machine for the patient - Refilled duonebs - Continue home inhalers - Can continue tylenol for myalgias - Closely monitor her oxygen levels, goal >88% With her presentation yesterday we initially thought she was having regular COVID testing, but was not the case and therefore tested for COVID, which returned positive. I called and discussed with her daughter who was present at her appointment yesterday and plays a large part in her medical care as the patient had just laid down for a nap. We discussed COVID as the main cause of her symptoms. Because of this we can still get blood work and CXR and will wait on abx until these tests are done for better evaluation for superimposed bacterial infection (rather than bacterial being the main culprit - as previously suspected). The daughter was in agreement with this plan. She is set up to get dialysis with the COVID+ placement. She plans to get testing later this week - difficulty with road conditions and dialysis, which is okay. We talked about monitoring her oxygen saturation at home. Currently it runs 89-90% without oxygen. We discussed less than 88% and not improving with oxygen, she should come to the ER. We also discussed the benefits from monoclonal antibodies and she was interested in this therapy. She plans to call to get information about scheduling an infusion. I told her to keep us closely informed of how the patient is doing as she is certainly high risk and she agreed. No other questions at this time.
Vorgeschichte
COPD (chronic obstructive pulmonary disease) Nephrotic syndrome, FSGS dx 2007 on bx HTN (hypertension) Biventricular heart failure with reduced left ventricular function OSA treated with BiPAP GERD (gastroesophageal reflux disease) Morbid obesity Anemia of chronic disease Nonischemic dilated cardiomyopathy, history of History of tobacco use Pulmonary hypertension SVT (supraventricular tachycardia) Itching Asterixis Chronic left-sided low back pain with left-sided sciatica Chronic respiratory failure with hypoxia Tricuspid regurgitation Gastrointestinal hemorrhage, unspecified gastrointestinal hemorrhage type History of kidney hematoma on left History of mesenteric infarction End stage renal disease on HD History of pneumonia Spinal stenosis of lumbar region Personal history of tobacco use, presenting hazards to health Controlled substance agreement signed Renal hematoma Paroxysmal atrial fibrillation with rapid ventricular response Nonischemic cardiomyopathy Other hyperparathyroidism Preop cardiovascular exam History of hyperlipidemia Hx of total hysterectomy History of hysterectomy including cervix Atrial fibrillation with RVR
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Bismuth Subsalicylate (PEPTO-BISMOL PO) calcitRIOL (ROCALTROL) 0.5 MCG capsule calcium acetate, Phos Binder, (PHOSLO
Allergien
PenicillinsHives, Swelling, Rash Aspirin Cefepime Ceftriaxone Codeine LatexHives, Rash Revaclear Dialysis MembraneItching
Vorherige Impfungen
-

VAERS 2052276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
75,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
19.04.2021
Beginn
10.01.2022
Tage bis Beginn
266,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Dyspnoea Infection Influenza A virus test negative Influenza B virus test Interstitial lung disease Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Patient is a 76 y.o. PMHx of HTN, T2DM, OSA, MI 1999 s/p heart catheterization, SSS 2009 s/p pacemaker admitted due to acute hypoxic respiratory failure due to COVID 19 pneumonia. Chest x ray demonstrated moderate interstitail prominence and increased perihilar fullness. No PE or pneumothorax. He was found to be COVID 19 positive on 1/11/22. He was treated with IV solumedrol and remdesivir. He did require 2L oxygen on NC, but quickly was able to maintain saturations on room air. He improved both clinically and in lab findings. Patient completed two days of Remdesivir prior to discharge. He was discharged home in stable condition to complete prednisone course 40mg for 5 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
2,0
Labordaten
DR CHEST SINGLE VIEW Resulted: 01/10/22 2302 Order Status: Completed Updated: 01/10/22 2304 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/10/2022 10:56 PM TECHNIQUE: Single view chest INDICATION: shortness of breath COMPARISON: 4/19/2018 chest x-ray ENCOUNTER: Not applicable _________________________ Impression: Moderate interstitial prominence and increased perihilar fullness which can be seen with pulmonary edema and/or potential atypical infection in the correct clinical setting. No evidence of pneumothorax or large pleural effusion. Cardiac silhouette appears mild to moderately enlarged. Left chest pacing device is in place. Influenza (Flu) A/B PCR (Normal) Collected: 01/10/22 2224 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 01/10/22 2246 Influenza A PCR Not Detected Not Detected Influenza B PCR Not Detected Not Detected COVID-19 PCR - Rapid (Abnormal) Collected: 01/10/22 2224 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 01/10/22 2238 COVID-19 PCR Detected
Aktuelle Erkrankungen
-
Vorgeschichte
Respiratory OSA (obstructive sleep apnea) Circulatory SSS (sick sinus syndrome) Benign essential hypertension CAD (coronary artery disease) Cardiac pacemaker in situ Endocrine/Metabolic DM type 2 (diabetes mellitus, type 2) Mixed hyperlipidemia Other Hx of myocardial infarction Leg length discrepancy Bilateral club feet
Andere Medikamente
amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 20 MG tablet benazepril (LOTENSIN) 20 MG tablet benzonatate (TESSALON) 100 MG capsule Coenzyme Q10 (CO Q 10) 10 MG CAPS doxazosin (CARDURA) 2 MG tablet dulaglutid
Allergien
Hctz [Hydrochlorothiazide] Rash
Vorherige Impfungen
-

VAERS 2051295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
GA
Alter
68,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
10.04.2021
Beginn
08.09.2021
Tage bis Beginn
151,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal operation Appendicectomy Colectomy Computerised tomogram thorax abnormal Deep vein thrombosis Large intestinal stenosis Postoperative thrombosis Pulmonary embolism Ultrasound Doppler abnormal Ultrasound abdomen abnormal

Symptomtext

Had Abdominal surgery to remove a colon stricture. Removed 2 feet of right colon and appendix. Developed post operative bilateral DVT and pulmonary emboli, documented by ultrasound and CT scans.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary embolism
Hospital-Tage
4,0
Labordaten
Ultrsound of leg veins and abdominal and chest CT scans Sept 8 2021
Aktuelle Erkrankungen
Crohn's colitis
Vorgeschichte
-
Andere Medikamente
Entiviyo Infusion Q8 weeks, Lialda 1.2gm qd. Bisoprolol 2.5 mg qd Ezetimibe 10 mg qd
Allergien
ACE inhibitors
Vorherige Impfungen
-

VAERS 2043540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
76,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
22.04.2021
Beginn
06.01.2022
Tage bis Beginn
259,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Anaemia Anticoagulant therapy Anticoagulation drug level above therapeutic Blood creatinine increased Blood lactic acid Blood pressure decreased Bronchoalveolar lavage Bronchoscopy COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic kidney disease Chronic obstructive pulmonary disease Condition aggravated Cough

Symptomtext

Hospitalized (1.6.22 - present - currently in ICU); COVID-19 positive (1.6.22); fully vaccinated (no booster) Admission date - 1.6.22: Brief history and medical decision making: 76 y/o F with PMHx of HFpEF, rheumatic fever s/p mechanical MV replacement on warfarin, CAD s/p CABG, CKD3, COPD who presented with worsening SOB and hypoxia in setting of positive COVID test 10 days PTA. She is admitted for acute hypoxic respiratory failure. Also found to have AKI on CKD3 and supratherapeutic INR. Patient's SOB improving with placement on HFNC. Will continue dexamethasone. Hold on remdesivir as pt received monoclonal antibody 2 days PTA and has eGFR < 30. Continue HFNC, wean as tolerated. Supportive care. Give gentle hydration and monitor renal function. Pt given vitamin K in ED, monitor INR. Hold warfarin but plan to resume once INR is at goal range of 2.5-3.5. ASSESSMENT / PLAN: Patient is a 76 y.o. female with a PMHx significant for rheumatic fever s/p mechanical mitral valve replacement on warfarin, HFpEF diastolic dysfunction, CKD III, CABGx1, CAD, HLD, HTN, COPD, CVA, essential tremor, microcytic anemia, hypothyroidism who presents with acute hypoxic respiratory failure in the setting of worsening SOB after positive Covid test 10 days ago. AHRF Covid-19 pneumonia COPD Exacerbation Worsening SOB, dyspnea and cough, O2 sat 50% on home pulse ox today. Wheezing on exam. satting 91% on 30 L HFNC 60% FIO2. Plan: -Decadron 6 mg x10 days -O2 supplementation O2 sat goal 90-904% -Albuterol breathing treatment now then 2 puff q 6 -Home Symbicort BID -Continuous pulse ox, tele -Tessalon for cough, saline nasal spray -If significant O2 desaturation, obtain repeat CXR, D-dimer, consider CTA Progress Note - 1.18.22: (sedated and intubated) Principal Problem / Chief Complaint Respiratory failure with hypoxia Admitted: 1/6/2022 11:05 AM Length of Stay: 12 days. Assessment and Plan Patient is a 76 y.o. female PMHx notable for HFpEF, rheumatic fever status post mechanical mitral valve, COPD, CKDIII, CAD s/p CABG x1, hypothyroidism who is admitted to the MICU for further management of acute hypoxic respiratory failure secondary to COVID 19 pneumonia and ARDS. # AHRF secondary to COVID-19 pneumonia Hx COPD Symptom onset 12/25, tested positive on 12/26, admitted on 01/06 and intubated 1/10. Status post monoclonal antibodies on 01/04. Vaccinated x2 but without booster. Bronchoscopy with BAL performed 1/10. Negative for legionella and strep. Cultures NGTD. Plan: o Tapering solumedrol, 30mg x3d (d2) o Lung protective ventilation; ARDS protocol o Completed 5 days Zosyn course o Continue COPD treatment: Albuterol every 6 hours, Symbicort twice a day, Spiriva daily o Diurese to goal net negative 1L- Lasix 80mg TID o Renal function stable # Leukocytosis WBC remains elevated but stable.Afebrile overnight with stable map. Continue to watch

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
12,0
Labordaten
HISTORY OF PRESENT ILLNESS: Patient is a 76 y.o. female with a PMHx significant for rheumatic fever s/p mechanical mitral valve replacement on warfarin, HFpEF diastolic dysfunction, CKD III, CABGx1, CAD, HLD, HTN, COPD, CVA, essential tremor, microcytic anemia, hypothyroidism who presents with acute hypoxic respiratory failure in the setting of worsening SOB after positive Covid test 10 days ago. Known covid-19 exposure over holiday. Fully vaccinated back in April 2021, has not received booster. Pt states she was maintaining good O2 sats in the 90s until this morning when she was in the 50s. She's had progressively worsening cough, dyspnea on exertion and decreased appetite. Received monoclonal antibody treatment 2 days ago. At the bedside, she is laying propped up with pillows in mild acute distress. Noticeable conversational dyspnea, saturating 91% on 30 L 60% HFNC with desaturation to 85% with speaking. We did confirm she wishes to be full code at this time. When asked about her supratherapeutic INR, she says her coumadin regimen was recently changed but that she was taking it as directed. She asked that we call her daughter with an update which I did shortly after speaking with her. Of note she was recently admitted to the hospital 12/9 for symptomatic anemia and received 1 unit of pRBC with Hgb of 7.7 on discharge. ED Course: In the ED, her blood pressure was slightly soft with a MAP of 56 and two 500 cc boluses were given. She was placed on supplemental oxygen. CXR obtained consistent with covid-19 pneumonia, no pleural effusion or pulmonary edema. EKG unchanged from prior, no signs of ischemia or arrhythmia. Labs significant for an INR of >8.0, mildly elevated LFTs, CR 1.91 from 1.28 on 12/9, Hgb 9.8, lactic acid 0.8. Vitamin K 5 mg given. Albuterol breathing treatment, tessalon ordered. Will hold antihypertensives, beta blocker, diuretic given hypotension and aspirin, coumadin given INR.
Aktuelle Erkrankungen
1.4.22: Sotrovimab infusion
Vorgeschichte
Coronary artery disease involving native coronary artery of native heart without angina pectoris Mitral insufficiency Essential hypertension History of CVA (cerebrovascular accident) Chronic obstructive pulmonary disease, unspecified OSA on CPAP Dyslipidemia Chronic kidney disease, stage 3 unspecified Hypothyroidism Depression Chronic diastolic (congestive) heart failure Severe anemia Mediastinal lymphadenopathy Morbid obesity Mixed stress and urge urinary incontinence History of mitral valve replacement Gout Essential tremor Anxiety Asymptomatic bacteriuria Bladder mass COVID-19 Acquired absence of both cervix and uterus Cardiac murmur, unspecified Hyperlipidemia, unspecified Hypertensive heart and chronic kidney disease with heart failure and stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease Iron deficiency anemia, unspecified Localized enlarged lymph nodes Mixed incontinence Monoarthritis, not elsewhere classified, right knee Presence of aortocoronary bypass graft Presence of prosthetic heart valve
Andere Medikamente
albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin EC 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet Ferrous Sulfate (IRON) 325 (65 Fe) MG TABS fluticasone-salmeterol (ADVAIR DISKU
Allergien
ErythromycinNausea and Vomiting Flonase [Fluticasone]Palpitations Lamictal [Lamotrigine]Hives Trileptal [Carbamazepine]Hives VancomycinRed man syndrome CodeineRash Ultram [Tramadol] Zetia [Ezetimibe]
Vorherige Impfungen
-

VAERS 2042996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MN
Alter
64,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
12.04.2021
Beginn
31.12.2021
Tage bis Beginn
263,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute respiratory failure Asthenia Back pain Blood albumin COVID-19 COVID-19 pneumonia Computerised tomogram head normal Computerised tomogram thorax abnormal Condition aggravated Confusional state Dementia Dyspnoea Fall Hypoalbuminaemia Hypotension Laboratory test abnormal Lung consolidation Lung infiltration

Symptomtext

HOSPITAL COURSE: Briefly, this is a 64-year-old female with multiple sclerosis, who was admitted on 1/8/2022, for worsening confusion and weakness in setting of COVID and bacterial PNA. Treating acute encephalopathy secondary likely toxic/metabolic. For more detail, including PMH, PSH, PFH, Social Hx and further info please see admission H&P. Hospital course dictated by problem: Acute hypoxic respiratory failure due to bacterial PNA Sepsis due to pneumonia, resolved Right lower lobe bacterial streptococcus pneumonia COVID-19 pneumonia Was vaccinated 4/2021, but overdue for booster. COVID positive in clinic, estimated around 12/31. Was seen in clinic then as was having weakness with one fall at home Had COVID treated with monoclonal antibody 1/6/22. Despite this continued to have progressive weakness, confusion and then developed shortness of breath. 1/8 presented to ED with weakness and confusion hypoxia requiring supplemental O2 via NC at 6L. CTPE neg for PE.RLL consolidation. + PCT, Urine St pneumo agn +.Studies c/w bacterial PNA w/ elevated procal, imaging. Per ID felt respiratory issues were not related to COVID PNA, more so bacterial PNA and 2/2 PTA sedative meds (tramadol, etc).- Per ID: her CT shows a lobar infiltrate but not diffuse infiltrates c/w COVID Would stop Decadron and monitor, if she appears to have worsening component of viral PNA (hypoxia, etc) would resume - does not appear her PTA Zeposia is assoc w/ more severe COVID sxs (per ID), ok to cont per neurology Therefore decadron was discontinued. Respiratory status has been stable since stopping decadron. Abx: was on rocephin, doxycycline. Doxy d/c 1/9 as pneumococcal urine Ag positive. Patient was fully treated for her pneumonia with ceftriaxone, stopped at time of discharge. ID signed off. Patient was stable on room air at time of discharge. She was seen by PT who did clear her to return home. Follow-up with PCP in 2 weeks. Needs follow-up imaging within 4 to 6 weeks including to rule out infiltrates also evaluate pleural effusions. Patient understands if she has any recurrent infectious symptoms to return immediately. Discharge plan was discussed in detail with her husband via phone. Good questions were asked and all were answered. Bilateral pleural effusions, hypoalbuminemia CT w/ bilateral pleural effusions - this likely related to hypoalbuminemia - s/p Albumin 12.5 mg q30min x 2 doses as hypotensive, hypoalbuminemic and bilateral effusions. -Consider outpatient chest x-ray in 4 weeks Acute metabolic/toxic encephalopathy -resolved In setting of above. Mild dementia at baseline and w/ MS hx. Bacterial PNA and COVID causing encephalopathy. - Head CT negative for acute intracranial processAlso more susceptible given PTA sedative medications such as tramadol. Tramadol initially held to help. Tramadol was slowly resumed by 1/10 improving. Alert to person and place. Said year 2021 but redirected to recent new year and later recalled accurate year.1/11- sl confusion re earlier events . By day of discharge she appeared to be at her baseline mentation without any obvious confusion. Tramadol had been continued on a slightly lower dose. Advised to continue that at home. PCP can additionally eval Generalized weakness-diffuse generalized weakness likely secondary to COVID-19 with acute worsening also contributed by her baseline MS. PT OT consulted. PT cleared to go back to her home, her husband is able to give her 24/7 supports, although she remains a chronic high fall risk. Multiple sclerosis-chronic-has outpatient neurologist,home dose Zeposia and Baclofen Recently had battery of MRIs and per husband MS considered stable., She was maintained on PTA tramadol. Follow-up - needs to reSchedule w OP Neurologist (was supposed to be on 1/10) History of cognitive impairment secondary to MS Per husband at baseline alert to person, place and time.- Not on any meds. F/u Neurology History of generalized anxiety disorder, chronic benzodiazepine use-patient maintained on PTA Cymbalta Per husband she takes 2 mg of Valium usually every afternoon but little other than that. He asked about dosing and advised if wanted they could decrease to q. OD. She has a as needed Xanax prior to MRI as ordered but does not take that. Further management per psych vs primary care. History of chronic opiate use, chronic low back pain- reports she has chronic low back pain has been on tramadol for a long time, reported as she became more clear that her back pain was increased here, wants her past tramadol resumed, seems Encephalopathy contributing to confusion regarding her reported dose tells me she did not take it daily but just intermittent a few doses a day max when she needed it. Appears PTA she takes 100 a.m./50 p.m./150 PM. That is higher than I would recommend. At time of discharge she seemed to be stable with mild pain on the lower tramadol dose of- 50mg am, 50mg 2pm, 100mg available as prn at bedtime. I recommend continue that for now. charted hx of alc abuse. Recommend follow-up with TC pain clinic re other modalities Hx UTI: 2 weeks ago -> rx antibiotics without improvement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
5,0
Labordaten
COVID POSITIVE 12/31/2021
Aktuelle Erkrankungen
-
Vorgeschichte
64-year-old female with a prior medical history of multiple sclerosis, generalized anxiety disorder, mild cognitive disorder secondary to MS
Andere Medikamente
-
Allergien
Amoxicillin, Azithromycin, Norco [hydrocodone-acetaminophen], and Penicillins
Vorherige Impfungen
-

VAERS 2034561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
OH
Alter
53,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
15.04.2021
Beginn
25.05.2021
Tage bis Beginn
40,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood disorder Myocardial infarction Pain Thrombosis

Symptomtext

blood clot in rt pinky; felt like a heart attack; Pain for several weeks; didnt bleed when I cut myself shaving/ Blood still thick; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 15Apr2021 10:00 (Lot number: EW0162) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Low level asthma" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Hydromet cough syrup, reaction(s): "allergy". Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: EN6202, Location of injection: Arm Left, Vaccine Administration Time: 10:00 AM), administration date: 12Mar2021, for COVID-19 immunization. The following information was reported: THROMBOSIS (medically significant) with onset 25May2021, outcome "unknown", described as "blood clot in rt pinky"; MYOCARDIAL INFARCTION (medically significant) with onset 25May2021, outcome "unknown", described as "felt like a heart attack"; PAIN (non-serious) with onset 25May2021, outcome "recovered" (2021), described as "Pain for several weeks"; BLOOD DISORDER (non-serious) with onset 25May2021, outcome "unknown", described as "didnt bleed when I cut myself shaving/ Blood still thick". The events "blood clot in rt pinky", "felt like a heart attack", "pain for several weeks" and "didnt bleed when i cut myself shaving/ blood still thick" were evaluated at the physician office visit. Therapeutic measures were taken as a result of thrombosis, myocardial infarction, pain, blood disorder. Addition information: it was reported that: believe clot eventually traveled to rt side of arm (june) to left side of neck (July 22) to left side of chest (23Jul2021), felt like heart attack. Covid prior vaccination was none. Covid tested post vaccination was none. Other vaccine in four weeks was none. Other medication in two weeks was none. Pain dimished within week. When it got to neck. Took aspirin 2 daily then one.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1500905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
60,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
19.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Chest X-ray Computerised tomogram Hepatic failure Near death experience Positron emission tomogram Vaccination site pain Vaccination site swelling Organ failure Sepsis Ultrasound scan

Symptomtext

She later added that she almost died. Her organs were shutting; blood infection; she almost died after getting the vaccine; her liver almost died/liver stormed; swelling in right arm above injection site and shoulder; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 60 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 19Apr2021 (Lot number: EW0162) at the age of 60 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: 20Feb2020 (unspecified if ongoing); "COVID-19", start date: Oct2020 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Batch/lot number: EP6955), administration date: 01Apr2021, when the patient was 60 years old, for COVID-19 immunization. The following information was reported: ORGAN FAILURE (hospitalization, life threatening) with onset Jun2021, outcome "unknown", described as "She later added that she almost died. Her organs were shutting"; SEPSIS (hospitalization) with onset 2021, outcome "recovering", described as "blood infection"; NEAR DEATH EXPERIENCE (hospitalization) with onset 2021, outcome "unknown", described as "she almost died after getting the vaccine"; HEPATIC FAILURE (hospitalization) with onset 2021, outcome "recovering", described as "her liver almost died/liver stormed"; VACCINATION SITE SWELLING (non-serious) with onset Apr2021, outcome "unknown", described as "swelling in right arm above injection site and shoulder". The patient was hospitalized for organ failure, sepsis, near death experience, hepatic failure (start date: Jun2021, discharge date: Jun2021, hospitalization duration: 3 day(s)). The events "she later added that she almost died. her organs were shutting", "blood infection", "she almost died after getting the vaccine", "her liver almost died/liver stormed" and "swelling in right arm above injection site and shoulder" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (2021) it was fine; (Jun2021) it was not okay, notes: on the 9th week; chest x-ray: (2021) fine; computerised tomogram: (2021) unknown result; ultrasound scan: (2021) fine. Therapeutic measures were taken as a result of organ failure, sepsis, near death experience. Clinical course: Caller states she has a couple of questions, States that on 01Apr2021 last year she had her first Pfizer Covd injection and on 19Apr2021 she had her second injection, states approximately 10 days after her second Pfizer injection her arm swelled up at the top above injection site on right arm, clarifies that her arm and shoulder started to swell. States she went to clinic and they thought she had sepsis, states she had a blood infection, states she was treated with Bactrim for 5 days, states this went on for 9 weeks, states she had her blood drawn every week and it was fine but then on the 9th week it was not okay, states she then went to the hospital and they said her organs were shutting down, states she had a CT scan and almost died due to contrast, no further information about contrast provided. States at this time she was treated, she states she received 26 bottles of blood. States the did a gall bladder sonogram and that was fine, states chest x-rays were fine, states they had a specialist come from 6 hours away, caller states she is not sure what medication they put in the bag but it kept her alive. States now in the mean time she has to pay all the medical bills, states she is living in the (withheld ) and had to have the vaccines to get on a plane to go home to her mother who was hemorrhaging to death. Caller states she is terrified to take the 3rd, 4th, or 5th booster vaccine, does not know where to go except her local doctor to get a letterhead to give to the airline for a medical exemption. Caller clarifies she was admitted to the hospital around the 6th or 07Jun2021 and was in the hospital for 3 days, exact dates are unknown. States that during the event, her liver stormed, states cannot wear make up now, not allowed a lot of stuff because her liver almost died, states she has improved though. Caller states she has two specific questions, caller wants to know in withheld they advise people wait 6 months between the injections, want to know why do they give it so close together in withheld. Are they giving them too close together. States she has had Covid twice before the injections. States she was diagnosed with Covid roughly 20Feb2020 and then in Oct2020. States then she gets the Covid injections and now she has those antibodies, is it advisable if you've already had Covid one or 2 times before should you get the vaccines? Her body went to war with itself since she had Covid antibodies already from having Covid before. States her doctor said there was another patient in clinic that had the same as her. No information provided or known of this patient. Caller states she has done in depth homework, has read all the reports, she is keeping on top of it, this is the first time she has called because she was compiling all this information. States she comes from a very intelligent town, states she is from a town in withheld and knows about the genetics and all of that. Caller states she got the vaccine because her daughter lives in withheld and takes care of her grandmother and the daughter was banging on and banging on about if she has to bury her grandmother, and was pushing the caller to get the vaccines and caller states she finally caved and got the vaccines and so she did, maybe she had them too close together and she should have spaced out, she does not know. Knows that everyone in withheld was shocked when she told them she got it 19 after. Caller asks can she get compensated, if she did not take the vaccine she could have recovered. She had the first dose of bnt162b2 in 01Apr2021 and the second dose on 19Apr2021. Caller reported that she experienced some AE with bnt162b2 including hospitalization for a blood infection. She had COVID infection, twice prior to getting the vaccine and have some antibodies. She is asking if it is even okay to get the vaccine even with prior infection. She later added that she almost died after getting the vaccine. Her organs were shutting and was unable to take medical exception from getting another booster or shot. Caller wants to know why in (withheld) the advise to get the second dose of bnt162b2, 6 months after the first dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Near death experience
Hospital-Tage
3,0
Labordaten
Test Date: 2021; Test Name: she had her blood drawn; Result Unstructured Data: Test Result:it was fine; Test Date: 202106; Test Name: she had her blood drawn; Result Unstructured Data: Test Result:it was not okay; Comments: on the 9th week; Test Date: 2021; Test Name: chest x-rays; Result Unstructured Data: Test Result:Fine; Test Date: 2021; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 2021; Test Name: gall bladder sonogram; Result Unstructured Data: Test Result:Fine
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1500905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
60,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
19.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Chest X-ray Computerised tomogram Hepatic failure Near death experience Positron emission tomogram Vaccination site pain Vaccination site swelling Organ failure Sepsis Ultrasound scan

Symptomtext

She later added that she almost died. Her organs were shutting; blood infection; she almost died after getting the vaccine; her liver almost died/liver stormed; swelling in right arm above injection site and shoulder; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 60 year-old female patient received bnt162b2 (COMIRNATY), administered in arm right, administration date 19Apr2021 (Lot number: EW0162) at the age of 60 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "COVID-19", start date: 20Feb2020 (unspecified if ongoing); "COVID-19", start date: Oct2020 (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Batch/lot number: EP6955), administration date: 01Apr2021, when the patient was 60 years old, for COVID-19 immunization. The following information was reported: ORGAN FAILURE (hospitalization, life threatening) with onset Jun2021, outcome "unknown", described as "She later added that she almost died. Her organs were shutting"; SEPSIS (hospitalization) with onset 2021, outcome "recovering", described as "blood infection"; NEAR DEATH EXPERIENCE (hospitalization) with onset 2021, outcome "unknown", described as "she almost died after getting the vaccine"; HEPATIC FAILURE (hospitalization) with onset 2021, outcome "recovering", described as "her liver almost died/liver stormed"; VACCINATION SITE SWELLING (non-serious) with onset Apr2021, outcome "unknown", described as "swelling in right arm above injection site and shoulder". The patient was hospitalized for organ failure, sepsis, near death experience, hepatic failure (start date: Jun2021, discharge date: Jun2021, hospitalization duration: 3 day(s)). The events "she later added that she almost died. her organs were shutting", "blood infection", "she almost died after getting the vaccine", "her liver almost died/liver stormed" and "swelling in right arm above injection site and shoulder" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood test: (2021) it was fine; (Jun2021) it was not okay, notes: on the 9th week; chest x-ray: (2021) fine; computerised tomogram: (2021) unknown result; ultrasound scan: (2021) fine. Therapeutic measures were taken as a result of organ failure, sepsis, near death experience. Clinical course: Caller states she has a couple of questions, States that on 01Apr2021 last year she had her first Pfizer Covd injection and on 19Apr2021 she had her second injection, states approximately 10 days after her second Pfizer injection her arm swelled up at the top above injection site on right arm, clarifies that her arm and shoulder started to swell. States she went to clinic and they thought she had sepsis, states she had a blood infection, states she was treated with Bactrim for 5 days, states this went on for 9 weeks, states she had her blood drawn every week and it was fine but then on the 9th week it was not okay, states she then went to the hospital and they said her organs were shutting down, states she had a CT scan and almost died due to contrast, no further information about contrast provided. States at this time she was treated, she states she received 26 bottles of blood. States the did a gall bladder sonogram and that was fine, states chest x-rays were fine, states they had a specialist come from 6 hours away, caller states she is not sure what medication they put in the bag but it kept her alive. States now in the mean time she has to pay all the medical bills, states she is living in the (withheld ) and had to have the vaccines to get on a plane to go home to her mother who was hemorrhaging to death. Caller states she is terrified to take the 3rd, 4th, or 5th booster vaccine, does not know where to go except her local doctor to get a letterhead to give to the airline for a medical exemption. Caller clarifies she was admitted to the hospital around the 6th or 07Jun2021 and was in the hospital for 3 days, exact dates are unknown. States that during the event, her liver stormed, states cannot wear make up now, not allowed a lot of stuff because her liver almost died, states she has improved though. Caller states she has two specific questions, caller wants to know in withheld they advise people wait 6 months between the injections, want to know why do they give it so close together in withheld. Are they giving them too close together. States she has had Covid twice before the injections. States she was diagnosed with Covid roughly 20Feb2020 and then in Oct2020. States then she gets the Covid injections and now she has those antibodies, is it advisable if you've already had Covid one or 2 times before should you get the vaccines? Her body went to war with itself since she had Covid antibodies already from having Covid before. States her doctor said there was another patient in clinic that had the same as her. No information provided or known of this patient. Caller states she has done in depth homework, has read all the reports, she is keeping on top of it, this is the first time she has called because she was compiling all this information. States she comes from a very intelligent town, states she is from a town in withheld and knows about the genetics and all of that. Caller states she got the vaccine because her daughter lives in withheld and takes care of her grandmother and the daughter was banging on and banging on about if she has to bury her grandmother, and was pushing the caller to get the vaccines and caller states she finally caved and got the vaccines and so she did, maybe she had them too close together and she should have spaced out, she does not know. Knows that everyone in withheld was shocked when she told them she got it 19 after. Caller asks can she get compensated, if she did not take the vaccine she could have recovered. She had the first dose of bnt162b2 in 01Apr2021 and the second dose on 19Apr2021. Caller reported that she experienced some AE with bnt162b2 including hospitalization for a blood infection. She had COVID infection, twice prior to getting the vaccine and have some antibodies. She is asking if it is even okay to get the vaccine even with prior infection. She later added that she almost died after getting the vaccine. Her organs were shutting and was unable to take medical exception from getting another booster or shot. Caller wants to know why in (withheld) the advise to get the second dose of bnt162b2, 6 months after the first dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Near death experience
Hospital-Tage
3,0
Labordaten
Test Date: 2021; Test Name: she had her blood drawn; Result Unstructured Data: Test Result:it was fine; Test Date: 202106; Test Name: she had her blood drawn; Result Unstructured Data: Test Result:it was not okay; Comments: on the 9th week; Test Date: 2021; Test Name: chest x-rays; Result Unstructured Data: Test Result:Fine; Test Date: 2021; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 2021; Test Name: gall bladder sonogram; Result Unstructured Data: Test Result:Fine
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2028255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
77,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
03.05.2021
Beginn
01.01.2022
Tage bis Beginn
243,0
Dosis
1
Route/Site
IM / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
COVID-19 Death Diarrhoea Dyspnoea Endotracheal intubation General physical health deterioration SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 4/12/2021 and 5/3/2021. Presented to ED on 1/1/2022 with complaints of shortness of breath and diarrhea, with reports of positive COVID test. Saturation on room air 80% on presentation. Started on remdesivir, dexamethasone, baricitinib, ceftriaxone and azithromycin. Continued to decline requiring intubation on 1/4/2022, and vasopressor support x3. Patient expired on 1/4/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Anxiety, CAD, Hyperlipidemia, Hypertension, Iron Deficiency, H/O MI, Peripheral vascular disease
Andere Medikamente
Albuterol NEBS QID, Amlodipine 10 mg QD, Aspirin 81 mg QD, Clopidogrel 75 mg QD, Ergocalciferol 1250 mcg QD, Fenofibrate 145 mg QD, Fluticasone Nasal QD, Metoprolol 100 mg QD, Nitroglycerin 0.4 mg SL PRN, Olmesartan 40 mg QD, Rosuvastatin 2
Allergien
Pneumococcal vaccine
Vorherige Impfungen
-

VAERS 2028255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
77,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
03.05.2021
Beginn
01.01.2022
Tage bis Beginn
243,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
COVID-19 Death Diarrhoea Dyspnoea Endotracheal intubation General physical health deterioration SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 4/12/2021 and 5/3/2021. Presented to ED on 1/1/2022 with complaints of shortness of breath and diarrhea, with reports of positive COVID test. Saturation on room air 80% on presentation. Started on remdesivir, dexamethasone, baricitinib, ceftriaxone and azithromycin. Continued to decline requiring intubation on 1/4/2022, and vasopressor support x3. Patient expired on 1/4/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Anxiety, CAD, Hyperlipidemia, Hypertension, Iron Deficiency, H/O MI, Peripheral vascular disease
Andere Medikamente
Albuterol NEBS QID, Amlodipine 10 mg QD, Aspirin 81 mg QD, Clopidogrel 75 mg QD, Ergocalciferol 1250 mcg QD, Fenofibrate 145 mg QD, Fluticasone Nasal QD, Metoprolol 100 mg QD, Nitroglycerin 0.4 mg SL PRN, Olmesartan 40 mg QD, Rosuvastatin 2
Allergien
Pneumococcal vaccine
Vorherige Impfungen
-

VAERS 2024746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
58,0
Geschlecht
M
Eingang
11.01.2022
Impfdatum
04.06.2021
Beginn
16.11.2021
Tage bis Beginn
165,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Anticoagulant therapy COVID-19 COVID-19 pneumonia Dyspnoea Hypoxia Pulmonary embolism SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient is COVID positive 11/16/2021. Patient is fully vaccinated. 58-year-old male presented to the ED with 10 days of worsening shortness of breath. He states that once he started exercising, he started to gasp for air and his caregiver called EMS. He has history of bilateral lower extremity DVT as well as history of PE. He was on Coumadin for 2 months before he stopped it in February as he said that it made him feel uncomfortable taking Coumadin. The patient denies any fever, chills, nausea, vomiting, or diarrhea at this point, though still having shortness of breath and is planned for thrombectomy today. Admitting DX: SOB, hypoxia, bilateral pulmonary embolism, Pneumonia due to COVID, Pulmonary embolus. Elevated troponin. Treatment: Completed 3 days Remdesivir/Vitamin D/ IV Decadron 6mg daily. Heparin drip transitioned to coumadin 2.5 mg daily. Maintained on albuterol inhaler. Discharged to home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary embolism
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2024597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
49,0
Geschlecht
M
Eingang
11.01.2022
Impfdatum
20.04.2021
Beginn
31.12.2021
Tage bis Beginn
255,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Glycosylated haemoglobin normal Hyperglycaemia Nasal congestion Oxygen saturation decreased Polyuria Pyrexia Refusal of treatment by patient Renal impairment SARS-CoV-2 test positive

Symptomtext

Hospitalized 1/1/2022; COVID-19 positive 12/31/2021; fully vaccinated Admit Date: 1/1/2022 3:23 AM Discharge Date: 1/7/2022 4:31 PM Hospital Course: Patient is a 50 year old male with history of hypertension, hyperlipidemia, CKD 4, morbid obesity, uncontrolled diabetes, obstructive sleep apnea noncompliant with CPAP, diabetic neuropathy, hypothyroidism presented to the ER with complaints of cough and fever. Patient also had nasal congestion but cough/SOB were at baseline. He was vaccinated for COVID but did nto yet receive booster. In the ER, he tested postive for COVID. CXR showed bilateral airspace disease consistent with COVID pneumonia. Patient was admitted for acute hypoxic respiratory failure due to COVID pneumonia. Patient was placed on supplemental oxygen and oral dexamethasone. Oxygen was gradually weaned off to room air at the time of discharge. Patient continued to have drop in oxygen saturations overnight. Refused to wear CPAP in the hospital. Patient prefers following up with his PCP for sleep study referral. Patient has uncontrolled diabetes which his outpatient endocrinologists have struggled with getting tight control with U500 insulin. Patient had significant hyperglycemia with steroids so DGMS was consulted. HbA1C is 8.3%. IV insulin was recommended, however patient refused it. Patient's blood sugars slowly improved. Nephrology was consulted for worsening renal function. Patient briefly received IV fluids with improvement in renal function. Lasix was held. As patient is having good diuresis Lasix was resumed at half the home dose. Patient was discharged to Home with services - COVID at home in stable condition.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
6,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Pneumonia due to COVID-19 virus HTN (hypertension) Vitamin D deficiency Obesity Membranous glomerulonephritis Group B streptococcal infection Venous stasis dermatitis Cellulitis of left lower extremity Type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin Nicotine dependence Nephrotic syndrome Stage 3 chronic kidney disease Dyslipidemia Severe sepsis Lumbar disc disease
Andere Medikamente
albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet Ascorbic Acid (VITAMIN C) 100 MG CHEW atorvastatin (LIPITOR) 20 MG tablet calcium carb-cholecalciferol (CALCIUM 500/D) 5
Allergien
Niacin
Vorherige Impfungen
-

VAERS 2001766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
70,0
Geschlecht
M
Eingang
04.01.2022
Impfdatum
09.04.2021
Beginn
08.12.2021
Tage bis Beginn
243,0
Dosis
2
Route/Site
IM / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute kidney injury Acute respiratory failure Ammonia increased Anticoagulant therapy Bronchoalveolar lavage abnormal COVID-19 Computerised tomogram head normal Computerised tomogram thorax abnormal Culture urine positive Death Dialysis Dyspnoea Encephalopathy Endotracheal intubation Enterococcus test positive Hyperammonaemia Infectious pleural effusion Mental status changes

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/18/2021 and 4/9/2021. On 12/8/2021 presented to ED for altered mental status. Also short of breath requiring HFNC. Admitted for acute respiratory failure due to COVID-19. Tx'd with dexamethasone, diuretics, heparin, hydrocortisone, broad spectrum antimicrobials, pressors, remdesivir, and dialysis. Developed pneumonia, pneumothorax, and para pneumonic effusion -> grew pseudomonas tx'd w/meropenem. Resp. status cont. to decompensate requiring intubation and proning, status c/b AKI, hyperammonemia and encephalopathy. Expired 12/27/21. Patient transitioned to comfort care and expired 12/27/2021 at 1526.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
19,0
Labordaten
Enterococcus faecalis; 12/23/21: ammonia 109; No acute intracranial abnormality on head CT on 12/20/21 and 12/25/21.
Aktuelle Erkrankungen
-
Vorgeschichte
Obesity, hyperlipidemia, hypertension, chronic kidney disease stage III, fatty liver disease, gout, neuropathy
Andere Medikamente
Allopurinol 300 mg daily, cartia XT 180 mg daily, vitamin B12, 1000 mcg daily, folic acid 400 mg, hydrochlorothiazide 25 mg daily, losartan 100 mg daily, valsartan-hydrochlorothiazide 320-25 mg daily
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 1999848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
CA
Alter
35,0
Geschlecht
M
Eingang
03.01.2022
Impfdatum
17.04.2021
Beginn
28.12.2021
Tage bis Beginn
255,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Bacterial sepsis Blood creatinine abnormal Blood lactic acid abnormal COVID-19 Culture positive Endotracheal intubation Full blood count Haemoglobin decreased Hypopituitarism Inflammation Liver function test abnormal Lumbar puncture normal Mental status changes Platelet count decreased Pneumonia bacterial SARS-CoV-2 test positive Septic shock Staphylococcal sepsis

Symptomtext

Patient was stabilized in the ED and extubated. Patient transferred to the floors where he returned to baseline mentation, with Cr and Lactate normalized and LFT's improving. Source of septic shock thought to be urinary or bacterial PNA. LP clean. Grew out MSSA. Discharge on course of PO Augmentin. Patient tested positive for COVID and received Remdesivir and Decadron, but patient not hypoxic and patient's presentation more consistent with bacterial sepsis than COVID respiratory failure. Patient has panhypopituitarism. Endocrine recommended starting Levothyroxine 50mcg, and continuing on on Decadron 5mg. Endocrine follow up outpatient. Patient had lower Hgb and Platelets, likely due to dilution from IVF and inflammation. Repeat CBC in 5 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Septic shock
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1967265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NJ
Alter
54,0
Geschlecht
F
Eingang
20.12.2021
Impfdatum
21.03.2021
Beginn
29.06.2021
Tage bis Beginn
100,0
Dosis
UNK
Route/Site
SC / -
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: unbekannt
Acute myocardial infarction Angina pectoris Cardiac stress test abnormal Dyspnoea Electrocardiogram abnormal Exercise tolerance decreased Loss of personal independence in daily activities Magnetic resonance imaging heart Pericarditis

Symptomtext

After second COVID vaccination by Phizer. Cardiac pain, NSTEMI caused by pericarditis.Required hospitalization and transfer to higher level hospital. Undergoing cardiac rehab presently. In shape hiker prior to vaccine .Able to hike at elevations over 12000 feet . Now am in cardiac rehab because I can't breathe due to pericarditis caused by this vaccine . My lifestyle has been ruined, thanks to Pfizer. It's been 6 months of tests and rehab and I'm still not able to even jog for 30 seconds.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
-
Labordaten
06/29/2021: EKG STRESS TEST - abnormal 12/16/2021: CARDIAC MRI - Indicating pericarditis
Aktuelle Erkrankungen
-
Vorgeschichte
High BP
Andere Medikamente
Ibuprofen, Fleicainide Losartan Potassium Troxendi XR Estradiol Magnesium Vit D3 Ubiquinol Multi Vit Vit C Probiotic
Allergien
Morphine , doxycycline,latex
Vorherige Impfungen
-

VAERS 1955598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
58,0
Geschlecht
M
Eingang
16.12.2021
Impfdatum
14.04.2021
Beginn
06.12.2021
Tage bis Beginn
236,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acquired diaphragmatic eventration Acute respiratory failure Angiogram pulmonary abnormal Arteriosclerosis coronary artery Atelectasis Bronchiectasis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Fatigue Fibrin D dimer Hypoxia Inappropriate schedule of product administration Influenza A virus test negative Influenza B virus test Lung infiltration

Symptomtext

Patient discharged following a (7) day inpatient admission for COVID 19. Patient is a 59 y.o. male who presented secondary to a chief complaint of ?cough". Patient states his symptoms started on 12/01/2021. He noted cough, shortness of breath, nausea and fatigue. He tested positive on a home COVID test a couple days after his symptoms started. In the emergency department, chest x-ray revealed bilateral infiltrates. The patient was hypoxic at 88% on room air. He was placed on 2 L nasal cannula. He was admitted for COVID-19 pneumonia to the hospitalist service. Patient was started on dexamethasone 6 mg daily as well as remdesivir. He completed 5 days of remdesivir therapy. Patient had elevated O2 requirements, requiring 50% venturi mask. A CT angiogram was obtained, which revealed bilateral infiltrates consistent with COVID-19 pneumonia, and ruled out pulmonary embolism. Patient was encouraged to lay prone, and utilize incentive spirometry. A procalcitonin was obtained and negative, NT proBNP was checked and normal. Patient was seen in consultation with Pulmonary Medicine for consideration of increased Steroid dosing. It was recommended that he complete the standard 6 mg of dexamethasone x 10 days. In regards to the patient's acute hypoxemic respiratory failure, this clinically improved, he will discharge on 3 L of O2. He is felt to be a good candidate for the COVID at home program. Pt is stable for DC home on 12/13/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
7,0
Labordaten
CT ANGIO THORAX WITH IV CONTRAST Resulted: 12/08/21 1627 Order Status: Completed Updated: 12/08/21 1629 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 12/8/2021 3:39 PM TECHNIQUE: Standard protocol CT angiogram images were obtained through the chest following the administration of intravenous contrast. Coronal and sagittal MIP 3-D reformations were performed. CONTRAST: The amount and type of contrast are recorded in the medical record. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: PE suspected, low/intermediate prob, positive D-dimer, COVID 19, worsening O2 requirements. COMPARISON: None ____________________ FINDINGS: Base of Neck & Axillae: There is no lymph node enlargement. Mediastinum & Hila: There is no mediastinal or hilar lymph node enlargement. The esophagus is unremarkable. Cardiovascular: Heart measures at the upper limits of normal in size. Calcified atherosclerotic plaque is present within left anterior descending coronary artery. The thoracic aorta is not aneurysmal and there is no dissection. There is no evidence for right heart strain. Pulmonary Arteries: No pulmonary embolism is present. Lungs & Airways: There is patchy semisolid and groundglass density infiltrate throughout both lungs involving all lobes. There is superimposed atelectasis in the right lower lobe with mild cylindrical bronchiectasis. There is also mild elevation of the right hemidiaphragm. Pleural Space: There are no measurable pleural effusions. There is no pneumothorax. Upper Abdomen: Included portions of the upper abdomen are unremarkable. Chest Wall & Musculoskeletal: No significant abnormality. ____________________ Impression: 1. There is no evidence of a pulmonary embolism 2. Bilateral bronchopneumonia typical of a Covid infection DR CHEST SINGLE VIEW Resulted: 12/08/21 0952 Order Status: Completed Updated: 12/08/21 0954 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/8/2021 9:35 AM TECHNIQUE: Single AP portable upright chest INDICATION: Shortness of Breath COMPARISON: 12/7/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: No supporting lines or tubes. Right diaphragm remains mildly elevated compared to the left. Lungs are slightly better expanded. There is no evidence of pneumothorax. Stable heart size. Pulmonary vasculature appears slightly less prominent. No evidence of hilar adenopathy or mass. No superior mediastinal widening. Stable aorta. Bilateral infiltrates appear mildly improved with the lungs slightly better expanded. No new pulmonary opacities. No large pleural effusion. Osseous structures are unchanged. _________________________ Impression: Mild improvement in bilateral infiltrates since yesterday. DR CHEST SINGLE VIEW Resulted: 12/07/21 0143 Order Status: Completed Updated: 12/07/21 0145 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/7/2021 12:36 AM TECHNIQUE: Single view chest INDICATION: COVID-19 x5 days, shortness of breath, cough COMPARISON: None. ENCOUNTER: Not applicable _________________________ FINDINGS: While lung volumes are exceedingly low, even allowing for this, there is at least moderate burden of patchy groundglass opacities more pronounced involving the left lung in the right lung. No lobar consolidation, sizable effusion or discernible pneumothorax. Heart size and visualized pulmonary vascularity are felt to be within normal limits for technique. There is for patient age, moderate calcification of the aortic knob. _________________________ Impression: Even allowing for low lung volumes, the findings are those suggestive of at least moderate Covid 19 pneumonia lung burden. COVID-19 PCR (Abnormal) Collected: 12/08/21 1251 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/08/21 1633 COVID-19 PCR Detected Abnormal Collected: 12/08/21 1251 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/08/21 1632 Influenza A PCR Not Detected Not Detected Influenza B PCR Not Detected Not Detected
Aktuelle Erkrankungen
-
Vorgeschichte
Hospital Cellulitis of left upper extremity Cellulitis Non-Hospital Elevated LFTs Anemia Essential hypertension Emotional depression Allergic rhinitis Osteoarthritis Contact dermatitis Left cervical radiculopathy Class 1 obesity in adult Pneumonia due to COVID-19 virus Acute hypoxemic respiratory failure due to COVID-19
Andere Medikamente
benzonatate (TESSALON) 200 MG capsule dexamethasone (DECADRON) 6 MG tablet fluticasone (FLONASE) 50 MCG/ACT nasal spray losartan (COZAAR) 50 MG tablet Omega-3 Fatty Acids (FISH OIL) 1000 MG capsule PARoxetine (PAXIL) 20 MG tablet
Allergien
Penicillins- Rash
Vorherige Impfungen
-

VAERS 1948214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
52,0
Geschlecht
M
Eingang
14.12.2021
Impfdatum
04.05.2021
Beginn
06.12.2021
Tage bis Beginn
216,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure Angiogram pulmonary abnormal Anticoagulant therapy COVID-19 COVID-19 pneumonia Cardiac telemetry Chest discomfort Chronic kidney disease Chronic lymphocytic leukaemia Computerised tomogram head Computerised tomogram neck Confusional state Cough Diarrhoea Dyspnoea Echocardiogram Ejection fraction decreased Electrocardiogram abnormal

Symptomtext

Hospitalized 12/6/2021-still admitted currently; COVID-19 positive 12/6/2021; fully vaccinated Procedures to be scheduled by PCP: see BW d/c summary Results/Procedures requiring PCP followup: see BW d/c summary Admission Date: 12/6/2021 Discharge Date: 12/12/2021 Details of Hospital Stay PRESENTING PROBLEM: CLL (chronic lymphocytic leukemia) (HCC) [C91.10] Acute respiratory failure with hypoxia (HCC) [J96.01] Acute hypoxemic respiratory failure due to COVID-19 (HCC) [U07.1, J96.01] COVID-19 virus infection [U07.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 53 y.o. male who presented to the emergency department with complaints of hallucinations and shortness of breath. Patient has a past medical history of CKD, CLL, and hyperlipidemia. Patient's pulse oximetry on arrival was 63% upon arrival to the emergency department. He was subsequently placed on a non-rebreather mask and oxygen saturation increased to 96%. Additionally, patient was tachycardic and tachypneic. He had a low-grade fever. Lab results were significant for hyperleukocytosis, hyperkalemia, and chronic kidney disease. EKG shows sinus tachycardia. COVID-19 was positive. Per report, patient had contracted COVID prior to Thanksgiving. CTA of the thorax showed no PE, however, there was diffuse bilateral lung opacities present. Upon assessment, patient was A&O x3, however, he was confused at times about situation. Suspect presenting symptoms were due to hypoxia related to COVID-19 pneumonia. Patient has been admitted for further evaluation and management of COVID-19 pneumonia. On night of 12/8, patient had significant event of decreased responsiveness and confusion. Patient was r/o for acute stroke. CT head, neck and MRI negative for acute ischemic event. Patient was initially started on lovenox for VTE prophylaxis and USV of left upper extremity showed superficial left cephalic vein thrombus and patient was started on therapeutic lovenox. Within 24 patient had decrease of platelets from 99 to 68 and medication was switched to eliquis for concern for H.I.T. Patient continued treatment for COVID pneumonia with use of high flo n/c canula. Patient also met sepsis criteria with concern for bacterial pneumonia and was given 5 days of IV zosyn and vancomycin due to positive MRSA screen. Patient developed severe diarrhea and c-diff testing was ordered but diarrhea stopped prior to collection and no sample was obtained. Patient had decreased oxygen need but c/o continued cough, chest heaviness, with continued tachycardia and tachypnea. Repeat CT thorax showed extensive right-sided pulmonary embolic burden extending to left side and with mild right heart strain. Hospitalist and PERT team discussed case and it was agreed to transfer patient for probable intervention. Patient remained in critical but stable condition for transfer. 12/12/2021 Admission Note (transferred to another hospital) -Diagnosed with COVID-19 on 12/6 - symptoms started prior to 11/26. Treated with Decadron - continue to complete 10 days. CTA 12/21/21: Interval improvement in moderate patchy ill-defined consolidative and groundglass airspace disease throughout the left greater than right upper lobes, greater than lower lobes -Completed 5 days of Vancomycin and Zosyn 12/6/21-12/11/21 (MRSA screen was positive) for possible bacterial co-infection. Elevated procalcitonin 1.94. -Requiring Hi-flow at Big Rapids with FIO2 40% - now tolerating the oximizer at 15 L. -Started on therapeutic Lovenox 12/7 for Left Cephalic Vein Thrombus. Platelets dropped from 99-- >68. Lovenox stopped with concern for HIT and Eliquis started. -Will start patient on Argatroban with concerns for HIT. HIT Ab pending. Hematology consulted -ECHO pending -US lower extremities pending -IR and Pulmonology consulted, planning thrombolysis on 12/13. NPO at midnight -Telemetry and continuous pulse oximetry -Supportive care with scheduled Mucinex, PRN anti-tussives Note 12/14/2021: - Patient underwent Bilateral pulmonary angio with right pulmonary thrombectomy on 12/13. - 2D ECHO prior to thrombectomy showed left ventricular ejection fraction is 52%. The right ventricle is normal size. The right ventricular systolic function is normal. - Currently on IV Argatroban for anticoagulation. Plan to transition to oral NOAC once platelet count normalizes. - Currently requiring 4L O2 via NC. Wean off O2 as able

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
8,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Acute respiratory failure with hypoxia (HCC) CLL (chronic lymphocytic leukemia) (HCC) Pneumonia due to COVID-19 virus Pulmonary embolism (HCC) HIT (heparin-induced thrombocytopenia) (HCC) Pulmonary embolism, unspecified chronicity, unspecified pulmonary embolism type, unspecified whether acute cor pulmonale present (HCC) History of alcohol abuse Bladder cancer (HCC) CKD (chronic kidney disease), stage III (HCC) Lower urinary tract symptoms (LUTS) Prediabetes Personal history of alcoholism (HCC) Hyperlipidemia Weakness
Andere Medikamente
acetaminophen (TYLENOL) tablet 1,000 mg acetaminophen (TYLENOL) tablet 500 mg albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 90 mcg inhaler (60 dose canister) argatroban 50 MG/50ML injection benzocaine-menthol (CEPACOL) lozenge 1 l
Allergien
NKA
Vorherige Impfungen
-

VAERS 1948073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
66,0
Geschlecht
F
Eingang
14.12.2021
Impfdatum
22.04.2021
Beginn
03.12.2021
Tage bis Beginn
225,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute respiratory failure Alanine aminotransferase increased Blood sodium decreased C-reactive protein increased COVID-19 COVID-19 pneumonia Cough Dyspnoea Hyponatraemia Laboratory test abnormal SARS-CoV-2 test positive

Symptomtext

Hospitalized 12/3/2021; COVID-19 positive 12/3/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider: DO Admission Date: 12/3/2021 Discharge Date: Dec 5, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute hypoxemic respiratory failure (HCC) [J96.01] COVID-19 [U07.1] HOSPITAL COURSE: 66-year-old female with PMH of hypertension, hypothyroidism, obesity, gastritis, depression anxiety, vitamin-D deficiency, who presented on 12/03/2021 with cough and shortness of breath since Sunday 11/28/21. Found to COVID-19 positive. Patient has been vaccinated x3. Admitted for COVID-19 pneumonia. Throughout admission, patient was requiring minimal oxygen requirement with only 2 liter nasal cannula. Hemodynamically stable. She was started on dexamethasone. Not a candidate for remdesivir or monoclonal antibody. She received Lovenox for DVT prophylaxis. Low suspicion for PE. She had some mild laboratory abnormalities, including mild hyponatremia 132. Home lisinopril-hydrochlorothiazide was held, replaced by lisinopril only during admission. Sodium normalized the following day. She also had mild elevated ALT 42, which normalized the following day. CRP on admission was 148, trended down to 49 on day of discharge. Given patient's overall benign clinical course, she was discharged with instructions to follow-up with COVID-19 at home program. Discharged home on 2 liters oxygen.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Acute hypoxemic respiratory failure (HCC) Pneumonia due to COVID-19 virus HTN (hypertension) Vasomotor instability Vitamin D deficiency C. difficile colitis Gastritis Obesity, morbid (HCC) Thyroid nodule Hypothyroidism Depression with anxiety Osteopenia
Andere Medikamente
albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet atorvastatin (LIPITOR) 40 MG tablet Calcium Citrate-Vitamin D 500-500 MG-UNIT PACK levothyroxine (SYNTHROID) 50 MCG tabl
Allergien
Vicodin
Vorherige Impfungen
-

VAERS 1941876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
OK
Alter
34,0
Geschlecht
F
Eingang
11.12.2021
Impfdatum
23.04.2021
Beginn
23.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Blood test Dizziness Dysphagia Electric shock sensation Electrocardiogram Electrocardiogram PR shortened Gait disturbance Head titubation Hypoaesthesia Muscle spasms Myocardial infarction Myocarditis Nystagmus Sleep disorder Tendon pain Throat tightness Vertigo Vitreous floaters

Symptomtext

throat felt tight; difficult to swallow; strange neck spasms; Experienced intense electrical zap sensations in brain; wake her out of sleep; nystagmus; floaters in eye; vertigo; Difficult to walk,; tendons sore; arms and legs completely "fell asleep"; internal vibrations in head like someone was constantly shaking head; dizziness; heart attack; heart inflammation; short PR syndrome; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 34 year-old female patient (not pregnant) received bnt162b2 (Pfizer COVID 19), administered in arm right, administration date 23Apr2021 16:45 (Lot number: EW0162) at the age of 34 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "None." The patient's concomitant medications were not reported. No covid prior vaccination, no covid tested post vaccination. No allergies. No other vaccine in four weeks. The following information was reported: THROAT TIGHTNESS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "throat felt tight"; DYSPHAGIA (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "difficult to swallow"; MUSCLE SPASMS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "strange neck spasms"; ELECTRIC SHOCK SENSATION (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "Experienced intense electrical zap sensations in brain"; SLEEP DISORDER (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "wake her out of sleep"; NYSTAGMUS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "nystagmus"; VITREOUS FLOATERS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "floaters in eye"; VERTIGO (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "vertigo"; GAIT DISTURBANCE (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "Difficult to walk,"; TENDON PAIN (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "tendons sore"; HYPOAESTHESIA (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "arms and legs completely "fell asleep""; HEAD TITUBATION (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "internal vibrations in head like someone was constantly shaking head"; DIZZINESS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "dizziness"; MYOCARDIAL INFARCTION (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "heart attack"; MYOCARDITIS (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "heart inflammation"; ELECTROCARDIOGRAM PR SHORTENED (hospitalization) with onset 23Apr2021 16:45, outcome "recovering", described as "short PR syndrome". The patient was hospitalized for throat tightness, dysphagia, muscle spasms, electric shock sensation, sleep disorder, nystagmus, vitreous floaters, vertigo, gait disturbance, tendon pain, hypoaesthesia, head titubation, dizziness, myocardial infarction, myocarditis, electrocardiogram pr shortened (hospitalization duration: 1 day). The events "throat felt tight", "difficult to swallow", "strange neck spasms", "experienced intense electrical zap sensations in brain", "wake her out of sleep", "nystagmus", "floaters in eye", "vertigo", "difficult to walk,", "tendons sore", "arms and legs completely "fell asleep"", "internal vibrations in head like someone was constantly shaking head", "dizziness", "heart attack", "heart inflammation" and "short pr syndrome" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: blood test: everything came back normal; electrocardiogram: possible heart inflammation and short pr syndrome. Therapeutic measures were not taken as a result of throat tightness, dysphagia, muscle spasms, electric shock sensation, sleep disorder, nystagmus, vitreous floaters, vertigo, gait disturbance, tendon pain, hypoaesthesia, head titubation, dizziness, myocardial infarction, myocarditis, electrocardiogram pr shortened. Clinical course: Hours after receiving vaccination her throat felt tight and difficult to swallow and then had strange neck spasms. Experienced intense electrical zap sensations in brain, both day and night, they would also wake her out of sleep. She experienced nystagmus and floaters in eye. She had vertigo. Difficult to walk, tendons sore. Her arms and legs completely "fell asleep" for 1 month. She had internal vibrations in head like someone was constantly shaking head. (This is the symptom she still feel today that has not gone away. The degree has lessened but is still there. Reading is now extremely difficult for her, as well as having a fan in a room...these things make the dizziness/vibration in head feeling intensely return. This was debilitating and traumatizing. She felt like she was having a heart attack 3 weeks after symptoms began and went to hospital. EKG showed possible heart inflammation and short PR syndrome. She had extensive blood tests and everything came back normal. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
1,0
Labordaten
Test Name: blood tests; Result Unstructured Data: Test Result:everything came back normal; Test Name: EKG; Result Unstructured Data: Test Result:possible heart inflammation and short PR syndrome
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1939712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
75,0
Geschlecht
F
Eingang
10.12.2021
Impfdatum
24.04.2021
Beginn
14.09.2021
Tage bis Beginn
143,0
Dosis
UNK
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Asthenia COVID-19 Cardiac arrest Death Decreased appetite Dyspnoea Endotracheal intubation Intensive care Mechanical ventilation Resuscitation SARS-CoV-2 test positive

Symptomtext

pt diagnosed positive for COVID on 9/14/21; treated with Omnicef, steroids, decadron, supplemental O2; dc'd to home; to ED with increasing dyspnea, poor appetite, and weakness; O2 requirement waxed and waned; respiratory status worsened requiring ICU, intubation with mechanical ventilation; pt experienced cardiac arrest , CPR administered, no ROSC achieved; spoke with daughter who elected to stop CPR, pt died in the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
21,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1897098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
OH
Alter
63,0
Geschlecht
M
Eingang
24.11.2021
Impfdatum
08.04.2021
Beginn
12.11.2021
Tage bis Beginn
218,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure COVID-19 Confusional state Dyspnoea Emotional distress Feeling abnormal Haemoptysis Laboratory test abnormal Productive cough

Symptomtext

Patient was fully vaccinated with Pfizer. Doses received 3/18/21 and 4/8/21. Patient was admitted approximately 1 week ago for acute hypoxic respiratory failure due to COVID-19. Patient was admitted for COVID at a different facility and discharged , he has declined. He continued to feel worse each day and developed a coughing fit. He called his granddaughter who came to see him and said he was acting confused and appeared to be in distress. She states that he said he felt like he was dying. She called the ambulance and they brought him to the hospital. Patient endorses shortness of breath and productive cough with some specks of blood. Patient was admitted 11/19/21 and is still in hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
5,0
Labordaten
+ 11/12/21
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1881307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MT
Alter
64,0
Geschlecht
F
Eingang
18.11.2021
Impfdatum
14.04.2021
Beginn
08.11.2021
Tage bis Beginn
208,0
Dosis
2
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Cardiac arrest Cerebral haemorrhage Death SARS-CoV-2 test positive

Symptomtext

Case suffered massive brain bleed and cardiac arrest while Covid positive 6 months after completing the Covid vaccine. Case died.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
-
Labordaten
Ordered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Status: Final Specimen Source: SOFT TISSUE SAMPLE Specimen Site: ENTIRE NASOPHARYNX Specimen Collection Date/Time: 2021-11-08 05:07:00.0 Results: * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: DETECTED Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2021-11-08 06:21:00.0 Performing Facility: HOSPITAL Interpretation: Very abnormal Result Method: LAB DEVICE: CEPHEID GENEXPERT DX SYSTEM Status: Final
Aktuelle Erkrankungen
Acid reflux Adenomatous polyp and FHx Colon Ca: repeat 5 yrs Back injury non surgical candidate per Dr Breast cancer screening she states yearly at Advanced Imaging and completed in 2013 and declines having my office set up another mammogram (OV 2/10/14) Degenerative arthritis of left knee s/p arthroscopy for meniscal tear (2014) Depression Diarrhea resolved/ negative colon biopsies DVT (deep venous thrombosis) (HCC) right common femoral to saphenous vein- Coumadin lifelong H/O Hashimoto thyroiditis dx'd by Bx by Dr; not on supplements Hx of bronchitis Immunization due tDAP 2009; receives yearly flu vaccines (OV 2/10/14) Lactose intolerance Migraine normal MRI/MRA CMC Multinodular goiter s/p thyroidectomy (2017) Neck pain Obesity negative overnight oximetry 3/2001; but continues to respectfully decline further sleepeval/study (OV 2/10/14) Pulmonary emboli (HCC) multiple PE's (2012); w/ h/o prior DVT: life long Coumadin Sinusitis Superficial phlebitis left leg Tubulovillous adenoma polyp of colon negative random bx for colitis
Vorgeschichte
Acid reflux Adenomatous polyp and FHx Colon Ca: repeat 5 yrs Back injury non surgical candidate per Dr Breast cancer screening she states yearly at Advanced Imaging and completed in 2013 and declines having my office set up another mammogram (OV 2/10/14) Degenerative arthritis of left knee s/p arthroscopy for meniscal tear (2014) Depression Diarrhea resolved/ negative colon biopsies DVT (deep venous thrombosis) (HCC) right common femoral to saphenous vein- Coumadin lifelong H/O Hashimoto thyroiditis dx'd by Bx by Dr; not on supplements Hx of bronchitis Immunization due tDAP 2009; receives yearly flu vaccines (OV 2/10/14) Lactose intolerance Migraine normal MRI/MRA CMC Multinodular goiter s/p thyroidectomy (2017) Neck pain Obesity negative overnight oximetry 3/2001; but continues to respectfully decline further sleepeval/study (OV 2/10/14) Pulmonary emboli (HCC) multiple PE's (2012); w/ h/o prior DVT: life long Coumadin Sinusitis Superficial phlebitis left leg Tubulovillous adenoma polyp of colon negative random bx for colitis
Andere Medikamente
Zoloft 100 My bid Maxalt 10 MGqd prn migraine Carafate 1 gm po bid Coumadin 7.5 MG po qd Desyrel 100 mg po qd Wellbutrin XL 300 mg po qd Pepcid 40 mg po bid Synthroid 175 mcg po qd Indocin 50 mg po tid
Allergien
PRoton pump inhibitors
Vorherige Impfungen
-

VAERS 1869708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

kritisch
Staat
AZ
Alter
45,0
Geschlecht
M
Eingang
15.11.2021
Impfdatum
23.04.2021
Beginn
28.04.2021
Tage bis Beginn
5,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute myocardial infarction Catheterisation cardiac abnormal Coronary arterial stent insertion Coronary artery occlusion

Symptomtext

patient had a STEMI 5 days after second dose of vaccine. Treated successfulyly with drug eluting stent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
3,0
Labordaten
cardiac catheterization with 100% occlusion of RCA.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
aspirin
Allergien
none
Vorherige Impfungen
-

VAERS 1861095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
52,0
Geschlecht
M
Eingang
11.11.2021
Impfdatum
03.04.2021
Beginn
10.11.2021
Tage bis Beginn
221,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cerebral haemorrhage Magnetic resonance imaging head abnormal Nausea Pyrexia Vomiting

Symptomtext

Pt with hx of pancreatic cancer, on chemotherapy via port for about 1 yr Presented to hospital with fever an nausea and vomiting. Brain Mri showed hemorrhagic foci now presumed to be metastatic foci

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral haemorrhage
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1860513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
UT
Alter
23,0
Geschlecht
F
Eingang
11.11.2021
Impfdatum
22.03.2021
Beginn
20.04.2021
Tage bis Beginn
29,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Anaphylactic shock Urticaria

Symptomtext

Hives the size of welts cover my body from head to toe on a daily basis. I've gone into anaphylectic shock twice and had to have an epi-pen injected during a five day span where I was unable to take any antihistamines because I was going to be allergy tested. I have to get Xolair injections becasue the antihistamines have stopped working. Symtoms started after first injection. i have not been given a diagnosis yet, but I have been suffering for almost a year.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic shock
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Cold, respitory
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1828774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TN
Alter
87,0
Geschlecht
M
Eingang
29.10.2021
Impfdatum
29.04.2021
Beginn
14.10.2021
Tage bis Beginn
168,0
Dosis
2
Route/Site
IM / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated with Pfizer. Second dose received 4/29/2021. Tested positive for COVID on 10/14/2021. Admitted to Hospital on 10/15/2021. Expired on 10/20/2021 while still hospitalized.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1821825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
WI
Alter
39,0
Geschlecht
M
Eingang
27.10.2021
Impfdatum
17.04.2021
Beginn
19.10.2021
Tage bis Beginn
185,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Acute respiratory failure Bronchial wall thickening C-reactive protein increased COVID-19 Cardiomegaly Chest X-ray abnormal Condition aggravated Fibrin D dimer normal Hypertensive emergency Malaise Procalcitonin increased SARS-CoV-2 test positive White blood cell count normal

Symptomtext

Pt fully vaccinated with the COVID-19 Pfizer vaccine, on 3/27/2021 and 4/17/2021 respectively. Pt presented to the hospital ED on 10/19/2021 with both symptoms of COVID and a hypertensive emergency. Hospital Course: Acute hypoxic respiratory failure -Transient, short-lived. Possibly secondary to Covid, but other etiology more likely - perhaps hypertensive emergency. -Supplemental oxygen only needed for a few hours overnight after admission. Weaned off oxygen. -as needed albuterol COVID -Symptom onset uncertain -Positive Covid test result 10/19/21 -Risk factors for severe disease BMI >34 -Vaccinated for covid -Dexamethasone 6mg started 10/19/21 -since he is already weaned off oxygen within just a few hours of admission, stopped dexamethasone. -Remdesivir not indicated -Tocilizumab/Baricitinib not indicated -Isolation: droplet/contact/N95 or PAPR/eye protection -DVT prophylaxis Lovenox -Lab trends: Mildly elevated CRP, but down trending D-dimer normal x2 days Normal white blood cell count Procalcitonin mildly elevated, but down trending -Imaging: Chest x-ray 10/19/2021 bronchial wall thickening in the perihilar regions, heart enlargement Things to follow-up as an outpatient: - covid vaccine booster candidate?

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
Hypertensive emergency with elevated troponin.
Vorgeschichte
Obesity
Andere Medikamente
Carvedilol
Allergien
no known allergies
Vorherige Impfungen
-

VAERS 1768665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
84,0
Geschlecht
M
Eingang
07.10.2021
Impfdatum
20.04.2021
Beginn
30.09.2021
Tage bis Beginn
163,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure Anticoagulant therapy Asthenia C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Critical illness Deep vein thrombosis Diarrhoea Fibrin D dimer increased Full blood count Immunology test Lung disorder Lung opacity Metabolic function test Pneumonia bacterial

Symptomtext

Hospitalized 9/30/2021; COVID-19 positive 09/30/2021; fully vaccinated CHIEF COMPLAINT: Pneumonia due to COVID-19 virus Weakness, found down at home Assessment/Plan ASSESSMENT/PLAN: Principal Problem: Pneumonia due to COVID-19 virus Sepsis due to COVID 19 PNA with concern for superimposed bacterial pneumonia Positive Test: 9/30 Symptoms Onset: 9/23 First Date of Eligible clearing of covid restrictions: pending review Symptoms: weakness, cough, emesis and diarrhea Tachycardic, tachypnic, WBC 27, LA 2.1 Treatment: Started on Decadron 6 mg and Remdesivir Supplemental O2, wean as able. Worsening tachypnea with RR 30s. STAT VBG pending. There was a question of a possible bacterial component in the ED and vanc cefepime ordered. CXR seems viral. Procal added and elevated - will cover for superimposed bacterial pneumonia with Rocephin/Zithromax Supportive Care with PRN anti-emetics, anti-tussives, anti-pyretics. Isolation and prone as much as possible and as frequently as possible. Daily CMP, daily complete blood count and D-dimer x3. VTE prophylaxis with Lovenox. Current oxygen requirement: SpO2: 94 % O2 Flow Rate (l/min): 2 l/min Note from 10/4/2021: Note from 10/4/2021: CHIEF COMPLAINT: Pneumonia due to COVID-19 virus Assessment/Plan ASSESSMENT / PLAN: Acute Hypoxic Respiratory Failure COVID19 Pneumonia Sepsis secondary to above S/P vaccination earlier this year Symptom onset was on 9/23, tested positive on 9/30 Initial CXR with diffuse abnormal parenchymal opacities, left greater than right Follow up CXR on 10/4 with increase bilateral airspace disease and less likely vascular congestion Currently requiring HFNC with 100 % FiO2 at rest- increased in past 24 hours Immune labs including CRP and D-dimer very elevated but improving Patient also with elevated Procalcitonin On Decadron 6 mg daily x 10 days Remdesivir started on 9/30 x 5 days Continue with antibiotics for superimposed bacterial pneumonia coverage x 5 total days Give one time dose if Diuril with findings of possible CHF component on follow up CXR Encourage proning Continue with anti tussive medication PRN Follow immune labs which are improving Lovenox SQ increased to treatment dose due to high d dimer and superficial thrombus seen on venous US Note from 10/7/2021: CHIEF COMPLAINT: Pneumonia due to COVID-19 virus Assessment/Plan ASSESSMENT / PLAN: Acute Hypoxic Respiratory Failure COVID19 Pneumonia Sepsis secondary to above S/P vaccination earlier this year. Symptom onset was on 9/23, tested positive on 9/30 Initial CXR with diffuse abnormal parenchymal opacities, left greater than right. Follow up CXR on 10/4 with increase bilateral airspace disease and less likely vascular congestion Currently requiring HFNC with 100 % FiO2 at rest Patient also with elevated Procalcitonin On Decadron 6 mg daily x 10 days Remdesivir 9/30 x 5 days Completed abx course x 5 total days Encourage proning. Lovenox 1mg/kg BID for DVT. Patient remains critically ill and receiving maximum non-invasive oxygen support. DNR/DNI

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
7,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
OSA (obstructive sleep apnea), moderate to severe, positional Chronic gout Pneumonia due to COVID-19 virus TIA (transient ischemic attack) Nephrolithiasis IFG (impaired fasting glucose) MG (myasthenia gravis) (HCC) Hx of Tubular adenoma Diverticulosis Vitamin D deficiency History of basal cell carcinoma (BCC) of skin RBBB
Andere Medikamente
allopurinol (ZYLOPRIM) 300 MG tablet aspirin 325 MG tablet Barberry-Oreg Grape-Goldenseal (BERBERINE COMPLEX PO) Cholecalciferol (VITAMIN D3) 1000 UNITS TABS fish oil-omega-3 fatty acids (FISH OIL) 1000 MG capsule Lactobacillus (PROBIOTIC A
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 1759209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
70,0
Geschlecht
M
Eingang
04.10.2021
Impfdatum
14.04.2021
Beginn
03.10.2021
Tage bis Beginn
172,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute myocardial infarction Acute respiratory failure Atrial fibrillation Chronic obstructive pulmonary disease Hypercapnia Hypoxia

Symptomtext

Acute respiratory failure with hypoxia and hypercapnia; COPD with hypoxia; permanent a-fib; Type 2 myocardial infarction

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1737367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MO
Alter
65,0
Geschlecht
F
Eingang
27.09.2021
Impfdatum
09.04.2021
Beginn
28.08.2021
Tage bis Beginn
141,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Death Intensive care Mechanical ventilation Respiratory disorder SARS-CoV-2 test positive

Symptomtext

On 8/28/21 after patient had been fully vaccinated, Patient became COVID positive. On 8/30/21, her respiratory status declined and she was admitted to Hospital. On 9/18/21 while still admitted as inpatient, she declined and required mechanical ventilation and ICU care. On 9/22/21 case died.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
24,0
Labordaten
8/28/21 PCR positive NP Swab
Aktuelle Erkrankungen
Unknown- Medical Records unavailable
Vorgeschichte
Unknown- Medical Records unavailable
Andere Medikamente
Unknown- Medical Records unavailable
Allergien
Unknown- Medical Records unavailable
Vorherige Impfungen
-

VAERS 1727109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TX
Alter
36,0
Geschlecht
M
Eingang
23.09.2021
Impfdatum
15.04.2021
Beginn
07.08.2021
Tage bis Beginn
114,0
Dosis
2
Route/Site
IM / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Activated partial thromboplastin time Acute respiratory failure Anticoagulant therapy Blood fibrinogen Blood gases Blood lactate dehydrogenase Blood magnesium Bradycardia C-reactive protein COVID-19 COVID-19 pneumonia Cardiac arrest Chest X-ray abnormal Computerised tomogram thorax abnormal Death Dyspnoea Endotracheal intubation Fibrin D dimer increased

Symptomtext

obese 35yoM who presents with acute SOB which was found in the ED due to acute COVID 19. He is diaphoretic, and speaks in only short sentences, frequently expressing varying preference for BPAP or facemask. He received the Moderna vaccine series several months prior, and had been in his usual state of good health prior to the abrupt onset of symptoms. He takes medication for hypertension. DISCHARGE DIAGNOSIS: 1. Acute hypoxic respiratory failure secondary to COVID- 19 pneumonia 2. COVID- 19 pneumonia with super-imposed bacterial pneumonia 3. Sepsis secondary to above on pressor support 4. Obesity with body mass index 57 5. Elevated D-dimer He was started on NRB and BPAP, as well as all COVID therapies of steroids, anticoagulation, Colchicine, and Ivermectin. He was also started on broad spectrum antibiotics for possible super-imposed bacterial pneumonia. His oxygenation worsened and he was intubated on 8/8. His O2 levels remained difficult to control and the AM of 8/9 he was proned with increasing PEEP. His oxygenation improved and he appeared to be overall stabilizing by 8/10. The afternoon of 8/10, he was getting suctioned by RT and was noted to become bradycardic, however, this quickly resolved with Atropine and was attributed to increased vasovagal tone secondary to prone positioning and increased PEEP. He remained HD stable and his O2 remained 90s (Last recorded VS HR 61, RR 24, BP 111/67, and O2 99%). Unfortunately, at approximately 2117 the patient developed an irregular heart rate before going into ventricular tachycardia and then asystole. He was started on medical management as per guidelines and CPR was initiated as soon as possible under the direction of Dr. was never obtained and Dr called at 2150. The patient's family was informed of his passing and all questions were answered. Cause of death appears to be cardiac arrest secondary to ventricular tachycardia secondary to hypoxic respiratory failure secondary to COVID- 19 pneumonia.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
3,0
Labordaten
CBC, CMP, PT, PTT, D DIMER, ABG'S, FIBRINOGEN, LFT, MAGNESIUM, LDH, FERRITIN, CRP. Labs concurrent with COVID pneumonia, sepsis, respiratory failure. CT, XRay chest done to assess lung status daily, continues to be concurrent with COVID pneumonia diminishing over stay.
Aktuelle Erkrankungen
unknown
Vorgeschichte
morbid obesity, HTN,
Andere Medikamente
hypertension medications
Allergien
No known drug allergies
Vorherige Impfungen
-

VAERS 1726809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
26,0
Geschlecht
F
Eingang
23.09.2021
Impfdatum
04.05.2021
Beginn
15.09.2021
Tage bis Beginn
134,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Angiogram cerebral normal Anxiety Arteriogram carotid normal Ataxia COVID-19 Cerebrovascular accident Cluster headache Computerised tomogram head normal Impaired work ability Migraine Nervous system disorder SARS-CoV-2 test positive Speech disorder Tachycardia Transient aphasia

Symptomtext

Hospitalized 9/19/2021 COVID-19 positive 9/15/2021; fully vaccinated Pt is a 26 y.o. female past medical history of POTS, episodic cluster headaches, anxiety, history of COVID infection who is presenting today with speech disturbance. Patient had worsening health since originally diagnosed with COVID in November 2020. She states she was off work for 6 months. She has been dealing with episodic cluster headaches. She is currently weaning off Elavil, she had been trying triptans but had severe side effects. Patient presented as stroke code to emergency department. Original NIH of 1. Patient was tachycardic but all other vital signs stable. NIHSS was 1 for LLE ataxia. Patient was emergently taken for advanced imaging. CT head revealed no evidence of acute infarction or hemorrhage. Tpa was not given due to low suspicion of stroke and low NIHSS. CTP revealed no evidence of core infarct or penumbra. CTA head/neck revealed no evidence of LVO or high grade stenosis. She was seen by Neurology who recommended treating for complex migraines. She did exhibit some degree of anxiety on exam, which was acknowledged by patient. It was unclear what the source of the patient's transient aphasia was however it may be related to complex migraine/anxiety/post COVID neurologic symptoms. She was prescribed ketorolac/Compazine/lorazepam to be taken in limited duration after discharge. She will follow-up with neurology. She was discharged home on 09/20/2021 in stable condition. COVID-19 - original + test 11/2020; positive again 9/15/2021. Status post monoclonal antibody 9/16/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Pure hypercholesterolemia 09/19/2021 ? Labyrinthitis ? Irritable bowel syndrome ? Eczema ? Bronchospasm ? COVID-19 ? POTS (postural orthostatic tachycardia syndrome) ? SOB (shortness of breath) ? Episodic cluster headache, not intractable ? Intermittent palpitations ? Anxiety state ? GERD (gastroesophageal reflux disease)
Andere Medikamente
albuterol sulfate (PROAIR RESPICLICK) 108 (90 Base) MCG/ACT inhalation powder Take 2 puffs by inhalation every 4 hours as needed for Wheezing. ? amitriptyline (ELAVIL) 10 MG tablet ? amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet
Allergien
Keflex
Vorherige Impfungen
-

VAERS 1726380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
64,0
Geschlecht
F
Eingang
23.09.2021
Impfdatum
08.04.2021
Beginn
16.09.2021
Tage bis Beginn
161,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute left ventricular failure Acute respiratory failure Ageusia Alanine aminotransferase increased Anosmia Aspartate aminotransferase increased Asthenia Blood albumin decreased Blood alkaline phosphatase increased Blood creatinine increased Blood glucose increased Blood sodium decreased Blood urea increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chest pain

Symptomtext

Hospitalized (9.21.21 - present); COVID-19 positive (9.16.21); fully vaccinated HISTORY OF PRESENT ILLNESS: Patient is a 65 y.o. female with a past medical history of sarcoidosis, OSA not on CPAP, CKD 3B, MGUS, and morbid obesity who presents today with hypoxia. Her current symptoms started on 9/14. Symptoms include fevers, chills, rigors, anorexia, dysgeusia, cough, weakness and diarrhea. She has not taken the majority of her medications in 1 week. She confirmed that she had not taken her Lasix in 1 week. The patient received a COVID test on 09/16 which was positive. She was to have the monoclonal antibody infusion today. When she went to her appointment, her oxygen level was noted to be in the 60s on room air and was sent to the ER. The patient arrived on 6 L of oxygen by nasal cannula. Her oxygen level at arrival was 77% on the 6 L. she was placed on non-rebreather at 15 L. She was transitioned to high-flow nasal cannula with an FiO2 of 90%. She was noted to be tachypneic in the ER with a respiratory rate of 30. She was also tachycardic with pulse of 107. Labs significant for sodium 133, BUN 25, creatinine 1.66, glucose 234, alk-phos 159, albumin 2.9, AST 137 ALT 100. CRP was 152.8. D-dimer 470. CXR with bilateral perihilar and left basilar opacities. This could represent central pulmonary edema. An atypical infection would be a differential consideration, although the distribution would be atypical for Covid 19 pneumonia. Patient was given 6 mg of Decadron as well as 40 mg of IV Lasix. ASSESSMENT / PLAN: Pneumonia due to COVID-19 virus Acute Respiratory failure with Hypoxia Lung Sarcoidosis Acute Systolic Congestive Heart Failure -CXR with bilateral perihilar and left basilar opacities. This could represent central pulmonary edema. An atypical infection would be a differential consideration, although the distribution would be atypical for Covid 19 pneumonia. Symptom onset: 9/14 - positive COVID-19 test 9/16 Symptoms: Chills, fevers, rigors, myalgias, head aches, anorexia, loss of taste and smell, productive cough, dizziness, chest pain, diarrhea, chest pain. Treatment: Remdesivir (starting 9/21 - will need to monitor kidney function and liver function daily), Decadron (started 9/21), Pulmonology consult (hx of Sarcoidosis), VTE prophylaxis with weight based Heparin, Prone PRN, IS, continuous pulse oximetry, supportive care with PRN Imodium, PRN anti-tussives, PRN anti-emetics, PRN albuterol inhaler. Given abnormal appearance of chest X-ray will continue IV Lasix 40 mg daily (adjust as necessary) -Not on current treatment for Sarcoidosis - has not taken her Lasix in one week 2/2 to poor oral intake/diarrhea -Daily weights with I/O, monitor urine output -Given reported chest pain - will obtain EKG now and place on telemetry -Pulm note 8/2021 regarding Sarcoidosis: Multiorgan involvement of sarcoidosis: liver, renal, lung. PET ct in July 2020 w/o evidence of sarcoidosis in heart. MTX stopped July 2020 and her PFTs have been stable since this. NOte from 9.23.21: Pneumonia due to COVID-19 virus Acute Respiratory failure with Hypoxia H/o pulmonary Sarcoidosis - CXR showed bilateral perihilar and left basilar opacities. - Symptom onset: 9/14, positive COVID test 9/16 - Remdesivir started 9/21 - plan to complete 5 day course - Decadron started 9/21 - plan to complete 10 days - Pulmonology consulted (hx of Sarcoidosis) - VTE prophylaxis with weight based Heparin - Encourage prone positioning and IS - Supportive care with anti tussives and anti emetics - Lasix decreased to 40mg IV daily Acute on chronic Systolic Congestive Heart Failure - ECHO from 2019 with LVEF 45-50%, normal diastolic function - LHC from 2020 without any significant arterial disease. EF not noted. - Takes Lasix 40mg PO daily at home - has not taken in one week - Pro BNP normal though may be falsely low due to BMI. CXR suggestive of pulmonary edema. - Continue on Lasix IV as above - Monitor daily weights, I&Os Pulmonary sarcoidosis - Per pulm note 8/2021 regarding Sarcoidosis: Multiorgan involvement of sarcoidosis: liver, renal, lung. PET ct in July 2020 w/o evidence of sarcoidosis in heart. MTX stopped July 2020 and her PFTs have been stable since this. - Not on active treatment - Pulm following - no need for an acute treatment. - Albuterol INH PRN CKD IIIB - Follows with Nephrology as outpatient - Creatinine is near baseline at 1.6 - GFR 38 - Monitor closely while diuresing and on Remdesivir - Lasix dosing as above - Daily weights, I/O

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
3,0
Labordaten
-
Aktuelle Erkrankungen
9.15.21 - called with symptoms 9.16.21 - COVID-19 positive 9.21.21 - antibody infusion
Vorgeschichte
Non-Hospital Anxiety Retinal neovascularization Degenerative progressive high myopia Dyslipidemia Gastroesophageal reflux disease Granuloma present on biopsy of liver Migraine headache Posterior vitreous detachment Histoplasmosis Hematuria CHF, chronic (HCC) MGUS (monoclonal gammopathy of unknown significance) Gout of left foot, unspecified cause, unspecified chronicity
Andere Medikamente
Outpatient Medications acetaminophen (TYLENOL) 500 MG tablet albuterol sulfate (PROAIR RESPICLICK) 108 (90 Base) MCG/ACT inhalation powder allopurinol (ZYLOPRIM) 100 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet brimoni
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1237758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
73,0
Geschlecht
F
Eingang
22.09.2021
Impfdatum
09.04.2021
Beginn
23.08.2021
Tage bis Beginn
136,0
Dosis
1
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal hernia Abdominal pain Acute respiratory failure Anaemia Blood alkaline phosphatase increased Blood creatinine increased Blood glucose increased Blood urea increased Brain natriuretic peptide increased COVID-19 Condition aggravated Cough Decreased appetite Drug screen positive Dyspnoea COVID-19 pneumonia Cardiac failure congestive Chest X-ray abnormal

Symptomtext

Hospitalized 8/29/21-9/8/21 COVID-19 positive 8/23/21; fully vaccinated

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
14,0
Labordaten
Patient is a 73 y.o. female with PMHx of CHF, HTN, Seizures, CAD post-CABG, CKD3, DM2 who presented to the ED on 8/29 with complaints of AMS, fatigue, fevers, and hypoxia. Patient tested positive for Covid on 8/23. She also complained of SOB, cough, HA, chronic abdominal pain, reduced appetite. She also tested for numbness in her lower left leg. She previously was hospitalized from 6/11-6/20 for acute CHF and found to have chronic diastolic heart failure. In the ED, she was significant for tachypnea and hypoxia, cocaine positive, anemia, thrombocytopenia. Her glucose was elevated at 239, BUN 62, Cr 1.89 (at baseline) and ALP of 244. She had elevated troponins with a 2 hour delta of +3, BNP of 17000+. CT of head was negative for acute changes. CT of abdomen revealed abdominal wall hernia. CXR showed findings consistent with Covid penumonia and mild congestion/pulmonary edema. She was started on Rocephin and azithromycin for suspected CAP and admitted into the hospital for Severe Covid infection with acute hypoxic respiratory failure and superimposed bacterial CAP. In the hospital, she was started on Decadron, remdesivir, covid panels. Rocephin and Azithromycin were continued to treat pneumonia. Lasix was started to treat CHF exacerbation. Seizure disorder was noted and continued on home medications. Dm2 was treated with insulin and HTN medications were continued. Other comorbidities were assessed and treated as needed. During her hospital stay, patient was notable for having focal seizures under 5 minutes. Patient used her vagal stimulator to help extinguish them. Decadron and remdesivir were subsequently discontinued for possibly lowering seizure threshold. The patient was transferred to the ICU due to protocol for needing a bear hugger. EGD was also performed to evaluate for a potential ulcer after tarry stools,but was negative for active bleeding. Patient finished antibiotic course and their respiratory status improved and was on room air by end of hospital course. She was discharged to facility in stable and improved condition Readmitted on 9/12-9/16/21 73 y.o. female with h/o known seizure disorder on AED's, CAD s/p CABG, SSS s/p PPM placement, HTN, HLD, GERD, hypothyroidism, depression/anxiety, and recent hospitalization for COVID-19 pneumonia, who presents to BW ER today now 4 days out from recent discharge with SAR staff concern for seizure-like episodes. She reportedly had 2 separate seizure-like events at this facility prior to presentation on 09/12, described by care staff as convulsing of bilateral arms and left leg initially, followed by convulsing of bilateral arms and bilateral legs. She also had another episode during the admitting physician's interview in which she was fully alert and talking, but also notably convulsing. Lamictal levels were noted to by supratherapeutic on admission. She was admitted for EEG monitoring and Lamictal dose was adjusted. Neurology followed and with patient back to her baseline with EEG completed and without seizures recorded, cleared patient for discharge and would plan on outpatient follow-up with epilepsy Clinic with recheck levels of Lamictal and zonisamide in 1 week. With patient stable she was discharged back to her facility. During this hospital stay patient was noted to be fluid positive both clinically and imaging that she was started on IV Lasix twice daily. Her volume status had been monitored and when clinically euvolemic she was transitioned back to her oral diuretics
Aktuelle Erkrankungen
She previously was hospitalized from 6/11-6/20 for acute CHF and found to have chronic diastolic heart failure
Vorgeschichte
CAD,CKD stage3, depression, diastolic CHF, Hypertension, Hypotension, seizure disorder, sick sinus Syndrome
Andere Medikamente
Tylenol, Norvasc, Vitamin C, Aspirin, Lipitor, Tums, Alphagan, Coreg, Vit D3, Catapres, Cardizem CD, Iron, Flonase, Lasiz, Apresoline, Vistaril, hyoscyamine, Insulin Aspart, Insulin detemir, Isordil, Lamictal, Levalbuterol, Synthroid, Anti
Allergien
paper tape, Zoloft (Selective Serotonin Reuptake Inhibitors)
Vorherige Impfungen
-

VAERS 1715804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
52,0
Geschlecht
F
Eingang
20.09.2021
Impfdatum
21.04.2021
Beginn
28.07.2021
Tage bis Beginn
98,0
Dosis
1
Route/Site
- / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
COVID-19 Death Decreased appetite Endotracheal intubation Fatigue Nausea Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

presented to ED with decrease in appetite, nausea, vomiting x approximately 1 wk; tested positive for COVID; fever and fatigue, decreased oxygen saturation; intubated on 8/7/21; condition worsened where she passed away at the hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
19,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1708911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
60,0
Geschlecht
M
Eingang
17.09.2021
Impfdatum
08.04.2021
Beginn
01.09.2021
Tage bis Beginn
146,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Acute respiratory failure Angiogram pulmonary normal Blood culture negative C-reactive protein increased COVID-19 Chest discomfort Chills Cough Diarrhoea Dyspnoea Haemoglobin decreased Hypoxia Inflammatory marker decreased Procalcitonin increased Productive cough Pyrexia SARS-CoV-2 test positive Sputum culture

Symptomtext

Hospitalized; COVID-19 positive (9.1.21; 9.8.21); fully vaccinated Admission Date: 9/8/2021 Discharge Date:9/17/2021 Discharge Disposition: home or self care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute hypoxemic respiratory failure due to COVID-19 HOSPITAL COURSE: Patient is a 60M with past medical history of HTN, CLL ( not on treatment), OSA and fully vaccinated against COVID-19 who is presenting with hypoxia and SOB. He tested positive for COVID 7 days ago (9/1) when he developed cough. He was scheduled to have monoclonial antibody infusion today however, was sent to the ED from the clinic due to hypoxia sats were at 87% prior to the infusion.He reports cough, chest heaviness, diarrhea and fevers. He has since been having worsening dyspnea, productive cough and persistent fever and chills. . He was febrile tachycardic and hypoxic on admission. He was placed on 2L oxygen with improvement in his oxygenation. Labs were notable for CRP 340.2, WBC 33.45, hgb 10.9. He was admitted for acute hypoxic respiratory failure related to COVID-19 infection and possible superimposed bacterial pneumonia. CT angiogram thorax showing no evidence of pulmonary embolism. He received 5 days of remdesivir, and 10 days of Decadron. He was noted to have elevated procalcitonin. Blood and sputum cultures were negative. He was placed on Rocephin and doxycycline for 7 days. He has had worsening respiratory status requiring placement of a HFNC. He was seen by pulmonary medicine. Inflammatory markers trended down. For his CLL he was diagnosed April 2021 with baseline WBC of 20. He is currently on not on active treatment. WBC level increased in the setting of infection and decadron use 9/17/2021 Pt S+E. Now on room air and stable at discharge. Patient in agreement with verbal instructions to return to ED if he experiences increased SOB. He will follow with his outpatient physicians

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
10,0
Labordaten
-
Aktuelle Erkrankungen
9.3.21: COVID-19 positive (SOB, COVID + 2 days ago, has leukemia, no tx at this time. Chest tightness and cough. BP stable but tachy in 140s, febrile, 93% on RA, tachypnic. Highest temp at home wasa 103.7. Pulse in 120s after 500ml fluids.) 9.8.21: Admitted
Vorgeschichte
NA
Andere Medikamente
Outpatient Medications amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG enteric coated tablet benzonatate (TESSALON) 100 MG capsule Cholecalciferol (VITAMIN D3 PO) citalopram (CELEXA) 20 MG tablet Multiple Vitamin (MULTIVITAMIN ADULT PO) onda
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1690161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NY
Alter
34,0
Geschlecht
M
Eingang
10.09.2021
Impfdatum
20.04.2021
Beginn
06.05.2021
Tage bis Beginn
16,0
Dosis
1
Route/Site
IM / AR
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Autopsy Death Gene mutation identification test negative Pericardial haemorrhage Toxicologic test normal

Symptomtext

Patient passed away on 05/06/2021, 16 days after the first Pfizer injection. He was a healthy 34 year old. Autopsy report showed no organ or other physical abnormalities. The autopsy report stated his cause of death was an hemopericardium (acute dissection of proximal thoracic aorta / fatal cardiac tamponade / rupture into pericardial sac).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
1) Genomic Sequencing and Deletion/Duplication Analysis of Genes Associated with Arterial Aneuryms and Dissections: No abnormailty identified in genes tested Toxicology Report: Examination of the specimen(s) submitted did not reveal any positive findings of toxicological significance by procedures outlined in the Analysis Summary.
Aktuelle Erkrankungen
-
Vorgeschichte
IBS,
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1678924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
73,0
Geschlecht
F
Eingang
07.09.2021
Impfdatum
03.05.2021
Beginn
23.08.2021
Tage bis Beginn
112,0
Dosis
1
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal hernia Abdominal pain Abdominal wall oedema Acute respiratory failure Anticoagulant therapy Atelectasis Blood alkaline phosphatase increased Brain natriuretic peptide increased COVID-19 Cardiac failure acute Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Chest pain Computerised tomogram abdomen Computerised tomogram abnormal Computerised tomogram head abnormal Condition aggravated

Symptomtext

Patient hospitalized with COVID-19; Still hospitalized (ICU); Fully vaccinated. Admission Note H&P: HISTORY OF PRESENT ILLNESS: Patient is a 73-year-old female with past medical history of diastolic CHF, hypertension, hyperlipidemia, seizure disorder s/p VNS, coronary artery disease status post CABG, sick sinus syndrome status post permanent pacemaker, CKD 3, diabetes type 2, GERD. Patient was recently hospitalized from 06/11/2021 to 6/20 3/21 for acute congestive heart failure found to have chronic diastolic CHF. Patient during this visit was suicidal and was EN route to facility when she developed chest pain and taken to Hospital. During hospitalization patient was noted to have chronic abdominal pain, a possible seizure that was followed up with an EEG and neuro evaluation all unremarkable. Patient denies suicidal ideations once admitted therefore no further psych placement needed and she was discharged to subacute rehab. Today patient is coming from facility with complaints of altered mental status from baseline, increased fatigue, fevers, and hypoxia. On 08/23 patient was diagnosed with COVID-19. Patient complains of some shortness of breath, cough, severe headache, abdominal pain but this appears chronic, numbness testing into her left lower leg. States having reduced appetite but no loss of taste or smell. ASSESSMENT/PLAN: Severe COVID-19 infection with acute hypoxic respiratory failure - First onset of symptoms: unknown, roughly week - Tested Positive: 8/23 - Decadron: 6mg PO daily, day #1 - continue home PPI - Give Remdesivir *Daily renal and liver function monitoring for kidney and liver toxicity due to Remdesvir is required. - Oxygen Requirements: 2L, wean as tolerated - COVID lab panel: - D-Dimer = ordered - CRP = ordered - alkaline phosphatase = 244 - DVT Prophylaxis: Heparin - treat CHF keeping euvolemic, encourage proning, IS - PRN albuterol, tessalon, tylenol Superimposed Bacterial CAP - procal mildly elevated at 0.29 - ER started Rocephin day 1/5 and Azithromycin day 1/3 - sputum culture, legionella, strep pneumoniae, blood cultures ordered Acute exacerbation of chronic diastolic CHF -last echo 6/12/21 EF 57%, diastolic dysfunction grade 2, right ventricle mildly to moderately decreased, mild MR, moderate TR right ventricular systolic pressure 43.1 mmHg -chest x-ray shows findings of mild congestion; BNP 17,476 -start Lasix 40 mg IV push 2 times a day *The patient is on IV Lasix which requires daily monitoring of electrolyte and renal function to monitor for the following toxicities: renal failure, hyper/hyponatremia, hypokalemia, metabolic alkalosis. -2 L fluid restriction, strict I&Os, daily weights Indeterminate high sensitivity troponins -trope 61 with a 2 hour delta of +3 -demand ischemia from CHF exacerbation and in the presence of CKD

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
11,0
Labordaten
Chest x-ray FINDINGS: Again, pacemaker generator pack in neural stimulator generator pack obscures portions of both the left and right chest. There is similar cardiomegaly. The visualized pulmonary vascularity does appear slightly congested. In addition to this, there are patchy areas of groundglass opacity right more pronounced than left. No sizable effusion or discernible pneumothorax. The adequately visualized portions of the implanted devices appear intact. __________________________________________________ CT head FINDINGS: 1. Patchy areas of hypodensity are noted in the periventricular and in the subcortical white matter. This is nonspecific but most likely represents chronic small vessel ischemic change of the white matter. There are no new areas of abnormal brain attenuation. No acute intracranial hemorrhage is identified. 2. The ventricles, sulci and the cisterns are prominent reflecting intracranial volume loss that is felt to be appropriate when allowing for the patient's age. No mass effect, midline shift nor extra-axial fluid collections are noted. 3. There is mild scattered mucosal thickening in the paranasal sinuses. The mastoid air cells are well aerated. 4. No skull abnormalities are noted. 5. Calcified atherosclerotic plaque is noted within the cavernous internal carotid arteries. ___________________________________________________ CT abdomen pelvis FINDINGS: Lung Bases: Multifocal small patchy opacities in the right middle lobe and right lower lobe likely representing pneumonia. Small layering right pleural effusion with prominent dependent atelectasis in the right lung base. Small left pleural effusion with mild dependent atelectasis in the left lung base. Mild cardiomegaly. Hepatobiliary: The liver has normal morphology and size with no focal lesion on this noncontrast study. The gallbladder is not identified likely due to a prior cholecystectomy. There is no biliary ductal dilatation. Pancreas: The pancreas is normal. Spleen: The spleen is normal. Adrenals: Poorly visualized. Kidneys, Ureters, & Bladder: There are bilateral renal cortical cysts. The kidneys are otherwise normal in appearance allowing for lack of intravascular contrast. There is no hydronephrosis. The ureters and bladder are normal. Gastrointestinal: The stomach, duodenum and remainder the small bowel are normal in appearance. There are no thick walled or abnormally dilated loops of small bowel. The colon is normal. No evidence of diverticulitis or acute colitis. Reproductive Organs: Status post hysterectomy. Lymphatic System: There is no lymph node enlargement within the abdomen or pelvis. Vasculature: There is severe calcific atherosclerotic disease involving the abdominal aorta and iliac arteries with extensive calcific atherosclerotic disease throughout the remainder of the abdomen. There is no abdominal aortic aneurysm. Peritoneum: Tiny amount of free fluid in the pelvis which is nonspecific. No other ascites. No free intraperitoneal air. Abdominal Wall & Musculoskeletal: There is a fat-containing abdominal wall hernia along the lateral margin of the left rectus sheath in the lower abdomen/high pelvic region. The ventral abdominal wall defect measures about 12 mm in diameter. The herniated fat measures up to 4.5 cm in diameter. There is extensive body wall edema. There is severe degenerative disc change at the L5-S1 level. There is no lumbar spine compression fracture. There is no lytic or blastic lesion involving the lumbar spine or bony pelvic ring. Assessment of the solid organs and soft tissues is limited as this is a noncontrast scan.
Aktuelle Erkrankungen
Hospitalized due to COVID-19 Found to be COVID positive 8.28.21. Iron infusions
Vorgeschichte
Diastolic CHF Hypertension Diabetes Depression Seizure disorder Sick Sinus Syndrome Chronic Kidney Disease Stage 3, GFR 30-59 mL/min Coronary artery disease (CAD) hypothyroidism Acute hypoxemic respiratory failure due to COVID-19
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet brimonidine (ALPHAGAN) 0.2 % ophthalmic solution calcium carbonate (TUMS) 500 MG chewable
Allergien
Tape Itching Zoloft [Serotonin Reuptake Inhibitors]
Vorherige Impfungen
-

VAERS 1493843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
-
Geschlecht
M
Eingang
28.08.2021
Impfdatum
12.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia Bedridden Bell's palsy Blindness Cerebrovascular accident Deformity thorax Hookworm infection Rash Coma Deafness Tooth loss Transient ischaemic attack Weight decreased

Symptomtext

Bell's Palsy; Stroke; TIA; Coma; Quarter of his hearing and eyesight gone; Quarter of his hearing and eyesight gone; Rash on cheek, scalp, groin, lower legs, and forearms; Weakness and was bedridden; Weakness and was bedridden; Teeth fell out; Lost weight; Sternum is projected; This is a spontaneous report from a contactable consumer (patient himself). A male patient of an unspecified age received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Solution for injection; Batch/Lot number was not reported) via an unspecified route of administration on 12Apr2021 as dose number unknown, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient begins call, by talking about his mother and her career as a nurse. The patient states he was slowly dying from the Pfizer vaccine, reclarified later as the Pfizer Covid 19 vaccine. On an unspecified date, patient experienced with Bell's Palsy, Rash on cheek, scalp, groin, lower legs, and forearms, Weakness and was bedridden, Coma, Teeth fell out, Quarter of his hearing and eyesight gone, Sternum was projected, Lost weight, TIA, Stroke. ADR as follows: 35 hours after the vaccine, on an unspecified date, he woke up with Bell's Palsy and his face will never be the same, rash on his cheek, scalp, groin, lower legs and forearms, weakness and was bedridden. He became homeless, then was in a coma, his teeth fell out and quarter of his hearing and eyesight was gone, his sternum was projected, he lost weight and he stated he will be dead by the end of the year. He got a TIA 3.5 months, after the vaccine. He had his car impounded with all of his possessions and had a stroke and needs financial assistance. Also stated Pfizer, lines the pockets of the medical system, they have legal immunity, he was pro-vaccine. He had been to 11 doctors, but Pfizer had lined their pockets, and those of the medical system. Investigation Assessment was not Provided. The outcome of all events was unknown. No further details were obtained. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1641754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
60,0
Geschlecht
M
Eingang
27.08.2021
Impfdatum
23.07.2021
Beginn
04.08.2021
Tage bis Beginn
12,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Acute kidney injury Acute respiratory failure Bilevel positive airway pressure COVID-19 COVID-19 pneumonia Cough Dyspnoea Hypertension Hyponatraemia Hypoxia Intensive care Pain Pneumonia Pyrexia Respiratory distress SARS-CoV-2 test positive Tachypnoea Transaminases increased

Symptomtext

08/04/2021: Admitted to ER with positive COVID test, shortness of breath, body aches, fever, and hypoxia on room air that began 3 days prior to admittance. Patient found to have AKI, Pneumonia, hyponatremia, hypertension, transaminitis, and acute respiratory failure with, tachypnea. 08/05/2021: AKI & hyponatremia resolved, hypertension controlled. Patient cough and 02 sat chief concern. 08/06/2021: Admitted to ICU for respiratory distress secondary to COVID induced pneumonia and placed on BiPAP. 08/07/2021-08/09/2021: Patient continued on BiPAP and remained stable with close monitoring. 08/10/2021: Patient taken off BiPAP and continued on high flow oxygen via nasal cannul. Showing signs of improvement. 08/11/2021: Oxygen requirements showed drastic improvement, still has elevated inflammatory markers. Moved out of ICU. 08/12/2021: Continued improvement, slowly working off of oxygen and antibiotics. 08/13/2021: Further improved and discharged on oxygen.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
9,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1431265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
73,0
Geschlecht
M
Eingang
19.08.2021
Impfdatum
19.04.2021
Beginn
01.08.2021
Tage bis Beginn
104,0
Dosis
2
Route/Site
IM / -
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Bacterial infection COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram neck Computerised tomogram normal Computerised tomogram thorax abnormal Condition aggravated Cough Death Fatigue Hypoxia Pneumonia SARS-CoV-2 test positive Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Endotracheal intubation

Symptomtext

Deceased. Date of Death: 8/11/21 Time of Death: 4:29 PM Preliminary Cause of Death: Respiratory failure with hypoxia Discharge Disposition: Deceased DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia of both lungs due to infectious organism, unspecified part of lung [J18.9] Acute hypoxemic respiratory failure [J96.01] a 73 year old male with PMH significant for follicular lymphoma, squamous cell carcinoma of face, recent COVID-19 pneumonia, pulmonary fibrosis, DVT hx s/p IVC filter on warfarin, HTN, hypothyroidism, who presented to the ED on 8/1 for evaluation following a syncopal episode, dyspnea on exertion and cough. Patient recent COVID-19 infection 6/15/21. Had remdesivir, steroids and antibiotic therapy, followed by pulm. He was placed on dexamethasone with taper 7/21. Started on Augmentin on 7/30. He had the syncopal episode on 8/1 and was found down by his wife. Negative CT after fall. Had desaturation to 83% in the emergency department. Started on vanc/zosyn. MRSA screen negative and vanc d/c'ed. CT chest in the emergency department showed no evidence of pulmonary embolism, did show prefer ground-glass infiltrates possible COVID-19 infection, also underlying interstitial lung disease. Pulmonology was consulted. He tested positive for COVID on 08/03/2021. ID was consulted. Thought to be new acute COVID infection rather than viral shedding. Started on dexamethasone 6 on 8/2. Received tocilizumab on 8/4. Due to worsening respiratory status, patient was transferred to ICU on 8/7. He was initially DNI. After conversation with patient and family on 8/8, he decided to be full code and pursue intubation. He was intubated on 8/8 and underwent bronch. Vancomycin was added. On 8/9 bactrim was started for empiric PJP treatment and zosyn was changed to meropenem for broader coverage. Patient developed DIC and was treated supportively with transfusions. Due to worsening respiratory status and poor prognosis, family decided to make patient DNR on 8/10. Decision was made to make patient comfort care on 8/11. Paralytics were held at 2:15 pm. Patient was terminally extubated at 3:49pm with comfort measures. Time of death 4:29pm. a 73 year old male with PMH significant for follicular lymphoma, squamous cell carcinoma of face, recent COVID-19 pneumonia, pulmonary fibrosis, DVT hx s/p IVC filter on warfarin, HTN, hypothyroidism, who was admitted on 8/1 for management of AHRF 2/2 repeat COVID-19 pneumonia. #Acute hypoxic respiratory failure #COVID-19 infection #idiopathic pulmonary fibrosis - AHRF etiology COVID vs ILD flare vs bacterial infection. Unlikely CHF exacerbation given echo with EF 62%. - pt volume up which may be contributing to respiratory status - possibility of PE. Known DVT in July, on warfarin. Will treat dvt with heparin which also treats possible PE. - d-dimer >35,000 since 8/5 - on 3 L O2 baseline - Recent covid infection on 6/15. Thought to be acute reinfection. - s/p tocuilizumab on 8/4 - diurese as needed to achieve net negative 1-2 L /24 hours - IV lasix 40 mg today - increase to decadron 6 mg BID #superimposed bacterial pna - CXR on 8/1 suggestive of bacterial pna - started on vanc/zosyn in ED - vanc d/c'ed after MRSA screen negative - continue zosyn (first dose 8/2) - given leukopenia and steroid use, consider addition bactrim for PCP prophylaxis. Will discuss with ID. #pancytopenia - likely related pt's prior chemo treatments - transfuse for hgb < 7, plts < 10

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
11,0
Labordaten
-
Aktuelle Erkrankungen
history of COVID in June 2021. Decreased O2 sats and sick visit scheduled with Pulmonary 7.21.21. . Hx of COVID-19 6/15/2021, with admission 6/17-6/20, in an immunocompromised host - He experienced initial improvement in symptoms with dexamethasone, but then worsening/persistent cough and exertional dyspnea symptoms since discontinuation of the steroids. Here today with new hypoxia. - Most recent CT imaging of the neck was reviewed from 6/28, which does provide some available slices of the bilateral upper lobes. There has been interval development of peripherally located GGO on top of pre-existing subpleural fibrotic changes. These findings are consistent with COVID-19 viral pneumonia, and I suspect his hypoxia is due to these changes on top of his chronic fibrotic lung disease. - His exertional hypoxia, as demonstrated on today's ambulatory pulse ox assessment, does qualify him for home oxygen therapy. Given his current symptomatology and ongoing hypoxia, will re-start steroids. I recommended prednisone taper, however, pt and his wife preferred dexamethasone as he had tolerated this previously without any adverse side effects. - Will start dexamethasone, 6 mg daily x 10 days, then 3 mg daily x 10 days. If feeling improved with steroids, can stop after completion, however, he may require a more prolonged steroid taper. Will forward message to his hematologist so he is aware. - Repeat CXR ordered - He did not have cough prior to COVID. If cough not improving with steroids, consider starting Atrovent inhaler 4 times daily. - Pt and his wife are scheduled to go out of town for 3 weeks in September, from 9/3-9/24. We will schedule him for follow up after return from their trip. I have ordered home oxygen to be used with ambulation in the interim, 3L per today's titration, however, if he still requires supplemental oxygen at the time of his trip, he will likely need oxygen during his flight and during travel, and we will discuss about getting him a portable oxygen concentrator. I have asked him to call and speak with one of the RN's in 20 days to give an update. 2. Chronic hypoxic respiratory failure - As above
Vorgeschichte
AKI (acute kidney injury) Pancytopenia Diverticulosis of sigmoid colon Family history of colon cancer Indolent non-Hodgkins lymphoma Hypothyroidism Chronic anticoagulation S/P insertion of IVC (inferior vena caval) filter Hypertension History of DVT (deep vein thrombosis) Erectile dysfunction, unspecified erectile dysfunction type Low testosterone in male Chronic venous stasis Chronic cough Dyslipidemia IPF (idiopathic pulmonary fibrosis) Agranulocytosis secondary to cancer chemotherapy Ankle impingement syndrome, left Arthritis of left ankle Exostosis of left tibia Squamous cell carcinoma, face COVID-19 virus infection Non-healing surgical wound Chemotherapy-induced peripheral neuropathy Chronic deep vein thrombosis (DVT) of right popliteal vein Platelets decreased Acute hypoxemic respiratory failure Syncope Left leg pain Elevated liver enzymes Goals of care, counseling/discussion
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet acyclovir (ZOVIRAX) 400 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Ascorbic Acid (VITAMIN C) 500 MG CAPS B Complex Vitamins (B COMPLEX 1 PO) dexameth
Allergien
amlodipine
Vorherige Impfungen
-

VAERS 1431265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MI
Alter
73,0
Geschlecht
M
Eingang
19.08.2021
Impfdatum
19.04.2021
Beginn
01.08.2021
Tage bis Beginn
104,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Bacterial infection COVID-19 COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram neck Computerised tomogram normal Computerised tomogram thorax abnormal Condition aggravated Cough Death Fatigue Hypoxia Pneumonia SARS-CoV-2 test positive Dyspnoea exertional Echocardiogram abnormal Ejection fraction decreased Endotracheal intubation

Symptomtext

Deceased. Date of Death: 8/11/21 Time of Death: 4:29 PM Preliminary Cause of Death: Respiratory failure with hypoxia Discharge Disposition: Deceased DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia of both lungs due to infectious organism, unspecified part of lung [J18.9] Acute hypoxemic respiratory failure [J96.01] a 73 year old male with PMH significant for follicular lymphoma, squamous cell carcinoma of face, recent COVID-19 pneumonia, pulmonary fibrosis, DVT hx s/p IVC filter on warfarin, HTN, hypothyroidism, who presented to the ED on 8/1 for evaluation following a syncopal episode, dyspnea on exertion and cough. Patient recent COVID-19 infection 6/15/21. Had remdesivir, steroids and antibiotic therapy, followed by pulm. He was placed on dexamethasone with taper 7/21. Started on Augmentin on 7/30. He had the syncopal episode on 8/1 and was found down by his wife. Negative CT after fall. Had desaturation to 83% in the emergency department. Started on vanc/zosyn. MRSA screen negative and vanc d/c'ed. CT chest in the emergency department showed no evidence of pulmonary embolism, did show prefer ground-glass infiltrates possible COVID-19 infection, also underlying interstitial lung disease. Pulmonology was consulted. He tested positive for COVID on 08/03/2021. ID was consulted. Thought to be new acute COVID infection rather than viral shedding. Started on dexamethasone 6 on 8/2. Received tocilizumab on 8/4. Due to worsening respiratory status, patient was transferred to ICU on 8/7. He was initially DNI. After conversation with patient and family on 8/8, he decided to be full code and pursue intubation. He was intubated on 8/8 and underwent bronch. Vancomycin was added. On 8/9 bactrim was started for empiric PJP treatment and zosyn was changed to meropenem for broader coverage. Patient developed DIC and was treated supportively with transfusions. Due to worsening respiratory status and poor prognosis, family decided to make patient DNR on 8/10. Decision was made to make patient comfort care on 8/11. Paralytics were held at 2:15 pm. Patient was terminally extubated at 3:49pm with comfort measures. Time of death 4:29pm. a 73 year old male with PMH significant for follicular lymphoma, squamous cell carcinoma of face, recent COVID-19 pneumonia, pulmonary fibrosis, DVT hx s/p IVC filter on warfarin, HTN, hypothyroidism, who was admitted on 8/1 for management of AHRF 2/2 repeat COVID-19 pneumonia. #Acute hypoxic respiratory failure #COVID-19 infection #idiopathic pulmonary fibrosis - AHRF etiology COVID vs ILD flare vs bacterial infection. Unlikely CHF exacerbation given echo with EF 62%. - pt volume up which may be contributing to respiratory status - possibility of PE. Known DVT in July, on warfarin. Will treat dvt with heparin which also treats possible PE. - d-dimer >35,000 since 8/5 - on 3 L O2 baseline - Recent covid infection on 6/15. Thought to be acute reinfection. - s/p tocuilizumab on 8/4 - diurese as needed to achieve net negative 1-2 L /24 hours - IV lasix 40 mg today - increase to decadron 6 mg BID #superimposed bacterial pna - CXR on 8/1 suggestive of bacterial pna - started on vanc/zosyn in ED - vanc d/c'ed after MRSA screen negative - continue zosyn (first dose 8/2) - given leukopenia and steroid use, consider addition bactrim for PCP prophylaxis. Will discuss with ID. #pancytopenia - likely related pt's prior chemo treatments - transfuse for hgb < 7, plts < 10

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
11,0
Labordaten
-
Aktuelle Erkrankungen
history of COVID in June 2021. Decreased O2 sats and sick visit scheduled with Pulmonary 7.21.21. . Hx of COVID-19 6/15/2021, with admission 6/17-6/20, in an immunocompromised host - He experienced initial improvement in symptoms with dexamethasone, but then worsening/persistent cough and exertional dyspnea symptoms since discontinuation of the steroids. Here today with new hypoxia. - Most recent CT imaging of the neck was reviewed from 6/28, which does provide some available slices of the bilateral upper lobes. There has been interval development of peripherally located GGO on top of pre-existing subpleural fibrotic changes. These findings are consistent with COVID-19 viral pneumonia, and I suspect his hypoxia is due to these changes on top of his chronic fibrotic lung disease. - His exertional hypoxia, as demonstrated on today's ambulatory pulse ox assessment, does qualify him for home oxygen therapy. Given his current symptomatology and ongoing hypoxia, will re-start steroids. I recommended prednisone taper, however, pt and his wife preferred dexamethasone as he had tolerated this previously without any adverse side effects. - Will start dexamethasone, 6 mg daily x 10 days, then 3 mg daily x 10 days. If feeling improved with steroids, can stop after completion, however, he may require a more prolonged steroid taper. Will forward message to his hematologist so he is aware. - Repeat CXR ordered - He did not have cough prior to COVID. If cough not improving with steroids, consider starting Atrovent inhaler 4 times daily. - Pt and his wife are scheduled to go out of town for 3 weeks in September, from 9/3-9/24. We will schedule him for follow up after return from their trip. I have ordered home oxygen to be used with ambulation in the interim, 3L per today's titration, however, if he still requires supplemental oxygen at the time of his trip, he will likely need oxygen during his flight and during travel, and we will discuss about getting him a portable oxygen concentrator. I have asked him to call and speak with one of the RN's in 20 days to give an update. 2. Chronic hypoxic respiratory failure - As above
Vorgeschichte
AKI (acute kidney injury) Pancytopenia Diverticulosis of sigmoid colon Family history of colon cancer Indolent non-Hodgkins lymphoma Hypothyroidism Chronic anticoagulation S/P insertion of IVC (inferior vena caval) filter Hypertension History of DVT (deep vein thrombosis) Erectile dysfunction, unspecified erectile dysfunction type Low testosterone in male Chronic venous stasis Chronic cough Dyslipidemia IPF (idiopathic pulmonary fibrosis) Agranulocytosis secondary to cancer chemotherapy Ankle impingement syndrome, left Arthritis of left ankle Exostosis of left tibia Squamous cell carcinoma, face COVID-19 virus infection Non-healing surgical wound Chemotherapy-induced peripheral neuropathy Chronic deep vein thrombosis (DVT) of right popliteal vein Platelets decreased Acute hypoxemic respiratory failure Syncope Left leg pain Elevated liver enzymes Goals of care, counseling/discussion
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet acyclovir (ZOVIRAX) 400 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler Ascorbic Acid (VITAMIN C) 500 MG CAPS B Complex Vitamins (B COMPLEX 1 PO) dexameth
Allergien
amlodipine
Vorherige Impfungen
-

VAERS 1272960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MN
Alter
54,0
Geschlecht
M
Eingang
18.08.2021
Impfdatum
15.04.2021
Beginn
20.04.2021
Tage bis Beginn
5,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Blindness Computerised tomogram head Ischaemic stroke Magnetic resonance imaging head Cerebrovascular accident Laboratory test Vertebral artery occlusion

Symptomtext

I had my first stroke 5 days after the Pfizer vaccine. And then my second stroke 8 days later. There is blockage in my right vertebral artery, but not in any other arteries. It is possible, but not certain, that the Pfizer vaccine caused some of the vertebral blockage to break off and cause my 2 strokes

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
8,0
Labordaten
Many many... I can get copies if you need them. Or you can access my medical records at the hospital.
Aktuelle Erkrankungen
Lymphoma
Vorgeschichte
Lymphoma
Andere Medikamente
None
Allergien
Cephalosporins
Vorherige Impfungen
-

VAERS 1905098

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
CA
Alter
49,0
Geschlecht
M
Eingang
13.08.2021
Impfdatum
19.04.2021
Beginn
20.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Breath sounds abnormal Crepitations Death Intensive care Laboratory test Myocardial infarction Syncope

Symptomtext

My husband, had a heart attack just one month after receiving the second dose of the vaccine. On May 21, 2021, his breathing didn't sound quite right. It was making a crackling sound. Shortly thereafter, he collapsed due to a heart attack. He had no history of heart problems himself. There is no history of heart problems in his family. Both doses of the vaccine were injected into his arm, but I don't remember which arm. He was admitted to hospital after he had a heart attack at home. They ran a multitude of tests, but I don't remember much. It was very traumatic. He was in the ICU for four days before he passed away on May 24, 2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
4,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Huntington's Disease
Andere Medikamente
Olanzapine
Allergien
None
Vorherige Impfungen
-

VAERS 1536552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
FL
Alter
64,0
Geschlecht
M
Eingang
09.08.2021
Impfdatum
19.04.2021
Beginn
27.07.2021
Tage bis Beginn
99,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acute myocardial infarction COVID-19 Chest pain Coronary arterial stent insertion Percutaneous coronary intervention SARS-CoV-2 test positive

Symptomtext

7/27/21: Patient came to ER due to acute onset chest pain and was found to have a STEMI, patient tested positive for COVID on 7/27/21. He underwent successful PCI s/p placement of DES in RCA. Patient was CP free after PCI. No COVID-related symptoms noted. 7/28/21: Patient was discharged home Note: patient previously was vaccinated with the Pfizer COVID-19 vaccine; 2nd dose administered in April 2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
2,0
Labordaten
SARS CoV 2 PCR COVID-19 positive on 7/27/2021
Aktuelle Erkrankungen
-
Vorgeschichte
HTN, HLD, GERD, post MI/LHC
Andere Medikamente
eszopiclone 3 mg oral tablet 3 mg PO at bedtime,
Allergien
Apples, codeine, milk products, peanuts, wheat
Vorherige Impfungen
-

VAERS 1519928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
WI
Alter
81,0
Geschlecht
M
Eingang
02.08.2021
Impfdatum
30.07.2021
Beginn
31.07.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

None

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Closed right hip fracture Acute respiratory failure
Vorgeschichte
DNR Hypertension Dementia
Andere Medikamente
Aspercream, Morphine and Tramadol both PRN, Aspirin 81mg, Baza Protec Cre, Ferrous Sulfate Elx-220/5ml, Ipratropium/sol Albuter, metoprol 25mg, MI-Acid SUS, Nystatin Pow 10000, Robafen Syp 100/5ml, Milk of Mag, Isosorb Mono 30mg, Omeprazole
Allergien
None
Vorherige Impfungen
-

VAERS 1503509

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
AZ
Alter
71,0
Geschlecht
F
Eingang
27.07.2021
Impfdatum
08.04.2021
Beginn
30.04.2021
Tage bis Beginn
22,0
Dosis
1
Route/Site
SYR / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Abdominal distension Asthenia Blood pressure immeasurable Cardiac arrest Cardiac dysfunction Central venous catheterisation Condition aggravated Death Decubitus ulcer Depressed level of consciousness Dialysis Fall Fatigue Gait inability Myocardial necrosis marker increased Oxygen saturation immeasurable Pulse absent Renal impairment

Symptomtext

after first vaccine was given 4/08, patient became very weak, tired and slept almost the entire 3 weeks, when it was time to take the second dose, on 4/29 she drove herself to the hospital, got the shot and went home, that evening she becan to feel very weak and fell down, calling an ambulance for help, the following day, she fell down once again, called 911 and got help getting to her feet, she began to realize her body was too weak to carry herself and when she fell the 3rd time called 911 and asked to go to the hospital. arriving she was immediately give blood transfusions, being told her kidneys had somehow gotten much much worse out of no where and they were no longer producing red blood cells properly, within the first week she was in the hospital, she was given 4 total blood transfusions and was told her heart was not functioning properly, There were elevated enzymes. She was beginning to bloat as her kidneys were not working at all anymore, she was no longer urinating. she was scheduled to have a dialysis port put in and she started dialysis. she was given medication and was sent to a rehab facility for a few weeks where she made no progress at all, she was still weak and unable to walk. due to her inability to walk she was sent home from the rehab, our family had to rally around her to help keep her clean, no bed was sent to us, no commode, we had to find money for all of these things, she quickly got bed sores and we tried all we could do to care for her with little help there was home health coming to see her twice a week, and we repeatedly asked if someone could look into the vaccine doing this to her no one cared to hear our suspicions of the vaccine doing this to our mother, she went to the dialysis clinic 3 times a week all the while paying for her own 800 dollar a week gurney transportation due to her inability to walk, on july 15th she finally got to see her dr, upon taking her vital signs they found no pulse, no blood pressure and no pulse ox but the dr did not seem to think this was a good reason to go to the hospital. we asked if the vaccine did this to her, the dr laughed it off, she went back home and was very tired, she went to sleep and the next morning when my father tried to wake her up for dialysis, she would not wake, 911 was called and she was once again rushed to the hospital, where her heart stopped within minutes of arriving.we asked the people in the ER if there was anyway we could talk to someone about the vaccine doing this to her. our mother is dead!! we were advised to call the health department, they told us to call the cdc, and i was directed to the compensation fund

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
30,0
Labordaten
no tests were ever completed due to the fact that, each time I suggested my mothers side effects/death might have been vaccine related, all medical professionals told me i was wrong.
Aktuelle Erkrankungen
no
Vorgeschichte
type 2 diabetes, renal dysfunction
Andere Medikamente
pioglitazone, levothyroxine, gabapentin, baclofen, furosemide,
Allergien
no
Vorherige Impfungen
-

VAERS 1498209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
PA
Alter
67,0
Geschlecht
M
Eingang
23.07.2021
Impfdatum
25.03.2021
Beginn
25.04.2021
Tage bis Beginn
31,0
Dosis
2
Route/Site
IM / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Agitation Computerised tomogram head Death Electroencephalogram General physical health deterioration Laboratory test Lumbar puncture

Symptomtext

Per family had progressive decline post vaccination with agitation. Significantly worse than prior baseline. He was hospitalized and transitioned to inpatient hospice. Time/Date of death 7/22/21 at 23:03pm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
Lumbar puncture, CT brain, EEG, infectious work-up.
Aktuelle Erkrankungen
advanced dementia presumed Alzheimer's (baseline AAox1), OSA, HTN, HLD
Vorgeschichte
See above
Andere Medikamente
alprazolam 0.5mg qhs, norvasc 10 daily, B complex, coreg 3.125 BID, D3, donepezil 5, Coromega, namenda 10 BID, MVI, sertraline 50, thiamine 100
Allergien
none
Vorherige Impfungen
-

VAERS 1490902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
37,0
Geschlecht
F
Eingang
21.07.2021
Impfdatum
15.07.2021
Beginn
19.07.2021
Tage bis Beginn
4,0
Dosis
2
Route/Site
IM / RA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood glucose normal Cardiac arrest Cardioversion Chest tube insertion Cyanosis Death Electrocardiogram abnormal Endotracheal intubation complication Mini-tracheostomy Muscle tightness Pulse absent Pupil fixed Resuscitation Reversal of opiate activity Unresponsive to stimuli Ventricular fibrillation

Symptomtext

Pfizer COVID vaccine dose #2 administered 15 Jul 2021 @ 07:59. ED physician documentation on 19 Jul 2021: "37-year-old female came the emergency department after found down by her husband. Has a history of attempted overdose in the past,, she was found down by her husband at 545, and unresponsive on scene. Medic was on scene and patient was noted to be in V. fib and therefore CPR was started, compressions were in progress upon arrival, however the patient remained in cardiac arrest. Other history was able to be gathered from the patient or family, however EMS stated that they had found that her glucose was 99 on scene, and she been given full dose Narcan as well on scene. And was shocked 3 times a 200 J, she was given 2 doses of epinephrine, as well as 300 of amiodarone. They attempted to intubate the patient however the patient was clamped down, and therefore they could not pass any sort of apparatus to control the airway, therefore they placed a nasal trumpet. Pertinent physical exam findings: Jaw clamped shut, pupils fixed, and was obviously cyanotic, no palpable pulses. No chest rise. EKG as interpreted by me (ED attending): Monitor showed that the patient was in asystole the entire time. Medical Decision making and plan of care: Patient was immediately moved from gurney onto bed, and chest compressions were continued without interruption. Given that the patient was in V. fib in the field, we did decide to place dual pads for dual sequential defibrillation, is on the plats however, the patient was noted to be in asystole, therefore chest compressions were continued, epinephrine, as well as calcium, as well as bicarb. See code chart for further details. IO was also placed in the patient's left proximal tibia. Regarding the patient's airway, several attempts were made to pass an ET tube, as well as paralyzed the patient with rocuronium, however tube passing was unsuccessful, and therefore I performed a cricothyrotomy. Followed by bilateral finger thoracostomies. See procedure notes below for further details. Despite 5 rounds of ACLS, with multiple doses of epinephrine, as well as bicarb and calcium carbonate administered, the patient remained in cardiac arrest, death was declared at 1851."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Sarcoidosis with recurrent syncope and possible tachyarrhythmia, concern for possible cardiac vs CNS sarcoid (7/9/21) Bipolar disorder Chronic pain/opioid use
Vorgeschichte
Opioid overdose and hospitalization (5/27/21) Asthma Autoimmune sensorineural hearing loss Bipolar disorder Constipation Elevated creatine kinase level Fibromyalgia Long term methotrexate user Low back pain Morbid obesity Neuropathy History of Non-Hodgkin lymphoma PTSD - Post-traumatic stress disorder Sarcoidosis Syncope Tachycardia
Andere Medikamente
diphenhydrAMINE/lidocaine/aluminum hydroxide/magnesium hydroxide/simethicone mucous membrane suspen , HX SIG - FOR REFERENCE ONLY: SWISH AND SPIT 5 ML BY MOUTH EVERY TWO HOURS AS NEEDED FOR SORE THROAT, MOUTH IRRITATION OR PAIN, Mouth or th
Allergien
morphine (Anaphylaxis) immune globulin intravenous (Rash)
Vorherige Impfungen
-

VAERS 1490039

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
PA
Alter
85,0
Geschlecht
F
Eingang
21.07.2021
Impfdatum
24.04.2021
Beginn
08.07.2021
Tage bis Beginn
75,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory failure Chest X-ray Condition aggravated Dyspnoea Productive cough

Symptomtext

Acute respiratory failure with hypoxia wet cough Shortness of breath

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
3,0
Labordaten
Chest X-ray
Aktuelle Erkrankungen
suspected liver cirrhosis.
Vorgeschichte
Nervous Coronary artery disease involving native coronary artery of native heart with angina pectoris (CMS/HCC) Osteoarthritis of thoracic spine with myelopathy Benzodiazepine dependence, episodic (CMS/HCC) Precordial chest pain Respiratory Chronic obstructive pulmonary disease (CMS/HCC) Cough Multifocal pneumonia Acute respiratory failure with hypoxia (CMS/HCC) Circulatory Aortic stenosis Essential hypertension External hemorrhoids ACS (acute coronary syndrome) (CMS/HCC) Congestive heart failure, unspecified HF chronicity, unspecified heart failure type (CMS/HCC) Digestive Gastroesophageal reflux disease Vitamin D deficiency BMI 40.0-44.9, adult (CMS/HCC) Genitourinary Type 2 diabetes mellitus with stage 4 chronic kidney disease, with long-term current use of insulin (CMS/HCC) Chronic kidney disease (CKD), stage III (moderate) (CMS/HCC) Infective urethritis Renal dysfunction Urinary tract infection without hematuria, site unspecified Musculoskeletal Arthritis Cellulitis of finger of right hand Abscess of right ring finger Endocrine/Metabolic Mixed hyperlipidemia Hypothyroidism Infectious/Inflammatory COVID-19 Immune Sjogren's syndrome (CMS/HCC)
Andere Medikamente
acetaminophen (TYLENOL EXTRA STRENGTH) 500 mg tablet albuterol 2.5 mg /3 mL (0.083 %) nebulizer solution albuterol HFA (PROAIR HFA) 90 mcg/actuation inhaler allopurinoL (ZYLOPRIM) 100 mg tablet amLODIPine (NORVASC) 10 mg tablet aspirin 81 m
Allergien
Hydrocodone-acetaminophenIndigestion / GI upset Iodinated Contrast MediaOther (document details in comments), Anaphylaxis IodineOther (document details in comments) Iodine Containing MultivitaminAnaphylaxis LisinoprilCoughing MeperidineNausea and Vomiting, Other (document details in comments) MorphineIndigestion / GI upset PenicillinsItching Propoxyphene N-acetaminophenNausea and Vomiting Sulfa (Sulfonamide Antibiotics)Itching PropoxypheneNausea And Vomiting Tramadol HydromorphoneOther (document details in comments)
Vorherige Impfungen
-

VAERS 1483747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
TN
Alter
69,0
Geschlecht
F
Eingang
18.07.2021
Impfdatum
09.07.2021
Beginn
11.07.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Atrial fibrillation Computerised tomogram thorax abnormal Electrocardiogram Hypoxia Pulmonary embolism

Symptomtext

On 7/11/2021 patient became hypoxic with oxygen saturation of 83% requiring supplemental oxygen. Did not improve and on 7/14/2021 and was sent to the hospital. She was diagnosed with bilateral pulmonary embolus and was found to be in A flutter with RVR.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary embolism
Hospital-Tage
2,0
Labordaten
7/14/2021 CT of thorax with PE protocol 7/14/2021 EKG
Aktuelle Erkrankungen
urinary tract infection
Vorgeschichte
dementia, hypertension, coronary disease
Andere Medikamente
Diltiazem, Lisinopril, atorvastatin, donepezil, olanzapine, depakote, vit d, pepcid, protonix, miralax, megace
Allergien
celebrex, zanaflex, neurtonin
Vorherige Impfungen
-

VAERS 1459755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
VA
Alter
48,0
Geschlecht
M
Eingang
09.07.2021
Impfdatum
16.04.2021
Beginn
15.06.2021
Tage bis Beginn
60,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Blindness Cerebrovascular accident Cognitive disorder Computerised tomogram head normal Computerised tomogram neck Hemiplegia Loss of consciousness Magnetic resonance imaging head abnormal Thalamic infarction

Symptomtext

Two months after receiving my second dose of the Pfizer COVID19 vaccine, I suffered a stroke. Symptoms included vision loss, complete left-side paralysis, loss of cognition, and loss of consciousness. Within ~15 minutes of the event, I was transported by ambulance to the nearest hospital and provided care. Within 3 hours of the event, I received tPA (Tissue Plasminogen Activator), and recovered fully.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
2,0
Labordaten
Two CT Scans of my head/neck were unremarkable. An MRI showed a "small acute right-side thalamic infarct". I recovered very quickly, and the doctor has indicated I should have no long-term impacts in terms of memory, cognition, or motor function. Note: my assumption is that this stroke had nothing to do with my receiving of the COVID19 vaccine (which occurred two months prior). However, followups with a cardiologist, neurologist, and my primary care physician have indicated no reason for the stroke to have occurred. I am reporting the incident as a data point (whether relevant or not), because I believe all data is important.
Aktuelle Erkrankungen
None
Vorgeschichte
Moderately high blood-pressure
Andere Medikamente
Olmesartan (40mg)
Allergien
Amoxicillin
Vorherige Impfungen
-

VAERS 1326260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
DE
Alter
58,0
Geschlecht
F
Eingang
06.07.2021
Impfdatum
13.04.2021
Beginn
26.04.2021
Tage bis Beginn
13,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: ja
Angioplasty Blood test Coronary arterial stent insertion Echocardiogram Electroencephalogram Myocardial infarction SARS-CoV-2 antibody test

Symptomtext

Heart attack, admission to hospital via ER, angioplasty and stent placement, medication and maintenance for the rest of my life.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
2,0
Labordaten
blood tests, EEG 4/26/21, blood tests, angioplasty, EEG, echocardiogram 4/27-28/21
Aktuelle Erkrankungen
none
Vorgeschichte
HBP, migraines, high cholesterol
Andere Medikamente
zyrtec
Allergien
bactrim
Vorherige Impfungen
-

VAERS 1326260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
DE
Alter
58,0
Geschlecht
F
Eingang
06.07.2021
Impfdatum
13.04.2021
Beginn
26.04.2021
Tage bis Beginn
13,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: ja
Angioplasty Blood test Coronary arterial stent insertion Echocardiogram Electroencephalogram Myocardial infarction SARS-CoV-2 antibody test

Symptomtext

Heart attack, admission to hospital via ER, angioplasty and stent placement, medication and maintenance for the rest of my life.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocardial infarction
Hospital-Tage
2,0
Labordaten
blood tests, EEG 4/26/21, blood tests, angioplasty, EEG, echocardiogram 4/27-28/21
Aktuelle Erkrankungen
none
Vorgeschichte
HBP, migraines, high cholesterol
Andere Medikamente
zyrtec
Allergien
bactrim
Vorherige Impfungen
-

VAERS 1447001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MO
Alter
33,0
Geschlecht
M
Eingang
05.07.2021
Impfdatum
09.04.2021
Beginn
17.04.2021
Tage bis Beginn
8,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Arterial injury Arterial repair Ascites Aspiration Aspiration pleural cavity Atelectasis Blood gases abnormal Brachiocephalic vein thrombosis Bronchial disorder Cardiac arrest Cardiac failure Cardiac imaging procedure abnormal Cardiac output Cardiogenic shock Cardiomegaly

Symptomtext

Other diseases of bronchus, not elsewhereclassified Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Acute respiratory failure with hypoxia Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Hypertensive heart disease with heart failure Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Heart failure, unspecified Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 ABG (arterial blood gas) abnormal Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Acute kidney failure, unspecified Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Polycythemia Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 Hyperglycemia, unspecified Onset: 20-Apr-20213:06 Comments: Onset Date: 20210417 ARDS (adult respiratory distress syndrome) Onset: 18-Apr-202116:37 Comments: Onset Date: 20210417 Shock Onset: 18-Apr-202116:37 Comments: Onset Date: 20210417 Acute respiratory failure Onset: 18-Apr-202116:37 Comments: Onset Date: 20210417 Aspiration pneumonitis Onset: 18-Apr-202116:37 Comments: Onset Date: 20210417 Abnormal CXR Onset: 18-Apr-202116:37 Comments: Onset Date: 20210417 Cardiogenic shock Onset: 17-Apr-202114:26 Comments: Onset Date: 20210417 Cardiac arrest Onset: 17-Apr-202114:26 Comments: Onset Date: 20210417 Pulmonary infiltrate Onset: 17-Apr-202112:23 Comments: Onset Date: 20210417 Acute respiratory failure with hypoxia Onset: 17-Apr-202112:23 Comments: Onset Date: 20210417 Aspiration into airway Onset: 17-Apr-202112:23 Abnormal EEG Onset: 25-May-202112:11 Comments: Onset Date: 20210419 Encephalopathy Onset: 25-May-202112:11 Comments: Onset Date: 20210419 Acute thrombosis of right cephalic vein Onset: 19-May-202111:49 Comments: Onset Date: 20210425 Cardiomegaly Onset: 30-Apr-20216:24 Comments: Onset Date: 20210426 Ventricular fibrillation Onset: 29-Apr-20212:21 Comments: Onset Date: 20210427 Coma Onset: 27-Apr-202114:09 Comments: Onset Date: 20210422 Postoperative hemorrhage involving circulatorysystem following circulatory system procedure Onset: 26-Apr-202112:27 Comments: Onset Date: 20210421 Personal history of ECMO Onset: 26-Apr-202112:23 Comments: Onset Date: 20210419 Presence of ventricular assist device Onset: 26-Apr-202112:23 Comments: Onset Date: 20210419 Frequent PVCs Onset: 24-Apr-202112:49 Comments: Onset Date: 20210424 Presence of other vascular implants and grafts Onset: 24-Apr-20215:43 Comments: Onset Date: 20210418 Obesity, unspecified Onset: 24-Apr-20214:58 Comments: Onset Date: 20210417 Body mass index [BMI] 45.0-49.9, adult Onset: 24-Apr-20214:58 Comments: Onset Date: 20210417 Hyperthermia Onset: 23-Apr-202121:40 Comments: Onset Date: 20210419 Ventricular tachyarrhythmia Onset: 23-Apr-202112:14 Comments: Onset Date: 20210423 This code is used to indicate to the billing staff thatservices have been rendered and the chargeneeds to be coded. Onset: 22-Apr-202113:08 Comments: Onset Date: 20210421 Cardiomyopathy Onset: 22-Apr-202111:48 Comments: Onset Date: 20210422

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
14,0
Labordaten
PO Diphenhydramine (Benadryl) [A9150] Date: 16-May-202119:48 Status: Completed Injection - Dexamethasone (Decadron) [J1100] Date: 16-May-202119:48 Status: Completed INSERT OF DEFIB GEN INTO CHESTSUBCU/FASCIA, OPEN APPROACH Date: 27-Apr-2021 INSERT SUBCU DEFIB LEAD IN CHESTSUBCU/FASCIA, OPEN Date: 27-Apr-2021 ASSISTANCE WITH RESPIRATORYVENTILATION, <24 HRS, CPAP Date: 23-Apr-2021 CONTROL BLEEDING IN LEFT FEMORALREGION, OPEN APPROACH Date: 21-Apr-2021 REMOVAL OF EXT HEART ASSIST FROMHEART, PERC APPROACH Date: 19-Apr-2021 REPAIR LEFT FEMORAL VEIN, OPENAPPROACH Date: 19-Apr-2021 REPAIR RIGHT INTERNAL JUGULAR VEIN,OPEN APPROACH Date: 19-Apr-2021 REPAIR RIGHT FEMORAL ARTERY, OPENAPPROACH Date: 19-Apr-2021 EXTRACORPOREAL OXYGENATION,MEMBRANE, PERIPHERAL VENO-VENOUS Date: 17-Apr-2021 HEART/LUNG RESUSCITATION CPR Date: 17-Apr-2021 INSERT NON-TUNNEL CV CATH Date: 17-Apr-2021 RESPIRATORY VENTILATION, GREATER THAN96 CONSECUTIVE HOURS Date: 17-Apr-2021 INSERTION OF MONITORING DEVICE INTO UPART, PERC APPROACH Date: 17-Apr-2021 MEASURE OF CARDIAC SAMPL & PRESSURE,L HEART, PERC APPROACH Date: 17-Apr-2021 FLUOROSCOPY OF MULT COR ART USING LOSM CONTRAST Date: 17-Apr-2021 INSERT EMERGENCY AIRWAY Date: 17-Apr-2021 INSERTION OF EXT HEART ASSIST INTOHEART, PERC APPROACH Date: 17-Apr-2021 DRAINAGE OF RIGHT LOWER LUNG LOBE,ENDO, DIAGN Date: 17-Apr-2021 ASSIST WITH CARDIAC OUTPUT USINGIMPELLER PUMP, CONTINUOUS Date: 17-Apr-2021 TRANSFUSE NONAUT RED BLOOD CELLS INPERIPH VEIN, PERC Date: 17-Apr-2021 - CARDIAC PROCEDURE CHEST 2VIEW Result: CARDIAC PROCEDURE CHEST CARDIACDEVICE PLACEMENT 71046 Exam: PA and lateral chest radiographs on4/28/2021 6:46 AM History: CARDIAC DEVICE PLACEMENT Comparison:4/22/2021 Findings: The cardiac silhouette is normal in size. The pulmonaryvasculature is distinct. The costophrenic angles are sharp. There is nopneumothorax. Lung volumes are low. There is increased density in bothlower lobes. Linear density at the right upper lobe. What may been implanteddefibrillator device is seen only on the lateral view is outside the field-of-viewthe frontal view. There is a single presternal subcutaneous lead new from theprior exam. Impression: 1. Low lung volumes with dependent atelectasis orconsolidation both lungs. 2. Linear density may represent scarring orresolving airspace opacity from the right upper lobe. 3. New implanteddefibrillator seen on the lateral view with a presternal subcutaneousdefibrillator lead. Date: 28-Apr-2021 8:11 Status: Completed - BRAIN MRI W/WO CONTRAST Result: BRAIN MRI W/WO CONTRAST post cardiacarrest 70553 EXAM: MRI Brain without IV and with 20 mL of IV Dotaremcontrast. HISTORY: Cardiac arrest, possible seizure COMPARISON: NoneFINDINGS: No intracranial masses or abnormal enhancement. No abnormalrestricted diffusion or evidence of evolving infarct. No evidence of intracranialhemorrhage. No hydrocephalus. No significant abnormal parenchymal signalabnormalities. Right frontal sinus secretions or mucocele. Sphenoid sinusmucosal thickening. Bilateral mastoid effusions. Remainder unremarkable.IMPRESSION: Normal appearance of the brain. Date: 25-Apr-2021 21:08 Status: Completed - CHEST AP ONLY Result: 4/20/2021 IMPRESSION: ETT at the level of the clavicularheads. Feeding tube to stomach. There is improved edema. There is infiltratein the left lower lobe. There is no pneumothorax. Cardiac size is similar. Date: 22-Apr-2021 15:45 Status: Completed ANGIO CHEST W/PE PROTOCOL Result: - Shortof breath 71275 CT pulmonary angiogram with IV contrast. Contrast: 128 ccof Isovue-370. PQRS Compliance Statement: One or more of the followingindividualized dose reduction techniques were utilized for this examination: 1.Automated exposure control. 2. Adjustment of the mA and/or kV according topatient size. 3. Use of iterative reconstruction technique. History: Shortness ofbreath. Technique: PE protocol. Images were timed to obtain maximumcontrast opacification of the pulmonary arteries. Maximum intensity projectionimages of the pulmonary arteries were created. Comparison: None.Pulmonary arteries: No pulmonary artery filling defect is identified.Lungs/pleura: Bilateral lower lobe atelectasis is present. Airspace disease isseen within the upper lobes and right middle lobe, and most confluent withinthe posterior right upper lobe. Small bilateral pleural effusions are present.The endotracheal tube tip is located 3 cm from the carina. Mediastinum/hilum:No enlarged mediastinal or hilar lymph nodes are identified. Cardiovascular:Cardiomegaly. The thoracic aortic caliber is within normal limits. Nopropagating dissection flap is evident. Upper abdomen: Evaluation of thesolid abdominal organs is limited due to the early phase of contrastenhancement and partial nonvisualization. A feeding tube coils within thestomach. Minimal perihepatic ascites is present. Bones: No suspicious lytic orblastic bone lesion is observed. Impression: 1. No pulmonary embolus. 2.Multilobar airspace disease, possibly due to pneumonia, ARDS, or edema. Date: 22-Apr-2021 11:58 Status: Completed - CHEST AP ONLY Result: Chest 4/19/2021 4:09 AM Comparison: April 18, 2021Findings: Tip of ET tube 4 cm proximal to the carina. Other tubes and linesunchanged in position. NG tube extends into the stomach. Impella leftventricular assist device is again noted. Venovenous ECMO cannulasunchanged in position Heart size cannot be accurately assessed due tomagnification from the AP technique. Diffuse bilateral airspace opacities. Noapparent pleural effusion or pneumothorax on the supine radiograph. Chest4/20/2021 4:38 AM: Findings: Tubes and lines unchanged in position. Stablediffuse bilateral airspace opacities, consistent with pulmonary edema and/orpneumonia. No apparent pleural effusion or pneumothorax on the supineradiograph. Date: 20-Apr-2021 12:18 Status: Completed - CHEST AP ONLY Result: Portable AP chest at 0 4:30 hours. Reason for exam: respiratory failure, ETtube, ECMO ET tube tip is at the inferior clavicular level. NG tube tip is in thestomach. Large bore cannula inserted through right internal jugular vein ispresent with its tip in right subclavian vein. Left ventricular impeller device ispresent. The lungs are not well inflated. There is mild cardiomegaly withpulmonary vascular congestion and bilateral pulmonary edema. Date: 20-Apr-2021 12:00 Status: Completed CHEST AP ONLY Result: AP chest dated April 17, 2021. History: ECMO. Findings:Extensive lung parenchymal opacities are essentially unchanged, and remainmost confluent within the upper lobes and retrocardiac lower lobe. Thecostophrenic sulci were not sharp. The cardiac silhouette is enlarged. Theendotracheal tube is below the thoracic inlet. Feeding tube coils within thegastric fundus. A left ventricular assist device is again seen. The tip of theright internal jugular ECMO cannula courses below the right atrium into theinferior vena cava, inferior to the field of view. Impression: Similar extensivemultilobar airspace disease, possibly due to pneumonia. Date: 18-Apr-2021 8:36 Status: Completed - CHEST AP ONLY Result: AP chest dated April 17, 2021 at 1114 hours. History:ECMO. Findings: Extensive lung parenchymal opacities are essentiallyunchanged, and are most confluent within the upper lobes. The costophrenicsulci were not sharp. The cardiac silhouette is enlarged. The endotrachealtube is below the thoracic inlet. Feeding tube coils within the gastric fundus. Aleft ventricular assist device has been placed. The tip of the right internaljugular ECMO cannula courses of a low the right atrium into the inferior venacava, inferior to the field of view. Impression: 1. Support lines as above. 2.Similar extensive multilobar airspace disease, possibly due to pneumonia. Date: 17-Apr-2021 18:04 Status: Completed - CHEST AP ONLY Result: Portable chest. Comparison: None. History: New admission.The client. Findings: Since the lung parenchymal opacities are present, andmost confluent within the right upper lobe. The costophrenic sulci were notimaged. The cardiac silhouette size cannot be accurately assessed. Theendotracheal tube tip is located below the thoracic inlet, 4.5 cm from thecarina. The feeding tube tip is within the gastric cardia. Impression: Extensivemultilobar airspace disease, possibly pneumonia. Date: 17-Apr-2021 12:21 Status: Completed - ANGIO CHEST W/WO+POST Result: CT angiography chest withcontrast PQRS statement: CT scans at this facility use dose reductionincluding either automated exposure control, iterative reconstructions, and /orweight based radiation dosing via mA and kV modification when appropriateto reduce radiation dose to as low as reasonably achievable. Contrast: 100mL Isovue-370 intravenous contrast with 3-D MIP reconstructions of thearteries acquired. HISTORY: Altered mental status. Status post code.FINDINGS: No pulmonary artery emboli. Endotracheal intubation tube tip 1cm above the carina. Heart size upper limits of normal. Mild fluid loweresophagus perhaps due to reflux. Aorta unremarkable. No adenopathy in thechest. No mediastinal hematoma. There is mild left axillary adenopathylargest lymph node measuring 2.2 x 1.5 cm. Extensive consolidated opacitiesand mild volume loss of the bilateral lower lobes and dependent denseconsolidated opacities of the bilateral upper lobes. There is a 1 cm nodulardensity within the dependent right distal mainstem bronchus. Bones areunremarkable. IMPRESSION: 1. No pulmonary emboli. 2. Extensiveconsolidated pulmonary opacities within the dependent upper and lowerlungs. This is likely the sequela of extensive aspiration pneumonitis.Pulmonary edema, pulmonary hemorrhage or multilobar pneumonia would bein the differential diagnosis. 3. 1 cm nodular density of the right distalmainstem bronchus. This is likely mucus. A endobronchial polyp is notexcluded. Attention on follow-up is advised. 4. Mild left axillary adenopathy Date: 17-Apr-2021 9:33 Status: Completed - HEAD W/O CONTRAST Result: CT scans at this facility use dose reduction including eitherautomated exposure control, iterative reconstructions, and /or weight basedradiation dosing via mA and kV modification when appropriate to reduceradiation dose to as low as reasonably achievable. HISTORY: Altered mentalstatus. Post code. FINDINGS: No intracranial hemorrhage, mass,hydrocephalus, extra-axial fluid collections or infarction. No acute ischemicchange. Partial opacification of the right frontal sinus and bilateral ethmoidsinuses. Orbits, mastoids and bones are unremarkable. IMPRESSION: Noacute intracranial CT abnormality. Mild frontal and ethmoid sinus disease. Date: 17-Apr-2021 9:10 Status: Completed - CHEST AP ONLY Result: Diffuse interstitial and alveolar opacities.No pleural effusion. No pneumothorax. Enlarged cardiac size. Endotrachealtube with tip 1.47 m above the carina. Impression: 1. Endotracheal tube withtip just above the carina. Recommend correlation for desired positioning. 2.Diffuse interstitial and alveolar opacities, may represent pulmonary edema,ARDS or infection including viral pneumonia. Date: 17-Apr-2021 9:04 Status: Completed
Aktuelle Erkrankungen
None
Vorgeschichte
Obese
Andere Medikamente
None
Allergien
Contact allergy to eucalyptus
Vorherige Impfungen
-

VAERS 1413046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
OR
Alter
70,0
Geschlecht
M
Eingang
19.06.2021
Impfdatum
12.04.2021
Beginn
15.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
UN / UN
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cardiac arrest Sudden death

Symptomtext

Sudden cardiac arrest 3 days after second vaccine

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiac arrest
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
History of atrial stenosis requiring atrial valve replacement x 2. History of atrial fibrillation in the last five years requiring multiple cardioversions. Recent hospitalization in the previous month for control. Sudden death occurred three days following second Covid vaccine. There had been a change of medications prior to the second COVID vaccine.
Vorgeschichte
Cardiomegaly and recurrent A-fib for which he had required multiple cardioversions however he was completely functional in all activities of daily living.
Andere Medikamente
Lisinopril Dofetilide Atorvastatin Furosemide Colchicine Warfarin Metroprolol Terazosin Amlodipine
Allergien
-
Vorherige Impfungen
-

VAERS 1399868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MN
Alter
76,0
Geschlecht
M
Eingang
15.06.2021
Impfdatum
20.04.2021
Beginn
20.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Family reported that the patient died 6 hours after being vaccinated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Unknown, none listed.
Vorgeschichte
Unkown, none listed
Andere Medikamente
Unkonwn
Allergien
None Known
Vorherige Impfungen
-

VAERS 1371183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
-
Alter
57,0
Geschlecht
F
Eingang
03.06.2021
Impfdatum
04.05.2021
Beginn
22.05.2021
Tage bis Beginn
18,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Acute kidney injury Acute respiratory failure Blood creatinine increased COVID-19 Convalescent plasma transfusion Endotracheal intubation Fibrin D dimer increased Intensive care SARS-CoV-2 antibody test SARS-CoV-2 test positive

Symptomtext

57 YO female pt presented to outside institution on 5/22 with acute respiratory failure, found to be COVID positive, also w AKI on admission (Cr 4.9). Denies cough, sputum production or fevers at home prior to presentation. She was intubated on arrival to outside institution 5/22 and admitted to ICU. She has been treated with dexamethasone 6mg IV and Remdesivir x1, convalescent plasma. Treated with empiric vanc/zosyn since admission for possible superimposed bacterial PNA. Also were empirically treating for PE due to elevated D-dimer though no CTPE. Transferred to this institution on 5/28. Pt is s/p mRNA vaccination on 4/13 and 5/4, but on immunosuppression with mycophenolate + sirolimus + prednisone...

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
5,0
Labordaten
COVID-19 IGG - SARS-COV-2 Spike (S) Protein Antibody NOT detected (5/28/2021) Novel Coronavirus PCR - SARS-COV-2 detected (5/28/2021)
Aktuelle Erkrankungen
-
Vorgeschichte
ESRD 2/2 diabetes s/p renal transplant (2014) now with CKD IV of transplant kidney, DM, HLD, HTN, and GERD
Andere Medikamente
Mycophenolate + sirolimus + prednisone + cyclosporine
Allergien
Lisinopril, losartan, tuberculin purified protein derivative
Vorherige Impfungen
-

VAERS 1365013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MN
Alter
41,0
Geschlecht
M
Eingang
01.06.2021
Impfdatum
08.04.2021
Beginn
26.04.2021
Tage bis Beginn
18,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Loss of consciousness Traumatic intracranial haemorrhage

Symptomtext

Patient presented to the ED and was subsequently hospitalized within 6 weeks of receiving COVID vaccination. Diagnosis was traumatic hemorrhage of left cerebrum with loss of consciousness.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Traumatic intracranial haemorrhage
Hospital-Tage
10,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1360502

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
GA
Alter
57,0
Geschlecht
U
Eingang
29.05.2021
Impfdatum
09.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Activated partial thromboplastin time Blood cholesterol increased Blood thyroid stimulating hormone Blood triglycerides Blood triglycerides increased Calcinosis Cerebrovascular accident Computerised tomogram Feeling abnormal Glycosylated haemoglobin increased Headache High density lipoprotein Hypoaesthesia Hypoaesthesia oral Lipids Low density lipoprotein Low density lipoprotein increased Metabolic function test

Symptomtext

right vision got more blurry; stroke on the left side of brain; felt weird; tongue started to go numb; Right side of face went numb; Headache; CBCT scan found nothing but calcification; overall cholesterol was 221; LDL was 124; triglyceride was 156; This is a spontaneous report from a contactable consumer (patient). A 57-year-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 09Apr2021 (lot number: EW0162), as 1st dose, single dose, at age 57 years old, for COVID-19 immunisation. Medical history included asthma, arthritis, environmental allergies, and allergy to grass ragweed, mold, tree pollen which triggers the asthma. Concomitant medications included celecoxib (CELEBREX) taken for arthritis from an unspecified date and ongoing; nicotinamide (VITAMIN B3); vitamin C; and vitamin b complex, taken for unspecified indications, start and stop dates were not reported. On 19Apr2021, between 19:30 to 20:00, the patient had a stroke on the left side of brain. It was also reported that on an unspecified date in Apr2021, the patient felt weird, tongue started to go numb, right side of face went numb, right vision got more blurry, and had headache. These events resulted to hospitalization on 20Apr2021 for 2 and a half days (as reported). In Apr2021, when the patient was in the hospital, laboratory tests were performed which included activated partial thromboplastin time (APTT), blood thyroid stimulating hormone (TSH), Hemoglobin A1C, lipid panel, basic metabolic panel, comprehensive metabolic panel, CBC platelet with automated differential, prothrombin INR, prothrombin time, i-STAT Troponin and Sonogram of carotid bilateral vascular in neck which were all normal; Triglycerides was 156, High density lipoprotein (HDL) was 53, Low density lipoprotein (LDL) was 124, Total cholesterol (overall cholesterol) was 221. On 10Apr2021, the patient underwent CBCT scan of the whole body which showed no aneurysm, no cancer, found nothing but calcification. The outcome of the events was unknown. Follow-up attempts are needed. Further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
-
Labordaten
Test Date: 202104; Test Name: APTT; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: TSH; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: Triglycerides; Result Unstructured Data: Test Result:156; Test Date: 20210410; Test Name: CBCT Scan; Result Unstructured Data: Test Result:calcification; Comments: showed no aneurysm, no cancer, found nothing but calcification; Test Date: 202104; Test Name: Hemoglobin A1C; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: HDL; Result Unstructured Data: Test Result:53; Test Date: 202104; Test Name: lipid panel; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: LDL; Result Unstructured Data: Test Result:124; Test Date: 202104; Test Name: basic metabolic panel; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: comprehensive metabolic panel; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: CBC platelet with automated differential; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: prothrombin INR; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: prothrombin time; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: Total cholesterol; Result Unstructured Data: Test Result:221; Test Date: 202104; Test Name: i-STAT Troponin; Result Unstructured Data: Test Result:Normal; Test Date: 202104; Test Name: Sonogram of carotid bilateral vascular in neck; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy to molds; Arthritis; Asthma; Environmental allergy; Seasonal allergy
Andere Medikamente
CELEBREX; VITAMIN B3; VITAMIN C [ASCORBIC ACID]; B COMPLEX (B50)
Allergien
-
Vorherige Impfungen
-

VAERS 1336515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
PA
Alter
82,0
Geschlecht
M
Eingang
21.05.2021
Impfdatum
07.04.2021
Beginn
08.05.2021
Tage bis Beginn
31,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute respiratory failure Adenovirus test Anticoagulant therapy Aortic valve stenosis Bilevel positive airway pressure Bordetella test Bordetella test negative COVID-19 Chest X-ray abnormal Chlamydia test negative Condition aggravated Coronavirus test negative Cough Dyspnoea Echocardiogram Echocardiogram abnormal Ejection fraction decreased Enterovirus test negative

Symptomtext

COVID-19 SOB (shortness of breath) Cough Suspected COVID-19 virus infection Care Coordination Progress Note RN (Registered Nurse) COVID 19 MAB Infusion Navigator Initial Patient Assessment Ordering Prescriber has completed required FDA EUA elements. COVID-19 Positive Result Date (and on chart/file): 5/8/21 Start of Symptoms Date: 5/6/21 Meets Criteria: ANY AGE: ? Body mass index (BMI) ?35 ? Chronic kidney disease ? Diabetes ? Immunosuppressive disease AGE SPECIFIC: ? ? 65 years of age ? ?55 years of age AND had Cardiovascular Disease OR Hypertension OR COPD/other chronic respiratory disease ED to Hosp-Admission Discharged 5/10/2021 - 5/18/2021 (8 days) Treatment team Sepsis due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (CMS/HCC) Principal problem Discharge Summary Discharge Summary BRIEF OVERVIEW Admitting Provider: MD Discharge Provider: DO Primary Care Physician at Discharge: MD Admission Date: 5/10/2021 Discharge Date: 5/18/2021 Discharge Diagnosis Medical Problems Hospital Problems POA * (Principal) Sepsis due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (CMS/HCC) Yes Overview Signed 5/14/2021 10:50 AM 05/11/2021 Dexamethasone 05/11/2021 Remdesivir Essential hypertension Yes CLL (chronic lymphocytic leukemia) (CMS/HCC) Yes OSA (obstructive sleep apnea) Yes Persistent atrial fibrillation (CMS/HCC) Yes DETAILS OF HOSPITAL STAY Presenting Problem/History of Present Illness/Reason for Admission Patient is an 82-year-old male with past medical history significant for CLL, obstructive sleep apnea, obesity and persistent atrial fibrillation who presented to the ER on 5/10 for evaluation of progressively worsening shortness of breath after recently being diagnosed with Covid?19. ER work-up concerning for severe sepsis with acute hypoxic respiratory failure for which he was admitted to the PCU under the hospitalist service. Hospital Course He was treated with dexamethasone and remdesivir but remained hypoxic requiring alternating trials of high flow nasal cannula and BiPAP for which pulmonology was consulted on 5/12. Unfortunately, he did not tolerate prone positioning. Despite his advanced age and several risk factors, he slowly but surely progressed from a pulmonary standpoint. He was weaned off high flow oxygen 2 days ago and deemed stable for downgrade to MedSurg with telemetry at that time. Since then he has continued to recover well, now requiring 6 L of oxygen with activity and 4 L at all other times. He is anxious to be discharged home and appears medically stable to do so with home health care services, remote patient monitoring and outpatient pulmonology follow-up with PAL as prior to hospitalization. Prior to discharge, all questions were answered and patient and his son expressed understanding, appreciation and agreement with the discharge plan at this time. Treatments: IV hydration, analgesia: acetaminophen, cardiac meds: metoprolol, furosemide and aldactone, anticoagulation: eliquis, steroids: dexamethasone, respiratory therapy: O2 and remdesivir

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
8,0
Labordaten
05/10/21 0853 Respiratory virus detection panel Collected: 05/10/21 0743 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected Narrative & Impression 05/10/2021 XR CHEST 2 VW IMPRESSION: Bilateral hyperinflated lungs representing underlying COPD changes. Mild to moderate prominence of interstitial lung markings, patchy groundglass haziness, probably represent subtle bilateral pulmonary infiltrates. Associated mild vascular congestion cannot be excluded. END OF IMPRESSION: INDICATION: Contact with and (suspected) exposure to covid-19 Shortness of breath Cough. TECHNIQUE: PA and lateral projections of the chest are acquired. COMPARISON: 2/21/2020 FINDINGS: Bilateral hyperinflated lungs representing underlying COPD changes. Mild to moderate prominence of interstitial lung markings, patchy groundglass haziness, probably represent subtle bilateral pulmonary infiltrates. Associated mild vascular congestion cannot be excluded. Heart size is within normal limits. Diffuse atherosclerotic calcifications and degenerative changes at visualized bones. This report was created using Voice Recognition software. Thank you for allowing us to participate in the car Pertinent Test Results: 5/8 XR CHEST 2 VW IMPRESSION: Bilateral hyperinflated lungs representing underlying COPD changes. Mild to moderate prominence of interstitial lung markings, patchy groundglass haziness, probably represent subtle bilateral pulmonary infiltrates. Associated mild vascular congestion cannot be excluded. 5/10 XR CHEST 1 VW PORT IMPRESSION: 1. Significant change. Asymmetric bilateral groundglass and patchy opacities, right lung greater than left. Commonly reported imaging features of COVID-19 pneumonia are present. Other processes that can cause a similar imaging pattern include but are not limited to: atypical infections (such as influenza virus, adenovirus, or organizing pneumonias) or noninfectious etiologies (such as asymmetric pulmonary edema, drug induced lung toxicity or connective tissue disease.) 2. Prominence of the cardiopericardial silhouette with retrocardiac density with diameter of approximately 11 cm. Question left atrial enlargement versus other mass. Could be hiatal hernia but suspect that there is a smaller hiatal hernia inferior to this and not related. 5/12 TTE CONCLUSIONS Abnormal Study: Yes Left ventricular ejection fraction is estimated at 56%. Normal left ventricular systolic function. Mild-moderate mitral valve regurgitation. Mild to Moderate aortic valve stenosis, mean gradient 15 mmHg, AVA 1.4 cm?.
Aktuelle Erkrankungen
-
Vorgeschichte
Respiratory OSA (obstructive sleep apnea) Dyspnea Lung nodules Circulatory Essential hypertension Persistent atrial fibrillation (CMS/HCC) Congestive heart failure (CMS/HCC) Heart murmur Spider angioma of skin Digestive Rectal polyp GERD (gastroesophageal reflux disease) Barrett's esophagus with dysplasia Genitourinary Malignant neoplasm of prostate (CMS/HCC) Benign prostatic hyperplasia with urinary obstruction Dysplasia of prostate Musculoskeletal Bilateral lower extremity edema Endocrine/Metabolic Hypercholesteremia Hematologic CLL (chronic lymphocytic leukemia) (CMS/HCC) Immune Sepsis due to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (CMS/HCC) Other Lymphedema Abnormal CT of the chest Advanced directives, counseling/discussion
Andere Medikamente
acetaminophen (TYLENOL) 325 mg tablet ascorbic acid, vitamin C, (ascorbic acid with rose hips) 500 mg tablet ASPIRIN ORAL b complex vitamins capsule coenzyme Q10 (CO Q10) 100 mg capsule ELIQUIS 5 mg tablet fluticasone propionate (FLONASE) 5
Allergien
PenicillinsHives / Urticaria
Vorherige Impfungen
-

VAERS 1333957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
PA
Alter
65,0
Geschlecht
F
Eingang
20.05.2021
Impfdatum
29.04.2021
Beginn
09.05.2021
Tage bis Beginn
10,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute respiratory failure COVID-19 Chest X-ray abnormal Chronic kidney disease Deep vein thrombosis Essential hypertension Granulomatosis with polyangiitis Hypothyroidism Influenza A virus test negative Influenza B virus test Insulin-requiring type 2 diabetes mellitus Lung infiltration Lung opacity Pain SARS-CoV-2 test positive Sepsis Swelling Ultrasound Doppler abnormal

Symptomtext

ED to Hosp-Admission Discharged 5/9/2021 - 5/11/2021 (2 days) Principal problem Discharge Summary Discharge Summary Hospitalist Medicine Date: 5/11/2021 Admission Date: 5/9/2021 Length of Stay: 2 Days Discharge Date: 5/11/2021 Admission Diagnosis Medical Problems Hospital Problems POA * (Principal) Sepsis Yes Type 2 diabetes mellitus, with long-term current use of insulin Not Applicable Benign essential hypertension Yes CKD (chronic kidney disease), stage IV Yes Gastroparesis Yes Granulomatosis with polyangiitis Yes Hypothyroidism Yes COVID-19 virus infection Yes DVT, lower extremity, proximal, acute, right Yes Acute on chronic respiratory failure with hypoxia Yes Monilial vulvitis No Hospital Course: Patient recently was admitted for possible sepsis picture. He was treated according to sepsis protocol including antibiotics for bacterial infection for pulmonary infiltrates however it was felt the pulmonary infiltrates are more related with COVID-19 pulmonary findings. Eliquis was started for DVT. Medical Center had been contacted Dr was the pulmonary attending and discussion is documented below- Attending hospitalist spoke to Dr from Medical Center. At this point they know that she has Wegener's granulomatosis involving her kidneys and causing her renal failure but they do not think that is what is going on in her lungs. They have still trying to work-up her infiltrates. She has it we obtain a nocturnal oximetry study. She was reassured that the patient is on her normal oxygen rate despite the DVT in her leg. She feels this should rule out a pulmonary embolism. If the patient is doing well from cardiopulmonary standpoint tomorrow she should be able to go home on Eliquis and follow-up with the specialist. She was continued on Monistat cream for 3 nights total. At this point patient will not require antibiotics will continue on Decadron and may be discharged to follow-up with her specialist.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
2,0
Labordaten
05/09/21 1734 COVID-19/Flu/RSV PCR - Asymptomatic screening for admission Collected: 05/09/21 1651 | Final result | Specimen: Swab from Nasopharynx Influenza A Not Detected Respiratory Synctial Virus Not Detected Influenza B Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical ED to Hosp-Admission Discharged 5/9/2021 Hospital ICU Imaging Results Procedure Component Value Ref Range Date/Time X-ray chest 1 view, Portable [3282331316] Resulted: 05/09/21 1949 Order Status: Completed Updated: 05/09/21 1949 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Faint areas of airspace consolidation with groundglass attenuation. This nonspecific imaging pattern can be seen with COVID-19. Other considerations include but are not limited to other infectious etiologies or noninfectious etiologies. END OF IMPRESSION: INDICATION: sepsis. TECHNIQUE: Portable view(s) of the chest are provided. COMPARISON: 3/26/2021 FINDINGS: The lungs are adequately inflated. Faint patchy airspace opacities are noted in the left midlung and right lung base with areas of groundglass attenuation. No effusion or pneumothorax identified. The cardiac silhouette, pulmonary vasculature and bony thorax are within normal limits for age. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. Ultrasound lower extremity venous right [3282316521] Resulted: 05/09/21 1649 Order Status: Completed Updated: 05/09/21 1650 Narrative: US LOWER EXTREMITY VENOUS RIGHT IMPRESSION: Examination positive for DVT from the right popliteal vein to the common femoral vein. END OF IMPRESSION: INDICATION: pain swelling. TECHNIQUE: High-resolution venous duplex with color flow technique was used to investigate the right lower extremity venous system where accessible to study. Permanently recorded images were obtained and stored. COMPARISON: None. FINDINGS: Intraluminal filling defect is noted in the right common femoral vein to the popliteal vein. The posterior tibial and peroneal veins demonstrate compressibility.. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient.
Aktuelle Erkrankungen
-
Vorgeschichte
Respiratory Acute on chronic respiratory failure with hypoxia Circulatory Benign essential hypertension Granulomatosis with polyangiitis Polyarteritis nodosa DVT, lower extremity, proximal, acute, right Digestive Gastroparesis Obesity Genitourinary CKD (chronic kidney disease), stage IV Hypertensive chronic kidney disease with stage 1 through stage 4 chronic kidney disease, or unspecified chronic kidney disease Monilial vulvitis Musculoskeletal Other specified disorders of bone density and structure, other site Endocrine/Metabolic Type 2 diabetes mellitus, with long-term current use of insulin Hypothyroidism Pure hypercholesterolemia Infectious/Inflammatory COVID-19 virus infection Immune Sepsis Other Adjustment disorder with mixed emotional features Edema Proteinuria Long term (current) use of insulin
Andere Medikamente
albuterol HFA (VENTOLIN HFA) 90 mcg/actuation inhaler, amLODIPine (NORVASC) 5 mg tablet apixaban (ELIQUIS) 5 mg tablet atorvastatin (LIPITOR) 10 mg tablet blood sugar diagnostic (FREESTYLE PRECISION NEO STRIPS) strip blood-glucose meter kit
Allergien
Sulfa (Sulfonamide Antibiotics)Rash Terbinafine HclRash
Vorherige Impfungen
-

VAERS 1289147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
PA
Alter
54,0
Geschlecht
M
Eingang
20.05.2021
Impfdatum
09.04.2021
Beginn
14.04.2021
Tage bis Beginn
5,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Acute respiratory failure Adenovirus test Angiogram pulmonary abnormal Bordetella test negative COVID-19 pneumonia Blood calcium Blood chloride normal Blood creatinine normal Blood potassium normal Blood sodium normal Blood urea normal Carbon dioxide normal Haematocrit decreased Chest X-ray abnormal Chills Condition aggravated Coronavirus test negative Dyspnoea

Symptomtext

Fever and chills Myalgia Viral syndrome ED to Hosp-Admission Discharged 4/18/2021 - 4/22/2021 (4 days) Hospital MD Last attending ? Treatment team Acute respiratory failure with hypoxia (CMS/HCC) Principal problem Presenting Problem/History of Present Illness/Reason for Admission Acute respiratory failure with hypoxia (CMS/HCC) [J96.01] Pneumonia due to COVID-19 virus [U07.1, J12.82] Hospital Course This pleasant 54-year-old gentleman with history of hypertension came in with increasing shortness of breath and hypoxia secondary to Covid pneumonia resulting in hypoxic respiratory failure and diffuse pulmonary infiltrates. Patient was hospitalized for management of severe sepsis secondary to Covid pneumonia resulting in acute hypoxic respiratory failure. Patient was also treated for possible secondary bacterial pneumonia given duration of Covid symptoms prior to coming into hospital. Patient made nice recovery and was able to wean off from high flow oxygen down to 2 L with exertion. Patient overall made nice recovery hence he was discharged home. Patient was noted to have rising D-dimers despite clinical improvement in Covid infection. He is at high risk for developing DVTs hence he was recommended to use Xarelto 10 mg daily for 1 month to prevent any risk of DVTs. Patient voiced understanding of this. In he was discharged home with home health care. His readmission potential is low to moderate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
4,0
Labordaten
04/18/21 1852 Respiratory virus detection panel Collected: 04/18/21 1714 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected 04/16/21 1839 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 04/16/21 0816 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result DetectedCritical 04/16/21 1839 COVID-19 PCR X-ray chest 1 view, Portable Result Date: 4/18/2021 XR CHEST 1 VW PORT IMPRESSION: Patchy ill-defined parenchymal opacities in the lungs bilaterally with a somewhat greater peripheral distribution, typical of Covid 19 pneumonia. END OF IMPRESSION: INDICATION: sob Covid sob Covid. TECHNIQUE: AP projection of the chest is acquired. COMPARISON: 4/20/2018 FINDINGS: Reduced lung volumes. There are patchy ill-defined parenchymal opacities in the lungs bilaterally, with a greater peripheral distribution. Though nonspecific, appearances are typical of Covid-19 pneumonia. No pneumothorax or pleural effusion. Normal cardiomediastinal silhouette. Regional osseous structures are unremarkable. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT angiogram chest pulmonary embolism with and without contrast Result Date: 4/18/2021 PROCEDURE INFORMATION: Exam: CTA Chest Without And With Contrast Exam date and time: 4/18/2021 10:00 PM Age: 54 years old Clinical indication: Other: Acute hypoxic respiratory fialure, covid, ? pe TECHNIQUE: Imaging protocol: Computed tomographic angiography of the chest without and with contrast. 3D rendering (Not supervised by radiologist): MIP and/or 3D reconstructed images were created by the technologist. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. Contrast material: OMNIPAQUE; Contrast volume: 80 ml; Contrast route: INTRAVENOUS (IV); COMPARISON: DX XR CHEST 1 VW 4/18/2021 5:45 PM FINDINGS: Pulmonary arteries: No pulmonary embolism within the pulmonary trunk, main pulmonary arteries, segmental, or subsegmental branches. Aorta: No aortic aneurysm. No aortic dissection. Lungs: Diffuse and multifocal groundglass attenuation of the pulmonary parenchyma with more focal consolidation in the bilateral upper lobes. Pleural spaces: No pneumothorax. Heart: No cardiomegaly. No pericardial effusion. Lymph nodes: No suspicious lymphadenopathy. Liver: Diffuse hepatic hypoattenuation consistent with hepatic steatosis. Bones/joints: Mild degenerative changes of the spine. No acute fracture or aggressive osseous lesion. Soft tissues: No acute abnormality. Other findings: Examination is somewhat limited by motion artifact. IMPRESSION: 1. Examination is somewhat limited by motion artifact. 2. No pulmonary embolism within the pulmonary trunk, main pulmonary arteries, segmental, or subsegmental branches. 3. Diffuse and multifocal groundglass attenuation of the pulmonary parenchyma with more focal consolidation in the bilateral upper lobes. Findings are suspicious for atypical infection. 4. Hepatic steatosis. 5. Chronic findings, as above. THIS DOCUMENT HAS BEEN ELECTRONICALLY SIGNED BY MD Physical Exam at Discharge Heart Rate: 67 Resp: 16 BP: 130/69 Temperature: 36.9 ?C (98.5 ?F) Weight: 118 kg (260 lb) Constitutional: Currently patient is in no apparent distress. HEENT: Pupils are equal react round with normal extraocular movements, no JVD, no neck rigidity. Cardiovascular: Pleasant, normal S2, regular rate rhythm, no obvious murmurs rubs or gallops. Respiratory: Good air entry bilaterally with no crackles or wheezes. Abdomen: Soft, nontender, good bowel sounds. CNS: Patient is alert and oriented x3, no focal motor or sensory deficits.
Aktuelle Erkrankungen
-
Vorgeschichte
Nervous Neck pain Stroke associated with COVID-19 (CMS/HCC) Cerebral infarction due to stenosis of right carotid artery (CMS/HCC) Respiratory Obstructive sleep apnea syndrome Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (CMS/HCC) Circulatory Essential hypertension Coronary artery disease involving native coronary artery of native heart without angina pectoris Symptomatic carotid artery stenosis, right Digestive Class 1 obesity due to excess calories without serious comorbidity with body mass index (BMI) of 34.0 to 34.9 in adult Musculoskeletal Avascular necrosis (CMS/HCC) Endocrine/Metabolic Hyperglycemia Mixed hyperlipidemia Immune Immunosuppression (CMS/HCC) Psoriasis Other High risk medication use Insomnia due to medical condition Male erectile disorder of organic origin History of non-ST elevation myocardial infarction (NSTEMI) Former smoker
Andere Medikamente
acetaminophen (TYLENOL) 325 mg tablet albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler amoxicillin 500 mg oral tablet aspirin tablet buPROPion XL (WELLBUTRIN XL) 150 mg 24 hr tablet cholecalciferol, vitamin D3, 2,000 unit capsule
Allergien
Sulfa (Sulfonamide Antibiotics)Other (document details in comments) Sulfamethoxazole-trimethoprimOther (document details in comments)
Vorherige Impfungen
-

VAERS 1324009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
MN
Alter
78,0
Geschlecht
M
Eingang
17.05.2021
Impfdatum
08.04.2021
Beginn
11.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
Cerebral haemorrhage

Symptomtext

Patient presented to the ED and was subsequently hospitalized for left-sided nontraumatic intracerebral hemorrhage. He is currently admitted for rehab.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral haemorrhage
Hospital-Tage
10,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1314603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NJ
Alter
68,0
Geschlecht
M
Eingang
13.05.2021
Impfdatum
22.04.2021
Beginn
23.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / AR
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia Back pain Blood test normal Chills Death Decreased appetite Dysgeusia Fatigue Illness Loss of consciousness Nausea Pyrexia Vomiting

Symptomtext

Illness set in either the day of the vaccination being administered or the day after, according to phone records. Signs include: nausea/vomiting, back aches, fever, chills, passing out, lack of appetite, extreme fatigue and low energy, bitter taste in the mouth and water tasting bitter.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
Physical and annual assessment was done 4/2021, patient was in good health. Blood test results came back ~ 5/3/21 (after his passing) ? results showed good health.
Aktuelle Erkrankungen
No illnesses
Vorgeschichte
Eczema
Andere Medikamente
Nausea medication
Allergien
None
Vorherige Impfungen
-

VAERS 1239205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
WA
Alter
38,0
Geschlecht
M
Eingang
11.05.2021
Impfdatum
15.04.2021
Beginn
17.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Activated partial thromboplastin time prolonged Acute myocardial infarction Arteriogram coronary normal Blood test Chest pain Angiogram Cardiovascular disorder Computerised tomogram Dyspnoea Computerised tomogram coronary artery normal Echocardiogram abnormal Electrocardiogram normal Myocarditis Troponin increased Echocardiogram Electrocardiogram SARS-CoV-2 antibody test SARS-CoV-2 test

Symptomtext

chest pains; short of breath; troponin at 4.6/Went up to 5.0/troponin peaked at 9.9; Echo shows decreased blood flow (50%); This is a spontaneous report from a contactable consumer (patient). A 38-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at same age, via an unspecified route of administration, administered in arm left on 15Apr2021 12:45 (Batch/Lot Number: EW0162) as single dose for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included loratadine/ pseudoephedrine (CLARIDIN-D). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at same age, administered in arm left on 25Mar2021 04:30 PM (Batch/Lot Number: ER8730) for covid-19 immunisation. The patient experienced chest pains, and short of breath both on 17Apr2021 22:00. Tried to sleep it off. 24 hours, didn't get better. On 17Apr2021, went to local ER, troponin at 4.6 ng/L. Doctors didn't believe it, did another blood draw. Went up to 5.0 ng/L. Ambulance to nearby hospital, troponin peaked at 9.9 ng/L. Echo showed decreased blood flow (50%) and EKG was irregular. Angiogram and CT scan show no blood clots or blockages. Patient was a healthy 38 male who was a distance runner. No history of chest pain or heart issues. Doctors determined incident almost certainly related to vaccine. The serious criteria for all events were hospitalization and duration were 2 days. The adverse events result in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Colchicine received as treatment for the adverse events. Prior to vaccination, the patient was not diagnosed with COVID 19. Since the vaccination, the patient has been tested for COVID 19. The patient underwent lab tests and procedures which included COVID test (COVID antibody blood test): negative on 20Apr2021, Covid test (Nasal Swab): negative on 18Apr2021. The outcomes of events were recovering.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
2,0
Labordaten
Test Date: 20210417; Test Name: Angiogram; Result Unstructured Data: Test Result:no blood clots or blockages; Test Date: 20210417; Test Name: CT scan; Result Unstructured Data: Test Result:no blood clots or blockages; Test Date: 20210417; Test Name: Echo; Test Result: 50 %; Comments: decreased blood flow; Test Date: 20210417; Test Name: EKG; Result Unstructured Data: Test Result:Irregular; Test Date: 20210420; Test Name: COVID test (COVID antibody blood test); Test Result: Negative ; Test Date: 20210418; Test Name: Covid test (Nasal Swab); Test Result: Negative ; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:peaked at 9.9 ng/L; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:Went up to 5.0 ng/L; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:4.6 ng/L
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
CLARIDIN-D
Allergien
-
Vorherige Impfungen
-

VAERS 1239205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
WA
Alter
38,0
Geschlecht
M
Eingang
11.05.2021
Impfdatum
15.04.2021
Beginn
17.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Activated partial thromboplastin time prolonged Acute myocardial infarction Arteriogram coronary normal Blood test Chest pain Angiogram Cardiovascular disorder Computerised tomogram Dyspnoea Computerised tomogram coronary artery normal Echocardiogram abnormal Electrocardiogram normal Myocarditis Troponin increased Echocardiogram Electrocardiogram SARS-CoV-2 antibody test SARS-CoV-2 test

Symptomtext

chest pains; short of breath; troponin at 4.6/Went up to 5.0/troponin peaked at 9.9; Echo shows decreased blood flow (50%); This is a spontaneous report from a contactable consumer (patient). A 38-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at same age, via an unspecified route of administration, administered in arm left on 15Apr2021 12:45 (Batch/Lot Number: EW0162) as single dose for covid-19 immunisation. The patient medical history was not reported. Concomitant medication included loratadine/ pseudoephedrine (CLARIDIN-D). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at same age, administered in arm left on 25Mar2021 04:30 PM (Batch/Lot Number: ER8730) for covid-19 immunisation. The patient experienced chest pains, and short of breath both on 17Apr2021 22:00. Tried to sleep it off. 24 hours, didn't get better. On 17Apr2021, went to local ER, troponin at 4.6 ng/L. Doctors didn't believe it, did another blood draw. Went up to 5.0 ng/L. Ambulance to nearby hospital, troponin peaked at 9.9 ng/L. Echo showed decreased blood flow (50%) and EKG was irregular. Angiogram and CT scan show no blood clots or blockages. Patient was a healthy 38 male who was a distance runner. No history of chest pain or heart issues. Doctors determined incident almost certainly related to vaccine. The serious criteria for all events were hospitalization and duration were 2 days. The adverse events result in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Colchicine received as treatment for the adverse events. Prior to vaccination, the patient was not diagnosed with COVID 19. Since the vaccination, the patient has been tested for COVID 19. The patient underwent lab tests and procedures which included COVID test (COVID antibody blood test): negative on 20Apr2021, Covid test (Nasal Swab): negative on 18Apr2021. The outcomes of events were recovering.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
2,0
Labordaten
Test Date: 20210417; Test Name: Angiogram; Result Unstructured Data: Test Result:no blood clots or blockages; Test Date: 20210417; Test Name: CT scan; Result Unstructured Data: Test Result:no blood clots or blockages; Test Date: 20210417; Test Name: Echo; Test Result: 50 %; Comments: decreased blood flow; Test Date: 20210417; Test Name: EKG; Result Unstructured Data: Test Result:Irregular; Test Date: 20210420; Test Name: COVID test (COVID antibody blood test); Test Result: Negative ; Test Date: 20210418; Test Name: Covid test (Nasal Swab); Test Result: Negative ; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:peaked at 9.9 ng/L; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:Went up to 5.0 ng/L; Test Date: 20210417; Test Name: Troponin; Result Unstructured Data: Test Result:4.6 ng/L
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
CLARIDIN-D
Allergien
-
Vorherige Impfungen
-

VAERS 1296125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NY
Alter
39,0
Geschlecht
F
Eingang
07.05.2021
Impfdatum
19.04.2021
Beginn
04.05.2021
Tage bis Beginn
15,0
Dosis
1
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Exposure during pregnancy Foetal death

Symptomtext

Two weeks after the first vaccine was administered the patient experience fetal death intrauterine. Pt was 18 weeks and 5 days. G4P3 EDD 10/3/21

Weitere VAERSDATA-Felder
Praegender Schweregrund
Foetal death
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
Nausea due to pregnancy
Vorgeschichte
Anxiety & depression
Andere Medikamente
Medical marijuana dextroamphetamine-amphetamine 25mg Prenatal vitamins famotidine 20mg Sertaline 100mg
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1294679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
VA
Alter
57,0
Geschlecht
F
Eingang
07.05.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anaphylactic shock Blood pressure increased Blood pressure measurement Dysphagia Loss of consciousness Oropharyngeal discomfort Paraesthesia

Symptomtext

anaphylactic shock; I started to pass out; tingle in her lip/her tongue was tingling; her BP was 150 something over 90 she thinks she heard 159 before they gave her; her throat is starting to close up; trouble swallowing; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in left arm on 17Apr2021 at 14:45 (Batch/Lot Number: EW0162), at the age of 57 year, as single dose for COVID-19 immunization. Medical history included anaphylactic reaction to spider bites, pruritus, ongoing hypersensitivity, ongoing allergy to arthropod sting. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took Lortab [hydrocodone bitartrate;paracetamol] and experienced drug hypersensitivity, singulair and experienced drug hypersensitivity. Concomitant medication included neocell super collagen, 6g collagen six per day as supplement. On 17Apr2021 the patient experienced anaphylactic shock, reported as medically significant. The patient reported "I started to pass out. She had tingle in her lip/her tongue was tingling. Her BP was 150 something over 90 she thinks she heard 159 before they gave her; her throat was starting to close up, she had trouble swallowing. She went to the hospital straight from the clinic where she received the vaccine. The patient reported the following: she went for shot at 14:30 and they didn't take her in until like 14:45. Patient stated after the shot, she sat down and knew she had to wait for at least 30 minutes because 10 years ago she had a couple events of anaphylactic shock due to spider bites. So patient stated she knew she should wait. Patient stated she started reading her book and had trouble swallowing at 5 minutes later, but she decided to keep reading book. Patient stated that 10 minutes she started to feel a tingle in her lip and then she started paying attention. Patient stated she then went over to the staff and found someone who was not busy and explained to them what was happening. Patient stated that staff member walked her over to the nurses station and at that time her tongue was tingling and this is not even 15 minutes later. The patient stated they gave her 10 ml of Benadryl and at about 15:05 at about 15:20 they had to give her the epinephrine because her throat was starting to close up and they called 911. The patient stated unfortunately the epi didn't; it may have slowed it down but she started to pass out. She don't know what her oxygen level was at that point. The patient recalled that her BP was 150 something over 90, she thinks she heard 159 before they gave her the Benadryl or at the same time. The patient stated once the EMT's showed up they gave her an IV and gave her steroids and that stopped her throat from closing and they gave her oxygen and that made her feel so much better. The patient stated it's like reliving the story here and her throat is starting to close up, patient clarified she is just choking up thinking about it and denied that her throat is actually closing up during call. The patient stated they did a lot of testing after did not show any signs of clotting which was good. Patient stated she did have trouble breathing, and they checked heart and her heart was fine. Patient states her throat, that is the part she needs to talk with her doctor about. Her throat didn't start to completely relax. Patient stated it was still tight on Sunday and Monday and that was a little concerning for her, but as far as lab work, no. Patient stated she was not admitted to the hospital, she spent 5 hours in the emergency room (ER) for observation and got sent home with an epi pen which she is not going to get and steroids which she finished yesterday. Patient stated she is not going to get the EpiPen because she does not foresee any need for it due to the amount of money it costs. Patient stated it costs $232 dollars and that is just too much, not to mention the amount of money she will have to give to hospital for the bill due to this event. Patient stated she is pretty clear that she won't or shouldn't get the next shot. The clinical outcome of Anaphylactic shock was recovered on 20Apr2021. The clinical outcome of her throat is starting to close up was not recovered. The clinical outcome of the remaining events was unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic shock
Hospital-Tage
-
Labordaten
Test Name: BP; Result Unstructured Data: Test Result:BP was 150 over 90; Comments: 150 something over 90; Test Name: BP; Result Unstructured Data: Test Result:159 over 90; Comments: something over 90 she thinks she heard 159 before they gave her the Benadryl
Aktuelle Erkrankungen
Allergic reaction; Allergy to arthropod sting
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylactic reaction; Itchy scalp
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1266861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
OH
Alter
69,0
Geschlecht
F
Eingang
28.04.2021
Impfdatum
15.04.2021
Beginn
16.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Cerebral haemorrhage Eye disorder Eye haemorrhage Incomplete course of vaccination Thrombosis

Symptomtext

4-16-21 @ 2PM SHE HAD A 'SHADOW IN HER RT EYE'. DROVE TO ER. DX WITH CLOT TO RT EYE AND LT OCCIPITAL AREA OF BRIAN. NO SURGERY. WAS GIVEN PLAVIX. HAS APPT WITH EYE DOCTOR ON MAY 3RD. SAW A NEUROLOGIST AND PCP. SHE IS DOING BETTER NOW AND RT EYE HAS 'CLEARED UP'. WILL NOT BE GETTING SECOND DOSE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral haemorrhage
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1238704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

kritisch
Staat
MN
Alter
45,0
Geschlecht
M
Eingang
27.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute myocardial infarction Anticoagulant therapy Arteriogram coronary normal Chest pain Echocardiogram abnormal Left ventricular dysfunction Myocarditis Troponin increased Dyspnoea Electrocardiogram Electrocardiogram ST segment elevation Ejection fraction Hyperhidrosis Pyrexia SARS-CoV-2 test Troponin

Symptomtext

Symptoms consistent with myocarditis; EKG showed very subtle diffuse ST elevations; chest pain; dyspnea; Troponin trended to 19; This is a spontaneous report from a contactable physician. A 45-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 08Apr2021 (Batch/Lot number and Expiration date were not reported) as a single dose for COVID-19 immunization. Relevant medical history included chronic back pain, degenerative disc disease, and Clostridium difficile (C. Diff) colitis; the patient had no risk factors for cardiac disease other than obesity; all from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient previously took cyclobenzaprine and pregabalin (LYRICA) and experienced allergies. It was unknown if the patient had other vaccine in four weeks. The patient had no COVID-19 prior vaccination. On 08Apr2021, 8 hours after the 2nd Pfizer vaccine was received, the patient developed chest pain with dyspnea. It was also reported that on 08Apr2021, troponin trended to 19; electrocardiogram (EKG) showed very subtle diffuse ST elevations; and the symptoms were consistent with myocarditis. All the adverse events (AE) resulted in a doctor or other healthcare professional office/clinic visit; an emergency room/department or urgent care; and hospitalization on an unspecified date for 3 days. The patient underwent lab tests and procedures, which included other/Xpert Xpress SARS-CoV-at assay: negative on 10Apr2021 (post vaccination). Therapeutic measures were taken as a result of all the events, which included colchicine and ibuprofen. The patient was recovering from all the events. Information on the batch/lot number has been requested.; Sender's Comments: Information provided was so limited to prevent a meaningful medical assessment. Other than a temporal association, there was no evidence or argument suggesting a causal relationship for BNT162B2 in the reported events, serious due to hospitalization. Otherwise, this patient did not show risk factors for cardiac disease, except for obesity. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute myocardial infarction
Hospital-Tage
3,0
Labordaten
Test Date: 20210408; Test Name: EKG; Result Unstructured Data: Test Result:very subtle diffuse ST elevations; Test Date: 20210410; Test Name: Other/Xpert Xpress SARS-CoV-at assay; Test Result: Negative ; Test Date: 20210408; Test Name: troponin; Result Unstructured Data: Test Result:trended to 19
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: C.difficile colitis; Chronic back pain; Degenerative disc disease; Obesity (no risk factors for cardiac disease other than obesity)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1257240

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
NY
Alter
30,0
Geschlecht
F
Eingang
25.04.2021
Impfdatum
13.04.2021
Beginn
14.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Angiogram Blood glucose Chest X-ray Differential white blood cell count Echocardiogram Electrocardiogram Fibrin D dimer Full blood count Metabolic function test Prothrombin time Pulmonary embolism SARS-CoV-2 test Syncope Ultrasound scan Urine analysis

Symptomtext

Vasovagal syncope and acute pulmonary embolism

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary embolism
Hospital-Tage
1,0
Labordaten
4/14: CBC and differential, comprehensive metabolic panel, POCT glucose, POCT iStat chem 8, POCT iStat troponin, POCT iStat VBG lactic acid, Protime INR, urinalysis, EKG 4/18-4/19: same as above, also echocardiogram, covid test, chest x-Ray, CT with contrast, D-dimer, leg ultrasound
Aktuelle Erkrankungen
None, seasonal allergies
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1204266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

kritisch
Staat
CA
Alter
94,0
Geschlecht
F
Eingang
13.04.2021
Impfdatum
08.04.2021
Beginn
09.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

Patient expired day after receiving second dose of Pfizer COVID-19 vaccine

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
UTI,
Vorgeschichte
Osteoporosis Dermatitis
Andere Medikamente
Metoprolol tartrate 100 mg nifedipine ER 30 mg Flomax 0.4 mg capsule Cipro 500 mg tablet Macrobid 100 mg benazepril 40 mg tamsulosin simivastatin 20 mg.
Allergien
Penicillin Sulfa Trimethoprim
Vorherige Impfungen
-

VAERS 2613637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PR
Alter
52,0
Geschlecht
F
Eingang
12.04.2023
Impfdatum
15.04.2021
Beginn
14.06.2022
Tage bis Beginn
425,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Arrhythmia Asthenia Back pain Blood pressure measurement Bone pain Carpal tunnel syndrome Deep vein thrombosis Depression Fatigue COVID-19 SARS-CoV-2 test Vaccination failure Haemorrhage Hypersensitivity Hypertension Hypoaesthesia Livedo reticularis

Symptomtext

Nasal Swab: Positive; Nasal Swab: Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 25Mar2021 as dose 1, single (Lot number: ER8730), in left arm and on 15Apr2021 as dose 2, single (Lot number: EW0162) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Congenital Protein S deficiency" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 14Jun2022, outcome "unknown" and all described as "Nasal Swab: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (14Jun2022) Positive, notes: Nasal Swab.; Sender's Comments: Linked Report(s) : PR-PFIZER INC-202300148624 same patient, same product, different dose and events.;PR-PFIZER INC-202300150204 same patient, same product, different dose and events.;

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deep vein thrombosis
Hospital-Tage
-
Labordaten
Test Date: 20220614; Test Name: SARS CoV-2 ANTIGEN; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Protein S deficiency
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2528318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AL
Alter
38,0
Geschlecht
M
Eingang
09.12.2022
Impfdatum
14.05.2021
Beginn
06.01.2022
Tage bis Beginn
237,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Angina pectoris Bundle branch block left Cardiac monitoring Cardiomyopathy Catheterisation cardiac Chest pain Dyspnoea Echocardiogram Ejection fraction decreased Electrocardiogram Hypertension Magnetic resonance imaging heart Myocarditis Scan myocardial perfusion

Symptomtext

SIGNS/SYMPTOMS Chest pain/angina SOB Reduced Ejection Fraction TREATMENT ECHO ECG/EKG Nuclear stress test Left heart catheterization Heart Monitor

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
4,0
Labordaten
ECHO - 01/06/22-01/09/22, 04/29/2022 ECG/EKG -multiple Nuclear stress test - 01/06/22-01/09/22 Left heart catheterization -03/01/2022 Heart Monitor - 02/18/2022 MRI cardiac - 03/17/2022 RESULTS Myocarditis LBBB (Left Bundle Branch Block) HTN Cardiomyopathy (resolved)
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Fish oil
Allergien
none
Vorherige Impfungen
-

VAERS 2510630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MA
Alter
49,0
Geschlecht
F
Eingang
17.11.2022
Impfdatum
22.05.2021
Beginn
22.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chest discomfort Dyspnoea Eyelid function disorder Facial paralysis Impaired driving ability Lacrimation increased Muscular weakness Neuropathy peripheral Pain in extremity Paraesthesia Peripheral swelling Pruritus Throat tightness Visual impairment

Symptomtext

She got her vaccine, 20 minutes later while she was walking home the first symptom was difficulty breathing. She felt like her chest and her throat were not able to expand to receive air. Her son has allergies and she called the allergy doctor but it was a Saturday so she did not receive an answer. She was a nursing student, and she went home and started taking things she had at home which was Prednisone, Albuterol, and an Epi-Pen and instructed her husband to use it if she needed it. Her breathing started getting better, but the itching on her face, scalp and her hands was very bad to the point that she wanted to remove the skin from her body. Then after a few hours something weird happened, her left eye was drooping, closing by itself and was tearing which started to come out. The right side was fine. The breathing was ok, itchiness. The next day she woke up the arm was extremely swollen and painful, which she felt it was a normal reaction. She put some cortisone cream around the area. After that the pins and needles feeling started from her lower scalp, neck, shoulder and all along both arms. Over the days she started to have weakness on her upper extremities, difficult for her to do anything with her arms, which was scary. She contacted her PCP, NP and she prescribed her a series of supplements to burst her immune system for 4 months, which was SPM active, Lysine, and also essential immunoacid, Turiva supplement, liposomal glutathione;, zinc, vitamins. Over 3 months the neuropathy was still there, it was random and not more constant on a daily basis, but randomly she had pins and needles on her shoulders, and especially on her skull on the back. She also had pins and needles randomly. The symptoms then went away around September of 2021. She saw an ENT/Allergist as he is her son's allergist where he gets shots, and saw him because she wanted to receive allergy testing. He said that there was nothing that he could do, and if he did the testing she would end up being positive which would be a false/positive. He told her that she could not have any vaccines right now and was not worth it to undergo testing. This was in another state. She moves and saw an allergist who told her that she was not a candidate for the vaccine and that she would test positive, and told her she could start a voluntary trial where they could inject smaller doses and she could be intubated if something should happen. She did not do this. The drooping of her mouth started while she was driving her car and had to stop driving as she was not able to see, but did go away after a few hours. She is still taking vitamin D, Vitamin C, omega 3 and other supplements now. She was advised by her doctor not to get any other vaccines, the NP. Months before she had Botox xoemin which did not work for her, and she had an allergic to that which was a local reaction on her face where the puncture was done, very swollen face as she had her forehead and crows-feet injected. She called her allergist and her NP which they gave her Prednisone. This was 3 months before the vaccine. She was informed by her allergist not to do it anymore. He felt that there was nothing that she should have been allergic to, but not to do it anymore. She went to Italy this summer and she has a plastic surgeon in the family and he injected her with Botox and did not have any reaction to that

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None.
Vorgeschichte
None.
Andere Medikamente
None.
Allergien
Oxycodone (couldn't talk or walk).
Vorherige Impfungen
-

VAERS 2500686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
45,0
Geschlecht
M
Eingang
07.11.2022
Impfdatum
27.04.2021
Beginn
09.09.2022
Tage bis Beginn
500,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 SARS-CoV-2 test positive Syncope

Symptomtext

09/09/22 presents to ED for "multiple episodes of syncope". PMHx of "heroin IV drug use still active, false positive hep C"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
09/10/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2324263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
60,0
Geschlecht
M
Eingang
20.06.2022
Impfdatum
20.11.2021
Beginn
28.02.2022
Tage bis Beginn
100,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Deep vein thrombosis Pain in extremity Ultrasound Doppler abnormal

Symptomtext

Arm soreness after injection, Right leg DVT - occlusive thrombus in the right popliteal vein as determined by peripheral venous ultrasound of the right leg on 03/01/2022. Patient had no prior change of medications, no travel, no extended time without movement, no trauma in the months prior to DVT

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deep vein thrombosis
Hospital-Tage
-
Labordaten
Peripheral venous ultrasound of the right leg on 03/01/2022
Aktuelle Erkrankungen
None
Vorgeschichte
Hypertension. HIV. hepatitis B. hepatitis C. Anal intraepithelial neoplasia. Adrenal adenoma. EtOH abuse . Diabetes Mellitus Type 2. Hyperlipidemia.
Andere Medikamente
?metFORMIN 500 mg tablet 1 tab(s) orally 2 times a day ?glipiZIDE 10 mg tablet 1 tab(s) orally once a day ?folic acid 1 mg tablet 1 tab(s) orally once a day ?doxycycline hyclate 100 mg capsule 1 cap(s) orally 2 times a day ?Biktarvy 50 mg-2
Allergien
None known
Vorherige Impfungen
-

VAERS 2315112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
38,0
Geschlecht
F
Eingang
10.06.2022
Impfdatum
02.05.2021
Beginn
02.05.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Inappropriate schedule of product administration Petechiae Syncope

Symptomtext

petechiae (5days after 2. vaccine); Prev dose administration date: 18Apr2021/ dose 2 administration date:02May2021; Fainting-like spells very 2-10mins for 3 hours - 13mins after 2. vaccine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02May2021 at 08:30 as dose 2, single (Lot number: EW0162) at the age of 38 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "low blood pressure" (unspecified if ongoing); "migraines" (unspecified if ongoing), notes: migraines (25+years); "endometriosis" (unspecified if ongoing); "meningioma" (unspecified if ongoing), notes: meningioma in left cavernous sinus. Concomitant medication(s) included: LEVONORGESTREL. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: EW0172, Location of injection: Arm Left, Vaccine Administration Time: 08:30 AM), administration date: 18Apr2021, when the patient was 38-year-old, for COVID-19 immunization, reaction(s): "Suspected vestibular migraine", "Fainting", "overactive stress response and sensory overload, sensitivity to light, sound, temperature change and smell causing dizziness", "electrical flash in brain after watching TV", "dizziness when reading on mobile and scrolling or switching windows on computer; dizziness when reading glossy pages", "erratic blood pressure: increased blood pressure by 20-30 points during most part of a day or too low when tired or after meals (85/55)", "increased heart rate", "heart palpitations", "increased body temperature by 1-2 degrees", "dermatitis-like rash", "dermatitis-like rash". The following information was reported: SYNCOPE (disability, medically significant) with onset 02May2021, outcome "not recovered", described as "Fainting-like spells very 2-10mins for 3 hours - 13mins after 2. vaccine"; INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 02May2021, outcome "unknown", described as "Prev dose administration date: 18Apr2021/ dose 2 administration date:02May2021"; PETECHIAE (disability) with onset 07May2021, outcome "not recovered", described as "petechiae (5days after 2. vaccine)". The events "fainting-like spells very 2-10mins for 3 hours - 13mins after 2. vaccine", "petechiae (5days after 2. vaccine)" and "prev dose administration date: 18apr2021/ dose 2 administration date:02may2021" required physician office visit. Therapeutic measures were taken as a result of syncope, petechiae. Clinical course: No other vaccine in four weeks. Treatment Meclizine, B2 vitamin. No covid prior vaccination. No Covid tested post vaccination. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Endometriosis; Low blood pressure; Meningioma (meningioma in left cavernous sinus); Migraine (migraines (25+years))
Andere Medikamente
LEVONORGESTREL
Allergien
-
Vorherige Impfungen
-

VAERS 2310802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
17,0
Geschlecht
F
Eingang
06.06.2022
Impfdatum
11.12.2021
Beginn
26.05.2022
Tage bis Beginn
166,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Adenovirus test positive Adrenal insufficiency Asymptomatic COVID-19 Bladder catheterisation Blood sodium increased Body temperature increased COVID-19 Chest X-ray normal Condition aggravated Diabetes insipidus Hypervolaemia Hypotension Hypovolaemic shock Intensive care Pyrexia SARS-CoV-2 test positive Sepsis Shock

Symptomtext

Hospitalized (5.26.22); COVID-19 positive (5.26.22); fully vaccinated PLUS booster BRIEF OVERVIEW: Primary Care Physician at Discharge: MD Admission Date: 5/26/2022 Discharge Date: 5/31/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Diabetes insipidus (HCC) [E23.2] Adrenal insufficiency (HCC) [E27.40] Acute febrile illness in child [R50.9] Sepsis, due to unspecified organism, unspecified whether acute organ dysfunction present (HCC) [A41.9] Sepsis (HCC) [A41.9] Hypovolemic shock (HCC) [R57.1] HOSPITAL COURSE: Overall Assessment: The patient is a 17 y.o. female with PMHx significant for spastic quadriplegic CP, hydrocephalus with VP shunt, epilepsy, schizencephaly, septo-optic dysplasia, 3rd nerve palsy, diabetes insipidus, adrenal insufficiency, secondary amenorrhea, g tube dependence,slow-transit constipation, short stature, global developmental delay, disordered sleep, and aggressive behavior who presented with fever and increased urine output, admitted to the PICU for steroid and fluid refractory shock. Respiratory/ENT: Patient remained on room air throughout her hospitalization Cardiovascular: Her multiple episodes of hypotension throughout her admission. She initially received to 60 mL per kg bolus of IV fluid. She was started on epinephrine and vasopressin both of which were eventually weaned off. She was dosed with stress dose steroids with 50 mg of hydrocortisone followed by 12.5 mg every 6 hours. Eventually she was weaned off the epinephrine. He was attempted to wean her onto her home dose of steroids but she did require further boluses of normal saline. This was likely secondary to her diabetes insipidus and excessive urine output. She will have a steroid taper at discharge. Her DDAVP was uptitrated throughout her hospitalization. Renal/Genitourinary: Patient was initially excessively fluid positive due to her shock. Following multiple doses of DDAVP and dose titration she was nearly euvolemic upon discharge. She did have a Foley catheter for urine output measured. FEN/GI: Patient's sodium levels fluctuate throughout her course. Upon discharge her sodium had been between 140 and 150 for multiple days. Her tube feeds were restarted after initially being held. Infectious Disease: Patient noted to be COVID + last week of April, asymptomatic at that time. Again tested positive on admission. Unclear if active COVID infection vs viral shedding. Noted to have rectal temp to 105.8 prior to admission. Film array positive for adenovirus and COVID 19. UA not suggestive of UTI. No focal consolidation on CXR. Possible related to MISC with prior COVID infection noted. Vanc and CTX started in the ED. Received 48 hours of empiric rocephin, cultures no growth to date, MISC workup noncontributory. Mom is also COVID positive with new symptoms. Endocrine: patient has a history of diabetes insipidus as well as adrenal insufficiency. See the above for stress dose steroid dosing. She require titration of her DDAVP prior to discharge. Discharge instructions have her taking 50 mcg of DDAVP at night and 100 mcg in the morning. Prior to admission she was taking at 50 mg nightly. We will have a 5 day steroid taper with hydrocortisone. These instructions were provided to the patient. Neurologic/Pain/Sedation/Psych: Throughout her hospitalization room we continued her home antiepileptic medications as well as her baclofen.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypovolaemic shock
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
3rd cranial nerve palsy, left Schizencephaly (HCC) Aggressive behavior Developmental delay Absence of septum pellucidum (HCC) Microcephaly (HCC) Epilepsy (HCC) Essential hypernatremia Dysphagia, s/p gastrostomy Septo-optic dysplasia (HCC) History of neurological testing - DO NOT EDIT Short stature Neuromuscular scoliosis Gastrostomy tube dependent (HCC) Adrenal insufficiency (HCC) Diabetes insipidus (HCC) Complex care coordination Strabismus Hydrocephalus s/p VP shunt Spastic quadriparesis (HCC) Septic shock (HCC) Agitation Sleep disturbance Slow transit constipation Dental caries, unspecified Secondary amenorrhea Vaccination not carried out because of caregiver refusal Incontinence of feces Muscle spasticity Moderate intellectual disabilities Childhood behavior problems Onychomycosis of great toe Skin lesion of back
Andere Medikamente
baclofen (LIORESAL) 10 MG tablet desmopressin (DDAVP) 0.1 MG tablet desmopressin (DDAVP) 0.1 MG tablet desmopressin (DDAVP) 0.1 MG tablet Enteral Nutrition Supplies MISC hydrocortisone (CORTEF) 10 MG tablet hydrocortisone (CORTEF) 5 MG tabl
Allergien
Vancomycin - rash Latex
Vorherige Impfungen
-

VAERS 2284783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
34,0
Geschlecht
F
Eingang
19.05.2022
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Heart rate increased Immediate post-injection reaction Syncope

Symptomtext

04/22/2021 I fainted and had a rapid heart rate right after the vaccine. I was treated by the nurse at the facility. They had me lie down, checked my blood pressure and kept me there for a while.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1854720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
58,0
Geschlecht
F
Eingang
11.05.2022
Impfdatum
10.04.2021
Beginn
02.11.2021
Tage bis Beginn
206,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dysarthria Facial paralysis Neck pain SARS-CoV-2 test positive Vision blurred

Symptomtext

11/2/21 presents to ED with "with slurred speech and right-sided facial droop" and "blurred vision and left-sided neck pain". PMHx "arthritis, carpal tunnel syndrome, osteopenia, cyst of the right kidney".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
11/2/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1854720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
58,0
Geschlecht
F
Eingang
11.05.2022
Impfdatum
10.04.2021
Beginn
02.11.2021
Tage bis Beginn
206,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dysarthria Facial paralysis Neck pain SARS-CoV-2 test positive Vision blurred

Symptomtext

11/2/21 presents to ED with "with slurred speech and right-sided facial droop" and "blurred vision and left-sided neck pain". PMHx "arthritis, carpal tunnel syndrome, osteopenia, cyst of the right kidney".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
11/2/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2268771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
52,0
Geschlecht
M
Eingang
10.05.2022
Impfdatum
16.04.2021
Beginn
16.03.2022
Tage bis Beginn
334,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 SARS-CoV-2 test positive Syncope

Symptomtext

03/16/22 presents to ED for "syncope". PMHx of "complicated renal transplant 2016 (on tacrolimus and mycophenolate), T2DM, HTN, diastolic dysfunction EF 55%"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
03/16/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2258369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
70,0
Geschlecht
M
Eingang
29.04.2022
Impfdatum
26.04.2021
Beginn
19.10.2021
Tage bis Beginn
176,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Anticoagulant therapy Atrial fibrillation Blood test Echocardiogram normal Electrocardiogram abnormal Fatigue Heart rate increased Loss of consciousness Ultrasound scan

Symptomtext

On the evening of October 19, 2021 at about 11:45pm, I felt my heart start to beat rapidly. At that time I believed it was because I was over tired so I went to bed. On the next morning about 7:30am I woke up and took my blood pressure and heart rate and my pressure was 82/55 and my heart rate was about 150. I called my family doctor and related the information to the nurse and they told me to go to the doctor's office - I went in about 1pm that afternoon. They did EKG and determined I was in A-Fib. Heart rate was 157. They called cardiologist team for instructions. I went back home after the visit. I drove into driveway they called and said go straight to ER. I went to ER and while in waiting room I passed out while in wheel chair. They took me into observation room and I "came to". They wanted to keep me overnight for observation, the 20th. Had an Echocardiogram and it was normal. Confirmed A-Fib and ordered blood thinners - Eliquis. Released from hospital on October 21, 2021. I have not had A-fib since that day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
1,0
Labordaten
EKG - A-Fib; Echocardiogram - normal; blood panel; ultrasound
Aktuelle Erkrankungen
None
Vorgeschichte
Ankylosing Spondylitis
Andere Medikamente
Tamsulosin HCL Lisinopril HCTZ Finasteride Diclofenac
Allergien
Penicillin; Bee Venom; Seasonal Allergies
Vorherige Impfungen
-

VAERS 2223910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CO
Alter
25,0
Geschlecht
F
Eingang
08.04.2022
Impfdatum
22.04.2021
Beginn
23.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Cold sweat Contusion Dizziness Feeling hot Foot fracture Headache Hyperhidrosis Limb injury Syncope X-ray abnormal

Symptomtext

Sometime that night after I got the shot I started getting a headache when I woke up the next day it was very severe. I eventually stopped work because my head was pounding. For the rest of the afternoon that day I felt very clammy and sweaty and warm. I got out of bed at 8pm to shower and at that point is when I got dizzy and fainted. I took Tylenol that afternoon for the headache. I went to urgent care the day after I fainted because my toe was very bruised from fainting and they found a fracture.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
X-ray
Aktuelle Erkrankungen
None
Vorgeschichte
Bechet's Disease; Chronic migraines; Hidradenitis Suppurativa; Mild Hypothyroidism
Andere Medikamente
Cimza; Omeprazole; Azathioprine; Fluoxetine; Propranolol; Levothyroxine; Vitamin D3
Allergien
Neosporin; Vancomycin
Vorherige Impfungen
-

VAERS 2209187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OK
Alter
66,0
Geschlecht
M
Eingang
31.03.2022
Impfdatum
29.09.2021
Beginn
07.01.2022
Tage bis Beginn
100,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia Blood glucose increased Blood test COVID-19 Cardiogenic shock Cardioversion Chest X-ray Coagulation test Dyspnoea Glycosylated haemoglobin Heart rate decreased Heart rate irregular Hyporesponsive to stimuli Intensive care SARS-CoV-2 test positive Tachycardia

Symptomtext

Tested positive for COVID on 01/07/2022. 01/09/2022 I went to the ER and I was sent home. 01/11/2022 I wasn't really responsive, and an ambulance was called because my heart beat had gotten down to 35 bpm. I was taken away by ambulance and they had to defibrillate me multiple times before I got into the ER. My blood sugar was at 546 and I was in the ICU for 4 days. I came home and I have had physical therapy and been trying to get my strength back walking for about a month. I tried getting my blood sugar back under control and I did increase glimepiride to 4 mg but I'm still not able to get it under control yet. I also had tachycardia and cardiogenic shock and an irregular heartbeat, and the tachycardia and irregular heartbeat has dissipated. My average blood sugar right now for 14 days is 166 and I'm trying to control my eating and I'm averaging 113 carbs a day. My projected A1C right now is 713. I also had shortness of breath.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cardiogenic shock
Hospital-Tage
4,0
Labordaten
COVID 01/07/2022 POSITIVE; Chest X-Ray, Blood Clot Test, Blood tests. (didn't have paperwork for results)
Aktuelle Erkrankungen
None
Vorgeschichte
CMT (charcot-marie-tooth), Hypertension, Type 2 Diabetes
Andere Medikamente
Low Dose Aspirin, Bupropion, Dexilant 60 mg, Edarbi 80 mg, Gemfibrozil 60 mg, Glimepiride 2 mg, Hydrochlorothiazide 12.5 mg, Pravastatin 20 mg, Zyrtec 10 mg.
Allergien
Nexium
Vorherige Impfungen
-

VAERS 2182259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
TX
Alter
31,0
Geschlecht
M
Eingang
16.03.2022
Impfdatum
09.06.2021
Beginn
19.06.2021
Tage bis Beginn
10,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cerebral venous sinus thrombosis Erectile dysfunction Headache

Symptomtext

Blood Clot: Cerebral venous sinus thrombosis (CVST). This included a sudden onset of the worst and most painful headache at the center top of my skull that I have ever had in my life about 1-2 weeks after the 2nd Pfizer vaccination. The headache's high severity persisted for about a week or two. Then had recurring headaches at the same spot for about 5 months on and also a little to the right of the middle of the skull and also at the back middle of my skull. The severity decreased over time. It was a type of headache that I have never had before, which is scary and makes me feel like I have something wrong with me and that I need to go to the hospital. It is now 10 months later and I very rarely have the headache, probably only once a month. I use to never ever take advil, but now I do sometimes. Also, Erectile Dysfunction, which was severe for 2 weeks immediately after vaccination, then gradually got back to normal at 5 months.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral venous sinus thrombosis
Hospital-Tage
-
Labordaten
I do not have medical insurance, so I did not go to the hospital although I should have.
Aktuelle Erkrankungen
None.
Vorgeschichte
None.
Andere Medikamente
None.
Allergien
None.
Vorherige Impfungen
-

VAERS 2180132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
64,0
Geschlecht
M
Eingang
15.03.2022
Impfdatum
23.04.2021
Beginn
21.02.2022
Tage bis Beginn
304,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia COVID-19 Diarrhoea Dyspnoea Influenza A virus test negative Influenza B virus test Respiratory distress Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

Patient presents with ? Diarrhea Since last thursday, pt has had diarrhea, weakness and shortness of breath ? Shortness of Breath HPI patient is a 65-year-old male presents the ED for respiratory distress. Patient reports he has been having diarrhea since last Thursday. Patient states has been very weak. Patient has had worsening shortness of breath. Patient today is unable to catch his breath and wife convinced him to come to the ER to be evaluated. Patient's wife reports that she was sick a week ago with flulike symptoms. Patient reports that they are both vaccinated against Covid. Patient has a previous history of a kidney transplant, hypertension, hyperlipidemia, A. fib, and GERD. Patient denies any chest pain, syncope, dizziness, recent trauma. Review of Systems CONSTITUTIONAL: no fever, no chills, no fatigue HEAD: no headache or loss of consciousness. EYES: no eye pain, redness or discharge. ENMT: no ear pain, no throat pain; no rhinorrhea or congestion. CARDIAC: No chest pain, no exercise intolerance, no palpations, no peripheral edema RESPIRATORY: no cough, wheezing, shortness of breath or trouble breathing. GI: no nausea, vomiting, diarrhea or abdominal pain. GU: no dysuria, no increased frequency, no hesitancy MSK: no muscle aches, joint pain or injury. NEURO: no dizziness, no change in vision, no seizure SKIN: no rashes; no lacerations or abrasions, no bruising. PSYCH: no recent changes in mood, affect, sleep, or thought processes

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory distress
Hospital-Tage
7,0
Labordaten
<NOCOVER> 1 HEALTH SYSTEM LABORATORY Chart Review Copy (65 yrs) PT CLASS: Inpatient DEPT: 2 SOUTH PCU PATIENT STATUS: Discharged GENDER: male BED: 2S/264 ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA (Order) Contains abnormal data Covid-19, Flu, RSV by NAA Order: Status: Final result Visible to patient: No (inaccessible in myChart) Next appt: 03/30/2022 at 02:30 PM in Cardiology Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 02/28/22 10:35 AM Last Resulted: 02/28/22 12:08 PM
Aktuelle Erkrankungen
? Atrial fibrillation (CMS/HCC) ? Chronic hepatitis B (CMS/HCC) ? Chronic kidney disease ? Hypertension ? Renal transplant recipient
Vorgeschichte
-
Andere Medikamente
APIXABAN (ELIQUIS) 5 MG PO TAB take 1 Tab by mouth twice daily. ATORVASTATIN (LIPITOR) 40 MG PO TAB take 40 mg by mouth once every night at bedtime. LOSARTAN (COZAAR) 100 MG PO TAB take 100 mg by mouth once daily. METOPROLOL
Allergien
No Known Allergies
Vorherige Impfungen
-

VAERS 2161791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
28,0
Geschlecht
F
Eingang
05.03.2022
Impfdatum
14.04.2021
Beginn
12.05.2021
Tage bis Beginn
28,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Heavy menstrual bleeding Thrombosis

Symptomtext

Second Dose: super severe periods, they got really really heavy, to the point she wanted to go to hospital because of the clots; Second Dose: super severe periods, they got really really heavy, to the point she wanted to go to hospital because of the clots; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 28 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 14Apr2021 (Lot number: EW0162) at the age of 28 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Asthma" (ongoing), notes: Additional Information for Other Conditions: Age 5; "Epstein-Barr virus infection" (ongoing), notes: Additional Information for Other Conditions: Age 19. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose Number:01, Lot: EL9264, Time the Vaccination Was Given: 10:45am, Anatomical Location of Administration of Pfizer vaccine considered as suspect: Arm Left, Verbatim:her toes are completely numb and she has loss of feeling in them, they are white), administration date: 17Mar2021, when the patient was 28 years old, for Covid-19 Immunization, reaction(s): "her toes are completely numb and she has loss of feeling in them, they are white", "she has a mottled skin color on her legs, they are purple", "increased and aggravated her migraines", "skin rash/the rash is oozing yellow and gross and somedays it really hurts", "Skin rash/the rash is oozing yellow and gross and somedays it really hurts", "Leg numbness". The following information was reported: THROMBOSIS (medically significant), HEAVY MENSTRUAL BLEEDING (non-serious) all with onset 12May2021, outcome "not recovered" and all described as "Second Dose: super severe periods, they got really really heavy, to the point she wanted to go to hospital because of the clots". Therapeutic measures were taken as a result of thrombosis. Clinical course: She reported side effects from the vaccine, it took her a while to report them, but she got vaccinated in March and had adverse reactions. PCP: Declines to provide information. she had super severe periods, they got really really heavy, to the point she wanted to go to hospital because of the clots. she has never had anything like that. Caller clarifies this was after the second dose and her toes are completely numb and she has loss of feeling in them, they are white. she has never had this issue before she is super healthy and this occurred after the first one. she has a mottled skin color on her legs, they are purple and states since she got the vaccine, within a day or two, she got a skin rash and has it ever since. Caller states the rash is oozing yellow and gross and somedays it really hurts. Caller states she knows it is a Pfizer thing because several people she knows that got it, now have eczema. Caller states this occurred after the first one and the vaccine has increased and aggravated her migraines and she had a 3 day severe migraine. Caller states she should have went to the hospital, it was super bad, the worst migraine of her life. Clarifies this was after the first dose. Caller states on the day of her first vaccine, her leg went numb for ten minutes. Caller states she will never be getting another Pfizer vaccine and she wishes she had never gotten the Covid vaccines.The patient did not received any vaccine prior with in 4 weeks ,The patient did not required to visit physician or emergency room informed to eurologist about increased Migraines and Dermatologist. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Asthma (Additional Information for Other Conditions: Age 5); Epstein-Barr virus infection (Additional Information for Other Conditions: Age 19)
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2157573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
83,0
Geschlecht
F
Eingang
04.03.2022
Impfdatum
22.04.2021
Beginn
01.03.2022
Tage bis Beginn
313,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Hypoxia Intensive care

Symptomtext

84-year-old female presents via EMS for hypoxia. Per EMS the patient was found at home with oxygen saturation in the 70% range. Family states the patient lives at home with them and they care for her. Family states the patient is a hospice patient though she is full code.Hx of colon cancer (h/o chemotherapy in 2020), HLP, PAD, h/o ivc filter. Patient admitted to ICU

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2140165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NV
Alter
56,0
Geschlecht
F
Eingang
25.02.2022
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Diarrhoea Fatigue Headache Hyperhidrosis Loss of consciousness Malaise Muscle disorder Seizure Tremor Vomiting

Symptomtext

Never recovered from Dose 1, continued to have additional issues after the fact including headache, tiredness extreme severe shaking uncontrollable, vomiting, muscle, and diarrhea. In addition, on a road trip began to feel unwell, excessively sweating head seizures and past out. Ambulance was called an taken to hospital locally, local hospital. Symptoms lasted 5 days was in hospital for 2 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
2,0
Labordaten
Contact Physician. Patient was unconscious.
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
No
Vorherige Impfungen
Dose 1, Pfizer-BioNTech.

VAERS 2086400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
17,0
Geschlecht
M
Eingang
24.02.2022
Impfdatum
24.01.2022
Beginn
28.01.2022
Tage bis Beginn
4,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Blood test abnormal Chest X-ray Chest pain Chills Delirium Blood test Dyspnoea Bradycardia Capillary nail refill test Chest discomfort Echocardiogram normal Echocardiogram Electrocardiogram Lethargy Myalgia Myocarditis Neuralgia Pain

Symptomtext

17 Y 7 M generally healthy male who presents with acute onset of chest pain/pressure worsening Friday. He received COVID booster on 1/24/22, had intense fevers, myalgias, "nerve pain" all over body the 24-36hours after the booster. He was pretty much recovering by Wednesday and went to school since Thursday. However, on Friday, by 11:30am, he was feeling very tired and out-of-it. He started feeling chest pressure and pain. Denies tingling/numbness/radiation. Currently, he says he feels a little pressure at the chest right above the epigastric area--more like pressure rather than sharp. At one point, he did feel sharp pain but the general sensation of pressure was more bothering. He was seen this afternoon and referred for labs. His troponin came back elevated at 0.4 and so he was directed to the emergency room for further evaluation. In ED: repeat troponin 0.44, bedside echocardiogram showed good LV function and no effusion. Rest of labs reassuring. After discussion with cardiology, patient admitted for further management. on 1/31/22:17 y.o. M with post COVID vaccine-related myocarditis, admitted with intermittent chest pain and elevated troponin, awaiting troponin level <0.5. Overall down-trended from peak troponin of 3.55 but with mild uptrend in troponin to 1.16 from 0.95. Chest pain improved with q8h motrin, now with only intermittent chest pain (at decr level from prior) and no SOB. Plan: Trending troponin q12h until trop <0.5. 1/28 EKG: NSR, RSR' in V1/V2 prob normal variant per Cards. Also on nicotine patch 14mg/24h started 1/29/22 in s/o hx vaping and desire to quit. Dispo plan & recs per Cardiology: Plan for outpt cards f/u appt, no strenuous activities for 30 days after discharge and no competitive sports for 3 months until he can be cleared with a normal treadmill test. Recheck troponin 1 week after discharge. Will need nicotine patch wean - should be on (14 mg/day) for 2 weeks then step down to step 3 (7 mg/day) for 2 weeks. Exam notable for CV: mildly bradycardic rate, normal rhythm, normal S1/S2, no point tenderness of chest on palpation. Cap refill < 2 sec, normal pulse. Pulm: CTAB. Abd: soft, NT, ND.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
3,0
Labordaten
Results for patient as of 2/24/2022 13:58 1/28/2022 16:48 TROPONIN I: 0.40 (H) 1/28/2022 20:40 TROPONIN I: 0.44 (H) 1/29/2022 04:15 TROPONIN I: 0.84 (H) 1/29/2022 16:25 TROPONIN I: 1.75 (H) 1/30/2022 03:40 TROPONIN I: 3.55 (H) 1/30/2022 15:35 TROPONIN I: 0.95 (H) 1/31/2022 03:50 TROPONIN I: 1.16 (H) 1/31/2022 16:30 TROPONIN I: 0.32 (H) 2/7/2022 16:35 TROPONIN I: <0.02
Aktuelle Erkrankungen
-
Vorgeschichte
h/o Vaping
Andere Medikamente
-
Allergien
Sulfur (not Sulfonamides)
Vorherige Impfungen
-

VAERS 1684315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
46,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blindness Disturbance in attention Dizziness Dysgeusia Feeling hot Dysstasia Loss of personal independence in daily activities Syncope Heart rate increased Hyperhidrosis Hypertension Muscular weakness Presyncope Tremor

Symptomtext

I felt fine for the first 25 minutes after the injection, then felt hot and dizzy. Medics helped me for the next 90 minutes and measured high blood pressure, 5 rounds of syncope, and shaking that looked like a seizure. I have a history of convulsive syncope with dysautonomia, and assume the 5 episodes were convulsive syncope. The shaking lasted 5 hours. I was dizzy and unable to stand much for 3 days. I continued to have dizziness episodes and was unable to function for 1 week. Full recovery took 4 weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Acquired Hypothyroidism Anemia, iron storage deficiency Antiphospholipid Antibodies/Syndrome Atlantoaxial Instability Celiac Disease Cervicogenic Headaches Cervical Instability Chronic Migraine Cubital Tunnel Syndrome Dysmenorrhea Dystonia of left foot Ehlers Danlos Syndrome, hypermobile type (hEDS) Facial weakness Irregular Menses Lung nodule, lung granuloma Mast Cell Activation Syndrome (MCAS) May Thurner Syndrome (iliac vein stent) Meibomian Gland Dysfunction Parasthesias (lower left leg) Pelvic Congestion Syndrome Pituitary microadenoma Prolactin, elevated Postural Orthostatic Tachycardia Syndrome (POTS) Post-Concussion Syndrome Obstructive Sleep Apnea Reynaud?s Disease Somatic Segmental Dysfunction CTLS Spine, Right upper extremity, bilateral feet Thoracic Outlet Syndrome Thrombosis of transverse sinus (CVST) Thyroid cancer Temporomandibular Joint Dysfunction (TMJ) Vertigo Visual Distortion (with dizziness & vertigo) Venous Insufficiency
Andere Medikamente
Armour Thyroid, Aspirin 325mg, Pyridostigmine, Diazepam, Meloxicam, Ketotifen, Famotidine, Xyzal, Cromolyn Sodium, Restasis, Iron, Probiotic, B vitamins (folate, B2, B6, B12), Vitamin C, Vitamin D, Vitamin E, glutathione, CoQ-10, Niacinamid
Allergien
Adhesive Tape, Benadryl, Nitrous Oxide, Versed/Midazolam, Fentanyl, Gabapentin, Tramadol, Sectral/Acebutolol, Lovenox, Progesterone, Tetanus vaccine; gluten
Vorherige Impfungen
-

VAERS 1684315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
46,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blindness Disturbance in attention Dizziness Dysgeusia Feeling hot Dysstasia Loss of personal independence in daily activities Syncope Heart rate increased Hyperhidrosis Hypertension Muscular weakness Presyncope Tremor

Symptomtext

I felt fine for the first 25 minutes after the injection, then felt hot and dizzy. Medics helped me for the next 90 minutes and measured high blood pressure, 5 rounds of syncope, and shaking that looked like a seizure. I have a history of convulsive syncope with dysautonomia, and assume the 5 episodes were convulsive syncope. The shaking lasted 5 hours. I was dizzy and unable to stand much for 3 days. I continued to have dizziness episodes and was unable to function for 1 week. Full recovery took 4 weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Acquired Hypothyroidism Anemia, iron storage deficiency Antiphospholipid Antibodies/Syndrome Atlantoaxial Instability Celiac Disease Cervicogenic Headaches Cervical Instability Chronic Migraine Cubital Tunnel Syndrome Dysmenorrhea Dystonia of left foot Ehlers Danlos Syndrome, hypermobile type (hEDS) Facial weakness Irregular Menses Lung nodule, lung granuloma Mast Cell Activation Syndrome (MCAS) May Thurner Syndrome (iliac vein stent) Meibomian Gland Dysfunction Parasthesias (lower left leg) Pelvic Congestion Syndrome Pituitary microadenoma Prolactin, elevated Postural Orthostatic Tachycardia Syndrome (POTS) Post-Concussion Syndrome Obstructive Sleep Apnea Reynaud?s Disease Somatic Segmental Dysfunction CTLS Spine, Right upper extremity, bilateral feet Thoracic Outlet Syndrome Thrombosis of transverse sinus (CVST) Thyroid cancer Temporomandibular Joint Dysfunction (TMJ) Vertigo Visual Distortion (with dizziness & vertigo) Venous Insufficiency
Andere Medikamente
Armour Thyroid, Aspirin 325mg, Pyridostigmine, Diazepam, Meloxicam, Ketotifen, Famotidine, Xyzal, Cromolyn Sodium, Restasis, Iron, Probiotic, B vitamins (folate, B2, B6, B12), Vitamin C, Vitamin D, Vitamin E, glutathione, CoQ-10, Niacinamid
Allergien
Adhesive Tape, Benadryl, Nitrous Oxide, Versed/Midazolam, Fentanyl, Gabapentin, Tramadol, Sectral/Acebutolol, Lovenox, Progesterone, Tetanus vaccine; gluten
Vorherige Impfungen
-

VAERS 2116081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NV
Alter
61,0
Geschlecht
M
Eingang
16.02.2022
Impfdatum
15.04.2021
Beginn
06.05.2021
Tage bis Beginn
21,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Amnesia Atrial tachycardia Blood test normal Cardiac ablation Cardiac imaging procedure normal Cardiac stress test normal Computerised tomogram normal Electrocardiogram normal Loss of consciousness

Symptomtext

05/6/2021 I was golfing, according to bystanders I passed out. I have no memory of this. I wake in the hospital. MD told me that I was brought in by ambulance with heart rate 183 BPM. Paramedics gave me an injection to slow my heart rate, I stayed overnight for observation. I was released the next day 5/7/2021, I followed up with my heart Dr. in 2 months and was scheduled for a heart ablation, procedure 11/2021, MD said everything looked good. MD said I have arterial tachycardia. There is no treatment for this.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
1,0
Labordaten
Blood work, MRI of the heart, CT scan, EKG, Stress test, all results were perfect.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vit B12; coq10; magnesium; potassium; glucosamine; fish oil; vit D3
Allergien
No
Vorherige Impfungen
-

VAERS 2109994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
61,0
Geschlecht
M
Eingang
14.02.2022
Impfdatum
22.04.2021
Beginn
17.12.2021
Tage bis Beginn
239,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Blood lactate dehydrogenase increased Blood sodium decreased C-reactive protein increased COVID-19 Catheter site pain Chest X-ray abnormal Chest tube insertion Dyspnoea Fibrin D dimer Haemoglobin decreased Influenza A virus test negative Influenza B virus test Influenza virus test negative Neutrophil count increased Oxygen saturation decreased Pneumothorax Respiratory distress Respiratory syncytial virus test negative

Symptomtext

This is a 62y.o. male with hx of COPD on 2-3L Home O2 and HTN, who presents to Facility with a chief complaint of respiratory distress. Patient arrived via EMS with SpO2 of 57%, which did not resolved with NRB and positional changes. Initial CXR demonstrated small left basilar pneumothorax with no appreciable mediastinal shift -- ER resident then placed L Chest Tube, which the patient tolerated with no reported issues, where SpO2 returned to low 90s. Patient currently on 1L NC, SpO2 96% and in no respiratory distress. Upon my examination s/p chest tube placement, patient denies any current SOB, palpitations, headache, or COV -- does not some tenderness at the site where the chest tube was placed. Patient found to be COVID+, received 2nd dose of Pfizer vaccine in April 2021. States for the last ~5 days he has had increasing SOB -- denies any fever/chills, productive cough, N/V/D Upon arrival to the ED: o Vitals: T 97.1?F, BP 145/104, HR 114, RR 18, SpO2 57% on RA. o Lab work obtained and remarkable for: ? COVID+ | WBC 14.4, Neutrophils 12.8 | Hgb 8.7 | Na 129 ? D-Dimer 1041, LDH 535, CRP 12.9 o Imaging demonstrates: ? CXR: small left basilar pneumothorax with no appreciable mediastinal shift o ID and Surgery has been consulted

Weitere VAERSDATA-Felder
Praegender Schweregrund
Respiratory distress
Hospital-Tage
18,0
Labordaten
HEALTH SYSTEM LABORATORY Chart Review Copy (62 yrs) PT CLASS: Inpatient DEPT: 4 SOUTH FH PATIENT STATUS: Discharged GENDER: male BED: 4SFH/474 ORD DR: AUTH DR: Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Status: Final result Visible to patient: No (inaccessible in myChart) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the FDA Emergency Use Authorization (EUA) for laboratories certified under CLIA to perform high complexity testing. This test has not been FDA cleared or approved. Specimen Collected: 12/18/21 10:47 PM Last Resulted: 12/18/21 11:58 PM Order Details View Encounter
Aktuelle Erkrankungen
? Chronic obstructive pulmonary disease (CMS/HCC) ? Hypertension
Vorgeschichte
? Chronic obstructive pulmonary disease (CMS/HCC) ? Hypertension
Andere Medikamente
Advair Diskus 500-50 MCG/DOSE INHAL AEROSOL POWDER, BREATH ACTIVATED inhale 1 Puff into the lungs every 12 hours. 12/18/2021 Unknown time albuterol (2.5 MG/3ML) 0.083% INHAL Nebu Soln inhale 2.5 mg using breathing machine every 8 hours as n
Allergien
Bee Venom
Vorherige Impfungen
-

VAERS 2102107

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
OK
Alter
34,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
01.04.2021
Beginn
03.05.2021
Tage bis Beginn
32,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Arthralgia Blood test Cerebral disorder Chest X-ray normal Chest discomfort Chest pain Dissociation Dizziness Dyspnoea Electric shock sensation Electrocardiogram PR prolongation Electrocardiogram abnormal Eye movement disorder Gait disturbance Head discomfort Heart rate increased Hypoaesthesia Joint swelling

Symptomtext

Paranthesias (arms, legs, head completely "asleep" and numb for months), tachycardia, pulsatile tinnitus, uncontrolled rapid eye movement-seems similar to nystagmus, electric shock sensation in head, body spasms- particularly in neck and head, chest pain and discomfort, shortness of breath, limb discomfort- difficulty to walk across the room, sore joints/tendons, knee pain, peripheral neuropathy, vertigo, tendonitis, temperature regulation issues, internal vibrations in brain, heaviness feeling in head, shooting sharp pain in arms/legs, burning skin feeling, blurred vision, sensitive scalp- unable to brush hair, heart palpitations, low grade fever, disconnected feeling, swollen ankles, dizziness, nerve pain especially with feet- warm water feels scalding & sometimes feels like stepping on glass, heart rate spikes when doing small tasks or taking a hot shower. Abnormal EKG- showed short PR syndrome and possible combined atrial enlargement. Visited Emergency room. Normal blood work.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
Chest xray-normal results Blood work extensive Ekg abnormal
Aktuelle Erkrankungen
N/a
Vorgeschichte
N/a
Andere Medikamente
N/a
Allergien
N/a
Vorherige Impfungen
-

VAERS 1493729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
35,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
24.05.2021
Beginn
02.06.2021
Tage bis Beginn
9,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Anticoagulant therapy Anxiety Computerised tomogram Condition aggravated Aspartate aminotransferase increased Basophil count Blood albumin Blood bilirubin Blood calcium AST to platelet ratio index Albumin globulin ratio Anticoagulation drug level Blood chloride Blood creatine phosphokinase Blood creatinine Blood glucose Blood immunoglobulin A

Symptomtext

Ovarian vein thrombosis; Microscopic colitis; Diverticulitis; Gestational diabetes mellitus; Elevated rheumatoid factor; Anticoagulation management encounter; Dehydration; Vaccine reaction; Chronic abdominal pain; Dizziness; GAD (generalized anxiety disorder); Generalized pain; Hypertriglyceridemia; Irritable bowel syndrome with diarrhea; Irritable bowel syndrome with diarrhea; Malaise and fatigue; Malaise and fatigue; Moderate episode of recurrent major depressive disorder; Severe anxiety; nausea; loss of appetite; vomiting; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 35 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm right, administration date 24May2021 13:15 (Lot number: EW0177) at the age of 35 years as dose 2, single for covid-19 immunisation. Vaccination facility type Workplace Clinic. Relevant medical history included: "appendectomy", start date: Nov2009, stop date: Nov2009, notes: Appendectomy Nov2009; "Sinus surgery x 2" (unspecified if ongoing), notes: Sinus surgery x 2, Sinus surgery 2014/2015; "anxiety" (unspecified if ongoing); "gestational diabetes" (unspecified if ongoing); "House dust mite allergy" (unspecified if ongoing). Family medical history included Maternal grand mother heart attack x 2, hyperlipidemia. Concomitant medication(s) included: CELEXA [CELECOXIB] taken for anxiety (ongoing); ATORVASTATIN; BUSPIRONE; CITALOPRAM; CLINDAMYCIN; CLONAZEPAM; IPRATROPIUM; IVERMECTIN; LEVONORGESTREL; OMEPRAZOLE; ONDANSETRON; SELZENTRY; QNASL taken for dust allergy (ongoing), ongoing Atrovent nasal spray for dust mite allergy. Vaccination history included: Bnt162b2 (Dose 1:Time: 4:00 Pm, Right arm, Intramuscular, Lot # EW0162), administration date: 20Apr2021, when the patient was 35 years old, for COVID-19 Immunization, reaction(s): "stomach ache/ Abdominal pain", "nausea/nauseous", "body aches all over/Body Aches/Pain", "Ovarian Vein Thrombosis", "Colitis", "Vomiting", "Diarrhea", "Fatigue/ tired/ felt exhausted", "Brain Fog", "Insomnia", "Panic Attacks", "Depression", "14% weight loss/lost 14% of her body weight", "high rheumatoid factor", "high inflammatory markers", "high cytokines", "Fear", "Blood clot", "Intestinal pain", "felt unwell", "arm soreness", "dizzy", "loss of appetite", "Chills". The following information was reported: OVARIAN VEIN THROMBOSIS (prolonged hospitalization, medically significant) with onset 02Jun2021, described as "Ovarian vein thrombosis"; COLITIS MICROSCOPIC (medically significant), described as "Microscopic colitis"; DIVERTICULITIS (medically significant), described as "Diverticulitis"; GESTATIONAL DIABETES (medically significant), described as "Gestational diabetes mellitus"; RHEUMATOID FACTOR, described as "Elevated rheumatoid factor"; ANTICOAGULATION DRUG LEVEL, described as "Anticoagulation management encounter"; DEHYDRATION, described as "Dehydration"; HYPERSENSITIVITY, described as "Vaccine reaction"; ABDOMINAL PAIN, described as "Chronic abdominal pain"; DIZZINESS, described as "Dizziness"; GENERALISED ANXIETY DISORDER, described as "GAD (generalized anxiety disorder)"; PAIN, described as "Generalized pain"; HYPERTRIGLYCERIDAEMIA, described as "Hypertriglyceridemia"; IRRITABLE BOWEL SYNDROME, DIARRHOEA, and all described as "Irritable bowel syndrome with diarrhea"; MALAISE, FATIGUE, and all described as "Malaise and fatigue"; DEPRESSION, described as "Moderate episode of recurrent major depressive disorder"; ANXIETY, outcome "unknown", described as "Severe anxiety"; NAUSEA, outcome "recovering", described as "nausea"; DECREASED APPETITE, outcome "recovering", described as "loss of appetite"; VOMITING, outcome "recovering", described as "vomiting". Outcome of other events were unknown. The patient prolonged hospitalization for ovarian vein thrombosis (hospitalization duration: 3 day(s)). The events "ovarian vein thrombosis" was evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: albumin globulin ratio: (20Aug2021) 1.9; (27Aug2021) 1.7; (22Sep2021) 1.9; (08Oct2021) 1.5; aspartate aminotransferase increased: (08Aug2021) 114; (20Aug2021) 95; (27Aug2021) 95; (22Sep2021) 95; ast to platelet ratio index: (08Aug2021) 22; (20Aug2021) 12; (27Aug2021) 14; (22Sep2021) 19; (08Oct2021) 22; basophil count: (08Aug2021) 0.9; (20Aug2021) 0.4; (20Aug2021) 0.03; (27Aug2021) 0.5; (27Aug2021) 0.04; (22Sep2021) 0.9; (22Sep2021) 0.06; (08Oct2021) 0.9; (08Oct2021) 0.04; (22Oct2021) 1.1; (22Oct2021) 0.06; blood albumin: (08Aug2021) 4.4; (20Aug2021) 4.2; (27Aug2021) 4.5; (22Sep2021) 4.6; (08Oct2021) 4.4; blood bilirubin: (20Aug2021) 0.8; (27Aug2021) 1.1; (22Sep2021) 0.8; (08Oct2021) 0.7; blood calcium: (08Aug2021) 9.3; (20Aug2021) 8.6; (27Aug2021) 9.4; (22Sep2021) 9.3; (08Oct2021) 9.3; blood chloride: (08Aug2021) 103; (20Aug2021) 109; (27Aug2021) 106; (22Sep2021) 106; (08Oct2021) 103; blood creatine phosphokinase: (02Jun2021) 30; blood creatinine: (08Aug2021) 0.6; (20Aug2021) 0.7; (27Aug2021) 0.7; (22Sep2021) 0.7; (08Oct2021) 0.6; (22Oct2021) 0.7; blood glucose: (08Aug2021) 91; (20Aug2021) h 111; (27Aug2021) 96; (22Sep2021) 87; blood immunoglobulin a: (28Jun2021) 0.20; (08Aug2021) 0.20; (13Aug2021) 0.30; (20Aug2021) 0.30; (27Aug2021) 0.30; (22Sep2021) 0.20; (08Oct2021) 0.20; (22Oct2021) 0.20; (08Aug2021) 0.01; (20Aug2021) 0.02; (27Aug2021) 0.02; (22Sep2021) 0.01; (08Oct2021) 0.01; (22Oct2021) 0.01; blood magnesium: (03Jun2021) 2.2; blood phosphorus: (08Aug2021) 54; (20Aug2021) 48; (27Aug2021) 50; (22Sep2021) 50; (08Oct2021) 54; blood pressure measurement: (07Jan2022) 100/67; blood sodium: (08Aug2021) 138; (20Aug2021) 141; (27Aug2021) 140; (22Sep2021) 140; (08Oct2021) 138; blood thyroid stimulating hormone: (13May2021) 1.84; blood urea: (08Aug2021) 9; (20Aug2021) 13; (27Aug2021) 11; (22Sep2021) 10; (08Oct2021) 9; body temperature: (07Jan2022) 36.9 Centigrade; carbon dioxide: (08Aug2021) 21; (20Aug2021) 23; (27Aug2021) 22; (22Sep2021) 24; (08Oct2021) 21; computerised tomogram: (02Jun2021) left gonadal vein thrombosis; (03Jun2021) small hemorrhagic cyst of right ovary; (08Jun2021) resolving thrombosis of left ovarian vein; c-reactive protein: (13May2021) 0.43; (02Jun2021) 0.36; (28Jun2021) 2; (10Jul2021) less than 0.30; (26Jul2021) 2; (04Aug2021) less than 0.30; eosinophil count: (08Aug2021) 0.4; (20Aug2021) 0.0; (20Aug2021) 0.00; (27Aug2021) 0.4; (27Aug2021) 0.03; (22Sep2021) 1.4; (22Sep2021) 0.09; (08Oct2021) 0.4; (08Oct2021) l 0.02; (22Oct2021) 1.3; (22Oct2021) 0.07; globulin: (08Aug2021) 3.0; (20Aug2021) 2.2; (27Aug2021) 2.7; (22Sep2021) 2.4; (08Oct2021) 3.0; glomerular filtration rate: (20Aug2021) 95; (27Aug2021) 95; (22Sep2021) 95; (08Oct2021) 114; glycosylated haemoglobin: (13May2021) 5.2; haematocrit: (28Jun2021) 39.6; (28Jun2021) 37.3; (10Jul2021) 41.9; (20Jul2021) 42.0, notes: POC Hct:43.0; (26Jul2021) 34.7; (04Aug2021) 38.5; (08Aug2021) 38.4; (10Aug2021) 40.8; (13Aug2021) 39.8; (20Aug2021) 36.0; (27Aug2021) 38.3; (22Sep2021) 38.2; (08Oct2021) 38.4; (22Oct2021) 39.6; haemoglobin: (13May2021) 13.9; (14May2021) l 10.8; (15May2021) 13.9; (02Jun2021) 13.8; (03Jun2021) 12.0; (08Jun2021) 14.4; (23Jun2021) 13.0; (28Jun2021) 12.7; (10Jul2021) 13.6; (20Jul2021) 14.4, notes: POC Hgb: 14.6; (26Jul2021) 11.8; (04Aug2021) 12.5; (08Aug2021) 12.7; (10Aug2021) 13.1; (20Aug2021) 11.6; (20Aug2021) 13.0; (27Aug2021) 12.6; (22Sep2021) 12.5; (22Sep2021) 13.9; (08Oct2021) 12.7; (22Oct2021) 12.9; heart rate: (07Jan2022) 16; hormone level abnormal: (08Aug2021) 17; (20Aug2021) 15; (27Aug2021) 20; (22Sep2021) 23; (08Oct2021) 17; immunology test: (04Jun2021) h 32.0; (28Jun2021) h 33.0; (26Jul2021) h 24.0; (04Aug2021) h 20.0; (20Aug2021) h 19.0; (27Aug2021) h 19.0; investigation: (08Aug2021) 14; (20Aug2021) 9; (27Aug2021) 12; (22Sep2021) 10; (08Oct2021) 14; (08Aug2021) 15; (20Aug2021) 19; (27Aug2021) 16; (22Sep2021) 14; (08Oct2021) 15; (13May2021) 103; (08Aug2021) 91; (20Aug2021) h 111; (27Aug2021) 96; (22Sep2021) 87; (08Oct2021) 91; (08Aug2021) 0.0; (20Aug2021) 0.0; (20Aug2021) 0.000; (27Aug2021) 0.0; (27Aug2021) 0.000; (22Sep2021) 0.0; (22Sep2021) 0.000; (08Oct2021) 0.0; (08Oct2021) 0.000; (22Oct2021) 0.0; (22Oct2021) 0.000; (08Aug2021) 4.6; (20Aug2021) 4.3; (27Aug2021) 4.3; (22Sep2021) 4.2; (08Oct2021) 4.6; (04Jun2021) h 32.00; (28Jun2021) h 33.0; (26Jul2021) h 24.0; (04Aug2021) h 20.00; (20Aug2021) h 19.0; (27Aug2021) h 19.0; (13May2021) negative; lymphocyte count: (08Aug2021) 32.4; (20Aug2021) 13.6; (27Aug2021) 16.6; (22Sep2021) 31.6; (08Oct2021) 32.4; (22Oct2021) 32.2; (08Aug2021) 1.45; (20Aug2021) l 0.95; (27Aug2021) 1.22; (22Sep2021) 2.03; (08Oct2021) 1.45; (22Oct2021) 1.68; mean cell haemoglobin: (13May2021) 29.9; (14May2021) 29.7; (15May2021) 29.2; (02Jun2021) 29.5; (03Jun2021) 29.9; (08Jun2021) 29.9; (23Jun2021) 30.0; (28Jun2021) 34.0; (28Jun2021) 30.2; (10Jul2021) 29.7; (20Jul2021) 30.8; (26Jul2021) 30.7; (04Aug2021) 30.1; (08Aug2021) 30.0; (10Aug2021) 29.8; (13Aug2021) 29.8; (20Aug2021) 30.0; (27Aug2021) 30.3; (22Sep2021) 30.0; (08Oct2021) 30.0; (22Oct2021) 29.8; mean cell haemoglobin concentration: (13May2021) 33.7; (14May2021) l 32.1; (15May2021) 33.1; (02Jun2021) 32.8; (03Jun2021) 32.6; (08Jun2021) 33.4; (23Jun2021) 33.7; (10Jul2021) 32.5; (20Jul2021) 34.3; (26Jul2021) 34.0; (04Aug2021) 32.5; (08Aug2021) 33.1; (10Aug2021) l 32.1; (20Aug2021) 32.2; (27Aug2021) 32.9; (22Sep2021) 32.7; (08Oct2021) 33.1; (22Oct2021) 32.6; mean cell volume: (13May2021) 88.6; (14May2021) 92.3; (15May2021) 88.2; (02Jun2021) 90.0; (03Jun2021) 91.8; (08Jun2021) 89.4; (23Jun2021) 89.1; (28Jun2021) 88.8; (10Jul2021) 91.5; (20Jul2021) 89.7; (26Jul2021) 90; (04Aug2021) 92.8; (08Aug2021) 90.6; (10Aug2021) 92.7; (13Aug2021) 91.3; (20Aug2021) 93.0; (27Aug2021) 92.1; (22Sep2021) 91.6; (08Oct2021) 90.6; (22Oct2021) 91.5; mean platelet volume: (13May2021) 10.3; (14May2021) 10.4; (15May2021) 10.4; (02Jun2021) 10.5; (03Jun2021) 10.5; (08Jun2021) 10.6; (23Jun2021) 10.3; (10Jul2021) 10.4; (20Jul2021) 11.0; (04Aug2021) 11.5; (10Aug2021) 11.4; monocyte count: (08Aug2021) 7.6; (20Aug2021) 3.4; (20Aug2021) 0.24; (27Aug2021) 4.2; (27Aug2021) 0.31; (22Sep2021) 5.5; (22Sep2021) 0.35; (08Oct2021) 7.6; (08Oct2021) 0.34; (22Oct2021) 5.2; (22Oct2021) 0.27; neutrophil count: (13May2021) 69.8; (14May2021) 48.8; (15May2021) 67.9; (02Jun2021) 80.7; (03Jun2021) 61.0; (08Jun2021) 73.3; (23Jun2021) 61.2; (28Jun2021) 61.6; (10Jul2021) 76.9; (20Jul2021) 78.9; (26Jul2021) 76; (04Aug2021) 73.4; (08Aug2021) 58.5; (08Aug2021) 2.62; (10Aug2021) 78.9; (13Aug2021) 80.0; (20Aug2021) 82.3; (20Aug2021) 5.74; (27Aug2021) 78.0; (27Aug2021) 5.74; (22Sep2021) 60.4; (22Sep2021) 3.88; (08Oct2021) 58.5; (08Oct2021) 2.62; (22Oct2021) 60.0; (22Oct2021) 3.13; platelet count: (13May2021) 342; (14May2021) 266; (15May2021) 333; (02Jun2021) h 390; (03Jun2021) 321; (08Jun2021) h 419; (23Jun2021) 310; (28Jun2021) 321; (10Jul2021) 361; (20Jul2021) 349; (26Jul2021) 277; (04Aug2021) 290; (08Aug2021) 237; (10Aug2021) 32.7; (13Aug2021) 312; (20Aug2021) 254; (27Aug2021) 250; (22Sep2021) 256; (08Oct2021) 237; (22Oct2021) 286; po2: (07Jan2022) 96 %; protein total decreased: (08Aug2021) 7.4; (20Aug2021) 6.4; (27Aug2021) 7.2; (22Sep2021) 7.0; (08Oct2021) 7.4; red blood cell count: (13May2021) 4.65; (14May2021) l 3.64; (15May2021) 4.76; (02Jun2021) 4.68; (03Jun2021) 4.01; (04Jun2021) 4.68; (28Jun2021) 4.20; (10Jul2021) 4.82; (20Jul2021) 4.33; (26Jul2021) 4.40; (08Aug2021) 4.24; (10Aug2021) 4.58; (20Aug2021) l 3.87; (27Aug2021) 4.16; (27Aug2021) 3.84; (22Sep2021) 4.17; (22Sep2021) 4.15; (08Oct2021) 4.24; (22Oct2021) 4.33; red cell distribution width increased: (13May2021) 12.2; (14May2021) 12.8; (15May2021) 12.7; (02Jun2021) 12.3; (03Jun2021) 12.4; (08Jun2021) 12.3; (23Jun2021) 12.2; (10Jul2021) 10.4; (20Jul2021) 11.0; (26Jul2021) 12.1; (04Aug2021) 11.5; (08Aug2021) 11.8; (10Aug2021) 11.4; (20Aug2021) 12.6; (27Aug2021) 12.4; (22Sep2021) 12.0; (08Oct2021) 11.8; (22Oct2021) l 11.5; respiratory rate: (07Jan2022) 16; thyroxine: (13May2021) 1.36; tri-iodothyronine: (13May2021) 2.5; ultrasound doppler: (03Jun2021) no dvt; white blood cell count: (13May2021) 7.86; (14May2021) 5.50; (15May2021) 7.42; (02Jun2021) 8.17; (03Jun2021) 7.62; (08Jun2021) 8.61; (23Jun2021) 7.64; (28Jun2021) 5.19; (10Jul2021) 8.94; (20Jul2021) h 12.11; (26Jul2021) 8.4; (04Aug2021) 7.44; (08Aug2021) 4.48; (10Aug2021) 6:27; (20Aug2021) 6.98; (27Aug2021) 7.36; (22Sep2021) 6.42; (08Oct2021) 4.48; (22Oct2021) 5.22. Therapeutic measures were taken as a result of ovarian vein thrombosis, abdominal pain, colitis microscopic, rheumatoid factor, anticoagulation drug level, dehydration, hypersensitivity. In summary, she had received the Pfizer COVID vaccine in Apr2021 and May2021. Soon after, she developed abdominal pain and found to have a left gonadal thrombosis on 03Mar2021. She was ultimately started on Eliquis. She had a hypercoagulation evaluation that was negative and has been working with COVID spe-cialists based in withheld who has started her on a protocol to help her ongoing symptoms of nau-sea, loss of appetite and abdominal pain. Since starting this protocol, she reports feeling better and now able to eat better with less nausea and vomiting. She reports ongoing intermittent abdominal pain and has now had multiple scans since Jun show-ing no acute pathology. Her abd MRI in Aug revealed resolution of her left gonadal vein thrombus. She reports no lower leg swelling and denies any chest pain, shortness of breath or cough. All other systems reviewed and are negative. Polytypic mature B cells are show a normal kappa to lambda ratio of 1.9:1. Unremarkable T cells are 85.3% of lymphocytes (CD4:CD8 ratio 1.21:1). NK cells are 5.3% of lym-phocytes. Diagnostic immunophenotypic features of involvement by a non-Hodgkin B or T cell lym-phoma are not identified. The final diagnosis is based upon flow cytometric analysis of the speci-men. Microscopic slides are examined for correlation. Gross Description: A: A specimen labeled with the patient's name and "peripheral blood" per container is received in 1-7mL EDTA tube and I-10mL heparin tube on 16Aug2021. Submitted entirely for flow cytometry. (mr/flow). Final Diagnosis: A: Right colon, biopsy: Colonic mucosa with focal active colitis. B: Left colon, biopsy: Colonic mucosa with focal active colitis. Comment: Both biopsies demonstrate focal active colitis of minimal inflammatory intensity, This is a nonspe-cific finding that can be seen in several conditions including infection, drug-induced gastrointestinal mucosal injury, and Crohn's disease despite the absence of granulomatous inflammation. No changes of ulcerative colitis are identified. There is no evidence of lymphocytic or collagenous coli-tis. No dysplasia or malignancy is identified. Clinical Information: Abdominal pain. Gross Description: A: Received in formalin, labeled with the patients name and "A. Right colon random biopsy", are nine, 0.2-0.7 cm, tan soft tissue fragments entirely submitted in A1-A2. B: Received in formalin, labeled with the patient's name and "B. Left colon random biopsy", are multiple, 0.1-0.7 cm, tan soft tissue fragments entirely submitted in B1-B2.jns VR). Current Treatment: Eliquis 5mg BID Physical Examination: Vitals: 07Jan2022 14:52 BP: 100/67;Pulse: 86 ;Resp: 16 ;Temp: 36.9 degree C ; SpO2: 96%; Ecog Performance Status, ECOG: 0; Constitutional: General: She is not in acute distress. Appearance: Normal appearance. She is normal weight. She is not ill-appearing, toxic-appearing or diaphoretic. Hent: Head: Normocephalic and atraumatic. Eyes: General: No scleral icterus. Extraocular Movements: Extraocular movements intact. Conjunctiva/sclera: Conjunctivae normal. Pupils: Pupils are equal, round, end reactive to light. Cardiovascular: Rate and Rhythm: Normal rate. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Abdominal: General: There is no distension. Neurological: General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time. Mental status is at baseline. Cranial Nerves: No cranial nerve deficit. Sensory: No sensory deficit. Motor: No weakness. Coordination: Coordination normal. Gait: Gait normal. Deep Tendon Reflexes: Reflexes normal. Psychiatric: Mood and Affect: Mood normal. Thought Content: Thought content normal. Judgment: Judgment normal. Laboratory Studies: 22Oct2021 LFTs normal. Imaging/Pertinent Studies: MRI pelvis 17Sep2021: Impression: 1. Improved left gonadal vein thrombus with near complete resolution. No new thrombus. 2. Normal ovaries. 3. Intrauterine device present in expected position.CT abd/pelvis Jun2021, Impression:1. No bowel obstruction or acute inflammatory process identified. 2. Suspicion of left gonadal vein thrombosis. Mixing artifact seems less likely given the homogeneous enhancement of other venous structures. 3. No free fluid or adenopathy. Assessment: Withheld has history of left gonadal vein thrombus that occurred in the context of getting the Pfizer COVID vaccine. We spent significant time reviewing the potential contribution of the vaccine to her recent blood clot but that this is not clear and difficult to prove. The clot certainly occurred within a period of weeks after her second vaccine. I discussed my limited expertise in COVID com-plications and defer any discussion about the association of her ongoing symptoms to the COVID vaccine. Given the spotty data about the association of blood clots with the vaccine could warrant a more prolonged period of anticoagulation. We discussed the risk of bleeding and very low risk of spontaneous bleeding on Eliquis which could be life threatening but very rare outside of an accident or trauma. With that in mind, I expressed my support to continue Eliquis for an extended period of time, maybe up to a year while she continues to sort out onoging symptoms post COVID vaccine. Plan: continued follow up with her "COVID' providers; continue Eliquis 5mg BID for now, likely plan for a year but will continue to discuss the risks/benefits of continued anticoagulation. Home Medications:Current Outpatient Medications:atorvastatin 10 MG tablet: No dose, route, or frequency recorded; busPlRone (BUSPAR): 15 mg, Oral, Daily; citalopram (CELEXA): 40 mg, Oral, Daily; clindamycin 1 % gel: 1 application, Topical Daily PRN; clonazePAM 0.5 MG tablet : 1 tablet, oral, Daily PRN; Eiquis: 5 mg, Oral, 2 times daily; ipratropium 0.03 % nasal spray: 2 sprays; ivermectin 3 MG tablet: 9mg po qAm / 3mg po qhs every 3 days, 0 Refill(s); levonorgestrel (Mirena) 52 mg (20 mcg/day) IUD: 1 each, Intrauterine, Every 6 months; omeprazole 20 MG DR capsule: No dose, route, or frequency recorded; ondansetron 4 MG disintegrating tablet: No dose, route, or frequency recorded; Qnasl 80 MCG/ACT nasal spray: 1 spray, Nasal, Daily PRN; Saline 0.9 % aerosol solution: 1 spray; Selzentry: 300 mg, Oral, Daily.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pelvic venous thrombosis
Hospital-Tage
3,0
Labordaten
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Test Name: Creatinine; Result Unstructured Data: Test Result:0.6; Test Date: 20211022; Test Name: Creatinine; Result Unstructured Data: Test Result:0.7; Test Date: 20210808; Test Name: Glucose; Result Unstructured Data: Test Result:91; Test Date: 20210820; Test Name: Glucose; Result Unstructured Data: Test Result:H 111; Test Date: 20210827; Test Name: Glucose; Result Unstructured Data: Test Result:96; Test Date: 20210922; Test Name: Glucose; Result Unstructured Data: Test Result:87; Test Date: 20210628; Test Name: ig; Result Unstructured Data: Test Result:0.20; Test Date: 20210808; Test Name: ig; Result Unstructured Data: Test Result:0.20; Test Date: 20210813; Test Name: ig; Result Unstructured Data: Test Result:0.30; Test Date: 20210820; Test Name: ig; Result Unstructured Data: Test Result:0.30; Test Date: 20210827; Test Name: ig; Result Unstructured Data: Test Result:0.30; Test Date: 20210922; Test Name: ig; Result Unstructured Data: Test Result:0.20; Test Date: 20211008; Test Name: ig; Result Unstructured Data: Test Result:0.20; Test Date: 20211022; Test Name: ig; Result Unstructured Data: Test Result:0.20; Test Date: 20210808; Test Name: IG; Result Unstructured Data: Test Result:0.01; Test Date: 20210820; Test Name: IG; Result Unstructured Data: Test Result:0.02; Test Date: 20210827; Test Name: IG; Result Unstructured Data: Test Result:0.02; Test Date: 20210922; Test Name: IG; Result Unstructured Data: Test Result:0.01; Test Date: 20211008; Test Name: IG; Result Unstructured Data: Test Result:0.01; Test Date: 20211022; Test Name: IG; Result Unstructured Data: Test Result:0.01; Test Date: 20210603; Test Name: Magnesium; Result Unstructured Data: Test Result:2.2; Test Date: 20210808; Test Name: Alkal phosphate; Result Unstructured Data: Test Result:54; Test Date: 20210820; Test Name: Alkal phosphate; Result Unstructured Data: Test Result:48; Test Date: 20210827; Test Name: Alkal phosphate; Result Unstructured Data: Test Result:50; Test Date: 20210922; Test Name: Alkal phosphate; Result Unstructured Data: Test Result:50; Test Date: 20211008; Test Name: Alkal phosphate; Result Unstructured Data: Test Result:54; Test Date: 20220107; Test Name: BP; Result Unstructured Data: Test Result:100/67; Test Date: 20210808; Test Name: Sodium Lvl; Result Unstructured Data: Test Result:138; Test Date: 20210820; Test Name: Sodium Lvl; Result Unstructured Data: Test Result:141; Test Date: 20210827; Test Name: Sodium Lvl; Result Unstructured Data: Test Result:140; Test Date: 20210922; Test Name: Sodium Lvl; Result Unstructured Data: Test Result:140; Test Date: 20211008; Test Name: Sodium Lvl; Result Unstructured Data: Test Result:138; Test Date: 20210513; Test Name: TSH; Result Unstructured Data: Test Result:1.84; Test Date: 20210808; Test Name: BUN; Result Unstructured Data: Test Result:9; Test Date: 20210820; Test Name: BUN; Result Unstructured Data: Test Result:13; Test Date: 20210827; Test Name: BUN; Result Unstructured Data: Test Result:11; Test Date: 20210922; Test Name: BUN; Result Unstructured Data: Test Result:10; Test Date: 20211008; Test Name: BUN; Result Unstructured Data: Test Result:9; Test Date: 20220107; Test Name: Temp; Result Unstructured Data: Test Result:36.9 Centigrade; Test Date: 20210808; Test Name: CO2; Result Unstructured Data: Test Result:21; Test Date: 20210820; Test Name: CO2; Result Unstructured Data: Test Result:23; Test Date: 20210827; Test Name: CO2; Result Unstructured Data: Test Result:22; Test Date: 20210922; Test Name: CO2; Result Unstructured Data: Test Result:24; Test Date: 20211008; Test Name: CO2; Result Unstructured Data: Test Result:21; Test Date: 20210602; Test Name: CT AIP; Result Unstructured Data: Test Result:Left gonadal vein thrombosis; Test Date: 20210603; Test Name: CT AIP; Result Unstructured Data: Test Result:Small hemorrhagic cyst of right ovary; Test Date: 20210608; Test Name: CT AIP; Result Unstructured Data: Test Result:Resolving thrombosis of left ovarian vein; Test Date: 20210513; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:0.43; Test Date: 20210602; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:0.36; Test Date: 20210628; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:2; Test Date: 20210710; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:less than 0.30; Test Date: 20210726; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:2; Test Date: 20210804; Test Name: C Reactive Prot; Result Unstructured Data: Test Result:less than 0.30; Test Date: 20210808; Test Name: eosinophil; Result Unstructured Data: Test Result:0.4; Test Date: 20210820; Test Name: eosinophil; Result Unstructured Data: Test Result:0.0; Test Date: 20210820; Test Name: eosinophil; Result Unstructured Data: Test Result:0.00; Test Date: 20210827; Test Name: eosinophil; Result Unstructured Data: Test Result:0.4; Test Date: 20210827; Test Name: eosinophil; Result Unstructured Data: Test Result:0.03; Test Date: 20210922; Test Name: eosinophil; Result Unstructured Data: Test Result:1.4; Test Date: 20210922; Test Name: eosinophil; Result Unstructured Data: Test Result:0.09; Test Date: 20211008; Test Name: eosinophil; Result Unstructured Data: Test Result:0.4; Test Date: 20211008; Test Name: eosinophil; Result Unstructured Data: Test Result:L 0.02; Test Date: 20211022; Test Name: eosinophil; Result Unstructured Data: Test Result:1.3; Test Date: 20211022; Test Name: eosinophil; Result Unstructured Data: Test Result:0.07; Test Date: 20210808; Test Name: Globulin; Result Unstructured Data: Test Result:3.0; Test Date: 20210820; Test Name: Globulin; Result Unstructured Data: Test Result:2.2; Test Date: 20210827; Test Name: Globulin; Result Unstructured Data: Test Result:2.7; Test Date: 20210922; Test Name: Globulin; Result Unstructured Data: Test Result:2.4; Test Date: 20211008; Test Name: Globulin; Result Unstructured Data: Test Result:3.0; Test Date: 20210820; Test Name: GFR; Result Unstructured Data: Test Result:95; Test Date: 20210827; Test Name: GFR; Result Unstructured Data: Test Result:95; Test Date: 20210922; Test Name: GFR; Result Unstructured Data: Test Result:95; Test Date: 20211008; Test Name: GFR; Result Unstructured Data: Test Result:114; Test Date: 20210513; Test Name: Hgb A1c; Result Unstructured Data: Test Result:5.2; Test Date: 20210628; Test Name: HCT; Result Unstructured Data: Test Result:39.6; Test Date: 20210628; Test Name: HCT; Result Unstructured Data: Test Result:37.3; Test Date: 20210710; Test Name: HCT; Result Unstructured Data: Test Result:41.9; Test Date: 20210720; Test Name: HCT; Result Unstructured Data: Test Result:42.0; Comments: POC Hct:43.0; Test Date: 20210726; Test Name: HCT; Result Unstructured Data: Test Result:34.7; Test Date: 20210804; Test Name: HCT; Result Unstructured Data: Test Result:38.5; Test Date: 20210808; Test Name: HCT; Result Unstructured Data: Test Result:38.4; Test Date: 20210810; Test Name: HCT; Result Unstructured Data: Test Result:40.8; Test Date: 20210813; Test Name: HCT; Result Unstructured Data: Test Result:39.8; Test Date: 20210820; Test Name: HCT; Result Unstructured Data: Test Result:36.0; Test Date: 20210827; Test Name: HCT; Result Unstructured Data: Test Result:38.3; Test Date: 20210922; Test Name: HCT; Result Unstructured Data: Test Result:38.2; Test Date: 20211008; Test Name: HCT; Result Unstructured Data: Test Result:38.4; Test Date: 20211022; Test Name: HCT; Result Unstructured Data: Test Result:39.6; Test Date: 20210513; Test Name: hgb; Result Unstructured Data: Test Result:13.9; Test Date: 20210514; Test Name: hgb; Result Unstructured Data: Test Result:L 10.8; Test Date: 20210515; Test Name: hgb; Result Unstructured Data: Test Result:13.9; Test Date: 20210602; Test Name: hgb; Result Unstructured Data: Test Result:13.8; Test Date: 20210603; Test Name: hgb; Result Unstructured Data: Test Result:12.0; Test Date: 20210608; Test Name: hgb; Result Unstructured Data: Test Result:14.4; Test Date: 20210623; Test Name: hgb; Result Unstructured Data: Test Result:13.0; Test Date: 20210628; Test Name: hgb; Result Unstructured Data: Test Result:12.7; Test Date: 20210710; Test Name: hgb; Result Unstructured Data: Test Result:13.6; Test Date: 20210720; Test Name: hgb; Result Unstructured Data: Test Result:14.4; Comments: POC Hgb: 14.6; Test Date: 20210726; Test Name: hgb; Result Unstructured Data: Test Result:11.8; Test Date: 20210804; Test Name: hgb; Result Unstructured Data: Test Result:12.5; Test Date: 20210808; Test Name: hgb; Result Unstructured Data: Test Result:12.7; Test Date: 20210810; Test Name: hgb; Result Unstructured Data: Test Result:13.1; Test Date: 20210820; Test Name: hgb; Result Unstructured Data: Test Result:11.6; Test Date: 20210820; Test Name: hgb; Result Unstructured Data: Test Result:13.0; Test Date: 20210827; Test Name: hgb; Result Unstructured Data: Test Result:12.6; Test Date: 20210922; Test Name: hgb; Result Unstructured Data: Test Result:12.5; Test Date: 20210922; Test Name: hgb; Result Unstructured Data: Test Result:13.9; Test Date: 20211008; Test Name: hgb; Result Unstructured Data: Test Result:12.7; Test Date: 20211022; Test Name: hgb; Result Unstructured Data: Test Result:12.9; Test Date: 20220107; Test Name: Pulse; Result Unstructured Data: Test Result:16; Test Date: 20210808; Test Name: ALT; Result Unstructured Data: Test Result:17; Test Date: 20210820; Test Name: ALT; Result Unstructured Data: Test Result:15; Test Date: 20210827; Test Name: ALT; Result Unstructured Data: Test Result:20; Test Date: 20210922; Test Name: ALT; Result Unstructured Data: Test Result:23; Test Date: 20211008; Test Name: ALT; Result Unstructured Data: Test Result:17; Test Date: 20210604; Test Name: Immunology; Result Unstructured Data: Test Result:H 32.0; Test Date: 20210628; Test Name: Immunology; Result Unstructured Data: Test Result:H 33.0; Test Date: 20210726; Test Name: Immunology; Result Unstructured Data: Test Result:H 24.0; Test Date: 20210804; Test Name: Immunology; Result Unstructured Data: Test Result:H 20.0; Test Date: 20210820; Test Name: Immunology; Result Unstructured Data: Test Result:H 19.0; Test Date: 20210827; Test Name: Immunology; Result Unstructured Data: Test Result:H 19.0; Test Date: 20210808; Test Name: AGAP; Result Unstructured Data: Test Result:14; Test Date: 20210820; Test Name: AGAP; Result Unstructured Data: Test Result:9; Test Date: 20210827; Test Name: AGAP; Result Unstructured Data: Test Result:12; Test Date: 20210922; Test Name: AGAP; Result Unstructured Data: Test Result:10; Test Date: 20211008; Test Name: AGAP; Result Unstructured Data: Test Result:14; Test Date: 20210808; Test Name: BUN/CRE; Result Unstructured Data: Test Result:15; Test Date: 20210820; Test Name: BUN/CRE; Result Unstructured Data: Test Result:19; Test Date: 20210827; Test Name: BUN/CRE; Result Unstructured Data: Test Result:16; Test Date: 20210922; Test Name: BUN/CRE; Result Unstructured Data: Test Result:14; Test Date: 20211008; Test Name: BUN/CRE; Result Unstructured Data: Test Result:15; Test Date: 20210513; Test Name: eAG; Result Unstructured Data: Test Result:103; Test Date: 20210808; Test Name: Glucose Lvl; Result Unstructured Data: Test Result:91; Test Date: 20210820; Test Name: Glucose Lvl; Result Unstructured Data: Test Result:H 111; Test Date: 20210827; Test Name: Glucose Lvl; Result Unstructured Data: Test Result:96; Test Date: 20210922; Test Name: Glucose Lvl; Result Unstructured Data: Test Result:87; Test Date: 20211008; Test Name: Glucose Lvl; Result Unstructured Data: Test Result:91; Test Date: 20210808; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20210820; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20210820; Test Name: NRBC; Result Unstructured Data: Test Result:0.000; Test Date: 20210827; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20210827; Test Name: NRBC; Result Unstructured Data: Test Result:0.000; Test Date: 20210922; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20210922; Test Name: NRBC; Result Unstructured Data: Test Result:0.000; Test Date: 20211008; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20211008; Test Name: NRBC; Result Unstructured Data: Test Result:0.000; Test Date: 20211022; Test Name: NRBC; Result Unstructured Data: Test Result:0.0; Test Date: 20211022; Test Name: NRBC; Result Unstructured Data: Test Result:0.000; Test Date: 20210808; Test Name: POC Na; Result Unstructured Data: Test Result:4.6; Test Date: 20210820; Test Name: POC Na; Result Unstructured Data: Test Result:4.3; Test Date: 20210827; Test Name: POC Na; Result Unstructured Data: Test Result:4.3; Test Date: 20210922; Test Name: POC Na; Result Unstructured Data: Test Result:4.2; Test Date: 20211008; Test Name: POC Na; Result Unstructured Data: Test Result:4.6; Test Date: 20210604; Test Name: RF Quant; Result Unstructured Data: Test Result:H 32.00; Test Date: 20210628; Test Name: RF Quant; Result Unstructured Data: Test Result:H 33.0; Test Date: 20210726; Test Name: RF Quant; Result Unstructured Data: Test Result:H 24.0; Test Date: 20210804; Test Name: RF Quant; Result Unstructured Data: Test Result:H 20.00; Test Date: 20210820; Test Name: RF Quant; Result Unstructured Data: Test Result:H 19.0; Test Date: 20210827; Test Name: RF Quant; Result Unstructured Data: Test Result:H 19.0; Test Date: 20210513; Test Name: Toxicology Studies; Test Result: Negative ; Test Date: 20210808; Test Name: lymphocytes; Result Unstructured Data: Test Result:32.4; Test Date: 20210820; Test Name: lymphocytes; Result Unstructured Data: Test Result:13.6; Test Date: 20210827; Test Name: lymphocytes; Result Unstructured Data: Test Result:16.6; Test Date: 20210922; Test Name: lymphocytes; Result Unstructured Data: Test Result:31.6; Test Date: 20211008; Test Name: lymphocytes; Result Unstructured Data: Test Result:32.4; Test Date: 20211022; Test Name: lymphocytes; Result Unstructured Data: Test Result:32.2; Test Date: 20210808; Test Name: Lymphocytes; Result Unstructured Data: Test Result:1.45; Test Date: 20210820; Test Name: Lymphocytes; Result Unstructured Data: Test Result:L 0.95; Test Date: 20210827; Test Name: Lymphocytes; Result Unstructured Data: Test Result:1.22; Test Date: 20210922; Test Name: Lymphocytes; Result Unstructured Data: Test Result:2.03; Test Date: 20211008; Test Name: Lymphocytes; Result Unstructured Data: Test Result:1.45; Test Date: 20211022; Test Name: Lymphocytes; Result Unstructured Data: Test Result:1.68; Test Date: 20210513; Test Name: MCH; Result Unstructured Data: Test Result:29.9; Test Date: 20210514; Test Name: MCH; Result Unstructured Data: Test Result:29.7; Test Date: 20210515; Test Name: MCH; Result Unstructured Data: Test Result:29.2; Test Date: 20210602; Test Name: MCH; Result Unstructured Data: Test Result:29.5; Test Date: 20210603; Test Name: MCH; Result Unstructured Data: Test Result:29.9; Test Date: 20210608; Test Name: MCH; Result Unstructured Data: Test Result:29.9; Test Date: 20210623; Test Name: MCH; Result Unstructured Data: Test Result:30.0; Test Date: 20210628; Test Name: MCH; Result Unstructured Data: Test Result:34.0; Test Date: 20210628; Test Name: MCH; Result Unstructured Data: Test Result:30.2; Test Date: 20210710; Test Name: MCH; Result Unstructured Data: Test Result:29.7; Test Date: 20210720; Test Name: MCH; Result Unstructured Data: Test Result:30.8; Test Date: 20210726; Test Name: MCH; Result Unstructured Data: Test Result:30.7; Test Date: 20210804; Test Name: MCH; Result Unstructured Data: Test Result:30.1; Test Date: 20210808; Test Name: MCH; Result Unstructured Data: Test Result:30.0; Test Date: 20210810; Test Name: MCH; Result Unstructured Data: Test Result:29.8; Test Date: 20210813; Test Name: MCH; Result Unstructured Data: Test Result:29.8; Test Date: 20210820; Test Name: MCH; Result Unstructured Data: Test Result:30.0; Test Date: 20210827; Test Name: MCH; Result Unstructured Data: Test Result:30.3; Test Date: 20210922; Test Name: MCH; Result Unstructured Data: Test Result:30.0; Test Date: 20211008; Test Name: MCH; Result Unstructured Data: Test Result:30.0; Test Date: 20211022; Test Name: MCH; Result Unstructured Data: Test Result:29.8; Test Date: 20210513; Test Name: MCHC; Result Unstructured Data: Test Result:33.7; Test Date: 20210514; Test Name: MCHC; Result Unstructured Data: Test Result:L 32.1; Test Date: 20210515; Test Name: MCHC; Result Unstructured Data: Test Result:33.1; Test Date: 20210602; Test Name: MCHC; Result Unstructured Data: Test Result:32.8; Test Date: 20210603; Test Name: MCHC; Result Unstructured Data: Test Result:32.6; Test Date: 20210608; Test Name: MCHC; Result Unstructured Data: Test Result:33.4; Test Date: 20210623; Test Name: MCHC; Result Unstructured Data: Test Result:33.7; Test Date: 20210710; Test Name: MCHC; Result Unstructured Data: Test Result:32.5; Test Date: 20210720; Test Name: MCHC; Result Unstructured Data: Test Result:34.3; Test Date: 20210726; Test Name: MCHC; Result Unstructured Data: Test Result:34.0; Test Date: 20210804; Test Name: MCHC; Result Unstructured Data: Test Result:32.5; Test Date: 20210808; Test Name: MCHC; Result Unstructured Data: Test Result:33.1; Test Date: 20210810; Test Name: MCHC; Result Unstructured Data: Test Result:L 32.1; Test Date: 20210820; Test Name: MCHC; Result Unstructured Data: Test Result:32.2; Test Date: 20210827; Test Name: MCHC; Result Unstructured Data: Test Result:32.9; Test Date: 20210922; Test Name: MCHC; Result Unstructured Data: Test Result:32.7; Test Date: 20211008; Test Name: MCHC; Result Unstructured Data: Test Result:33.1; Test Date: 20211022; Test Name: MCHC; Result Unstructured Data: Test Result:32.6; Test Date: 20210513; Test Name: MCV; Result Unstructured Data: Test Result:88.6; Test Date: 20210514; Test Name: MCV; Result Unstructured Data: Test Result:92.3; Test Date: 20210515; Test Name: MCV; Result Unstructured Data: Test Result:88.2; Test Date: 20210602; Test Name: MCV; Result Unstructured Data: Test Result:90.0; Test Date: 20210603; Test Name: MCV; Result Unstructured Data: Test Result:91.8; Test Date: 20210608; Test Name: MCV; Result Unstructured Data: Test Result:89.4; Test Date: 20210623; Test Name: MCV; Result Unstructured Data: Test Result:89.1; Test Date: 20210628; Test Name: MCV; Result Unstructured Data: Test Result:88.8; Test Date: 20210710; Test Name: MCV; Result Unstructured Data: Test Result:91.5; Test Date: 20210720; Test Name: MCV; Result Unstructured Data: Test Result:89.7; Test Date: 20210726; Test Name: MCV; Result Unstructured Data: Test Result:90; Test Date: 20210804; Test Name: MCV; Result Unstructured Data: Test Result:92.8; Test Date: 20210808; Test Name: MCV; Result Unstructured Data: Test Result:90.6; Test Date: 20210810; Test Name: MCV; Result Unstructured Data: Test Result:92.7; Test Date: 20210813; Test Name: MCV; Result Unstructured Data: Test Result:91.3; Test Date: 20210820; Test Name: MCV; Result Unstructured Data: Test Result:93.0; Test Date: 20210827; Test Name: MCV; Result Unstructured Data: Test Result:92.1; Test Date: 20210922; Test Name: MCV; Result Unstructured Data: Test Result:91.6; Test Date: 20211008; Test Name: MCV; Result Unstructured Data: Test Result:90.6; Test Date: 20211022; Test Name: MCV; Result Unstructured Data: Test Result:91.5; Test Date: 20210513; Test Name: MPV; Result Unstructured Data: Test Result:10.3; Test Date: 20210514; Test Name: MPV; Result Unstructured Data: Test Result:10.4; Test Date: 20210515; Test Name: MPV; Result Unstructured Data: Test Result:10.4; Test Date: 20210602; Test Name: MPV; Result Unstructured Data: Test Result:10.5; Test Date: 20210603; Test Name: MPV; Result Unstructured Data: Test Result:10.5; Test Date: 20210608; Test Name: MPV; Result Unstructured Data: Test Result:10.6; Test Date: 20210623; Test Name: MPV; Result Unstructured Data: Test Result:10.3; Test Date: 20210710; Test Name: MPV; Result Unstructured Data: Test Result:10.4; Test Date: 20210720; Test Name: MPV; Result Unstructured Data: Test Result:11.0; Test Date: 20210804; Test Name: MPV; Result Unstructured Data: Test Result:11.5; Test Date: 20210810; Test Name: MPV; Result Unstructured Data: Test Result:11.4; Test Date: 20210808; Test Name: monocytes; Result Unstructured Data: Test Result:7.6; Test Date: 20210820; Test Name: monocytes; Result Unstructured Data: Test Result:3.4; Test Date: 20210820; Test Name: monocytes; Result Unstructured Data: Test Result:0.24; Test Date: 20210827; Test Name: monocytes; Result Unstructured Data: Test Result:4.2; Test Date: 20210827; Test Name: monocytes; Result Unstructured Data: Test Result:0.31; Test Date: 20210922; Test Name: monocytes; Result Unstructured Data: Test Result:5.5; Test Date: 20210922; Test Name: monocytes; Result Unstructured Data: Test Result:0.35; Test Date: 20211008; Test Name: monocytes; Result Unstructured Data: Test Result:7.6; Test Date: 20211008; Test Name: monocytes; Result Unstructured Data: Test Result:0.34; Test Date: 20211022; Test Name: monocytes; Result Unstructured Data: Test Result:5.2; Test Date: 20211022; Test Name: monocytes; Result Unstructured Data: Test Result:0.27; Test Date: 20210513; Test Name: neutrophil; Result Unstructured Data: Test Result:69.8; Test Date: 20210514; Test Name: neutrophil; Result Unstructured Data: Test Result:48.8; Test Date: 20210515; Test Name: neutrophil; Result Unstructured Data: Test Result:67.9; Test Date: 20210602; Test Name: neutrophil; Result Unstructured Data: Test Result:80.7; Test Date: 20210603; Test Name: neutrophil; Result Unstructured Data: Test Result:61.0; Test Date: 20210608; Test Name: neutrophil; Result Unstructured Data: Test Result:73.3; Test Date: 20210623; Test Name: neutrophil; Result Unstructured Data: Test Result:61.2; Test Date: 20210628; Test Name: neutrophil; Result Unstructured Data: Test Result:61.6; Test Date: 20210710; Test Name: neutrophil; Result Unstructured Data: Test Result:76.9; Test Date: 20210720; Test Name: neutrophil; Result Unstructured Data: Test Result:78.9; Test Date: 20210726; Test Name: neutrophil; Result Unstructured Data: Test Result:76; Test Date: 20210804; Test Name: neutrophil; Result Unstructured Data: Test Result:73.4; Test Date: 20210808; Test Name: neutrophil; Result Unstructured Data: Test Result:58.5; Test Date: 20210808; Test Name: neutrophil; Result Unstructured Data: Test Result:2.62; Test Date: 20210810; Test Name: neutrophil; Result Unstructured Data: Test Result:78.9; Test Date: 20210813; Test Name: neutrophil; Result Unstructured Data: Test Result:80.0; Test Date: 20210820; Test Name: neutrophil; Result Unstructured Data: Test Result:82.3; Test Date: 20210820; Test Name: neutrophil; Result Unstructured Data: Test Result:5.74; Test Date: 20210827; Test Name: neutrophil; Result Unstructured Data: Test Result:78.0; Test Date: 20210827; Test Name: neutrophil; Result Unstructured Data: Test Result:5.74; Test Date: 20210922; Test Name: neutrophil; Result Unstructured Data: Test Result:60.4; Test Date: 20210922; Test Name: neutrophil; Result Unstructured Data: Test Result:3.88; Test Date: 20211008; Test Name: neutrophil; Result Unstructured Data: Test Result:58.5; Test Date: 20211008; Test Name: neutrophil; Result Unstructured Data: Test Result:2.62; Test Date: 20211022; Test Name: neutrophil; Result Unstructured Data: Test Result:60.0; Test Date: 20211022; Test Name: neutrophil; Result Unstructured Data: Test Result:3.13; Test Date: 20210513; Test Name: Platelet; Result Unstructured Data: Test Result:342; Test Date: 20210514; Test Name: Platelet; Result Unstructured Data: Test Result:266; Test Date: 20210515; Test Name: Platelet; Result Unstructured Data: Test Result:333; Test Date: 20210602; Test Name: Platelet; Result Unstructured Data: Test Result:H 390; Test Date: 20210603; Test Name: Platelet; Result Unstructured Data: Test Result:321; Test Date: 20210608; Test Name: Platelet; Result Unstructured Data: Test Result:H 419; Test Date: 20210623; Test Name: Platelet; Result Unstructured Data: Test Result:310; Test Date: 20210628; Test Name: Platelet; Result Unstructured Data: Test Result:321; Test Date: 20210710; Test Name: Platelet; Result Unstructured Data: Test Result:361; Test Date: 20210720; Test Name: Platelet; Result Unstructured Data: Test Result:349; Test Date: 20210726; Test Name: Platelet; Result Unstructured Data: Test Result:277; Test Date: 20210804; Test Name: Platelet; Result Unstructured Data: Test Result:290; Test Date: 20210808; Test Name: Platelet; Result Unstructured Data: Test Result:237; Test Date: 20210810; Test Name: Platelet; Result Unstructured Data: Test Result:32.7; Test Date: 20210813; Test Name: Platelet; Result Unstructured Data: Test Result:312; Test Date: 20210820; Test Name: Platelet; Result Unstructured Data: Test Result:254; Test Date: 20210827; Test Name: Platelet; Result Unstructured Data: Test Result:250; Test Date: 20210922; Test Name: Platelet; Result Unstructured Data: Test Result:256; Test Date: 20211008; Test Name: Platelet; Result Unstructured Data: Test Result:237; Test Date: 20211022; Test Name: Platelet; Result Unstructured Data: Test Result:286; Test Date: 20220107; Test Name: SpO2; Test Result: 96 %; Test Date: 20210808; Test Name: Total protein; Result Unstructured Data: Test Result:7.4; Test Date: 20210820; Test Name: Total protein; Result Unstructured Data: Test Result:6.4; Test Date: 20210827; Test Name: Total protein; Result Unstructured Data: Test Result:7.2; Test Date: 20210922; Test Name: Total protein; Result Unstructured Data: Test Result:7.0; Test Date: 20211008; Test Name: Total protein; Result Unstructured Data: Test Result:7.4; Test Date: 20210513; Test Name: rbc; Result Unstructured Data: Test Result:4.65; Test Date: 20210514; Test Name: rbc; Result Unstructured Data: Test Result:L 3.64; Test Date: 20210515; Test Name: rbc; Result Unstructured Data: Test Result:4.76; Test Date: 20210602; Test Name: rbc; Result Unstructured Data: Test Result:4.68; Test Date: 20210603; Test Name: rbc; Result Unstructured Data: Test Result:4.01; Test Date: 20210604; Test Name: rbc; Result Unstructured Data: Test Result:4.68; Test Date: 20210628; Test Name: rbc; Result Unstructured Data: Test Result:4.20; Test Date: 20210710; Test Name: rbc; Result Unstructured Data: Test Result:4.82; Test Date: 20210720; Test Name: rbc; Result Unstructured Data: Test Result:4.33; Test Date: 20210726; Test Name: rbc; Result Unstructured Data: Test Result:4.40; Test Date: 20210808; Test Name: rbc; Result Unstructured Data: Test Result:4.24; Test Date: 20210810; Test Name: rbc; Result Unstructured Data: Test Result:4.58; Test Date: 20210820; Test Name: rbc; Result Unstructured Data: Test Result:L 3.87; Test Date: 20210827; Test Name: rbc; Result Unstructured Data: Test Result:4.16; Test Date: 20210827; Test Name: rbc; Result Unstructured Data: Test Result:3.84; Test Date: 20210922; Test Name: rbc; Result Unstructured Data: Test Result:4.17; Test Date: 20210922; Test Name: rbc; Result Unstructured Data: Test Result:4.15; Test Date: 20211008; Test Name: rbc; Result Unstructured Data: Test Result:4.24; Test Date: 20211022; Test Name: rbc; Result Unstructured Data: Test Result:4.33; Test Date: 20210513; Test Name: RDW; Result Unstructured Data: Test Result:12.2; Test Date: 20210514; Test Name: RDW; Result Unstructured Data: Test Result:12.8; Test Date: 20210515; Test Name: RDW; Result Unstructured Data: Test Result:12.7; Test Date: 20210602; Test Name: RDW; Result Unstructured Data: Test Result:12.3; Test Date: 20210603; Test Name: RDW; Result Unstructured Data: Test Result:12.4; Test Date: 20210608; Test Name: RDW; Result Unstructured Data: Test Result:12.3; Test Date: 20210623; Test Name: RDW; Result Unstructured Data: Test Result:12.2; Test Date: 20210710; Test Name: RDW; Result Unstructured Data: Test Result:10.4; Test Date: 20210720; Test Name: RDW; Result Unstr
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anxiety; Appendectomy (Appendectomy Nov2009); Gestational diabetes; House dust mite allergy; Sinus operation (Sinus surgery x 2 Sinus surgery 2014/2015)
Andere Medikamente
CELEXA [CELECOXIB]; ATORVASTATIN; BUSPIRONE; CITALOPRAM; CLINDAMYCIN; CLONAZEPAM; IPRATROPIUM; IVERMECTIN; LEVONORGESTREL; OMEPRAZOLE; ONDANSETRON; SELZENTRY; QNASL
Allergien
-
Vorherige Impfungen
-

VAERS 2037855

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
43,0
Geschlecht
M
Eingang
15.01.2022
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Anxiety Blood test Cardiac flutter Chest pain Computerised tomogram Dizziness Dyspnoea Dysstasia Electrocardiogram Electroencephalogram Fatigue Hyperhidrosis Insomnia Magnetic resonance imaging Nausea Neuropathy peripheral Palpitations Syncope

Symptomtext

After 1st Dose: Extreme fatigue, shortness of breath, extreme anxiety, anxiety attack, palpitations, heart pounding, heart flutter, extreme sweating, severe chest pains, insomnia, fainting upon standing, dizziness, blurred vision, nausea, vomiting, lasting for 8-10 weeks. After 2nd Dose: Peripheral Neuropathy,

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
ER visit 04/26/2021, EKG, Blood Test ER visit 07/01/2021, EKG, Blood Test, MRI, CT Scan Neurologist: EEG, EMG, Blood Test
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Nexium 20mg Daily Citalopram 40mg Daily Trazadone 100mg at Bedtime Adult Multi-Vitamin, 1 Daily Vitamin D3 50 mcg, 1 Daily
Allergien
None that are known.
Vorherige Impfungen
-

VAERS 2020860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
51,0
Geschlecht
M
Eingang
10.01.2022
Impfdatum
17.03.2021
Beginn
09.01.2022
Tage bis Beginn
298,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Syncope

Symptomtext

Pt is a resident of County Jail where he states several people have been positive for COVID-19. Pt is being admitted due to syncope.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1985142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
30,0
Geschlecht
M
Eingang
08.01.2022
Impfdatum
17.12.2021
Beginn
17.12.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Activated partial thromboplastin time Chest X-ray Chest pain Differential white blood cell count Echocardiogram Immunisation Myocarditis SARS-CoV-2 test Electrocardiogram Fibrin D dimer Full blood count International normalised ratio Lipids Magnetic resonance imaging Metabolic function test Platelet count Prothrombin time Scan with contrast

Symptomtext

Myocarditis; Strong chest pain; Booster Dose; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 17Dec2021 (Lot number: 330308D) at the age of 30 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "No" (unspecified if ongoing), notes: other medical history: No. There were no concomitant medications. Vaccination history included: Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose lot number=EW0162, Prev dose lot unknown=False, Prev dose administration date=28Apr2021, Prev dose dose number=2, Prev dose vaccine location=Left arm), administration date: 28Apr2021, when the patient was 29 years old, for COVID-19 immunization; Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose lot number=ER8734, Prev dose lot unknown=False, Prev dose administrationdate=02Apr2021, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 02Apr2021, when the patient was 29 years old, for COVID-19 immunization. The following information was reported: MYOCARDITIS (Medically significant and hospitalization) with onset 21Dec2021 03:00, outcome "recovering", described as "Myocarditis"; CHEST PAIN (Medically significant and hospitalization) with onset 21Dec2021 03:00, outcome "recovering", described as "Strong chest pain, Immunisation (Medically significant and hospitalization) with onset 17Dec2021, outcome "unknown", describes as Booster dose. The patient was hospitalized for myocarditis, chest pain (hospitalization duration: 2 day(s)). The events "myocarditis" and "strong chest pain" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (21Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of myocarditis, chest pain. reported as Prescription medications (unspecified). Clinical information: Strong chest pain diagnosed as Myocarditis after being admitted to the hospital for 2 days. It was reported that, the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was unknown, Prior to vaccination, if the patient was diagnosed with COVID-19. Since the vaccination, the patient has been not tested for COVID-19. Reported as no known allergies. The lot number for BNT162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
2,0
Labordaten
Test Date: 20211221; Test Name: COVID/FLU/RSV BY PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: No, Comment: other medical history: No
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2015582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
DC
Alter
63,0
Geschlecht
F
Eingang
07.01.2022
Impfdatum
06.12.2021
Beginn
07.12.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bell's palsy Ear discomfort Facial paralysis Facial paresis

Symptomtext

Starting with onset of symptoms (pressure in left ear) on evening of 7 December, the day following booster vaccine, and developing through 8/9 December, developed partial facial paralysis (Bell's Palsy) on left side of face. Was prescribed a course of steroids (prednisone) and anti-virals (valacyclovir) which had no effect in alleviating symptoms. Paralysis continues 4 weeks later, with about 20-30 % of muscle movement regained on affected side of face.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
Doctor's visit on 9 December.
Aktuelle Erkrankungen
had suffered migraine 3-4 days prior
Vorgeschichte
-
Andere Medikamente
atorvastatin
Allergien
none
Vorherige Impfungen
-

VAERS 2000274

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MD
Alter
38,0
Geschlecht
F
Eingang
03.01.2022
Impfdatum
17.04.2021
Beginn
21.12.2021
Tage bis Beginn
248,0
Dosis
2
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Bell's palsy Ear pain Facial paralysis Herpes zoster Laboratory test Neurological examination Pain

Symptomtext

Develope Bell?s palsy. Right side facial paralysis and throbbing pain under the ear. One doctor says could be caused by shingles outbreak without the rash. I think the vaccine triggered this. Meds steroids and antivirals. 2 weeks duration of healing my face.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
Saw a neurologist given test in office. Also lime disease test. Haven?t gotten results yet
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
Multiple vitamin, D3, omega 3, probiotic
Allergien
No
Vorherige Impfungen
-

VAERS 1981164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MO
Alter
52,0
Geschlecht
M
Eingang
26.12.2021
Impfdatum
04.06.2021
Beginn
10.06.2021
Tage bis Beginn
6,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Brain natriuretic peptide C-reactive protein increased Cardiac stress test Chest pain Differential white blood cell count Echocardiogram Feeling abnormal Full blood count Inflammation Lipase Metabolic function test Pericarditis Scan myocardial perfusion Troponin I Urine analysis

Symptomtext

Kept feeling chest pains, some days worse than others. Wasn't until at work felt like having heart attack in Sept that my supervisor and director of operations took me to hospital. Sept 13th ran all kinds of tests. B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS, everything looked good, kept saying healthy, then Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSION SPECT STRESS AND REST, TRANSTHORACIC ECHO (TTE) COMPLETE, still was told healthy. It wasn't until Oct 13th my Cardiologist asked when I had my vaccination did he order the next test CBC W/ AUTO DIFFERENTIAL, C-REACTIVE PROTEIN, CBC WITH DIFFERENTIAL. With the C-REACTIVE PROTEINS that high couple medications for inflammation stating Pericarditis. Colchicine was one of the meds. Sept 13th . B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSION SPECT STRESS AND REST, TRANSTHORACIC ECHO (TTE) COMPLETE, Oct 13th my Cardiologist asked when I had my vaccination did he order the next test CBC W/ AUTO DIFFERENTIAL, C-REACTIVE PROTEIN, CBC WITH DIFFERENTIAL. With the C-REACTIVE PROTEINS that high he put me on Colchicine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
Sept 13th . B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS, Sept 20th Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSIO
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Advil
Allergien
Codeine
Vorherige Impfungen
-

VAERS 1981164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MO
Alter
52,0
Geschlecht
M
Eingang
26.12.2021
Impfdatum
04.06.2021
Beginn
10.06.2021
Tage bis Beginn
6,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Brain natriuretic peptide C-reactive protein increased Cardiac stress test Chest pain Differential white blood cell count Echocardiogram Feeling abnormal Full blood count Inflammation Lipase Metabolic function test Pericarditis Scan myocardial perfusion Troponin I Urine analysis

Symptomtext

Kept feeling chest pains, some days worse than others. Wasn't until at work felt like having heart attack in Sept that my supervisor and director of operations took me to hospital. Sept 13th ran all kinds of tests. B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS, everything looked good, kept saying healthy, then Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSION SPECT STRESS AND REST, TRANSTHORACIC ECHO (TTE) COMPLETE, still was told healthy. It wasn't until Oct 13th my Cardiologist asked when I had my vaccination did he order the next test CBC W/ AUTO DIFFERENTIAL, C-REACTIVE PROTEIN, CBC WITH DIFFERENTIAL. With the C-REACTIVE PROTEINS that high couple medications for inflammation stating Pericarditis. Colchicine was one of the meds. Sept 13th . B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSION SPECT STRESS AND REST, TRANSTHORACIC ECHO (TTE) COMPLETE, Oct 13th my Cardiologist asked when I had my vaccination did he order the next test CBC W/ AUTO DIFFERENTIAL, C-REACTIVE PROTEIN, CBC WITH DIFFERENTIAL. With the C-REACTIVE PROTEINS that high he put me on Colchicine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
Sept 13th . B-TYPE NATRIURETIC PEPTIDE, LIPASE, COMPREHENSIVE METABOLIC PANEL, TROPONIN I, URINALYSIS, Sept 20th Sept 20th STRESS TEST WITH MYOCARDIAL PERFUSION, NM HEART PERFUSIO
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Advil
Allergien
Codeine
Vorherige Impfungen
-

VAERS 1893301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0162

schwer
Staat
NM
Alter
71,0
Geschlecht
F
Eingang
18.12.2021
Impfdatum
11.11.2021
Beginn
13.11.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood test normal Epistaxis Mouth haemorrhage Platelet count normal Thrombosis Choking sensation Cough Fatigue Feeling abnormal

Symptomtext

1st Event: Blood started streaming from my nose while I was eating supper. It drenched paper towel after paper towel in rapid succession. Went to bathroom to stand over sink while pinching the very end (soft part) of my nose. Blood continued to come through my nose onto paper towel and back up in my nose and simultaneously stream from my mouth. When I released my pinch to clear my nose, blood streamed out. Early on, a large puddle the consistency of loose pudding came out and stayed in a large puddle in my sink. It maintained it form w/o any slow seeping down the sink. After 30 minutes approx. of blood streaming, I manage to call the 24-hour nurse who stayed on the phone with me for almost 2 1/2 hours until I could tell her the streaming might be very, very slightly slowing. Meanwhile she was telling me I would have to go to medical facility if it didn't stop. After 3 hours it did start to slow down though still flowing from my mouth and nose. Finally it stopped and then I started passing very large clots from my mouth. 11:00 pm was when the last clot passed. Total time from 5:30 pm until 11:00 pm. 2nd event was 11-19-21: 7:00 a.m. blood started drippin from my nose. I pinched my nose and after about 4 minutes, it stopped. 3rd event was 12-1-21: 5.45 a.m. I was lying in bed awake and all of a sudden I felt like I needed to blow my nose. I got up and saw blood soaking my pillow, bed linens, etc. This lasted until 9:00 a.m. when I passed the last clot through my mouth. Bleeding streamed from before 5:45 a.m. until about 8:30 a.m.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
Blood test after 3rd event -- 2 days after -- showed normal platelet level.
Aktuelle Erkrankungen
none
Vorgeschichte
restrictive cardiomyopathy (due to long-term effects of radiation therapy 1977), post-radiation specific myalgia, osteoporosis, Gerd, post-operative hypothyroidism, osteoarthritis
Andere Medikamente
Escitalopram, Levothyroxine, multi-vitamin, Glucosamine w/MSM, B6, D3.
Allergien
Pistachio nuts, boniva, prolia, penicillin, warfarin (combined with escitalopram), Hydrochlorothiazide, lovenox, calcitonin Salmon, Lisinopril
Vorherige Impfungen
-

VAERS 1958068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
16,0
Geschlecht
M
Eingang
17.12.2021
Impfdatum
02.05.2021
Beginn
31.07.2021
Tage bis Beginn
90,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Myocarditis SARS-CoV-2 test

Symptomtext

Myocarditis; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 16 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02May2021 (Lot number: EW0162) at the age of 16 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing) and no other medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (previous COVID-19 vaccine product also Pfizer product and lot number is ER8730, dose1, administrated in the left arm), administration date: 11Apr2021, when the patient was 16 years old, for Covid-19 Immunization. The following information was reported: MYOCARDITIS (hospitalization, disability, life threatening) with onset 31Jul2021 06:00, outcome "not recovered", described as "Myocarditis". The patient was hospitalized for myocarditis (hospitalization duration: 3 day(s)). The event "myocarditis" was evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test (Nasal Swab): (31Jul2021) negative. Therapeutic measures were taken as a result of myocarditis included Ibuprofen.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
3,0
Labordaten
Test Date: 20210731; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Penicillin allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1952445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NJ
Alter
20,0
Geschlecht
M
Eingang
15.12.2021
Impfdatum
07.05.2021
Beginn
14.06.2021
Tage bis Beginn
38,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Anti-GAD antibody positive Autoimmune thyroiditis Blood glucose increased Blood ketone body Blood thyroid stimulating hormone normal Diabetic ketoacidosis Glycosylated haemoglobin increased Hypothyroidism Insulin C-peptide Intensive care Laboratory test Type 1 diabetes mellitus

Symptomtext

Three months after receiving the second dose of the vaccine, I was admitted into the ICU (September 7th, 2021) and treated for being in DKA. My blood sugar was +500, and A1C was 12.6 and estimated by doctors that my average blood sugar for the past 3 months was 300. My thyroid hormone levels also pointed to hypothyroidism. I was given 2 kinds of insulin and levothyroxine to take daily. Later, I was officially diagnosed with Type 1 Diabetes and Hashimotos disease.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
5,0
Labordaten
Routine Chem labs showed A1C 12.6% September 10th 06:38AM, BSR 195 mg/dL September 10th 06:38AM. C-Peptide read 0.4 ng/mL September 10th 06:38AM. TSH read 7.79 ulU/mL. Glucose read >= 500 mg/dL September 8th 1:48AM Ketones 80 mg/dL September 8th 1:48AM. GAD Ab 1278.2 U/Ml September 9th 07:30AM.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1944160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
63,0
Geschlecht
F
Eingang
13.12.2021
Impfdatum
21.04.2021
Beginn
05.12.2021
Tage bis Beginn
228,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Alveolar lung disease Blood bilirubin increased Blood creatinine increased Blood urea increased COVID-19 Chest X-ray abnormal Computerised tomogram head normal Cough Dizziness Dyspnoea Endotracheal intubation Head injury Influenza like illness Intensive care Loss of consciousness Malaise Nausea Positive airway pressure therapy

Symptomtext

Flu "I feel like I have the flu for the past few days." ? Syncope "I passed out this morning and I think I hit my head." Source of Information: Patient and Available medical record History of Present Illness: This is a 64y.o. female with pmh of Hypertension H/o renal transplant in 2001,on immmunosuppresants ckd following transplant Presented to ed with c/o fever,malaise,which started last week, along with this symptoms she develop cough and sob with nausea,also feeling lightheaded.she is vaccinated for covid,but did not get her booster shot yet. V/s were normal and o2 sat 95 % on ra,at the time of arrival Admission labs were bun/cr of 45/4.09,bilirubin of 2.0,ua with wbc of 11 to 20 but with squamous cells of >50. Ct head shows no acute process Chest xray with rt basilar air space disease covid -19 positive

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
7,0
Labordaten
Currently hospitalized- not discharged yet, in Critical Care, was intubated but now is on BiPap
Aktuelle Erkrankungen
? Hyperlipidemia ? Hypertension ? Kidney disease
Vorgeschichte
? Hyperlipidemia ? Hypertension ? Kidney disease
Andere Medikamente
amLODIPine (NORVASC) 2.5 MG PO Tab take 5 mg by mouth once daily. Unknown Unknown time Med Note ( Tue Dec 7, 2021 3:18 AM) Pt unsure if she's still taking: last filled 10/11/21 (90 day supply) aspirin 81 MG PO Chew Tab take 81 mg b
Allergien
Pentazocine
Vorherige Impfungen
-

VAERS 1925196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
19,0
Geschlecht
M
Eingang
06.12.2021
Impfdatum
26.11.2021
Beginn
26.11.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Blood creatine phosphokinase MB increased Blood creatine phosphokinase increased C-reactive protein increased Catheterisation cardiac normal Chest pain Ejection fraction normal Electrocardiogram ST segment elevation Glycosylated haemoglobin Liver function test increased Malaise Myocarditis Pain Pain in extremity Painful respiration Symptom recurrence Troponin increased

Symptomtext

Myocarditis, chest pain, elevated troponin. Patient presented to ED on 11/29/2021 with 3 day history of chest pain. Patient stated he started to feel sick in the evening after he had his COVID-19 booster shot. He reported pain in the middle of the chest, radiating to the left. EKG showed ST elevation in ant leads, labs showed elevated trops of 234. CPK 427, CPK MB 26, CRP cardiac marker 54. Mild elevated LFTs. Hba1c 5. on admission. patient was taken to cath lab for LHC, which revealed a normal ejection fraction and normal coronaries. Patient was discharged on 11/30/21 but came back on 12/1/21 with complaints of recurrent chest pain. He admits the pain is somewhat worse with deep inspiration but not movement. He describes it as a midsternal pain that can radiate to his left arm, occurs and resolves spontaneously.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
3,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Autism
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1801652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
67,0
Geschlecht
M
Eingang
23.11.2021
Impfdatum
15.04.2021
Beginn
29.04.2021
Tage bis Beginn
14,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Angiogram cerebral normal Angiogram pulmonary normal Asthenia Biopsy artery normal Catheterisation cardiac normal Arthritis Dyspnoea Giant cell arteritis Headache Magnetic resonance imaging head Chest pain Computerised tomogram thorax normal Dyspnoea exertional Echocardiogram normal Fatigue Magnetic resonance imaging head normal Presyncope Migraine

Symptomtext

Sent to ER, Dx migraine; arthritis; dyspnea; Headache; This is a spontaneous report from a contactable healthcare professional. A 67-year-old male patient received the first dose of BNT162B2 at 67-year-old, intramuscularly in arm left on 15Apr2021 (Batch/Lot Number: EW0162) at single dose for COVID-19 immunisation. Medical history included COVID-19, ongoing coronary artery disease (CAD) from Sep2020, ongoing hypogonadism from 15May2021, ongoing anxiety, ongoing depression, ongoing osteopenia, ongoing osteoarthritis, ongoing obstructive sleep apnoea syndrome (OSA), and coronary artery bypass (CABG) from Sep2020. Concomitant medications included alendronate sodium (ALENDRONATE), atorvastatin, acetylsalicylic acid/ascorbic acid (ASPIRIN), buspirone, isosorbide dinitrate (ISOSORBIDE), metoprolol, omeprazole, potassium chloride, prasugrel, vitamin d3, and fluoxetine. Patient experienced headache on 29Apr2021, had a MRI, MRA, saw cardiology and optimists SED rate negative, MRA. Developmental hypoplasia vs chronic conclusion. MRI, WNL sent to ER, Dx migraine not improved. Had cardiac Cath on 14May2021 to PCL not improved sent to neurology. Artery bx negative but exam c/w GCA a temoral arthritis. Had on high dose prednisolone with some relief. Continued to have increased dyspnea. Palm said covid longer to chronic steroid use. Back in hospital in Oct2021 for Dyspnea near (Withheld), cardiac clearance, rheumatological work up pending. Relevant tests in May2021: MRI brain (magnetic resonance imaging head): Negative; MRA brain: Negative; Temporary artery: Negative; SED rate: Negative. Outcome of event migraine was not resolved, and of other events was unknown.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal relationship between the event Migraine and suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
Test Date: 202105; Test Name: Temporal arteritis; Test Result: Negative ; Test Date: 202105; Test Name: MRA; Test Result: Negative ; Test Date: 202105; Test Name: MRI brain; Test Result: Negative ; Test Date: 202105; Test Name: Sed rate; Test Result: Negative
Aktuelle Erkrankungen
Anxiety; Coronary artery disease; Depression; Hypogonadism; Obstructive sleep apnoea syndrome; Osteoarthritis; Osteopenia
Vorgeschichte
Medical History/Concurrent Conditions: CABG; COVID-19
Andere Medikamente
ALENDRONATE; ATORVASTATIN; ASPIRIN [ACETYLSALICYLIC ACID;ASCORBIC ACID]; BUSPIRONE; ISOSORBIDE [ISOSORBIDE DINITRATE]; METOPROLOL; OMEPRAZOLE; POTASSIUM CHLORIDE; PRASUGREL; VITAMIN D3; FLUOXETINE
Allergien
-
Vorherige Impfungen
-

VAERS 1854449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
CT
Alter
43,0
Geschlecht
M
Eingang
09.11.2021
Impfdatum
18.04.2021
Beginn
28.10.2021
Tage bis Beginn
193,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anticoagulant therapy Deep vein thrombosis Erythema Pain in extremity Peripheral swelling Thrombosis Ultrasound Doppler abnormal

Symptomtext

Developed swelling, redness and pain in right leg. Symptoms started 10/28/21. Went to ER on 10/30/21 confirmed 2 DVTs in right leg Currently being treated on Eliquis (anti coagulant) since 10/30/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deep vein thrombosis
Hospital-Tage
-
Labordaten
Ultrasound 10/30/21.
Aktuelle Erkrankungen
NO
Vorgeschichte
Factor V Leiden (1 copy of gene)
Andere Medikamente
NONE
Allergien
OMOXICILLAN
Vorherige Impfungen
-

VAERS 1846928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IL
Alter
38,0
Geschlecht
F
Eingang
05.11.2021
Impfdatum
08.06.2021
Beginn
02.08.2021
Tage bis Beginn
55,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal distension Fatigue Heavy menstrual bleeding Menstruation irregular Pain Thrombosis Urinary tract infection

Symptomtext

Starting in August 2021, I started having irregular and heavy menstrual cycles. I have been on the birth control pill after giving birth in 2017. I have always taken the pill at the exact same time each day and every day. I have always had a very light period that only lasted about 2 days each month. This was consistent every month while on birth control. I have never had a heavy period. Each month after August 2021, I continued to have a more heavy period with blood clots and had a period almost 20 days out of 30-31 days. I called my doctor 3 times and they increased my birth control to prevent the constant bleeding. November 4th, 2021, I got an IUD inserted and my OBGYN also noticed many blood clots in my cervix while she was inserting it during the procedure. I have also felt more fatigued and bloated lately, all during this constant menstrual cycle over the past few months. I have also had 5 urinary tract infections since getting my 2nd dose of the vaccine causing physical pain each time. It took longer than usual for my antibiotics and pain medicine prescribed to me for my urinary tract infections to take affect.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
8/6/2021 -Urinary tract infection 9/10/2021 - Birth control increased 11/4/2021- Intrauterine device inserted
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Adderall
Allergien
None
Vorherige Impfungen
-

VAERS 1843179

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
TN
Alter
47,0
Geschlecht
M
Eingang
04.11.2021
Impfdatum
14.04.2021
Beginn
20.04.2021
Tage bis Beginn
6,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Bell's palsy

Symptomtext

Bell's Palsy onset 04/20 for 2 weeks

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
-
Allergien
none
Vorherige Impfungen
-

VAERS 1833534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
32,0
Geschlecht
F
Eingang
01.11.2021
Impfdatum
21.04.2021
Beginn
21.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood culture COVID-19 Chest X-ray Chills Dizziness Electrocardiogram Electrocardiogram ambulatory Immediate post-injection reaction Muscular weakness Palpitations Pyrexia Syncope Throat tightness

Symptomtext

On 04/21/2021, immediately after the vaccination- my throat started getting tight and it felt like it was closing up. The nurse on site gave me Benadryl. On 04/22/2021, by the next day I got up, I had chills, my legs felt weak and would give out from underneath me. I was dizzy, fever, my heart would race, and this kept continuing for a couple of days. I went to the Emergency Room as well. My heartrate was resting around 120- 130, and it would just rise and fall really fast and I would just collapse. I had to wear a heart monitor. The doctor could not determine what was happening. There was no cause why that was happening. I would get heart palpitations. The heartrate last for like 3 months. It had decreased some. Every once in a while I would feel my heart race up until August. It wasn't as bad as the beginning. By August, it was occasionally. I was still being affected from my fast heartrate and dizziness, up until I got COVID-19. I got COVID-19 08/21/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Holter Heart Monitor Chest X-Ray EKG Bloodwork Blood Culture
Aktuelle Erkrankungen
N/A
Vorgeschichte
PCOS Asthma Migraines
Andere Medikamente
Claritin 10mg Topamax 100mg Protonix 40mg Zoloft 150mg Pepcid 40mg Epi-Pen as needed Camrese 0.15mg
Allergien
Morphine Cephalosporins Honey Shellfish
Vorherige Impfungen
-

VAERS 1833367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IL
Alter
52,0
Geschlecht
M
Eingang
01.11.2021
Impfdatum
09.04.2021
Beginn
14.10.2021
Tage bis Beginn
188,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: nein
Cerebral venous sinus thrombosis Computerised tomogram head Jugular vein thrombosis Magnetic resonance imaging head Transverse sinus thrombosis Venogram

Symptomtext

Occlusive Dural venous sinus thrombosis involving the right sigmoid sinus and visualized right internal jugular vein with non occlusive dural sinus thrombosis of the right transverse sinus

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral venous sinus thrombosis
Hospital-Tage
8,0
Labordaten
MRI brain 10/15/21 CT Brain and venogram 10/14/2021
Aktuelle Erkrankungen
None
Vorgeschichte
No history
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2650170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
-
Geschlecht
U
Eingang
28.10.2021
Impfdatum
09.04.2021
Beginn
16.04.2021
Tage bis Beginn
7,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cardiac stress test normal Chest pain Echocardiogram normal Myocarditis Scan myocardial perfusion Sleep disorder

Symptomtext

I received the Pfizer Covid-19 vaccines and developed myocarditis 7 days after the 2nd dose. The first dose was injected on 3/19/2021 at hospital. Lot number pfizer EN6205, second injection was administered on 4/9/2021 at hospital Lot# EW0162. I am a 58 Y/O male with the chest pain occurring each night for 5 days in a row waking me up. The pain was similar to having a tooth ache over my left enter mediastina and seem to resolve after 5 days. I went for a cardiac workup including cardiac echo, exercise stress test w/o nuclear then with nuclear imaging. All test results came back normal.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
-
Labordaten
NUCLEAR STRESS TEST 10-Sep-2021 Negative; UNKNOWN CARDIA ECHO 15-Sep-2021 Normal TREADMILL STRESS TEST (NON NUCLEAR) 21-Sep-2021 normal
Aktuelle Erkrankungen
Non smoker and rarely drink alcohol.
Vorgeschichte
Overweight.
Andere Medikamente
Only men's multivitamins. Once daily multivatamin, 2,000 IU's Vitamin D; 50mg Zinc,
Allergien
None known.
Vorherige Impfungen
-

VAERS 1813324

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IL
Alter
59,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
23.04.2021
Beginn
24.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blindness Chills Concussion Diarrhoea Disorientation Dizziness Fatigue Head injury Headache Loss of consciousness Magnetic resonance imaging Pyrexia Swelling Vomiting

Symptomtext

Severe diarrhea, vomiting, headache, fever, chills, and fatigue. Had diarrhea and vomiting for hours. During my last trip to the bathroom, I became dizzy, disoriented, and was unable to see. Then I passed out. When I came to, I was on the floor and had a lump on my head. Doctor diagnosed me with a concussion.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
MRI, May 2021 Two-hour neurological consult, June 2021 Follow-up neurological consult, August 2021
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vitamin D and calcium supplement (raw calcium by Garden of Life)
Allergien
None
Vorherige Impfungen
Flu shot

VAERS 1795246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NH
Alter
59,0
Geschlecht
F
Eingang
18.10.2021
Impfdatum
16.04.2021
Beginn
17.09.2021
Tage bis Beginn
154,0
Dosis
2
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anaemia Blood test Chest X-ray Computerised tomogram Electrocardiogram Headache Syncope Transfusion X-ray with contrast upper gastrointestinal tract

Symptomtext

Symptomatic anemia, syncope event, suspected upper GI bleed secondary to NSAIDS, chronic headache following Covid infection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
CT scan, chest X-ray, Loads of blood work, vitals, EKGs, blood transfusion.
Aktuelle Erkrankungen
COPD, depression, high cholesterol all under control
Vorgeschichte
COPD, depression, high cholesterol all under control.
Andere Medikamente
225mg venlafaxine, 40mg atorvastatin, multivitamin, 1200mg fish oil, 600mg calcium, 25mcg D3, 1000mcg B-12
Allergien
Nicotine gum
Vorherige Impfungen
-

VAERS 1785199

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IL
Alter
70,0
Geschlecht
M
Eingang
14.10.2021
Impfdatum
23.04.2021
Beginn
29.09.2021
Tage bis Beginn
159,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Acute kidney injury Blood creatinine increased Cough Dehydration Syncope

Symptomtext

Had multiple syncope episodes, cough. Admitted for dehydration, acute kidney injusry. Pt was discharged 10/09/2021

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Creatnine 4.1
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetic Colon cancer Hypertension CAD, elevated cholesterol
Andere Medikamente
-
Allergien
Lisinopril
Vorherige Impfungen
-

VAERS 2654794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
CT
Alter
38,0
Geschlecht
M
Eingang
12.10.2021
Impfdatum
18.04.2021
Beginn
18.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: unbekannt Erholt: unbekannt
Asthenia Autonomic nervous system imbalance Biopsy skin abnormal Electromyogram Hypoaesthesia Magnetic resonance imaging head Neuralgia Neuropathy peripheral Noninfective encephalitis Paralysis Peripheral swelling Postural orthostatic tachycardia syndrome Small fibre neuropathy Tinnitus Tremor Vasculitis

Symptomtext

Pfizer covid vaccine diagnosed with small fiber neuropathy, bilateral ulnar neuropathy, brain inflammation, tinnitus. All my limbs are numb tinnitus pots dysautonomia, nerve pain everywhere swelling hands can't close my fist extreme weakness legs drop out temporary paralysis tremors neuropathy of the whole body vascular inflammation everywhere including the brain This vaccine has ruined tens of thousands of people's lives causing a whole array of neurological damage. I don't know how you can keep hiding this

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paralysis
Hospital-Tage
-
Labordaten
EMG BRAIN MRI SFN BIOPSY, 30-JUNE-2021, POSITIVE SFN, ulnar neuropathy
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1768962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
MO
Alter
39,0
Geschlecht
F
Eingang
07.10.2021
Impfdatum
05.04.2021
Beginn
02.05.2021
Tage bis Beginn
27,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Nerve injury Neuralgia Thrombosis

Symptomtext

left arm blood clot and nerve damage

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
blood clot found 5/ 5/2021 nerve pain continued after and hasn't let up since getting diagnosed with blood clot
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
esteraylla- birth control for left side pain sprionolatone for acne on the face nifedepine for raynauds and a multi viatmin
Allergien
codenine nepoxen
Vorherige Impfungen
-

VAERS 1760688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MO
Alter
19,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
01.07.2021
Beginn
11.08.2021
Tage bis Beginn
41,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Electrocardiogram Illness Supraventricular extrasystoles Syncope

Symptomtext

After day one I was extremely sick to the point where I could not move. During the month after my vaccination I started having severe chest pain and was recently diagnosed with PAC (premature atrial contractions) which cause syncope at random times.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
EKG - 10/01/21
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Nexplanon arm implant
Allergien
none
Vorherige Impfungen
-

VAERS 1437413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NY
Alter
53,0
Geschlecht
F
Eingang
28.09.2021
Impfdatum
29.03.2021
Beginn
30.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Balance disorder Disorientation Headache Hypoaesthesia Hypoaesthesia oral Immediate post-injection reaction Laboratory test normal Loss of consciousness Migraine Vertigo Vomiting

Symptomtext

Migraine headache; This is a spontaneous report from a contactable consumer. A 53-year-old female patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration in arm left on 29Mar2021 afternoon at 53 years (Lot Number: ER8727) as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. Previously, in Dec2020 at 52 years, the patient received the following vaccines all for immunization, with no adverse effect: tuberculosis vaccines (unknown manufacturer), influenza vaccine (unknown manufacturer), varicella zoster vaccine (unknown manufacturer), unspecified vaccine. The patient experienced migraine headache (medically significant) on 30Mar2021 with outcome of not recovered. It was reported that the next day migraine presented along with additional symptoms that were thought to be natural and normal side effects. All other side effects dissipated, but the migraines continued. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : -PFIZER INC-202101057859 Same patient/drug, different dose/event

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1715856

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
DC
Alter
56,0
Geschlecht
F
Eingang
20.09.2021
Impfdatum
12.05.2021
Beginn
08.06.2021
Tage bis Beginn
27,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Computerised tomogram normal Dysarthria Dyskinesia Facial paralysis Lip swelling Magnetic resonance imaging normal Swelling face

Symptomtext

Suddenly had swelling of upper lip while driving home from a follow-up doctor appointment from foot surgery in December 2020. When I got home, left side of face felt swollen from temple to neck. Attempted to eat a sandwich when I couldn't open my mouth to bite. Called a friend and parent to ask what should I do. Was still able to move around and move legs and arms. Friend came over and noticed the right side of my face drooping. I had slurred speech because I couldn't fully open my mouth. Ambulance called to check my pressure, etc. There was concern I was having a stroke. I was taken to Hospital Emergency Room where a nurse and doctor surmised I had facial paralysis and I was sent home with a prednisone and valacyclovir (routine treatment). I saw my primary physician 2 days later with orders for a CT scan and an MRI. Results didn't show anything unusual. Began taking B12 complex liquid form. First appointment available to see a neurologist and ophthalmologist was in August. Since then received referral for physical therapy. Initial visit was late August with accompanying appointments beginning in October. In the interim, I was given exercises.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Diabetes; Hypertension
Andere Medikamente
Prescribed: Carvedilol, Amlodipine, Losartan, Lovastatin, Tresiba, Bupropion, Citalopram Hydrobromide, Trazadone OTC and Dietary Supplements: Biotin, Calcium Citrate Magnesium and Zinc, Vitamin B12 and B6, Vitamin D3, Vitamin C, Natrol 5-
Allergien
None other than celery.
Vorherige Impfungen
-

VAERS 1692764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
35,0
Geschlecht
F
Eingang
11.09.2021
Impfdatum
20.04.2021
Beginn
20.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal pain upper Antibody test Anxiety Chills Colitis Colonoscopy Computerised tomogram Cytokine increased Cytokine test Decreased appetite Depression Diarrhoea Dizziness Fatigue Fear Feeling abnormal Inflammatory marker increased Inflammatory marker test

Symptomtext

Ovarian Vein Thrombosis; Colitis; Vomiting; Diarrhea; Fatigue/ tired/ felt exhausted; Brain Fog; Insomnia; Panic Attacks; Anxiety; Depression; high rheumatoid factor; high inflammatory markers; high cytokines; Fear; 14% weight loss/lost about 7% of my body weight; nausea/nauseous; body aches all over/Body Aches/Pain; felt unwell; arm soreness; dizzy; loss of appetite; Chills; stomach ache; sleep is very poor; This is a spontaneous report from a contactable consumer (patient). A 35-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EW0162), via an unspecified route of administration, in right arm on 20Apr2021 16:00 (at the age of 35-years-old) as dose 1, single for COVID-19 immunization. Medical history included chronic sinusitis, indoor allergies, appendectomy, septra allergy, intolerance to Augmentin, sulfa allergy and other allergies. Concomitant medications included citalopram, cetirizine hydrochloride (ZYRTEC), melatonin, beclometasone dipropionate (QNASL), celecoxib (CELEXA), ipratropium bromide (ATROVENT) and ipratropium. The patient experienced nausea, body aches all over, body aches, pain, 14% weight loss/lost about 7% of my body weight, arm soreness, felt unwell, dizzy, loss of appetite, chills, stomach ache and poor quality sleep on 20Apr2021 17:00 and ovarian vein thrombosis, colitis, vomiting, diarrhea, fatigue, tired, felt exhausted, brain fog, insomnia, panic attacks, anxiety, depression, high rheumatoid factor, high inflammatory markers, high cytokines and fear on 20Apr2021 20:00. The patient was hospitalized for the events for 7 days. The patient underwent lab tests and procedures which included antibody test: negative in Aug2021, colonoscopy: unknown result and computerised tomogram: unknown result on an unspecified date, cytokine test: high, rheumatoid factor: high and inflammatory marker test: high on 20Apr2021, nucleic acid test: negative on 28Apr2021 Nasal Swab, sars-cov-2 test: negative in Apr2021 Blood test, sars-cov-2 test: negative on 28Apr2021 Nasal Swab. Therapeutic measures were taken as a result of the events. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Ovarian vein thrombosis
Hospital-Tage
7,0
Labordaten
Test Date: 202108; Test Name: UW Nucapsulated Antibody Test; Test Result: Negative ; Test Name: colonoscopy; Result Unstructured Data: Test Result:Unknown result; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210420; Test Name: cytokines; Result Unstructured Data: Test Result:high; Test Date: 20210420; Test Name: inflammatory markers; Result Unstructured Data: Test Result:high; Test Date: 20210428; Test Name: NAAT (COVID-19); Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210420; Test Name: rheumatoid factor; Result Unstructured Data: Test Result:high; Test Date: 202104; Test Name: Nasal Swab; Test Result: Negative ; Comments: Blood test; Test Date: 20210428; Test Name: SARS-CoV-2; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy (other medical history: Indoor Allergies, Sinusitis, appendectomy); Allergy (other medical history: Chronic Sinusitis, allergies); Appendectomy (other medical history: Indoor Allergies, Sinusitis, appendectomy); Chronic sinusitis (other medical history: Chronic Sinusitis, allergies); Sinusitis (other medical history: Indoor Allergies, Sinusitis, appendectomy); Sulfonamide allergy (known allergies: Sulfa, Augmentin (intolerance))
Andere Medikamente
CITALOPRAM; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; MELATONIN; QNASL; CELEXA [CELECOXIB]; ATROVENT; IPRATROPIUM
Allergien
-
Vorherige Impfungen
-

VAERS 1682824

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
KY
Alter
70,0
Geschlecht
M
Eingang
08.09.2021
Impfdatum
05.04.2021
Beginn
07.09.2021
Tage bis Beginn
155,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 pneumonia Syncope

Symptomtext

Patient presented to ED after having syncopal episode, denied shortness of breath of cough. Patient admitted for COVID PNA and is still undergoing inpatient treatment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1646903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
21,0
Geschlecht
M
Eingang
07.09.2021
Impfdatum
10.06.2021
Beginn
13.06.2021
Tage bis Beginn
3,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Chest X-ray Chest pain Dizziness Dyspnoea Electrocardiogram Magnetic resonance imaging Presyncope Myocarditis

Symptomtext

6/13/21 Woke up w/chest Pain, difficulty breathing, and dizzy enough to almost pass out. Admitted to hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
2,0
Labordaten
ECG/ MRI Chest XRay
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
NA
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 1646903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
21,0
Geschlecht
M
Eingang
07.09.2021
Impfdatum
10.06.2021
Beginn
13.06.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Chest X-ray Chest pain Dizziness Dyspnoea Electrocardiogram Magnetic resonance imaging Presyncope Myocarditis

Symptomtext

6/13/21 Woke up w/chest Pain, difficulty breathing, and dizzy enough to almost pass out. Admitted to hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
2,0
Labordaten
ECG/ MRI Chest XRay
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
NA
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 1651888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MT
Alter
43,0
Geschlecht
F
Eingang
28.08.2021
Impfdatum
05.05.2021
Beginn
05.05.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Electric shock sensation

Symptomtext

I had SSRI withdrawal brain zaps; This is a spontaneous report from a contactable consumer, the patient. A 43-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the arm left on 05May2021 at 15:00 (at the age of 43-year-old) as a single dose for COVID-19 immunisation. Medical history included depression, colectomy (two colon resection) and total abdominal hysterectomy with bilateral salpingo-oophorectomy. Concomitant medications included citalopram (MANUFACTURER UNKNOWN), cetirizine hydrochloride (ZYRTEC), pantoprazole (MANUFACTURER UNKNOWN) ,loperamide hydrochloride (IMODIUM) and amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) from unknown date for unknown indication. It was reported that the patient had no allergies to medications, food, or other products. The patient did not receive any vaccination within four weeks prior to the COVID-19 vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 05May2021 at 17:00, the patient experienced had SSRI withdrawal brain zaps. The patient reported that after the 2nd dose, patient had SSRI withdrawal brain zaps, but patient had not missed or taken the citalopram late, that occurred for about 30 hours total, and began within about two hours of the vaccination. The patient did not receive any treatment for the events. The events do not resulted in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the event SSRI withdrawal brain zaps was on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Colectomy (other_medical_history: two colon resection); Depression; Total abdominal hysterectomy with bilateral salpingo-oophorectomy (other_medical_history: TAH w/ BSO)
Andere Medikamente
CITALOPRAM; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; PANTOPRAZOLE; IMODIUM; ADDERALL
Allergien
-
Vorherige Impfungen
-

VAERS 1646310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NJ
Alter
60,0
Geschlecht
F
Eingang
28.08.2021
Impfdatum
15.04.2021
Beginn
17.04.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Blood pressure increased Blood pressure measurement Cerebral venous sinus thrombosis Headache SARS-CoV-2 test

Symptomtext

Severe headaches; increased high blood pressure; Diagnosed with acute cerebral venous sinus thrombosis.; This is a spontaneous report from a non-contactable consumer (patient). A 60-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EW0162), via an unspecified route of administration, administered in arm right on 15Apr2021 08:30 (at the age of 60-years-old) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced severe headaches, increased high blood pressure and was diagnosed with acute cerebral venous sinus thrombosis on 17Apr2021. The patient was hospitalized for the events for 3 days. The clinical course was as follows: Severe headaches began 2 days following vaccine which continued straight for 2 1/2 weeks followed by extremely increased high blood pressure. Sent to hospital emergency. Admitted and diagnosed with acute cerebral venous sinus thrombosis. The patient underwent lab tests and procedures which included blood pressure measurement: increased (Extremely increased high blood pressure), SARS-COV-2 test: negative (Nasal Swab), both on 03May2021. The adverse events resulted in Emergency room/department or urgent care. Therapeutic measures were taken as a result of all events (Blood Thinners and BP Medication). The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebral venous sinus thrombosis
Hospital-Tage
3,0
Labordaten
Test Date: 20210503; Test Name: Blood pressure; Result Unstructured Data: Test Result:Increased; Comments: Extremely increased high blood pressure; Test Date: 20210503; Test Name: Rapid Test/PCR; Result Unstructured Data: Test Result:Negative; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1295440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
56,0
Geschlecht
F
Eingang
28.08.2021
Impfdatum
14.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Ageusia Autism spectrum disorder Balance disorder Bladder pain Blood urine present Burning sensation Derealisation Dizziness Echocardiogram Electrocardiogram Faeces discoloured Haematochezia Hyperacusis Hypoaesthesia Loss of consciousness Magnetic resonance imaging Melaena Musculoskeletal stiffness

Symptomtext

Caller states she has been having sensory problems such as dizziness, balance issues, chills related to her nervous system; sensory of her skin; blood in her urine and blood in stools along with having had 2 periods even though she is postmenopausal; a red rash on both of her arms and a swollen arm in the arm she received vaccination; a red rash on both of her arms and a swollen arm in the arm she received vaccination; she is now having visual problems.; numbness and tingling that started at her feet and stopped at her knees but went also from her neck to her arms; numbness and tingling that started at her feet and stopped at her knees but went also from her neck to her arms; burning on the feet; her neck was so stiff she couldn't tip it back; Caller states her arms were beat red and the left arm from her first vaccine still swollen; Caller states her arms were beat red and the left arm from her first vaccine still swollen; couldn't walk; unexplained black stools and rectal bleeding for 20 minutes; Raynaud's; bladder hurt so bad; can't taste; states her hearing, vision, and sense of touch is unreal; sensory issues triggering a blackout; blood in her urine and blood in stools along with having had 2 periods even though she is postmenopausal; she felt like she had Parkinson's.; blood in her urine and blood in stools along with having had 2 periods even though she is postmenopausal; melena; unexplained black stools and rectal bleeding for 20 minutes; autism; Caller states she has been having sensory problems such as dizziness, balance issues, chills related to her nervous system; sensitive hearing; This is a spontaneous report from a contactable nurse (patient herself). A 56-year-old female patient received second dose of BNT162B2 (Solution injection; Batch/Lot Number: EW0162), via an unspecified route of administration on 14Apr2021 as single dose for covid-19 immunisation. Medical history included asthma and migraine. The patient's concomitant medications were not reported. The patient previously received first dose of bnt162b2 (Solution injection; Batch/Lot Number: ER2613), via an unspecified route of administration in left arm on 20Mar2021 as single dose for covid-19 immunisation and experienced Rash on arm, vaginal bleeding, Hearing problems, Flu symptoms, balance problems, rushes of chills, Nausea, ringing in the right ear, Patient states her arms were beat red and the left arm from her first vaccine still swollen, Patient states she was a little dizzy from her first dose. Patient states she has been having sensory problems such as dizziness, balance issues, chills related to her nervous system, sensitive hearing, sensory of her skin, and sensory issues triggering a blackout. Patient states that in the beginning when a sound or sensation bothered her, she couldn't move and felt like she was blacking out. Patient states she also had blood in her urine and blood in stools along with having had 2 periods even though she is postmenopausal. Patient states she also had a red rash on both of her arms and a swollen arm in the arm she received vaccination. Patient states that the first day after her second shot she felt like she had Parkinson's. She was not able to walk into the store or drive a car. Patient states she was using a walker and if she felt dizzy she had to hold onto something, and then it would get black all of a sudden. Patient states that she is now having visual problems. Patient states she usually would workout 3 hours a day until two days after her first dose on 22Mar2021, but now can't walk on the treadmill or look at the screen of a music video it throws her balance off. Patient states that at Physical Therapy, they told her that for person her age, she is now 89% disabled. Patient states she has numbness and tingling that started at her feet and stopped at her knees but went also from her neck to her arms. Patient states she is now on Neurontin, Meclizine, and Phenergan for nausea. Patient states that she couldn't hold a mug and when sitting in a chair closing her eyes and fast-forwarding the DVR it makes her dizzy and so do ceiling fans, and when planes are flying over she couldn't take the noise. Patient states it has taken months to walk outside without falling and to be able to wear headphones and she can listen to music now. Patient states that it reminds her of autism, it is affecting her sensory. Patient states she can now drive on a backroad, but with nothing on the side of her or a car in front of her. Patient states the wind throws her off balance and a car going by on the street does too. Patient states she couldn't get out of bed first 3 weeks due to numbness and tingling and burning on the feet. Patient states she took 100mg of meclizine a day at the beginning, her neck was so stiff she couldn't tip it back. Patient also states she is in menopause, but had vaginal bleeding times two and saw gynecologist. Patient states she then had black stools and took to her primary who said it is maybe an ulcer, but she was already treated for h. Pylori. Patient states he diagnosed her with melena and dizziness and her RBCs were normal. Patient states her arms were beat red and the left arm from her first vaccine still swollen. Patient states she was tested for covid and didn't have it. She states her hearing, vision, and sense of touch is unreal and she is now on 900mg Neurontin. She stated that she still cannot drive. The Patient has numbness and tingling, like Parkinson's. The Patient is in therapy for this. The Patient did a test at therapy and it showed that she has severe balancing issues, she is 98% impaired. The Patient was told to take Neurontin and Dramamine. Because of the vaccine the Patient husband is driving her all over to her appointments. The first 3 weeks after the vaccine the Patient thought she was going to die. She stated that there were plenty of doctors around to give you the vaccine but none that want to see you after the vaccine if you have a reaction. She asked if there were any doctors that the Patient can see. The Patient can't see a neurologist until January. The Patient was having a hard time to get in to see her PCP. The Patient has gone to the emergency room several times. They keep telling the Patient to take Dramamine and give it another week, take Dramamine and give it another week, take Dramamine and give it another week. The numbness and tingling started in the Patient feet and came up her legs. The Patient arms were sore with a rash, and her legs felt like a rubber band. The Patient had to drag her legs behind her to walk because she couldn't walk. The nurse didn't want give the Patient the second dose. The Patient requested a half dose of the vaccine for her second dose but they couldn't do that. The Patient still isn't driving, she has sound sensitivity. The fast forwarding on the DVR makes her sick, she has to close her eyes. After the first dose the Patient had nausea and couldn't stand in the shower, it knocked out her vestibular system. The Patient also has problems with hot and cold- its her autonomic system. The Patient couldn't tolerate talking on the phone for the first 2 months. Planes flying overhead was a problem. The Patient has fallen 3 times- once inside and two times outside. Anytime the Patient looks up she almost blacks out. None of these side effects were on the Patient check out sheet- nothing about blacking out. The Patient was in menopause and has had vaginal bleeding. The Patient was checked for yeast and a UTI but they didn't find anything. The Patient has had unexplained black stools and rectal bleeding for 20 minutes. Both of the Patient arms rashed up all the way down. The Patient arm was still swollen from the first shot and numb. The Patient had to use the walker to walk because of the numbness and tingling. For the first 3 weeks if the Patient looks up she felt like she was going to black out. The Patient husband had to hold a plate and cup because she couldn't use them because of her depth perception issues. Patient stated that after the second dose everything amplified. The Patient wasn't able to ride the exercise bike and felt like she was going to black out when she looked around. The vaccine messed up the Patient sensory- her ears are messing up and so are her eyes. The Patient can't take anything in front of her face. The Patient couldn't tolerate the water on her legs in the shower or tilt her head back because her neck was so stiff. The Patient has only washed her hair 4 times since she received the vaccines because of this. The Patient neck felt colder whenever the nurse pulled back the plunger and the nurse put the vaccine in the Patient higher than other people do. After the second dose the Patient arms, she thought it was Raynaud's, her blood vessels were having a reaction. It looked like the Patient has been in the sun but she hasn't. It was an inflammatory response and histamines. The Patient was taking Meclizine after Benadryl. The Patient wants to know why after 4 months was she taking meclizine. Are the Patient symptoms going to go away. The ringing in the right ear started after the first vaccine off and on, but she noticed it yesterday. The Patient menstrual bleeding happened twice and they checked her and didn't find anything. The Patient went back to the gynecologist because her bladder was hurting. The gynecologist did a urine test and it showed she had blood in her urine. The Patient had black stools and was diagnosed with dizziness and melena. The Patient felt wet and went to the bathroom and there was blood, bright red blood when she wiped and no answers. They checked the Patient hemoglobin and no answers. Within that month, in June, the Patient bladder hurt so bad. The Patient took peridium for weeks and Azo because it hurt so bad. They did another urine test a couple of weeks later and there was no blood. All this time the Patient was still having the numbness and tingling and extreme dizziness. The Patient was having to take 100 mg of meclizine, with 75 mg of Benadryl, with nausea medicines, and Neurontin and she was so sleepy. The Patient can now walk to the mailbox as long as there isn't a lot of noise without assistance. The Patient feels like somehow the vaccine hit her sensory. The Patient can't taste and was tested for covid and that was negative. The hot, and cold and noise bother the Patient. The Patient eyes are blurry still in the morning, her depth perception was off, and she can't take the sensory. The Patient saw part of a stool with black in it. The Patient red blood cell count was fine and that was it. The emergency room said as long as you're not having a stroke or heart attack to send her home. The Patient visited the emergency room multiple times but was never admitted as a patient. The first 3 weeks the Patient thought she was going to stop breathing. Every breath out was chills, it was a sensory thing. The Patient still has this, it was almost like autism. The chills run down her arms. The numbness an tingling can be increased by sound. If a plane flew over it was almost like she would black out. The Patient doesn't know what's causing it. The Patient was also given steroids after the vaccine. Since the Patient has migraines the doctors think that's why she has had this reaction. The Patient had blood in the urine, but its gone now. The Patient had an MRI and they thought they saw a tumor on her spine. The Patient had another MRI and the tumor was gone. The Patient has had 3 EKGs. 2 of them said left ventricle possible infarcts. The first EKG was normal. The Patient went to the emergency room every Friday for 3 weeks. The doctor saw something on the Patient heart and ordered a cardiac ultrasound and whatever was there was gone. Everything that was there for one test then disappeared. Sometimes there's irritation and they can't give her a reason why. The Patient has been in menopause for 2 years and doesn't know why the blood showed up. 4 months later and the Patient is still having symptoms. Patient asks if there are doctors who only treat people with vaccination symptoms and wants to know if this was damaging her body. The Patient wanted to know what was causing the numbness and tingling. Some doctors say that meclizine dampens the chemicals in her brain so don't take it, then some say go ahead and take it, then some say to only take it for emergency reasons. No one was telling the Patient the reason for these things. The Patient thinks that there should be a doctor that was able to see patients who have reactions to vaccines. The Patient knows that this is rare but was she was better than she was 2 months ago, she missed more this summer than last summer. The outcome of the events was unknown.; Sender's Comments: Based on available information and the drug temporal relationship, the causality between the events "Loss of consciousness, post-menopausal hemorrhage, Parkinson's disease, Haematochezia, melena, Rectal haemorrhage, Autism spectrum disorder" and the suspect drug "BNT162B2" cannot be completely excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Test Name: cardiac ultrasound; Result Unstructured Data: Test Result:whatever was there was gone; Comments: whatever was there was gone; Test Name: EKG; Result Unstructured Data: Test Result:left ventricle possible infarcts; Comments: caller has had 3 EKGs. 2 of them said left ventricle possible infarcts; Test Name: EKG; Result Unstructured Data: Test Result:normal; Comments: first EKG was normal.; Test Name: MRI; Result Unstructured Data: Test Result:saw a tumor on her spine; Comments: saw a tumor on her spine; Test Name: MRI; Result Unstructured Data: Test Result:tumor is gone; Comments: caller had another MRI and the tumor is gone; Test Name: RBC; Result Unstructured Data: Test Result:Normal; Test Name: covid; Result Unstructured Data: Test Result:she was tested for covid; Comments: Caller states she was tested for covid; Test Name: urine test; Result Unstructured Data: Test Result:blood in her urine; Comments: she had blood in her urine
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Migraine
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1642035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
CA
Alter
36,0
Geschlecht
F
Eingang
27.08.2021
Impfdatum
12.04.2021
Beginn
13.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Chronic obstructive pulmonary disease Dyspnoea Echocardiogram Epistaxis Gingival bleeding Pericardial effusion Pericarditis Rectal haemorrhage

Symptomtext

Bleeding gums nose and rectal bleeding. Pericardial effusion and pericarditis. Shortness of breath COPD

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
3,0
Labordaten
Echo
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Compazine Reglan
Vorherige Impfungen
-

VAERS 1641770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
38,0
Geschlecht
M
Eingang
27.08.2021
Impfdatum
16.04.2021
Beginn
24.08.2021
Tage bis Beginn
130,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest discomfort Chest pain Echocardiogram Electrocardiogram Pericarditis

Symptomtext

Pericarditis chest tightness... Pain... Weird pulse rates. Cant lie flat when sleeping.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
Ekg.... Heart echo
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
Albuterol inhaler
Allergien
Tea mushrooms codeine
Vorherige Impfungen
-

VAERS 1589089

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
-
Geschlecht
U
Eingang
20.08.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Central venous catheterisation Computerised tomogram head Computerised tomogram neck Laryngeal disorder Palatal disorder Paralysis Scan

Symptomtext

Paralyzed soft palate for 26 days and paralyzed right vocal chord for 2 1/2 months and counting

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paralysis
Hospital-Tage
-
Labordaten
Picc line placement and removal CT scan of head neck and chest videostroboscopy
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1407003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
50,0
Geschlecht
M
Eingang
16.08.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Abdominal distension Ageusia Ammonia abnormal Anosmia Blood disorder Chills Diarrhoea Dyspnoea Blood lactic acid increased Blood test Bloody discharge COVID-19 Chest discomfort Cirrhosis alcoholic Coagulopathy Computerised tomogram Confusional state Contusion

Symptomtext

Covid 19 Test positive on 1/14/2021 Full on symptoms: high fever, chills, aches, pains, no taste & or smell, brain fog,extreme tiredness, no appetite, wheezing, right chest and dizziness. Primary prescribed inhaler, tylenol , and antibiotic. 3/8/221 Follow up with dr. Refilled inhaler. Continue to have systems above and increased bruising and tiredness. 4/27/2021 First dose of Pfisher vaccine. Within 12hrs, all core Covid symptoms came back with extreme fever, aches & pain, brian fogm and no smell & taste. First week of May began to turn jaundice, yellowing of the eyes, vision, confusion, bruising & no clotting of cuts, very unsteady on feet, high fevers, swelling of stomach and non appetite. May 7,2021 Fever of 104.3 and uncountable chills and shaking. Along with all the symptoms above along with being unable to get out of bed. Extreme jaundice,yellowing of eyes, and confusion. Used tylenol to treat the fever and fluids. Due to vomiting and diarrhea. May 11, 2021 Saw primary physician and had blood work drawn. Advised to go home, try to rest and increase food and fluids intake. May 13, 2021 Saw primary physician and advised extreme high and low blood counts. Due to the extreme jaundice possible stone or liver issues. The Doctor was going to set up a CT Scan of the liver for the high bilirubin and other blood levels. May 15, 2021 Extreme high fever over 103.6, blood discharge from penis, vomiting , severe diarrhea , confusion, and increased chills & fever spell as from May 7th, 2021. Call 911 to be taken to hospital. May 15- June 1 remained in hospital along with 3 days in CCU. First time we have even been advised about the advanced liver disease, blood factor issues , extreme jaundice, fluid on abdomen, and low blood pressure. Within hours many tests were run, medications, scans, mri?s, ct?s, blood tests, urgliosts, hemototlglists, GI dr?s, and ect. We were advised to have matters in order as it was thought he would have made it through all the infections and the shutdown of the liver, spleen , blood pressure levels, and etc. We have not recovered from the dose of the vaccine as he continues to have motor skill issues, confusion, low blood pressure, mixed-blood cell issues with red and white cells, jaundice, and etc..Doctors are saying we will not know if he will survive until after 6mths as his body is still fighting to heal. He has now been smoke and alcohol-free since May 15, 2021. He will never be able to take another drink or he will be dead in 2 weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
23,0
Labordaten
Medical Tests Blood full panel 5/11/21 Blood full panels 5/15/21 constantly throughout the hospital stay June 1st, 2021 CT Scan, MRI, Ultrasounds May 5/15/21 constantly throughout the hospital stay June 1st, 2021 June 1, 2021, to current blood pressure check, oxygen levels, and pulse 3x a week performed by PT and OT therapy staff. May 26, 2021 - Parcenesits removal of 2.6L of fluid in the abdomen. July 6th Full panel blood work July 20th Full panel blood work Doctors appointments June 15, 2021, was his last dr appointment with primary Dr. June 24, 2021, was his first follow-up appointment with GI dr. July 6, 2021, first appointment with new primary, Dr. July 20, 2021 - 2 week check-up with primary Dr. August 10, 2021 - check-up with primary Dr. Advised to eat more to gain weight added medication for depression/anxiety: Escitalopram 5mg, take 1 tablet every day. The next visit is August 24, 2021, for a checkup and bloodwork. Along with adding OTC meds to help with constipation and juices. Missed dr appointment : August 5, 2021, with GI PT/ OT at the house: PT at the house : 6/9,6/14,6/18,6/21,6/23,6/28,7/2,7/7,7/9,7/13,7/15,7/19,7/21,8/10 OT at the house: 6/10.6/14,6/17,6/22,6/30.7/8,7/14,7/23 7/25/2021 thru 7/28/2021 Called 911 for being nonresponsive. He was taken by ambulance. Frist blood test his ammonia level was 126. Elevated lactic acid level Hepatic Encephalopathy Hyperbilirubinemia Liver cirrhosis, alcoholic Pancytopenia Bleeding and large blood clots in the upper right gums and would not stop with the blood flow. Consulted on-call Dr on 8/3/2021 at primary. Advised to apply pressure, if not better to call in the am for further direction. Consulted with Dr on call and his GI dr early am. Advised to take to ER as soon as possible for blood tests to check the clotting and possible need for platelets. Drove to ER. Sat in ER waiting for 4 1/2 hrs before taken back to the room. Released with to keep eye on bleeding - do not remove the clot on the gums, soft foods, and keep GI appt for 8/5/2021. ( Blood bank was tested for transfusion if needed ) Cirrhosis Gingival bleeding Bloodwork attached ( items circled are too high or too low ) 8/5/2021 thru 8/6/2021 Called 911 for being nonresponsive. He was taken by ambulance. Frist blood test his ammonia level was 148. Was admitted. Coagulopathy Hepatic Encephalopathy Liver cirrhosis, alcoholic Pancytopenia Thrombocytopenia Removed 2 drugs that may be one of the factors for high ammonia levels Alprazolam 05mg at bedtime Trazodone 200mg at bedtime Follow up with primary Dr on August 10th
Aktuelle Erkrankungen
-
Vorgeschichte
Alcoholism
Andere Medikamente
Trazadone 2tab at night 100mg tab Alprazolam .05mg at night Pantoprazole 1tab in the morning - 40mg Tylenol Extra Strength 500 mg tabs standard 2 tabs when needed
Allergien
PCN
Vorherige Impfungen
-

VAERS 1407003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
50,0
Geschlecht
M
Eingang
16.08.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Abdominal distension Ageusia Ammonia abnormal Anosmia Blood disorder Chills Diarrhoea Dyspnoea Blood lactic acid increased Blood test Bloody discharge COVID-19 Chest discomfort Cirrhosis alcoholic Coagulopathy Computerised tomogram Confusional state Contusion

Symptomtext

Covid 19 Test positive on 1/14/2021 Full on symptoms: high fever, chills, aches, pains, no taste & or smell, brain fog,extreme tiredness, no appetite, wheezing, right chest and dizziness. Primary prescribed inhaler, tylenol , and antibiotic. 3/8/221 Follow up with dr. Refilled inhaler. Continue to have systems above and increased bruising and tiredness. 4/27/2021 First dose of Pfisher vaccine. Within 12hrs, all core Covid symptoms came back with extreme fever, aches & pain, brian fogm and no smell & taste. First week of May began to turn jaundice, yellowing of the eyes, vision, confusion, bruising & no clotting of cuts, very unsteady on feet, high fevers, swelling of stomach and non appetite. May 7,2021 Fever of 104.3 and uncountable chills and shaking. Along with all the symptoms above along with being unable to get out of bed. Extreme jaundice,yellowing of eyes, and confusion. Used tylenol to treat the fever and fluids. Due to vomiting and diarrhea. May 11, 2021 Saw primary physician and had blood work drawn. Advised to go home, try to rest and increase food and fluids intake. May 13, 2021 Saw primary physician and advised extreme high and low blood counts. Due to the extreme jaundice possible stone or liver issues. The Doctor was going to set up a CT Scan of the liver for the high bilirubin and other blood levels. May 15, 2021 Extreme high fever over 103.6, blood discharge from penis, vomiting , severe diarrhea , confusion, and increased chills & fever spell as from May 7th, 2021. Call 911 to be taken to hospital. May 15- June 1 remained in hospital along with 3 days in CCU. First time we have even been advised about the advanced liver disease, blood factor issues , extreme jaundice, fluid on abdomen, and low blood pressure. Within hours many tests were run, medications, scans, mri?s, ct?s, blood tests, urgliosts, hemototlglists, GI dr?s, and ect. We were advised to have matters in order as it was thought he would have made it through all the infections and the shutdown of the liver, spleen , blood pressure levels, and etc. We have not recovered from the dose of the vaccine as he continues to have motor skill issues, confusion, low blood pressure, mixed-blood cell issues with red and white cells, jaundice, and etc..Doctors are saying we will not know if he will survive until after 6mths as his body is still fighting to heal. He has now been smoke and alcohol-free since May 15, 2021. He will never be able to take another drink or he will be dead in 2 weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
23,0
Labordaten
Medical Tests Blood full panel 5/11/21 Blood full panels 5/15/21 constantly throughout the hospital stay June 1st, 2021 CT Scan, MRI, Ultrasounds May 5/15/21 constantly throughout the hospital stay June 1st, 2021 June 1, 2021, to current blood pressure check, oxygen levels, and pulse 3x a week performed by PT and OT therapy staff. May 26, 2021 - Parcenesits removal of 2.6L of fluid in the abdomen. July 6th Full panel blood work July 20th Full panel blood work Doctors appointments June 15, 2021, was his last dr appointment with primary Dr. June 24, 2021, was his first follow-up appointment with GI dr. July 6, 2021, first appointment with new primary, Dr. July 20, 2021 - 2 week check-up with primary Dr. August 10, 2021 - check-up with primary Dr. Advised to eat more to gain weight added medication for depression/anxiety: Escitalopram 5mg, take 1 tablet every day. The next visit is August 24, 2021, for a checkup and bloodwork. Along with adding OTC meds to help with constipation and juices. Missed dr appointment : August 5, 2021, with GI PT/ OT at the house: PT at the house : 6/9,6/14,6/18,6/21,6/23,6/28,7/2,7/7,7/9,7/13,7/15,7/19,7/21,8/10 OT at the house: 6/10.6/14,6/17,6/22,6/30.7/8,7/14,7/23 7/25/2021 thru 7/28/2021 Called 911 for being nonresponsive. He was taken by ambulance. Frist blood test his ammonia level was 126. Elevated lactic acid level Hepatic Encephalopathy Hyperbilirubinemia Liver cirrhosis, alcoholic Pancytopenia Bleeding and large blood clots in the upper right gums and would not stop with the blood flow. Consulted on-call Dr on 8/3/2021 at primary. Advised to apply pressure, if not better to call in the am for further direction. Consulted with Dr on call and his GI dr early am. Advised to take to ER as soon as possible for blood tests to check the clotting and possible need for platelets. Drove to ER. Sat in ER waiting for 4 1/2 hrs before taken back to the room. Released with to keep eye on bleeding - do not remove the clot on the gums, soft foods, and keep GI appt for 8/5/2021. ( Blood bank was tested for transfusion if needed ) Cirrhosis Gingival bleeding Bloodwork attached ( items circled are too high or too low ) 8/5/2021 thru 8/6/2021 Called 911 for being nonresponsive. He was taken by ambulance. Frist blood test his ammonia level was 148. Was admitted. Coagulopathy Hepatic Encephalopathy Liver cirrhosis, alcoholic Pancytopenia Thrombocytopenia Removed 2 drugs that may be one of the factors for high ammonia levels Alprazolam 05mg at bedtime Trazodone 200mg at bedtime Follow up with primary Dr on August 10th
Aktuelle Erkrankungen
-
Vorgeschichte
Alcoholism
Andere Medikamente
Trazadone 2tab at night 100mg tab Alprazolam .05mg at night Pantoprazole 1tab in the morning - 40mg Tylenol Extra Strength 500 mg tabs standard 2 tabs when needed
Allergien
PCN
Vorherige Impfungen
-

VAERS 1531572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
UT
Alter
31,0
Geschlecht
F
Eingang
06.08.2021
Impfdatum
14.05.2021
Beginn
30.05.2021
Tage bis Beginn
16,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Arthralgia Chest X-ray abnormal Chest pain Dyspnoea Electrocardiogram abnormal Fatigue Magnetic resonance imaging heart Pain in extremity Pericarditis

Symptomtext

Developed Pericarditis. Severe chest pain, trouble breathing, shoulder and arm pain, extreme fatigue. Went to a 24-hour medical clinic and they thought it was muscular and prescribed Prednisone. The chest pain continued to be severe and I began to have trouble breathing. At this point I went to the Emergency Room, where I was diagnosed with Pericarditis. **My first Covid Vaccine's LOT # was changed: someone crossed out the last number on the lot number (that was stamped on my card) and hand wrote a different number on top of it. The original lot number was: EW0169, but when I received the card, a 2 was hand-written over the 9. This was my first Covid vaccine, given on 04/17/2021

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
EKG, MRI, chest xray: 8/2/2021 - Diagnosed with Pericarditis, prescribed Colchicine and after a follow up visit the next day with my Doctor, gabapentin.
Aktuelle Erkrankungen
None
Vorgeschichte
Borderline High Blood Pressure
Andere Medikamente
Norethindrone, Labetalol, Ibuprofen
Allergien
Penecillan
Vorherige Impfungen
-

VAERS 1524152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
49,0
Geschlecht
F
Eingang
03.08.2021
Impfdatum
18.04.2021
Beginn
20.05.2021
Tage bis Beginn
32,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Asthenia Depressed level of consciousness Dizziness Intensive care Laboratory test Malaise Musculoskeletal disorder

Symptomtext

Lost function of each hand for about 1 week after the shot except after the 2 nd dose my wife?s weakness continued on to the other arm and then one day she wasn?t feeling well and felt dizzy and when I got home she was extremely weak and not very arousable was taken to hospital where she spent 36 day in icu and almost died

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
60,0
Labordaten
Multiple tests done at hospital 5/20 - 7/24
Aktuelle Erkrankungen
Nothing!
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1396012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CT
Alter
38,0
Geschlecht
M
Eingang
31.07.2021
Impfdatum
18.04.2021
Beginn
27.04.2021
Tage bis Beginn
9,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Arthralgia Arthritis Blood creatine phosphokinase Blood magnesium Blood test Asthenia Confusional state Electric shock sensation Hypoaesthesia Blood thyroid stimulating hormone Burning sensation C-reactive protein Disability Dizziness Dyspnoea Dysstasia Electrocardiogram Erythema

Symptomtext

numb hands; paresis; numb face; loss of functions in legs; temporary paralysis of body; throat swelling shut; weak muscles giving out. calves give out; brain zaps; constant muscle spasms; convulsions; tinnitus; extreme pain; weakness; confusion; extreme nerve pain in arms hands and back; scapula, biceps in pain; injection area hurts stille very bad/throbs; numb feet; numb scalp; cannot make a fist or grab a cup; still disabled cannot work or function; This is a spontaneous report from a contactable consumer or other non-health care professional (patient). A 38-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number: EW0162 and Expiry date: Unknown), via an unspecified route of administration, administered in arm left on 18Apr2021 17:00 (at the age of 38-year-old) as single dose for COVID-19 immunization at Public Health Clinic facility. The patient medical history was reported as none. The patient had no known allergies. Concomitant medication included ibuprofen (MANUFACTURER UNKNOWN) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. Prior to vaccination, patient was not diagnosed with Covid 19 and has been tested for Covid-19 since the vaccination. On 27Apr2021 12:00, the patient experienced numb hands, paresis, numb face, loss of functions in legs, temporary paralysis of body, throat swelling shut, weak muscles giving out. calves give out, brain zaps, constant muscle spasms, convulsions, tinnitus, cannot make a fist or grab a cup, extreme pain, weakness, confusion, extreme nerve pain in arms hands and back, scapula, biceps in pain, injection area hurts still very bad/throbs, numb feet, numb scalp, like a nerve is seized in them. Injection area hurts still very bad/throbs, all ongoing for 3 months still disabled cannot work or function. The patient was hospitalized for 1 day. The events resulted in doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The patient did not receive any treatment for the events. The seriousness of the events was assessed as life threatening. The patient underwent lab tests and procedures which included sars-cov-2 test (Nasal Swab): negative on 23May2021. The outcome of all events was not resolved. Device Date was reported as 19Jul2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paralysis
Hospital-Tage
1,0
Labordaten
Test Date: 20210523; Test Name: SARS-CoV-2; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
IBUPROFEN
Allergien
-
Vorherige Impfungen
-

VAERS 1515783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AR
Alter
31,0
Geschlecht
F
Eingang
30.07.2021
Impfdatum
21.04.2021
Beginn
24.05.2021
Tage bis Beginn
33,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Blood test Computerised tomogram abnormal Computerised tomogram thorax normal Dizziness Echocardiogram normal Electrocardiogram abnormal Electrocardiogram ambulatory Gait disturbance Heart rate increased Lymphadenopathy Mammogram normal Orthostatic hypotension Postural orthostatic tachycardia syndrome Presyncope Splenomegaly Stress Tachycardia

Symptomtext

First two days, swollen supraclavicular node. I still have this. Two weeks later, swollen node under right armpit. I still have this. I had ultrasound and mammogram of breasts. No cancer. One month later I had abdominal pain so my doctor ordered a ultrasound and CT scan. It showed enlarged spleen at 15cm and several pericical lymph nodes measuring 1cm. Waiting to see a hematologist on this issue. Then, July 6th I had a sudden episode of tachycardia reaching 150 bmp. Blood pressure 170 over something. Near syncope. Went to hospital several times until I was admitted. The high heart rate abated but returns as soon as I stand. This comes along with postural hypotension as well according to discharge diagnosis. The hospital did EKG, echocardiogram, 24hr holter, x-ray, chest CT, blood work, and nothing showed up except my EKG was abnormal one time. They didn't really explain. I went to my cardiologist because I couldn't hardly walk after these episodes. The dizziness was so bad and I felt like if pass out if I stood. Dr. said I have POTS, (Postural Orthostatic Tachycardia Syndrome) and they're gonna do more testing. I'm seeing an electrophysiologist soon as well as getting a sleep study. I have started on antidepressants and any anxiety meds since from all this stress. I still have all the symptoms except I can walk now around my house and a little outside.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
3,0
Labordaten
5/26/2021 ultrasound
Aktuelle Erkrankungen
Hypothyroidism, depression, anxiety, ovarian cysts
Vorgeschichte
Hypothyroidism, depression, anxiety, ovarian cysts
Andere Medikamente
Euthyrox 150 mcg, cytomel 5 mcg, Taytulla 20mg, B12, multivitamin
Allergien
None that I'm aware of
Vorherige Impfungen
-

VAERS 1510737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NJ
Alter
54,0
Geschlecht
F
Eingang
28.07.2021
Impfdatum
19.04.2021
Beginn
18.05.2021
Tage bis Beginn
29,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Ear pain Electromyogram Facial paralysis Headache Herpes zoster Herpes zoster oticus Magnetic resonance imaging Nerve conduction studies Oral mucosal blistering Pyrexia Vertigo

Symptomtext

Headache, fever, vertigo, ear pain, blisters in mouth, facial paralysis on right side. Symptoms began May 18/2021, ER visit 5/23 resulting in diagnosis of Ramsay Hunt Syndrome : shingles (herpes zoster virus) on 7th cranial nerve.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
MRI 7/13/2021 EMG/Nerve conduction test 7/20/2021
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 1502756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
15,0
Geschlecht
M
Eingang
26.07.2021
Impfdatum
12.07.2021
Beginn
12.07.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood glucose normal Body temperature increased COVID-19 Dizziness Influenza like illness Presyncope SARS-CoV-2 test positive

Symptomtext

Experienced a vasovagal syndrome 5 minutes after COVID vaccine. c/o feeling dizzy, denied itching, shortness of breath, nausea or headache. On exam by Health Care Provider, vitals BP 90/60 rt arm, 106/62 left arm, pulse 59-71, resp rate 20, glucose 102, temp 97.3 with 98% pulse ox. PT transported by EMS to medical clinic for evaluation, In medical clinic, given Pediatlye, monitored and released after feeling better. COVID vacine given on Jul 12th. On Jul 15th, pt c/o flu like symptoms, rapid test neg-fluids given. On Jul 16th, pt temp was 102, HR 98, BP 114/52 and tested positive for COVI. Placed in isolation and will be released on jul 27th

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
None performed
Aktuelle Erkrankungen
07/10/21 Covid Test Neg, c/o HA and treated
Vorgeschichte
No chronic conditions known
Andere Medikamente
None routinely given; given Tylenonl x 1 for a headache
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 1413300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MT
Alter
61,0
Geschlecht
M
Eingang
24.07.2021
Impfdatum
09.04.2021
Beginn
28.05.2021
Tage bis Beginn
49,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Heart rate decreased Syncope Thrombosis Stent placement Thrombectomy

Symptomtext

Fainting spell; blood clot; low heart rate for extended period of time; This is a spontaneous report from contactable consumer (patient). A 61-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 09Apr2021 09:30 (Batch/Lot Number: EW0162) as dose 2, single for Covid-19 immunization. The patient received the 1st dose of Comirnaty (Lot number: ER8727) on 19Mar2021 09:30 AM (at the age of 61years) in left arm for Covid-19 Immunization (no reaction). Medical history included femoral artery aneurysm from Jan2020 to an unknown date. Concomitant medications included atorvastatin calcium (ATORVASTATIN CALCIUM) taken for an unspecified indication, start and stop date were not reported; and acetylsalicylic acid (ASAPRIN) taken for an unspecified indication, start and stop date were not reported. The patient previously took codeine and experienced hypersensitivity. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. On 28May2021 16:00, the patient experienced fainting spell, blood clot, and low heart rate for extended period of time. The patient was hospitalized for the events for 6 days. The events resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The treatment received for the adverse events included Stent inserted and heart rate monitor implanted. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was recovered with sequel on an unspecified date. Seriousness criteria was reported as hospitalization, life threatening illness (immediate risk of death from the event), disability or permanent damage].

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
6,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Femoral artery aneurysm
Andere Medikamente
ATORVASTATIN CALCIUM; ASAPRIN
Allergien
-
Vorherige Impfungen
-

VAERS 1413300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MT
Alter
61,0
Geschlecht
M
Eingang
24.07.2021
Impfdatum
09.04.2021
Beginn
28.05.2021
Tage bis Beginn
49,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Heart rate decreased Syncope Thrombosis Stent placement Thrombectomy

Symptomtext

Fainting spell; blood clot; low heart rate for extended period of time; This is a spontaneous report from contactable consumer (patient). A 61-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 09Apr2021 09:30 (Batch/Lot Number: EW0162) as dose 2, single for Covid-19 immunization. The patient received the 1st dose of Comirnaty (Lot number: ER8727) on 19Mar2021 09:30 AM (at the age of 61years) in left arm for Covid-19 Immunization (no reaction). Medical history included femoral artery aneurysm from Jan2020 to an unknown date. Concomitant medications included atorvastatin calcium (ATORVASTATIN CALCIUM) taken for an unspecified indication, start and stop date were not reported; and acetylsalicylic acid (ASAPRIN) taken for an unspecified indication, start and stop date were not reported. The patient previously took codeine and experienced hypersensitivity. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. On 28May2021 16:00, the patient experienced fainting spell, blood clot, and low heart rate for extended period of time. The patient was hospitalized for the events for 6 days. The events resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The treatment received for the adverse events included Stent inserted and heart rate monitor implanted. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was recovered with sequel on an unspecified date. Seriousness criteria was reported as hospitalization, life threatening illness (immediate risk of death from the event), disability or permanent damage].

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
6,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Femoral artery aneurysm
Andere Medikamente
ATORVASTATIN CALCIUM; ASAPRIN
Allergien
-
Vorherige Impfungen
-

VAERS 1497482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
58,0
Geschlecht
F
Eingang
23.07.2021
Impfdatum
19.04.2021
Beginn
05.07.2021
Tage bis Beginn
77,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Bell's palsy

Symptomtext

Bell's Palsy; This is a spontaneous report from a contactable consumer (reported for herself). A 58-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EW0177), dose 2 via an unspecified route of administration, administered in arm left on 19Apr2021 at 17:00 (at the age of 58-years-old) as dose 2, single for covid-19 immunization at Pharmacy or Drug Store. Medical history included ongoing blood cholesterol and ongoing nephropathy. The patient did not receive any other vaccines within four weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Device Date was reported as 11Jul2021.Concomitant medication within 2 weeks of vaccination included rosuvastatin (ROSUVASTATIN). The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EW0162), dose 1 via an unspecified route of administration, administered in arm left on 19Apr2021 at 17:00 (at the age of 58-years-old) as dose 1, single for covid-19 immunisation. Since the vaccination, the patient had not been tested for COVID-19. On 05Jul2021 at 09:00, the patient experienced bell's palsy. The case assessed as serious (Disabling/Incapacitating, medically significant). There was no Prolonged hospitalization. The adverse event result in Emergency room/department or urgent care. Therapeutic measures were taken as a result of event and treatment included with Prednisone, Valacyclovir and Systane. The outcome of the event was not resolved. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Cholesterol; Nephropathy
Vorgeschichte
-
Andere Medikamente
ROSUVASTATIN
Allergien
-
Vorherige Impfungen
-

VAERS 1376892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
17,0
Geschlecht
M
Eingang
22.07.2021
Impfdatum
18.05.2021
Beginn
02.06.2021
Tage bis Beginn
15,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
C-reactive protein normal Chest X-ray normal Chest discomfort Chest pain Dyspnoea Dyspnoea exertional Echocardiogram normal Electrocardiogram ST segment elevation Pericarditis Red blood cell sedimentation rate normal Electrocardiogram Fibrin D dimer normal Full blood count normal Metabolic function test Troponin normal

Symptomtext

Dx:Pericarditis He complains of retrosternal chest pain that he first noted 01 Jun 2021. He stated he first noted it after eating some warm food at lunchtime yesterday and described it as an "achy" discomfort that does not radiate. It was intermittently mild throughout the day yesterday but worse when he woke up today. Stated that does make him feel mildly short of breath. Pt c/o acute chest pain with dyspnea upon exertion Seems like a straight forward very mild case. Had f/u cardiology appointment on 6/11. Normal CRP and ESR 6/11. ECG 6/11 still with diffuse ST elevation. Scheduled for ECHO. Phone message later stated ECHO normal

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
Vitals: Temp 36.9 Celsius Resp: 16 HR: 71 BP 115/71 O2: 98 CXR: 02 Jun -WNL EKG of June 2, 2021 at 11: 24 shows a normal sinus rhythm with ventricular rate of 67, minimal diffuse ST elevation consistent with pericarditis, no blocks Troponin Levels: 02 Jun- Normal
Aktuelle Erkrankungen
N/A-Information pulled from State level pulled report, details limited-report indicated no comorbidities.
Vorgeschichte
N/A-Information pulled from State level pulled report, details limited-report indicates no comorbidities.
Andere Medikamente
N/A-Information pulled from State level pulled report, details limited.
Allergien
N/A-Information pulled from State level pulled report, details limited
Vorherige Impfungen
-

VAERS 1483819

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MO
Alter
71,0
Geschlecht
F
Eingang
18.07.2021
Impfdatum
05.06.2021
Beginn
06.06.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Appendicectomy Appendicitis Blood culture positive Computerised tomogram abdomen Computerised tomogram abnormal Escherichia infection Intensive care Sepsis

Symptomtext

Acute appendicitis and associated gram negative (E. coli) sepsis which occurred within 24 hours after administration of her second Pfizer COVID-19 vaccination

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
10,0
Labordaten
CT of the abdomen/pelvis 6/6/2021 revealing acute appendicitis. Positive blood cultures for E. coli 6/6/21 and 6/7/21. Admission to the hospital with the need for surgical ICU care and appendectomy which was done 6/7/21.
Aktuelle Erkrankungen
None
Vorgeschichte
Chronic illnesses of Rheumatoid arthritis, mechanical valve replacement (anticoagulation therapy), hypothyroidism, and hypertension.
Andere Medikamente
Warfarin, Losartan, levothyroxine, hydroxychloroquine, diltiazem, Tylenol. None of these medications were new at the time of adverse reaction.
Allergien
No known drug allergies
Vorherige Impfungen
-

VAERS 1471311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
19,0
Geschlecht
F
Eingang
14.07.2021
Impfdatum
26.04.2021
Beginn
01.05.2021
Tage bis Beginn
5,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Blood test abnormal Dizziness Dyspnoea Fatigue Intensive care Nausea Palpitations Temperature intolerance Type 1 diabetes mellitus Urine analysis abnormal Vomiting Weight decreased

Symptomtext

Pronounced weight loss began within two weeks of the first dose. Patient lost 30 pounds in 3 months. She was diagnosed as a Type 1 diabetic July 12, 2021. Her symptoms during those three months included weight loss, dizziness, fatigue, sensitivity to heat, racing heart, easily out of breath, nausea and vomiting.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
3,0
Labordaten
Blood and urine tests done in Dr. office at 10:30am on 7/12/21. The same day, she went to an endocrinologist where more bloodwork was done, and she ended up in the ER and ICU at .
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none known
Vorherige Impfungen
-

VAERS 1446248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
KY
Alter
17,0
Geschlecht
F
Eingang
13.07.2021
Impfdatum
15.06.2021
Beginn
30.06.2021
Tage bis Beginn
15,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Facial paralysis Feeling abnormal Hypoaesthesia

Symptomtext

Pt is a 17 yr/o female who presents with numbness to right side of her face that started on Thursday. She reports Wednesday it felt funny but no numbness or paralysis. Patient reports Thursday she went to PMD for vaccinations face still felt funny but not numb or inability to smile or raise eyebrow. Patient reports Friday and today she is unable to lift eyebrow or smile on the right side. She has not had any blurry vision, no speech abnormality, no headaches, no extremity weakness. Patient with no difficulty ambulating. She has not had any recent illness, no hx of HSV or herpes, no hx of tick bites or removal of ticks from body and no recent fevers or rash. Mom did mention that she did have the covid vaccine pfizer on 6/15. She did not have any symptoms after the vaccines and did well until Thursday. She did receive vaccinations on 7/1, hep a and menigococcal B and conjugate vaccine. She has never had any previous reactions to vaccines. She is otherwise interactive gcs 15.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
augmentin, cobalt, nickel
Vorherige Impfungen
-

VAERS 1464552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NC
Alter
75,0
Geschlecht
F
Eingang
12.07.2021
Impfdatum
03.05.2021
Beginn
17.05.2021
Tage bis Beginn
14,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Bell's palsy

Symptomtext

Patient developed symptoms that appear like Bell's Palsy on May 17, 2021 and reported to the ED on May 18, 2021. She was treated with a short course of prednisone and Valtrex. Symptoms improved within 2 weeks, but continue to linger about 8 weeks later.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
type 2 diabetes, hypertension,
Andere Medikamente
Aspirin, metformin, amlodipine, Probiotic OTC, omega 3 fish oil OTC, CoQ10 OTC, chromium OTC, Vitamin B12 OTC, famotidine, zinc OTC, magnesium OTC, cholecalciferol OTC, ascorbic acid OTC
Allergien
codeine (vomiting) lisinopril and losartan (leg cramps)
Vorherige Impfungen
-

VAERS 1457652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
17,0
Geschlecht
M
Eingang
08.07.2021
Impfdatum
25.04.2021
Beginn
25.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Syncope

Symptomtext

Syncopal episode after receiving vaccine. Adult emergency called. Pt awake and alert within 1-2 mins. To ACC for evaluation

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
zoloft
Allergien
none
Vorherige Impfungen
-

VAERS 1446524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NH
Alter
44,0
Geschlecht
F
Eingang
04.07.2021
Impfdatum
20.05.2021
Beginn
20.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Abnormal dreams Asthenia Autoimmune disorder Blood test Chest pain Chills Dizziness Electric shock sensation Electrocardiogram Head discomfort Headache Immediate post-injection reaction Loss of personal independence in daily activities Paraesthesia Peripheral swelling Pyrexia Tinnitus

Symptomtext

Normal immune reaction: fever, chills, headache Abnormal immune reactions developed immediately including tinnitus in left ear, brain zaps or head rushes constantly throughout the day and night with and without dizziness and tingling and swelling in extremities. This has not resolved six weeks post-vaccine. Developed chest pain, vivid dreams, and head pressure/pain. I've seen an ENT specialist and the Neurologist who are calling these long-haul autoimmune reactions. It feels as if my nervous system is in overdrive and inflamed. It is debilitating and is inhibiting my daily life. I am a healthy 44-year-old woman who was in great health prior to this vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
EKG Full panel blood work MRI to be conducted 7/12/21
Aktuelle Erkrankungen
None
Vorgeschichte
Vestibular issues in the left ear but have been resolved for years.
Andere Medikamente
Vybrid 10 milligrams
Allergien
Sulfa
Vorherige Impfungen
tetannis shot at age 10 and had adverse reaction, sick for over a week with flu like symptoms.

VAERS 1446446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
37,0
Geschlecht
M
Eingang
03.07.2021
Impfdatum
01.04.2021
Beginn
05.04.2021
Tage bis Beginn
4,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Blood test Electromyogram abnormal Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Lumbar puncture Magnetic resonance imaging Muscular weakness Neuropathy peripheral X-ray

Symptomtext

Four days following first dose, sudden numbness developed followed by weakness in right leg. Initially attributed to peroneal neuropathy and did not seek medical help. Second dose was received and left foot numbness developed followed by weakness. Symptoms ascended to knees the next few days and was admitted to the hospital. MRI's, x-rays, blood work, lumbar puncture were performed. Treated with 4 days of IVIG. EMG performed to diagnose with Guillain-Barre Syndrome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Guillain-Barre syndrome
Hospital-Tage
5,0
Labordaten
MRI - 5/7/21 Lumbar Puncture - 5/10/21 EMG - 6/17/21
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
Erythromycin
Vorherige Impfungen
-

VAERS 1439941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
SC
Alter
-
Geschlecht
F
Eingang
01.07.2021
Impfdatum
08.06.2021
Beginn
08.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood glucose abnormal Blood pressure measurement Cold sweat Dizziness Heart rate Pallor Respiratory rate Seizure like phenomena

Symptomtext

Patient exhibited a seizure like episode that lasted approximately 15 seconds.; feel dizzy; pale and clammy skin; pale and clammy skin; This is a spontaneous report from a contactable other hcp (nurse). An adolescent non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0162 and expiry date: unknown), dose 1 via intramuscular on 08Jun2021 as dose 1, single for covid-19 immunisation. The patient's medical history included syncope when patient was younger (had syncopal episode after a vaccination). The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no allergies. On 08Jun2021 the patient experienced exhibited a seizure like episode that lasted approximately 15 seconds. Patient was placed on the ground in a supine position where she regained consciousness. Patient with clammy and pale skin. Attempted to put patient in chair, once in chair she began to feel dizzy and was placed back on the ground in a supine position. Patient was able to sit up on the ground and was given juice and crackers. Patient continued to have pale and clammy skin. Alert and oriented x 3. EMS arrived and patient transported to hospital. The patient underwent lab tests and procedures which included Blood sugar at 14:13 was 92, at 14:05 BP was 122/69, at 14:10 BP was 122/58, at 14:05 heart rate was 100, at 14:05 respiratory rate was 18 on 08Jun2021. The outcome of all the events was unknown.; Sender's Comments: Based on the information available and temporal association, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events. . The case will be reassessed once new information is available The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure like phenomena
Hospital-Tage
-
Labordaten
Test Date: 20210608; Test Name: Blood sugar; Result Unstructured Data: Test Result:92; Comments: Blood sugar at 14:13 was 92.; Test Date: 20210608; Test Name: BP; Result Unstructured Data: Test Result:122/69 mmHg; Comments: AT 14:05 BP was 122/69; Test Date: 20210608; Test Name: BP; Result Unstructured Data: Test Result:122/58 mmHg; Comments: At 14:10 BP was 122/58; Test Date: 20210608; Test Name: HR; Result Unstructured Data: Test Result:100; Comments: AT 14:05 HR 100; Test Date: 20210608; Test Name: RR; Result Unstructured Data: Test Result:18; Comments: AT 14:05 RR 18; Test Date: 20210608; Test Name: RR; Result Unstructured Data: Test Result:20; Comments: AT 14:10 RR was 20
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Syncopal attack (when patient was younger, unknown age, had syncopal episode after a vaccination)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1434021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OK
Alter
14,0
Geschlecht
M
Eingang
29.06.2021
Impfdatum
24.06.2021
Beginn
24.06.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood glucose normal Diarrhoea Dizziness Feeling abnormal Flushing Headache Loss of consciousness

Symptomtext

My son experience after the vaccine around 03:40pm, he felt dizzy, started to black out and passed out. I gave him fluids and called his PCP. I made him eat since he did not eat earlier that day. He states he felt off, I gave him some Tylenol medication. He also had a headaches and started with diarrhea. The next day he stayed in bed, continued with flushed bright red cheeks, diarrhea and the headaches. The day after that he started to feel bit better, I think his symptoms lasted between 36-48 hours. His glucose level was 90.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
thrombocytosis, psoriasis disease
Andere Medikamente
-
Allergien
Gluten, psoriasis disease
Vorherige Impfungen
Flu and MMR vaccines- his arm would swell up and he would get a super local reaction to his arm.

VAERS 1430319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
56,0
Geschlecht
F
Eingang
27.06.2021
Impfdatum
14.05.2021
Beginn
04.06.2021
Tage bis Beginn
21,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Bell's palsy Eye movement disorder Facial paralysis

Symptomtext

Sought treatment on June 5th for drooping right side of mouth and inability to independently operate right eye (unable to close/blink)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
Diagnosed with Bells Palsy
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Multivitamin, Advil, Allegra, Vitamin B, Vitamin D, Vitamin C
Allergien
N/A
Vorherige Impfungen
-

VAERS 1429398

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
17,0
Geschlecht
M
Eingang
26.06.2021
Impfdatum
21.04.2021
Beginn
22.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Chest pain Myocarditis SARS-CoV-2 test

Symptomtext

had his second shot on 21Apr2021 and was in the hospital for chest pains/pressure on April 23-25, diagnosed with Myocarditis,; Myocarditis; had his second shot on 21Apr2021 and was in the hospital for chest pains/pressure on April 23-25, diagnosed with Myocarditis,; This is a spontaneous report from a contactable consumer (patient). A 17-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, lot number: EW0162), via an unspecified route of administration in left arm on 21Apr2021 (at the age of 17-year-old) and as single dose for COVID-19 immunisation. Medical history reported as none, patient had no known allergies. Concomitant medication included escitalopram, dose: 10 mg taken for an unspecified indication, start and stop date were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, lot number: ER8732), via an unspecified route of administration in Arm Left on 31Mar2021. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Reported that patient received Escitalopram 10 mg within 2 weeks of vaccination. Patient was not diagnosed with COVID-19 prior to vaccination and patient did not test for COVID-19 since the vaccination. It was reported that patient had his second shot on 21Apr 2021 and was in the hospital for chest pains/pressure on April 23-25, diagnosed with Myocarditis. The patient was hospitalized for the events for 2 days on 23Apr2021 to 25Apr2021. On 24Apr2021, the patient underwent lab tests and procedures which included blood test for covid test and result with negative. Patient received treatment for events with 10+ ekg's or so, ibuprofen. The outcome of the events was recovered on an unspecified date in 2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
2,0
Labordaten
Test Date: 20210424; Test Name: Blood test; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
ESCITALOPRAM
Allergien
-
Vorherige Impfungen
-

VAERS 1427111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MN
Alter
16,0
Geschlecht
M
Eingang
25.06.2021
Impfdatum
13.05.2021
Beginn
03.06.2021
Tage bis Beginn
21,0
Dosis
1
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein
Balance disorder Demyelination Dysarthria Dysphemia Facial paralysis Gait disturbance Hemiplegia Hypoaesthesia Immunoglobulin therapy Magnetic resonance imaging abnormal Magnetic resonance imaging head abnormal Magnetic resonance imaging spinal abnormal Motor dysfunction Multiple sclerosis Muscular weakness Neuromyelitis optica spectrum disorder Plasmapheresis Toxic leukoencephalopathy

Symptomtext

6/3/21 at 1230 pm: Sudden onset of right arm numbness progressing to transient blurry vision, difficulty walking, right lower extremity weakness, difficulty moving his mouth, stuttering, imbalance, and right sided facial droop. He was admitted to hospital on 6/4/21. Found to have a demyelinating process (see imaging report below). He received IVIG treatment and IV steroids with some (but incomplet)e improvement and was discharged to Rehab on 6/16/21 on oral steroids. However, he had recurrence and progression of symptoms and was sent back to hospital on 6/19/21 with worsening right sided hemiplegia. He underwent repeat high dose IV steroids and initiation of plasmapharesis. He has currently (as of 6/25/21) completed 3 of 5 runs of plasmapharesis with marked improvement in symptoms but still has significant right sided motor deficits. Neurologists here now feel comfortable making a diagnosis of multiple sclerosis. He will likely be discharging home for ongoing therapy and treatment after he completes plasmapharesis on 6/28/21.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
21,0
Labordaten
Extensive testing done including MRI brain (6/3/21 and 6/4/21): "Multifocal T2 hyperintensity within the left centrum semiovale, left middle cerebellar peduncle, subcortical right superior frontal gyrus near the motor cortex and right posterior periventricular white matter adjacent to splenium of the corpus callosum. Questionable T2 hyperintensity of the left optic nerve although exam is not dedicated for optic nerve evaluation therefore finding is equivocal. Largest left centrum semiovale lesion is likely more acute and demonstrates diffusion restriction with faint contrast enhancement. Overall, findings are primarily concerning for a demyelinating process, such as multiple sclerosis, anti-MOG disease or NMO. Acute toxic leukoencephalopathy is also a possibility but considered much less likely. Similar findings on MRI orbits and cervical spine on 6/7 as well as repeat cervical spine MRI 6/23.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
none
Allergien
Morphine
Vorherige Impfungen
-

VAERS 1421157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NC
Alter
53,0
Geschlecht
M
Eingang
23.06.2021
Impfdatum
13.04.2021
Beginn
24.04.2021
Tage bis Beginn
11,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Angiogram cerebral normal Arthralgia Asthenia Balance disorder CSF oligoclonal band absent CSF protein increased CSF test abnormal Chest X-ray normal Computerised tomogram head normal Cough Electrocardiogram normal Eyelid ptosis Facial paralysis Fall Fatigue Full blood count normal Guillain-Barre syndrome Headache

Symptomtext

The patient is a 53 yo previously healthy male who experienced GBS temporally associated with receipt of Pfizer BioNTech COVID vaccine (lot # EW0162 )13 APR 2021. He denies any illness symptoms such as fever, malaise, cough, URI symptoms, n/v/d in the preceding month. He denies any immediate reaction suggestive of IgE mediated event. He reports his initial only side effect was local site tenderness. Approximately 11 days after receipt he had been playing basketball with his kids during the. day and he noted unusual fatigue that evening, pain in his shoulders/neck, took ibuprofen and went to be early. In the morning (Day 14), his right leg slipped and he fell when standing after getting out of bed. He took a few steps and discovered he had no balance and fell again. Family brought him to ER. He was evaluated but no definitive diagnosis and discharged home. He reports on 29 APR 21 (day 16) he was brushing his teeth and couldn't retain water in his mouth. He noted facial drooping, his speech was affected and he returned to ER. ER eval was inconclusive but he was admitted for further evaluation. after multiple tests including LP he was diagnosed with atypical GBS. He received IVIG and was transferred to hospital. He states he improved dramatically after a few days. He was transferred back to hospital and then to rehab for one week and then discharged home. He reports currently he estimates strength at about 60%. He is continuing to improve but fatigues easily. . ER note 27 APR documents c/o body aches x2 days, cough, weakness, HA, perioral numbness and sinus pressure. Also states family member had URI symptoms. Diagnostics included ECG (1st degree block), CXR, CT head, CBC, Chem, LFT, Trop and COVID-19 which were are WNL. A UA showed 2+ ketones. Dx was viral syndrome or possible side effects from COVID vaccine and discharged home, but placed on isolation due to concern for COVID because of symptoms. ER note c/o oral and extremity paresthesias for this date. Triage diagnosis was vaccine reaction. ER note documents c/o facial droop, eye lid droop, left arm weakness. Neuro exam documents facial droop, unable to lift left arm above head. Diagnostics included plain films left femur and hip, ECG, CT/CTA head, MRI brain, MR venography were normal. Neuro consult did not think was CVA but he was admitted for further eval. Symptoms continued to progress to include increased weakness, DTR 1+ throughout, difficulty managing excretions. LP 01 MAY 2021 was positive for protein and neg for oligoclonal bands, or evidence of infection. He was diagnosed with atypical GBS, started on IVIG, and transferred to hospital. He was transferred back 06 MAY after completing IVIG and then transferred for rehab therapy x1 week followed by discharge home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
None reported
Allergien
NKA
Vorherige Impfungen
-

VAERS 1413592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
38,0
Geschlecht
M
Eingang
21.06.2021
Impfdatum
21.04.2021
Beginn
11.05.2021
Tage bis Beginn
20,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Acoustic stimulation tests normal Blood test normal Cardiac monitoring Disturbance in attention Dizziness Electrocardiogram normal Feeling abnormal Head discomfort Headache Hypoaesthesia Lacrimation increased Muscle spasms Muscle twitching Muscular weakness Pain Panic attack Paraesthesia Paranasal sinus discomfort

Symptomtext

1st covid shot: 10 minutes after I felt light headed and numbness\tingles throughout my entire body for up to a minute. (didn't eat prior) 2nd covid shot: felt similar symptoms but only lasted a few seconds. (ate that day) ------------------------------------------------ Issues\Symptoms Week 1 May 2-8 Right eye started slowly watering on Sunday and kept going for a week Dizzy moment on a trip. Eye stopped watering mostly by Saturday ----------------------------------- Week 2 Dizzy moment again at a friend's house(hadn't eaten that day). Numbness through arms/weakness. May 10th: Panic attack. I was driving home and felt the numbness go through my arms so I pulled off and called friends to come and get me and take me home. Ended up calling another firend who is a nurse and she had me squeeze someone's hand and check my face for sign of a stroke etc. She thought I was having a panic attack and said to get some food, take some melatonin and try to calm down and goto sleep which I did. May 11th: Saw General doc who ordered blood work and heart monitor. No recommendations for immediate issue. EKG looked fine. Through the week Numbness and tingles in arms and head Ringing in ears, lots of head/sinus pressure, unable to focus, brain fog. ----------------------------- Week 3 May 19th: Had blood drawn for testing: Night before getting heart monitor I couldn't sleep because it felt like not breathing fast enough made me light headed to the point I could pass out and was getting worried. May 20th: Fitted with a heart monitor for 48 hours. I was freaking out when we got to the hospital and almost went to the ER but we went to cardiology and saw the nurse who helped calm me down and did another EKG which looked good. Blood pressure was high that day possibly from the anxiety. Stayed at my dad's the next few days with the monitor, had tingles a couple times, some pressure, but slept well. ------------------------------ Week 4 May 24th: Followup with General doc said blood tests looked good, not diebetic, blood pressure fine, no signs of heart problems. Gave me 6 days of prednisone and Nasonex for possible inflammation of Eustachian tube. (didn't feel like they helped any) through the week: Felt okish for a day and a half, drove to work and then towards the end of the day started feeling off, right side feels like it's floating up and down, sensation down through leg which lasted about a week. Pushed in between nose and cheek on right side and felt numbness/pain shoot through my head on that side Periods of ringing again though not as much but also periods of head pressure and pain if resting head on hands etc. --------------------------- Week 5 Muscle spasms in both arms lasting a couple minutes, finger twitching on left hand. Also had muscle spasms in legs since. ENT visit June 2nd: Audiologist tested hearing and saw no issues. ENT gave me an exam and did not find any issues with the Eustachian tube or any other problems. Suggested to do see if the symptoms continue to lessen and if they dont then do a VNG test and if that doesn't provide anything that he would have to refer me to a Neurologist next to see if they can find anything. After the visit I came upon a web site and found that there are 300 pages of other people posting having the same symptoms as I have been experiencing for varying lengths of time, some upwards of 10 weeks. https://vestibular.org/forum/dizziness/covid-19-vaccine-side-effects/ At this point I am absolutely convinced my issues have been as a result of some sort of reaction from the covid vaccine. There are way too many people having the same issues in a similar timeframe for not to be true. In the few weeks since I still have symptoms that come and go but don't last nearly as long when they do. However it can still be quite disruptive depending on the circumstance.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
Blood work Heart Monitor Hearing and Vestibular tests
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1412847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OR
Alter
31,0
Geschlecht
M
Eingang
19.06.2021
Impfdatum
18.06.2021
Beginn
18.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Fall Fatigue Head injury Somnolence Syncope

Symptomtext

15 minutes after vaccination, I was severely tired and groggy which was to be expected. That lasted for a few hours then I felt more normal. Around 6.5 hours after vaccination, while standing in my kitchen, I rapidly became very dizzy and fainted, falling to the kitchen floor. My girlfriend was there and said I hit my head on the floor, and was passed out for about 5 seconds before regaining consciousness and slowly coming back to myself. I reminded dizzy for another 20-30 minutes and had to stay laying down, before I was able to come to my feet and feel not dizzy anymore. I had plenty of food and water, so this event felt directly related to the vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
None.
Vorgeschichte
None.
Andere Medikamente
Taken at 6:00 AM: one pill of Sumatriptan/Imitrex 50mg to treat a mild migraine the morning of my vaccine.
Allergien
None.
Vorherige Impfungen
-

VAERS 1366332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NJ
Alter
44,0
Geschlecht
M
Eingang
17.06.2021
Impfdatum
13.04.2021
Beginn
20.04.2021
Tage bis Beginn
7,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia Back pain Chest pain Dyspnoea Fatigue Erythema Headache Injection site pain Lymphadenopathy Neck pain Pain Loss of consciousness Pruritus Pulmonary pain Rash SARS-CoV-2 test negative Sensitive skin

Symptomtext

Passed out; Had troub breathing/couldn't catch breath when went upstairs; Chest pain; Felt like lungs were hurting in back; Weak; Tired; This is spontaneous report received from a contactable consumer (patient). This is the first of two reports with the events related to the first vaccine dose. A 44-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in arm left on 13Apr2021 at 19:00 (Batch/Lot Number: ew0162) as 1st dose, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. No other vaccine received in four weeks. After vaccination on 13Apr2021, no issue w/injection site. a week later had trouble breathing, chest pain, felt like lungs were hurting in back, weak, tired, couldn't catch breath when he went upstairs, almost passed out. No treatment received for adverse event. No covid prior vaccination. No covid tested post vaccination. No known allergies. The outcome of events was not recovered.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021636737 Same reporter/patient/product; different doses/events.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1395021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
15,0
Geschlecht
M
Eingang
13.06.2021
Impfdatum
13.06.2021
Beginn
13.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Feeling hot Head injury Loss of consciousness Seizure

Symptomtext

PATIENT BECAME FAINT, AND HOT AFTER RECEIVING VACCINE. PATIENT THEN WENT UNCONCIOUS, HIT HEAD ON FLOOR AND IS BELIEVED TO SEIZED FOR APPROXIMATELY 20 SECONDS. PATIEN THEN BECAME CONSCIOS, STATED HE WAS STILL FAINT AND LIGHT HEADED AND WAS SEATED UNTIL EMT ARRIVED. EMT CHECKED PATIENTS VITALS, RECOMMEND PATIENT BE SEEN AT NEARBY HOSPITAL TO EXAMINE PATIENT. PATIENT THEN WALKED OUT OF STORE WITH EMT PERSONELL AND GOT IN AMBULANCE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NONE KNOWN
Vorgeschichte
UNKNOWN
Andere Medikamente
UNKNOWN
Allergien
NONE
Vorherige Impfungen
-

VAERS 1391506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
26,0
Geschlecht
F
Eingang
11.06.2021
Impfdatum
16.03.2021
Beginn
18.05.2021
Tage bis Beginn
63,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Condition aggravated Dyspnoea Facial paralysis Fatigue Headache

Symptomtext

Stroke like symptoms: fatigue, headache, facial droop, shortness of breath

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
05/18 please contact doctor for them
Aktuelle Erkrankungen
-
Vorgeschichte
Fatigue, migraines, panic attacks, stroke like symptoms
Andere Medikamente
Nexplenon
Allergien
-
Vorherige Impfungen
-

VAERS 1391000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
-
Geschlecht
F
Eingang
11.06.2021
Impfdatum
16.04.2021
Beginn
17.04.2021
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Blepharospasm Circumstance or information capable of leading to medication error Dizziness Fatigue Feeling abnormal Headache Lymph node pain Neurological symptom Oropharyngeal pain Pain Pain in extremity Sinus pain Somnolence Thrombosis

Symptomtext

a possible clot behind her right calf muscle in her right leg; Right eye is now twitching every so often but not constantly; She was afraid that she was going to have a stroke; Even gets headaches; Extreme pressure and pain in her sinus, lymph, right side of her face and her ear; Extreme pressure and pain in her sinus, lymph, right side of her face and her ear; The right side of her face and her head don't feel right; Pain and pressure in her lymph gland on the right side of her throat; Has extreme tiredness and fatigue; Almost felt like she had a possible clot behind her right calf muscle in her right leg. It was a pain near that calf muscle between her knee and the bottom of her heel; She felt slightly dizzy; Slept more; She didn't go back for the 2nd dose because she considers her reaction to be severe; some neurologic side effects; extreme pressure and pain in her right lymph gland, sinus cavities, her eye, her ear, her temple; This is a spontaneous report from a non-contactable consumer (patient herself). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was: EW0162; Expiry date: unknown) via an unspecified route of administration, administered in Arm Right on 16Apr2021 as 1ST DOSE, SINGLE DOSE for COVID-19 immunization. The patient medical history include anaphylactic shock in 2010 died and was brought back and concomitant medications were not reported. The patient had not taken any other products. She worked in the drug industry for so many years and she did not take medications other than occasionally she would take vitamins or supplements like fish oil or krill oil and maybe vitamin D but nothing on a regular basis and she had not been on any prescription drugs for a very long time. Caller said that she was calling because she got the vaccination on 16APR2021 and she had very severe adverse reactions within 24 hours of getting it. She got her COVID vaccine late Friday afternoon and by Saturday night she had experienced extreme pressure and pain in her right lymph gland, sinus cavities, her eye, her ear, her temple, the right side of her head and her right gland still was not normal. She was trying to avoid going to the doctor because she had a high deductible but she probably would have to go because her right eye was now twitching every so often but not constantly. She really regrated getting the vaccine. She didn't go into a computer system to sign up for her vaccine, someone else did it for her and whatever she agreed to she did not agree to it anymore. She didn't go back for the 2nd dose because she considers her reaction to be severe because she had been extremely healthy for the past few years and not needed to go to the doctor for hardly anything so she was afraid that she was going to have a stroke. Now, over a month and a half later her right gland did not feel right. She even got headaches and the right side of her face and her head did not feel right. She did experience an anaphylactic shock in 2010 died and was brought back, no further details provided. When she got her shot, they kept her for 1/2 an hour because of this. She felt slightly dizzy but for the most part she seemed okay but 24 hours later she literally was curled up and she thought that she was going to die. It was extreme pressure and pain in her sinus, lymph, right side of her face and her ear. Everything began approximately 24 hours after the COVID vaccination except for the eye twitching, that only started about a week ago and it was not constant but she had never experienced anything like that in her life before and it had happened a dozen times in the past two weeks.She was concerned that she might have some neurologic side effects. She said all of her other side effects have subsided somewhat but the real persistent side effect was the pain and pressure in her lymph gland on the right side of her throat. That had been pretty persistent since she got her vaccine, as far as the others, they came and went. She also had extreme tiredness and fatigue. She had slept more since she got the COVID vaccine than normal and she woke up and was awoke for a few hours and then she was tired again and wanted to sleep. The other day she probably slept for 16 out of the 24 hours that day which was quite excessive, it was not normal. This was not constant though. The tiredness was constant. She was sleeping more than she was used to sleeping or that she ever had. In the recent past she did not normally sleep as much. She said that the eye twitching didn't occur today, it occurred yesterday and the day before but she had never experienced anything like that before. Her 2nd dose was supposed to be 07MAY2021 . Another thing that she had that was highly unusual was that she almost felt like she had a possible clot behind her right calf muscle in her right leg. It was a pain near that calf muscle between her knee and the bottom of her heel and it was pretty persistent for few days as well. She didn't bump it on anything. She used a massage cream to massage it out which helped a little bit. It was a little bit strange. The outcome of all events was unknown. followup attempts are possible, additional information has been requested.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylactic shock (died and was brought back)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1390946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
45,0
Geschlecht
M
Eingang
11.06.2021
Impfdatum
15.04.2021
Beginn
13.05.2021
Tage bis Beginn
28,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Angiogram Investigation Pericarditis

Symptomtext

Acute pericarditis; This is a spontaneous report received from a contactable consumer (patient). A 45-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EW0162), via an unknown route in the left arm, on 15Apr2021 (at the age of 45-year-old) at single dose for COVID-19 immunisation. Historical vaccine includes the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number ER8730) administered in Mar2021 for COVID-19 immunisation. No relevant medical history was provided. The patient was not diagnosed with COVID-19 before vaccination. The patient did not have concomitant medications. No other vaccine was received in four weeks. On 13May2021 at 13:00, the patient was found to have acute pericarditis. The event was assessed serious because requiring hospitalization. An angiogram was done, and results were not provided. On 14May2021, a Nasal Swab was done and resulted negative. The patient was recovering from the event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
Test Date: 2021; Test Name: angiogram; Result Unstructured Data: Test Result:unknown results; Test Date: 20210514; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1389761

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
35,0
Geschlecht
M
Eingang
10.06.2021
Impfdatum
10.06.2021
Beginn
10.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dyspnoea Erythema Immediate post-injection reaction Loss of consciousness Muscle contractions involuntary Unresponsive to stimuli

Symptomtext

About one minute following vaccine administration, the patient said he was going to pass out. He lost consciousness but was making snorting/snoring noises and was having muscle contractions that left him rolling around in his chair. This lasted about 2 minutes. He then turned very red and it appeared that he wasn't breathing. I removed his facemask and yelled his name/patted his chest and he began to regain consciousness. He sat for several minutes and said he felt fine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1384573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NH
Alter
57,0
Geschlecht
F
Eingang
10.06.2021
Impfdatum
09.04.2021
Beginn
11.04.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Arteriogram carotid normal Balance disorder Blood pressure increased Burning sensation Central nervous system inflammation Computerised tomogram Deafness Disorientation Dizziness Computerised tomogram head Computerised tomogram normal Disturbance in attention Echocardiogram normal Electrocardiogram ambulatory normal Electrocardiogram normal Feeling abnormal Gait disturbance Echocardiogram

Symptomtext

loss of balance 4/11/21 dizziness / unsteady walking 4/11 lightheaded / near falling to ground 4/24 vertigo 4/28 - ER and hospialized for 2 days (4/28-4/30) Increased blood pressure Increased hear rate blurred vision, trouble concentrating, brain fog, short term memory impacted nystagmus hearing loss inflamation of 7th and 8th nerves, face twitching itchy head, tinglingly pain / burning in feet, achy hands joints,

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
MRI with and without contrast- brain 4/28 normal CT scan with and without contrast- brain and carotoid artery- 4/28 normal ekg, echo caridagram, Holter monitor 4/28 normal 6/3 to 6
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
Lisinipril 10 mg, vitamin c, d3, omega 3, magnesium
Allergien
amolicillin (possible)
Vorherige Impfungen
-

VAERS 1385123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MO
Alter
41,0
Geschlecht
F
Eingang
09.06.2021
Impfdatum
08.06.2021
Beginn
08.06.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Blood glucose Cold sweat Hypotonia Loss of consciousness Nervousness Unresponsive to stimuli

Symptomtext

Pt was very nervous about the injection. It was determined that she had anxiety related to the injection. She passed out and was unresponsive at times, cold sweats, limp. There were no signs of swelling or throat closing. and airways were clear. All vitals were normal following the event, 911 was called and arrived within 5-10 minutes and check vitals again then administered oxygen and she became more responsive. Blood sugar was also checked with a hand-held device and finger stick blood sample. It was determined that she should go top the hospital for additional care and tests.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
No further information available for pt..
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1381876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
SC
Alter
17,0
Geschlecht
F
Eingang
08.06.2021
Impfdatum
08.06.2021
Beginn
08.06.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood glucose normal Cold sweat Dizziness Loss of consciousness Pallor Seizure like phenomena

Symptomtext

Patient exhibited a seizure like episode that lasted approximately 15 seconds. Patient was placed on the ground in a supine position where she regained consciousness. 911 was notified at 1401. Patient with clammy and pale skin. At 1405 BP was 122/69, HR 100, RR 18. Attempted to put patient in chair, once in chair she began to feel dizzy and was placed back on the ground in a supine position.. At 1410 BP was 122/58, RR 20. Blood sugar at 1413 was 92. Patient was able to sit up on the ground and was given juice and crackers. Patient continued to have pale and clammy skin. Alert and oriented x 3. EMS arrived and patient transported to hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Blood sugar at 1413 was 92.
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
No
Vorherige Impfungen
When patient was younger, unknown age, had syncopal episode after a vaccination.

VAERS 1374299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
45,0
Geschlecht
F
Eingang
04.06.2021
Impfdatum
16.04.2021
Beginn
21.05.2021
Tage bis Beginn
35,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Angiogram cerebral normal Anxiety Blood test normal Computerised tomogram head abnormal Dizziness Echocardiogram normal Fatigue Full blood count normal Headache Ischaemic stroke Magnetic resonance imaging head abnormal Metabolic function test normal Thrombosis Ultrasound Doppler Ultrasound scan normal Visual impairment

Symptomtext

PT STARTED EXPERIENCING INTENSE HEADACHES ON THE MORNING OF 5/21/2021. THE HEADACHES CONTINUED ON AND OFF FOR SEVERAL DAYS UNTIL ON 5/24/2021 AT 3 PM, SHE HAD A DEBILITATING HEADACHE WITH DIZZINESS THAT COULD NOT BE RELIEVED. THEN ON THE AFTERNOON OF 5/25/2021, SHE STARTED EXPERIENCING VISUAL CHANGES WITH BLACK SPOTS IN HER VISION. SHE WAS ABLE TO SEE HER DOCTOR ON 5/27/2021 AT 10 AM. HE SENT HER FOR A CT SCAN OF HER HEAD WHICH WAS FOLLOWED BY A MRI OF HER BRAIN. THE MRI AND CT SCAN REVEALED THAT SHE HAD A LEFT FRONTAL ISCHEMIC STROKE. SHE WAS ADMITTED TO THE HOSPITAL ON 5/27 AND DISCHARGED HOME ON THE AFTERNOON OF 5/28. SHE HAD A CT ANGIOGRAM OF THE BRAIN, AN ECHO OF THE HEART, ULTRASOUND OF THE CAROTIDS AND A HYPERCOAGULATION BLOOD PANEL. ALL OF WHICH WERE NORMAL AND SHOWED NO EVIDENCE OF WHERE THE BLOOD CLOTS CAME FROM THAT CAUSED HER STROKE. SHE CONTINUES TO HAVE HEADACHES WITH DIZZINESS, FATIGUE, AND NOW BAD ANXIETY.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Ischaemic stroke
Hospital-Tage
2,0
Labordaten
CBC, BMP, HYPERCOAGULATION PANEL, LIPID PANEL - 5/28/2021 - WNL CT ANGIOGRAM, ECHO, U/S CAROTIDS - 5/28/2021 - ALL NORMAL
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
LEXAPRO
Allergien
NONE
Vorherige Impfungen
-

VAERS 1364598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OK
Alter
14,0
Geschlecht
M
Eingang
01.06.2021
Impfdatum
26.05.2021
Beginn
26.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Confusional state Electrocardiogram Fatigue Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

Ten minutes after receiving vaccine patient had syncopal event. He was unconscious approximately 5-10 seconds. After event patient was extremely diaphoretic, pale and slightly confused for <5 minutes. He complained of feeling very tired. Patients systolic bp unable to be detected, HR 57, O2 97%. Patient was laid in modified Trendelenburg position. BP rechecked after 5 minutes and was in the 90s systolic. Mother said he had a history of a heart murmur that nothing needed to be done about until he was an adult. Advised to go to ER for EKG d/t unknown cardiac condition.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1360642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
-
Geschlecht
U
Eingang
29.05.2021
Impfdatum
20.04.2021
Beginn
24.05.2021
Tage bis Beginn
34,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Peripheral swelling Thrombosis

Symptomtext

I didn't know if this could be a blood clot forming as result of the vaccination or this just regard could still be a blood clot.; I have too swelling in my lower left leg just below the knee; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EW0162; NDC / UPC number of COVID Vaccine: Unknown; Expiration Date: 31Jul2021), via an unspecified route of administration on 20Apr2021 as 2nd dose, single for covid-19 immunisation. Medical history included blood clot and stated as I do have blood clot in my past case history. My mother died at blood clot to the heart. Concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (Lot Number: ER8734; Expiration date: 31Jul2021) for COVID-19 immunisation. On 24May2021, the patient experienced i didn't know if this could be a blood clot forming as result of the vaccination or this just regard could still be a blood clot and i have too swelling in my lower left leg just below the knee. Additional Context was received as, I was calling in regard to my vaccination did I had. The first shot I had on 30Mar2021 and then the second one was on 20Apr2021. Further patient stated, that's what I am really not sure about I am not sure of this, if this is a COVID related vaccine issue or not. I have swelling too in my lower left leg just below the knee. I noticed this first time yesterday and notice this again today few minutes ago looking better and I didn't know if this could be a blood clot forming as result of the vaccination or this just regard could still be a blood clot and I wasn't sure if there was any relation to the vaccine. Patient stated, I am going to try to see my doctor tomorrow, helps to get into see him tomorrow. Like I said I am trying to see my doctor tomorrow. I am trying to see him hopefully he will able to help me. I have concerned about the swelling because I do have blood clot in my past case history. My mother died at blood clot to the heart I had in never and stroke and that is why I concerned. So that's why I go to the doctor tomorrow. Outcome of the events was recovering. Further probing could not be done as consumer was not willing to complete the report. Hence limited information available over the call.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood disorder (My mother died at blood clot to the heart); Blood disorder (I do have blood clot in my past case)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1357350

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
36,0
Geschlecht
F
Eingang
28.05.2021
Impfdatum
29.04.2021
Beginn
30.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia Dizziness Dyspnoea Headache Pulmonary thrombosis Thrombosis

Symptomtext

Blood clots in lung and leg; Blood clots in lung and leg; Dizziness; Weakness; Headache; shortness of breath; This is a spontaneous report from a contactable consumer (patient). A 36-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in the left arm on 29Apr2021 16:00 (Batch/Lot Number: EW0162) as 2nd dose, single dose for COVID-19 immunization. The patient received the first dose of COVID-19 vaccine on 08Apr2021 17:45 left arm for COVID-19 immunization. Medical history included fibromyalgia and had covid-19 prior to vaccination. Concomitant medications included gabapentin; ethinylestradiol, norgestimate (ORTHO-CYCLEN); and diclofenac sodium (DICLOFENAC SODIUM); all taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 30Apr2021 05:00, the patient had blood clots in lung and leg, dizziness, weakness, headache (still after a month) and shortness of breath. As a result of the events, the patient visited doctor or other healthcare professional and has been to the emergency room. The events required hospitalization and was considered a life-threatening illness (immediate risk of death from the event). The patient was hospitalized for two days. The patient was put on blood thinners as treatment for the events. The patient has not recovered from the events.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary thrombosis
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19; Fibromyalgia
Andere Medikamente
GABAPENTIN; ORTHO-CYCLEN; DICLOFENAC SODIUM
Allergien
-
Vorherige Impfungen
-

VAERS 1357229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IN
Alter
43,0
Geschlecht
F
Eingang
28.05.2021
Impfdatum
13.05.2021
Beginn
13.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bell's palsy Dizziness Ear pain Headache Hypoaesthesia Hypoaesthesia oral Oropharyngeal pain Paraesthesia Paraesthesia oral Pharyngeal hypoaesthesia

Symptomtext

sore throat/her throat started hurting very bad and it does not have any signs of stopping; concerned about signs of Bell's palsy; numbness that goes under her chin and down throat then from her tongue to the back of her throat/cheeks and lips went numb/numbness was all over her face bilaterally/numbness tongue down her throat; numbness that goes under her chin and down throat then from her tongue to the back of her throat/cheeks and lips numb; numbness that goes under her chin and down throat then from her tongue to the back of her throat/cheeks and lips numb; lip and right cheek got very tingly/tingling in cheeks and lips; lip and right cheek got very tingly/tingling in cheeks and lips; pounding headache; lightheadedness and dizziness; severe left ear pain; This is a spontaneous report from a contactable nurse (patient). A 43-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right arm on 13May2021 at 09:30 am (at the age of 43 years old) (Lot Number: EW0162; Expiration Date: Jul2021) as 1st dose, single for COVID-19 immunization. Medical history and concomitant medications reported as none. The patient reported that she got the first dose of the Pfizer COVID-19 vaccine on 13May2021 at 09:30am. At 09:54am, she noticed her lip and right cheek got very tingly/tingling in cheeks and lips and at 10:04 am she had numbness that goes under her chin and down throat then from her tongue to the back of her throat/both cheeks and lips went numb. Then at 12:00 noon, the intense numbness was all over her face bilaterally and had numbness tongue down her throat. At 13:45, her throat started hurting very bad and it does not have any signs of stopping and so she is concerned about signs of Bell's palsy. The patient confirmed that she did not have loss of muscle control, she can still swallow and breathe. She confirmed that she has no signs of stroke. But had severe left ear pain since the vaccine. The patient did not think this is an emergency. She was told to report these to Pfizer. The patient was not sure if she should get the second vaccine and wondered if these were all normal. She declined to provide primary care provider details stating she hasn't been seen by one in a while. She stated that the soreness/hurting of throat was not there at first but is getting worse and also her tongue is also going numb and it's going down the throat. She did not have any weakness, but has pounding headache, some lightheadedness and dizziness, and sore throat on 13May2021. She has not been seen by provider and has not been to emergency room. She did call her family doctor and was instructed to go to the emergency room, but she wanted to see if the symptoms would subside first and notify Pfizer. No other vaccines given the same time on 13May2021 and no other vaccines 4 weeks prior. No problems with vaccines in the past. Outcome of the event severe ear pain was unknown, while not yet recovered from the remaining events. The events Bell's palsy, lip and right cheek got very tingly/tingling in cheeks and lips, numbness that goes under her chin and down throat then from her tongue to the back of her throat/cheeks and lips went numb/numbness was all over her face bilaterally/numbness tongue down her throat, sore throat/her throat started hurting very bad and it does not have any signs of stopping, pounding headache, and lightheadedness and dizziness were assessed as serious (medically significant). Information on Lot/Batch number was available. Additional information has been requested.; Sender's Comments: A causal association between BNT162B2 and the reported events cannot be excluded based on a temporal relationship. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1349551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MD
Alter
23,0
Geschlecht
F
Eingang
26.05.2021
Impfdatum
17.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest pain Dyspnoea Fatigue Hypoaesthesia oral Oropharyngeal pain Peak expiratory flow rate Pulmonary oedema Throat irritation

Symptomtext

the back of her tongue felt numb/developed a numb tongue; throat was itchy then sore/her throat was sore and itchy; throat was itchy then sore/her throat was sore and itchy; chest pain; not quite normal breathing/uncomfortable breathing/heavy breathing that was more of an irregular breathing; Fatigue; her lungs felt swollen; This is a spontaneous report from a Pfizer-sponsored program via a consumer reported for a patient (reporter's mother). A 23-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Right on 17Apr2021 (Lot Number: EW0162) (at the age of 23-year-old) as single dose for covid-19 immunization. Medical history included asthma and diagnosed at age 2, allergy and allergy to bull dogs. Concomitant medications included budesonid taken for allergy, start and stop date were not reported; formoterol fumarate dihydrate taken for allergy, start and stop date were not reported. The patient experienced her lungs felt swollen in Apr2021, the back of her tongue felt numb/developed a numb tongue on 17Apr2021, throat was itchy then sore/her throat was sore and itchy on 17Apr2021, chest pain on 17Apr2021, not quite normal breathing/uncomfortable breathing/heavy breathing that was more of an irregular breathing/out of breath walking up the steps on 17Apr2021 and fatigue on 17Apr2021. A family member had some reaction to the first pfizer covid-19 vaccine. Wanted to know where can she find information to determine if the second vaccine shot is safe. 40 minutes from the time of the injection the back of her tongue felt numb and her throat was itchy then sore. About 40 minutes after that those symptoms went away. Later in the day she had chest pain and not quite normal breathing. After using her asthma inhaler twice in a short time this dissapated. Fatigue remained for about a week. Her daughter was prescribed Metronidazole 500mg (she initially thought it was penicillin) and the packaging information of the antibiotic says not to receive any vaccines. She was scheduled for her second dose next Tuesday (18May2021) and wanted to know if it would this be applicable to the Pfizer BioNTech Covid 19 vaccine. Mother calling on behalf of daughter who received the first dose of the Pfizer BioNTech Covid 19 vaccine on 17Apr2021. She was told to wait 30 minutes after the vaccine and was okay, however after 40 minutes after the vaccine she developed a numb tongue, her throat was sore and itchy. This subsided within about 30 minutes (also reported as 40 minutes). About 4 hours after the vaccine she developed chest pain and uncomfortable breathing. Her daughter states her lungs felt swollen, and was out of breath walking up the steps. She did use her AuviQ and albuterol inhaler and the first dose of AuviQ didn't work so she repeated it and it helped. She called the doctor and used her peak flow meter and the doctor on call stated that her reading was okay and did not need further medical attention. After that evening those side effects went away. Caller has a past medical history of asthma and allergies to bulldogs. If she was even around someone who has been near a bull dog she will develop chest symptoms. Mother spoke with CDC and they told her as long as her daughter didn't go to the ER it was okay for her to receive the vaccine and wanted to know if she get her second dose of the Pfizer BioNTech Covid 19 vaccine. She is scheduled to receive it next Tuesday (18May2021). Her doctor said that some people react to the polyethylene glycol and want to know if she could get tested for that. After the patient received the vaccine, her tongue was numb and her throat was sore and itchy but it went away. This started 40 minutes after the patient received the vaccine. 4 hours after the patient received the vaccine, she had chest pain and heavy breathing. The caller is nervous because the patient has only had this chest pain during a severe allergic reaction in the past. The patient do about the second dose. The patient was also prescribed an antibiotic this week and the antibiotic paperwork said not to have any vaccines while taking that product. The patient is due for the second dose of the vaccine this week, is it okay to get because she will still be on the penicillin. This event happened after receiving the first dose of the vaccine on 17Apr2021. The patient also had fatigue for a week. The patient had the heavy breathing that was more of an irregular breathing. The patient's lungs felt swollen, it felt like there was weight on her chest, it was uncomfortable breathing. The caller felt out of breath walking up the steps. The caller used her inhaler twice. The patient underwent lab test included investigations: the on call doctor had the patient do the peak flow meter and it was fine, over 550 on 17Apr2021. No more information was available. The doctor also had the patient press her chest to see if there was pain when she touched it and there was not so the on call doctor felt comfortable not making the patient go to the emergency room. Caller reports that her daughter received her first vaccine dose on 17Apr2021 and afterwards experienced a severe reaction with symptoms including, tongue swelling, sore throat, and Chest pain. Caller reported that it didn't getm severe enough for her to need an Epi pen. Caller reports that they have an appointment to see her doctor as well, for further discussion. She calls today to ask if symptoms with the second dose are expected to be worse than they were with the first shot and timing of the second dose. We refer you to speak to your healthcare provider about the risks of the vaccine compared to the risks of potentially not being fully protected against COVID- 19 infection. Your healthcare provider knows your health situation and has access to information that can better help inform this decision. The outcome of the event her lungs felt swollen was unknown, the event fatigue was recovered in Apr2021, the other events was recovered on 17Apr2021. Information on lot/batch is available; further information has been requested.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary oedema
Hospital-Tage
-
Labordaten
Test Date: 20210417; Test Name: Peak flow; Result Unstructured Data: Test Result:over 550; Comments: peak flow meter and it was fine, over 550 More information available (Y/N): NO
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy (the patient has only had this chest pain during a severe allergic reaction in the past.); Allergy to animal; Asthma (Diagnosed at age 2)
Andere Medikamente
BUDESONID; FORMOTEROL FUMARATE DIHYDRATE
Allergien
-
Vorherige Impfungen
-

VAERS 1347707

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
76,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
13.04.2021
Beginn
28.04.2021
Tage bis Beginn
15,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Adenovirus test Aortic arteriosclerosis Aortic valve stenosis Arteriosclerosis coronary artery Atelectasis Bilevel positive airway pressure Blood glucose increased Blood magnesium increased Bordetella test negative COVID-19 Chest X-ray abnormal Chest pain Chlamydia test negative Computerised tomogram thorax abnormal Diastolic dysfunction Dyspnoea Ejection fraction decreased Emphysema

Symptomtext

Hypoxia & Shortness of breath Chief Complaint Patient presents with ? Shortness of Breath x 3 days, denies any cough, congestion, or fever. daughter is with her. Oxygen very low 74, provider notified right away and he came into room. ED to Hosp-Admission Discharged 4/15/2021 - 4/17/2021 (2 days) Last attending ? Treatment team Aspiration pneumonia of left lower lobe, unspecified aspiration pneumonia type (HCC) Principal problem Hospital Course HPI: a 76 y.o. female presenting to the ED with chief complaint of chest pain and shortness of breath. Patient is being seen in the emergency department for evaluation of the above, here with her daughter. Patient was seen and evaluated by local urgent care and referred here for evaluation. Is reported that patient was hypoxic. Patient's daughter also states that they have been monitoring her oxygen saturation at home and it has been in the 60s and 80%. Patient does report a cough. She has been using her inhaler more frequently. Received her Covid vaccination 2 days ago. Hospital Course: Patient was admitted and placed on supplemental O2. Chest x-ray 4/15/2021 showed some opacity at the left costophrenic angle effusion with some areas of atelectasis possible. Chest CT performed on 4/16/2021 revealed small areas of consolidation/infiltrate in the right upper and left lower lobes of the lungs, emphysema, and a 3 mm pulmonary nodule in the left upper lobe. Small bilateral pleural effusions have decreased since CT of12/11/2020. Initial CBC revealed white blood cell count of 9.3. Hemoglobin and hematocrit were stable at 8.8 and 29.4. Renal function was stable as well. Glucose on 4/16/2021 fasting was 222. Magnesium was at goal at 2.5. Procalcitonin levels were performed and were 0.19. She was initially started on IV vancomycin and cefepime as well as Flagyl due to possible aspiration pneumonia. On 4/17/2021, patient was adamant on being discharged. She did discuss possibly signing out AMA. I did explain to her the ramifications of that. She voiced understanding. I also discussed this with her daughter, as well. She required 4 L of supplemental O2 and achieved an O2 sat of 93%. On room air patient was 78%. Therefore, home O2 was ordered. IV antibiotics were changed to oral Levaquin 250 mg to take 1 by mouth daily (based on renal function) for 7 days and generic Flagyl 500 mg to take 1 3 times a day for 7 days. She was instructed to take antibiotics as prescribed as well as use supplemental O2. She was also advised that if symptoms worsened she was to return to the emergency room. At time of discharge she was stable with supplemental O2 in place. ED to Hosp-Admission Discharged 4/28/2021 - 5/4/2021 (6 days) Last attending ? Treatment team Hospital Course HPI: a 76 y.o. female with a past medical history of systolic and diastolic heart failure, diabetes mellitus type 2, above-the-knee amputation of left lower extremity, who comes from home where her oxygen saturation as per the daughter was 25%. She was recently discharged from here on 4/17/2021 for left lower lobe pneumonia. She does not want to be in the hospital. She states that she felt fine when she came in this time. She was evaluated by the ICU who stated she is a DNR/DNI and felt that with BiPAP modification she was satting better. She was adamant that she wanted to leave the last time she was here and went home with oral Levaquin and Flagyl. When she arrived, nursing states that there was dried stool on her bottom. The patient denies any current shortness of breath. She wants her BiPAP mask removed as it is uncomfortable to her. After explaining it as needed she agreed to have it on. She denies any abdominal pain, she denies any chest pain. She denies any fevers or chills. Hospital Course: Patient was admitted for acute on chronic diastolic CHF, acute on chronic hypoxic respiratory failure secondary to CHF and COVID-19. Patient was also treated for elevated blood pressures. Cardiology was consulted, patient was placed on Lasix twice daily and was started on hydralazine for blood pressure. From pneumonia standpoint, patient started on Zosyn, for COVID-19 patient was started on Decadron and remdesivir. Patient finished a course of remdesivir in the hospital. Patient went from using 5 L oxygen to only 1 L, meanwhile chronically she has been using 3 L at home prior to coming into the hospital. Patient has not been requiring any further BiPAP. She has been afebrile for more than 48 hours. Today nephrology recommended to lower Lasix down to once daily instead of twice daily to avoid kidney injury. Patient is medically stable for discharging home today to finish her course of Augmentin and Decadron. Patient appears to be very hesitant about having to continue self isolating. Family understands the need for further isolation. Patient will receive a remote monitoring kit upon discharge. ED to Hosp-Admission Discharged 5/10/2021 - 5/17/2021 (7 days) Last attending ? Treatment team Pneumonia due to COVID-19 virus Principal problem Hospital Course HPI: Patient was admitted with hypoxia and pneumonia due to COVID-19 virus. For details please see the history and physical. Hospital Course: Patient had previously been diagnosed with COVID-19 pneumonia about 3 weeks ago and had been treated with remdesivir Decadron and antibiotics. She was now admitted with pneumonia and hypoxemia. Her oxygen requirement went up and she was at 1 point requiring high flow oxygen up to 15 L/min. Subsequently her oxygen requirement was able to be tapered. She was treated with steroids during this hospitalization. Her oxygen requirement is now down to 4 L/min. She is feeling better. She is now felt stable for discharge with outpatient follow-up with her PCP. Steroids have been stopped on discharge. Her daughter was regularly updated during this hospitalization. I called and left a message at the time of discharge today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
13,0
Labordaten
04/28/21 1119 Respiratory virus detection panel Collected: 04/28/21 1000 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected ED to Hosp-Admission Discharged 4/15/2021 Imaging Results Procedure Component Value Ref Range Date/Time Transthoracic echo (TTE) limited (Abnormal) Resulted: 04/16/21 1704 Order Status: Completed Updated: 04/16/21 1704 MV E/E' septal 22.44 MV E' tissue velocity septal 0.06 m/s Valve area - Index 0.7 cm2/m2 LVEF, A2C 42 >50 % LVEF, A4C 40 >50 % LVOT SI 19.70 ml/m2 AoV Vmax (trace/curve) 1.82 m/s Aortic root 2.5 cm LA volume index A2C 44.70 mL/m2 LA volume index A4C 26.90 mL/m2 LVEF, 2D 40 % AoV VTI 34.49 cm AoV peak gradient 14 mmHg AoV mean gradient 8 mmHg AVA peak vel 1.5 2.0 cm2 LVOT max velocity 0.88 m/s LVOT peak VTI 18.05 cm LVOT peak gradient 3 mmHg LVOT mean gradient 2.0 mmHg LVOT diameter 2 cm FS 19Abnormal 28 - 44 % IVSd 1.1 0.6 - 1.1 cm LVIDd 4.70 3.70 - 5.60 cm LVIDs 3.80 2.00 - 3.80 cm LVEDV 103 mL EF 40 >50 % LVESV 62 mL LVPWd 1.1 0.6 - 1.1 cm LADs 4.2Abnormal 1.9 - 4 cm MV deceleration time 116 msec MV peak A velocity 0.94 m/s MV peak E velocity 1.41 m/s MV E/A ratio 1.50 MV E' tissue velocity lateral 0.06 cm/s AVA by cont VTI 1.6 2.0 cm2 LVOT stroke volume 56.68 mL LA Volume Index 35.8 mL/m2 LV Diastolic Volume Index 3.8 Narrative: ? Left Ventricle: Left ventricle visualization improved with use of imaging enhancing agent. Left ventricle cavity appears normal. ? Left Ventricle: Hypokinetic basal to mid lateral wall, hypokinetic basal to middle portion of the anterior wall. ? Left Ventricle: Systolic function is mildly decreased with an ejection fraction of 40-45%. ? Left Ventricle: Wall thickness is normal. ? Left Ventricle: There is grade II (moderate) diastolic dysfunction and elevated left atrial pressure. ? Right Ventricle: Systolic function is normal. ? Aortic Valve: There is mild stenosis. AVA=1.7 cm 2 Peak/mean gradient=14/8 mm Hg ? Mitral Valve: There is mild to moderate regurgitation with a centrally directed jet. ? Tricuspid Valve: RV systolic was not estimated due to inadequate jet. X-ray chest 1 view - Portable Resulted: 04/16/21 0737 Order Status: Completed Updated: 04/16/21 0737 Narrative: XR CHEST 1 VW PORT INDICATION: Shortness of breath. Female, 76 years COMPARISON: Chest radiograph from None. FINDINGS: Single frontal view of the chest shows some streaky interstitial changes. There is blunting left costophrenic angle. Heart is mildly prominent size. No pneumothorax. Surgical clips in right axilla. The bones are osteopenic. IMPRESSION: Some opacity at the left costophrenic angle. Effusion with some areas of atelectasis possible. END OF IMPRESSION: This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT chest without contrast (Abnormal) Resulted: 04/16/21 0125 Order Status: Completed Updated: 04/16/21 0125 Narrative: PROCEDURE INFORMATION: Exam: CT Chest Without Contrast; Diagnostic Exam date and time: 4/16/2021 12:11 AM Age: 76 years old Clinical indication: Shortness of breath, hypoxia. TECHNIQUE: Imaging protocol: Diagnostic computed tomography of the chest without contrast. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. COMPARISON: CT Chest 12/11/2020 5:53 PM FINDINGS: Small area of consolidation with adjacent airspace disease in the right upper lobe of the lung which is similar to the comparison examination. Mild dependent atelectasis and few small patchy areas of new consolidation are present in the left lower lobe of the lung. Mild dependent atelectasis in the right lower lobe of the lung. Emphysema is present. 3 mm nodular focus is present in the left upper lobe of the lung at the lung apex which is not clearly seen on the comparison examination. Large airways are patent. Small bilateral pleural effusions which are decreased in size relative to the comparison examination. Heart is normal in size. No significant pericardial effusion. Trace fluid remains in the superior pericardial recess. Aortic and coronary artery atherosclerotic calcification. No thoracic aortic aneurysm. Few small stable mediastinal lymph nodes, none pathologic by size criteria. Liver is decreased in attenuation compatible with fatty infiltration. Visualized upper abdominal contents are otherwise unremarkable by unenhanced examination. Post right mastectomy with surgical clips in the right axilla. Osseous structures are intact. Mild degenerative changes involve the spine. IMPRESSION: 1. Small areas of consolidation/infiltrate in the right upper and left lower lobes of the lungs, similar on the right and new on the left relative to the comparison examination. 2. Mild lower lobe atelectasis. 3. Emphysema. 4. 3 mm pulmonary nodule in the left upper lobe of the lung which is not clearly seen on the comparison examination. 5. Small bilateral pleural effusions which have decreased in size relative to the comparison examination. 6. Atherosclerotic vascular disease which includes coronary artery disease. 7. Fatty infiltration of the liver. 8. Post right mastectomy. Results Procedure Component Value Ref Range Date/Time CT chest without contrast Resulted: 04/28/21 2114 Order Status: Completed Updated: 04/28/21 2114 Narrative: CT CHEST WO CONTRAST IMPRESSION: Small bilateral pleural effusions Unchanged infiltrate right upper lobe slightly worsened infiltrate in the right lower lobe and stable infiltrate in the left lower lobe compared with 4/16/2021. END OF IMPRESSION: INDICATION: covid/pneumonia/HF exacerbation. TECHNIQUE: The thorax was scanned from the diaphragm to the lung apex without intravenous contrast administration and axial, coronal, and sagittal views were obtained. Up-to-date CT equipment and radiation dose reduction techniques were employed. CTDIvol: 13.1 mGy. DLP: 446 mGy-cm. COMPARISON: Chest x-ray 4/28/2021, chest CT 4/16/2021 FINDINGS: Lungs and pleura: There is a focal area of consolidation in the right upper lobe with thickening of the fissure in the right upper lobe which is relatively unchanged. There is fluid in the inferior right major fissure. Persistent consolidation is identified in the left lung base which is unchanged and slightly worsened in the right lung base. There are small bilateral pleural effusions. Mediastinum and hila: Normal. Heart, aorta and pericardium: Normal. Bones and soft tissues: Normal. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view, Portable Resulted: 04/28/21 1924 Order Status: Completed Updated: 04/28/21 1924 Narrative: XR CHEST 1 VW PORT ,4/28/2021 6:36 PM EDT IMPRESSION: There are worsening infiltrates in the left and right lung bases. This appears be a combination of airspace infiltrate and interstitial infiltrate. There are also mild increased interstitial markings in the left and right midlung zone that are more prominent END OF IMPRESSION: INDICATION: dyspnea. Covid 19 positive 76 years, Female TECHNIQUE: Portable AP view of the chest. COMPARISON: 4/20/2021 chest x-ray obtained at 10:20 AM FINDINGS: The heart is borderline in size. There are worsening infiltrates in the left and right lung bases. This appears be a combination of airspace infiltrate and interstitial infiltrate. There are also mild increased interstitial markings in the left and right midlung zone are more prominent. No pleural effusion. There is no pneumothorax. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view Resulted: 04/28/21 1031 Order Status: Completed Updated: 04/28/21 1031 Narrative: XR CHEST 1 VW PORT IMPRESSION: Left lower lobe opacity where pneumonia is suspect worsened/new END OF IMPRESSION: INDICATION: Shortness of Breath. TECHNIQUE: Portable COMPARISON: 4/15/2021 FINDINGS: Opacities seen in the left lung base which is worsened. Heart size vascularity mediastinum are normal. Postsurgical changes are demonstrated in the right axilla. Imaging Results Procedure Component Value Ref Range Date/Time X-ray chest 1 view Resulted: 05/10/21 1730 Order Status: Completed Updated: 05/10/21 1730 Narrative: XR CHEST 1 VW IMPRESSION: Mild interval increasing Covid type infiltrates in the lungs bilaterally. END OF IMPRESSION: INDICATION: SOB. 76 years TECHNIQUE: AP chest COMPARISON: 4/28/2021 FINDINGS: The heart is normal in size. Patchy linear and hazy opacities are noted throughout the lungs suggesting Covid type pneumonia. Findings are mildly worsened. There is no pleural effusion. There is no pneumothorax.
Aktuelle Erkrankungen
-
Vorgeschichte
Respiratory Asthma Pneumonia due to infectious organism, unspecified laterality, unspecified part of lung Acute hypoxemic respiratory failure (HCC) COPD exacerbation (HCC) Hemoptysis Acute respiratory failure with hypoxia (HCC) Aspiration pneumonia of left lower lobe, unspecified aspiration pneumonia type (HCC) Pneumonia due to COVID-19 virus Circulatory Peripheral vascular disease (HCC) Essential hypertension Pulmonary hypertension (HCC) Accelerated hypertension Chronic systolic CHF (congestive heart failure) (HCC) CAD (coronary artery disease) Genitourinary CKD stage 4 due to type 2 diabetes mellitus (HCC) Chronic kidney disease, stage 3b Musculoskeletal Arthritis Osteoporosis Primary osteoarthritis of right knee Closed nondisplaced intertrochanteric fracture of left femur with routine healing, subsequent encounter Endocrine/Metabolic Type 2 diabetes mellitus (HCC) Hypertriglyceridemia Hypothyroidism Hematologic Leucocytosis Infectious/Inflammatory COVID-19 Other Anxiety disorder History of above-knee amputation of left lower extremity (HCC) Cancer (HCC) S/P ORIF (open reduction internal fixation) fracture Weakness Personal history of malignant neoplasm of breast Suspected urinary tract infection
Andere Medikamente
albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler ALPRAZolam (XANAX) 0.25 mg tablet aspirin 81 mg chewable tablet cholecalciferol (VITAMIN D3) 1,250 mcg (50,000 unit) capsule furosemide (LASIX) 40 mg tablet gabapentin (NEURONTIN)
Allergien
Erythromycin Flu Vac Ts 2014 (18-64yrs)(pf) Plavix [Clopidogrel]
Vorherige Impfungen
-

VAERS 1347480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
58,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
09.04.2021
Beginn
28.04.2021
Tage bis Beginn
19,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Acute respiratory distress syndrome Culture throat SARS-CoV-1 test SARS-CoV-2 test

Symptomtext

Acute respiratory disease Dx

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory distress syndrome
Hospital-Tage
-
Labordaten
04/28/21 1305 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 04/28/21 0843 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result DetectedCritical
Aktuelle Erkrankungen
-
Vorgeschichte
Nervous Cervical dystonia Other Disorder of eye movements
Andere Medikamente
botulinum toxin Type A (BOTOX) 100 unit glucosamine-chondroitin (Osteo Bi-Flex) 250-200 mg tablet multiple vitamins (HEXAVITAMIN) tablet tablet omega 3-dha-epa-fish oil (Fish Oil) 1,000 mg (120 mg-180 mg) capsule
Allergien
NKA
Vorherige Impfungen
-

VAERS 1346965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
17,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

Patient fainted within 15 minutes of vaccination. She had not eaten that day. Given some food; no treatment needed and she was released to home with a parent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1346955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
16,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope Vomiting

Symptomtext

Patient fainted and vomited within 15 minutes of vaccination. No treatment needed. Patient released to home with parent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1346868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
58,0
Geschlecht
M
Eingang
25.05.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

Patient had syncopal episode within 15 minutes of vaccination. Patient had not eaten that morning. Felt better after resting and was released to home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1346833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
29,0
Geschlecht
M
Eingang
25.05.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Syncope

Symptomtext

Patient had syncopal episode within 15 minutes of vaccination. Has occurred with other vaccinations. Patient released to home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1346813

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
47,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Generalised tonic-clonic seizure

Symptomtext

Patient was described as having a "Grand mal" seizure within 15 minutes of vaccination. Patient was observed, refused transport to ER, and was released to home when she felt better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Generalised tonic-clonic seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1334553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
52,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anaphylactic reaction Feeling hot Hypoaesthesia Pharyngeal hypoaesthesia Throat tightness

Symptomtext

Patient felt warm, numbness in arms and legs, throat got numb and "tight." Patient given Benedryl 50mg IV and transported to ER by EMS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1334553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
52,0
Geschlecht
F
Eingang
25.05.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Anaphylactic reaction Feeling hot Hypoaesthesia Pharyngeal hypoaesthesia Throat tightness

Symptomtext

Patient felt warm, numbness in arms and legs, throat got numb and "tight." Patient given Benedryl 50mg IV and transported to ER by EMS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1343558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PR
Alter
46,0
Geschlecht
F
Eingang
24.05.2021
Impfdatum
14.04.2021
Beginn
07.05.2021
Tage bis Beginn
23,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Computerised tomogram Dyskinesia Echocardiogram Echoencephalogram Laboratory test Magnetic resonance imaging head Scan with contrast Syncope

Symptomtext

Syncope, R25.9 Unspecified abnormal involuntary movements. R55 Syncope and Collapse. I don't remember how it happen just collapse, ambulance took me to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
3,0
Labordaten
Hospital Record have everything. They did, Head MRI with contrast, CT, Encephalogram, Echocardiogram, routine labs.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Wellbutrin 300mg, Nexium 20mg, Linzess 290mg every other day.
Allergien
Aspirin
Vorherige Impfungen
-

VAERS 1340340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AR
Alter
65,0
Geschlecht
F
Eingang
22.05.2021
Impfdatum
26.04.2021
Beginn
26.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anaphylactic reaction Blood pressure increased Blood pressure measurement Chills Fatigue Headache Nausea Pharyngeal swelling Pyrexia Thinking abnormal Vaccination site erythema Vaccination site pruritus Vaccination site swelling

Symptomtext

Throat was swollen, started having anaphylaxis; Throat was swollen, started having anaphylaxis; Blood pressure got totally out of control, it just spiked; had like a fever; Injection site turned red, swollen, angry, itching; Injection site turned red, swollen, angry, itching; Injection site turned red, swollen, angry, itching; got a very bad headache; nausea; chills; Brain fog; fatigue; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number: EW0162 and expiration date not provided), via an unspecified route of administration, in left arm, on 26Apr2021 09:30 (at the age of 65-year-old), at single dose, for COVID-19 immunization. Medical history included blood pressure, patient had anaphylaxis to other drugs in the past, the medication was an ace inhibitor caller took years ago when trying to help blood pressure. Family Medical History provided as "no". Concomitant medications included losartan for blood pressure (patient had been on this medication for years); and progesterone (began taking this medication probably last summer). The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0153 and expiration date not provided), via an unspecified route of administration, in left arm, on 05Apr2021 13:30 (at the age of 65-year-old), at single dose, for COVID-19 immunization. No additional vaccines administered on same date. The patient got a very bad headache from 26Apr2021 (about an hour after received second vaccine); nausea from 26Apr2021; chills from 26Apr2021; brain fog from 26Apr2021; fatigue from 26Apr2021; throat was swollen, started having anaphylaxis from 28Apr2021 (in the evening) to 02May2021 (it had eased up enough and patient could swallow); blood pressure got totally out of control, it just spiked from 28Apr2021, patient was still having trouble getting it back down. Patient had to double up on blood pressure medication. Patient stated it was persisting a little bit. Patient's blood pressure was going way higher than what it would normally. Patient only took 25mg of losartan. Patient's blood pressure usually never went over 125. Injection site turned red, swollen, "angry", itching and had like a fever from 28Apr2021. On 26Apr2021, patient got a very bad headache, nausea, chills and fatigue. Patient was expecting all of this. Patient was sick on 26Apr2021 and 27Apr2021 and had to stay in bed, clarified she was sick with headache, chills and fatigue. On 28Apr2021 (Wednesday), patient's throat was swollen, started having anaphylaxis. The outcome of the events "headache, nausea, chills, brain fog" was recovered on 27Apr2021; of "fatigue" was recovering; of "throat was swollen, started having anaphylaxis" was recovered on 02May2021; of "blood pressure got totally out of control, it just spiked" was not recovered; of "injection site turned red, swollen, angry, itching and had like a fever" was recovered on 03May2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Anaphylactic reaction
Hospital-Tage
-
Labordaten
Test Name: Blood pressure; Result Unstructured Data: Test Result:usually never went over 125
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylactic reaction to drug (an ace inhibitor caller took years ago when trying to help blood pressure); Blood pressure abnormal
Andere Medikamente
LOSARTAN; PROGESTERONE
Allergien
-
Vorherige Impfungen
-

VAERS 1331209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
15,0
Geschlecht
F
Eingang
19.05.2021
Impfdatum
19.05.2021
Beginn
19.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Bradycardia Dizziness Hypotension Nausea Pallor Presyncope Vital signs measurement

Symptomtext

Vasovagal reaction of c/o dizziness with nausea. bradycardia, hypotension. color pallor. Vital signs- 126/66 P-51 R-20 Temp 98.3 reaction subsided within 30 minutes. intervention required observation of s/s

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 1327724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
40,0
Geschlecht
F
Eingang
18.05.2021
Impfdatum
15.04.2021
Beginn
05.05.2021
Tage bis Beginn
20,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Exposure during pregnancy Haemorrhage Premature separation of placenta Stillbirth Thrombosis Vasculitis

Symptomtext

Placental abruption (with heavy bleeding) occurred two days short of week 36 in first pregnancy (which was achieved via IVF with PGS-tested embryo), resulting in stillbirth on 5/6/2021; baby was 4lb 8oz upon delivery. Due date was June 4, 2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
2,0
Labordaten
Placenta pathology report showed vasculitis and blood clots may have caused or contributed to the abruption.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Prenatal vitamins, low-dose aspirin, magnesium supplement, vitamin B2 supplement
Allergien
Codeine, shellfish
Vorherige Impfungen
-

VAERS 1327514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
38,0
Geschlecht
M
Eingang
18.05.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure measurement Immediate post-injection reaction Syncope

Symptomtext

Patient fainted immediately following vaccination. Initial BP was 147/107; decreased to 132/88 within about 30 minutes and patient was released to home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1320843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
OK
Alter
34,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
30.04.2021
Beginn
03.05.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blepharospasm Blood test Chest X-ray normal Chest discomfort Chest pain Electric shock sensation Electrocardiogram normal Endoscopy upper gastrointestinal tract Eye movement disorder Insomnia Limb discomfort Muscle spasms Neuropathy peripheral No reaction on previous exposure to drug Pyrexia Tendonitis

Symptomtext

Chest pain/tightness. Went to ER. Chest xray and EKG came back normal. Felt like I was having a heart attack. Weird eye movement, eyes flutter especially when closed and I cannot sleep because of it. I have also have brain zap sensations. Neuropathy, legs and feet have been off and on asleep. Constant low grade fever. Tendonitis. Spasms in legs and arms. I have an appointment to see a neurologist. I am 34 years old and never had a medical issue before until after I took this vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
May 14 EKG chest pain, test for ulcer, lots of blood work.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Lidocaine
Vorherige Impfungen
-

VAERS 1320708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
35,0
Geschlecht
M
Eingang
15.05.2021
Impfdatum
05.05.2021
Beginn
05.05.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Atrial fibrillation Chest pain Dizziness Dyspnoea Heart rate increased Loss of consciousness Seizure

Symptomtext

According to my wife, 10 minutes post shot I had what appeared to be a mild seizure and lost consciousness for 1-2 minutes. Prior to that happening, I told her I felt light headed. She notified personnel while we were in the 15 min wait holding area and when I regained consciousness two EMTs were checking me out. They took my vitals, asked me questions and had me get out of the car and walk around. I was monitored for several minutes. It was recommended I visit a hospital or urgent care if I continued to feel unwell. My wife & I left the vaccine site and decided on the way home to go to the hospital just to ensure everything was all right. We went back home for about 30-60 minutes. During this time my heart rate continued to remain elevated and it felt like I had adrenaline coursing through my system. I attributed the feeling to recovering from passing out, but it did not dissipate. Upon arrival to the ER I began having trouble trying to breathe and chest pain. During the triage EKG it was discovered I was experiencing atrial fibrillation. I was given treatment, fluids and monitored for several hours before being released. Estimated time from receiving shot to being diagnosed with afib was approximately 2.5-3 hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
All tests/results happened 5/5/21 during ER visit; unsure exactly what everything is so I copied verbatim from the clinical discharge summary: - ECG / cardiovascular, - Consult / consult MD, - Cardiac monitor / patient care, - ED triage, chest pain CS / patient care, - IV insertion / patient care, - RN cont pulse oximeter / patient care, - Oxygen therapy / respiratory tx/proc, - Auto diff / general lab, - BMP / general lab, - CBC/diff / general lab, - CMP / general lab, - Est CrCl (CG) / general lab, - Pro BNP / general lab, - Rental funct index / general lab, - TSH / general lab - Trop T / general lab, - XR Chest 1V / radiology.
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 1320617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IN
Alter
43,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
13.05.2021
Beginn
13.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Cough Dizziness Ear pain Facial paralysis Headache Hypoaesthesia Hypoaesthesia oral Laboratory test Limb discomfort Oropharyngeal pain Pharyngeal hypoaesthesia

Symptomtext

5 mins after inject, dizziness 0954: Severe left ear pain, that minimized and I developed bilateral cheek/mouth numbness 1004: Numbness developed in my mouth, tongue and throat 1030: Sitting up right and with feeling of left sided drift 1230: Numbness going down my chin and throat 1530: Drinking water, coughing up water, severe throat pain, numbness all over face, RUE, and going down chest. Took a dose of PO Zyrtec OTC 1600: Spouse and son noticed right sided face mouth drooping, right side of lip not moving. RLE felt like weight on my leg 1715: Went to ER, rec'd 1L of NS, IV Benadryl, IV Solu-Medrol, IV Pepcid 2300: Noticed my face was symmetrical and RLE heaviness gone 5/14: Continued with numbness around mouth. No RUE, Throat or RLE pain 05/15: 1050: Feeling better, mild HA. on PO Prednisone taper

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
ER visits, IV medications and Labs
Aktuelle Erkrankungen
None
Vorgeschichte
Mild HTN, Thyroid Disease
Andere Medikamente
Allegra, Synthroid, Prilosec, Rhinocort
Allergien
PCN and latex
Vorherige Impfungen
-

VAERS 1320243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
GA
Alter
49,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bone pain Gait disturbance Hypoaesthesia Musculoskeletal pain Myalgia Paralysis

Symptomtext

Severe muscle soreness (paralyzing); Severe muscle soreness (paralyzing); soreness in tissue and bones; soreness in tissue and bones; unable to walk straight; numbness in hands, arms, and feet.; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm left on 15Apr2021 11:00 (Batch/Lot Number: EW0162) at the age of 49 years, as 0.3 ml single for covid-19 immunisation. Previously the patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) Lot: EN6207, on 25Mar2021 at 11:00 AM at 0.3 ml single in left arm. Medical history included calcium deposits and mitral valve prolapse, from an unknown date and unknown if ongoing. The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's concomitant medications were not reported. On 15Apr2021 at 18:00 the patient experienced severe muscle soreness (paralyzing), soreness in tissue and bones, unable to walk straight, numbness in hands, arms, and feet (severe symptoms as such for 4 days). The outcome of the events was resolving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paralysis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Calcium deposits; Mitral valve prolapse
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1320132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NC
Alter
50,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
08.04.2021
Beginn
23.04.2021
Tage bis Beginn
15,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Bell's palsy Dysgeusia Hypoaesthesia oral

Symptomtext

Bell's palsy; metallic, numb sensation on end of tongue; metallic, numb sensation on end of tongue; This is a spontaneous report received from a contactable consumer (patient). A non-pregnant 50-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 08Apr2021 at 09:45 AM (at the age of 50 years old) (Lot Number: ew0162, unknown expiration) as 1st dose, single for COVID-19 immunization. Medical history included chronic atopic dermatitis, mild asthma, sulfa allergies, latex allergies, allergies of peanuts and almond, banana peel allergies, allergy to tomatoes, sesame allergy, and shrimp allergy. Concomitant medications included dupilumab (DUPIXENT); hydroxyzine hcl; and ibuprofen. The patient experienced metallic, numb sensation on end of tongue and Bell's palsy on 23Apr2021. The events resulted in emergency room/department or urgent care visit. The patient received prednisone and valacyclovir as treatment for the events. No other vaccine in four weeks. The patient has no COVID prior to vaccination and was not tested for COVID post vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had not yet recovered from the events. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy to nuts; Asthma; Atopic dermatitis; Food allergy; Fruit allergy; Latex allergy; Shellfish allergy; Sulfonamide allergy
Andere Medikamente
DUPIXENT; HYDROXYZINE HCL; IBUPROFEN
Allergien
-
Vorherige Impfungen
-

VAERS 1278094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
42,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
23.04.2021
Beginn
23.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Fatigue Feeling abnormal Headache Heart rate increased Insomnia Nausea Syncope

Symptomtext

fainting; Extreme fatigue; chills; headache; insomnia; elevated resting heart rate; nausea; brain fog; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EW0162), via an unspecified route of administration, administered in right arm on 23Apr2021 08:15 as 2nd dose, single for COVID-19 immunization. The patient's medical history included allergic to chocolate. The patient's concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: ER8727), in the right arm on 02Apr2021 08:15 AM for COVID-19 immunization. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 was administered was clinic (Public Health Clinic/Veterans Administration facility). The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. There were no other medications received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient experienced extreme fatigue, chills, headache, insomnia, elevated resting heart rate, nausea, fainting, brain fog, all on 23Apr2021 at 13:00. These started about 5 hours after injection, worsened for about 35 hours, then improved over the next 48 hours. No treatment was received for the events. The outcome of the events were recovered on an unspecified date. Follow-up attempts are needed. Information about lot/batch number is available.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Food allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1278094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
42,0
Geschlecht
F
Eingang
15.05.2021
Impfdatum
23.04.2021
Beginn
23.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Fatigue Feeling abnormal Headache Heart rate increased Insomnia Nausea Syncope

Symptomtext

fainting; Extreme fatigue; chills; headache; insomnia; elevated resting heart rate; nausea; brain fog; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EW0162), via an unspecified route of administration, administered in right arm on 23Apr2021 08:15 as 2nd dose, single for COVID-19 immunization. The patient's medical history included allergic to chocolate. The patient's concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: ER8727), in the right arm on 02Apr2021 08:15 AM for COVID-19 immunization. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 was administered was clinic (Public Health Clinic/Veterans Administration facility). The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. There were no other medications received within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The patient experienced extreme fatigue, chills, headache, insomnia, elevated resting heart rate, nausea, fainting, brain fog, all on 23Apr2021 at 13:00. These started about 5 hours after injection, worsened for about 35 hours, then improved over the next 48 hours. No treatment was received for the events. The outcome of the events were recovered on an unspecified date. Follow-up attempts are needed. Information about lot/batch number is available.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Food allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1307379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
36,0
Geschlecht
M
Eingang
11.05.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Disorientation Fall Loss of consciousness Memory impairment

Symptomtext

Patient (36-year-old male, , first dose in left arm, Pfizer Lot # EW0162, expiration date 04/18/2021) was vaccinated by RN at 1453. Patient arrived alert and oriented x3, answered "no" to all screening questions, and revealed to nurse that he had a fear of needles. Nurse then offered to vaccinate patient in the zero gravity chair, patient refused stating that it would be embarassing. Patient also stated if he looked away from the needle, he would be fine. Patient received the vaccine in his left arm, nurse directed patient to sit in the front of the observation area by the EMT table, patient agreed. Patient was alert and oriented when leaving vaccine station #3. When patient made his way to the front of the EMT station to have a seat, he ended up falling at 1459. It is unclear if he loss consciousness and then fell or fell then loss consciousness. Lead RN was then alerted at 1500 by the lead ancillary, , who I ) instructed to call EMS. The recorded time of the EMS phone call is 1501. While waiting for EMS, I attempted to rouse patient by calling his name and rubbing his sternum for several minutes and obtained a set of vitals. Vitals are as followed: BP: 119/76, O2: 100%, P: 59 taken at 1502. Patient exhibited eye movements when name was called repetitively and then patient opened his eyes at 1504 stating "Somebody just hit me", while attempting to gesture to the juncture where his neck met his skull. While patient was alert, he was oriented x1. Patient could not remember where he was, what had happened, or what day it was. Patient only remembered first and last name but could not remember his age. While speaking to patient, patient loss consciouness for a second time at 1505. Another set of vitals were obtained at 1506, BP: 104/80. After getting a reading of the blood pressure, patient suddently roused at 1508 and began erratically moving his arms and legs, attempting to stand while yelling out "Somebody just hit me! Get off me! Who are you?!" Patient insisted on getting up, RN and I assisted patient to transfer into the zero-gravity chair. EMS arrived at 1510 and assumed care of patient. Patient was continually yelling during EMS assessment. EMS left with patient at 1515, hospital ER unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1303446

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
61,0
Geschlecht
F
Eingang
10.05.2021
Impfdatum
04.05.2021
Beginn
06.05.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Flank pain Pulmonary thrombosis

Symptomtext

pain in side, blood clots in lung

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary thrombosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
penicillin
Vorherige Impfungen
-

VAERS 1302226

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WI
Alter
63,0
Geschlecht
M
Eingang
10.05.2021
Impfdatum
16.04.2021
Beginn
29.04.2021
Tage bis Beginn
13,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Bell's palsy Computerised tomogram head normal Eyelid ptosis Facial paralysis Headache

Symptomtext

Right sided Bells Palsy with right facial droop and right eye ptosis. Also had headache. Currently on prednisone. Mild improvement noted

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
CT of the head negative
Aktuelle Erkrankungen
No
Vorgeschichte
DM 2, Hypertension, atrial fibrillation, coronary artery disease, diastolic dysfunction
Andere Medikamente
None
Allergien
No
Vorherige Impfungen
-

VAERS 1301259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WI
Alter
16,0
Geschlecht
M
Eingang
09.05.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
General physical condition abnormal Syncope

Symptomtext

Patient fainted in store about 5 minutes after receiving vaccination, patient seemed anxious when vaccine was given

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Blood pressure was normal after incident
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1299326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IL
Alter
19,0
Geschlecht
F
Eingang
08.05.2021
Impfdatum
21.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Ear pain Illness Nausea Syncope Vomiting

Symptomtext

I almost fainted; Nausea; Feeling sick and throw up; Feeling sick and throw up; felt very light headed/dizzy; Ear pain (right); This is a spontaneous report from a contactable consumer (patient). A 19-year-old female patient received first dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration in arm left, on 21Apr2021 at 18:00 (Lot Number: EW0162), as single dose, for COVID-19 immunisation. Medical history was not reported. Concomitant medication included unspecified nasal spray. The patient experienced almost fainted (medically significant) on an unspecified date with outcome of unknown, nausea (non-serious) on an unspecified date with outcome of unknown, feeling sick and throw up (non-serious) on an unspecified date with outcome of unknown, felt very light headed/dizzy (non-serious) on an unspecified date with outcome of unknown, ear pain (right) (non-serious) on an unspecified date with outcome of unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1299252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WI
Alter
85,0
Geschlecht
F
Eingang
08.05.2021
Impfdatum
10.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Investigation Peripheral swelling Thrombosis

Symptomtext

blood clot it is from my hip all the way down to my left leg to my ankle; blood clot but it is the big one from my hip all the way down to my foot; foot going down the swelling went up to my leg/foot and my leg is swelled my toes all over up to my leg swelled; This is a spontaneous report from a contactable consumer (patient). An 85-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: EW0162), via an unspecified route of administration, administered in left upper arm on 10Apr2021 at the age of 85-years-old as single dose for COVID-19 immunization. The patient's medical history included ongoing arthritis and ongoing chronic obstructive pulmonary disease (COPD). The patient reported that she was not taking anything for arthritis, just some Tylenol once in a while over the counter (it was not prescription). The patient was taking an inhaler for COPD. The patient was taking unspecified concomitant medications. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: ER2613), administered in left upper arm on 20Mar2021 at the age of 85-years-old for COVID-19 immunization and experienced bladder infection and viral infection. The patient got the first Pfizer vaccine on 20Mar2021 and was alright for a few days afterwards. Then all of a sudden, she started getting infections on 28Mar2021, 8 days after she had the first vaccine. She got a real bad bladder infection then she went to the doctor and she got medication for that. She was with bladder infection then she came down with the viral infection. The patient reported that she has not even been going anywhere because of the virus and she has been staying home. She just goes to the grocery store and clinic to the doctor, that was it. The patient had an antibiotic for the bladder infection. Sulfamethoxazole was the name of the medication that was for bladder infection. They didn't give the medication for the viral infection. The patient reported that it was just a viral infection, it was not the Covid. Since then, she had her second dose of the vaccine on 10Apr2021 and from an unspecified date in 2021, her foot started, her foot swelled up and she didn't know. She takes lot of retention pills, so she thought maybe it was that. So she took her pills and everything and washed and start getting but the next day instead of the foot going down, the swelling went up to her leg and then the next day it went all away up to her hip. The swelling on the left side from the foot all away up to the hip. She went to urgent care on 21Apr2021 (reported as "21st") and saw a doctor and she was tested and she had blood clots. Regarding lab test, the patient reported she had two infections and then she got the blood clot that was from her hip all the way down to her left leg to her ankle. She could not figure out that they called the test and what they tested. But they had a lab work done then one has a test, veins, and everything. She can't remember. The patient reported that her foot and her leg was swelled, her toes all over up to her leg swelled. She had a fat foot and a fat leg just one side. She would say since she has started taking medicines for that, she took the first dose at the evening of 21st (21Apr2021), the day she went to the urgent care, and she would say it was not any worse. The medication was supposed to break up the blood clot, but it was the big one from her hip all the way down to her foot. Just a little bit better. The outcome of the events was recovering.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
Test Name: test; Result Unstructured Data: Test Result:blood clots
Aktuelle Erkrankungen
Arthritis (not taking anything for arthritis may be just some Tylenol once in a while over the counter); COPD (taking an inhaler for COPD)
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1296762

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
45,0
Geschlecht
F
Eingang
07.05.2021
Impfdatum
15.04.2021
Beginn
16.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dysmenorrhoea Heavy menstrual bleeding Polymenorrhoea Thrombosis

Symptomtext

Had an additional mensural cycle with heavy clotting and cramping.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Green caps, Allegra,
Allergien
none
Vorherige Impfungen
-

VAERS 1295776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
29,0
Geschlecht
M
Eingang
07.05.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Hyperhidrosis Syncope

Symptomtext

pt with known anxiety to vaccines. fainted. EMT notified, oxygen placed. pt diaphoretic. recovered after 30 minutes of monitoring. refused ED and discharged home at 1310

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1294160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
25,0
Geschlecht
M
Eingang
06.05.2021
Impfdatum
06.05.2021
Beginn
06.05.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Fall Head injury Refusal of treatment by patient Seizure Syncope

Symptomtext

25yo male patient fainted about 5min after receiving the vaccine while sitting in an observation chair. He fell to the side off his chair and hit head on the concrete floor, with his body still on the chair. Patient had convulsion-like movements. It was unclear if it was seizure-type activity or if his body was struggling to sit up from the supine position laying on the chair. Patient was attended to immediately by pharmacist - he responded immediately to my talking to him and touching his shoulders. Patient was guided to an upright seated position, then helped to floor and asked to lie on floor with legs elevated. 911 was called and Seattle Fire Dept arrived about 5min later. Patient was fully aware of surroundings, his name, etc. Evaluated him and took multiple blood pressure readings with him laying on floor and eventually sitting up. His pressure was initially low but recovered to normal over 15-30 minutes. Ambulance was called but patient declined as his parents were on their way. Patient's blood pressure recovered to normal and he was able to sit and stand, was fully conversational throughout the episode. Patient left building of his own accord with his family to seek medical follow-up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None reported
Vorgeschichte
None reported
Andere Medikamente
None reported
Allergien
None reported
Vorherige Impfungen
-

VAERS 1293698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OK
Alter
50,0
Geschlecht
M
Eingang
06.05.2021
Impfdatum
06.05.2021
Beginn
06.05.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Loss of consciousness

Symptomtext

Patient came in to get his second pfizer vaccine. He waited his 15 minutes of observation, I told him his time was up and he walked around the pharmacy area a little bit and talked with one of the technicians. He left the store and passed out in the parking lot. An ambulance was called because he was not coherent and the EMS said his blood pressure was over 200 systolic. We informed them he was a diabetic but we weren't told what his blood sugar level was before taking him to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
unknown
Aktuelle Erkrankungen
unknown
Vorgeschichte
diabetes, high blood pressure
Andere Medikamente
gabapentin 300mg, cetirizine 10mg, albuterol hfa, fluticasone nasal spray, gvoke 21mg/0.2ml, carvedilol 25mg, tresiba 200unit, humalog kwikpen 100U, pravastatin 20mg. lisinopril 40mg, amlodipine 10mg
Allergien
lithium
Vorherige Impfungen
-

VAERS 1293590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
31,0
Geschlecht
F
Eingang
06.05.2021
Impfdatum
04.05.2021
Beginn
05.05.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Electric shock sensation Headache Musculoskeletal stiffness Myalgia

Symptomtext

In addition to commonly reported side effects (headache, mild muscle pain and stiffness), approximately 18 hours post-injection distinctive systems normally associated with escitalopram withdrawal, mainly electric shock sensations in face and 'brain zaps,' began occurring. Symptoms disappeared within approximately an hour of taking normal daily dose of escitalopram (20 mg). Approximately 10 hours later, symptoms reappeared with similar severity, and a half-dose of of escitalopram was taken (10 mg). Again, within about an hour symptoms disappeared. No further symptoms have occurred as of >48 hours post-injection. No additional effects observed, and overall recovery from other post-vaccine symptoms proceeded quickly.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
insomnia, hypersomnia bordering on narcolepsy
Andere Medikamente
Escitalopram 20 mg/day; Modafinil 200 mg/day; Trazodone 12.5 mg/day; Nortel 35 mg/day
Allergien
Mild dairy allergy
Vorherige Impfungen
-

VAERS 1292829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
48,0
Geschlecht
M
Eingang
06.05.2021
Impfdatum
08.04.2021
Beginn
12.04.2021
Tage bis Beginn
4,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Chest pain Computerised tomogram thorax abnormal Dyspnoea Echocardiogram normal Ejection fraction normal Generalised oedema Peripheral swelling Pulmonary oedema Rash Rash erythematous Skin warm Ultrasound Doppler Urine protein/creatinine ratio decreased

Symptomtext

48-year-old male healthy presented with increased shortness of breath. He mentioned he had COVID-19 vaccine first dose almost 3 weeks ago then symptoms started of having shortness of breath with swollen upper and lower extremity not improving since it started. One week after vaccine developed generalized swelling in hands and feet up to thighs with firey red rash now on arms and inner thighs, felt warm. No itching. Reports some shortness of breath and chest pain. Treated outpatient with lasix without improvement, therefore required hospitalization for generalized anasarca. CT- pulmonary edema. Urine Protien/Cr ratio 0.16 - nephrotic syndrome unlikely, B/L lower extremity duplex negative for DVT, 2D echo showing normal EF of 60%

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pulmonary oedema
Hospital-Tage
4,0
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
Moderate episode of recurrent major depressive disorder Thoracic aortic aneurysm without rupture
Andere Medikamente
Venlafaxine
Allergien
None
Vorherige Impfungen
-

VAERS 1291200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
40,0
Geschlecht
M
Eingang
05.05.2021
Impfdatum
10.04.2021
Beginn
17.04.2021
Tage bis Beginn
7,0
Dosis
UNK
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bell's palsy

Symptomtext

I've developed bell's Palsey; This is a spontaneous report from a contactable consumer. A 40-years-old male patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Arm Left on 10Apr2021 (Batch/Lot Number: EW0162) as a single dose for covid-19 immunisation. Medical history and concomitant medications were not reported. The patient did not have any other vaccinations within 4 weeks. The patient reported that on 17Apr2021, he developed bell's palsey. The outcome of the event was not reported. The patient did not have COVID prior to vaccination not was tested post vaccination.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1291184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
46,0
Geschlecht
M
Eingang
05.05.2021
Impfdatum
18.04.2021
Beginn
19.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Body temperature Dehydration Dizziness Feeling abnormal Hyperhidrosis Night sweats Peripheral swelling Pyrexia Thrombosis

Symptomtext

This is a spontaneous report from a contactable consumer (patient's fiance). A 46-year-old male patient received the first dose bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Arm Left on 18Apr2021 11:20 (Lot Number: EW0162) (received at the age of 46-years-old) as SINGLE DOSE for COVID-19 immunisation. Medical history included right knee pain. Concomitant medications were not reported. The patient received the Pfizer 1st shot 18Apr2021 11:20 am. On 19Apr2021, at midnight, he had low grade fever then swelling right leg. On the day of the report, 20Apr2021, he had swelling to both legs. The patient had taken ibuprofen as treatment beside propping legs up. The reporter wanted more information on the swelling and if it's related to taking ibuprofen. It was further reported that the patient experienced severe swelling from the knees down to the calves on both legs on 19Apr2021. He also experienced night sweats, fever, lightheadedness and dizziness on 19Apr2021. They want to know if there are any reports regarding the swelling side effects and if it is from the vaccine. The first dose of the vaccine was given 2 days ago (18Apr2021) and the second dose is due on 09May2021. The patient got his first shot on 18Apr2021 about 11:20am. After about 15 hours he developed swelling in one leg, she later clarified this to be his right leg, and now reports that both of his legs are swollen at the time of report (20Apr2021). She noted that patient told her his legs are not painful. She doesn't know if it's a blood clot or if they needed to go to the hospital. She also wanted to know if there is information about this as a side effects or if other people are having this too. She then reported that the patient started experiencing a fever, profuse sweating, and was spacey about 12 hours after the vaccine, a little after midnight 19Apr2021. She doesn't know if the dehydration made it worse. His fever was low-grade 99.8 degrees and lasted 4 and a half to 5 hours and has now resolved. When asked if patient received any treatment for fever, caller said it was so recent, and that was listed as a common side effect that goes away. Reported the patient drank fluids and she kept an eye on him. Leg swelling was about 15 hours after the vaccine, early morning 19Apr2021. She noted that the swelling in the right leg got bigger and didn't go down, but the left leg did. But today the left was more swollen and more prominent today. She further clarified that the patient takes ibuprofen for pre-existing right knee pain. Caller also reported that the patient propped his legs to alleviate the swelling, it has improved some but the swelling did not go away. The adverse events did not require a visit to the physician office or emergency room. Outcome of the event fever was resolved on 19Apr2021 (lasted 4 and a half to 5 hours); outcome of the event "severe swelling from the knees down to the calves on both legs" was not resolved; outcome of the remaining events was unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
Test Date: 20210419; Test Name: fever; Result Unstructured Data: Test Result:low-grade 99.8 degrees
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Knee pain
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1290064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WI
Alter
24,0
Geschlecht
M
Eingang
05.05.2021
Impfdatum
13.04.2021
Beginn
15.04.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia Back pain Balance disorder Blood creatine phosphokinase normal Blood creatinine increased Blood folate normal C-reactive protein normal CSF protein increased Cough Echocardiogram normal Hyperhidrosis Hypoaesthesia Immunoglobulin therapy Influenza like illness Limb discomfort Lumbar puncture Magnetic resonance imaging head normal Mobility decreased

Symptomtext

He states he had the first Pfizer COVID-19 vaccine in the series on 4/13/2021. He states that two days later on 4/15/2021 he felt like his feet were heavy. He continues to experience that sensation in his feet, and even feeling like his feet are asleep at nighttime and when he first gets up in the morning. The asleep feeling in the feet gets better when he gets up and moves around but the heavy sensation in the legs does not get better. He states that his mobility is affected though that his legs feel heavy and he is not as easily mobile as he used to be. He feels his balance is off. Patient later reported that he did have and episode of syncope about 5 minutes after he got the vaccine but otherwise was doing okay until 4/15/2021. He presented to the ED with these symptoms on 5/3/2021 at approximately 7:14pm and was admitted to the hospital for evaluation. Patient states that he normally exercises regularly and has been having a great deal of difficulty especially with squatting and now has difficulty walking up stairs, feels very weak and his legs feel heavy. He reports that the numbness and tingling sensation of his feet when sleeping is new and he has never had it in the past. Symptoms get worse with exertion and prolonged activity. Neurologist was consulted and several tests were ordered. Neurology consult noted that patient had a prior COVID 19 infection in November 2020. Per neurologist notes: His symptoms first started about two days after he received Pfizer COVID vaccine on April 13, 2021. He recalled feeling his feet heaviness and it was hard to pick them up. He also had some calf pain. He also had difficulty with doing his stretches and yoga positioning. A week ago, he began to have difficulty with picking up a ball or anything from the ground. He also developed pins and needles at the fingertips at the same time he developed tingling sensation of his feet. He also has lower back pain. He tested positive for SARS-COV-2 antigen on November 12, 2020. He recalled having symptoms lasting for a few days consisting of diaphoresis, cough, and flu-like symptoms. Per neurologist, symptoms seem to resemble acute inflammatory demyelinating polyneuropathy (AIDP). Patient was treated with IVIG for 5 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
MRI of the head without contrast May 4, 2021 No evidence of intracranial mass, mass effect, or shift of the midline structures. No evidence of intracranial hemorrhage or other abnormal fluid collection. No acute ischemic change or other restricted diffusion throughout the brain. Normal cortical gray-white matter differentiation is present throughout the brain in the white matter structures demonstrate normal signal. Echocardiogram May 4, 2021 Left ventricular systolic function is normal. Ejection Fraction = 60-65%. There is no hemodynamically significant valvular heart disease. There is no pericardial effusion. There are no prior studies for comparison Lumbar puncture: Check NIF and Vital capacity one time. Will also check vitamin B12/folate, thiamine, vitamin D25 hydroxy level, ANA, rheumatoid factor, CRP, SPEP, Lyme antibody IgG and IgM. CSF protein elevated at 92 (ref range 10-45) mg/dL CK is within normal limits Normal B12 and folate, normal CRP Cr. 1.31, although possibly due to dehydration. Will trend EMG ordered
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1289217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
58,0
Geschlecht
F
Eingang
05.05.2021
Impfdatum
29.04.2021
Beginn
01.05.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Chills Deep vein thrombosis Fatigue Imaging procedure abnormal Joint range of motion decreased Pain in extremity Peripheral swelling Pyrexia Ultrasound Doppler

Symptomtext

Pt presented with persisting right leg pain that seemed to spread to the hip. Pain appeared approximately 1 day after receiving second dose of Pfizer COVID vaccine. Second dose received on 4/29/2021. Additionally, the patient experienced fever, chills, and fatigue, which had resolved by her presentation to the clinic on 5/3/2021. Pt noted the pain was partially positional, but was constant and found little relief with tylenol purchased over the counter. On physical exam, swelling of the lower extremity was noted with decreased hip ROM. Pain was ellicted on palpation of the calf. No erythema was noted. Pt was sent for Venous Duplex Ultrasound of both legs which was positive for deep vein thrombosis in the right leg.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Deep vein thrombosis
Hospital-Tage
-
Labordaten
Venous Duplex Ultrasound of b/l lower extremities: May 6, 2021 -- DVT in RLE extending from mid-femoral to popliteal and proximal posterior tibial veins
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Daily Multivitamin
Allergien
None
Vorherige Impfungen
-

VAERS 1288911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MD
Alter
34,0
Geschlecht
F
Eingang
05.05.2021
Impfdatum
13.04.2021
Beginn
21.04.2021
Tage bis Beginn
8,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Heavy menstrual bleeding Oligomenorrhoea Thrombosis

Symptomtext

Period lasting over 14 days (still on going). Multiple pads filled in a 2 hour window. A piece of uterine lining came out of body, approximately 2 inches long and an inch across.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Birthcontrol- levonirgeatrel and ethical estradiol tablets
Allergien
Touch allergy to latex
Vorherige Impfungen
-

VAERS 1285204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
ND
Alter
26,0
Geschlecht
M
Eingang
04.05.2021
Impfdatum
27.04.2021
Beginn
28.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Angioedema Diarrhoea Full blood count Influenza A virus test Influenza B virus test Loss of consciousness Metabolic function test Muscle fatigue Myalgia Pyrexia SARS-CoV-2 test Sensation of foreign body Urticaria Vomiting

Symptomtext

Initial event was hives that didn't itch appearing on elbows, they continued to spread for about a day. The doctor said to start Zyrtec, pepcid and ibuprofen. Hours later vomiting, diarrhea, and a blackout followed along with a fever of 102. This time ER gave IV fluids, acetaminophen, ketorolac, ondansetron, and sodium chloride .9%. At this time no mention or notice was made of the hives previously looked at. After this Zyrtec, Pepcid and acetaminophen were being taken regularly. Throughout the rest of that day the hives got worse along with pretty severe angioedema. Also, a feeling of swollowing around a lump in my throat. No change through the night into next day (Friday) for the hives,swelling and lump feeling in throat. Went to walk in clinic where I was prescribed prednisone tapered for 16 days. After the first day of steroids not much change. After 2 there was some improvement. As of today one week after receiving the 2nd dose of the vaccine approximately 90% of the hives are gone, only mild swelling and some muscle fatigue and pain left.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
4/29/21 Comprehensive metabolic panel Hemogram/diff Influenza a and b Stat sars-cov-2 Rna
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1281360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
31,0
Geschlecht
F
Eingang
03.05.2021
Impfdatum
03.05.2021
Beginn
03.05.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Flushing Hyperhidrosis Presyncope Tachycardia

Symptomtext

patient with h/o Potts Dz. onset of tachycardia, presyncope, diaphoresis and facial flushing 5 mins after vaccination. had similar physiologic response after first dose that lasted 24 hours. no prev h/o issues with vaccinations, injections or blood draws

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Potts Disease
Andere Medikamente
Vitamin D3, Tumeric, Probiotic
Allergien
-
Vorherige Impfungen
similar response to previous Covid vaccine 3 weeks prior

VAERS 1281349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
IN
Alter
40,0
Geschlecht
F
Eingang
03.05.2021
Impfdatum
30.04.2021
Beginn
01.05.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fatigue Loss of consciousness Pyrexia

Symptomtext

Tired Fever Dizzy/Passed Out Treatment-rest, plenty of fluids, Advil Outcomes-feeling better

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
Paxil
Allergien
NA
Vorherige Impfungen
-

VAERS 1278103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
35,0
Geschlecht
M
Eingang
01.05.2021
Impfdatum
29.04.2021
Beginn
30.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Axillary pain Fatigue Flushing Headache Heart rate increased Hyperhidrosis Injection site pain Insomnia Pain Syncope

Symptomtext

First vaccine, no major symptoms (04/09/2021) besides sore arm and flush feeling for ~1 hour around 7 hours after vaccine issued. Second vaccine (04/29/2021), slight headache after about 6 hours?woke up at 2:30am (11 hours after second vaccine) with flush feeling/light sweating but no fever. Triggered my vasovagal syncope (had this happen with other vaccines before so no big deal) to have a heavier heartbeat (about 10-20bpm higher than normal) for about 2 hours. Insomnia until about 6am. Next day 4/30 minor soreness, fatigue, soreness at injection site and ?blah? feeling with headache. 5/1/2021: woke up feeling great, other than soreness in my left arm and armpit area. By noon 5/1 most soreness gone with little to no other symptoms?

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None
Vorgeschichte
Syncope and history of SVT
Andere Medikamente
Diltiazem ER 180mg
Allergien
None
Vorherige Impfungen
-

VAERS 1262194

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
16,0
Geschlecht
M
Eingang
01.05.2021
Impfdatum
22.04.2021
Beginn
24.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Angiogram abnormal Cardiac imaging procedure abnormal Chest pain Echocardiogram Electrocardiogram ST segment elevation Myocarditis Troponin Immunoglobulin therapy Pyrexia Troponin T increased Ventricular extrasystoles Ventricular tachycardia

Symptomtext

Patient had fever one day after his vaccine. Two days after his vaccine, he had acute onset chest pain that was described as 10/10. He was admitted to hospital on 4/25 due to EKG showing diffuse ST elevations and troponin T being elevated up to 1700. During the hospitalization, he was found to have a run of ventricular tachycardia and occasional pre ventricular contractions. He was found to have myocarditis after cardiac MRI was performed on 4/26. After confirmation of the myocarditis, he was treated with 2/kg of IVIG and two days of Solumedrol followed by outpatient steroid taper. He was discharged on 4/29/21.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myocarditis
Hospital-Tage
5,0
Labordaten
Echocardiograms: 4/25/21 and 4/26/21 Electrocadiograms: done daily during the admission (initially showed diffuse ST elevations, improved on dishcarge) Cardiac MRI: 4/26, showed findings consistent with myocarditis MRA chest: 4/26 Daily troponin checked: 4/25: 1503, 1774, 1627 4/26: 1229, 1062, 992, 1001, 871 4/27: :1172, 1411 4/28: 665 4/29: 952
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1229319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NV
Alter
62,0
Geschlecht
F
Eingang
01.05.2021
Impfdatum
16.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Chills Dizziness Dyskinesia Facial paralysis Blood pressure increased Blood pressure measurement Electric shock sensation Fatigue Headache Hypertension Immediate post-injection reaction Injection site pain Hangover Hypoaesthesia Malaise Pain in extremity Vertigo

Symptomtext

blood pressure (BP) was usually 110/70 however 8 hours after shot BP was 145/85; really bad vertigo and dizziness; really bad vertigo and dizziness; facial palsy; vision in her right eye got fuzzy; face got numb on the right side; hot electrical nerve zinging entire right arm, right shoulder blade and right calf; sore arm; feel sick; hangover; vomiting; This is a spontaneous report from a contactable consumer (patient) via the medical information team. A 62-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in the right arm on 16Apr2021 11:15 (Batch/Lot Number: EW0162) as single dose (at the age of 62-years-old) for COVID-19 immunisation. Medical history included anaphylaxis: carries an epi pen, and has allergies to wasps. The patient also took unspecified dietary supplements. The patient had no other vaccine in four weeks. The patient got her first vaccine dose on 16Apr2021 and reported having a history of anaphylaxis and carried an epi pen. She stayed at the vaccination facility for an hour and a half and she got facial palsy and her vision in her right eye got fuzzy. Then her face got numb on the right side. It took 4 hours for it to go away but by dinner she felt ok. She added that immediately after the shot (16Apr2021), she experienced hot electrical nerve zinging entire right arm, right shoulder blade and right calf that lasted 30 minutes; blurry vision right eye started 15 minutes after shot, recurred off and on for 6 hours; facial palsy on right side that started about 30 minutes after shot that lasted 4 1/2 hours; vertigo/dizziness that started 7 hours after the shot; and blood pressure (BP) was usually 110/70 however 8 hours after shot BP was 145/85. She filed a report online when her symptoms began to subside. A couple hours later, she began to feel sick again and went to bed. When she walked to her mailbox, she was feeling ok but when she bent over to get the mail, that made it all worse. She woke up feeling as if she had a hangover and reported vomiting right away after getting out of bed. She had really bad vertigo and dizziness. She also had a sore arm (unspecified which arm) and stated that she was "experiencing everything on the freaking list." The patient wanted to know if this was normal and asked if she should get the second dose. She was advised that if she had a severe allergic reaction after a previous dose of the vaccine, she should not get the Pfizer-BioNTech Covid-19 vaccine. She also wanted to know if her symptoms got worse over the weekend and wanted to know what were the signs if she should go to the hospital. The patient did not receive any treatment for the adverse effects. The patient did not have COVID prior to vaccination and was not COVID tested post vaccination. The patient recovered from hot electrical nerve zinging entire right arm, right shoulder blade and right calf 16Apr2021 11:45; face got numb on the right side on 16Apr2021 15:15 and facial palsy on 16Apr2021 16:15. The outcome of the remaining events was unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
Test Name: BP; Result Unstructured Data: Test Result:110/70; Test Date: 20210416; Test Name: BP; Result Unstructured Data: Test Result:145/85; Comments: 8 hours after shot
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylaxis (carries an epi pen); Wasp sting
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1229319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NV
Alter
62,0
Geschlecht
F
Eingang
01.05.2021
Impfdatum
16.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Chills Dizziness Dyskinesia Facial paralysis Blood pressure increased Blood pressure measurement Electric shock sensation Fatigue Headache Hypertension Immediate post-injection reaction Injection site pain Hangover Hypoaesthesia Malaise Pain in extremity Vertigo

Symptomtext

blood pressure (BP) was usually 110/70 however 8 hours after shot BP was 145/85; really bad vertigo and dizziness; really bad vertigo and dizziness; facial palsy; vision in her right eye got fuzzy; face got numb on the right side; hot electrical nerve zinging entire right arm, right shoulder blade and right calf; sore arm; feel sick; hangover; vomiting; This is a spontaneous report from a contactable consumer (patient) via the medical information team. A 62-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in the right arm on 16Apr2021 11:15 (Batch/Lot Number: EW0162) as single dose (at the age of 62-years-old) for COVID-19 immunisation. Medical history included anaphylaxis: carries an epi pen, and has allergies to wasps. The patient also took unspecified dietary supplements. The patient had no other vaccine in four weeks. The patient got her first vaccine dose on 16Apr2021 and reported having a history of anaphylaxis and carried an epi pen. She stayed at the vaccination facility for an hour and a half and she got facial palsy and her vision in her right eye got fuzzy. Then her face got numb on the right side. It took 4 hours for it to go away but by dinner she felt ok. She added that immediately after the shot (16Apr2021), she experienced hot electrical nerve zinging entire right arm, right shoulder blade and right calf that lasted 30 minutes; blurry vision right eye started 15 minutes after shot, recurred off and on for 6 hours; facial palsy on right side that started about 30 minutes after shot that lasted 4 1/2 hours; vertigo/dizziness that started 7 hours after the shot; and blood pressure (BP) was usually 110/70 however 8 hours after shot BP was 145/85. She filed a report online when her symptoms began to subside. A couple hours later, she began to feel sick again and went to bed. When she walked to her mailbox, she was feeling ok but when she bent over to get the mail, that made it all worse. She woke up feeling as if she had a hangover and reported vomiting right away after getting out of bed. She had really bad vertigo and dizziness. She also had a sore arm (unspecified which arm) and stated that she was "experiencing everything on the freaking list." The patient wanted to know if this was normal and asked if she should get the second dose. She was advised that if she had a severe allergic reaction after a previous dose of the vaccine, she should not get the Pfizer-BioNTech Covid-19 vaccine. She also wanted to know if her symptoms got worse over the weekend and wanted to know what were the signs if she should go to the hospital. The patient did not receive any treatment for the adverse effects. The patient did not have COVID prior to vaccination and was not COVID tested post vaccination. The patient recovered from hot electrical nerve zinging entire right arm, right shoulder blade and right calf 16Apr2021 11:45; face got numb on the right side on 16Apr2021 15:15 and facial palsy on 16Apr2021 16:15. The outcome of the remaining events was unknown.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
Test Name: BP; Result Unstructured Data: Test Result:110/70; Test Date: 20210416; Test Name: BP; Result Unstructured Data: Test Result:145/85; Comments: 8 hours after shot
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylaxis (carries an epi pen); Wasp sting
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1225473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
62,0
Geschlecht
F
Eingang
01.05.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Laboratory test Pericarditis Pleurisy SARS-CoV-2 test

Symptomtext

Pericarditis; Pleuritis; This is a spontaneous report from a contactable consumer, the patient. A 62-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot: EW0162), via an unspecified route of administration in the left arm on 15Apr2021 at 12:30 (at the age of 62-years-old) as a single dose for COVID-19 immunization. Medical history included thalassemia minor, fibromyalgia, migraines, depression, Barrett's Esophagus, hiatal hernia, restless leg syndrome (RLS), asthma, hypothyroidism, moderate sleep apnea, osteoarthritis, valvular heart disease, hyperlipidemia, degenerative disc disease (DDD), osteopenia, benign essential tremor, hypertension (HTN). The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medications were not reported, but the patient did receive other unspecified medications within two weeks of the vaccine. The patient did not receive any other vaccinations within 4 weeks of the vaccine. The patient previously took morphine, pregabalin (LYRICA) and methylphenidate hydrochloride (CONCERTA) and experienced allergies. On 15Apr2021 at 21:30, the patient had shortness of breath and chest pain and could only tolerate leaning forward. She went to the emergency room and was admitted to the hospital for pericarditis and pleuritis. She was informed not to take the second vaccine as it would kill her. The patient was hospitalized as of an unspecified date for 2 days and treated with steroids, anti-inflammatory and pain medication. Since the vaccination, the patient was tested for COVID-19 via nasal swab on 16Apr2021 with negative results. The clinical outcome of pericarditis and pleuritis was resolving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
2,0
Labordaten
Test Date: 20210416; Test Name: COVD-19 Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Barrett's esophagus; Benign essential tremor; Degenerative disc disease; Depression; Fibromyalgia; Heart disorder; Hiatal hernia; Hyperlipidemia; Hypertension; Hypothyroidism; Migraine; Osteoarthritis; Osteopenia; Restless legs syndrome; Sleep apnea; Thalassemia minor
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1225473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
62,0
Geschlecht
F
Eingang
01.05.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Chest pain Computerised tomogram thorax Dyspnoea Echocardiogram Laboratory test Pericarditis Pleurisy SARS-CoV-2 test

Symptomtext

Pericarditis; Pleuritis; This is a spontaneous report from a contactable consumer, the patient. A 62-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot: EW0162), via an unspecified route of administration in the left arm on 15Apr2021 at 12:30 (at the age of 62-years-old) as a single dose for COVID-19 immunization. Medical history included thalassemia minor, fibromyalgia, migraines, depression, Barrett's Esophagus, hiatal hernia, restless leg syndrome (RLS), asthma, hypothyroidism, moderate sleep apnea, osteoarthritis, valvular heart disease, hyperlipidemia, degenerative disc disease (DDD), osteopenia, benign essential tremor, hypertension (HTN). The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medications were not reported, but the patient did receive other unspecified medications within two weeks of the vaccine. The patient did not receive any other vaccinations within 4 weeks of the vaccine. The patient previously took morphine, pregabalin (LYRICA) and methylphenidate hydrochloride (CONCERTA) and experienced allergies. On 15Apr2021 at 21:30, the patient had shortness of breath and chest pain and could only tolerate leaning forward. She went to the emergency room and was admitted to the hospital for pericarditis and pleuritis. She was informed not to take the second vaccine as it would kill her. The patient was hospitalized as of an unspecified date for 2 days and treated with steroids, anti-inflammatory and pain medication. Since the vaccination, the patient was tested for COVID-19 via nasal swab on 16Apr2021 with negative results. The clinical outcome of pericarditis and pleuritis was resolving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
2,0
Labordaten
Test Date: 20210416; Test Name: COVD-19 Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Barrett's esophagus; Benign essential tremor; Degenerative disc disease; Depression; Fibromyalgia; Heart disorder; Hiatal hernia; Hyperlipidemia; Hypertension; Hypothyroidism; Migraine; Osteoarthritis; Osteopenia; Restless legs syndrome; Sleep apnea; Thalassemia minor
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1274799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
16,0
Geschlecht
F
Eingang
30.04.2021
Impfdatum
30.04.2021
Beginn
30.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood glucose normal Electrocardiogram Eye movement disorder Hyperhidrosis Pallor Syncope Unresponsive to stimuli

Symptomtext

Patient fainted post-vaccination. Observed patient beginning to lean forward and RN was able to prevent her from falling. Patient's eyes observed to roll upward while patient became unresponsive to stimuli and diaphoretic. No incontinence. EMS called while patient assisted simultaneously to gurney by multiple staff. Upon lying down, patient awoke and become alert and oriented to person, place, time, and situation, though stayed pale and diaphoretic for several minutes. VS @ 12:55: BP 120/80, P 59, SAO2 99%, resp unlabored. VS @ 13:00: BP 138/83, P 62, R 20, SAO2 99% VS @ 13:04: BP 123/73, P 54, SAO2 99% VS @ 13:10: BP 100/69, P 78, SAO2 98% Sitting at edge of bed without symptoms at 13:05, alert and conversing with staff and mother. EMS arrived at 13:07 - their monitor showed NSR, random blood sugar = 93. Ate a snack and drank juice, symptoms completely resolved. Mother declined transport to ED. Discharged home with mother with post-vaccination instructions, will receive 2nd dose while lying down.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
EKG rhythm strip performed 4/30/2021 by EMS = NSR Random blood sugar performed 4/30/2021 by EMS = 93 mg/dL
Aktuelle Erkrankungen
-
Vorgeschichte
Depression
Andere Medikamente
Prozac
Allergien
None known
Vorherige Impfungen
-

VAERS 1274146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
62,0
Geschlecht
M
Eingang
30.04.2021
Impfdatum
14.04.2021
Beginn
16.04.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Angiogram Computerised tomogram Magnetic resonance imaging Seizure

Symptomtext

Seizure

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
6,0
Labordaten
CT, ct-a, mri
Aktuelle Erkrankungen
None
Vorgeschichte
Coronary artery disease
Andere Medikamente
Crestor Zetia aspirin gabapentin Flomax Allegra prilosec melatonin meloxicam Plavix metoprolol vitamin D
Allergien
Penicillin ancef sulfa
Vorherige Impfungen
-

VAERS 1273428

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
46,0
Geschlecht
F
Eingang
30.04.2021
Impfdatum
28.04.2021
Beginn
30.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Loss of consciousness Pain in extremity

Symptomtext

10 minutes after injection "passed out in vehicle", unsure for how long. Then regained consciousness and passed out 2 more times. RN came to vehicle and took BP and was normal. Pt given crackers and juice and was able to stay alert and oriented and then able to drove home. Later that pm about 8:00 states passed out again for about 1 hr. No other symptoms present other than continued sore arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Fibromyalgia, epilepsy, bipolar, mild asthma, mild heart failure, high cholesterol, high blood pressure, Factor 5 lighten, back pain
Andere Medikamente
Fluoxitine, metoperal, B 12, Seraquil, Gabapentin, Simbastatin, Montelukast, Toperamate, triliptal, Suboxone, Xarelto, melatonin, Tylenol, MVI, Vit. C with iron
Allergien
Morphine, Demerol, Celebrex, Zofran
Vorherige Impfungen
several vaccines received in 2007 (Hep. A/Hep. B/ MMR, Flu) high fever

VAERS 1272422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
23,0
Geschlecht
F
Eingang
29.04.2021
Impfdatum
29.04.2021
Beginn
29.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Syncope

Symptomtext

15 minutes after vaccination. Patient felt light headed and fainted for couple seconds. She returned to consciousness immediately and sat down for an additional 20 minutes before heading out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Erythromycin, Penicillin, Sulfacetamide
Vorherige Impfungen
-

VAERS 1272319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
50,0
Geschlecht
F
Eingang
29.04.2021
Impfdatum
27.03.2021
Beginn
27.03.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Headache Loss of consciousness Nausea Paraesthesia Pyrexia Sluggishness Vomiting

Symptomtext

9-10 hours after 1st dose my left arm tingled like it was asleep. Then my hands and feet started tingling as well. My arm tingling stopped after a few minutes but I have tingling in my fee quite often. 12 hours after 2nd dose I got a fever, 17 hours after I threw up and had a the worst headache, 21 hours after I still had a fever headache nausea and I passed out. I started to feel a little better 30 hours after my 2nd dose, but was sluggish for another 2 days. Then 2 days after the tingling in my feet came back and is almost constant.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
I saw Doctor but she didn't seem to know and suggested I see a cardiologist.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Vitamin C, D, collagen booster, fish oil, quercetin, multi vitamin focusing on hair, skin and nails
Allergien
none
Vorherige Impfungen
-

VAERS 1272052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CO
Alter
16,0
Geschlecht
F
Eingang
29.04.2021
Impfdatum
29.04.2021
Beginn
29.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness Tremor Tunnel vision Unresponsive to stimuli

Symptomtext

Patient was a client at a drive-through COVID-19 clinic. Patients Father was driving and the patient was seated in the front passenger seat. After receiving vaccine, FOC drove forward and parked in an observation lot that was staffed by 3 RNs. FOC reported to an observation lot attendant that patient, Patient was losing vision (narrowing), shaking, and then stopped responding. The observation lot attendant noted loss of consciousness, reclined patient in the seat and elevated feet above the heart by placing them on the car dashboard. At 1535, 911 was notified by RN. When car door was opened by the attending observation lot worker, client began regaining consciousness. Client was given apple juice and crackers and vitals were taken. At 1540, Patient blood pressure measured 91/60, pulse oximeter reading of 96% saturation, and heart rate 72bpm. Paramedics arrived to the scene at 1545 and assessed the client; patient was not transported. Father was instructed by paramedics of warning signs and when to seek further care. FOC and patient were advised to inform PCP and to report this instance when receiving future vaccines. FOC and patient remained onsite for 15 minutes following Paramedic care and were dismissed when patient and FOC reported that they felt comfortable leaving.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1271246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
28,0
Geschlecht
F
Eingang
29.04.2021
Impfdatum
01.04.2021
Beginn
29.04.2021
Tage bis Beginn
28,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hallucination Nausea Seizure

Symptomtext

Hallucinations, seizures, severe nausea.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Epilepsy, Bronchiectasis, developmental delay, ASD (repaired), severe reflux, hypotonia, choreoathetoid cerebral palsy
Andere Medikamente
Zonisamide, Lansoprazole, senna
Allergien
Vancomycin
Vorherige Impfungen
-

VAERS 1271110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
70,0
Geschlecht
M
Eingang
29.04.2021
Impfdatum
17.04.2021
Beginn
27.04.2021
Tage bis Beginn
10,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bell's palsy

Symptomtext

Bells palsy

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
Made appointment at PCP office related
Aktuelle Erkrankungen
None
Vorgeschichte
None reported
Andere Medikamente
Not available
Allergien
None
Vorherige Impfungen
-

VAERS 1212395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
41,0
Geschlecht
F
Eingang
29.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal discomfort Abdominal pain Dizziness Hypersensitivity Nausea Blood test Loss of consciousness Pallor Post-traumatic stress disorder Pulse abnormal Presyncope Tinnitus Vision blurred Vital capacity

Symptomtext

Feeling of blacking out; Nauseous/nausea; Light headed; Vision clouded over; Ears started ringing loudly; Pale; Vasovagal response; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported), on the left arm on 14Apr2021 (15:15) as a single dose, with route of administration unspecified, for COVID-19 immunization. Medical history included hypothyroidism, allergies and sulfa allergies. The patient was not pregnant at the time of vaccination. Concomitant medication included thyroid (ARMOUR THYROID). On 13Apr2021 (15:15), the patient had a feeling of blacking out; nauseous/nausea; light headed; vision was clouded over; ears had started ringing loudly; was pale; and had vasovagal response. The events had resulted in doctor or other healthcare professional office/clinical visit and emergency room/department or urgent care. The patient had received an anti-nausea medication, fluids and antacids as treatment for the reported events. The patient's bloodwork was fine and vitals were good, both on 13Apr2021. The outcome of the events was unknown. The patient was not diagnosed with COVID-19 prior to the vaccination, and had not been tested post-vaccination. Information on the lot/batch number has been requested.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Test Date: 20210413; Test Name: Bloodwork; Result Unstructured Data: Test Result:fine; Test Date: 20210413; Test Name: Vitals; Result Unstructured Data: Test Result:good
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy; Hypothyroidism; Sulfonamide allergy
Andere Medikamente
ARMOUR THYROID
Allergien
-
Vorherige Impfungen
-

VAERS 1266426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
17,0
Geschlecht
F
Eingang
28.04.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood pressure decreased Syncope

Symptomtext

Pt had an episode of syncope for 10 seconds after getting vaccinated . Blood pressure dropped to 90/50, Hr 48. After repositioning the pt and giving some fluid Blood pressure raised to 113/96 Hr 72.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
paramedic were notified. Patient transferred to the hospital for further evaluation .
Aktuelle Erkrankungen
No per pt.
Vorgeschichte
Hx of appendectomy.
Andere Medikamente
No per pt
Allergien
N/A per pt
Vorherige Impfungen
-

VAERS 1264883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
CA
Alter
47,0
Geschlecht
M
Eingang
27.04.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Abdominal pain upper Aphasia Dyskinesia Hypoaesthesia oral Pallor Paraesthesia Syncope Tension Tremor

Symptomtext

At 1118 patient fainted, had fixed shaking, pale, loss of speech. Once patient reactted he was able to speak and gave Past medical history of Asperger syndrome and no fainting spells before. Patient complained of stomach pain. numb lip, tingling sensation on fingers. Hands began to flexion and tense up. Vital signs were with in normal range. clinet began to show normalized sign and symptoms. Ems was still called and was taken to hospital for furhter observation at 1153.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Asperger Syndrome
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1264676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
25,0
Geschlecht
M
Eingang
27.04.2021
Impfdatum
27.04.2021
Beginn
27.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cold sweat Dizziness Feeling cold Syncope

Symptomtext

At 1248 patient fainted, began to feel, cold and clammy, vital signs within normal rage. Patient reported light headedness while seating down. Reported no previous medical history. EMS called and released patient. We kept patient for 30 minutes in observation until father picked him up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None stated
Vorgeschichte
-
Andere Medikamente
-
Allergien
Benadryl
Vorherige Impfungen
-

VAERS 1263480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MT
Alter
17,0
Geschlecht
F
Eingang
27.04.2021
Impfdatum
21.04.2021
Beginn
22.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Amnesia Blood culture Blood glucose decreased Blood pressure decreased Blood test Body temperature increased Cardiac murmur Chest X-ray Chills Computerised tomogram head Computerised tomogram thorax Confusional state Dizziness Dysphemia Full blood count Headache Incoherent Inflammatory marker increased

Symptomtext

At 2am 4/22 patient started to feel sick and sent a text that I didn't read until 630 as I was asleep. She had severe muscle aches, hurt to move, hurt to breathe and felt like she was having a heart attack. She felt like she might pass out and had some blurred vision. At 630am, I saw her texts and immediately brought her 2 tylenol and a large glass of water. She went back to bed. She woke up around 10:45 and was feeling decent except for a headache but no fever or anything so we went to try on some Prom dresses. At the dress shop, she collapsed and had a seizure lasting around a minute. She lost her bladder and was completely confused and incoherent. She's never had a seizure before. I scooped her up, brought her to the ER where they ran every test and scan imagineable. Full blood work up and cultures, a chest xray, a CT scan of her brain and lungs. Her temp was high 103-104 and she had full body chills and a pounding headache. Her BP kept dropping and got as low as 81/36. They threw 2 bags of IV fluids into her and admitted her to the hospital. She had also developed a heart murmur. Over the course of the night, her BP stabilized but her temp continued to spike and come back down with Tylenol/Ibuprofen. She also had IV Tordahl for the headache. Her inflammatory markers were high at 15.3 which we were told should be less than 1. They reran labs in the morning but everything can back really low which they felt was a dilution effect from all the fluids so wanted us to follow up with her primary care on Monday. On Saturday night, he lymph nodes were swollen to the size of ping pong balls but have since slowly reduced in size although still there. Her labs were better from discharge and her white blood cell count was within range and her inflammatory marker was down to 1.7. Her blood sugar was a little low. She did pass out and have seizure like response to giving blood in the doctors office, lost bladder control again, shot pupils, etc. She is still stuttering over words, has some short term memory retention and has some motor function issues which they think is a result of the initial seizure and should resolve itself over time. Her liver function tests were totally normal in the hospital but are a high now so they will be checking her out again next week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
1,0
Labordaten
4/22: Chest Xray, CT Scan of Brain and Lungs, 4/22 & 4/23 & 4/26 Full CBC/Blood Cultures for drugs and infections/viruses, etc. Clinic would have results from those labs.
Aktuelle Erkrankungen
None
Vorgeschichte
PCOS, exercised induced asthma
Andere Medikamente
Sprintec (birth control for PCOS), Melatonin
Allergien
None known
Vorherige Impfungen
-

VAERS 1262462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
19,0
Geschlecht
F
Eingang
27.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness Loss of consciousness

Symptomtext

Dizziness for 5 minutes after vaccination. Passed out for less than 30 seconds. Patient stable, released from vaccination site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1260536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
CA
Alter
42,0
Geschlecht
F
Eingang
26.04.2021
Impfdatum
19.04.2021
Beginn
23.04.2021
Tage bis Beginn
4,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Heavy menstrual bleeding Thrombosis

Symptomtext

Heavier period than normal, bigger blood clots expelled

Weitere VAERSDATA-Felder
Praegender Schweregrund
Thrombosis
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Nothing
Vorgeschichte
supraventricular tachycardia
Andere Medikamente
Nothing
Allergien
Peach, cherry, plum, hazelnut
Vorherige Impfungen
-

VAERS 1260057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
46,0
Geschlecht
F
Eingang
26.04.2021
Impfdatum
25.04.2021
Beginn
25.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bone pain Dizziness Fatigue Headache Myalgia Pruritus Respiratory tract congestion Rhinorrhoea Syncope

Symptomtext

Dizziness, syncope, systemic pain (muscular, bone, headache), extreme fatigue, congestion, runny nose, pruitis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Sulfa, pineapple
Vorherige Impfungen
-

VAERS 1258702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
30,0
Geschlecht
M
Eingang
26.04.2021
Impfdatum
20.04.2021
Beginn
20.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Clonus Presyncope Tonic clonic movements

Symptomtext

1525 vaccinated 1530 per EMT & family, witnessed vasovagal response to vaccine HX of vasovagal response post vac's & blood draws. hx severe PTSD. 1540 witnessed sz like symptoms clonic/tonic . X2 patient is on anti-sz meds with no previous 525, pt down on the floor x3 with legs elevated. assisted to W/C x2 people. X2 witnessed vasovagal response per mom 0 medical intervention needed and would be counter predictive due to PTSD hx. respected mother request. Pt transferred to car x2 people legs elevated BP 112/72 - o2 97%. 1700 pt appears stable, escorted EMT & myself assisted to private car. Mother was thankful not to have called for transfer.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1191760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
41,0
Geschlecht
F
Eingang
25.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fatigue Nausea Syncope

Symptomtext

Fainting; Nausea; Dizziness; Fatigue; This is a spontaneous report from a contactable consumer (Patient). A 41-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Formulation: Solution for injection, Lot number: EW0162) via unspecified route of administration on arm left at a single dose on 08Apr2021 17:00 for COVID-19 immunization. The patient medical history. Concomitant medication was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 08Apr2021 at 17:15 patient experienced nausea, fainting, dizziness and fatigue. The outcome of the events was recovered on an unspecified 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1191760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
41,0
Geschlecht
F
Eingang
25.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fatigue Nausea Syncope

Symptomtext

Fainting; Nausea; Dizziness; Fatigue; This is a spontaneous report from a contactable consumer (Patient). A 41-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Formulation: Solution for injection, Lot number: EW0162) via unspecified route of administration on arm left at a single dose on 08Apr2021 17:00 for COVID-19 immunization. The patient medical history. Concomitant medication was not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 08Apr2021 at 17:15 patient experienced nausea, fainting, dizziness and fatigue. The outcome of the events was recovered on an unspecified 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1252664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NY
Alter
34,0
Geschlecht
M
Eingang
24.04.2021
Impfdatum
24.04.2021
Beginn
24.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

After receiving the vaccine and sitting, the patient fainted for a brief moment. After waking, he said that he's fainted before when he gets cuts. He drank some water and sat for another half an hour and we measured his blood pressure twice. First it was 90/70. He sat for a while longer and we measured it again at 108/73 and he said he was feeling better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 1252643

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
VA
Alter
34,0
Geschlecht
M
Eingang
24.04.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Presyncope

Symptomtext

He had a vasovagal reaction few minutes after receiving the vaccine. Recovered after being placed in supine position with feet elevated. Initial systolic bp of 80, HR of 40, O2 sat 97%. No CP / Neuro Sxs / breathing difficulties / skin changes. He was fasting for religious reason; also has h/o fainting when he tried to donate blood. SBP came up to 100 after about 10mins. He felt better after several bottles of water and a banana and was symptom free when he left the clinic about 30-40 minutes later.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
None
Vorgeschichte
none
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1252055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AZ
Alter
16,0
Geschlecht
M
Eingang
24.04.2021
Impfdatum
19.04.2021
Beginn
21.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Distributive shock Eosinophil count abnormal Full blood count normal Metabolic function test Respiratory viral panel Syncope Urticaria

Symptomtext

Diffuse urticarial reaction leading to mild distributive shock and syncope

Weitere VAERSDATA-Felder
Praegender Schweregrund
Distributive shock
Hospital-Tage
3,0
Labordaten
CBC normal, respiratory pathogen panel normal, CMP normal, absolute eosinophils 0.1
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1248300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NE
Alter
42,0
Geschlecht
F
Eingang
23.04.2021
Impfdatum
20.04.2021
Beginn
21.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Blood test Computerised tomogram Dysarthria Ear pain Electrocardiogram Facial paralysis Headache Hypoaesthesia Magnetic resonance imaging Neck pain Pain Pain in jaw Paraesthesia

Symptomtext

Patient received 1st Pfizer vaccine at 3:10pm on 4/20/21 and felt only numbness/tingling in arm within the first hour, then felt fine rest of day into the following day 4/21/21, until about 2:00pm when she developed a headache that got worse with time. Headache turned into pain that radiated to her ears, jaw, and neck. When patient got home close to 6pm that evening (4/21/21), she looked in the mirror and noted her face looked droopy. She went to go speak to her husband, who realized immediately that her speech was slurred. He took her to hospital where she was admitted for observation and tests were run.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
1,0
Labordaten
CAT Scan, MRI, EKG, blood work on 4/21/21.
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes Type 2
Andere Medikamente
Daily multivitamin, Pravastatin 40mg, Jardiance 10mg, Tamoxifen 20mg
Allergien
Allergies to Codeine, Hydrocodone, Metformin, Oxycodone, Pork, Latex, Sulfa, Vesicare
Vorherige Impfungen
-

VAERS 1247836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
20,0
Geschlecht
M
Eingang
23.04.2021
Impfdatum
23.04.2021
Beginn
23.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

Patient fainted and was lowered to the floor. He came around quickly and received water to drink and stayed until feeling better-about 30 minutes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
UNKNOWN
Vorgeschichte
NONE LISTED
Andere Medikamente
UNKNOWN
Allergien
NONE LISTED
Vorherige Impfungen
-

VAERS 1246648

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
NV
Alter
48,0
Geschlecht
M
Eingang
23.04.2021
Impfdatum
10.04.2021
Beginn
19.04.2021
Tage bis Beginn
9,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Bell's palsy Blood test Computerised tomogram Electrocardiogram Erythema Facial paralysis Headache Hypoaesthesia Laboratory test Magnetic resonance imaging Paraesthesia oral SARS-CoV-2 test

Symptomtext

Red patch on arm for about 10 days, he in size to 4"x6". Tingling on tongue. Pain on back of head for several days, still continuing. Numbness in left jaw, Loss of muscle use on left side of face. Went to ER where they indicated Bell's palsy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
4.21.2021 - at ER: ekg, CT scan, mri, covid test, blood labs
Aktuelle Erkrankungen
None
Vorgeschichte
Diabetic Hypertension Asthma
Andere Medikamente
Synjardy, lisinopril, atorvastatin, symbicort, buprprion, onglyza, fluticasone, montelukast
Allergien
IVP dyes
Vorherige Impfungen
-

VAERS 1246349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MD
Alter
24,0
Geschlecht
F
Eingang
23.04.2021
Impfdatum
17.04.2021
Beginn
18.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bell's palsy Facial paralysis Hypoaesthesia

Symptomtext

I started to develop Bell's palsy ~24hrs after receiving the vaccine (got the vaccine Saturday 1pm, noticed symptoms periodically through Sunday). I recognized the early symptoms from one previous episode of Bell's palsy ~7mo ago (knot next to/under nose with the feeling of tightness and slight loss of feeling). I took 800mg ibuprofen every 3 hours upon the advice of my aunt, a nurse practitioner, to hopefully stop it before it progressed to full palsy, but on Wednesday woke up with facial droop and numbness primarily focused around the nose and upper lip on the right side. I went to Urgent Care facility, and received Prednisone for the Bell's palsy and Valacyclovir to cover in case it was a viral infection that flared when my immune system dropped after receiving the vaccine. The facial numbness is getting better but is not yet resolved (Friday). I am in the process of scheduling a follow up with a neurologist.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
mild idiopathic arthritis/ mild joint pain
Andere Medikamente
Zyrtec, glucosamine, melatonin (daily), vitamin D, magnesium, cranberry extract, probiotic (every other day)
Allergien
Augmentin (mild allergy)
Vorherige Impfungen
-

VAERS 1243847

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
29,0
Geschlecht
F
Eingang
22.04.2021
Impfdatum
19.04.2021
Beginn
20.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Generalised tonic-clonic seizure Headache

Symptomtext

Per mother, patient had severe headache within 3 hours of administration, then had tonic clonic seizure the following morning requiring rescue medication

Weitere VAERSDATA-Felder
Praegender Schweregrund
Generalised tonic-clonic seizure
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
epilepsy, intractable lennox-gastaut syndrome without status epilepticus, encephalopathy, urge incontinence, developmental delay, vagus nerve stimulation device in place (first placed in 2006), ostepenia
Andere Medikamente
tylenol, clobazam, diazepam, divalproex, ibuprofen, nayzilam, vimpat, xcopri
Allergien
lacosamide, banzel, tegretol, topamax, rufinamide
Vorherige Impfungen
-

VAERS 1243127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
29,0
Geschlecht
F
Eingang
22.04.2021
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Pt in observation, resting in chair with husband. Pt had 1-2 minute LOC while sitting in chair and responded with touch and talk. W/C to med eval. station and placed in supine position on cot. VS 106/67 75P 18R. Pale and diaphoretic. Husband present with medical Hx. Fluids offered and ortho static BP done, stable with Gatorade and 16oz water. VS 130/86 60P 20 100% sat, sitting & 136/93 70P 18R 100%sat standing and discharged ambulatory with husband at 1215. Educate pt for return visit for 2nd dose to be placed in med eval cot and recovery, verbalized understanding RS, NP.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
CLINDAMYCIN
Vorherige Impfungen
-

VAERS 1242750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TN
Alter
22,0
Geschlecht
M
Eingang
22.04.2021
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Loss of consciousness

Symptomtext

Pt. reported loss of consciousness approximately 10 minutes after vaccination. Pt. alerted observation staff immediately. Pt. reported he had not eaten or had anything to drink this morning. Pt. was given pack of crackers and juice. Pt. was A&Ox3 with no confusion and reported anxiety only. Heart rate-58, P02-98%. Pt. was observed for 30 additional minutes with no additional complications.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
Pt. denies taking any medications.
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1242497

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0162

schwer
Staat
-
Alter
23,0
Geschlecht
M
Eingang
22.04.2021
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Syncope

Symptomtext

PT RECEIVED VACCINE AND FAINTED WHEN STANDING IN LINE FOR CHECKOUT. PT STATED HE DID NOT EAT BREAKFAST. EMS ASSIST WAS CALLED AND PT ESCORTED TO ER

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1239449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
24,0
Geschlecht
M
Eingang
21.04.2021
Impfdatum
21.04.2021
Beginn
21.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Hyperhidrosis Loss of consciousness

Symptomtext

Patient received first vaccination dose and immediately reported feeling faint and "blacking out" to nurse administrating vaccination. Nurse instructed patient to lay down and prop legs on chair. At 4:18pm nurse altered pharmacist of patient feeling faint. Pt with pulse of 58 BP 112/59, patient with sweat on brow, reporting no issues with breathing or other allergic symptoms. Pharmacist evaluating patient found that patient had had a large meal, had exercised for ~25 minutes, and may be dehydrated. Pharmacist provider patient with bottle of water, patient refusing snacks and or food. 4:22 patient reports feeling 80% better, was able to sit down. Pt denies EMS services, and discloses to pharmacist that while he is not afraid of needles; however, he has generalized anxiety and believes it may have contributed to event, pulse 66, BP 119/59. 4:30 pulse 56, BP 119/66. 4:38 pulse 53, BP 114/65. 4:53 pulse 52, BP 116/59 patient reports feeling fine. 4:55 patient leaves pharmacy to shop in store. 5:03 Patient comes back to pharmacy and signed that he is doing well, pharmacist requests call when patient makes it home safely. 5:23 Patient calls from home reporting he is okay.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Generalized anxiety disorder
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
Pt unable to recall, but said that he had similar reaction in late teens to vaccination

VAERS 1238057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
MO
Alter
41,0
Geschlecht
M
Eingang
21.04.2021
Impfdatum
21.04.2021
Beginn
21.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Immediate post-injection reaction Loss of consciousness

Symptomtext

Right after receiving the vaccine (approximately 5 minutes after), patient said they were feeling light-headed. I went to go get patient water and a granola bar since he hadn't eaten breakfast and patient passed out. Patient was resting after receiving the 1st dose of the vaccine, and was propped against the wall in the corner on a chair, so he was just leaned up against the wall (didn't fall to the ground). Several patients helped me move the patient to the ground so he was lying horizontal and he woke up almost immediately (max 10 seconds). He wasn't quite oriented to what had just happened but knew he was on the ground. Within 1 minute, patient knew where he was, was feeling fine and wanted to sit back on the chair. He was carrying on a full conversation and did not feel feverish, sweating, tired, faint, or have a headache, just embarrassed. Patient stayed for a full 30 minutes and wanted to drive himself home because he felt completely back to normal. Vaccine administrator calling to check up on patient during next available break.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
No previous reactions, NO HIV, COVID-19 etc
Vorgeschichte
Patient answered NONE to this question
Andere Medikamente
No seizure medications, blood thinners, MAB drugs or vaccines within 4 weeks,
Allergien
No allergies listed, no previous reaciton to vaccines
Vorherige Impfungen
-

VAERS 1237681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
WA
Alter
30,0
Geschlecht
M
Eingang
21.04.2021
Impfdatum
21.04.2021
Beginn
21.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Pallor Panic attack Syncope

Symptomtext

Person went to car for 15 minute wait period with partner. Began feeling faint upon sitting down. Per partner, had a brief syncopal episode (less than 30 seconds). On site EMT's summoned. Found patient pale. BP initially 70/0 P48. Moved patient to a cot supine and gave O2 2L via nasal cannula. BP came up to 110/80 and 5 minutes later was 130/90 with P 68. Color returned. Another 5 minutes sat patient up, BP 140/90, remained consistent when standing. Pt. stated he was had panic attacks and this felt like one. Was anxious about shot before arriving. This was a typical reaction for him.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vitamin D
Allergien
None
Vorherige Impfungen
-

VAERS 1232601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NC
Alter
29,0
Geschlecht
F
Eingang
20.04.2021
Impfdatum
20.04.2021
Beginn
20.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Syncope Vital signs measurement

Symptomtext

immediately after infection, pt reported dizziness, EMT and MD notified, pt then experienced syncope for approx 20 seconds, spontaneously resolved. normal vital signs. tolerated food/drink after, talkative and in good spirits shortly after regaining consciousness, no head trauma or fall. pt arranged for someone to drive her home. did not require hospital evaluation.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
seizures, hypoglycemia
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1232076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
FL
Alter
61,0
Geschlecht
F
Eingang
20.04.2021
Impfdatum
20.04.2021
Beginn
20.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Confusional state Syncope

Symptomtext

Patient suffered a syncopal episode and confusion while under observation following her booster vaccination. Patient has a history of diabetic related emergencies but this syncope/confusion resolved itself while under the care of on site paramedics. Patient was transported to a hospital of her choosing.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
BGl: 203 BP: 117/90 HR: 57
Aktuelle Erkrankungen
-
Vorgeschichte
Chronic Renal Failure
Andere Medikamente
Insulin
Allergien
Codeine
Vorherige Impfungen
-

VAERS 1231009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
32,0
Geschlecht
M
Eingang
19.04.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Confusional state Dizziness Hot flush Joint instability Loss of consciousness Mydriasis Nausea Pallor Skin abrasion Skin disorder

Symptomtext

Patient received the 1st COVID-19 Vaccine (Pfizer, Lot #: EW0162, expiration date: 07/31/2021) at 10:00. At 10:12 patient ambulated to Medic in the observation area, asking to use the restroom due to complaints of nausea. Patient was advised by Hospital that he would not be able to use the restroom due to his physical presentation of pale, warm, moist skin, pupils becoming greater than or equal to 9 mm, and a look of confusion. Medic attempted to assist the client with ambulation to anti- gravity chair, when the patient?s knees buckled and he was assisted to the floor. Nurse and Nurse responded to assist Medic. Patient lost consciousness and was then assisted into anti-gravity chair and sternal rub applied. Per Medic , patient?s loss of consciousness subsided after 3 seconds and became conscious, alert, and oriented to person, place, time, and event (CAOX4). Patient stated he has ?syncopal episodes every time he has a procedure done that involves needles.? Baseline vitals were obtained by Medic at 1015, while patient was sitting: blood pressure: 98/50, heart rate: 60, respiratory rate: 18, pupils equal and reactive to light at 5 mm. Patient claimed that about 2 minutes status post- vaccine, he began to feel ?lightheaded, nauseous, and had a hot flash. Patient stated he has similar reactions every time. Patient denied chest pain, headache, vomiting, abdominal pain, and blurry vision. Patient was given water to sip on. At 1020, second set of vitals were taken by Medic, while patient was sitting: blood pressure: 90/60, respiratory rate: 16, heart rate: 97, and patient was conscious, alert, and oriented to person, place, time, and event (CAOX4). Patient?s skin was normal color, warm, and dry. Pupils were 3 mm and equal and reactive to light. Patient claimed last oral intake was on 04/15/2021 with minimal fluid intake as well. Patient denied any complaints and claimed he was feeling better. ALS interventions offered by Medic for further evaluation and care, but patient refused. Third set of vitals were obtained by Medic, while patient was standing, at 1030: blood pressure: 118/76, heart rate: 82, respiratory rate: 14, and patient was conscious, alert, and oriented to person, place, time, and event (CAOX4). Patient was negative for orthostatic pressures and was released into the care of his spouse, after waiting in the observation area for about 1 hour. Patient drank a full 12 ounce water bottle and was able to walk out on his own, with a steady gait and in no distress.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None.
Vorgeschichte
Syncopal (needles).
Andere Medikamente
None.
Allergien
Pet dander allergies.
Vorherige Impfungen
-

VAERS 1230275

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
23,0
Geschlecht
F
Eingang
19.04.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Fall Seizure Syncope

Symptomtext

Patient fainted, dropped out of the chair, had a seizure

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1229968

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NH
Alter
56,0
Geschlecht
F
Eingang
19.04.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood pressure decreased Blood pressure measurement Chills Decreased appetite Dizziness Dysgeusia Electrocardiogram Fatigue Feeling abnormal Gait disturbance Loss of consciousness Loss of personal independence in daily activities Nausea Palpitations Throat irritation Vision blurred

Symptomtext

12 minutes after the injection, I felt very dizzy, nauseous, a few minutes later, I totally blacked out, they took me into the emergency room and took my blood pressure, which was very low and my heart was racing. I came to about 7-10 minutes later with very dizzy feeling, a itchy throat and was feeling very dizzy. The hospital staff gave me water and took a EKG - I was told to just rest. I got the chills and felt waves of dizzy/nauseous for a while. After about an hour, I felt strong enough to go home. I went home and was very tired and still dizzy. I was tired and was too tired to do anything other than stay in bed for three days. I lost my appetite, had weird metal taste in my mouth and had a few dizzy episodes the next day where I couldn't walk to the bathroom without help. I am usually a very healthy person, never have passed out before and now three days later, I can only work a few hours a day without getting tired and my brain feels foggy - hard to focus.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
The hospital took my blood pressure and an EKG. No results were provided to me. They sent me home and told me I would be fine.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Juice Plus Whole Food Vitamin Supplement that I have taken for over 20 years.
Allergien
Allergic to Penicillin, some light food allergies, seasonal allergies
Vorherige Impfungen
-

VAERS 1229782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
43,0
Geschlecht
F
Eingang
19.04.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Ear discomfort Headache Nausea Syncope Vomiting

Symptomtext

At approximately 11:47, patient presented with syncope, nausea and vomiting, headache, and ear pressure. EMS was notified at approximately 11:49 and arrived at 11:54. Pt agreed to transport to hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Pt recently had a breast biopsy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1229184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
57,0
Geschlecht
F
Eingang
19.04.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Hyperhidrosis Malaise Presyncope Syncope

Symptomtext

Patient became diaphoretic stating "I don't feel good". Pt had syncopal episode. Patient placed on stretcher, +pulse and +resp., Pt immediately regained consciousness and talking. Pt taken to ER. Determined to have vasovagal response and discharged.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1225876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
NY
Alter
57,0
Geschlecht
M
Eingang
18.04.2021
Impfdatum
18.04.2021
Beginn
18.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Electrocardiogram Loss of consciousness Pallor Sinus bradycardia Syncope

Symptomtext

49yr patient with hx of Hashimoto who had received second dose at 10:58M, was observed to pass out while sitting on the observation area, as per paramedic patient (who was sitting right in front of him) pass out for 30 seconds while sitting on his chair. On my arrival patient awake, alert and oriented x3, seem a little pale, he was sitting up drinking water, he was taken to the examination room, laying flat on the stretcher, initial vital signs were BP 93/58 HR 48 RR 20, Sat 100% on room air, EKG long strip was done with showed sinus bradicardia, subsequent BP after 18 mins were 104/70 and then 114/69 HR 60. Patient denies shortness of breath, itchining or rash. fingerstick was 102mg/dL. (see below)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
see above
Aktuelle Erkrankungen
None
Vorgeschichte
Hashimoto Thyroiditis
Andere Medikamente
Ambient
Allergien
None
Vorherige Impfungen
-

VAERS 1225859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
18,0
Geschlecht
F
Eingang
18.04.2021
Impfdatum
18.04.2021
Beginn
18.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope Tooth injury

Symptomtext

Patient fainted (syncope) within 2 minutes. Fell off her chair and hit her front tooth which broke off. 911 was called, her vitals were taken. Cleared by medical staff. Patient and mother refused to be taken to the Hospital. Both signed waivers of fact. Patient walked off without assistance.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
na
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1225206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
CA
Alter
16,0
Geschlecht
M
Eingang
18.04.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Flushing Hyperhidrosis Pallor Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Additional Details: After getting the vaccine, patient was feeling lightheaded while he was sitting down. He tripped over the chair and fell over when he tried to get up too quickly. Patient fainted briefly as we were trying to get him to a chair and was pale initially. 911 was called. After he was given water and the paramedics arrived patient got better. paramedics tested vitals and everything was in normal range. patient reported being nervous about getting the vaccine. paramedics left after collecting info

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1222867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
-
Geschlecht
F
Eingang
17.04.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope Vomiting

Symptomtext

Fainting, vomiting

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
clonazepam and xanax prior to vaccination due to needle phobia
Allergien
unknown
Vorherige Impfungen
-

VAERS 1222859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
KS
Alter
-
Geschlecht
U
Eingang
17.04.2021
Impfdatum
-
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Heart rate increased Hypotension Syncope Vomiting

Symptomtext

Pt reported dizziness, and fainted, woke up quickly and vomited. Ambulance was called for. Blood pressure was extremely low and pulse rate was high as reported by ems. pt became more alert and did decline ambulance ride to the hospital. spoke later to spouse and they did go to emergency room.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
unknown in emergency room-- on clinic site, low bp and high pulse rate, o2 normal
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1222044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
26,0
Geschlecht
M
Eingang
17.04.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Bradycardia Hyperhidrosis Hypotension Oxygen saturation decreased Presyncope

Symptomtext

Vagal reaction. Patient was diaphoretic, altered, hypotensive, bradycardic and oxygen sats were in the low 90's. Patient was responsive but not answering questions appropriately. 911 was activated by myself and Ambulance responded. They evaluated the patient who's vital signs improved and patient signed a refusal to be transported to the emergency room.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Denies
Vorgeschichte
None
Andere Medikamente
Denies
Allergien
Denies
Vorherige Impfungen
-

VAERS 1220655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
31,0
Geschlecht
M
Eingang
16.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Loss of consciousness

Symptomtext

Pt fell forward on the table and was assisted to the ground; BP 135-137/92-94; HR 88-106; RR 18, SpO2 99%

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1220049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MT
Alter
38,0
Geschlecht
M
Eingang
16.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Immediate post-injection reaction Presyncope

Symptomtext

Patient experienced near syncope immediately following first dose of vaccine. Patient reports that this is a common occurrence following any procedure involving needles. Patient recovered quickly and refused any further treatment prior to leaving the vaccine POD.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1219876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
25,0
Geschlecht
M
Eingang
16.04.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Condition aggravated Loss of consciousness Muscle spasms Musculoskeletal stiffness Syncope

Symptomtext

At 1455 client had a vasovagal syncopal reaction following 1st dose of Pfizer vaccine. Client stated he had a history of syncope and anxiety with injections and blood draws. No injuries were sustained and client regained consciousness with sternal rub and verbal prompts. Client was unconscious for less than 20 seconds. Vital signs were obtained and were within normal limits. Client denied shortness of breath, headache, nausea, vomiting, diarrhea, dizziness or blurry vision. Client's pupils were PERRLA. Client complained of feeling stiffness and cramping in hands and arms. Paramedic was able to flex hands and arms without resistance, capillary refill was less than 2 seconds. Client offered 911 evaluation and declined three times. Client left via wheelchair and released to care of significant other following a 60 minute observation time and stated resolution of symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None Stated
Vorgeschichte
None Stated
Andere Medikamente
None stated
Allergien
None stated
Vorherige Impfungen
-

VAERS 1219477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
26,0
Geschlecht
M
Eingang
16.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness Flushing Hyperhidrosis Syncope

Symptomtext

Syncope, Flushing/sweating, Dizziness; provided hydration + rest

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1219290

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
45,0
Geschlecht
M
Eingang
16.04.2021
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness

Symptomtext

HE PASSED OUT ABOUT 7 MINUTES AFTER RECEIVING THE VACCINE. ON SITE EMS RESPONDED. VITALS LISTED BELOW. HE SAYS HE HAS A HISTORY OF PASSING OUT. HE RECOVED AND DID NOT WANT TO GO TO ER, SO HE WAS RELEASED TO HOME.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
BP 124/80 HR 76 AND 98% O2 ON ROOM AIR
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
famotadine
Allergien
-
Vorherige Impfungen
-

VAERS 1216548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
19,0
Geschlecht
F
Eingang
15.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

Parient fainted after receiving Pfizer vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1215872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
27,0
Geschlecht
F
Eingang
15.04.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fall Head injury Syncope

Symptomtext

Patient received first dose of vaccine and about 5 to 10 minutes later patient fainted and hit her head while waiting in pharmacy area after receiving the shot. She quickly regained consciousness and two pharmacists had her sit on ground to elevate her legs. Also gave her water. Had her stay in pharmacy waiting area until she was ok to leave.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
No
Vorherige Impfungen
Patient says she has a history of fainting (unknown vaccine types or dates)

VAERS 1214812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CT
Alter
55,0
Geschlecht
F
Eingang
15.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood pressure increased Dizziness Electrocardiogram Fatigue Loss of consciousness Nausea Palpitations Paraesthesia Sensation of foreign body

Symptomtext

Started with dizziness, then nausea, tingling sensation, lump in throat. Then racing heart and heart palpitations. Blood pressure dangerously high. Then extreme tiredness and passed out. Then ambulance was called

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
They did an EKG and monitored my heart rate and blood pressure.
Aktuelle Erkrankungen
None
Vorgeschichte
Low thyroid, kidney stone problems
Andere Medikamente
Levothyroxine 50MCG, Chlorthalidone 50 MG, Potassium Citrate 120 MG
Allergien
Penicillin, Cechlor
Vorherige Impfungen
-

VAERS 1214208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
KS
Alter
21,0
Geschlecht
F
Eingang
15.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Head injury Syncope

Symptomtext

The patient received the Pfizer vaccination and had filled out their consent form having everything checked no. After given their immunization they were instructed to sit for the required 15 minutes. AMA the patient got up from chair and approached the counter to ask if they could use a restroom. When the pharmacist approached her, she fainted and bumped her head on the dividing partition on her way down. Pharmacist went out immediately to the patient. 911 was called. The patient was already conscious again. The paramedics to her with them, as they wanted to check her. She was still orthostatic, and they advised to her they felt it would be a good idea. Employee tried to call on 4/14/21 and the patient did not answer.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Pt blood pressure take at pharmacy by paramedics and pt was orthostatic
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
unknown
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1210980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OR
Alter
31,0
Geschlecht
M
Eingang
15.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Fall Syncope

Symptomtext

Syncope: After instructed to sit in the lobby for a 15 minute observation time, the patient walked 20 feet over to my consultation window after a couple minutes reporting lightheadedness/dizziness and requested a seat in my vaccination room. Upon making my way through the pharmacy to open the door the patient collapsed from a standing position to the floor. The patient regained conscience almost immediately after the fall and reported no injuries. EMS was also on scene by coincidence, shopping. The patient declined their assistance.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1211054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
SC
Alter
29,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dyspnoea Gait disturbance Hypopnoea Loss of consciousness Trismus Unresponsive to stimuli

Symptomtext

29 yo Female reported after last vaccine hives that resolved next day with Benadryl and single brief dizziness described as insignificant before vaccine. Upon walking to the bathroom during the 30 minute wait time, escort noted patient appeared to be in need of assistance so he offered her a chair. Upon sitting, she slumped against him so he asked for medical assistance. EMS called. On the ground patient was unresponsive with shallow breathing; neck was hard to move but attributed to her large bun. Stethoscope used to hear breath sounds as nurse reported she was breathing but did not appear to be strong breaths. Pulse ox 96% or higher with BP appropriate, HR in 90s. She awoke to sternal rub, nurse asked her if she had difficulty breathing after noting her jaw was rigid and unable to open. Patient indicated yes to difficult breathing so epinephrine was given. ~ 30 seconds after epinephrine patient alert and breathing deeply, began to respond to questions. After reporting breathing was still moderately difficulty (a few minutes later), epinephrine second dose given. Patient transport via EMS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Shellfish - Vomiting; Sweet Potato - Uticaria
Vorherige Impfungen
Pt reported Hives with first dose of Pfizer COVID vaccine, resolved with diphenhydramine

VAERS 1210672

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
SC
Alter
37,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Confusional state Cough Dyspnoea Loss of consciousness Pallor Presyncope Retching Seizure like phenomena

Symptomtext

37 yo obese dependent female with severe vasovagal reaction after a 30 minute wait time someone walking by noticed patient was not looking well and informed the observation staff. Nurse called for assistance and began talking with the patient. Provider arrived and patient was pale, slumped in chair but conversive. Upon assisting patient to the floor she became unconscious and we laid her down. EMS was requested. Over the next few minutes had 3 episodes of LOC with brief ~5 seconds of breathing cessation and seizure like activity with significant head shaking sometimes involving upper torso followed by coughing and retching without actual vomiting. Due to this she was placed in left lateral recumbent position with the first episode. Each time she awoke she appeared confused but was able to answer questions. Oxygen was applied with pulse oximetry but unable to obtain BP during this time. After the third episode she suddenly asked what happened and mentation returned to normal. Upon Fire/EMS arrival was conversing normally on the floor on her left side. Reported multiple food/environmental allergies and metformin allergy. History of suspected seizure but nothing proven. Reported before her vaccine that last time she experienced a brief LOC hours ~12 hours after her first vaccine. She had arranged for someone to stay with her tonight in case she felt faint again.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Multiple Food Allergies/Environmental Allergies and allergy to metformin
Vorherige Impfungen
Patient reported had syncope event after first dose of vaccine

VAERS 1210302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
24,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness

Symptomtext

Patient Allergies: NKA 14:53 patient received the covid vaccine Pfizer Lot:EW0162 Expiration:7/21 dose 0.3ml in left deltoid, then slid off the chair, nurse caught her and slid her to the ground provided support for her head, ensure the area was clear, she went unconscious for 15 seconds then regain conscious, vitals were taken, BP-133/89, Pulse-81, SPO2 97%, numeric pain scale 0/10. Patient was A &O x 4 person, time, place, and situation-----------------------------------------------RN 14:56 reassessed vitals BP-131/68, Pulse- 71, R-16 even and unlabored, Spo2 98%, numeric pain scale 0/10, she was A&O x 4 person, person, place and situation, patient denies chest pain, denies shortness of breath, denies hx of going unconscious, she was moved to a chair for observation, will continue to monitor------------------------------------------------------------RN 15:07 contacted to alert her of the situation and to follow next step of protocol, will continue to monitor the patient-------------------------------------------------RN 15:15 patient denies any chest pain, denies shortness of breath, denies dizziness, A&Ox4 person, place, time, and situation-----------------------------------------------------------------RN 15:24 reassessed the patient vitals BP-108/63, Pulse-70, SPO2-99% , numeric pain scale 0/10, denies chest pain, denies shortness of breath, denies dizziness, A&Ox4 person, place, time, and situation, had patient raise for chair slowly reported no dizziness, had patient walk back and forth w/ no assistance, observed a steady and even gait, patient denies any dizziness, provided education to follow up with primary care or head to urgent care, if patient starts to experience shortness of breath or anaphylaxis to call 911, both patient and partner verbalized understanding, the partner verbalized that he would be driving the patient home---------------------------------------------------------------------------------------------------------------------------------

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
NA
Allergien
NA
Vorherige Impfungen
-

VAERS 1209236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
32,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Hot flush Nausea Syncope Unresponsive to stimuli Vomiting

Symptomtext

Patient felt hot and then she felt syncopal then appeared to have a grand mall seizure. She displayed posturing and was unresponsive for ~ 10-15 seconds. No loss of bladder control. BP 125/78 HR 42. Squad was called. BP 136/76 HR 75 O2 sat 99% Squad arrived. Patient is now responsive. Nursing staff has called her husband. He states this happens when she has an injection. He stated that he will come pick her up and he did not want her going with the squad. Patient spoke to her husband. Patient is refusing transport with squad stating that her husband is a PA and is on his way to pick her up. BP 126/80 HR 69 O2 Sat 98%. Squad left. Patient states that she feels better, She sat up. Patient now reports that she feels nauseated. Patient vomited. BP 127/55 HR 76 O2 Sat 99%. Patient's husband has arrived. Patient reports feeling well. Vitals standing BP 117/86 HR 69 O2 Sat 100%.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Zoloft
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1208279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
16,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Facial paralysis Hypoaesthesia Paraesthesia Pupillary reflex impaired

Symptomtext

Patient started feeling a numbness/tingling sensation in her right pinky that slowly moved up her arm and to her elbow about 20 minutes after she received the vaccine. Her right eye started to droop as well and her right pupil was slow to react to light upon assessment by EMT. Patient usually feels dizzy at baseline but felt even more dizzy after the vaccine. The numbness and tingling sensation in the right arm started to subside at 1500 and was completely gone by 1520. Vital signs were taken by EMT, BP 110/70, O2 99%, and P 73 which is patient's baseline. Patient's side effects subsided and she was escorted out to the car by her mother and EMT and her mother drove her home. RN and EMT advised patient to call her primary care provider to explain the adverse effects of the vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial paralysis
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Mast Cell Disease, chronic migraines, exercise induced hives, Asthma
Andere Medikamente
Pepcid, Zyrtec, Singulair
Allergien
Penicillin, Cephalosporins
Vorherige Impfungen
-

VAERS 1207815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
AR
Alter
27,0
Geschlecht
M
Eingang
14.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Bradycardia Hypotension Seizure like phenomena Syncope

Symptomtext

Syncope with seizure like activity. Bradycardia and hypotension, HR 30-40 BMP

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure like phenomena
Hospital-Tage
-
Labordaten
patient refused
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1207379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
40,0
Geschlecht
F
Eingang
14.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure measurement Heart rate Oxygen saturation Syncope

Symptomtext

3:41PM PT STATES SHE FEELS LIKE 'SHE MAY PASS OUT'. PLACED IN WHEEL CHAIR - SYNCOPE X30-60 SEC. MOVED TO COT; NOW RESPONSIVE. BP 150/90, HR 96, R 16, 02 SAT 99%. PT CALLED HUSBAND TO COME PICK HER UP. 3:46PM PT STATES 'THIS IS HER TYPICAL POTS EPISODE'. STATES SHE WAS WORKING ON HER KITCHEN AND PROBABLY JUST OVER DID IT. BP 128/80. STATES SHE FEELS BETTER NOW. 3:50PM A/O, PINK, W/D, RESP WITH EASE. BP 132/78, HR 77. 4PM SITTING UP - DRINKING WATER. STATES 'FEELS PRETTY GOOD'. 4:08PM TO EXIT PER WHEEL CHAIR; ASSISTED INTO AUTO TO BE TAKEN HOME PER HUSBAND. A/O, PINK, W/D, RESP WITH EASE. 4-14-21 9:30AM TC: PT STATES SHE 'FEELS SO MUCH BETTER NOW'.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
POTS SYNDROME/PASSES OUT
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1207314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
OH
Alter
27,0
Geschlecht
M
Eingang
14.04.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dizziness Fall Head injury Loss of consciousness

Symptomtext

Patient arrived for his vaccine. Vaccine was administered by nurse. Patient then stated that he does not do well with shots and then he passed out. The nurse attempted to break his fall. He fell out of the chair and onto the floor hitting his head on the ground. He was passed out for about 20-30 seconds. His legs were elevated and he woke up. VS were taken BP 137/80 HR 68 O2 sat 100% Squad was called. VS retaken BP 141 HR 70 O2 sat 100% Squad arrived. Patient feels lightheaded. Assisted to chair. VS retaken BP 114/93 HR 60 O2 sat 98 % Patient taken to hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1206361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
27,0
Geschlecht
M
Eingang
14.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Syncope

Symptomtext

Syncope; BP 101/55; HR 67 improved to 121/72; HR 80. RR stable at 18

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1204277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
64,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Presyncope

Symptomtext

Near syncope, revived immediately with and amonia inhalant.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1203298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
CA
Alter
42,0
Geschlecht
F
Eingang
13.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Loss of consciousness

Symptomtext

1027 patient asked for assistance and promptly lost consciousness, Patient assisted to the ground by LVN and LVN. Interventions and vitals initiated. Patient lost consciousness for about 15 seconds. Patient sternal rubbed. Patient slowly started to blink and start to correctly answer questions. Patient legs elevated on chair. BP 119/71, Pulse 74, SaO2 98%, Resp 22, Temp 98.2. Patient slowly lifted and sat upright on the ground. Tolerated water. 1035 vitals, BP 117/62, Pulse 69, SaO2 98%, Temp 97.2, Respirations 18. Patient tolerated standing and moved to the back of observation to sit down on the ground once again. 1038 Patient stated she felt dizzy, so she was laid down again, vitals WNL, alert and oriented. 1045, BP 119/68, Pulse 64, SaO2 99%, Resp 20. Patient is sitting and alert. Patient tolerating sitting on chair upright. Partner at her side. 1100 patient vitals BP 124/74, Pulse 69, SaO2 98%, Temp 97.2, Resp 20. Patient educated on getting some rest and water and avoid any strenuous activity. If symptoms return or worsen to seek medical attention. Patient left site without further incident.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1202543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
NY
Alter
22,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fall Head injury Seizure

Symptomtext

Pt fell and hit his head, An eyewitness said pt was having a seizure, but pt said he does not have seizure disorder. Ambulance was called. Pt was alert and oriented. Patients dad was going to take him to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
unknown
Aktuelle Erkrankungen
not known
Vorgeschichte
no
Andere Medikamente
not known
Allergien
none
Vorherige Impfungen
-

VAERS 1201086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0162

schwer
Staat
MI
Alter
35,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
13.04.2021
Beginn
13.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Hyperhidrosis Presyncope

Symptomtext

Vasovagal symptoms - diaphoresis, lightheaded, dizzy

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Duloxetine, Flonase, Singulair
Allergien
NKDA; Seasonal allergies
Vorherige Impfungen
Meningitis vaccine - about 15 years ago

VAERS 1200296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
-
Alter
19,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Syncope

Symptomtext

syncope, history of syncope due to vaccinations. monitored for 30 mins and symptoms resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1198132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
28,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
11.04.2021
Beginn
11.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Computerised tomogram Dizziness Fall Seizure Syncope

Symptomtext

I got the Covid 19 Vaccine Pfizer at the pharmacy. After I got the Vaccine I was waiting in the waiting room for 15 minutes but before my time was up and it was my time to leave I felt really dizzy & light headed as I was sitting down on a chair. Then I just felt some one tell me to wake up because I had fainted, fell face down to the floor & convulsed for 5 seconds.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
CAT scan at MC Sunday 04/11/2021
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
No
Vorherige Impfungen
-

VAERS 1198132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
TX
Alter
28,0
Geschlecht
M
Eingang
13.04.2021
Impfdatum
11.04.2021
Beginn
11.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Computerised tomogram Dizziness Fall Seizure Syncope

Symptomtext

I got the Covid 19 Vaccine Pfizer at the pharmacy. After I got the Vaccine I was waiting in the waiting room for 15 minutes but before my time was up and it was my time to leave I felt really dizzy & light headed as I was sitting down on a chair. Then I just felt some one tell me to wake up because I had fainted, fell face down to the floor & convulsed for 5 seconds.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
CAT scan at MC Sunday 04/11/2021
Aktuelle Erkrankungen
No
Vorgeschichte
No
Andere Medikamente
No
Allergien
No
Vorherige Impfungen
-

VAERS 1198752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
25,0
Geschlecht
F
Eingang
12.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Hyperhidrosis Hyperventilation Injection site pain Loss of consciousness Nausea Vision blurred

Symptomtext

Pt c/o pain at injection site during vaccination administration. Pt became nauseous, blurred vision, LOC x2 episodes, and diaphoresis. Pt repeatedly stated, "I can't see." Pt hyperventilating at time of arrival to med obs. Assisted in slowing breathing with positive effect. Pt assisted to stretcher from w/c and place in position. Pt reports vision back to almost baseline after repositioning. Pt given apple juice and crackers. Prior to d/c to home, pt reported left eye remained slightly burred and requested her father pick her up at staff suggestion for safety. VS at 1702: BP 57/44, recheck 68/44 (placed in trendelenburg position), HR 65, RR 24, O2 sat 100% on RA. VS at 1710: BP 106/82, HR 66, RR 18, O2 sat 100% on RA. VS at 1715: BP 104/73, HR 61, RR 18, O2 sat 99% on RA. VS at 1728: BP 109/80, HR 62, RR 17, O2 sat 99% on RA. VS at 1733: BP 106/80,, HR 68, RR 18, O2 sat 98% on RA. No s/s of distress at time of discharge. Pt escorted to exit via w/c with staff per protocol.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
junelle, spironolcatone
Allergien
sulfa
Vorherige Impfungen
-

VAERS 1198584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

schwer
Staat
AZ
Alter
33,0
Geschlecht
F
Eingang
12.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Heart rate increased Paraesthesia Presyncope Taste disorder

Symptomtext

Rapid heart rate within 2 minutes of injection, the feeling of pins and needles in my face. Waited at site for 30 minutes, sucked on candy and drank water. Laid down in my car. Left after 30 min. Sat up, and it happened again. Every ten minutes my face would be tingly. Bad taste in mouth. Was told by onsite physician, I had a vasovagal response. 2 hours post injection and I feel better.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Peanuts
Vorherige Impfungen
-

VAERS 1196129

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
PA
Alter
35,0
Geschlecht
M
Eingang
12.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Loss of consciousness Tunnel vision

Symptomtext

Pt reports feeling tunnel vision, dizziness, and LOC. Pt briefly lost consciousness and assisted to floor by staff. BLE elevated on chair while pt in supine position on floor PTA of med obs team with stretcher. Pt placed in stretcher, able to stand and ambulate independently without difficulty. Pt given water, refused snack d/t gluten intolerance. VS at 0934: BP 139/79, HR 51, RR 17, O2 sat 100% RA. VS at 0944: BP 124/84, HR 60, RR 16, O2 sat 100% on RA. VS at 0951: BP 119/83, HR 59, RR 17, O2 sat 96% on RA. VSS at time of discharge. Pt escorted to exit via w/c by staff per protocol.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
depression
Andere Medikamente
lexapro
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1195920

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
39,0
Geschlecht
F
Eingang
12.04.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Aphasia Dizziness Dysphonia Feeling hot Retching Syncope Throat irritation Throat tightness Tremor

Symptomtext

pt received 1st dose of Pfizer Covid vaccine at 0710; began complaining of feeling HOT only and was fanning self; writer offered a bottle of water and began talking to pt at 0715 at 0720 pt stated that HER throat was becoming ITCHY and began gagging; vitals bp 144/92, HR 105, 02 sat 99% on RA. 0721 pt received STAT EPI in Left thigh; stat call made. Repeat vitals 02 sat 100 % hr 93. Pt began feeling better stating THROAT itching was better, however she had trouble speaking as voice was raspy and weak and she kept clearing her throat; almost sounded like slight audible wheeze which didn't progress any further. Stat team arrived; when pt stood up she had felt dizzy and mentioned she had some shakiness but was able to ambulate to WC on own. vitals 0723 bp 132/88 HR 96 02sat 99%. Pt was taken to ED via WC 0725 for further evaluation.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1195563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
26,0
Geschlecht
F
Eingang
12.04.2021
Impfdatum
10.04.2021
Beginn
10.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Blood pressure increased Loss of consciousness

Symptomtext

Patient passed out, states it happens on occasion. BP 114/73 HR71 RR16, then 5 minutes later 124/75, HR72, RR16. Patient came up to provider, asked to lay down, then passed out. States she has fainted in the past when she saw others past out. Left in stable condition

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1195558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
17,0
Geschlecht
M
Eingang
12.04.2021
Impfdatum
10.04.2021
Beginn
10.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Blood glucose Fall Head injury Headache Hypotension Loss of consciousness Syncope

Symptomtext

Patient fainted and fell while standing, hit head on floor, brief loss of consciousness, pupils PERRLA. Minor head pain, BP hypotensive (80/54) in wheelchair. Gave juice and crackers (hadn't eaten that day), glucose 91. Patient stable upon leaving, recommended ER visit for head evaluation.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1194809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
19,0
Geschlecht
M
Eingang
11.04.2021
Impfdatum
11.04.2021
Beginn
11.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Presyncope

Symptomtext

Near syncope. Trendelenburg position. Cold water bottle on neck.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
No
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
-
Allergien
no
Vorherige Impfungen
-

VAERS 1194291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
46,0
Geschlecht
M
Eingang
11.04.2021
Impfdatum
10.04.2021
Beginn
11.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Loss of consciousness Nausea Pyrexia

Symptomtext

Pfizer-BioNTech COVID-19 vaccine EUA Patient passed out after waking up at 3 AM the day after the shot was administered. Symptoms included nausea and dizziness. Fever around 100?F begin the following day April 11, 2021 and persisted throughout the day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
None conducted.
Aktuelle Erkrankungen
None
Vorgeschichte
Lower back herniated disc
Andere Medikamente
Chondroitin Vitamin C Mg supplement
Allergien
None known
Vorherige Impfungen
-

VAERS 1193654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
27,0
Geschlecht
M
Eingang
11.04.2021
Impfdatum
11.04.2021
Beginn
11.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Contusion Dizziness Loss of consciousness

Symptomtext

Patient has the vaccine and then got dizzy and started to put self on floor, passed out and hit face on the floor. Patient has a red bruise on his forehead and nose. Patient was advise that he should go to ER to get checked out because he passed out and hit his head. Patient refused and went home with girlfriend. They were advised as to what signs to look out for and then if the patient gets these symptoms to take him to the ER to get evaluated

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
no
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
no
Allergien
no
Vorherige Impfungen
-

VAERS 1191365

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
29,0
Geschlecht
M
Eingang
10.04.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dry mouth Fear of injection Hyperhidrosis Syncope

Symptomtext

Patient received their vaccine at 4:25pm, and fainted at 4:30pm, and at 4:35pm the patient was back to baseline. He drank a bottle of water and felt normal. He initially was sweaty, had a dry mouth immediately fainted. He stated he only had a pretzel before the vaccine, and had an issue with needles in the past.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 1190595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
48,0
Geschlecht
M
Eingang
10.04.2021
Impfdatum
10.04.2021
Beginn
10.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cold sweat Loss of consciousness Tunnel vision

Symptomtext

Patient stated he was sitting in the chair and he started feeling clammy tunnel vision and blacked out. he doesnt remember being brought over to the observation room. He was encouraged to drink fluids, patient stated he was feeling better and reported no further tunnel vision, he was escorted out with his son accompanying him. vital signs @ 1024 HR 62, BO 98/60 RR 18, pulse ox 96%, at 1027, HR 81, BO 111/65, RR 18 and pulse ox 95% on RA, at 1044 HR 62, BP 111/ 69, RR 18 and Pox 97%. He was released at 1045 by himself to the exit of the facility.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
Unknown
Vorgeschichte
high cholesterol
Andere Medikamente
Nystatin
Allergien
None
Vorherige Impfungen
-

VAERS 1189724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MI
Alter
46,0
Geschlecht
M
Eingang
10.04.2021
Impfdatum
10.04.2021
Beginn
10.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Bradycardia Heart rate decreased Hyperhidrosis Loss of consciousness Pallor Syncope

Symptomtext

syncopal episode x3. Loss of consciousness each time less than 1 minute. pale, diaphoretic. Bradycardic, HR low 50's. Blood pressure stable. Neurologically intact. EMS notified and transported to Hospital for further evaluation. 7:36 to 800:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none at this time. Transported to Hospital
Aktuelle Erkrankungen
states none
Vorgeschichte
History of lymphoma, completed chemo 2018
Andere Medikamente
states no medications
Allergien
states no know allergies
Vorherige Impfungen
-

VAERS 1186607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
PA
Alter
46,0
Geschlecht
M
Eingang
09.04.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bradycardia Dizziness Hyperhidrosis Paraesthesia Presyncope

Symptomtext

patient admits to vagal response and passing out in past. few mins after vaccine became diaphoretic and near syncopal. arrived to obs and placed in tredelenberg, bp 119/80 hr 58 rr 18 sats 98% on ra. offered snack and water, refused snack. few mins later, diaphoresis resolved. stretcher sat up, bp 123/78 hr 50 rr 18 sats 98% on ra; states baseline is bradycardic around 50's. sat up to side of bed with feet dangling, bp 116/81 hr 52, then 112/80 hr 58, then standing bp 104/70 hr 63, patient started to feel dizzy and needed to lie back down, once laying down bp returned to 123/81 hr 50. 5 mins later, sitting bp 118/81 hr 53, standing 111/75 hr 58, few mins of standing had bp 90/63 hr 57, tingling in fingers and dizziness, causing patient to need to lay back down. few mins later lying bp 109/69 hr 59 sitting bp 113/70, 114/79, 121/86. standing bp checks 121/87, 114/82, and stabilized with final bp at 117/83. no further s/s of issues or orthostatic hotn. escorted with spouse, who was driving, to exit with no issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
hx of vagal response with donating blood and receiving vaccinations
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1186371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
-
Alter
24,0
Geschlecht
M
Eingang
09.04.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Muscle rigidity Pallor Screaming Seizure Syncope

Symptomtext

Sitting in general observation area, began screaming and holding his head with clenched arms and hands. 1000 became rigid, suspect seizure, EMT reports syncopal episode. Assisted per EMT to w/c and taken to private observation area. BP 84/52 HR 54 O2 96% on room air. Color pale. EMT remains present. Offered patient water. Patient oriented x 3, Educated on taking next vaccine while lying down. Sister states patient has history of passing out while donating blood. Patient has needle phobia 1011 patient eating cookies and drinking water without difficulty. PB 105/79 HR 80 O2 98%. Denies dizziness, lightheadedness, Denies headache. 1015. STood at w/c - no dizziness. Patient states he feels well enough to leave, gait steady, ambulated to POV

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
asthma
Andere Medikamente
ADHD meds, meds for seasonal allergies, asthma inhaler
Allergien
none
Vorherige Impfungen
-

VAERS 1182493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
21,0
Geschlecht
F
Eingang
08.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Blood pressure decreased Dizziness Hyperhidrosis Loss of consciousness Nausea Syncope Tunnel vision

Symptomtext

Pt became anxious, sweaty and dizzy. Developed tunnel vision and loss of consciousness. Staff with pt at time of syncopal episode and assisted pt to floor. Pt regain consciousness within 1 minute. Pt placed on stretcher and arrived to med obs at 1558. Vitals obtained. At this time pt states she is feeling normal. At 1611 c/o dizziness and nausea. BP rechecked and notably dropped. Pt placed in the trendelenburg position. BP increased. Nausea and dizziness resolved. Snacks and water given. Pt left facility 1712, friend driving. Vitals as follows; 1600 BP 107/74 HR 85 RR 22 spo2 98% 1611 BP 97/68 HR 78 RR 20 spo2 100% 1625 BP 109/76 HR RR 18 spo2 99% 1705 BP 95/66 (standing, asymptomatic)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
-
Vorgeschichte
anxiety, depression
Andere Medikamente
zoloft
Allergien
penicillin, amoxicillin, shellfish, bananas, cats
Vorherige Impfungen
-

VAERS 1181894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
PA
Alter
41,0
Geschlecht
M
Eingang
08.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Feeling abnormal Hyperhidrosis Loss of consciousness

Symptomtext

started to sweat and felt "not right" post injection a few minutes, states has happened several times in past when getting injections. staff assisted to floor and states did lose consciousness for a moment. felt better once in obs, 1517 bp 119/68 hr 83 rr 20 sats 98% on ra. 1530 bp 138/72 hr 67 rr 17 sats 98% on ra. states s/s resolved, stood up with no issues, escorted to personal vehicle with no issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 1180551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
PA
Alter
35,0
Geschlecht
M
Eingang
08.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cold sweat Dizziness Fall Head injury Hyperhidrosis Loss of consciousness Pallor Pulse abnormal Skin abrasion

Symptomtext

had complaints of dizziness, diaphoresis after shot while sitting in chair, was about to notify someone and had witnessed fall to ground, head first out of chair, fell to ground and had 15 sec syncopal episode, with thready pulse noted, barely palpable, pale, and clammy. feet put up on chair, ammonia tx, regained consciousness, and rolled onto backboard and transported to obs via stretcher, answering appropriately at this time. left forehead abrasions noted. 1105: bp 137/85 hr 76 rr 18 sats 99% on ra. PERRL. 1115: bp 136/86 hr 88 rr 16 sats 100% on ra, feeling better per patient. advised to go via ems for further eval for possible imaging by md and nurses, refusing, as has syncopal episodes in past similar to this with falls. 1124: bp 144/90 hr 81 lying, bp 135/88 hr 82 sitting, bp 126/89 hr 81 standing; asymptomatic. patient states feeling back to baseline. instructed on ss to monitor for and to go to ed. escorted to private vehicle with no further issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
na
Vorgeschichte
syncopal episodes x2
Andere Medikamente
none
Allergien
nka
Vorherige Impfungen
-

VAERS 1180447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

schwer
Staat
MN
Alter
28,0
Geschlecht
F
Eingang
08.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

Nearly fainted after vaccine. Moved to cot and recovered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
Fainted in past

VAERS 1179888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

schwer
Staat
PA
Alter
33,0
Geschlecht
M
Eingang
08.04.2021
Impfdatum
08.04.2021
Beginn
08.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chest discomfort Cold sweat Dizziness Feeling hot Syncope

Symptomtext

0933: few minutes after receiving vaccine, c/o dizziness, chest tightness, feeling hot, starting to black out. patient then experienced syncopal episode, feeling clammy, while being placed on stretcher, thready pulse noted. regained counsciousness once laying flat on stretcher. arriving to obs 0936: bp 111/71 hr 68 rr 18 sats 96%. patient arousable and reports feeling better. 0941: bp 110/69 hr 74 rr 18 sats 98%. patient able to sit up with ease, reports feeling back to baseline 0945: bp 120/86 hr 78 rr 18 sats 98% on ra. no further s/s of complications. departed to personal vehicle 0956.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
na
Vorgeschichte
mental health issues, social anxiety
Andere Medikamente
none
Allergien
nka
Vorherige Impfungen
-

VAERS 2681289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
50,0
Geschlecht
M
Eingang
12.09.2023
Impfdatum
08.04.2021
Beginn
31.12.2021
Tage bis Beginn
267,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Presents to the ED for shortness of breath, Tested positive for COVID,remdesivir, Decadron.Supplemental O2

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2612429

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
AK
Alter
16,0
Geschlecht
M
Eingang
10.04.2023
Impfdatum
11.05.2021
Beginn
16.05.2021
Tage bis Beginn
5,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Orthostatic hypotension Tunnel vision

Symptomtext

Severe Orthostatic Hypotension anytime follow laying down or sitting for > 5 minutes severe requiring holding on to objects or sitting back down with tunnelvision that would pass after 1-2 mintues provided slowly getting back to upright positiion

Weitere VAERSDATA-Felder
Praegender Schweregrund
Orthostatic hypotension
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NONE NOTED
Vorgeschichte
Asthma
Andere Medikamente
FLovent, albuterol
Allergien
KNDA
Vorherige Impfungen
-

VAERS 2596715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
68,0
Geschlecht
M
Eingang
14.03.2023
Impfdatum
13.04.2021
Beginn
24.11.2021
Tage bis Beginn
225,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 COVID-19 pneumonia Chest X-ray Diarrhoea Imaging procedure abnormal Lung disorder Oropharyngeal pain Oxygen saturation decreased Productive cough SARS-CoV-2 test positive

Symptomtext

Patient is a 69-year-old vaccinated(COVID) gentleman with past medical history significant for partial seizures, prostate cancer in remission (status post RT) who presented to the emergency department on 11/24/2021 for evaluation of symptoms of sore throat, productive cough, diarrhea since 11/17/2021. In the emergency department was noted to have desaturations to the 88% requiring 2 L via nasal cannula. his COVID screen was positive and imaging showed bilateral airspace disease. COVID-19 pneumonia was suspected, patient started on IV Decadron and admitted to internal medicine for continued care. Post admission patient's pro callus noted to be elevated. Patient was started on super added antibio

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
3,0
Labordaten
DR CHEST SINGLE VIEW Resulted: 11/24/21 1440 Order Status: Completed Updated: 11/24/21 1442 Narrative:
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2581560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

moderat
Staat
OR
Alter
83,0
Geschlecht
M
Eingang
14.02.2023
Impfdatum
19.04.2021
Beginn
20.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / UN
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Blood disorder Cardiac disorder Laboratory test Nasopharyngitis Pancreatic disorder Tremor

Symptomtext

shaking all over, cold, heart, pancreous , blood affected spent four days in hospital

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
4,0
Labordaten
multiple tests
Aktuelle Erkrankungen
diabetes, high blood pressure,
Vorgeschichte
diabetes, high blood pressure
Andere Medikamente
simvastatin tansulosin finasteride metformin
Allergien
-
Vorherige Impfungen
-

VAERS 2577739

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CT
Alter
52,0
Geschlecht
F
Eingang
09.02.2023
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Arthralgia Condition aggravated Fatigue Headache Neck pain COVID-19 Disease recurrence SARS-CoV-2 test Vaccination failure Pain in extremity Psoriasis Psoriatic arthropathy Tinea pedis

Symptomtext

psoriatic arthritis; I still was not having relief and it worsened; severe pain in all joints; exhausted; sore arm; headache; severe neck pain; had a severe psoriasis breakout on the bottom of my feet; it was athletes foot i tried several remedies; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 17Apr2021 as dose 2, single (Lot number: EW0162) at the age of 52 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "endometriosis" (unspecified if ongoing); "mild psoriasis" (unspecified if ongoing), notes: mild psoriasis; "high cholesterol" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Flagyl, reaction(s): "Known allergies: Flagyl". Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Batch/Lot No: ER8732, Location of injection: Arm Left), administration date: 27Mar2021, when the patient was 51-year-old, for COVID-19 immunization. The following information was reported: PSORIASIS (disability) with onset 17Apr2021, outcome "not recovered", described as "had a severe psoriasis breakout on the bottom of my feet"; HEADACHE (disability) with onset 17Apr2021, outcome "not recovered"; TINEA PEDIS (disability) with onset 17Apr2021, outcome "not recovered", described as "it was athletes foot i tried several remedies"; NECK PAIN (disability) with onset 17Apr2021, outcome "not recovered", described as "severe neck pain"; PAIN IN EXTREMITY (disability) with onset 17Apr2021, outcome "not recovered", described as "sore arm"; PSORIATIC ARTHROPATHY (disability, medically significant), outcome "unknown", described as "psoriatic arthritis"; CONDITION AGGRAVATED (disability), outcome "unknown", described as "I still was not having relief and it worsened"; ARTHRALGIA (disability), outcome "unknown", described as "severe pain in all joints"; FATIGUE (disability), outcome "unknown", described as "exhausted". The events "psoriatic arthritis", "sore arm", "headache", "severe neck pain", "had a severe psoriasis breakout on the bottom of my feet", "it was athletes foot i tried several remedies", "i still was not having relief and it worsened", "severe pain in all joints" and "exhausted" required physician office visit. Therapeutic measures were taken as a result of psoriatic arthropathy, pain in extremity, headache, neck pain, psoriasis, tinea pedis, condition aggravated, arthralgia, fatigue. Clinical course: Patient did not took other vaccine in four weeks and other medication in two weeks. Immediate adverse effects sore arm for days also headache and upon 2nd shot severe neck pain from the time patient received the shot to several months after went to a chiropractor for several months after not thinking it was from shot but I thought it was. Patient also had a severe psoriasis breakout on the bottom of her feet thinking it was athletes foot she tried several remedies eventually got a steroid prescribed but that did not help finally went to dermatologist as she still was not having relief and it worsened they prescribed me with another topical also by now having symptoms of psoriatic arthritis which she was looking into now with a biologic prescription of Skyrizi and she was scheduling with a rheumatologist for further help with this issue as she was in severe pain in all joints and am exhausted. AE resulted in: Doctor or other healthcare professional office/clinic visit, Disability or permanent damage. For AE treatment Prescribed steroidal ointments and biologic. Patient did not had COVID prior vaccination. COVID tested post vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300053075 same patient, different events after different doses of the vaccine;

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Endometriosis; High cholesterol; Psoriasis (mild psoriasis)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2576383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
71,0
Geschlecht
F
Eingang
06.02.2023
Impfdatum
01.12.2021
Beginn
04.01.2023
Tage bis Beginn
399,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

01/04/23 presents to the ED for "shortness of breath". PMHx of "COPD on 2 L, CAD, hyperlipidemia"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
01/04/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2570527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
81,0
Geschlecht
M
Eingang
30.01.2023
Impfdatum
13.12.2021
Beginn
29.12.2022
Tage bis Beginn
381,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/29/22 presents to ED for "shortness of breath". PMHx of "hypertension, CAD, CHF, A. fib on Eliquis, and emphysema"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
12/29/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2557475

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
55,0
Geschlecht
F
Eingang
11.01.2023
Impfdatum
16.03.2021
Beginn
14.12.2022
Tage bis Beginn
638,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/14/22 presents to EC ED for "shortness of breath". PMHx of "Crohn's with ostomy"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
12/15/22 SARS-CoV-2 (COVID-19) detected.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2549656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
UT
Alter
60,0
Geschlecht
F
Eingang
04.01.2023
Impfdatum
19.04.2021
Beginn
18.01.2022
Tage bis Beginn
274,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Dysgeusia Herpes zoster Hypoaesthesia Neuropathy peripheral COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Covid test date= 18Jan2022, covid test result= Positive; Covid test date= 18Jan2022, covid test result= Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 29Mar2021 as dose 1, single (Lot number: ER8727), in right arm and on 19Apr2021 as dose 2, single (Lot number: EW0162) at the age of 60 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: IBUPROFEN. Vaccination history included: Shingrix (I had had Shingrix vaccine 2 dose in Jan2019), administration date: Jan2019, when the patient was 58 years old, for Immunization. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 18Jan2022, outcome "unknown" and all described as "Covid test date= 18Jan2022, covid test result= Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jan2022) Positive; (29Dec2021) Negative; (03Jan2022) Negative. Additional information: facility type vaccine: Other. No other vaccine in four weeks. No covid prior vaccination. covid tested post vaccination. No known allergies.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201399101 same reporter/patient, different dose/event;

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Test Date: 20220118; Test Name: COVID 19 Test; Test Result: Positive ; Test Date: 20211229; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20220103; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
IBUPROFEN
Allergien
-
Vorherige Impfungen
-

VAERS 2529082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MO
Alter
89,0
Geschlecht
F
Eingang
12.12.2022
Impfdatum
07.05.2021
Beginn
05.12.2022
Tage bis Beginn
577,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Cough Dyspnoea Nasopharyngitis

Symptomtext

Symptom onset was 12/04/2022 with a severe cold, cough and SOB. Admitted to hospital 12/05/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
3,0
Labordaten
unknown
Aktuelle Erkrankungen
unknown
Vorgeschichte
none reported
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2526159

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
53,0
Geschlecht
F
Eingang
07.12.2022
Impfdatum
15.04.2021
Beginn
22.06.2022
Tage bis Beginn
433,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Amnesia Cardiac monitoring normal Distractibility Disturbance in attention Electrocardiogram normal Fatigue Impaired work ability Loss of personal independence in daily activities Magnetic resonance imaging normal Palpitations Panic attack SARS-CoV-2 test negative Tachycardia Tremor

Symptomtext

On 06/22 after the 2nd dose I had panic attacks symptoms. I would wake up with panic attacks and sleep with panic attacks. My heart was racing. I couldn't focus at all. I was lack of memory. At work I get distracted easily. I had 5 panic attacks each of them lasted for weeks. 2 months later while I was driving the panic attack happened again. I called my doctor he said to track it. After 30 days later I went to a cardiologist after speaking to my doctor. The Cardiologist diagnosed me with Hyper Tachycardia. They did MRI and everything came back as normal. I am a healthy person. I ran marathons, now I can't even run or do the things I used to do regularly. I get tired easily. My hand shakes when I get panic attacks. The second Cardiologist I went to did EKG, and had me on a heart monitor for 24 hours. The result came out good. My doctor said they are keeping an eye on me to see why I kept getting panic attacks out of nowhere.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
07DEC2022 COVID-19 test negative
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multivitamins
Allergien
None
Vorherige Impfungen
-

VAERS 2433432

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
50,0
Geschlecht
F
Eingang
08.09.2022
Impfdatum
19.03.2021
Beginn
15.08.2022
Tage bis Beginn
514,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Catheterisation cardiac normal Chest pain Coronary artery disease Diarrhoea Dizziness Echocardiogram abnormal Malaise Palpitations SARS-CoV-2 test positive Sinusitis Visual impairment

Symptomtext

52-year-old female presents with chest pain and episodes of palpitations feeling lightheaded which she describes as dizzy and feeling visual spots. Patient has been lightheaded with standing more recently. She was working here in the food service area when she began to feel the symptoms and came to the emergency department for evaluation. Patient has been seen in urgent care last week and placed on Augmentin for sinus infection. She has had diarrhea since being placed on the Augmentin recently. She had an echo with some wall motion abnormalities, albeit smaller are, in the septum. Due to this and risk factors, she was advised to have an ischemic eval - due to COVID precautions and inability to get her HR to a target for a CTA, she had a cardiac cath with essentially normal coronaries (one report did mention "nonobstructive CAD" but the cath report does not mention lesions or stenosis). She will follow with cardiology.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
7,0
Labordaten
8/15 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2420998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
66,0
Geschlecht
M
Eingang
26.08.2022
Impfdatum
04.05.2021
Beginn
21.08.2022
Tage bis Beginn
474,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Body temperature increased COVID-19 Chest pain Dyspnoea Fatigue SARS-CoV-2 test positive Tachycardia

Symptomtext

Pt to ED 8/21 for fatigue x3 days. Pt tachy in triage at 115 with low grade temp. Pt reporting intermittent CP/shortness of breath. COVID+ 8/21. 8/23 bed without any gait disturbances. Pt denies any CP, nausea, vomitng and SOB. Pt discharged 8/23.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
3,0
Labordaten
see above
Aktuelle Erkrankungen
None
Vorgeschichte
Gastroesophageal reflux disease ... Gastroesophageal reflux disease Chronic idiopathic constipation Weight loss Hematochezia Abdominal bloating General weakness
Andere Medikamente
Acetaminophen 500 MG PO Cap ... Acetaminophen 500 MG PO Cap Alendronate Sodium 70 MG PO Effer Tab aspirin 81 MG PO Chew Tab atorvastatin (LIPITOR) 20 MG PO Tab hydrocortisone (CORTEF) 10 MG PO Tab Levothyroxine Sodium (SYNTHROID PO) lisinop
Allergien
Penicillins
Vorherige Impfungen
-

VAERS 1971642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
66,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
29.04.2021
Beginn
02.08.2022
Tage bis Beginn
460,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Chest discomfort Cough Dyspnoea SARS-CoV-2 test positive Diarrhoea Feeling cold Nausea Pyrexia

Symptomtext

chills, fever, diarrhea, nausea

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
8,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1971642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
66,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
29.04.2021
Beginn
02.08.2022
Tage bis Beginn
460,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Chest discomfort Cough Dyspnoea SARS-CoV-2 test positive Diarrhoea Feeling cold Nausea Pyrexia

Symptomtext

chills, fever, diarrhea, nausea

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
8,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2388891

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NY
Alter
65,0
Geschlecht
M
Eingang
25.07.2022
Impfdatum
07.05.2021
Beginn
01.05.2021
Tage bis Beginn
-
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Joint swelling Palpitations

Symptomtext

Intense heart pounding/banging after exercise; highly swollen ankles for 5 weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
N/A.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Multivitamins
Allergien
Slight allergy to Kiwis
Vorherige Impfungen
-

VAERS 2368750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
VA
Alter
43,0
Geschlecht
M
Eingang
14.07.2022
Impfdatum
29.04.2021
Beginn
30.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure increased Fatigue Feeling abnormal Hypertension Hypotonia

Symptomtext

Elevated Blood Pressure: In the weeks following the shot my blood pressure increased to hypertension 2 with readings going up to 170/118 occasionally. This reduced to readings up to 150s/100s over time, before I started taking blood pressure medication. This was accompanied by fatigue, brain fog, muscle loss, etc. I have been on blood pressure medication (Olmesartan) ever since to keep it under control

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
hypothyroidism
Andere Medikamente
Levothyroxine, Vitamin D supplements
Allergien
-
Vorherige Impfungen
-

VAERS 2357656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
45,0
Geschlecht
M
Eingang
05.07.2022
Impfdatum
08.04.2021
Beginn
29.06.2022
Tage bis Beginn
447,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Chest discomfort Palpitations SARS-CoV-2 test positive

Symptomtext

6/29 46y.o. male with a PMH significant for Wolf parkinson, Afib S/P ablation and cardioversion (on eliquis), Wolf parkinson, HFrEF ( 35-40%). HTN. Presented from home with a chief complaint of palpitations and chest tightness of 2 days duration

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
6/29 SARS-CoV-2 by NAA, Detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2328830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
61,0
Geschlecht
M
Eingang
23.06.2022
Impfdatum
10.04.2021
Beginn
15.06.2022
Tage bis Beginn
431,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Endotracheal intubation Hypotension Hypoxia Mental status changes Resuscitation SARS-CoV-2 test positive Somnolence

Symptomtext

6/15 62y.o. male patient presenting to the ED with altered mental status. In the EC, patient became increasingly somnolent, hypoxic to 80% and was intubated for airway protection. He became hypotensive and was resuscitated with 30cc/kg fluids then started on Levophed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
-
Labordaten
6/15 Sars-Cov-2 by NAA, detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2328829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
60,0
Geschlecht
F
Eingang
23.06.2022
Impfdatum
10.04.2021
Beginn
15.06.2022
Tage bis Beginn
431,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dizziness Dyspnoea Nausea SARS-CoV-2 test positive

Symptomtext

6/15 61y.o. female with PMH HFpEF, COPD, HLD, HTN, GERD, OSA on BIPAP, chronic pain presenting for lightheadedness, dyspnea, nausea.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
6/15 Sars-Cov-2 by NAA, detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2325665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
IL
Alter
60,0
Geschlecht
F
Eingang
21.06.2022
Impfdatum
28.03.2021
Beginn
05.04.2021
Tage bis Beginn
8,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Balance disorder Dysstasia Gait disturbance Gait inability Magnetic resonance imaging head normal Magnetic resonance imaging neck Magnetic resonance imaging spinal normal Mobility decreased Walking aid user

Symptomtext

Severe balance issues. Sometimes unable to get up and extreme difficultly in walking and standing. Have had to use a cane on occasions. Have to hold on to people or things to walk. Some days are good and others bad. It is very unpredictable still to this day. I can feel fine one minute and then the next I am unable to walk.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
Have had MRI's of the brain, cervical spine, thoracic spine and lumbar spine. All have been normal. Currently doing vestibular therapy, with little relief.
Aktuelle Erkrankungen
-
Vorgeschichte
Vertigo, but new symptoms are totally different than my usual.
Andere Medikamente
Lorazepam, Betahistine, Premarin, Omeprazole, Flonase, Symbicort
Allergien
-
Vorherige Impfungen
-

VAERS 2310808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
69,0
Geschlecht
M
Eingang
06.06.2022
Impfdatum
23.11.2021
Beginn
24.05.2022
Tage bis Beginn
182,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cellulitis Chemotherapy Computerised tomogram neck Deformity Dizziness Electroencephalogram abnormal Encephalopathy Face oedema Febrile neutropenia Gastrostomy Hypotension Infection Laryngoscopy abnormal Mental status changes Neck mass Post procedural complication Pyrexia

Symptomtext

Hospitalized (5.24.22); COVID-19 positive (5.24.22); Fully vaccinated PLUS booster BRIEF OVERVIEW: Hematologist/Oncologist: MD Primary Care Physician at Discharge: DO Admission Date: 5/24/2022 Discharge Date: 06/06/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Neutropenic fever (HCC) COVID-19 HOSPITAL COURSE: The patient is a 69-year-old male with past medical history significant for squamous cell carcinoma of the right mandible and right posterior lateral tongue status post surgical resection. Patient is currently receiving weekly cisplatin and concurrent radiation.The patient was recently admitted 5/3 -5/6/22 with sepsis secondary to right facial and neck cellulitis. Patient was seen in the office on the day of admission ( 5/24) for his weekly cisplatin and found to be febrile and tachycardic and sent to the emergency department for further evaluation. In the emergency department he tested positive for Covid-19, patient was started on cefepime and vancomycin with Infectious workup. CT neck 5/24/22 - interval decrease in size of several heterogenous masses right lateral neck suggesting favorable treatment response. Some of these masses could represent superinfection which is improving. No new or enlarging neck masses. Persistent prominent right facial swelling and edema suggestive of cellulitis. ENT assessed the patient and did a flexible laryngoscopy, no airway obstruction was noted, but he was noted to have a right-sided asymmetry in hypopharynx and lateral pharyngeal wall. Steroids were started to help with swelling. They recommended moisturized air and mucolytics. ID was asked to see and were concerned some of the erythema was radiation induced. He had repeat fevers and AMS. He was changed to merrem and neurology was asked to see for AMS. EEG was done showing encephalopathy. Neurology initially felt he needed a LP as part of the work up for encephalitis. But that resolved and the concern for encephalitis was resolved. Antibiotics were DC'd on 6/4. He was stable for DC on 6/6. He had RT prior to DC and was sent on a steroid taper of 4 Mg TID x3 days, 4 MG BID x 3 days and 4 mg daily x 3 days, then 2 mg daily x 3 days and stop. He has follow-up as listed above.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypotension
Hospital-Tage
13,0
Labordaten
-
Aktuelle Erkrankungen
5.3.22 - hospitalized 5.3.22 - 5.6.22 - for sepsis - Discharge summary: This is a 69 y.o. year old patient who was admitted on 5/3/2022 with PMH of HTN, GERD, OSA, prostate cancer s/p resention 2012 as well as right mandibular squamous cell carcinoma and T1 squamous cell carcinoma of the right posterior lateral tongue s/p surgical resection currently on weekly Cisplatin. He is currently on XRT but this was held due to fever/hypotension during his XRT attempt at treatment. Pt presented to ER from XRT with fever 39, hypotension with syst 90's, dizzy and with increased right facial swelling and secretions. Patient was admitted for further evaluation treatment of sepsis and cellulitis. Patient underwent a CT of the neck on 05/03/2022 which showed right facial and lateral neck cellulitis that was thought to be secondary to postop changes versus RT versus infectious. Per discussion with radiation oncologist, these changes are not expected already with radiation so suspected that these were actually acute cellulitis findings. Infectious Disease team was consulted given severe nature patient's sepsis and inconclusive CT scan. Ultimately effect ultimately Infectious Disease team did recommend prior to discharge transitioning IV antibiotics to Augmentin as well as linezolid via PEG tube through 05/17/2022. Prior authorization was obtained obtained on linezolid at time of discharge. Undergoing chemotherapy and radiation therapy (for malignant neoplasm of overlapping sites of tongue)
Vorgeschichte
OSA on CPAP Prostate cancer (HCC) - s/p resection 4/20/2012 Gastroesophageal reflux disease without esophagitis Herpes zoster, ocular - 1/21/2018 Glaucoma suspect of both eyes Choroidal nevus, right eye Overweight (BMI 25.0-29.9) Hypertension, essential, benign Malignant neoplasm of overlapping sites of tongue (HCC) Chronic ulcer of left leg with fat layer exposed (HCC) At risk for falls Cancer of oral cavity (HCC) Primary osteoarthritis of left hip Primary osteoarthritis of right knee Dysphagia Sepsis (HCC) Febrile neutropenia (HCC) Cancer related pain Nausea Loose stools Acute hypoxemic respiratory failure (HCC) Squamous cell carcinoma of right posterior lateral tongue (HCC), and right mandible Cellulitis of mouth Transient alteration of awareness
Andere Medikamente
SILAPAP 160 MG/5ML liquid DENTA 5000 PLUS 1.1 % CREA dexamethasone (DECADRON) 4 MG tablet gabapentin (NEURONTIN) 250 MG/5ML solution gabapentin (NEURONTIN) 300 MG/6ML solution guaiFENesin 100 MG/5ML SOLN LORazepam (ATIVAN) 1 MG tablet LORaz
Allergien
Norco - dizziness
Vorherige Impfungen
-

VAERS 2309608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
36,0
Geschlecht
F
Eingang
04.06.2022
Impfdatum
04.02.2022
Beginn
04.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Burning sensation Injection site hypoaesthesia Injection site pain Injection site paraesthesia Joint range of motion measurement Laboratory test Loss of personal independence in daily activities Pain Pain in extremity Paraesthesia

Symptomtext

Pain and numbness to the right deltoid. Pain is a burning sensation that radiates down to the right wrist and has a shooting sensation of pins and needles, when I move my arm forwards, backwards, flex and raise above elbow length. The center of my right deltoid has constant tingling sensation. The pain has become so intolerable that I am unable to perform my daily activities without the constant use of Ibuprofen and Tylenol, that only dulls my pain and my children are now having to assist me with dressing, grooming, and bathing. The pain has increased from 6/10 to 10/10 with certain movements, and the medications are upsetting my stomach.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site paraesthesia
Hospital-Tage
-
Labordaten
06/03/2022 failed range of motion test due to pain, labs were drawn and now pending from same date visited the urgent care facility.
Aktuelle Erkrankungen
none
Vorgeschichte
coccidioidomycosis
Andere Medikamente
Daily multi-vitamin, Topamax
Allergien
Cytotec, meloxicam
Vorherige Impfungen
-

VAERS 2290826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
60,0
Geschlecht
F
Eingang
23.05.2022
Impfdatum
16.04.2021
Beginn
01.05.2022
Tage bis Beginn
380,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood 1,25-dihydroxycholecalciferol increased Blood calcium increased Blood glucose increased Blood test abnormal Chest X-ray abnormal Chest scan Dyspnoea Exercise tolerance decreased Fatigue Glycosylated haemoglobin increased Inflammation Inflammatory marker increased Injection site erythema Injection site pain Loss of personal independence in daily activities Pyrexia Vomiting Walking aid user

Symptomtext

I had a fever the second day after the shot pain and redness at the injection site. The second morning after the 2nd shot I vomited in the morning, but just once. Then it was fatigue for the rest of the day, drinking fluids and monitoring temperature which the highest was 101. used Tylenol to bring down, it was just fatigue after that, all other sx went away by the 3rd day, but the fatigue stayed. I went to the doctor about 2-3 weeks later due to the lasting fatigue, shortness of breath and exhaustion after very little exertion. Blood work was done in May or June showed elevated calcium in the blood and elevated Vitamin D125. She ordered another blood test for inflammation markers and it showed high inflammation. Blood sugar and AC was high and it was recommended to make dietary changes which I did. She also did Chest x-rays, chest scan, full body scan At that point I was referred to specialist endocrinology, ENT and cardiologist. Started feeling better after being prescribed Trulicity. Exercising was very difficult. I am now walking with a cane and I do a few household chores and I can not do them with out being exhausted so quickly.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Blood work was done in May or June - Abnormal results Chest x-rays, chest scan, full body scan - abnormal
Aktuelle Erkrankungen
no
Vorgeschichte
HBP, High cholesterol
Andere Medikamente
Lisinopril / HCTZ 20mg/10mg, tri core 145mg, omeprazole 20mg, C-PAP therapy, Voltaren gel, Ashwagandha
Allergien
NKDA, pistachios
Vorherige Impfungen
flue vaccine every year I would get the flu for 3-4 days this happened while active duty in the Air Force, maybe 1991. Since I g

VAERS 2280516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NJ
Alter
44,0
Geschlecht
F
Eingang
17.05.2022
Impfdatum
11.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest X-ray Chills Echocardiogram Heart rate increased Hypertension Positron emission tomogram Pyrexia Ultrasound scan

Symptomtext

fever; chills; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: (159558). A 45-year-old female patient received BNT162b2 (BNT162B2), on 11Apr2021 as dose 1, single (Lot number: EW0162) at the age of 44 years for covid-19 immunisation. The patient's relevant medical history included: "stage I breast cancer" (unspecified if ongoing), notes: she had stage I breast cancer 10 years ago; "mastectomy" (unspecified if ongoing), notes: She had a mastectomy done. The patient's concomitant medications were not reported. The following information was reported: PYREXIA (non-serious), outcome "recovered", described as "fever"; CHILLS (non-serious), outcome "recovered". Relevant laboratory tests and procedures are available in the appropriate section.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200699539 same patient, same product, different dose, different events;US-PFIZER INC-202200700343 same patient, same product, different dose, different events

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
Test Name: chest x-ray; Result Unstructured Data: Test Result:Unknown results; Comments: the emergency department took a chest x-ray; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown results; Test Name: high heart rate; Result Unstructured Data: Test Result:High heart rate; Comments: She went to the emergency department and high blood pressure and high heart rate; Test Name: high blood pressure; Result Unstructured Data: Test Result:High Blood pressure; Comments: She went to the emergency department and high blood pressure; Test Name: pet scan; Result Unstructured Data: Test Result:Unknown results; Test Name: ultrasound; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Breast cancer stage I (she had stage I breast cancer 10 years ago); Mastectomy (She had a mastectomy done)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2271074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
78,0
Geschlecht
M
Eingang
11.05.2022
Impfdatum
17.04.2021
Beginn
07.02.2022
Tage bis Beginn
296,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/07/22 presents to ED for "SOB". PMHx of "AF on coumadin, ischemic cardiomyopathy (EF 20%) s/p AICD, MVR, CKD stage III, HLD, HTN, hypothyroidism"

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
02/07/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2266963

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
57,0
Geschlecht
F
Eingang
07.05.2022
Impfdatum
01.04.2021
Beginn
10.05.2021
Tage bis Beginn
39,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hemiparesis Injected limb mobility decreased Injection site pain Insomnia Muscular weakness Pain X-ray

Symptomtext

Constant pain in area of injection site; some limited movement and pain with movement; some weakness in left arm; sometimes painful to sleep on left arm; physical therapy has not helped; no prior injury or problems with left arm or shoulder

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
X-ray 3/22/22 MRI scheduled
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2266566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
75,0
Geschlecht
M
Eingang
06.05.2022
Impfdatum
25.03.2021
Beginn
01.08.2021
Tage bis Beginn
129,0
Dosis
2
Route/Site
SC / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: unbekannt
Exercise tolerance decreased Functional endoscopic sinus surgery Joint stiffness Mobility decreased Muscular weakness Pain Swelling

Symptomtext

Several months after receiving the second shot I started experiencing muscular weakness, then joint stiffness, then both plus pain and swelling. It got so bad I couldn't get out of bed in the morning and get dressed. In Dec2021 I had FESS sinus surgery and part of the post surgery treatment included a six day course of steroids. By day two all my muscle and joint symptoms were gone, but they came back within a month. Another dose of steroids for my sinuses yielded immediate relief for my joints and muscles again. Prior to these problems I walked at least a mile a day in our neighborhood or on our treadmill plus I utilized my Sneakers Program at a local gym a few times a week. After the symptoms came. came back again and after discussing the problems with my physician I decided to start a very slow introduction of Ibuprophen, first one pill a day and then two. Within a couple of days the symptoms were around 75% gone and I'm living with it because I don't want to go back on steroids. There is no history of joint or muscle problems in my family history and prior to this I could sit on the floor with legs crossed and stand up without using my hands. I can't prove this was caused by the vaccine but the timing is quite suspect as there were no other probabilities.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
SPORADIC HIGH BLOOD PRESSURE
Andere Medikamente
OLMESARTAN/AMLODIPINE/MONTELUCAST
Allergien
CERTAIN PROCESSED WHEAT
Vorherige Impfungen
-

VAERS 2263342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
35,0
Geschlecht
F
Eingang
04.05.2022
Impfdatum
21.04.2021
Beginn
27.04.2022
Tage bis Beginn
371,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 CSF white blood cell count increased Chest pain Culture negative Fatigue Headache Lumbar puncture abnormal Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Pain Paraesthesia SARS-CoV-2 test positive

Symptomtext

Patient is fully vaccinated. COVID positive on 4/27/2022 at hopitalization. 36-year-old female that presented with bilateral lower extremity paresthesias and severe headaches. She also had general body aches, chest pain, fatigue. She did not require oxygen. Lumbar puncture was done. CSF showed mild increase in WBCs. Cultures have been negative however and so have MRIs of brain and spine. Discussed this at length with neurology and they recommended close follow-up as an outpatient. Patient symptoms have resolved and she was feeling well on discharge.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2256861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
31,0
Geschlecht
M
Eingang
28.04.2022
Impfdatum
21.04.2021
Beginn
07.01.2022
Tage bis Beginn
261,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Asthenia COVID-19 Chills Cough Disturbance in attention Fatigue Feeling abnormal Headache Mobility decreased Muscle fatigue Pain SARS-CoV-2 test positive

Symptomtext

I worked out one day and I had not worked out for a while. I had muscle fatigue all over that started on the second day and it got worse on the third day. I had a headache and took Tylenol and I developed a slight cough. The next day, I was extremely fatigued, and I could barely move I was so tired and sore. I took an at home test and it was positive, and I went to the Urgent Care to get tested. I tested Positive for COVID-19 on 01/09/2022. The next day I was very tired with tiredness, chills and coughing. I felt better on the fourth day. My head felt fuzzy and I had trouble focusing. I had no loss of taste or smell that was noticeable. I was fully recovered but I still had little energy and my brain fog lingered until a full week after it started.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
COVID-19 Positive 01/09/2022
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
Seasonal Allergies
Vorherige Impfungen
-

VAERS 2251990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
45,0
Geschlecht
F
Eingang
26.04.2022
Impfdatum
20.04.2021
Beginn
21.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dyspnoea Fatigue Productive cough Pyrexia Secretion discharge Upper respiratory tract infection

Symptomtext

Fever, difficulty breathing , coughing up mucus, shortness of breath, and extreme fatigue. Received prescriptions. Doctor stated upper respiratory infection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
Hypertension
Andere Medikamente
Amoxicillin 500ml, Abuteral (inhaler), and emergency Vitamin C packet .
Allergien
Erythromyein.
Vorherige Impfungen
-

VAERS 2250195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
VA
Alter
48,0
Geschlecht
F
Eingang
25.04.2022
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Cardiac monitoring Chest pain Condition aggravated Dry eye Extrasystoles Eye pain Inappropriate schedule of product administration Neck pain Pain Palpitations Rash

Symptomtext

I have left eye pain for one month. I scaled the pain to be a 6. I went to see an optometrist. They found nothing but dry eye. I knew this 5 years ago, but it did not cause pain. I went to another doctor, after my 2nd dose, the eye pain was worse. It lasted much longer, gradually it goes away and comes back. It is not as bad anymore. I also have chest palpitations and pain; this was 10 days after my 2nd dose. The position related, when I sit and lean forward, I feel pain. I feel like it was puerilities, the feeling of pain is happening but, not as often. They doctors are saying I have premature heartbeat. I have never had this before and I have no family history of heart problems. I also have a rash on both hands and joint pain on left ankle front side. This is not normal for me. I had seen a neurologist due to neck pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Heart Monitor
Aktuelle Erkrankungen
2 Weeks before the vaccine I had a little eye pain; I did not pay attention to this when I took the vaccine.
Vorgeschichte
Neck pain
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2241698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew 0162

moderat
Staat
IN
Alter
42,0
Geschlecht
F
Eingang
19.04.2022
Impfdatum
03.12.2021
Beginn
04.04.2022
Tage bis Beginn
122,0
Dosis
2
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal discomfort Abdominal pain Appendicectomy Appendicitis Arthralgia Computerised tomogram abdomen abnormal Condition aggravated Diarrhoea Endometriosis Fatigue Full blood count Intra-abdominal haemorrhage Menstruation irregular Ovarian cyst Pyrexia SARS-CoV-2 test Scan with contrast abnormal Urine analysis

Symptomtext

I'm not sure the vaccine had any impact one way or another. However, will share: On about 3/28/22 had a low grade fever, abdominal discomfort, achy joints, increased tiredness etc. These symptoms lasted for about a week. I took 2 covid tests during that week because i could not figure out what was wrong with me. Then on 4/4 the abdominal pain intensified, some diarrhea, vomiting, but no fever. After it did not get better and instead got a bit worse, I went to Urgent Care the morning of 4/6. They determined that I was having a flare up of endometriosis, have 4.5 cm cysts on each ovary, uterine fibroids AND acute appendicitis. I was directed to drive myself to the ER for consult and surgery. During the surgery to remove my appendix and inspect the rest of the situation, they determined that the endo flare up caused a significant amount of hemorrhagic fluid in my abdomen thus infecting my appendix. (For the last 3-4 months my periods have been significantly worse which is likely due to the endometriosis)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
full panel of blood and urine tests CT with contrast of abd.
Aktuelle Erkrankungen
n/a
Vorgeschichte
Endometriosis, PCOS, Depression, Anxiety
Andere Medikamente
Mulit-vitamin
Allergien
Oats, formaldehyde, some adhesives
Vorherige Impfungen
I've had the usual flu-like symptoms after all 3 vaccinations.

VAERS 2236134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
32,0
Geschlecht
F
Eingang
15.04.2022
Impfdatum
21.04.2021
Beginn
26.04.2021
Tage bis Beginn
5,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood test Hypoaesthesia Lymphadenopathy Paraesthesia Ultrasound scan abnormal

Symptomtext

I noticed pins and needles and numbness in the lower right side of my body. I took Benadryl and had an extreme reaction to Benadryl. It was like a heart attack symptoms and that worsened the pins and needles feeling on my right side of my body. This lasted 6-8 weeks. I went to my PCP for a blood test and general exam. I got an ultrasound on my neck due to swollen lymph nodes which was inflamed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
Blood work, Ultrasound.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Birth control
Allergien
None
Vorherige Impfungen
-

VAERS 2233667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
48,0
Geschlecht
F
Eingang
14.04.2022
Impfdatum
28.04.2021
Beginn
30.04.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthma Condition aggravated Hyperaesthesia Lip swelling Pharyngeal swelling Pruritus Urticaria

Symptomtext

I experienced itching around tight clothing area, whelps developed, my lips began to swell, my throat began to swell shut, and I had to take Benadryl for that reaction. After I recovered from the reaction my asthma has been flaring up more than normal. When I went to the doctors office for the reaction I was prescribed a steroid pack. It took 2 weeks to recover and return to normalcy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
Womens Multivitamin
Allergien
Shellfish; Avocado
Vorherige Impfungen
-

VAERS 1463271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
PA
Alter
61,0
Geschlecht
F
Eingang
06.04.2022
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal distension Anosmia Back pain Decreased appetite Diarrhoea Asthenia Blood test COVID-19 Condition aggravated Fatigue Feeding disorder Feeling abnormal Illness Immediate post-injection reaction Gastrointestinal disorder Memory impairment Mobility decreased Pain

Symptomtext

Immediately after vaccine, I came home and felt horrible. I had no strength and worsening pains. I could not function and I laid in bed for 7 days. I was extremely fatigues and my back pain increased worse than its ever been. I could not eat. I also got COVID-19 in December 28th. I had was sick for 10 days. I was put back on steroids after being off of them and that seemed to help. I was told by my doctor that I have long COVID due to cognitive issues with memory and sleep pattern disruption.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Positive COVID-19 test, blood work
Aktuelle Erkrankungen
-
Vorgeschichte
Back surgery 01/2021
Andere Medikamente
Steroids, Blood pressure meds, Gabapentin, Flexeril, oxycodone
Allergien
None
Vorherige Impfungen
-

VAERS 1463271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
PA
Alter
61,0
Geschlecht
F
Eingang
06.04.2022
Impfdatum
16.04.2021
Beginn
16.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal distension Anosmia Back pain Decreased appetite Diarrhoea Asthenia Blood test COVID-19 Condition aggravated Fatigue Feeding disorder Feeling abnormal Illness Immediate post-injection reaction Gastrointestinal disorder Memory impairment Mobility decreased Pain

Symptomtext

Immediately after vaccine, I came home and felt horrible. I had no strength and worsening pains. I could not function and I laid in bed for 7 days. I was extremely fatigues and my back pain increased worse than its ever been. I could not eat. I also got COVID-19 in December 28th. I had was sick for 10 days. I was put back on steroids after being off of them and that seemed to help. I was told by my doctor that I have long COVID due to cognitive issues with memory and sleep pattern disruption.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Positive COVID-19 test, blood work
Aktuelle Erkrankungen
-
Vorgeschichte
Back surgery 01/2021
Andere Medikamente
Steroids, Blood pressure meds, Gabapentin, Flexeril, oxycodone
Allergien
None
Vorherige Impfungen
-

VAERS 2209125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
51,0
Geschlecht
F
Eingang
31.03.2022
Impfdatum
29.11.2021
Beginn
04.02.2022
Tage bis Beginn
67,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Acute kidney injury Anaemia COVID-19 Culture urine negative Imaging procedure abnormal Leukocytosis Metastasis Neoplasm malignant Pyrexia Red blood cell transfusion SARS-CoV-2 test positive Sepsis Tachycardia Urinary tract infection White blood cell count abnormal

Symptomtext

Patient up to date on COVID vaccinations who admitted to hospital with COVID positive test (no respiratory issues during stay) for sepsis from UTI and active metastatic cancer. Provider discharge note below: "Significant Findings and Invasive Procedures) the patient presented with fever, tachycardia and leukocytosis found to be septic from complicated UTI. Mild hydro on imaging and she has ureteral stent. She also had AKI. aki improved as did fever/wbc. Urology recommended outpatient follow up and early stent exchange but not until out of covid isolation, especially given the fact she has resolution of aki and was feeling improved. She was given 1u prbc due to symptomatic anemia though she was not far from baseline and without observed hemorrhage. She was offered a second unit given 7.5 hgb and mild tachycardia but she declined. Will complete 7 day course with cipro, ucx was negative but was collected after cefepime given. Gen: in NAD. Non toxic. Appears improved. HEENT: mucosa moist CV: borderline tachycardic rate, regular rhythm Resp: clear to auscultation bilaterally Abd: soft Ext: left lower extremity with trace pittign lower extremity edema, right lower extremity without any significant edema Skin: warm, dry Neuro: alert, oriented x4 No flank pain. Issues Requiring Follow Up: (Who, what, when, and how communicated?) follow up urology for stent exchange in 1-2 weeks."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tachycardia
Hospital-Tage
3,0
Labordaten
COVID "detected" PCR on 02/04/2022
Aktuelle Erkrankungen
-
Vorgeschichte
SLE (systemic lupus erythematosus) (*) Vitamin D deficiency Generalized osteoarthrosis, involving multiple sites Synovitis of knee History of splenectomy Hypertension Leukopenia B12 deficiency Iron deficiency anemia due to chronic blood loss Iron malabsorption Acute pericarditis associated with systemic lupus erythematosus (SLE) (*) Sinus tachycardia Chronic deep vein thrombosis (DVT) of femoral vein of left lower extremity (*) Lupus anticoagulant positive Elevated lipase Endometrial cancer (*) Metastasis to liver (*) Anemia due to antineoplastic chemotherapy Retroperitoneal lymphadenopathy Hypomagnesemia Malignant neoplasm of uterus (*) Class 2 obesity with body mass index (BMI) of 35.0 to 35.9 in adult AKI (acute kidney injury) (*) Liver dysfunction
Andere Medikamente
Vitamin B12 Decadron (after chemotherapy Chemotherapy Colace Vitamin D2 Iron Folic acid Neurontin Norco Mag-Ox Cellcept Compazine
Allergien
Plaquenil [Hydroxychloroquine]: Maculopathy Bactrim [Sulfamethoxazole-trimethoprim]: Itching Celebrex [Celecoxib]: Itching
Vorherige Impfungen
-

VAERS 2201402

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
63,0
Geschlecht
F
Eingang
28.03.2022
Impfdatum
21.10.2021
Beginn
01.01.2022
Tage bis Beginn
72,0
Dosis
3
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood test Chest X-ray Dizziness Dyspnoea Electrocardiogram Hyperhidrosis Hypothyroidism Palpitations Paraesthesia Thirst

Symptomtext

Woke up thirsty, went to get something to drink. Got dizzy while standing by fridge. Sat down started having palpitations. Broke out in sweats, hands and feet got tingly. Shortness of breath. After a while of it not going away I went to the ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Bloodwork; EKG; chest X-ray - my thyroid was low
Aktuelle Erkrankungen
No
Vorgeschichte
Thyroid problem; cholesterol issues; blood pressure
Andere Medikamente
Zyrtec, Albuterine, Spironeurolatone, Losartan, Estrotest, Potassium Chloride, Probiotic, Levothyroxine, Rosvastatin, Cingular, Folic Acid, Galaxine
Allergien
Doxycycline; Augmentin; quinine; Robaxin
Vorherige Impfungen
-

VAERS 2189224

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
32,0
Geschlecht
F
Eingang
20.03.2022
Impfdatum
26.03.2021
Beginn
16.04.2021
Tage bis Beginn
21,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cognitive disorder Condition aggravated Crying Feeling abnormal Headache Impaired work ability Influenza like illness Migraine Myalgia Nausea Pain Pain in extremity Vomiting Weight decreased

Symptomtext

I was okay with the first dose; mild arm soreness, and mild flu-like symptoms later that evening (achiness, mild headache)--synptoms mostly cleared by the next day. The second dose, however, sparked an 8-day-long migraine that was so intense that I had to call out of work for several days and work lightly from home the rest of the time out of necessity. I was vomiting from the pain, hiding in my darkened bedroom in tears for days on end, and by days 4-5 I was scheduling massages and other therapies out of sheer desperation, looking for anything that would help. I have never, ever had a migraine last that long, or maintain such intensity for such a long period of time with no relief. Over-the-counter pain medications had no effect, and I lost approx. 5-6 lbs in 7 days due to an inability to keep food down. I will never forget waking up on Day 9 realizing for the first time in what felt like an eternity, that the pain had finally subsided. I felt hungover that day, as though I'd had been drinking the night before; nauseous, clouded/impaired cognitive function, sore muscles as though I'd been working out; but the migraine was finally gone. So far I have been too terrified of a repeat episode to get a booster shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma, Eczema, migraines 3-7 times per year that last approx. 24-48 hours at maximum
Andere Medikamente
-
Allergien
Benadryl, Doxycycline
Vorherige Impfungen
-

VAERS 2178485

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0162

moderat
Staat
PR
Alter
25,0
Geschlecht
M
Eingang
14.03.2022
Impfdatum
18.04.2021
Beginn
20.05.2021
Tage bis Beginn
32,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Fatigue Heart rate increased Testicular pain

Symptomtext

I have pain in the testicles and my heart go so fast also i am very tired every day .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Pain in the testicle and my heart go so fast
Vorgeschichte
Pain in testicles i an tired all the time
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2134535

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
90,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
30.04.2021
Beginn
09.12.2021
Tage bis Beginn
223,0
Dosis
1
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Acute kidney injury Blood creatinine increased COVID-19 Central venous catheterisation Computerised tomogram thorax normal Condition aggravated Dyspnoea Dyspnoea exertional Hypoxia Malaise Mental status changes Myalgia Nasopharyngitis Positive airway pressure therapy SARS-CoV-2 test positive Sleep apnoea syndrome Sleep disorder

Symptomtext

Provider summary "91 YO male with a PMHx of asthma, OSA, pulmonary hypertension, CKD stage 3, type 2 diabetes, obesity who presents with dyspnea on exertion and cold-like symptoms for a few days. Patient is an incredibly poor historian and frequently falls asleep during exam. He cannot tell me even why he came to the hospital. He denies any current pain and denies any current trouble breathing. Called patient's DPOA and left voicemail. Also discussed with daughter. She told me that patient had been feeling sick for approximately a week. He predominantly complained of myalgias and not trouble breathing. ER notes that he complained of shortness of breath for the last few days. Reportedly was vaccinated with 2 doses of the vaccine but did not obtain booster. In the ED: Initially required non-rebreather due to hypoxia PICC. Quickly weaned to room air, but needs oxygen while sleeping due to known OSA. Labs notable for COVID positive, AKI with a creatinine of 1.9. CT pulmonary embolism negative for PE. He was weaned fairly quickly off of BiPap support to nasal cannula. His mentation quickly improved as well. He was continued on dexamethasone and remdesevir while admitted. He was eventually weaned to room air but needed O2 with activity. He was seen by PT/OT recommended SNF v home with assist. He adamantly refuse SNF placement. His care was discussed wit his daughter and caregiver. They all agreed that he could come home. He was discharged in stable condition with strict return precautions. "

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
4,0
Labordaten
Positive COVID PCR test 12/9/2021
Aktuelle Erkrankungen
-
Vorgeschichte
Morbid obesity with BMI of 50.0-59.9, adult (*) Diabetes (*) Hypertension History of arthroplasty of right knee OSA (obstructive sleep apnea) Hyperlipidemia BPH (benign prostatic hyperplasia) COVID-19 Acute respiratory failure with hypoxia (*) Resolved AKI (acute kidney injury) (*) Resolved
Andere Medikamente
acetaminophen 650 mg Oral every 4 hours PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation EVERY 6 HOURS PRN allopurinol 100 mg Oral Daily amlodipine besylate/benazepril 10-20 mg 1 capsule Oral Daily benzocaine 10 % Mouth/Throat
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2127211

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
-
Geschlecht
M
Eingang
19.02.2022
Impfdatum
21.04.2021
Beginn
21.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Tremor

Symptomtext

My hand on which I had the shot is numb kind of my hand is kind of shaky; My hand on which I had the shot is numb kind of my hand is kind of shaky; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Apr2021 (Lot number: EW0162) as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: TREMOR (non-serious), HYPOAESTHESIA (non-serious) all with onset 21Apr2021, outcome "unknown" and all described as "My hand on which I had the shot is numb kind of my hand is kind of shaky". No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2126638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TN
Alter
17,0
Geschlecht
F
Eingang
19.02.2022
Impfdatum
22.04.2021
Beginn
22.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Burning sensation Headache Paraesthesia Vaccination site warmth

Symptomtext

Tingling and burning up and down back/for Tingling in face, side of right cheek; Tingling and burning up and down back; Headache; Warm at injection site; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A 17 year-old female patient received bnt162b2 (BNT162B2), administration date 22Apr2021 09:30 (Lot number: EW0162, Expiration Date: 31Jul2021) at the age of 17 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Headache" (unspecified if ongoing), notes: Tylenol every once in while for headaches in the last 2 week. Concomitant medication(s) included: TYLENOL taken for headache. Vaccination history included: Meningitis a (Route: injection, Anatomical Location: right arm), for immunisation. The following information was reported: PARAESTHESIA (non-serious) with onset 22Apr2021 09:45, outcome "not recovered", described as "Tingling and burning up and down back/for Tingling in face, side of right cheek"; BURNING SENSATION (non-serious) with onset 22Apr2021, outcome "not recovered", described as "Tingling and burning up and down back"; HEADACHE (non-serious) with onset 22Apr2021, outcome "recovered" (22Apr2021), described as "Headache"; VACCINATION SITE WARMTH (non-serious) with onset 22Apr2021, outcome "not recovered", described as "Warm at injection site". Therapeutic measures were not taken as a result of paraesthesia, burning sensation, headache, vaccination site warmth. Additional information: The patient had tingling and burning up and down her back, neck and tingling in her face. Had the vaccine 9:30 this morning. It started almost as soon as she had it. Also had a headache that went away. The patient was told to wait the 15 minutes to see if there were any side effects. When she left, she started feeling the burning sensation in her back. When she got home, she felt the tingling, like acupuncture. It was still burning and felt the same way. Has not gotten any worse, its the same. Tingling in face, side of right cheek: Is by her nose on the right side. Started about an hour or 2 ago. Still feels the same. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Headache (Tylenol every once in while for headaches in the last 2 week.)
Andere Medikamente
TYLENOL
Allergien
-
Vorherige Impfungen
-

VAERS 2117046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
56,0
Geschlecht
F
Eingang
16.02.2022
Impfdatum
19.10.2021
Beginn
29.01.2022
Tage bis Beginn
102,0
Dosis
3
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Computerised tomogram neck Dysphagia Dysphonia Exposure to SARS-CoV-2 Laryngeal oedema Mobility decreased SARS-CoV-2 test positive Secretion discharge Swollen tongue White blood cell count increased

Symptomtext

Patient was admitted because of sensation of tongue swelling gradually got worse to the point that she has a difficulty swallowing. She was seen in emergency department 1st time she was evaluated by CT scan of the neck that was essentially negative. She was given Augmentin 1 dose of Diflucan and prednisone tapering dose and discharged home. Next day her symptoms got worse with tongue swelling and mucus-like secretion in the mouth that she have a difficulty clearing. She was experiencing difficulty raising her head with swelling in the tongue. Denies any cough or shortness of breath. She was positive for COVID 19 home test 10 days ago. First emergency room visit cope with test was done that also resulted positive . She was gi ven IV Solu-Medrol, IV Unasyn. IMPRESSION: 1. Dysphagia. 2. Mild edema of the larynx and hoarseness. 3. Symptoms likely related to her COVID-19 exposure.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
5,0
Labordaten
COVID-19 positive on January 29, 2022. WBC count is elevated at 16.87 ( started on Prednisone).
Aktuelle Erkrankungen
-
Vorgeschichte
History of lumbar fusion Migraine
Andere Medikamente
ALPRAZolam (XANAX) 0.5 MG tablet cyclobenzaprine (FLEXERIL) 5 MG tablet famotidine (PEPCID) 20 MG tablet HYDROcodone-acetaminophen (NORCO) 7.5-325 MG tablet Quercetin 50 MG tablet zolpidem (AMBIEN) 10 MG tablet
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2110836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
69,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
18.05.2021
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Angiogram pulmonary normal COVID-19 Chest X-ray abnormal Chest pain Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Cough Decreased appetite Diarrhoea Dyspnoea exertional Exposure to communicable disease Hypoxia Myalgia Nausea Oxygen saturation decreased Pain Platelet count decreased

Symptomtext

70 y/o female with history of COPD, hypothyroidism who p/w n/v and body aches. Patient states saw Dr. on Tuesday for covid testing due to n/v/d and her 2 daughters had covid. She tested negative at that time. She has had myalgias, no fever, persistent cough that has caused chest soreness. She states diarrhea has improved, but has not had anything to eat in 2 days due to emesis. She has been covid vaccinated, and had covid last year as well and received monoclonal ab treatment. She has not had a booster. In the ER, cxr shows only chronic changes of copd, but covid is positive. ER physician wanted to send patient home, but O2 dropped into the mid 80s upon any exertion. Admission requested. DISCHARGE: Diagnosed with COVID in ED. She had mild oxygen desaturations with activity, so admitted overnight. CTA showed no COVID pneumonia, no PE or other acute process. She is an active smoker with advanced emphyxema on CT. This is likely chronic/subacute hypoxemia from progressive COPD and no acute process identified to treat. No active wheezing. Discharged home on supplemental oxygen, for which she qualified. Mildly low WBC and platelets likely from COVID infection. Recommend CBC in one week to re-assess.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
258227
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2110836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
69,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
18.05.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Angiogram pulmonary normal COVID-19 Chest X-ray abnormal Chest pain Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Cough Decreased appetite Diarrhoea Dyspnoea exertional Exposure to communicable disease Hypoxia Myalgia Nausea Oxygen saturation decreased Pain Platelet count decreased

Symptomtext

70 y/o female with history of COPD, hypothyroidism who p/w n/v and body aches. Patient states saw Dr. on Tuesday for covid testing due to n/v/d and her 2 daughters had covid. She tested negative at that time. She has had myalgias, no fever, persistent cough that has caused chest soreness. She states diarrhea has improved, but has not had anything to eat in 2 days due to emesis. She has been covid vaccinated, and had covid last year as well and received monoclonal ab treatment. She has not had a booster. In the ER, cxr shows only chronic changes of copd, but covid is positive. ER physician wanted to send patient home, but O2 dropped into the mid 80s upon any exertion. Admission requested. DISCHARGE: Diagnosed with COVID in ED. She had mild oxygen desaturations with activity, so admitted overnight. CTA showed no COVID pneumonia, no PE or other acute process. She is an active smoker with advanced emphyxema on CT. This is likely chronic/subacute hypoxemia from progressive COPD and no acute process identified to treat. No active wheezing. Discharged home on supplemental oxygen, for which she qualified. Mildly low WBC and platelets likely from COVID infection. Recommend CBC in one week to re-assess.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
258227
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2110217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
96,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
20.04.2021
Beginn
27.08.2021
Tage bis Beginn
129,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 COVID-19 pneumonia Haemorrhage intracranial Pneumonia SARS-CoV-2 test positive

Symptomtext

Admit originally for intracranial hemorrhage and pna. Found to be COVID + after admit. Fully vaccinated. COVID pna with possible aspiration pna as well. Was on RA to start but did eventually require O2 by NC. Started on steroids, cefepime, merrem, zinc, vit-D, singulair. Palliative care following. D/C to inpatient hospice.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
25,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
52,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
08.04.2021
Beginn
09.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Fatigue Influenza like illness Mobility decreased Pain Pain in extremity

Symptomtext

I was weak, tired, and achy all over that lasted the whole day. As if I had the flu. I may have had a low grade temp. and I stayed in bed all day. I took Tylenol. I felt better by the next morning. My arm hurt intermittently off and on for about a month. When I moved it would hurt.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Diabetes, Coronary artery disease, hypothyroidism , high blood pressure, endometriosis, PCOS
Andere Medikamente
Lipitor 80mg 1x/day, Toprol xl 25mg 1x/day, prinzide 20/25 1x/day, Synthroid 75mg 1x day, Wellbutrin 300mg xl 1x/day, aygestin 5mg (1) 2x day, Humulin R U-500 100 units plus coverage for meals, Zyrtec 10mg/ daily, Women multi vitamin, 2 bab
Allergien
None
Vorherige Impfungen
-

VAERS 2108457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
48,0
Geschlecht
F
Eingang
12.02.2022
Impfdatum
12.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Pain Pain in extremity

Symptomtext

My right thumb is the worst, it's killing me. My right hand is worse than my left hand.; My right thumb is the worst, it's killing me. My right hand is worse than my left hand.; The pain is really bad; Due to the pain being really bad, she had to get up last night and put an ice pack but the pain got worse; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program. The reporter is the patient. A 48 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 12Apr2021 12:10 (Lot number: EW0162) at the age of 48 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose number - 01, Lot number: ER2613 , Location: Left arm), administration date: 22Mar2021, when the patient was 48 years old, for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), PAIN IN EXTREMITY (non-serious) all with onset Apr2021, outcome "unknown" and all described as "My right thumb is the worst, it's killing me. My right hand is worse than my left hand."; PAIN (non-serious) with onset Apr2021, outcome "unknown", described as "The pain is really bad"; CONDITION AGGRAVATED (non-serious) with onset Apr2021, outcome "unknown", described as "Due to the pain being really bad, she had to get up last night and put an ice pack but the pain got worse". Therapeutic measures were taken as a result of pain in extremity, pain in extremity, pain, condition aggravated. Additional Information: No additional vaccines administered on same date of the Pfizer suspect. No AE(s) require a visit to ER or MD office. If the patient was hospitalized, how many days was the hospital stay was not applicable. No prior vaccinations (within 4 weeks). No relevant tests. Caller state she had to stay at the facility after her Pfizer COVID Vaccines for each dose due to her allergies she was under observation. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy; Ankle arthroplasty (she had ankle replacement surgery and had stopped taking her Xeljanz XR a week before that surgery); Incision site infection (By this past Thursday, it's pretty much healed); Rheumatoid arthritis (She was diagnosed with Rheumatoid arthritis in 1991); Shoulder replacement (Had her right shoulder done twice); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2096663

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (OTHER) · Charge EW0162

moderat
Staat
OH
Alter
61,0
Geschlecht
F
Eingang
08.02.2022
Impfdatum
07.12.2021
Beginn
08.12.2021
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Feeding disorder Lymphadenopathy Migraine Myalgia Pain Toothache

Symptomtext

My two infected molars forwich I had been on antibiotics for several days and was in no pain with, began hurting me excruciatingly to the point that I could only eat with my front teeth for the next five days. I felt like I had swollen glands, migraines of my whole head that came and went, extreme upper torso soreness. My neck muscles were so sore and I was rubbing them all the time. I was in my pajamas for five days. On the 6th day I woke up pain free and able to eat anything I wanted. What a journey.. ihad had no problems with the vaccines.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes, high cholesterol, thyroid, high blood pressure,
Andere Medikamente
Losartin,naltraxone,levothyroxine,magnesium,folic acid,glimperiride,duloxetine,topiramite,quetiapine, vitamin d3,metformin,metoprolol,pravastatin,colestipol
Allergien
Lisinipil
Vorherige Impfungen
-

VAERS 2096264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
53,0
Geschlecht
F
Eingang
08.02.2022
Impfdatum
15.09.2021
Beginn
15.09.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dyspnoea Palpitations Pharyngeal swelling

Symptomtext

Throat swelled, Hard time breathing, Heart racing

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Sulfa, Vancomycin, Latex
Vorherige Impfungen
Flu Shot

VAERS 2087998

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CO
Alter
56,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
14.04.2021
Beginn
13.06.2021
Tage bis Beginn
60,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Asthenia Biopsy skin abnormal Blood immunoglobulin M increased Histology normal Limb discomfort Malaise Mobility decreased Neuropathy peripheral Paraesthesia

Symptomtext

Acute-onset weakness, pins and needles, tingling, nerve blankets, limb nausea in full body. Worsened from June to October 2021, symptoms improved a little from October to present. At present, full body paresthesia, worst in feet and legs. No treatment to date as potential diagnosis discovered a week ago. Outcome to date: post exertional malaise and feet condition means I cannot be as active as before onset.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
TS-HDS AUTOANTIBODY Resulted on 01/26/2022. Abnormal. IgM vs TS-HDS: 17,000. Normal Value: <10,000. SKIN BIOPSY REPORT Date Reported: 12/8/2021. Epidermal Nerve Fiber Analysis (PGP 9.5 stain): Abnormal intraepidermal nerve fiber density at all sites. This is consistent with a neuropathy affecting small nerve fibers. Sweat gland nerve fiber density was normal M.D. Board Certified in Neurology Skin Histology (H & E stain): Routine hematoxylin and eosin stained sections show no evidence of small vessel vasculitis or other histologic abnormalities. M.D. Board Certified in Dermatopathology
Aktuelle Erkrankungen
None
Vorgeschichte
Cardiac arrhythmia (PACs)
Andere Medikamente
Diltiazem 180 mg Flecainide 100 mg x2
Allergien
None known
Vorherige Impfungen
-

VAERS 2087538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
31,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
19.03.2021
Beginn
19.03.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Back pain Dysmenorrhoea Heavy menstrual bleeding Inappropriate schedule of product administration Migraine Polymenorrhoea

Symptomtext

same thing as before heavy bleeding/menstrual cycle changed to heavy flows after the vaccine; After my second dose, my menstrual cycle was two weeks earlier; horrible menstrual cramps; lower back pain; migraines; Dose number=1 Administration date=19Mar2021/ dose number: 2 vaccine date:19Mar2021; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 19Mar2021 (Lot number: EW0162) at the age of 31 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "mild back aches" (unspecified if ongoing), notes: This never happens with me usually its none to mild back aches.; "birth control" (unspecified if ongoing), notes: Although I was on birth control pill and I always get my period on time. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Product COVID 19, brand=Pfizer,, Lot number: EP7534,, Vaccine location=Left arm,, Dose number=1), administration date: 19Mar2021, when the patient was 31 years old, for COVID-19 immunisation, reaction(s): "my menstrual cycle was late two weeks", "had horrible cramps which never happens". The following information was reported: INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) with onset 19Mar2021, outcome "unknown", described as "Dose number=1 Administration date=19Mar2021/ dose number: 2 vaccine date:19Mar2021"; HEAVY MENSTRUAL BLEEDING (non-serious) with onset 27Mar2021, outcome "unknown", described as "same thing as before heavy bleeding/menstrual cycle changed to heavy flows after the vaccine"; POLYMENORRHOEA (non-serious) with onset 27Mar2021, outcome "unknown", described as "After my second dose, my menstrual cycle was two weeks earlier"; DYSMENORRHOEA (non-serious) with onset 27Mar2021, outcome "unknown", described as "horrible menstrual cramps"; BACK PAIN (non-serious) with onset 27Mar2021, outcome "unknown", described as "lower back pain"; MIGRAINE (non-serious) with onset 27Mar2021, outcome "unknown", described as "migraines". Therapeutic measures were not taken as a result of heavy menstrual bleeding, polymenorrhoea, dysmenorrhoea, back pain, migraine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Back ache (This never happens with me usually its none to mild back aches.); Birth control (Although I was on birth control pill and I always get my period on time)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2080347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NC
Alter
34,0
Geschlecht
F
Eingang
01.02.2022
Impfdatum
21.12.2021
Beginn
23.12.2021
Tage bis Beginn
2,0
Dosis
1
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dyspnoea Heart rate increased Palpitations

Symptomtext

I've noticed that my heart rate has been elevated since my booster shot given on 12/21. I experience breathlessness, heart palpitations, and high heart rate when completing normal, every day activities. My smart watch has noted that my heart rate has been trending higher for 7 weeks, starting 2 days after my booster shot. My resting heart rate has increased by 11 beats per minute.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
My smart watch has noted that my heart rate has been trending higher for 7 weeks, starting 2 days after my booster shot. My resting heart rate has increased by 11 beats per minute.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
ibuprofen, tylenol
Allergien
none
Vorherige Impfungen
-

VAERS 2075637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
68,0
Geschlecht
M
Eingang
31.01.2022
Impfdatum
30.03.2021
Beginn
27.01.2022
Tage bis Beginn
303,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cough Dyspnoea Wheezing

Symptomtext

Pt has increased cough and wheezing and called EMS due to worsening shortness of breath. Pt does have COPD and diabetes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1489808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

moderat
Staat
MI
Alter
59,0
Geschlecht
M
Eingang
27.01.2022
Impfdatum
08.04.2021
Beginn
11.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: unbekannt
Acoustic stimulation tests Antibody test negative Anxiety Blood pressure increased Blood test normal Blindness Feeling abnormal Headache Hypertension Botulinum toxin injection Computerised tomogram head normal Deafness Decreased activity Depersonalisation/derealisation disorder Depression Diarrhoea Disability Ear, nose and throat examination

Symptomtext

Severe Vertigo three days after 2nd vaccination requiring hospitalization. High blood pressure (180/110)and headaches two weeks after. Massive headaches requiring hospitalization May 30, 2021. Visits to ENT, Neurologist, Allergist, and Primary care Physician for several weeks following. Additional symptoms, increasing blood pressure, headaches, insomnia, sleep apnea, diareah for 2 months, tinnitus, hearing loss, extreme neck pain, extreme anxiety, and depression. Treatments over the following three months included CPAP therapy, blood pressure medication, hearing tests, depression medication, anxiety medication, Migraine medication, Botox shots for neck pain which also helped with headaches, facett block.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
2,0
Labordaten
ECG, EEG, CT Head Scan, Blood Tests of all forms, antibody tests, genetic testing, Ultrasound, Urinalysis, sleep test, and sinus scope. All test results normal, healthy physically.
Aktuelle Erkrankungen
None
Vorgeschichte
Mild Athsma, Seasonal Allergies
Andere Medikamente
Trilogy, Flonase SEnsimist
Allergien
Walnuts
Vorherige Impfungen
-

VAERS 1489808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
59,0
Geschlecht
M
Eingang
27.01.2022
Impfdatum
08.04.2021
Beginn
11.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: unbekannt
Acoustic stimulation tests Antibody test negative Anxiety Blood pressure increased Blood test normal Blindness Feeling abnormal Headache Hypertension Botulinum toxin injection Computerised tomogram head normal Deafness Decreased activity Depersonalisation/derealisation disorder Depression Diarrhoea Disability Ear, nose and throat examination

Symptomtext

Severe Vertigo three days after 2nd vaccination requiring hospitalization. High blood pressure (180/110)and headaches two weeks after. Massive headaches requiring hospitalization May 30, 2021. Visits to ENT, Neurologist, Allergist, and Primary care Physician for several weeks following. Additional symptoms, increasing blood pressure, headaches, insomnia, sleep apnea, diareah for 2 months, tinnitus, hearing loss, extreme neck pain, extreme anxiety, and depression. Treatments over the following three months included CPAP therapy, blood pressure medication, hearing tests, depression medication, anxiety medication, Migraine medication, Botox shots for neck pain which also helped with headaches, facett block.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
2,0
Labordaten
ECG, EEG, CT Head Scan, Blood Tests of all forms, antibody tests, genetic testing, Ultrasound, Urinalysis, sleep test, and sinus scope. All test results normal, healthy physically.
Aktuelle Erkrankungen
None
Vorgeschichte
Mild Athsma, Seasonal Allergies
Andere Medikamente
Trilogy, Flonase SEnsimist
Allergien
Walnuts
Vorherige Impfungen
-

VAERS 2065436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
94,0
Geschlecht
M
Eingang
26.01.2022
Impfdatum
04.05.2021
Beginn
13.01.2022
Tage bis Beginn
254,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Atelectasis COVID-19 COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Hyperglycaemia Hypoglycaemia Hypoxia Lung opacity SARS-CoV-2 test positive Somnolence

Symptomtext

Hospitalized 01/13/2022; COVID-19 positive 01/13/2022; Fully vaccinated BRIEF OVERVIEW: Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 1/13/2022 Discharge Date: 01/25/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia due to COVID-19 virus COVID-19 HOSPITAL COURSE: Patient is a 94-year-old male who presented to the emergency department with shortness of breath. In the emergency department, patient was found to be hypoxemic on room air and required supplemental oxygen. Chest x-ray showed patchy mild right pulmonary opacities consistent with atelectasis and/or pneumonia. Patient was found to be positive for COVID-19. He was admitted to the Internal Medicine service and started on Decadron and remdesivir. Endocrinology was consulted for steroid induced hyperglycemia. Patient was started on an insulin drip and transitioned to BBI. He had some morning hypoglycemia, so this was adjusted to just corrective insulin. His oxygenation improved and remained stable. Physical & occupational therapy recommended subacute rehab, but the patient's daughter wanted to take him home. He was set up with the COVID at home program, but ultimately given continued somnolence, his advanced age, and illness, the patient's daughter asked to be set up with Hospice. Patient was discharged home with Hospice.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
12,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Acute bronchitis due to other specified organisms Pneumonia due to COVID-19 virus CAD (coronary artery disease) HTN (hypertension) Right bundle branch block Gastroesophageal reflux disease, esophagitis presence not specified Parainfluenza infection Dementia with behavioral disturbance Chronic renal insufficiency Benign prostatic hyperplasia, unspecified whether lower urinary tract symptoms present Dyslipidemia Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet acetaminophen (TYLENOL) 650 MG suppository aspirin 81 MG tablet bisacodyl (DULCOLAX) 10 MG suppository brimonidine (ALPHAGAN) 0.15 % ophthalmic solution dutasteride (AVODART) 0.5 MG capsule haloperidol
Allergien
Hydrocodone-acetaminophen Lexiscan (Edetic-Acid)
Vorherige Impfungen
-

VAERS 2043380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
56,0
Geschlecht
M
Eingang
18.01.2022
Impfdatum
22.04.2021
Beginn
21.12.2021
Tage bis Beginn
243,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Chest pain Cough Dizziness Headache Insomnia Nausea

Symptomtext

Chief Complaint: Cough and Chest Pain Source of Information: Patient and spouse at bedside History of Present Illness: This is a 57y.o. male with a history of asthma, COPD, HTN, psoriasis, chronic back pain, dyslipidemia, morbid obesity and OSA who presents to local-ED with chief complaint of SOB and chest pain. Patient states that these symptoms started 4 days ago. He admits to a non-productive cough and chest pain that is worse with coughing. He states his chest pain is left-sided and sometimes radiates to the right side of his chest. Patient admits to headaches, lightheadedness, generalized abdominal pain, mild nausea and a decrease in sleep for the past 4 days. Patient states that he has been taking Robitussin and DayQuil without relief. Patient is vaccinated against COVID, but has not received the booster. He states that he started vaping a few months ago, and that he takes ~5 hits daily. He also admits to drinking alcohol, approximately 2-3 shots of liquor per week, and occasional marijuana use. Denies fevers, chills, vomiting, diarrhea, constipation or lower extremity edema. ED course:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Chief Complaint: Cough and Chest Pain Source of Information: Patient and spouse at bedside History of Present Illness: This is a 57y.o. male with a history of asthma, COPD, HTN, psoriasis, chronic back pain, dyslipidemia, morbid obesity and OSA who presents to local-ED with chief complaint of SOB and chest pain. Patient states that these symptoms started 4 days ago. He admits to a non-productive cough and chest pain that is worse with coughing. He states his chest pain is left-sided and sometimes radiates to the right side of his chest. Patient admits to headaches, lightheadedness, generalized abdominal pain, mild nausea and a decrease in sleep for the past 4 days. Patient states that he has been taking Robitussin and DayQuil without relief. Patient is vaccinated against COVID, but has not received the booster. He states that he started vaping a few months ago, and that he takes ~5 hits daily. He also admits to drinking alcohol, approximately 2-3 shots of liquor per week, and occasional marijuana use. Denies fevers, chills, vomiting, diarrhea, constipation or lower extremity edema. ED course:
Aktuelle Erkrankungen
? Arthritis ? Asthma ? Chronic neck pain ? Dyslipidemia ? Hypertension ? Kidney stone ? Morbid obesity with BMI of 50.0-59.9, adult (CMS/HCC) ? Obstructive sleep apnea wears CPAP at home, machine broke, waiting ? Psoriasis ? Pyelonephritis
Vorgeschichte
? Arthritis ? Asthma ? Chronic neck pain ? Dyslipidemia ? Hypertension ? Kidney stone ? Morbid obesity with BMI of 50.0-59.9, adult (CMS/HCC) ? Obstructive sleep apnea wears CPAP at home, machine broke, waiting ? Psoriasis ? Pyelonephritis
Andere Medikamente
albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln inhale 2 Puffs into the lungs every 4 hours as needed for FOR SHORTNESS OF BREATH. (disp insurance-pref prod) Patient taking differently: inhale 2 Puffs into
Allergien
? Grass Other Sneezing and eyes water
Vorherige Impfungen
-

VAERS 2043254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
69,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
13.07.2021
Beginn
28.12.2021
Tage bis Beginn
168,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia COVID-19 Cough Hypertension Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

I had sore throat and running nose. Then, I my blood pressure was really high. Then, I had no energy and very weak. I had a lot of mucus and congestive. I had body aches as well. I was also coughing and sneezing. These symptoms are still ongoing since Dec 28th, so about 3 weeks now. On Dec 30th, I was tested positive for Covid-19. I went on Jan 12th for another Covid-19 test, negative results for that one. I do have an appointment on Jan 21th, to see my doctor about this.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
Covid-19 test
Aktuelle Erkrankungen
n/a
Vorgeschichte
HTN, type 2 diabetic, chronic back pains
Andere Medikamente
n/a
Allergien
blood pressure medicine, antibiotics
Vorherige Impfungen
flu

VAERS 2043200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
68,0
Geschlecht
M
Eingang
18.01.2022
Impfdatum
29.04.2021
Beginn
05.01.2022
Tage bis Beginn
251,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
COVID-19 Chest pain Dyspnoea SARS-CoV-2 test positive

Symptomtext

short of breath, chest pain

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
12,0
Labordaten
+ COVID test
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2037868

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
75,0
Geschlecht
F
Eingang
15.01.2022
Impfdatum
15.04.2021
Beginn
04.01.2022
Tage bis Beginn
264,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt
COVID-19 Pneumonia SARS-CoV-2 test positive

Symptomtext

pneumonia

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pneumonia
Hospital-Tage
11,0
Labordaten
+ COVID test
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2034906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
53,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
10.05.2021
Beginn
10.01.2022
Tage bis Beginn
245,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Chest X-ray normal Chills Computerised tomogram thorax abnormal Cough Dyspnoea Lung infiltration Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Covid19 breakthrough. 1st Vaccine received on 04/19/2021. 53 y/o PMH Asthma, COPD, Metastatic Breast Cancer/Left mastectomy, OSA, Diastolic HF, CAD, Pulm emboli presents to ED with 1 day history of c/o SOB, dry cough, sore throat, fevers, chills and generalized body aches. CXR negative. CT chest with multifocal patchy groundglass infiltrates RLL. Pt requiring O2 at 2L NC sats 94%. Treated with IV Steroids/IV ABX and Remdesivir.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
SARS CoV 2 PCR Covid19-Detected 01/10/2022
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma, Stage IV Metastatic Breast Cancer/Left mastectomy, COPD, OSA, Diastolic HF, CAD, Pulm emboli
Andere Medikamente
-
Allergien
No known allergies
Vorherige Impfungen
-

VAERS 2032288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
IL
Alter
43,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
20.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Tinnitus

Symptomtext

I have tinnitus already. After the second vaccine it became much worse. It is louder and very disruptive.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Migraines; sinusitis
Andere Medikamente
Magnesium; Melatonin; Omeprazole; Stool softner
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 2028520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
72,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
05.06.2021
Beginn
10.01.2022
Tage bis Beginn
219,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dyspnoea Influenza A virus test Influenza B virus test SARS-CoV-2 test

Symptomtext

shortness of breath

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen
-
Vorgeschichte
Arthritis ? Diabetes mellitus (CMS/HCC) ? End stage renal disease ? High cholesterol ? Hypertension ? Overactive bladder ? Post-operative nausea and vomiting ? SOB (shortness of breath) on exertion
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2025017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MN
Alter
96,0
Geschlecht
F
Eingang
11.01.2022
Impfdatum
29.04.2021
Beginn
05.01.2022
Tage bis Beginn
251,0
Dosis
1
Route/Site
SYR / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Asthenia COVID-19 COVID-19 pneumonia Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pfizer vaccines on 4/8/21, 4/29/21 COVID positive by PCR on 1/5/22. admit to hospital 1/5/22 d/t SOB, weakness; diagnosis of acute COVID-19 pneumonia, PE

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2021297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
68,0
Geschlecht
M
Eingang
10.01.2022
Impfdatum
07.05.2021
Beginn
08.01.2022
Tage bis Beginn
246,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cough Dyspnoea Hypoxia

Symptomtext

Cough, SOB, Hypoxia

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2014745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
29,0
Geschlecht
F
Eingang
07.01.2022
Impfdatum
18.04.2021
Beginn
26.12.2021
Tage bis Beginn
252,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
COVID-19 Cough Dyspnoea Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

congestion, cough, short of breath + COVID test

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2014071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
44,0
Geschlecht
M
Eingang
07.01.2022
Impfdatum
14.07.2021
Beginn
21.12.2021
Tage bis Beginn
160,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Cough Palpitations Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

congestion, cough, palpitations + COVID test

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2010495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
72,0
Geschlecht
F
Eingang
06.01.2022
Impfdatum
20.05.2021
Beginn
08.11.2021
Tage bis Beginn
172,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 COVID-19 pneumonia Cough Fibrin D dimer increased Nausea Pain SARS-CoV-2 test positive

Symptomtext

COVID 19 virus positive on 11/8/2021. She was having cough, nonproductive with generalized body aches, some nausea, no vomiting, no abdominal discomfort. D-dimer 1,564, This patient was admitted because of COVID-19 pneumonia. The patient was fluctuating between 4 and 3 L nasal cannula. The patient is known to have oxygen at home at 4 L. The patient has been on decadron IV every 24 hours. Discharged to home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
9,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2002927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
74,0
Geschlecht
M
Eingang
04.01.2022
Impfdatum
07.04.2021
Beginn
25.12.2021
Tage bis Beginn
262,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Anticoagulant therapy Atelectasis Blood creatinine normal Blood potassium normal Brain natriuretic peptide decreased C-reactive protein normal COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Chest discomfort Chronic left ventricular failure Condition aggravated Cough Decreased appetite Dyslipidaemia Dyspnoea

Symptomtext

Hospitalized (12.25.21); COVID-19 positive (12.25.21); fully vaccinated Admission Date: 12/25/2021 Discharge Date: Dec 28, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Shortness of breath [R06.02] Acute on chronic congestive heart failure, unspecified heart failure type (HCC) [I50.9] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient is a 74 yo man who was admitted to Hospital 12/25/21 with chest heaviness, increasing chronic LE edema, shortness of breath and orthopnea, all progressively worse over 3 weeks. Symptoms were severe enough over the 10 days PTA to affect his quality of life whereby he felt he would be better off dead. He had been vaccinated against Covid x2 with booster due several weeks prior but felt unwell so did not get this. He has chronic systolic heart failure, ICM EF 25% with ICD. He has a remarkable deranged lipid management concern (hyperlipidemia/dyslipidemia) that had led to CAD w/ 5v CABG 2009, PAD w/ left LE stent, renal artery stenosis w/ bilateral stents 2012, left subclavian artery stenosis and bilateral carotid artery occlusions. Additionally, he carries dx of hypertension, pulmonary hypertension, hx of lung cancer w/ left lower lobectomy 2018, hx of 15 pack year tobacco with COPD not on oxygen (may use tiotropium INH but this was not clarified), and BPH. ER staff gave him a dose of Lasix with impressive volume out and immediate improvement if not resolution of his chest heaviness and shortness of breath. An acute exacerbation of chronic systolic heart failure was diagnosed. His renal function was excellent w/ creatinine 0.7, eGFR >60, with Lasix continued and chronic edema of bilateral lower extremities improved over his brief stay whereby they were smaller than they had been in a long time per his report. BNP was 22K but CXR was without clear support for either vascular congestion nor Covid PNA, former not an uncommon finding attributed to lymphatic management of excess fluid, despite respiratory symptom and chronic 3rd spacing. BNP decreased to 11K by discharge. Cardiology helped guide his care. Echo revealed ejection fraction 25%, lower by 10% from prior review. Valsartan was stopped and Entresto started. He discharged with a script sent to the pharmacy at hospital, informed the 1st month would be free. This was done after he questioned if a delay in picking up scripts at his preferred pharmacy, for 2-3 days would be OK. Advised it was not so for convenience, a 30 day supply of all his meds were sent to the pharmacy including furosemide 20 daily (new) and potassium chloride 20 daily (new, due to a consistent potassium level of 3.5 while here) with emphasis on his picking these up before his wife collected him at the door. In an attempt to avoid his ever being out of med, refills of all 3 meds were e-scribed to his preferred pharmacy. Coreg was continued without change. He understood not to continue valsartan, that this was a component of his new Entresto. Heart failure recommendations and rule of 2s was placed in his chart by his Cardiology team. Standing weights at admission and discharge were 73.3 (accuracy of a first measure from a bed scale, 78.3, was in question and the first standing wt was likely collected after his first dose Lasix) and 72.3 respectively. Troponins slightly elevated but flat; 57, 55 so ACS was not considered a diagnosis on presentation, rather, was thought to be a reflection of myocardial injury related to CHF and Covid infection. Additional symptoms since 12/17/21 included fatigue, mild cough and poor appetite. His wife tested positive for Covid several weeks prior. Our patient tested negative for Covid 12/16/21, likely around the same time his wife tested positive. He was positive on admission 12/25/21 but symptoms were subtle, distinguished from shortness of breath, chest heaviness and orthopnea rapidly relieved with Lasix, helped make the distinction between these concurrent conditions. Chest x-ray revealed some atelectasis and/or airspace disease at his right lung base. D-dimer was consistently and significantly elevated, 4K-5K. Doppler ultrasound lower extremity was negative for VTE. He never required oxygen nor had fever, tachycardia, nor chest pain to suggest PE. CRP was <3 further supporting lack of evidence for robust inflammatory response related to a Covid infection. Lovenox 40 SQ daily was administered throughout his stay. He had no indication for Decadron or remdesivir given no O2 in use, and he was not a monoclonal antibody candidate given sx onset was >7 days PTA. Medications at discharge: ASA 81 d Atorvastatin 80 d Coreg 12.5 BID Imdur 60 BID Entresto 24-26 BID (new) Lasix 20 d (new) KCl 20 d (new) Flomax Tiotropium INH (unclear if in use regularly) Cardiology arranged a BMP 1/3/22 A 2 gm sodium restricted diet was instituted but curiously, no a 2 liter fluid restriction. He enjoys potato chips when home but eats only a few at a time. Fluid restriction of 2L daily was advised at discharge. He was full code He discharged home 12/28/21 feeling much better that at presentation, in good condition, but he understands his heart is not well and the gravity of such a diagnosis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
3,0
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
Peripheral vascular disease with claudication s/p lower ext stent Benign prostatic hyperplasia with urinary obstruction Coronary artery disease (Cabg x 5 in 2009) Hypercholesterolemia Acute on chronic systolic heart failure (HCC) Stenosis of carotid artery Emphysema (HCC) Biventricular ICD (implantable cardioverter-defibrillator) in place Chronic osteoarthritis Benign essential HTN Renal artery stenosis (HCC) History of smoking greater than 50 pack years Chronic hyponatremia Anemia, unspecified type Personal history of other malignant neoplasm of bronchus and lung Shortness of breath
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet aspirin 81 MG tablet atorvastatin (LIPITOR) 80 MG tablet carvedilol (COREG) 12.5 MG tablet docusate (COLACE) 100 MG capsule furosemide (LASIX) 20 MG tablet isosorbide mononitrate CR (IMDUR) 60 MG 24 hr
Allergien
Chantix [Varenicline]Hallucinations LisinoprilCough
Vorherige Impfungen
-

VAERS 1995806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NJ
Alter
63,0
Geschlecht
F
Eingang
31.12.2021
Impfdatum
17.04.2021
Beginn
29.12.2021
Tage bis Beginn
256,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Admitted with increased shortness of breath and coughing

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
3,0
Labordaten
12/29/2021 - SARS-CoV-2 Antigen (++)
Aktuelle Erkrankungen
-
Vorgeschichte
Breast cancer, CAD, dyslipidemia, HTN
Andere Medikamente
amlodipine 10 mg po daily anastrozole 1 mg po daily atorvastatin 40 mg po daily metoprolol 50 mg XL po daily clopidogrel 75 mg po daily
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1988712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
65,0
Geschlecht
M
Eingang
29.12.2021
Impfdatum
20.04.2021
Beginn
11.08.2021
Tage bis Beginn
113,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 pneumonia Sepsis

Symptomtext

Patient admitted to hospital with severe sepsis secondary to COVID-19 associated pneumonia.He was started on IV antibiotics,IV steroids and remdesivir.His condition gradually improved.He is weaned down to 3 L oxygen by nasal cannula and has been stable at this level.He will be discharged home today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
15,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1981833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
58,0
Geschlecht
F
Eingang
27.12.2021
Impfdatum
01.12.2021
Beginn
03.12.2021
Tage bis Beginn
2,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Heart rate increased Heart rate irregular Injection site erythema Injection site pain Injection site rash Injection site swelling Ocular discomfort Paraesthesia Rash erythematous Rash pruritic Swelling Urticaria

Symptomtext

Booster - Painful, red spot appeared two days after vaccine. Lasted a week. Then turned into a red, itchy rash with welts and swelling and prickly. Continued to spread for a week over upper left arm, shoulder, collar bone, down chest, other areas popped out such as middle and side of left torso, left wrist, left shoulder blade and under arm pit. Topical treatment of cortisone and benedry didn't help. Doctor prescribed Prednisone 20 mg/day for 7 days. Greatly improved the situation. 2nd Vaccine - Vascular issues developed about a month after vaccine and continued for several months which included rapid heart rate, irregular beats, busted eye vessels, swollen in vein in calf.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Autoimmune - connective tissue
Andere Medikamente
Plaquenil, baby aspirin, multi-vitamin, imodium
Allergien
Penicillin, sulfa, macrobid, cipro
Vorherige Impfungen
-

VAERS 1981689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
45,0
Geschlecht
F
Eingang
27.12.2021
Impfdatum
10.12.2021
Beginn
10.12.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Chest discomfort Condition aggravated Dyspnoea Fatigue Feeling cold Headache Hypoaesthesia Lymphadenopathy Paraesthesia Paraesthesia oral Pruritus Swollen tongue Upper respiratory tract infection Vaccine positive rechallenge

Symptomtext

Patient reported difficulty breathing, numbness / tingling; tongue swelling and itchy neck following vaccination. Reported to have occurred within 5 to 10 minutes after 12.10.2021 dose. Reported with prior doses as well. Patient's words / communication to Allergist: "I received my 3rd vaccine on Friday and I had another reaction to it. As before, I received the Pfizer vaccine and this time between 5-10 minutes after receiving the shot my tongue and lips started tingling then my tongue started swelling. I had taken benadryl right after I got the shot. But basically my symptoms matched what I reported to you when I saw you and when I messaged you after 2nd shot but with the added tongue swelling and lips tingling. So it appears that my reaction to the Pfizer shot is worsening." Allergists response: "In my experience, patients have similar symptoms with both the Pfizer and Moderna vaccines. Due to the risk of thrombosis, I do not recommend the Johnson and Johnson vaccine for someone your age. In the future, I would recommend taking Benadryl before you get the vaccine. We could also consider adding Singulair (prescription) which can sometimes help. Please contact me before your next dose and I will prescribe this." Patient description of concern with 2nd dose: received the shot at 1:19pm At 1:30 the arm where I got the injection felt tingly and weirdly cool. Like there was an ice cube or an icicle along my arm. 1:35 the finger in my hands started tingling -- note: at 1:46 the finger tingling started to feel itchy under my finger nails like under the nail itself and not the ends of the fingers but on the pink above the moon. 1:43 my toes started tingling. 1:45pm I started feeling chest tightness - it was fairly mild -- enough that I noticed it but not so bad that I was worried. Less tight than before, JSYK. 1:55pm I took 2 benadryl after talking with the RN and EMTs at the vaccine administration site. 2:02pm My tongue started to tingle and swelled slightly 2:19 pm My jaw and nose started to itch. 3:19pm All of the reactions subsided 3:30pm Benadryl sleepiness overwhelmed me and I slept for about 6 hours until 9:30pm. When I woke, all was back to normal. Or at least my version of normal ^_^ Per the watch I wear which has a heart rate monitor, my heart rate was 85 BPM after the vaccine which is a slightly higher resting heartrate than normal Per the app it's between 69-73bpm. But it wasn't enough to concern me. I'm getting all of the fatigue, swollen lymph nodes, headache, and achy joints as before. As a note: this is one of my allergy seasons. I am allergic to tree pollen. And well *gestures at the trees*. So it is possible that my immune system is just annoyed at life in general. I did go down with a chest/upper respiratory infection on Tuesday, but that's not unexpected. I get this about 3 times a year because of my allergies.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
12.2.21 - US head / neck: IMPRESSION: 1. There are 3 indeterminate thyroid nodules that meet criteria for biopsy. 2. The first nodule meeting criteria for biopsy is on the right thyroid lobe and is best seen on images 9-11. The second nodule meeting criteria for biopsy is on the right thyroid lobe and is best seen on images 12-13. The third nodule meeting criteria for biopsy is on the left thyroid lobe and is best seen on images 22-24. Fine-needle aspiration biopsy of these 3 nodules is advised to exclude malignancy. 3. Enlarged heterogeneous hyperemic thyroid gland. In the setting of normal TSH and elevated thyroid antibodies is is suspicious for Hashimoto's thyroiditis. Please correlate clinically. The orange significant findings protocol was initiated at 12/3/2021 2:24 PM. The presence of a significant findings result is to be communicated with a clinician and/or clinical staff by support staff.
Vorgeschichte
Heavy menstrual bleeding Borderline personality disorder (HCC) GAD (generalized anxiety disorder) PTSD (post-traumatic stress disorder) Multiple environmental allergies Multiple drug allergies Obesity Vertigo Mild intermittent asthma without complication Multiple thyroid nodules PCOS (polycystic ovarian syndrome) Intractable migraine with aura without status migrainosus
Andere Medikamente
albuterol (VENTOLIN) 108 (90 BASE) MCG/ACT inhaler B Complex Vitamins (VITAMIN B COMPLEX) tablet Cholecalciferol (VITAMIN D3) 2000 UNITS TABS DiphenhydrAMINE HCl (BENADRYL PO) Drospirenone 4 MG TABS EPINEPHrine 0.3 MG/0.3ML auto-injector ga
Allergien
CatsAsthma/Shortness of Breath, Cough, Itching, Shortness of Breath, Skin Rashes/Hives, Sneezing, Throat swelling DustAsthma/Shortness of Breath, Cough, Headache, Itching, Sneezing, Swelling PollenItching, Shortness of Breath, Sneezing Red DyeDermatitis, Itching, Rash, Shortness of Breath, Swelling ScallopsAnaphylaxis, Anxiety, Asthma/Shortness of Breath, Itching, Palpitations, Shortness of Breath, Swelling, Throat swelling Adhesive TapeDermatitis, Itching, Rash, Swelling Amoxicillin Artificial SweetenersDiarrhea, Nausea and Vomiting Contrast Dye [Ivp Dye, Iodine Containing] CopperDermatitis, Itching, Rash, Skin Rashes/Hives Covid-19 (Mrna) Vaccine (Pfizer)Itching Diamox [Acetazolamide] IsotretinoinNausea and Vomiting Latex NickelDermatitis, Itching, Rash, Skin Rashes/Hives, Swelling Other Saccharin Sulfa Drugs TetracyclineNausea and Vomiting
Vorherige Impfungen
Reported the same reactions with 1st, 2nd, and booster of COVID Pfizer vaccine. See dates above.

VAERS 1981267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NH
Alter
55,0
Geschlecht
F
Eingang
26.12.2021
Impfdatum
14.12.2021
Beginn
14.12.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Acoustic stimulation tests abnormal Condition aggravated Erythema Pruritus Tinnitus Urticaria Vaccination complication

Symptomtext

Shot 2 Tinnitus - has not gone away but has lessened Shot 3 - Covid Arm (welt, red, itchy, 1 week) and Tinnitus - got worse again

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
hearing test for the tinnitus
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
HRT
Allergien
Codeine
Vorherige Impfungen
-

VAERS 1963152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
PA
Alter
56,0
Geschlecht
M
Eingang
20.12.2021
Impfdatum
12.12.2021
Beginn
13.12.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Dizziness Headache Hypoaesthesia Muscle spasms Pain Paraesthesia Trismus

Symptomtext

Minor Aches and Chills, Headache developed approx. 16 hours after booster shot. At approx. the 22 hour mark, I experienced severe lightheadedness followed by numbness and tingling in both arms and legs, along with cramping in both hands, both calves and jaw. Symptoms lasted approx. 30 minutes. I was completely symptom free in a few hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
I did not seek medical attention
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Simvastatin, Lisinopril/HTZ, OTC Multivitamin
Allergien
None
Vorherige Impfungen
-

VAERS 1961836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NV
Alter
52,0
Geschlecht
M
Eingang
18.12.2021
Impfdatum
10.04.2021
Beginn
10.05.2021
Tage bis Beginn
30,0
Dosis
2
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Atrial fibrillation Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Palpitations Specialist consultation Ventricular tachycardia

Symptomtext

Heart Palpitations were going on starting the second week of May then I went to the cardiologist in July that gave me a Holter Monitor that came back with atrial flutter and Non-sustained ventricular tachycardia. I was given an echocardiogram and EKG. Now symptoms are only present when heartbeat is elevated during exercise or excitement, however, it is not during the normal day to day activities.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
EKG and Echocardiogram and Holter Monitor that showed atrial flutter and Non-sustained ventricular tachycardia.
Aktuelle Erkrankungen
N/A
Vorgeschichte
Mild Asthma and Grave's Disease for 20 years, Celiac disease.
Andere Medikamente
Iron Supplement 65MG, Methimazole
Allergien
Dizzy spells from Ibuprofen
Vorherige Impfungen
-

VAERS 1959035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
59,0
Geschlecht
M
Eingang
17.12.2021
Impfdatum
22.04.2021
Beginn
17.12.2021
Tage bis Beginn
239,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chills Cough Dyspnoea

Symptomtext

presents to hospital EC with SOB, cough and chills; has underlying hx of COPD

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1955630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
55,0
Geschlecht
M
Eingang
16.12.2021
Impfdatum
07.04.2021
Beginn
14.12.2021
Tage bis Beginn
251,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Acute kidney injury Bladder catheterisation Blood creatinine increased Blood urine present COVID-19 Chills Computerised tomogram abdomen abnormal Computerised tomogram head normal Condition aggravated Dehydration Diarrhoea Full blood count Glomerular filtration rate decreased Haemoglobin decreased Hypophagia Migraine Myalgia

Symptomtext

Currently admitted at (2) inpatient admission . H & P: Patient is a 55 y.o. male with a history of liver cirrhosis due to hep C status post treatment, Crohn's disease status post colostomy, substance abuse in remission on Suboxone, depression with anxiety, and migraines who presents to the ER with 4-5 day history of inability to urinate, as well as fevers, chills, myalgias, he T. patient was vaccinated against COVID-19 with 2 doses of Pfizer vaccine in April this year. He lives at home with his elderly mother and great niece who have had upper respiratory symptoms for the past few days as well. Patient denies prior history of urinary retention or enlarged prostate. He denies flank pain, urinary incontinence, hematuria, dysuria. He has been trying to hydrate at home, drinking 5 bottles of water every day. He has been compliant with his other medications including Bumex. He has noticed increased loose stools from his ostomy despite his normal regimen of fiber and Imodium. Patient has had very poor oral intake due to worsening nausea with intermittent vomiting. Patient endorses 25 lb weight loss since May of this year. Currently, patient complains of severe migraine headache with nausea and photosensitivity. He typically takes Imitrex at home for code of therapy but has not yet taken that today. In the ER, patient was febrile 101.5 F, not tachycardic, or tachypneic. Blood pressure soft 99/57. O2 sat 92% on room air. Patient tested positive for COVID-19 and received monoclonal antibodies. Patient had significant body aches and received Robaxin, Haldol, and dilaudid IV. Nausea not improved with Zofran. He received 2 L IV hydration. Labs showed AKI with creatinine 1.69, GFR 44 down from baseline creatinine 1.0. Complete blood count with acute on chronic pancytopenia, WBC 3.3, hemoglobin 11.9. Platelets 21000. Foley catheter was placed with 450 mL out. Urinalysis showed trace ketones, trace blood, hyaline casts, but no signs of infection. CT abdomen and pelvis with IV contrast redemonstrated known cirrhosis, splenomegaly, varices, but no urinary abnormality, hydronephrosis, or obstruction. The patient complained of ongoing migraine headache, and did not feel comfortable discharging home with AKI and urinary retention. The patient was placed in observation with Internal Medicine for further evaluation and treatment. ASSESSMENT / PLAN: AKI Dehydration 2/2 poor oral intake and diarrhea on diuretic Urinary retention, ?BOO Unable to void x 4-5 days, output 450 ml with foley placement in ED Cr 1.62, up from baseline 1.0 CT AP w/contrast showed known cirrhosis, splenomegaly and varices. No urinary abnormality/obstruction. UA showed trace ketones, trace blood, hyaline casts, no concern for infection - avoid nephrotoxins, renally dose meds - received 2L IV fluid, continue 100 ml/hr overnight - continue foley for now - Urology consulted - trend renal function COVID-19 infection Previously vaccinated x2 doses Pfizer in April 2021 Onset symptoms: 12/10 Positive test: 12/14 Monoclonal antibodies: 12/14 - not hypoxic, monitor closely - supportive care with anti-pyretics, anti-emetics, anti-tussives, anti-diarrheal, and analgesics Migraine headache Give imitrex (50 mg now) Pt does not want migraine cocktail "that has made it worse before" Liver cirrhosis 2/2 hepatitis C (s/p Harvoni) Hx ascites, esophageal varices, hepatic encephalopathy Follows with U of M hepatology, no current plans for liver transplant Continue home xifaxin, nadolol, PPI Hold home bumex in AKI Pancytopenia, chronic Evaluated by hematology in the past, bone marrow biopsy, attributed to cirrhosis Trend Hx crohn's disease s/p iliectomy with colostomy formation Surgery at facility, several subsequent intestinal blockages s/p surgery Monitor bowel function Hx opioid abuse/dependence in remission Continue home suboxone Depression with anxiety Insomnia Continue home xanax nightly and seroquel Unintentional weight loss Down > 25lbs since May this year Nutrition consulted Diet: general with 2g Na restriction VTE ppx: lovenox subq (HIGH risk in COVID) Code status: FULL, per discussion with patient on admission Patient care was reviewed with Dr. whose input is reflected above. Disposition: placed in observation for urology eval of urinary retention and also monitoring of dehydration in COVID infection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
2,0
Labordaten
CT HEAD WITHOUT IV CONTRAST Resulted: 12/15/21 1315 Order Status: Completed Updated: 12/15/21 1317 Narrative: EXAMINATION: CT Head without Contrast EXAM DATE: 12/15/2021 12:21 PM TECHNIQUE: Multiple axial noncontrast images of the brain were obtained and reformatted according to the standard protocol. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Headache, classic migraine, r/o bleeding, plts 11 COMPARISON: None HAND DOMINANCE: Unknown ENCOUNTER: Not applicable ____________________ FINDINGS: Intracranial hemorrhage: None. Infarct/Vascular: No CT evidence of acute infarct. Intracranial Mass: No evidence of intracranial mass. CSF Spaces: The ventricles, sulci, and cisterns are normal. Calvarium and Scalp: Unremarkable. Paranasal Sinuses and Orbits: Visualized paranasal sinuses show mild mucosal thickening at the left sphenoid sinus and minimal mucosal thickening within the bilateral maxillary sinuses. Orbits are unremarkable. ____________________ Impression: 1. No acute intracranial abnormality. CT ABDOMEN AND PELVIS WITH IV CONTRAST Resulted: 12/14/21 1444 Order Status: Completed Updated: 12/14/21 1447 Narrative: EXAMINATION: CT Abdomen and Pelvis with IV Contrast EXAM DATE: 12/14/2021 1:28 PM TECHNIQUE: CT imaging of the abdomen and pelvis was performed with intravenous contrast. Coronal and sagittal images were reconstructed. CONTRAST: The amount and type of contrast are recorded in the medical record. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Abdominal pain, acute, nonlocalized COMPARISON: 10/8/2020 ENCOUNTER: Not applicable ____________________ FINDINGS: Lung Bases: Included extent of the lung bases are clear. Hepatobiliary: The liver is small with a nodular surface. The portal veins are patent. The gallbladder is absent. There is no biliary dilatation. Pancreas: The pancreas is normal. Spleen: The spleen is markedly enlarged. There are no splenic lesions. Adrenals: The adrenal glands are normal. Kidneys, Ureters, & Bladder: Both kidneys have a normal size and there is no hydronephrosis. Both ureters have a normal caliber. The urinary bladder is unremarkable. Gastrointestinal: The stomach and small bowel are normal with no obstruction or inflammation. Small bowel resection has been performed with loop ileostomy in the right lower quadrant. The appendix is normal. The large bowel is normal. Reproductive Organs: The uterus is absent. Lymphatic System: There is no lymph node enlargement within the abdomen or pelvis. Vasculature: Normal caliber abdominal aorta. There is a mesenteric and perigastric varices. Peritoneum: No free fluid, free air, or inflammation. Abdominal Wall & Musculoskeletal: No significant abnormality. ____________________ Impression: 1. No acute inflammatory process in the abdomen or pelvis. 2. Hepatic cirrhosis with marked splenomegaly and varices. Collected: 12/14/21 1244 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/14/21 1332 COVID-19 PCR Detected
Aktuelle Erkrankungen
-
Vorgeschichte
Hospital Migraine, unspecified, without mention of intractable migraine without mention of status migrainosus Dehydration Counseling regarding advanced care planning and goals of care Multiple comorbid conditions AKI (acute kidney injury) COVID-19 virus infection Hypotension Non-Hospital Cirrhosis of liver due to hepatitis C Tobacco use Chronic migraine Esophageal varices determined by endoscopy Mental health disorder Opioid use disorder, severe, dependence Personality disorder Anxiety Splenomegaly Abnormal EKG Crohn's disease of small intestine with intestinal obstruction Pancytopenia Secondary biliary cirrhosis Psychophysiological insomnia Healthcare maintenance Hypokalemia Lumbar back pain Weight loss, unintentional Change in stool Ileostomy care Former smoker Skin lump of leg, left Urinary retention
Andere Medikamente
albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.25 MG tablet ALPRAZolam (XANAX) 1 MG tablet bumetanide (BUMEX) 1 MG tablet buprenorphine (SUBUTEX) 2 MG SUBL Calcium Carb-Cholecalcif
Allergien
PollenHeadache Shellfish AllergyDiarrhea Buprenorphine-naloxoneHeadache Ileostomy Restricted Foods Midazolam Nsaids
Vorherige Impfungen
-

VAERS 1947834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
WI
Alter
27,0
Geschlecht
M
Eingang
14.12.2021
Impfdatum
28.04.2021
Beginn
07.12.2021
Tage bis Beginn
223,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Cough Dyspnoea Fatigue Hypophagia Malaise SARS-CoV-2 test positive

Symptomtext

Patient presents to ER with 6 days of feeling ill, and tested positive for COVID 12/1. Admitted on 12/08/21. Primarily has fatigue, nonproductive cough, mild sob; decreased oral intake. Patient has past medical history of end-stage renal disease due to medullary cystic disease (interstitial nephritis suggestive of nephrononopthisis and FSGS on June 2020 biopsy) status post kidney transplant December 2020.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
acetaminophen, acyclovir, calcium-cholecalciferol, mycophenolate sodium, predniSONE, sulfamethoxazole-trimethoprim , tacrolimus
Allergien
-
Vorherige Impfungen
-

VAERS 1944253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
59,0
Geschlecht
F
Eingang
13.12.2021
Impfdatum
12.04.2021
Beginn
29.11.2021
Tage bis Beginn
231,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Chills Cough Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

11/29/21 presents to EC ED for "shortness of breath, chills, fatigue, and cough". PMHx of "coronary artery disease, asthma, COPD, diabetes mellitus type 2, GERD, hypercholesterolemia, hypertension, morbid obesity, OSA, TIA, lumbar radiculopathy".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
11/30/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1944076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
60,0
Geschlecht
F
Eingang
13.12.2021
Impfdatum
23.04.2021
Beginn
26.11.2021
Tage bis Beginn
217,0
Dosis
2
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Condition aggravated Cough Decreased appetite Dyspnoea Exposure to SARS-CoV-2 Fatigue Headache Influenza A virus test negative Influenza B virus test Influenza virus test negative Loss of personal independence in daily activities Nausea Neuralgia Productive cough SARS-CoV-2 test positive Wheezing

Symptomtext

This is a 61y.o. female with PMH significant for RA and emphysema with home O2 use at 2LNC presents to ED with c/o coronavirus concern. Pt has been feeling fatigued with progressive worsening x 7 days. Pt states she is unable to complete her ADLs without feeling SOB and tired which is not normal for her. Associated symptoms include cough with scant clear sputum production, wheezing, decreased appetite, and nausea without vomiting. Pt has been exposed to coronavirus recently via family members. Pt is vaccinated against coronavirus x 2 in April 2021 with pfizer vaccine. Pt notes chronic headache and neuropathy pain from shingles outbreak from 2 years ago. Pt denies fever, chills, sinus pressure, rhinorrhea, purulent sputum, abdominal pain, diarrhea, constipation or dysuria.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
5,0
Labordaten
Contains abnormal data SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC Order: 1270192130 Status: Final result Visible to patient: Yes (not seen) Next appt: None 0 Result Notes Ref Range & Units 11 d ago FLU A Not Detected Not Detected FLU B Not Detected Not Detected SARS Not Detected Detected Abnormal Performed By MD Specimen Collected: 12/02/21 9:32 PM Last Resulted: 12/02/21 9:52 PM
Aktuelle Erkrankungen
Emphysema of lung (CMS/HCC) ? Rheumatoid arthritis (CMS/HCC)
Vorgeschichte
Emphysema of lung (CMS/HCC) ? Rheumatoid arthritis (CMS/HCC)
Andere Medikamente
albuterol (2.5 MG/3ML) 0.083% INHAL Nebu Soln inhale 2.5 mg using breathing machine every 6 hours as needed. Past Week Unknown time albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln inhale 4 Puffs into the lu
Allergien
Iodinated Diagnostic Agents Fainting/Syncope
Vorherige Impfungen
-

VAERS 1943933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0162

moderat
Staat
MI
Alter
75,0
Geschlecht
M
Eingang
13.12.2021
Impfdatum
20.04.2021
Beginn
12.12.2021
Tage bis Beginn
236,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

Covid + SOB

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
2,0
Labordaten
Abbott rapid test
Aktuelle Erkrankungen
unknown
Vorgeschichte
Diabetes type 2, hypertension, hypothyroidism bipolar, and schizophrenia
Andere Medikamente
unknown
Allergien
seroquel
Vorherige Impfungen
-

VAERS 1942112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
41,0
Geschlecht
F
Eingang
11.12.2021
Impfdatum
09.04.2021
Beginn
10.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Ageusia Anosmia Condition aggravated Lymphadenopathy

Symptomtext

patient reported that she lost sense of smell and taste with each vaccine, temporarily. She also reports swollen lymph nodes under each arm that continues with no relief.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
patient does not do anything to assist with side effects. Not majorly concerned, but felt it should be reported. No lab tests have been done for this situation.
Aktuelle Erkrankungen
Patient had covid-19 in November of 2020 and lost taste/smell. This side effect occurred with the vaccines both time.
Vorgeschichte
allergies
Andere Medikamente
Vitamin D (OTC)
Allergien
NKDA
Vorherige Impfungen
only with the pfizer vaccines

VAERS 1938964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
64,0
Geschlecht
F
Eingang
10.12.2021
Impfdatum
07.04.2021
Beginn
07.12.2021
Tage bis Beginn
244,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Abdominal lymphadenopathy Adrenal mass Angiogram abnormal Aortic stenosis Ascites Asthenia Atrial fibrillation Blood albumin decreased Blood creatinine increased Blood urea increased Chills Computerised tomogram abdomen abnormal Condition aggravated Cough Decreased appetite COVID-19 Calculus urinary Cardiomegaly

Symptomtext

12/7/2021 - present (3 days) inpatient admission HISTORY OF PRESENT ILLNESS: a 65 y.o. female with a PMH of venous insufficiency , chronic kidney disease, psoriasis on Humira, OSA with nightly BiPAP dependence, mild MR, mild AS, hypertension, anxiety and chronic anemia who presents today with weakness, fatigue, cough, anorexia, headaches and dizziness. The patient has known exposures to people with COVID-19. She received both Pfizer vaccines, last 07/14/2021. She has not had a chance to get her booster shot as of yet. She states that prior to Thanksgiving her sister was hospitalized with COVID-19 and she had been in contact with her. She states that on Thanksgiving she stayed home because she did not feel well. She has had sweats, chills, generalized malaise, altered taste and smell in addition to the above initial complaints. She denies any chest pain. She has noticed increased swelling in her lower extremities. She did not take any of her home medications prior to arriving today. In the ER, the patient was tachycardic with a pulse of 106, mildly febrile with a temperature of 37.9? C. Tachypnea with a respiratory rate of 33. The patient was not hypoxic on ambient air. Labs significant for BUN 23, creatinine 1.28, albumin 2.3, lipase 88, NT proBNP 2855, WBC 12.33, hemoglobin 7.2. COVID-19 PCR was positive. CXR with mild cardiomegaly with pulmonary vascular congestion. FOBT obtained in the ER was heme positive. The patient received 1 g of Tylenol, 1 L of IV fluids and 20 mg of IV Lasix. The patient will be admitted for further evaluation and treatment. ASSESSMENT / PLAN: Acute on chronic blood loss anemia Gross hematuria -Suspect urinary source given patient report of gross hematuria - history of recent right lithotripsy on 10/21. Has a history of post lithotripsy hematoma during a past lithotripsy. -Trend hemoglobin Q 8 hours, transfuse for Hgb <7. Pt signed blood consent in ER. Given to ER secretary. The consent will be tubed to the floor for scanning once she arrives. -Consult Urology. Have asked RN to straight cath for urinalysis as patient is incontinent. -FOBT was positive in ER, however tarry or red stool not noted. Patient reports no rectal bleeding or tarry stool. She does take iron so her stool is dark. EGD/Colonoscopy 7/2019 with normal EGD exam. No bleeding lesions or cause for anemia. Colonoscopy with moderate pandiverticulosis moderate. 15 mm sessile polyp, located in the cecum, which was completely removed but specimen was unable to be retrieved. Small polyps could have been missed. -Hold ASA for now Acute on chronic congestive heart failure with preserved ejection fraction New onset Atrial Fibrillation -NT-pro BNP up 1116 (July/2021) -- > 2855 upon arrival -CXR with mild cardiomegaly with pulmonary vascular congestion -Lower extremity edema noted on exam -Given 20 mg of IV lasix in ER (had received 1 L of IVF) -Continue home dose oral lasix going forward - monitor daily weights, I/O, 2 G NA restriction, 2 L fluid resriction -EKG with A-fib (no previous episodes on EKGs), monitor on telemetry, check TSH. With chronic anemia and intermittent bleeding - likely would be a poor candidate for OAC -ECHO 7/23/21: LVEF 58%, mild AS, mild MR, diastolic function indeterminate. COVID-19 infection -Vaccinated x 2 - had not had a chance to get booster. On Humira. -Symptom onset 11/26 or earlier. Not a candidate for MAB. -Symptoms: Generalized weakness, cough, rhinorrhea, anorexia, dizziness, headaches, sweats and chills, altered taste and smell -CXR without signs of COVID-19 -If patient develops further symptoms such as hypoxia - Decadron can be started. She is out of the therapeutic window for Remdesivir. -Unable to offer VTE prophylaxis with Lovenox given possible active bleeding. SCDs are ordered. -Supportive care with anti-tussives, PRN Tylenol for any fevers Hypertension -Continue metoprolol and norvasc within parameters. OSA with nightly Bi-pap dependence -OSA power plan ordered -Continuous pulse oximetry Psoriasis -Receives Humira every 14 days FULL CODE Diet: Heart Healthy, 2 L fluid restriction, 2 G NA VTE Prevention: This patient is high risk per the VTE risk assessment tool, however pharmacologic prophylaxis is contraindicated due to bleeding. SCDs have been ordered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
3,0
Labordaten
CT ABDOMEN AND PELVIS WITH IV CONTRAST [357398943] Resulted: 12/09/21 1907 Order Status: Completed Updated: 12/09/21 1909 Narrative: EXAMINATION: CT Abdomen and Pelvis with IV Contrast EXAM DATE: 12/9/2021 4:38 PM TECHNIQUE: CT imaging of the abdomen and pelvis was performed with intravenous contrast. Coronal and sagittal images were reconstructed. CONTRAST: The amount and type of contrast are recorded in the medical record. QPP DOCUMENTATION: At least one of the following dose reduction techniques was utilized: Iterative reconstruction, and/or Automatic Exposure Control, and/or mA/kV adjustment based on body size. INDICATION: Hematuria, unknown cause COMPARISON: None ENCOUNTER: Not applicable ____________________ FINDINGS: Lung Bases: Bilateral lower lobe consolidation, greater on the right. There is a small right pleural effusion Hepatobiliary: Hepatic contour is slightly serrated. No biliary dilatation or focal hepatic mass is demonstrated There is no biliary dilatation and the gallbladder is unremarkable with no calcified stones. Pancreas: The pancreas is normal. Spleen: The spleen has a normal size and there are no splenic lesions. Adrenals: There is a 15 mm left adrenal nodule, stable since July 2021 Kidneys, Ureters, & Bladder: The left kidney is unremarkable except for small nonobstructing cysts in the lower pole the right kidney is abnormal with moderate hydronephrosis. There are 2 obstructing calculi at the UPJ measuring 2 and 3 mm in diameter respectively. Beyond the obstruction, the right ureter is unremarkable to the bladder. The left ureter is unremarkable throughout. Portions of the pelvis obscured by artifact from right hip arthroplasty. There are multiple nonobstructing intrarenal calculi bilaterally. The urinary bladder is unremarkable. Gastrointestinal: The stomach and small bowel are normal with no obstruction or inflammation. Moderate left-sided diverticulosis without diverticulitis Reproductive Organs: Portions of the pelvis are obscured. The uterus is not identified Lymphatic System: There is mild adenopathy in the upper abdomen and retroperitoneum. Particularly, there is a 15 mm retrocrural lymph node and scattered. Aortic lymph nodes superior to the renal veins. Vasculature: Normal caliber abdominal aorta. The main abdominal aortic branch vessels including the celiac, mesenteric, and renal arteries appear patent with no evidence of a stenosis. There is no evidence for mesenteric venous thrombosis. Peritoneum: Minimal ascites is present Abdominal Wall & Musculoskeletal: Postoperative changes right hip. DJD lumbar spine. ____________________ Impression: 1. The principal abnormality is 2. Obstructing stones at the right UPJ. There is abnormal enhancement of the mucosa of the right intrarenal collecting system suggesting urinary tract infection. No focal renal abscesses are seen. 3. Cirrhotic changes in the liver. 4. Lower lobe consolidation on the right the right effusion 5. Abnormal but nonspecific upper abdominal adenopathy 6. Stable left adrenal adenoma 7. Bilateral intrarenal calculi DR CHEST SINGLE VIEW [348158796] Resulted: 12/07/21 1433 Order Status: Completed Updated: 12/07/21 1435 Narrative: EXAMINATION: Single View Chest EXAM DATE: 12/7/2021 2:08 PM TECHNIQUE: Single view chest INDICATION: SOB/ Chest Pain. COMPARISON: CTA chest 7/23/2021. ENCOUNTER: Not applicable _________________________ FINDINGS: Mild cardiomegaly with pulmonary vascular congestion. No consolidation, substantial pleural effusion, or pneumothorax. _________________________ Impression: Mild cardiomegaly with pulmonary vascular congestion. Collected: 12/07/21 1327 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 12/07/21 1434 COVID-19 PCR Detected Abnormal
Aktuelle Erkrankungen
-
Vorgeschichte
OSA (obstructive sleep apnea) Essential hypertension, benign Stage 3a chronic kidney disease Heart failure with preserved ejection fraction SARS pneumonia Gross hematuria non-Hospital insomnia with sleep apnea Environmental allergies Overactive bladder Primary osteoarthritis involving multiple joints Psoriasis Impaired fasting glucose Dense breasts History of total hysterectomy Hypertriglyceridemia, essential Degenerative disc disease, lumbar Mixed stress and urge urinary incontinence Venous insufficiency of both lower extremities Class 2 severe obesity due to excess calories with serious comorbidity in adult Anemia, unspecified type Thrombocytopenia, acquired BiPAP (biphasic positive airway pressure) dependence Atherosclerosis of abdominal aorta Osteopenia of neck of left femur Aortic stenosis, mild Mild mitral regurgitation Iron deficiency anemia due to chronic blood loss Acute on chronic blood loss anemia Acute on chronic heart failure with preserved ejection fraction Acute on chronic anemia
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet adalimumab (HUMIRA) 40 MG/0.8ML injection amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) capsule ferrous sulfate 325 (65 Fe) MG tablet fluti
Allergien
Bandaids Hives Codeine Hives
Vorherige Impfungen
-

VAERS 1938572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
64,0
Geschlecht
F
Eingang
10.12.2021
Impfdatum
15.11.2021
Beginn
06.12.2021
Tage bis Beginn
21,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Cardiac flutter Heart rate increased Palpitations

Symptomtext

Periodic feelings of having a fast-beating, fluttering, or pounding in center of chest. It happens several times a day. Symptoms started about a week ago. No problem with breathing or chest pain. Also having some joint pain in fingers

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
Haven't seen a doctor yet
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Acidics and sensitive to Vicodin
Vorherige Impfungen
-

VAERS 1935605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
63,0
Geschlecht
U
Eingang
09.12.2021
Impfdatum
19.03.2021
Beginn
27.11.2021
Tage bis Beginn
253,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Cough Diarrhoea Dyspnoea Myalgia Respiratory tract congestion

Symptomtext

11/27/21 presents to ED for "shortness of breath, cough, congestion, diarrhea, myalgias". PMHx of "COPD".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1935246

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0162

moderat
Staat
NY
Alter
41,0
Geschlecht
M
Eingang
09.12.2021
Impfdatum
20.04.2021
Beginn
14.05.2021
Tage bis Beginn
24,0
Dosis
2
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dyspnoea Pyrexia Tremor

Symptomtext

Had shortness of breath while doing everyday active over multiple days multiple times a day. Avoided exercise as a result, was usually active but afraid to exercise due to the reaction. Initially had a terrible reaction to the 2nd dose the night of the second dose had some trouble breathing, fever, shakes, felt as bad as I've ever felt, but slowly disappeared over a about 4 days.... Then had issues of shortness of breath after these episodes. I don't remember exactly when the shortness of breath started but remember it clearly two weeks after may have started earlier.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
-
Vorgeschichte
Vocal granuloma
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1928955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MN
Alter
27,0
Geschlecht
M
Eingang
07.12.2021
Impfdatum
12.04.2021
Beginn
03.12.2021
Tage bis Beginn
235,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Ageusia Anosmia Asthma Chest discomfort Chills Condition aggravated Diarrhoea Headache Nasal congestion Oropharyngeal pain Pain Productive cough Pyrexia Respiratory tract congestion Sinus congestion

Symptomtext

Moderate persistent asthma presents today with 3 day history of fever-101.3 oral temp, chills, diarrhea, body aches, headache, sore throat, productive cough, loss of taste, loss of smell, diarrhea, sinus congestion, nasal congestion, chest congestion, chest tightness. starting 12/3/21

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
ADHD; major depression, asthma without complications
Andere Medikamente
Taking Cyclobenzaprine HCl 10 MG Tablet 1 tablet Orally three times a day as needed, Taking Advair Diskus 250-50 MCG/DOSE Aerosol Powder Breath Activated 1 puff Inhalation Twice a day, Taking Ventolin HFA 108 (90 Base) MCG/ACT Aerosol Solut
Allergien
pineapple: throat swelling - Allergy.
Vorherige Impfungen
-

VAERS 1925115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
56,0
Geschlecht
M
Eingang
06.12.2021
Impfdatum
28.04.2021
Beginn
12.05.2021
Tage bis Beginn
14,0
Dosis
2
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Blood immunoglobulin E increased Bronchitis Dyspnoea Symptom recurrence

Symptomtext

Within two weeks of the second dose of the vaccine I got Bronchitis and I was having trouble breathing. I have been having Bronchitis repeatedly since I got my vaccines. I am now taking Montelukast, and I have been hospitalized once and I had Bronchitis in May, June September, October and November. I was tested for Asthma and it was negative. My IGE was very high. I used to run regularly.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
5,0
Labordaten
Dose 3: 11/09/2021 no number, Pharmacy
Aktuelle Erkrankungen
N/A
Vorgeschichte
MI history
Andere Medikamente
Simvastatin; Adderall; Amitriptyline; Vitamin D; Multivitamin
Allergien
Penicillin as a child
Vorherige Impfungen
-

VAERS 1921804

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NJ
Alter
43,0
Geschlecht
F
Eingang
03.12.2021
Impfdatum
14.04.2021
Beginn
14.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Breast tenderness Cardiac discomfort Fatigue Immediate post-injection reaction Paraesthesia

Symptomtext

Tingling down legs and arms immediately after 1st shot. Felt sensation up spine and around skull too. Heart sensations. Tingling in all limbs lasted for several weeks. Heart sensations on and off. Extremely tender breast for two weeks on top of fatigue. Sat at clinic longer hoping symptoms would go away, never did. EMT wasn't helpful (she didn't take my name, just said she needed to make sure I didn't get palsy of the face) so I left. Made an appointment with my primary doctor and he didn't know how to advise since data not out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
just vitamins
Allergien
none
Vorherige Impfungen
-

VAERS 1920910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
51,0
Geschlecht
M
Eingang
03.12.2021
Impfdatum
08.04.2021
Beginn
27.11.2021
Tage bis Beginn
233,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Cough Diarrhoea Dyspnoea Feeling abnormal Pyrexia SARS-CoV-2 test positive Swelling Vaccine breakthrough infection

Symptomtext

COVID breakthrough. SOB and cough for one week(starting around 11/27/21). Per patient he started to feel poorly with fever and had diarrhea then he became increasingly swollen and SOB. He went to ED on 12/2/2021 and his COVID test came back positive

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
2,0
Labordaten
COVID PCR+ on 12/2/2021
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes and Hypertension
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1920860

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
AZ
Alter
34,0
Geschlecht
M
Eingang
03.12.2021
Impfdatum
26.03.2021
Beginn
01.04.2021
Tage bis Beginn
6,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Anxiety Anxiety disorder Biopsy site unspecified normal Blood cholesterol increased Blood test Chest X-ray Chest pain Cholelithiasis Colonoscopy Computerised tomogram abdomen Computerised tomogram abdomen abnormal Computerised tomogram thorax normal Electrocardiogram Endoscopy Panic attack Panic disorder Sleep disorder

Symptomtext

Note: I have no history of anxiety or panic attacks. Roughly one week after the first dose, I had what was ultimately described as a panic attack - I went to the ER thinking it was a heart attack, where they did blood panels, x-ray, and a chest CT. I was later discharged. The problem recurred (but worse) the next day. I have been chasing this ever since. What happened - Six ish days after the first dose of Pfizer, I began having chest/abdomen pains, panic/anxiety problems. Symptoms have lessened over time but returned later. Symptoms - chest pain in middle-to-upper-left; panic/anxiety attacks began; unable to sleep many nights due to pain/constantly waking up with "impending doom" fears What has been done - Four ER visits, several GP followups and lots of testing. X-rays, chest/abdomen/pelvis CTs, blood panels, endoscopy and colonoscopy. Diet changes. All doctors (GP, ER) I've mentioned the timing to have mostly shrugged-off the timing with the vaccine, however, no other causes have been identified to-date, and the symptoms are still occurring - some days are better than others. At this point, I'm wondering about the booster shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
2021-04-02 - ER visit; blood panel, chest x-ray, chest CT (no significant findings) 2021-04-03 - ER visit; blood panel, chest x-ray 2021-04-05 - GP visit, blood panel (slight elevated cholesterol, not of significant concern) 2021-04-12 - abdomen and pelvis CT; at least one small 7 to 8 mm gallstone noted (not of significant concern) 2021-05-25 - endoscopy, colonoscopy (no significant findings, biopsies came back clear) 2021-08-07 - ER visit; EKG, blood clot test (no significant findings) 2021-08-12 - ER visit; EKG, chest x-ray, blood panels (no significant findings) 2021-11-15 - abdomen CT; radiopaque gallstone but no sign of acute cholecystitis (not of significant concern)
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Occasional multivitamin.
Allergien
Minor allergy to bermuda grass.
Vorherige Impfungen
-

VAERS 1920708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
42,0
Geschlecht
F
Eingang
03.12.2021
Impfdatum
10.09.2021
Beginn
10.09.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Blood pressure increased Chest discomfort Dizziness Palpitations Panic attack Throat tightness

Symptomtext

Patient called to report that she doesn't want second covid vaccine because she experienced side effects 30 to 45 minutes after getting first Pfizer vaccine on 9/10/21. She said she waited in the lobby for 15 to 20 minutes, then left and went shopping. She experienced light headedness. So she went home, then started experiencing her heart racing and a a friend gave her 100mg of Benadryl and took her to the ER. She said she felt heavy chested and throat tightness, but never had difficulty breathing or swallowing and never lost consciousness. She says her blood pressure was elevated at the ER. She said she was told she had a panic attack and was released and in 5 hours from receiving the vaccine she was feeling normal.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1905914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
68,0
Geschlecht
M
Eingang
29.11.2021
Impfdatum
12.04.2021
Beginn
18.11.2021
Tage bis Beginn
220,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 COVID-19 pneumonia Condition aggravated Dyspnoea Dyspnoea exertional Hyponatraemia Hypoxia Oxygen saturation decreased Pyrexia SARS-CoV-2 test positive

Symptomtext

Hospitalized 11/18/2021; COVID-19 positive 11/18/2021; fully vaccinated BRIEF OVERVIEW: Discharge Provider: MD, MPH Primary Care Provider at Discharge: MD Admission Date: 11/18/2021 Discharge Date: 11/20/2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hyponatremia [E87.1] Pneumonia due to COVID-19 virus [U07.1, J12.82] HOSPITAL COURSE: Patient admitted with SOB, fevers and hypoxia down to 88%. On admission patient was started on dexamethasone. He required up to 2L of nasal cannula but weaned to room air at rest in the am of 11/20/21. Patient was still desatting to 87% with activity and so was discharged with home O2. CONSULTS / RECOMMENDATION: Further wean O2 at home. Patient was given a pulse ox to assist with weaning at home. Goal oxygen concentration of 92%.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
OSA (obstructive sleep apnea) Pneumonia due to COVID-19 virus Coronary artery disease Hypertension Left-sided carotid artery disease Anemia due to recent lower GI bleed Hyperlipidemia Hyponatremia
Andere Medikamente
aspirin 81 MG tablet atorvastatin (LIPITOR) 80 MG tablet benzonatate (TESSALON) 100 MG capsule buPROPion (WELLBUTRIN XL) 150 MG 24 hr tablet lisinopril (ZESTRIL) 2.5 MG tablet metoprolol-XL (TOPROL-XL) 25 MG tablet Multiple Vitamins-M
Allergien
NKA
Vorherige Impfungen
-

VAERS 1904696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
37,0
Geschlecht
M
Eingang
29.11.2021
Impfdatum
30.04.2021
Beginn
06.05.2021
Tage bis Beginn
6,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest discomfort Dyspnoea Head discomfort Headache Paraesthesia

Symptomtext

Approx. four days to a week later, shortness of breath while leaning back on floor. Never happened before without exertion of any kind. Recall some pounding in chest. - NOTE: Shortness of breath resolved. Lasted for a few days. Chest tightness, pressure in chest, uncomfortable feelings persisted pretty consistently ever since almost every day to some degree, often in the morning in bed. Note: Continues. Recent to the time of reporting this, i) November 28th, unusual sensations in different areas around the top of the skull, sometimes as a minor headache, sometimes sensation with no pain. Note: New occurrence, becoming fairly common, at least one or twice daily. ii) Finally so tingling sensations in the lower extremities, very minor sensations close to the skin, around joints, blood vessels; very minor but I know my body and not something I've experienced before the shot. Usually subsides with movement.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None so far, doctor asked questions to rule out any "anxiety from the shot" differential diagnosis, (it was not immediate after shot, myocarditis was being heard more commonly for younger men, so it was considered probable). Because of messaging from by health agencies and media... I was not offered testing but I will go tomorrow to ask for a diagnostic as least for peace of mind. Interested in Echocardiogram: (pericarditis) Troponin & other enzymatic markers for myocarditis (PULS heart test, general heart?) D-Dimer blood clots Anything if relevant and prudent for nuerological systems related to my head.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
cetirizine
Allergien
none
Vorherige Impfungen
-

VAERS 1896988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
52,0
Geschlecht
M
Eingang
24.11.2021
Impfdatum
01.04.2021
Beginn
16.11.2021
Tage bis Beginn
229,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Endotracheal intubation Fatigue Influenza virus test Nasal congestion Pyrexia Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

Pt received Pfizer vaccines on 04/01/21 and 04/25/2021. Pt presented to the ED on 11/16/21 with complaints of SOB, cough, nasal congestion, fever, and fatigue. Pt was found to be COVID positive. CXR showed COVID pneumonia. Pt required supplemental oxygen leading to intubation. Pt was transferred to another Hospital for ECMO.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
-
Labordaten
COVID-19, Flu, RSV positive for SARS-COV-2 on 11/16/21
Aktuelle Erkrankungen
-
Vorgeschichte
Obesity
Andere Medikamente
-
Allergien
none
Vorherige Impfungen
-

VAERS 1894788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
39,0
Geschlecht
F
Eingang
23.11.2021
Impfdatum
30.04.2021
Beginn
06.11.2021
Tage bis Beginn
190,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

11/6/21 presents to EC ED "with concerns about covid. Patient began experiencing cough and shortness of breath 3 days prior after contact with COVID+ individual. Patient tested positive 2 days prior to presentation." PMHx "polycystic kidney disease, deceased donor renal transplant on CellCept".

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
11/07/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1885469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
83,0
Geschlecht
F
Eingang
19.11.2021
Impfdatum
18.03.2021
Beginn
16.11.2021
Tage bis Beginn
243,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 COVID-19 pneumonia Chest X-ray abnormal SARS-CoV-2 test positive

Symptomtext

Pt received pfizer vaccine on 03/18/21 and 04/08/21. While inpatient, pt tested positive for COVID. CXR showed developing COVID pneumonia.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19 pneumonia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
COPD, CAD, GERD, HLD, HTN, CVA, obstructive sleep apnea
Andere Medikamente
norvasc, lipitor, plavix, apreesoline, synthroid, cozaar, effexor, advair
Allergien
-
Vorherige Impfungen
-

VAERS 1885014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0162

moderat
Staat
NY
Alter
54,0
Geschlecht
F
Eingang
19.11.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal distension Adnexa uteri pain Asthenia Chest discomfort Dyspnoea Dysuria Gait disturbance Impaired work ability Laboratory test Myalgia Pharyngeal swelling Pyrexia Swelling Ultrasound scan Urinary retention Visual impairment

Symptomtext

Swelling throughout the body Swelling and eyes Diminished vision 10 minutes after injection, swollen throat, Contacted primary doctor. Was given a prescription for an EpiPen 4/17/21. Due to diminished vision visited I doctor Needed another new prescription for glasses (my current prescription was already a recent one) paid $300 out-of-pocket for I already received a prescription less than a year ago through my optical insurance sharp pains in muscles throughout the body which continued for the first five weeks Chest tight hard to breathe For five weeks Weakness throughout the body needed assisting walking Day two to day 12 after injection One month of ovarian pain which I have never experienced past menopause and was bleeding for an entire week! Missed 10 days of work Lower abdomen very swollen the first two weeks unable to urinate ureters swollen resulting in urinary retention fevers and an ER visit at Hospital on 4/24/21 Required antibiotics. Another 100 dollar co-pay for that.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Had laboratory test at ER 4/24/21 I know I had a sonogram a few days before that because there?s not much time to submit all this information this is all I can send at the moment
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma heart murmur, Spine injury
Andere Medikamente
Alprazolam .25 at bedtime, Vitamin D 1000 IU daily, B12 50 MCG daily, Probiotic GNC brand eight strain chewable
Allergien
Penicillin Clindamycin Ceftin. Doxycycline
Vorherige Impfungen
-

VAERS 1884208

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
57,0
Geschlecht
M
Eingang
19.11.2021
Impfdatum
11.04.2021
Beginn
11.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Arthralgia Dyspnoea Fatigue Inappropriate schedule of product administration Somnolence

Symptomtext

Constant fatigue; joint pain; shortness of breath when I try to excersise; Sleeping a minimum of 12-14 hours a day; dose number 1, 25Mar2021, dose number 2, 11Apr2021; This is a spontaneous report from a contactable consumer (patient) reported for himself that: A 57 years old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in Arm right on 11Apr2021 10:00 (Batch/Lot Number: EW0162) as DOSE 2, SINGLE for covid-19 immunisation .Age at vaccination 57 years. Hitorical vaccine included: first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) administered on 25Mar2021 at 09:00 AM on left arm Lot# ER8730.Medical history included Abdominal aortic aneurysm (AAA) from 2015 to an unknown date Concomitant medication(s) included labetalol taken for an unspecified indication, start and stop date were not reported; amlodipine besilate (NORVASC) taken for an unspecified indication, start and stop date were not reported; benazepril (BENAZEPRIL) taken for an unspecified indication, start and stop date were not reported; duloxetine (DULOXETINE) taken for an unspecified indication, start and stop date were not reported. On 01Jul2021 the patient reported Constant fatigue and joint pain, shortness of breath when I try to exercise. Sleeping a minimum of 12-14 hours a day.The outcome of the event dose number 1, 25Mar2021, dose number 2, 11Apr2021 was unknown. The outcome of the other events was not recovered.Additional information:Facility where the most recent COVID-19 vaccine was administered: School or Student Health Clinic,No other vaccines within 4 weeks prior to the COVID vaccine.Prior to vaccination, no diagnosis with COVID-19.Since the vaccination, the patient hasn't been tested for COVID-19 Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Abdominal aortic aneurysm (AAA)
Andere Medikamente
LABETALOL; NORVASC; BENAZEPRIL; DULOXETINE
Allergien
-
Vorherige Impfungen
-

VAERS 1879654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NJ
Alter
56,0
Geschlecht
F
Eingang
18.11.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood test Body temperature Cold sweat Colonoscopy Decreased appetite Diarrhoea Dizziness Muscle spasms Nausea Pain in extremity Paraesthesia Urine alcohol test X-ray

Symptomtext

cold sweats; finger tingling; nauseous/extreme nausea; Cramps/cramping; didn't eat all that much; Diarrhea; dizzy again; arm was sore; This is a spontaneous report from contactable consumer (patient) reported for herself. A 56-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EW0162, Expiration date: unknown) via an unspecified route of administration, administered in right arm (right upper arm) on 12Apr2021 at 08:45 am (age at vaccination was 56 years) as dose 2, single for COVID-19 immunization. The patient's medical history included seasonal allergies, food poisoning, stomach flu and dehydrated. The patient had been to hospital 3 times, 2 time were to deliver her babies and one time was for food poisoning 15 or 18 years ago, she went in and had to get hydration because she dehydrated. Concomitant medications included escitalopram oxalate (LEXAPRO) taken for anxiety and bereavement depression from 05Sep2020 and ongoing (she had been taking this for about 9 months), levothyroxine taken for thyroid from 31Oct2014 and ongoing, ascorbic acid (VITAMIN-C) from an unspecified start date and ongoing (she had been taking this for about 10 years), trametes versicolor (TURKEY TAIL MUSHROOM) from an unspecified start date and ongoing (she had been taking this for about 10 years), biotin from an unspecified start date and ongoing (she had been taking this for about 10 years), origanum vulgare (OREGANO) from an unspecified start date and ongoing (she had been taking this for about 10 years), 1,2-octanediol; ascorbic acid, butyrospermum parkii; glycerol; helianthus annuus; oenothera biennis; olea europaea; persea americana; retinol; rosa moschata; vaccinium vitis-idaea fruit; vitamin E NOS from an unspecified start date and ongoing, magnesium from an unspecified start date and ongoing (she had been taking this for about 10 years), melatonin from an unspecified start date and ongoing (she had been taking this for about 10 years), vitamin B complex (B COMPLEX (B50) from an unspecified start date and ongoing (she had been taking this for about 10 years), colecalciferol, folate sodium, magnesium, omega-3 fatty acids, pyridoxine hydrochloride, vitamin b12 nos, vitamin e nos (SUPER OMEGA 3 [COLECALCIFEROL; FOLATE SODIUM; MAGNESIUM;OMEGA-3 FATTY ACIDS; PYRIDOXINE HYDROCHLORIDE; VITAMIN B12 NOS;VITAMIN E NOS]) from an unspecified start date and ongoing (she had been taking this for about 10 years), 1,2-octanediol;ascorbic acid; butyrospermum parkii; glycerol; helianthus annuus; oenothera biennis; olea europaea; persea americana; retinol; rosa moschata; vaccinium vitis-idaea fruit; vitamin e nos (1,2-OCTANEDIOL; ASCORBIC ACID; BUTYROSPERMUM PARKII; GLYCEROL; HELIANTHUS ANNUUS; OENOTHERA BIENNIS;OLEA EUROPAEA; PERSEA AMERICANA; RETINOL; ROSA MOSCHATA; VACCINIUM VITIS-IDAEA FRUIT; VITAMIN E NOS) from an unspecified start date and ongoing; vitamin D3 from an unspecified start date and ongoing (she had been taking this for about 10 years), andrographis paniculata, echinacea purpurea root, olea europaea leaf (IMMUNE SUPPORT) (she had been taking this for about 10 years) and adult women's vitamin (she had been taking this for about 10 years) all taken for an unspecified indication. The patient took vitamins every day for at least 10 years. These were the things that have helped her avoid the flu and cold, she never had the flu or cold, she gets seasonal allergies, she thought they work for her, it could be all in her head but she was not going to make any changes. She said the cancer institute recommended turkey tail. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: ER8727, Expiration date: unknown) via an unspecified route of administration, administered in right arm (right upper arm) on 22Mar2021 at 08:45 am (age at vaccination was 56 years) as dose 1, single for COVID-19 immunization and experienced severe stomach cramps, diarrhea, very extreme nausea/nauseous again, like that same feeling, cold sweats, fingers felt tingly/tingling, tired, dry heaving, didn't eat all that much, cramps, dehydrated, she wasn't feeling good and she was in pain. No additional vaccines were administered on same date of the Pfizer suspect. The patient declined being sick at the time of vaccination. She said she didn't get sick like that, she had allergies, has had the stomach flu, she has never had flu felt like she felt after the shot, it was excruciating. She didn't think it was the shot, the first one and second one the symptoms were within 48 hours of each other. The facility where the most recent COVID-19 vaccine was administered was not a Military Facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 05Apr2021, the patient underwent lab test which included blood test, urine test and x-ray and the results were normal. All the tests from the ER came back clean, all blood levels were normal, there were no high white blood cells and her doctor said everything came back normal. They checked her all out and could not figure out why she was so nauseas, why she was having diarrhea, all the test came back fine, there was no infection and no obstruction. She said all the tests from the ER came back clean. The patient's body temperature: normal (she did not have a fever) and colonoscopy: result unknown on an unspecified date. The patient's second shot was that past Monday, 12Apr2021 at the same facility, same time, same place, same everything. She said she got the shot, everything was fine, her arm was sore that evening on 12Apr2021 just like what everybody was experiencing, she didn't think anything of it, she was prepared to call off, to not be in, to not feel good, for it to be a nightmare. She said she even went to the gym Monday night to do her workout, everything was fine. She had a sore arm on Tuesday. Wednesday, she was at work again and, like clockwork, the same times, the same channel, the same symptoms happened again. The symptoms started on 14Apr2021. On 14Apr2021, the patient experienced cold sweat, dizzy again, finger tingling, nauseous, exactly to the minute to the time of the first shot, same symptom problem. She sat back in her chair, texted her doctor, and that she did not want to got to the ER. She thought that something was wrong, the shot, it was cramping, she had extreme nausea, she could not eat a lot on 14Apr2021. She said she had no body ache, no fever, just cramping and diarrhea on 14Apr2021. She wanted to fight through it, she wanted to go home and use the toilet, the telemedicine doctor said he didn't think that was gastritis. She said the doctor told her that he had some patients got diarrhea and vomiting issues on shots too with Pfizer. She was prescribed the same medicines again, confirmed Zofran and Bentyl, she went home, took it, it was good, it calmed down, she has been on it ever since. She said it was the same amount of time, she was mortified of another attack. The outcome of all the events was resolved on 15Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
Test Date: 20210405; Test Name: Blood test; Result Unstructured Data: Test Result:Normal; Comments: All blood levels were normal, there were no high white blood cells. No infection and no obstruction; Test Name: Body temperature; Result Unstructured Data: Test Result:Normal; Comments: She did not have a fever; Test Name: Colonoscopy; Result Unstructured Data: Test Result:Result unknown; Test Date: 20210405; Test Name: urine test; Result Unstructured Data: Test Result:Normal; Comments: No infection and no obstruction; Test Date: 20210405; Test Name: X-ray; Result Unstructured Data: Test Result:Normal; Comments: No infection and no obstruction
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Food poisoning (Food poisoning 15 or 18 years ago, she went in and had to get hydration because she dehydrated..); Pregnancy (The patient had been to hospital 3 times, 2 time were to deliver her babies.); Seasonal allergy (She gets seasonal allergies, she thinks they work for her); Stomach flu (She has never had flu felt like she felt after the shot); Water excessive loss of (Food poisoning 15 or 18 years ago, she went in and had to get hydration because she dehydrated.)
Andere Medikamente
LEXAPRO; LEVOTHYROXINE; VITAMIN-C; TURKEY TAIL MUSHROOM; BIOTIN; OREGANO; 1,2-OCTANEDIOL;ASCORBIC ACID;BUTYROSPERMUM PARKII;GLYCEROL;HELIANTHUS ANNUUS;OENOTHERA BIENNIS;OLEA ; MAGNESIUM; MELATONIN; B COMPLEX (B50); SUPER OMEGA 3 [COLECALCIF
Allergien
-
Vorherige Impfungen
-

VAERS 1876028

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
56,0
Geschlecht
F
Eingang
17.11.2021
Impfdatum
28.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Body temperature Condition aggravated Fatigue Lymph node pain Myalgia Pain in extremity Pyrexia Vaccination site pain

Symptomtext

pain at injection site; intense pain in lymph node; fever 100-103 degrees- down to 99 with tylenol; severe fatigue; Severe muscle and joint/rib pain, pain at injection site (entire arm) 1st and 2nd shot- worse; Severe muscle and joint/rib pain, pain at injection site (entire arm) 1st and 2nd shot- worse; Severe muscle and joint/rib pain; Severe muscle and joint/rib pain; This is a spontaneous report from a contactable consumer (patient). This 56-year-old non-pregnant female (Not Hispanic Or Latino Caucasian) patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0162) via an unspecified route of administration in left arm on 28Apr2021 at 10:30 (at the age of 56-year-old) as DOSE 2, SINGLE for covid-19 immunization. Facility type vaccine reported as other. Medical history included High bp, generalized anxiety disorder, autoimmune history. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient concomitant medications included Bisoprolol, Lisinopril, Xanax for an unspecified indication and Tylenol for pyrexia, start and stop date were not reported. The patient had known allergies for sulfur. No covid prior vaccination. No covid tested post vaccination. The patient did not receive any other vaccines within four weeks. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: Ew0151) on unspecified route in right arm on 07Apr2021 at 15:00 (at the age of 56-year-old) as DOSE 1, SINGLE for covid-19 immunization and on 07Apr2021 at 18:00 patient had severe muscle and joint/rib pain, joint/rib pain, pain at injection site and severe fatigue. On an unspecified date, after second dose patient experienced Severe muscle and joint/rib pain, pain at injection site (entire arm) 1st and 2nd shot- worse w/ 2nd dose, intense pain in lymph node (under arm), fever 100-103 degrees- down to 99 with Tylenol, severe fatigue. Treatment received for the event fever 100-103 degrees was Tylenol and for rest of the event patient did not receive any treatment. On an unknown date, patient underwent lab tests and procedures which included body temperature: 100-103 degrees- down to 99 with Tylenol. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Test Name: Body temperature; Result Unstructured Data: Test Result:100-103 Centigrade; Comments: degrees; Test Name: Body temperature; Result Unstructured Data: Test Result:99 Centigrade; Comments: down to 99 with Tylenol.
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Autoimmune disorder; Blood pressure high; Generalized anxiety disorder.
Andere Medikamente
BISOPROLOL; LISINOPRIL; XANAX; TYLENOL.
Allergien
-
Vorherige Impfungen
-

VAERS 1873364

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MN
Alter
70,0
Geschlecht
M
Eingang
16.11.2021
Impfdatum
15.04.2021
Beginn
07.11.2021
Tage bis Beginn
206,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chills Cough Dizziness Dyspnoea Exposure to SARS-CoV-2 Headache Pyrexia Vaccine breakthrough infection

Symptomtext

This case meets criteria for vaccine breakthrough review. Known exposures. SxS include 6 days of fevers, chills, SOB, cough, dizziness, headaches.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1870421

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
49,0
Geschlecht
F
Eingang
15.11.2021
Impfdatum
15.04.2021
Beginn
16.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Balance disorder Blood glucose normal Cystitis Full blood count normal Headache Hepatitis C test negative Inflammation Injection site paraesthesia Magnetic resonance imaging normal Skin reaction Tremor

Symptomtext

The initial symptoms were tingling on the injection area and the next day I didn't have balance, I had trimmers on my upper body and hands, my balance was bad that I was given Prednisone and I had skin reaction. I was also having body inflammation and I did end up with cystitis and severe headaches.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site paraesthesia
Hospital-Tage
-
Labordaten
MRI results came back normal 08/09/2021 CBC Normal Hepatitis C Negative Glucose Level was 110
Aktuelle Erkrankungen
N/A
Vorgeschichte
Allergies
Andere Medikamente
Ibuprofen
Allergien
Did not want to list allergies
Vorherige Impfungen
-

VAERS 1865188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
-
Alter
38,0
Geschlecht
F
Eingang
12.11.2021
Impfdatum
01.03.2021
Beginn
01.04.2021
Tage bis Beginn
31,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Asthenia Condition aggravated Contusion Dysstasia Fatigue Impaired healing Postural orthostatic tachycardia syndrome Tilt table test Vitamin D decreased

Symptomtext

After vaccine - Extreme POTS symptoms and Vitamin D level dropped - on 50,000 IU Vitamin D/week ever since vaccine; was taking 2,000 IU/day prior to testing; recently put on Metoprolol due to ongoing orthostatic tachycardia. Symptoms since April include extreme weakness, fatigue, orthostatic tachycardia up to 140s/150s when standing, unable to stand for extended periods of time, some days unable to stand for more than thirty seconds, slow healing bruises, etc.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Tilt table test 09/2021; Vitamin D test 04/2021. Failed tilt table test due to inability to stand for the entire test. Was taking Vitamin D supplements prior to testing as Vitamin D had been lower in the past. While on 2000 IU/day, my level at testing had dropped into the 20s.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1861133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
WA
Alter
28,0
Geschlecht
F
Eingang
11.11.2021
Impfdatum
01.04.2021
Beginn
04.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Basedow's disease Chest pain Hypertension Hypothyroidism Laboratory test Nodule Pain Thyroid dermatopathy

Symptomtext

May 2 2021- current Severe pain Leg nodules Pre-tibial bi-lateral myxedema Graves disease Hypothyroidism Chest pain High blood pressure + more

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
2,0
Labordaten
Countless tests were done and can be found in my medical records if need be
Aktuelle Erkrankungen
None
Vorgeschichte
Seizures
Andere Medikamente
Gabapentin Fluoxetine Buspirone Aripriprozole
Allergien
N/A
Vorherige Impfungen
-

VAERS 1846667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
WI
Alter
36,0
Geschlecht
F
Eingang
05.11.2021
Impfdatum
14.04.2021
Beginn
20.04.2021
Tage bis Beginn
6,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthma Condition aggravated Respiratory disorder

Symptomtext

Prior to the shots I had mile asthma where I used my rescue inhaler once a year. Since then I have needed my inhaler once to twice a week, and I am on a daily medication to help with breathing issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Mild asthma, WPW
Vorgeschichte
-
Andere Medikamente
Zyrtec
Allergien
-
Vorherige Impfungen
-

VAERS 1839277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
49,0
Geschlecht
F
Eingang
03.11.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Dizziness Electrocardiogram Hyperhidrosis Inflammation Insomnia Nervousness Skin swelling

Symptomtext

Now she is scared; Chest pain; Sweating; Dizziness; not able to sleep; skin jumping left side of her face/skin jumping right leg; inflammation and swelling in the skin over her chest; inflammation and swelling in the skin over her chest; This is a spontaneous report from a contactable consumer or other non HCP (Patient). A 49-years-old female patient received first dose of bnt162b2 (BNT162B2, PFIZER-BIOTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0162), via an unspecified route of administration, administered in Arm Right on 15Apr2021 14:00 (Age at vaccination: 49-years-old) as Dose 1, Single for covid-19 immunization. Medical history included mini-stroke from 2000 to an unknown date. The patient concomitant medications were not reported. patient not had any other vaccine within 4 weeks. On 15-APR-2021 14:00 patient experienced Chest pain, Sweating, Dizziness, not able to sleep, skin jumping left side of her face/skin jumping right leg, inflammation and swelling in the skin over her chest and on an unspecified date experienced Now she is scared. It was reported patient has a question, on the 15 she had the first dose for the Pfizer. Just a couple of minutes after she received it, she had chest pain really strong, she was unsure if this was a normal side effect and wanted to give it some time. Later when she got home the chest pain returned. She was unable to sleep due to the chest pain. Now she is scared because the second does is coming on 06May2021. She need recommendation whether she should get the next dose of the vaccine. Chest Pain: The last time was yesterday, it was something that was minimum. It was on 1% of the pain she felt before. It is fleeting came and went as it pleased. Felt like there is some lingering inflammation in the skin over her chest , swelling in chest, that started on the date of the vaccine but now it is to a minimum. She has not taken Tylenol. Slight pain with a minimum amount of swelling. Sweating: she had the sweating with the chest pain, and had it again yesterday, but it was reduced, just a little bit of sweating. Dizzy - She has none, not anymore. It also came with the chest pain as the chest pain started reducing itself, the dizziness reduced until she no longer felt it. Not able to sleep: first night was the hardest. She just woke up at night, four times the second night. skin jumping: the first night her left side of her face felt like it moved, jumping, skin on the left side on the first night. And she felt a similar sensation on her right leg two days later. On her right leg it has happened at least four times. They gave her Ibuprofen for the swelling in her muscle in the chest area. Adverse events resulted in Emergency Room visit. Adverse events not resulted in Physician Office visit. The patient underwent lab tests and procedures which included electrocardiogram: normal on Apr2021. The outcome for the event Chest pain, Sweating, inflammation and swelling in the skin over her chest, inflammation and swelling in the skin over her chest was reported as resolving and for event Now she is scared was reported as unknown and for event Dizziness outcome was resolved on an unspecified date in Apr2021, not able to sleep was resolved on 16Apr2021. skin jumping left side of her face/skin jumping right leg was resolved on 15Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Test Date: 202104; Test Name: EKG; Result Unstructured Data: Test Result: normal.
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Stroke (Reports in 2000 she had a mini-stroke. She didn't know if this would help or not).
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1836999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
PA
Alter
90,0
Geschlecht
F
Eingang
02.11.2021
Impfdatum
19.04.2021
Beginn
18.10.2021
Tage bis Beginn
182,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 SARS-CoV-2 test positive

Symptomtext

Contact with and (suspected) exposure to other viral communicable diseases - issues with her O2 saturations and shortness of breath & COUGH Registered Nurse Progress Notes Signed Encounter Date: 10/21/2021 Signed Hide copied text Hover for details Verified the following for the patient prior to giving injections: Code status:Full Code Allergies: No known drug allergies Weight: 174 Positive test date: 10/18/21 Symptoms patient is experiencing today are: Administered casirivimab 600mg along with imdevimab 600mg as 4 subcutaneous injections of 2.5ml each. Lot #: 8408100007 Exp. Date: 05/31/2023 Time injections administered:1650 Injection sites: 2.5ml subcutaneous - Left upper arm,back 2.5mg subcutaneous - Right upper arm,back 2.5mg subcutaneous - Left outer thigh 2.5mg subcutaneous - Right outer thigh Patients response to injections: Tolerated well Patient was re-evaluated at: 1750 Vitals signs at re-evaluation are: stable Injection sites at re-evaluation are: (description) No redness, swelling, or bruising Report given to charge nurse prior to leaving the facility.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
10/18/2021 0944 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 10/18/21 0944 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result Detected Critical
Aktuelle Erkrankungen
-
Vorgeschichte
Problem List 10 items Respiratory Chronic seasonal allergic rhinitis Digestive Obesity Chronic idiopathic constipation Genitourinary Stage 3 chronic kidney disease (CMS/HCC) Musculoskeletal Lower extremity edema Closed fracture of right hip with routine healing Endocrine/Metabolic Hypercholesterolemia Other History of CVA (cerebrovascular accident) Requires daily assistance for activities of daily living (ADL) and comfort needs Ambulatory dysfunction
Andere Medikamente
aspirin tablet docusate sodium (COLACE) 100 mg capsule simvastatin (ZOCOR) 80 mg tablet
Allergien
NKA
Vorherige Impfungen
-

VAERS 1836180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
IN
Alter
40,0
Geschlecht
F
Eingang
02.11.2021
Impfdatum
22.03.2021
Beginn
26.03.2021
Tage bis Beginn
4,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Back pain Mobility decreased Muscle spasms

Symptomtext

Within a week after both shots I suffered debilitating, crippling lower back pain. I could barely walk or move and was in constant severe pain. After the first shot I didn't realize the vaccine was the cause, I thought I had just injured my back. I made multiple trips to my chiropractor to see what the issue was, and not surprisingly he couldn't find anything mechanically wrong. It wasn't until after the second shot when I was on my way to the ER due to a resurgence in the lower back pain that I made the connection to the vaccine. Both shots I received on a Monday, and both times on Friday I was in severe pain. They gave me a shot of a steroid and something for the pain at the ER, but that didn't really do anything to ease the pain so a few days later I visited my family doctor. He diagnosed it as severe spasms due to my immune response to the vaccine and placed me on Prednisone, which I took for about a month or so. That seemed to ease the pain so I could at least get around and be mobile.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
NA
Allergien
None
Vorherige Impfungen
-

VAERS 1824646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
12,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
02.06.2021
Beginn
03.06.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Body temperature Dyspnoea Fatigue Heart rate Palpitations Pyrexia

Symptomtext

fever of around 100 degrees F; abnormal racing heart of 126 bpm; shortness of breath; fatigue; This is a spontaneous report from a contactable consumer (Patient's Parent). A 12-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0162) via an unspecified route of administration, administered in Arm Right on 02Jun2021 at 13:45 (at the age of 12-year-old) as dose 2, single for COVID-19 immunisation. Medical history included atrial septal defect ASD level 1 from an unknown date and unknown if ongoing. There were no concomitant medications. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0162) via an unspecified route of administration, administered in Arm Right on unknown date in May2021 (at the age of 12-year-old) as dose 1, single for COVID-19 immunisation. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No other medications in two weeks reported. On 03Jun2021 at 06:00 the patient experienced fever of around 100 degrees Fahrenheit, abnormal racing heart of 126 bpm, shortness of breath, fatigue. The patient underwent lab tests and procedures which included body temperature: 100 Fahrenheit, heart rate: 126 on 03Jun2021 (bpm abnormal racing). Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient was not tested for COVID-19. Patient did not receive treatment for the events. Outcome of the events were resolved on unknown date in 2021. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Test Date: 20210603; Test Name: fever; Result Unstructured Data: Test Result:100 Fahrenheit; Test Date: 20210603; Test Name: heart; Result Unstructured Data: Test Result:126; Comments: bpm abnormal racing
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Atrial septal defect
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1824329

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
KY
Alter
48,0
Geschlecht
M
Eingang
28.10.2021
Impfdatum
05.05.2021
Beginn
06.05.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Asthenia Chills Diarrhoea Dizziness Dyspnoea Headache Heart rate increased Lymphadenopathy Malaise Myalgia Nausea Pyrexia Renal pain SARS-CoV-2 test Vaccination site pain Vomiting

Symptomtext

Nausea; Headache; Extreme weakness/ So weak; Dizziness/ dizzy; Fast heart beat (sometimes wake me from sleep); Difficulty breathing; Sore at injection site; Sore muscles and joints; Sore muscles and joints; Chills; Fever; Swollen under arm Lymph node on same side as injection; One time vomiting (possibly unrelated to vaccine); Some diarrhea; Pain in kidney areas, sometimes left side, some time both sides; General feeling sick; This is a spontaneous report from a contactable consumer, the patient. A 48-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the left arm on 05May2021 at 14:30 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. Medical history included asthma and allergy to penicillin. Concomitant medications included montelukast (MANUFACTURER UNKNOWN) for an unknown indication from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within four weeks prior to the COVID-19 vaccine. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 14Apr2021 at 14:30 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. On 06May2021 at 05:30, the patient experienced nausea, headache, extreme weakness, dizziness, fast heartbeat (sometimes woke the patient from sleep), difficulty breathing, sore at injection site, sore muscles and joints, chills, fever, general feeling sick, swollen under arm lymph node on same side as injection, one time vomiting (possibly unrelated to vaccine), some diarrhea, pain in kidney areas, sometimes left side, sometime both sides, so weak and dizzy that he had to miss two days of work and too dizzy to drive. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had been tested for COVID-19. On an unknown date in 2021, the patient underwent antigen test via nasal swab and the result was negative. The clinical outcome of the events nausea, headache, extreme weakness/so weak, dizziness/dizzy, fast heartbeat (sometimes woke the patient from sleep), difficulty breathing, sore at injection site, sore muscles and joints, chills, fever, general feeling sick, swollen under arm lymph node on same side as injection, one time vomiting (possibly unrelated to vaccine), some diarrhea and pain in kidney areas, sometimes left side, sometime both sides was resolving at the time of the report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Test Date: 2021; Test Name: Antigen test; Test Result: Negative ; Comments: nasal swab
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Penicillin allergy (known allergies: penicillin)
Andere Medikamente
MONTELUKAST
Allergien
-
Vorherige Impfungen
-

VAERS 1824043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
42,0
Geschlecht
F
Eingang
28.10.2021
Impfdatum
09.04.2021
Beginn
09.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Back pain Chest pain Gait disturbance Maternal exposure during pregnancy Muscular weakness Paraesthesia Spinal pain

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 42-year-old pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EW0162) via an unspecified route of administration in the left arm on 09Apr2021 at 12:00 (vaccination at the age of 42-year-old and pregnant at the time of vaccination), as DOSE 1, SINGLE for COVID-19 immunisation. The patient's medical history of the patient included diabetic 2 and hsv2. The patient had a history of allergies to latex and penicillin on an unknown date and unknown if ongoing or not. Concomitant medications were reported as none. The patient gestation period was 9 weeks and delivery date was on 04Nov2021. It was reported that the patient last menstrual date was on 13Jan2021. The patient did not receive any other medications within two weeks prior to the vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient was pregnant during the vaccination on 09Apr21. On 11Apr2021 at 17:00, the patient's spine hurts and having trouble walking, weakness in the legs and chest pain, lower back pain felt like something sharp was poking. No therapeutic measures were taken for the events. The adverse events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The outcome of the events spine hurts, trouble walking, weakness in legs, chest pain and lower back pain felt like something sharp was poking was not recovered at the time of report.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Herpes simplex type II (hsv2); Latex allergy; Penicillin allergy; Type 2 diabetes mellitus (diabetic2.)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1818147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NH
Alter
63,0
Geschlecht
F
Eingang
26.10.2021
Impfdatum
23.04.2021
Beginn
19.06.2021
Tage bis Beginn
57,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Arrhythmia Blood test Cardiac flutter Dehydration Dizziness Echocardiogram Electrocardiogram Hypotension

Symptomtext

I had become dehydrated. June 19th - I had worked out really heavily in the day and I got dizzy that night. I tried to hydrate up. In the morning, I had a galloping heart - an arrhythmia - I went to ER dept. in the mid morning. They did a lot of testing. They gave me a medicine that I didn't tolerate. They gave me a beta blocker (Metoprolol) - and my heart started galloping all over the place - so they created more of an arrhythmia because I have low blood pressure. I went back two days later - they just sent me home but kept me on it. I communicated with my primary care doctor - and I had to wean have the drug - took two weeks to do that. . He gave me magnesium/potassium supplement and I've been fine since. Oh and they had given me Ziopatch - they had given me that at ER on the 20th. They took it off and read the report and it helped show why the doctor why was comfortable taking me off of the blood thinner. I have not had galloping, feeling dizzy times since being off the beta blocker and being on the magnesium/potassium. I still have minor heart flutters still have but have had that my whole life from time to time. I have stopped: alcohol, caffeine and chocolate - have stopped those triggers to help lessen things. I have a cardiologist now.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arrhythmia
Hospital-Tage
-
Labordaten
Blood work - metabolic ; EKG - showed PVCs (doublets and triplets - the arrhythmias); echocardiogram - that showed my heart function was okay - was functioning; magnesium phosphorus; blood gases; troponin - everything was normal. By that time I was rehydrated by that time and so my numbers were pretty good.
Aktuelle Erkrankungen
no
Vorgeschichte
Asthma - cold induced; Raynaulds Syndrome; Osteoarthritis
Andere Medikamente
no
Allergien
no
Vorherige Impfungen
-

VAERS 1817962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
VA
Alter
49,0
Geschlecht
F
Eingang
26.10.2021
Impfdatum
21.04.2021
Beginn
28.04.2021
Tage bis Beginn
7,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Condition aggravated Contusion Fatigue Headache

Symptomtext

Prior to receiving the vaccine, my platelet levels were in the normal range. After the 1st vaccine, I noticed fatigue within 1st 24 hrs. for several weeks. With the second vaccine, I had fatigue as well but now experience bruising that I did not have before. I have not received any treatments. My hematologist did not think the numbers were so severe that the needed to be treated. I was told to return to follow up and see where my number are. I also experienced headaches for the first month or so after the first vaccine. The same thing occurred after the second dose. I do not usually get headaches, so this is not normal for me.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Regular blood work to check platelet counts
Aktuelle Erkrankungen
None
Vorgeschichte
Chronic idiopathic hives ITP Herniated disc in neck
Andere Medikamente
Ritalin Xyzal multivitamin B12 D3 Gabapentin
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 1817536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
50,0
Geschlecht
F
Eingang
26.10.2021
Impfdatum
23.04.2021
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Dizziness Headache Nausea

Symptomtext

Killer headaches; Dizziness; Nausea; Has been experiencing "killer" headaches. She states that this morning it is "really bad"; This is a spontaneous report from a contactable consumer or other non hcp (patient) via medical information team. A 50-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection; batch or lot Number: EW0162) via an unspecified route of administration, administered in right arm on 23Apr2021 morning at 9:30 (at the age of 50-years-old) as dose 1, single dose for covid-19 immunization. The patient medical history included high blood pressure from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported but patient stated took small dose of medication for high blood pressure. On an unspecified date, the patient experienced killer headaches, this morning it is really bad and stated that she is also having dizziness and nausea. Patient received the first dose yesterday but she is experiencing a severe headache. She already took Ibuprofen orally one last night and one this morning, took one 800 mg tablet it's the prescription that she had last year for something else but it helped little but today it got worse. Patient concerned that she had a headache yesterday and this morning it's getting worse, and she took Ibuprofen last night but today it's not helping. She would like to know if it is safe to take Excedrin to treat her symptoms, as she is worried about a potential interaction between it and the vaccine. Response received as there is no information regarding a potential interaction between the vaccine and Excedrin. Spoke from the attached document to let caller know about CDCs considerations that medications used to reduce pain can be taken after vaccination to treat symptoms, but let caller know that it does not specify Excedrin. Referred caller to HCP for further guidance. Unaddressed medical questions referred or forwarded to medical Information. Therapeutic measures were taken as a result of all the events. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high.
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1815673

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NV
Alter
47,0
Geschlecht
F
Eingang
25.10.2021
Impfdatum
20.04.2021
Beginn
20.05.2021
Tage bis Beginn
30,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Mobility decreased Muscle spasms Pain Pain in extremity Tendonitis X-ray limb abnormal

Symptomtext

My arm hurts. Sometimes I get spasms. I could only raise it to a certain level and it begins to hurt. I saw a doctor and they gave me a shot for the pain. The shot helped a little bit but my arm still hurts a little bit and that bothers me. Tiredness; fatigue all the time. General body aches-especially on my left-side.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
X-ray on my left shoulder-found tendinitis.
Aktuelle Erkrankungen
None
Vorgeschichte
High Blood Pressure; Arthritis
Andere Medikamente
Lisinopril 20mg; Euthyrox 25mg; Vitamin D 25mg; Montelukast 10mg Ibuprofen 800mg
Allergien
None
Vorherige Impfungen
-

VAERS 1814698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NV
Alter
67,0
Geschlecht
F
Eingang
25.10.2021
Impfdatum
16.04.2021
Beginn
08.06.2021
Tage bis Beginn
53,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Herpes zoster Paraesthesia Rash

Symptomtext

I had tingling and rash on my right face. It took two or three weeks to go away. I went to see my doctor about this. They told me that I had Shingles. They gave me an antivirus medicine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
Codeine
Vorherige Impfungen
-

VAERS 1812312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
IN
Alter
55,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
23.04.2021
Beginn
24.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Condition aggravated Contusion Inappropriate schedule of product administration Incorrect route of product administration SARS-CoV-2 test negative Vaccination site erythema Vaccination site swelling Vaccination site warmth

Symptomtext

the dose was administered "too low, and into the fatty part of my arm".; dose 1st dose on 20Apr2021 and 2nd dose on 23Apr2021; have redness and swelling near the injection site, which traveled down her arm, and around to her back; have redness and swelling near the injection site, which traveled down her arm, and around to her back; the area is "very warm to the touch"; brusing; Spread past injection site from back of arm to back side of torso; This is a spontaneous report from a contactable consumer (patient). A 55-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, lot number: EW0162, Expiry date: unknown) (age at the time of vaccination was 55 years, patient was non-pregnant at the time of vaccination), administered in Arm Right on 23Apr2021 as dose 2, single for COVID-19 immunization. The patient's medical history included seizure, asthma, drug allergy to phenergan. The patient's concomitant medication included Lamotrigin, montelukast, cetrizine and losartan. The patient did not take any other vaccine in four weeks prior COVID -19 vaccine. She was not diagnosed with COVID prior vaccination and tested negative with COVID post vaccination. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: ER975), via an unspecified route of administration, administered in Arm Right on 20Apr2021 at 12:00 as dose 1, single for COVID-19 immunization. On 24Apr2021, the patient started to have redness and swelling near the injection site, which traveled down her arm and around her back. The patient reported that the area was warm to touch. The patient has been seen by primary care and visited the emergency room and they told to take an antihistamine treatment. The patient believe that the dose may have been given incorrectly. The patient stated that the person who administered the dose was joking around, walking too much and not paying attention to what she was doing, and thinks that the dose was administered too low and into the fatty part of her arm. On 20Apr2021 the patient took first dose and on 23Apr2021 the patient took the second dose. The patient's treatment included antibiotic. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Test Date: 20201128; Test Name: Spit Test; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Seizure
Andere Medikamente
LAMOTRIGIN; MONTELUKAST; CETRIZINE; LOSARTAN
Allergien
-
Vorherige Impfungen
-

VAERS 1812252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NC
Alter
38,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
20.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Breast pain Fatigue Malaise Musculoskeletal chest pain Paraesthesia oral Stomatitis Tremor

Symptomtext

Tongue got tingly; Mouth is like if she's eating a sour gummy bear, it was very watery; Very tired; Not feeling well; Body was shaking when she was awake; Weird pain on her right side on her rib; pain shoulder; Pain under my breast; This is a spontaneous report from a contactable consumer. This consumer (patient) reported for herself that, A 38-years-old female patient received bnt162b2 (BNT162B2, Formulation: Solution for injection, Batch/Lot Number: EW0162) (at the age of 38 years old), dose 1 via an unspecified route of administration on 20Apr2021 as dose 1, single for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. On an unspecified date in Apr2021, the patient experienced, she did not remember when she had her first shot. She received the first shot on 20Apr2021. When she had her first shot, her tongue got tingly, like a tingly sensation, and her mouth was like she was eating a sour gummy bear, it was very watery. She further described as it would come and go for the first day she took the vaccine, she thought the second one too. She was very tired, not feeling well, her body was shaking when she was awake. She also had this weird pain on her right side on her rib. She did not know what it was, it was still not going away. It was not like she broke something, but she had herself doing exercise or something, it was kind of there, the pain. She had never had the pain before, she did not know if it was due to vaccine. She had pain under her breast and shoulder and a few days after she received the shot, she had sour taste in her mouth, the latter has resolved in 2021. The outcome of all the events was unknown, and the outcome of the event mouth is like if she's eating a sour gummy bear, it was very watery was recovered on an unspecified date in 2021 and Weird pain on her right side on her rib was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Musculoskeletal chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1811441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NY
Alter
38,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
17.04.2021
Beginn
22.04.2021
Tage bis Beginn
5,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Dyspnoea Fatigue Feeling abnormal Pain SARS-CoV-2 test

Symptomtext

Severe body aches; Shortness of breath; Chest pains; Brain fog; Fatigue; This is a spontaneous report from a contactable consumer, the patient. A 38-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the left arm on 17Apr2021 at 13:45 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included unspecified birth control medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took sulfur (MANUFACTURER UNKNOWN) and experienced drug allergy. On 22Apr2021 at 23:00, the patient experienced severe body aches, shortness of breath, chest pains, brain fog and fatigue. On 23Apr2021, the patient underwent SARS-CoV-2 test (blood test) and the result was negative. The event resulted in emergency room/department or urgent care. No therapeutic measures were taken as a result of the events. Since the vaccination, the patient had been tested for COVID-19. The clinical outcome of the events severe body aches, shortness of breath, chest pains, brain fog and fatigue was resolving at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Test Date: 20210423; Test Name: SARS-CoV-2 test; Test Result: Negative ; Comments: Blood test
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1811015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
41,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Headache Myalgia Neuralgia Pain Paraesthesia

Symptomtext

This is a spontaneous report from a contactable consumer, the patient. A 41-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the right arm on 19Apr2021 at 10:15 (at the age of 41-years-old) as a single dose for COVID-19 immunisation. Medical history included rheumatoid arthritis, exercise-induced asthma and known allergies to sulfa, tomatoes, dust mites, and ragweed. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included fluoxetine hydrochloride (PROZAC), meloxicam (MANUFACTURER UNKNOWN), bupropion hydrochloride (WELLBUTRIN) and trazodone (MANUFACTURER UNKNOWN); all from unknown dates for unknown indications and unknown if ongoing. The patient previously received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8732) via an unspecified route of administration in the right arm on 29Mar2021 at 10:00 (at the age of 41-years-old) as a single dose for COVID-19 immunisation. The patient previously received chlorhexidine gluconate (HIBICLENS), ciprofloxacin hydrochloride (CIPROFLOXACIN) and levofloxacin (LEVAQUIN) on unknown dates for unknown indications and experienced drug allergy. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 19Apr2021 at 11:00, the patient experienced pain between scapulae and ribs and it felt like nerve pain, a light tingling sensation in arms, muscle aches, bad headache and chills. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events pain between scapulae and ribs, nerve pain, light tingling sensation in arms, muscle aches, bad headache and chills were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Arthritis rheumatoid; Asthma exercise induced; Fruit allergy (Known allergies: Tomatoes); House dust mite allergy (Known allergies: Dust mites); Ragweed allergy (Known allergies: Ragweed); Sulfonamide allergy (Known allergies: Sulfa.)
Andere Medikamente
PROZAC; MELOXICAM; WELLBUTRIN; TRAZODONE.
Allergien
-
Vorherige Impfungen
-

VAERS 1238624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
56,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
19.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure measurement Bone pain Headache Hypertension Myalgia Nausea Pyrexia Vomiting

Symptomtext

Headache; All over bone/muscle aches; All over bone/muscle aches; Nausea; Vomiting; High blood pressure; This is a spontaneous report from a contactable consumer, the patient. A 56-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the right arm on 19Apr2021 at 10:30 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. Medical history included irritable bowel syndrome (IBS), high blood pressure, high cholesterol, and sulfonamide allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient had received other medication which was not specified within two weeks of vaccination for unknown indication on unknown date. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER2613) via an unspecified route of administration in the right arm on 29Mar2021 at 10:30 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. The patient previously took sulfur (MANUFACTURER UNKNOWN) and experienced drug allergy known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unknown date in Apr2021 at 03:00, the patient experienced headache, all over bone and muscle aches, nausea, vomiting, high blood pressure. Therapeutic measures were not taken as a result of the events. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, all over bone and muscle aches, nausea, vomiting, high blood pressure was resolved on an unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
Test Date: 202104; Test Name: Blood pressure; Result Unstructured Data: Test Result:High Blood Pressure; Comments: at 03:00
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; High cholesterol; Irritable bowel syndrome (IBS); Sulfonamide allergy (known allergies: sulfa/sulfer)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1238624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
56,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
19.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure measurement Bone pain Headache Hypertension Myalgia Nausea Pyrexia Vomiting

Symptomtext

Headache; All over bone/muscle aches; All over bone/muscle aches; Nausea; Vomiting; High blood pressure; This is a spontaneous report from a contactable consumer, the patient. A 56-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the right arm on 19Apr2021 at 10:30 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. Medical history included irritable bowel syndrome (IBS), high blood pressure, high cholesterol, and sulfonamide allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient had received other medication which was not specified within two weeks of vaccination for unknown indication on unknown date. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER2613) via an unspecified route of administration in the right arm on 29Mar2021 at 10:30 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. The patient previously took sulfur (MANUFACTURER UNKNOWN) and experienced drug allergy known allergies. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unknown date in Apr2021 at 03:00, the patient experienced headache, all over bone and muscle aches, nausea, vomiting, high blood pressure. Therapeutic measures were not taken as a result of the events. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events headache, all over bone and muscle aches, nausea, vomiting, high blood pressure was resolved on an unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
Test Date: 202104; Test Name: Blood pressure; Result Unstructured Data: Test Result:High Blood Pressure; Comments: at 03:00
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; High cholesterol; Irritable bowel syndrome (IBS); Sulfonamide allergy (known allergies: sulfa/sulfer)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1235392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NY
Alter
38,0
Geschlecht
F
Eingang
23.10.2021
Impfdatum
16.04.2021
Beginn
20.04.2021
Tage bis Beginn
4,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Feeling hot Paraesthesia Pruritus Rash erythematous Flushing

Symptomtext

"My" neck began to itch, "I" rubbed it with "my" hands for a few minutes and then it started to tingle; "I" went to look in the mirror and noticed that "my" neck and "my" face, were red.; "I" then began to feel a warm sensation on "my" arms and legs/ The warm, rushing sensation in "my" extremities lasted for about 5 minutes.; upon looking at them, "I" noticed red rashes around "my" elbows and knees/Around 2 hours later, the rashes were completely gone.; "My" neck began to itch, "I" rubbed it with "my" hands for a few minutes and then it started to tingle; This is a spontaneous report from a contactable consumer, the patient. A 38-year-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the right arm on 16Apr2021 at 09:15 (at the age of 38-years-old) as a single dose for COVID-19 immunisation. The medical history included fibromyalgia, anxiety, panic disorder, depression, kidney stones, allergy to nickel which caused dermatitis and allergy to contrast dye which caused anaphylaxis. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The concomitant medications included escitalopram (MANUFACTURER UNKNOWN), vitamin b complex (VITAMIN B), ascorbic acid (VITAMIN C), vitamin d nos (VITAMIN D) and probiotic (unspecified); all for unknown indications from unknown dates and unknown if ongoing. On 20Apr2021, around 11:10, the patient's neck began to itch, she rubbed it with her hands for a few minutes and at 11:15, it started to tingle, she went to look in the mirror and noticed that her neck and her face were red. The patient then began to feel a warm sensation on her arms and legs and upon looked at them, she noticed red rashes around her elbows and knees. The warm, rushing sensation in her extremities lasted for about 5 minutes. The rashes were began to subside at that point. Around 2 hours later, the rashes were completely gone. The adverse events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events neck began to itch, then it started to tingle, neck and face were red was unknown, while the clinical outcome of the event felt a warm sensation on arms and legs was resolved on 20Apr2021 at 11:20 and red rashes around elbows and knees was resolved on 20Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Anaphylaxis (Allergy to Contrast dye (anaphylaxis)); Anxiety; Contrast media allergy (Allergy to Contrast dye (anaphylaxis)); Depression; Dermatitis (Allergy to Nickel (dermatitis)); Fibromyalgia; Kidney stones; Nickel sensitivity (Allergy to Nickel (dermatitis)); Panic disorder
Andere Medikamente
ESCITALOPRAM; VITAMIN B [VITAMIN B COMPLEX]; VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]
Allergien
-
Vorherige Impfungen
-

VAERS 1229740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
37,0
Geschlecht
M
Eingang
23.10.2021
Impfdatum
29.03.2021
Beginn
30.03.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Adverse drug reaction Chest discomfort Dyspnoea Lung disorder

Symptomtext

Shortness of breath. It wasn't a heart attack. It was just as if "I" could not get a full breath.; As if "my" chest was tight/restricted from expanding all the way.; Beyond the common side-effects, which lasted for one week, I also had shortness of breath.; This is a spontaneous report from a contactable consumer, the patient. A 37-year-old male patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8732) via an unspecified route of administration in the arm left on 29Mar2021 at 10:30 (at the age of 37-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient was not a smoker and didn't have any underlying health issues. The patient exercise frequently and eat healthy. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The concomitant medications included methylphenidate hydrochloride (RITALIN); for an unknown indication from an unknown date and unknown if ongoing. On an unknown date in 2021, the patient experienced beyond the common side-effects, which lasted for one week. On 30Mar2021, the patient also experienced shortness of breath. It wasn't a heart attack. It was just as if he could not get a full breath. As if the patient's chest was tight/restricted from expanding all the way. The shortness of breath lasted for about two weeks. The adverse events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events chest tight/restricted from expanding all the way was recovering, while the clinical outcome of event shortness of breath/ could not get a full breath was recovered on an unknown date in Apr2021 and beyond the common side-effects, which lasted for one week resolved on unspecified date in 2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
RITALIN
Allergien
-
Vorherige Impfungen
-

VAERS 1807810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
61,0
Geschlecht
F
Eingang
22.10.2021
Impfdatum
20.04.2021
Beginn
20.05.2021
Tage bis Beginn
30,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arrhythmia Cardiac monitoring Cardiac stress test Computerised tomogram coronary artery Condition aggravated Echocardiogram Electrocardiogram Ultrasound Doppler Ventricular extrasystoles

Symptomtext

A month after the vaccine, 05/20/2021- my arrhythmia from Micro Valve Prolapse got significantly worse. I don't know if that is the vaccine or if that is just age, I just don't know. I went to my PCP, and he referred me to Cardiologist.. It was in August, before I saw Dr. They put me through several heart related test. And now have me taking a Beta blocker, Metoprolol 25 mg once a day. The outcome was that my Calcium Score was only 16. My heart was strong. the heart monitor showed 23 PVC's a minute.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arrhythmia
Hospital-Tage
-
Labordaten
EKG echocardiogram Stress Test Calcium Scoring Heart Monitor for 48 hours aortic scan - fine
Aktuelle Erkrankungen
Joint Pain
Vorgeschichte
High Cholesterol Micro Valve Prolapse Acid Reflux
Andere Medikamente
Simvastatin 20 mg Once a day Multivitamins
Allergien
Hay Fever Type Allergies Aleve
Vorherige Impfungen
-

VAERS 1804792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
VA
Alter
43,0
Geschlecht
F
Eingang
21.10.2021
Impfdatum
20.04.2021
Beginn
12.09.2021
Tage bis Beginn
145,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Ageusia Anosmia COVID-19 Chills Fatigue Feeling abnormal Feeling cold Injected limb mobility decreased Injection site pain Night sweats Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On the day I received my second dose I had soreness in my left arm and could not lift it. I also had body aches, low grade fever, chills and night sweats that lasted about 12 hours. On 09/12/2021 I felt like I was cold and was having body aches and runny nose and congestion. My symptoms worsened for the next few days. I started having night sweats and chills and a fever of 100.1. On 9/15/2021 I have a virtual visit with my doctor, and they thought I had bad allergies and prescribed steroids. The next day I lost my sense of taste and smell. The fever had improved but I was still fatigued and having night sweats, congestion, and drainage. I got a COVID-19 test on 9/21/2021 and tested positive. At that point my symptoms were improving so I just isolated at home, drank fluids, and took Tylenol. I experienced brain fog and fatigue for another 2 weeks. I learned several people I had been with all the same symptoms. Five of us in total. However, everyone else that was tested, tested negative.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injected limb mobility decreased
Hospital-Tage
-
Labordaten
COVID-19 test 9/21/2021- positive
Aktuelle Erkrankungen
None
Vorgeschichte
Hypothyroidism Prediabetes Obesity High blood pressure PCOS
Andere Medikamente
Levothyroxine 88mcg once daily Montelukast 10 mg once daily Cymbalta 20mg once daily Allegra 180 mg once daily Metformin 100mg twice daily Vitamin d 4000iu daily Odactra 12sq hdm once daily
Allergien
ChloraPrep with dye causes rash
Vorherige Impfungen
-

VAERS 1801795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TN
Alter
69,0
Geschlecht
F
Eingang
20.10.2021
Impfdatum
20.04.2021
Beginn
15.05.2021
Tage bis Beginn
25,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Condition aggravated Culture stool Dehydration Impaired work ability Irritable bowel syndrome Laboratory test Pyrexia

Symptomtext

Went to the ER and was really dehydrated. I had constant IBS and it was every day. I had a fever and weakness and headaches. On May 16 I had an IBS attack, and on the 24th. It lasted until the 28th. I couldn't go to work, it just wouldn't stop. I started an antibiotic on the 31st of May. I had a fever on the 3rd of June. Until the 11th of June. They gave me extra sugar through an IV. I'm on my second round of antibiotics, I had an attack on Monday. I'm taking Xifaxan 550 mgs twice a day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
A had a few test at the hospital but I don't remember. Nothing came back bad. I had a stool test performed.
Aktuelle Erkrankungen
None
Vorgeschichte
Epilepsy; IBS issues; but not like what I'm experiencing right now.
Andere Medikamente
Tremadone; atorvastatin; lisinopril; vitamins I take a lot; Alive! women's 50 plus; Biactive with calcium K; D; D3
Allergien
Dilantin; Tegretol; Zarontin; antibiotics; ciprofloxacin
Vorherige Impfungen
-

VAERS 1801784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
PA
Alter
70,0
Geschlecht
F
Eingang
20.10.2021
Impfdatum
16.04.2021
Beginn
24.04.2021
Tage bis Beginn
8,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Antinuclear antibody Arthritis Blood folate Blood thyroid stimulating hormone Blood uric acid Fatigue Glomerular filtration rate Glycosylated haemoglobin Inflammation Injection site pain Lipids Loss of personal independence in daily activities Magnetic resonance imaging Metabolic function test Mobility decreased Pain Rheumatoid factor Vitamin B12

Symptomtext

Starting at the end of April I started feeling pain in my left shoulder. Finally on May 20th I went to a Chiropractor office. I had continued pain in my left shoulder so I was hoping they would relieve it. I went to them through June. Then finally on May 26th I went to my primary care physician for a check up. I continued on June 22nd with my primary care physician. I had an inflammation of PMR above the shoulder and hip joints. It seemed to be something was wrong with my rotator cuff. They thought it was a possible tear or tendon. That was the initial feeling. From there it progressed to my right shoulder but not at the rotator cuff. It progressed to my hips and my legs and essentially to my eyes and my skin. During those five months I was in complete agony and was going to physical therapy. I found it difficult to get out of bed in the morning due to the pain. During the morning I would also be very fatigued. Over the period of five months I was pretty much not able to be active as I had been. Currently I'm on prednisone under the care of a rheumatologist. I have improved with the prednisone, I was prescribe at 15mg for 15 weeks. Currently I'm at 12.5mg for 15 weeks until my next appointment with her. In between the rheumatologist appoint. I became under the care of a man who had a business called "Restorative Pain Care" and he changed my medication from Escitalopram and Bupropion to Cymbalta. Now I'm on Prednisone and Cymbalta. The prednisone has been very effective at this point. I feel better and more energetic.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
Test Done on 05/26/2021 Blood test -Glomerular Filtration rate estimated, Lipids Screen, H hema profile HME, TSHW Profile T4, Comprehensive metabolic panel, Vitamin B12 Level, Folate, RPR, X-Ray, MRI. Test Done on 07/26/2021 Hemoglobin A1C, Rheumatoid Factor ASSAY, Cyclyc Citiul Peptide ABIGG, Anti Nuclear anti body, Sedimentation Rate, CRP Non Cardiac, Uric Acid
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Escitalopram 10mg, Bupropion HCL 300mg
Allergien
-
Vorherige Impfungen
-

VAERS 1795251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
88,0
Geschlecht
F
Eingang
18.10.2021
Impfdatum
07.05.2021
Beginn
09.10.2021
Tage bis Beginn
155,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Anaemia Blood folate normal COVID-19 Condition aggravated Cytopenia Decreased appetite Diarrhoea Electrophoresis protein Hypersomnia Nausea Respiration abnormal SARS-CoV-2 test positive Vitamin B12 normal Vomiting

Symptomtext

Hospitalized; COVID-19 positive (10.9.21); Fully vaccinated Attending Physician: MD Date of Admission: 10/9/2021, Hospital Day: 5 Date of Discharge: 10/13/2021 PRESENTING PROBLEM: COVID-19 virus infection [U07.1] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 88 y.o. female with a history of chronic expressive aphasia secondary to TBI in 2018 as well as hypertension, B12 deficiency, chronic osteoarthritis with hip pain, who lives with her daughter and son-in-law. At baseline the patient has expressive aphasia, but is able to understand speech and follow commands. Patient is able to feed herself and is independent in her ADLs. Patient's daughter reports that she had noted the patient to be panting yesterday, and also noted decreased appetite. She also observed her mother to be sleeping most of the day yesterday. Today she had an episode of explosive diarrhea with nausea and vomiting. The patient did have C difficile in May of 2021, and because of her diarrhea she was brought to the emergency department. The patient nausea, vomiting and diarrhea slowly improved. Likely due to COVID-19. She was treated supportively. Her diet was advanced and tolerated. Her diarrhea resolved. Hematology evaluated her due to her anemia and thrombocytopenia which they feel is reactive. Her folate and B12 levels were checked and were normal. SPEP pending. Patient will follow up with PCP. Daughter indicated that she is looking for a nursing home for the patient as her husband (daughter's) just had a heart attack and has hip pain and inability to take care of patient for too long. The patient will isolate until 10/19. PT/OT evaluated her and recommended home with assist. She was discharged with daughter to her home in the meantime in stable and improved condition. Active Issues Requiring Follow-up Issue: covid infection Recommended follow-up provider/specialty: pcp for cytopenias What is needed: CBC, possible hematology referral if does not resolve (hematology felt that this is reactive due to covid)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
5,0
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
History of adenomatous polyp of colon Primary osteoarthritis involving multiple joints Diverticulosis Spinal stenosis Essential hypertension Osteopenia B12 deficiency Recurrent major depressive disorder, in partial remission Generalized anxiety disorder Pure hypercholesterolemia Altered mental status History of Clostridioides difficile colitis Expressive aphasia Vascular dementia without behavioral disturbance Nausea vomiting and diarrhea Thrombocytopenia
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet Calcium-Phosphorus-Vitamin D (CALCIUM GUMMIES PO) citalopram (CELEXA) 20 MG tablet gabapentin (NEURONTIN) 100 MG capsule losartan (COZAAR) 25 MG tablet Multiple Vitamins-Minerals (ZINC PO) traMADol (ULT
Allergien
NKDA
Vorherige Impfungen
-

VAERS 1793232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MA
Alter
41,0
Geschlecht
M
Eingang
16.10.2021
Impfdatum
19.04.2021
Beginn
19.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal discomfort Diarrhoea Erythema Gastrointestinal disorder Pain in extremity Palmar erythema Paraesthesia

Symptomtext

Left hand erythema/Lines in his hands seemed to be exaggerated; Left hand erythema/Lines in his hands seemed to be exaggerated; Upset stomach; Some diarrhea; Soreness in arm; His GI complaints started about maybe 2 to 3 hours after the vaccine.; Tingling in his scalp on the left side/Tingling on lateral aspect of abdominal wall; This is a spontaneous report from a contactable other hcp (patient). A 41-years-old male patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EW0162) via an unspecified route of administration on 19Apr2021 at 10:30 (at the age of 41-year-old) as dose 1, single for COVID-19 immunisation. The patient medical history included he has put on a few pounds from lockdown. Concomitant medications were not reported. History of all previous immunization with the Pfizer vaccine considered as suspect was reported as none. Historical vaccine reported as He has gotten flu shots. Additional vaccines administered on same date of the Pfizer Suspect was reported as none. Prior Vaccinations (within 4 weeks) was reported as none. Patient family medical history was reported as none. Relevant Tests reported as none. On 19Apr2021 the patient experienced left hand erythema/lines in his hands seemed to be exaggerated, tingling in his scalp on the left side/tingling on lateral aspect of abdominal wall, upset stomach, some diarrhea, soreness in arm, his gi complaints started about maybe 2 to 3 hours after the vaccine. It reported that about 4 to 6 hours later on the same side of his body that he had the shot he started having some symptoms. On his left hand he had some erythema, and the lines in his hands seemed to be exaggerated where the lines were deeper. He had tingling in his scalp on the left side. Also on the lateral aspect of his abdominal wall he had the same type of sensation. He didn't see anything on his abdominal wall and he didn't shave to see his scalp. It was reported that like his symptoms would appear and disappear over the course of a day. It was reported that 2 to 3 hours after he got the shot he had an upset stomach and some diarrhea. The patient stated that when his hand thing showed up his wife said it looked like it would be itchy. It was not itchy but he could tell it was not normal.It was not burning or itching but there was something wrong with his hand how he described. He is wondering if it is still safe to get the second shot. It was reported that the erythema was coming and going. It is weird how things were transient, and it was kind of rotating between 3 different spots. Other than the soreness everything has recovered completely. Patient not received treatment for the events. Outcome of the event soreness in arm was not recovered and other events was recovered on 19Apr2021. No follow-up attempts are needed. No further information is expected

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Weight gain
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1793134

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
KY
Alter
31,0
Geschlecht
F
Eingang
16.10.2021
Impfdatum
14.04.2021
Beginn
15.04.2021
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Epistaxis Migraine Muscle spasms Myalgia

Symptomtext

Migraine; Nosebleed; extreme Charlie Horse type pain in my legs; some muscle pain for several more in legs andupper arms.; This is a spontaneous report from a contactable nurse. A 31-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the right arm on 14Apr2021 at 10:45 (at the age of 31-year-old) as a single dose for COVID-19 immunisation. The patient did not have any medical history and no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included adapalene (DIFFERIN) from an unknown date for an unknown indication and was unknown if ongoing. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 15Apr2021 at 02:00, in the early morning hours after getting the vaccine, the patient experienced extreme Charlie Horse type pain in the leg which abruptly woke the patient and was hurt badly for about an hour. It was slowly calmed down but later on the same day, the patient had some muscle pain for several more in her legs and upper arms. On 16Apr2021, day two, the patient had a migraine which was not normal for the patient and also had a nosebleed. It was reported that she did not have a nosebleed for many years. The events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and the emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events extreme Charlie Horse type pain in legs and muscle pain recovered on an unknown date in Apr2021 while that of the event migraine and nosebleed was recovered on 16Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
DIFFERIN
Allergien
-
Vorherige Impfungen
-

VAERS 1792987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
DC
Alter
31,0
Geschlecht
M
Eingang
16.10.2021
Impfdatum
15.04.2021
Beginn
16.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Dizziness Fatigue Headache Heart rate Heart rate increased Hyperhidrosis Pain Paraesthesia SARS-CoV-2 test Tremor

Symptomtext

Chills; Sweating; Body aches; Poking sensation in bicep away from where the shot was given; Headache; Shaking/jittery; Extreme tiredness; Dizziness; Resting heart rate doubled from normally 40 to nearly 90bpm; This is a spontaneous report from a contactable consumer, the patient. A 31-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the left arm on 15Apr2021 at 11:45 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. Medical history included allergy. It was reported that the patient was fairly healthy and the patient's family has history of heart issues. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included fluticasone propionate (FLONASE) for allergy from an unknown date and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6208) via an unspecified route of administration in the left arm on 26Mar2021 at 11:30 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. On 16Apr2021 at 00:00 the patient experienced chills; then followed by sweating; body aches; poking sensation in bicep away from where the shot was given, not near it; headache; shaking/jittery; extreme tiredness; dizziness and resting heart rate doubled from normally 40 to nearly 90bpm (beats per minute). The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No therapeutic measures were taken as a result of the events. On 14Apr2021, the patient underwent nasal swab test (SARS-CoV2-test) and the result was negative. Since the vaccination, the patient had been tested for COVID-19. The clinical outcome of the events chills; then followed by sweating; body aches; poking sensation in bicep away from where the shot was given, not near it; headache; shaking/jittery; extreme tiredness; dizziness and resting heart rate doubled from normally 40 to nearly 90bpm was recovering at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
Test Date: 20210416; Test Name: Resting heart rate; Result Unstructured Data: Test Result:90 bpm; Comments: Doubled from normally 40 to nearly 90bpm; Test Date: 202104; Test Name: Resting heart rate; Result Unstructured Data: Test Result:40bpm; Test Date: 20210414; Test Name: SARS-CoV-2 test; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy
Andere Medikamente
FLONASE [FLUTICASONE PROPIONATE]
Allergien
-
Vorherige Impfungen
-

VAERS 1792936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
29,0
Geschlecht
M
Eingang
16.10.2021
Impfdatum
15.04.2021
Beginn
15.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Contusion Fall Feeling abnormal Feeling hot Oxygen saturation Tremor

Symptomtext

Patient was sitting in a chair after given the Covid-19 vaccine and felt fuzzy; fell to the ground; and hit his face with some bruising; Witness notice he was shaking for a few seconds after the fall.; His skin felt fine warm when touch.; This is a spontaneous report received from a contactable Pharmacist. A 29-years-old male patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EW0162) dose 1, intramuscularly administered in Arm Left on 15Apr2021 at 12:15 (at the age of 29-year-old) as dose 1, single for covid-19 immunization. Patient medical history was reported as none and patient's concomitant medications were not reported. other medications in 2 weeks was unknown. Patient was not covid positive before vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and patient has not been tested for COVID-19 since the vaccination. On 15Apr2021 at 12:30 Patient was sitting in a chair after given the Covid-19 vaccine and felt fuzzy and fell to the ground and hit his face with some bruising. Witness notice he was shaking for a few seconds after the fall. He recovered conscious quickly and breath normal and said he was fine. His skin felt fine warm when touch. Paramedics came really quick and measure his oxygen levels and left shortly as his vitals are fine. Relevant laboratory tests included oxygen levels; result was unknown on 15April2021.They instructed him to seek emergency room if any symptoms arise. No treatment was received for the events. The outcome of event was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
Test Date: 20210415; Test Name: oxygen levels; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1792923

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
GA
Alter
17,0
Geschlecht
M
Eingang
16.10.2021
Impfdatum
14.04.2021
Beginn
15.04.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Dyspnoea Insomnia Nasopharyngitis Restlessness

Symptomtext

unable to sleep or rest comfortably; cold; feeling like he couldn't breathe; felt like his chest was being compressed and was very restless; felt like his chest was being compressed and was very restless; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). A 17-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EW0162), dose 2 via an unspecified route of administration, administered in Arm Left on 14Apr2021 at 11:45 (age at the time of vaccination was 17 years) as DOSE 2, SINGLE for covid-19 immunisation at Hospital. Medical history included occassional vasovagal syncope from an unknown date and unknown if ongoing and known allergies were reported as no. Concomitant medication(s) and other medications in two weeks included ibuprofen (ADVIL [IBUPROFEN]) and vitamins nos (FLINTSTONES) both taken for an unspecified indication, start and stop date were not reported. Historically the patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EP6955) via an unspecified route of administration, administered in Arm Left on 25Mar2021 at 11:30 (age at the time of vaccination was 17 years) as DOSE 1, SINGLE for covid-19 immunisation. Other vaccine in four weeks was reported as no. The patient did not have covid prior to vaccination. On n 15Apr2021 at 05:30, the patient was unable to sleep or rest comfortably, cold, feeling like he couldn't breathe and felt like his chest was being compressed and was very restless. It was reported that, the patient woke up in the middle of the night, cold, and feeling like he couldn't breathe. He felt like his chest was being compressed and was very restless. The chest compression scared him and caused him to be unable to sleep or rest comfortably. He has since recovered and was feeling better. The patient was not tested for covid post vaccination. The treatment for ae was not received. The outcome of all the events was recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Vasovagal symptoms
Andere Medikamente
ADVIL [IBUPROFEN]; FLINTSTONES
Allergien
-
Vorherige Impfungen
-

VAERS 1792883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NY
Alter
54,0
Geschlecht
M
Eingang
16.10.2021
Impfdatum
12.04.2021
Beginn
12.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Axillary pain Chest pain Dyspnoea Pain in extremity Vaccination site swelling

Symptomtext

Swelling at injection site; Severe pain shooting through arm to armpit and allthe way to middle of chest.; Shortness of breath; Severe pain shooting through arm to armpit and allthe way to middle of chest.; Severe pain shooting through arm to armpit and allthe way to middle of chest.; This is a spontaneous report from a contactable consumer, the patient. A 54-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the arm left on 12Apr2021 at 09:00 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. Medical history included chiari and high blood pressure. Concomitant medications included morphine hydrochloride (MORPHINE), hydrocodone bitartrate (HYDROCODONE), tizanidine (MANUFACTURER UNKNOWN) and amlodipine besilate (AMLODIPINE) started on an unknown date for unknown indication and unknown if ongoing. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: UNKNOWN) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 12Apr2021 at 20:00, the patient experienced swelling at injection site, severe pain shooting through arm to armpit and all the way to middle of chest and shortness of breath. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events swelling at injection site, severe pain shooting through arm to armpit and all the way to middle of chest and shortness of breath were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high (high blood pressure); Chiari malformation (Chiari)
Andere Medikamente
MORPHINE; HYDROCODONE; TIZANIDINE; AMLODIPINE
Allergien
-
Vorherige Impfungen
-

VAERS 1785695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NJ
Alter
30,0
Geschlecht
M
Eingang
14.10.2021
Impfdatum
17.04.2021
Beginn
17.04.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia Imaging procedure Paraesthesia

Symptomtext

Leg/knee numbness and tingling

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
Radiology - DVT - Negative Approx. 1 week after vaccine
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma
Andere Medikamente
-
Allergien
Caffeine, Albuterol (intolerance), Amoxicillin (intolerance)
Vorherige Impfungen
-

VAERS 1785252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
AZ
Alter
24,0
Geschlecht
F
Eingang
14.10.2021
Impfdatum
15.04.2021
Beginn
21.09.2021
Tage bis Beginn
159,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Ageusia Anosmia COVID-19 Chills Cough Dyspnoea Headache Malaise Myalgia Nasal congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Complaint of shortness of breath, difficulty breathing, cough, chills, headache, runny nose/congestion, loss of taste and smell, myalgia and malaise.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Positive Covid-19 test at an Urgent care, unknown type.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1782846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
AK
Alter
62,0
Geschlecht
F
Eingang
13.10.2021
Impfdatum
11.04.2021
Beginn
14.04.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthma Blood glucose increased Blood pressure increased Blood test Condition aggravated Cough Wheezing

Symptomtext

Blood sugar was high and that was the first thing that happened. It eventually went back to normal. Some time in the summer during the first week of July, I had a flare up of asthma with lots of wheezing and coughing. I had to go back on rescue meds. And at some point in the summer, I also had a great increase in my blood pressure. I?m not sure when that started because I had only been doing virtual visits, but at a doctor visit my BP was really high and had to go to my PCP. We?re still working on that now and I?m currently on several medications and my BP is still not where it needs to be.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
N/A at the time, but has had blood tests, heart tests, and everything came back the same as it was before the vaccine.
Aktuelle Erkrankungen
N/A
Vorgeschichte
Diabetes Type 2, Asthma, Hypertension, IBS, Arthritis
Andere Medikamente
? Multivitamin daily ? Vitamin D3 1000iu daily ? Spiriva 2.5 - 2 puffs in the morning daily ? Symbicort ? 160/4.5 1 puff morning & 1 puff evening ? Desipramine ? 75mg daily at night ? Atenolol 25mg daily at night ? Montelukast Sodium ? 10mg
Allergien
Penicillin, Sulfa medications, Avalox, Contrast dyes used for scans, pollen allergies & bee stings
Vorherige Impfungen
Swollen arm & high fever to a flu shot

VAERS 1782280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MN
Alter
52,0
Geschlecht
F
Eingang
13.10.2021
Impfdatum
14.04.2021
Beginn
28.04.2021
Tage bis Beginn
14,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Condition aggravated Hunger Hyperthyroidism Thyroid function test abnormal Weight decreased

Symptomtext

2 weeks after receiving vaccine had weakness, hunger and weight loss. Believed the vaccine triggered her hyperthyroidism to come back. Had to restart Methlmazole medication from her Endocrinologist.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Checked patients thyroid levels and started back on medication.
Aktuelle Erkrankungen
None.
Vorgeschichte
Asthma, Graves Disease.
Andere Medikamente
Advair, Calcium, Multivitamin, Methlmazole.
Allergien
Zoloft.
Vorherige Impfungen
-

VAERS 1776296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
42,0
Geschlecht
F
Eingang
11.10.2021
Impfdatum
08.10.2021
Beginn
08.10.2021
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Lymphadenopathy Neuralgia Oedema peripheral Pain Pain in extremity Palpitations Pyrexia

Symptomtext

on 10/08/2021 around 10PM at the vaccine administration site, developed left arm pain, continues to have left arm pain, developed swollen area under left axilla, noticed swelling to left armpit/throbbing pain 10/08/2021, reports on 10/09/2021 left axilla lymph node swelling continued to increase in size. Reports she also developed chills, fever, left arm nerve pain, heart palpation around 24 hours after vaccine. Reports all other symptoms including heart palpations resolved except left arm pain and swollen lymph node to left axilla. Reports she took ibuprofen and applied ice pack to left arm/armpit for her symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
none.
Aktuelle Erkrankungen
none
Vorgeschichte
None
Andere Medikamente
Camaese Birth Control
Allergien
none
Vorherige Impfungen
-

VAERS 1774467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
TX
Alter
44,0
Geschlecht
F
Eingang
09.10.2021
Impfdatum
14.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Asthenia Grip strength decreased Loss of personal independence in daily activities Pain in extremity Paraesthesia Peripheral coldness Speech disorder

Symptomtext

Her fingertips are very cold and hurt; Pain at the thumb joint/pain started yesterday around the thumb joint in her right hand; Loss of strength in arm and hand; Hard to grip things, and when I can grip it's hard to carry; All her fingers are ice cold and her thumb is ice cold also; Shortly thereafter, I started getting tingling sensation in my hand, getting worse the tinging/now it's prickling, vibration, tingling; It is hard to grip things and she lost her grip and is not carrying many things; Can't even talk right now; This is a spontaneous report from a contactable consumer. This female consumer (patient) reported for herself that: A 44-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot Number: EW0162 via an unspecified route of administration, administered in Arm Right on 14Apr2021 at 09:04 am (44-year-old at the time of vaccination) as dose 1, single for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient took the vaccine because of the pandemic and stated she wanted to do her part. The patient was not administered with additional Vaccines on same date of BNT162B2. The patient had not received any vaccine within four weeks. On 14Apr2021, shortly thereafter the vaccination, the patient experienced getting tingling sensation in my hand, getting worse the tinging/now it's prickling, vibration, tingling, loss of strength in arm and hand, hard to grip things, and when i can grip it's hard to carry, all her fingers are ice cold and her thumb is ice cold also, hard to grip things and she lost her grip and is not carrying many things. On 15Apr2021, the patient experienced pain at the thumb joint/pain started yesterday around the thumb joint in her right hand. On 16Apr2021, the patient experienced her fingertips are very cold and hurt. On an unspecified date in Apr2021, the patient experienced can't even talk right now. The patient got shot first dose of Pfizer in right arm and all of this is on right side, got the vaccine on Wednesday, shortly thereafter, the patient started getting tingling sensation in her hand, getting worse the tinging subsided, not having the same tingling, it is not like when your arm fells asleep, now it's prickling, vibration, tingling. Also with pain at the thumb joint and loss of strength, hard to grip things and when the patient can grip it's hard to carry, due to less strength. The patient wanted to know how to make this go away. All the patient's friends research said to take supplements, she was already taking Vitamin D and Zinc. The patient stated she can not even talk right now. The patient stated today which is Friday and the 3rd day she has had lost strength in her arm and tingling and prickly feeling still and her fingertips are very cold and hurt. The patient stated the tingling went down but the prickly feeling occurred and was really tingling that is like when you fall asleep and it was an asleep type of tingling most of the day and the next day the tingling subsided quite a bit and now it is a prickly tingling type. The patient stated that the pain started yesterday around the thumb joint in her right hand and the pain is not in her other fingers on that hand and the pain is ongoing and getting worse. The patient stated that she keeps touching her hand to see if it does still hurt and it does still hurt and all her fingers are ice cold and her thumb is ice cold also, states the ice cold feeling began on Wednesday and it is ongoing and is getting worse. Stated they are getting a cold front with weather and she does not know if the cold is weather related but her right hand is colder than her other hand. The patient stated she has the loss of strength and it began when the tingling started and she is not picking up things and can't tell if the loss of strength began on Wednesday and it is definitely there on Thursday and today, stated on her arm and hand, it is hard to grip things and she lost her grip and is not carrying many things but is a realtor and went to get a sign out of a yard and put in in her car and carrying the sign was an endeavor. Stated the loss of strength is ongoing and worse than yesterday, stated on Wednesday and Thursday it was more of an annoyance but this is the 3rd day and the loss of strength is more than an annoyance now. The patient stated she is not a healthcare professional but does self medicate. Stated she has not seen her HCP in a couple of years. The patient stated that she had an appointment on Tuesday for the Johnson and Johnson vaccine and it was cancelled so she scrambled to find something. The patient stated she did not require treatment for the reported events. The events required no visit to emergency room or physician office. Therapeutic measures were taken as a result of shortly thereafter, i started getting tingling sensation in my hand, getting worse the tinging/now it's prickling, vibration, tingling (paraesthesia), pain at the thumb joint/pain started yesterday around the thumb joint in her right hand (arthralgia), loss of strength in arm and hand (asthenia), hard to grip things, and when i can grip it's hard to carry (loss of personal independence in daily activities), it is hard to grip things and she lost her grip and is not carrying many things (grip strength decreased). The outcome of the events Hard to grip things, and when I can grip it's hard to carry, Can't even talk right now, It is hard to grip things and she lost her grip and is not carrying many things and Her fingertips are very cold and hurt were unknown while other events were not recovered. No follow-up attempts are needed. No further information is expected

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1765237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NH
Alter
44,0
Geschlecht
F
Eingang
06.10.2021
Impfdatum
06.05.2021
Beginn
01.06.2021
Tage bis Beginn
26,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Burning sensation Chest X-ray Dizziness Electrocardiogram Electroencephalogram Headache Heart rate increased Immune reconstitution inflammatory syndrome Magnetic resonance imaging head Magnetic resonance imaging neck Magnetic resonance imaging thoracic Muscle twitching Neuropathy peripheral Paraesthesia

Symptomtext

Diagnosed with post vaccine inflammatory syndrome Five months of chronic head pain/zaps, dizziness, peripheral neuropathy with tingling and burning, and twitching. rapid heart rate

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
MRI of brain, cervical (neck) and thoracic spine. EEG, EKG, chest x-ray
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Vybrid 10 mlg
Allergien
Sulfa - slight allergy
Vorherige Impfungen
-

VAERS 1761703

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OK
Alter
32,0
Geschlecht
F
Eingang
05.10.2021
Impfdatum
17.09.2021
Beginn
17.09.2021
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dyspnoea Hyperhidrosis Hypertension Throat tightness

Symptomtext

SOB; throat tightening; hypertension; sweating

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
LoLoEstrin Fe-Birth Control
Allergien
Sulfa drugs
Vorherige Impfungen
-

VAERS 1756369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OR
Alter
31,0
Geschlecht
F
Eingang
02.10.2021
Impfdatum
16.04.2021
Beginn
19.04.2021
Tage bis Beginn
3,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest pain Dysmenorrhoea Heavy menstrual bleeding Menstrual disorder

Symptomtext

Extreme abnormal mentsrual cycle; intense cramps and bleeding; intense cramps and bleeding; Severe chest pain when lying down; This is a spontaneous report from a contactable consumer (patient). A 31-year-old female non-pregnant patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EW0162, Expiration Date: not reported) via an unspecified route of administration in Left Arm on 16Apr2021 18:30 as dose 1, single for COVID-19 immunization (at the age of 31-year-old, non-pregnant). Medical history included attention deficit hyperactivity disorder (ADHD) from an unknown date and unknown if ongoing. Patient had no known allergies. Patient had no covid prior vaccination and was not covid tested post vaccination. Concomitant medication(s) (in two weeks) included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) taken for attention deficit hyperactivity disorder, start and stop date were not reported. Patient did not receive any other vaccine in four weeks. The patient experienced extreme abnormal mentsrual cycle, intense cramps and bleeding, severe chest pain when lying down on 19Apr2021. Patient was sent for two days. Ae resulted in doctor or other healthcare professional office/clinic visit. The patient did not receive treatment for the events. The outcome of the events was not recovered. No follow up attempts are possible; no further information expected

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: ADHD
Andere Medikamente
Pfizer, Inc. EUA 027034
Allergien
-
Vorherige Impfungen
-

VAERS 1756353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
OH
Alter
72,0
Geschlecht
F
Eingang
02.10.2021
Impfdatum
10.04.2021
Beginn
10.04.2021
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal discomfort Body temperature Chest pain Dizziness Headache Hypersensitivity Musculoskeletal discomfort Oropharyngeal pain Pain in extremity Pharyngeal swelling Pyrexia SARS-CoV-2 test Swollen tongue

Symptomtext

Fever like 100.8; Pain to chest/says it felt like a rubber band was wrapped around her chest and back; Sick on your stomach; Dizzy; felt like a rubber band was wrapped around her chest and back; throat and tongue swelling like an allergy; Throat and tongue swelling; Throat and tongue swelling; Sore Throat; Headache; Pain in Arm; This is a spontaneous report from a contactable consumer (patient). A 72-years-old female patient received BNT162b2 (Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number: EW0162, Expiration date: 31Jul2021, NDC number was unknown), via an unspecified route of administration on 10Apr2021 at 08:15 hours as dose 1, single (at the age of 72-years-old) for COVID-19 immunisation. The patient medical history included ongoing pacemaker (implanted 2 years ago), ongoing high blood pressure diagnosed 2 years ago, cholesterol, (diagnosed about 2 years ago), 2 stomach surgeries (many years ago), Back Surgery (many years ago), Diverticulitis (many years ago), removal of part of intestines (about 3 and a half years ago), several allergies (patient cannot take pain medications or most antibiotics, stated they made her sick, patient cannot eat red meat, lactose, cannot digest some meats, chest pain that felt like a rubber band around her chest and back before, unrelated to the vaccine, regulate heart rate, cannot take any pain medications, as they make her throw up and feel sick, had issues when taking almost all antibiotics, sick for about 7 weeks from Nov 2020 to unknown if ongoing, in about Nov 2020 for about 7 weeks, patient had horrible, horrible symptoms, patient was sick to the stomach, throwing up, same chest pain with feeling like a rubber band was around her body, losing weight, difficulty breathing, and fever, called her doctor and got antibiotics, antibiotics were hard for her to take. Patient took two rounds of antibiotics and was still sick. Patient went to Emergency Room and tested negative for COVID. Doctor thought false negative because of her symptoms. Patient stated that there was lot of health issues in her family such as heart disease and cancer. Historical vaccine included flu vaccine every year with no issues for immunisation. Patient had no history of all previous immunizations with the Pfizer vaccine considered as suspect. Patient had no prior vaccinations (within 4 weeks). Concomitant medications included unknown medications for high blood pressure and unknown medication to regulate heart rate. Patient was worried about getting the vaccine at first; she did not want to do it because she gets sick from everything. On 10Apr2021, about an hour after the vaccination, patient throat and tongue began swelling a little; like an allergy, sore throat, also had a slight headache and pain in her arm. Patient stated that throat and tongue swelling lasted for about 8 hours. On 11Apr2021, patient had a fever 100.8 degrees, had pain across her chest and stated that it felt like a rubber band was wrapped around her chest and back, was sick on her stomach and dizzy, had a headache, and the fever. Patient asked if it was normal to have side effects after the first shot. Patient heard from everybody not to worry about the first dose, it does not have side effects. They said the side effects come with the second dose. Patient does not know if it was safe for her to get the second dose. Patient had no emergency room and physician office visit for all the events. No relevant tests were performed. The outcome of throat and tongue swelling and throat and tongue swelling like an allergy was recovered on 10Apr2021, Headache, fever like 100.8, pain to chest/says it felt like a rubber band was wrapped around her chest and back, Sick on your stomach, Dizzy was recovered on 12Apr2021, pain in arm was recovering, unknown for felt like a rubber band was wrapped around her chest and back and not recovered for sore throat. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Test Date: 20210411; Test Name: Fever 100.8 degrees; Result Unstructured Data: Test Result:100.8; Comments: Degrees; Test Name: Covid test; Result Unstructured Data: Test Result:Negative
Aktuelle Erkrankungen
Artificial cardiac pacemaker user (implanted 2 years ago.); Blood cholesterol abnormal (Diagnosed about 2 years ago.); Blood pressure high (Diagnosed about 2 years ago)
Vorgeschichte
Medical History/Concurrent Conditions: Allergy NOS; Allergy to antibiotic (had several allergies); Back surgery (many years ago.); Chest discomfort; Chest pain; Difficulty breathing; Diverticulitis (many years ago.); Drug allergy (had several allergies); Fever; Gastrointestinal surgery (many years ago.); Heart disease, unspecified; Heart rate abnormal; Intestinal operation NOS (about 3 and a half years ago.); Lactose intolerance; Loss of weight; Meat allergy; Sickness; Stomach discomfort; Vomiting
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 1749865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
FL
Alter
30,0
Geschlecht
F
Eingang
30.09.2021
Impfdatum
29.09.2021
Beginn
30.09.2021
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia Immediate post-injection reaction Lymphadenopathy Muscular weakness Pain Pain in extremity Paraesthesia Tenderness

Symptomtext

Reports immediately after IM injection of second dose of COVID vaccine, developed shooting pain into left arm/left side of collar bone. Reports she woke up this morning - noticed left supraclavical lymph node swelling and tenderness and "tingling like pins and needles" from knees extending to feet bilaterally. Reports onset of symptoms 09/30/2021 at 0530 am treatment: follow up with PCP or seek medical attention right away (ER or 911) should symptoms worsen, weakness/numbness or worsening tingling to bilateral lower extremity, shortness of breath, chest pain, or change in neurological status. will follow up with team member health care clinic in 5-7 days or sooner as needed

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
observation, referral to PCP, follow up in 5-7 days. Instructed to go immediately to ER if symptoms should worsen, weakness/numbness or if her symptoms increase.
Aktuelle Erkrankungen
09/01/2021- allergies- took Zyrtec which resolved symptoms. Took COVID test: negative
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 1741945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
AZ
Alter
57,0
Geschlecht
F
Eingang
28.09.2021
Impfdatum
11.04.2021
Beginn
20.06.2021
Tage bis Beginn
70,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Anticoagulant therapy Blood test Cardiac pacemaker insertion Cardioversion Chest X-ray Computerised tomogram Echocardiogram Electrocardiogram Heart rate increased Pneumonia

Symptomtext

I was hospitalized, I was put on IV antibiotics for pneumonia, oxygen. Rapid heart rate 174 bpm. Metoprolol, diltiazem, Eliquis. Eventually they put me on pacemaker. I'm on ENTRESTO, NATOPHEROL, warfarin. Since I have been home since the pacemaker I have felt pretty normal.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pneumonia
Hospital-Tage
18,0
Labordaten
EKG, echocardiogram, full blood panel, chest x-rays, CT scans, cardioversion.
Aktuelle Erkrankungen
-
Vorgeschichte
Psoriatic arthritis; hypothyroid
Andere Medikamente
Levothyroxine; norethindrone; estradiol; vit d; zinc; vit c; calcium; Claritin; Allegra
Allergien
-
Vorherige Impfungen
-

VAERS 1741077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
MI
Alter
56,0
Geschlecht
M
Eingang
28.09.2021
Impfdatum
07.04.2021
Beginn
20.09.2021
Tage bis Beginn
166,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
positive for covid on admission
Aktuelle Erkrankungen
-
Vorgeschichte
Pneumothorax, hyponatremia
Andere Medikamente
Albuterol, methocarbamol, metoprolol,
Allergien
-
Vorherige Impfungen
-

VAERS 1731551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
NC
Alter
78,0
Geschlecht
M
Eingang
24.09.2021
Impfdatum
06.05.2021
Beginn
18.05.2021
Tage bis Beginn
12,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain Arthralgia Chest pain Pain Pain in extremity

Symptomtext

On physical eversion pain occurred in upper abdomen, rest would make it go away, Over time (two weeks) the pain moved up through the lower chest, the upper chest, shoulders, the into my upper arms. To date (9/24/2021) the pain has not gone away it is still in my upper arms , lower arms, and fingers.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Doctor gave me cortisone shots in both arms - had no effect.
Aktuelle Erkrankungen
Type 2- AIC 6.2
Vorgeschichte
Polio - Physical Exertions can lead to mussel soreness
Andere Medikamente
Aspirin 81mg Multi Vitamin Centrum Sliver Vitamin D 5000 units Zyrtec
Allergien
Z-PACK
Vorherige Impfungen
-

VAERS 1718499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0162

moderat
Staat
CA
Alter
47,0
Geschlecht
F
Eingang
21.09.2021
Impfdatum
17.04.2021
Beginn
01.04.2021
Tage bis Beginn
-
Dosis
2
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Chills Diarrhoea Dizziness Headache Herpes zoster Myalgia Neuralgia Pain Pain in extremity Palpitations Pyrexia Rash Skin burning sensation

Symptomtext

pain in her left big toe, left ankle, left knee, & left hip; a rash on her left leg; Shingles rash started; nerve pain from Shingles; she started to feel a burning skin sensation on the left side of her thigh; Diarrhea; joint pain; heart palpitations; dizzy; Chills; Headache; Muscle pain; Fever; she had a shooting pain in her left leg; This is a spontaneous report from a contactable consumer or other non-healthcare professional. A 47-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0162), second dose via intramuscular, administered in left arm on 17Apr2021 at 08:45 (at the age of 47-year-old) as dose 2, 0.3 ml single for COVID-19 immunisation; hydroxychloroquine (HYDROXYCHLOROQUINE), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) and ongoing, at 200 mg, 2x/day for Sjogren's syndrome. Medical history included Sjogren's syndrome from Sep2020 and ongoing Sjogren's disease took Hydroxychloroquine (or Plaquenil) 200mg, twice a day, palpitations from Dec2020 and ongoing, hypertension from Dec2020 and ongoing, hypersensitivity from an unknown date and unknown if ongoing she took 1 Allegra daily for seasonal allergies for 7 to 8 years. No concomitant medications were not reported. Report is not related to a study or programme. No investigation assessment was reported. Vaccine was not administered at military facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other vaccines on same date COVID vaccine was administrated. Historical vaccine given to patient previously was bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: ER8730, Expiration Date: Jul2021), first dose via unspecified route of administration on 27-MAR-2021 (at the age of 47-year-old) as dose 1, single for COVID-19 immunisation and experienced she wasn't feeling well, High blood pressure and Palpitations. It was reported that caller stated she wanted to report side effects for the COVID-19 Vaccine. She said she had an autoimmune disease, and her rheumatologist wanted her to get the COVID-19 Vaccine, as soon as possible. Reported she had her first COVID-19 Vaccine in her left arm on 27Mar2021, providing Pfizer Lot Number: ER8730 and Expiration Date: Jul2021. She said she had her second COVID-19 Vaccine in her left arm on 17Apr2021 at 8:45, providing Pfizer Lot Number: EW0162. She said she did not have expiration date for the second COVID-19 vaccine dose, or the vaccine NDC Number. Reported she saw her rheumatologist this morning, and her rheumatologist traced back her symptoms to the date she received her second COVID-19 Vaccine dose. She said after she received her second COVID-19 Vaccine dose on 17Apr2021, she started to feel severe joint pain on 23Apr2021. She said she thought she had gout and contacted her rheumatologist. She said on 26Apr2021, she started to feel a burning skin sensation on the left side of her thigh. She said she waited a couple days, and on Sunday (02May2021), she woke up with Shingles. She said her doctor told her the Shingles might be related to the COVID-19 Vaccine because after her second COVID-19 Vaccine dose, all of sudden, she was not feeling too well, and her symptoms were bad. She said her doctor prescribed her Shingles medication. Reported Shingles was pretty painful. She said she had severe pain while taking a shower when the water drops hit her skin. She said she experienced that severe pain (clarified as a burning sensation) before she had the Shingles rash. She clarified on 26Apr2021 she had a burning sensation start, and the burning sensation was killing her when she took a shower, and when she was wearing a dress. She said she did not email her doctor until 28Apr2021 that something was not quite right. She said on Sunday (02May2021), the burning sensation improved, and then she saw a rash on her left leg, and the Shingles rash started. She said when she talked with her doctor today (03May2021), her doctor confirmed she had Shingles. She said at first, she thought what she was experiencing was Lupus because of her recent Sjogren's disease diagnosis (in Sep2020). Reported she had been contacting her rheumatologist because she had discomfort and this and that. She said her rheumatologist traced down her symptoms to her second COVID-19 Vaccine dose. She said she had problems with her left side, and her rheumatologist said the second COVID-19 Vaccine dose triggered the problems. Reported after she had her first COVID-19 Vaccine dose, she experienced heart palpitations. She said the COVID-19 Vaccine facility called paramedics or EMTs. She said her blood pressure increased too, but she didn't remember what her blood pressure readings were because she wasn't feeling well. She clarified she had a previous problem with palpitations and high blood pressure before the COVID-19 Vaccine. She said the paramedics or EMTs monitored her for a whole hour, and then released her to the COVID-19 Vaccine facility staff, who monitored her for another 20 minutes. She said the paramedics or EMTs offered to take her to the hospital, but she said she would be OK. She said she took her heart palpitation medicine earlier that day (clarified as Metoprolol 25mg) and didn't take anything to treat the heart palpitations she experienced after her first COVID-19 Vaccine dose. She did not have her Metoprolol 25mg prescription to provide the NDC, Lot, and Expiration Date. Reported after her second COVID-19 Vaccine, she experienced the same issue with heart palpitations. She said the COVID-19 Vaccine facility wanted to call the paramedics or EMTs again, but she told them she didn't want that. She said her husband was with her at the time, so the COVID-19 Vaccine facility made her wait for 45 minutes. She said she was also dizzy and told the COVID-19 Vaccine facility she just wanted to go home and lie down. She said after she got home from her second COVID-19 Vaccine, she rested and was fine. Reported later in the day on 17Apr2021, she experienced all the COVID-19 Vaccine side effects listed on Pfizer's website. She clarified she had chills, headache, joint pain, muscle pain, fever, and diarrhea. Chills, Headache, Muscle pain, Fever, Diarrhea. Reported she took Tylenol Arthritis, and nothing for the diarrhea. She said she knew the diarrhea would stop eventually. She said she was at work and did not have the Tylenol Arthritis NDC, Lot, and Expiration Date. Reported she took Hydroxychloroquine (or Plaquenil) 200mg, twice a day, for Sjogren's Disease. She said the Hydroxychloroquine normally helped her joint pain pretty good, but this time, the Hydroxychloroquine didn't work for her joint pain. She said her joints were killing her, and the joint pain got worse, and worse, on her daily (Hydroxychloroquine 200mg) medication. She said the Hydroxychloroquine 200mg did not actually help. Reported she was at work and didn't have her Hydroxychloroquine 200mg prescription bottle to provide the NDC, Lot, and Expiration Date. Reported she first started Hydroxychloroquine 200mg, twice a day in Dec2020. She said she had severe palpitations at that time, so her rheumatologist put the Hydroxychloroquine 200mg on hold, and sent her to a cardiologist. She said she had been seeing the cardiologist since Dec2020. She clarified after the cardiologist did all his exams, he put her on Metoprolol 25mg, twice a day, to lower her heart rate, and blood pressure. She said she had been taking the Metoprolol 25mg since Feb2021, and did not have the NDC, Lot, and Expiration Date. She said she restarted the Hydroxychloroquine 200mg, twice a day, in Mar2021. Reported her doctor told her she prescribed an anti-viral, and she needed to pick-up her prescription from the pharmacy. She said she did not know the name of the anti-viral, and did not have the NDC, Lot, and Expiration Date. She said the doctor told her if her Shingles becomes too painful, she would prescribe something stronger for pain. No further details provided. Reported her doctor told her that part of the pain she had been experiencing since her second COVID-19 Vaccine could be nerve pain from Shingles. She said she had left side pain that had worsened. She said she had pain in her left big toe, left ankle, left knee, and left hip. She said she had a shooting pain in her left leg. Reported she took 1 Allegra daily for seasonal allergies for 7 to 8 years. She said she did not have her Allegra with her to provide the UPC/NDC, Lot, and Expiration Date. Caller asked if anyone else had reported getting Shingles after the second COVID-19 Vaccine. The caller was offered transfer to Pfizer Medical Information and declined. She said her doctor had told her yes, that others had reported getting Shingles after the COVID-19 Vaccine. She said her husband had also sent her an article of a few cases of people with autoimmune diseases that experienced Shingles. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available): COVID-19 Vaccine, Lot Number: ER8730, Expiry Date: Jul2021, Route: Intramuscular, Anatomical Location: Arm, Left, No. of Previous Doses: None, Date: 27Mar2021. Reported after her first COVID-19 Vaccine dose, she experienced heart palpitations. She said her blood pressure increased too, but she did not remember what her blood pressure readings were because she was not feeling well. She said after her second COVID-19 Vaccine, she experienced the same issue with heart palpitations. She said later in the day on 17Apr2021, she experienced all the COVID-19 Vaccine side effects listed on Pfizer's website. She clarified she had chills, headache, joint pain, muscle pain, fever, and diarrhea. She said after she received her second COVID-19 Vaccine dose on 17Apr2021, she started to feel severe joint pain on 23Apr2021. She said she thought she had gout and contacted her rheumatologist. She said on 26Apr2021, she started to feel a burning skin sensation on the left side of her thigh. She said on Sunday (02May2021), the burning sensation improved, and then she saw a rash on her left leg, and the Shingles rash started. She said when she talked with her doctor today (03May2021), her doctor confirmed she had Shingles. Patient reported she had severe joint pain after her second COVID-19 Vaccine. She said she took Hydroxychloroquine 200mg, twice a day, for Sjogren's Disease. She said the Hydroxychloroquine normally helped her joint pain pretty good, but this time, the Hydroxychloroquine did not work for her joint pain. She said her joints were killing her, and the joint pain got worse, and worse, on her daily Hydroxychloroquine 200mg medication. She said the Hydroxychloroquine 200mg did not actually help. Reported she was at work and did not have her Hydroxychloroquine 200mg prescription bottle to provide the NDC, Lot, and Expiration Date. Adverse event did not require a visit to emergency room but visited to physician office. No relevant tests were reported. The outcome of the events rash on her left leg, shingles rash, joint pain, she had a shooting pain in her left leg was not recovered. The outcome of the event she started to feel a burning skin sensation on the left side of her thigh was recovering. The outcome of the events nerve pain from shingles and pain in her left big toe, left ankle, left knee, & left hip was unknown. The outcome of the events heart palpitations, dizzy, chills, headache, muscle pain, fever and diarrhea were recovered on an unspecified date. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Blood pressure high; Palpitations; Sjogren's disease (Sjogren's disease took Hydroxychloroquine (or Plaquenil) 200mg, twice a day.)
Vorgeschichte
Medical History/Concurrent Conditions: Allergy (she took 1 Allegra daily for seasonal allergies for 7-8 years)
Andere Medikamente
HYDROXYCHLOROQUINE
Allergien
-
Vorherige Impfungen
-