VAERS Reports #EW0169

VAERS 2723162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 12.12.2023
Impfdatum: 21.04.2021
Beginn: 22.01.2022
Tage bis Beginn: 276,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Diarrhoea Dyspnoea Hypoxia Lung opacity SARS-CoV-2 test positive Vomiting

Symptomtext

brought to ER for evaluation of cough, shortness of breath, vomiting and diarrhea. In the ER patient was noted to be hypoxic with the O2 saturation 82% and placed on oxygen 6 L by nasal cannula. CRP elevated. Tested positive for COVID-19. Chest x-ray notable for bilateral pulmonary opacities consistent with pneumonia. Patient has received 2 doses for COVID-19 but not the booster. Patient is admitted with the COVID-19 pneumonia, placed on IV Decadron, remdesivir and supportive treatment failure. For acute hypoxic respiratory failure due to COVID-19 patient has been placed on supplemental oxygen. Patient's symptoms significantly improved. Inflammatory markers were improving. Patient needed home oxygen and was arranged. Patient was discharged home.

Weitere VAERSDATA-Felder

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

VAERS 2671142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 94,0
Geschlecht: F
Eingang: 15.08.2023
Impfdatum: 29.04.2021
Beginn: 16.01.2022
Tage bis Beginn: 262,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Multiple organ dysfunction syndrome Septic shock Urinary tract infection

Symptomtext

Admitted w/septic shock with multiorgan failure, UTI, COVID-19, possible RUL pna and C.diff infection. Tx w/abx, steroids, O2, zinc; poor prognosis, palliative care consulted; pt transitioned to hospice

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2660021

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 24.07.2023
Impfdatum: 28.05.2021
Beginn: 01.03.2023
Tage bis Beginn: 642,0
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: Peritoneal Cancer, Breast Cancer, GERD , Peripheral neuropathy
Andere Medikamente: Ativan, hydromorphone
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2657729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 67,0
Geschlecht: F
Eingang: 18.07.2023
Impfdatum: 26.04.2021
Beginn: 08.01.2022
Tage bis Beginn: 257,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure COVID-19 pneumonia Dyspnoea

Symptomtext

Presented to ED w/SOB; admitted for COVID-19 pna & acute resp failure w/hypoxia; tx w/02, steroids, abx, zinc; dc 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 2656553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 14.07.2023
Impfdatum: 20.04.2021
Beginn: 19.04.2023
Tage bis Beginn: 729,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Anticoagulant therapy Anxiety Atrial fibrillation Blood glucose increased Blood sodium decreased COVID-19 Cardiac failure Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Chronic obstructive pulmonary disease Coagulopathy Condition aggravated Cough Depression Diabetes mellitus inadequate control Dyspnoea

Symptomtext

Patient is a 59 y.o. female patient of, MD with history of Atrial fibrillation/flutter, COPD, DM type 2, Depression, Hypertension, parkinson's disease who presented to Hospital with shortness of breath was found to have acute hypoxic respiratory failure, COVID infection, COPD, and CHF exacerbation. Acute hypoxic respiratory failure Covid-19 Virus Infection Date of onset of symptoms: 4/15/2023 Symptoms present on admission: cough and shortness of breath Date of covid positive test: 4/19/23 Vaccination status: vaccinated Imaging: CXR with mild CHF and background pHTN pattern consistent with COPD Oxygen requirements on admission: 2LNC Current oxygen requirements: 1LNC (not on home O2) Medical therapy: remdesivir and steroids Consultants following: none Anticipated special isolation end date: 4/29/23 Home O2 eval revealed no home O2 needs and patient declined home O2 setup even if qualified as family members are smokers and she is concerned for fire Acute COPD exacerbation Dyspnea, coughing CXR mild CHF and COPD changes Improved with albuterol inhalation Continue spiriva, xopenex, symbicort, azithromycin decadron Wean O2 to RA, did not qualify for home O2 Acute on chronic HFpEF exacerbation Dyspnea and hypoxia on admit CXR with mild CHF vascular congestion Received IV lasix x1 with clinical improvement TTE 08/2022 with EF 70% with severe MS Lowered home PO lasix with renal recovery Clinically appears euvolemic 4/21 Severe mitral valve stenosis Afib with RVR Warfarin induced coagulopathy Trop 15-17, flat HR 140's in RVR on 4/19 Due to hypoxia/COVID and albuterol inh Resumed home metoprolol and cardizem Goal HR<120 prn lopressor IVP Switched albuterol to xopenex INR 3.7 on warfarin, pharmacy to dose HR controlled since 4/20, INR 1.9 Uncontrolled DM type 2 BG 422, not in DKA; HbA1c 10.3 Suspect due to systemic steroids for COVID/COPD and lack of home insulin Uncontrolled despite home lantus and SSI Increased lantus to 50 U BID in addition to lispor 25U Qac and home metformin Adjust insulin as needed for optimal control Pseudohyponatremia Na 129 due to hyperglycemia Corrected Na normal on 4/21 Depression and anxiety Wellbutrin Obesity BMI 44.29 Lifestyle changes recommended

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615306

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge EW0169

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 14.04.2023
Impfdatum: 03.11.2021
Beginn: 01.10.2022
Tage bis Beginn: 332,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Death Pain SARS-CoV-2 test positive

Symptomtext

3RD DOSE PFIZER COVID VACCINE GIVEN 6/16/22 #FP7135; pt had a positive COVID test 10/3/22 at a local health care facility (SNF); pt admitted to a local hospice facility on 10/14/22; with PVD dx and GIP for pain; pt passed away in the hospice facility

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PVD, HTN, CVA, BPH, CAD, ATRIAL FIBRILLATION, MULTIPLE INFARCTS WITH CARDIAC EMBOLI, MITRAL VALVE INSUFFICIENCY, DM, DEMENTIA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2593839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 93,0
Geschlecht: F
Eingang: 09.03.2023
Impfdatum: 19.08.2021
Beginn: 01.08.2022
Tage bis Beginn: 347,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Death Dysgeusia Failure to thrive Gastrointestinal disorder Hypotension Renal impairment SARS-CoV-2 test positive

Symptomtext

3RD DOSE PFIZER COVID VACCINE GIVEN 3/3/22, #FJ1620; pt admitted to hospital on 8/26/22 with vague abdominal sx, hypotension, FTT; found to be positive for COVID; respiratory status stable on RA; dysgeusia, given zinc; Decadron; holding Remdesivir due to kidney function; pt requested comfort care and hospice; DNR; pt dc'd on 9/4/22 to Hospice Facility where she passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CKD STAGE 3, CAD S/P CABG X3 AND STENTING, PACEMAKER, HTN, HLD, CHF, GERD, HYPOTHYROIDISM, IBS, OSTEOPOROSIS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2591840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 06.03.2023
Impfdatum: 14.05.2021
Beginn: 01.08.2022
Tage bis Beginn: 444,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Anticoagulant therapy COVID-19 Death Dyspnoea Haemoptysis SARS-CoV-2 test positive

Symptomtext

Pt brought to ED with SOB and hemoptysis; approximately a month ago, pt dx with PE, on Eliquis; found to be positive for COVID in ED; Dexamethasone, Remdesivir, O2 supplementation; transitioned to DNR, comfort care; passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, DM, ASTHMA, CAD, HLD, ARTHRITIS
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2590452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

kritisch

Staat: ID
Alter: 57,0
Geschlecht: F
Eingang: 02.03.2023
Impfdatum: 26.08.2021
Beginn: 22.02.2022
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Angiogram Angiogram cerebral Cerebrovascular accident Echocardiogram Headache Scan brain Speech disorder

Symptomtext

In January 2022 my husband noticed problems with my speech, went to doctor and after scans they found I had 3 CVA events. Currently taking medication Crestor, speech therapy, physical therapy, and continuing to work through headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Brain w/o Cont, MRA Head Angio w/o Cont 2/18/2022; CDA ECHO 6/23/22; Echocardiogram 6/23/22
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety, depression
Andere Medikamente: Trazadone & citropram
Allergien: None
Vorherige Impfungen: -

VAERS 2562939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

kritisch

Staat: WI
Alter: 69,0
Geschlecht: M
Eingang: 19.01.2023
Impfdatum: 19.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Cerebrovascular accident SARS-CoV-2 test

Symptomtext

Stroke of unknown origin on 02May2021, that caused Permanent disability; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 19Apr2021 as dose 1, single (Lot number: Ew0169) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history included: "High cholesterol at that time only, minor other unrelated health concerns" (unspecified if ongoing), notes: High cholesterol at that time only, minor other unrelated health concerns; "known allergies: New stings" (unspecified if ongoing), notes: known allergies: New stings; "if COVID prior vaccination: Yes" (unspecified if ongoing), notes: if COVID prior vaccination: Yes. The patient's concomitant medications were not reported. The following information was reported: CEREBROVASCULAR ACCIDENT (hospitalization, disability, medically significant, life threatening) with onset 02May2021 at 08:00, outcome "not recovered", described as "Stroke of unknown origin on 02May2021, that caused Permanent disability". The patient was hospitalized for cerebrovascular accident (hospitalization duration: 30 day(s)). The event "stroke of unknown origin on 02may2021, that caused permanent disability" required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown result, notes: If COVID tested post vaccination: Yes. COVID test type post vaccination was Nasal Swab. Therapeutic measures were taken as a result of cerebrovascular accident. Clinical course: It was reported that Serious: patient received more than 3 doses. No other vaccine informers. Stroke of unknown origin on 02May2021 that caused Permanent disability. Then on 19Aug2021 diagnosed with acute kidney failure determined to be caused by terminal multiple myeloma. AE resulted in: [Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event), Disability or permanent damage]. Treatment AE with Stroke rehab.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 30,0
Labordaten: Test Name: COVID tested: Nasal Swab; Result Unstructured Data: Test Result:Unknown result; Comments: If COVID tested post vaccination: Yes. COVID test type post vaccination was Nasal Swab.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to sting (known allergies: New stings); COVID-19 (if COVID prior vaccination: Yes); High cholesterol (High cholesterol at that time only, minor other unrelated health concerns)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2562172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: AL
Alter: 46,0
Geschlecht: M
Eingang: 18.01.2023
Impfdatum: 11.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Blindness unilateral Cerebrovascular accident Hypoaesthesia Magnetic resonance imaging head abnormal

Symptomtext

I sustained a punctate right occipital stroke in a cortical location confirmed by MRI on brain. I suffered Left side numbness and left eye blindness for around 2 hrs and continued partial loss of left eyesight for several days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: I sustained a punctate right occipital stroke in a cortical location confirmed by MRI on brain
Aktuelle Erkrankungen: None
Vorgeschichte: Testosterone Treatment since 2009
Andere Medikamente: Zoloft 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 2539104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 21.12.2022
Impfdatum: 06.04.2021
Beginn: 05.10.2022
Tage bis Beginn: 547,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Aortic dissection Asthenia COVID-19 Computerised tomogram thorax Ex-tobacco user Fatigue Renal aneurysm SARS-CoV-2 test positive

Symptomtext

Pt admitted to Hospital with a dissection of his descending thoracic aorta. While there he developed acute respiratory insufficiency that required high flow oxygen therapy. Concomitantly he was also noted to have a infrarenal aneurysm measuring up to 5.7 to 6 cm in diameter. Radiology measurements were 5.4 cm but not deemed accurate because of the measurement technique. He states he is now not smoking. He is fatigued but otherwise slowly regaining strength. His infrarenal aneurysm was not treated during that admission due to his other acute problems. His thoracic aortic dissection actually appeared to be improving on subsequent CT imaging.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 10/7 SARS-CoV-2 -COVID-19, Micro -- detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2478630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

kritisch

Staat: MN
Alter: 63,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 31.12.2021
Beginn: 13.10.2022
Tage bis Beginn: 286,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient expired 10/13/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Benign essential hypertension Mixed hyperlipidemia Quadriplegia Osteomyelitis of pelvis Esophageal candidiasis Dysphagia Constipation Sinus tachycardia Bilateral heel pressure ulcer Right ankle pressure ulcer Spinal Cord injury of thoracic region Partial quadriplegia Bladder spasms GERD Moderate malnutrition in the context of acute illness Hypocalcemia PAD Chronic anemia
Andere Medikamente: Unknown
Allergien: Lisinopril, quinolones, glycerin, docusate
Vorherige Impfungen: -

VAERS 2456299

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SD
Alter: 66,0
Geschlecht: M
Eingang: 23.09.2022
Impfdatum: 02.12.2021
Beginn: 14.07.2022
Tage bis Beginn: 224,0
Dosis: 2
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal hernia Anastomotic leak COVID-19 Death General physical health deterioration SARS-CoV-2 test positive Small intestinal obstruction Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 04/05/2021, 04/26/2021, and 12/02/2021. They presented to hospital on 06/24/2022 with a strangulated ventral hernia and a small bowel obstruction. They were admitted same day. They experienced further complications of an anastomotic leak. They were transferred to a different hospital on 07/12/2022 for nursing care after their health continued to deteriorate. They transitioned to comfort care only. They tested positive for COVID-19 on 07/14/2022 and died on 07/15/2022. It is not well understood if the individual experienced COVID-19 symptoms since this was a medically complex situation and the individual had several underlying medical conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 22,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Kidney Disease, Osteoarthritis, Morbid Obesity with past gastric bypass; Hypothyroid (past thyroidectomy for non-follicular thyroid neoplasm), Hypertension, Likely Renal Cell Carcinoma (further work up not done); Lung Mass/nodule (further work up not done) At the time of the adverse event, they were experiencing complications related to a strangulated ventral hernia and a small bowel obstruction.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2436943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SD
Alter: 56,0
Geschlecht: F
Eingang: 09.09.2022
Impfdatum: 11.12.2021
Beginn: 17.07.2022
Tage bis Beginn: 218,0
Dosis: 2
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 COVID-19 pneumonia Death Dyspnoea Hypoxia Inappropriate schedule of product administration Pneumonia mycoplasmal Pulmonary embolism SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Pfizer product on 03/30/2021, 04/21/2021, and 12/11/2021. They were admitted to hospital on 06/24/2022 with a primary complaint of shortness of breath. COVID-19 test on 06/24/2022 was negative. They were found to be experiencing complications of hypoxia and acute bilateral pulmonary thromboembolic tic disease. They were also diagnosed with mycoplasma pneumonia. A second test on 07/17/2022 was positive. They were also diagnosed with COVID-19 pneumonia. They remained hospitalized until their death on 07/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 24,0
Labordaten: Negative COVID-19 test on 06/24/2022. Positive COVID-19 test on 07/18/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Mycoplasma Pneumonia, Severe Pulmonary Hypertension, Hypothyroidism, GERD, heparin-induced thrombocytopenia, Unspecified Anemia,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 25.06.2021
Beginn: 17.08.2022
Tage bis Beginn: 418,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure Anticoagulant therapy Arterial thrombosis Atrial fibrillation COVID-19 pneumonia Condition aggravated Deep vein thrombosis Intensive care Respiratory failure SARS-CoV-2 test positive

Symptomtext

66 y/o F with PMH significant for severe COPD, pulmonary HTN, a-fib, pancreatic ca s/p Whipple, and dementia, who was initially admitted to the ICU for acute on chronic hypoxic respiratory failure from COVID-19 PNA requiring HFNC/NRB. Pt was treated with remdesivir and soul-medrol for her COVID-19 PNA. Her hospitalization was otherwise significant for a-fib with rvr, LLE DVT, and a new dx of chronic thrombus in the RLL artery . Pt was treated with anticoagulation with IV heparin. She was ultimately transferred out of the ICU after goals of care were addressed and her code status was changed to DNR/DNI. ICU consultation was requested by the primary team on 9/2 for escalating FiO2 requirements on HFNC. No dyspnea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 8/17 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2430942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 06.10.2021
Beginn: 08.10.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Pulmonary embolism

Symptomtext

Narrative: Patient developed pulmonary embolism two days after receiving vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2419260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TN
Alter: 86,0
Geschlecht: F
Eingang: 24.08.2022
Impfdatum: 06.05.2021
Beginn: 16.02.2022
Tage bis Beginn: 286,0
Dosis: 2
Route/Site: SYR / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute left ventricular failure COVID-19 Death Hypotension Lethargy Pneumonia Respiratory failure Sepsis

Symptomtext

The patient was brought back to Hospital on 02/26/2022. The patient previously had a 30-day admission at the facility for PNA, acute diastolic heart failure, and was found to have COVID towards the end of her hospitalization. She was brought back to the facility for respiratory failure, hypotension, and lethargy. In the ED the patient was found to be septic and have a new PNA. The family agreed to perform only comfort measures. The patient expired on 02/27/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2391133

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 26.07.2022
Impfdatum: 19.04.2021
Beginn: 01.11.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Acute respiratory failure COVID-19 Death Fall General physical health deterioration Haematoma Hypotension Intensive care SARS-CoV-2 test positive Shock haemorrhagic

Symptomtext

11/19/21 pt had a positive COVID test (outpatient) at facility; 11/23/21 pt to ED with AHRF; right leg hematoma after a fall; given Decadron, Remdesivir, Baricitinib; pt became hypotensive in spite of vasopressors; hemorrhagic shock; transferred to ICU; pt's condition continued to deteriorate; pt chose comfort care and passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM, HTN, asthma, obesity s/p gastric bypass
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2357959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SD
Alter: 66,0
Geschlecht: M
Eingang: 05.07.2022
Impfdatum: 31.08.2021
Beginn: 14.10.2021
Tage bis Beginn: 44,0
Dosis: 3
Route/Site: SYR / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac arrest Death Dyspnoea SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/17/2021, 03/10/2021, and 08/31/2021. They tested positive for COVID-19 twice on 10/14/2021. They were also admitted to hospital on 10/14/2021 after presenting to emergency department with a primary complaint of shortness of breath. The individual experienced complications of acute kidney injury, cardiac arrest, acute hypoxic respiratory failure, COVID-19 pneumonia, and acute respiratory distress syndrome. After aggressive treatments did not improve their condition, they were transitioned to comfort care and died on 10/25/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: Two positive COVID-19 tests on 10/14/2021 despite being vaccinated and boosted.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Immunosuppression, Obesity, Chronic Kidney Disease, Hypertension, Type II Diabetes, Atrial Fibrillation, kidney transplant recipient approx 14 years before the adverse event, hypothyroidism.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2347576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TN
Alter: 73,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 20.04.2021
Beginn: 25.09.2021
Tage bis Beginn: 158,0
Dosis: 2
Route/Site: SYR / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute respiratory failure Asthenia COVID-19 Death General physical health deterioration Mechanical ventilation Polyuria

Symptomtext

/Patient was admitted to a Medical Center on 09/25/2021 for acute hypoxemic respiratory failure d/t Covid-19. She was started on Decadorn but did not quality for remdesivir d/t her liver and kidney disease. Patient was attempted to be diuresed but developed an acute kidney injury and Nephrology felt she may have hepatic renal syndrome. She was noted to have a significant decline and functional status and increased weakness during hospitalization. On 10/05/2021 patient was placed on V60 machine, and expired on 10/06/2021.

Weitere VAERSDATA-Felder

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

VAERS 2328943

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 23.06.2022
Impfdatum: 18.05.2021
Beginn: 01.01.2022
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Anticoagulant therapy COVID-19 Death Diarrhoea General physical health deterioration Hypophagia Hyporesponsive to stimuli Hypothermia SARS-CoV-2 test positive Sepsis Vomiting

Symptomtext

1/12/22 pt brought to Ed via EMS reporting poor oral intake; O2 sats 85% on RA; placed on NRB; decreased responsiveness, diarrhea x 2 days, vomiting 1 x; admitted started on ABX and fluids; found to be positive for COVID; given Remdesivir, Heparin; pt's condition worsened became hypothermic requiring Bair Hugger blanket; severe sepsis; poor prognosis; DNR; in patient hospice where he expired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: dementia, HTN,HLD, NIDDM
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2320351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 15.06.2022
Impfdatum: 14.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 262,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal pain upper COVID-19 Cardiac arrest Condition aggravated Cough Death Dyspnoea Endotracheal intubation Hyperhidrosis Intensive care Malaise Pericardial effusion SARS-CoV-2 test positive

Symptomtext

PFIZER COVID VACCINE #3 GIVEN 9/8/21, LOT #FF2589; 1/13/22 pt to ED with increasing SOB and cough; states had a positive COVID test 2 days prior to coming to ED; sx have worsened; positive COVID test in ED; pt diaphoretic and c/o epigastric pain without radiation; found to have moderate to large pericardial effusion; during hospitalization, pt experienced cardiac arrest - repeat episodes; intubated; transferred to MICU; given IV ABX and IV pressors; family then made pt a DNR, comfort care; pt extubated and he passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: scleroderma, pericardial effusion, CKD, HLD, HTN, gout, hypothyroidism, GERD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 29.04.2021
Beginn: 09.09.2021
Tage bis Beginn: 133,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory distress syndrome Acute respiratory failure COVID-19 pneumonia Death Endotracheal intubation Extubation Pneumonia

Symptomtext

During the hospitalization , patient was treated for following diagnosis 1. Acute hypoxic respiratory failure with ARDS secondary to COVID-19 bilateral pneumonia (POA): Patient was intubated on 09/12/2021 Patient was extubated on 09/18/2021 and within few minutes of extubation patient passed away comfortably with family members bedside Patient was pronounced dead at 12:31 p.m. on 09/18/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2303656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 06.05.2021
Beginn: 01.02.2022
Tage bis Beginn: 271,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury COVID-19 Chemotherapy Death Encephalopathy Hypercalcaemia Plasma cell myeloma Pulseless electrical activity SARS-CoV-2 test positive

Symptomtext

Pfizer COVID vaccine #3 given 12/17/2021, lot # FE3594; pt had a positive COVID test on 2/11/2022, ordering facility Hospital; 3/30/22 admitted to hosp with acute renal failure, acute hypercalcemia, acute encephalopathy, dx with multiple myeloma; took 3 rounds of chemotherapy; no renal failure improvement; suffered 2 PEA arrests and did not survive the second one.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 29,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TN
Alter: 63,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 12.03.2021
Beginn: 12.04.2022
Tage bis Beginn: 396,0
Dosis: 3
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death and COVID pos S/p COVID vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD Hypertension
Andere Medikamente: loratadine methotrexate montelukast prednisone folic acid
Allergien: amoxicillin codeine
Vorherige Impfungen: -

VAERS 2278520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 16.05.2022
Impfdatum: 04.05.2021
Beginn: 01.11.2021
Tage bis Beginn: 181,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Cardiac arrest Chest tube insertion Death Endotracheal intubation General physical health deterioration Haemoptysis Intensive care Mental status changes Pneumothorax Pulmonary mass SARS-CoV-2 test positive

Symptomtext

pt presented to ED with altered mental state and coughing up bloody secretions; left pneumothorax, right lung mass; positive for COVID; given IVFs, ABX, dexamethasone; intubated, Chest tube placed; transferred to ICU; pt's condition declined; DNR; pt went into asystole and never recovered; death certificate and medical records sent per VAERS request

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: lung CA, COPD, HTN, CHF, lupus, stroke
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2273571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SD
Alter: 97,0
Geschlecht: M
Eingang: 12.05.2022
Impfdatum: 27.04.2021
Beginn: 27.09.2021
Tage bis Beginn: 153,0
Dosis: 2
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 Death Dyspnoea Ischaemic stroke SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 04/06/20221 and 04/27/2021. They tested positive for COVID-19 on 09/27/2021 x4. They were briefly admitted to hospital on 09/29/2021 after presenting to emergency department for shortness of breath, but were discharged back to the nursing home at which they were a resident. The individual was a DNR and on comfort care only. They died later on the same day, on 09/29/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID-19 tests x4 on 09/27/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Type II Diabetes, Previous Cerebrovascular Accident, Hypothyroidism, Chronic Kidney Disease (Stage III) Ischemic Stroke about 3 weeks prior to the adverse event. The individual was a resident of the nursing home indicated in the address portion of this form.
Andere Medikamente: -
Allergien: Codeine (reaction: other, not specified) Aspirin (reaction: other, not specified)
Vorherige Impfungen: -

VAERS 2265869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NC
Alter: 40,0
Geschlecht: M
Eingang: 06.05.2022
Impfdatum: 14.04.2021
Beginn: 21.08.2021
Tage bis Beginn: 129,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Pulmonary embolism Thrombosis

Symptomtext

Blood clot in left lower leg, Pulimonary Embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2260603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: AZ
Alter: 45,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 01.05.2021
Beginn: 01.12.2021
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Agitation Alopecia Angina pectoris Anosmia Arthralgia Blood test Cardiac stress test normal Constipation Diarrhoea Echocardiogram normal Electrocardiogram abnormal Headache Hepatic enzyme increased Injection site pain Joint swelling Laboratory test Malaise Myocardial infarction

Symptomtext

On the 12-03-2021 I got COVID-19 symptoms lasted till 12-13-2021, with symptoms for fever and headaches, body aches. I lost sense of smell. Right after Christmas, I started to feel agitated, pain in my left shoulder radiating to my heart. Went to see my PCP and she checked my vitals, said everything was okay, lungs were clear. I also had an EKG which shoed I had a heart attack, lower myocardia-infarction. I went to see a cardiologist on 01-06-2022 and another EKG was done with same results. The cardiologist sent me for an echocardiogram and nuclear stress test and these exams were normal. I was told my symptoms were viral and was dismissed on 04-07-2022 and myocarditis had disappeared. In mid march 2022, I started to have pain in my joints, hair was falling and my right ankle was swollen and pain in every joint in my body. I also had diarrhea and constipation. I went to my PCP again and my vitamin D was low. My liver enzymes were high as well. I am now also going to see a rheumatologist to check in the joints. I do not know if my symptoms are related to the vaccine or due to COVID-19. They also gave me a prescription for Pantoprazole 20mg from my gastroenterologist. I had also some pain in my left arm after my vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: EKG performed, lab blood panel on 04-06-2022
Aktuelle Erkrankungen: COVID-19
Vorgeschichte: MASH, Fatty Liver Stage II, Sleep Apnea
Andere Medikamente: Hydrochlorothiazide
Allergien: NKDA
Vorherige Impfungen: Flu shot, 5-6 years ago, I got bronchitis.

VAERS 2241905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OR
Alter: 48,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 15.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram cerebral Arteriovenous fistula Arteriovenous malformation Brain scan abnormal Cerebral haemorrhage Cerebral thrombosis Diplopia Dizziness Headache Impaired work ability Magnetic resonance imaging Migraine Transient ischaemic attack Venogram

Symptomtext

I experienced a severe headache, with double vision which came and went for 2 days, then I developed a severe migraine that would not abate with medication which lasted for 6 days. After the headache went away I was still experiencing double vision. Doctors thought it could be a transient ischemic neurological event and the vision would return to normal as it cleared itself, which took 2 months. 4 months after the vaccine I began experiencing dizziness and when they performed a head scan they found a clot, arterial venous malformation fistula, and evidence of a bleed. I am under ongoing care from physicians. I was out of work due to double vision and neurological procedure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: MRI; MRV scan; Neuro Angiogram
Aktuelle Erkrankungen: No
Vorgeschichte: Hypertension; Overweight; Intercranial Hypertension; Migraine with Aura
Andere Medikamente: Clenbuterol, Zyrtec, Multivitamin, Vitamin D
Allergien: Onion; Seasonal Allergies; Erythromycin; Bee Stings
Vorherige Impfungen: -

VAERS 2231147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 13.04.2022
Impfdatum: 05.10.2021
Beginn: 01.01.2022
Tage bis Beginn: 88,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Death General physical health deterioration Intensive care Respiratory failure SARS-CoV-2 test positive

Symptomtext

pt brought to hospital; in hypoxic respiratory failure; found to be positive for COVID; admitted to ICU; high flow O2; ABX, dexamethasone and remdesivir given; pt's condition worsened; status changed to DNR/DNI; transitioned to comfort care and passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD on O2 at home
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1216702

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MN
Alter: 45,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 09.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Brain stem infarction Cerebrovascular accident Hemiparesis Imaging procedure abnormal Motor dysfunction Brain stem stroke Ischaemic stroke Neurological symptom

Symptomtext

Pontine stroke symptoms 3 days after the first immunization on 4/9/2021. Resolution of symptoms after brief hospitalization. Recurrent stroke 6/5/2021 resulting in significant hemiparesis and functional impairment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: Hospitalization 4/15 - 4/18/2021 and 6/6-6/10/21. Brain imaging confirmed pontine stroke
Aktuelle Erkrankungen: Longstanding Diabetes mellitus, diabetic nephropathy, retinopathy, neuropathy, hypertension, hyperlipidemia
Vorgeschichte: Longstanding Diabetes mellitus, diabetic nephropathy, retinopathy, neuropathy, hypertension, hyperlipidemia
Andere Medikamente: -
Allergien: Multiple environmental allergies, mold, pollen, dust mites
Vorherige Impfungen: -

VAERS 2223156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 22.04.2021
Beginn: 09.10.2021
Tage bis Beginn: 170,0
Dosis: 2
Route/Site: UN / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute kidney injury Acute respiratory failure COVID-19 pneumonia Cardio-respiratory arrest Death Dialysis Dyspnoea Intensive care

Symptomtext

Presented to the ER 10/9 with c/o SOB; admitted 10/9 for acute hypoxic resp failure & PNA d/t COVID & tx w/steroids, zinc, Vit C, & pepcid; 10/10 added Zithromax; 10/11 added Cefipime; 10/12 tx to ICU d/t increased resp demand & increased WOB on Max AirVo settings. Pt also developed AKI and was started on dialysis; 10/23 pt coded and ROSC unable to be achieved & pt expired.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 49,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 06.05.2021
Beginn: 01.01.2022
Tage bis Beginn: 240,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Acute myocardial infarction Arrhythmia COVID-19 Cardiac arrest Computerised tomogram head abnormal Death Drug screen positive Endotracheal intubation Fall Life support Metabolic acidosis Pulseless electrical activity Resuscitation SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

pt brought to hosp by EMS after pt fell at home and was unresponsive; family initiated CPR; EMS found pt in PEA arrest; treated and ROSC obtained; intubated; to ED; positive for COVID; given steroids; positive for cocaine; metabolic acidosis; suspected NSTEMI versus alternative arrhythmia; CT brain scan showed possible encephalomalacia; stroke work up; pt experienced multiple cardiac arrests with PEA; ACLS; reintubated; ROSC achieved; pt had another PEA arrest and passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD on dialysis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218140

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 19.08.2021
Beginn: 01.12.2021
Tage bis Beginn: 104,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal distension Asymptomatic COVID-19 Death Endotracheal intubation Hepatic encephalopathy Hypotension Intensive care Mental status changes Pulse absent Resuscitation SARS-CoV-2 test positive Unresponsive to stimuli Urinary incontinence

Symptomtext

pt to ED with altered mental status, swollen abdomen, urinary incontinence; had a previous hospitalization with hepatic encephalopathy, no lactulose given; spoke with PCP and he advised him to go to ED when arrives back home; positive test for COVID; asymptomatic; pt was found unresponsive in the bathroom and pulseless; CPR x 3; ROSC obtained; transferred and intubated; hypotensive; vasopressors; family updated with pt's condition and the decided to make him a DNR; pt died in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: alcoholic cirrhosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 76,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 22.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: UN / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute pulmonary oedema Acute respiratory failure Death

Symptomtext

Patient was fully vaccinated Pfizer on 4/5/21, 4/26/21 and received booster on 12/22/21. Facility received death abstract. confirmed Patient was admitted on 12/28/21 to Hospital. Patient Died 12/31/21 at 00:20 due to Acute Hypoxic Respiratory failure and flash pulmonary edema. No further information provided to facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2170732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 85,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 29.04.2021
Beginn: 06.10.2021
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 pneumonia

Symptomtext

pt admitted to hosp , ARF with Hypoxia secondary to COVID pneumonia; treated with steroids, ABX, dexamethasone, O2 supplementation; worsening respiratory failure; pt was transitioned to comfort care

Weitere VAERSDATA-Felder

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

VAERS 2157714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 55,0
Geschlecht: M
Eingang: 04.03.2022
Impfdatum: 15.04.2021
Beginn: 10.01.2022
Tage bis Beginn: 270,0
Dosis: 2
Route/Site: IM / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death Hypoxia Pyrexia Terminal state Tremor Viral test

Symptomtext

per report received. it appears patient was a resident of long term acute care facility. 1/9/2022 became feverish, shaky and hypoxic. patient was diagnosed with COVID-19 and it was determined that patient was terminal. Patient was transferred to Hospice. Comfort measures including parentally controlled substances per order. Patient died 1/11/2022 at 04:15

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: PCR
Aktuelle Erkrankungen: unknown
Vorgeschichte: Endocarditis Aortic and mitral valve replacements. CHF PEA arrest- required tracheostomy
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2110741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 57,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 19.05.2021
Beginn: 16.07.2021
Tage bis Beginn: 58,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2098753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: PA
Alter: 31,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 08.05.2021
Beginn: 29.10.2021
Tage bis Beginn: 174,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abortion spontaneous Foetal death Maternal exposure before pregnancy Second trimester pregnancy Ultrasound foetal abnormal Uterine cervix dilation procedure Uterine dilation and evacuation

Symptomtext

2nd trimester missed miscarriage detected on 10/29/2021 (18th week of pregnancy). Fetal demise is believed to have occurred at 16 weeks. Treated with dilation and evacuation procedure on 11/5/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: 1,0
Labordaten: Ultrasound 10/29/21 Laminaria placement 11/4/21 D&E outpatient procedure 11/5/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: Cats Mold
Vorherige Impfungen: -

VAERS 2098653

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 84,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 17.04.2021
Beginn: 28.01.2022
Tage bis Beginn: 286,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac arrest Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Death Emphysema Endotracheal intubation Intensive care Lung opacity Mental status changes Pleural effusion Pseudomonas test positive Pulseless electrical activity SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/27/2021 and 4/17/2021. Presented to the ED with altered mental status.Admitted for acute hypoxic resp failure 2/2 Covid PNA and COPD exacerbation. Received: vitamin C, budesonide, methylprednisolone, zinc, redesivir, tocilizumab, and antibiotics. Mentation initially improved but 2/1/2022 transferred back to ICU due respiratory decompensation. On 2/2/2022 had a brief cardiac arrest following mechanical intubation. CRRT was initiated in the evening and patient subsequently had another PEA arrest. Patient expired at 2139.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: 1/28/2022: COVID positive and chest x-ray showed emphysema, small bilateral pleural effusions, and hazy opacities. 2/2/2022: respiratory culture positive pseudomonas.
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, diverticulitis, dementia, CHF, CKD, diabetes, anemia, GERD, dyslipidemia, emphysema
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2087699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 02.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Acute respiratory failure Ageusia Anosmia COVID-19 COVID-19 pneumonia Chest discomfort Chest pain Computerised tomogram thorax abnormal Dyspnoea Exposure to SARS-CoV-2 Lung opacity Malaise Procalcitonin Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient presented to ED with worsening SOA and increased O2 requirements. States that she had a loss of taste and sense of smell starting early this week and was tested a couple days after her daughter tested positive for Covid and tested positive herself. States that she received casirivimab and imderimab infusions on 12/29. Patient states that this am her SOA and chest pain/tightness became worse, prompting her to come to the ED. Patient states that her family was going to initially get together for the holidays, however when her brother tested Covid positive, they cancelled all plans; then her daughter and husband became sick and she is now sick. Patient received both Covid vaccines and the booster. Hospital medicine consulted for admission. Acute hypoxic respiratory failure sec to COVID 19 pneumonia 63yo F w/ CML s/p BMT c/b CGVH, previous hx of bilateral DVT ( completed treated ), HTN, neuropathy, GERD presenting with worsening respiratory failure due to COVID19 requiring oxygen. -COVID positive on 12/31. -CT PE - negative for PE. Multifocal GGO. procalcitonin elevated to 0.22 on admission and trended down to 0.09 without any treatment -12/30: started remdesivir and dexamethasone. Finished 5 days of remdesivir. Discharged with dexamethasone to finish until 1/9/22 dexa for total 10 days. Resume home prednisone 30 mg daily after that. -required up to 5 L NC . Improved to 2 L NC at rest and on exertion. -she was discharged with home oxygen 2 L NC at rest and exertion. Recommended to check oxygen twice a day. Discharge Disposition/Condition Disposition: Home with Home Health Condition: Stable (s/sx potential problems absent or manageable)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: COVID PCR positive on 12/31/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: Past Medical History CML s/p BMT (allogeneic) T2DM GERD Chemo induced cardiomyopathy Peripheral neuropathy
Andere Medikamente: Acyclovir Allopurinol Amitriptyline HCl Cyclobenzaprine HCl Dexametha
Allergien: Latex
Vorherige Impfungen: -

VAERS 2072131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 49,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 22.05.2021
Beginn: 25.01.2022
Tage bis Beginn: 248,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Death related to complications of COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSC: DM; idiopathic subglottic tracheal stenosis; HTN; HLD; obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2072000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 69,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 24.08.2021
Beginn: 14.01.2022
Tage bis Beginn: 143,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Blood pressure abnormal COVID-19 COVID-19 pneumonia Cough Death Dyspnoea Endotracheal intubation Intensive care Pyrexia SARS-CoV-2 test positive Septic shock

Symptomtext

Pfizer COVID-19 Vaccine: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/1/2021, 3/30/2021 and 8/24/2021. Presented to ED 1/14/2022 with complaints of shortness of breath, cough, and fever of 7 days duration. Admitted to MICU for acute hypoxemic respiratory failure due to Covid PNA. Started on remdesivir and decadron and given 1 dose Toci per ID recommendations. Intubated 1/19/21. Developed septic shock requiring levophed to maintain blood pressure. Increased to 3 pressors 1/22. Code status changed to DNR/COT 1/22/22. Required a 4th pressor 1/23/22. Expired on 1/23/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: Positive COVID-19 on 1/5/2022 using the Hologic Panther System platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Allergic rhinitis, Anemia, Asthma, Automatic implantable cardioverter-defibrillator in situ, Cardiomyopathy, COPD, Muscular dystrophy, GERD, Gout, Obesity, Sleep Apnea, Osteoarthritis, Osteoporosis, Ventricular tachycardia, hypopituitism on chronic prednisone
Andere Medikamente: Acetaminophen, Albuterol, Amoxicillin, Budesonide, Calcitonin,Diclofenac gel, Ergocalciferol, Famotidine, Fluticasone Nasal, Ibuprofen, Ketorolac Ophthalmic, Levalbuterol, Levofloxacin, Magnesium, Nystatin, Olopatadine, Pantoprazole, Potass
Allergien: Azithromycin, Bactrim, Penicillin, Benzonatate
Vorherige Impfungen: -

VAERS 2050857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

kritisch

Staat: MO
Alter: 56,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 10.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death Mechanical ventilation SARS-CoV-2 test positive

Symptomtext

case tested positive on 1/1/22 at hospital . ventilated on 1/4. died 1/15

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: CLL (leukemia)
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2218956

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 18.08.2021
Beginn: 03.01.2022
Tage bis Beginn: 138,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Anticoagulant therapy Aortic arteriosclerosis Atelectasis COVID-19 Cardiac failure acute Cardiomegaly Chest X-ray abnormal Chronic kidney disease Dyspnoea Electrocardiogram abnormal Hypervolaemia Left ventricular failure Lung opacity Oedema peripheral Pleural effusion Pulmonary oedema SARS-CoV-2 test positive

Symptomtext

Narrative: Admitted JAN 3,2022@21:01:20 Discharged JAN 11,2022@16:07 Assessment: 1. Acute-on-Chronic Diastolic Heart Failure 2. Acute Hypoxic Respiratory Failure 3. CKD Stage 3 67 yo male with PMH HTN, HLD, recently ESRD on HD (6/21-8/21) but now CKD 3a, DM, h/o prostate cancer, s/p right 2nd/3rd toe amputations, and left foot osteomyelitis, former smoker who presented to the Emergency Dept on 1/3/22 with worsening bilateral lower extremity edema and shortness of breath in setting of COVID complicated by acute hypoxic respiratory failure. He was admitted with Acute hypoxic respiratory failure secondary to COVID (Despite being COVID vaccinated x 2) with volume overload. Continued on home Lasix PO 40 mg BID. Completed Rocephin 1/8/2022 for CAP coverage. Completed 5 day course of remdesivir and dexamethasone and anticoagulated with Intermediate dose anticoagulation. Required 2L NC. Walk test on 1/10 with desat to 86% pm RA. Arranged for home O2 on discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Date Test Name Result 01/10/2022@12:00 COVID-19 SCREENING (Alinity-M) POSITIVE 01/03/2022@16:40 COVID-19_(XPRESS PCR) DETECTED Exam Date/Time 01/03/2022 14:25 Procedure Name CHEST-1 VIEW (AP/PA) Impression Again demonstrated are cardiopulmonary findings most consistent with congestive heart failure, including pulmonary edema, small, bilateral layering pleural effusions, and suspected bibasilar compressive atelectasis. An interstitial infectious or inflammatory process is not excluded. Correlation with patient's signs and symptoms is recommended. Report EXAM: AP portable upright chest dated 01/03/22 14:25:00 COMPARISON: 10/11/21 FINDINGS: EKG leads overlie the chest. Allowing for portable technique, there is redemonstration of borderline cardiomegaly. There is redemonstration of diffuse bilateral central interstitial opacity. There is hazy and patchy bibasilar opacity redemonstrated, with a mild linear component at the right lung base. There is redemonstration of aortic calcification tortuosity. Postsurgical changes of the left glenoid are again demonstrated.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2005680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 29.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

vaccinated-covid related death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute UTI; cellulitis; COPD; asthma; DM2; CKD stage 3; CAD; HTN; HLD; morbid obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1997540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: IL
Alter: 34,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 09.09.2021
Beginn: 11.09.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Chest X-ray abnormal Chest wall tumour Computerised tomogram Death Hepatomegaly Intensive care

Symptomtext

Unprecedented and unexplained tumor growth throughout chest cavity. Liver 3 times normal size. Quotes from oncologist, thoracic surgeon, ICU doctor and cardiologist "I've never seen anything like this" "We thought we were looking at someone else's scans" Vaccine given 9/9/2021, patient death 10/4/2021, less than 30 days post vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: CT scans, Chest X-ray, blood work
Aktuelle Erkrankungen: Malignant Mesothelioma
Vorgeschichte: None
Andere Medikamente: Bumex, Cholecalciferol, Digoxin, Gabapentin, Robitussin, Norco, Motrin, Corlanor, Magnesium Oxide, Melatonin, Robaxin, Metolazone, Metoprolo XL, Protonix, KDUR, Pericolace, Zoloft
Allergien: NKA
Vorherige Impfungen: -

VAERS 1961966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 63,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 13.09.2021
Beginn: 16.12.2021
Tage bis Beginn: 94,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

fully vaccinated, covid related death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM2; PVD; HTN; HLD; asthma; history of immunosuppressive therapy; hx of CVAs; obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1940497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: KS
Alter: 88,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 28.08.2021
Beginn: 01.10.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal lymphadenopathy Activated partial thromboplastin time shortened Acute kidney injury Acute respiratory failure Agitation Alanine aminotransferase increased Aspartate aminotransferase increased Asthenia Atelectasis B-cell small lymphocytic lymphoma Biopsy bone marrow abnormal Blood bilirubin increased Blood creatinine increased Blood fibrinogen decreased Blood lactate dehydrogenase increased Blood triglycerides increased Chest X-ray abnormal Chronic lymphocytic leukaemia

Symptomtext

Note 1 Nov 2021: 88 y.o. male with history of CLL on acalabrutinib, CAD s/p stent directly admitted from Clinic on 10/26 for neutropenic fever with pancytopenia. IVIG was given on 10/27 for suspected ITP due to covid vaccine,, and patient had an infusion reaction. Increased oxygen requirements, fever, and encephalopathy requiring transfer to ICU on 10/29. Hematology is consulted for continuity of care. # CLL # Pancytopenia # Acute DIC # Concern for HLH - Diagnosed 8/2019, peripheral blood flow revealed immunophenotype c/w CLL and FISH showed del13 and del6 - 7/2021: started acalabrutinib due to progressive symptoms and cytopenias - Treatment on hold since 10/20 for cytopenias - Hgb 11.4 with MCV 90 on admission (baseline Hgb 12-14) -- > 8.7 - Platelets 8 on admission, s/p IVIG 1gm/kg 10/27 & 28 for suspected ITP -- > 9K with last transfusion 10/31 - Haptoglobin <30, fibrinogen 52-- > 48 with last 5 pack of cryo 10/31, INR 1.6, PTT 34, D-dimer 2211, LDH 1632-- >2536, TB 1.4, Ferritin >7500, TG 236 - WBC 2 with ANC 1100 and ALC 980 on admission -- > 23 with ANC 760 - s/p BMBx 10/28:Residual chronic lymphocytic leukemia/small lymphocytic lymphoma, interstitial pattern, involving approximately 20-30% of cellular elements in hypercellular bone marrow (60-70%) with decreased granulopoiesis, increased erythropoiesis, dyserythropoiesis, and 3% blasts. - 10/29: RRT called for hypoxia, agitation; transferred to ICU - started on dexamethasone for HLH from 10/29/21 - remains on high flow oxygen, and pressors # Acute Hypoxemic Respiratory Failure # IVIG Reaction # Neutropenic Fever - Patient with low-grade fevers and dry cough for several weeks, Tmax 101-102F usually at night - CXR (10/26): bilateral small pleural effusion and bilateral opacities at the bases - IVIG reaction (10/27): RRT called for tachycardia, high-grade fever, AMS, hypotension (SBP 90s); given steroids and Benadryl. No hives, angioedema, or rash. Oxygen requirement up to 6L, patient with intermittent AMS afterwards - CT chest (10/28): bibasilar atelectasis and mild pleural effusions - CT A/P (10/28): lymphadenopathy (increased in abdomen, decreased in pelvis) and new mild-moderate hepatosplenomegaly - ID consulted, concern for disseminated fungal infection given new hepatosplenomegaly - Currently on meropenem # Severe Dysphagia # Weight Loss # Melena - Patient reports decreased appetite noticed as early as September 2021, increasing difficulty with swallowing of solids, unintentional 10-15lb weight loss since July, and black stools - Last endoscopy/HRM in 2016 unremarkable - GI consulted, plan for EGD once patient is more stable # AKI - Scr 1.14 on admission (baseline 0.7-0.8) -- > 4.07 # Transaminitis - AST/ALT normal on admission -- > AST 238, ALT 66 Recommendations: ?Discussed in details with the patient and the family about his previous and recent labs, imaging findings, his diagnosis, possible management options and prognosis. We explained that his HLH is not responding as we expected with the steroids, he has been on the steroids for 3 days by now. Briefly explained about use of etoposide in HLH but also expressed the concern about tolerability of chemotherapy in a frail elderly patient, in ICU, on pressors with severe cytopenias. Patient and his family understand the severity of the disease and agree with the plan. We will plan to continue the steroids for now. - Continue dexamethasone 10mg/m2 with plans for tapering as follows for suspected HLH: - Week 1 and 2: 10mg/m2 - Week 3 and 4: 5mg/m2 - Week 5 and 6: 2.5mg/m2 - Week 7: 1.25mg/m2 - Week 8: taper to zero - unfortunately he ultimately died of complications stemming from tx of ITP 2/2 covid vaccines given 1/28/2021, 2/22/2021, and 8/28/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: see note
Andere Medikamente: -
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 1932902

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NC
Alter: 48,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 04.05.2021
Beginn: 10.06.2021
Tage bis Beginn: 37,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Cough Pulmonary embolism Thrombosis

Symptomtext

Dry cough, blood clot in left thigh and right calf, blood clot burst causing pulmonary embolism; was put on blood thinners.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Ulcerative colitis
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1917807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 19.04.2021
Beginn: 22.11.2021
Tage bis Beginn: 217,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acidosis Agitation Anuria Blood alkaline phosphatase normal Blood bicarbonate Blood creatinine increased Blood lactic acid Blood pH decreased Blood potassium increased COVID-19 Cough Death Dyspnoea Encephalopathy Fall COVID-19 pneumonia Chest X-ray abnormal Computerised tomogram head normal

Symptomtext

Patient is deceased (11.26.21); Hospitalized 11.25.21; COVID-19 positive (11.22.21); fully vaccinated Admission Date: 11/25/2021; Discharge Disposition: Deceased (11.26.21) DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Pneumonia due to COVID-19 virus [U07.1, J12.82] Septic shock (HCC) [A41.9, R65.21] HOSPITAL COURSE: Patient is a 64-year-old woman past medical history significant for type 2 diabetes, peptic ulcer disease, paroxysmal atrial fibrillation not on home anticoagulation was admitted for septic shock secondary to COVID-19 pneumonia. Upon arrival to the emergency department, patient was initially hypothermic, tachypneic, hypotensive, hypoxic requiring high-flow nasal cannula and peripheral pressors. Initial labs were notable for pH of 6.78, creatinine 8.36, potassium 6, bicarb to, ALP 112, lactic acid 16.2. CXR demonstrated patchy multifocal opacities. Patient was administered 1 L of normal saline, calcium chloride 3 g, 1 amp of bicarb. While awaiting transfer to the medical intensive care unit, patient underwent a fall in her room. CT head was negative, CT C-spine was notable for severe motion degradation artifact but no evidence of C-spine injury on visualized segments. No injuries noted secondary to fall. Upon arrival to the medical intensive care unit, patient was significantly encephalopathic and agitated. Discussion with her son at bedside confirmed wishes for code status of do not resuscitate/DNI as identified in the emergency department by the social worker. Patient was altered and agitated. She was gasping for air while attempting to get up from bed. She is requiring pressor support, continues to be tachycardic and tachypnic and HFNC @ 50% FiO2. Patient is not producing urine. Fluid status +5.5L since admission. She remained profoundly acidemic with 3 pressors but still had low blood pressures. With her agitation, it will be difficult to place a dialysis catheter without complications or needing to intubate her to place the vascath. Patient's current condition, treatments, and prognosis was shared with the patient , and family. Patient continued at this point have worsening septic shock requiring 3 pressors this morning and worsening renal function for which she would be a candidate for renal replacement therapy. To further pursue renal replacement therapy, patient would likely need to be intubated. At this point, both son and husband wished to pursue and respect patient's wishes she previously expressed "that she would not want to be on a mechanical ventilator lifelong, or even for short duration if this was only brief while requiring renal replacement therapy." Patient was deemed DNR/DNI per their wishes. After husband arrived to the hospital, patient was transitioned to comfort care and shortly thereafter Dr. was contacted of patient's passing. Dr's saw the patient at bedside and performed a death examination. Patient was pronounced dead at 5:45 pm likely due to profound shock. I requested for a medical examiner because the patient died within 24 hours of admission and also had a fall while in the emergency department. I spoke with Dr. from the Medical Examiner's office who determined this is not a medical examiner case and does not require autopsy therefore autopsy will not be performed. Ok to release to funeral home.

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Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: 11.22.21 - Urgent Care visit - COVID-19 positive - Urgent Care with COUGH (fatigue, cough, loss of appetite for about 1 week. no OTC meds. ) - did not receive Monoclonal antibody treatment
Vorgeschichte: Essential hypertension Hyperlipidemia Type 2 diabetes mellitus without complication, with long-term current use of insulin (HCC) Atrial fibrillation (HCC) Esophageal stricture Gastric outlet obstruction Iron deficiency anemia due to chronic blood loss Osteoarthritis of both knees Septic shock (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet Blood Glucose Monitoring Suppl (BLOOD GLUCOSE MONITOR SYSTEM) w/Device KIT blood glucose test strips chlorthalidone (HYG
Allergien: Ampicillin Erythromycin Ibuprofen PenicillinsRash
Vorherige Impfungen: -

VAERS 1881317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: KY
Alter: 49,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 08.05.2021
Beginn: 30.10.2021
Tage bis Beginn: 175,0
Dosis: 1
Route/Site: UN / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Activated partial thromboplastin time normal Acute left ventricular failure Acute pulmonary oedema Acute respiratory failure Alanine aminotransferase normal Albumin globulin ratio decreased Alcohol abuse Anion gap normal Anticoagulant therapy Arteriosclerosis Ascites Aspartate aminotransferase normal Atrial fibrillation Basophil count decreased Basophil percentage decreased Blood albumin decreased Blood alkaline phosphatase increased Blood bilirubin increased

Symptomtext

11/3/21 Altered Mental Status Per EMS, neighbors called for altered mental status, unknown last known well. Per neighbors, pt is usually A&Ox4. Per EMS, pt follows commands, unable to answer any questions. Cardiogenic shock Procedures: 1. CT head: No acute disease 2. CT chest noncontrast: Acute on chronic pulmonary vascular congestion. Marked cardiomegaly. 3. CT abdomen/pelvis: Perihepatic and upper abdominal and pelvic ascites with moderate body wall edema. Advanced atherosclerosis. Mild diverticular disease 4. Renal ultrasound: Normal 5. Blood cultures: No growth 6. COVID-19: Negative 7. Hemoglobin A1c: 8.4 8. TSH: 6.8 10/30/21: This patient was a 49-year-old male with a past medical history significant for chronic systolic CHF with EF 14%, type II poorly controlled diabetes mellitus, LV thrombus on Eliquis, hypertension, chronic kidney disease, history of alcohol abuse, and a history of medical noncompliance who presented to hospital secondary to an altered mental status. She was admitted to the intensive care unit for cardiogenic shock secondary to an acute on chronic systolic CHF and metabolic encephalopathy. The patient was seen and evaluated by the heart failure group at which time it was noted that this patient has remained noncompliant in the outpatient setting as well. Over the course of his hospitalization, multiple discussions took place regarding his status. He eventually agreed to DNR status. He did require multiple continuous drips that included dopamine, Neo-Synephrine, Levophed, vasopressin, milrinone, heparin, amiodarone, Bumex, Precedex, and dopamine drips during the hospitalization. Unfortunately, given his noncompliance, there was little that could be done. Despite multiple continuous drips, the patient eventually expired on November 3, 2021 at 1924.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: Results for patient as of 11/18/2021 17:58 11/3/2021 10:34 Sodium: 118 (LL) Potassium: 4.5 Chloride: 86 (L) CO2: 13 (L) Glucose: 326 (H) BUN: 61 (H) Creatinine: 1.97 (H) BUN/Creat Ratio: 31.0 Total Protein: 6.5 Albumin: 2.7 (L) Globulin: 3.8 Albumin/Globulin Ratio: 0.7 (L) Calcium: 7.5 (L) Bilirubin-Total: 5.3 (H) ALT/SGPT: 33 AST/SGOT: 28 Alkaline Phosphatase: 338 (H) Estimated GFR: 36 (L) Estimated GFR: 44 (L) Phosphorus: 3.4 Magnesium: 1.8 Anion Gap: 19 (H) PTT: 63.2 (H) WBC: 24.41 (H) RBC: 3.70 (L) HGB: 11.1 (L) HCT: 35.3 (L) MCV: 95.4 MCH: 30.0 MCHC: 31.4 Platelet Count: 89 (L) MPV: 13.0 (H) Differential Type: Hospital CBC w/AutoDiff NEUT%: 46.6 LYM%: 51.2 (H) Mono%: 1.5 EOS%: 0.1 BASO%: 0.2 IG%: 0.4 EOS#: 0.02 NRBC%: 0 Absolute Neutrophil Count: 11.38 (H) Baso#: 0.04 Red Cell Distribution Width-CV: 17.3 (H) Absolute Lymphocyte Count: 12.50 (H) Monocyte Absolute: 0.37 Immature Granulocyte Abs: 0.10 10/30/21 COVID-19 RESULT Not Detected Not Detected
Aktuelle Erkrankungen: -
Vorgeschichte: 1. Acute on chronic systolic CHF (congestive heart failure) (8/11/2021) 2. Metabolic acidosis, 3. Leukocytosis (10/30/2021) 4. Metabolic encephalopathy (10/30/2021) 5. Acute respiratory failure with hypoxia (11/2/2021) 6. Acute pulmonary edema with congestive heart failure (11/2/2021) 7. Elevated alkaline phosphatase level (8/11/2021) 8. Hyponatremia (10/30/2021) 9. Abnormal LFTs (10/30/2021) 10. New onset atrial fibrillation (10/31/2021) 11. History of alcohol abuse (8/11/2021) 12. Left ventricular thrombus (8/15/2021) 13. Chronic anticoagulation with Eliquis (8/21/2021) 14. Alcohol abuse (10/30/21) 15. Thrombocytopenia (10/30/2021) 16. Hypothyroidism (11/2/2021)
Andere Medikamente: ampicillin-sulbactam 3 g Intravenous Q6H o aspirin 81 mg Oral Daily o digoxin 125 mcg Intravenous Every Other Day o furosemide 80 mg Intravenous Q8H o LORazepam o mupirocin 0.5 g Nasal BID o tamsulosin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1877255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 83,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.05.2021
Beginn: 06.11.2021
Tage bis Beginn: 185,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cellulitis Death Dyspnoea Fatigue Oxygen saturation decreased Pain in extremity Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 4/14/2021 and 5/5/2021. Covid-19 + in September, 2021. Patient presented to ED on 11/6/2021 for leg pain and diagnosed with severe cellulitis, denies injury to leg, found to be Covid-19 + upon admission. On 11/10/2021 patient began to complain of fatigue and increased dyspnea with increased oxygen requirements. Family elected for palliative care due to declining oxygen saturations despite NIPPV. Patient expired on 11/11/21.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID Positive on 11/6/2021 using Cepheid GeneXpert, 10/1/2021 using the Hologic Panther System, 9/25/2021 using Cepheid GeneXpert
Aktuelle Erkrankungen: -
Vorgeschichte: Cellulitis, Hypertension, Osteoarthritis, Asthma, COPD, OSA, Atrial Fibrillation, Interstitial Lung disease, Anemia
Andere Medikamente: Acetaminophen PRN, Diphenhydramine PRN, Albuterol PRN, Augmentin 500 mg BID, Apixaban 5 mg BID, Arformoterol BID, Azelastine Nasal QD, Budesonide Nebs BID, Carvedilol 3.125 mg BID, Cetirizine 10 mg QD, Furosemide 40 mg QD, Gabapentin 100 mg
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 1876598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: KY
Alter: 46,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 09.04.2021
Beginn: 20.10.2021
Tage bis Beginn: 194,0
Dosis: 2
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Death

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Rotator cuff tear
Vorgeschichte: Musculoskeletal and Integument Osteoarthritis of right knee, unspecified osteoarthritis type Medial meniscus tear Primary osteoarthritis of right knee Primary osteoarthritis of knee Chondromalacia, patella Greater trochanteric bursitis of left hip Genitourinary Uterovaginal prolapse, incomplete Other Fibromyalgia Impingement syndrome of right shoulder Encounter for gynecological examination Health care maintenance
Andere Medikamente: diclofenac (VOLTAREN) 75 MG EC tablet DULoxetine (CYMBALTA) 30 MG capsule DULoxetine (CYMBALTA) 60 MG capsule levothyroxine (SYNTHROID) 100 MCG tablet nitrofurantoin, macrocrystal-monohydrate, (MACROBID) 100 MG capsule oxyCODONE-acetam
Allergien: Penicillin V PenicillinsRash
Vorherige Impfungen: -

VAERS 1857775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 13.04.2021
Beginn: 22.10.2021
Tage bis Beginn: 192,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Aspartate aminotransferase increased COVID-19 COVID-19 pneumonia Condition aggravated Electrolyte imbalance Hypokalaemia Hypomagnesaemia Lipase increased SARS-CoV-2 test positive Tachycardia

Symptomtext

COVID PNEUMONIA ACUTE HYPOXEMIC RESPIRATORY FAILUTRE TACHYCARDIA ELECROLYTE ABNORMALITIES HYPOKLEMIA HYPOMAGNESEMIA ELEVATED AST ELEVATED LIPASE

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: COVID POSITIVE 10/28/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: fluticasone propionate (FLONASE) 50 mcg/act nasal suspension metFORMIN (GLUCOPHAGE) 1000 mg oral tablet albuterol (VENTOLIN HFA;PROVENTIL HFA;PROAIR) 108 (90 BASE) MCG/ACT inhalation inhaler metoprolol (TOPROL XL) 100 mg oral XL tabl
Allergien: -
Vorherige Impfungen: -

VAERS 1857453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 69,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 11.05.2021
Beginn: 08.11.2021
Tage bis Beginn: 181,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure COVID-19 COVID-19 pneumonia

Symptomtext

Acute respiratory failure with hypoxia; COVID-19 virus infection; Pneumonia due to COVID-19 virus

Weitere VAERSDATA-Felder

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

VAERS 1850145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

kritisch

Staat: IL
Alter: 65,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 24.04.2021
Beginn: 20.10.2021
Tage bis Beginn: 179,0
Dosis: UNK
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Death

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1839942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 18.04.2021
Beginn: 02.11.2021
Tage bis Beginn: 198,0
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 Sepsis

Symptomtext

Acute hypoxemic respiratory failure due to COVID-19; SEPSIS due to COVID-19 Pneumonia

Weitere VAERSDATA-Felder

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

VAERS 1833236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 21.04.2021
Beginn: 26.07.2021
Tage bis Beginn: 96,0
Dosis: 2
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Cerebral infarction Chills Death Dyspnoea Hyperglycaemia Hypoxia Magnetic resonance imaging head abnormal Mental status changes Positive airway pressure therapy Pyrexia SARS-CoV-2 test positive

Symptomtext

pt comes to ED and states he was diagnosed positive for COVID 2 days ago; presents to ED with increasing SOB, fever, chills, hypoxic, placed on 3 L O2 via NC; COVID test is positive; pt is hyperglycemic; received insulin, steroids, antibiotics, remdisivir, thromboembolic prophylaxis; eventually switched to BiPAP; mental status worsened; MRI of brain shows widespread, extensive acute infarctions; his condition worsened and he eventually passed away in the hospital

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Praegender Schweregrund: Death
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1786567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 29.04.2021
Beginn: 04.10.2021
Tage bis Beginn: 158,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Adenovirus test Alanine aminotransferase normal Angiogram pulmonary abnormal Aspartate aminotransferase normal Atrial fibrillation Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride decreased Blood creatinine normal Blood culture Blood culture negative Blood glucose Blood lactic acid Blood potassium normal Blood sodium decreased Blood urea normal

Symptomtext

10/04/21 Fever or Chills Difficulty breathing Fatigue 10/05/2021 CARE Cough (Primary Dx); SOBOE (shortness of breath on exertion); COPD with acute exacerbation (HCC); Pulmonary HTN (HCC); New onset type 2 diabetes mellitus (HCC) ED to Hosp-Admission Discharged 10/8/2021 - 10/12/2021 (4 days) Hospital Acute on chronic respiratory failure with hypoxia (CMS/HCC) Hospital Problems POA * (Principal) Acute on chronic respiratory failure with hypoxia (CMS/HCC) Yes Plan chief complaint: Worsening shortness of breath Acute on chronic hypoxic respiratory failure secondary to COVID-19 pneumonia -Patient uses 3 LPM of O2 at baseline. At the ED, she required 4 LPM. She was very dyspneic at rest and on exertion. D-dimer was elevated. CTA chest is negative for pulmonary embolism. There is diffuse interstitial disease with mild groundglass opacity of the right lung apex that is nonspecific. -Continue O2 supplementation. DuoNeb 4 times a day and as needed. Start Mucinex, incentive spirometry and OPEP. Consult pulmonary service Severe sepsis secondary to COVID-19 pneumonia -Patient presented with tachypnea, blunted tachycardia due to beta-blocker and calcium channel blocker use, with respiratory source of infection and lactic acidosis. CT chest showed diffuse interstitial disease with groundglass opacity of the right lung apex. -Start dexamethasone 6 mg once daily. She is agreeable to start remdesivir. Start remdesivir once daily. Check CRP. Procalcitonin low. She was started on ceftriaxone and azithromycin at the ED. Monitor procalcitonin and if it remains low, consider discontinuing antibiotics in the next 24 hours. Follow-up blood cultures. Lactic acidosis -Likely due to hypoxia and sepsis. Lactic acid on admission 2.5. Patient received a total of 1 L NS bolus at the ED. -Addendum: Repeat lactic acid 2.9. O2 sat 95% on 4 LPM. She is volume overloaded on exam. I think that lactic acidosis may also be due to hypoperfusion from CHF. Will give IV diuretic and monitor. Check TTE Acute exacerbation COPD Pulmonary hypertension -dexamethasone and remdesivir as above. DuoNeb 4 times daily and as needed. Continue Breo inhaler. Patient states that she uses BiPAP at night. Will order BiPAP while admitted. Consult pulmonary service. Paroxysmal atrial fibrillation -Continue diltiazem, metoprolol, flecainide and digoxin. Continue Xarelto. Currently on sinus rhythm on my examination. Check EKG Intermittent chest pain -Patient states that she has intermittent chest pain but this is her baseline. Check EKG and troponins. Addendum: troponin 0.04 x 2. No EKG changes. Will monitor Hyponatremia -pt had decreased appetite in the past few days but looks volume overloaded on exam. Sodium on admission is 126. She received a total of 1 L NS bolus at the ED. Repeat sodium 130. She looks volume overloaded on exam. I will continue her on diuretic. Continue to monitor sodium Bilateral leg swelling - She has bilateral leg swelling at baseline which has worsened in the past few days. Continue bumetanide and spironolactone. D-dimer is elevated. I will order ultrasound of the lower extremities to rule out DVT Type 2 diabetes -Hold Metformin. I will put her on insulin sliding scale while admitted. Closely monitor blood sugars since she is on dexamethasone. Adjust insulin dose as needed Anxiety/depression -Continue sertraline. She takes temazepam nightly. She also takes lorazepam as needed. I offered to call her family but she declined. 1. Nutrition: Consistent carbohydrate, heart healthy diet 2. VTE prophylaxis: SCD, on Xarelto 3. Disposition: Admit to 3 S. 4. Code Status: DNI but okay for CPR -discussed with patient 5. Estimated length of stay: At least 4 more day(s) 6. Time Spent: 70 minutes was spent face-to-face with the patient, greater than 50% of the time was spent counseling the patient and family at the bedside regarding treatment, medications, chart review and lab results and coordination of care. History of Present Illness Pt is an 50 y.o. female who presented to the ED with worsening cough and shortness of breath. Patient has a past medical history of COPD on home O2, atrial fibrillation, pulmonary hypertension, diastolic heart failure, hypertension, anxiety/depression, type 2 diabetes. She has chronic hypoxic respiratory failure from COPD, using 3 LPM of O2 at home. Her symptoms started 6 days ago. She had worsening cough compared to her baseline. She also had worsening shortness of breath at rest and on exertion. She has chronic bilateral leg swelling that is also worse. She has had poor appetite. No diarrhea or abdominal pain. She also complains of intermittent chest pain which is usual for her. She was diagnosed with COVID-19 on October 5, 2021 at an urgent care center. She had an x-ray done at urgent care which showed multifocal pneumonia. She was advised to go to the hospital but she did not want to. She has persistent symptoms so she eventually went to the emergency department. Patient received only 1 dose of Pfizer vaccine in January 2021. She states that she did not receive the second dose because she thought that she had a reaction to the first dose -she claims that she had more coughing and dyspnea after first dose. At the ED, patient was tachypneic with RR 24, she was requiring 4 LPM of O2 at the ED. D-dimer was elevated 0.79. CTA of the chest is negative for PE. There is diffuse interstitial disease with mild groundglass opacity of the right lung apex that is nonspecific. Lactic acid was 2.5. Patient was given NS bolus 1 L at the ED. Patient will be admitted for treatment of acute on chronic hypoxic respiratory failure secondary to COVID-19 pneumonia. She is at high risk for deterioration given COPD and heart disease. Review of Systems Constitutional: Positive for activity change, appetite change and fatigue. Negative for chills and fever. HENT: Negative for nosebleeds and trouble swallowing. Respiratory: Positive for cough, shortness of breath and wheezing. Cardiovascular: Positive for chest pain and leg swelling. Negative for palpitations. Gastrointestinal: Negative for abdominal distention, abdominal pain, constipation, diarrhea, nausea and vomiting. Genitourinary: Negative for dysuria and hematuria. Musculoskeletal: Negative for joint swelling and myalgias. Neurological: Negative for dizziness, seizures, syncope, facial asymmetry, speech difficulty, light-headedness, numbness and headaches. Psychiatric/Behavioral: Negative for agitation, behavioral problems, confusion and hallucinations. The patient is not nervous/anxious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 10/08/2021 2327 Respiratory virus detection panel Collected: 10/08/21 2327 | 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 Detected Critical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Syncytial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected 10/05/2021 1214 COVID-19 EXTERNAL (NON WELLSPAN OR NON INTERFACED LAB) Collected: 10/05/21 1214 | Final result | Specimen: Swab from Nasopharynx COVID-19 Overall Result External Detected Critical Procedure Note MD - 10/05/2021 Formatting of this note might be different from the original. EXAM: XR CHEST 2 VIEWS HISTORY: Productive cough, shortness of breath COMPARISON: None FINDINGS: Upright PA and lateral views of the thorax are provided for interpretation. There is an implantable cardiac loop recorder. There are hazy airspace opacities in both lung bases which could represent atelectasis but are concerning for focal infiltrates. There is no pleural effusion or pneumothorax. The cardiomediastinal silhouette is mildly enlarged. There are no acute osseous abnormalities. IMPRESSION: Bibasilar airspace opacities concerning for multifocal pneumonia. LABORATORY RESULTS: CBC: Results from last 7 days Lab Units 10/08/21 2326 WBC AUTO K/mcL 6.9 HEMOGLOBIN g/dL 11.5 HEMATOCRIT % 37.5 PLATELETS K/mcL 216 NEUTROS PCT AUTO % 71 LYMPHS PCT AUTO % 21 MONOS PCT AUTO % 7 EOS PCT AUTO % 0 CHEMISTRY: Results from last 7 days Lab Units 10/08/21 2326 SODIUM mmol/L 126* POTASSIUM mmol/L 4.9 CHLORIDE mmol/L 97* CO2 mmol/L 20* BUN mg/dL 10 CREATININE mg/dL 0.78 CALCIUM mg/dL 8.5* TOTAL PROTEIN gm/dL 6.9 BILIRUBIN TOTAL mg/dL 0.3 ALK PHOS IU/L 81 ALT IU/L 26 AST IU/L 28 COAGULATION: Results from last 7 days Lab Units 10/09/21 0200 INR 1.0 OTHER TESTS: 0 Lab Value Date/Time TROPONINI 0.03 (H) 01/05/2021 0436 TROPONINI 0.03 (H) 01/05/2021 0152 TROPONINI 0.04 (H) 01/04/2021 2125 TROPONINI 0.03 (H) 10/21/2019 0132 TROPONINI 0.03 (H) 10/20/2019 2305 TROPONINI <0.03 01/22/2018 0642 TROPONINI <0.03 01/22/2018 0255 TROPONINI <0.03 01/21/2018 2145 TROPONINI <0.03 05/03/2017 1545 TROPONINI <0.03 05/03/2017 1025 TROPONINI 0.04 (H) 04/12/2017 1118 TROPONINI 0.04 (H) 04/12/2017 0812 TROPONINI 0.03 (H) 04/12/2017 0341 TROPONINI 0.03 (H) 04/01/2017 2143 TROPONINI 0.03 (H) 02/02/2017 1420 TROPONINI <0.10 04/27/2010 0755 CULTURE RESULTS: Lab Results Component Value Date URCULT No Growth at 1:1000 dilution 02/01/2020 Lab Results Component Value Date BLOODCX No growth at 120 hours 01/04/2021 IMAGING: X-ray chest 1 view, Portable Result Date: 10/9/2021 XR CHEST 1 VW PORT IMPRESSION: Likely pulmonary edema and congestive failure. END OF IMPRESSION: INDICATION: sob. TECHNIQUE: Portable AP projection of the chest is acquired. COMPARISON: 1/8/2021 FINDINGS: There is mild cardiomegaly allowing for position. Pulmonary vascular prominence and interstitial opacity is demonstrated. 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: 10/9/2021 CTA CHEST PULMONARY EMBOLISM W WO CONTRAST IMPRESSION: No evidence of pulmonary thromboembolus. Nonspecific lymphadenopathy which was also present previously. Diffuse interstitial disease is noted with mild ground glass opacity of the right lung apex that is nonspecific. Pulmonary Artery Embolism: None. Cardiomegaly: None. RV/LV ratio: N/A END OF IMPRESSION: INDICATION: Short of breath. Rule out pulmonary emboli Assess for pulmonary artery embolism. TECHNIQUE: Contrast-enhanced helical CT scan of the chest was performed from the lung apices to below the diaphragm. Multiplanar, MIP and 3D reconstructions were performed under concurrent radiologist supervision on an independent 3D workstation and reviewed. Automated dose reduction technique utilized. Total number of CT examinations at this institution in the past 12 months: 1 CONTRAST: 100mL of IOHEXOL 350 MG IODINE/ML INTRAVENOUS SOLUTION administered INTRAVENOUS. Quality of contrast opacification was Adequate. Other limitations: None COMPARISON: 1/5/2021 FINDINGS: There is no evidence of a filling defect in the pulmonary arterial system. There is no evidence of cardiac or aortic enlargement. There is diffuse nonspecific lymph node prominence up to approximate 14 mm diameter. Mediastinal lymph nodes are also present are mildly prominent. There is no evidence of axillary lymphadenopathy. Mildly nodular thyroid is noted. There is no esophageal dilatation. There is no evidence of pleural or pericardial effusion. There is no evidence of osseous lesion with mild degenerative change. There appears to be a mild degree of diffuse bilateral interstitial thickening and there is nonspecific groundglass opacity in the right lung apex. Pleural effusion is no longer present. No significant abnormality in the upper abdomen is demonstrated. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. Medical Decision Making/ Level of Risk: high
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Angina pectoris (CMS/HCC) Chest pain Epigastric pain Syncope Syncope, unspecified syncope type Unstable angina pectoris (CMS/HCC) Respiratory Chronic lung disease Difficulty breathing Obstructive sleep apnea syndrome Sleep apnea Obstructive sleep apnea Chronic obstructive pulmonary disease (CMS/HCC) Orthopnea Asthma Interstitial lung disease (CMS/HCC) Lung mass Panlobular emphysema (CMS/HCC) Acute respiratory failure with hypoxemia (CMS/HCC) Tachypnea Oxygen dependent Community acquired pneumonia COPD exacerbation (CMS/HCC) Circulatory Disease of pulmonary circulation (CMS/HCC) Essential hypertension Irregular heart rhythm Palpitations Tachycardia Paroxysmal atrial fibrillation (CMS/HCC) Pulmonary hypertension (CMS/HCC) Diastolic CHF, chronic (CMS/HCC) Demand ischemia (CMS/HCC) Acute diastolic congestive heart failure (CMS/HCC) Digestive Barrett's esophagus Benign neoplasm of colon Bile-induced gastritis Constipation Dysphagia Gastroesophageal reflux disease Pseudopolyposis of colon (CMS/HCC) Intestinal malabsorption Nausea Nausea and vomiting Gastric ulcer Stricture of esophagus Esophageal dysphagia Gastroesophageal reflux disease without esophagitis Morbid obesity (CMS/HCC) Gastroesophageal reflux disease with esophagitis, unspecified whether hemorrhage Musculoskeletal Arthritis Hiatal hernia Bilateral edema of lower extremity Endocrine/Metabolic Hypercholesterolemia Pure hypercholesterolemia Mixed hyperlipidemia Lactic acidosis New onset type 2 diabetes mellitus (CMS/HCC) Hypomagnesemia Type 2 diabetes mellitus without complication, without long-term current use of insulin (CMS/HCC) Hematologic Iron deficiency anemia Anemia Immune Sepsis (CMS/HCC) Severe sepsis (CMS/HCC) Other Malignant neoplastic disease (CMS/HCC) History of colonic polyps Hypersomnia with sleep apnea Epigastric abdominal tenderness Anxiety Edema Hx of adenomatous colonic polyps Elevated alkaline phosphatase level Elevated glucose level Bandemia Depression
Andere Medikamente: albuterol 2.5 mg /3 mL (0.083 %) nebulizer solution albuterol HFA (PROVENTIL HFA) 90 mcg/actuation inhaler bumetanide (BUMEX) 2 mg tablet cyclobenzaprine (FLEXERIL) 10 mg tablet dexAMETHasone (DECADRON) 6 mg tablet dexlansoprazole (DEX
Allergien: CodeineShortness of breath / Dyspnea, Palpitations Sulfamethoxazole-trimethoprimSwelling , Rash Valium [Diazepam]Nausea and Vomiting, Chest Pain / Tightness Versed [Midazolam]Nausea and Vomiting, Chest Pain / Tightness Amoxicillin-pot ClavulanateOther (document details in comments) Hydrocodone-acetaminophenOther (document details in comments) TramadolOther (document details in comments)
Vorherige Impfungen: -

VAERS 1783820

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: GA
Alter: 78,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 20.04.2021
Beginn: 22.09.2021
Tage bis Beginn: 155,0
Dosis: UNK
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Death

Symptomtext

Patient fully vaccinated and died due to Covid related causes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Lung disease, diabetes, high blood pressure
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1778972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 43,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 25.06.2021
Beginn: 11.10.2021
Tage bis Beginn: 108,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure COVID-19 Diabetic neuropathy Dialysis End stage renal disease Insulin-requiring type 2 diabetes mellitus

Symptomtext

Hospitalization - acute respiratory failure with hypoxia; ESRD on dialysis; COVID-19; T2M with diabetic polyneuropathy with long-term current use of insulin

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

VAERS 1771652

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OH
Alter: 15,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 03.06.2021
Beginn: 02.10.2021
Tage bis Beginn: 121,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram Blood test Computerised tomogram abdomen Echocardiogram Muscle strain Pleural effusion Pulmonary embolism Pulmonary infarction

Symptomtext

Patient had a pulmonary embolism and infarct to his right lung, pleural effusions bilaterally and right heart strain from the clot.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: He was admitted to the hospital 10/5-6. He had CT of the abdomen and pelvis, and a CTA. He had numerous blood tests, he had an echocardiogram.
Aktuelle Erkrankungen: -
Vorgeschichte: autism, ADHD, depression/anxiety, insulin resistance, allergies and asthma
Andere Medikamente: Klonopin 2mg qhs, Cogentin ER 2mg qhs, wellbutrin XL 300mg qd, risperidal 1.5 mg po bid, topamax 100mg bid, neurontin 300mg qd, lithium 450mg bid, metformin 500mg bid, xyzal 5mg qam, fish oil, melatonin, vitamin D, albuterol hfa 90 mcg 2 pu
Allergien: Amoxicillin/Penicillins
Vorherige Impfungen: -

VAERS 1759243

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: PA
Alter: 72,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 21.04.2021
Beginn: 13.09.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Acute kidney injury Acute respiratory failure Adenovirus test Aortic valve incompetence Atelectasis Atrial fibrillation Blood culture negative Bordetella test negative COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Cardiomegaly Central venous catheterisation Chest X-ray abnormal Chest tube insertion Chlamydia test negative Chronic obstructive pulmonary disease

Symptomtext

ED to Hosp-Admission Discharged 8/27/2021 - 9/15/2021 (19 days) Last attending ? Treatment team Acute on chronic diastolic (congestive) heart failure Final Summary for Deceased Patient BRIEF OVERVIEW Admitting Provider: MD Discharge Provider: MD Primary Care Physician at Discharge: MD Admission Date: 8/27/2021 Discharge Date: 9/15/2021 Final Diagnosis Principal Problem: Acute on chronic diastolic (congestive) heart failure Active Problems: Paroxysmal A-fib Pulmonary hypertension, moderate to severe Chronic obstructive pulmonary disease with acute exacerbation Pleural effusion on right End stage COPD Congestive heart failure, unspecified HF chronicity, unspecified heart failure type Endocarditis Lactic acidosis DETAILS OF HOSPITAL STAY Date and time of death: September 15, 2021, 12:11 PM Cause of death: Septic shock from COVID-19 pneumonia Acute respiratory failure from COVID-19 and systolic heart failure Secondary diagnoses: Severe aortic insufficiency Superimposed bacterial pneumonia Acute renal failure Lactic acidosis Possible endocarditis Atrial fibrillation with rapid ventricular response End-stage COPD Elevated LFTs Coagulopathy from malnutrition and acute illness Hospital Course Patient is a 72-year-old female with history of COPD, atrial fibrillation on Coumadin, systolic heart failure, recent TMVR presented to the hospital with systolic heart failure. She is admitted to medical service and seen by the heart failure team. Echocardiogram showed severe aortic insufficiency and was being considered for valve intervention. She was treated with IV diuretics however her respiratory status did not improve. Hospital course was prolonged and she was hospitalized for 18 days. There is consideration of endocarditis given possible vegetations noted on aortic valve. CT surgery recommended aggressive antibiotic regimen and stated she was high risk for surgery. Initially was plan for IV antibiotics through October 4. She was treated with Lasix infusion, however urine output became marginal. Patient's x-ray developed progressive infiltrates and on September 14 she was found to have COVID-19 infection. She was started on steroids and received plasma as well. Antibiotics were also broadened to cover potential superimposed bacterial pneumonia. Despite this, her clinical condition deteriorated. She developed progressive renal failure as well as elevated LFTs and coagulopathy. She became more somnolent and oxygen requirement escalated. She became progressively critically ill and was requiring vasopressors, and was maxed on norepinephrine. Unfortunately, she continued to deteriorate and passed away on September 15. I passed along my condolences to the patient's son.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 19,0
Labordaten: 09/13/21 1432 Respiratory virus detection panel Collected: 09/13/21 1319 | 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 Detected Critical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Syncytial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected Procedure Component Value Ref Range Date/Time X-ray chest 1 view, Portable [3302832002] Resulted: 09/14/21 1407 Order Status: Completed Updated: 09/14/21 1407 Narrative: XR CHEST 1 VW PORT IMPRESSION: Persistent diffuse interstitial opacities bilaterally, similar to prior radiographs. END OF IMPRESSION: INDICATION: CHF, COVID 19 with increased O2 req. TECHNIQUE: AP upright projection of the chest is acquired. COMPARISON: Radiographs of 9/13/2021. FINDINGS: There is unchanged cardiomegaly. Right-sided PICC catheter and TAVR again noted. Right basilar chest tube again noted. Persistent diffuse interstitial opacities bilaterally, similar to prior radiographs. No evidence of pneumothorax. Hiatal hernia is noted. Little significant interval change compared to prior radiographs. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. Ultrasound liver [3302633235] Resulted: 09/13/21 1016 Order Status: Completed Updated: 09/13/21 1017 Narrative: US LIVER IMPRESSION: Nonobstructive calculus in the right lower pole of the kidney, 8 mm. Small right pleural effusion. Otherwise, no sonographic abnormality in the remaining right upper quadrant of the abdomen. END OF IMPRESSION: INDICATION: Elevated LFTs. TECHNIQUE: Grayscale ultrasonography and color Doppler of the right upper quadrant of the abdomen was performed. Permanently recorded images were obtained and stored. COMPARISON: Correlation made with CT of the abdomen and pelvis dated 8/15/2021 LIMITATIONS: None. FINDINGS: Liver size: Normal. Length: 14.1 cm. Liver echogenicity: Normal. Liver contour: Smooth. Liver mass: None. Liver vasculature: Normal. Bile ducts: Intrahepatic and extrahepatic bile ducts not dilated. Common bile duct: 2 mm. Gallbladder: Surgically absent. Pancreas: Head, body, and tail appear normal. Right kidney: No pelvicalyceal dilatation. Echogenic focus in the lower pole, 8 mm. Length: 11.4 cm. Perfusion: Normal. Inferior vena cava: Visualized portions appear normal in caliber. Ascites: None. Small right pleural effusion. Normal values: Liver length 15-18 cm; common duct <= 6 mm; gallbladder wall <= 3 mm, length <= 8-12 cm, and width <= 4 cm; kidney 9.5-11.5 +/-1.3 cm. 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 [3302574370] Resulted: 09/13/21 0733 Order Status: Completed Updated: 09/13/21 0733 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Stable chest. 2. See below report. END OF IMPRESSION: INDICATION: F/U hypoxia. TECHNIQUE: Single AP projection of the chest is acquired. COMPARISON: Chest radiograph dated September 11, 2021. FINDINGS: Cardiomegaly changes are stable. Cardiac valve repair changes are stable. Right-sided PICC line with tip in the SVC/RA junction is stable. Diffuse interstitial edema or infiltrates in perihilar region are stable. Cannot exclude perihilar pneumonia changes versus CHF. Right basilar chest tube is stable. Small left basilar effusion changes are stable. 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 [3302413288] Resulted: 09/11/21 0721 Order Status: Completed Updated: 09/11/21 0721 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Some increasing diffuse interstitial alveolar lung infiltrates. Increasing in the right upper lung. 2. Findings may be a combination of CHF and possible underlying pneumonia. 3. Otherwise stable chest. 4. See below report. END OF IMPRESSION: INDICATION: Congestion. TECHNIQUE: Single AP projection of the chest is acquired. COMPARISON: Chest radiograph dated September 9, 2021. FINDINGS: Moderate cardiomegaly changes are stable. Diffuse interstitial alveolar lung infiltrates are somewhat increased in the right lung. Right-sided PICC line with the tip in the SVC/RA junction is stable. Cardiac valve replacement changes are reidentified. No pneumothorax is noted. Patient is rotated to the right. Small bibasilar effusion changes are stable. 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 [3301777237] Resulted: 09/09/21 0846 Order Status: Completed Updated: 09/09/21 0846 Narrative: XR CHEST 1 VW PORT IMPRESSION: Interval worsening of pulmonary edema. END OF IMPRESSION: INDICATION: Hypoxia. TECHNIQUE: AP upright projection of the chest is acquired. COMPARISON: AP chest 9/7/2021. FINDINGS: There has been interval worsening of diffuse interstitial opacities in bilateral lungs, indicating worsening of pulmonary edema. No additional changes are noted since the prior study. 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 [3301430639] Resulted: 09/07/21 1416 Order Status: Completed Updated: 09/07/21 1416 Narrative: XR CHEST 1 VW PORT IMPRESSION: Bilateral perihilar and diffuse interstitial opacities slightly improved from prior likely reflecting improving interstitial edema. END OF IMPRESSION: INDICATION: hypoxia. TECHNIQUE: AP portable upright projection of the chest is acquired. COMPARISON: September 1, 2021 FINDINGS: Prosthetic cardiac valve stent is again noted. There is a right upper extremity PICC unchanged. There are bilateral perihilar and diffuse interstitial opacities slightly improved from prior likely reflecting improving interstitial edema. There is no significant pleural effusion. There is no pneumothorax. The cardiomediastinal silhouette is unchanged in size. Pleurx catheter at the right lung base is unchanged. 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 [3300502907] Resulted: 09/01/21 1239 Order Status: Completed Updated: 09/01/21 1239 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Prominence of the vascular pattern, worrisome for vascular failure. 2. Bibasilar atelectasis. 3. Improved right basilar opacity. END OF IMPRESSION: INDICATION: PNEUMOTHORAX pleural effusion. TECHNIQUE: AP upright projection of the chest is acquired. COMPARISON: Radiographs of 8/31/2021. FINDINGS: The cardiomediastinal silhouette is unchanged. Right-sided PICC catheter and right basilar Pleurx drainage catheter are unchanged position. Transarterial aortic valve replacement is unchanged. There is an intra-arterial occlusion device, unchanged. Even allowing for inspiratory effort, the vascular pattern is prominent and worrisome for vascular failure. Improved opacity at the right lung base. There is mild bibasilar atelectasis. 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 [3300337828] Resulted: 08/31/21 1308 Order Status: Completed Updated: 08/31/21 1308 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Small right-sided pleural effusion, slightly improved compared to prior radiographs. 2. Persistent small right apical pneumothorax with Pleurx catheter in place. 3. Mild pulmonary edema bilaterally. END OF IMPRESSION: INDICATION: PNEUMOTHORAX pleural effusion. TECHNIQUE: AP upright projection of the chest is acquired. COMPARISON: Radiographs of 8/31/2021. FINDINGS: There is unchanged cardiomegaly. Persistent right-sided pleural effusion, slightly improved compared to prior radiographs. Right-sided Pleurx catheter is in unchanged position. Right basilar opacity is again noted which may reflect atelectasis or reexpansion edema. There is mild pulmonary edema bilaterally. Redemonstrated is a small right apical pneumothorax. Right-sided PICC catheter is unchanged in position. 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 [3300337830] Resulted: 08/31/21 0711 Order Status: Completed Updated: 08/31/21 0711 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. New small right apical pneumothorax. 2. Right greater than left pleural effusions and adjacent hazy airspace opacities, with improved aeration of the right lower lobe compared to the prior study. 3. Unchanged cardiomegaly. END OF IMPRESSION: INDICATION: sob, s/p pleurx cath today for effusion. TECHNIQUE: AP upright portable projection of the chest is acquired. COMPARISON: Chest radiograph performed on August 30, 2021. FINDINGS: Unchanged cardiomegaly. There is a small moderate right pleural effusion with adjacent hazy airspace opacity, decreased compared the prior study, with improved aeration of the right lower lobe. Hazy left lower lobe opacity, unchanged from the prior study, with probable minimal left pleural fluid. Unchanged prominence of the bilateral interstitial markings. There is a small right apical pneumothorax, new compared to the prior study. A right-sided chest catheter terminates in the right lower lung zone. A right-sided PICC line terminates in the atriocaval junction. An aortic stent is noted. Calcification of the aortic arch is identified. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. IR pleurx pleural catheter insertion [3300337812] Resulted: 08/30/21 1624 Order Status: Completed Updated: 08/30/21 1624 Narrative: IR PLEURX PLEURAL CATHETER INSERTION IMPRESSION: Right-sided tunneled pleural catheter placement with immediate drainage of 1400 mL of amber fluid. Plan: Tunneled pleural catheter ready for immediate use. Contact interventional radiology if issues with drainage. END OF IMPRESSION: _______________________________________________________________ Procedural Personnel Attending physician(s): M.D. Fellow physician(s): None Resident physician(s): None Advanced practice provider(s): None Pre-procedure diagnosis: Pleural effusion Post-procedure diagnosis: Same Indication: Non-malignant pleural effusion Additional clinical history: None Complications: No immediate complications. PROCEDURE SUMMARY: - Ultrasound and fluoroscopic-guided tunneled pleural catheter placement - Additional procedure(s): None PROCEDURE DETAILS: Pre-procedure Consent: Informed consent for the procedure including risks, benefits and alternatives was obtained and time-out was performed prior to the procedure. Preparation: The site was prepared and draped using maximal sterile barrier technique including cutaneous antisepsis. Anesthesia/sedation Level of anesthesia/sedation: No sedation Anesthesia/sedation administered by: Not applicable Total intra-service sedation time (minutes): 0 Limited thoracic ultrasound Limited thoracic ultrasound was performed. A safe window for catheter insertion was identified. Findings: There is a large right pleural effusion. Tunneled pleural catheter placement Local anesthesia was administered. The pleural cavity was accessed with a 17G needle and a wire was placed. A subcutaneous tunnel was anesthetized adjacent to the puncture site and the catheter was tunneled through the subcutaneous tissues. Serial dilation of the pleural access point was performed, and a peel-away sheath was placed. The catheter was passed into the sheath as it was peeled away. Pleural access technique: Real-time ultrasound guidance Catheter placed: BD PleurX Closure The pleural access site was closed and the catheter was secured to the skin. A sterile bandage was applied. Access site closure technique: Tissue adhesive Catheter securement technique: Non-absorbable suture Contrast Contrast agent: None Contrast volume (mL): 0 Radiation Dose Fluoroscopy time (minutes): 0.2 Reference air kerma (mGy): 1.35 Kerma area product (Gy-cm2): 0 Additional Details Additional description of procedure: None Equipment details: None Specimens removed: Pleural fluid Estimated blood loss (mL): Less than 10 Standardized report: SIR_TunneledPleuralCatheter_v3 Attestation Signer name: WITHHELD I attest that I was present for the entire procedure. I reviewed the stored images and agree with the report as written. 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 [3300239920] Resulted: 08/30/21 0838 Order Status: Completed Updated: 08/30/21 0838 Narrative: XR CHEST 1 VW PORT IMPRESSION: Cardiomegaly with mild pulmonary venous cephalization and bilateral pleural effusions, right greater than left are not significantly changed. END OF IMPRESSION: INDICATION: Pneumothorax. Pleural effusion. TECHNIQUE: An AP upright portable projection of the chest was obtained on 8/30/2021 at 0539 hours. COMPARISON: 8/29/2021 FINDINGS: The heart size remains enlarged with evidence of valve repair. Mild pulmonary venous cephalization is noted. A right-sided PICC line terminates at the cavoatrial junction. A moderate-sized right pleural effusion and a small left pleural effusion are noted. There is associated right basilar atelectasis. 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 [3300134426] Resulted: 08/29/21 0842 Order Status: Completed Updated: 08/29/21 0843 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. No change large right pleural effusion obscuring the inferior right hemithorax. 2. New minor left base atelectasis. END OF IMPRESSION: INDICATION: pleural effusion. TECHNIQUE: AP portable projection of the chest is acquired. COMPARISON: 8/27/2021 FINDINGS: Prior transcatheter valve replacement. Left lung clear except for minor opacity partly obscuring the left hemidiaphragm. No change large right pleural effusion obscuring the inferior hemithorax. Stable heart and mediastinum. Bones and soft tissues unchanged. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 2 views [3299258969] Resulted: 08/27/21 1512 Order Status: Completed Updated: 08/27/21 1512 Narrative: XR CHEST 2 VW IMPRESSION: New right pleural effusion. END OF IMPRESSION: INDICATION: SOB. TECHNIQUE: PA and lateral views of the chest were obtained. COMPARISON: August 23, 2021 FINDINGS: There is a moderate-sized right pleural effusion increased from prior study. Heart is enlarged. There is been aortic valve replacement. There is a PICC in the SVC. Results Procedure Component Value Ref Range Date/Time Respiratory virus detection panel [3302633241] (Abnormal) Collected: 09/13/21 1319 Order Status: Completed Specimen: Swab from Nasopharynx Updated: 09/13/21 1432 Adenovirus Not Detected Not Detected Chlamydophila pneumoniae Not Detected Not Detected COVID-19 SARS-CoV-2 Overall Result Detected Critical Not Detected Coronavirus Not Detected Not Detected Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected Metapneumovirus Not Detected Not Detected Mycoplasma pneumoniae Not Detected Not Detected Parainfluenza Not Detected Not Detected Enterovirus/Rhinovirus Not Detected Not Detected Respiratory Syncytial Virus Not Detected Not Detected Bordetella pertussis Not Detected Not Detected Bordetella parapertussis Not Detected Not Detected Narrative: Testing performed by real-time polymerase chain reaction (PCR) and reverse transcriptase polymerase chain reaction (RT-PCR). The Dept. of Health has been notified of this result. Clostridium difficile PCR - Once [3302574341] (Normal) Collected: 09/12/21 1702 Order Status: Completed Specimen: Stool from Per Rectum Updated: 09/12/21 1807 C. diff PCR Not Detected Not Detected Narrative: Testing performed by real time polymerase chain reaction (PCR). Blood culture [3300502914] Collected: 09/01/21 1215 Order Status: Completed Specimen: Blood, Venous Updated: 09/06/21 1302 Blood Culture No growth at 120 hours Blood culture [3300502915] Collected: 09/01/21 1212 Order Status: Completed Specimen: Blood, Venous Updated: 09/06/21 1302 Blood Culture No growth at 120 hours Fungal culture - pleural, RIGHT [3300239957] Collected: 08/30/21 1606 Order Status: Sent Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/03/21 2304 Narrative: The following orders were created for panel order Fungal culture - pleural, RIGHT. Procedure Abnormality Status --------- ----------- ------ Fungal culture, (Sputum...[3300337801] In process Fungal smear (Sputum/Ti...[3300337803] Final result Please view results for these tests on the individual orders. Fungal smear (Sputum/Tissue/Body Fluid/Urine) [3300337803] Collected: 08/30/21 1606 Order Status: Completed Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/03/21 2304 Fungal Stain SEE BELOW Comment: SOURCE : BODY FLUID Result/Comment: No fungus seen on microscopic examination. Anaerobic culture - pleural, RIGHT - Tube 3 [3300239954] (Normal) Collected: 08/30/21 1606 Order Status: Completed Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/02/21 1006 Anaerobic Culture No anaerobes isolated Body fluid culture - pleural, RIGHT - Tube 3 [3300239955] Collected: 08/30/21 1606 Order Status: Completed Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/02/21 1006 Narrative: The following orders were created for panel order Body fluid culture - pleural, RIGHT - Tube 3. Procedure Abnormality Status --------- ----------- ------ Body fluid culture[3300337797] Final result Anaerobic culture[3300337799] Please view results for these tests on the individual orders. Body fluid culture [3300337797] Collected: 08/30/21 1606 Order Status: Completed Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/02/21 1006 Body Fluid Culture No growth Body Fluid Culture Gram Stain Few Polymorphonuclear leukocytes No bacteria seen Specimen concentrated for Gram stain AFB culture - pleural, RIGHT - Tube 3 [3300239948] Collected: 08/30/21 1606 Order Status: Sent Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/01/21 1037 Narrative: The following orders were created for panel order AFB culture - pleural, RIGHT - Tube 3. Procedure Abnormality Status --------- ----------- ------ AFB Culture Progressive...[3300337789] In process Mycobacteria Stain, Aci...[3300337791] Final result Please view results for these tests on the individual orders. Mycobacteria Stain, Acid-Fast, Fluorochrome [3300337791] Collected: 08/30/21 1606 Order Status: Completed Specimen: Body Fluid from Pleural Cavity, Right Updated: 09/01/21 1037 AFB Stain SEE BELOW Comment: Mycobacteria Stn,AF,Fluor SOURCE : BODY FLUID Result/Comment: No acid-fast bacilli seen. Mycobacteria smear result should be used as an adjunct to culture in diagnosing mycobacterial disease (e.g. tuberculosis). If intended, please ensure an order for Mycobacteria (Acid-Fast-Bacilli) culture has also been submitted. AFB Culture Progressive TB/MAI Probes, ID and TB/MAI Sensitivity [3300337789] Collected: 08/30/21 1606 Order Status: Sent Specimen: Body Fluid from Pleural Cavity, Right Updated: 08/30/21 1615 Fungal culture, (Sputum/Tissue/Body Fluid/Urine) [3300337801] Collected: 08/30/21 1606 Order Status: Sent Specimen: Body Fluid from Pleural Cavity, Right Updated: 08
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Chronic obstructive pulmonary disease with acute exacerbation Obstructive sleep apnea Acute respiratory failure with hypoxia Pleural effusion on right Hypoxia End stage COPD Circulatory Paroxysmal A-fib Hypotension Pulmonary hypertension, moderate to severe Aortic valve sclerosis Mitral stenosis Cerebral microvascular disease Left atrial thrombus Chronic diastolic congestive heart failure due to valvular disease Acute on chronic diastolic (congestive) heart failure Vegetation of heart valve Congestive heart failure, unspecified HF chronicity, unspecified heart failure type Endocarditis Digestive Obesity (BMI 35.0-39.9 without comorbidity) GERD (gastroesophageal reflux disease) Genitourinary History of urinary infection Endocrine/Metabolic Lactic acidosis Hematologic Erythrocytosis Relative polycythemia Other Positive blood culture History of cholecystectomy History of tonsillectomy Current smoker Unintended weight loss Dark stools Ground glass opacity present on imaging of lung Advanced directives, counseling/discussion
Andere Medikamente: acetaminophen (TYLENOL) 650 mg 8 hr tablet acetaminophen (TYLENOL) 650 mg 8 hr tablet albuterol HFA (VENTOLIN HFA) 90 mcg/actuation inhaler alendronate (FOSAMAX) 70 mg tablet amLODIPine (NORVASC) 2.5 mg tablet ascorbic acid, vitamin C,
Allergien: MorphineShortness of breath / Dyspnea AcetazolamideHives / Urticaria Sulfa (Sulfonamide Antibiotics)Hives / Urticaria Golden Rod Ragweed CyclobenzaprineJittery / shaky DiclofenacDizziness / Lightheaded
Vorherige Impfungen: -

VAERS 1718551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 14.04.2021
Beginn: 20.09.2021
Tage bis Beginn: 159,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure COVID-19 COVID-19 pneumonia SARS-CoV-2 test positive

Symptomtext

Hospitalized 9/20/21 from skilled nursing facility, SARS-CoV-2 positive 9/20/21, acute hypoxic respiratory failure due to Covid 19 Pneumonia

Weitere VAERSDATA-Felder

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

VAERS 1715538

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TN
Alter: 62,0
Geschlecht: U
Eingang: 20.09.2021
Impfdatum: 03.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 17,0
Dosis: UNK
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Ageusia Bradycardia COVID-19 pneumonia Death Dyspnoea Fatigue General physical health deterioration Hospitalisation Mechanical ventilation Myocarditis Oxygen saturation decreased PO2 decreased Productive cough Pyrexia

Symptomtext

Patient had diabetes, breast cancer and hypertension. Presented to the ED with a fever of 104, productive cough, shortness of breath, loss of taste, fatigue, and low oxygen saturations. She was diagnosed with COVID one week ago. Patient was admitted with COVID PNA and was placed on a ventilator on 8/22/2021. Patient developed significant bradycardia due to COVID myocarditis. She had only received her first dose of Moderna 8/3/2021. She continued to deteriorate and family chose to terminally extubate her and she expired on 9/4/2021.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: po2-46
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1685687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 65,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 30.04.2021
Beginn: 17.08.2021
Tage bis Beginn: 109,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure abnormal COVID-19 Cough Death Decreased appetite Diabetic ketoacidosis Dialysis Diarrhoea Endotracheal intubation General physical health deterioration Hypoxia Nausea Prone position Pyrexia Renal impairment Respiratory acidosis Resuscitation SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 4/7/2021 and 4/30/2021. Presented to ED on 8/17/2021 with cough, nausea, vomiting, diarrhea fever of 102, loss of appetite, and decreased UOP. Treated initially for DKA, and placed on HFNC. DKA resolved, and transitioned off insulin gtt 8/21. Due to increasing oxygen requirements, patient intubated on 8/23, and subsequently required proning. Developed septic shock, requiring norepinephrine and vasopressin gtt. Worsening renal function prompted Vascath placement and initiation of dialysis 8/29. Patient continued to deteriorate clinically, requiring the addition of epinephrine for blood pressure support, and worsening respiratory acidosis and hypoxemia. He developed wide complex tachycardia requiring 1 shock, after which family was called for goals of care discussion. Transitioned patient to comfort care, and he expired shortly thereafter.

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Praegender Schweregrund: Death
Hospital-Tage: 14,0
Labordaten: Positive COVID Tests on 8/17 and 8/18 .
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia of Chronic Disease, BPH, Chronic diastolic CHF, CHronic gout without tophus, Chronic ulcer of toe (left foot), Chronic venous insufficiency, CKD stage 3, CAD involving native artery of transplanted heart without angina pectoris, diabetic peripheral neuropathy associated with type 2 DM, Essential hypertension, H/O depression, H/O heart transplant, H/O nephrolithiasis, H/O shingles, hyperlipidemia, long-term immunosuppression, metabolic bone disease, obesity, Obstructive sleep apnea on CPAP, primary urethral papillary carcinoma.
Andere Medikamente: Aspirin 81 mg QD, Atorvastatin 40 mg QD, Cholecalciferol 1000 units BID, Cyanocobalamin 100 mcg QD, Fish Oil BID, Glimepiride 4 mg BID, Hydralazine 50 mg TID, Insulin aspart 20 units TID, Insulin glargine 30 units QD, Isosorbide dinitrate 2
Allergien: Gabapentin (altered mental status)
Vorherige Impfungen: -

VAERS 1582297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 21.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Angiogram cerebral Anticoagulant therapy Arteriogram carotid Atrial septal defect Cerebrovascular accident Computerised tomogram Echocardiogram Facial paralysis International normalised ratio Magnetic resonance imaging head abnormal Neurological symptom Prothrombin time Scan with contrast Speech disorder Transient ischaemic attack Ultrasound Doppler

Symptomtext

I woke up with stroke symptoms (right side facial drooping, speech deficit) in the morning on 4/30/2021. I went to the ER where I had many tests, including a MRI that confirmed the stroke. The doctors also discovered that I have a PFO in my heart which was closed on 7/9/3032. I had a TIA on 6/6/2021. I am taking Plavix, Asprin 81mg, atorvastatin, and immediately stopped use of microgestin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: CT scan without contrast MRI without contrast MRI with contrast MR Angiography Head without IV Contrast MR Angiography Neck without IV Contrast Prothrombin Time w/INR Transthoracic Echo (TTE) TCD Emboli Monitoring w/O Iv Saline - Hits Study
Aktuelle Erkrankungen: -
Vorgeschichte: migraine with aura
Andere Medikamente: microgestin fe 1/20, adderall XR 10mg, fiber, unisom
Allergien: -
Vorherige Impfungen: -

VAERS 1540952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OK
Alter: 52,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 04.08.2021
Beginn: 08.08.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac arrest Death

Symptomtext

Cardiac arrest resulting in death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, morbid obesity, hypertension, alcoholism
Andere Medikamente: Seroquel, guanfacine, fluoxetine, lisinopril, omeprazole, ondansetron, naltrexone
Allergien: none known
Vorherige Impfungen: -

VAERS 1524888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MD
Alter: 72,0
Geschlecht: M
Eingang: 04.08.2021
Impfdatum: 29.06.2021
Beginn: 01.07.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Coma Dyspnoea Illness SARS-CoV-2 test

Symptomtext

so sick that he could not breathe; so sick that he could not breathe; Coma; tested positive for COVID-19; This is a spontaneous report from a contactable consumer (Patient 's son) reported for a patient (Father). This is a report received from a Pfizer-sponsored program. A 72-years-old male patient received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0169 and Expiry date: Unknown), via an unspecified route of administration on 29Jun2021 at 17:00 (at the age of 72-yers-old) as DOSE 1, SINGLE for Covid-19 immunisation. The patient medical history included hypertension (Blood pressure high) (Caller says his father has high blood pressure, unknown when diagnosed, and he doesn't remember what medication he took). The patient concomitant medications were not reported (Caller says his father got no other vaccinations the same day as they got the COVID-19 vaccine or recently beforehand, and started no new medications. He says his father has high blood pressure). The patient had experienced so sick that he could not breathe on 04Jul2021 (the reporter says his father on the 3rd and on the 4th was so sick that he could not breathe, so they called the ambulance on 4th and he received treatment in the ICU, which he doesn't know what they did since he cannot see him), coma on Jul2021, tested positive for covid-19 on 02Jul2021. The patient received the first dose of the Pfizer COVID-19 vaccine on June 29th and then two days later he tested positive for COVID-19 and he wants to know if he still gets the second dose of vaccine as well. The patient was hospitalized for so sick that he could not breathe and coma for 18 days. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 27Jun2021, sars-cov-2 test: positive on 02Jul2021 (the reporter says that before they did the shot they did test two things, and on June 27th they were all negative for COVID-19, which was what make us like doesn't know what is going on, since on the 29th they were all positive after vaccine). Therapeutic measures were taken as a result of so sick that he could not breathe. Outcome of the events so sick that he could not breathe, Coma and tested positive for COVID-19 was unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma
Hospital-Tage: 18,0
Labordaten: Test Date: 20210627; Test Name: COVID-19 PCR test; Result Unstructured Data: Test Result:negative; Test Date: 20210702; Test Name: COVID-19 PCR test; Result Unstructured Data: Test Result:positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Verbatim: Blood pressure high)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1485986

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

kritisch

Staat: NY
Alter: -
Geschlecht: F
Eingang: 30.07.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angiogram cerebral abnormal Arteriogram carotid abnormal Cerebrovascular accident Computerised tomogram head abnormal Electrocardiogram abnormal Immune thrombocytopenia Gait inability Lacunar infarction Pericardial effusion Transient ischaemic attack Vasculitis Venogram abnormal

Symptomtext

ITP, Immune Thrombocytopenia Purpura; She has been told she is at risk for stroke; This is a spontaneous report received from a contactable consumer or other non-health care professional. A female patient of an unspecified age received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Batch/Lot Number: was not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced itp, immune thrombocytopenia purpura, she has been told she was at risk for stroke on an unspecified date. The events assessed as serious (medically significant). The letter references Pfizer BioNTech COVID19 Vaccine, BNT162B2, also Moderna BNT162B2. While providing information for the follow up caller stated one of her friends has ITP, Immune Thrombocytopenia Purpura, and now she has been told she was at risk for stroke. Maybe she had the Pfizer vaccine and it was aggravating her condition. Her friend was just in the Emergency Room and they told her that she was at risk for stroke. Caller declined to do report for her friend. The outcome of the events was reported as unknown. Information about lot/batch number has been requested.

Weitere VAERSDATA-Felder

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

VAERS 1509694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NH
Alter: 63,0
Geschlecht: M
Eingang: 28.07.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cerebrovascular accident Headache Neuralgia

Symptomtext

I had a stroke. My headaches were only on the left side of my temple. I've been getting a lot of nerve pain all on the left side on my body, back and leg. This pain has been occurring for over two months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: No medical test or laboratory results.
Aktuelle Erkrankungen: No Other illnesses at the time of vaccination and up to one month prior
Vorgeschichte: No Chronic or long-standing health conditions
Andere Medikamente: High blood pressure medications
Allergien: No Allergies to medications; food; other products
Vorherige Impfungen: -

VAERS 1493186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 22.07.2021
Impfdatum: 14.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Appetite disorder Asthenia Bacterial infection Blood glucose Blood glucose abnormal Cardiomegaly Cerebrovascular accident Decreased appetite Endocarditis Fall Hip fracture Hyperpyrexia Illness Mobility decreased Musculoskeletal discomfort Pyrexia Sepsis Somnolence

Symptomtext

Fall/ The second fall put him back in the hospital; He had a fever of 104; Endocarditis; got sick; sepsis; stroke; fell and broke his hip; weak; get a partial hip replacement; enlarged heart; know which bacteria caused it; his blood sugar was in the 600s; sleeping all of the time; lost his appetite; could not get out of bed; Patient was not eating or drinking; This is a spontaneous report received from a Pfizer sponsored program. A 66-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: EW0169) via an unspecified route of administration, administered in Arm on 14Apr2021 around 15:00 to 15:30 as dose 1, single for covid-19 immunisation. The patient's medical history included atrial fibrillation, patient was diagnosed years ago, before his stroke in 2015, a long time ago, cardiac failure congestive, aortic valve disease, cerebrovascular accident, diabetes mellitus, hypertension, last year patient had a blood infection, so he had to take four antibiotics. The patient's concomitant medications included rivaroxaban (XARELTO) taken for atrial fibrillation. It was reported that patient received the first dose of the vaccine in mid-April and got sick 2 days later(18Apr2021). Patient had a fever of 104. Caller took him to the doctor and patient was diagnosed sepsis. Patient was in the hospital and was then tested for and diagnosed with Endocarditis due to the sepsis. Patient was currently in a rehab facility and was weak. The rehab facility wanted to give patient the second dose of the covid vaccine. But the rehab facility was not sure if they will get the Pfizer covid vaccine. Reporter was worried about patient getting a second dose of anything. This was not the first-time patient has had endocarditis. Patient has been diagnosed with it before. Patient has a history of congestive heart failure, a bad aortic value, past stroke, and diabetes. They do not know if patient still had endocarditis, but patient has completed the antibiotics. They are unable to test patient again for endocarditis because he is in such bad shape. Patient had one side that was weak, and then he fell and broke his hip. Patient was not a candidate for open heart surgery because of his enlarged heart. Before patient received the first dose of the covid vaccine, patient was sleeping all the time and reporter thought it was due to the sepsis. The doctor told reporter that the sepsis was there before patient got the first dose of the covid vaccine. Patient has A-Fib and takes Eliquis. It was reported that patient had a stroke while he was in the hospital. Patient fell because of the weakness from his stroke. The second fall put him back in the hospital. Patient was in poor shape; his blood sugar was in the 600s. Before patient went to the hospital, he was sleeping all of the time, and he lost his appetite. They did not know if patient still has endocarditis because he could not have the follow up procedure done because he was in bad shape. Patient had weakness and fell and broke his hip. Patient was currently in rehab for physical therapy. Reporter clarifies that she took patient to the emergency room, and then he was admitted to the hospital. Patient's fever did not start out at 100 degrees, it gradually went up to 104 degrees. By the second or third day, patient's fever got up to 104 degrees. Reporter is back to square one for help. Reporter is asking if there is anyone who would know what to do. Patient's cardiologist said for patient to get the second dose of the covid vaccine. Reporter knows that no one had that in the clinical trial. Before the covid vaccine, patient was having a crown done in his mouth. Last year patient had a blood infection, so he had to take four antibiotics. Reporter thinks they were called amoxicillin, and they were 500mg each. Patient had to take them all at once as a preventive. Patient is on a lot of things, that reporter does not even know. Patient has had a lot of things done to his heart. Patient has had to have ablations. Patient has a very bad heart. Patient has a question about herself. She had the covid vaccine and had no reactions. She is on Celebrex 200mg. Reporter stopped taking a day and a half before the covid vaccine. Reporter is asking if she could have messed herself up by taking an anti-inflammatory, and if taking Celebrex could have prevented her from getting the full effect. Prior to taking Covid vaccine her husband has had Endocarditis, congestive heart failure, bad heart valve and a stroke. 1st dose of vaccine mid-April. 2 days later had a fever of 104 and was admitted to the hospital with sepsis. The sepsis caused endocarditis again. Husband is in rehab facility, and they want him to take a second dose. Should he be getting 2nd dose of Pfizer or a different Covid vaccine. Wife wondering if husband should get 2nd dose at all. Reporter does not think that this has anything to do with the covid vaccine, since they know which bacteria caused it. Reporter thinks that maybe patient getting the first dose of the covid vaccine put patient over the edge. This is the second time that patient has had vegetation, the first time was last year. Reporter thinks that all of patient's doctors are panicking over the covid vaccine. Reporter knows that patient is in bad shape. In the clinical trial, there was nothing in there about congestive heart failure, or nothing about endocarditis. Patient may still have endocarditis. Reporter does not know what will happen to patient if he gets the second dose of the covid vaccine. Reporter states that unfortunately patient does not go to the best cardiologist. Reporter thinks that patient is so bad off, that he could be on palliative care. The only reason reporter waited so long to call Pfizer is because patient is in rehab now, and they might be getting in the Pfizer covid vaccine. They asked reporter if she wanted patient to get the second dose of the Pfizer covid vaccine. They should get them in on 16Jul2021. Reporter said yes, about a week ago, but it has been on her mind to call and ask the source. Reporter took patient to the hospital, and the doctors diagnosed him with sepsis: Patient was not willing to go to the hospital at first. Patient could not get out of bed. Patient was not eating or drinking. Reporter was trying to give him stuff. Reporter is not a scientist. An infectious disease doctor told reporter that patient already had sepsis before the covid vaccine. Patient was in terrible shape. Patient had a stroke while he was in the hospital. They figured out he had a stroke about five days after being in the hospital. After the stroke, patient had two weeks of physical therapy there. Dates of Hospitalization: He was in the hospital for a few weeks. Patient was home for two days he fell because of the weakness from his stroke. The second fall put him back in the hospital. Patient had to get a partial hip replacement. For about a week now, patient has been in rehab. Patient has A-Fib, since the stroke, he is not on Eliquis. Patient was not on Eliquis before. Patient also has hypertension, but it is under control. Therapeutic measures were taken as a result of endocarditis and fell and broke his hip. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Name: blood sugar; Result Unstructured Data: Test Result:600; Test Name: Fever; Result Unstructured Data: Test Result:104 degrees
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Aortic valve disease (a bad aortic value); Atrial fibrillation (Patient was diagnosed years ago, before his stroke in 2015, a long time ago.); Congestive heart failure; Diabetes; Hypertension; Infection (Last year patient had a blood infection so he had to take four antibiotics.); Stroke
Andere Medikamente: XARELTO
Allergien: -
Vorherige Impfungen: -

VAERS 1463308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: IL
Alter: 54,0
Geschlecht: F
Eingang: 11.07.2021
Impfdatum: 23.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Arthritis Asthenia C-reactive protein Cardiac arrest Chills Computerised tomogram Dehydration Exposure to SARS-CoV-2 Gait disturbance Hot flush Immobile Influenza like illness Lumbar vertebral fracture Magnetic resonance imaging Mental impairment Nerve injury Osteoporosis Pain in extremity

Symptomtext

heart stopped, had to code her; weakness; Caller states she is pretty much grounded/because she couldn't get up the stairs/couldn't get up off floor/having trouble walking; pretty much crippled her; superficial blood clot in left leg; having trouble thinking; compression fracture L5; hot flashes; chills; set off arthritis from top of head to the bottom of her feet; arthritis in every bone ever broken; Dehydrated; Uncontrollable urine; nerve damage, where she can barely hold the phone; because she was having all kinds of pain in legs.; the normal flu-like body aches / just like a little bit of the flu; she had family and her boyfriend, someone tested positive; This is a spontaneous report from a contactable consumer (patient). This 54-year-old female patient received the first dose of BNT162B2 (, Lot No. EW0169) at Left arm at single dose for COVID-19 immunisation on 23Apr2021 (54-year-old at vaccination). Relevant history included PTSD (diagnosed in 1995, 1996, 2000, been for years, unsure of exact year), Bipolar disorder (a mental disorder; a cross between bipolar disorder and PTSD (Post-traumatic stress disorder); last hospitalization for this was in Jan2019), Carpal tunnel in right and left hand (being treated for this prior to the shot), lower back injury (took Tylenol for a lower back injury from about 30 years ago, she fell down a flight down of stairs with her daughter, when she was first born, states her daughter will be 34 at the end of this month. Caller states she saw an orthopedic doctor, who said not to do anything about it, just keep taking what she's taking), Blood pressure abnormal which was diagnosed about 5-7 years ago, diabetic non-insulin dependent, also provided hypoglycemia as a medical condition, Sleep apnoea which was diagnosed about 15 years ago, history of blood clots, fall in Apr2021 (Easter Sunday, being treated). Relevant concomitant drug included lorazepam (ATIVAN) for PTSD and mental disorder, paracetamol (TYLENOL) for carpal tunnel and general pain and she had a lower back injury, and furosemide for blood pressure abnormal. On 23Apr2021, the patient took the first shot, and didn't have too bad of reaction, just like a little bit of the flu. Caller states in between first shot and just before the second shot, she's had some reactions, and in & out of the hospital quite a few times, trying to figure out what's going on. Caller states she was at place on 13Apr, 14Apr, and then 15Apr. Caller states they had to code her, she's been unable to work, it has set off arthritis from the top of her head to the bottom of her feet, it's pretty much crippled her to point to where they've now figured out that it is the covid shot that the side effects. Caller states she just saw her family doctor yesterday, finally able to go in and see him physically, and she has piles of paperwork she's having to go through, and that's why she started back with paperwork from # Hospital, dated 15Apr. Caller states she had the shot on 23Apr. Caller confirms first shot was 23Apr2021. Caller states there's more, it's just started a bunch of things, she's got stacks of papers, and she's sicker than a dog right now, because she got an infection just after, not sure if it's tied into this. Caller states she's having trouble thinking at times, has caused nerve damage, where she can barely hold the phone. Caller states she is pretty much grounded; this is the first time she's been able to get into her apartment, because she couldn't get up the stairs, so she has all the time in the world right now. Reporter details: Type: Caller states she is a home health aide, clarifies not a nurse. But she's recently been working with #, and #, and was emailed papers for the type of leave for COVID-19, and extended leave of absence from work. Caller states the last time she worked was 05Apr, seventh, ninth, tenth, something like that. HCP details: Caller states she can't think right now; she's in and out of it due to medications. HCP Email: Caller declines to provide. Patient details: Caller provided name at the beginning of call as #. Height: States, depends on who's measuring it, five two, five three, five one. Caller clarifies as five two. Product: Caller confirms the product as Pfizer covid shot. Caller states she had to get vaccinated because it was required. First dose: 23Apr2021, Lot EW0169, NDC and Expiration Date: Unknown, Left arm Second dose: 14May2021, Lot EW0179, NDC and Expiration Date: Unknown, Left arm. Caller adds on 15Apr, she had family and her boyfriend, someone tested positive, so from 13Apr until 27Apr, she quarantined herself in a hotel, close to her work. Caller initially provided date of second dose as three weeks after first dose on 15May2021, but then clarifies correct date as 14May2021. History: Caller states she was just taking her normal medications, and states she does not want to go through those at this minute. Caller states she had an appointment to get first shot, but they spelled her name wrong, and the # had to do a VIP thing. Before she went to get the shot she was trying to ask the medical doctor from the # some questions because she had concerns, but before she could tell them any part of her history, the doctor just said to go ahead and give her the shot. States the reason she got the number for Pfizer was from when, on 15Apr, she went to #, to begin with, and they tested her for covid, and gave her instructions, she was off of work. Caller clarifies she never got a phone call, when agent asks for test results of the test. Caller confirms this test was done before her shot. Event details: Caller states she got first shot and a couple days later, it was the normal flu-like body aches; she was told to got to store and get stuff for allergies, and for the flu, but she already had Tylenol and Benadryl for allergies. Caller clarifies she was told this by the #; they gave the shot, had them sit down and wait 15-20 minutes, then let them go, and told them what to do. Caller states these symptoms only lasted a couple of days. States that she doesn't remember if she actually took the Tylenol or Benadryl as treatment for the flulike body aches. States that she has all this paperwork that is going back to 15Apr, and she does not remember at the moment what she took for treatment of symptoms. Caller states she has everything journaled written down, states in between the first and second shot, she was in and out of emergency rooms, trying to figure out what was going on. States she had to go back to medical facility because she was having reactions, she was in the emergency room for weakness, and other things, and had to be checked for blood clots, so she had to go back. She was there on 13May, 14May, they did a venous doppler on everything because she was having all kinds of pain in legs. Then on 15May, she had to go back to be checked for something, right after she got out of emergency room, and after she had the test, she was medically to get the second shot, and after she got the second shot, it's been downhill from there. Caller states she was admitted into # Hospital, and was in and out of the hospital. States she coded, they had to do CPR on her, and this has affected all of her nerves. Caller states they gave both shots in her left arm and it has set off everything and all the nerve damage. Caller states this is scaring her because she is the only family member who has had the Pfizer shot. Everybody else is out of the state and had the Johnson and Johnson, or all the other vaccines, and she's the only one who's had this shot, and the one who has had the most damage. Call handler made multiple attempts to clarify information provided and get further details, but asks to move on because all the questions are setting her off. Caller states maybe she should have had the case worker call. Caller clarifies, she did not have arthritis prior to this. Caller states 31May2021, she was rushed to Place because she couldn't get up off the floor, they weren't sure what was going on with her, her bladder, so they put her on prednisone for a week. Caller did not finish statement regarding her bladder. Caller states all hospitals she has been in have been #, with exception of one in #. Caller provides #, when agent asks for spelling or clarification. Caller states she can't hold the phone very long, and she can't sit up for very long either. States she has a hard time pronouncing the letters, when agent asks her to spell the hospital name. Caller states the problem is agent is on a headset and her phone is set up for handicap for an ear that can't hear properly, so she states the agent being on a headset is why agent can't hear her. Caller states she has hearing loss and can't hear the consonants. Caller states she is due to take medicine and can't take it while on the phone. Caller asks if there a fax number to fax the rest of this to. Caller states all of the hospitals, #, are all under #, it's a whole medical group with all different hospitals in different towns. Caller states prior to emergency room visit, she was in # Hospital because she couldn't walk, was having trouble walking. She coded while they were admitting her; her heart stopped and they had to code her. Caller adds she has not had a paycheck since 09Apr or tenth, states landlord hasn't thrown her out but she's close to being evicted because she hasn't worked, it's been determined the side effects have caused more damage. Caller states 15Apr2021 she got Pfizer's phone number when she was tested for covid. Caller states that's when they did the test but she never heard anything back regarding the results of the test. She quarantined at a hotel, and had to be away from work. Caller states it's been # Hospital where it started. Caller states maybe agent needs to call back and finish report because she has all of hospital papers dissected with dates. Caller states she was given a huge packet on 15Apr, when she was tested for covid. at medical facility which is the only local medical facility, and she went there on 15Apr because her boyfriend's sons' girlfriend tested positive and he's in #, and they gave her a note for her work with instructions. Caller clarifies they gave her a huge packet so that's where she got all the paperwork in Apr before she got the shot. Caller states after the first shot she had 48 hours of hot flashes, the chills, typical flu-like symptoms; only lasted 48 hours, and then from the twenty third she's had different symptoms, and has been in an out of hospitals, trying to figure out what was going on with her. States she was healthy and working until 07Apr, 08Apr, or 09Apr, is the last time she worked. Then she quarantined from 13Apr until 27Apr, and then they had to get vaccinated, so she registered, and when she went there, they spelled her name wrong with a # instead of #, she she started asking questions trying to give medical history before the shot. She had not given any of her history and doctor said to just give it. They gave the shot in her left arm and from then on the damage hit and it has been one thing after another. Caller states she previously had a test done in 2017, electrical shock from toes to head, and acupuncture same day, and only thing showed up was carpal tunnel in right and left hand. She was being treated with 1000 mg Tylenol, and she was fine working at #, and #, since 2018. States she was physically fine and is 54 years old, the oldest one working there and now she's been back and forth from hospitals. Caller states she was in # in the hospital with weakness 10Jun2021 or 07Jun2021. Caller states this has been a continuous thing going to hospitals for weakness, bladder is just letting go like just having uncontrollable urine, she got dehydrated. She only had to be inpatient at #Hospital in #. Caller states right after admitted there, primary doctors found a superficial blood clot in left leg and started her on #, and they discharged her and transferred her by from main hospital to the emergency room satellite. She was there to do an MRI and had to sedate her because she's claustrophobic. They found an L5 compression fracture, which caller clarifies is new since the shot. Caller states the back specialist said not going to do anything it, it will heal on it's own. Caller states she was sent to get her car and had a major allergic reaction to a drug given while in hospital but the nurse didn't listen, they let her drive her car from ##, which is satellite for # Hospital. States she stopped at a #, paid for Benadryl and had to park the car while she took two Benadryl for having major symptoms. Caller states when she felt she was ok, she drove back to hotel, but when she got there she couldn't get out of car so the manager called 911, and # they came and assessed her. Her cognitive level was fine, but she was sitting in urine and couldn't get out of car, so they rushed her to # Hospital and she was admitted on an orthopedic floor, this was 20May or 21May, and she went unresponsive while they were admitting her, so they coded her. States that she still has bruises on her ribcage. A cardiologist came and actually he listened to her. They did three different cat scans and determined that she now has arthritis in every bone ever broken. It's very painful. States that she is sitting with 5 piles of paperwork from 15Apr to her most current one which would have been at # Hospital just a couple of days ago. She has been diagnosed with so many different things because the doctor's couldn't figure out what was going on. Call handler attempted to query the name of the medication that caused her allergic reaction. Caller stated that there are 4 medications that she reacts to, two are muscle relaxers that she is allergic to, and one of them was given to her at # hospital. States that the problem is that people look at your mental disabilities first, they don't look at your other history, and nurses are over worked, so even though she told the nurse to call her doctor because she was having a major reaction and she knew what it was, they were still discharging her. Call handler again asked for the name of the product. Caller became upset and stated that she is physically in pain and is getting ready to pee herself right now. Caller started yelling that there are 5 medications that she is allergic to. No further details provided. Caller stated that the next call is going to the governor of #. Call was abruptly disconnected. The outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Test Name: CAT scan; Result Unstructured Data: Test Result:Arthritis everywhere; Test Name: CPR; Result Unstructured Data: Test Result:affected all of her nerves.; Comments: affected all of her nerves.; Test Name: MRI; Result Unstructured Data: Test Result:L5 compression fracture,; Comments: L5 compression fracture,; Test Date: 20210415; Test Name: SARS-CoV-2 test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back injury (from about 30 years ago, she fell down a flight down of stairs with her daughter, took Tylenol); Bipolar disorder (a mental disorder; a cross between bipolar disorder and PTSD; hospitalized in Jan2019); Blood pressure abnormal (Diagnosed about 5-7 years ago); Carpal tunnel syndrome (being treated for this prior to the shot); Clot blood; Diabetes mellitus non-insulin-dependent (Also provided hypoglycemia as a medical condition); Drug allergy (unknown drug name); Fall (being treated); Hypoglycemia; Post-traumatic stress disorder (diagnosed in 1995, 1996, 2000, been for years, unsure of exact year); Sleep apnoea (Diagnosed about 15 years ago)
Andere Medikamente: ATIVAN; TYLENOL; FUROSEMIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1449307

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MN
Alter: 38,0
Geschlecht: M
Eingang: 06.07.2021
Impfdatum: 07.05.2021
Beginn: 21.06.2021
Tage bis Beginn: 45,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Blood cholesterol normal Myocardial infarction

Symptomtext

Heart attack within 1.5 months of receiving final dose. 38 year old, physically fit patient has excellent cholesterol, blood pressure, and resting heart rate numbers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1440521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: LA
Alter: 66,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 29.06.2021
Beginn: 29.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Ataxia Cerebrovascular accident Dysarthria Magnetic resonance imaging head abnormal

Symptomtext

66 y/o male presents to the ED with generalized weakness, slurred speech, ataxia that started yesterday at 5:00pm while he was driving. He had his second dose of the Covid vaccine at 4:30pm. He woke this morning (6/30), still having symptoms, so his son brought him to the ED. Diagnosis of stroke, acute CVA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: -
Vorgeschichte: Acid reflux, Arteriosclerosis of coronary artery bypass graft, back pain, diastolic dysfunction; Hx of CABG, Hyperlipidemia, Obesity with body mass index greater than 30
Andere Medikamente: smokes cigarettes
Allergien: -
Vorherige Impfungen: -

VAERS 1432207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OH
Alter: 65,0
Geschlecht: M
Eingang: 28.06.2021
Impfdatum: 19.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aphasia Chills Death Hot flush

Symptomtext

Trouble speaking, cold chills, hot flashes. Death on 5/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: epilepsy, high blood pressure, high cholesteral, overweight
Andere Medikamente: -
Allergien: unknown
Vorherige Impfungen: -

VAERS 1431067

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MN
Alter: 39,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 10.05.2021
Beginn: 24.06.2021
Tage bis Beginn: 45,0
Dosis: UNK
Route/Site: - / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Exposure during pregnancy Maternal death during childbirth

Symptomtext

Pt died during child birth on 06/24/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Maternal death during childbirth
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1401971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SC
Alter: 62,0
Geschlecht: F
Eingang: 16.06.2021
Impfdatum: 19.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Chemotherapy Chest X-ray abnormal Computerised tomogram abnormal Death Drug hypersensitivity Dyspnoea Fatigue Feeding disorder Gait disturbance Laboratory test Pneumonia Rash Renal failure Sepsis Small cell lung cancer

Symptomtext

Few days after receiving the vaccine around 4/25, my mother complained to me that she was feeling very weak and tired, she was unable to hold anything down. She also had a rash. She became weaker and weaker so suddenly and unable to even drink protein drinks. She finally went to the ER on 5/4 because she could barely walk, unable to eat anything and was short of breath. They diagnosed her with pneumonia and a possible lung mass. She was diagnosed simultaneously 10 days later with small cell lung cancer however she had no symptoms prior. She received first dose chemo on 5/20/21 and had a reaction to the chemo that the doctor stated was very rare. They then had to try a different type of chemo for second dose 2 days later. She progressively got worse suddenly after chemo dose #3 and was in renal failure the day following chemo completion. She died on 5/27/2021. Her primary death diagnosis was sepsis, pneumonia and small cell lung cancer. I am reporting this for my mother because the vaccine has not been tested on cancer or chemo patients. It can and should not be regarded as coincidental. It needs to be tracked in case there are future reports regarding cancer patients.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: lab work, xrays, cat scans
Aktuelle Erkrankungen: umbilical hernia / hiatal hernia
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1375050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 64,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 14.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Client was screened as per CDC guidelines and had no contraindications for receiving the vaccine on 4/14/2021. LCHD had no notice of any adverse issues. He did not present to the 2nd dose clinic and follow up phone calls revealed that he had died on 4/28/2021.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: none known
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 1371952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MN
Alter: 71,0
Geschlecht: M
Eingang: 03.06.2021
Impfdatum: 16.04.2021
Beginn: 12.05.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Acute myocardial infarction Chest pain

Symptomtext

Patient presented to the ED with chest pain and was subsequently hospitalized. Diagnosis was NSTEMI. This was within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1371756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 85,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 14.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Cerebrovascular accident

Symptomtext

Patient presented to the ED and was subsequently hospitalized for cryptogenic stroke within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1256367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 57,0
Geschlecht: U
Eingang: 03.06.2021
Impfdatum: 25.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction Anaphylactic shock Flatulence Hypersensitivity Chest discomfort Cough Pharyngeal swelling Wheezing

Symptomtext

Anaphylactic shock; Gassing which can't stop; Allergic reaction; 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, solution for injection), dose 2 via an unspecified route of administration, administered in right arm on 25Apr2021 (Batch/Lot Number: EW0169) at the age of 57 years old, as 2ND DOSE, SINGLE for COVID-19 immunisation. Medical history included hypothyroidism, Sjogren's syndrome, rheumatoid arthritis, depression, asthma and ICP (unspecified). Concomitant medications included levothyroxine taken for hypothyroidism; paroxetine taken for depression; omeprazole taken for acid reflux; all from unknown start and stop date. The patient was taking unspecified "locale" medication for Sjogren's syndrome. Historical vaccination included first dose of BNT162B2 on 04Apr2021 at the age of 57 years old, (lot number: ER8732) for COVID-19 immunization and patient did not get any reaction to it. On 25Apr2021, the patient experienced anaphylactic shock, gassing which can't stop and allergic reaction. Clinical course of events was reported as follows: The patient had the COVID Shot on 25Apr2021 and went to anaphylactic shock and the patient was sent to the emergency room. The patient has some issues like gassing which cannot stop. The patient was out of work for 2 weeks. The patient thought, an allergic reaction because of the COVID shot. The patient was also brought to the ICU. The patient just wanted to know more information about that because the doctor could not tell the patient. Treatment for the adverse events: Albuterol inhaler as the patient was asthmatic. Zyrtec 10 mg twice a day. Docusate 100 mg for two days, Prednisone 40mg to lower a down for 4 days. Senna 1 tab bed time. Acetaminophen, Hydrochloroquine, Lower peroxin, Melatonin, Methazole, and Paroxetine all these medications were given to the patient when the patient was discharged from hospital on 30Apr2021. The patient was hospitalized for all the events from 25Apr2021 to 30Apr2021. The patient recovered with sequelae from all the events on 30Apr2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Depression; Hypothyroidism; Rheumatoid arthritis; Sjogren's syndrome
Andere Medikamente: LEVOTHYROXINE; PAROXETINE; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1256367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 57,0
Geschlecht: U
Eingang: 03.06.2021
Impfdatum: 25.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction Anaphylactic shock Flatulence Hypersensitivity Chest discomfort Cough Pharyngeal swelling Wheezing

Symptomtext

Anaphylactic shock; Gassing which can't stop; Allergic reaction; 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, solution for injection), dose 2 via an unspecified route of administration, administered in right arm on 25Apr2021 (Batch/Lot Number: EW0169) at the age of 57 years old, as 2ND DOSE, SINGLE for COVID-19 immunisation. Medical history included hypothyroidism, Sjogren's syndrome, rheumatoid arthritis, depression, asthma and ICP (unspecified). Concomitant medications included levothyroxine taken for hypothyroidism; paroxetine taken for depression; omeprazole taken for acid reflux; all from unknown start and stop date. The patient was taking unspecified "locale" medication for Sjogren's syndrome. Historical vaccination included first dose of BNT162B2 on 04Apr2021 at the age of 57 years old, (lot number: ER8732) for COVID-19 immunization and patient did not get any reaction to it. On 25Apr2021, the patient experienced anaphylactic shock, gassing which can't stop and allergic reaction. Clinical course of events was reported as follows: The patient had the COVID Shot on 25Apr2021 and went to anaphylactic shock and the patient was sent to the emergency room. The patient has some issues like gassing which cannot stop. The patient was out of work for 2 weeks. The patient thought, an allergic reaction because of the COVID shot. The patient was also brought to the ICU. The patient just wanted to know more information about that because the doctor could not tell the patient. Treatment for the adverse events: Albuterol inhaler as the patient was asthmatic. Zyrtec 10 mg twice a day. Docusate 100 mg for two days, Prednisone 40mg to lower a down for 4 days. Senna 1 tab bed time. Acetaminophen, Hydrochloroquine, Lower peroxin, Melatonin, Methazole, and Paroxetine all these medications were given to the patient when the patient was discharged from hospital on 30Apr2021. The patient was hospitalized for all the events from 25Apr2021 to 30Apr2021. The patient recovered with sequelae from all the events on 30Apr2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Depression; Hypothyroidism; Rheumatoid arthritis; Sjogren's syndrome
Andere Medikamente: LEVOTHYROXINE; PAROXETINE; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1368625

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 23.04.2021
Beginn: 16.05.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Acute respiratory failure Blood bicarbonate decreased Blood chloride normal Blood creatinine increased Blood glucose increased Blood lactate dehydrogenase normal Blood potassium normal Blood sodium normal Blood urea increased C-reactive protein increased COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Diarrhoea Ear pain Fibrin D dimer normal

Symptomtext

5/16/21 Pt presented to a free standing ED with complaints of cough, body aches, nasal congestion and otalgia that started around 5/11/21. In the ED she had audible wheezing, mild tachypnea (RR19) and her RA pulse ox was 88-943%. She was placed on oxygen and found to be positive for SARS-CoV-2. CXR showed possible pneumonia and she was transferred to a tertiary care facility for admission. She was discharged on 5/21/21 Acute hypoxic respiratory failure, resolved Covid-19 Virus Infection Date of onset of symptoms: Approximately 7 days prior (5/15/2021) Symptoms present on admission: Nasal congestion, myalgias, productive cough of yellow-green sputum, diarrhea Date of covid positive test: 5/16 Vaccination status: vaccinated, received only first dose Imaging: CXR with lobar pneumonia Oxygen requirements on admission: 2 L Current oxygen requirements: None Medical therapy: Oral prednisone, not a candidate for remdesivir Inflammatory markers: CRP 18.1, ferritin 111, D-dimer 0.62, LDH 174 Community-acquired pneumonia Given lobar appearance on CXR and productive cough of green/yellow sputum I do feel it prudent to cover the patient for community-acquired pneumonia Treated with Azithromycin, Augmentin Acute on chronic kidney disease Baseline serum creatinine approximately 1.1-1.2, presenting serum creatinine 1.94 Prerenal versus intrinsic renal 2/2 infection Creatinine trending down to 1.24 at time of discharge COPD with acute exacerbation IV Solu-Medrol initially, transition to oral prednisone Schedule bronchodilators Started Symbicort per hospital formulary, and held home Flovent while hospitalized Antibiotic coverage as above

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: 5/16/21 NP Swab + SARS-CoV-2, negative influenza A/B Na 138, K+ 4.5, CL 106, HCO3 20, BUn 42, Cr 1.94, glucose 174 WBD 7.49, Hgb 10.0, Hct 38.1, Plt 206 Normal hepatic function and pro BNP CXR Airspace opacity at the left lung base, may be related to atelectasis versus pneumonia
Aktuelle Erkrankungen: N/A
Vorgeschichte: anemia anxiety arthritis carotid stenosis cataract COPD CAD depression insulin requiring type 2 DM hypothyroidism GERD hypertension hyperlipidemia kidney stones psoriasis stroke obesity BMI 35.75
Andere Medikamente: Albuterol MDI QID prn SOB ASA 81mg daily atorvastatin 80mg QHS carvedilol 25mg BID clopidogrel 75mg daily cetirizine 10mg daily cyclosporine 0.05% 1 gtt OU BID doxazosin 2mg QHS ferrous sulfate 35mg QD Fluticasone propionate 220mcg one puff
Allergien: sulfa
Vorherige Impfungen: -

VAERS 1271213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 27.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acidosis Acute hepatic failure Acute kidney injury Alanine aminotransferase increased Aspartate aminotransferase increased Asthenia Atelectasis Blood creatinine increased Blood ethanol normal Blood gases abnormal Blood glucose increased Blood ketone body increased Blood lactic acid increased Cardiac arrest Chronic kidney disease Blood lactic acid Cerebral atrophy Cerebral small vessel ischaemic disease

Symptomtext

Felt ill shortly after getting the vaccine. Weakness, nausea and vomiting. Developed AMS. Presented to the ER and was found to be in acute hepatic failure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 2,0
Labordaten: INR 2.6 ABG 6.99/28/165 CR 3.02 up from 1.71 AST 2742 ALT 1305 Normal LFTs 12/23/2020 Glucose 550 - which arguably goes against hepatic failure Lactic Acid 15.6 Tylenol < 10 COVID negative Beta-Hydroxybutyrate 1.4 Ethanol negative CT of abdomen: 1. Hepatic steatosis. No significant abnormalities of the liver are otherwise demonstrated on this exam. 2. Cholelithiasis. 3. Bilateral pleural effusion with associated atelectasis. 4. The appendix is normal. CT Head: 1. No acute intracranial CT abnormalities. 2. Diffuse cerebral atrophy and white matter hypoattenuation consistent with chronic microvascular ischemic change. 3. Small punctate foci of gas are demonstrated within the region of the carotid siphon bilaterally and the superior right orbit. The etiology of this gas is unknown.
Aktuelle Erkrankungen: -
Vorgeschichte: DM2 CKD3 CAD HTN ICD PVD Chronic Systolic heart failure
Andere Medikamente: unknown
Allergien: Cipro Doxycycline Rosuvastatin - myalgia Simvastatin - myalgia
Vorherige Impfungen: -

VAERS 1271213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: PA
Alter: 80,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 27.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acidosis Acute hepatic failure Acute kidney injury Alanine aminotransferase increased Aspartate aminotransferase increased Asthenia Atelectasis Blood creatinine increased Blood ethanol normal Blood gases abnormal Blood glucose increased Blood ketone body increased Blood lactic acid increased Cardiac arrest Chronic kidney disease Blood lactic acid Cerebral atrophy Cerebral small vessel ischaemic disease

Symptomtext

Felt ill shortly after getting the vaccine. Weakness, nausea and vomiting. Developed AMS. Presented to the ER and was found to be in acute hepatic failure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 2,0
Labordaten: INR 2.6 ABG 6.99/28/165 CR 3.02 up from 1.71 AST 2742 ALT 1305 Normal LFTs 12/23/2020 Glucose 550 - which arguably goes against hepatic failure Lactic Acid 15.6 Tylenol < 10 COVID negative Beta-Hydroxybutyrate 1.4 Ethanol negative CT of abdomen: 1. Hepatic steatosis. No significant abnormalities of the liver are otherwise demonstrated on this exam. 2. Cholelithiasis. 3. Bilateral pleural effusion with associated atelectasis. 4. The appendix is normal. CT Head: 1. No acute intracranial CT abnormalities. 2. Diffuse cerebral atrophy and white matter hypoattenuation consistent with chronic microvascular ischemic change. 3. Small punctate foci of gas are demonstrated within the region of the carotid siphon bilaterally and the superior right orbit. The etiology of this gas is unknown.
Aktuelle Erkrankungen: -
Vorgeschichte: DM2 CKD3 CAD HTN ICD PVD Chronic Systolic heart failure
Andere Medikamente: unknown
Allergien: Cipro Doxycycline Rosuvastatin - myalgia Simvastatin - myalgia
Vorherige Impfungen: -

VAERS 1364581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 57,0
Geschlecht: F
Eingang: 01.06.2021
Impfdatum: 28.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Angiogram cerebral normal Asthenia Computerised tomogram head normal Dysarthria Dyskinesia Dyspnoea Facial paralysis Headache Paraesthesia Respiratory arrest Scan with contrast normal Unresponsive to stimuli

Symptomtext

Patient complaining of a pricking needles to head. At 10:30, patient was constantly jerking and not responding to questioning. Episode lasted 2 minutes. 911 called. Placed patient in supine position and at 10:30 patient showed visible signs of not breathing, holding throat, gasping for air. EpiPen given. Patient transported to ED at 11:17. Upon arrival to ED at 11:19 am, left sided facial droop and weakness with slurred speech and complaints of a severe headache noted. Patient received keppra 3000 mg intravenous x 1 dose at 1211. Patient was discharged from emergency department 5/28/21 at 1330 with prescription for keppra 500 mg by mouth twice daily and ambulatory referral to neurology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: CT head without contrast: No acute intracranial process identified (5/28/21) CT angio head with contrast: No large vessel occlusion identified (5/28/21)
Aktuelle Erkrankungen: urinary tract infection
Vorgeschichte: alcohol use, asthma, epilepsy, stroke, migraines, mixed hyperlipidemia, osteoarthritis, tobacco use
Andere Medikamente: tylenol #3 take 1 tablet by mouth every 8 hours as needed for pain, albuterol HFA inhaler 90 mcg/actuation inhale 2 puffs every 6 hours as needed for wheezing or shortness of breath, atorvastatin 40 mg by mouth daily, breo ellipta 100-25 mc
Allergien: Adhesive, aspirin, band-aid plus antibiotic, influenza vaccine latex, morphine, penicillin
Vorherige Impfungen: influenza vaccine at age 5-6 years resulting in ICU stay, unknown symptoms and vaccine brand

VAERS 1351602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: TX
Alter: 43,0
Geschlecht: F
Eingang: 26.05.2021
Impfdatum: 17.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Abdominal pain Computerised tomogram abdomen Computerised tomogram abnormal Hydronephrosis Mass Pyrexia Septic shock Vaginal discharge

Symptomtext

Patient presented to ED with increased abdominal pain, vaginal drainage, fever to 39.2, pulse in 140's and SPB in the 90s, septic shock presumed pelvic abscess. abdominal pain worse than usual with sudden increase 5/17 -5/19. Clinical suspicion for vaccine-related AE is low.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: -
Labordaten: 5/19 - CT abdomen pelvis: -3.1 x 6.9 cm collection noted with some superior to the bladder and some possible phlegmon developing as well. Some soft stranding is increased with some inflammation likely due to the pseudotumor. -some vaginal drainage is present, likely related to known fistula -s/p IR drainage 05/22 of retropubic abscess with hx of fistula: -+ Ecoli, Efaecalis, strep anginosus -s/p right PCN placement by IR 5/22 for bilateral hydronephrosis
Aktuelle Erkrankungen: pelvic abscess with drain placement 4/6/21 and abx: moxifloxacin and minocycline to continue through 5/11/21.
Vorgeschichte: history of pelvic myofibroblastic inflammatory pseudotumor in the rectovesical pouch s/pTURBT complicated by nonfunction bladder hydronephrosis and recurrent UTIs
Andere Medikamente: morphine, promethazine, apixaban minocycline, and moxifloxacin completed 5/11/21
Allergien: cyclobenzaprine (anaphylaxis) chlorhexidine (burn, blisters) amoxicllin, meperidine, oxycodone (GI intolerance, N/V) adhesives, fentanyl, latex, biopatch, daptomycin, meropenem, alcohol swabs, tegaderm silver (rash) sulfa (unknown) hydromorphone (urinary retention, GI intolerance)
Vorherige Impfungen: -

VAERS 1341523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: SD
Alter: 49,0
Geschlecht: M
Eingang: 23.05.2021
Impfdatum: 18.05.2021
Beginn: 21.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood culture positive Chest X-ray abnormal Disseminated intravascular coagulation Drug screen Dyspnoea Echocardiogram Electrocardiogram Haemoglobin decreased Intensive care International normalised ratio increased Laboratory test abnormal Multiple organ dysfunction syndrome Pneumonia Renal failure Respiratory failure Septic shock Shock Staphylococcal sepsis

Symptomtext

Post vaccine #2 on 5/18 he developed hives, shortness of breath and reportedly did not feel with fatigue. Symptoms worsened and he was admitted to ICU on May 21st via the ED for multiorgan failure including respiratory failure with R pneumonia, Shock, Renal failure, Disseminated intravascular coagulation, shock liver failure requiring invasive vent support and treatment for septic shock including vasopressor support and antibiotic therapy. He was started on CRRT on the 22nd. His INR continues to rise and Hb dropping consistent with worsening DIC. Blood cultures are positive for MRSA. He will likely die from progressive septic shock and MSOF.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: Extensive labs and chest xrays. Echo and EKGs. Drug screen.
Aktuelle Erkrankungen: -
Vorgeschichte: Severe Emphysema, Methamphetamine/THC abuse, Migraines, hypothyroidism.
Andere Medikamente: Trelegy, Albuterol
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1321430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 27.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Blood test Chest X-ray Computerised tomogram Echocardiogram Electrocardiogram Pulmonary embolism Pulmonary infarction Ultrasound Doppler SARS-CoV-2 test

Symptomtext

multiple pulmonary embolisms in both lungs; Lung infarction occurred in left lung; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received the 2nd dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration in arm left, on 27Apr2021 at 08:00 AM at 30 years (Lot# EW0169) as single dose, for COVID-19 immunisation. The patient was not pregnant and was not pregnant at time of vaccination. Medical history was none. Patient had no known allergies. It was unknown if patient experienced COVID-19 prior to vaccination. Concomitant medication in two weeks included multivitamin. The patient did not receive any other vaccine in four weeks. Previously the patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech) for COVID-19 immunisation on 06Apr2021 at 01:30 PM in left arm (Lot# ER8734) at 30 years. The patient experienced multiple pulmonary embolisms in both lungs (caused hospitalization, life threatening) on 04May2021 at 03:00 PM with outcome of recovering, lung infarction occurred in left lung (caused hospitalization, life threatening) on 04May2021 at 03:00 PM with outcome of recovering. The patient was hospitalized from 05May2021 to 08May2021. The events also required emergency room visit. Patient was tested for COVID-19 post vaccination (nasal swab): negative on 05May2021. Therapeutic measures were taken as a result of the events and included treatment with Lovenox injections, pain management, oral blood thinner.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Date: 20210505; Test Name: COVID-19 virus test (nasal swab); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1321430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 27.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Blood test Chest X-ray Computerised tomogram Echocardiogram Electrocardiogram Pulmonary embolism Pulmonary infarction Ultrasound Doppler SARS-CoV-2 test

Symptomtext

multiple pulmonary embolisms in both lungs; Lung infarction occurred in left lung; This is a spontaneous report from a contactable consumer (patient). A 30-year-old female patient received the 2nd dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), via an unspecified route of administration in arm left, on 27Apr2021 at 08:00 AM at 30 years (Lot# EW0169) as single dose, for COVID-19 immunisation. The patient was not pregnant and was not pregnant at time of vaccination. Medical history was none. Patient had no known allergies. It was unknown if patient experienced COVID-19 prior to vaccination. Concomitant medication in two weeks included multivitamin. The patient did not receive any other vaccine in four weeks. Previously the patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech) for COVID-19 immunisation on 06Apr2021 at 01:30 PM in left arm (Lot# ER8734) at 30 years. The patient experienced multiple pulmonary embolisms in both lungs (caused hospitalization, life threatening) on 04May2021 at 03:00 PM with outcome of recovering, lung infarction occurred in left lung (caused hospitalization, life threatening) on 04May2021 at 03:00 PM with outcome of recovering. The patient was hospitalized from 05May2021 to 08May2021. The events also required emergency room visit. Patient was tested for COVID-19 post vaccination (nasal swab): negative on 05May2021. Therapeutic measures were taken as a result of the events and included treatment with Lovenox injections, pain management, oral blood thinner.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: Test Date: 20210505; Test Name: COVID-19 virus test (nasal swab); Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1331132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 19.05.2021
Impfdatum: 17.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Basal ganglia infarction Cerebral infarction Cerebrovascular accident Haemorrhage Intensive care Internal capsule infarction Lacunar infarction Magnetic resonance imaging head abnormal Microangiopathy

Symptomtext

We do not have immunization info for dose 1 New onset stroke symptoms/Stroke Alert 5.18.21 @ 1244pm following second dose of vaccine administered 5.17.2021. MRI + acute stroke, emergent TPA administered. Currently remains inpatient on ICU level of care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: 5. 18.2021 MRI: 1. Lacunar infarction involving the right corona radiata and adjacent basal ganglia and internal capsule measuring approximately 1.4 x 1.1 x 1.8 cm without mass effect or hemorrhagic conversion. While there is a punctate focus of susceptibility at the very inferior margin, it is possible that this is due to petechial hemorrhage versus a punctate focus of chronic microhemorrhage. Follow-up imaging recommended. 2. Within the right cerebellum there is a punctate focus of susceptibility with surrounding edema consistent with microhemorrhage that may be acute microhemorrhage. Findings in this location may be seen with hypertension, however a very small cavernoma may appear similar. 3. Additional foci of chronic microhemorrhage seen within the deep gray nuclei and the cerebellum as well as the pons, which may be seen associated with hypertension. 4. Chronic lacunar infarctions within the left thalamus and within the pons. 5. Mild degree of white matter T2 hyperintensity is nonspecific and likely due to chronic microangiopathic change.
Aktuelle Erkrankungen: appendectomy, cholecystectomy
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1330783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 19.04.2021
Beginn: 27.04.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Complication of pregnancy Foetal death Maternal exposure before pregnancy

Symptomtext

Patient had an intrauterine fetal demise at 40 5/7 weeks. Most likely unrelated but wanted it reported that she had vaccine during pregnancy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Foetal death
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Pregnancy
Vorgeschichte: N/A
Andere Medikamente: Prenatal complete
Allergien: No known Allergies
Vorherige Impfungen: -

VAERS 1305781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 23.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure measurement Dizziness Dyspnoea Fatigue Headache Hypoaesthesia Lethargy Limb discomfort Muscular weakness Myocardial infarction Nausea Oxygen saturation Palpitations Paraesthesia

Symptomtext

difficulty breathing; racing heart; Dizzy; nauseated; headache; heart attack; fingers started tingling and going numb; fingers started tingling and going numb; arms became heavy; lethargic; feeling exhausted; Arms are still weak; This is a spontaneous report from a contactable consumer (patient). A 35-year-old female 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 23Apr2021 09:00 (Batch/Lot Number: EW0169) as single dose for covid-19 immunisation. Medical history included scoliosis. The patient's concomitant medications were not reported. Patient was received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: CR8733), at age of 35 years old, administered in arm left on 02Apr2021 05:00 PM, for covid-19 immunisation. The patient experienced dizzy and nauseated with a headache at 3:00am 26Apr2021. At 7:00am patient woke up again with the same symptoms but strong nausea, difficulty breathing and racing heart. Her fingers started tingling and going numb once she was up (on 26Apr2021). Her arms became heavy and she started feeling lethargic (on 26Apr2021). Patient thought she was having a heart attack on 26Apr2021. Blood pressure was normal and pulse ox was normal. Most symptoms subsided by 11:00am. Arms are still weak at 7:47pm. Still feeling exhausted. Events resulted in doctor or other healthcare professional office/clinic visit. No other vaccine administered in four weeks. No other medications in two weeks. No treatment was received. No covid prior vaccination. No covid tested post vaccination. No known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcomes of events were recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:normal; Test Name: pulse ox; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Scoliosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1299278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: NC
Alter: 57,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Cerebrovascular accident Computerised tomogram Dysarthria Echocardiogram Facial paralysis Feeling abnormal Headache Hypoaesthesia Hypotension Investigation Magnetic resonance imaging Muscle twitching Vaccination site movement impairment

Symptomtext

stroke like symptoms; on his left side he had face droop; he had a speech slur; he couldn't move his left arm/couldn't lift his left arm; low blood pressure; his face was numb; his lip was twitching; bad headache; brain fog; This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in the left arm on 21Apr2021 14:00 (Batch/Lot Number: EW0169) as single dose (at the age of 57-years-old) for COVID-19 immunisation. Medical history included stroke from 02Feb2020 to 02May2020 (not ongoing). The patient had 3 stroked last year and he was put on ELIQUIS and baby aspirin and a regimen for his strokes. The last one he had was 02May2020 and he has had no problems since then. Last year when he had strokes it wasn't because of his heart it was because of an artery in his brain that went 90 degrees. In Jun2020 they found out that the problem was an artery and that's when the doctor to do the double dose baby aspirin and then everything was fine and he had no episodes at all. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN), lot number: P116218, expiration date: Jan2022 taken for stroke from 02Feb2020 to an unspecified stop date; and apixaban (ELIQUIS), lot number: 1796050, expiration date: Sep2023 taken for stroke from 02Feb2020 to an unspecified stop date. The patient had no additional vaccines on the same date as Pfizer vaccine and had no prior vaccine within 4 weeks. The patient had his first shot of the Pfizer COVID vaccine on 21Apr2021 at 14:00 and stated that they made him go wait for 15 minutes in his car. 10 minutes into waiting after the COVID vaccine, he had to call over the EMT because he had stroke like symptoms. On his left side he had face droop, he had a speech slur and he couldn't move his left arm. The patient was transferred to the hospital and was hospitalized. His CT scan was fine, the CT scan with dye was fine, his MRI was fine, and his heart was fine. The patient wanted to know if he should get the second COVID vaccine because of the reaction that he had from the first COVID vaccine. The patient got the COVID vaccine on 21Apr2021 and on 23Apr2021 he was still having a bad headache, brain fog and there was a deficit on his left side. He can't grab and hold something in his left hand and he has a slight deficit on the left side corner of his mouth. The patient was planning on seeing the provider in the first week of May2021. The patient added that he was told to wait 15 minutes and then 10 minutes in he could feel his face was numb and his lip was twitching and he couldn't lift his left arm. He laid on the horn and the EMS came over and they said that he had stroke like symptoms so they transferred him out of his car and into an ambulance where he had vitals taken and he had another episode of stroke like symptoms. They took him into a different ambulance and had another episode in that ambulance when they were on the way to the hospital. He didn't have anything after that except a bad headache and a slight deficit on his left side, according to them, and just a brain fog like when he was trying to figure out how to put things together and he was still having those at the time of the report. The patient was discharged from the hospital on 22Apr2021. The patient stated that his last stroke was on 02May2020 and he has had no headaches since until he had the COVID vaccine on 21Apr2021. According to the doctors and the neurologist at the hospital he could've had a stroke, he could've had low blood pressure from the vaccine or he could've had a multitude of other things but they recommended him to call Pfizer and CDC for the report. While in the hospital, he had a CT scan without contrast, a CT with contrast on 21Apr2021; an MRI without contrast on 21Apr2021; an echocardiogram without dye and with dye on 22Apr2021 and they did another MRI but of his neck on 22Apr2021; all were normal. The patient was hospitalized for stroke like symptoms, on his left side he had face droop, he had a speech slur and he couldn't move his left arm from 21Apr2021. The event stroke like symptoms resolved with sequel on 22Apr2021. The patient recovered from on his left side he had face droop, he had a speech slur, and he couldn't move his left arm on 22Apr2021. The patient has not recovered from bad headache, brain fog. The outcome of his face was numb was unknown, his lip was twitching and low blood pressure was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Test Date: 20210421; Test Name: CT scan with/without contrast; Result Unstructured Data: Test Result:normal; Test Date: 20210422; Test Name: echocardiogram with dye; Result Unstructured Data: Test Result:normal; Test Date: 20210422; Test Name: echocardiogram without dye; Result Unstructured Data: Test Result:normal; Test Date: 202104; Test Name: heart; Result Unstructured Data: Test Result:fine; Test Date: 20210421; Test Name: MRI; Result Unstructured Data: Test Result:normal; Test Date: 20210422; Test Name: MRI neck; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Stroke
Andere Medikamente: BABY ASPIRIN; ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 1295527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Brain stem infarction Cerebrovascular accident Computerised tomogram head normal Confusional state Dysarthria Hemiparesis Magnetic resonance imaging head abnormal NIH stroke scale

Symptomtext

Pt is a 59 YOF who received her first COVID-19 Pfizer vaccination on 4/16/21. She has PMH significant for diabetes mellitus type II, hypertension, COPD. Almost immediately post vaccine, patient started exhibiting signs of slurred speech and right side weakness. Patient started improving when being moved to triage ? however after a few minutes, slurred speech and confusion returned. 911 called and patient transported to ED. On admission neurology consulted and initial CT head negative. Patient received IV tPA and MRI brain was obtained which showed left medial pontine infarct. Diagnosis: Left pontine stroke. NIH 4 on admission and discharge. No history of TIA nor stroke. Unclear if stroke is related to vaccine...

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus type II, hypertension, COPD
Andere Medikamente: Duloxetine DR, dulaglutide, acetaminophen, albuterol,...
Allergien: Codeine, gabapentin, Vicodin
Vorherige Impfungen: -

VAERS 1289683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0169

kritisch

Staat: OH
Alter: 70,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 20.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure Blood creatinine increased Blood glucose normal Blood urea normal COVID-19 COVID-19 pneumonia Chills Computerised tomogram thorax Computerised tomogram thorax abnormal Diarrhoea Haemoptysis Headache Hilar lymphadenopathy Influenza A virus test negative Influenza virus test negative Legionella test Lung opacity Lymphadenopathy mediastinal

Symptomtext

4/22/21 Patient admitted to hospital for COVID D/C summary: Clinical Summary a 70 y.o. male with a history of HTN, prostate cancer, chronic pain, T2DM, OSA noncompliant with CPAP who presented to ED 4/22/2021 with scant hemoptysis. Found to be COVID+ and hypoxic requiring 2L NC. Cr. 1.4. He was transferred for further evaluation and management. Improved with Remdesivir and steroid therapy. Patient completed 3 doses of remdesivir, recommended completion of steroid therapy (5/2) and repeat outpt CT Chest. 1. Acute Hypoxic Respiratory Failure: requiring 2-3L NC on admission in setting of COVID-19 pneumonia. CTPA with no PE, patchy multifocal ground glass opacities, mildly enlarged mediastinal and hilar LAD, likely reactive. Pulmonary hygiene. Weaned off of O2 4/24/21. Home o2 evaluation with patient desaturating to 91% with exertion. 2. COVID-19 Pneumonia: symptoms began 4/20/2021 with headache, fever, chills and diarrhea. Presented with scant hemoptysis. COVID + 4/22/21. Febrile to 101 on admission. CTPA as described. Hypoxia as described. Started decadron (stop date 5/2), scheduled albuterol, mucinex. Monitor respiratory status. Pulmonary followed, initiated Remdesivir 4/23 following improvement in renal function. Recommended completion of 10 days of steroid therapy. Recommend repeat CT chest in 4-6 weeks for resolution.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 4/22/21 BUN 14, Cr 1.45, normal electrolytes, glucose 109 NP swab + SARS-CoV-2, Neg influenza A/B, 4/23 NS MRSA DNA-negative, urine Legionella Ag and strep pneumo Ag both negative 4/23 CTA 1) No evidence of pulmonary embolism. 2)Imaging features in the lungs which can be seen with COVID-19 pneumonia, though are nonspecific and can occur with a variety of infectious and noninfectious processes. 3) Mildly enlarged mediastinal and hilar lymphadenopathy, presumably reactive.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN prostate CA chronic pain type 2 DM OSA GERD morbid obesity (BMI 42.9) history of tobacco abuse
Andere Medikamente: amlodipine 10mg QD atorvastatin 40mg QD Chantix 1mg BID empagliflozin 25mg QD lisinopril 20mg BID loratadine 10mg QD melatonin 3mg QHS omeprazole 40mg QD oxybutynin XL 15mg QD oxycodone/APAP 10/325mg one up to 5 times daily as needed for pa
Allergien: NKA
Vorherige Impfungen: -

VAERS 1289022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 05.05.2021
Impfdatum: 21.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

Patient passed away on 4/29/2021. A member of our staff noticed his name on the obituary section of our local news. We do not know of any other details.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Past Medical History: Rosacea, HTN, Hyperlipidemia, Diabetes Type 2, degenerative disease
Andere Medikamente: Jan 2020: Ativan, Ambien, Tulicity, Kenalog, Glucophage, Lisinopril
Allergien: PCN - GI intolerance
Vorherige Impfungen: -

VAERS 1282295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: MT
Alter: 40,0
Geschlecht: M
Eingang: 03.05.2021
Impfdatum: 27.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute myocardial infarction Catheterisation cardiac abnormal Chest pain Dyspnoea Echocardiogram abnormal Ejection fraction decreased Electrocardiogram ST segment elevation Electrocardiogram abnormal Hyperhidrosis Left ventricular dysfunction Ventricular hypokinesia Vomiting

Symptomtext

Awakened at 2 am 5/1/21 with acute onset of chest pain, SOB, and diaphoresis. No cardiac history; no history of similar episode. Reported that, following his second dose of COVID vaccine, he was ill for 1 day with vomiting. Chest pain continued upon arrival to ER 5/1/21 about 7 am. EKG indicated STEMI. Adm with Acute ST elevation myocardial infarction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: 5/1 EKG - Anterolateral infarct, acute (LAD) - INTERPRETATION: ST elevation, consider inferior injury 5/1 Echocardiogram - CONCLUSIONS: 1. Left ventricular ejection fraction, by visual estimation, is 30 to 35%. 2. Severely decreased global left ventricular systolic function. 3. Mild to moderately increased left ventricular internal cavity size. 4. Severe global hypokinesis of the left ventricle. 5/1 Cardiac cath - Final Impression: 1. No epicardial coronary artery disease is noted; 2. Severe global reduction in left ventricular systolic function with an estimated ejection fraction of 30%.
Aktuelle Erkrankungen: Genital Herpes
Vorgeschichte: Asthma, Seasonal Allergies
Andere Medikamente: Testosterone Cypionate 200mg IM q 2 wk; Valacyclovir 500 mg tab 2 tabs daily for 5 days
Allergien: NKA
Vorherige Impfungen: -

VAERS 1256687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 43,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arrhythmia Body temperature Cardiac arrest Computerised tomogram head Echocardiogram Electrocardiogram Seizure Exercise electrocardiogram abnormal Fall Investigation Pyrexia SARS-CoV-2 test Troponin

Symptomtext

Seizure; Cardiac arrest; Arrhythmia; Began convulsing and then tipped over; Began convulsing and then tipped over; 12 lead EKG without ischemic changes, arrhythmia; Febrile 38+; This is a spontaneous report from a contactable other HCP. A 43-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0169) via intramuscular route in arm left on 23Apr2021 at 12:45 as single dose for covid-19 immunisation. Historical Vaccine included first dose of bnt162b2 (Lot Number: EW0150) via intramuscular, administered in arm left on 02Apr2021at 14:15 for covid-19 immunisation. Medical history included obstructive sleep apnea, food allergy and intolerant of peanuts-causes sneezing and there were no concomitant medications. On 23Apr2021 at 18:30 the patient experienced a seizure resulting in cardiac arrest. Witnesses described patient began convulsing and then tipped over. AED applied with no shock advised. Unknown down time prior to initiation of CPR. Rhythm PEA upon arrival of EMS. 7 mins CPR before ROSC obtained. Initial Troponin 12. 12 lead EKG without ischemic changes, arrhythmia, etc. Transthoracic echo without regional wall abnormalities or significant findings. CT of head negative for acute intracranial process. No history of seizure, cardiac issues, drug use, etc. Intubated and sedated. Febrile 38+ on arrival requiring active cooling measures to maintain normothermia. The case classified as serious emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). On 23Apr2021, the patient underwent lab tests and procedures which included body temperature: 38+ on arrival requiring active cooling measures to maintain normothermia, computerised tomogram head: negative for acute intracranial process, echocardiogram: without regional wall abnormalities or significant findings, electrocardiogram: without ischemic changes, arrhythmia, investigation: pea, sars-cov-2 test: negative Nasal Swab and troponin: 12. Treatment received included multiple life support measures, treatment for seizures, etc. No covid prior vaccination. Patient had covid tested post vaccination. No other vaccine in four weeks. The outcome of the events was not recovered.; Sender's Comments: Based on strong temporal association the causal association between the reported events seizure, cardiac arrest, arrhythmia, began convulsing and then tipped over, febrile 38+ and the usage of the vaccine are considered related. 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: Cardiac arrest
Hospital-Tage: -
Labordaten: Test Date: 20210423; Test Name: Febrile; Result Unstructured Data: Test Result:38+; Comments: on arrival requiring active cooling measures to maintain normothermia; Test Date: 20210423; Test Name: CT of head; Test Result: Negative ; Comments: for acute intracranial process; Test Date: 20210423; Test Name: Transthoracic echo; Result Unstructured Data: Test Result:Without regional wall abnormalities; Comments: or significant findings; Test Date: 20210423; Test Name: EKG; Result Unstructured Data: Test Result:without ischemic changes, arrhythmia; Test Date: 20210423; Test Name: Rhythm; Result Unstructured Data: Test Result:PEA; Test Date: 20210423; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210423; Test Name: Troponin; Result Unstructured Data: Test Result:12
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obstructive sleep apnea syndrome; Peanut allergy; Sneezing
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1256687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: WI
Alter: 43,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arrhythmia Body temperature Cardiac arrest Computerised tomogram head Echocardiogram Electrocardiogram Seizure Exercise electrocardiogram abnormal Fall Investigation Pyrexia SARS-CoV-2 test Troponin

Symptomtext

Seizure; Cardiac arrest; Arrhythmia; Began convulsing and then tipped over; Began convulsing and then tipped over; 12 lead EKG without ischemic changes, arrhythmia; Febrile 38+; This is a spontaneous report from a contactable other HCP. A 43-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EW0169) via intramuscular route in arm left on 23Apr2021 at 12:45 as single dose for covid-19 immunisation. Historical Vaccine included first dose of bnt162b2 (Lot Number: EW0150) via intramuscular, administered in arm left on 02Apr2021at 14:15 for covid-19 immunisation. Medical history included obstructive sleep apnea, food allergy and intolerant of peanuts-causes sneezing and there were no concomitant medications. On 23Apr2021 at 18:30 the patient experienced a seizure resulting in cardiac arrest. Witnesses described patient began convulsing and then tipped over. AED applied with no shock advised. Unknown down time prior to initiation of CPR. Rhythm PEA upon arrival of EMS. 7 mins CPR before ROSC obtained. Initial Troponin 12. 12 lead EKG without ischemic changes, arrhythmia, etc. Transthoracic echo without regional wall abnormalities or significant findings. CT of head negative for acute intracranial process. No history of seizure, cardiac issues, drug use, etc. Intubated and sedated. Febrile 38+ on arrival requiring active cooling measures to maintain normothermia. The case classified as serious emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). On 23Apr2021, the patient underwent lab tests and procedures which included body temperature: 38+ on arrival requiring active cooling measures to maintain normothermia, computerised tomogram head: negative for acute intracranial process, echocardiogram: without regional wall abnormalities or significant findings, electrocardiogram: without ischemic changes, arrhythmia, investigation: pea, sars-cov-2 test: negative Nasal Swab and troponin: 12. Treatment received included multiple life support measures, treatment for seizures, etc. No covid prior vaccination. Patient had covid tested post vaccination. No other vaccine in four weeks. The outcome of the events was not recovered.; Sender's Comments: Based on strong temporal association the causal association between the reported events seizure, cardiac arrest, arrhythmia, began convulsing and then tipped over, febrile 38+ and the usage of the vaccine are considered related. 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: Cardiac arrest
Hospital-Tage: -
Labordaten: Test Date: 20210423; Test Name: Febrile; Result Unstructured Data: Test Result:38+; Comments: on arrival requiring active cooling measures to maintain normothermia; Test Date: 20210423; Test Name: CT of head; Test Result: Negative ; Comments: for acute intracranial process; Test Date: 20210423; Test Name: Transthoracic echo; Result Unstructured Data: Test Result:Without regional wall abnormalities; Comments: or significant findings; Test Date: 20210423; Test Name: EKG; Result Unstructured Data: Test Result:without ischemic changes, arrhythmia; Test Date: 20210423; Test Name: Rhythm; Result Unstructured Data: Test Result:PEA; Test Date: 20210423; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20210423; Test Name: Troponin; Result Unstructured Data: Test Result:12
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Obstructive sleep apnea syndrome; Peanut allergy; Sneezing
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1258266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: DC
Alter: 23,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 16.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 8,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Angiogram pulmonary abnormal Anticoagulant therapy Cardiomegaly Dyspnoea Fibrin D dimer Pleuritic pain Pneumomediastinum Pulmonary embolism Rheumatoid arthritis Ultrasound Doppler normal

Symptomtext

Dyspnea and pleuritic chest pain onset 4/22-23, prompting presentation to ED. Found in ED on 4/24 to have central R pulmonary embolus extending into interlobar, segmental, subsegmental branches of RUL & RLL, mild R heart enlargement without evidence to suggest RH strain, and mild pneumomediastinum most notable at the thoracic inlet. Tolerating RA. Started on AC with heparin drip, transitioned to xarelto at discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 3,0
Labordaten: D-dimer 1500 -- CTA chest: 1. Central right pulmonary embolus with extends into interlobar, segmental, and subsegmental branches of the right upper and lower lobes. Few subsegmental defects suggested in the left lower lobe as well. 2. Mild right heart enlargement without evidence to suggest right heart strain. 3. Mild pneumomediastinum observed most notable at the thoracic inlet. LE dopplers (bilateral) without evidence of DVT.
Aktuelle Erkrankungen: none
Vorgeschichte: migraine headache
Andere Medikamente: fremanezumab, naratriptan, rizatriptan, topiramate
Allergien: NKA
Vorherige Impfungen: -

VAERS 1256112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: AZ
Alter: 48,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 22.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

My husband received the shot on the 22nd. He died in his sleep on the 24th. He was complaining how the second shot really was giving him a lot of trouble, but nothing that would indicate life-threatening symptoms

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Emphysema, Peripheral Arterial Disease, High BP
Vorgeschichte: Emphysema, Peripheral Arterial Disease, High BP
Andere Medikamente: Equate one daily multivitamin, turkey tail mushroom, coq10, magnesium, glucosamine, fish oil/flax, holy basil, 6-mushroom blend (piping rock brand)
Allergien: NA
Vorherige Impfungen: -

VAERS 1214118

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

kritisch

Staat: VA
Alter: 21,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Flushing Loss of consciousness Palpitations Respiratory arrest

Symptomtext

Patient loss consciousness. Vaccine administered around 1240, approximately at 1250 patient pass out. Observer called for help and EMS was activated at 1250. Patient was flushed and not breathing, observer pushed EpiPen 0.3mL (Lot #0FM200 Exp: OCT2021)for 10 seconds at 1252. Patient woke up, helped arrived and was moved into private patient room. Fire was called at 1254 arrived at 1303. Vital signs taken at 1258 BP: 71/39 HR:73 O2: 100% Temp:98.7 degrees Celsius. Second Vital signs taken at 1300 BP: 86/49 HR:97 O2: 99% Temp:98.7 degrees Celsius. Patient stated before passing out symptoms of light headedness and heart racing and flushed. Patient improving symptoms, transported to the Hospital at 1307.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Fire ants anaphylaxis
Vorherige Impfungen: -

VAERS 2561387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 35,0
Geschlecht: M
Eingang: 17.01.2023
Impfdatum: 21.05.2021
Beginn: 01.10.2021
Tage bis Beginn: 133,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Abdominal discomfort Anticoagulant therapy Biopsy liver abnormal Computerised tomogram liver abnormal Dizziness Full blood count Hepatomegaly Internal haemorrhage Liver scan abnormal Oesophageal disorder Oesophageal variceal ligation Platelet count decreased Portal vein cavernous transformation Portal vein thrombosis Splenomegaly Transfusion Ultrasound liver abnormal

Symptomtext

Initially after getting the shot I had no major symptoms. After a while I started getting dizzy and went to see my PCP who asked for a full CBC blood work. Found out that my platelets count was low so the investigation started to find out why and after seeing several doctors (PCP, GI, Surgeon, Hematologist, Hepatologist) and doing several tests and imaging, the results showed that I have a cavernous transformation of the portal vein (Something that I never had before). The issues continued with my liver and spleen being enlarged causing pressure in the veins in my stomach and oesophagus which eventually busted causing me to have internal bleeding. An emergency endoscopy was performed and banding of the oesophageal varices was performed. Additionally, a blood clot was found in my portal vein that is causing more stress to the functions of the liver and surrounding organs. All my blood counts are very low and I had to get blood transfusions and Iron transfusions. The treatment is ongoing to figure out what needs to happen with the clots and if blood thinners are a good option since I'm constantly bleeding from tiny veins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Portal vein thrombosis
Hospital-Tage: 10,0
Labordaten: CBC performed every 4-5 months Ultrasound with and without Iodine Full comprehensive CT scan Liver biopsy Liver Fibroscan Blood transfusion Iron transfusion All the above is being conducted every 6 to 10 weeks to check the progress
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Allergic to Asprin, Food allergy to Lactose
Vorherige Impfungen: -

VAERS 2318934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 44,0
Geschlecht: M
Eingang: 14.06.2022
Impfdatum: 16.06.2021
Beginn: 13.05.2022
Tage bis Beginn: 331,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Bradycardia COVID-19 Chest X-ray normal Computerised tomogram head normal Cough Dizziness Fatigue Hypotension Myalgia SARS-CoV-2 test positive Syncope

Symptomtext

Patient is fully vaccinated and boosted. Tested COVID positive. 45-year-old male presenting to the ED for dizziness, lightheadedness, and multiple syncopal episodes. Hypotensive and bradycardic on arrival. Positive for cough, fatigue, myalgias. BP 99/58 | Pulse 57 | Temp 97.3 ?F (36.3 ?C) (Oral) | Resp 16 | Ht 180.3 cm (5' 11") | Wt 113 kg (250 lb) | SpO2 96% CT of head: no acute pathology. CXR: no acute process. Medications: fluids, rocephin, decadron. discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2269033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CT
Alter: 43,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Alopecia Anxiety Arrhythmia Arthralgia Asthenia Autonomic nervous system imbalance Blood pressure increased Bone pain Carpal tunnel syndrome Chest discomfort Chest pain Choking sensation Condition aggravated Decreased appetite Diarrhoea Discomfort Dysphagia Dyspnoea

Symptomtext

Within 3.5 hours of my injection, I felt an intense heaviness crawl up my arm and to my head. It felt like heavy weights were resting on my head and shoulders. I could do not much more than just go lay down. I was surprised that with my first dose I was feeling anything at all. There is no way that I had any exposure to Covid, (as I had been strictly staying home, having groceries delivered since March 2020)and I had heard that only people who had had prior exposure or reacting on the first shot. As the night went on, I had hot and cold flashes that went through the morning. The next day, my period started, a week early. Through the next week I felt extremely fatigued, and could barely lift my left arm. I thought I started feeling better with the exception of my arm, which was also feeling very crampy. The pain and cramping moved further towards my left side of my chest. Even lifting my left arm would cause me to become breathless and cause tightening in my chest. I took care to avoid over doing it for a while hoping it would go away. The tightness and pain were crawling up over my shoulders and to my neck at this point. Every time I turned my head left or right there was a crunching noise. There were times I felt like my head was dislocating from my neck. One evening I experienced the worst migraine of my life. I have experienced many migraines before, and this was something entirely different. The pounding was so hard I was terrified that the end was upon me, and I did not even feel stable enough to get to the hospital. I asked my husband to bring children to me and silently said my goodbyes just in case. Almost three weeks in to this experience, I developed extreme pains in my chest that were also extremely exhausting, I felt like gravity was five times heavier than normal, and knew that something was deeply wrong. My ribs ached and I was in severe pain if I wore a bra. I then developed severe diarrhea and I could not eat anything at all. It?s like all of my saliva went dry and swallowing mechanism no longer knew how to work.. My arms were hulky looking, with the veins bulging out, my muscles ached, I had carpal tunnel and the thoracic outlet syndrome all acting up and making my arms go numb constantly through the night as I tried to sleep. It was disturbed and I was constantly awoken with feelings of doom and deep primal anxiety. I had a horrible burning feeling under my skin that felt like lava coursing through my veins all of the time, like the worst body aches of the worst flu ever. I was due for my next shot. 10 minutes before leaving for my appointment, I listened to the strongest feeling I've ever felt in my gut, cancel the appointment and called my doctor instead. I could barely get myself to the appointment. They took my blood pressure and then they made me wait a very long time before they came back and took it again. The reason why is because even after waiting 20 minutes quietly in a room, my blood pressure was only down to the dangerously high 174/100, my usual is 115/70. While my doctor listened to my concerns and acknowledged them, advising me not to get the second shot. When I expressed hesitancy to my doctor about taking a heart medicine, she insisted it would be important especially if I possibly had myocarditis. She did many kinds of blood work, and it showed I had high white blood cells. She also had me take an an EKG there in the office, which was normal. My doctor gave me amlodipine for blood pressure, which I took for the next six months before my blood pressure suddenly returned to my normal low and I was able to stop taking it. It was that sixth month that my periods finally returned to normal as well, after being very much off schedule, very heavy, and with horrible, debilitating PMS worse than anything Ive ever experienced before. After that appointment with the doctor, I did my best to take care of myself and just try to survive. I had little hope that the doctors could do much for me, and was feeling too unwell to even pursue further answers as far as testing or specialists go. Not to mention the expense, particularly now that I was too unwell to work. The horrible pain with in my bones and joints and muscles was working its way down my body. I noticed it had moved from my head, down my back, to my legs and finishing with my feet, taking about 8 weeks to make it through my toes. Incredible pain, joints subluxating, inflammation, bulging veins, an incredible weakness like my nerves weren't able to communicate to my muscles anymore. It was like what people describe MS to feel like. Later I learned that what I experienced was similar to and possibly transverse myelitis. My allergies seemed worse than ever and eating made my head stuffy instantly, my GI track crampy, and I would feel my heart beat change. to slow, too fast, pounding, skipping, feelings of doom or intense anxiety, and a bright red flushing that looked like a sunburn. Often these flares would lead back to me not being able to eat at all. It's like my entire G.I. system would shut down. I would then go into starvation mode and my muscles would start losing their tone and ache like lava was under my skin again. I became very afraid to eat anything except a few safe foods. I went on a low histamine diet and fared a little better. Foods like garlic and onion that I had eaten daily all of my life were now causing me horrible dysautonomia flares, sending all of my body systems into chaos and high alert. I have also been experiencing hives all over my chest, arms, and face like I never have in my life since my shot. Another alarming sign was the amount of hair I was loosing. It far surpassed the amount I lost after having babies. It has slowed down a little now (a year later) but for about six months so much was coming it out my hairline was changing and I could see my scalp through my once very thick and plentiful hair. During all of this I was also experiencing a lot of neurological issues like vision problems with my left eye, intense pressure and lots of floaters. Bright lights were completely intolerable, and standing under a light gave me a sensation that made me feel like I was going to have a seizure, especially if I looked up at it. Sometimes it would trigger a rapid heartbeat, which was starting to become more of a common problem. My heart rate would go from being 65 beats a minute to 165 beats a minute within seconds and race for many minutes. I eventually learned a vasovagal maneuver to stop it, but for a long time it was absolutely terrifying. My ears rang with tinnitus and continue to do so to this day with a constant high pitched electronic whine like a chorus of a thousand little mice singing in a monotone unison. Also, I while I have essential tremor that is pretty well controlled with a low dose of propranolol taken daily for the past 17 years, my tremor was much more intense than usual, and I often felt a deep internal tremor, particularly right around my midsection in near my diaphragm. Walking around the house made me breathless as my heart was bouncing in my chest with irregular beats. I often had the sensation of the wind being sucked from my lungs, and sometimes presyncope followed by racing heart. I started improving slowly with time until 4 1/2 months and I had another six weeks of major setbacks. I had issues with constantly choking on food, as if the muscles in my throat had forgotten how to swallow somehow. I am a former professional opera singer, and have very good awareness and use of my throat muscles so this was very disturbing. Food would often get stuck halfway down, or trapped partially under my epiglottis as I swallowed, keeping it from closing properly. I had three consecutive flares, two weeks long each. My systems would go into full dysautonomia, my GI system shut down; I couldn't eat, no saliva, extreme nausea, extreme fatigue, irregular heart rhythms. More starvation and muscle wasting, neuropathic pain, unable to eat for two weeks at a time except small amounts of soup, yogurt, or smoothies. When I started to make a turn for the better again, my muscles would twitch and my legs would bounce on their own for a day or so. Strangely enough I was optimistic that this was my nerves trying to heal. At six months into this nightmare, My arrhythmias were getting near constant, and it was presenting as something called postural orthostatic tachycardia syndrome. My blood pressure had come down, and now it was going down too low, especially when I stood up, so I stopped the blood pressure medicine. That was the same month my periods finally returned to normal. I have slowly been trying to regain my strength since then, and only have had one major flare since. It was in February; for four days I was unable to eat, my heart was jumping around again, and I was extremely short of breath and weak. The flares I've gotten shorter and I hope they continue to. I am very careful about what I eat and avoid all trigger foods. A supplement I take is called d-ribose has been helping my arrhythmias so I can work around the house again and lightly exercise. It is usually taken for heart failure. I have also taken zyrtec and pepcid and followed a low-histamine diet since last summer to try and manage the histamine overload. I hope I can one day return to my previous strength and health. This experience was terrifying and took a year of my life. I spent a total of three months in bed, six barely able to walk around the house, and only now am feeling well enough to lightly exercise again. My husband had to take care of myself and our small children--thankfully he was able to work from home or I don't know how we would have survived it. I only very recently began meeting one real estate client because it was too unsafe for me to go anywhere with my heart issues until now as my arrhythmias are fewer and I have some warning of a flare. During the most dangerous times the main reason I never went to the ER during the very worst of my adverse reaction was because I didn't feel physically stable enough to get myself there. I am still working to my strength. This has undoubtedly been the worst health crisis of my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: High White Blood Cells on June 11th which resolved a month later. High Blood Pressure 174/100.
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: Possible Ehlers-Danlos Syndrome but have not pursued official diagnosis yet due to expense and difficulty of finding a doctor who can diagnose it, as well as the pandemic keeping me home since I cannot be fully vaccinated now. Had some racing heart issues following childbirth. Essential tremor since childhood. Celiac Disease. Symptoms of Mast Cell Activation Syndrome. History of migraines (this is why I take propranolol, as well as for the essential tremor.)
Andere Medikamente: Zyrtec; Pepcid; Tylenol; Propranolol; Multivitamin
Allergien: Celiac disease (gluten); Latex allergy
Vorherige Impfungen: -

VAERS 2264659

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MO
Alter: 75,0
Geschlecht: M
Eingang: 05.05.2022
Impfdatum: 26.10.2021
Beginn: 22.04.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bell's palsy

Symptomtext

Have Bell's Palsy. Took prednisone 60 mg for 7 days and 3 grams of valacyclovir for 7 days. Taking Tylenol (325 mg) every 4-6 hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: None - Clearly visible on face
Aktuelle Erkrankungen: None
Vorgeschichte: seasonal allergy
Andere Medikamente: 100 mcg Levothyroxin, 75 mcg Vit D. AREDS 2, Flonase (1 spray in one nostril) - all daily
Allergien: None
Vorherige Impfungen: -

VAERS 2242043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 25,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Blood pressure increased Cardiac monitoring Dyspnoea Immunisation reaction Periorbital swelling Pharyngeal erythema Pharyngeal swelling Rash SARS-CoV-2 test positive Swelling face Throat tightness Tremor Urticaria

Symptomtext

Patient experienced an anaphylactic reaction to the COVID-19 Pfizer vaccine. (difficulty breathing, swelling of face and throat, rash - within 4 hours; emergency treatment sought) Immediately after administering the COVID-19 booster dose - patient complained of some tightness is the throat and was shaking. Office Notes: "He was feeling some tightness in his throat when I arrived and was talking to him. He was not having any respiratory distress. We examined the heart lungs and he appeared to have a regular rate and rhythm along with normal breath sounds. No wheezing audible. I asked him if he had a history of anxiety which he stated he did. I also asked if he had any reaction to the 1st or 2nd COVID-19 vaccinations and he stated he did not. We discussed that this could just be an anxiety provoked reaction. I reassured the patient that everything looks good and sounds good Obviously we cannot examine the inside of his throat to look at his airway but I advised him to drink some water while he waited the 15 minutes he was also sent after receiving the COVID vaccination. I checked on the patient multiple times throughout the 15 minutes. Each time I spoke with him his symptoms were improving. We discussed that if he was having an anaphylactic reaction the water would not improve the symptoms and it would have worsened. I gave him reassurance that this is likely just related to anxiety and there is no indication for us to call EMS or inject steroids at this time. He was advised that if his symptoms were worsening he should call 911 for further evaluation. Patient in agreement the plan." Telemedicine appointment 2 hours after vaccine - "Wheezing, some dyspnea, throat feels tight after COVID 19 vaccination 2 hours ago. I have escalated patient to in person at the ER. His parents will drive him now." When to Emergency Department - 4.11.22 - DIAGNOSIS at time of disposition: 1. Anaphylaxis due to COVID-19 vaccine. HISTORY OF PRESENT ILLNESS: Patient is a 25-year-old male with the chief complaint of a possible allergic reaction. Patient explains that this morning he received his booster dose of the Pfizer COVID-19 vaccination. Patient describes that immediately after the shot he noticed chest tightness and sore throat, describing this as tight. He notified his PCP of his symptoms who told him they were likely related to anxiety and told him to take a dose of his anxiety medication when he returned home. Patient describes that upon returning home he noticed continued chest tightness along with wheezing. He also describes a rash to his neck, abdomen, and back. Patient notes that he took a dose of Benadryl and Ativan around 1130. He notes that he was not feeling particularly anxious prior to the vaccination. He received both doses of the Pfizer COVID-19 vaccination in March 2021 and April 2021 without similar reaction. He notes that he tested positive for COVID-19 February 2022. Denies fever. He reports that he does have peanut allergies and has an EpiPen at home. 1336: On exam he does have some bilateral expiratory wheezing, rash on his back neck and arms with some urticaria where he has scratched the rash. Oropharynx is clear, voice is normal and there is no oral swelling. Some erythema to the posterior pharynx noted I did order IV Solu-Medrol, IV Benadryl and Pepcid, fluids and albuterol for wheezing. I do not feel patient needs EpiPen at this time. 1338: Patient's rash was worsening, he started having swelling around his eyes. He continued to have wheezing. We decided to give him epinephrine and move him to a monitored room. Patient was placed on a cardiac monitor, administered epinephrine will continue to monitor his symptoms. 1620: Patient was reassessed around 3:30 p.m., his rash had resolved, he was having no sensation of throat swelling, wheezing had resolved and he fell back to baseline. Will continue to monitor the patient until around 4:30 p.m 1636: Patient reassessed again, no recurrent symptoms, no wheezing, pulse ox 99%, no facial swelling, no rash. I did offer to observe the patient for an hour or 2 longer but they were comfortable going home at this point in time with no recurrent symptoms. I will prescribe prednisone 40 mg for 2 more days, have him continue Benadryl every 6 hours and follow up with this with his doctor. He has an EpiPen at home that is not expired and he is educated about symptoms that require using it and calling 911. He is welcome to come back with any new or worsening symptoms. He is advised never to receive a COVID-19 vaccine again due to the severe allergy. + elevated BP - to be evaluated by PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Unspecified constipation Peanut allergy Simple Renal cyst Family hx of colon cancer GAD (generalized anxiety disorder) Recurrent major depressive disorder, in full remission (HCC) Panic disorder Hashimoto's disease Multiple food allergies Insomnia Mixed hyperlipidemia
Andere Medikamente: EPINEPHrine 0.3 MG/0.3ML auto-injector LORazepam (ATIVAN) 0.5 MG tablet Magnesium 300 MG CAPS MULTIPLE VITAMIN PO Omega-3 Fatty Acids (OMEGA 3 PO) Probiotic Product (PHILLIPS COLON HEALTH PO) traZODone (DESYREL) 150 MG tablet
Allergien: NutsHives Lortab [Codeine]Itching, Rash Peanuts [Peanuts]Swelling TetracyclineItching, Rash Vicodin [Hydrocodone-acetaminophen]Itching, Rash Wellbutrin [Bupropion]
Vorherige Impfungen: -

VAERS 2219826

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MO
Alter: 46,0
Geschlecht: F
Eingang: 07.04.2022
Impfdatum: 20.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Balance disorder Bell's palsy Blood culture Blood glucose abnormal Blood lactic acid Blood lactic acid increased Body temperature Condition aggravated Diabetes mellitus Feeling abnormal Glycosylated haemoglobin Headache Pyrexia Swelling face Trigeminal neuralgia

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 46 year-old female patient received bnt162b2 (BNT162B2), administration date 20Apr2021 (Lot number: EW0169) at the age of 46 years as dose 2, single for Covid-19 immunisation. Relevant medical history included: "Bell's palsy" (unspecified if ongoing); "Trigeminal neuralgia" (unspecified if ongoing). Concomitant medication(s) included: LYRICA. Vaccination history included: Bnt162b2 (Dose: 01, Lot: ER8733), administration date: 30Jan2021, when the patient was 46 years old, for Covid-19 immunization. The following information was reported: DIABETES MELLITUS (hospitalization, medically significant) with onset Jan2022, outcome "unknown", described as "Diagnosed with diabetes"; BELL'S PALSY (hospitalization, medically significant), outcome "not recovered", described as "She also has bell's palsy"; HEADACHE (hospitalization) with onset Apr2021, outcome "unknown", described as "Head was pounding"; PYREXIA (hospitalization) with onset Apr2021, outcome "unknown", described as "High fever"; ASTHENIA (hospitalization) with onset Apr2021, outcome "unknown", described as "No energy at all"; BALANCE DISORDER (hospitalization) with onset Apr2021, outcome "unknown", described as "Felt off balance, kind of like her equilibrium was off"; BLOOD LACTIC ACID INCREASED (hospitalization), outcome "unknown", described as "Lactic acid was elevated"; SWELLING FACE (hospitalization), outcome "unknown", described as "Facial swelling"; TRIGEMINAL NEURALGIA (hospitalization), outcome "recovered", described as "She has trigeminal neuralgia behind her left eye"; CONDITION AGGRAVATED (hospitalization), outcome "unknown", described as "Clarifies that the flare up started before she received the vaccine but got worse after the second dose and she could not bear the pain anymore."; FEELING ABNORMAL (non-serious), outcome "unknown", described as "head was real foggy". The patient was hospitalized for headache, pyrexia (start date: 21Apr2021, discharge date: 24Apr2021, hospitalization duration: 3 day(s)). The patient underwent the following laboratory tests and procedures: blood culture: (unspecified date) negative, notes: Her doctor thought she was severely sepsis, but her results were negative; blood glucose abnormal: (unspecified date) high; blood lactic acid: (unspecified date) elevated; body temperature: (Apr2021) high, notes: High fever; glycosylated haemoglobin: (unspecified date) diabetes, notes: She asked to check her A1C and she was then diagnosed with diabetes. Therapeutic measures were taken as a result of trigeminal neuralgia. Clinical course: Symptoms after 2nd dose of Pfizer Vaccine: Head was pounding, high fever, no energy at all, felt off balance and what she means by that is her head was real foggy, kind of like her equilibrium was off. All started 6-8 hours after the 2nd dose was given. Symptoms after 3rd dose: 104.3 Fever, headache, loss of appetite, aches. only lasted 24 hours and then she bounced right back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Test Name: Blood culture; Test Result: Negative; Comments: Her doctor thought she was severely sepsis, but her results were negative; Test Name: Blood sugars; Result Unstructured Data: Test Result: High; Test Name: Lactic acid; Result Unstructured Data: Test Result: Elevated; Test Date: 202104; Test Name: Body temperature; Result Unstructured Data: Test Result: High; Comments: High fever; Test Name: A1C; Result Unstructured Data: Test Result: Diabetes; Comments: She asked to check her A1C and she was then diagnosed with diabetes.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bell's palsy; Trigeminal neuralgia
Andere Medikamente: Lyrica
Allergien: -
Vorherige Impfungen: -

VAERS 2162528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 70,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 16.04.2021
Beginn: 06.03.2022
Tage bis Beginn: 324,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Blood gases Loss of consciousness

Symptomtext

Patient found by family at home passed out in her bathroom and weakness. Brought to hospital for assessment. Treatment plan includes: Therapy, ABGs, Oxygen titration, blood pressure monitoring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, COPD, Obesity, CAD, GERD, Asthma
Andere Medikamente: -
Allergien: Azithromycin, Ceclor, Cephalexin
Vorherige Impfungen: -

VAERS 2126272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 61,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Dizziness Presyncope

Symptomtext

Feeling dizzy like I am going to pass out; Feeling dizzy like I am going to pass out; Weakness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 14Apr2021 (Lot number: EW0169) at the age of 61 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing); "Hypertension" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN ER taken for diabetes mellitus; LEVOTHYROXINE taken for hypothyroidism; LOSARTAN HCTZ taken for hypertension; BABY ASPIRIN. The following information was reported: DIZZINESS (non-serious) with onset 16Apr2021, outcome "not recovered", PRESYNCOPE (non-serious) with onset 16Apr2021, outcome "unknown" and all described as "Feeling dizzy like I am going to pass out"; ASTHENIA (non-serious) with onset 16Apr2021, outcome "unknown", described as "Weakness". Therapeutic measures were taken as a result of dizziness, presyncope, asthenia. Additional information: Clinical course: The patient received the Pfizer vaccine on 14Apr2021 and the first couple of days, she was okay, starting that third day, when she woke up and she was feeling dizzy like she was going to pass out and was kind of weak. Patient looked for the side effect at the sheet that was given to her at the vaccine site. Patient drank plenty of fluids and fluids have electrolyte in it for the events. Events seemed to get any better, but patient still felt the dizziness. The patient was querying if dizziness and weakness were severe reaction to the vaccine. Patient stated that she wanted to report it and wanted the authority to be responsible for anything that will happen to her body because she has no other insurance of anything else. It was reported that the patient took Tylenol extra strength 500mg (2 tablet, once) by mouth on April 15. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetes; Hypertension; Hypothyroidism
Andere Medikamente: METFORMIN ER; LEVOTHYROXINE; LOSARTAN HCTZ; BABY ASPIRIN
Allergien: -
Vorherige Impfungen: -

VAERS 2028289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: DC
Alter: 36,0
Geschlecht: F
Eingang: 12.01.2022
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: unbekannt Erholt: ja

Angina pectoris Blood thyroid stimulating hormone Body temperature increased Cardiac monitoring Chest X-ray Dizziness Ear pain Electrocardiogram Feeling abnormal Full blood count Hypoaesthesia Immediate post-injection reaction Injection site reaction Loss of consciousness Lymphadenopathy Metabolic function test Muscle twitching Nausea

Symptomtext

Immediate severe nausea and neck swelling sensation on injection side. About 30 minutes later experienced vasovagal response (typical for me), including lightheaded/passing out, turning A certain color, increased body temperature, severe nausea. I laid down for about 20 minutes and was given an anti-nausea pill before sent home. About 1 -1.5 hours after my shot, I was standing at my sink and felt like I had the wind suddenly knocked out of me. I then experienced severe heart pain - it felt like someone had scooped a chunk out of my heart. I am a young health avid runner and I have never experienced such severe pain in my life. My entire right arm (injection arm) also became numb and tingly, and I was unable to get a pulse-oxy reading for about 30 minutes from my finger on right hand. My severe pain, heart pounding/rapid and strong palpitations, numb and tingling arm lasted for about 2 hours until it subsided. I failed to go to the hospital when I should have in that moment (in hindsight I should have). About 36-48 hours after my shot, I started to develop other symptoms over the course of two weeks. It started with what felt like loss of bladder control and excessive thirst. I also had constant eye twitching in my right eye for about 10-12 days, numbness along my lower right side extremities (my right leg and foot were numb for a few days), bad episodes of mental brain fog, and more. About 3-5 days after my shot I woke up in the middle of the night grasping for air, heart rapidly pounding, and eyes rolled back. Again, something I have never experienced before. For about 3 months after my shot I had random episodes of rapid heart palpitations (especially when laying down in bed), brain fog, light headiness, right ear pain, and swollen lymph nodes in right side of neck.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: CBC, TSH, T4, Basic Metabolic Panel, CMP 14, chest xray, neck ultrasound, chest ultrasound, EKG, heart monitor
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Align (probiotic)
Allergien: N/A
Vorherige Impfungen: Gardasil, age 21, likely vasovagal response (passed out about 15 minutes after the shot)

VAERS 2024555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 60,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 15.04.2021
Beginn: 10.01.2022
Tage bis Beginn: 270,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Hospitalisation SARS-CoV-2 test positive

Symptomtext

HOSPITALIZED COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hospitalisation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 20,0
Geschlecht: M
Eingang: 26.12.2021
Impfdatum: 22.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Chest pain Echocardiogram abnormal Feeling abnormal Heart rate increased Hyponatraemia Hypotension Malaise Pericarditis Pyrexia Troponin increased

Symptomtext

Shot #3 at pharmacy 12/22/2021- Patient reported feeling very unwell 12/25/2021 around 8 am complaining of " feels like I'm having a heart attack". Fever of 101.1 around 4 pm same day. Requested to go to ER 12/26/21 around 12 am due to terrible chest pain. He is still in ER at Medical Clinic. DX is pericarditis. No prior history of cardiac events. Moderate malaise during 12/21 to 12/24. Being treated currently with heparin, toradol, nitroglycerin, K+.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: Pericarditis via echocardiogram 12/26 as per nurse via phone. Abnormal elevated troponin levels on admittance. Hyponatrimia. Low blood pressure 88/60?. Heart rate (resting) as high as 94 bpm.
Aktuelle Erkrankungen: Scalp dermatitis
Vorgeschichte: Possible past Lyme Disease, dysthymia
Andere Medikamente: None known
Allergien: Possible banana, wheat, dairy, rice allergies (Doctor has specific info)
Vorherige Impfungen: Dose #2 pfizer

VAERS 1545397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 26.04.2021
Beginn: 19.05.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Anticoagulant therapy Cerebral venous sinus thrombosis Computerised tomogram head abnormal Headache Impaired work ability Migraine Neck pain SARS-CoV-2 test Sleep disorder Vomiting

Symptomtext

a CVST blood clot in my brain; vomit; headache; neck pain; migraine; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Apr2021 (Lot number: EW0169) at the age of 35 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "known allergies Cashews and other tree nuts" (unspecified if ongoing). The patient took concomitant medications (birth control). No other vaccine in four weeks. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left), administration date: 05Apr2021, when the patient was 35 years old, for COVID-19 immunization. No covid prior vaccination. The following information was reported: CEREBRAL VENOUS SINUS THROMBOSIS (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "a CVST blood clot in my brain"; VOMITING (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "vomit"; HEADACHE (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "headache"; NECK PAIN (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "neck pain"; MIGRAINE (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "migraine". The patient was hospitalized for cerebral venous sinus thrombosis, vomiting, headache, neck pain, migraine (hospitalization duration: 2 day(s)). The events "a cvst blood clot in my brain", "vomit", "headache", "neck pain" and "migraine" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (17Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of cerebral venous sinus thrombosis, vomiting, headache, neck pain, migraine. Clinic course included on the morning of 19May2021, patient woke up with the worst headache/neck pain she had ever had in life. This caused patient to vomit a few times before going to the ER. Once at the ER, she explained that she thought she had a migraine and vomited a couple more times. Once seen by the medical staff, patient was informed that had a CVST blood clot in brain. Patient was given Heparin and was put on oral blood thinners once discharged from the hospital, where she took them for the next 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 2,0
Labordaten: Test Date: 20211117; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1545397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 26.04.2021
Beginn: 19.05.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Anticoagulant therapy Cerebral venous sinus thrombosis Computerised tomogram head abnormal Headache Impaired work ability Migraine Neck pain SARS-CoV-2 test Sleep disorder Vomiting

Symptomtext

a CVST blood clot in my brain; vomit; headache; neck pain; migraine; 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 (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Apr2021 (Lot number: EW0169) at the age of 35 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "known allergies Cashews and other tree nuts" (unspecified if ongoing). The patient took concomitant medications (birth control). No other vaccine in four weeks. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left), administration date: 05Apr2021, when the patient was 35 years old, for COVID-19 immunization. No covid prior vaccination. The following information was reported: CEREBRAL VENOUS SINUS THROMBOSIS (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "a CVST blood clot in my brain"; VOMITING (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "vomit"; HEADACHE (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "headache"; NECK PAIN (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "neck pain"; MIGRAINE (hospitalization, life threatening) with onset 19May2021, outcome "recovered", described as "migraine". The patient was hospitalized for cerebral venous sinus thrombosis, vomiting, headache, neck pain, migraine (hospitalization duration: 2 day(s)). The events "a cvst blood clot in my brain", "vomit", "headache", "neck pain" and "migraine" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (17Nov2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of cerebral venous sinus thrombosis, vomiting, headache, neck pain, migraine. Clinic course included on the morning of 19May2021, patient woke up with the worst headache/neck pain she had ever had in life. This caused patient to vomit a few times before going to the ER. Once at the ER, she explained that she thought she had a migraine and vomited a couple more times. Once seen by the medical staff, patient was informed that had a CVST blood clot in brain. Patient was given Heparin and was put on oral blood thinners once discharged from the hospital, where she took them for the next 6 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 2,0
Labordaten: Test Date: 20211117; Test Name: Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1955695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MO
Alter: 16,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 28.04.2021
Beginn: 13.12.2021
Tage bis Beginn: 229,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bell's palsy Eye movement disorder Facial paralysis Hyperacusis Lacrimation increased Neck pain

Symptomtext

Partial paralysis on the right side of face. Neck pain. Sensitivity to sound. Right eye watery and trouble blinking/closing eye

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Saw Dr who diagnosed with Bells Palsy.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1919680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 26.04.2021
Beginn: 27.09.2021
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Heart rate Heart rate decreased Investigation SARS-CoV-2 test Vaccination failure Syncope

Symptomtext

Covid test result - Positive / Covid test date 27Sep2021; Covid test result - Positive / Covid test date 27Sep2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old [non-pregnant] adult female received COVID-19 immunisation with the first dose of intramuscular BNT162B2 (solution for injection; Lot ER8733 expiry information not reported) as a single dose in the left arm on 05Apr2021 (at 55-years-old) and the second dose of intramuscular BNT162B2 (solution for injection; Lot EW0169 expiry information not reported) as a single dose in the left arm on 26Apr2021 (at 55-years-old). Relevant medical history included known sulfonamide and shellfish allergies; the patient described other medical history as multiple. The patient denied receiving any other vaccine within four weeks of this vaccine; It was unknown if the patient was diagnosed with COVID prior to vaccination; and the patient was not pregnant at the time of vaccination. Concomitant medications included omeprazole (PRILOSEC); topiramate (TOPAMAX); escitalopram oxalate (LEXAPRO); ropinirole; and buspirone hydrochloride (BUSPAR). The patient previously received treatment for unspecified indications with oxycodone hydrochloride/oxycodone terephthalate/paracetamol (PERCOCET), codeine, prochlorperazine maleate (COMPAZINE), and metoclopramide (REGLAN) and experienced a drug allergy with each. On 27Sep2021 the patient tested positive for COVID via nasal swab. The outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210927; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: PRILOSEC; TOPAMAX; LEXAPRO; ROPINIROLE; BUSPAR
Allergien: -
Vorherige Impfungen: -

VAERS 1919680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 55,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 26.04.2021
Beginn: 27.09.2021
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Heart rate Heart rate decreased Investigation SARS-CoV-2 test Vaccination failure Syncope

Symptomtext

Covid test result - Positive / Covid test date 27Sep2021; Covid test result - Positive / Covid test date 27Sep2021; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 56-year-old [non-pregnant] adult female received COVID-19 immunisation with the first dose of intramuscular BNT162B2 (solution for injection; Lot ER8733 expiry information not reported) as a single dose in the left arm on 05Apr2021 (at 55-years-old) and the second dose of intramuscular BNT162B2 (solution for injection; Lot EW0169 expiry information not reported) as a single dose in the left arm on 26Apr2021 (at 55-years-old). Relevant medical history included known sulfonamide and shellfish allergies; the patient described other medical history as multiple. The patient denied receiving any other vaccine within four weeks of this vaccine; It was unknown if the patient was diagnosed with COVID prior to vaccination; and the patient was not pregnant at the time of vaccination. Concomitant medications included omeprazole (PRILOSEC); topiramate (TOPAMAX); escitalopram oxalate (LEXAPRO); ropinirole; and buspirone hydrochloride (BUSPAR). The patient previously received treatment for unspecified indications with oxycodone hydrochloride/oxycodone terephthalate/paracetamol (PERCOCET), codeine, prochlorperazine maleate (COMPAZINE), and metoclopramide (REGLAN) and experienced a drug allergy with each. On 27Sep2021 the patient tested positive for COVID via nasal swab. The outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210927; Test Name: Nasal Swab; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shellfish allergy; Sulfonamide allergy
Andere Medikamente: PRILOSEC; TOPAMAX; LEXAPRO; ROPINIROLE; BUSPAR
Allergien: -
Vorherige Impfungen: -

VAERS 1928059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OR
Alter: 41,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anaphylactic reaction Asthenia Body temperature Bone pain Chest pain Chills Dysstasia Fatigue Hyperhidrosis Loss of consciousness Muscle spasms Pain Pyrexia Seizure Sleep disorder

Symptomtext

full body pain; chest pain; My body convulsed/ had muscle spasms constantly for 7 days/nights; passed out when body was exhausted; My body convulsed/ had muscle spasms constantly for 7 days/nights; passed out when body was exhausted; Couldn't stand; walk pain was extreme; Too weak to sit up; chills; massive sweats around the clock.; Didn't sleep; I had the most excruciating full body pain every bone in my body/Every bone in body,all teeth,joints, felt like being crushed & broken 100% at all times no break; Anaphylactic reaction; fever/fever of 102; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 41 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 15Apr2021 09:00 (Lot number: EW0169) at the age of 41 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing), notes: Other medical history:asthma. There were no concomitant medications. Past drug history included: Cefaclor, reaction(s): "Known allergies: Cefaclor", notes: Known allergies:Cefaclor. Vaccination history included: Bnt162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer, Prev dose brand unknown=False, Prev dose lot number=ER8727, Prev dose lot unknown=False, Prev dose administration date=25Mar2021 , Prev dose administration time= 09:00 AM, Prev dose dose number=1, Prev dose vaccine location=Left arm), administration date: 25Mar2021, when the patient was 41 years old, for Covid-19 immunization. The following information was reported: ANAPHYLACTIC REACTION (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "Anaphylactic reaction"; PYREXIA (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "fever/fever of 102"; PAIN (life threatening), outcome "unknown", described as "full body pain"; CHEST PAIN (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "chest pain"; SEIZURE (life threatening), MUSCLE SPASMS (life threatening) all with onset 15Apr2021 15:00, outcome "recovered" and all described as "My body convulsed/ had muscle spasms constantly for 7 days/nights"; LOSS OF CONSCIOUSNESS (life threatening), FATIGUE (life threatening) all with onset 15Apr2021 15:00, outcome "recovered" and all described as "passed out when body was exhausted"; DYSSTASIA (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "Couldn't stand"; PAIN (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "walk pain was extreme"; ASTHENIA (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "Too weak to sit up"; CHILLS (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "chills"; HYPERHIDROSIS (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "massive sweats around the clock."; SLEEP DISORDER (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "Didn't sleep"; BONE PAIN (life threatening) with onset 15Apr2021 15:00, outcome "recovered", described as "I had the most excruciating full body pain every bone in my body/Every bone in body,all teeth,joints, felt like being crushed & broken 100% at all times no break". The events "anaphylactic reaction", "fever/fever of 102", "chest pain", "my body convulsed/ had muscle spasms constantly for 7 days/nights", "passed out when body was exhausted", "my body convulsed/ had muscle spasms constantly for 7 days/nights", "passed out when body was exhausted", "couldn't stand", "walk pain was extreme", "too weak to sit up", "chills", "massive sweats around the clock.", "didn't sleep" and "i had the most excruciating full body pain every bone in my body/every bone in body,all teeth,joints, felt like being crushed & broken 100% at all times no break" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: body temperature: (15Apr2021) 102. Therapeutic measures were taken as a result of anaphylactic reaction, pyrexia, pain, chest pain, seizure, loss of consciousness, muscle spasms, fatigue, dysstasia, pain, asthenia, chills, hyperhidrosis, sleep disorder, bone pain. Additional information: The patient reported about covid vaccine. The patient was not covid prior vaccination, the patient had not covid tested post vaccination. Anaphylactic reaction 3pm sudden fever,full body pain,chest pain,called 911 was triaged- as healthy vital signs by ambulance.took 1 Benedril.Couldn't stand unsupported could barely walk pain was extreme. For the next 7, 24 hour days, I had the most excruciating full body pain every bone in my body, a fever of 102- just low enough, ER told me to stay home. patient body convulsed/ had muscle spasms constantly for 7 days/nights, I had firey fever pain chills,massive sweats around the clock.Didn't sleep. passed out when body was exhausted. Every bone in body, all teeth,joints, felt like being crushed & broken 100% at all times no break,no relief 7 solid days,no break in fever or excruciating full body pain. Too weak to sit up. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210415; Test Name: Body temperature; Result Unstructured Data: Test Result:102
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Other medical history:asthma)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 17.08.2021
Beginn: 12.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Bell's palsy Drooling Facial paralysis Nausea Oropharyngeal pain Swelling face Vomiting

Symptomtext

NauseaVomiting sx similar to Bells Palsey, facial drooping, facial/cheek swollen Narrative: Previous 2 yrs ago of Bells palsey. Now is c/o of drooling on L side mouth and facial swelling. N/V, sore throat Advised to go to Emergency Room

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1921094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 43,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 12.05.2021
Beginn: 16.09.2021
Tage bis Beginn: 127,0
Dosis: UNK
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

C-reactive protein abnormal Chest X-ray Echocardiogram Electrocardiogram Full blood count Inflammation Metabolic function test Pericardial effusion Pericarditis Red blood cell sedimentation rate Stress echocardiogram Troponin I

Symptomtext

pericardial effusion, pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC with auto differential 9/16/2021 basic metabolic panel 9/16/2021 EKG 12 lead 9/16/2021 Chest x-ray PA and Lateral 9/16/2021 Troponin I 9/16/2021 Troponin I (again) 9/16/2021 Echo Stress Echocardiogram 9/30/2021 ESR 10/12/2021 CRP Inflammation 10/12/2021 EKG 12 lead 10/15/2021 Troponin I 10/15/2021 Echocardiogram, 11/12/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Sjogren's syndrome, depression
Andere Medikamente: trintellix, meloxicam, cyclobenzaprine, multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1850688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 84,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 13.04.2021
Beginn: 26.10.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 Intensive care SARS-CoV-2 test positive

Symptomtext

Pt completed initial Pfizer COVID 19 Vaccination (on 3/23/2021 and 4/13/2021 respectively), plus the Pfizer booster on 10/19/2021. COVID test was positive 10/26/2021 and he was transferred from a smaller hospital to this hospital for higher level of care. Pt eventually needed ICU level care here, but has since improved enough to be cared for in our ICU department.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anemia, CAD, cardiomyopathy, CHF, chronic Afib, current use of long term anticoagulation, diverticulosis, enlarged prostate without urinary obstruction, HTN, gout, hyperlipidemia, hypothyroidism, asthma, MRSA, osteoarthrosis, peptic ulcer, pulmonary hypertension, rheumatic disorders of both mitral and aortic valves, OSA, venous stasis ulcers, vitamin D deficiency.
Andere Medikamente: allopurinol, budesonide-formoterol, bumetanide, carvedilol, celecoxib, ergocalciferol, fluticasone, levothyroxine, losartin, omega 3s, potassium chloride, rosuvastatin, spironolactone, warfarin.
Allergien: Lisinopril, niacin
Vorherige Impfungen: -

VAERS 1843205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 20.04.2021
Beginn: 28.10.2021
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Atrial fibrillation Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac imaging procedure abnormal Chest X-ray abnormal Chest discomfort Computerised tomogram thorax abnormal Condition aggravated Cough Dyspnoea Echocardiogram abnormal Ejection fraction decreased Fatigue Haematocrit increased Haemoglobin increased Hypoxia

Symptomtext

75-year-old female presented with nausea, chest tightness, and shortness of breath. Patient did have some mild fatigue and a mild cough 2 weeks prior. After getting her flu shot, about 4 hours later, she developed nausea, vomiting, and chest tightness. This was then followed by progressive shortness of breath with orthopnea. Upon presentation to the emergency department, patient was found to be in atrial fibrillation with RVR which is new for her. She was also hypoxic at 87% on room air. CT angiogram thorax showed no PE but there was bilateral infiltrates, pulmonary edema versus infectious. Her COVID test came back positive. She also had significantly elevated troponin at 683 with an elevated BNP at 4000. Patient has been vaccinated for COVID. Upon discussion with Cardiology, patient was started on a heparin drip and daily aspirin. Patient was started on Decadron and remdesivir for COVID pneumonia. Her presentation was thought to be multifactorial cause by pulmonary edema, AFib with RVR, and COVID pneumonia. Patient was placed on Cardizem drip. Her symptoms and hypoxia quickly resolved after her rate was controlled. An echocardiogram showed a decreased ejection fraction of 40% with hypokinetic distal and apical segments. A cardiac MRI was then done which showed findings consistent with stress-induced cardiomyopathy (apical type). There was no MRI evidence of myocardial infarction or myocarditis. Left ventricular ejection fraction was 48%. Patient was given a dose of Lasix with very good response and urine output. Follow-up chest x-ray the next day showed improvement of her bilateral infiltrates which points more towards resolving pulmonary edema. With improvement of her symptoms, patient was discharged home with plans to have a follow-up echocardiogram in 4 weeks. Patient's metoprolol dose was increased to 75 mg daily. She was discharged on atorvastatin 40 mg daily, Lasix 20 mg daily, and transition to Eliquis 5 mg twice a day for atrial fibrillation. She will follow-up with cardiology as an outpatient.

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 2,0
Labordaten: Recent Labs 10/28/21 10/29/21 10/30/21 WBC 21.68* 18.66* 24.17* HGB 16.7* 14.1 13.6 HCT 47.8* 40.2 40.1 PLATELET 293 223 194
Aktuelle Erkrankungen: -
Vorgeschichte: Circulatory Hypertension Left carotid artery stenosis Splenic artery aneurysm NSTEMI (non-ST elevated myocardial infarction) Atrial fibrillation with RVR (HCC)Endocrine/Metabolic Hypercholesterolemia Hypothyroidism due to acquired atrophy of thyroid
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 40 MG tablet CALCIUM PO Cholecalciferol (VITAMIN D3 PO) furosemide (LASIX) 20 MG tablet levothyroxine (SYNTHROID
Allergien: Ibu [Nsaids] LovastatinNausea Only, GI Upset Pravastatin
Vorherige Impfungen: -

VAERS 1832311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 39,0
Geschlecht: F
Eingang: 31.10.2021
Impfdatum: 30.03.2021
Beginn: 16.04.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Heavy menstrual bleeding Impaired work ability Loss of personal independence in daily activities Menstrual disorder Polymenorrhoea Thrombosis Tinnitus

Symptomtext

I had extreme fatigue for approximately 3 weeks. After 3 weeks the fatigue lasted into August; the fatigue kept me from working to my full potential and completing all the daily tasks. My menstrual cycle in April - present has been affected by the vaccine as well. I have a very regular menstrual cycle and since April it has swayed between being very light and shorter days to extremely heavy flow for up to 3 weeks and with apple sized blood clots. I am still experiencing these symptoms and never know what to expect month to month. I have also experienced an increase of ringing in the ears after the vaccine. I would get ringing 1-2 times year normally, but after the vaccine it was constant and daily. This picked up after the 2nd shot.

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: No tests were ordered by my OB
Aktuelle Erkrankungen: none
Vorgeschichte: Chronic sinusitis
Andere Medikamente: Daily Multi vitamin, Vitamin D Supplement, Magnesium supplement, probiotic
Allergien: bacitracin, peanuts
Vorherige Impfungen: Per mother, MMR, age of 3. Inconsolable, extreme crying for hours. I remember this event and recall not feeling right or well. N

VAERS 1825141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 15,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 13.08.2021
Beginn: 12.10.2021
Tage bis Beginn: 60,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute motor axonal neuropathy Central venous catheterisation Diplegia Flavivirus test negative Gait disturbance Guillain-Barre syndrome Immunoglobulin therapy Inflammation Laboratory test normal Loss of personal independence in daily activities Lumbar puncture Magnetic resonance imaging abnormal Mobility decreased Muscular weakness Pain Plasmapheresis Syncope Walking aid user

Symptomtext

Patient was diagnosed with Acute Guillain-Barre Syndrome. She had a weak ankle on Tuesday, 10/12/2021 and saw a physical therapist who referred her to another PT the next day. On 10/13/2021, she collapsed getting out of bed with weakness in her legs. She saw PT, who referred her to a neurologist, who then sent her to the ER for an MRI, who then sent her to Hospital for that MRI. The MRI happened early morning of 10/14/2021. It showed inflammation consistent with GBS so they put her under to install a central line and do a spinal tap. By hen, she was only able to move her head a couple inches. No movement in her arms and legs, but there was pain everywhere. The tests came back verifying GBS and the Neurologist said it was Acute Motor Axonal Neuropathy. Plasmapheresis began the evening of 10/14/2021 (7 bottles) and IVIG right after. Patient had a total of 5 treatments of plasmapheresis over 10 days, every other day (Thursday, Saturday, Monday, Wednesday and Friday). IVIG then followed on Saturday and another Sunday. Patient worked with PT and OT every day after movement started again. She worked on standing the Friday of the last plasmapheresis, worked on walking with a walker on Saturday and Sunday and could walk on her own a little Monday. She will be working on walking more each day and start outpatient PT at hospital TIRR on November 8, 2021. Please note, patient is 15 and the youngest Studio Company This is really effecting her and her future job opportunities that she has been training for since she was 2 years old!

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 14,0
Labordaten: I was told she was tested for Wast Nile, Zika and other pathogens that have been shown to set off the GBS. She was negative to all. The MRI showed no structural issues, only the inflammation consistent with GBS.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D, Calcium & Cranberry Concentrate
Allergien: None
Vorherige Impfungen: -

VAERS 1818489

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 26.10.2021
Impfdatum: 12.05.2021
Beginn: 17.10.2021
Tage bis Beginn: 158,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Anticoagulant therapy Arthropathy Asthenia Blood lactic acid increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Haematemesis Haemoglobin normal Hepatic steatosis Hyperbilirubinaemia Hypoxia Lung opacity Magnetic resonance imaging spinal abnormal Nausea Presyncope SARS-CoV-2 test positive Spinal osteoarthritis

Symptomtext

Hospitalized 10/17/2021; COVID-19 positive 10/17/2021; fully vaccinated BRIEF OVERVIEW: Hematologist/Oncologist: No care team member to display Admission Date: 10/17/2021 Discharge Date: 10/21/21 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: COVID-19 HOSPITAL COURSE: No notes on file This is a 66 y.o. patient with a past medical history significant for HTN, CAD, Atrial Fibrillation, Depression, DM type II, neuropathy associated with MM, HLD and Multiple myeloma who presented with symptoms of weakness and near syncope at home per spouse at bedside 10/17/21. In the ED, patient was found to be hypoxic and nauseous, and improved with 2 L NC and Zofran. A CXR revealed patchy diffuse bilateral airspace opacities, compatible with COVID 19 pneumonia and his lactic acid ws slightly elevated, covid swab was positive. Patient was admitted for further tx. ID followed. Patient was placed on dexamethasone 6 mg daily, Remdesevir, and monoclonal antibodies given 10/18/21. Weaned off 2L to RA. MRI of lumbar/sacrum 10/18/21 no aggressive focal lesions, no fracture or mass. Mild progressive facet arthropathy L3-4. Multilevel lumbar spondylosis. PT/OT evaluated while inpatient. Patient also had coffee - ground emesis 10/18/21, GI followed. Protonix gtt started -- transitioned to PPI PO BID for 8 weeks, then will have EGD on outpatient basis when covid pna resolves. Eliquis initially held, then restarted as hgb stayed stable. Also noted hyperbilirubinemia 10/17 of 1.9 and had RUQ US which showed hepatic steatosis and mild splenomegaly, no biliary tree dilation. While inpatient team followed and adjusted insulin tx.

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Praegender Schweregrund: Presyncope
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: OSA (obstructive sleep apnea) AF (paroxysmal atrial fibrillation) CAD (coronary artery disease) Hypertension Sustained SVT PVC's (premature ventricular contractions) Orthostatic hypotension Class 1 obesity due to excess calories with serious comorbidity and body mass index (BMI) of 33.0 to 33.9 in adult Constipation due to opioid therapy COVID-19 Kappa light chain Multiple myeloma Cancer related pain Neuropathy associated with multiple myeloma Syncope, unspecified syncope type Dyslipidemia Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin Steroid-induced hyperglycemia
Andere Medikamente: acyclovir (ZOVIRAX) 400 MG tablet apixaban (ELIQUIS) 5 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet Cholecalciferol (VITAMIN D3 PO) DARATUMUMAB IV dexamethasone (DECADRON) 4 MG tablet empagliflozin (JARDIANCE) 10 MG tablet FLUoxetine (
Allergien: NKA
Vorherige Impfungen: -

VAERS 1818261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: AZ
Alter: 40,0
Geschlecht: F
Eingang: 26.10.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bedridden Bell's palsy Chills Condition aggravated Dysgeusia Fatigue Headache Herpes zoster Injection site erythema Injection site pain Joint range of motion decreased Joint swelling Myalgia Nausea Pyrexia Tinnitus

Symptomtext

My arm got really stiff. At the injection site, it was red and sore for a day. Later that night, that is when the other side effects came (the adverse side effects). Severe fatigue; really bad headache; muscle pain that on a lot of days I was needing to take 6 Advil during the course of the day - really painful. Also, the Bell's palsy symptoms started up that night. It was like a really bad case of flu that wouldn't go away. A constant fever for about a week. I had chills. The nausea was full-blown for about 6 weeks. It also swelled up my joints so that in the morning or at night I couldn't move my hands or arms. I do get side effects with medications that I take. I took natural supplements and was bedridden for about the first week because the muscle pain and inflamed joints were so bad. I did acupuncture for Bell's palsy - that was onset after the vaccine. Bell's Palsy- usually my symptoms for chronic condition are nonexistent, but each time I had the COVID-19 vaccine, it made me have the worse Bell's palsy symptoms that I've had in my life. My eye that wouldn't close; my drooling from my mouth because I couldn't move it. Ringing in the ears, and metallic taste in my mouth. A week and a half after the side effects lessened, I got shingles - from June 18th and ended before my birthday on August 22nd. My doctors think I got it because of the vaccine. Shingles symptoms lasted about 8 weeks, and it was pretty painful. Growing across my head and over my eyes. They gave me an anti-viral and I also took olive leaf extract and I used EMU oil as well; with those, it stopped growing. Doctor said it was the vaccine that brought the symptoms. My body was under duress. I had a relapse of the shingles- the beginning of September. It was a minute about of it; they thought it was pseudo pain from the shingles which I may have re-occur for 6 months. October 1st, I had my flu shot. My prior flu shot was August 30, 2020.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Diabetes Asthma Bell's Palsy - Bilateral Compromised Immune System
Andere Medikamente: Diabetic Medications Vitamin Supplements
Allergien: Flonase Latex
Vorherige Impfungen: Flu shot: because I'm allergic to latex and I guess that was what caused it - I had a little difficulty breathing for about a da

VAERS 1815466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 25.10.2021
Impfdatum: 24.03.2021
Beginn: 24.10.2021
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arterial disorder Arteriogram carotid abnormal COVID-19 Chest X-ray abnormal Chest pain Chest tube insertion Dyspnoea Fall Intensive care Mediastinal shift Musculoskeletal chest pain Pneumomediastinum Pneumothorax Rib fracture SARS-CoV-2 test positive Subcutaneous emphysema Swelling face

Symptomtext

REASON FOR ADMISSION Fall, right sided rib fractures, right pneumothorax HISTORY OF PRESENT ILLNESS a 70 y.o. man who presents to the Hospital with chest pain, increased work of breathing and massive subcutaneous emphysema status post falling off a 6 ft roof yesterday. Patient did not hit his head. He denies loss of consciousness. He is not on any blood thinner. He presented to the ED and daily chest x-ray demonstrated several right-sided rib fractures and a small pneumothorax. Patient was discharged pain meds. The patient later developed worsening facial swelling and returned to the ED due to concern for an allergic reaction. Patient was given epinephrine and prednisone and was discharged home. Patient awoke this morning with increased chest pain and difficulty breathing and presented to Emergency Department. Initial chest x-ray showed a left-sided pneumothorax with some mediastinal shift. A left-sided chest tube was placed. Imaging demonstrated right-sided rib fractures 1 through 7, large right pneumothorax, and large volume pneumomediastinum and subcutaneous emphysema. Patient also had a left-sided 1st rib fracture. A CTA of the neck was obtained which showed abnormal mild kinking of the left subclavian/axillary artery at the 1st rib. Patient was also COVID positive. Patient was transported up to the ICU for right chest tube placement and further management. Upon arrival, patient had HR 80-90's, SBP in 160-170's, and saturating greater than 98% on 3 L nasal cannula. Patient denies any allergies. He reports right-sided chest wall pain. His area decision maker would be his wife. A right-sided chest tube was placed under moderate sedation and confirmed by x-ray.

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Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 10/24/2021Coronavirus 2 PCR Detect, V symptomatic DETECTED
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1786555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 21.04.2021
Beginn: 02.07.2021
Tage bis Beginn: 72,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Deep vein thrombosis Pain in extremity Ultrasound Doppler abnormal

Symptomtext

2nd dose of covid vaccine on 4/21/21, last week of June I started having extreme pain in my left calf. On july 2nd ultrasound showed i had 4 DVTs in my left leg.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound of left leg
Aktuelle Erkrankungen: No illness
Vorgeschichte: HTN, HYPOTHYROIDISM, ANXIETY, FACTOR V LEIDEN MUTATION
Andere Medikamente: Lisinopril, levothyroxine & buspar
Allergien: None
Vorherige Impfungen: -

VAERS 1786555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 21.04.2021
Beginn: 02.07.2021
Tage bis Beginn: 72,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Deep vein thrombosis Pain in extremity Ultrasound Doppler abnormal

Symptomtext

2nd dose of covid vaccine on 4/21/21, last week of June I started having extreme pain in my left calf. On july 2nd ultrasound showed i had 4 DVTs in my left leg.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ultrasound of left leg
Aktuelle Erkrankungen: No illness
Vorgeschichte: HTN, HYPOTHYROIDISM, ANXIETY, FACTOR V LEIDEN MUTATION
Andere Medikamente: Lisinopril, levothyroxine & buspar
Allergien: None
Vorherige Impfungen: -

VAERS 1786182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 72,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 30.04.2021
Beginn: 17.09.2021
Tage bis Beginn: 140,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Atelectasis COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Computerised tomogram abdomen Computerised tomogram thorax abnormal Condition aggravated Dizziness Emphysema Haematocrit decreased Haemoglobin decreased Hypotension Laboratory test Lung consolidation Lung disorder Mean cell volume decreased Occult blood negative Pneumonia

Symptomtext

This is an elderly 72-year-old female who is an ongoing smoker with a known history of COPD on home O2 at the nursing home, possibly 2 L p.r.n. was out smoking and then had an unwitnessed syncopal episode. Was sent to the emergency room on 9/17/21 where she was found to be hypotensive and in respiratory distress. Her hemoglobin was found to be only 4.3. Patient was started on a BiPAP and then the hospitalist service was called for admission. Patient denies any history of epistaxis, hemoptysis, hematemesis, melena, hematochezia, hematuria, and she is not on any blood thinning medications. Her rectal exam revealed OB negative stool. The patient is denying abdominal pain. She does complain of feeling lightheaded. She does have a history of chronic anemia, but her baseline hemoglobin runs around 9.3, which was there in February of this year. At that point of time, her MCV was 88.6. Currently, her H and H is 4.7 and 18.5 with an MCV of 61.5. I have ordered stat anemia workup on her and a CT abdomen and pelvis and chest as well. Her COVID test did come back as positive. She will be going up to the IMC as an inpatient. Started her on Rocephin because her urinalysis is abnormal and the chest x-ray, there is a possibility of some COVID related pneumonia as well. Patient rececived and completed all 5 doses of remdesivir and 10 days of dexamethasone. Placed on ampicillin on 10/2/21. Discharged on 10/14/2021

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Praegender Schweregrund: Respiratory distress
Hospital-Tage: 27,0
Labordaten: 9/17/2021 COVID19- positive 9/17/21 chest xray: Bibasilar tissue prominence may reflect interstitial inflammation/infection or interstitial edema. 9/18/21 CT chest: Findings consistent with emphysema with mild traction atelectasis moving the mediastinum to the right. In addition there is severe fibrotic changes of the right lung with a superimposed pneumonia. 10/13/21 chest xray: COPD changes. Extensive consolidation within the right lung redemonstrated. Overall, this is probably mildly worse when compared to the prior study specially within the right lower lung. Left basilar airspace disease could represent atelectasis or additional pneumonia. This also appears mildly worse.
Aktuelle Erkrankungen: -
Vorgeschichte: Consists of hypertension, hyperlipidemia, COPD, chronic hypoxemic respiratory failure on home O2 at 2 L mostly p.r.n., osteoporosis, GERD, history of peptic ulcer disease, restless legs syndrome, osteoarthritis, anxiety, smoker.
Andere Medikamente: Albuterol PRN, alendronate, clopidogrel, donepezil, folic acid, losartan, memantine, metoprolol tartrate, nicotine patch, nitro PRN, omeprazole, pravastatin, ropinirole, thiamine, tramadol
Allergien: Aspirin, codeine, levofloxacin
Vorherige Impfungen: -

VAERS 1780326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 12.10.2021
Impfdatum: 11.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bell's palsy

Symptomtext

Bell's palsy

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1776881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 20.09.2021
Beginn: 20.09.2021
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

Dizziness, then syncopal episode. Syncopal episode lasted for <30 seconds. Recovered fully within25 mins with just water and snacks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Ibuprofen
Allergien: NKDA, no other allergies
Vorherige Impfungen: -

VAERS 1762114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TN
Alter: 14,0
Geschlecht: F
Eingang: 05.10.2021
Impfdatum: 15.05.2021
Beginn: 25.05.2021
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Brain natriuretic peptide increased C-reactive protein increased Cardiac imaging procedure abnormal Chest pain Condition aggravated Echocardiogram normal Full blood count Inflammatory marker increased Laboratory test Lymphocyte count Neutrophil count increased Pericardial effusion Pericarditis Platelet count increased Red blood cell sedimentation rate increased SARS-CoV-2 antibody test positive Troponin normal White blood cell count increased

Symptomtext

She is a 14 yo girl who has been seeing Cardiology for chronic idiopathic pericarditis, referred to ID to investigate potential causes, including if there might be a link to the COVID vaccine that she received. The infectious disease testing was overall unremarkable, except that her COVID IgG was negative (sent because she had a history of presumed COVID), and a sendout for COVID Spike protein IgG was positive (likely showing response to the vaccine). timeline of events: July 2020 ? patient with presumed COVID-19, symptomatic with a viral illness and multiple family members with similar symptoms tested + for COVID-19 September 2020 ? began experiencing intermittent episodes of chest pain ? seen by PCP only at several visits with normal EKG (9/9/2020, 1/27/21), estimated 5-6 episodes total 5/15/21 ? 1st dose of Pfizer COVID-19 vaccine Week of 5/25/21 ? started to have more significant symptoms of chest pain that lasted for longer than previously, seen by PCP 6/3/21, 6/14/21, 6/17/21 and started on naproxen 6/5/21 ? 2nd dose of Pfizer COVID-19 vaccine 6/21/21 ? first seen by Cardiology, had elevated inflammatory markers and trivial pericardial effusion, diagnosed with likely recurrent pericarditis 6/22/21 ? seen by Rheum, added colchicine 7/13/21 ? f/u with Cards, symptoms improved, echo normal 8/23 ? f/u with Cards, symptoms resolved, normalized inflammatory markers, stopped naproxen 8/31 ? f/u with Rheum, symptoms remain resolved 9/9 ? cardiac MRI done, some delayed enhancement noted in the pericardium but no thickening or effusion 9/17/21 ? seen by ID, symptoms remain resolved

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Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Labs 9-17-21: COVID IgG negative, COVID IgG spike >100 Labs 8-16-21: ESR 5, Crp 0.5, WBC 6.7, plt 340 Labs 7-9-21: ESR 50, Crp 56, WBC 10.5, plt 444 Labs from 06/22/21: ESR 104, Crp 113, WBC 9.8, plt 523, BNP 102, Labs from 06/17/21: CRP: 160.7, WBC: 20.8, plt 519, ANC 18k, ALC 1050 Labs from 06/14/21: ESR 18, Crp 90, CBC WBC 7.4, plt 559, Troponin: normal at less than 0.01
Aktuelle Erkrankungen: recurrent chest pain
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1760292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

schwer

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 15.05.2021
Beginn: 10.08.2021
Tage bis Beginn: 87,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Cardiac disorder Catheterisation cardiac Condition aggravated Fatigue Impaired driving ability Impaired work ability Magnetic resonance imaging head Malaise Pericarditis

Symptomtext

Pericarditis, heart problems that I?m still being treated for. Fatigue, ill, can?t function to drive or work

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 15,0
Labordaten: Every test from brain Mri to heart cath. Spent 15 days total in hospital and still living with effects to the point I can?t drive or work. Was very healthy til now, tests from August 10, 2021 to present date of October 4, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: Pericarditis, heart problems that are not yet resolved. Fatigue, low blood pressure and fibrillation. Suddenly cannot do daily functions. Can?t drive or work due to padding out and dizziness.
Andere Medikamente: Pantaprazole 40 mg oxycodone 5 mg
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1759175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 65,0
Geschlecht: M
Eingang: 04.10.2021
Impfdatum: 04.09.2021
Beginn: 18.09.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Blood urine present Catheter placement Cystoscopy abnormal Irrigation therapy Pyrexia Thrombosis

Symptomtext

That Saturday the 18th, I started urinating blood. I did not think much of it at first and then it continued to get worse I was afraid I would bleed out. I went to the Clinic, I was admitted and they immediately catheterized me and irrigated me for days and Wednesday they operated on me It was called a cystoscopy an evacuation of clots. After I was home with a catheter I developed a high fever that would come and go.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 5,0
Labordaten: Blood Panel
Aktuelle Erkrankungen: -
Vorgeschichte: High Blood pressure, slow urination,
Andere Medikamente: nifedipine ER, Flomax
Allergien: -
Vorherige Impfungen: -

VAERS 1750113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 07.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Dyspnoea Fatigue Injection site pain Malaise Nausea Pain Syncope

Symptomtext

Deep fatigue, body aches, dizzy spells, shortness of breath lasting for 3-4 months. Arm pain at injection site was intermittent and lasted for several months. The dizzy spells were severe and were most acute within one month of the second dose; at one point I fainted. Nausea after the first several weeks of taking the second dose. I still don't feel as well as I felt before the vaccinations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Low thyroid.
Andere Medikamente: T3/T4 compounded thyroid medication
Allergien: Allergy to dairy and fragrances.
Vorherige Impfungen: -

VAERS 1696482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: SC
Alter: 22,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Angiogram normal Laboratory test normal Magnetic resonance imaging head normal Seizure Angiogram Chest X-ray Chills Computerised tomogram head Computerised tomogram spine Dizziness Full blood count Injection site induration Injection site pain Injection site swelling Injection site warmth Magnetic resonance imaging head Migraine Nausea

Symptomtext

Migraine, drowsiness, light headed Injection arm hot - stiff-hard and bump. Chills Nausea Stinging feeling from injection area up to neck

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 1,0
Labordaten: CBC - 09/12/21 Urine test 09/11/21 Cat Scan - CT Cervical Spine w/o IV cont - 09/11/21 Cat Scan - CT Head w/o IV Cont - 09/11/21 Chest X-Ray 09/11/21 MRI BrainWO/W Cont inc MRA - 09/12/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis in back
Andere Medikamente: Women's daily multiviatamin
Allergien: Egg allergy as a child
Vorherige Impfungen: -

VAERS 1696482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: SC
Alter: 22,0
Geschlecht: F
Eingang: 21.09.2021
Impfdatum: 10.09.2021
Beginn: 10.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Angiogram normal Laboratory test normal Magnetic resonance imaging head normal Seizure Angiogram Chest X-ray Chills Computerised tomogram head Computerised tomogram spine Dizziness Full blood count Injection site induration Injection site pain Injection site swelling Injection site warmth Magnetic resonance imaging head Migraine Nausea

Symptomtext

Migraine, drowsiness, light headed Injection arm hot - stiff-hard and bump. Chills Nausea Stinging feeling from injection area up to neck

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 1,0
Labordaten: CBC - 09/12/21 Urine test 09/11/21 Cat Scan - CT Cervical Spine w/o IV cont - 09/11/21 Cat Scan - CT Head w/o IV Cont - 09/11/21 Chest X-Ray 09/11/21 MRI BrainWO/W Cont inc MRA - 09/12/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis in back
Andere Medikamente: Women's daily multiviatamin
Allergien: Egg allergy as a child
Vorherige Impfungen: -

VAERS 1317064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 47,0
Geschlecht: F
Eingang: 19.09.2021
Impfdatum: 12.05.2021
Beginn: 10.09.2021
Tage bis Beginn: 121,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest X-ray Dizziness Dyspnoea Rash Chest discomfort Computerised tomogram head Feeling abnormal Headache Nausea Seizure Syncope Tremor

Symptomtext

Nausea, chest pressure, headache/fuzzy brain, convulsions at 9am at home at 11am in family doctor's office. Nurse and doctor called 911, taken to ER by ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Head CT scan
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: probiotics
Allergien: none
Vorherige Impfungen: Same symptoms and ER visit reported to VAERS on May 14,2021.

VAERS 1704763

MERCK & CO. INC. · EBOLA ZAIRE (ERVEBO) · Charge EW0169

schwer

Staat: WA
Alter: 42,0
Geschlecht: F
Eingang: 16.09.2021
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

Anaphylactic reaction Dyspnoea Hot flush Throat tightness

Symptomtext

13 minutes after shot hot flush over body, Then anyphalactic reaction: throat closing, difficulty breathing. Benadryl as treatment. x 2. Symptoms lasted until next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: -
Allergien: Ceclor Morphine
Vorherige Impfungen: -

VAERS 1694566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OK
Alter: 59,0
Geschlecht: F
Eingang: 13.09.2021
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Facial paralysis Fatigue Hyperhidrosis Muscle spasms Pain

Symptomtext

initially I had generalized body aches, sweats and fatigue. Last week it progressed to muscle spasms in my feet, legs, hands and arms with some facial dropping. Over the past weekend I started having muscle spasms in my back in addition to the other things already mentioned

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: none -- I was instructed to hydrate, rest and take ibuprofen. I already had flexeril prn as a sleep aid so I have been taking those twice daily for past 4 days. I was instructed to go to the ER for any new muscle weakness.
Aktuelle Erkrankungen: Diabetes, Thyroid, high cholesterol, low Vitamin D
Vorgeschichte: Diabetes, Thyroid, high cholesterol, low Vitamin D
Andere Medikamente: Trulicity 1.5 mg/ 0.5 ml SQ weekly, Cyclobenzaprine 10 mg prn nightly sleep, Levothyroxin 75 mg daily, Atorvastatin 20 mg at bedtime, Glimepiride 2 mg daily, Xigduo XR 5-1000mg daily, Vitamn D 5000 units weekly
Allergien: Morphine, Codeine
Vorherige Impfungen: -

VAERS 1674139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 22.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Amnesia Body temperature Insomnia Loss of consciousness Malaise Pyrexia Scratch Speech disorder Vomiting

Symptomtext

I actually blacked out./But the blackout was scary; trouble sleeping; fevered; sick feeling; don't remember much from Friday morning at all; threw up the tylenol; scratches; could not form coherent sentences; This is a spontaneous report from a contactable consumer (patient). This 33-year-old non-pregnant female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Right on 22Apr2021 16:15 (Batch/Lot Number: EW0169) as DOSE 2, SINGLE (at the age of 33 years) for covid-19 immunisation. Historical vaccine included BNT162B2 for Covid-19 immunization as DOSE 1 SINGLE (at the age of 33 years) on 01Apr2021 16:30 in the right arm Brand: Pfizer Lot number: ER8732 and experienced insomnia. The patient had no other vaccine other than BNT162B2 in four weeks. The patient medical history was not reported. The patient reported she did not have any known allergies. The patient did not have Covid prior vaccination. Concomitant medications included topiramate (TOPAMAX) taken for an unspecified indication, start and stop date were not reported; paroxetine hydrochloride (PAXIL [PAROXETINE HYDROCHLORIDE]) taken for an unspecified indication, start and stop date were not reported. The patient experienced "I actually blacked out./but the blackout was scary " on 23Apr2021 04:00 with outcome of recovered, trouble sleeping on 23Apr2021 04:00 with outcome of recovered , got up at 4am running a fever on 23Apr2021 04:00 with outcome of recovered, sick feeling on 23Apr2021 04:00 with outcome of recovered, threw up the Tylenol on 23Apr2021 with outcome of recovered, scratches on 23Apr2021 with outcome of recovered, could not form coherent sentences on 23Apr2021 with outcome of recovered, "don't remember much from Friday morning at all" on 23Apr2021 with outcome of recovered, "The next thing I remember is my dog waking me up by licking my face about 20 mins later. I was laying face down in the hallway between the bathroom and the bedroom. Other than some scratches, I didn't get hurt. I also could not form coherent sentences while trying to call my husband to tell him to come home from work. I don't remember much from Friday morning at all. It is all a fog. But the blackout was scary. I was fevered and sick feeling for 24 hours and then was fine again." The patient underwent lab tests and procedures which included body temperature: fever on 23Apr2021. Therapeutic measures were taken as a result of fevered (Tylenol). Fever and sick feeling resolved on 24Apr2021. All other events recovered in 2021. The patient did not have a Covid test-post-vaccination. No follow-up attempts are required. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021458876 same reporter/patient, different vaccine dose and event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210423; Test Name: body temperature; Result Unstructured Data: Test Result:fever
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: TOPAMAX; PAXIL [PAROXETINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 1667116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CT
Alter: 20,0
Geschlecht: M
Eingang: 02.09.2021
Impfdatum: 13.05.2021
Beginn: 26.08.2021
Tage bis Beginn: 105,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Blood creatine phosphokinase MB Blood creatine phosphokinase increased Cardiac dysfunction Conduction disorder Echocardiogram abnormal Ejection fraction decreased Electrocardiogram abnormal Headache Immunoglobulin therapy Inflammatory marker increased Myocarditis N-terminal prohormone brain natriuretic peptide increased Pain Troponin I increased

Symptomtext

Patient was admitted for myocarditis on 8/29/21 with diffuse ST changes on EKG and elevated inflammatory markers. It is unclear if this event was related to vaccination as it was several months removed from the second shot it the series. there was significant heart dysfunction on echo with EF of 38%. Heart function quickly recovered to normal EF of 63% 3 days later after having support with milrinone and enalapril. Patient also received IVIG. the quick improvement of function fits more with vaccine related myocarditis as opposed to viral myocarditis. Infectious workup negative to date. Possible viral trigger with symptoms of headache and body aches for 3 days before presentation. Unclear at this time whether vaccine related or from an unknown viral etiology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 5,0
Labordaten: EKG significant for ST elevations, mild interventricular conduction delay, and PR depressions. Maximum lab values as follows: Troponin I 20/98, CK 1,258, CK-MB, 79.5, pro-BNP 655. Echo demonstrating reduced function with EF of 38%.
Aktuelle Erkrankungen: unknown
Vorgeschichte: history of Kikuchi Disease. Obesity
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1666425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 12,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 02.09.2021
Beginn: 02.09.2021
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 Nausea

Symptomtext

Pt became light headed, felt nauseas, and began to passout. PT Doctor entered room and provided care. Pt provided juice and recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1658792

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

schwer

Staat: -
Alter: 51,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Chills Dizziness Flushing Heart rate increased Hyperhidrosis Hypertension Loss of consciousness Nausea Paraesthesia oral

Symptomtext

During monitoring period post Pfizer COVID-19 vaccine, pt experienced hypertension, flushing, dizziness, lightheadedness, faint feeling, chills, nausea, rapid heart rate. VS: 155/98, P 101, R 25, O2 98%. Upon assessment, patient oriented x 4, states she was "blacking out" sweating profusely. Stated some tingling of bottom lip. Patient initially refused emergency medication after about 10 minutes agreed to IM Benadryl 25mg x 1. Patient remained in extended Observation for an hour and a half. Ice applied, water, blanket. Notified family members via phone that she had a reaction but began to feel better after an hour and 30 minutes. Patient discharged to home. VS: 125/71, P 59, R 19, O2 100%

Weitere VAERSDATA-Felder

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

VAERS 1624215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MS
Alter: 46,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 28.07.2021
Beginn: 28.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Syncope Tachycardia

Symptomtext

Fainted after shot, returned 8/20/21 and made us aware he has had unspecified persistent tachycardia (>100 bpm) since receiving shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1912456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 14,0
Geschlecht: F
Eingang: 19.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood pressure decreased Headache Heart rate decreased Nausea Pallor Poor peripheral circulation Presyncope Tremor

Symptomtext

Patient is a 14 year old female brought in by mother for COVID Vaccination, dose # 1 of the Pfizer BioNTech vaccine under emergency use authorization. Screening Prior to Vaccination: Is there a current illness or fever? No Has the patient ever had a severe (anaphylactic) reaction to any trigger? No Has the patient had a severe (anaphylactic) reaction to any vaccine or vaccine component? No Has the patient ever had myocarditis? no Does the patient have a bleeding disorder or use a blood thinner? no Is the patient immunocompromised? no For Females: Is the patient pregnant, planning to become pregnant or breast feeding? No Has the patient ever fainted from a vaccination? no Has the patient received a COVID vaccination before? No Patient Assessment Patient's temperature is 97.5 degrees, taken by contactless forehead method. Consent Verbal informed consent was obtained by parent. . Monitoring and Discharge Patient was monitored for 15 minutes following vaccination. There were any reactions. The patient was noted to have nausea and pallor 10 minutes after vaccine administration.. The patient required brief rest in supine position and epinephrine. Additional details about the reaction: see below. Patient received her first dose of the covid vaccine around 2:15pm. Approximately 5-10 minutes later, patient's mother alerted the nurse that patient was experiencing nausea. Nurse followed mother to the bathroom where patient was kneeling on the floor in front of the toilet. Patient was extremely pale, shaky, and complaining of nausea. Nurse brought patient water, a chair to sit in, and took her pulse and oxygen level with pulse oximeter machine. Pulse ox was in 97-99% range, and heart rate was in the upper 90s. Due to the patient's ill appearance, nurse went to get a BP cuff and alerted physician of the situation as she was getting one. Physician arrived in the bathroom. Nurse took BP- 110/72 at this time. Physician did a physical exam of patient and instructed nurse to have patient lie down with feet elevated and monitor her. Nurse took patient back to the exam room, laid her in supine position, elevated feet with a pillow, and left the room for approximately another 4-5 minutes. Mother again alerted nurse that pulse oximeter machine was beeping, and nurse returned to room. Patient was still complaining of nausea and appeared very pale. Patients pulse was in the 50s and low 60s, and her pulse ox was holding stead at 97-99% range. Nurse took a manual heart rate with stethoscope to verify accuracy of pulse oximeter machine- 60bpm. Nurse took BP again- 92/62. Nurse alerted physician. Physician came to exam room, examined patient. Patient was still complaining of severe nausea. Patient was still extremely pale. Physician BP- 98/58. HR still in 50s and 60s. Decision was made by physician to give 0.3mg of epinephrine to patient and call 911. Nurse alerted front office staff to call 911. Nurse drew up 0.3mg of epi, dose was verified by physician and second nurse. Nurse administered 0.3mg of epi to patient at 2:49pm. Ambulance arrived approximately 5 minutes later. Ambulance team took over monitoring patient vitals. Ambulance team advised mom that if she went to the hospital she would just have to wait and then be sent home. Mom requested to speak with physician, who advised mom that patient needed to go to the hospital for monitoring. After physician left the room, ambulance team member told mom that she had worked at the hospital, and she knew that the care patient would receive at the hospital would not be different than the care elsewhere. Nurse communicated with mom that physician recommended patient be taken via ambulance to be seen at the hospital as she had a serious allergic reaction to the COVID vaccine, and she needs to be under observation. Discussed option to be monitored at hospitals' urgent care versus ER to save on cost. Mom was concerned about the cost of an expensive ambulance ride, and she ultimately opted to drive to an alternate hospital (across the street from the office) against the advice of the physician and nurse. Nurse advised mom that she needed to drive immediately to the alternate hospital. Instructed mom that if patient deteriorated in the car to call 911 immediately. Mom agreed. At the time of patient leaving, she was still complaining of nausea. She was no complaining of headache as well. Color had improved. Blood pressure was up, 110s over 70s. Heart rate was still in 60s. Immediately after patient left nurse notified physician of mom's decision to drive to alternate hospital. Note: Epinephrine Lot #: 27670 Epinephrine Expiration Date: 09/2022 Administered in left vastus lateralis muscle - Nurse --- Agree with above. Initially, felt reaction was likely vasovagal response to vaccine (although had not occurred for her with prior vaccines/bloodwork). No wheezing, difficulty breathing, cough, or rash. Timing seemed prolonged for a vasovagal event and was worsening over 30 minutes of monitoring. Due decreasing BP, decreasing HR (although lower than her norm based on prior vitals- not tachycardic), poor perfusion, pallor, headache, and persistent nausea- even after laying down with feet elevated, drinking water, resting, and monitoring, decided to give epi for possible allergic reaction and send to the ER for monitoring. Per mom, patient was monitored at a hospital. ER doctor felt most likely a vasovagal response rather than anaphylactic reaction. She is doing better. Physician Assessment Need for vaccination Plan Orders COVID-19 ? 8/12/2021 Admin COVID dose 1 ? 8/12/2021 Instructions Pfizer BioNTech fact sheet given and reviewed. Side effects listed on the fact sheet include allergic reactions (severe and non severe), myocarditis, pericarditis, injection site pain and/or swelling, fatigue, fever, chills, muscle pain, headache. Signs of myocarditis for which to call include chest pain, palpitations or fluttering or pounding heart, shortness of breath. Call or seek emergency care if these signs occur.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1587110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: AL
Alter: 18,0
Geschlecht: M
Eingang: 19.08.2021
Impfdatum: 17.08.2021
Beginn: 17.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Pyrexia Seizure Syncope Vomiting

Symptomtext

Approximately 12 hours after injection, Pt spiked a high fever, chills and vomiting. By 9:00am he collapsed and had two seizures. He was administered Tylenol and Ibuprofen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1583171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 14.08.2021
Beginn: 14.08.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Refusal of examination Syncope

Symptomtext

Syncope after dose 1, assisted to stretch, allowed to rest, patient's father refused further evaluation

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1513430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MT
Alter: 15,0
Geschlecht: F
Eingang: 18.08.2021
Impfdatum: 23.06.2021
Beginn: 21.07.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Activated partial thromboplastin time prolonged Anticoagulant therapy Axillary vein thrombosis Basophil count Blood creatinine normal Blood electrolytes normal Blood fibrinogen decreased Blood glucose normal Blood lactic acid normal Blood magnesium normal Blood urea nitrogen/creatinine ratio Blood urea normal Brachiocephalic vein thrombosis Discomfort Erythema Full blood count normal Haematocrit normal Haemoglobin normal

Symptomtext

COVID in 04/2021 and received 2 doses of COVID vaccine, completing her course towards the end of June. COVID-19, mRNA, LNP-S, PF, 30 mcg/0.3 mL dose (COVID-19 VACCINE (PFIZER)) 6/23/2021, 6/3/2021 7/21/2021 Right arm axillosubclavian thrombosis 8/17/2021 Admitted for procedure INFRA CLAVICULAR FIRST RIB RESECTION AND RIGHT UPPER EXTREMITY VENOGRAM, Balloon angioplasty of subclavian vein (Right)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1574114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 24,0
Geschlecht: F
Eingang: 16.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Asthenia Fatigue Headache Heavy menstrual bleeding Hyperhidrosis Malaise Nausea Presyncope Thrombosis Tremor Vision blurred

Symptomtext

On the day of vaccination, I had a heavy menstrual cycle with extremely painful abdominal cramps. around 6:00 PM I noticed large blood clots with white tissue after wiping my perineal area. Today is day 5 after vaccination and I am still having a heavy menstrual cycle. On day 2 following vaccination, I woke up with the same excruciating headache. Upon getting out of bed I suddenly felt very weak and nauseous. About 2 minutes later I experienced blurry vision, extreme diaphoresis, and my entire body was shaking. I believed I was going to faint so I sat down on the floor. My symptoms did not reside for 30 minutes. From around 6:00 PM after Vaccination to today (day 5 after vaccination) I have has a persistent headache and I am still experiencing fatigue and malaise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control
Allergien: NKA
Vorherige Impfungen: -

VAERS 1569263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 15,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 15.07.2021
Beginn: 02.08.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Facial paralysis

Symptomtext

Pt. developed partial facial paralysis on her left side, around 1-2 weeks after her first COVID-19 vaccine injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1562832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 15.08.2021
Impfdatum: 24.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Colitis ischaemic Colon adenoma Colonoscopy abnormal Constipation Dehydration Diarrhoea Dizziness Endoscopy abnormal Fatigue Gastritis Gastrointestinal disorder Haemorrhoids Large intestinal ulcer Nausea Oesophagitis Presyncope Sick relative

Symptomtext

The day after I got my 2nd shot, I felt really sick. I was dizzy, nauseous, extremely fatigued to where I almost passed out a couple times. My biggest concern was the fatigue and my blood pressure tanking. It got down to 90/60. The issue is that for the months following I had really bad gastrointestinal issues. I was constipated at times, and had diarrhea at other times, going about 8-10 times before it even hit noon (my average before this was once a day or not at all). I was dehydrated from using the bathroom so much so I was dizzy nauseous, light-headed, and fatigued constantly. I had a lot of abdomen pain and soreness. All of these symptoms occured after I got my 2nd dose and have continued until this very day. I went to my primary doctor in May/June, but she believed that I was having too many unrelated symptoms and that it was probably something I was eating (since I do have a few food allergies). I basically wasn?t having it and I went to get a second opinion at a diagnostic gastrointestinal doctor. I got a colonoscopy and endoscopy from him back in July and it was concluded that I had an ulcer in my colon, among other things like a polyp (also in my colon), gastritis, esophagitis, and internal hemorrhoids. Now the only one that is really important to this story, however, is the ulcer. I was told by the doctor?s assistant in my follow up appointment that I also have ischemic colitis and that that was how my ulcer was most likely formed- just having a drop in blood pressure for an extended period of time, not getting enough blood flow to my colon, causing an ulcer. She told me the ulcer will heal as my blood pressure rises, but I?m my whole life I?ve always had lower than average blood pressure so it can?t get high enough and I?m in a bit of a pickle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Colonoscopy and endoscopy: July 2, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: Trazodone, abilify, lexapro, birth control
Allergien: Eggs, wheat, dairy, grass
Vorherige Impfungen: -

VAERS 1558292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 12,0
Geschlecht: M
Eingang: 14.08.2021
Impfdatum: 14.08.2021
Beginn: 14.08.2021
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 Malaise Pallor Seizure

Symptomtext

Less than 5 minutes after receiving the Pfizer Covid 19 vaccine, the patient slumped to the side hitting his head on the wall. He started to seize. His father moved him down to the ground. He came to and opened his eyes. His lips were pale and he said he didn't feel well. His father kept talking to him to keep him awake. The father stated he had seizures in the past. 911 was called and an EpiPen was given. Paramedics arrived. The patient was able to walk to the gurney. Paramedics took him away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: -

VAERS 1545553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: PA
Alter: 15,0
Geschlecht: F
Eingang: 11.08.2021
Impfdatum: 11.08.2021
Beginn: 11.08.2021
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

Symptomtext

passed out, clamy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: na/
Andere Medikamente: n/a
Allergien: cats, dogs, dust
Vorherige Impfungen: -

VAERS 1540467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CT
Alter: 33,0
Geschlecht: M
Eingang: 10.08.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort Angiogram cerebral normal Anxiety Arteriogram carotid normal Condition aggravated Electric shock sensation Full blood count normal Magnetic resonance imaging head normal Magnetic resonance imaging neck Mechanical urticaria Neuralgia Pruritus Sensory disturbance

Symptomtext

Patient had ongoing symptom described as 'bubbling' or 'fizzing' in back of head or as 'bubbles flowing up a corridor in the back of the head' for ~1 year prior to 1st vaccine dose . Symptom would only occur once every few days/weeks and would occur momentarily or for a few minutes of the day then dissipate. After receiving 1st vaccine dose, patient noticed symptom as they proceeded to waiting area but then it had gone away. About an hour later the symptom returned and persisted almost non stop. Symptom has since persisting and occurring daily but has changed and feels more like "electricity" or smaller bubbled/fluid/fizzing being forced or moved around in back of head and neck. It seems to occur more frequently simultaneously with stomach symptoms like stomach growling. Also causes 'impending doom' feeling. MRI and MRA of the head and neck were performed and were unremarkable. Patient was treated with Topamax for nerve pain and it did seem to help subdue symptom but did not resolve. Topamax was d/c because of itchiness of the skin and dermatographism. 5 weeks post after d/c of Topamax, itchiness/dermatographism are persisting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: MRI/MRA of Head and Neck - Unremarkable CBC - normal
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: Copaxone 40 MG, M,W,F Multivitamin Vitamin D
Allergien: -
Vorherige Impfungen: -

VAERS 1537161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: FL
Alter: 54,0
Geschlecht: M
Eingang: 09.08.2021
Impfdatum: 20.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Anticoagulant therapy Anxiety disorder Blood test Chest discomfort Computerised tomogram abnormal Dyspnoea Pulmonary thrombosis Thrombosis Ultrasound Doppler abnormal

Symptomtext

SHORTNESS OF BREATH AND TIGHTNESS OF CHEST. 1ST EMERGENCY ROOM VISIT PATIENT WAS SENT HOME DISAGNOSED WITH ANXIETY DISORDER. SOB AND TIGHTNESS CONTINUES DURING FOLLOWING WEEKS. PATIENT RETURNS FOR 2ND VISIT AT SAME EMERGENCY ROOM AT UNION HOSPITAL WITH SEVERE SHORTNESS OF BREATH. CAT SCAN OF LUNGS AND ULTRASOUND OF LEG REVEALLED MULTIPLE BLOOD CLOTS IN BOTH LUNGS AND BEHIND KNEE. PATIENT WAS ADMITTED TO HOSPITAL. PATIENT WAS PLACED ON IV BLOOD THINNERS DURING STAY. PATIENT WAS RELEASED ON ELIQUIS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 5,0
Labordaten: FIRST ER VISIT.....NO TESTS END ER VISIT....ULTRASOUND OF LEG, CAT SCAN OF LUNGS. BLOODWORK
Aktuelle Erkrankungen: ANXIETY; SARCOIDOSIS; KIDNEY DISEASE
Vorgeschichte: ANXIETY ; KIDNEY DISEASE
Andere Medikamente: NEXIUM 20MG; PAROXETINE 37.5MG; CHLORDIAZEPOXIDE/CLIDINIUM; PREDNISONE 20MG; SIMETHICONE
Allergien: PENICILLIN; VITAMIN D2
Vorherige Impfungen: -

VAERS 1528941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WY
Alter: 13,0
Geschlecht: M
Eingang: 05.08.2021
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Decreased appetite Feeling cold Muscle rigidity Nausea Pallor Syncope

Symptomtext

Patient was sitting in waiting chair for 15 min observation time while nurse was administering siblings vaccine. Mom looked at patient and stated he looked pale. Nurse got patient juice, sucker and ice pack. Patient leaned over in chair appeared he may vomit, then he sat straight up with hands clenched and was rigid, then leaned back over and had an episode of syncope. Patient came to almost immediately but did not remember what happened. Patient was nervous about needles and family has a history of syncope and needle fear with vaccines. Nurse and patients dad helped pt to lie on the floor per patient request, allowed pt to lie on floor with an ice pack and take small sips of juice until he felt like he could sit up, pt reports he felt hot. Allowed pt to sit up on floor for 5 mins, then assisted pt to chair. After 5-10 mins pt felt as though he could leave, pt reports he feels cold at this time. Nurse walked with pt and dad to their vehicle to make sure pt did not get dizzy and fall. I recommended that pt not be left alone; mom will stay home with him. I called and checked on pt (1000) and mom reports he stated "I feel pretty dang good." Mom reports pt still feels cold and doesn't have an appetite. Pt had not eaten prior to vaccine. Nurse educated that pt should eat prior to next vaccine and we will use an ice pack on is neck, provide juice and sucker prior and following injection.

Weitere VAERSDATA-Felder

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

VAERS 1528642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OK
Alter: 46,0
Geschlecht: F
Eingang: 05.08.2021
Impfdatum: 30.07.2021
Beginn: 01.08.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Dyspnoea Magnetic resonance imaging Pain in extremity Thrombosis Ultrasound Doppler abnormal

Symptomtext

Pt. states that after receiving the 1st dose Phizer 07/30/2021 (Noted 07/30/2021 MMR 1st dose received), started experiencing symptoms 08/01/2021 of pain throughout the right leg and shortness of breath. 08/02/2021 Primary visit and was determined to have a blood clot located in the PVT calf. Prescribed a blood thinner. (Previous history of DVT 13yrs). Recommendation to continue prescription with follow up to ER if continue or shortness of breath.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound 08/02/2021 MRI 08/02/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Adivan
Allergien: N/A
Vorherige Impfungen: -

VAERS 1520228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 17,0
Geschlecht: M
Eingang: 02.08.2021
Impfdatum: 02.08.2021
Beginn: 02.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Loss of consciousness Syncope

Symptomtext

Patient stood up after receiving vaccination and fainted into mother's arms. Patient regained consciousness after a few minutes. 911 was called. EMT arrived and took patient to hospital for evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1505361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 27.07.2021
Impfdatum: 19.04.2021
Beginn: 09.06.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram head normal Electrocardiogram normal Facial paralysis Headache Magnetic resonance imaging head normal Muscular weakness Neck pain Paraesthesia Scan with contrast normal

Symptomtext

Headache Neck Pain Subtle tingling in hands and feet Muscle weakness Facial Droop

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 1,0
Labordaten: 6/30/21 - CT Head Scan without contrast - No acute intracranial abnormality. 6/30/21 - CT Head Scan with contrast - No evidence of high-grade stenosis, occlusion, dissection, or aneurysm within the arteries of the head and neck. 6/30/21 - EKG - Normal. 7/1/21 - MRI Brain without contrast - No acute intracranial abnormality. 7/1/21 - MRI Brain with contrast - No evidence of intracranial hemorrhage or acute infarct.
Aktuelle Erkrankungen: -
Vorgeschichte: Bullous Pemphigoid Lichen Planus obstructive sleep apnea Iron deficiency anemia polycystic ovarian syndrome
Andere Medikamente: Yasmin Clobetasol Iron Calcium, Magnesium, Vitamin D
Allergien: Amoxicillin Sulfa Drugs Azathioprine Mycophenolate Doxycycline
Vorherige Impfungen: Flu vaccine caused Bullous Pemphigoid to flare. Vaccine given in October 2017, patient 40 years old. Don't know brand name.

VAERS 1502309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 14,0
Geschlecht: M
Eingang: 26.07.2021
Impfdatum: 11.06.2021
Beginn: 11.07.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Angiotensin converting enzyme Anti-ganglioside antibody negative Bacterial test negative Blood creatine phosphokinase increased Blood glucose decreased C-reactive protein increased CSF test abnormal Cytomegalovirus test negative Electromyogram abnormal Enterovirus test negative Epstein-Barr virus test negative Facial paresis Gait disturbance Guillain-Barre syndrome Immunoglobulin therapy Movement disorder Muscular weakness Nerve conduction studies abnormal

Symptomtext

Presented with bilateral facial weakness on 7/11. Prescribed 3 day course of steroids (7/14-7/16) without improvement. Presented again on 7/18 with worsening facial weakness in addition to bilateral upper and lower extremity weakness and difficulty walking. Admitted to hospital on 7/19. On the second day of his hospitalization he was no longer ambulatory. Diagnosed with likely AIDP based on CSF studies (albuminocytologic dissociation, negative infectious work-up). Treated with 3-day course of IVIG (7/21-7/23), after which he showed significant improvement in his upper/lower extremity and facial strength and ambulation. He is being discharged with ongoing outpatient physical therapy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 7,0
Labordaten: CK 535, ESR 35, CRP 12.6 EMG/NCS: evidence of a severe, generalized polyradiculoneuropathy most consistent with AIDP. R Tib motor n with prolonged latency. R ulnar m nerve with reduced amplitude with abs F-wave. Sensory responses normal. EMG with decr recruitment CSF studies: WBC 4, Protein 165, Glu 71, Enterovirus Neg, CMV Neg, VZV neg, EBV neg, Pending: ACE, Lyme Serum: EBV positive (likely false positive as it was obtained after IVIg was given), Lyme (negative), Ganglioside pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1502269

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 26.07.2021
Impfdatum: 15.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electric shock sensation Electromyogram Lymphadenopathy Mammogram Paraesthesia

Symptomtext

Swollen lymph nodes was found under the left armpit. And a tingling sensation in my lower back and fingers, like a shooting nerve feeling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Mammogram; EMG
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Yes
Allergien: Yes
Vorherige Impfungen: -

VAERS 1494109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 22.07.2021
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

Blood test normal Differential white blood cell count Dizziness Dyspnoea Electric shock sensation Electrocardiogram normal Exercise tolerance decreased Fatigue Full blood count Hyperhidrosis Loss of personal independence in daily activities Nausea Pain Pruritus Troponin

Symptomtext

As soon as I received the shot my arm felt like lightning went through it. I began having shortness of breath. I walked to get some water and started having more trouble breathing. I was sweating, I felt dizzy. The EMS came and took me to the hospital where I was for 4-5 hours. I was given Benadryl. I was going to get medicine for nausea, but I felt better and was afraid to take anything because of the reaction. I was very lightheaded, dizzy and nauseous. At the hospital, I was observed. I was getting better but I was still itchy. The Doctor was going to prescribe some prednisone but wanted to hold off on any medication to allow the vaccine to do its job. I was given a prednisone pack and a Benadryl pack. I felt better so I didn't take the prednisone. I was told to continue taking Benadryl and if that did not help, I was to take prednisone. Currently, I still experience extreme achiness and fatigue. This is something I have never experienced before. I am on medication for the achiness that my doctor believes to be arthritis but it is not helping. I was able to run 3 miles a day but now I am unable to even walk it. It is difficult getting up and down stairs which the medication has helped with some.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Blood work: normal; EKG: normal; CBC differential; Troponin: negative
Aktuelle Erkrankungen: Yes
Vorgeschichte: Thyroid issue, muscle aches
Andere Medikamente: Euthyrox
Allergien: Yes
Vorherige Impfungen: -

VAERS 1487228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: KS
Alter: 17,0
Geschlecht: F
Eingang: 20.07.2021
Impfdatum: 14.05.2021
Beginn: 15.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

The morning of the day after of getting the second Covid shot my daughter fainted. (Same thing happened to my other daughter) neither daughter has ever fainted before and neither daughter has anxiety from shots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1471066

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge Ew0169

schwer

Staat: AZ
Alter: 18,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 21.04.2021
Beginn: 12.05.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram Dizziness Electroencephalogram Magnetic resonance imaging Nausea Seizure Tremor

Symptomtext

Nausea dizzy tremors seizurez

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 3,0
Labordaten: Ctscan Mri Eeg Two hospitals, tital 6 days in hodoutal
Aktuelle Erkrankungen: No
Vorgeschichte: Heart and Sydenhams Chorea
Andere Medikamente: Prozac and lamitcal and pencillan
Allergien: Late
Vorherige Impfungen: -

VAERS 1470251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 42,0
Geschlecht: F
Eingang: 14.07.2021
Impfdatum: 06.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Activated partial thromboplastin time Differential white blood cell count Dizziness Electrocardiogram Full blood count Hypotension Lipase Loss of consciousness Metabolic function test Prothrombin time Unresponsive to stimuli

Symptomtext

dizziness, loss of consciousness, several minutes unable to regain consciousness, blood pressure remained low, after trip to ER required two bags of liquids to bring blood pressure up to a safe level for discharge

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ECG, ECG 12-LEAD, LIPASE, COMPREHENSIVE METABOLIC PANEL, COMPLETE BLOOD COUNT WITH DIFFERENTIAL, ACTIVATED PARTIAL THROMBOPLASTIN TIME, PROTHROMBIN TIME , all completed on 5/7/2021
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: amoxicillin
Vorherige Impfungen: -

VAERS 2612818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 13.07.2021
Impfdatum: 23.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein

Aphasia Asthenia Autonomic nervous system imbalance Chest discomfort Chest pain Computerised tomogram head Conversion disorder Dysarthria Echocardiogram Electrocardiogram Electrocardiogram ambulatory Electroencephalogram Head discomfort Heart rate increased Hypoaesthesia Immunisation reaction Laboratory test Magnetic resonance imaging head

Symptomtext

Fainting, rapid heart rate, pressure in head, seizures (non epileptic), chest pain and pressure, loss of speech and slurring speech, paralysis, weakness, numbness, tingling. I already called in the first time she was hospitalized and my report # is 543719. Hospitalized 5/22/21 thru 5/26/2021 and on 6/20/21 thru 6/22/21 with multiple Emergency Room visits in between hospital stays Diagnosed with Functional Neurological Disorder and Dysautonomia - POTS (Postural Orthostatic Tachycardia Syndrome which the doctor did say that the vaccine caused. She was a healthy 17 yr ols before she got the vaccine. She is treated with Propranolol 20 mg 2 times a day and takes 430 mg of Salt Caps 3 times a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: -
Labordaten: MRI of the brain,EEG, ECHO, EKG, multiple lab work, CT of head, holter monitor done during hospital stay
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety, Depression
Andere Medikamente: Guanfacine 3 mg extended tabs PO every day, Sertraline 200 mg
Allergien: Amoxicillin, Penicillins
Vorherige Impfungen: -

VAERS 1295866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

schwer

Staat: PA
Alter: 52,0
Geschlecht: M
Eingang: 01.07.2021
Impfdatum: 20.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Anticoagulant therapy Blood test abnormal Computerised tomogram abnormal Erythema Peripheral swelling Thrombectomy Thrombosis Ultrasound Doppler abnormal

Symptomtext

3 days after vaccine pt woke up to swollen arm . Blood clot had developed in left arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: Went to ER and was transfered to hospital . kepted on blood thinners until Monday the 24th. Surgery was done to remove blood clot. on the 25th another clot was found surgery was performed . Discharged- on 26th .
Aktuelle Erkrankungen: no
Vorgeschichte: heart condition, high blood pressure and high cholesterol
Andere Medikamente: Prestation, Proplanalon, Verapamil, asprin
Allergien: Penicillin , blueberry, Benadryl Toradol,
Vorherige Impfungen: -

VAERS 1431562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CT
Alter: 43,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure increased Blood test Cardiac monitoring Cardiac stress test Cardiac valve disease Chest pain Dizziness Echocardiogram Electrocardiogram Fatigue Heart rate increased Impaired work ability Loss of consciousness Palpitations Pyrexia Seizure Skin discolouration Ventricular extrasystoles

Symptomtext

The day of the vaccine I felt really tired after a few hours. I normally have low grade fevers so I was not concerned with that. During the night I woke up and I passed out and had some symptoms of seizure when I got up. I am still experiencing symptoms and it has been twelve weeks and my heart rate is high. I continued having a high fever for two weeks, it was running at 102-103 degrees instead of my normal low grade fever at times 99-100 degrees. My heart rate was also very high exaggerated heart rate since getting the vaccine Even if I do normal activity I feel palpitations and my heart rate is elevated. My blood Pressure had been elevated and I have been experiencing dizziness. Some tests are showing leaky valves and PVCs. I have experienced chest pain which is recently resolved. I feel tired and dizzy. At one time the backs of my hands turned blue for a few days. I was unable to work for the first month after the second dose of the vaccine. I have been working but I am still very tired and I have used all of my time off. I have seen a Cardiologist, Neurologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Stress Test Heart Echo EKG, Heart Monitor Blood Work
Aktuelle Erkrankungen: -
Vorgeschichte: Poly Cystic Ovary Syndrome Asthma, Post Concussion Syndrome Migraines Von Willebrand's Disease Arthritis, Double String and ANA Positive
Andere Medikamente: Nortriptyline 10mg Seroquel 25mg Yazmin Advair inhaler Epipen PRN Claritin 20mg 2 times daily Vitamin C, Vitamin B12 Complex, Calcium with D
Allergien: Lactose Intolerance Seasonal Allergy Cats Mosquito Bites
Vorherige Impfungen: Multiple as an infant

VAERS 1321723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 25.06.2021
Impfdatum: 18.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood test Computerised tomogram Electrocardiogram Electromyogram Gait disturbance Electromyogram abnormal Guillain-Barre syndrome Hypoaesthesia Immunoglobulin therapy Intensive care Headache Magnetic resonance imaging Paraesthesia Mechanical ventilation Muscular weakness Sinus pain Sinusitis

Symptomtext

Pt started with headaches sinus pain. Was treated at her family doctor for a sinus infection. These symptoms did not go away and on 5/7/2021 she started getting tingling and numbness in her hands and feet. On 5/8/2021 she was taken to the Hospital and blood work and MRI was taken but did not see anything. She was told to follow up with her family physician on Monday 5/10/2021. She got worse in the evening and had trouble walking. She was taken to another hospital at 4:00 A M on 5/9/2021. On 5/9/2021 the neurologist thought she may have a chemical imbalance. After getting and MRI, blood work and and EMG on 5/10/2021 she was diagnosed with Gillian Barre syndrome and treatments

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 47,0
Labordaten: MRI, EKG, Blood work, EMG , Cat Scan 5/10/21
Aktuelle Erkrankungen: None
Vorgeschichte: Diverticulitis
Andere Medikamente: Atorvastatin, Amoxicillin, Triamterene
Allergien: None
Vorherige Impfungen: -

VAERS 1417111

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 29,0
Geschlecht: M
Eingang: 22.06.2021
Impfdatum: 22.06.2021
Beginn: 22.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Hallucination Hyperhidrosis Loss of consciousness Musculoskeletal stiffness Nausea Pallor Paraesthesia Vomiting

Symptomtext

Pt getting shot felt tingling 30 seconds after then nausea and lightheaded. He got stiff, gasped and passed out. Per pt, he had a "hallucination". Pt experienced LOC for approx 5 seconds, he "took a deep snort" and came back. Pt pale and diaphoretic, vomited and moved to med obs 1. VSS. Resolution of symptoms within 20 minutes, and released.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1410135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 36,0
Geschlecht: M
Eingang: 18.06.2021
Impfdatum: 29.04.2021
Beginn: 14.06.2021
Tage bis Beginn: 46,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Myocarditis

Symptomtext

Myocarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1410018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

schwer

Staat: TX
Alter: 27,0
Geschlecht: M
Eingang: 18.06.2021
Impfdatum: 05.05.2021
Beginn: 15.06.2021
Tage bis Beginn: 41,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bell's palsy Facial paralysis Swelling face

Symptomtext

Bell?s Palsy Paralysis and swelling on the left side of the face Prednisone for treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine Lisinopril Atomoxetine Zolpidem ER Hydrochlorothiazide Lorazepam
Allergien: None
Vorherige Impfungen: -

VAERS 1392109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: SC
Alter: 16,0
Geschlecht: M
Eingang: 11.06.2021
Impfdatum: 03.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Brain natriuretic peptide Cardiac dysfunction Chest pain Myocarditis SARS-CoV-2 antibody test Troponin increased

Symptomtext

Myocarditis (CP, elevated troponin, cardiac dysfunction). Steroid burst with normalization of function and improvement in troponins

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: Troponin, COV-2 IGG Panel (Disease), COV-2 IGG (Vaccine Immunity), BNP
Aktuelle Erkrankungen: Had COVID on 4/19/2021 with mild, brief cough
Vorgeschichte: None
Andere Medikamente: None
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1321541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 23.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Feeling abnormal Frustration tolerance decreased Pain Pain in extremity Ultrasound scan X-ray Pruritus Rash Thrombosis Vaccination site pain

Symptomtext

blood clot already eliminated; pain; This is really miserable because it persisting and it is always there; I feel like frustrated; light pink rashes in the back from knee above in both legs; both of my legs below the knees had really bad itches; mild pain in the back of the upper left leg; sharp pain at a spot in my left hip joint; Sore in the injection area; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 23Apr2021 15:30 (Batch/Lot Number: EW0169; Expiration Date: 31Aug2021) as 1ST DOSE, SINGLE DOSE for covid-19 immunisation, age at vaccination 62 years old. Patient is not pregnant at vaccination time. Medical history included diabetes mellitus from Sep2020 to and blood pressure (abnormal) from an unknown date. Concomitant medications included metformin taken for diabetes mellitus, start and stop date were not reported; dapagliflozin propanediol monohydrate (FARXIGA) taken for diabetes mellitus, start and stop date were not reported; levothyroxine (LEVOTHYROXINE) taken for an unspecified indication, start and stop date were not reported; lisinopril (LISINOPRIL) taken for blood pressure (abnormal), start and stop date were not reported. Clinical course was reported as follows: On 24Apr2021 noon (12:00), patient suddenly felt a shar at a spot in her left hip joint. It was then moved to the mild pain in the back of the upper left leg, which never disappeared. The pain there got a lot worse, so severe, also reported as now just a mild pain. Patient went to bed around 12 am on 25Apr2021, both legs below the knees had really bad itches; by next day 6 AM it was gone and never returned. On 26Apr2021, in late afternoon, in the back of both of the legs started bad it itches, and patient saw light pink rashes in the back from knee above in both legs, which disappeared by midnight, and never again noted. Sore in the injection area (Apr2021) similar to flu vaccine, which was gone after a few days. Patient stated adverse reaction getting worse and asked how it can be resolved because he can't function normally because of adverse effect. Patient stated that this is really miserable because it is persisting, and it is always there. He stated he is a normal person his breath, he still sees, still read, and is sound. He feels he is in constant pain, mild pain is annoying, but this week is so worse. Patient stated his "blood clot already eliminated" (onset date unspecified, event not clarified). Patient felt frustrated. Second dose was scheduled on 14May2021, but he didn't take it, he cancelled the second dose because of pain. Treatment was not given for the events (does not take medications). Outcome of the events "blood clot already eliminated" was recovered on an unspecified date, "both of my legs below the knees had really bad itches" was recovered on 26Apr2021, "light pink rashes in the back from knee above in both legs" and "Sore in the injection area" was recovered on Apr2021. Outcome of "sharp pain at a spot in left hip joint" and "mild pain in the back of the upper left leg" was not recovered (persisting for three weeks). Outcome of the other events was unknown. Seriousness reported as non-serious. Follow up needed, further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal (Verbatim: Blood pressure); Diabetes (Verbatim: Diabetes)
Andere Medikamente: METFORMIN; FARXIGA; LEVOTHYROXINE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1321541

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 10.06.2021
Impfdatum: 23.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Feeling abnormal Frustration tolerance decreased Pain Pain in extremity Ultrasound scan X-ray Pruritus Rash Thrombosis Vaccination site pain

Symptomtext

blood clot already eliminated; pain; This is really miserable because it persisting and it is always there; I feel like frustrated; light pink rashes in the back from knee above in both legs; both of my legs below the knees had really bad itches; mild pain in the back of the upper left leg; sharp pain at a spot in my left hip joint; Sore in the injection area; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 23Apr2021 15:30 (Batch/Lot Number: EW0169; Expiration Date: 31Aug2021) as 1ST DOSE, SINGLE DOSE for covid-19 immunisation, age at vaccination 62 years old. Patient is not pregnant at vaccination time. Medical history included diabetes mellitus from Sep2020 to and blood pressure (abnormal) from an unknown date. Concomitant medications included metformin taken for diabetes mellitus, start and stop date were not reported; dapagliflozin propanediol monohydrate (FARXIGA) taken for diabetes mellitus, start and stop date were not reported; levothyroxine (LEVOTHYROXINE) taken for an unspecified indication, start and stop date were not reported; lisinopril (LISINOPRIL) taken for blood pressure (abnormal), start and stop date were not reported. Clinical course was reported as follows: On 24Apr2021 noon (12:00), patient suddenly felt a shar at a spot in her left hip joint. It was then moved to the mild pain in the back of the upper left leg, which never disappeared. The pain there got a lot worse, so severe, also reported as now just a mild pain. Patient went to bed around 12 am on 25Apr2021, both legs below the knees had really bad itches; by next day 6 AM it was gone and never returned. On 26Apr2021, in late afternoon, in the back of both of the legs started bad it itches, and patient saw light pink rashes in the back from knee above in both legs, which disappeared by midnight, and never again noted. Sore in the injection area (Apr2021) similar to flu vaccine, which was gone after a few days. Patient stated adverse reaction getting worse and asked how it can be resolved because he can't function normally because of adverse effect. Patient stated that this is really miserable because it is persisting, and it is always there. He stated he is a normal person his breath, he still sees, still read, and is sound. He feels he is in constant pain, mild pain is annoying, but this week is so worse. Patient stated his "blood clot already eliminated" (onset date unspecified, event not clarified). Patient felt frustrated. Second dose was scheduled on 14May2021, but he didn't take it, he cancelled the second dose because of pain. Treatment was not given for the events (does not take medications). Outcome of the events "blood clot already eliminated" was recovered on an unspecified date, "both of my legs below the knees had really bad itches" was recovered on 26Apr2021, "light pink rashes in the back from knee above in both legs" and "Sore in the injection area" was recovered on Apr2021. Outcome of "sharp pain at a spot in left hip joint" and "mild pain in the back of the upper left leg" was not recovered (persisting for three weeks). Outcome of the other events was unknown. Seriousness reported as non-serious. Follow up needed, further information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal (Verbatim: Blood pressure); Diabetes (Verbatim: Diabetes)
Andere Medikamente: METFORMIN; FARXIGA; LEVOTHYROXINE; LISINOPRIL
Allergien: -
Vorherige Impfungen: -

VAERS 1300044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 10.06.2021
Impfdatum: 04.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Arteriogram coronary normal Blood test Chest X-ray normal Chest pain Computerised tomogram thorax normal Cardiac imaging procedure normal Echocardiogram normal Headache Myocarditis Electrocardiogram normal Laboratory test Troponin increased

Symptomtext

Adverse event: highly elevated triponin levels, chest pain (felt like a heart attack) Treatment: overnight hospital stay, various tests, ECG, bloodwork Outcome: Sent home next day after confirmation of no structural damage to heart; instructed to take ibuprofen to handle any pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: 5/7/21: Heart test review and report, Emergency services, Laboratory services, Chest x-ray, Ct scan of heart and arteries
Aktuelle Erkrankungen: None
Vorgeschichte: Scoliosis
Andere Medikamente: Tylenol Extra Strength (2 pills; for headache)
Allergien: lactose
Vorherige Impfungen: -

VAERS 1382523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 19,0
Geschlecht: M
Eingang: 08.06.2021
Impfdatum: 28.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Chest pain Echocardiogram normal Magnetic resonance imaging heart Myocarditis Troponin increased

Symptomtext

Patient presented with severe crushing chest pain and was found to have elevated troponin levels. He was diagnosed with myocarditis. Echo showed normal heart function. Cardiac MRI was also done and showed normal heart function with a faint scar suggestive of myocarditis. Overall, findings suggested post vaccine related myocarditis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Abnormal troponin- 2.82
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1381983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 14,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 08.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Presyncope Respiratory rate increased Tremor

Symptomtext

COVID-19 Post Vaccine #2 Vasovagal reaction. EMS notified due to patients history of anxiety and increase in RR, patient stated she feels "shaky". Patient stated she feels better with legs elevated. Patient lowered to the ground, legs elevated and moved to the litter. VS taken and EMS notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: History of Anxiety
Vorgeschichte: None
Andere Medikamente: Denied any medication use to include any OTC.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1378276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: KY
Alter: 57,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 04.05.2021
Beginn: 07.06.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Deep vein thrombosis

Symptomtext

1. Acute deep vein thrombosis (DVT) of tibial vein of left lower extremity (CMS/HCC) No history of any DVT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: asa
Vorherige Impfungen: -

VAERS 1377037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 07.06.2021
Impfdatum: 31.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Influenza like illness Lethargy Pain Seizure Tremor Vaccine positive rechallenge

Symptomtext

After first shot - felt severe flu-like symptoms. Very lethargic, no energy, boy ached ALL over. Lasted two days. After second shot, at 1 am, I woke up with EXTREME convulsions. Entire body was shaking all over, looked like I was being electrocuted. Conditioned worsened over next 30 minutes. I then asked my husband to hold me as tight as possible to stop the shaking. He did so and it took over 30 min. for the extreme convulsions to cease.I was not "hot nor cold", meaning no fever. The next two days I had the same symptoms as after the first vaccine - felt severe flu-like symptoms. Very lethargic, no energy, boy ached ALL over

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tamoxifen
Allergien: None
Vorherige Impfungen: -

VAERS 1376861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 06.06.2021
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: ja

Blood test normal Blood urine C-reactive protein increased Computerised tomogram pelvis Cystoscopy Fatigue Magnetic resonance imaging normal Pyrexia Thrombosis Urine analysis normal Urobilinogen urine X-ray normal

Symptomtext

Elevating fever, extreme fatigue, body aches- 9th day bleeding while urinating: 10th day- BLOOD CLOT while urinating 2nd vaccine - milder fever, less fatigue, fewer body aches. 5th day, blood in urine. End of side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: UTI - negative, urine tests, blood culture tests( negative) , inflammation tests ( high), X-ray of kidneys and bladder - negative 5.5.2021, MRI abdomen Pelvis UROGRAM ( negative) URO CYSTOCSOPY ( negative.
Aktuelle Erkrankungen: Autoimmunity
Vorgeschichte: Multiple autoimmune diseases, primary immune disease, asthma
Andere Medikamente: Klonepin, Gabepentin, Plaquenil, Estradiol, Flinstone vitamin, vit D, Calcium, Tylenol
Allergien: Aspirin, bees, clindamycin, diclofenac, Imuunoglobulin(IgG), Levaquin, Cipro, Avelox, propofol, Valcyclovir
Vorherige Impfungen: Flu vaccine - 2014

VAERS 1371386

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 03.06.2021
Impfdatum: 24.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 38,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Deep vein thrombosis Exposure during pregnancy Oedema peripheral Pain in extremity Peripheral vein occlusion Thrombosis Ultrasound Doppler abnormal

Symptomtext

30yof, 36w pregnant, came to clinic on 6/1 with 2 week history of lower leg tenderness and edema. Doppler confirmed on 6/1 that patient had an acute proximal DVT in the left lower extremity, with occlusive thrombus within the distal femoral vein. She denies personal history of clot; this is her 2nd pregnancy; she notes no family history of clot; this pregnancy is complicated by excessive weight gain (current BMI 32.28 kg/m2). Pt received Pfizer COVID vaccine on 4/24/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 2,0
Labordaten: Doppler confirmed
Aktuelle Erkrankungen: No others listed per H&P; excessive weight gain with this pregnancy.
Vorgeschichte: None per H&P
Andere Medikamente: Prenatal Vitamin daily
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1369331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 02.06.2021
Impfdatum: 12.05.2021
Beginn: 28.05.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Computerised tomogram Dyspnoea Pulmonary thrombosis Ultrasound Doppler

Symptomtext

Dose #1 received on 4/21/21. Dose #2 received on 5/12/21. Difficulty breathing beginning on 5/5/28/21. Diagnosed with multiple blood clots in right lung on 5/30/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: CT scan 5/30/21 Ultrasound of legs 5/30/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1368816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 15.05.2021
Beginn: 31.05.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy heart Cardiac failure acute Catheterisation cardiac abnormal Dyspnoea exertional Echocardiogram Echocardiogram abnormal Ejection fraction decreased Histiocytosis Myocarditis Necrosis Respiratory viral panel

Symptomtext

Myocarditis with histiocytic involvment on pathology. Presented with new onset acute heart failure with reduced ejection fraction of 15%. Had several days of dyspnea on exertion approximately 5 days prior to presentation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: 5/31: TTE with EF 15% 5/31: Complete Respiratory Virus panel negative 6/1: Right heart catheterization and endomyocardial biopsy with histiocytic involvement and necrosis.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1368422

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 03.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 26,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Electroencephalogram Loss of consciousness Seizure

Symptomtext

passing out episodes, seizures, hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: edg on brain
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety/depression
Andere Medikamente: sertraline 200mg, guanfacine er 3mg
Allergien: amoxicillin, penicillin
Vorherige Impfungen: -

VAERS 1368008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 63,0
Geschlecht: F
Eingang: 02.06.2021
Impfdatum: 17.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory distress syndrome Asthenia Blood electrolytes normal Blood lactic acid COVID-19 Chest X-ray abnormal Chest tube insertion Cough Diarrhoea Endotracheal intubation Fall Full blood count normal Glycosylated haemoglobin increased Hypoxia Influenza A virus test negative Influenza B virus test Intensive care Lung infiltration

Symptomtext

4/28/21 Pt presented to the ED with complaints of a cough that started 2 weeks ago and was getting worse and weakness with several falls. She also admitted to intermittent diarrhea. She was found to be febrile with a temp to 101.1, tachypneic w/RR of 20. Sats were in the low 90's. NP was was positive for SARS-CoV-2. CXR showed bilateral opacities and she was admitted for PNA and sepsi. She was given Rocephin and Z-max in ED and both were discontinued upon admission. She was started on Decadron in ED 4/30 she had increasing hypoxemia and was placed on a non rebreather. She was transferred to critical care and given tocilizumab. Her respiratory status continued to worsen and she was intubated. She subsequently developed a pneumothorax that persisted despite 2 chest tubes. She developed a large air leak and she was not a surgical candidate. Family ultimately decided to w/draw care on 5/15/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: 17,0
Labordaten: 4/9/21 Preprocedure NP swab was negative for SARS-CoV-2 4/28/21 NP swab positive for SARS-CoV-2, negative influenza A/B Normal CBC. Electrolytes unremarkable. Lactic acid 2.3, Hgb A1c 11.3, procalcitonin 0.88 (nl < 50ng/ml) CXR Bilateral patchy hazy opacities are seen, suspicious for bilateral patchy hazy infiltrates. 5/12/21 CXR Increasing bibasilar infiltrates compared to the recent study 5/14/21 CXR IMPRESSION: 20% right-sided pneumothorax. Endotracheal tube tip terminates 3 cm above carina. Diffuse bilateral airspace left progressed when compared to prior exam 5/15/21 CXR IMPRESSION: 1. Slight improvement in right apical pneumothorax. 2. Stable diffuse pulmonary opacities consistent with edema, pneumonia or ARDS. 3. No other significant change
Aktuelle Erkrankungen: None
Vorgeschichte: arthritis hypertension type 2 DM-uncontrolled fibromyalgia GERD hyperlipidemia OSA-non compliant with CPAP obesity-BMI 32
Andere Medikamente: atorvastatin 40mg daily clopidogrel 75mg daily glipizide 20mg BID losartan 25mg QD metformin 500mg BID pantoprazole 40mg daily It is unclear which if any of these meds patient was taking on adm. Non-compliance due to financial issues
Allergien: duloxetine
Vorherige Impfungen: -

VAERS 1341688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 12,0
Geschlecht: F
Eingang: 31.05.2021
Impfdatum: 17.05.2021
Beginn: 23.05.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood glucose normal Blood lactic acid Blood sodium normal Generalised tonic-clonic seizure Postictal state Blood test Electroencephalogram Magnetic resonance imaging Seizure Urine analysis

Symptomtext

Patient had a seizure on Sunday may 23 at 715am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 1,0
Labordaten: MRI, EEG 10 hours, EEG 48 hours, Blood tests, Urine tests
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamins (flinstone?s gummy bears); Ritalin XR 10mg
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1360445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 18,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 20.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Angina pectoris Asthenia Blood pressure measurement Cardiac disorder Chest X-ray Chest pain Chills Dizziness Dyspnoea Electrocardiogram Fatigue Headache Hyperhidrosis Hypersensitivity Hypotension Inflammation Loss of consciousness

Symptomtext

Problems with her heart; Shortness of breath; Pain the chest; Low blood pressure; Passed out; Started shaking "like a seizure"; Started shaking "like a seizure"; Dizziness; Tiredness; Stomach pain; Chills; Fever; Sweats; Nausea; Vomiting/throwing up; Inflammation in the chest, muscle or maybe heart inflammation; Inflammation in the chest, muscle or maybe heart inflammation; Inflammation in the chest, muscle or maybe heart inflammation; Pain in the heart; Not feeling well; Had a severe allergic reaction; Headache; Weak; This is a spontaneous report from a contactable consumer (patient's mother). An 18-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW0169; Expiration date was not reported) on the left arm on 20Apr2021 as a 1st dose, single dose, with route of administration unspecified, for COVID-19 immunization. The patient had no relevant medical history and concomitant medications. On 20Apr2021, the patient had passed out; started shaking "like a seizure"; dizziness; tiredness; stomach pain; chills; fever; sweats; vomiting/throwing up; and nausea. The patient was brought to urgent care/emergency room (ER) due to the reported events. On 21Apr2021, the patient had shortness of breath; pain in the chest; and low blood pressure. On 22Apr2021, the patient had problems with her heart. The patient was brought to urgent care/emergency room (ER) due to the reported events, and for cardiac work up. On an unspecified date in 2021, the patient was not feeling well; had a severe allergic reaction; headache; and was weak. In Apr2021, the patient had "inflammation in the chest, muscle or maybe heart inflammation". The patient received treatment for the events, pain in the chest and "inflammation in the chest, muscle or maybe heart inflammation" (double dose of naproxen. The patient's laboratory tests included normal blood pressure on 22Apr2021; chest x-ray on 21Apr2021 (results were not provided); echo sonogram on 22Apr2021 (results were not provided); electrocardiogram (EKG) was normal on 21Apr2021, 22Apr2021 and 23Apr2021. The outcome of the events was not recovered for tiredness; was recovered on an unspecified date in 2021 for chills, sweats, vomiting/throwing up; was recovering for pain in the chest; and was unknown for all the other events. The patient's primary care provider was writing a doctor's note recommending that she not receive the second dose based on her reaction to the first dose, and the PCP recommended that the mother call Pfizer as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210421; Test Name: Blood pressure; Result Unstructured Data: Test Result:low; Test Date: 20210422; Test Name: Blood pressure; Result Unstructured Data: Test Result:normal; Test Date: 20210421; Test Name: xray; Result Unstructured Data: Test Result:unknown results; Test Date: 20210421; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20210422; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20210423; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Date: 20210422; Test Name: Echo sonogram; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1358645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: ID
Alter: 15,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 27.05.2021
Beginn: 27.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Nausea Syncope

Symptomtext

Nausea and faintness with vaccination Vitals: BP 125/70 HR 95 Resp 18 O2Sat 97 Skin Signs: Warm and dry, Other - pale Circulation: Cap refill <2sec Respiratory: Breath sound clear bilaterally Initial Treatment: Supine on cot, feet elevated. Feeling better already. 7:00 PM Vitals: BP 118/60 HR 66 Resp 18 O2Sat 99 Skin Signs: Warm and dry Circulation: Cap refill <2sec Respiratory: Breath sound clear bilaterally Follow up Treatment: Nausea disappeared. Ready to leave. Home with mother.

Weitere VAERSDATA-Felder

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

VAERS 1357221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 22.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blood count Blood pressure measurement Dehydration Hypotension Loss of consciousness Malaise White blood cell count White blood cell count increased

Symptomtext

passed out; blood pressure is low/blood pressure was 80 something over 50 something; white blood count is high; dehydrated; not feeling well; This is a spontaneous report from a contactable consumer (patient). A 57-years-old male patient received bnt162b2 (PFIZER COVID 19 VACCINE, Batch/Lot Number: EW0169), via an unspecified route of administration, administered in Arm Left on 22Apr2021 08:00 (57-years-old) as 1st dose, single for COVID-19 immunization (his cardiologist recommended him to get it and signed him up for it). Medical history included ongoing coronary stents (Has 18 coronary stents in total. The last three stents were put in 2018), burning of nerves in the back from Apr2021 (The burning of nerves was done through injection), underlying heart issue, neuropathy, diabetes, blood pressure, Cholesterol. Concomitant medications included metformin taken for diabetes from an unspecified start date and ongoing; pantoprazole from an unspecified start date and ongoing; lorazepam from an unspecified start date and ongoing; gabapentin like a nerve block for neuropathy and diabetes from an unspecified start date and ongoing; isosorbide taken for slow release nitro for heart from an unspecified start date and ongoing; carvedilol taken as beta blocker and helps blood pressure and stuff from an unspecified start date to 10May2021; rosuvastatin taken for cholesterol from an unspecified start date and ongoing; ticagrelor (BRILINTA) taken as blood thinner; losartan taken for blood pressure from an unspecified date and unspecified date; acetylsalicylic acid (ASPRIN, Bayer) from an unspecified start date and ongoing; magnesium from an unspecified start date and ongoing; furosemide taken as water pill from an unspecified date and unspecified date; metoprolol from 10May2021 to an unspecified stop date; amlodipine from an unspecified date and from May2021; chlorthalid tabniva taken as water pill (25mg at night at the time of the shot, couple of days ago he had to start cutting it in half, now he is only taking 12.5mg at night). The patient previously took Plavix (Brilinta replaced Plavix to keep his stents open. He was on Plavix over 6 years ago), Fentanyl, and Versed. The patient experienced passed out (hospitalization) on 04May2021, blood pressure is low/blood pressure was 80 something over 50 something (hospitalization) on 01May2021, not feeling well on Apr2021, white blood count is high on an unspecified date, dehydrated on an unspecified date. The patient was hospitalized for passed out and blood pressure is low/blood pressure was 80 something over 50 something from 04May2021 to 05May2021. The patient underwent lab tests and procedures which included blood count: 13 on 12May2021. The patient received Pfizer COVID vaccine and reported after 1st dose received on 22Apr2021 he is not feeling well, he has an underlying heart issue and a history of stents placed, white blood cells are high and has a low blood pressure. His Dr. asked him to call Pfizer to ask if this could have been reported as side effects from vaccination. He was asking if he should get the second dose. He had Pfizer shot and has got to get the second one on Saturday. He doesn't know if it is related or not. He has been going to the doctor. He has underlying conditions and takes heart medications and has stents. He has not been feeling good since getting the shot. He is not sure if it is affiliated. His white blood count is high and he has to go to the doctor. His doctor is advising him to hold off on getting the second one and told him to call and ask if anyone else has had side effects like that. He clarified shot as COVID19 Vaccine. He saw his cardiologist yesterday and they thought it was interesting that he started having problems. They wanted him to call the phone number and see if he can postpone the second one. He is not sure if it is related to the shot. His blood pressure has been really low (01May2021) since taking the shot. He takes a ton of medications and they are having to adjust his medications since. Not been feeling good is ongoing. It started 3 to 4 days after getting shot. White blood count is high information reported as he was in the hospital and they didn't say anything about his white count. They did his blood count yesterday and they said it was 13 and want him to see his primary care. He just found out about that yesterday. He is going to see his primary care today. He was in the hospital from 04May2021 to 05May2021 because he passed out because his blood pressure was 80 something over 50 something. Blood pressure is low has improved but they have adjusted his medications to help it improve. COVID19 Vaccination Card: it says first dose COVID19. It doesn't have how much was administered. There is a number 42221 on the vaccination card, but he is not sure what it is. At first caller had said he got the vaccine on 24Apr2021, but then clarified that he got the vaccine on 22Apr2021. The patient went to Emergency Room. His wife had to call the ambulance because his wife thought it was his heart. They took him to the ER. They were treating him for his heart and then realized it was his blood pressure was extremely low. Prior Vaccinations (within 4 weeks): No vaccine, but he did have burning of nerves in the back at Pain Clinic done in Apr2021. The burning of nerves was done through injection. He has had it done many times. They give him a local anesthetic when they do it and also Fentanyl and Versed. He has had Fentanyl and Versed many times, due to having stents. Family Medical History Relevant to AE: No. His sisters have gotten it and they are fine. His brother has gotten it and he is fine. Patient did not wish to do a report about his siblings experience with the vaccine. His brother has issues like caller and takes medications, but he hasn't had any side effects from the vaccine. The outcome of the event blood pressure is low/blood pressure was 80 something over 50 something was recovering, not feeling well was not recovered, while for other events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 1,0
Labordaten: Test Date: 20210512; Test Name: blood count; Result Unstructured Data: Test Result:13; Test Name: blood pressure; Result Unstructured Data: Test Result:low; Test Name: white blood cells; Result Unstructured Data: Test Result:high
Aktuelle Erkrankungen: Coronary stent user (Has 18 coronary stents in total. The last three stents were put in 2018)
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal; Cholesterol; Diabetes; Heart disorder; Neuropathy; Radiofrequency ablation (The burning of nerves was done through injection)
Andere Medikamente: METFORMIN; PANTOPRAZOLE; LORAZEPAM; GABAPENTIN; ISOSORBIDE; CARVEDILOL; ROSUVASTATIN; BRILINTA; LOSARTAN; ASPRIN; MAGNESIUM; FUROSEMIDE; METOPROLOL; AMLODIPINE
Allergien: -
Vorherige Impfungen: -

VAERS 1354940

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: DC
Alter: 47,0
Geschlecht: F
Eingang: 27.05.2021
Impfdatum: 14.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Disorientation Dizziness Head injury Injury Joint injury Loss of consciousness Nausea Syncope

Symptomtext

I experienced dizziness, nausea, disorientation and fainted while standing. I hurt my head, knee and thumb, but was otherwise ok. I don't know how long I was out and woke up on the floor. :(

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Hypothyroidism
Andere Medikamente: Armour Thyroid, Liothyronine
Allergien: Basil
Vorherige Impfungen: -

VAERS 1343829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TN
Alter: 47,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 17.05.2021
Beginn: 19.05.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Chest pain Endocarditis Pain Pericarditis

Symptomtext

Pericarditis, after experiencing achy joints Excruciating stabbing pain in back through to chest

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: On 5/20 doctor explained that I had inflamed heart lining and fluid retention around heart. The kept me under observation for 2 days
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bulging discs in neck
Andere Medikamente: Progesterone, Estrodiol .05, Adderall 20mg
Allergien: N/A
Vorherige Impfungen: -

VAERS 1341094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: KY
Alter: 15,0
Geschlecht: F
Eingang: 22.05.2021
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: ja

Dizziness Loss of consciousness Presyncope

Symptomtext

Light headed, passing out. Vasovagal response to needle stick.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1340725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 17,0
Geschlecht: M
Eingang: 22.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
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

Client Fainted ~5min after the vaccine. BP 86/42, repeat 97/40, HR 71, 99% pulse ox. Patient lowered to the ground, vitals obtained, wheeled to Health office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: BP 86/42, repeat 97/40, HR. 99% pulse Ox
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1337491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: AL
Alter: 30,0
Geschlecht: M
Eingang: 21.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood pressure decreased Disorientation Dizziness Hyperhidrosis Immediate post-injection reaction Nausea Syncope

Symptomtext

Syncope about 10 minutes after the COVID19 Vaccine was received, followed by a brief state of disorientation, nausea, lightheadedness and diaphoresis. No vomiting. Patient's initial SBP was 99 and it quickly dropped to 88. HR 32, Epinephrine administered. SBP rose to 91, HR to 42. 2nd dose of Epinephrine was administered and EMS called and took patient to the ED at hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Unknown since patient was managed in the field, then brought to ED on 20MAY2021 by EMS.
Aktuelle Erkrankungen: No acute or recent illness.
Vorgeschichte: None
Andere Medikamente: No meds
Allergien: Coconut
Vorherige Impfungen: -

VAERS 1333740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: KY
Alter: 15,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 20.05.2021
Beginn: 20.05.2021
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

Symptomtext

Patient passed out about 15 minutes after receiving the vaccine. She stated that she had not eaten since breakfast and is the reason she felt lightheaded. Staff provided water and a snack for the patient and sat with her until she felt ready to stand up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 1332840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 18,0
Geschlecht: M
Eingang: 20.05.2021
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

Dizziness Fear Irritability Loss of consciousness Nervousness Syncope

Symptomtext

Fainted within 30 seconds/Passed out completely after shot; Passed out completely after shot; Some intermittent light headedness and dizziness; Some intermittent light headedness and dizziness; Irritating; scary/ fearful; scary/ fearful; This is a spontaneous report from a contactable consumer (patient's mother). An 18-year-old male patient received the first dose of BNT162B2 (Pfizer-Biontech Covid-19 Vaccine, Lot. EW0169) at single dose, on 22Apr2021 at 17:30, for COVID-19 immunization. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. Relevant medical history and concomitant medications were unknown. Patient's mother reported that her son fainted within 30 seconds of receiving the Pfizer vaccine 1st dose and since then he had experienced some intermittent light headedness and dizziness. He passed out completely after shot. Adverse events were described as following: "patient is due to get his second dose of the shot later this evening but is having periods of lightheadedness and dizziness. Patient's mother states that her son also feels like he is going to pass out. She states that this started 30 seconds after the first shot. Her son only passed out once, completely right after the shot, it was a bad experience. She's glad he actually wants the other one today, but he is concerned because he is still lightheaded and dizzy after 3 weeks. Patient's mother states that he has been trying to function, work, and live his life but its irritating to him and scary. The doctor suggested that he should get his second dose but her son is a little fearful". Physician Office Visit required. The patient did not recover from intermittent light headedness and dizziness, while clinical outcome of the other events was unknown.; Sender's Comments: Based on known drug safety profile and strong temporal relationship there is reasonable possibility of causal association between the reported events and the suspect drug. 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: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1268220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NV
Alter: 19,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 23.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blindness COVID-19 Fall Loss of consciousness Migraine Dizziness Hypotension Nausea Pain SARS-CoV-2 test

Symptomtext

lost vision in both eyes; passed out; dizzy; severe nausea set in with severe body pain; severe nausea set in with severe body pain; worst migraine of my life; low blood pressure; This is a spontaneous report received from a contactable consumer (patient). A 19-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (at the age of 19-years-old), administered in Arm Left on 23Apr2021 13:00 (Lot Number: EW0169) as 1st dose, single for COVID-19 immunization. Medical history included anxiety, and allergies to mosquitoes, hotdogs, and sausage. The patient was not pregnant at the time of vaccination. Concomitant medications included citalopram and drospirenone, estradiol (EOS), IUD, daily supplements. The patient previously took oxycodone ("oxicodone") and percocet [oxycodone hydrochloride;oxycodone terephthalate;paracetamol] and experienced allergies. The patient, 48 hrs later, lost vision in both eyes, became dizzy, passed out multiple times. Later severe nausea set in with severe body pain. Went to Urgent Care the following day and was told side effects. That night had worst migraine of her life, low blood pressure, and continued nausea. Given some meds and sent home to rest. Took 2 full days to feel okay again. Onset date and time of events reported as 25Apr2021 13:00. The adverse events resulted in Emergency room/department or urgent care. Therapeutic measures were taken as a result of the events. Treatment received for the adverse events included Toradol, Benadryl, and Reglan. The patient underwent lab tests and procedures which included sars-cov-2 test: negative (Nasal Swab) on 27Apr2021. The outcome of the events was recovered with sequelae. The events "lost vision in both eyes" and "passed out" were considered as serious (medically significant). Facility where the most recent COVID-19 vaccine was administered was Clinic/facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. No follow-up attempts are possible, no further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210427; Test Name: SARS-CoV-2 by PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to arthropod bite; Anxiety; Food allergy
Andere Medikamente: CITALOPRAM; EOS
Allergien: -
Vorherige Impfungen: -

VAERS 1268220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NV
Alter: 19,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 23.04.2021
Beginn: 25.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blindness COVID-19 Fall Loss of consciousness Migraine Dizziness Hypotension Nausea Pain SARS-CoV-2 test

Symptomtext

lost vision in both eyes; passed out; dizzy; severe nausea set in with severe body pain; severe nausea set in with severe body pain; worst migraine of my life; low blood pressure; This is a spontaneous report received from a contactable consumer (patient). A 19-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (at the age of 19-years-old), administered in Arm Left on 23Apr2021 13:00 (Lot Number: EW0169) as 1st dose, single for COVID-19 immunization. Medical history included anxiety, and allergies to mosquitoes, hotdogs, and sausage. The patient was not pregnant at the time of vaccination. Concomitant medications included citalopram and drospirenone, estradiol (EOS), IUD, daily supplements. The patient previously took oxycodone ("oxicodone") and percocet [oxycodone hydrochloride;oxycodone terephthalate;paracetamol] and experienced allergies. The patient, 48 hrs later, lost vision in both eyes, became dizzy, passed out multiple times. Later severe nausea set in with severe body pain. Went to Urgent Care the following day and was told side effects. That night had worst migraine of her life, low blood pressure, and continued nausea. Given some meds and sent home to rest. Took 2 full days to feel okay again. Onset date and time of events reported as 25Apr2021 13:00. The adverse events resulted in Emergency room/department or urgent care. Therapeutic measures were taken as a result of the events. Treatment received for the adverse events included Toradol, Benadryl, and Reglan. The patient underwent lab tests and procedures which included sars-cov-2 test: negative (Nasal Swab) on 27Apr2021. The outcome of the events was recovered with sequelae. The events "lost vision in both eyes" and "passed out" were considered as serious (medically significant). Facility where the most recent COVID-19 vaccine was administered was Clinic/facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. No follow-up attempts are possible, no further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210427; Test Name: SARS-CoV-2 by PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to arthropod bite; Anxiety; Food allergy
Andere Medikamente: CITALOPRAM; EOS
Allergien: -
Vorherige Impfungen: -

VAERS 1324062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 23,0
Geschlecht: F
Eingang: 17.05.2021
Impfdatum: 22.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Dizziness Fall Heart rate increased Heavy menstrual bleeding Hypokinesia Menstruation irregular Syncope

Symptomtext

I felt dizzy so I grabbed the edge of the bathroom counter, the next thing I knew I was on the bathroom floor and couldn't move. My mom said I was out for 1-2 minutes before she found me. I have never fainted before ever. This only happened once. But the following week my heart rate when standing would reach 130-145 bpm. The following weekend I experienced a longer than normal menstrual cycle with heavier bleeding than normal, even while I was still on my birth control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: blood tests and a referral to a cardiologist.
Aktuelle Erkrankungen: -
Vorgeschichte: PCOS Migraines Iron Deficiency Anemia
Andere Medikamente: Xulane Tylenol Naproxen
Allergien: Vancomycin Compazine Caffeine Tree nuts Seeds
Vorherige Impfungen: -

VAERS 1324017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 39,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Deep vein thrombosis Erythema Metastasis Peripheral swelling Ultrasound scan abnormal

Symptomtext

Patient recently diagnosed with DVT and was taking enoxaparin 80mg subq q12h. Presented to ED after receiving vaccination with increased swelling and redness in RLE. worsening of DVT on imaging.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 4,0
Labordaten: 5/14 US RLE: IMPRESSION: 1. Progression of deep venous thrombosis with complete occlusion of the right common femoral vein. 2. Stable near complete occlusive deep venous thrombosis in the right superficial femoral vein.
Aktuelle Erkrankungen: RLE DVT
Vorgeschichte: metastatic rhabdomycosarcoma (temozolomide 200mg PO daily x 5, 4/27 -5/1; irinotecan 60mg IV daily x 5, 4/27 - 5/1 ; vincristine 2mg IV x 1, 4/27)
Andere Medikamente: enoxaparin 80mg subq q12h; tramadol 50mg q6h prn moderate pain, temozolomide 200mg daily x 5 days
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1323875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: MN
Alter: 51,0
Geschlecht: F
Eingang: 17.05.2021
Impfdatum: 21.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Pericarditis

Symptomtext

She presented to the ED on 4/30/21 due to left sided chest pain. She was found to have acute pericarditis with no identifiable source. Unclear if vaccine is related but did receive vaccine on 4/21/21 before this developed. currently being managed by cardiology with.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: depression, asthma, environmental allergies
Andere Medikamente: flexeril, gabapentin, cymbalta, singulair, ibuprofen, albuterol, flovent
Allergien: codeine
Vorherige Impfungen: -

VAERS 1323651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 12,0
Geschlecht: M
Eingang: 17.05.2021
Impfdatum: 16.05.2021
Beginn: 16.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

Fainted soon after the injection. Came too soon after and walked out on his own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Daily: probiotic, vitamin C, quercetin, bromelain
Allergien: Dairy
Vorherige Impfungen: -

VAERS 1321960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 44,0
Geschlecht: F
Eingang: 16.05.2021
Impfdatum: 19.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: UN / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Electric shock sensation Nausea Pyrexia Sensitive skin

Symptomtext

Fever of 101 degrees, nausea, and skin felt hypersensitive to touch for about 48 hours. Ongoing symptom of intermittent sensations in arms and face that feels like quick "zings" of electricity. This happens usually when I am exercising or make fast movements. It seems to be improving over the weeks since I got the vaccine and is not impacting daily activities too much at the point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Migrane on the day of the vaccine, otherwise healthy.
Vorgeschichte: None
Andere Medikamente: Vitamin D supplement, Allicin (garlic) supplement, and one dose of ibuprofen for headache taken 1 hr prior to vaccine.
Allergien: None
Vorherige Impfungen: -

VAERS 1317771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: KS
Alter: 20,0
Geschlecht: M
Eingang: 14.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

1305 Fainted from Sitting position in observation room, no trauma noted. Assisted to supine position with legs elevated on chair, regained consciousness. BP 70/42. HR 106. At 1315 Resting BP now 94/50, HR 86, O2 Sat 98%, assisted to W/C and taken to EMS room to lie down on cot. Snack given. At 1330 Feeling better now. BP 110/60, HR 61, O2 sat 98%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Denied
Vorgeschichte: denied
Andere Medikamente: Denies
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1317615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: UT
Alter: 16,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 19.04.2021
Beginn: 06.05.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Continuous positive airway pressure Culture negative Cytomegalovirus test negative Differential white blood cell count Enterovirus test negative Epstein-Barr virus test negative Frequent bowel movements Full blood count HIV test negative Haemoglobin decreased Intensive care Lymphocyte count decreased Neutrophil count decreased Pancytopenia Parvovirus B19 test negative Platelet count decreased Pyrexia

Symptomtext

16-year-old medically complex female, JIA, bronchiectasis and chronic nighttime oxygen requirement who presented to the hospital on 5/6 with fever, increased stool output, and perianal skin breakdown. Her course was complicated by respiratory failure (requiring ICU admission for CPAP), pancytopenia, diarrhea with buttock skin breakdown requiring rectal tube for wound and stool management, and extensive workup which was unrevealing for an infectious cause. She clinically improved with respect to pancytopenia with discontinuation of felbamate, and completed a treatment course with Zosyn for suspected buttock SSTI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: 5/7 CBCd WBC 1.1, Hgb 6.7, Plts 23, ANC 0.8, ALC 0.7; Cultures negative. 5/5 COVID PCR negative, 5/9/2021 COVID Ab positive Viral workup included negative Biofire respiratory film array 2.1 (5/5), BioFire GI-film array 5/6, and serum HIV, EBV, CMV, parvovirus, parecho/enterovirus and adenovirus PCRs.
Aktuelle Erkrankungen: JIA, encephalopathy, central line dependence
Vorgeschichte: JIA, encephalopathy, central line dependence, cerebral palsy
Andere Medikamente: Enbrel, Epidiolex, felbamate, keppra, topiramate
Allergien: cephalosporins, erythromycin, ketamine, metronidazole
Vorherige Impfungen: -

VAERS 1317517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 23,0
Geschlecht: F
Eingang: 14.05.2021
Impfdatum: 13.05.2021
Beginn: 13.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Diarrhoea Dizziness Nausea Syncope Vomiting

Symptomtext

Dizzy and syncope post vaccine with staring into space for 5-10 seconds. No loss of tone, shaking/clonic activity, no falls, no incontinence, immediate return to alert and oriented. States has similar episodes in past with drug intolerance. Had nausea and vomitting with delayed diarrhea s/p the episode of syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: norethindrone-e.estradiol-iron
Allergien: Clindamycin, sulfa
Vorherige Impfungen: -

VAERS 1314774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 17,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 30.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Muscle twitching Seizure Syncope

Symptomtext

school nurse filled out incident report per their policies. Incident highlights: "Pt got her mom?s attention and started to slump down, Mom and volunteer? Were able to assist her to the floor. No injuries during the episode, did not hit her head. She has twitching of her extremities which appeared to be a seizure. Mom stated there was no seizure history. EMS was called. Pt was alert when EMS arrived, they assessed her and it was determined that she should get an evaluation but EMS gave the option to transport themselves for follow up as she appeared stable." unable to contact mother, no additional information available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1312592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Pallor Syncope

Symptomtext

Attendee was found laying on his back on the floor of the observation area and appeared pale skin, eyes open. breathing effortlessly. Attendee was assessed by me and I asked him his name. No response. Said Hello, can you hear me? Attendee responded "yes". I asked patient to tell me how he was feeling and he said I feel dizzy. Blood pressure was taken 152/ 66 pulse 76 SpO2 98%. Attendee informed he appeared to have fainted. Stated he did not have any symptoms or problems like this after first dose. States he did have breakfast. Remembers walking to chair after shot and was watching Anime on his phone and then I asked him if he could hear me. Patient denies SOB, chest pain, no S/S of swelling, itching , redness, denies headache. Sat up with assistance on floor. Offered saltine crackers and Nestle sugar water which he drank. Patient stood with assistance back to chair. No symptoms of nausea, vomiting, headache or dizziness. Second BP taken 132/66 Pulse 66, SPO2 99%. Attendee rerported he drove himself to clinic. Advised to call for ride home. Patient called his father who arrived and identified to pick him up at 11:58. Observed patient until father came and answered questions from father. Home care instructions reiterated. Attendee walked to exit by me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: None reported
Vorgeschichte: None reported
Andere Medikamente: None reported
Allergien: None reported
Vorherige Impfungen: -

VAERS 1310127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 50,0
Geschlecht: F
Eingang: 12.05.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Presyncope Syncope Tunnel vision

Symptomtext

Lightheaded, tunnel vision, then syncopal episode. Vasovagal reaction, monitored for 30 mins, offered PO fluids, released with BP and symptoms improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Scleroderm, asthma, celiac disease
Andere Medikamente: Dexilant, Flonase, Vit D, advair, albuterol,
Allergien: PCN, NSAID, arythromycin
Vorherige Impfungen: -

VAERS 1309553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 23.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Erythema Thrombosis Ultrasound scan

Symptomtext

blood clot in one of his leg; leg became red; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 23Apr2021 (at the age of 73 years old) (Lot Number: EW0169, unknown expiration) as 1st dose, single for COVID-19 immunization. Medical history and concomitant medications were reported as none. The patient received his first dose of COVID-19 vaccine on 23Apr2021. In the night of 24Apr2021, his leg became red and he spoke to his doctor. The experienced a blood clot in one of his leg on 25Apr2021. The patient received Eliquis for the events to be taken for 45 days. He would like to consult if he should receive the second dose after the side effect from the first dose. Patient would like to know if there have been reports of blood clots after receiving the COVID-19 vaccine. The patient is scheduled to receive his second dose on 14May2021. The patient underwent lab tests and procedures which included blood test and ultrasound on leg: unknown results on 26Apr2021. Outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210426; Test Name: blood test; Result Unstructured Data: Test Result:unknown result; Test Date: 20210426; Test Name: Ultrasound on leg; Result Unstructured Data: Test Result:unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1306598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 16,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 06.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Bilevel positive airway pressure Dyspnoea Fatigue Hypotension Intensive care Cardiogenic shock Electrocardiogram ST segment elevation Haemoptysis Hypoxia Laboratory test Oxygen saturation decreased Pain Pericarditis Myocarditis Nausea Respiratory failure Troponin increased Vomiting

Symptomtext

Youth had his second dose of Pfizer COVID vaccine on 5/6/21. On 5/7/21 he woke up reporting body ache and fatigue. Treated with Tylenol and rest. On 5/9/21 he was reporting that he felt short of breath, blood pressure and 02 sats were low. He was taken to the ER for evaluation. Determined he had pericarditis and was flown via helicopter to ER Hospital where he remains in the PICU on bipap and cardiac IV drips.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiogenic shock
Hospital-Tage: -
Labordaten: Labs per at Hospital
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: VYVANSE 40 MG QAM CLONIDINE 0.2 MG QHS ABILIFY 15 MG QAM
Allergien: NKA
Vorherige Impfungen: -

VAERS 1306197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 11.05.2021
Impfdatum: 24.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Dyskinesia Lip swelling Moaning Muscle rigidity Seizure

Symptomtext

Twelve hours after the second shot, I had convulsions; About 5 hours after the second shot, my lips started to swell; I had a pain that started in my left armpit, shot down to my inner elbow, and caused my whole arm to get rigid; I had a pain that started in my left armpit, shot down to my inner elbow, and caused my whole arm to get rigid; Then my body would jerk and I groaned; Then my body would jerk and I groaned; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0169) at left arm on 24Apr2021 09:45 AM at second dose, single for COVID-19 immunisation. Medical history included chronic rhinitis and Lyme disease. Patient previously received Morphine, cefzil and grass. Patient previously received the first dose of BNT162B2 on 03Apr2021 09:45 AM (lot number: EP7533) on Left arm for Covid-19 Immunization. Concomitant medication included loratadine, astaxanthin (BIOASTIN), spirulina spp. the patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. About 5 hours after the second shot (also reported as 24Apr2021 22:00), her lips started to swell. she took her allergy medicine and she felt better. Twelve hours after the second shot, she had convulsions. she had a pain that started in her left armpit, shot down to her inner elbow, and caused her whole arm to get rigid. Then her body would jerk and she groaned. It stopped and started in intervals, with calm in between. It was unknown prior to vaccination, if the patient diagnosed with COVID-19. Not tested for COVID-19. Outcome of the events was recovering. Follow-up information requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic rhinitis; Lyme disease
Andere Medikamente: LORATADINE; BIOASTIN; SPIRULINA SPP.
Allergien: -
Vorherige Impfungen: -

VAERS 1299961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 04.05.2021
Beginn: 06.05.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Antinuclear antibody Blood test normal Blood thyroid stimulating hormone normal Chest pain Coxsackie virus test Dyspnoea Echocardiogram normal Electrocardiogram ST segment elevation Full blood count normal HIV test negative Hepatitis B surface antigen Intensive care Magnetic resonance imaging abnormal Malaise Metabolic function test normal Myalgia Myocarditis Nausea

Symptomtext

Patient is a previously healthy 16 year-old M presenting with acute onset chest pain, shortness of breath, nausea, vomiting, malaise, fever and myalgia to ED on 5/6/2021 at 20:44. He started experiencing symptoms on 5/6/2021 morning a t06:07 AM. He received his second dose of Pfizer COVID-19 vaccine on 5/4/2021 10:: AM. In the ED, CBC, CMP and UA was within normal limits. EKG at 20:46 and again at 21:14 showed ST segment elevation in inferolateral leads with possible myocardial injury, ischemia or pericarditis. Troponin 0 hour was 835 and at 2 hours 1674. Patient was admitted to the PICU for further evaluation and management. Echo on 5/6/2021 showed normal LV systolic function with SF 31% . Cardiac MRI on 5/7 showed contrast enhancement of inferolateral wall consistent with myo-pericarditis with small pericardial effusion. Troponins were trended every 12 hours and plateaued in the 1800's on 5/8/2021. Patient was diagnosed with acute myo-pericarditis. Respiratory viral PCR and COVID-19 PCR on 05/06/2021 were negative. Thyroid studies were normal. ANA titer is pending. Viral serology for HbsAg was negative and HIV was non-reactive. Results for additional viral serologies for Coxsackie viruses, EBV, CMV and HHV6 are awaited. Patient was treated with NSAIDs and Colchicine. IVIG was not given based on clinical judgement. Pediatric Cardiology was involved in patient's care and clinical decision making. Patient remained hemodynamically stable on room air throughout his PICU course. He was discharged on 5/9/2021 with Pediatric Cardiology outpatient follow up in 2-3 weeks. He will continue Ibuprofen 600 mg every hours and Famotidine 20 mg 2 times daily until his follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: EKG 5/6/2011 Echo 5/6/2011 Cardiac MRI - 5/7/2011 Troponin T -5/6/2021-5/9/2021 TSH, FT4 - 5/7/2021 HIV, HbsAg- 5/7/2021 Respiratory viral PCR - 5/6/2021 COVID-19 PCR - 5/6/2021
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma, well controlled, not on medications.
Andere Medikamente: Zyrtec PRN, Flonase PRN
Allergien: none
Vorherige Impfungen: -

VAERS 1299223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 14.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Cold sweat Dyspnoea Investigation Muscle spasms Pain Syncope

Symptomtext

nearly fainted twice; I've been having weird pains in several spots inside my muscles all over the place in my legs, feet, arms, neck, chest, face and even my left hand ring finger tip. It's pain that is in spots, it feels; I've been having weird pains in several spots inside my muscles all over the place in my legs, feet, arms, neck, chest, face and even my left hand ring finger tip. It's pain that is in spots, it feels; pains in chest; catching my breath; very cold and clammy; This is a spontaneous report from a contactable consumer (the patient). A 45-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EW0169), via an unspecified route of administration, on 14Apr2021 at 11:30 (at the age of 45-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history included cardiac disorder from an unknown date and unknown if ongoing, irregular heart beat and depression from an unknown date and unknown if ongoing. Concomitant medication included metoprolol (METOPROLOL) taken for an unspecified indication, start and stop date were not reported. The patient did not have any other vaccines within four weeks prior to the vaccination. The patient stated that when he first got the shot he actually nearly fainted twice and had to lay on the floor for a while. It was very scary, he thought he was going to die. He got very cold and clammy and had pains in chest and had a hard time catching his breath. They checked his vital signs a couple times and said they looked good. But he still felt sick and they said if he did not feel better soon they may have to call for an ambulance for him. Eventually he felt better enough to where he was able to get up off the floor and on handicap cart to drive out of there. Also, he's been having weird pains in several spots inside his muscles all over the place in his legs, feet, arms, neck, chest, face and even his left hand ring finger tip. It's pain that is in spots, it feels like mini-charley-horses that lasts anywhere from 20 something to 30 something seconds. Now it's mostly continuous pains in his thigh muscles between his legs. And a pain in one spot in his left arm bicep. This has been happening for days." The patient experienced "nearly fainted twice" on 15Apr2021 with outcome of not recovered, chest pain, got very cold and clammy and had a hard time catching his breath on 15Apr2021 with outcome of not recovered. He also reported that he has been having weird pains in several spots inside his muscles all over the place in his legs, feet, arms, neck, chest, face and even his left hand ring finger tip. it's pain that is in spots, it feels starting on 15Apr2021 with outcome of not recovered. The patient underwent lab tests and procedures which included unspecified investigation: myalgias on an unspecified date . Therapeutic measures (unspecified) were taken as a result of the events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Name: lab tests; Result Unstructured Data: Test Result:Myalgias
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cardiac disorder (irregular heart beat); Depression
Andere Medikamente: METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1295999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 26,0
Geschlecht: M
Eingang: 07.05.2021
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fall Feeling hot Hyperhidrosis Syncope

Symptomtext

Patient was sitting in chair after vaccine waiting the required 15 minutes. He states he was staring sown watching his phone and he felt hot and then woke up on the floor with people around him. He fainted. He felt hot and sweaty afterward. Episode seemed to pass within about 10 minutes all together. Paramedics came and checked him out since he hit his head when he fell. Patient didn't want to go to hospital and was picked up from the store by family member.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Paramedics took BP once they arrived and reading was within normal range.
Aktuelle Erkrankungen: Patient stated he fainted 2-3 weeks prior to this fainting spell. That incident was unrelated to any vaccination.
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1295343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 19,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Hyperhidrosis Hypotension Presyncope Vision blurred

Symptomtext

Suspected vasovagal episode, blurry vision, sweaty, hypotension, eval by EMS, transported to ER via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1294515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 54,0
Geschlecht: F
Eingang: 07.05.2021
Impfdatum: 23.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Discomfort Heavy menstrual bleeding Hypomenorrhoea Menstrual disorder Menstruation irregular Pain Pollakiuria Thrombosis Ultrasound scan vagina abnormal

Symptomtext

After receiving the first dose on 4/1/21 Lot# ER8733, I had light spotting for 2 days. Second dose given 04/23/21 and by 04/28/2021 I started bleeding again And by the second day I was soaking through pads and huge clots were coming out. This has never happened to me before. After 7 days of bleeding heavily I woke up on May 5th at 4:00 a.m. with intense abdominal cramping The only way I can describe was labor. I felt back labor, pelvic pressure, frequent urination and intense pain. I reached out to my gynecologist And he immediately told me to remove my estrogen patch and later that morning he started me on progesterone treatment for 10 days to stop the bleeding. After 7 hours of pain on May 5th, I went to the emergency department and an ultrasound revealed a blood clot. From ultrasound results "there is a complex area in the area of the cervix measuring 5.7 x 3.6 x 2.6 cm." After several hours I was released from the emergency room taking toradol for pain. That evening I passed a huge blood clot! I'm very grateful it was where it was and I could expel it. But there's no doubt the second vaccine caused this issue that has never happened to me before. I still get my periods though irregular and very light. So this event was highly unusual and very painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 5/5/2021 US PELVIC COMPLETE AND TRANSVAGINAL and other regular blood tests upon ER admission.
Aktuelle Erkrankungen: -
Vorgeschichte: Bipolar depression
Andere Medikamente: Estradiol 1 mg patch twice a week. Lamotrigine 150 mg Vibryd 10 mg Olmesartan Vitamins 50+ Trazodone 150mg
Allergien: N/a
Vorherige Impfungen: -

VAERS 1292370

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 60,0
Geschlecht: F
Eingang: 06.05.2021
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: nein

Bell's palsy Blood test normal Facial paralysis

Symptomtext

Facial drooping on right side of face, began after shot, about 10:30pm was the first indication. Still couldn't spit out my toothpaste properly in the morning, doctor's office told me to go into the Emergency room, which I did. Diagnosis of Bell's Palsy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: 5/6/2021 - blood drawn, normal levels, nothing unusual. All motor functions and eye movements controlled. Just the one side of the face - no motor control and numbness to the right side of the face.
Aktuelle Erkrankungen: none
Vorgeschichte: seasonal allergies
Andere Medikamente: atenolol, atorvastatin, cetirizine, multivitamin, omega-3 fatty acid
Allergien: none
Vorherige Impfungen: -

VAERS 1292170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
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 / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Head injury Syncope

Symptomtext

Pt felt dizzy, had vasovagal syncope, hit head on metal stanchion and then the ground.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Vitals monitored q 10 mins for 40 mins.
Aktuelle Erkrankungen: Denies
Vorgeschichte: Admits Hx vasovagal reactions
Andere Medikamente: Denies
Allergien: Denies
Vorherige Impfungen: -

VAERS 1285106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 63,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 03.05.2021
Beginn: 03.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood pressure increased Bradycardia Feeling cold Pallor Presyncope Tunnel vision

Symptomtext

Right after vaccination recipient became pale, cool, had narrowing vision, near syncopal episode, bradycardia, and increased BP. Recipient was stabilized by onsite EMS and transferred to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1283970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 16.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Confusional state Headache Magnetic resonance imaging Nausea Photophobia Seizure

Symptomtext

Headache, nausea, confusion, photophobia, seizure requiring a call to 911 and a visit the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: MRI
Aktuelle Erkrankungen: breast cancer
Vorgeschichte: metastasis breast cancer
Andere Medikamente: Claritin non-drowsy 24 hour, Citalopram 40 mg, Whole Foods Women's Multi
Allergien: latex
Vorherige Impfungen: -

VAERS 1282898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TX
Alter: 17,0
Geschlecht: M
Eingang: 03.05.2021
Impfdatum: 02.05.2021
Beginn: 02.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dizziness Hypotension Presyncope

Symptomtext

Vasovagal event with hypotension and dizziness after vaccine (patient stated did not eat that morning)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1282810

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 39,0
Geschlecht: F
Eingang: 03.05.2021
Impfdatum: 15.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Bell's palsy

Symptomtext

Bell's Palsy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Viral pharyngitis with symptoms starting on 04/19/2021
Vorgeschichte: Malignant neoplasm of the breast right undergoing current radiation.
Andere Medikamente: BuSpar 30 mg b.i.d., lorazepam 0.5 mg p.r.n., acetaminophen a 1000 mg p.r.n., clindamycin 1% gel, sertraline 200 mg daily, omeprazole 20 mg b.i.d..
Allergien: Adhesives, chlorhexidine
Vorherige Impfungen: -

VAERS 1281950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0169

schwer

Staat: WI
Alter: 18,0
Geschlecht: F
Eingang: 03.05.2021
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: ja

Dizziness Loss of consciousness

Symptomtext

CLIENT PASSED OUT OR FAINTED AFTER RECEIVING THE VACCINE WHILE VACCINATOR WAS PROVIDING HER WITH INSTRUCTIONS. CLIENT WAS ASSISTED TO THE FLOOR. NO INJURIES OBTAINED. CLIENT CAME TO IN SECONDS AND EXPLAINED SHE OFTEN FAINTS AFTER VACCINATION. CLIENT REMAINED UPRIGHT FOR 10 MINUTES AND DRANK WATER. WHEN ABLE TO WALK, CLIENT WAS ESCORTED TO A COT IN THE MONITORING AREA AND LAID DOWN. CLIENT WAS STABLE AND REMAINED AT FACILITY FOR 30 MINUTES UNTIL ABLE TO WALK AND WAS NO LONGER LIGHT HEADED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE.
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKOWN
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1280077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 16,0
Geschlecht: M
Eingang: 02.05.2021
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Fall Head injury Loss of consciousness

Symptomtext

Pt fell off chair and hit head on ground. EMS and 2 vaccinator RN's came to help. Pt lost consciousness for few seconds. Pt vitals and glucose were stable. Pt alert and oriented when awoke. Pt transported to hospital with EMS with mother.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1279108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 38,0
Geschlecht: M
Eingang: 01.05.2021
Impfdatum: 26.03.2021
Beginn: 07.04.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Asthenia Chest discomfort Dyspnoea Electrocardiogram ambulatory Electrocardiogram normal Feeling abnormal Full blood count normal Malaise Metabolic function test Palpitations Presyncope Skin discolouration Visual impairment

Symptomtext

First vaccine dose 3/26/21 First health event 4/7/21: pre-syncope and palpitations Second vaccine dose 4/16/21 4/18/21: strange heart feelings on any exertion, pre-syncope, weakness, malaise, winded by even walking the dog, hands turn purple, weird thump/click in chest, visual changes (seeing colors or spots, greying of vision, migraine-like hallucinations), shortness of breath Episodes like the one described on 4/18 daily, especially in the morning and on exertion until now, 5/1/21 Seen in the ER on 4/19/21 and 5/1/21. EKGs normal, CBC and metabolic panel largely normal. Holter monitor 4/21/21-4/26/21 placed by healthcare Center; hasn't been read yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Seen in the ER on 4/19/21 and 5/1/21. EKGs normal, CBC and metabolic panel largely normal. Holter monitor 4/21/21-4/26/21 placed by healthcare Center; hasn't been read yet.
Aktuelle Erkrankungen: Elevated lipase levels intermittently for one year; no clear diagnosis
Vorgeschichte: Elevated lipase levels intermittently for one year; no clear diagnosis
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1277363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

schwer

Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 01.05.2021
Impfdatum: 13.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Loss of consciousness Seizure Vomiting

Symptomtext

unconscious; seizure; throwing up while unconscious; This is a spontaneous report from a contactable other healthcare professional (patient). A 23-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: Ew0169), dose 1 intramuscular, administered in Arm Right on 13Apr2021 14:45 (at the age of 23years) as single dose for Covid-19 immunization. The patient is not pregnant at the time of vaccination. There were no medical history and concomitant medications. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that on 14Apr2021 (10:15 PM), the patient was unconscious for about 15 seconds, having a seizure for 5 seconds, and throwing up while unconscious. The adverse events resulted in Emergency room/department or urgent care. There was no treatment received for the adverse event. The patient has not been tested for COVID-19 since the vaccination. The outcome of events was recovering.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events loss of consciousness, seizure, vomiting and the suspect vaccine BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer drug 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: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1274408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 30.04.2021
Impfdatum: 30.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dysphagia Loss of consciousness Miliaria Pharyngeal swelling

Symptomtext

1-5 minutes after both shots: sensation of mild swelling in throat, in addition to mild dizziness/faintness which passed after 5-10 minutes (no phobia of needles). Feeling of swelling in throat/difficulty swallowing lasted until about 4 hours after vaccine was given, and was more intense after second dose, though not enough to seek medical attention. In addition, after the second dose, a feeling of prickling/heat on skin, which began within 1-5 minutes of receiving the vaccine and lasted for about 5 minutes after symptoms began. No respiratory effects. No other symptoms which resembled an allergic reaction (itchy mouth, rash, adrenaline rush, etc.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Prescribed Adderall 7.5 MG, taken at 1:45 PM.
Allergien: Severely allergic to tree nuts (3 prior anaphylactic reactions, one requiring ER treatment). Also allergic to grass/tree pollen and cats. Prior adverse reaction (vomiting) to either codeine or the after-effects of anesthesia after wisdom tooth extraction. No known medication allergies.
Vorherige Impfungen: -

VAERS 1272938

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 37,0
Geschlecht: F
Eingang: 30.04.2021
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: ja Erholt: ja

Dizziness Fall Flushing Head injury Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Pt was wearing bullet proof vest and jacket as part of security uniform. Pt was ok after receiving vaccine. Roughly 10 minutes after administration, pt became lightheaded and fell out of chair in waiting area. Pt's head hit the floor. Pt stated they did not need EMS, however on-site medical staff recommended pt be seen due to head injury.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1272051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 35,0
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: ja Erholt: ja

Cyanosis Generalised tonic-clonic seizure Loss of consciousness Unresponsive to stimuli

Symptomtext

FOLLOWING PATIENTS FIRST PFIZER COVID -19 INJECTION, PATIENT PASSED OUT, BECAME UNRESPONSIVE AND CYANOTIC IN THE LIPS AND THAN HAD A TONIC CLONIC SEIZURE FOR 45 SECONDS. PATIENT WAS TAKEN TO ER BY EMS WITH HER HUSBAND.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: -
Labordaten: UNKNOWN
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 1270928

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
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 / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness

Symptomtext

Patient passed out during monitoring, observation period. She was alert and oriented and EMS was contacted. She sat up and drank some water. EMS monitored her heart rate and blood pressure and she was released to her father.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood pressure Pulse Ox Heart rate
Aktuelle Erkrankungen: Patient states she has extreme anxiety during medical procedures and was nervous prior to the vaccine. She had not eaten anything that day.
Vorgeschichte: none
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1268231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 16,0
Geschlecht: M
Eingang: 28.04.2021
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

Fall Head injury Loss of consciousness

Symptomtext

had his injection at 12:15pm without incident and went to monitoring area and sat at table. lost consciousness and fell to the floor, staff alerted RN who came over to . regained consciousness right away. stated that he remembered leaning forward over the table looking at his phone and texting his sister and then he was on the floor. A wheel chair was brought over and was laid down on the cot where he stated he already felt better. PHN assessed for injuries. He denies pain, no injuries noted except for right eyebrow that is red and starting to swell. At 12:20pm BP 108/64, P-63, Os Sats 96% and R-18.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Denies
Vorgeschichte: Denies
Andere Medikamente: Denies
Allergien: Denies
Vorherige Impfungen: -

VAERS 1263623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NH
Alter: 21,0
Geschlecht: F
Eingang: 27.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

Patient had a syncopal episode after vaccine adminsitration. Normal reaction for patient after injections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Syncopal episodes after previous vaccinations

VAERS 1259701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 16,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 26.04.2021
Beginn: 26.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anxiety Panic attack Seizure Wheezing

Symptomtext

Patient was vaccinated and left with her mother to sit in her car for 30 minute monitoring period. Patient's mother stated patient was experiencing extreme anxiety getting the vaccine and after 20 minutes was wheezing. She brought patient inside and a Pharmacist came to check on her and her mother stated that she has had a reaction to a medication in the past and just needed Benadryl. Benadryl was given to her and she took it orally. Her pulse and blood oxygen were measured with a finger pulse oximeter and were both normal. Shortly after she was panicking more and had a seizure. Her mother reported that she has frequent seizures when she has anxiety/panic episodes. Her seizures were persisting so 911 was called. Paramedics arrived shortly after and took patient to the hospital. A few hours later the patient's mother came back to us to inform us that she was released from the hospital and was feeling fine and back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: psychogenic non-epileptic seizures panic disorder anxiety
Andere Medikamente: none
Allergien: cephalosporins
Vorherige Impfungen: -

VAERS 1258029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 26.04.2021
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

Dizziness Syncope Vital signs measurement

Symptomtext

Patient did not stay and refused observation at time of vaccine. Came back 10 minutes later with reported syncopal episode after pulling off the road nearby for lightheadness. Patient taken to medical tent for observation and medical director called. VS Stable Kept until 210pm. No adverse reaction symptoms noted. Will observe for 30 minutes during second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: BCP
Allergien: NA
Vorherige Impfungen: -

VAERS 1257954

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 26.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Dizziness Heart rate decreased Hypotension Nausea Nervousness Syncope Tremor

Symptomtext

Patient became very nervous five minutes after having vaccination, fainted to the floor with body tremors, BP 81/38 P45, Resp. 18, EMT at side with nursing staff, was put on stretcher, and complained of dizziness, nausea and lightheadedness, Later BP 114/55, P67 Resp.17. Patient transferred to ER. Recovered, no medications administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1257637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: NY
Alter: 25,0
Geschlecht: F
Eingang: 26.04.2021
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: ja Erholt: nein

Anaphylactic reaction Anxiety Asthenia Chest discomfort Chills Confusional state Dizziness Dysphagia Dyspnoea Feeling cold Flushing Hyperhidrosis Hypersensitivity Hyperventilation Nausea Rash Throat tightness Tremor

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Severe, Systemic: Allergic: Rash Generalized-Mild, Systemic: Chills-Severe, Systemic: Confusion-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hyperventilation-Mild, Systemic: Nausea-Mild, Systemic: Shakiness-Severe, Systemic: Weakness-Mild, Additional Details: Patient recieved vaccination. 15 minutes later patient stated she wanted to stay a little longer with a feeling of uneasiness and muscle trembling/shaking and feeling cold. 27 minutes later patient stated she felt a sudden tightness in her chest and a shortness of breathing. Patient requested to get an epi-pen injection due to the difficulty in breathing. Patient had epi-pen injected into left thigh at 4:46 pm .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1247353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OR
Alter: 19,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 18.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Loss of consciousness Muscle twitching Seizure Tonic clonic movements

Symptomtext

Patient notified us that she has a history of a seizure disorder with stress events. They are not associated with decreased respiratory effort. Approx 3 minutes after receiving vaccination, patient's head fell back to pillow and her arms and eye lids started twitching. Dr notified and immediately came to bedside. Started monitoring VS. All vitals remained stable. Seizure went from calm, sleep state, to slight twitching, to brief tonic/clonic episodes. Total seizure time lasted about 12 minutes. Awake and comfortable with no further symptoms by 15 minutes post vaccination. Waited with Pulse ox on for another 15 then wheeled out with father and brother accompanying her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: non epileptic seizures
Vorgeschichte: GAD MDD non-epileptic seizures excema
Andere Medikamente: ferrous sulfate oral contraceptive mirtazapine melatonin loratadine duloxetine fluticasone nasal
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1251831

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 17,0
Geschlecht: F
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: ja Erholt: nein

Seizure

Symptomtext

Pt received vaccine at 306p and at 316p began to have seizure like activity for 30 seconds. VSS EMS here to assess pt, pt to ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1251126

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: TN
Alter: 37,0
Geschlecht: M
Eingang: 24.04.2021
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Bell's palsy

Symptomtext

Developed Bell?s Palsy the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: Office visit to PCP for diagnosis and treatment.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: asteline, Flonase, Allegra, omeprizole
Allergien: -
Vorherige Impfungen: -

VAERS 1248500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: MN
Alter: 18,0
Geschlecht: M
Eingang: 23.04.2021
Impfdatum: 19.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac imaging procedure abnormal Myocarditis Troponin increased

Symptomtext

Acute myocarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 2,0
Labordaten: Elevated troponin Cardiac MRI consistent with myocarditis
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1247848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: IL
Alter: 32,0
Geschlecht: F
Eingang: 23.04.2021
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

Dizziness Hyperhidrosis Loss of consciousness Pallor

Symptomtext

PASSED OUT IN THE OBSERVATION AREA ,DIZZY, SWEATY, PALE. BP72/48 LAYDOWN ,LEGS ELAVATED WITH MEDICS FOR 30 MINUTES. 9:50 AM FEELING BETTER ATE SOME FOOD AND DRINK WATER.. WENT HOME AND BP 116/72

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1247497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: MN
Alter: -
Geschlecht: U
Eingang: 23.04.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hyperhidrosis Loss of consciousness Pallor Vomiting

Symptomtext

Patient got pale, diaphoretic and pasted out for approx. 15 sec., after 5 min after getting the injection. Patient aroused. She reports that she had not eaten anything today. Given graham crackers and water for oral intake. Shortly after eating the crackers and drinking the water, patient vomited. She reports that she felt better after the emesis. Patient able left per ambulatory status, after 30 min of monitoring patient.

Weitere VAERSDATA-Felder

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

VAERS 1246600

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 25,0
Geschlecht: F
Eingang: 23.04.2021
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: ja Erholt: nein

Dizziness Hypoaesthesia Joint stiffness Seizure Vision blurred

Symptomtext

Patient Came into observation and said she felt like she was going to have a seizure, subject layed down and complained of feeling dizzy, blurry vision, stiffness and both arms are numb. Empress transported to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1243977

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 30,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Headache Loss of consciousness Myalgia Pain Pyrexia Syncope

Symptomtext

Fever, Headache, Muscle pains, Body aches, Weakness, Fainted, Lost consciousness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1241656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 32,0
Geschlecht: M
Eingang: 22.04.2021
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

Loss of consciousness Vital signs measurement

Symptomtext

Patient with a history of syncope after injections of any kind. Afraid of needles. Approximately 7 minutes post injection patient passed out in observation. LOC less than 20 seconds. Awake and oriented x3 and VS stable and within normal limits. Dr. , medical director, consulted. No further orders. Observed for 30 minutes and wife called. Patient released to self. He will bring a driver for dose 2 and let staff know he has syncope with injections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Syncope with all injections

VAERS 1241612

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 22.04.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

Tod: nein Lebensbedrohlich: nein Hospital: unbekannt Disable: unbekannt ER: nein Erholt: unbekannt

Confusional state Dizziness Fear of injection Flushing Hyperhidrosis Nausea Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Additional Details: Patient informed immunizing pharmacist of \"fear of needles\"" before vaccine was administered. Pharmacist talked to patient prior to injecting to distract her. Immediately after puncturing and prior to injecting

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Y
Aktuelle Erkrankungen: -
Vorgeschichte: PHM
Andere Medikamente: -
Allergien: 04/22/2021
Vorherige Impfungen: -

VAERS 1238587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: DE
Alter: 16,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 21.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Balance disorder Gait disturbance Loss of consciousness

Symptomtext

Patient start walking unstable after getting up from vaccination table loss consciousness after being sited on the chair but quickly regain consciousness shortly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1237710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 24,0
Geschlecht: F
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

Muscular weakness Nervousness Syncope Tremor

Symptomtext

Patient denied symptoms during 15-minute required observation period. When she got up from chair to pick up vaccination card, endorsed near-syncope and bilateral lower extremity weakness like "she felt she was walking in sand." Denies visual symptoms, oral swelling, dyspnea, pruritis, nausea. Patient sat back down and was attended to. She was noticeably nervous (hand/leg shaking). SpO2 99%, HR 62. Patient endorses history of anxiety that is treated with beta blocker. Patient felt back to her baseline after approximately 15 additional minutes of rest and sipping on water. Trial of ambulation at that time with complete resolution of symptoms. She was cleared to return to work with return precautions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1237357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 21,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 20.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chills Electrocardiogram Eye injury Laboratory test Pyrexia SARS-CoV-2 test negative Syncope

Symptomtext

chills, 102.9 fever, syncopal event, laceration above left eye

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG, labs, COVID-19 PCR test-all negative 6 stitches
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1237248

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MN
Alter: 18,0
Geschlecht: F
Eingang: 21.04.2021
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: nein

Anxiety Malaise Syncope Vital signs measurement

Symptomtext

Within minutes of pt receiving covid vaccine, verbalized to 'not feel well' and fainted. A friend and staff members gently assisted pt to the floor. Immediate assessment of vital signs and pt taken to private area for monitoring. Pt may have had vasovagal response due to anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: anxiety, ADHD, depression, disordered eating
Andere Medikamente: celexa, wellbutrin XL, ritalin
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1233019

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NH
Alter: 17,0
Geschlecht: F
Eingang: 20.04.2021
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

Dizziness Syncope

Symptomtext

Transient lightheadedness with brief syncope. Subsequent NV controlled with position of comfort. Patient had not eaten anything today and had only coffee so far. Pt was given fruit, muffin and water and was monitored for an additional 45 minutes with continued improvement and no other symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1232217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 19,0
Geschlecht: M
Eingang: 20.04.2021
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

Dizziness Hyperhidrosis Presyncope

Symptomtext

POST VACCINE, PATIENT HAD NEAR SYNCOPAL EPISODE, S/S WERE DIZZINESS, DIAPHORESIS, LIGHTHEADEDNESS. BROUGHT BACK TO OBS VIA WC. ASSISTED TO STRETCHER TO LAY DOWN. REPORTED S/S RESOLVED AFTER A FEW MINUTES. VSS. ESCORTED TO EXIT WITH NO ISSUES AT 1537. 1526 LYING BP 127/70 HR 60 RR 16 SATS 99% RA 1533 SITTING BP 136/76 HR 58 RR 16 SATS 100% RA 1535 STANDING BP 125/75 HR 68 RR 18 SATS 99% RA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1231335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 19.04.2021
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: ja Erholt: nein

Asthenia Blood glucose normal Depressed level of consciousness Feeling abnormal Hyperhidrosis Hypoaesthesia Loss of consciousness Nausea Pallor

Symptomtext

1735 Pt reported nausea to obs staff. RN responds as pt loses consciouness x3-5 sec. Regains consciousness, but is weak, pale, diaphoretic. Other 2 RN's respond, help pt to right side on cot. Semi-conscious, reponds to verbal. States she "feels bad." 1737 BP 80/40, P26-55, R14, O2 100%. 911 called. Next door (clinic backup) MFD ALS crew x4 on scene at 1740. Care turned over. BP 68/37, P66, R14, O2 100%, bl gluc 105. 1747 Pt more alert, but still weak and pale. IV access by medic in right arm. IVF wide open. 1750 BP 96/53, P 67, R16, O2 100%. Pt eyes now open, talking, pink lips. Pt. reports her right hand/arm feel numb (vacc inj side). 1755 BP 99/58, P 64, R 16, O2 100%. Transport by amb to ER at 1755.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: blood glucose finger stick = 105 IV fluid ~500cc infused prior to transport
Aktuelle Erkrankungen: "covid longhaulers"
Vorgeschichte: history of eating disorder, covid longhaulers: migraines, nausea, fatigue, decreased appetite
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1231174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: GA
Alter: 31,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Feeling abnormal Palpitations Syncope Visual impairment

Symptomtext

Patient with light headed feeling, heart palpitations, Feels dazed and syncopal. Stated visual defect present. VS stable. EMS called for consultation. Evaluated. Orange juice given and pretzels. Released to family after refusing transport to local healthcare facility. Patient will eat before dose 2 in 21 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: PCN and Amoxcillin
Vorherige Impfungen: -

VAERS 1230433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 21,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Asthenia Dizziness Laboratory test Loss of consciousness Malaise Nausea Pallor Pregnancy test urine negative Seizure like phenomena Syncope Urinary incontinence Vomiting

Symptomtext

WEAKNESS, NAUSEA, VOMITING, SYNCOPE WITH URINARY INCONTINENCE. DESCRIBED FEELING WEAK AND NOT GOOD BEING UP EVERY HOUR WITH NAUSEA. WOKE UP AT 7AM, VOMITED AND PASSED OUT ON BATHROOM FLOOR WITH INCONTINENCE OF URINE. ROOMMATE DESCRIBED SEIZURE LIKE ACTIVITY WHILE PT WAS ON THE FLOOR. PALLOR. DIZZINESS. PT GIVEN 1L NS, CT SCAN AND LABS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NEGATIVE URINE PREGNANCY. UNCERTAIN OF OTHER LAB RESULTS AT THIS TIME.
Aktuelle Erkrankungen: None
Vorgeschichte: UNKNOWN TO WRITER
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1229858

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 16,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Dizziness Presyncope Syncope

Symptomtext

Patient with near syncope, provided juice, ice pack and rest, continued to feel dizzy, moved to the cot to lay down, then a syncope episode occurred, Medics on site, transfer to local Emergency Department via squad. Vital Signs: B/P 120/73 P: 103 R: 18 Pulse ox: 100%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None at the School Location
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None on file at this time
Allergien: No allergies to any medications or foods
Vorherige Impfungen: -

VAERS 1229809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 45,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Abdominal pain upper Anaphylactic reaction Asthenia Blood glucose increased Blood pressure increased Chest pain Chills Cough Dizziness Dysphonia Fatigue Gait disturbance Heart rate increased Hyperacusis Injection site bruising Injection site pain Nausea Pollakiuria

Symptomtext

15 minutes after the injection I had an intense allergic/anaphylactic reaction. I was watched and treated on site by EMS for 2 hours with Benadryl, oxygen and rest. We did not use epi because I was still able to breath (minus some wheezing, coughing, hoarseness and lung irritation). I felt the reaction hit when I started seeing green spots and my vitals dramatically increased (BP 181/111, HR 142 and weak). I then experienced the following symptoms: rash/hives on neck and chest, fatigue and weakness, dizzy and lightheaded and needed wheelchair for moving around, chills and shaking, blurry vision, nausea, stomach pain, headache, chest pain and increased urination. I also had elevated glucose (147). During those two hours my vitals decreased a little, but the rest of my symptoms persisted. I was not getting better and my vitals started to increase again at the two hour mark so EMS called an ambulance and transported me to hospital. I was treated with solumedrol and observed for several hours. The meds helped enough to send me home. (I did have to continue taking Benadryl at home that night and the next day because I continued to have an allergic response). I also had severe injection site pain and bruising.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Chiari malformation, dysautonomia, Ehlers-Danlos syndrome, Mast Cell Activation Syndrome, polyneuropathy, autoimmune disease, migraines
Andere Medikamente: Zyrtec, pepcid, zafirlukast, LDN
Allergien: Singulair, regadenoson, gabapentin, topamax, iv contrast
Vorherige Impfungen: -

VAERS 1229678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 30,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
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 Syncope

Symptomtext

POST VACCINE, PATIENT LOST CONSCIOUSNESS FOR ABOUT 30 SECONDS PER SIG OTHER. ASSISTED TO FLOOR, PLACED ON STRETCHER IN TRENDELENBERG AND TAKEN TO OBS AT 1315. PATIENT STATES S/S RESOLVED ONCE ARRIVING TO OBS. VSS AND MAINTAINED UNTIL STANDING POSITION. PER ON SITE MD, PT EXPERIENCED CLASSIC SYNCOPAL VASOVAGAL REACTION- RESOLVED. PATIENT RELEASED WITH NO ISSUES AT 1330. 1320 INITIAL BP 154/89 HR 74 SATS 97% RA 1325 SITTING BP 150/78 HR 80 SATS 98% RA 1330 STANDING BP 139/87 HR 80 SATS 99% RA

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 1229442

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 19.04.2021
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: unbekannt

Hyperhidrosis Loss of consciousness

Symptomtext

Patient passed out in observation area, another patient called out for assistance. Patient appeared diaphoretic, bp 85/50. I have patient water and observed him for an additional 15 mins afterward. Retook blood pressure, 110/78. patient awake, talking to father. States he "feels much better".

Weitere VAERSDATA-Felder

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

VAERS 1225396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 28,0
Geschlecht: F
Eingang: 18.04.2021
Impfdatum: 18.04.2021
Beginn: 18.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Discomfort Dysphagia Gaze palsy Seizure Unresponsive to stimuli Visual impairment

Symptomtext

Patient presented to clinic today for 1st Covid vaccine. After receiving vaccine, patient complaining of seeing "colored spots". Patient brought to reclining chair from waiting room. Patient has multiple comorbidity's - please see list in CMR. Patient's aunt in room with patient. 0807: Patient c/o having a "heavy face". VS 159/98, 89, 96% on RA. Patient denies any issues with breathing. Per patient when she swallowed some water, she felt as if it was hard to get down. Patient given 50 mg PO Benadryl (own supply). 0811: Patient stating that colored spots are now gone. VS: 169/95, 87, 98% on RA. 0817: VS 133/90, 96, 93%. Patient had small seizure in room; patient eyes rolled back, patient appeared to be non-responsive. Total time for seizure was approximately 30 seconds. After seizure, patient responsive and alert X3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: Blood Pressure
Aktuelle Erkrankungen: Obesity Hypercholesterolemia and hypertriglyceridemia PCOS. Patient was treated with Metformin Dysmenorrhea. Menometrorrhagia Major depression. Anxiety Dysautonomia. Migraines Conversion disorder Photophobia Chronic pain (has tried morphine, HYDROcodone, oxyCODONE, traMADol, lyrical and Cymbalta in the past) Hypothyroidism, subclinical and history of thyroid nodules Seronegative inflammatory arthritis/seronegative RA versus psoriatic arthritis. Fibromyalgia. Raynaud's. Degenerative arthritis of the LS spine, L5-S1 spondylolisthesis. Chronic sinusitis Allergic rhinitis. Esophageal spasms. History of Vitamin D deficiency. Eczema History of POTS History of pulmonary nodule (10/2015) History of microscopic hematuria (2015) Gait disorder Paresthesias bilateral legs Hidradenitis suppurativa (seen by Dermatology) Vertigo Plantar fasciitis (see by Podiatry)
Vorgeschichte: Obesity Hypercholesterolemia and hypertriglyceridemia PCOS. Patient was treated with Metformin Dysmenorrhea. Menometrorrhagia Major depression. Anxiety Dysautonomia. Migraines Conversion disorder Photophobia Chronic pain (has tried morphine, HYDROcodone, oxyCODONE, traMADol, lyrical and Cymbalta in the past) Hypothyroidism, subclinical and history of thyroid nodules Seronegative inflammatory arthritis/seronegative RA versus psoriatic arthritis. Fibromyalgia. Raynaud's. Degenerative arthritis of the LS spine, L5-S1 spondylolisthesis. Chronic sinusitis Allergic rhinitis. Esophageal spasms. History of Vitamin D deficiency. Eczema History of POTS History of pulmonary nodule (10/2015) History of microscopic hematuria (2015) Gait disorder Paresthesias bilateral legs Hidradenitis suppurativa (seen by Dermatology) Vertigo Plantar fasciitis (see by Podiatry)
Andere Medikamente: Acetaminophen Acetaminophen **Office Administered** Albuterol Sulfate (Ventolin HFA?) Inhalation Aluminum Hydroxide-Magnesium Carbonate (Gaviscon?) AmLODIPine ARIPiprazole Benzoyl Peroxide Topical BuPROPion HCl (Wellbutrin SR?) Calcium Carb
Allergien: Amitriptyline: Muscle cramps ?Duloxetine (Cymbalta?): Aggressive behavior, adult ?Hydrochlorothiazide: Hives / by patient history ?HYDROcodone-Acetaminophen: Auditory hallucinations; Visual hallucinations ?Penicillin: Itching; Rash ?PredniSONE: Rapid heart rate; Irritability / by patient history ?Pregabalin (Lyrica?): Weight gain, abnormal ?Venlafaxine: Mood swings Non-Drug Allergies/Adverse Reactions: ?Cats: Sneezing; Runny nose ?Cayenne pepper: Rash / by patient history / Also capsaicin ?Dogs: Hives / by mother's report ?Nuts: Hives; Wheezing ?Ragweed: Stuffy nose; Runny nose ?Walnuts: Hives; Rash
Vorherige Impfungen: -

VAERS 1223444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 51,0
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

Dizziness Hyperhidrosis Loss of consciousness

Symptomtext

3 MIN POST VACCINE PT BECAME SWEATY AND DIZZY. PT WAS ASSISTED TO FLOOR BY STAFF. WHILE LYING ON THE FLOOR, PT EXPERIENCED LOC FOR 3 SEC. TRANSPORTED TO MED OBS VIA STRETCHER AT 1300. SIGNIFICANT OTHER AT BEDSIDE. PT PLACED IN A REVERSE TRENDELENBERG POSTION. VITALS OBTAINED AND MONITORED THROUGHOUT. VSS. PT REPORTS FEELING DIZZY AND LIGHTHEADED. WATER AND SALTINE CRACKERS GIVEN. PT SLOWLY TRANSITIONED TO A SITTING AND THEN STANDING POSITION. ALL SYMPTOMS RESOLVED. PT RELEASED WITH SIGNIFICANT OTHER AT 1334. ESCORTED TO EXIT WITH STAFF, NO FURTHER ISSUES. VITALS AS FOLLOWS: 1301 BP 151/78 HR 82 SPO2 98 1306 BP 147/98 HR 69 SPO2 99 1311 BP 137/89 HR 70 SPO2 99 1321 BP 142/91 HR 62 SPO2 99 1331 SITTING BP 139/92 HR 71 1333 STANDING BP 141/98 HR 71 SPO2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: HASHIMOTO DX
Andere Medikamente: NONE
Allergien: NKA
Vorherige Impfungen: -

VAERS 1223045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
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 / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Fatigue Immediate post-injection reaction Loss of consciousness Nausea

Symptomtext

Immediately following vaccination pt felt like he was going to pass out. Pt experienced LOC in the chair with significant other at side. Pt was safely lowered to floor by staff. Pt regained consciousness while on floor. Per staff LOC duration was 10 sec. Pt then transported to med obs at 0943 via stretcher. Pt reports dizziness and nausea. Pt placed in reverse trendelenburg position. Pt was slowly transitioned to a sitting position. Water and goldfish given. Nausea returned. Pt back to lying position. Pt feeling better and again slowly transitioned to a sitting and then standing position. Pt reports feeling fatigued but all other symptoms resolved. Pt released to home with significant other driving at 1054. Pt escorted to exit by staff and significant other with no further issues. Vitals as follows: 0945 BP 128/78 HR 57 SPO2 99 0950 BP 134/82 HR 56 SPO2 100 0955 BP 124/82 HR 76 SPO2 100 1002 BP 129/85 HR 62 SPO2 99 1001 BP 126/85 HR 64 SPO2 100 1015 SITTING BP 131/74 HR 69 SPO2 100 1030 SITTING BP 134/87 HR 73 1050 STANDING BP 121/82 HR 80 SPO2 100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: SULFA DRUGS
Vorherige Impfungen: -

VAERS 1220209

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Syncope

Symptomtext

Patient had a syncopal episode approximately 5 minutes after receiving COVID 19 vaccine. Patient was immediately placed on gurney. Syncopal episode lasted approximately 10 seconds. Patient was under medical supervision the entire time and did not hit his head. Initial vitals signs were: BP 110/70, pulse 55, O2 100%. paramedics did arrive on scene and evaluate the patient. Patient felt much better and refused transport to ER. Patient signed out AMA with paramedics. Note: Patient admitted to history of syncopal episodes in the past during previous blood draws and vaccine administrations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1220094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NC
Alter: 28,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Eye movement disorder Feeling abnormal Loss of consciousness Muscle twitching Seizure Vomiting

Symptomtext

patient sitting in post-vaccination area has a witnessed seizure at 1525, patient had twitching, LOC and eye rolling. EMT and RN were there and observed. Patient returned to consciousness, and moved behind curtin. Patient had another witnessed seizure @ 1532 lasting 10 seconds, with LOC, twitching, eyerolling and vomiting. Patient came to and placed on floor, alert and awake, able to answer questions but feeling foggy. EMS was called during 1st seizure. EMS arrived and took patient to hospital @ 1558.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1219735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 37,0
Geschlecht: F
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 Fall Head injury Syncope

Symptomtext

Syncope, dizziness; Pt hit her head on the stairs. No open wounds, neuro check wnl. BP 93/69; HR 65 RR 17 SpO2 100%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1219698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 21,0
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 Fall Flushing Head injury Hyperhidrosis Pallor Syncope

Symptomtext

Syncope, flushing/sweating. Another pt witnessed pt fall and hit his head on doorway, no LOC. Pt A&O x3, but dizzy/sweaty/pale. RN assisted pt on wheelchair to obs tent + provider called. VS initially 84/45. BP improved, pt pupils + neuro checked by provider. Given multiple PO fluids + crackers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1218975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MO
Alter: 64,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Syncope

Symptomtext

Minutes after vaccination patient became syncopal, clinical team was nearby, patient difficult to rouse. EMS responded. HR was 36, BP 60/30, patient was responsive but within a few minutes had an additional syncopal episode. Patient was responsive again, bp was 85/40, Blood sugar was normal, EMS set up IV line and monitored patient briefly. HR recovered to 80, and BP e179/50. 12 lead administered, but unclear. Patient was transported by EMS to Emergency Room for further assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1218897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 51,0
Geschlecht: F
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

Anxiety Blood pressure measurement Cold sweat Feeling cold Heart rate Paraesthesia Respiratory rate Syncope Vital signs measurement

Symptomtext

Clammy, tingling in bilat hands, anxiety. Pt stated she fainted before - feels cold, clammy beforehand. She felt this way w/ bilat tingling & called for nurse. A&O x4. Vitals stable. Gave water - hasn't drank since 10 AM. After drinking water, pt stated she is feeling better. Offered w/c for exit, declined. Vitals still stable. Pt left Yahoo in stable condition. BP 123/63; HR 72; RR 18, SpO2 97%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Hydrocodone-Vomiting
Vorherige Impfungen: -

VAERS 1218765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: OH
Alter: 18,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Cold sweat Fall Head injury Headache Loss of consciousness Paraesthesia

Symptomtext

Patient recieved vaccine without any issues on 4/16/21. Patient walked to waiting area with pharmacist, was not having any issues or concerns, and was observed for several minutes by the RPH. Approximately 5 minutes after receiving the COVID-19 shot, the patient passed out, fell out of his chair, and hit his head. The patient immediately regained concousness and sat back in his chair. The RPH immediately had a pharmacy associate call 911 and observed the patient. Patient stated he felt a liquid tingle go down his arm from where he received his vaccine then passed out. Patient stated he had a headache and appeared clammy. RPH provided an instant ice pack and observed patient until EMS arrived. EMS provided care to patient and determined he did not need to go to the hospital. Patient was advised to go to hospital if he becomes nauseus. Patient claimed he was okay and just has a headache. Patient's mother took him home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Anxiety, SAD
Andere Medikamente: Abilify, Buspar, Effexor, Vitamin D
Allergien: none
Vorherige Impfungen: Gardisal - syncope at age 13

VAERS 1218607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 28,0
Geschlecht: F
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

Loss of consciousness Syncope

Symptomtext

Patient received vaccine and proceeded to observation area. While patient was sitting she had a brief episode of syncope but quickly regained consciousness. Patient was place on the floor to lay down and given juice. She stated that she felt much better almost right away. We observed her for 20-30 minutes until the patient felt well enough to leave on her own.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None known.
Vorgeschichte: Unknown.
Andere Medikamente: Aviane 0.1-20 mg/mcg tablets (one daily) Metronidazole 500 mg tablets (twice daily for 7 day total duration, day 6 of 7 at time of immunization)
Allergien: No known drug allergies.
Vorherige Impfungen: Patient has experience syncope before with blood draws.

VAERS 1218361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 28,0
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

Heart rate irregular Hyperhidrosis Pulse absent Syncope

Symptomtext

Patient had syncopal episode with out loss of consciousness. Patient became diaphoretic with a palpable irregular heart rate. He was closely observed and placed in a laying position with his feet elevated. Biox was 99% with an irregular HR of 78. Patient recovered to his baseline in approximately 45 minutes and left the facility with his driver and recommendations to follow up with urgent care and to contact his healthcare provider.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Recommendation to follow up with his healthcare provider and or to see an urgent care as soon as possible; this recommendation was well received by his driver who was a relative and by the patient.
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: Unknown.
Andere Medikamente: None indicated on patient record.
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 1215577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 36,0
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

Dizziness Feeling abnormal Loss of consciousness

Symptomtext

Pt felt light headed and warm several minutes after the vaccine. She has passed out with blood draws in the past and says her symptoms now are similar to previous episodes. Transported to med obs at 1500. Pt given water and crackers and almost immediately feels better. Pt released to home by self via public transportation at 1522. Vitals as follows: 1500 BP 135/91 HR 85 SPO2 98 1505 BP 125/80 HR 91 SPO2 98 1510 BP 125/80 HR 82 SPO2 99 1515 SITTING BP 125/84 HR 85 SPO2 100 1520 STANDING BP 150/88, 124/79 HR 93 SPO2 100

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: ORAL CONTRACEPTIVE
Allergien: NKA
Vorherige Impfungen: -

VAERS 1215142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 23,0
Geschlecht: M
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

Consciousness fluctuating Dizziness Nausea Seizure like phenomena Sneezing Vomiting

Symptomtext

Post vaccine pt experienced multiple sneezes and became lightheaded. Pt assisted to floor by staff. Transported to med obs at 1300 via stretcher. Vitals obtained and monitored. While in med obs pt became nauseated and had several episodes of emesis. Water and saltine crackers given. All symptoms resolved. Pt released to home by self at 1405. After pt was released, med obs staff was informed by vaccinator that pt appeared to have seizure like activity after vaccine was given. Pt was then in and out of consciousness and was assisted to the floor at that time. Vitals as followed: 1303 LYING BP 115/64 HR 61 RR 12 SPO2 94% 1310 LYING BP 123/59 HR 63 RR 12 SPO2 96% 1314 LYING BP 102/45 HR 86 RR 14 SPO2 95% 1322 LYING BP 113/59 HR 65 RR 14 SPO2 95% 1337 SITTING BP 93/66 HR 67 RR 14 SPO2 97% 1339 SITTING BP 115/67 HR 74 RR 14 SPO2 96% 1343 STANDING BP 108/66 HR 69 RR 14 SPO2 96% 1354 STANDING BP 132/65 HR 64 RR 14 SPO2 97%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: asthma, depression, anxiety
Andere Medikamente: singular, buspar, lexapro
Allergien: seasonal allergies
Vorherige Impfungen: -

VAERS 1214517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 72,0
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

Anxiety Dizziness Heart rate increased Hypertension Nausea Panic reaction Presyncope Tunnel vision

Symptomtext

Immediate warmth, dizziness, mild nausea, and progession to tunnel vision after her shot. She had a sensation of rapid heart beat with a normal range pulse here in observation. She was very anxious and hesitant to come for the vaccine. BP was initially high for her, 162/87, with a pulse of 79. Normal O2 sats. BP improved with observation. Classic Anxiety/Panic symptoms with mild vasovagal symptoms. All resolved. patient to exit with wheelchair and staff

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1214495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 17,0
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: ja Erholt: ja

Blood glucose normal Electrocardiogram normal Immediate post-injection reaction Presyncope

Symptomtext

Client had vasovagel response immediately after she stood up from getting the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: EKG was performed in the ER, along with labs (mom unaware of which labs that were done). EKG appeared to be normal. Blood sugar was 106, O2 level was at 99%, client was given fluids.
Aktuelle Erkrankungen: No
Vorgeschichte: Previous vasovagel response that happened in school once.
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1213520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 17,0
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

Dizziness Eye movement disorder Hyperhidrosis Loss of consciousness

Symptomtext

Dizziness, mild sweating, and a temporary loss of hearing a few minutes after the shot before brief LOC. Mother reported "eyes rolling up" and a respiratory gasp. Rapid recovery with fully orientation on the floor. VS stable in observation. No nausea or visual changes reported by the patient. No orthostasis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None needed
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1213390

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: CA
Alter: 34,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Confusional state Hyperhidrosis Loss of consciousness Myoclonus

Symptomtext

Pt lost consciousness approximately 2 minutes after vaccine with full body myoclonic jerks for 30 second duration. Pt had confusion for 10 minutes, HR 50 bpm, diaphoretic. Pt transported to ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Syncope Possible seizures
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 1213103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 61,0
Geschlecht: F
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Electrocardiogram normal Hyperhidrosis Syncope

Symptomtext

Within 15 minutes of vaccination, patient became diaphoretic. Shortly after, had syncopal episode and was taken to urgent care for EKG evaluation. No abnormal findings, and patient was discharged in alert, stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG (normal)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1213031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 22,0
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

Deafness Dizziness Feeling hot Presyncope

Symptomtext

Warmth, dizziness, temporary loss of hearing shortly after vaccination. No nausea, diaphoresis, or tunnel vision. Near syncope prevented by lying down quickly. Typical vasovagal reaction for her. Rapid recovery with all normal vital signs. No orthostasis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None needed
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1212841

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 29,0
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

Dizziness Hyperhidrosis Nausea Presyncope

Symptomtext

Pre vaccine pt reports being anxious. Post vaccine pt developed nausea, dizziness, and became sweaty. Pt transferred to meds obs at 0939 via wc, accompanied by significant other. Vitals obtained and monitored. Symptoms resolved. Per on site physician pt experienced classic non syncopal vasovagal reaction - resolved. Pt released home with significant other at 1007. Vitals as follows: 0940 Lying BP 106/71 HR 67 RR 16 SPO2 100 0948 Sitting BP 102/71 HR 64 RR 18 SPO2 100 0956 Standing BP 96/56 HR 79 RR 18 SPO2 98 (asymptomatic)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: anxiety, depression, vasovagal reaction, adhd
Andere Medikamente: adderall, klonopin
Allergien: nka
Vorherige Impfungen: -

VAERS 1212774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

schwer

Staat: PA
Alter: 48,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Nausea Presyncope

Symptomtext

Post vaccine pt developed dizziness, nausea and became sweaty. Pt transferred via wc and arrived to obs at 0905. Vitals obtained and monitored. Symptoms resolved. Per physician, pt experienced classic non syncopal vasovagal reaction - resolved. Pt released to home by self at 0920. Vitals as follows: 0909 Lying BP 123/83 HR 67 RR 20 SPo2 96 0915 Sitting BP 134/84 HR 67 RR 18 SpO2 99 0916 Standing BP 119/83 HR 70 RR 18 SpO2 98

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: vasovagal syncope
Andere Medikamente: vytorin, zyrtec
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1212663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: PA
Alter: 17,0
Geschlecht: M
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

Dizziness Hyperhidrosis Nausea Presyncope

Symptomtext

Post vaccine pt became dizzy, sweaty and experienced nausea. Pt transferred to med obs. Accompanied by parents. Pt reports immediately feeling better after lying down on stretcher. Vitals obtained and monitored. Per on site physician - pt experienced classic non syncopal vasovagal reaction - resolved. Pt released at 0857 with parents. Vitals as follows: 0845 LYING BP 120/83 HR 65 RR 18 SpO2 97% 0840 SITTING BP 113/67 HR 78 RR 18 SpO2 100% 0850 STANDING BP 130/75 HR 93 RR 18 SpO2 96%

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: nka
Vorherige Impfungen: -

VAERS 1212316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 26,0
Geschlecht: M
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: unbekannt Erholt: ja

Presyncope

Symptomtext

patient had vasovagal reaction post vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: trendelburg reaction, vital signs, and oxygen saturation
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1211213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 15.04.2021
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: unbekannt

Presyncope

Symptomtext

Vasovagal. Legs elevated then proceeded to med bay. VS stable. BP 125/59; 114/60, HR 85; 77, RR 12 x2, SpO2 100% RA x2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1209342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: WI
Alter: 30,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort Anxiety Dizziness Dyspnoea Headache Hyperhidrosis Respiratory distress Wheezing

Symptomtext

Six minutes after administration of the clients second dose of BioNTech Pfizer vaccine she began to have difficulty breathing and audible wheezing. She reported GI upset, headache, feeling dizzy, and impending doom. She self-administered puffs from her albuterol inhaler. Pulse ox remained above 97% , pulse 113, BP- 160/100. EMS was activated. Epi 0.5mg administered into left deltoid at 12:25 pm. Transferred client from chair to floor without difficulty. Continued to experience respiratory distress and became diaphoretic. Administered second dose epinephrine 0.5mg to left vastus lateralis at 12:30pm. Fire and Rescue arrived at 12:33pm. Transferred client to ED via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma
Vorgeschichte: Asthma
Andere Medikamente: -
Allergien: Imitrex, aspirin, & mushrooms Patient reported liver and kidney failure with large amounts of aspirin consumption.
Vorherige Impfungen: While client was supine on floor, she stated that she did not tell the truth about feeling ill after her first dose of the Pfize

VAERS 1208536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: MI
Alter: 16,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Blood glucose Seizure

Symptomtext

had a seizure shortly after receiving his first dose of Pfizer Covid 19 vaccine. After EMS arrived they performed a fingerstick to check blood sugar and he had another seizure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1207785

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 31,0
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

Hypotension Syncope

Symptomtext

Patient had syncopal episode post vaccine, and was hypotensive

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Trendelburg position and vital signs
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1207768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

schwer

Staat: NY
Alter: 50,0
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: ja Erholt: nein

Dizziness Hyperhidrosis Laboratory test Syncope

Symptomtext

Patient had a syncopal episode post vaccine, as well as dizziness, diaphoresis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Labs
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperlipidemia, GERD, seizures
Andere Medikamente: atorvastatin, calcium carbonate, metoprolol ER, Lovaza, pantoprazole, famotidine, Colace, diclofenac, Trileptal
Allergien: Lactose
Vorherige Impfungen: -

VAERS 2723149

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 44,0
Geschlecht: F
Eingang: 12.12.2023
Impfdatum: 21.04.2021
Beginn: 08.01.2022
Tage bis Beginn: 262,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

C-reactive protein increased COVID-19 pneumonia Fibrin D dimer increased Surgery

Symptomtext

Received vitamin C, antibiotics, decadron, Lovenox, and zinc. COVID-19 pneumonia patient not requiring any oxygen. But in the light of elevated CRP and D-dimer will start her on Lovenox and steroids. Cleared Lovenox with Dr since patient's less than 24 hours after surgery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2710737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 49,0
Geschlecht: M
Eingang: 07.11.2023
Impfdatum: 20.04.2021
Beginn: 07.12.2021
Tage bis Beginn: 231,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Atrial flutter COVID-19 pneumonia Cough Dyspnoea Fatigue Myalgia Sepsis

Symptomtext

Presented with fatigue, myalgies, cough and dyspnea ; patient was diagnosed with sepsis due to COVID pneumonia , And treated with remdesivir and dexamethasone ; patient initially required 15 O2 for adequate oxygenation , and was also seen by Pulmonary and Critical Care Service ; patient had 1 episode of atrial flutter which has resolved by discharge , and no further intervention needed per Cardiology . By discharge, patient was breathing much better , has Much Less Cough , and down to 1 L oxygen to maintain adequate oxygenation with ambulation .

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2697727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 49,0
Geschlecht: M
Eingang: 18.10.2023
Impfdatum: 07.05.2021
Beginn: 10.11.2021
Tage bis Beginn: 187,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia COVID-19 pneumonia Cough Diarrhoea Dyspnoea Procalcitonin Pyrexia SARS-CoV-2 test positive Sepsis

Symptomtext

to ED c/o SOB, weakness, fever, cough, diarrhea; + COVID pneumonia and sepsis, TX: zithromax, merrem, remdesevir, Vit C, Zinc, Singulair, Solu-medrol, lovenox, O2 15 lpm, abx stopped d/t procalcitonin less than 0.25.; upon discharge home, O2 decrease 2 lpm

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2696832

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 45,0
Geschlecht: M
Eingang: 16.10.2023
Impfdatum: 18.08.2021
Beginn: 19.08.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Dyshidrotic eczema Eczema Inflammation

Symptomtext

Extreme full body eczema flare up that lasted about five months. Treated with oral prednisone which unusually did not help subdue the inflammation. Severe dyshidrosis on hands, feet, and legs which has been an ongoing condition

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma and eczema
Andere Medikamente: -
Allergien: eggs
Vorherige Impfungen: -

VAERS 2679579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 06.09.2023
Impfdatum: 21.04.2021
Beginn: 22.12.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Blood lactic acid C-reactive protein COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Fibrin D dimer normal Lung opacity Mental status changes Oxygen saturation decreased Procalcitonin SARS-CoV-2 test positive White blood cell count normal

Symptomtext

presented with altered mental status and SOB; positive for COVID-19 pneumonia;CXR revealed bilateral opacities subjectively they are mild in nature. admitted to the hospital and was noted to have drop in oxygen saturation up to 86% on ambulation. Labs: D-Dimer was negative, serum WBC negative, lactic unremarkable. CRP 6.35, Procal 0.07 Tx: IV dexamethasone and remdesivir, also rec'd maxipine, Vit C, Lovenox, Singulair, and zind. His oxygenation has improved; room air at d/c.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2668577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 70,0
Geschlecht: M
Eingang: 09.08.2023
Impfdatum: 14.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 48,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arrhythmia supraventricular Dizziness Echocardiogram Electrocardiogram Electrocardiogram ambulatory abnormal Nervousness Palpitations Ventricular extrasystoles

Symptomtext

PALPITATIONS, NERVOUSNESS, DIZZINESS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia supraventricular
Hospital-Tage: -
Labordaten: CARDIOLOGY EVALUATION, ECHOCARDIOGRAPHY, MULTIPLE ECG'S HOLTER MONITOR DEMONSTRATING LOW ATRIAL BASELINE RHYTHM HIGH PVC BURDEN
Aktuelle Erkrankungen: PROSTATE CA, MS, HTN
Vorgeschichte: PROSTATE CA, MS, HTN
Andere Medikamente: PRAVASTATIN, LISINOPRIL, HCTZ
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2659640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: SC
Alter: 48,0
Geschlecht: F
Eingang: 23.07.2023
Impfdatum: 23.07.2021
Beginn: 23.07.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Ageusia Amnesia Anosmia Balance disorder Blood test Brain fog Burning sensation Chills Cognitive disorder Computerised tomogram Computerised tomogram head Cough Deafness Decreased appetite Depression Dizziness Dyspnoea Fall

Symptomtext

I started feeling tingly shooting sensations on the right side of my face, ear, and traveled to the right side of my head after about 10 minutes of receiving the vaccine. When my husband was driving me home, I started feeling dizzy and felt like I was intoxicated and sea sick. After I got home I was extremely nauseous, dizzy and felt even more intoxicated. I laid down and rested for a while and kept feeling worse. I took a shower that evening and lost my balance and stumbled and fell down. The next morning I felt dizzy and nauseous and I called the doctor at the Express Care where I received the vaccine. They told me if I started feeling like I was having a heart attack or pass out to go to the emergency room I rested the whole weekend and felt dizzy, balance issues, nauseous and had no appetite. My head would feel hot inside but not to the touch. I woke up on Monday and my right arm and shoulder felt heavy and partially numb. The same arm that received the vaccine. I still had the dizziness, balance issues, nausea. My ears were also ringing. I was feeling shooting tingly sensations starting at my shoulder down my right arm. My appetite was basically nonexistent. My husband had to force me to eat and cook bland food. I initially missed two weeks of work after the vaccine. My heart started beating heavy and my apple watch gave me notifications that my heart rate was too low. It got down to 40 beats per minute. My oxygen saturation level also got on the low side and I felt like I could hardly breathe. I could not sleep through the night and I ended up going to cardiac emergency room on August 2nd or 3rd. They ran tests and checked for myocarditis which was negative at that time. The ER doctor told me that I had a prolonged vaccine reaction. I felt like I had symptoms of covid. I was coughing, I had chills, nausea, loss of smell and taste. My legs started shaking uncontrollably at night. I went back to Express Care and they tested my for covid which was negative and could not figure out what was going on. I started feeling pressure in my head and tingling and pain in my right side of my face around August 16th. The pressure got worse as the week went on and the right side of my head around my temple area started hurting constantly. It felt like someone hit me on the head with a baseball bat. I also started feeling what we figured out to be brain fog. I went to my family doctor ( at Facility. He had me go do bloodwork. I went back to Express Care on August 22nd with the head pressure and pain and numbness and shooting sensations in my right shoulder/arm and I had the tingling sensations shooting through the right side of my face. The pain was so excruciating that I was in tears. They advised me to go to the ER because they were worried about a possible stroke. My husband drove me to ER downtown the evening of August 22nd 2021. They did blood tests and I had a CAT scan of my brain. They gave me IV medications for the head pain and medication for the extreme nausea. The ER doctor advised me to go the a neurologist for further testing. The next day I felt my vision had changed and my hearing was sometimes fading out. The brain fog was intense. My brain also started feeling like it was on fire. The fire in the brain feeling has not subsided since. It happens every day 24 hours a day. The ER doctor advised me to go to a neurologist to follow up and do more testing. I went to Neurological Clinic a day later. Dr. ordered MRI of my brain and neck. Dr. told me that I had a reaction to the vaccine. He had patients that had similar symptoms but had had covid (which is now known as long covid). So essentially I had suffered long covid from the vaccine. (which was not known at that time) My health deteriorated from there. I have not worked full time since. I was out of work from September through December of 2021. My family doctor told me he could not help me and referred me to specialty doctors. I have been going to every type of specialty doctor and alternative medicine doctors and providers for relief since then. One of my doctors told me I had neural inflammation due to vaccine because of the symptoms of brain fog, dizziness and brain on fire that I had not ever had previous to the vaccine. My quality of life has been significantly altered. I could not follow simple instructions to heat a microwave lunch for my son. I could not cook anything. I could not even read correctly. When I would try to read a book or article, my brain would guide my eyes to read from right to left. I could not remember what I had just read. I would read over and over again the same paragraph and the information would just not stick in my head. I could not do simple math. I could not form sentences. I felt like I had dementia. I still have a hard time processing and absorbing information and reading. My short term memory is almost non existent. I had to try hard to remember how to take a shower and dress myself and I could not work due to the tremendous brain fog and dizziness. I could not drive. I had to live with my mother in law and have her and my sister in law take care of me during the day since my husband had to work. My marriage has suffered and my son has suffered from this adverse event. I ended up having extreme depression from dealing with this horrible life altering reality. I have spent thousands of dollars trying to get better and had to have help from my family since I could not work and have been working reduced hours. I experience extreme fatigue daily and brain fog on a daily basis. I had no health issue to speak of before I received the vaccine. My daily symptoms now are almost too much to list. I went from being a healthy 48 year old mother and full time paralegal of 20 years who could do many things at one time and pretty much remember everything to all the sudden not being able to remember anything short term and feeling like I had dementia and have not been able to work full time since. Everyday feels like I am living a nightmare that keeps repeating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Cardiac ER multiple tests (August 2nd or 3rd 2021) ER CAT scan and bloodwork August 16, 2021 MRI September 1st and 3rd 2021 Facility Blood tests September 2021 Medical Care Dr., Blood testing Dr. (blood testing)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None at that time (occasional vitamin c)
Allergien: None known
Vorherige Impfungen: -

VAERS 2652944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NC
Alter: 46,0
Geschlecht: M
Eingang: 05.07.2023
Impfdatum: 07.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Atrial fibrillation Atrial flutter Cardiac ablation Cardiac stress test normal Cardioversion Computerised tomogram normal Dyspnoea Electrocardiogram abnormal Scan with contrast normal Sinus rhythm Tachycardia

Symptomtext

3 days after receiving shot 1 on 7 April 2021, I developed severe shortness of breath while doing trivial tasks. On April 13th, 2021, I went to my PCM for a scheduled appointment and told him how I was feeling. He listened to my heart and lungs and suspected I was in Afib. He confirmed his suspicions by conducting a 12 lead EKG. I was then referred to an Electrophysiologist who conducted a full work up to include stress test and CT scan with contrast. All normal. Electrophysiologist felt was an isolated incident as I had never had any heart issues prior. Worked for 25 years where my health was monitored regularly including yearly heart work ups once I turned 40 with no heart issues ever recorded. On 27 April 2021 received shot 2. On 30 April 2021 I went into Afib again with Tachycardia. Heart rate exceeded 200 BPM. Ended up in the ER of a local Hospital where I spent the weekend. Heart converted through medication to sinus rhythm on that Sunday. Decision was made to conduct cardiac ablation after continued repeated episodes of Afib with Tachycardia when treatment with Propophenon did not control. Was ablated in August of 2021 and continued treatment for the following year with Flecanide twice daily. After medication withdrawal in November of 2022 the Afib returned. Underwent 2nd Ablation in January of 2023 and it was discovered heart was continuing to make new pathways versus previous ablation reconnections. Treatment is continuing with Flecanide and Diltiazem but still having frequent episodes of Afib, severe atrial flutter, and Tachycardia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 8,0
Labordaten: Multiple EKGs, CT scans, stress tests, 2 x Ablation procedures, continued treatment with Flecanide and Diltiazem.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Celebrex, Lisinopril, Prilosec, Atrovostatin, Neurotin,
Allergien: NKA
Vorherige Impfungen: -

VAERS 2639637

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 37,0
Geschlecht: F
Eingang: 01.06.2023
Impfdatum: 27.03.2021
Beginn: 18.04.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: JET / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Back pain Chest pain Disability Fatigue Impaired work ability Laboratory test normal Loss of personal independence in daily activities Myalgia Pain in extremity

Symptomtext

Severe muscle ache, back pain , fatigue, chest pain, leg pain started after receive first dose, the pain stop. The same thing happen after the second dose and it continue. My symptoms are so severe that I am disable , struggling to do normal daily tasks, and I am unable to work.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I did so many tests and everything came back normal . My providers could not figure out what is wrong with me.
Aktuelle Erkrankungen: Grace disease/ hyperthyroidism
Vorgeschichte: none
Andere Medikamente: Prescription : Levothyroxine, methocarbamol Over the counter: tylenol, multivitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2627491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 05.05.2023
Impfdatum: 15.04.2021
Beginn: 21.02.2023
Tage bis Beginn: 677,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/21/23 presents to ED for "cough" "shortness of breath". PMHx of "COPD, CKD, GERD, obesity, diabetes"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/21/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2610478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NM
Alter: 69,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 21.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia Blood test Brain fog Decreased appetite Dehydration Dizziness Dyspnoea Fatigue Feeding disorder Feeling hot Fluid retention Lymphadenopathy Myalgia Nausea Pain Respiratory tract congestion Swelling

Symptomtext

My lymphatic system is in a state of dysfunction. I have had swelling all over my body, came on gradually to the point of it being probably 12-15 lbs of lymphatic fluid in my body. Fluctuations can be pounds daily of ever day or two. Loss of appetite, smell, tastes, desire to eat almost anything and everything. Feeling of dehydration, dizziness, fog brain, feverish with no fever, shortness of breath, fatigue, muscle, body aches, congestion of head, throat and waves of nausea.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: I have had extensive blood work, kidney ultra sound, neck ultra sound, a mammogram and breast ultra sound scheduled for this week, request for a CT scan to eliminate and tumors or c
Aktuelle Erkrankungen: no other illnesses was fine....not fine now
Vorgeschichte: CHF, Fabry disease
Andere Medikamente: -
Allergien: I do have allergies to medications, foods & flu vaccination.
Vorherige Impfungen: Flu shot vaccination in 2017

VAERS 2603036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 52,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 23.05.2021
Beginn: 01.06.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Allergy test Angiogram Asthma Blood test Chest pain Computerised tomogram Dyspnoea Investigation Magnetic resonance imaging Palpitations Positron emission tomogram Pulmonary function test Pulmonary mass Rash Tuberculin test Urticaria X-ray

Symptomtext

Chest pain; Heart palpitation; Shortness of breath; Rash/Started to face; Asthma; Nodule grew the lung; Hives; The initial case was missing the following minimum criteria: no adverse effect. Upon receipt of follow-up information on 20Mar2023, this case now contains all required information to be considered valid. This is a spontaneous report received from a 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 23May2021 at 08:00 as dose 1, single (Lot number: EW0169) at the age of 52 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "thyroid" (ongoing), notes: Thyroid; "penicillin Allergy" (unspecified if ongoing); "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19: Yes; "Cholesterol" (ongoing). Family medical history relevant to Adverse events (AES): Grandmother-Diabetes, Mom-High blood pressure, Dad-Cancer, Brother-Diabetes, High blood pressure. Concomitant medication(s) included: ARMOUR THYROID oral taken for thyroid disorder (ongoing); ATORVASTATIN oral taken for blood cholesterol (ongoing). The following information was reported: ASTHMA (non-serious) with onset 01Jun2021, outcome "not recovered"; CHEST PAIN (non-serious) with onset 01Jun2021, outcome "not recovered"; PALPITATIONS (non-serious) with onset 01Jun2021, outcome "not recovered", described as "Heart palpitation"; RASH (non-serious) with onset 01Jun2021, outcome "not recovered", described as "Rash/Started to face"; DYSPNOEA (non-serious) with onset 01Jun2021, outcome "not recovered", described as "Shortness of breath"; URTICARIA (non-serious) with onset Jun2021, outcome "not recovered", described as "Hives"; PULMONARY MASS (medically significant) with onset Jun2021, outcome "not recovered", described as "Nodule grew the lung". The events "nodule grew the lung", "chest pain", "heart palpitation", "shortness of breath", "rash/started to face", "hives" and "asthma" required physician office visit. The patient underwent the following laboratory tests and procedures: Angiogram: (28Jun2021) negative, notes: The procedure was negative; (05Nov2021) Unknown results, notes: Comments: dr. concluded not heart; Computerised tomogram: (28Jun2021) nodule showing on CAT scan; Magnetic resonance imaging: (28Jun2021) Unknown result, notes: Further test; (15Oct2021) Unknown result; Positron emission tomogram: (15Oct2022) Comments: Nodule increased; (23Jan2023) Comments: Nodule increased; Pulmonary function test: (15Oct2021) Unknown result; (15Oct2022) Unknown result; X-ray: (15Oct2021) Comments: Nodule of lungs; Blood test: (unspecified date) Unknown results; Allergy test: (unspecified date) Unknown results; Tuberculin test: (unspecified date) Unknown results; vein testing: (unspecified date) Unknown results; (unspecified date) Unknown results. Clinical course: Vaccination facility type was reported as Public health clinic. In Jun2021, after 1st vaccine started to experience chest pain, shortness of breath, heart palpitations, hives. I went to my Dr. in Jun2021 and was sent to Cardiologist. I went the tests and CAT scan. There was a nodule showing on CAT scan. I was then sent for an angiogram to determine if there were any blockages. The procedure was negative. I went back to primary care was sent to lung specialist. I went the blood tests, Allergy test, TB tests, vein testing, XRAY, MRI, CT scan, PET scan. The nodule grew the lung or felt. I should see a surgeon. Now I am schedule for a surgery 11Apr2023. I never had asthma or breathing issues. All started after vaccine. I went for two and my symptoms did not improve.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300082818 Same reporter, patient/ different dose;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Allergy test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210628; Test Name: angiogram; Test Result: Negative ; Comments: The procedure was negative.; Test Date: 20211105; Test Name: angiogram; Result Unstructured Data: Test Result:Unknown results; Comments: Comments: dr. concluded not heart; Test Name: blood tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210628; Test Name: CAT scan; Result Unstructured Data: Test Result:nodule showing on CAT scan; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: vein testing; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210628; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result; Comments: Further test; Test Date: 20211015; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result; Test Date: 20221015; Test Name: PET scan; Result Unstructured Data: Test Result:Comments: Nodule increased; Test Date: 20230123; Test Name: PET scan; Result Unstructured Data: Test Result:Comments: Nodule increased; Test Date: 20211015; Test Name: Lung test; Result Unstructured Data: Test Result:Unknown result; Test Date: 20221015; Test Name: Lung test; Result Unstructured Data: Test Result:Unknown result; Test Name: TB tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211015; Test Name: X-RAY; Result Unstructured Data: Test Result:Comments: Nodule of lungs
Aktuelle Erkrankungen: Cholesterol; Thyroid disorder (Thyroid)
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19: Yes); Penicillin allergy
Andere Medikamente: ARMOUR THYROID; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2593203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: WI
Alter: 52,0
Geschlecht: M
Eingang: 08.03.2023
Impfdatum: 21.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Arthralgia Autoimmune thyroiditis Chest pain Dizziness Dry skin Dyspepsia Dyspnoea Erythema Heart rate irregular Laboratory test abnormal Massage Muscle spasms Muscle tightness Myalgia Pain in extremity Palpitations Skin exfoliation Tendon pain

Symptomtext

Initially muscle tightness, cramping and painful tendons from wrist through shoulder. All muscle groups. That never completely subsided but was able to recover with massage. A few months later, started having irregular heart beats. Heart was racing when I was falling asleep. Had shortness of breath, difficult to describe chest pain, dizziness, digestion issues and skin issues (dry, flaky and red).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Checked with ER and found nothing irregular with heart. Went to clinic and was tested for thyroid issues. Was diagnosed with a thyroid disorder. Began taking medication. Later, was tested to determine what type of thyroid disorder I have. Found it was an auto immune disorder (Hashimotos disease).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2592254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 07.03.2023
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Bone pain Burning sensation Decreased appetite Fatigue Insomnia Laboratory test Loss of personal independence in daily activities Mobility decreased Neuropathy peripheral Pain Pain in extremity Paraesthesia

Symptomtext

THE NIGHT OF THE 1ST DOSE ON (3/26), i EXPERIENCED SEVERE BONE PAIN IN BOTH OF MY LEGS. I TOOK OVER SOME PRESCEIBED PAIN MEDICATION I HAD (VICODIN) AND IT DID ABSOLUTELY NOTHING TO RELIEVE THE PAIN. i COULD NOT FALL ASLEEP FOR MORE THAN 30 MINUTE SPURTS. i was in too much pain to eat and was just stuck in bed for 4 days. upon getting the 2nd dosage, i experienced the same pain but the severity was worse. Again, i could not fall asleep or eat. Upon getting the 3rd dosage on top of the severe joint pain, inability to fall asleep, i began to experience neuropathy (fire and pin and needles on the bottom of my both feet all day every day). as months went on, my symptoms have stayed and have increase in severity. By september 2022, both my knees, both hips and finger joints in both hands are affected with pain and now I require medication to help me fall asleep. I am constantly feeling fatigue and can't do most of the every day things I used to be able to do. Running an errand now takes twice as long and actually must plan out which errand or chores i will choose to do each day since I'm only able to do 1 each day before I end up in extreme pain at night standing on my feet too long.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: regualr lab work
Aktuelle Erkrankungen: BACK PAIN SCIATICA
Vorgeschichte: BACK PAIN SCIATICA
Andere Medikamente: TRAMADOL, GABAPENTIN
Allergien: PITTED FRUIT APPLES POMEGRANIT
Vorherige Impfungen: -

VAERS 2580412

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 10.12.2021
Beginn: 18.01.2023
Tage bis Beginn: 404,0
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

01/23/23 presents to ED for "breathing problem". PMHx of "metastatic triple negative BCA w/malignant effusion s/p thoras & L VATS"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/18/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 92,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 17.04.2021
Beginn: 25.12.2022
Tage bis Beginn: 617,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/25/22 presents to ED for "cough, SOB". PMHx of "HTN, HLD, SSS s/p PPM"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 12/25/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 11.01.2023
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia Body temperature increased COVID-19 pneumonia Dysstasia Fall Respiratory failure

Symptomtext

Patient brought to the ED by EMS on 11/2 for evaluation of a fall. The patient's wife found patient lying on the floor next to his bed, possibly down for two hours. Patient reported he rolled out of bed onto the floor. Patient was unable to get up, so EMS was called. While in the ED, he was found to have a temperature of 100.5 F and O2 sats around 89%. Additionally, his COVID PCR test came back positive in the ED. Patient was admitted 11/2 - 11/4 for evaluation of the fall/generalized weakness and mild hypoxic respiratory failure secondary to COVID-19 pneumonia. Patient was placed on 2L O2 but was quickly weaned off oxygen. He has received the primary COVID vaccine series and two boosters.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2539036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 21.12.2022
Impfdatum: 14.04.2021
Beginn: 26.09.2022
Tage bis Beginn: 530,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal lymphadenopathy COVID-19 Cardiac stress test normal Computerised tomogram thorax abnormal Cough Dyspnoea Echocardiogram normal Ejection fraction normal Hilar lymphadenopathy Hypertension Lymph node calcification Oesophagram Procalcitonin SARS-CoV-2 test positive Troponin normal

Symptomtext

This is a 72y.o. female with PMHx significant for CAD prior PCI, HTN, sarcoidosis, CHF diastolic dysfunction who presented for shortness of breath progressively worsening over the last few weeks. She endorses mild SOB at baseline and does not use supplemental O2 or CPAP at home. Endorses a dry cough. She is vaccinated against COVID and did not test positive in the past until 9/26. Recently hospitalized for HTN. States she has a hx Pulmonary embolism from early 2000s. Denies chest pain, abdominal pain, nausea, vomiting, paresthesia, fever, chills. During ED eval, chest CT showed no PE, but a bulky calcified lymphadenopathy in the hila and upper abd. Trop negative, COVID positive. procalcitonin 7.32. Admit for further eval and management. covid precautions removed 10/6 and sats stable on RA now. She completed IV decadron and Remdesivir 10/1. ID was following and completed ceftin . She has hx of Dysphagia S/p dilation on 7/21 via EGD. Esophagram showing no evidence of obstruction and Esophageal dysmotility and she is tolerating reg diet. Per cardio, CP likely due to MS in nature. ECHO with EF 55% and stress test neg with EF 70%. Psych was following and trazadone increased, continue xanax. PT/OT recommending SAR and pt agreeable. She is stable for d/c with close Op follow up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 10,0
Labordaten: 9/26 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2525619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 54,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 22.04.2021
Beginn: 22.04.2022
Tage bis Beginn: 365,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypertension Tinnitus

Symptomtext

Ongoing tinnitus and high blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Although my doctor admits to hearing the tinnitus, he claims he had not heard of any association between the vaccine and tinnitus/high blood pressure, so he has dismissed my complaints
Aktuelle Erkrankungen: Heartburn
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: Avonex prefilled syringe, RX, Esomeprazole OTC
Allergien: None
Vorherige Impfungen: -

VAERS 2512861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 48,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 18.11.2021
Beginn: 11.07.2022
Tage bis Beginn: 235,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anti-cyclic citrullinated peptide antibody Arthralgia Autoimmune disorder Blood immunoglobulin G Blood test normal COVID-19 Cough Fatigue Headache Laboratory test Lethargy Mobility decreased Oropharyngeal pain Pain in extremity Peripheral swelling Respiratory symptom Rheumatoid factor positive SARS-CoV-2 test positive

Symptomtext

It started with a sore throat. I had headaches and I got a lot of respiratory symptoms like a cough. I felt super tired and lethargic. I felt okay and I thought I was good to go and I was up doing stuff all over the house. I took a downhill turn because I would do too much. After that, that's when the coughing and respiratory stuff started. They gave me an oral steroid treatment and the z-pack antibiotic. By day 14 of COVID-19, my right hand and wrist started really hurting. At first, they thought it was cellulitis because I've had that before and it was similar. My hand swelled a little bit, and the pain was similar. The last day of my treatment, my left hand immediately started the same pain. This wasn't the same as cellulitis and I went to the ER a couple of times. My doctor ran initial tests and he was suspicious about it being an autoimmune issue. He tested me and noted I was high in some factors for rheumatoid arthritis. I couldn't see the rheumatologist until October 17. I was on steroids several times, went to the ER several times, and was trying to control the pain until I could get into the rheumatologist. All the doctors said that they noticed that if you possibly have an underlying autoimmune condition, COVID-19 can possibly bring that up to the surface, so that's probably what happened. On October 18, I did start treatment for RA. The medication I'm currently talking is sulfasalazine. Hands are still experiencing pain daily. The mobility in my hands has decreased, especially in the morning. Some days are better than others. I also take celecoxib and more supplements.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 07/12/2022 COVID-19 test positive; 08/11/2022 Autoimmune panel, factors indicating possible Rheumatoid Arthritis; X-rays on wrists and hands; Labs; 10/17/2022 tests done at Rheumatologist; Rheumatoid factor screen positive, Cyclic Citrul Peptide, AB IGG; 11/17/2022 blood work normal
Aktuelle Erkrankungen: Recently menopausal (last 2 years)
Vorgeschichte: None
Andere Medikamente: ADDERALL; desvenlafaxine; spironolactone; gabapentin; vitamin B12; zinc; vitamin D3; CITRACAL PETITE
Allergien: ZOFRAN; CYMBALTA
Vorherige Impfungen: -

VAERS 2512491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CT
Alter: 21,0
Geschlecht: F
Eingang: 20.11.2022
Impfdatum: 01.04.2021
Beginn: 05.05.2021
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest pain Dyspnoea Electrocardiogram normal

Symptomtext

5/5/21 at work had very bad chest pain and shortness of breathe. Went to the ER where they did a ECG. ECG came back abnormal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ECG 5/5/21 Blood work. They did not do c reactive protein or (ESR).
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 52,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 25.03.2021
Beginn: 19.09.2022
Tage bis Beginn: 543,0
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

09/19/22 presents to ED for "shortness of breath". PMHx of "Crohn's disease, CVA, atrial fibrillation, CKD, acute thrombus of left ventricle"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/19/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2503174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 61,0
Geschlecht: U
Eingang: 09.11.2022
Impfdatum: 25.03.2021
Beginn: 10.09.2022
Tage bis Beginn: 534,0
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

09/10/22 presents to ED for "breathing problem". PMHx of "CAD status post multiple coronary stents, hypertension, hyperlipidemia, insulin-dependent diabetes mellitus"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/10/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CT
Alter: 47,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 05.05.2021
Beginn: 01.10.2021
Tage bis Beginn: 149,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Abdominal pain Angiopathy Back pain Blood test Catheterisation cardiac abnormal Chest pain Dyspnoea Endothelial dysfunction Fatigue General physical health deterioration Headache Malaise Pain Pain in extremity

Symptomtext

About 5 months after receiving my second dose, I started to feel ill. I experienced extreme fatigue, chest pain that radiated to the left side of my head, arm, back and abdomen, shortness of breath and it continued to decline. In December 2021, I was diagnosed with coronary endothelial dysfunction. In January 2022 through May 2022, I had therapy and I have had a partial recovery. In July/August, I had another significant decline. This September, I was diagnosed with coronary microvascular dysfunction. I am continuing to decline. I see my cardiologist regularly. I'm hoping to participate in a clinical trial where they will insert a sinus reducer called NEOVASC, in December 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: Cardiac catheterization with provocative test; blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Perimenopause
Andere Medikamente: Omegas; vitamins; norethindrone
Allergien: Surgical tape; propranolol; fluoxetine
Vorherige Impfungen: -

VAERS 2488436

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 55,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 14.04.2021
Beginn: 24.10.2022
Tage bis Beginn: 558,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Atrial fibrillation COVID-19 Dyspnoea Fatigue Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt with PMH of hypertension and obesity has had 1-2 days of fever, dyspnea, and fatigue. He is found to be COVID-19 positive and has Afib with RVR.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 14.05.2021
Beginn: 14.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Aneurysm Blood immunoglobulin M increased Blood phosphorus decreased Blood potassium decreased Blood sodium decreased Dizziness Electrolyte imbalance Exercise tolerance decreased Fatigue Gastrooesophageal reflux disease Hyperacusis Idiopathic intracranial hypertension Intracranial pressure increased Magnetic resonance imaging Migraine Palpitations Paraesthesia Photophobia

Symptomtext

After first shot, I had severe fatigue, exercise intolerance, migraines, dizziness. Afrer second shot, I had the same fatigue, exercise intolerance, migraine, dizziness, tachycardia, electrolyte imbalances, pins and needles all over my skin, light and sound sensitivity, GERD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Idiopathic intracranial hypertension
Hospital-Tage: -
Labordaten: IGM Elevated (12/2021 Low Sodium, Potassium, Phosphorus (9/2021, 10/2021, and other dates) MRI w/ Contrast, Intracranial Hypertension, pseudotumor cerebri, Aneurysm, Transverse sinus stenosis POTS, Postural orthostatic tachicardia syndrome Palpitations
Aktuelle Erkrankungen: None
Vorgeschichte: Varicose Veins on left leg from pregnancy
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2485621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 57,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 16.04.2021
Beginn: 31.08.2022
Tage bis Beginn: 502,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain Dizziness SARS-CoV-2 test positive

Symptomtext

08/31/22 presents to ED for "chest pain" "lightheadedness". PMHx of "heavy alcohol use, DVT, subdural hematoma, delirium tremens, Warnicke encephalopathy"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/31/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2471882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 83,0
Geschlecht: F
Eingang: 07.10.2022
Impfdatum: 08.04.2021
Beginn: 14.09.2022
Tage bis Beginn: 524,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Biopsy brain Bradycardia COVID-19 Condition aggravated Fall Hypertension Muscle contracture SARS-CoV-2 test positive

Symptomtext

Pt to ED 9/10 for unintentional left arm contractions after fall. 9/13 pt Hypertensive and bradycardic. 9/14 pt COVID+, rx remdesivir for 3 days, no alleviating or aggravating factors. 9/16 no new complaints noted; stable; no acute cardiac issues noted. 9/18 pt to OR for brain biopsy. 9/19 pt A&OX4, VSS, Patient has no complaints of pain. 9/20 no overnight issues, pt feeling better. 9/23 pt discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Cerebrovascular accident (CVA), unspecified mechanism A hypertension Cerebral hemorrhage Vasogenic cerebral edema ICH (intracerebral hemorrhage) Brain tumor
Andere Medikamente: amLODIPine (NORVASC) 10 MG PO Tab cloNIDine (CATAPRES) 0.1 MG PO Tab hdrALAZINE (APRESOLINE) 50 MG PO Tab levETIRAcetam (KEPPRA) 500 MG PO Tab
Allergien: None
Vorherige Impfungen: -

VAERS 2446606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NH
Alter: 56,0
Geschlecht: F
Eingang: 15.09.2022
Impfdatum: 04.12.2021
Beginn: 04.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test COVID-19 Flank pain Infection Lymph node pain Lymphadenopathy Malaise Mammogram Mobility decreased Parotid gland enlargement

Symptomtext

I had the first 2 injections at a drive through clinic and the 3rd dose was at a pop up clinic. I was hard hit in recovering from the vaccine 5 days in bed and pain in several places along my left side, which I now believe are all lymph node sites based on their locations. In April I became ill with an infection that started in my head and swollen lymph nodes and parotid glands as well. It lasted for 3 months and I took 4 rounds of antibiotics between the end of April and the end of July. The swelling hasn't gone away but gets a little better then a little worse. I've had a mammogram and a bunch of other blood tests to rule our cancer, heart disease etc since they are all on my left side. Then I got covid on August 31, took Paxlovid because I'm high risk. The lymph nodes are increasingly swollen and painful and have a general feeling of not being fully well. I'm also still experiencing some symptons of covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Mammogram and various blood tests to rule of breast cancer and cancer in general. I'm have an echocardigram next week to rule out heart issues and the following week I'll have an ultrasound of the axillary glands. I believe there are four nodes that are impacted, 2 in my armpit, 1 in my breat and one near my spleen that is also swollen and painful.
Aktuelle Erkrankungen: Osteoarthritis, sub clinical thyroid disease
Vorgeschichte: ADHD, ASD, allergies and asthma,
Andere Medikamente: Zytec, Flonase nasal spray, Advair inhaler, albuterol inhaler when needed
Allergien: Environmental allergies, pollen, grass, mold,trees, cats, dogs, latex, metals, and cross reactions some some foods outlined in charts Had a one time reaction to Ampicillin when I had mono (EBV) which helped to diagnosis me
Vorherige Impfungen: -

VAERS 2442975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 73,0
Geschlecht: F
Eingang: 13.09.2022
Impfdatum: 20.01.2022
Beginn: 08.09.2022
Tage bis Beginn: 231,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury Ageusia Asthenia COVID-19 Decreased appetite Dizziness Fatigue Gastritis Hypotension Nausea SARS-CoV-2 test positive Vaccine breakthrough infection Vomiting

Symptomtext

Patient seen in the ED on 9/8 for hypotension. She reported being diagnosed with COVID about 3 weeks prior (8/18/22). For the past 3 weeks she has been experiencing dizziness, generalized weakness, fatigue, decreased appetite, nausea, and vomiting. While in the ED, patient tested positive again for COVID by PCR. She was admitted to the hospital from 9/8-9/11 with discharge diagnoses including nausea, vomiting, and loss of taste, suspect related to COVID gastritis; hypotension; and AKI, improving. Patient has received vaccine and 1 booster for COVID-19. This meets criteria for COVID vaccine breakthrough case review.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient with history of rheumatoid arthritis.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2422660

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 29.08.2022
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arteriospasm coronary Cardiac stress test Catheterisation cardiac Chest pain Dizziness Hypertension Immediate post-injection reaction Laboratory test Magnetic resonance imaging Microvascular coronary artery disease

Symptomtext

Instant elevated high blood pressure - 190/100 Dizziness Now suffer from incontrollable high blood pressure and also coronary vasospasm's. I have been hospitalized several times and have constant chest pain. Now also diagnosed with Coronary Microvascular Disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 3,0
Labordaten: High Blood pressure the day of vaccination 03/31/2021 Cardiac Cath - 07/2021 - due to coronary vasospams Lab work - 07/2021 Lab Work 12/2021 Lab work - 02/2022 Lab work - 07/2022 Cardiac Stress MRI - 08/2022
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: None
Allergien: none
Vorherige Impfungen: -

VAERS 2439961

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 18.02.2021
Beginn: 27.04.2022
Tage bis Beginn: 433,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Arthralgia Asthenia COVID-19 COVID-19 pneumonia Chest pain Cough Myalgia Productive cough Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received four doses of Pfizer COVID 19 Vaccine. Pt had his 4th shot booster for COVID 19 with the Pfizer vaccine in April 2022 at an outside facility. About 1-2 days after that, he started developing some generalized weakness, cough with white phlegm, runny nose/congestion, myalgias and arthralgias. The patient tested positive for COVID 19 on 27 April 2022. The patient presented to the ED with symptoms above and was admitted with COVID pneumonia, cough, and chest pain. The patient was treated with iv antibiotics. The patient was discharged on 29 April 2022 in stable condition. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2420924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 26.08.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angiogram Electrocardiogram Heart rate increased Hypersensitivity Injection site erythema Injection site swelling Muscle spasms No reaction on previous exposure to drug Paraesthesia Rash Sinus tachycardia Swelling face Ultrasound Doppler

Symptomtext

REACTION TO BOOSTER no issues with first 2 vaccines. Had covid first week of december. 4 weeks later was told to get booster. Redness/swelling at injection site hours after vaccine Delayed allergic response 24 hours later ER visit for allergic response. Elevated HR, Rash face,chest, and arms, leg spasms, tingling in both left and right legs,face puffy, sinus tachcardyia Issues still not resolved coming out of ER ER Visit multiple times after For reaction not being resolved Eventually seen by allergist who starts anthistimaine medication round the clock

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Jan 12, 2022 at 5:45 pm Electrocardiogram Jan 15, 2022 at 6:17 pm Chest CTA Jan 15, 2022 at 4:15 pm Venous Duplex
Aktuelle Erkrankungen: post Covid had Covid first week of December
Vorgeschichte: None
Andere Medikamente: none
Allergien: bee sting*
Vorherige Impfungen: -

VAERS 2420881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 06.01.2021
Beginn: 06.08.2022
Tage bis Beginn: 577,0
Dosis: 1
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Arthralgia COVID-19 Confusional state Dysarthria Joint swelling Lethargy Pneumonia aspiration Pyrexia SARS-CoV-2 test positive

Symptomtext

Pt to ED 8/3 for bilateral ankle swelling and pain. 8/4 pt is A&Ox4, cooperative. Respirations are even, unlabored. 8/5 Pt confused and lethargic. 8/6 pt COVID+. 8/7 Pt more oriented (x4) w/ intermittent confusion and slurred speech. Pt still lethargic, fever of 101.1. 8/11 Pt aox1,confused, on 3L 02 NC not in distress. 8/12 O2 requirements increased; possible component of aspiration pneumonia; remdesivir rx completed. 8/13 pt is aox3-4, with period of confusion. 8/15 Fever (resolved) likely secondary to COVID, now on RA O2 possible component of aspiration pneumonia.8/16 pt alert,orient x3. No distress noted. 8/17 pt is A&OX4, VSS no complaints or discomfort. Pt discharged 8/17.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia aspiration
Hospital-Tage: 15,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Alcoholic cirrhosis (CMS/HCC) ...
Andere Medikamente: acetaminophen (TYLENOL) suppository 650 mg ...
Allergien: None
Vorherige Impfungen: -

VAERS 2376658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 21.07.2022
Impfdatum: 21.04.2021
Beginn: 14.07.2022
Tage bis Beginn: 449,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dyspnoea

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2347623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 01.07.2022
Impfdatum: 14.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Electromyogram normal Feeling abnormal Headache Hyperacusis Hypoaesthesia Laboratory test normal Magnetic resonance imaging head normal Magnetic resonance imaging neck Magnetic resonance imaging normal Neck pain Paraesthesia Spinal X-ray normal Tinnitus Vertigo

Symptomtext

I woke up 5 days later with severe pain in my neck and upper back, headache. Numbness and tingling in my hand and feet . Ringing in my ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Spine x-ray negative. Got sent to PT for 6 weeks. Referred to Neurology, they did MRI of my neck and back, negative. Trigger point injections. EMG testing on my hands and feet, negative. Multipul labs all negative. Saw Rheumatologist, more labs all negative. Sent to Chiropractor, more PT. Episode of Vertigo that sent me to ER, did MRI of my brain, negative. Following this I have even worsening ringing in my ears. Told to see ENT and audiology. Moderate hearing loss with hyperacucity. Was told only help was hearing aides and they might not help. Was advised and tried antidepressants which made me sick. It's now over a year later, I'm still miserable, again trying an antidepressant.
Aktuelle Erkrankungen: none
Vorgeschichte: Osteoporosis
Andere Medikamente: Multivitamins, Calcium, Vitamin C, Vitamin D, Alendronate
Allergien: Psyllium
Vorherige Impfungen: -

VAERS 2336037

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 27.06.2022
Impfdatum: 14.04.2021
Beginn: 09.11.2021
Tage bis Beginn: 209,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Albumin CSF Albumin urine Antinuclear antibody positive Asthenia Balance disorder Blood glucose normal Blood iron decreased Blood thyroid stimulating hormone decreased Borrelia test negative C-reactive protein normal CSF immunoglobulin G index CSF lymphocyte count CSF monocyte count CSF oligoclonal band absent CSF protein increased Dehydration Diabetic ketoacidosis Electromyogram normal

Symptomtext

Pfizer mRNA vaccines given April and May of 2021. No personal history of diabetes. Diagnosed with type 1 diabetes in DKA 11-9-21. Given perceived higher risk status with the diabetes diagnosis had the Pfizer booster 12-15-21. Among the hospitalization and booster developed severe constellation of symptoms including muscle aches all over, skin hyperesthesia, mental fog, forgetfulness, insomnia, weakness particularly in both lower legs, poor balance particularly going down stairs. Pain was the most bothersome.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 3,0
Labordaten: 11-9-21: Admission for DKA, significant testing done at hospitalization but all related to typical DKA testing. 02/09/2022: Iron and TIBC indicative of iron deficiency, ferritin 19, normal urine albumin excretion, CMP overall normal except glucose 156 and otherwise consistent with dehydration, TSH 1.2, VIT D 60, Rheumatoid Factor normal, ESR/CRP normal, ANA speckled at 1:80 dilution, b12 high, lyme ab negative, 3/6/22: MRI brain with and without IV contrast: Few nonspecific white matter hyperintensities. No acute abnormality. No abnormal enhancement. 3/6/22: MRI cervical and thoracic spine with and without IV contrast: Impression: Minimal degenerative changes at C4-5. Minimal reversal of the cervical curvature. Barely appreciable scoliosis of the thoracic spine. No altered signal or abnormal enhancement in the spinal cord to suggest demyelinating disease. No acute abnormality of the spine. Mild annular bulging at L5-S1. 3/23/22 EMG: Essentially normal electrodiagnostic study of the lower extremities 4/20/22: INR 1.1, CBC normal other than microcytic at 78, Lumbar Puncture 4/20/22: LP: Negative for malignant cells, scattered lymphocytes and monocytes, protein CSF 56 mg/dl (reference 15-45), IGG synthesis rate essentially normal other than albumin high at 36.5 mg/dl, serum and CSF oligoclonal banding normal
Aktuelle Erkrankungen: none
Vorgeschichte: Depression, anxiety, chronic fatigue syndrome
Andere Medikamente: none
Allergien: Bactrim, Sudafed
Vorherige Impfungen: -

VAERS 2309689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 28,0
Geschlecht: M
Eingang: 05.06.2022
Impfdatum: 10.04.2021
Beginn: 01.06.2021
Tage bis Beginn: 52,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Cardiac failure congestive Catheterisation cardiac abnormal Dyspnoea Echocardiogram Fluid retention Pericardial effusion

Symptomtext

About a month after the second shot I experienced shortness of breath, I retained fluid in legs, stomach, and chest, went to hospital several times for treatment in the months after. In November 2021 I went in to hospital for a Right Heart catheterization. Dr then diagnosed me with congestive heart faliure due to all of the fluid around my heart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: 9/30/21- Cardiologist Visit 10/21/21- Refered by Cardiologist to Heart Faliure Specialist Dr. visited at clinic for initial visit 10/29/21- Echocardiogram Procedure ordered by Dr. 11/11/21- Hospital procedure Right Heart Catheterization performed by Dr. 11/11/21- Admitted to the ER Hospital for two days for congestive heart faliure
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertrophic Cardiomyopathy
Andere Medikamente: Metoprolol 50 MG Daily
Allergien: None
Vorherige Impfungen: -

VAERS 2292696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OR
Alter: 44,0
Geschlecht: F
Eingang: 24.05.2022
Impfdatum: 18.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac disorder Hypertension Palpitations

Symptomtext

I noticed my heart felt different about 2 weeks after my fist vaccination. What I noticed was my heart felt like it was working harder. it Felt like it was palpitating differently that it had been before. I didn't schedule an appointment for it on it's own, but I went to some already made appointments with my dentist and endocrinologist who took my blood pressure. Every appointment that I went to showed a hypertension level blood pressure. I scheduled an appointment with my family practitioner to have her look into this.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: 04/06/2022 - (Dentist Office) Blood Pressure x2 - 145/99 and 157/94
Aktuelle Erkrankungen: none
Vorgeschichte: Pituitary Tumor
Andere Medikamente: Bromocriptine 2.5mg 1xday, Multivitamin
Allergien: none
Vorherige Impfungen: Fever and Chills - Meningitis Vaccine - Nov 2015 - 38

VAERS 2290472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: IL
Alter: 55,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 15.04.2022
Beginn: 18.05.2022
Tage bis Beginn: 33,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Fatigue Headache Lethargy Mobility decreased Nasal congestion Productive cough Pulmonary congestion SARS-CoV-2 test positive Throat irritation

Symptomtext

I clicked on the text to do my VSAFE check in and one of the questions was have you contracted COVID and I clicked YES and then a few days later you guys called, so here I am. My 2nd booster was given on APRIL 15th and on MAY 18th I woke up with massive nasal and chest congestion, very lethargic, couldn't and didn't want to get out of bed, extreme fatigue, massive headache, scratchy throat (yet it didn't hurt to swallow), flemmy cough on and off through the day. On MAY 19th took an at home test and came back positive. On MAY 20th I called our area CLINIC and spoke to nurse who was able to get a prescription for PAXLOVID through pharmacy which I started that evening and am currently on course to complete by WED MAY 25th when I'll see if it worked or if I rebound. Backing up a bit....my entire family is fully vaxxed and boosted, my adult kids are all at home. After Mothers Day my 20 year old daughter went back to her apartment (on May 10th) for college, she told me she spent the next 4 days on her bathroom floor with similar symptoms but she had a fever over 100 ( my temp stayed around 98). She took TWO at home tests while there and both came back negative while she was still experiencing symptoms. She returned back home here on May 14th Saturday, still sick (again she tested negative twice). Long story short, on Wednesday May 18th, My 28 year old son and my 24 (soon to be 25 the next day) daughter and I all woke up with the same symptoms of stuffy congested nose and chest, cough etc. My son coughed so hard he almost vomited and then hepassed out on the floor. Later that day my son and daughter do an at home test and they come back positive. I test May 19th Im postive too. My husband tests negative and has no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none that I'm aware of
Andere Medikamente: multi vitamin, probiotic supplement, fiber supplement
Allergien: none that I'm aware of
Vorherige Impfungen: -

VAERS 2287091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 68,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 16.04.2021
Beginn: 01.01.2022
Tage bis Beginn: 260,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Dyspnoea Pyrexia SARS-CoV-2 test positive Wheezing

Symptomtext

SOB, COUGH, WHEEZING, FEVER, CHILLS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: POSITIVE COVID TEST 5/17/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety Diverticulitis Enlarged prostate Esophageal thickening Heartburn Prostate disease Hypothyroidism
Andere Medikamente: atorvastatin (LIPITOR) 20 mg Oral Tab citalopram (CELEXA) 20 mg Oral Tab famotidine (PEPCID) 20 mg oral tablet levothyroxine (SYNTHROID) 112 mcg Oral Tab traZODone (DESYREL) 50 mg Oral Tab
Allergien: Percocet [Oxycodone-Acetaminophen]
Vorherige Impfungen: -

VAERS 2286996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 28,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 07.05.2021
Beginn: 28.01.2022
Tage bis Beginn: 266,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Chills Cough Dyspnoea Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I tested positive for COVID 01/28/2022 with a home test. At was a mild to moderate. I didn't have to go to the hospital. I had trouble breathing, a cough, chills, fever, and body ache. I spent most of the time in bed. I had it for about 5 days. I had COVID twice. I can't remember the first time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID home test
Aktuelle Erkrankungen: No
Vorgeschichte: Fibromyalgia, Bipolar Type 2 and ADHD
Andere Medikamente: Venlafaxin 300mg, Lamotrigine, Baclosen 10mg, Fluoxetine 20mg, Dexmethylphenidate and CBD Oil.75ml,
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2284782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 31,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 20.11.2021
Beginn: 17.05.2022
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Dizziness Dyspnoea Nausea Pyrexia SARS-CoV-2 test positive Vomiting

Symptomtext

Received Pfizer vaccines on 3/31/21, 4/21/21, 11/21/21; tested positive for COVID by PCR on 5/17/22; admitted to hospital on 5/18/22 d/t fever, N/V, cough, dyspnea, dizziness. Underlying congenital heart disease w/ tricuspid atresia and a-fib on Warfarin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 15.04.2021
Beginn: 17.01.2022
Tage bis Beginn: 277,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

01/17/22 presents to EC ED for "chest pain". PMHx of "DM2, HTN, HLD, asthma"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/18/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 37,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 21.04.2021
Beginn: 16.02.2022
Tage bis Beginn: 301,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute kidney injury COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/16/22 presents to ED for "AKI and shortness of breath". PMHx of "IgA nephropathy s/p renal transplant, HTN, and hypothyroidism"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/17/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PR
Alter: 63,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 11.05.2021
Beginn: 03.06.2021
Tage bis Beginn: 23,0
Dosis: 2
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Blepharitis Cheilitis Eye inflammation Inflammation Injected limb mobility decreased Mechanical ventilation Puncture site oedema

Symptomtext

THE PATIENT PRESENT INFLAMATION IN THE FOREHEAD (IN THE CENTER) AND PASSAGE TO THE EYES, EYELIDS, NOSE, CHEEKS, LIPS AND NECK. IMMOBILITY OF THE LEFT ARM AND EDEMA IN THE PUNCTURE AREA. REQUIRED TREATMENT WITH PREDNISONE, LEVOPHED, FERROUS SULFATE, AUGMENTIN. HE WAS ON MECHANICAL VENTILATOR FROM MARCH 6, 2022 TO MARCH 23, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: HYPOTHYROIDISM
Andere Medikamente: NONE
Allergien: YES- SULPHA
Vorherige Impfungen: -

VAERS 1403467

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 36,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 01.04.2021
Beginn: 01.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Bedridden Dizziness Echocardiogram normal Fall Fatigue Blood test Chest X-ray Computerised tomogram Dysstasia Palpitations Feeling abnormal Gait inability Immediate post-injection reaction Influenza like illness Laboratory test normal Mobility decreased Movement disorder Postural orthostatic tachycardia syndrome

Symptomtext

This is a 36 year old previously healthy woman. She had COVID Vaccine (Pfizer, first dose) on April 2021 and immediately after the vaccination, she started experiencing dizziness and ringing sound in her ears. She went back home and these symptoms continued to get worse. Ten days after vaccination, she felt very tired, dizzy and heart racing then she fell down but didn't pass out and was transferred to ER. At the ER she had a lot of work up done and was normal and was given some IV fluids then sent home. After going home she continued to have worsening symptoms and went to the ER again and repeated work up was negative and was sent home. She continued to feel worse and from April to June 2021 she was staying at bed and not able to walk or move. On August, she started to improve gradually and be able to get out of bed and do some upright activities. On November she contracted a viral infection form her kids but didn't get tested for COVID as her symptoms looked like regular flu and she had a relapse with worsening symptoms and being bedridden. By beginning of December 2021 she started to experience some improvement in her symptoms and went to see a physical therapist who instructed her to do squatting exercises and once she started doing it, her symptom got worse again and spent the whole month of January 2022 in bed again. She continued to have gradual improvement and was able to get out of bed by February and by March 2022 she contracted another viral infection from her kids but she tested negative for COVID and she didn't experience worsening of her symptoms after that infection. On March 25th she had a tilt table testing at hospital. The testing showed inappropriate sinus tachycardia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Echocardiogram wnl Tilt table test with significant tachycardia and orthostatic tachycardia.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: no
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2263534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MO
Alter: 54,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 21.04.2021
Beginn: 30.04.2022
Tage bis Beginn: 374,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chest pain Dyspnoea Respiratory tract congestion

Symptomtext

Symptom onset was 04/29/2022, SOB, congestion and chest pain/pressure. Admitted to hospital 04/30/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Chronic Kidney and Urinary Tract Infections
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2263418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 91,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 21.04.2021
Beginn: 08.09.2021
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 COVID-19 pneumonia Dyspnoea SARS-CoV-2 test positive

Symptomtext

Presented with SOB; Covid + in ED; Admitted to medical facility with Covid PNA, tx with steroids, merrem, remdesivir, pulmicort, Vit C, Baricitinib, symbicort, zinc; supplemental O2 required..up to 12 LPM; back to 4LPM baseline at d/c The facility that she came from will not be able to take her for 10 days after the initial COVID test. She is able to go to another facility for now until she is able to go back to her skilled nursing facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2252283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 71,0
Geschlecht: F
Eingang: 26.04.2022
Impfdatum: 17.09.2021
Beginn: 07.03.2022
Tage bis Beginn: 171,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Dyspnoea Fatigue Productive cough SARS-CoV-2 test positive

Symptomtext

COVID related hospitalization after being vaccinated with Pfizer series + booster (9/17/2021, 3/25/2021, 3/4/21). Admitted 3/7/22 to Hospital: Presents with shortness of breath, fatigue and productive cough Tested positive for Covid 3/2/2022 Chronically on 2L nasal cannula around the clock , on hospice care at long term care facility On admission needed oxygen 3L nasal cannula Given steroids for covid and antibiotics for possible community acquired pneumonia during hospitalization Receives 4mg of dexamethasone at baseline. Increased steroids during hospitalization Received IV hydration Improved and back to baseline 2L of oxygen at discharge Discharged 3/9/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of metastatic lung cancer Former smoker-quit 2001 COPD Anxiety depression
Andere Medikamente: Acetaminophen suppository-prn Albuterol inhaler Bisacodyl suppository-prn Calcium carbonate 600mg Dexamethasone 2mg tab-two times daily Docusate sodium 100mg Famotidine 40mg Fentanyl 37.5mcg Flonase Folic acid Gabapentin 300mg Hu
Allergien: morphine and Vioxx
Vorherige Impfungen: -

VAERS 2244087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 29,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthritis Blood test normal Dizziness Eye disorder Fatigue General physical condition abnormal Glassy eyes Imaging procedure abnormal Impaired work ability Irritability Lymphadenopathy Myositis Nausea Nerve conduction studies normal Nerve injury Pain Pain in extremity Palpitations

Symptomtext

About 10 minutes after the shot I had heart palpitations, racing heart, and felt dizzy. That lasted about 10 minutes. About 2 hours later, I noticed my lymph nodes on my neck were getting larger. About 5 hours later, I felt really exhausted and irritable and my arm was sore. About 8 hours later is when my husband noticed I looked unwell. My eyes were dark and glassy and I felt nauseous. 11 hours after the shot was when the very intense body aches kicked in, joints, muscles, and everything felt very inflamed and my fever started. Throughout the night, all of that worsened until about when I woke up the next morning around 11AM. Everything felt better. I was mildly sore and everything improved throughout the day. The tendonitis and nerve issues in my arm started a few months after the shot. I saw Dr. (Privacy) first. He prescribed me with tizanidine and meloxicam. He was hopeful that it would improve in about a month, but asked me to come back or give him a call if it did not. He thought it was tendonitis or ulnar nerve entrapment. I waited about a month and half and it had slightly improved but started to get worse again. I am an (privacy) so I thought that might have something to do with it but I had never had problems with it before. I cut my hours in half and that still wasn't helping. I took a couple of weeks off of work and that didn't help either. That's when I decide to call him again. He referred me to an arm specialist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Imaging of Arm and Neck - everything looked normal except for a little bit of loss of curvature in my neck; Nerve Test - everything looked fine with my nerves; Bloodwork - looked normal.
Aktuelle Erkrankungen: None
Vorgeschichte: Allergies; asthma
Andere Medikamente: Centrum Women's Vitamin, Xyzal 5mg, Mirena IUD
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2243203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 12.04.2021
Beginn: 26.08.2021
Tage bis Beginn: 136,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Aphasia COVID-19 Dyspnoea Exposure to SARS-CoV-2 Malaise SARS-CoV-2 test positive

Symptomtext

8/26/21 presents to urgent care requesting COVID-19 testing due to experiencing COVID-19 symptoms and exposure to COVID-19 8/27/21 PMH of CAD s/p PCI, HTN, Hyperlipidemia, COPD, Tobacco Abuse, Obesity and RA who presented to ER with c/o SOB and difficulty with speech

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 8/26/21 SARS-CoV-2 (COVID-19) by PCR, Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2235965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 57,0
Geschlecht: F
Eingang: 15.04.2022
Impfdatum: 22.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Dizziness Dyspnoea Echocardiogram Erythema Feeling abnormal Feeling hot Influenza like illness Injected limb mobility decreased Malaise Neck pain Pain Peripheral swelling Pulmonary function test Pyrexia Vision blurred

Symptomtext

I woke up the next morning and I was just on fire. My entire body was red and I was burning up with a fever up to 103.0, chills and body aches all over. My husband put cool rags on me and we called the hospital. We did not go since the ER told us that was common symptoms over the phone. My fever did go down the next day but I felt lightheaded and felt like I had the flu. This lasted almost 2 weeks. Within a couple of days of the vaccine, I could not lift my left arm that was vaccinated. I also had pain all the way up to the left side of my neck at the same time as the arm. After 3 weeks, my feet became swollen and my vision became blurred. I then started going to the doctor and he prescribed fluid medicine then sent me to a cardiologist for a check up. I also started having trouble catching my breath at 3 weeks after vaccination so then I was sent to a lung specialist. No other medications. This lasted 4-5 months. I don't feel sick anymore but I still don't feel myself yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Cardiac Ultrasound and Echocardiogram at Hospital possibly June 2021. I went into a chamber to check out my lungs at the same hospital above in possibly July 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Hypothyroid
Andere Medikamente: Synthroid 125mcg daily; Hydrochlorothiazide daily
Allergien: None
Vorherige Impfungen: -

VAERS 2235914

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 13.04.2022
Impfdatum: 17.08.2021
Beginn: 28.09.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Electrocardiogram abnormal Sinus tachycardia Supraventricular tachycardia

Symptomtext

Multiple recurrent episodes of supraventricular tachycardia noted on 09/28/2021, 10/22/2021, 12/15/2021, 02/21/2022, 03/09/2022 x 3 episodes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Sinus tachycardia
Hospital-Tage: -
Labordaten: ER visit 09/28/21- EKG Sinus Tachycardia results Vitals HR-141 EKG 3/01/224- Sinus Tachycardia 03/09/22-Pulse 152
Aktuelle Erkrankungen: None
Vorgeschichte: Schizophrenia paranoia, constipation, hyperlipidemia, history of traumatic brain injury
Andere Medikamente: Lipitor, Cogentin, Clozapine, Depakote, Luvox, Invega Sus, Dss,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2228675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 22.04.2021
Beginn: 06.05.2021
Tage bis Beginn: 14,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Magnetic resonance imaging Mobility decreased Myalgia Pain Product administered at inappropriate site Ultrasound scan

Symptomtext

A couple of weeks after vaccine, my shoulder would hurt to move. I could not move my shoulder. I went to my doctor. I was told that I was giving the vaccine in the wrong place. My muscles were hurting. I waited 2 more weeks and the pain was so bad that I could not move it. I went back to my doctor and got a steroid injection. That did not help. I was referred to another doctor for sports medicine. I have seen him twice now. I had an MRI, ultrasound, and a steroid injection. That helped for maybe 2 weeks. I went back again and got another steroid injection that actually worked. I was referred to get Physical Therapy. I have that appointment tomorrow due to the pain being excruciating again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: MRI, ultrasound.
Aktuelle Erkrankungen: None
Vorgeschichte: Burn victim; Prosthetic leg; Past tracheostomy surgeries
Andere Medikamente: Seroquel; Famotidine; Chlorthalidone; Pregabalin; Omeprazole; Amlodipine/Losartan; Vitamin D3 2000iu; Potassium; Magnesium; Multivitamin
Allergien: Antibiotics
Vorherige Impfungen: -

VAERS 2220980

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 19,0
Geschlecht: F
Eingang: 07.04.2022
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: ja Erholt: nein

Anxiety Chest pain Dizziness Hypoaesthesia Hypoaesthesia oral Movement disorder Speech disorder

Symptomtext

Within 10-15 mins after receiving my vaccination, I started to feel lightheaded and dizzy. I had numbness in my fingers, toes, face and mouth. I wasn't able to speak or move for about 4-5 mins. After about 1-2 minutes, I started to have severe chest pain on left side which was the same side as the vaccine. This chest pain lasted about 1.5 weeks. Each incident would last between 5-20 mins at a time. Numbness on face and mouth has continued. About two days later, I decided to go to urgent care. They told me I was having an anxiety attack and sent me home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin, Zyrtec
Allergien: Seasonal Allergies, Peanuts
Vorherige Impfungen: -

VAERS 2213113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MO
Alter: 46,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 25.08.2021
Beginn: 01.01.2022
Tage bis Beginn: 129,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood culture Blood glucose abnormal Blood lactic acid Body temperature Condition aggravated Drug ineffective Investigation Suspected COVID-19 Decreased appetite Glycosylated haemoglobin Headache Pain Pyrexia

Symptomtext

she came down with Covid in Jan2022; she came down with Covid in Jan2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non-HCP) from product quality group. The reporter is the patient. A 46-year-old female patient received bnt162b2 (BNT162B2), administration date 25Aug2021 (Batch/Lot number: unknown) at the age of 46 years as dose 3 (booster), single, administration date 20Apr2021 (Lot number: EW0169) as dose 2, single and administration date 30Mar2021 (Lot number: ER8733) as dose 1, single for covid-19 immunisation. Relevant medical history included: "Trigeminal neuralgia" (unspecified if ongoing), notes: Trigeminal neuralgia; "Bell's palsy" (unspecified if ongoing), notes: Bell's palsy; "Covid-19", start date: Sep2020 (unspecified if ongoing), notes: she was diagnosed but was asymptomatic. Concomitant medication(s) included: LYRICA. The following information was reported: DRUG INEFFECTIVE (medically significant), SUSPECTED COVID-19 (medically significant) all with onset Jan2022, outcome "unknown" and all described as "she came down with Covid in Jan2022". The patient underwent the following laboratory tests and procedures: blood culture: negative; blood lactic acid: not provided; investigation: not provided. Additional information: She is glad that she had it because she came down with Covid in Jan2022, she had Covid twice. Once before she was vaccinated in Sep2020, she was diagnosed but was asymptomatic. That scared her she didn't have any symptoms other than little bit of a fever. she was living with her brother and his girlfriend and babysitting full time for them. Then got Covid again, states the boyfriend refuses to get vaccinated. Her symptoms were mild only lasted 24 hours, could not say had covid because it did not feel like it only had a fever for 24 hours. Bounced back to herself, she was scared because she has a compromised autoimmune system multiple and takes injection that lowers immune system to fight things. Description of Product Complaint: Description of complaint: Hydrochlorothiazide: there is a diuretic in the hydrochlorothiazide too as she does retain water, she doesn't think it helps with her blood pressure too much to be honest. Adds she is glad that she had it because she came down with Covid in Jan2022. Patient did not administer any other vaccines on same day. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Test Name: Blood culture; Test Result: Negative ; Test Name: Lactic acid; Result Unstructured Data: Test Result:Not Provided; Test Name: A1C; Result Unstructured Data: Test Result:Not Provided
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bell's palsy; COVID-19 (she was diagnosed but was asymptomatic); Trigeminal neuralgia
Andere Medikamente: LYRICA
Allergien: -
Vorherige Impfungen: -

VAERS 2217939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 19.07.2021
Beginn: 29.12.2021
Tage bis Beginn: 163,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 COVID-19 pneumonia Cough Lower respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Narrative: 61 year old male who presented to ED on 12/29/2021 with complaints of cough and chest congestion. Dx with COVID pneumonia. PMH of DM, obesity, sleep apnea, HTN, and depressive disorder. admitted and treated with dexamethasone (12/29-12/31) Discharged on 12/31/21 with dexamethasone 6mg PO daily for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Positive COVID test on 12/29/2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 10.04.2021
Beginn: 06.01.2022
Tage bis Beginn: 271,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Anxiety COVID-19 Cough Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

01/06/22 presents to ED for "fatigue, dyspnea, cough" "increasing shortness of breath and anxiety". "history of smoking and obesity"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 01/06/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 21.05.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Loss of personal independence in daily activities Magnetic resonance imaging Mobility decreased Muscle discomfort Musculoskeletal disorder Pain in extremity Tendonitis X-ray

Symptomtext

It gave me tendinitis in my left arm; my left arm or hand lost mobility; Muscles are frozen so I am unable to use my arm.; I am unable to use my arm to wash my back ; to pull my bra; putting on my blouse or shirt; stretching for things.; I have to always sleep on my right because it''s so painful; I can''t sleep on my left side; Any form of weight lifting anything I get I am unable to use my arm to do; limited mobility from my left arm that has become extremely painful; my muscles are frozen; assist with getting back full function of my left hand; administered a cortisone shot to help with relieving the pain in my left hand; This is a spontaneous report received from a contactable reporter (Consumer or other non HCP). The reporter is the patient. A 39 year-old female patient received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 21May2021 08:30 (Lot number: EW0169, Expiration Date: Jul2021) at the age of 39 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1, Lot number:EW0179, Time: 8:30, Route of admin: Intramuscular), administration date: 30Apr2021, when the patient was 39 years old, for COVID-19 Immunization. The following information was reported: TENDONITIS (non-serious), outcome "unknown", described as "It gave me tendinitis in my left arm; my left arm or hand lost mobility; Muscles are frozen so I am unable to use my arm."; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious), outcome "unknown", described as "I am unable to use my arm to wash my back ; to pull my bra; putting on my blouse or shirt; stretching for things."; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "I have to always sleep on my right because it''s so painful; I can''t sleep on my left side; Any form of weight lifting anything I get I am unable to use my arm to do"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "limited mobility from my left arm that has become extremely painful"; MUSCLE DISCOMFORT (non-serious), outcome "unknown", described as "my muscles are frozen"; MUSCULOSKELETAL DISORDER (non-serious), outcome "unknown", described as "assist with getting back full function of my left hand"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "administered a cortisone shot to help with relieving the pain in my left hand". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of tendonitis, loss of personal independence in daily activities, pain in extremity, mobility decreased, muscle discomfort, musculoskeletal disorder, pain in extremity. Additional information: It was reported that the patient started to realize that the events in the ending of Jun30 and July and it was Jul2021. Lab tests were the findings was the tendinitis so no arteries and nerve were damage so there was no prominent damage to my arm however it caused the tendinitis where the patient was unable, the muscle were frozen so the patient was unable to use her arm. Relevant tests included: MRI: Result were Stiffness (Shoulder) on 31Jan2022, Stiffness (Arm) on 01Feb2022 and Stiffness (neck) on 02Feb2022 and Chest X-ray: Results unknown. There was no relevant test for thromboembolic events with Thrombocytopenia. The patient visited an orthopedic surgeon who recommended physical therapy twice a week and who also administered a cortisone shot on 16Feb2022 to help with the pain in her left arm. He also recommended her doing physical therapy twice a week to assist with getting back full function of left hand. The doctor only recommended her for getting 3 MRI on her shoulder, neck and arm. The patient did not taken any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. She stated that she was reaching out, not just for awareness, but also to see if there was anything could be done to assist with the out-of-pocket expense this was costing her. Each visit to the physical therapy cost (Dollar sign) 40 and she had to pay a copay for all MRI and visits to the Orthopedic doctor. In addition to that there was the cost of travelling expense. She would be very grateful if she would receive a response from someone on the Pfizer legal team regarding this and the consideration and help with the matter at hand. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20220131; Test Name: MRI; Result Unstructured Data: Test Result:stiffness; Comments: Shoulder; Test Date: 20220201; Test Name: MRI; Result Unstructured Data: Test Result:stiffness; Comments: Arm; Test Date: 20220202; Test Name: MRI; Result Unstructured Data: Test Result:stiffness; Comments: Neck; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2181869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 19.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Lymphadenopathy Migraine Pyrexia

Symptomtext

Extreme pain in joints; chills; fever; migraine; swollen lymph nodes in underarm and groin; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 34-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 19Apr2021 15:00 (Lot number: EW0169) at the age of 33 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing); "allergies" (unspecified if ongoing); "heart murmur" (unspecified if ongoing); "Allergies: Walnuts" (unspecified if ongoing); "Allergies: latex" (unspecified if ongoing); "Allergies: Bees" (unspecified if ongoing); "seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: PRILOSEC [OMEPRAZOLE]; SINGULAIR; NASONEX. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8733, Location of injection: Arm Left, Vaccine Administration Time: 03:00 PM), administration date: 29Mar2021, when the patient was 33 years old, for COVID-19 immunization. The following information was reported: ARTHRALGIA (non-serious) with onset 2021, outcome "recovering", described as "Extreme pain in joints"; CHILLS (non-serious) with onset 2021, outcome "recovering", described as "chills"; PYREXIA (non-serious) with onset 2021, outcome "recovering", described as "fever"; MIGRAINE (non-serious) with onset 2021, outcome "recovering", described as "migraine"; LYMPHADENOPATHY (non-serious) with onset 2021, outcome "recovering", described as "swollen lymph nodes in underarm and groin". Therapeutic measures were not taken as a result of arthralgia, chills, pyrexia, migraine, lymphadenopathy. Additional information: The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient did not test positive for COVID-19. 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: Allergic reaction to bee sting; Allergy; Allergy to nuts; Asthma; Heart murmur; Latex allergy; Seasonal allergy
Andere Medikamente: PRILOSEC [OMEPRAZOLE]; SINGULAIR; NASONEX
Allergien: -
Vorherige Impfungen: -

VAERS 2180204

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge EW0169

moderat

Staat: PA
Alter: 57,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 08.05.2021
Beginn: 26.05.2021
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anticoagulant therapy Asthenia Cardiovascular disorder Chest discomfort Dyspnoea Exercise lack of Hiccups Impaired work ability Lethargy Pulse absent Stent placement Thrombectomy Weight increased

Symptomtext

I got two doses of the Pfizer vaccine on April 15th and May 8th of 2021. Since then I have been going through all manner of health issues. I have not had any health issues before then. I had surgery to remove blood clot from my groin (they put a stent inside of me) because the blood was not flowing to my left leg. That leg was without a pulse. I went to the doctor and they sent me immediately to the hospital. That when I had the surgery. I have been having shortness of breath and hiccups ever since... The doctor told me today, March 4, 2022 that they will have to do an endoscopy on March 24th. The hiccups are every day for several months now, they are almost violent. I have been going through a lot ever since the vthe vaccine. I have been taking clopidogrel (blood thinner) since the surgery. I also find that my chest tightens up from time to time, which scares me a lot. I have not done the booster because of the changes in my body since the first two shots. I have been lethargic and do not have the energy I use to have to do my exercises, which caused me to gain weight gradually. I am concerned that there are things that the medical professionals do not know about the vaccine and how it affects us individually. I am now thinking that I did the wrong thing by taking this vaccine recommended by the CDC. How do we resolve this issue? What should my next step be? I see a lot of new data coming out about the vaccine that I think we all should have been informed of before taking the vaccine. I am a Singer and this hiccup thing is causing major problems for me. I cannot go through an entire song without it interfering, which is causing major problems for me doing a live performance. I can get away with it in the studio because we can always stop and start again, but it poses a major problem for me singing live.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2176822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Dehydration Dry eye Dry skin Myalgia Palpitations Thirst Urine output decreased

Symptomtext

Joint pain; Muscle pain; Heart racing; Extreme thirst; Feeling of excessive dehydration; body, skin, eyes, feel dry; body, skin, eyes, feel dry; feeling of decreased urination; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 50 year-old female patient received bnt162b2 (COMIRNATY), administered in arm left, administration date 31Aug2021 (Lot number: EW0169) at the age of 50 years 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: THIRST (non-serious) with onset 31Aug2021, outcome "not recovered", described as "Extreme thirst"; PALPITATIONS (non-serious) with onset Sep2021, outcome "not recovered", described as "Heart racing"; ARTHRALGIA (non-serious), outcome "not recovered", described as "Joint pain"; MYALGIA (non-serious), outcome "not recovered", described as "Muscle pain"; DEHYDRATION (non-serious) with onset 31Aug2021, outcome "not recovered", described as "Feeling of excessive dehydration"; DRY SKIN (non-serious), DRY EYE (non-serious) all with onset 31Aug2021, outcome "unknown" and all described as "body, skin, eyes, feel dry"; URINE OUTPUT DECREASED (non-serious) with onset 31Aug2021, outcome "unknown", described as "feeling of decreased urination". The events "extreme thirst" and "feeling of excessive dehydration" were evaluated at the physician office visit. Additional information: Patient did not receive any other vaccines within four weeks prior to the suspect administration. Patient had received one allergy shot but no vaccine. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2176548

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: IL
Alter: 57,0
Geschlecht: M
Eingang: 12.03.2022
Impfdatum: 26.08.2021
Beginn: 26.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest pain

Symptomtext

Chest pain; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program (159558). The reporter is the patient. A 58 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 26Aug2021 (Lot number: EW0169) at the age of 57 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "eczema" (unspecified if ongoing). There were no concomitant medications. The following information was reported: CHEST PAIN (non-serious) with onset 26Aug2021, outcome "recovered" (Sep2021), described as "Chest pain". The event "chest pain" was evaluated at the physician office visit and emergency room visit. Additional information included: The report was related to a study or programme. The patient did not receive any additional vaccines administered on same date of the Pfizer Suspect. For the event Chest Pain, patient was not admitted to the hospital though. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccines was None. Time the Vaccination Was Given: between 0800-0900. Expiry Date of Covid-19 Vaccine: Unknown. The patient did not receive other Products. He thought that, the chest pain started right after the vaccine and lasted few days after that. He clarified that it started immediately and continued on for about 10 days. Skin inflammation started after the second dose. He had a history of eczema and it caused him to flare up. It has improved and is under control now. It got out of control in the beginning of Nov2021. The patient Patient's Medical History (including any illness at time of vaccination): None. Family Medical History Relevant to AE(s): none. There were no relevant tests. Investigation Assessment: No. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Eczema
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2175218

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: AL
Alter: 53,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 25.08.2021
Beginn: 05.09.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injected limb mobility decreased Investigation Pain in extremity Peripheral swelling Vaccination site pain

Symptomtext

Whole left side that I got the shot on, I was in so much pain, I could not move, could nobody touch me and it was awful; Whole left side that I got the shot on, I was in so much pain, I could not move, could nobody touch me and it was awful; On my left side that I got the shot, under my arm it is swollen up real bad and even hurting; On my left side that I got the shot, under my arm it is swollen up real bad and even hurting; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 25Aug2021 09:00 (Lot number: EW0169) at the age of 53 years as dose 1, single and administered in arm left, administration date 15Sep2021 09:39 (Lot number: 30135BA) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (ongoing), notes: Verbatim: Blood pressure. Concomitant medication(s) included: LISINOPRIL taken for blood pressure abnormal. The following information was reported: PERIPHERAL SWELLING (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 2021, outcome "unknown" and all described as "On my left side that I got the shot, under my arm it is swollen up real bad and even hurting"; VACCINATION SITE PAIN (non-serious), INJECTED LIMB MOBILITY DECREASED (non-serious) all with onset 05Sep2021, outcome "recovered" (13Sep2021) and all described as "Whole left side that I got the shot on, I was in so much pain, I could not move, could nobody touch me and it was awful". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of peripheral swelling, pain in extremity, vaccination site pain, injected limb mobility decreased. Additional information: Dates for On my left side that I got the shot, under my arm it is swollen up real bad and even hurting: (From: Unspecified To: Unspecified). Dates for Whole left side that I got the shot on, I was in so much pain, I could not move, could nobody touch me and it was awful: (From: Unspecified To: Unspecified). Is COVID 19 Vaccine a Pfizer product? Yes. COVID 19 Vaccine manufacturer: Unspecified. Dates for COVID 19 Vaccine: (Start: Unspecified Stop: Unspecified). NDC number of COVID 19 Vaccine: Unknown. UPC number of COVID 19 Vaccine: Unknown. Expiry Date of COVID 19 Vaccine: Unknown. Other Products: Yes: Dates for Concomitant Products Lisinopril: (Start: Unspecified Stop: Unspecified). Patient History: Yes: Patient history: Blood pressure (From: Unspecified To: Unspecified). Investigation Assessment: Yes. Additional Context: This case is the first case out of two cases in which reporter is reporting for herself. Consumer stated, "I just called, I got the Pfizer shot on the 25Aug and a couple of days after I got the shot, on my left side that I got the shot, my arm, under my arm it is swollen up real bad and even hurting, but I put ice pack on it and it went down. But on 05Sep till the 13th, I had on my whole left side, the whole left side that I got the shot on I could not, I was in so much pain, I could not move, could nobody touch me and it was awful. So, I do not know, I looked on my phone and I tried to ask (Name withheld) about the pain, what do I need to do and they say something about, I could have kidney, it could be my kidney, my pancreas or blood clot or something (further clarification unknown hence not captured as events). So on the 12th that night I got up and I took me some Baby Aspirin, I know Baby Aspirin is (voice not clear), if you got blood clot it do so. That night it kind of eased all so I have been, I have totally been taking Baby Aspirins and it have been my easing the pain but for those few days that I am 'asking you that' it turns out very so bad (further clarification unknown), it was (further clarification unknown). And today I just went and get my last shot. So I found out that the girl in the office had the same side effect but she had it of her second dose (hence split made). So, they just told me to call and report it. So it could be like a side effect I guess because I did not know that, there nobody else had, he said she had, she has it so many times (further clarification unknown), she went in and done X-Rays and stuff and they could not find that. So I am thinking this probably, she got the same shot that I got, so I am feeling this problem from the same thing. But after I took the Baby Aspirin, I have been taking it for a couple of days now and it is like it eased that, so I do not know what this shot, the second shot is going to do so." Concern paraphrased: Consumer stated, "Well I 'want to see', I just got my second shot today so I don't know what (voice not clear) and so I do not know. I was just trying to see, so far I am good." Consumer was informed about the role of Pfizer Medical Information. Vaccine Name: Pfizer COVID 19 Vaccine. Consumer was offered with the number for Pfizer Medical Information. Consumer stated, "Is it the same number the (Withheld)?" Consumer was provided with the number of Pfizer Medical Information (Withheld) and was requested to select option 3, timings as and 8 am to 8 pm Monday to Fridays as per (EST). Consumer was informed about the role of Pfizer Drug Safety and requested to probe. Reporter Type: Consumer stayed, "No, I am a patient (hence captured as Consumer or other non-health professional)." Other Medical Conditions: Consumer stated, "No." Other Medications: Consumer stated, "I take blood pressure pills and I take vitamins." Laboratory Test: Consumer stated, "Oh yeah, I just had lab work done the same day I got the, the week before I got the shot." Name and Result of Laboratory Test: Consumer stated, "I do not have then but everything but good on my, I mean the place that I gave you they done my lab work so they have all my information there." Treatment: Consumer stated, "No, only thing I have taken was Baby Aspirins and Tylenol." Additional questions: Time of vaccination: Consumer stated, "The time, today it was at, today dose it was at 09:39 (am) when I came out. The first one, it was at 9, I had my appointment at 9, it was at 9 o'clock." When probed if consumer had any other vaccination 4 weeks prior to COVID 19 Vaccine, Consumer stated, "No." Route of administration: Consumer stated, "No, I do not even know what you are talking about." Relevant Family Medical History related to events: Consumer stated, "No."(withheld) is cross-linked(withheld). Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Lab work; Result Unstructured Data: Test Result:Unknown result; Comments: Laboratory Test: Consumer stated, "Oh yeah, I just had lab work done the same day I got the, the week before I got the shot."
Aktuelle Erkrankungen: Blood pressure abnormal (Verbatim: Blood pressure).
Vorgeschichte: -
Andere Medikamente: LISINOPRIL.
Allergien: -
Vorherige Impfungen: -

VAERS 2162187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 28,0
Geschlecht: F
Eingang: 06.03.2022
Impfdatum: 17.09.2021
Beginn: 01.01.2022
Tage bis Beginn: 106,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Fatigue Illness Maternal exposure during breast feeding Pain Pyrexia Suppressed lactation

Symptomtext

Within 8 hours after both doses (it was worse after each dose), I became extremely ill. Body aches, fever, short breath, fatigue. It resolved within 24 hours. What I really want to report is that I was breastfeeding at the time of getting the vaccine. My supply started to slowly dip a couple of weeks afterward.... and by November, I had to slowly start supplementing with formula. It is now March and my milk supply is barely existent. My right breast has almost dried up. My menstrual cycle also restarted in Januray (I hadn't had my period prior to this since pre-pregnancy). Prior to the vaccine, I was an "over producer"...able to pump so much milk, I could freeze as much as I wanted (and I so wish I had froze more). I used to be able to pump several days ahead. Aside from the vaccine, nothing in my life/health changed. I am so upset by this and I regret the day I got the shot. Breastfeeding was/is so important to me and it breaks my heart that I have to supplement with formula when I had such a strong supply prior to the vaccine. Vaccine Dates: dose one: 09/17/2021, dose 2: 10/08/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Anemia
Andere Medikamente: Prenatal vitamins and iron.
Allergien: None.
Vorherige Impfungen: -

VAERS 2161068

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: IA
Alter: 22,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 05.08.2021
Beginn: 05.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Lacrimation increased Nausea Tremor Vertigo

Symptomtext

Sudden eyes watering; nausea; vertigo; violent body shaking; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 05Aug2021 14:00 (Lot number: Ew0169) at the age of 22 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: LACRIMATION INCREASED (non-serious) with onset 05Aug2021 15:00, outcome "recovering", described as "Sudden eyes watering"; NAUSEA (non-serious) with onset 05Aug2021 15:00, outcome "recovering", described as "nausea"; VERTIGO (non-serious) with onset 05Aug2021 15:00, outcome "recovering", described as "vertigo"; TREMOR (non-serious) with onset 05Aug2021 15:00, outcome "recovering", described as "violent body shaking". The events "sudden eyes watering", "nausea", "vertigo" and "violent body shaking" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of lacrimation increased, nausea, vertigo, tremor. Additional information: The patient did not receive other vaccine in four weeks. The patient did not receive other medications in two weeks. The patient had not covid prior vaccination. The patient had not covid tested post vaccination. The patient had not known allergies. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
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 2150836

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: PA
Alter: 48,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 19.05.2021
Beginn: 23.06.2021
Tage bis Beginn: 35,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood pressure fluctuation Dizziness Hypertension

Symptomtext

Since July of 2021, second vaccine date in May, my blood pressure has been hypertension stage 1, or elevated, or normal. I was looking at my blood pressure history on my phone and the first case of hypertension was 133/69 on July 23rd. A value as high as 149/87 on February the 6th. I am continuing to monitor. I reported this to my doctor in December they advised I come in however I lost my job and benefits. I did not become worried about my circulation until December when I felt lightheaded after a meal in the evening. I did contact my doctor however I did not make an appointment because I had lost my health insurance. Presently I'm monitoring my blood pressure daily and it fluctuates.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: None
Vorgeschichte: BMI -- 26
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1992217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NH
Alter: 53,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Injected limb mobility decreased Magnetic resonance imaging Pain Pain in extremity Muscle strain X-ray

Symptomtext

Continual strain and pain in my left fore arm. between my elbow and wrist; Continual strain and pain in my left fore arm. between my elbow and wrist; 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 22Apr2021 (Lot number: EW0169) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing), notes: handled with medication; "Sulfa Drug Allergy" (unspecified if ongoing). Concomitant medication(s) included: ABILIFY; TOPIRAMATE; DULOXETINE; PRIMIDONE. Vaccination history included: Bnt162b2 (Dose 1, lot number: EN6205, vaccine location: left arm), administration date: 23Mar2021, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: MUSCLE STRAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 22Apr2021, outcome "not recovered" and all described as "Continual strain and pain in my left fore arm. between my elbow and wrist". Therapeutic measures were not taken as a result of muscle strain, pain in extremity. Additional Information: Facility type vaccine was reported as other. The patient reported that, "continual strain and pain in my left fore arm. between my elbow and wrist. I sometimes can not even pick up a soda can or shuffle a deck of cards." No pain at the injection site. Started immediately after receiving the second vaccine and had not lessened. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression (handled with medication); Sulfonamide allergy
Andere Medikamente: ABILIFY; TOPIRAMATE; DULOXETINE; PRIMIDONE
Allergien: -
Vorherige Impfungen: -

VAERS 1992217

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NH
Alter: 53,0
Geschlecht: F
Eingang: 26.02.2022
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: nein

Arthralgia Injected limb mobility decreased Magnetic resonance imaging Pain Pain in extremity Muscle strain X-ray

Symptomtext

Continual strain and pain in my left fore arm. between my elbow and wrist; Continual strain and pain in my left fore arm. between my elbow and wrist; 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 22Apr2021 (Lot number: EW0169) at the age of 53 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Depression" (unspecified if ongoing), notes: handled with medication; "Sulfa Drug Allergy" (unspecified if ongoing). Concomitant medication(s) included: ABILIFY; TOPIRAMATE; DULOXETINE; PRIMIDONE. Vaccination history included: Bnt162b2 (Dose 1, lot number: EN6205, vaccine location: left arm), administration date: 23Mar2021, when the patient was 53 years old, for COVID-19 immunization. The following information was reported: MUSCLE STRAIN (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 22Apr2021, outcome "not recovered" and all described as "Continual strain and pain in my left fore arm. between my elbow and wrist". Therapeutic measures were not taken as a result of muscle strain, pain in extremity. Additional Information: Facility type vaccine was reported as other. The patient reported that, "continual strain and pain in my left fore arm. between my elbow and wrist. I sometimes can not even pick up a soda can or shuffle a deck of cards." No pain at the injection site. Started immediately after receiving the second vaccine and had not lessened. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression (handled with medication); Sulfonamide allergy
Andere Medikamente: ABILIFY; TOPIRAMATE; DULOXETINE; PRIMIDONE
Allergien: -
Vorherige Impfungen: -

VAERS 2134605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KS
Alter: 34,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 19.02.2022
Beginn: 19.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Palpitations

Symptomtext

Patient in for booster dose 2/19/2022, patient received booster dose Pfizer dose 33025BD in observation area and stated she felt like heart was racing and high anxiety noted. Vitals taken P87, O2 100%, BP 120/82, R 20 patient given sips of H20 and visited w patient. States increased anxiety was because days after 1st dose Pfizer her right eye became irritated and red, Went to eye dr. and he stated she has had a reaction to something. No treatment needed. After 20 minutes she was calmer and states feeling better. 4:50 pm vitals were BP 116/60 , R 18, P 84, 02 98% Recommended if any issues contact physician or go to ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: 1st dose, Pfizer Covid 19 vaccine 4/6/2021

VAERS 2641338

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 22.02.2022
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

Asthenia Dizziness Hypoaesthesia Paraesthesia

Symptomtext

Intermittent tingling & Numbness of Right arm approx 10 minutes after injection to Left arm. Dizziness and generalized weakness ~ 10 minutes after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None as of 4/14/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Iron
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2130036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 10.05.2021
Beginn: 10.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Headache Lethargy Mobility decreased Somnolence

Symptomtext

went outside and planted and it took her 15 minutes when it should of taken her 5 minutes; severe lethargy; Severe Backache; head ache; Sleeps a lot; 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 46 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10May2021 09:00 (Lot number: EW0169) at the age of 46 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: LETHARGY (non-serious) with onset 10May2021, outcome "not recovered", described as "severe lethargy"; BACK PAIN (non-serious) with onset 10May2021, outcome "not recovered", described as "Severe Backache"; HEADACHE (non-serious) with onset 10May2021, outcome "not recovered", described as "head ache"; SOMNOLENCE (non-serious) with onset 10May2021, outcome "not recovered", described as "Sleeps a lot"; MOBILITY DECREASED (non-serious), outcome "unknown", described as "went outside and planted and it took her 15 minutes when it should of taken her 5 minutes". Therapeutic measures were taken as a result of lethargy, back pain, headache. Additional information: Treatment: Bed and Tylenol, Rexall Sports Rubbing Alcohol Cream, Muscle Freeze like Icy Hot, Acetaminophen. AEs did not require a visit to Emergency Room or Physician Office. Prior Vaccinations (within 4 weeks), AE(s) following prior vaccinations, Family Medical History Relevant to AE(s), Relevant Tests: None. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
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 2127071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 38,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 15.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Pain in extremity Paraesthesia

Symptomtext

pain to the left leg; tingly feeling to his feet; 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 male patient received bnt162b2 (BNT162B2), administration date 15Apr2021 (Lot number: EW0169) at the age of 38 years 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: PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "pain to the left leg"; PARAESTHESIA (non-serious) with onset 2021, outcome "unknown", described as "tingly feeling to his feet". The events "pain to the left leg" and "tingly feeling to his feet" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of pain in extremity, paraesthesia. Additional Information: The patient received first dose of Pfizer Covid Vaccine on 15Apr2021 and he is complaining of pain to the left leg and a tingly feeling to his feet, specifically his left pinky toe. He went to urgent care and they examined him and told him there was nothing wrong with his leg and prescribed him Ibuprofen. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2126865

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 24,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 14.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Migraine Nausea Pain Vaccination site pain Vomiting

Symptomtext

Mild episodes of Migraine; Arm pain where I received the shot; Nauseous; Throwing up several times; This cost me some hours with my work because of this pain; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 24 year-old male patient received bnt162b2 (BNT162B2), administered in arm, administration date 14Apr2021 (Lot number: EW0169) at the age of 24 years as dose 1, single for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: MIGRAINE (non-serious), outcome "unknown", described as "Mild episodes of Migraine"; VACCINATION SITE PAIN (non-serious), outcome "unknown", described as "Arm pain where I received the shot"; NAUSEA (non-serious), outcome "unknown", described as "Nauseous"; VOMITING (non-serious), outcome "unknown", described as "Throwing up several times"; PAIN (non-serious), outcome "unknown", described as "This cost me some hours with my work because of this pain". Additional information: Other Products and Investigation Assessment are reported as NO No follow-up attempts are possible. 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: -
Allergien: -
Vorherige Impfungen: -

VAERS 2126529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 55,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Paraesthesia

Symptomtext

feel tingly & kind of numb; feel tingly & kind of numb; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55 year-old female patient (not pregnant) received BNT162B2, administered in arm right, administration date 21Apr2021 11:00 (Lot number: EW0169, Expiration date: Unknown) at the age of 55 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Discoid lupus erythematosus (Skin lupus, NOT systemic lupus)" (unspecified if ongoing), notes: Discoid lupus erythematosus (Skin, lupus, NOT systemic lupus). Concomitant medication(s) included: SYNTHROID. Past drug history included: Known allergies: sulfa, reaction(s): "drug allergy", notes: Sulfa. Vaccination history included: Bnt162b2 (Product: COVID 19, Brand: mRNA/Pfizer, Lot number: ER8733, Lot unknown: False, Administration date: 23Mar2021, Administration time: 11:00am, Vaccine location: Right arm, Dose number: 1), administration date: 23Mar2021, when the patient was 55 years old, for Covid-19 Immunisation, reaction(s): "feel tingly & kind of numb". The following information was reported: PARAESTHESIA (non-serious), HYPOAESTHESIA (non-serious) all with onset 22Apr2021 11:15, outcome "recovering" and all described as "feel tingly & kind of numb". Therapeutic measures were not taken as a result of paraesthesia, hypoaesthesia. Additional information: No other vaccine in four weeks. No COVID prior vaccination. No COVID tested post vaccination. 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: Discoid lupus erythematosus (Discoid lupus erythematosus (Skin lupus, NOT systemic lupus))
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 2118686

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 12.10.2021
Beginn: 12.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Gait disturbance Lymph node pain Migraine Nausea

Symptomtext

migraine; joints hurt so that I could walk barely; joints hurt so that I could walk barely; armpits hurt very badly; nausea; chills; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 12Oct2021 15:00 (Lot number: EW0169) at the age of 63 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Neuropathies" (ongoing), notes: secondary to chemo 2006; "Raynaud's" (ongoing), notes: secondary to chemo 2006; "spinal stenosis" (ongoing); "arthritis" (unspecified if ongoing); "Migraine", start date: 1988 (ongoing), notes: since 1988- occasional; "pain issues" (unspecified if ongoing); "cholesterol" (unspecified if ongoing); "SI Joint" (unspecified if ongoing); "sleep" (unspecified if ongoing); "Periodic asthma" (unspecified if ongoing). Concomitant medication(s) included: FLUZONE QUADRIVALENT, administration date 07Oct2021; CYCLOBENZAPRINE taken for sacroiliac joint dysfunction (ongoing); HYDROCODONE taken for arthritis, stenosis, migraine (ongoing); MAGNESIUM OXIDE; TYLENOL taken for pain (ongoing); PRAVASTATIN taken for blood cholesterol abnormal (ongoing); ALPRAZOLAM taken for sleep disorder (ongoing). Past drug history included: Allergy: codein, reaction(s): "Allergy: Codein"; Allergy: demerol, reaction(s): "Allergy: demerol"; Allergy: ultram, reaction(s): "Allergy: ultram"; Allergy: ergotamine, reaction(s): "Allergy: ergotamine". Vaccination history included: Pfizer (Dose Number: 2, Batch/Lot No: ER8733, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 09Apr2021, when the patient was 63 years old, for COVID-19 Immunization; Pfizer (Dose Number: 1, Batch/Lot No: EN6207, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 19Mar2021, when the patient was 63 years old, for COVID-19 Immunization; Flu shot (Anatomical Site of injection: R. Arm), administration date: 07Oct2021, when the patient was 63 years old. The following information was reported: MIGRAINE (non-serious) with onset 12Oct2021 21:00, outcome "recovering", described as "migraine"; GAIT DISTURBANCE (non-serious), ARTHRALGIA (non-serious) all with onset 12Oct2021 21:00, outcome "recovering" and all described as "joints hurt so that I could walk barely"; LYMPH NODE PAIN (non-serious) with onset 12Oct2021 21:00, outcome "recovering", described as "armpits hurt very badly"; NAUSEA (non-serious) with onset 12Oct2021 21:00, outcome "recovering", described as "nausea"; CHILLS (non-serious) with onset 12Oct2021 21:00, outcome "recovering", described as "chills". Therapeutic measures were taken as a result of migraine, gait disturbance, arthralgia, lymph node pain, nausea, chills. Additional information: The Booster had much more severe side effects than the first two doses. My joints hurt so that I could walk barely and my armpits hurt very badly. I felt the same level of nausea, migraine, and chills. I'm glad I didn't know beforehand because I might have missed the booster. I understand these effects to be a strong immune response which is good news and I'm very grateful to Pfizer and (Privacy) for providing these vaccines. I won't tell anyone how awful I feel bec I would not deter anyone. At one point though the side effects were scary and I thought how awful for those suffering Covid in the hospitals and dying. I am tryi g to convince my son who is in a Frontline occup to get the booster. Still, I thought you should know the side effects were pretty rough. Still, I'm very grateful. Took hydrocodone though I had been greatly reduc. pain subsided after 2.5 days. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Weakened immune system. Specific Relevant Test For Thromboembolic Events with Thrombocytopenia was unknown. Patient did not need emergency medical treatment due to the Booster. Children will be very wary if they have similar side effects. (Praying) No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine (since 1988- occasional); Neuropathy (secondary to chemo 2006); Raynaud's syndrome (secondary to chemo 2006); Spinal stenosis
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Asthma; Blood cholesterol abnormal; Pain; Sacroiliac joint dysfunction; Sleep disorder
Andere Medikamente: CYCLOBENZAPRINE; HYDROCODONE; MAGNESIUM OXIDE; TYLENOL; PRAVASTATIN; ALPRAZOLAM
Allergien: -
Vorherige Impfungen: -

VAERS 2113058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 65,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 14.05.2021
Beginn: 09.02.2022
Tage bis Beginn: 271,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Alanine aminotransferase normal Albumin globulin ratio Anion gap Anticoagulant therapy Aspartate aminotransferase increased Asthenia Basophil count normal Basophil percentage Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium normal Blood chloride normal Blood creatinine decreased Blood glucose normal Blood potassium normal Blood sodium normal Blood urea decreased

Symptomtext

2/9/22 66-year-old male with history of congestive heart failure, hypertension, hyperlipidemia, essential thrombocythemia, CVA presented to the emergency department with shortness of breath. Diagnosed with coronavirus most week ago, no nausea or vomiting, no diarrhea. No abdominal pain. No chest pain. Patient is on chronic Xarelto for history of stroke. Denies any complaints. Onset: 6 days, Timing: Intermittent, Location: Chest Quality: Shortness of breath, Radiation: None, Severity: Moderate, worsened by: Exertion, Relieved by: Rest, Associated symptoms: None, Review of Systems, Constitutional: Positive for activity change and fatigue. Negative for chills and fever. HENT: Negative for congestion and sore throat. Eyes: Negative for pain and discharge. Respiratory: Positive for shortness of breath. Negative for cough.Cardiovascular: Negative for chest pain, palpitations and leg swelling. Gastrointestinal: Negative for abdominal pain, nausea and vomiting. Genitourinary: Negative for dysuria, frequency and urgency. Musculoskeletal: Negative for back pain and myalgias. Skin: Negative for color change and rash. Neurological: Negative for light-headedness and headaches. 2/10/22 Discharge summary: Patient is a 66-year-old male who presents the hospital with complaints of shortness of breath. He was diagnosed with COVID-19 6 days prior to admission and did feel weak and congested, however he began having dyspnea with exertion just prior to admission. He went to the ICC where he was found to have O2 saturations in the mid 80s on room air. He was placed on oxygen and sent to the ER for further evaluation where he was admitted for treatment of hypoxia related to COVID-19 viral pneumonia. He was started on IV steroids and Remdesivir and had significant improvement in his symptoms over the last 24 hours. He was able to ambulate without any significant DOE but will require oxygen temporarily on discharge. This will be arranged for the patient and I will also discharge him on a course of oral Decadron. The patient will be discharged home with referral to the virtual hospital as well. He should also follow-up with PCP in 1 week. He is stable for discharge at this time and anticipate he will likely need O2 for the next 1 to 2 weeks at most. He is vaccinated and received a booster dose as well, although he is immunocompromised and therefore likely had a slightly worse course of illness due to this reason.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 1,0
Labordaten: 2/9/22 XR Chest 1 Vw CONCLUSION: No active disease, Comprehensive Metabolic Panel (CMP), Collection Time: 02/09/22 4:03 PM, Result Value Ref Range, Sodium 136 136 - 145 mmol/L, Potassium 4.6 3.5 - 5.1 mmol/L, Chloride 103 98 - 107 mmol/L, Carbon Dioxide 25 22 - 29 mmol/L, Anion Gap 8 5 - 13 (arb'U), Glucose 188 (H) 74 - 99 mg/dL, Blood Urea Nitrogen (BUN) 8 8 - 26 mg/dL, Creatinine-Blood 0.58 (L) 0.73 - 1.18 mg/dL, BUN/Creatinine Ratio 13.8 RATIO, Estimated GFR >60 >60 /1.73 m2, Estimated GFR if African-American >60 >60 /1.73 m2, Total Protein 7.3 6.2 - 8.0 g/dL, Albumin 3.8 3.2 - 4.6 g/dL, Globulin 3.5 1.5 - 4.5 g/dL, Albumin/Globulin Ratio 1.1 1.1 - 2.5 RATIO, Calcium 9.3 8.4 - 10.2 mg/dL, Total Bilirubin 0.3 0.2 - 1.2 mg/dL, AST/SGOT 40 (H) 5 - 34 U/L, ALT/SGPT 36 0 - 55 U/L, Alkaline Phosphatase 85 40 - 150 U/L, Type Natriuretic Peptide, Collection Time: 02/09/22 4:03 PM, Result Value Ref Range, B-Type Natriuretic Peptide 17.6 3 - 160 pg/mL, Troponin, Collection Time: 2/09/22 4:03 PM, Result Value Ref Range, Troponin <0.010 0.000 - 0.034 ng/m, CBC w/Diff Collection Time: 02/09/22 4:03 PM. Result Value Ref Range, White Blood Count 9.29 4.5 - 11.0 10*3/uL, Red Blood Count 3.74 (L) 4.5 - 5.9 10*6/uL, Hemoglobin 11.4 (L) 13.5 - 17.5 g/dL, Hematocrit 36.8 (L) 41.0 - 53.0 %, Mean Corpuscular Volume 98.4 80.0 - 100.0 fL, Mean Corpuscular Hemoglobin 30.5 26.0 - 34.0 pg, Mean Corpuscular HGB Conc 31.0 31.0 - 37.0 g/dL, Red Cell Distribution Width-CV 17.1 (H) 12.0 - 16.8 %, Platelet Count 882 (H) 140 - 440 10*3/uL, Mean Platelet Volume 9.5 8.4 - 12.4 fL, Diff Type Hospital CBC w/AutoDiff (arb'U), Neutrophils % 65.2 45 - 80 %, Lymphocyte % 24.3 15 - 50 %, Monocyte % 7.5 0 - 15 %, Eosinophil% 0.9 0 - 7 %, BASO% 0.5 0 - 2 %, Immature Granulocyte% 1.6 (H) 0.0 - 1.0 %, Nucleated RBC % 1 (H) 0 /100 (WBC), Neutrophil Abs 6.05 2.0 - 8.8 10*3/uL, Lymphocyte-Absolute 2.26 0.7 - 5.5 10*3/uL, Monocyte Absolute 0.70 0.0 - 1.7 10*3/uL, EOS-Absolute 0.08 0.0 - 0.8 10*3/uL, Basophil Abs 0.05 0.0 - 0.2 10*3/uL, Immature Granulocyte Abs 0.15 (H) 0.00 - 0.10 10*3/L,
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, Asthma, CHF (congestive heart failure) 12/23/2015, Gallstones, Gout, Hyperlipidemia, Hyperlipidemia Hypertension Leukemia Myocardial infarction 1992 Polycythemia Shingles 12/21/13 Stroke 1992 Umbilical hernia
Andere Medikamente: allopurinol (ZYLOPRIM) 300 MG tablet Take 300 mg daily, allopurinol (ZYLOPRIM) 300 MG tablet Take 300 mg by mouth daily cyclobenzaprine (FLEXERIL) 10 MG tablet Take 10 mg by mouth 2 (two) times daily as needed ferrous sulfate 325 (6
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2110287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 79,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 20.04.2021
Beginn: 30.01.2022
Tage bis Beginn: 285,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal pain Asthenia COVID-19 pneumonia Cough Dyspnoea Fatigue Oropharyngeal pain Wheezing

Symptomtext

recent diagnosis of COVID pneumonia on 1/30/22 in the setting of increasing fatigue, sore throat, cough, wheezing, shortness of breath, abdominal pain, and generalized weakness. She was hospitalized from 1/30 - 2/06/22 in the setting of her pneumonia and was discharged home with new oxygen requirements. Patient states that she normally does not use oxygen at home, but has been using 1L of supplemental oxygen since her COVID diagnosis. She endorses an ongoing cough, wheezing, and shortness of breath but has otherwise been back to her normal state of health.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2109076

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Autonomic nervous system imbalance Chronic fatigue syndrome Disease recurrence Mast cell activation syndrome Menstrual disorder Post viral fatigue syndrome Postural orthostatic tachycardia syndrome SARS-CoV-2 test Vertigo

Symptomtext

Worst relapse of ME/CFS I''ve ever had in 18 years. Have been bed bound since, never returned to baseline.; Worst relapse of ME/CFS I''ve ever had in 18 years. Have been bed bound since, never returned to baseline.; Worst relapse of ME/CFS I''ve ever had in 18 years. Have been bed bound since, never returned to baseline.; vertigo; dysautonomia; POTS; MCAS; menstrual cycle changes; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 13Apr2021 15:00 (Lot number: EW0169) at the age of 48 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "ME/CFS" (unspecified if ongoing); "ME/CFS" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing); "PCOS" (unspecified if ongoing); "Sleep apnea" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN ER; GABAPENTIN; VENLAFAXINE XR; LAMICTAL. Past drug history included: Septra, reaction(s): "Known allergies:Septra". The following information was reported: CHRONIC FATIGUE SYNDROME (disability), POST VIRAL FATIGUE SYNDROME (disability), DISEASE RECURRENCE (disability) all with onset 13Apr2021 18:00, outcome "not recovered" and all described as "Worst relapse of ME/CFS I''ve ever had in 18 years. Have been bed bound since, never returned to baseline."; VERTIGO (disability) with onset 13Apr2021 18:00, outcome "not recovered", described as "vertigo"; AUTONOMIC NERVOUS SYSTEM IMBALANCE (disability) with onset 13Apr2021 18:00, outcome "not recovered", described as "dysautonomia"; POSTURAL ORTHOSTATIC TACHYCARDIA SYNDROME (disability) with onset 13Apr2021 18:00, outcome "not recovered", described as "POTS"; MAST CELL ACTIVATION SYNDROME (disability) with onset 13Apr2021 18:00, outcome "not recovered", described as "MCAS"; MENSTRUAL DISORDER (disability) with onset 13Apr2021 18:00, outcome "not recovered", described as "menstrual cycle changes". The events "worst relapse of me/cfs i''ve ever had in 18 years. have been bed bound since, never returned to baseline.", "vertigo", "dysautonomia", "pots", "mcas" and "menstrual cycle changes" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: sars-cov-2 test: (14Jan2022) negative, notes: Blood test; (10Dec2021) negative, notes: Nasal Swab. Therapeutic measures (MCAS labs, Valtrex, Claritin, Pepcid AC, Benadryl) were taken as a result of chronic fatigue syndrome, post viral fatigue syndrome, disease recurrence, vertigo, autonomic nervous system imbalance, postural orthostatic tachycardia syndrome, mast cell activation syndrome, menstrual disorder. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Postural orthostatic tachycardia syndrome
Hospital-Tage: -
Labordaten: Test Date: 20220114; Test Name: IGG Autobodies; Test Result: Negative ; Comments: Blood test; Test Date: 20211210; Test Name: PCR Nasal Swab; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic fatigue syndrome; Fibromyalgia; Myalgic encephalomyelitis; Polycystic ovary; Sleep apnea
Andere Medikamente: METFORMIN ER; GABAPENTIN; VENLAFAXINE XR; LAMICTAL
Allergien: -
Vorherige Impfungen: -

VAERS 2105029

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 71,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 21.04.2021
Beginn: 10.02.2022
Tage bis Beginn: 295,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain SARS-CoV-2 test positive

Symptomtext

Pt was admitted on 2/6 for chest pain and was a direct admit from an outlying facility. She was tested for COVID on admission and was negative. She was re-tested on 2/10 pre-operatively and found to be positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2101797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: WI
Alter: 62,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 01.12.2021
Beginn: 26.01.2022
Tage bis Beginn: 56,0
Dosis: UNK
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Angiogram pulmonary Anticoagulation drug level above therapeutic Blood creatinine normal Blood culture negative COVID-19 Cough Culture urine positive Dehydration Dyspnoea Fatigue Gastrointestinal disorder Hypoxia International normalised ratio Oxygen saturation decreased Positive airway pressure therapy Productive cough Respiratory failure Respiratory tract congestion

Symptomtext

Patient is a 62 y.o. male with PMH of a-fib, CAD s/p CABG, mechanical aortic and mitral valve replacements on warfarin, renal transplant x2 (most recently '18), DM1, pancreatic transplant, adrenal insufficiency, OSA on CPAP and remote hx of DVT who presents in transfer from hospital where he has been admitted with covid since 1/17. His symptoms started on 1/14 per outside H&P with chest congestion, rhinorrhea and cough. He originally presented there on 1/17 due to dehydration from <24h of vomiting. At that time was mildly hypoxic requiring 2L O2 NC. He was treated with IVF, 2 days of remdesivir and dexamethasone. There was a question of UTI so he received ceftriaxone x3 days, but UCx grew mixed flora an it was stopped. BCx were negative. He had been doing well enough that they were considering discharge on home O2, but then during the last 24 hours his respiratory failure worsened to the point of requiring high flow oxygen, and then bipap was started last night due to increased WOB. He received tocilizumab yesterday. Attempts were made to transfer to the transplant center, but they were full with a waiting list. Therefore, he was transferred here while awaiting bed. Of note, his creatinine has been stable throughout the stay at hospital and his INRs have been therapeutic and supratherapeutic. Because of that, CTA for PE was felt to be low yield. He did receive stress dose steroids for a period of time after he had increased abdominal symptoms. At this time he is on 6mg dex bid at direction of transplant center. His other immunosuppressants are being held. Upon arrival here, he states he feels fatigued and has a minimally productive cough, but otherwise feels ok. Denies chest pain, presyncope, orthopnea, leg swelling, abdominal pain, current n/v. We attempted to wean him off Bipap to HF mask 100% 70L and he desaturated to 85%, so we put him back on CPAP of 10, at 80% FiO2 with O2 sat of 96%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2069351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 79,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 04.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 34,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal distension Asthenia Blood pressure fluctuation Computerised tomogram abdomen abnormal Computerised tomogram normal Decreased appetite Fatigue Feeling abnormal Gait inability Laboratory test Malaise Motor dysfunction Pain Pneumonia Tremor Weight decreased Wheelchair user White blood cell count increased

Symptomtext

Cannot say an exact date, but early December 2021, I started feeling bad; gradually feeling worse and worse. Dec 20, I had an appointment with my doctor, and told him I was very tired. My blood pressure was up and down. I was hurting all over. He found I had an elevated white blood count. He prescribed an antibiotic and ordered a CT scan, since my stomach was enlarged some. Dec 23, I was taken to ER at a regional hospital and found to have pneumonia. I was very weak and not eating much. I was given an IV of antibiotics and prednisone. Jan 2, was my second trip to ER at a regional hospital now very, very weak, not eating and still elevated white blood count. I was released with nothing done because they couldn't find an issue. Jan 7, a CT scan was performed. Nothing found they say. I was so sick, I had to be in wheelchair because I couldn't walk. I was shaking very bad. I was so sick I couldn't function. I've lost about 20 to 25 pounds since this started.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: I went to a clinic and they are ran all sorts of tests to find the issue. No results yet.
Aktuelle Erkrankungen: COPD, high blood pressure
Vorgeschichte: COPD, high blood pressure
Andere Medikamente: Vitamins D, C, B, Zinc, Magnesium, Finasteride 5mg, Lorartan 100mg
Allergien: Sulfa drug
Vorherige Impfungen: -

VAERS 2065744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 50,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 20.09.2021
Beginn: 27.12.2021
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Chest X-ray abnormal Chills Diarrhoea Dyspnoea Headache Lung opacity Pain Parosmia Productive cough Respiratory tract congestion Taste disorder

Symptomtext

Patient is fully vaccinated. Pt. presents to ED with cough, congestion times one week. Reports that he tested positive COVID on 12/22. Patient reports that he's having mild shortness of breath, no chest pain, has cough- productive, congestion, body aches, changes in smell and taste but denies losing his taste. Reports he has had some bouts of diarrhea. No nausea or vomiting. Denies fever. Positive for chills, headaches. BP 114/67 | Pulse 62 | Temp 97.9 ?F (36.6 ?C) (Oral) | Resp. 18 | HT 165.1 cm (5' 5") | WT 88.5 kg (195 lb.) | SpO2 97% | BMI 32.45 kg/m? CXR: Subtle interstitial opacities bilaterally may reflect Covid 19 pneumonia. Sent information over for monoclonal infusion they will contact patient. Pt discharged from ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2065392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 48,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 05.05.2021
Beginn: 18.01.2022
Tage bis Beginn: 258,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Asthenia Bacterial test Blood culture negative Blood urine present COVID-19 Chest X-ray abnormal Clostridium test negative Cough Culture stool negative Culture urine positive Diarrhoea Headache Imaging procedure Influenza virus test negative Laboratory test Legionella test Lung consolidation

Symptomtext

Hospitalized 01/18/2022; COVID-19 positive 01/18/2022; fully vaccinated DATE OF ADMISSION: 01/18/2022 DATE OF DISCHARGE: 01/21/2022 Attending physician, covering for Dr. HOSPITAL COURSE The patient is a very pleasant 49-year-old male with past medical history as listed above including non-small cell lung cancer, actively on chemotherapy and immunotherapy with Dr., who presented to ED with symptoms of intermittent fevers, cough, headache, diarrhea, and generalized weakness. Initial laboratory studies and imaging can be found per Epic review. Of note, COVID positive in the ED on January 18. He was negative for influenza. The patient is vaccinated, but has not had his booster. Chest x-ray showed new patchy nodular airspace disease in the left lower lobe consistent with new organizing pneumonia. Stable right upper lobe consolidation. Legionella strep pneumo and MRSA were negative. He was started on Zosyn empirically in the ED. He was transferred for further evaluation. He was started on remdesivir x3 doses. Monoclonal antibodies have no affect against Omicron variant and he would not qualify. Discussed this with Infectious Disease. The patient had complaints of significant diarrhea. C diff and stool for enteric pathogens were obtained and both were negative. There was concern for immune mediated colitis. He was started on high-dose Solu-Medrol with plan to transition to oral prednisone probably or with likely prolonged taper. He had no fevers during the hospital stay. UA showed leukocytes, blood, and few bacteria. Urine culture showed resident flora. Blood cultures have remained negative to date. Zosyn was discontinued at discharge. There was no need for Zarxio as the patient has already reached his nadir. He had mild AKI on presentation and was treated with IV fluid hydration. This has normalized. Overall, he did well during the course of the hospital stay. He remained hospitalized to receive 3 doses of remdesivir. He was felt medically stable for discharge on 01/21/2022. Planned desat walk prior to discharge to ensure he does not require any home oxygen with ambulation. He is encouraged to call our office if he has any respiratory decline or present to the emergency department if needed. DISCHARGE INSTRUCTIONS The patient has followup with Dr. on January 31 at 11:40 a.m. Chemotherapy on hold until followup with Dr.

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Praegender Schweregrund: Organising pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Non-small cell cancer of right lung COPD (chronic obstructive pulmonary disease) OSA (obstructive sleep apnea) Squamous cell lung cancer, right Aortic valve regurgitation Essential hypertension Leukocytoclastic vasculitis Pulmonary emboli Acute anemia Neutropenic fever Chronic bilateral low back pain with sciatica Metastasis to kidney AKI (acute kidney injury) Sepsis Personal history of PE (pulmonary embolism) Port-A-Cath in place Adrenal mass Endogenous depression Immunocompromised Tobacco use disorder
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet apixaban (ELIQUIS) 5 MG tablet benzonatate (TESSALON) 200 MG capsule budesonide/fo
Allergien: NKA
Vorherige Impfungen: -

VAERS 2058869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 71,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 19.05.2021
Beginn: 16.01.2022
Tage bis Beginn: 242,0
Dosis: 2
Route/Site: IM / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia COVID-19 Chest pain Confusional state Dyspnoea SARS-CoV-2 test positive

Symptomtext

Hospitalized for COVID with shortness of breath, chest pains, weakness, and confusion on 1/16/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: positive COVID test on 1/16/2022
Aktuelle Erkrankungen: unknown
Vorgeschichte: history of cirrhosis, history of esophageal varices, coronary heart disease, stage 3 chronic kidney disease, hypertension, hyperlipemia, and sleep apnea
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2058589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 51,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 19.04.2021
Beginn: 08.01.2022
Tage bis Beginn: 264,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Ammonia increased Angiogram cerebral normal Anticoagulant therapy Blood culture positive Blood glucose normal Brain oedema COVID-19 COVID-19 pneumonia Cerebral haematoma Cerebral mass effect Child-Pugh-Turcotte score increased Chronic disease Compression garment application Computerised tomogram head abnormal Condition aggravated Craniocerebral injury Dysphagia Faecal volume increased

Symptomtext

TRAUMA PROGRESS NOTE 1/21/2022 REMAINS HOSPITALIZED 1/24/2022 ASSESSMENT/PLAN: The patient is a 52 y.o. male who was admitted on 1/13 with R-sided weakness and abnormal speech after unwitnessed fall on 1/8. HCT with left temporal lobe parenchymal hematoma with surrounding cerebral edema and local mass effect. He was also discovered to have COVID pneumonia, he was treated for CAP with 5 day course of ABX. Repeat HCT 1/14 was stable, MRI/MRA 1/14 without evidence of underlying vascular lesion, tumor, or pathologic reason for left temporal lobe hemorrhage. He did receive lactulose for elevated ammonia in context of ongoing encephalopathy likely attributed to TBI and medications. He was transferred to the floor 1/17. Tube feeds were initiated but he ended up self pulling this 1/18, however he is cleared for PO diet and he is doing well with this so decision was made to defer replacement of FT for now. Active Hospital Problems Fall - tertiary completed Left temporal lobe parenchymal hematoma with mass effect complicated by Acute Metabolic encephalopathy - nsgy consulted. - Repeat HCT 1/14 was stable - MRI/MRA 1/14 without evidence of underlying vascular lesion, tumor, or pathologic reason for left temporal lobe hemorrhage. - Na goal 140-145 - Na tabs 2g TID. - Free Water restricted 1L - SBP goal <160 and maintaining Prediabetes - A1C 6.2 - low SSI - BS goal <180 and maintaining. Did have a single reading of 190s last night but since his PO intake is somewhat inconsistent, will hold off on Lantus for now. COVID pneumonia - Finished Zithromax and Rocephin course 5 days to cover for CAP - on RA. - Deep breathing exercises, IS therapy. Up as able. - DDIMER 1.6 1/18 from 4.4. - given TBI and thrombocytopenia, contraindicated for therapeutic AC. Continue on heparin ppx. - PCT 1/17 0.04, no leukocytosis, afebrile. - Blood cultures on admission 1 of 2 showing GPC. Likely contaminant. Hold off on ABX. Repeat BC pending. No growth so far. - Off full barrier precautions on Sunday. Chronic Pancytopenia due to chronic disease Chronic thrombocytopenia - Outpatient records with PLT at ~50s. Now trend ~30s. Trend every other day. If continues to decrease will reevaluate ppx therapy, consider repeat HCT and stop dvt ppx if PLT <25. hgbs are stable. No evidence of active bleeding Dysphagia - Due to TBI - Speech following, diet per them - much improved, having better PO intake Urinary incontinence - UA neg, monitor. - Strict I&Os Left upper arm hematoma - from in hospital fall - mark with marker and compression wrapping - XRs negative for fracture. Hx of hepatic cirrhosis, unspecified hepatic cirrhosis type, unspecified whether ascites present (HCC) - Child-Pugh class B - avoid hepatotoxic medications. - hold lactulose due to large vol. Stools. Ammonia 49 improved to 43. Low suspicion for encephalopathy of hepatic origin, suspect is largely due to TBI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 12,0
Labordaten: COVID PCR POSITIVE 1/13/2022
Aktuelle Erkrankungen: -
Vorgeschichte: He was admitted almost two years ago with an UGI bleed- was found to have cirrhosis (attributed to etoh) with esophageal varices (banded). A CT scan was obtained showing possible liver lesions. He was to have a repeat EGD and a liver MRI-which I see no evidence of having occurred. He has been chronically thrombocytopenic as well, though did not have splenomegaly on CT 2 years ago.
Andere Medikamente: -
Allergien: NO KNOWN
Vorherige Impfungen: -

VAERS 2058252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: UT
Alter: 27,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Angina pectoris Arthralgia Blood test normal Chest discomfort Chest pain Electrocardiogram normal Hypoaesthesia Muscle spasms X-ray normal

Symptomtext

After 3rd dose, later in the day started feeling aching on left side of chest/shoulder. This quickly moved directly around heart area and included sharp pain around heart. Heart felt very tight and was aching. Kept getting worse throughout week. Left arm went numb 6 days after vaccine. Went to ER on day 6 once arm numbness started. They took EKG, blood work and xray. Found nothing immediately wrong. Gave anti-inflammatory shot and 5 day anti-inflammatory prescription. A few days after prescription ended chest pain kicked up again, being very tight and painful at times. Would take ibuprofen to help pain. Started taking quercetin, vitamin c and zinc daily which seems to b helping. A month later has gotten better but still aches and feels like a cramp around heart from time to time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, blood work, x ray
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2057317

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 33,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 21.05.2021
Beginn: 02.06.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Dyspnoea Heart rate irregular SARS-CoV-2 test

Symptomtext

Chest pains; Shortness of breath; Irregular heart beat; This is a spontaneous report from a contactable reporter (consumer or other non-HCP). The reporter is the patient. A 33-year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21May2021 at 15:00 (Lot number: EW0169) at the age of 33 years as dose 2, single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?: Yes. Concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot Number: ER8731; Anatomical Location: Arm Left; Administration time: 15:00; Route of administration: Unspecified), administration date: 29Apr2021, when the patient was 33 years old, for COVID-19 immunisation. The following information was reported: CHEST PAIN (non-serious) with onset 02Jun2021, outcome "not recovered", described as "Chest pains"; DYSPNOEA (non-serious) with onset 02Jun2021, outcome "not recovered", described as "Shortness of breath"; HEART RATE IRREGULAR (non-serious) with onset 02Jun2021, outcome "not recovered", described as "Irregular heart beat". The events "Chest pains", "Shortness of breath" and "Irregular heart beat" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: It was unknown whether any therapeutic measures were taken as a result of the events. The patient had no known allergies. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19 and the results were unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 28.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Angiogram pulmonary abnormal Arteriosclerosis coronary artery Arthralgia Asthenia Bacterial test Blood culture negative COVID-19 Cardiomegaly Chest X-ray abnormal Chills Cholecystectomy Condition aggravated Cough Dyspnoea Fall Goitre Gram stain positive Haemodialysis

Symptomtext

Still hospitalized. This is a 75-year-old immunocompromised female with a PMH of breast cancer on tamoxifen, HFpEF, IDDM2, HTN, GERD, and ESRD who presented to the ER 1/11/22 with a CC of generalized weakness x 1 week and a positive home COVID test. CXR showed mild bilateral patchy opacities. Pt was given Tylenol, Decadron, 500 mL IVF bolus and transferred to facility for hospital admission. On interview, telephone interpreter was utilized throughout. Pt states she has been progressively weak with shortness of breath, cough, fever and chills x 1 week. she states she was too weak to get up and ambulate with her walker as she typically would. She states she fell and hurt her right knee trying to walk up steps yesterday. She states she was started on hemodialysis approximately 2 weeks ago. She states she cannot recall the name of her nephrologist or cardiologist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 9,0
Labordaten: CT ANGIO THORAX WITH IV CONTRAST Resulted: 01/17/22 2027 Order Status: Completed Updated: 01/17/22 2029 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 1/17/2022 7:55 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: worsening respiratory failure, covid. COMPARISON: None ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: No adenopathy. Enlarged and heterogenous thyroid gland with several coarse calcifications throughout the right thyroid lobe. Consider nonemergent thyroid ultrasound to further evaluate. Mediastinum & Hila: No suspicious mediastinal or hilar lymphadenopathy. Enlarged mediastinal lymph nodes are likely reactive. Cardiovascular: The heart is mildly enlarged. Mild coronary artery calcifications. The thoracic aorta is normal in caliber. Left chest port catheter terminates within the right atrium. No findings of right heart strain. Pulmonary Arteries: No pulmonary embolism is identified. Lungs & Airways: Extensive widespread consolidative and groundglass opacities throughout both lungs. Pleural Space: No pleural effusion or pneumothorax. Upper Abdomen: Post cholecystectomy. Chest Wall & Musculoskeletal: No suspicious osseous lesions. ____________________ Impression: 1. Widespread bilateral airspace disease, concordant with history of COVID-19 pneumonia. 2. No pulmonary embolism. DR CHEST SINGLE VIEW Resulted: 01/16/22 1602 Order Status: Completed Updated: 01/16/22 1604 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/16/2022 3:42 PM TECHNIQUE: Single view chest INDICATION: increased o2 demands, covid COMPARISON: 1/14/2022 and 1/11/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: There is persistent scattered airspace opacities involving both lungs greatest in the right upper lobe. There is more confluence opacification in the right lower lobe and persistent essentially unchanged left upper lobe airspace disease. Retrocardiac airspace disease is also stable. No evidence of effusion or pneumothorax. Left IJ port tip in right atrium without change. _________________________ Impression: Slight interval increase in right upper and lower lung opacities with stable left lung opacities. DR CHEST SINGLE VIEW Collected: 01/14/22 1910 Order Status: Completed Updated: 01/14/22 1912 Narrative: EXAMINATION: Single View Chest EXAM DATE: 1/14/2022 6:06 PM TECHNIQUE: Single view chest INDICATION: increased O2 demands, covid COMPARISON: 1/11/2022 ENCOUNTER: Not applicable _________________________ FINDINGS: Cardiac views also is unchanged in size and contour. There is increased right greater than left airspace opacities. No pneumothorax or effusion. _________________________ Impression: Interval worsening of right greater the left airspace opacities consistent with clinical history of Covid pneumonia Dictated by: MD on 1/14/2022 7:10 PM. Electronically signed by: MD on 1/14/2022 7:11 PM. DR KNEE RIGHT MINIMUM 4 VIEWS Resulted: 01/12/22 1712 Order Status: Completed Updated: 01/12/22 1714 Narrative: EXAMINATION: Knee Right Complete, Four or More Views EXAM DATE: 1/12/2022 5:04 PM TECHNIQUE: Frontal, lateral, oblique and sunrise view INDICATION: fall, right knee pain COMPARISON: None ENCOUNTER: Initial _________________________ FINDINGS: There is no acute fracture or dislocation involving the right knee. The medial and lateral joint spaces are relatively well-maintained. There is significant degenerative narrowing of the patellofemoral joint space particularly along the lateral aspect of the joint where there is subchondral sclerosis on the femoral condyle and articular surface of the patella. There is no evidence for knee joint effusion and there are no suspicious bone lesions. _________________________ Impression: No acute fracture or dislocation involving the right knee with patellofemoral joint osteoarthritis Peripheral Blood Culture Collected: 01/16/22 0914 Order Status: Completed Specimen: Blood, Venous Updated: 01/21/22 1101 Cult Blood Peripheral No bacteria or yeast isolated Peripheral Blood Culture Collected: 01/16/22 1737 Order Status: Completed Specimen: Blood, Venous Updated: 01/20/22 2201 Cult Blood Peripheral No Growth 4 Days Sputum Culture Collected: 01/13/22 0212 Order Status: Completed Specimen: Body Fluid from Sputum Updated: 01/15/22 0751 Bacterial culture, sputum Normal Upper Respiratory Flora, no MRSA or Pseudomonas aeruginosa isolated Gram stain Many WBCs Few Squamous Epithelial Cells Many Gram Positive Cocci Moderate Gram Negative Rods Moderate Gram Positive Rods Few Gram Negative Cocci COVID-19 PCR - Rapid (Abnormal) Collected: 01/12/22 1740 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 01/12/22 1830 COVID-19 PCR Detected Abnormal
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD (end stage renal disease) Immunocompromised Chronic diastolic heart failure HTN (hypertension) IDDM2 Class 3 severe obesity with body mass index (BMI) of 40.0 to 44.9 in adult, unspecified obesity type, unspecified whether serious comorbidity present hx of Breast cancer Chronic anemia Generalized weakness Non-Hospital HLD (hyperlipidemia) Osteoarthritis CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Visual acuity reduced Postmenopausal bone loss Noncompliance with diabetes treatment Acute on chronic kidney failure Acute on chronic renal failure Chronic combined systolic and diastolic heart failure Dependence on renal dialysis Secondary hyperparathyroidism of renal origin
Andere Medikamente: Outpatient Medications Accu-Chek Aviva Plus Blood Glucose Monitor Accu-Chek FastClix Lancets allopurinol (ZYLOPRIM) 100 MG tablet amLODIPine (NORVASC) 10 MG tablet atorvastatin (LIPITOR) 20 MG tablet B Complex-C-Folic Acid 0.8 MG TABS BD PE
Allergien: No known allergies.
Vorherige Impfungen: -

VAERS 2051216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 03.05.2021
Beginn: 11.01.2022
Tage bis Beginn: 253,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Dyspnoea Myalgia SARS-CoV-2 test positive

Symptomtext

short of breath, myalgias

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: + COVID test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2039534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 17.01.2022
Impfdatum: 22.04.2021
Beginn: 06.01.2022
Tage bis Beginn: 259,0
Dosis: 2
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

cough, short of breath

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 8,0
Labordaten: + COVID test
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2032864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 58,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 14.04.2021
Beginn: 04.01.2022
Tage bis Beginn: 265,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Dyspnoea Nasal congestion Sinus congestion

Symptomtext

cough- shortness of breath- sinus congestion- nasal congestion. starting on 1/4/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Tob abuse. Anxiety/depression. HTN.
Andere Medikamente: ?hydroCHLOROthiazide 25 MG Tablet 1 tablet in the morning Orally Once a day ?Metoprolol Succinate ER 100 MG Tablet Extended Release 24 Hour 1 tablet Orally Once a day Not-Taking ?Ibuprofen 200 MG Tablet 1 tablet with food or milk as n
Allergien: Augmentin: Allergy
Vorherige Impfungen: -

VAERS 2031517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NC
Alter: 27,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 22.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 19,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Condition aggravated Vitiligo

Symptomtext

I was born with vitiligo on my right leg (pattern was unchanged for my entire life, never spread, never changed). After my covid vaccination, the two covid injection sites now have over a quarter sized vitiligo mark that has stayed for months and gotten more prominent. I have been absolutely traumatized by the way it looks. I can not wear tops that show my arms anymore. I have never had this kind of reaction from any other vaccine (including flu) and I haven?t had this reaction when having covid naturally.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid
Vorgeschichte: Vitiligo
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2219955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 20.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain Musculoskeletal stiffness Myalgia Paraesthesia

Symptomtext

Myalgia injection site pain, stiff neck, tingling in arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2024577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 71,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 20.04.2021
Beginn: 10.01.2022
Tage bis Beginn: 265,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Dehydration Diarrhoea Malaise Pyrexia Vomiting

Symptomtext

Patient received 2 COVID vaccines on 4/20/21, and 3/30/21, and was hospitalized with COVID on 1/10/22, and remains hospitalized today with COVID symptoms for 2 weeks that have led to weakness, emesis, diarrhea, fever and dehydration

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2010504

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: IL
Alter: 94,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 20.04.2021
Beginn: 05.01.2022
Tage bis Beginn: 260,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia Bacteriuria Blood creatinine increased Blood electrolytes normal COVID-19 Chest X-ray normal Cognitive disorder Cough Impaired self-care Laboratory test abnormal Mobility decreased SARS-CoV-2 test positive Urine analysis abnormal White blood cell count normal

Symptomtext

95 y.o female with history of a fib not on anticoagulation, CAD, HTN, HLD, IFG, and CKD who presents with generalized weakness. Patient has perhaps mild cognitive impairment at baseline, but is able to provide reasonable history at admission. She lives at home alone in generally functions well. It seems that she has developed generalized weakness in the past few days. This has been progressive to the point that she was unable to get up out of chairs or in the bathroom today, even despite assistance from family members. Has had a mild nonproductive cough in the past few days but denies shortness of breath. Denies fevers, chills, or any localizing symptoms of infection including dysuria. Due to her weakness, she was brought to the ED today for evaluation. There, vitals were stable without hypoxia. Labs were significant for normal electrolytes, creatinine 1.2 (baseline), WBC 6.2. Urinalysis revealed bacteriuria, but as above patient was asymptomatic. COVID testing returned positive. Chest x-ray was clear. As patient is unable to care for herself at home, she has been admitted to the medicine team for further care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2005543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 17.04.2021
Beginn: 25.12.2021
Tage bis Beginn: 252,0
Dosis: 2
Route/Site: UN / UN

Tod: ja Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

12/25/2021: Event occurred after 2nd vaccine. 83-year-old male who comes emergency department today for shortness of breath. as feeling okay and then today became short of breath and he went to the ER to be evaluated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 10,0
Labordaten: Sars COV2 -Positive- 12/25/2021
Aktuelle Erkrankungen: unknown
Vorgeschichte: post CABG, hypertension, hypothyroidism
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2005477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 69,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood test Chest pain Computerised tomogram Diarrhoea Electrocardiogram Headache Magnetic resonance imaging Ventilation/perfusion scan

Symptomtext

I had diarrhea for 2 days, severe headache and chest pains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG - sent to ER for further testing - CT Scan, MRI, Blood work, Lung Scan referred to a Cardiologist.
Aktuelle Erkrankungen: NA
Vorgeschichte: Joint pain from previous from Knee Replacement, Costochondritis
Andere Medikamente: Motrin as needed
Allergien: Shellfish, Contrast Dye
Vorherige Impfungen: -

VAERS 2001294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CT
Alter: 32,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 27.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Computerised tomogram Magnetic resonance imaging Migraine Vision blurred Visual impairment

Symptomtext

After receiving the vaccine, two days later while I was working on my computer, I couldn't see my right hand on my computer. I was waving my right hand in front of my face and realized it was blur spot in my eye. I went to the emergency room and they put me on stroke protocol. After the MRI and CT scan, they diagnosed me with an ocular migraine. The neurologist informed me if I continued to received migraines after diagnosis, I would be prescribed migraine medication. The blurred vision was reduced before being discharged so no medication was given to me to help relieve the problem.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: CT & MRI scan--04/29/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1988960

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 23.09.2021
Beginn: 26.12.2021
Tage bis Beginn: 94,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Dyspnoea Exposure to SARS-CoV-2 Influenza A virus test positive Influenza B virus test positive Pain SARS-CoV-2 test positive

Symptomtext

12/26 cough, body aches, shortness of breath, tested positive for covid on 12/29 after roommates tested positive o

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification, POC 12/29/21 detected
Aktuelle Erkrankungen: -
Vorgeschichte: DM2, COPD, CHF
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1985280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OR
Alter: 68,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 18.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Balance disorder Burning sensation Condition aggravated Motor dysfunction Neuropathy peripheral Peripheral sensorimotor neuropathy Peroneal nerve palsy Sensory loss

Symptomtext

I want to advise you that I had a very painful sensory and motor post (11 days post vaccine; lasting about 3 months) Pfizer #2 vaccine for Covid. I am a generally healthy 69 years old. The presenting symptoms (day 11) were a left foot drop, severe burning pain in all 4 extremities and a transient (about 3 weeks) unilateral supraclavicular (sensory) complete sensory loss. My post vaccine neuropathy was a painful exacerbation of my underlying idiopathic slowly progressive idiopathic length dependent neuropathy. Now 6 months later, the underlying neuropathy has a new worse pain at baseline and decline in balance, motor control and sensation in my hands and feet. I realize that there may be a much larger group of patients with peripheral neuropathy; many of these patients (like myself) have not had their reaction documented by the FDA or CDC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic idiopathic length dependent neuropathy, Obstructive sleep apnea, Coronary artery disease, Iron deficiency anemia
Andere Medikamente: Aspirin 81mg
Allergien: -
Vorherige Impfungen: -

VAERS 1982171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 17.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Injected limb mobility decreased Injection site pain Magnetic resonance imaging

Symptomtext

Left shoulder pain, unable to lift my arm, started shortly after I got Covid vaccine #1. on April 17.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: I did PT( 5/28, 6/25, 7/9), and MRI on Aug 1.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 21.10.2021
Beginn: 12.12.2021
Tage bis Beginn: 52,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Dyspnoea Inappropriate schedule of product administration Myalgia SARS-CoV-2 test positive

Symptomtext

Patient was fully vaccinated + booster with Pfizer (7/1/21, 7/21/21, and 10/21/21). Patient has had a cough, SOB, and myalgias since 12/12/21. Patient was admitted with COVID 12/22/21 and is currently hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: +COVID 12/22/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974723

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 62,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 21.10.2021
Beginn: 12.12.2021
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Dyspnoea Inappropriate schedule of product administration Myalgia SARS-CoV-2 test positive

Symptomtext

Patient was fully vaccinated + booster with Pfizer (7/1/21, 7/21/21, and 10/21/21). Patient has had a cough, SOB, and myalgias since 12/12/21. Patient was admitted with COVID 12/22/21 and is currently hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: +COVID 12/22/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974639

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 60,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 13.04.2021
Beginn: 21.12.2021
Tage bis Beginn: 252,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Diarrhoea Dyspnoea Dysuria Exposure to SARS-CoV-2 Feeling abnormal Headache Malaise Pyrexia SARS-CoV-2 test positive Taste disorder Urine output decreased

Symptomtext

From history and physical 12/21/21: Patient is a 61 y.o. female with a PMH significant for ESRD on HD M/W/F, diabetes mellitus type 2, HTN, HLD, chronic hypoxic respiratory failure on 2 L home O2, history of stroke who presents to the ED due to shortness of breath. Patient reports recent exposure to COVID-19. She was tested positive outpatient for COVID-19 on 12/14/2021, she was asymptomatic at that time. She reports that she began to feel poorly over the next 4-5 days. She complains of nonproductive cough, shortness of breath, low-grade fever, diarrhea, malaise, headache, change in taste. Today, patient reports shortness of breath not relieved with her home oxygen. Due to difficulty breathing she came to the ED. Patient is a small amount of urine in has current complaints of dysuria.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1955362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 34,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 16.04.2021
Beginn: 14.12.2021
Tage bis Beginn: 242,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Dyspnoea Headache Nasal congestion Pain Sinus congestion Upper-airway cough syndrome

Symptomtext

headache, cough, shortness of breath, body aches, sinus congestion, nasal congestion, post nasal drainage. starting 12/14/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none.
Vorgeschichte: hypertension.
Andere Medikamente: Lisinopril.
Allergien: none.
Vorherige Impfungen: -

VAERS 1948014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 17,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 14.05.2021
Beginn: 01.10.2021
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Alopecia Chest X-ray Chest pain Electrocardiogram

Symptomtext

Hair loss and chest pain five months post vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG, Chest X-ray reported normal at Urgent Care on 10/2021.
Aktuelle Erkrankungen: Patient was complaining of chest pain, sometimes related to exercise, anxiety or laughter. Patient also complaining of hair loss associated with hair thinning in the scalp region.
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1946996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 22.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 10,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Insomnia Loss of personal independence in daily activities Magnetic resonance imaging Pain Paraesthesia X-ray

Symptomtext

couldn't sleep; had severe paresthesia of the right side of my scalp down my neck on the right side; I couldn't sleep nor function normally; pain; pulling and tingling sensation; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 22Apr2021 06:15 (Lot number: EW0169) at the age of 60 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Asthma" (unspecified if ongoing); "pencillin" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose:1, Dose administration time:3.30am, dose vaccine location: left arm, Lot number:EW0150, Dose brand: Pfizer, Dose product: COVID-19), administration date: 01Apr2021, when the patient was 60 years old, for Covid-19 immunization. The following information was reported: INSOMNIA (non-serious) with onset 02May2021, outcome "recovered with sequelae", described as "couldn't sleep"; PARAESTHESIA (non-serious) with onset 02May2021, outcome "recovered with sequelae", described as "had severe paresthesia of the right side of my scalp down my neck on the right side"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 02May2021, outcome "recovered with sequelae", described as "I couldn't sleep nor function normally"; PAIN (non-serious) with onset 02May2021, outcome "recovered with sequelae", described as "pain"; PARAESTHESIA (non-serious) with onset 02May2021, outcome "recovered with sequelae", described as "pulling and tingling sensation". The events "couldn't sleep", "had severe paresthesia of the right side of my scalp down my neck on the right side", "i couldn't sleep nor function normally" and "pain" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of insomnia, paraesthesia, loss of personal independence in daily activities, pain, paraesthesia. Additional information: No other vaccine in four weeks and no Other medications in two weeks. Patient had severe paresthesia of the right side of her scalp down my neck on the right side starting at about 2 weeks after the 2nd shot. she couldn't sleep nor function normally due to the pain, pulling and tingling sensation, it has since subsided considerably but has not gone away. This lasted several weeks and went to the dr and insisted on an MRI as she couldn't tell if this was her scalp or inside my head. It was reported that patient did not have covid prior to vaccination nor tested covid post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Test Date: 20210502; Test Name: MRI; Result Unstructured Data: Test Result:scalp or inside my head; Comments: I couldn't tell if this was my scalp or inside my head.; Test Name: x-ray; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma; Penicillin allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1944295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 63,0
Geschlecht: U
Eingang: 13.12.2021
Impfdatum: 21.04.2021
Beginn: 03.12.2021
Tage bis Beginn: 226,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea exertional SARS-CoV-2 test positive Tachycardia

Symptomtext

12/03/21 presents to ED for "tachycardia and dyspnea w exertion ". PMHx of "Covid diagnosis last month".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 12/03/21 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1936237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 10.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mobility decreased Myalgia Pain in extremity Sleep disorder Vaccination site mass

Symptomtext

76 year old Hispanic female experiencing sore left arm (muscle pain) on left arm when the first dose of the covid vaccine was given to her on 6/10/2021 to the present (12/9/2021). Got her second covid vaccine on 6/30/2021 and still was experiencing sore left arm (muscle pain) . She can't sleep on her left side or bend her arm to the back and say's that there is a hard lump in that area where the vaccine was given that developed when she got the vaccine. She reported to her health care provider Dr. The symptom of the sore left arm muscle pain is still ongoing and has gotten worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1936237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 10.06.2021
Beginn: 10.06.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mobility decreased Myalgia Pain in extremity Sleep disorder Vaccination site mass

Symptomtext

76 year old Hispanic female experiencing sore left arm (muscle pain) on left arm when the first dose of the covid vaccine was given to her on 6/10/2021 to the present (12/9/2021). Got her second covid vaccine on 6/30/2021 and still was experiencing sore left arm (muscle pain) . She can't sleep on her left side or bend her arm to the back and say's that there is a hard lump in that area where the vaccine was given that developed when she got the vaccine. She reported to her health care provider Dr. The symptom of the sore left arm muscle pain is still ongoing and has gotten worse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1935750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 20.04.2021
Beginn: 03.12.2021
Tage bis Beginn: 227,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 12/3/21
Aktuelle Erkrankungen: -
Vorgeschichte: ? COPD (chronic obstructive pulmonary disease) ? HTN (hypertension) ? MI (myocardial infarction)
Andere Medikamente: ALBUTEROL-IPRATROPIUM, CONC: 3-0.5MG/3ML, (DUO-NEB) INHL NEBULIZER SOLUTION SPIRIN 81 MG ORAL ENTERIC COATED TABLET CHOLECALCIFEROL, VITAMIN D3, 25 MCG, 1000 UNIT, 25 MCG (1,000 UNIT) ORAL TABLET FINASTERIDE (PROSCAR) 5 MG ORA
Allergien: Sulfa (Sulfonamide Antibiotics)
Vorherige Impfungen: -

VAERS 1928955

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

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: 2
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 1923809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 23.04.2021
Beginn: 01.05.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anti-saccharomyces cerevisiae antibody Antinuclear antibody positive Dyspnoea Electrocardiogram abnormal Muscular weakness Sinus bradycardia Somnolence

Symptomtext

Weakness in both arms, especially the left arm with lack of control over left hand on occasion. Shortness of breath and overall drowsiness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: From blood drawn on 11/30: ? Anti Nuclear Antibodies, IFA: Positive, Flag A ? S cereviaiae IgG: Flag H ? Fana Staining Patterns, Speckled Pattern: Flag H ? EKG with Interpretation: Sinus Bradycardia Tests scheduled for 12/13/2021 ? EMG ? MRI BRAIN W/O&W CON
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Montelukast 10mg, mulit-vitamin
Allergien: Crab meat, red wine
Vorherige Impfungen: -

VAERS 2565387

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: -
Alter: 21,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 20.08.2021
Beginn: 20.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anxiety Dizziness Palpitations

Symptomtext

Dizziness & Palpitations Narrative: Employee started experiencing anxiety ready team called and employee taken to ER for observation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1923253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NM
Alter: 49,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 26.04.2021
Beginn: 30.04.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Mobility decreased

Symptomtext

Numbness and loss of dexterity in my left arm. It started four days after second shot and still continues today. I have had multiple doctors look at it and they cannot see a reason why there is this loss of function.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: August 20, 2021 October 11, 2021 November 8, 2021 November 10, 2021
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa, cranberries
Vorherige Impfungen: -

VAERS 2570268

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 03.09.2021
Beginn: 27.08.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Fatigue Headache Nausea Vomiting

Symptomtext

Headache, NauseaVomiting, SOB-RESLOVED, INCREASED FATIGUE Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1916724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: WA
Alter: 19,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 22.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Allergy to arthropod bite Dyspnoea Fatigue Menstruation irregular Palpitations

Symptomtext

Shortness of breath, heart palpitations, fatigue, rapid heart rate Irregular periods (after 2.5 years on IUD with no menstruation cycles) Allergic reactions to bug bites (intense swelling and pain) (did not previously have these issues)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro Wellbutrin
Allergien: -
Vorherige Impfungen: Influenza (2019, 2020)

VAERS 1913044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: AL
Alter: 37,0
Geschlecht: M
Eingang: 01.12.2021
Impfdatum: 26.04.2021
Beginn: 04.06.2021
Tage bis Beginn: 39,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Asthenia Blood test General physical health deterioration Hypoaesthesia Magnetic resonance imaging Nerve conduction studies Pain Paraesthesia Scan brain Scan with contrast Surgery Weight decreased X-ray

Symptomtext

Started as numbness/tingling. Within hours grew into chronic debilitating pain. One month later, 3 mris, 2 xrays, down 20 lbs , it was deemed to have cervical surgery. Here we are 12/1/21, supposedly ?fully recovered? from surgery, another 4 mris?s including brain scan (w/contrast), 11 xrays , countless blood tests, muscle and nerve studies, tons of nerve meds, muscle relaxers, advise, Tylenol, topicals, oils, breathing exercises, praying, I?m still in excruciating pain. 210 lbs 6/1/21. 175 soaking wet 12/1/21. I keep getting passed around from specialist to specialist with 0 piece of mind , or even a hint as to what is going on with me. Until now I haven?t entertained the notion all this came from the vaccine, but with multiple dr?s now telling me I need to have my primary check into it because others are now reporting the same issues month or so out from their vaccine. Perfect health up to this point and now I?m on verge of death, I feel like my body is eating itself. Please help as no one else came figure it out. I have all medical docs to provide whoever can assist. I emailed cdc, fda, local news, federal government. I?m at a loss and have no where to turn.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Nothing that explains what?s happening to me.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: 1 a day vitamin, fenugreek, adderall
Allergien: No
Vorherige Impfungen: -

VAERS 1909771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 21.04.2021
Beginn: 25.11.2021
Tage bis Beginn: 218,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Cough Dyspnoea Dyspnoea exertional Fatigue Feeling abnormal Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

presents to ED complaining of shortness of breath, general weakness and fatigue, cough and sore throat for past 3 days. Pt had a positive at home covid test on 11/25/21. He was feeling OK then but has steadily been feeling worse. Today he is losing his breath with any activity. He has occasional cough, which has been dry but is hacking when it occurs

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 19.04.2021
Beginn: 27.11.2021
Tage bis Beginn: 222,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

November 26th with shortness of breath. Was COVID positive. Her vital signs were significant for blood pressure 153/96, heart rate of 76, temperature of 36.7?, respiratory rate of 24, oxygen saturation of 74% on room air required 4 L of oxygen to maintain saturation above 90%.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 82,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 21.04.2021
Beginn: 04.06.2021
Tage bis Beginn: 44,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Paraesthesia Pruritus

Symptomtext

Numbness, itching and tingling sensation in hands and fingers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Vitamins
Allergien: None.
Vorherige Impfungen: -

VAERS 1906131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: MO
Alter: 38,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 27.03.2021
Beginn: 26.11.2021
Tage bis Beginn: 244,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Cough Dyspnoea Fatigue Ocular hyperaemia Respiratory tract congestion

Symptomtext

Cough, congestion, fatigue, Shortness of breath and eye redness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1896796

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 14.04.2021
Beginn: 16.11.2021
Tage bis Beginn: 216,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 COVID-19 pneumonia Endotracheal intubation Influenza virus test Respiratory syncytial virus test SARS-CoV-2 test positive

Symptomtext

Pt received Pfizer vaccines on 04/14/21 and 05/11/21. Pt presented to the ED on 11/16/21 due to recently testing positive for COVID while at a rehabilitation center. CXR showed COVID pneumonia. Pt required intubation

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: COVID-19, flu, RSV by NAA positive for SARS-COV-2 on 11/16/21
Aktuelle Erkrankungen: -
Vorgeschichte: DM2, dementia, HTN
Andere Medikamente: Lipitor, claritin, namenda, glucophage, toprol, bactroban, senokot, lamisil
Allergien: Heparin
Vorherige Impfungen: -

VAERS 1884927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 13.05.2021
Beginn: 10.06.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest pain Dyspnoea Hypoaesthesia Palpitations

Symptomtext

After 2nd Dose 2 weeks later Numbness in Arms Chest Pain, Short of Breath, Heart Racing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No issue detected.
Aktuelle Erkrankungen: None
Vorgeschichte: PCOS, Antiphospholipid Syndrome Antibodies
Andere Medikamente: Pre Natal Vitamin
Allergien: Shellfish, IV Contrast
Vorherige Impfungen: -

VAERS 1881388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 51,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RL

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia Back pain Blood test Cardiac disorder Cardiac function test Cardiac stress test Chest pain Computerised tomogram Dyspnoea Electrocardiogram Fatigue Feeling abnormal Fibrin D dimer Headache Hemianaesthesia Hypertension Hypoaesthesia Impaired work ability

Symptomtext

04/23/2021 09:00PM 6 hours right side of face, body down to leg went numb. Sick in bed no energy, fatigue, and headaches throughout the weekend. Two weeks later she was feeling off and foggy with her mind set on Friday night exactly two weeks from vaccination had pain in chest and back and could not catch her breath and was taken to the hospital by her husband over the weekend. High blood pressure sent her home on Sunday. Tuesday to hospital to do a D-dimer. Was out of work sick for a week. Friday heart condition May, June, July for high blood pressure. Possible breast cancer with biopsy. Still having side effects.

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Praegender Schweregrund: Chest pain
Hospital-Tage: 1,0
Labordaten: Stress test Blood test EKG CAT Scan without the dye D-dimer Ultrasound on leg and sent her home with high blood pressure medicine, pain medicine MRI for stroke and checked for with contrast and out Heart test to blow out the arteries
Aktuelle Erkrankungen: No
Vorgeschichte: No Stomach Issue with Diarrhea with Certain Foods No Gallbladder
Andere Medikamente: Low Dose Hormone Birth Control
Allergien: No
Vorherige Impfungen: -

VAERS 1869900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 30.03.2021
Beginn: 08.11.2021
Tage bis Beginn: 223,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 11/11/21
Aktuelle Erkrankungen: -
Vorgeschichte: Personal history of colonic polyps tubular adenoma 4/2011, repeat due 10/2011 Hypertension 3/28/2011 Cesarean Delivery 2/14/2011 Tobacco Abuse 2/22/2011 Diabetes mellitus type II (HRC) Varicella Asthma (HRC) intermittent per patient Arthritis (HRC) right knee replacement Rheumatoid arthritis involving multiple sites with positive rheumatoid factor (HRC) 5/13/2019 Hyperlipidemia (HRC)
Andere Medikamente: insulin aspart, NOVOLOG, (NOVOLOG) 100 unit/mL SubQ Soln insulin aspart, NOVOLOG, (NOVOLOG) 100 unit/mL SubQ Soln lisinopril (PRINIVIL) 5 mg Oral Tab ondansetron (ZOFRAN ODT) 4 mg Oral ODT ondansetron (ZOFRAN ODT) 4 m
Allergien: -
Vorherige Impfungen: -

VAERS 1864953

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 88,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 25.03.2021
Beginn: 10.11.2021
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Arteriosclerosis Asthenia Atrial fibrillation Biliary dilatation Bladder dilatation Blood bicarbonate increased Blood creatinine increased Blood gases Blood lactic acid Blood pH normal Blood potassium normal Blood sodium decreased Blood urea increased Bronchial secretion retention COVID-19 Chest pain Computerised tomogram abdomen normal Computerised tomogram thorax abnormal

Symptomtext

Pfizer vaccine 3/25/21, 4/20/21 CHIEF COMPLAINT Patient unsure but shortness of breath, cough and chest pain per ED HISTORY OF PRESENT ILLNESS Pt is a 88 y.o. female with complex medical comorbidities who presented to ED in city via EMS for 1-2 days duration of weakness, shortness of breath, and chest pain by report. She was reportedly tachypneic and hypoxic in the 80s % on room air, and SpO2 was 100% on 3L of supplemental oxygen by nasal canula. Evaluation at local ED included positive SARS-CoV-2 PCR on 11/10. Labs were otherwise significant for WBC 17.4 with neutrophilia and lymphopenia, hemoglobin 8.2 (10.1 on 10/31), platelet count 418, creatinine 1.06 (comparing to 0.8 at baseli

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 11/10/2021 Coronavirus 2 PCR Detect, V symptomatic POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Hypertension Essential Primary Hyperlipidemia Mixed Chronic Obstructive Pulmonary Disease Without Exacerba
Andere Medikamente: -
Allergien: Ciproflaxcin
Vorherige Impfungen: -

VAERS 1851331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 56,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 16.04.2021
Beginn: 05.11.2021
Tage bis Beginn: 203,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Anosmia Chills Cough Dyspnoea Ear discomfort Eye pruritus Nasal congestion Rhinorrhoea Sneezing Upper-airway cough syndrome

Symptomtext

nonproductive cough, chills, shortness of breath, loss of taste, loss of smell, nasal congestion, post nasal drainage, sneezing, itchy eyes runny nose, ear fullness. starting on 11/5/2021

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: History of Depression. Menopause at age 44.
Andere Medikamente: ?Vitamin D 2000 UNIT Tablet 3 capsules Orally Once a day ?Multi For Her - Tablet as directed Orally
Allergien: none
Vorherige Impfungen: -

VAERS 2579453

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 19.08.2021
Beginn: 19.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Diarrhoea Dyspnoea Headache Pruritus Rash Swelling face Urticaria Vision blurred

Symptomtext

BlurredVision, Headache, SkinRash, UrticariaPruritus, Diarrhea, SOB,Facial swelling, Narrative:

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1846430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 31,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Exposure during pregnancy Fatigue Feeling abnormal Headache Palpitations

Symptomtext

Patient called nurse triage line on 11.2.21. Reported racing heart (HR 95-105 all day", mild headache, increased fatigue with activity and "brain fog" after getting the Pfizer booster on 11.1.21. She reported that it started around 8AM on 11.2.21. Patient reports being 27 weeks pregnant. LMP 4.26.21.

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Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Patient is 27 weeks pregnant
Vorgeschichte: Asthma Migraines EE (eosinophilic esophagitis) GERD (gastroesophageal reflux disease) Barrett esophagus Multiple food allergies Multiple respiratory allergies Hypersomnia Anxiety and depression
Andere Medikamente: albuterol HFA (ALBUTEROL) 108 (90 Base) MCG/ACT inhaler buPROPion (WELLBUTRIN SR) 150 MG 12 hr tablet busPIRone (BUSPAR) 7.5 MG tablet cetirizine (ZYRTEC ALLERGY) 10 MG tablet methylphenidate (RITALIN) 5 MG tablet montelukast (SINGULAIR) 10
Allergien: Cats Dogs Other Seasonal Allergies, Unspecified
Vorherige Impfungen: -

VAERS 1843676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NC
Alter: 20,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 14.10.2021
Beginn: 17.10.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Chest X-ray Chest pain Chromaturia Culture urine Electrocardiogram Full blood count Metabolic function test Painful respiration Urine analysis

Symptomtext

10-18-21 Sent to ER for left-sided chest pain worse on deep breaths. ER did not think related to vaccine. Had EKG and released 10-28-21 Seen back in the office for Dark urine was sent to ER for possible rhabdomyolysis. Patient was admitted from ER and was Discharged on 11-1-21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: EKG, Chest Xray, CBC, CMP, Ua and Ua Culture
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1843235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 04.11.2021
Impfdatum: 19.04.2021
Beginn: 28.10.2021
Tage bis Beginn: 192,0
Dosis: 2
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acquired diaphragmatic eventration Adenovirus test Angiogram abnormal Anticoagulant therapy Aortic arteriosclerosis Aortic dilatation Arteriosclerosis Arteriosclerosis coronary artery Asthenia Atelectasis Atrial fibrillation Atrial flutter Bacterial test negative Bacterial test positive Blood culture negative Bordetella test negative Bronchiolitis Bronchitis

Symptomtext

Patient is a 79 y.o. male with a PMH of COPD, HLD, hypothyroidism, HTN, DM, and corectal cancer. Patient presented to the ED for generalized weakness and fatigue x 1-2 days. Stated prior to coming to the ED he had a mechanical fall. + Dry cough that started 1 night PTA. + SOB, mildly worse than his baseline. + Conversational dyspnea; patient stated that is his baseline 2/2 to his COPD. + BLE edema; unchanged from baseline per patient. The patient was admitted for further evaluation and management. He had a positive urine culture for enterococcus. He was initially treated with Rocephin, then Zosyn prior to changing to Amoxicillin 1 g PO TID to complete a 7 day course. The patient was also positive for Covid. He was given dexamethasone in the ED, and Regeneron on 10/29 with subjective improvement in symptoms per patient. Cardiology was consulted for new onset afib. The patient's metoprolol was increased to 100 mg daily and they recommended a Ziopatch which was placed prior to discharge. He was also started on Lovenox during his admission and changed to Eliquis at time of discharge. Prior to discharge, the CM arranged additional services as the patient will be quarantined through 11/11 and lives alone. The patient was eating and ambulating at the time of discharge. Answered all questions and the patient was comfortable with the discharge plan. Medications as listed below. The patient will follow up with Dr. after his quarantine ends.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: Procedure Component Value Ref Range Date/Time CV Patch Monitor w/hookup- 14day Resulted: 10/31/21 1231 Order Status: Sent Updated: 10/31/21 1311 DR CHEST SINGLE VIEW Resulted: 10/30/21 0324 Order Status: Completed Updated: 10/30/21 0326 Narrative: EXAMINATION: Single View Chest EXAM DATE: 10/30/2021 2:05 AM TECHNIQUE: Single view chest INDICATION: fever w/u COMPARISON: Chest CT 10/29/2021 ENCOUNTER: Not applicable _________________________ FINDINGS: Normal heart size. Calcified aorta. Right-sided port in good position. Elevated right hemidiaphragm. Prior right shoulder surgery. Old right clavicle fracture. The lungs are fairly well-inflated without consolidation. No effusion or pneumothorax. There are multiple granulomas. _________________________ Impression: No acute airspace process. CV Echo Complete With Contrast Collected: 10/29/21 0925 Order Status: Completed Updated: 10/29/21 1131 Narrative: LIMITED ECHOCARDIOGRAPHY REPORT Name: (PRIVACY) Study Date: 10/29/2021 Patient Location: Emergency Department DOB: (PRIVACY) Patient Class: Inpatient Gender: Male Ordering Physician: (PRIVACY) Age: 79 yrs Height: 180 cm Weight: 101 kg Resting HR: 111 BSA: 2.2 m2 Resting BP: 121/76 mmHg Reason For Study: Atrial fibrillation/flutter (AF), Dyspnea on exertion (DOE), atrial fibrillation/flutter, New onset A-fib History/Symptoms: hypertension, diabetes, COPD, history of smoking, Peripheral arterial disease, COVID 19 (10/21) Electronically signed by: MD on 10/29/2021 11:31 AM Interpretation Summary Limited TTE: Upper septal hypertrophy (sigmoid septum), normal variant. Left ventricular systolic function is normal. The left ventricular ejection fraction is 65%. No regional wall motion abnormalities noted. The right ventricle is mildly dilated. The right ventricular systolic function is normal. There is moderate mitral annular calcification. No mitral valve stenosis. Left atrium is at least moderately dilated by visual estimation. There is no comparison study available. STUDY PERFORMED/QUALITY: AORTIC VALVE: A two-dimensional transthoracic The aortic valve is not well echocardiogram with color flow and visualized. There is no aortic valve spectral flow Doppler was performed in stenosis. limited views only. The technical quality of the exam was fair. The MITRAL VALVE: apical views were difficult to obtain There is moderate mitral annular and are suboptimal in quality. Due to calcification. There is no mitral limited acoustic windows, Definity was valve stenosis. administered. LEFT VENTRICLE: TRICUSPID VALVE: The left ventricle is normal in size. There is no tricuspid stenosis. There Upper septal hypertrophy (sigmoid is mild tricuspid regurgitation. The septum), normal variant. Left estimated right ventricular systolic ventricular systolic function is pressure is 27 mmHg. normal. The left ventricular ejection fraction is 65%. The LV ejection fraction was determined utilizing visual estimation. There was insufficient diastolic data to allow for diastolic function assessment. No regional wall motion abnormalities noted. LEFT ATRIUM: Left atrium is at least moderately dilated by visual estimation. The interatrial septum is not well visualized. RIGHT ATRIUM: Right atrial size is normal. RIGHT VENTRICLE: The right ventricle is mildly dilated. The right ventricular systolic function is normal. INFERIOR VENA CAVA: The IVC is dilated (>2.1 cm) with normal collapse during patient sniff (>50% collapse). The estimated RA pressure is 8 mm Hg (5-10 mm Hg)). Left Ventricle Tricuspid Valve IVSd: 1.1 cm TR max vel: 2.22 m/sec LVPWd: 1.1 cm TR max PG: 20.0 mmHg LVIDd: 5.9 cm LVIDs: 4.0 cm ______________________________________________________________________________ Great Vessels IVC diam: 2.2 cm Reference Table: Normal Mild ModerateSevere Men LVEF > 52% 41-51% 30-40% <30% Women LVEF > 54% 41-53% 30-40% <30% Men LVIDd 4.2-5.8 5.9-6.3 6.4-6.8 >6.8 Women LVIDd 3.8-5.2 5.3-5.6 5.7-6.1 >6.1 LA Volume (ml/m^2) < 34 35-41 42-48 >48 ______________________________________________________________________________ Electronically signed by: MD on 10/29/2021 11:31 AM All sources of data reside in the Cardiology EJECTION FRACTION ECHO Collected: 10/29/21 0925 Order Status: Completed Updated: 10/29/21 1131 EJECTION FRACTION ECHO 65 % CT ANGIO THORAX WITH IV CONTRAST Resulted: 10/29/21 0146 Order Status: Completed Updated: 10/29/21 0148 Narrative: EXAMINATION: CT Angiography of the Thorax EXAM DATE: 10/29/2021 12:07 AM 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: Chest trauma, mod-severe. History of colon and hepatocellular cancer. COMPARISON: Chest, abdomen and pelvis CT 6/25/2021 ENCOUNTER: Not applicable ____________________ FINDINGS: Base of Neck & Axillae: Similar appearance to mildly prominent bilateral axillary nodes without interval suspicious change. Mediastinum & Hila: Similar appearance to slightly prominent and mildly enlarged multicompartmental nodes. No mediastinal hematoma or frank mass. No pneumomediastinum. The esophagus is within normal limits for technique. Cardiovascular: Heart size and pericardium are within normal limits. Similar minimal to mild coronary artery calcifications. Similar ectasia of the ascending thoracic aorta to approximately 4.5 to 4.6 cm. No dissection or aneurysm. Similar atherosclerotic disease. There is no evidence for right heart strain. Pulmonary Arteries: No pulmonary embolism is present. Lungs & Airways: No evidence of consolidation to suggest lobar pneumonia or contusion. Minimal dependent atelectasis present. There are a few subtle areas of mild bronchocentric groundglass opacity scattered throughout both upper lobes slightly more pronounced on the right than on the left suggestive of process such as minimal respiratory bronchiolitis. No change in the subcentimeter solid nodules of the middle lobe at the fissure and inferolateral left upper lobe pleural-based nodule continuing to measure approximately 9 and 7 mm respectively. No interval suspicious pulmonary nodule. Pleural Space: There are no pleural effusions. There is no pneumothorax. Upper Abdomen: Evaluation of the upper abdomen is limited by early phase enhancement but no interval acute change or suspicious finding within the limits of the exam. Stable cirrhotic appearance of the liver with hypertrophy of the caudate noted. There is similar partially visualized splenomegaly. Cholelithiasis again noted without acute inflammatory change. Similar enlarged gastrohepatic ligament nodes. Chest Wall & Musculoskeletal: Visualized soft tissues are intact without acute or suspicious finding. Bone windows likewise show no acute or suspicious finding. ____________________ Impression: 1. No traumatic appearing finding of the chest noted. 2. No evidence of pulmonary embolus. 3. Minimal groundglass bronchocentric opacities of the upper lobes right greater than left suggest resolving or evolving acute process such as bronchitis or respiratory bronchiolitis. No consolidating pneumonia. 4. Stable appearance to pulmonary nodules. 5. No acute interval change the appearance of the visualized upper abdomen within the limits of the exam. Procedure Component Value Ref Range Date/Time Peripheral Blood Culture Collected: 10/31/21 0854 Order Status: Completed Specimen: Blood, Venous Updated: 11/04/21 1001 Cult Blood Peripheral No Growth 4 Days Central Line Blood Culture (Normal) Collected: 10/30/21 0149 Order Status: Completed Specimen: Blood, Central Line Updated: 11/04/21 0301 Cult Blood Central Line No bacteria or yeast isolated Central Line Blood Culture (Normal) Collected: 10/29/21 0543 Order Status: Completed Specimen: Blood, Central Line Updated: 11/03/21 0702 Cult Blood Central Line No bacteria or yeast isolated Peripheral Blood Culture Collected: 10/29/21 0041 Order Status: Completed Specimen: Blood, Venous Updated: 11/03/21 0300 Cult Blood Peripheral No bacteria or yeast isolated Peripheral Blood Culture Collected: 10/28/21 2234 Order Status: Completed Specimen: Blood, Venous Updated: 11/03/21 0002 Cult Blood Peripheral No bacteria or yeast isolated Urine Culture (Abnormal) Collected: 10/29/21 0046 Order Status: Completed Specimen: Urine, clean catch Updated: 10/31/21 0742 Bacterial culture, urine >=100,000 CFU/mL Enterococcus faecalis Abnormal Susceptibility Enterococcus faecalis Not Specified Ampicillin Susceptible Levofloxacin Susceptible Nitrofurantoin Susceptible Tetracycline Susceptible Vancomycin Susceptible Linear View Clostridioides difficile Toxin (Normal) Collected: 10/29/21 2312 Order Status: Completed Specimen: Stool from Rectum Updated: 10/30/21 0533 C difficile Toxin Negative Negative Respiratory Pathogens (Abnormal) Collected: 10/28/21 2234 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 10/29/21 0614 Adenovirus PCR Film Array Not Detected Not Detected Coronavirus 229E PCR Film Array Not Detected Not Detected Coronavirus HKU1 PCR Film Array Not Detected Not Detected Coronavirus NL63 PCR Film Array Not Detected Not Detected Coronavirus OC43 PCR Film Array Not Detected Not Detected COVID-19 PCR Detected Abnormal Not Detected Comment: COVID-19 (SARS-CoV-2) test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status. This test has received Emergency Use Authorization (EUA) by the FDA, but performance has not been evaluated for asymptomatic patients. Testing was performed using a nucleic acid amplification method. The specimen source may have been changed from the original order per patient situation or symptoms. See website for additional information. Metapneumovirus PCR Film Array Not Detected Not Detected Rhinovirus-Enterovirus PCR Film Array Not Detected Not Detected Influenza A PCR Film Array Not Detected Not Detected Influenza A H3 PCR Film Array Not Detected Not Detected Influenza A H1 PCR Film Array Not Detected Not Detected Influenza A 2009 H1 PCR Film Array Not Detected Not Detected Influenza B PCR Film Array Not Detected Not Detected Parainfluenza 1 PCR Film Array Not Detected Not Detected Parainfluenza 2 PCR Film Array Not Detected Not Detected Parainfluenza 3 PCR Film Array Not Detected Not Detected Parainfluenza 4 PCR Film Array Not Detected Not Detected Respiratory Syncytial Virus PCR Film Array Not Detected Not Detected Bordetella pertussis PCR Not Detected Not Detected Bordetella parapertussis PCR Not Detected Not Detected Chlamydia pneumoniae PCR Not Detected Not Detected Mycoplasma pneumoniae PCR Not Detected Not Detected COVID-19 PCR (Abnormal) Collected: 10/28/21 2234 Order Status: Completed Specimen: Swabbed Collection from Nasopharynx Updated: 10/28/21 2328 COVID-19 PCR Detected Abnormal Not Detected Comment: COVID-19 (SARS-CoV-2) RT-PCR test is positive. Clinical correlation with patient history and other diagnostic information is necessary to determine infection status. This test has received Emergency Use Authorization (EUA) by the FDA, but performance has not been evaluated for asymptomatic patients. Testing was performed using a nucleic acid amplification method. The specimen source may have been changed from the original order per patient situation or symptoms. See website for additional information. This test was performed at Laboratory. Covid 19 Result Comment See Comment Comment: COVID-19 results reported as "detected" means COVID-19 positive. Positive patients should self-isolate for 10 days or 24 hours after fever resolves and other symptoms are improving, whichever is longer: - Stay home except to get medical care and wear a facemask if you must leave - Separate yourself from other people in your home, known as home isolation - Cover your coughs and sneezes - Wash your hands often - Avoid sharing household items - Clean high-touch surfaces everyday - If you have a medical emergency and need to call 911, notify dispatch personnel that you may have COVID-19 and put on a facemask before emergency medical services arrive. If the result is "inconclusive" or "invalid" and you have not been contacted by a medical professional from medical facility about your result or if you have questions about COVID-19, your symptoms, or need a return to work/school note, please contact your primary care provider (PCP). If you do not have a PCP, visit website.
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory COPD (chronic obstructive pulmonary disease) Circulatory Hypertension associated with diabetes Peripheral arterial disease Digestive Squamous cell carcinoma of anal canal Primary liver hepatocellular carcinoma Malignant neoplasm of overlapping sites of rectum, anus and anal canal Colon cancer Infectious/Inflammatory Gout of right knee COVID-19 virus infection Acute cystitis Hematologic Anemia, blood loss Platelets decreased Nervous Bilateral leg weakness Chemotherapy-induced peripheral neuropathy Genitourinary Right renal mass - right 20 mm Endocrine/Metabolic Type 2 diabetes mellitus without complication, without long-term current use of insulin Hypothyroidism due to medication Other Primary osteoarthritis of knees, bilateral Former Smoker Left adrenal mass- indeterminate Bilateral lower extremity edema Generalized weakness
Andere Medikamente: amoxicillin (AMOXIL) 500 MG capsule apixaban starter pack (ELIQUIS) 5 MG TBPK tablet benazepril-hydrochlorothiazide (LOTENSIN HCT) 20-25 MG per tablet benzocaine-menthol (CEPACOL) 15-3.6 MG LOZG benzonatate (TESSALON) 100 MG capsule gabapen
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 1659075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 45,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Antinuclear antibody Basophil count Blood bilirubin Blood creatine phosphokinase Chest X-ray normal Chest discomfort Chills Cold sweat Arthralgia Injection site pain Laboratory test Blood glucose Blood glucose increased Blood thyroid stimulating hormone Blood uric acid Brain natriuretic peptide C-reactive protein

Symptomtext

does not feel her immune system is the same; hasn't had a voice/ hasn't been able to talk with her regular voice; wheezing; cough stuff up; couldn't breathe; her blood sugar is elevated; a lot of stomach pain; Headache; Chest pressure; D Dimer test that was high/ some sort of an infection maybe; Respiratory infection; Enlarged Lymph nodes; pain/ like it was burning, throbbing/ in different locations of her body; cold sweats; This is a spontaneous report from a contactable nurse (patient). A 45-year-old female patient received the second dose of bnt162b2 (COMIRNATY, Lot Number: EW0169), via an unspecified route of administration, administered in right arm on 30Aug2021 (45-year-old at time of vaccination) as single dose for COVID-19 immunization. Medical history included tachycardia, insomnia, depression, obesity, "sleep". Concomitant medications included amitriptyline (AMITRIPTYLINE) taken for sleep (she was already prescribed amitriptyline prior to receiving the vaccines as needed for sleep, but she doesn't like to take medicine she rarely took that); propranolol (PROPRANOLOL) taken for tachycardia. The patient previously received levofloxacin (LEVAQUIN) and experienced drug allergy; previously received doxycycline (DOXYCYCLINE) and experienced drug allergy. The patient previously received the first dose of bnt162b2 (COMIRNATY, Lot Number: EW0169), via an unspecified route of administration, administered in right arm on 09Aug2021 (45-year-old at time of vaccination) as single dose for COVID-19 immunisation and experienced "lymph nodes are enlarged on her neck and armpit area" and pain in the neck. Narrative: Patient states that both first and second dose of the Pfizer covid vaccine have the same Lot Number EW0169. She got both doses on the dominant arm, on her right arm. She received first vaccination dose on 09Aug2021, after she has been having issues with her lymph nodes. On the right side the lymph nodes are enlarged on her neck and armpit area. She got an ultrasound done with labs. Her HCP still recommended her to get the 2nd Pfizer vaccine. She got the second dose on 30Aug2021 ever since then she has had a headache (later clarified as "started 3 days after the second dose"). She has a neurologist appointment coming up. The first night after the second dose (30Aug2021) she had cold sweats, the next day (31Aug2021) she woke up with excruciating pain, it was different type of pain, like it was burning, throbbing, and she feels the pain at the same time in different locations of her body. Her pain was bad that she could not be touched. She called the doctor the next day (01Sep2021) because she was chest pressure, the pain is still there but not as excruciating. She went to urgent care and they did labs, a D Dimer test that was high (0.58 on 02Sep2021), they did an emergency CT Scan with contrast of the chest, and the doctor said that was negative. The doctor said that she felt like D Dimer test indicated she had some sort of an infection maybe. Patient states that she was back to her doctor because the pain was random, it was like ice picks would stab in random parts of body. She can't get rid the of headache. They ran more tests, she has started to feel better with exception of the headache. She is on medication that she was not on before. She has a follow up with neurology. Two and half weeks ago (Sep2021) she got a respiratory infection, she tested negative for flu (Sep2021) and COVID-19 (22Sep2021). They put her on an inhaler, steroids, and antibiotics, and she is still sick. She does not feel her immune system is the same. She hasn't had a voice in 2.5 weeks. They gave her another round of antibiotics, she still needed an inhaler because she developed wheezing. She has never had this before, all of this is ongoing since the second vaccination. Event details: Enlarged Lymph nodes: It started about 2 days after the first dose, it started off with pain in the neck, she did not have a sore throat but when moving the neck she could feel it pull, she then physically felt the enlargement by feeling it with touch. It had subsided after a week and a half. Then after the second vaccination it came back, however it wasn't until 2.5 weeks after the second dose it enlarged again. The second time around it subsided about a week later (Sep2021) and ended beginning of Oct2021. Headache: It started 3 days after the second dose. She is on medication for it now, for the headache. Outcome: some days are better than others, she still feels the tight band around the head. Treatment for headaches: She takes amitriptyline every night because it helps with the headache, she was already on propranolol, she was also given a migraine medication, a new one that she cant remember the name of. She is schedule for a MRI on 28Oct2021. Pain: It started the day after the second dose (31Aug2021), it's random pain that she didn't have before. It feels like ice picks now, like she will have nerve pain on cuticle of the toe. It's weird spots it comes up. The severity comes on fast, on a pain scale her pain is between 7-8 out of 10. When it comes it doesn't last long. Chest Pressure: It started on 01Sep2021, the day before she went to urgent care, she called the doctor and she actually wanted her to call 911 the day before but she didn't. She went to urgent care on 02Sep2021. Outcome: Her Chest still feels tight however she does not know if it's the respiratory infection. Patient clarified she did not go to an emergency room in a hospital, she went to an urgent care facility that was attached to the big organization and so they were able to send her to different places within the facility for tests. Respiratory infection: She happens to love her Nurse practitioner but she is tired of seeing her. When she goes for her yearly exams she is overweight but not unhealthy. She saw the Nurse practitioner on 16Sep2021 because she couldn't breathe. Outcome: She is on the second round of antibiotics, it's got better from where it was before. She is now actually able to cough stuff up but she still has wheezing, She hasn't been able to talk with her regular voice since this started. Treatment: The 1st antibiotic she was given was a Z-Pak and the steroid is prednisone 20mg twice a day. The Second antibiotic is Augmentin twice a day, the doctor gave her steroids because she is still tight but not wheezing as much, the doctor told her to try not to take the steroids if she can help it, since her blood sugar is elevated (on 02Sep2021). She was also given an albuterol inhaler. She has not Lot numbers to provide for Amitriptyline, Migraine Medication with unknown name, Propranolol, Z-Pak, Augmentin, or Prednisone, they are not physically with her at this moment. Patient states that the Antibiotic was taken twice a day. Investigation: Before she only had yearly checks up and that's it. Patient states that she has had a lot of lab work done starting on 18Aug2021. 20Aug2021: She has an ultrasound of soft neck tissue with the result of a nonspecific anterior neck lymph nodes with first one having measurements of 1.0cm by 0.9cm by 0.4cm and the other one being 1.2cm by 1.3cm by 0.3cm. 02Sep2021: She had many tests. Her BMP for the most part was good, the glucose was elevated. She had a CBC in which the White Blood Cells was fine, Red Blood Cells was fine, the Hemoglobin was fine, her MCHC was 31.4, and the MPV 11.2, She has 59% neutrophils, 27% lymphocytes, 8% monocytes, 5% eosinophils, and 1% basophils. She has an Abdominal Ultrasound that was normal, an Abdominal obstruction Series that was normal, she clarified that she was also having a lot of stomach pain (on 02Sep2021). She has a CT of the Chest to rule out a PE, it was normal, she had a 12 lead EKG that showed sinus rhythm. 22Sep2021: On this day she went back to doctor, and they drew a CBC which had abnormal hematocrit 43.2, her neutrophil was 69%, lymphocytes was 23%, monocytes 5%, eosinophils 3%, and the basophil was back to normal at 0%. Her CMP (comprehensive metabolic panel) showed her glucose was still elevated but she is on steroids. 13Oct2021: She went to the doctor because they wanted to listen to lungs a second time. She is allergic to Levaquin and Doxycycline. Patient would also like to add her upcoming appointments She see's Neurology on 21Oct2021 for the headaches. She has an Ultrasound schedule for 20Oct2021 at 3:10PM. She has a MRI schedule 27Oct2021. Other test data: On 18Aug2021: Mono: Negative; comprehensive metabolic panel: Normal; Strep Group A: Negative. On 02Sep2021: ANA: normal; CK: normal; Chest X-ray: fine; C-reactive protein: Elevated 0.82; BNP, Test for Heart Failure: 27, Normal; Lipase: 17, Normal; Liver Panel: Bilirubin on 02Sep202: 0.1, low; Urine analysis: normal. On 22Sep2021: Sediment: 17; Rheumatoid factor: Normal; Uric acid: normal; CT Scan without Contrast: normal. On 13Oct2021: TSH: normal; Hemoglobin A1C: normal. The case was reported as non-serious. The outcome of enlarged lymph nodes was recovered in Oct2021; headache and "pain/ like it was burning, throbbing/ in different locations of her body" were not recovered; respiratory infection was recovering; outcome of other events was unknown.; Sender's Comments: Based on the temporal relationship, the association between the event respiratory infection with COMIRNATY use can not be fully 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210902; Test Name: ANA; Result Unstructured Data: Test Result:normal; Test Date: 20210902; Test Name: basophils; Test Result: 1 %; Test Date: 20210922; Test Name: basophils; Test Result: 0 %; Comments: back to normal; Test Date: 20210902; Test Name: Liver Panel: Bilirubin; Result Unstructured Data: Test Result:0.1; Comments: Low; Test Date: 20210902; Test Name: CK; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: glucose/ blood sugar; Result Unstructured Data: Test Result:elevated; Test Date: 20211013; Test Name: TSH; Result Unstructured Data: Test Result:normal; Test Date: 20210922; Test Name: Uric acid; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: BNP, Test for Heart Failure; Result Unstructured Data: Test Result:27; Comments: Normal; Test Date: 20210902; Test Name: Chest X-ray; Result Unstructured Data: Test Result:fine; Test Date: 20210922; Test Name: CT Scan without Contrast; Result Unstructured Data: Test Result:normal; Test Date: 20210902; Test Name: Chest CT; Result Unstructured Data: Test Result:Normal; Comments: to rule out a PE; Test Date: 20210902; Test Name: C-reactive protein; Result Unstructured Data: Test Result:Elevated 0.82; Test Date: 20210902; Test Name: 12 lead EKG; Result Unstructured Data: Test Result:Sinus Rhythm; Test Date: 20210902; Test Name: eosinophils; Test Result: 5 %; Test Date: 20210922; Test Name: eosinophils; Test Result: 3 %; Test Date: 20210902; Test Name: D-Dimer; Result Unstructured Data: Test Result:0.58; Comments: high, indicated she had some sort of an infection maybe; Test Date: 20210818; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: CBC; Result Unstructured Data: Test Result:White Blood Cells was fine, Red Blood Cells was fi; Comments: White Blood Cells was fine, Red Blood Cells was fine, the Hemoglobin was fine, her MCHC was 31.4, and the MPV 11.2, She has 59% neutrophils, 27% lymphocytes, 8% monocytes, 5% eosinophils, and 1% basophils; Test Date: 20210922; Test Name: CBC; Result Unstructured Data: Test Result:abnormal hematocrit 43.2, her neutrophil was 69%,; Comments: abnormal hematocrit 43.2, her neutrophil was 69%, lymphocytes was 23%, monocytes 5%, eosinophils 3%, and the basophil was back to normal at 0%.; Test Date: 20211013; Test Name: Hemoglobin A1C; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: hematocrit; Result Unstructured Data: Test Result:43.2; Comments: abnormal; Test Date: 20210902; Test Name: Hemoglobin; Result Unstructured Data: Test Result:fine; Test Date: 202109; Test Name: flu test; Test Result: Negative ; Test Date: 20210818; Test Name: Mono; Test Result: Negative ; Test Date: 20210902; Test Name: lipase; Result Unstructured Data: Test Result:17; Comments: Normal; Test Date: 20210902; Test Name: lymphocytes; Test Result: 27 %; Test Date: 20210922; Test Name: lymphocytes; Test Result: 23 %; Test Date: 20210902; Test Name: MCHC; Result Unstructured Data: Test Result:31.4; Test Date: 20210902; Test Name: MPV; Result Unstructured Data: Test Result:11.2; Test Date: 20210902; Test Name: BMP; Result Unstructured Data: Test Result:glucose was elevated; Comments: for the most part was good; Test Date: 20210818; Test Name: comprehensive metabolic panel; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: comprehensive metabolic panel; Result Unstructured Data: Test Result:Glucose Elevated; Test Date: 20210902; Test Name: monocytes; Test Result: 8 %; Test Date: 20210922; Test Name: monocytes; Test Result: 5 %; Test Date: 20210902; Test Name: neutrophils; Test Result: 59 %; Test Date: 20210922; Test Name: neutrophils; Test Result: 69 %; Test Date: 20210902; Test Name: Red Blood Cells; Result Unstructured Data: Test Result:fine; Test Date: 20210922; Test Name: Sediment Rate; Result Unstructured Data: Test Result:17; Test Date: 20210922; Test Name: Rheumatoid factor; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20210818; Test Name: Strep Group A; Test Result: Negative ; Test Date: 20210902; Test Name: Abdominal Ultrasound; Result Unstructured Data: Test Result:Normal; Test Date: 20210820; Test Name: Ultrasound of the Soft Neck; Result Unstructured Data: Test Result:a nonspecific anterior neck lymph nodes with first; Comments: a nonspecific anterior neck lymph nodes with first one having measurements of 1.0cm by 0.9cm by 0.4cm and the other one being 1.2cm by 1.3cm by 0.3cm; Test Date: 20210902; Test Name: Urine analysis; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: White Blood Cells; Result Unstructured Data: Test Result:fine; Test Date: 20210902; Test Name: Abdominal obstruction series; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Insomnia; Obesity; Sleep disorder; Tachycardia
Andere Medikamente: AMITRIPTYLINE; PROPRANOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1659075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 45,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 30.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Antinuclear antibody Basophil count Blood bilirubin Blood creatine phosphokinase Chest X-ray normal Chest discomfort Chills Cold sweat Arthralgia Injection site pain Laboratory test Blood glucose Blood glucose increased Blood thyroid stimulating hormone Blood uric acid Brain natriuretic peptide C-reactive protein

Symptomtext

does not feel her immune system is the same; hasn't had a voice/ hasn't been able to talk with her regular voice; wheezing; cough stuff up; couldn't breathe; her blood sugar is elevated; a lot of stomach pain; Headache; Chest pressure; D Dimer test that was high/ some sort of an infection maybe; Respiratory infection; Enlarged Lymph nodes; pain/ like it was burning, throbbing/ in different locations of her body; cold sweats; This is a spontaneous report from a contactable nurse (patient). A 45-year-old female patient received the second dose of bnt162b2 (COMIRNATY, Lot Number: EW0169), via an unspecified route of administration, administered in right arm on 30Aug2021 (45-year-old at time of vaccination) as single dose for COVID-19 immunization. Medical history included tachycardia, insomnia, depression, obesity, "sleep". Concomitant medications included amitriptyline (AMITRIPTYLINE) taken for sleep (she was already prescribed amitriptyline prior to receiving the vaccines as needed for sleep, but she doesn't like to take medicine she rarely took that); propranolol (PROPRANOLOL) taken for tachycardia. The patient previously received levofloxacin (LEVAQUIN) and experienced drug allergy; previously received doxycycline (DOXYCYCLINE) and experienced drug allergy. The patient previously received the first dose of bnt162b2 (COMIRNATY, Lot Number: EW0169), via an unspecified route of administration, administered in right arm on 09Aug2021 (45-year-old at time of vaccination) as single dose for COVID-19 immunisation and experienced "lymph nodes are enlarged on her neck and armpit area" and pain in the neck. Narrative: Patient states that both first and second dose of the Pfizer covid vaccine have the same Lot Number EW0169. She got both doses on the dominant arm, on her right arm. She received first vaccination dose on 09Aug2021, after she has been having issues with her lymph nodes. On the right side the lymph nodes are enlarged on her neck and armpit area. She got an ultrasound done with labs. Her HCP still recommended her to get the 2nd Pfizer vaccine. She got the second dose on 30Aug2021 ever since then she has had a headache (later clarified as "started 3 days after the second dose"). She has a neurologist appointment coming up. The first night after the second dose (30Aug2021) she had cold sweats, the next day (31Aug2021) she woke up with excruciating pain, it was different type of pain, like it was burning, throbbing, and she feels the pain at the same time in different locations of her body. Her pain was bad that she could not be touched. She called the doctor the next day (01Sep2021) because she was chest pressure, the pain is still there but not as excruciating. She went to urgent care and they did labs, a D Dimer test that was high (0.58 on 02Sep2021), they did an emergency CT Scan with contrast of the chest, and the doctor said that was negative. The doctor said that she felt like D Dimer test indicated she had some sort of an infection maybe. Patient states that she was back to her doctor because the pain was random, it was like ice picks would stab in random parts of body. She can't get rid the of headache. They ran more tests, she has started to feel better with exception of the headache. She is on medication that she was not on before. She has a follow up with neurology. Two and half weeks ago (Sep2021) she got a respiratory infection, she tested negative for flu (Sep2021) and COVID-19 (22Sep2021). They put her on an inhaler, steroids, and antibiotics, and she is still sick. She does not feel her immune system is the same. She hasn't had a voice in 2.5 weeks. They gave her another round of antibiotics, she still needed an inhaler because she developed wheezing. She has never had this before, all of this is ongoing since the second vaccination. Event details: Enlarged Lymph nodes: It started about 2 days after the first dose, it started off with pain in the neck, she did not have a sore throat but when moving the neck she could feel it pull, she then physically felt the enlargement by feeling it with touch. It had subsided after a week and a half. Then after the second vaccination it came back, however it wasn't until 2.5 weeks after the second dose it enlarged again. The second time around it subsided about a week later (Sep2021) and ended beginning of Oct2021. Headache: It started 3 days after the second dose. She is on medication for it now, for the headache. Outcome: some days are better than others, she still feels the tight band around the head. Treatment for headaches: She takes amitriptyline every night because it helps with the headache, she was already on propranolol, she was also given a migraine medication, a new one that she cant remember the name of. She is schedule for a MRI on 28Oct2021. Pain: It started the day after the second dose (31Aug2021), it's random pain that she didn't have before. It feels like ice picks now, like she will have nerve pain on cuticle of the toe. It's weird spots it comes up. The severity comes on fast, on a pain scale her pain is between 7-8 out of 10. When it comes it doesn't last long. Chest Pressure: It started on 01Sep2021, the day before she went to urgent care, she called the doctor and she actually wanted her to call 911 the day before but she didn't. She went to urgent care on 02Sep2021. Outcome: Her Chest still feels tight however she does not know if it's the respiratory infection. Patient clarified she did not go to an emergency room in a hospital, she went to an urgent care facility that was attached to the big organization and so they were able to send her to different places within the facility for tests. Respiratory infection: She happens to love her Nurse practitioner but she is tired of seeing her. When she goes for her yearly exams she is overweight but not unhealthy. She saw the Nurse practitioner on 16Sep2021 because she couldn't breathe. Outcome: She is on the second round of antibiotics, it's got better from where it was before. She is now actually able to cough stuff up but she still has wheezing, She hasn't been able to talk with her regular voice since this started. Treatment: The 1st antibiotic she was given was a Z-Pak and the steroid is prednisone 20mg twice a day. The Second antibiotic is Augmentin twice a day, the doctor gave her steroids because she is still tight but not wheezing as much, the doctor told her to try not to take the steroids if she can help it, since her blood sugar is elevated (on 02Sep2021). She was also given an albuterol inhaler. She has not Lot numbers to provide for Amitriptyline, Migraine Medication with unknown name, Propranolol, Z-Pak, Augmentin, or Prednisone, they are not physically with her at this moment. Patient states that the Antibiotic was taken twice a day. Investigation: Before she only had yearly checks up and that's it. Patient states that she has had a lot of lab work done starting on 18Aug2021. 20Aug2021: She has an ultrasound of soft neck tissue with the result of a nonspecific anterior neck lymph nodes with first one having measurements of 1.0cm by 0.9cm by 0.4cm and the other one being 1.2cm by 1.3cm by 0.3cm. 02Sep2021: She had many tests. Her BMP for the most part was good, the glucose was elevated. She had a CBC in which the White Blood Cells was fine, Red Blood Cells was fine, the Hemoglobin was fine, her MCHC was 31.4, and the MPV 11.2, She has 59% neutrophils, 27% lymphocytes, 8% monocytes, 5% eosinophils, and 1% basophils. She has an Abdominal Ultrasound that was normal, an Abdominal obstruction Series that was normal, she clarified that she was also having a lot of stomach pain (on 02Sep2021). She has a CT of the Chest to rule out a PE, it was normal, she had a 12 lead EKG that showed sinus rhythm. 22Sep2021: On this day she went back to doctor, and they drew a CBC which had abnormal hematocrit 43.2, her neutrophil was 69%, lymphocytes was 23%, monocytes 5%, eosinophils 3%, and the basophil was back to normal at 0%. Her CMP (comprehensive metabolic panel) showed her glucose was still elevated but she is on steroids. 13Oct2021: She went to the doctor because they wanted to listen to lungs a second time. She is allergic to Levaquin and Doxycycline. Patient would also like to add her upcoming appointments She see's Neurology on 21Oct2021 for the headaches. She has an Ultrasound schedule for 20Oct2021 at 3:10PM. She has a MRI schedule 27Oct2021. Other test data: On 18Aug2021: Mono: Negative; comprehensive metabolic panel: Normal; Strep Group A: Negative. On 02Sep2021: ANA: normal; CK: normal; Chest X-ray: fine; C-reactive protein: Elevated 0.82; BNP, Test for Heart Failure: 27, Normal; Lipase: 17, Normal; Liver Panel: Bilirubin on 02Sep202: 0.1, low; Urine analysis: normal. On 22Sep2021: Sediment: 17; Rheumatoid factor: Normal; Uric acid: normal; CT Scan without Contrast: normal. On 13Oct2021: TSH: normal; Hemoglobin A1C: normal. The case was reported as non-serious. The outcome of enlarged lymph nodes was recovered in Oct2021; headache and "pain/ like it was burning, throbbing/ in different locations of her body" were not recovered; respiratory infection was recovering; outcome of other events was unknown.; Sender's Comments: Based on the temporal relationship, the association between the event respiratory infection with COMIRNATY use can not be fully 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: Dyspnoea
Hospital-Tage: -
Labordaten: Test Date: 20210902; Test Name: ANA; Result Unstructured Data: Test Result:normal; Test Date: 20210902; Test Name: basophils; Test Result: 1 %; Test Date: 20210922; Test Name: basophils; Test Result: 0 %; Comments: back to normal; Test Date: 20210902; Test Name: Liver Panel: Bilirubin; Result Unstructured Data: Test Result:0.1; Comments: Low; Test Date: 20210902; Test Name: CK; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: glucose/ blood sugar; Result Unstructured Data: Test Result:elevated; Test Date: 20211013; Test Name: TSH; Result Unstructured Data: Test Result:normal; Test Date: 20210922; Test Name: Uric acid; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: BNP, Test for Heart Failure; Result Unstructured Data: Test Result:27; Comments: Normal; Test Date: 20210902; Test Name: Chest X-ray; Result Unstructured Data: Test Result:fine; Test Date: 20210922; Test Name: CT Scan without Contrast; Result Unstructured Data: Test Result:normal; Test Date: 20210902; Test Name: Chest CT; Result Unstructured Data: Test Result:Normal; Comments: to rule out a PE; Test Date: 20210902; Test Name: C-reactive protein; Result Unstructured Data: Test Result:Elevated 0.82; Test Date: 20210902; Test Name: 12 lead EKG; Result Unstructured Data: Test Result:Sinus Rhythm; Test Date: 20210902; Test Name: eosinophils; Test Result: 5 %; Test Date: 20210922; Test Name: eosinophils; Test Result: 3 %; Test Date: 20210902; Test Name: D-Dimer; Result Unstructured Data: Test Result:0.58; Comments: high, indicated she had some sort of an infection maybe; Test Date: 20210818; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: CBC; Result Unstructured Data: Test Result:White Blood Cells was fine, Red Blood Cells was fi; Comments: White Blood Cells was fine, Red Blood Cells was fine, the Hemoglobin was fine, her MCHC was 31.4, and the MPV 11.2, She has 59% neutrophils, 27% lymphocytes, 8% monocytes, 5% eosinophils, and 1% basophils; Test Date: 20210922; Test Name: CBC; Result Unstructured Data: Test Result:abnormal hematocrit 43.2, her neutrophil was 69%,; Comments: abnormal hematocrit 43.2, her neutrophil was 69%, lymphocytes was 23%, monocytes 5%, eosinophils 3%, and the basophil was back to normal at 0%.; Test Date: 20211013; Test Name: Hemoglobin A1C; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: hematocrit; Result Unstructured Data: Test Result:43.2; Comments: abnormal; Test Date: 20210902; Test Name: Hemoglobin; Result Unstructured Data: Test Result:fine; Test Date: 202109; Test Name: flu test; Test Result: Negative ; Test Date: 20210818; Test Name: Mono; Test Result: Negative ; Test Date: 20210902; Test Name: lipase; Result Unstructured Data: Test Result:17; Comments: Normal; Test Date: 20210902; Test Name: lymphocytes; Test Result: 27 %; Test Date: 20210922; Test Name: lymphocytes; Test Result: 23 %; Test Date: 20210902; Test Name: MCHC; Result Unstructured Data: Test Result:31.4; Test Date: 20210902; Test Name: MPV; Result Unstructured Data: Test Result:11.2; Test Date: 20210902; Test Name: BMP; Result Unstructured Data: Test Result:glucose was elevated; Comments: for the most part was good; Test Date: 20210818; Test Name: comprehensive metabolic panel; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: comprehensive metabolic panel; Result Unstructured Data: Test Result:Glucose Elevated; Test Date: 20210902; Test Name: monocytes; Test Result: 8 %; Test Date: 20210922; Test Name: monocytes; Test Result: 5 %; Test Date: 20210902; Test Name: neutrophils; Test Result: 59 %; Test Date: 20210922; Test Name: neutrophils; Test Result: 69 %; Test Date: 20210902; Test Name: Red Blood Cells; Result Unstructured Data: Test Result:fine; Test Date: 20210922; Test Name: Sediment Rate; Result Unstructured Data: Test Result:17; Test Date: 20210922; Test Name: Rheumatoid factor; Result Unstructured Data: Test Result:Normal; Test Date: 20210922; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20210818; Test Name: Strep Group A; Test Result: Negative ; Test Date: 20210902; Test Name: Abdominal Ultrasound; Result Unstructured Data: Test Result:Normal; Test Date: 20210820; Test Name: Ultrasound of the Soft Neck; Result Unstructured Data: Test Result:a nonspecific anterior neck lymph nodes with first; Comments: a nonspecific anterior neck lymph nodes with first one having measurements of 1.0cm by 0.9cm by 0.4cm and the other one being 1.2cm by 1.3cm by 0.3cm; Test Date: 20210902; Test Name: Urine analysis; Result Unstructured Data: Test Result:Normal; Test Date: 20210902; Test Name: White Blood Cells; Result Unstructured Data: Test Result:fine; Test Date: 20210902; Test Name: Abdominal obstruction series; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Insomnia; Obesity; Sleep disorder; Tachycardia
Andere Medikamente: AMITRIPTYLINE; PROPRANOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1839301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: -
Geschlecht: U
Eingang: 03.11.2021
Impfdatum: 22.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain

Symptomtext

chest pain; This is a spontaneous report from a contactable consumer (patient). A patient of an unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EW0169, expiration date: unknown) via an unspecified route of administration on 22Apr2021 as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced chest pain. Stated never had it before any chest pain nothing and wanted to know about what should be done. Outcome of the event was unknown at the time of reporting. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1839273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest X-ray Computerised tomogram Decreased appetite Dyspnoea Electrocardiogram Fatigue Fibrin D dimer Full blood count Insomnia Ultrasound scan

Symptomtext

not been sleeping; shortnessof breath; tired; Dose 2: Appetite is gone; This is a spontaneous report from a contactable consumer (patient). A 54-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number EW0169), via an unspecified route of administration, administered in Arm Left on 28Apr2021 11:00 AM (at the age of 54-year-old) as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient had the first dose on 07Apr2021 in her left arm, lot: EW0158 for Covid-19 immunization and experienced Shortness of breath, awful cough, decreased appetite and tired. No prior Vaccinations (within 4 weeks). The patient's concomitant medications were not reported. On 28Apr2021 dose 2: appetite is gone, shortness of breath, tired. On an unspecified date, not been sleeping. She had her first dose of the Covid-19 Vaccine on 07Apr2021 and her second dose yesterday 28Apr2021. The patient happened to be tired on 28Apr2021. After the 15 min of second dose patient experienced shortness of breath and felt like she was gasping for air, due to this she was she laying down. Her appetite was gone and she has an issue breathing. The patient underwent lab tests and procedures which included chest x-ray: negative, computerised tomogram: negative on an unspecified date, electrocardiogram: normal, fibrin d dimer: normal, full blood count: normal, ultrasound scan: negative, the patient got negative for Covid. The outcome of shortness of breath was recovering, the outcome of dose 2: appetite is gone, was not recovered. The outcome of not been sleeping and tired was unknown. PSCC Communication: Caller provides multiple times for second dose administration, clarifies second dose was given at 11:15 AM. Referred caller to her physician for medical advice.Caller disconnected while on hold. Medical Information agent states she will call them back with the number provided. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Chest X-ray; Result Unstructured Data: Test Result:negative; Test Name: CT; Result Unstructured Data: Test Result:negative; Test Name: EKG; Result Unstructured Data: Test Result:Normal; Test Name: D dimer; Result Unstructured Data: Test Result:Normal; Test Name: CBC; Result Unstructured Data: Test Result:Normal; Test Name: Ultrasound; Result Unstructured Data: Test Result:negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2596742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 07.10.2021
Beginn: 07.09.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Cough Diarrhoea Dyspnoea Fatigue SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 12/28/2020, Pfizer, dose #1 01/19/2021, Pfizer, dose #2 10/07/2021, Pfizer dose #3 09/07 cc: cough, diarrhea, fatigue, dyspnea exposure: unknown 09/09 COVID swab, result: detected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09/09 COVID swab, result: detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1837416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KY
Alter: 56,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 01.07.2021
Beginn: 02.07.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tachycardia Tinnitus

Symptomtext

1 -Tachycardia for several hours, starting at 1 AM on 07/02/2021. 2 - Ringing in the right ear, high frequency ringing, started on 07/03/2021 and still continues on today (11/02/2021) and getting louder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Barrett's esophagus, twisted colon, asthma
Andere Medikamente: omeprazole, Famotidine, Vit D, potassium
Allergien: penicillin, sulfa drugs, eggs and banana's
Vorherige Impfungen: Flu vaccine 2 years ago. Arms & hands tingle/go numb, trouble breathing. Both within 15 minutes of receiving the vaccine.

VAERS 1835787

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 52,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 14.05.2021
Beginn: 01.05.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Bronchial secretion retention Chest pain Chills

Symptomtext

Chills; Slight pains in the chest; Didn't cough up phlegm anymore; This is a spontaneous report from a contactable consumer or other non hcp (patient herself).A 52-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EW0169, Expire Date: unknown) via an unspecified route of administration in left upper arm on 14May2021 (at the age of 52 years-old) as dose 2, 0.3mL single for COVID-19 immunization (reported as because she has COPD and didn't want to get sick) Patient medical history included ongoing COPD (chronic obstructive pulmonary disease) diagnosed in 2020, maybe June 2020, ongoing high blood pressure (hypertension) had it for years maybe 5 or 6 years, physical problems (malaise), but nothing with breathing. The concomitant medications reported as none. Historical vaccine includes BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EW0151, Expiry Date: Unknown) via an unspecified route of administration in left upper arm on 02Apr2021 at 09:30 in the morning as dose 1, 0.3mL single for COVID-19 immunization and experienced didn't cough up phlegm anymore, It was just the next couple of days of getting the first vaccine. That has continued. She has not coughed up phlegm since then and Slight pains in the chest, but it was come and go. Vaccine was not administered at military facility. Additional vaccines administered on same date of the pfizer suspect was reported as none. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine was not provided. The adverse events following prior vaccinations was none. No family medical history relevant to adverse events. The patient experienced chills, slight pains in the chest (Pain is not like pain, but is a nagging), didn't cough up phlegm anymore on May2021. COVID19 shot first dose was given on 02Apr2021 and second dose given on 14May2021. Reporter states she was late to get second dose. Before she took the shot, she had phlegm that she coughed up in the morning. When she took the first shot, she didn't cough up phlegm anymore and same with second. She had not been coughing up phlegm since. She is wondering if she should be concerned. Maybe the fluid is not leaving the lungs and is still in there. Her primary care doctor is at Health Center, she doesn't have a specific doctor it is just a clinic. The slight pains in the chest after second shot, it is constant now. The pain is in the left side. The time of onset of events was not provided. The events were not resulted in any emergency room visit and physician office visit. The patient underwent lab tests and procedures after the first dose which included blood test (Blood work): normal on an unspecified date maybe less than a month ago in 2021. They said everything was alright. She hadn't had a chest x-ray since having the vaccine.The clinical outcome of events chills was unknown while that of slight pains in the chest, didn't cough up phlegm anymore was not recovered. Information on Lot/Batch number was available. Additional information has been requested. No follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Blood work; Result Unstructured Data: Test Result:Normal; Comments: They said everything was alright.
Aktuelle Erkrankungen: Blood pressure high (Verbatim: high blood pressure); COPD (Verbatim: COPD diagnosed in 2020, maybe June 2020,)
Vorgeschichte: Medical History/Concurrent Conditions: Physically unwell (Verbatim: physical problems)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1832870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 35,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 28.04.2021
Beginn: 02.05.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anxiety Blood thyroid stimulating hormone normal Electrocardiogram normal Full blood count normal Metabolic function test normal Palpitations Panic attack Tension Vitamin B12 decreased Vitamin D decreased

Symptomtext

From the 2nd day of my second covid shot, I have been experiencing anxiety related symptoms for last 6 months. On 05/01/2021 around night 11PM est - I suddenly had racing heart beat for some hours that I never had. on 05/02/2021- I visited PCP on 05/02/2021 to understand the symptoms and to get treatment My TSH level, B12, D vitamin and Blood pressure was checked. TSH was around 8.5 and B12, D were very low. Blood pressure was above normal too on the day of the my PCP visit. To control my blood pressure, I cut down the salt completely from my food intake.I was taking Levothyorixine every alternative day, and was also taking medications for B12 and D. But my symptoms were not gone. I still used to feel lot of uneasiness in the body and used to feel anxiety and tension all the time. If I was fine for one day, I used to be having anxiety symptoms for rest of the week. The symptoms continued for entire May month. I used to feel heavy headed sometimes. Light headed sometimes. Racing heart beat continued most of the time. PCP did complete blood tests CBC and Metabolic panel on 06/11/2021 and they all came out normal. PCP said it is general anxiety and will go away eventually after few months. In a month of june and July, I had some kind of panic attacks which made me visit Urgent care and Emergency care each time. They said I have some anxiety related symptoms. My PCP gave hydroxizine HCL 25 mg to treat anxiety as needed but I never used that as I was trying to heal the anxiety on it's own. But even after 6 months from my vaccination ,I have been experiencing anxiety symptoms every day. No improvements. This is impacting my daily activities a lot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: CBC, Metabolic test, ECG for heart taken. All came out normal.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1831301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 57,0
Geschlecht: M
Eingang: 30.10.2021
Impfdatum: 29.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dysstasia Loss of personal independence in daily activities Nausea Speech disorder Tremor Visual impairment Vomiting

Symptomtext

am unable to go to work, so I am on short-term disability as a result; was at work when I suddenly was unable to stand. I dropped to my knees and started vomiting. I couldn't open my eyes because everything was shaking or moving. I was admitted to emergency room; was at work when I suddenly was unable to stand. I dropped to my knees and started vomiting. I couldn't open my eyes because everything was shaking or moving. I was admitted to emergency room; nauseous.; My vision is still off; could not stand; difficulty talking; This is a spontaneous report from a contactable consumer (patient). A 57-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0169), via an unspecified route of administration, administered in Arm Right on 29Apr2021 15:00 (at the age of 57-year-old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included none. Patient did not have known allergies. Concomitant medication(s) included pantoprazole sodium sesquihydrate (PANTOPRAZOL A) taken for an unspecified indication, start and stop date were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EW0151), administered in Arm Right on 08Apr2021 15:00 (at the age of 57-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Patient did not receive any other vaccine in four weeks. The patient stated that on 29Apr2021, he was at work when he suddenly was unable to stand. He dropped to his knees and started vomiting. He could not open his eyes because everything was shaking or moving. He was admitted to emergency room. He could not stand or open his eyes without being nauseous. Everything was still shaking. He had severe vomiting. He was released and sent home. He was unable to stand or open eyes for 48 hours. He had difficulty talking without vomiting. On day 3, he was able to sit up and walk with assistance. He was also slowly able to hold down food. It was day 11 and he was still unsteady on his feet. His vision was still off. It was still very hard to focus. He was unable to go to work, so was on short-term disability as a result. Patient did not have covid prior vaccination and covid was not tested post vaccination. Patient did not receive any treatment. The outcome of events was not recovered. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente: PANTOPRAZOL A
Allergien: -
Vorherige Impfungen: -

VAERS 1827695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 29.10.2021
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: nein

Asthenia Bronchial irritation Dizziness Myalgia Oesophagectomy Palatal swelling Palpitations

Symptomtext

racing heartbeat; dizziness; lightheaded; weakness; esophageal restriction; swelling in roof of mouth; bronchial irritation; muscle pain; This is a spontaneous case from a contactable consumer (Patient) reported that: A 78-years-old non-pregnant female patient received BNT162B2 (Pfizer BioNTech solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 16Apr2021 09:45 (Batch/Lot Number: EW0169) as DOSE 1, SINGLE for covid-19 immunization (Age at vaccination 78 years). The patient past medical history included Allergy (drug hypersensitivity) from an unknown date and unknown if ongoing highly sensitive to all medications. Concomitant medication included calcium (CALCIUM) taken for an unspecified indication, start and stop date were not reported and Vitamin d (VITAMIN D [VITAMIN D NOS]) taken for an unspecified indication, start and stop date were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within 4 weeks prior to covid-19 vaccination. the patient was not diagnosed with COVID-19. On 16Apr2021 After 4 hours the patient experienced racing heartbeat, dizziness, lightheaded and weakness. After 9 hours experienced esophageal restriction, swelling in roof of mouth and bronchial irritation and after 20 hours reported muscle pain all over body. No treatment was received. The event outcome was Recovering. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (highly sensitive to all medications)
Andere Medikamente: CALCIUM; VITAMIN D [VITAMIN D NOS]
Allergien: -
Vorherige Impfungen: -

VAERS 1825876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 58,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 31.03.2021
Beginn: 26.10.2021
Tage bis Beginn: 209,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Dyspnoea Ear pain Headache Lymphadenopathy Nasal congestion Oropharyngeal pain Pain Productive cough Sinus congestion Sneezing Wheezing

Symptomtext

headache- sore throat- chills- productive cough- shortness of breath- body aches- ear pain- sinus congestion- nasal congestion- swollen glands- wheezing- sneezing starting 10/26/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Anemia. Rt breast lumpectomy. Depression. 1/03 left hemmorrhagic cyst. G3P3. R abdomen shingles. Allergic rhinitis. GERD. Nicotine dependence. scoliosis, chronic neck pain. cervical DDD. colon/EGD 4/2015 esophagitis & colon polyps repeat q 5 yrs. Asthma/ reactive airway disease. Elevated cholesterol.
Andere Medikamente: ?Triamcinolone Acetonide 0.1 % Cream 1 application Externally twice a day ?Fluticasone Propionate 50 MCG/ACT Suspension 2 sprays Nasally Once a day ?Vitamin D ?Albuterol Sulfate HFA 108 (90 Base) MCG/ACT Aerosol Solution 2 puffs a
Allergien: PENICILLIN DRUGS: hives - Allergy Doxycycline Monohydrate: skin burning, feet swelling
Vorherige Impfungen: -

VAERS 1824543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: SC
Alter: 73,0
Geschlecht: F
Eingang: 28.10.2021
Impfdatum: 15.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Mouth swelling Paraesthesia Swelling face

Symptomtext

Face started tingling like someone sticking me with pins; Mouth started swelling; Face started swelling around mouth and cheeks; This is a spontaneous report from a contactable consumer, the patient. A 73-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the right arm on 15Apr2021 at 11:00 (at the age of 73-years-old) as a single dose for COVID-19 immunisation. Medical history included juvenile asthma as a child that no longer affected her and known allergies to tree nuts cosmetics and perfumes. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included colecalciferol (VITAMIN D3), boron (MANUFACTURER UNKNOWN), prunus cerasus (TART CHERRY) and Ascorbic acid, Pyridoxine hydrochloride, Biotin, Folic acid, Colecalciferol, Retinol, Pantothenic acid, Riboflavin, Phytomenadione, Nicotinamide, Betacarotene, Iron, Magnesium, Manganese, Potassium, Chromium, Copper, Zinc, Calcium, Iodine, Phosphorus, Selenium, Vitamin b12 nos, Xantofyl, Lycopene, Vitamin b1 nos, Vitamin e nos (CENTRUM SILVER); all for unknown indication, on unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. 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 22Mar2021 at 01:00 (at the age of 72-years-old) as a single dose for COVID-19 immunisation and the patient also previously received guaifenesin/pseudoephedrine hydrochloride (SUDAFED), alendronate sodium (FOSAMAX) and experienced drug allergy. On 15Apr2021 at 11:15, after waiting 15 at site, the patient started driving home and her face started tingling like someone sticking her with pins, mouth started swelling and face started swelling around mouth and cheeks. This was all in a matter of 15 to 30 minutes. The patient reported that she always carried diphenhydramine hydrochloride (BENADRYL), because of allergic reactions to different things. The events had not resulted in doctor/other health care professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were taken as a result of the events and included treatment with diphenhydramine hydrochloride (BENADRYL). The clinical outcome of the events face started tingling like someone sticking her with pins, mouth started swelling and face started swelling around mouth and cheeks was resolved on 15Apr2021. 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: Allergy to nuts (Known allergies: Tree nuts); Childhood asthma (Had juvenile asthma as a child, no longer effected); Cosmetic allergy (Known allergies: Cosmetics); Perfume sensitivity (Known allergies: Perfumes)
Andere Medikamente: VITAMIN D3; BORON; TART CHERRY; CENTRUM SILVER [ASCORBIC ACID;BETACAROTENE;BIOTIN;CALCIUM;CHROMIUM;COLECALCIFEROL;COPPER;FOLIC ACID;
Allergien: -
Vorherige Impfungen: -

VAERS 1821857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 33,0
Geschlecht: F
Eingang: 27.10.2021
Impfdatum: 01.04.2021
Beginn: 03.10.2021
Tage bis Beginn: 185,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Dyspnoea Ear pain Headache Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

cough, shortness of breath, headache, sore throat- off and on, ear pain. tested positive for covid19 10/5/21 LOT #1 not available

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: mild asthma; wolff-parkinon-white syndrom; hypertensionl lichen sclerosus
Andere Medikamente: Benzonate; Doxycycline; Clobetasol; Dizepam; Sprintec
Allergien: none
Vorherige Impfungen: -

VAERS 1815513

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: VA
Alter: 24,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Condition aggravated Conversion disorder Diarrhoea Fatigue Gait disturbance Headache Injection site pain Nausea Pain Post-acute COVID-19 syndrome Pyrexia Tinnitus Tremor Visual impairment

Symptomtext

My acute COVID-19 infection in April 2020 triggered further postviral complications, including Functional Neurological Disorder (FND). Both my Pfizer doses severely exacerbated my long covid/FND symptoms and created new setbacks in my disabilities. Pfizer #1: Severe symptoms for 6 days with new onset of constant, mild ringing ears that I still experience. Worse nausea, fatigue, and headache for 4-5 days. Worse functional arm/hand tremor, functional gait, injection site pain, and diarrhea for 3 days. Chills and a sense of warm postnasal drip for 2 days. Pfizer #2: Severe symptoms for 15 days, many of my FND symptoms still not back to baseline. Ringing ears became slightly louder after second dose. Worse functionalhand/arm tremor, functional gait, ringing ears, and diarrhea for 15+ days. Worse fatigue for 8 days. Worse headache for 7 days. Worse nausea for 5 days. Worse injection site pain and body aches for 5 days. Chills for 3 days and feverish for 2 days. I messaged my neurologist about the worse FND symptoms following COVID vaccinations but we did not take further action as FND can naturally have ups and downs. I do not think the COVID vaccine itself made me sicker, but I think there may be an interesting relationship between my previous contraction of COVID-19 in early 2020, my reactivity to COVID and development of Long Covid, the triggering of my FND, and the possibility that the COVID vaccine ellicits severe symptoms in me. I received a flu shot in September 2021 and did not have any abnormal or severe symptoms like I did with the Pfizer COVID vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Long Covid (acute COVID-19 infection April 2020) Postviral Fatigue Syndrome (triggered by acute COVID infection)Functional Neurological Disorder (FND) (functional gait and tremor disorders, triggered by long covid), Post Traumatic Vision Syndrome (diagnosed April 2021 but began before 1st Pfizer dose, triggered by long covid or FND) ,
Andere Medikamente: Flovent HFA inhaler 110mcg, Sprintec birth control
Allergien: Mild seasonal allergies
Vorherige Impfungen: -

VAERS 1815298

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 62,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Blood test Cardiac disorder Cardiac monitoring Cardiac stress test Dyspnoea Echocardiogram Electrocardiogram Tachycardia

Symptomtext

I dealing with rhythms, tachycardia, and SOB. I was having serve joint pain in my back and hands that have resolved. But the heart problem is still a problem. The heart problem have been ongoing for 5 months now. I went to the hospital on Oct 5th because it has gotten worst. I was hospitalized for 1 day. They did blood work for heart attack, serve EKG, echo cardio gram, and a stress test. I am wearing a heart monitor for two weeks now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: blood work, EKG, Echo cardio gram, stress test
Aktuelle Erkrankungen: N/A
Vorgeschichte: arthritis
Andere Medikamente: N/A
Allergien: TB shot, BBI 2000
Vorherige Impfungen: -

VAERS 1815083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 25.10.2021
Impfdatum: 21.04.2021
Beginn: 22.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Cardiac flutter Chills Condition aggravated Cough Dental caries Dyspnoea Electrocardiogram Headache Rash Sensitive skin Taste disorder Visual impairment

Symptomtext

About 8 hours after the vaccine, it started with a really bad headache first. And then I had no fever but very bad chills. I had a rash on my neck. I had difficulty breathing. I had extreme hypersensitivity to touch on my skin. That lasted about 6 hours. After that I had received at least one EKG because I had a heart flutter. I had a vision change, I had trouble seeing. Went to the eye doctor recently. They checked my eyes and my vision had changed since I had been there which had been less than a year. I had a significant change in my left eye. At my annual dentist appt, my dentist identified three cavities in my molars which are all sealed. I have never had any cavities before, so have been going to the doctor to deal with the cavities and other sensitivities that I didn't have prior. I am still maintaining with my long COVID symptoms which has been ongoing. It could be a lifetime, they said, of dealing with these symptoms. I am having continued cough, shortness of breath, and taste aversion and joint pain. I did an urgent care televisit after this injection. They gave me a new inhaler to take, albuterol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG through my primary care at the time, they said it was probably from COVID and to wait it out.
Aktuelle Erkrankungen: Long COVID, I got COVID in January 2021 (1/4/2021), still was having difficulty breathing; migraine; scarring on my right lung; Taste and smell was altered.
Vorgeschichte: Asthma; Difficulty breathing.
Andere Medikamente: Wixela; Albuterol; Famotidine; Pirazolac; Topamax; Prednisone; Nebulizer.
Allergien: Penicillin.
Vorherige Impfungen: COVID-19 Dose 1, 03/31/2021, I had really bad headache, hypersensitive to touch. Those symptoms lasted about 16 hours.

VAERS 1812843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 04.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Head discomfort Nausea Pain in extremity Paraesthesia Pyrexia

Symptomtext

left arm pain and tingling; left arm pain and tingling; fevers; nausea; heaviness of her head; This is a spontaneous from a contactable physician reported that. A 64-years-old female patient received BNT162B2 (BioNTech/Pfizer vaccine solution for injection), dose 1 intramuscular, administered in Arm Left on 04Apr2021 (Batch/Lot Number: EW0169) as DOSE 1, SINGLE for covid-19 immunization (Age at vaccination 64 years). Facility where the most recent COVID-19 vaccine was administered: Hospital. The patient past medical history included hypertension from an unknown date and unknown if ongoing, Allergies to Chamomile, codeine, latex, mango, Pineapple and shellfish. The patient's concomitant medications were not reported. The patient previously took codeine and experienced drug hypersensitivity. 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 did not receive any other vaccine within 4 weeks prior to covid-19 vaccination. The patient has not received other medications in two weeks. On 13Apr2021 the patient developed left arm pain and tingling, fevers, nausea and what she describes as heaviness of her head. The adverse event results Doctor or other healthcare professional office/clinic visit. The patient received a treatment with Pepcid. The event outcome was Not recovered. Device Date: 04Jun2021 Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to plants; Fruit allergy; Hypertension; Latex allergy; Shellfish allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1811807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: WA
Alter: 21,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 24.04.2021
Beginn: 24.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Hypoaesthesia Paraesthesia

Symptomtext

Numbness; Tingling from shoulder down to hand; Wrist pains; This is a spontaneous report from a contactable consumer, the patient. A 21-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 24Apr2021 at 12:15 (at the age of 21-years-old) as a single dose for COVID-19 immunisation. Medical history included gastroesophageal reflux disease (GERD), generalized anxiety disorder, carpal tunnel and sulfonamide allergy. Prior to 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. Concomitant medications included fluoxetine hydrochloride (POZAC), methylphenidate hydrochloride (CONCERTA), atomoxetine hydrochloride (STRATTERA), glycopyrronium tosylate (QBREXZA) and Rethinylestradiol, norgestimate (MILI) from an unknown date for an unknown indication and unknown if ongoing. On 24Apr2021 at 13:15, after about 35-45 minutes, the patient experienced numbness and tingling from shoulder down to hand accompanied by wrist pains. She was unsure if that is a common side effect, but it was not listed so she wanted to report it anyways. 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 outcomes of the events numbness, tingling from shoulder down to hand and wrist pain were 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: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Carpal tunnel syndrome (Carpal Tunnel); Gastroesophageal reflux disease (GERD); Generalized anxiety disorder; Sulfonamide allergy (Known allergies: Sulfa)
Andere Medikamente: PROZAC; CONCERTA; STRATTERA; QBREXZA; MILI [ETHINYLESTRADIOL;NORGESTIMATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1811606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 48,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dry mouth Lymphadenopathy Paraesthesia Paraesthesia oral Pharyngeal swelling

Symptomtext

Tingling in tongue; Minor internal throat swelling; Severe dry mouth; Swollen glands in throat; Tingling in hands; This is a spontaneous report from a contactable consumer, the patient. A 48-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 20Apr2021 at 12:30 (at the age of 48-years-old) as a single dose for COVID-19 immunisation. Medical history included multiple sclerosis (MS) and known allergies to penicillin and sulfa. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included phentermine (MANUFACTURER UNKNOWN) for unknown indication from an unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 20Apr2021 at 13:15, the patient experienced tingling in hands, tingling in tongue, severe dry mouth, swollen glands in throat and minor internal throat swelling. The events did not result 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. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events tingling in hands, tingling in tongue, severe dry mouth, swollen glands in throat and minor internal throat swelling were resolved on an unknown date in Apr2021. 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: Multiple sclerosis (MS); Penicillin allergy (known allergies to penicillin); Sulfonamide allergy (known allergies to sulfa)
Andere Medikamente: PHENTERMINE
Allergien: -
Vorherige Impfungen: -

VAERS 1811544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain Asthenia Chest pain Fatigue Flatulence Headache Muscular weakness Myalgia Pain in extremity

Symptomtext

Abdominal/ stomach pain (mild to moderate) gas; Headache; Mild chest pain; Extreme weakness and fatigue; Upper body muscle weakness and pain, especially in left arm; Upper body muscle weakness and pain, especially in left arm; Upper body muscle weakness and pain, especially in left arm; extreme weakness and fatigue; upper abdominal/stomach pain (mild to moderate).; This is a spontaneous report from a contactable consumer, the patient. A 43-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 20Apr2021 at 13:00 (at the age of 43-years-old) as a single dose for COVID-19 immunisation. Medical history included gastroesophageal reflux disease (GERD) and hernia hiatal. The patient had no known allergies. Concomitant medications included cyanocobalamin (oral B-12) (MANUFACTURER UNKNOWN), iron supplement (MANUFACTURER UNKNOWN) and multi vitamin (MANUFACTURER UNKNOWN) for unknown indication from unspecified date, unknown if ongoing. Prior to 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 20Apr2021, on the day of vaccination, the patient experienced upper abdominal/stomach pain (mild to moderate). On 22Apr2021, 2 days after vaccination, the patient experienced headache, mild chest pain, gas, extreme weakness, fatigue, upper body muscle weakness and pain, especially in left arm. The symptoms were persistent for 3 days at the time of this report. 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 abdominal/ stomach pain (mild to moderate), gas, headache, mild chest pain, extreme weakness, fatigue, upper body muscle weakness and pain, especially in left arm was 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: GERD; Hernia hiatal
Andere Medikamente: B-12; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1811235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 60,0
Geschlecht: M
Eingang: 23.10.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest pain Dizziness Headache

Symptomtext

At 14 hours headache was worse with upper chest pain; At 14 hours headache was worse with upper chest pain and non stop "dizzyness"; About 12 hours after shot started with headache; This is a spontaneous report from a contactable consumer, the patient. A 60-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 16Apr2021 at 09:00 (at the age of 60-years-old) as a single dose for COVID-19 immunisation. Medical history included high blood pressure and type 2 diabetes. 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 received other vaccines within four weeks prior to the vaccination. The patient did not receive any concomitant medications. The patient previously received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8730) via an unspecified route of administration in the right arm on 26Mar2021 (at the age of 60-years-old) as a single dose for COVID-19 immunisation. On 16Apr2021 at 21:00, about 12 hours after the shot, the patient experienced headache. On 16Apr2021 at 23:00, at 14 hours after the shot, the headache was worse with upper chest pain and non-stop dizziness. Felt better on 18Apr2021 at 12:00. 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 about 12 hours after shot started with headache and at 14 hours headache was worse with upper chest pain and non-stop dizziness was resolved on 18Apr2021 at 12:00. 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); Type 2 diabetes mellitus (Type 2 diabetes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1811130

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: OR
Alter: 24,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 15.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Chills Dyspnoea Headache Nausea Palpitations Pyrexia

Symptomtext

Heart palpitations; Tightness in chest; Shortness of breath; Fever; Chills; Headache; Nausea; This is a spontaneous report from a contactable consumer, the patient. A 24-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0169) via an unspecified route of administration in the left arm on 15Apr2021 at 13:00 (at the age of 24-years-old) as a single dose for COVID-19 immunisation. Medical history included COVID-19 and had known allergies to wheat and gluten. 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 vitamin d (MANUFACTURER UNKNOWN), vitamin B (MANUFACTURER UNKNOWN), ascorbic acid (VITAMIN C), levoglutamide (L GLUTAMINE) and iron (MANUFACTURER UNKNOWN) all from an unknown date for unknown indication and unknown if ongoing. On 16Apr2021, the first two days, the patient experienced fever, chills, headache and nausea, felt fine but had these symptoms again. On 21Apr2021 at 03:00 (about 6 days after vaccination), the patient woke up with heart palpitations, tightness in chest and shortness of breath. 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 reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events fever, chills, headache, nausea, heart palpitations, tightness in chest and shortness of breath was not recovered at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19; Food allergy (known allergies: Wheat); Gluten intolerance (known allergies : Gluten)
Andere Medikamente: VITAMIN D NOS; VITAMIN C [ASCORBIC ACID]; L GLUTAMINE; IRON; VITAMIN B [VITAMIN B COMPLEX]
Allergien: -
Vorherige Impfungen: -

VAERS 1412945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 27.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Burning sensation Erythema Flushing Breast pain Hypoaesthesia Movement disorder Musculoskeletal pain Nausea Neck pain Neuralgia Pain in extremity Paraesthesia Pain Physical disability

Symptomtext

was in both hands, that numbing sensation; painful arm, so painful she couldn't even lift it or move it; she could not get up; Nauseous was reported as worsened; the palms of her hands turned very red, it looked like she had a glove on; felt pins and needles in her hands; severe left sided arm pain; arm pain which radiated to her shoulder blades, neck, back under her am/ she feels all painful and achy/ the whole area was so severe; thought the vaccine might have hit a nerve; The shoulder, neck, back, shoulder blade, it just feels like it's burning; severe left sided arm pain which radiated to her shoulder blades; severe left sided arm pain which radiated to her shoulder blades, neck; severe left sided arm pain which radiated to her shoulder blades, neck, back under her am/ upper back; severe left sided arm pain which radiated to her shoulder blades, neck, back under her am, and left breast; This is a spontaneous report from a contactable consumer (patient) reporting herself. A 69-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number EW0169) via an unspecified route of administration, administered in left arm on 27Apr2021 at 14:15-14:30 (age at the time of vaccination was 69-years-old) as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. She did not take any medication. No other products were administered. There were no any history of all previous immunizations with the Pfizer vaccine considered as suspect and no additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations within 4 weeks and no any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No adverse events following prior vaccinations. There was no patient's medical history (including any illness at time of vaccination) and no family medical history relevant to adverse events. No relevant tests. It was reported that, after receiving first dose, the patient has felt pins and needles in her hands. Aside from this, she had severe left sided arm pain which radiated to her shoulder blades, neck, back under her am, and left breast. She was feeling all these stabbing pins and needles in her hands, worse in her left hand. She said this has been going on for 2 weeks now. Nauseous was reported as worsened. She wanted to know if this was a known side effect associated with the Pfizer-BioNTech Covid-19 Vaccine, and if it would go away. Consumer also wanted to know if this might had been caused by the vaccine not being administered properly and did not go into the muscle. She thought the vaccine might have hit a nerve, but she did not that the pins and needles in her hands have already subsided. She stated her hands, the palms of her hands turned very red. She stated it looked like she had a glove on but she experienced such a painful arm, so painful she could not even lift it or move it, it was been severe, it was into her shoulder, neck, shoulder blade, upper back, the whole area was so severe. She stated into the back of her neck, shoulder, her whole back, shoulder blade on left side, under her arm, and into the breast on her left side. She was supposed to go back for another shot, she did not think so. She stated at that point, it was in both hands, that numbing sensation and she was showing to her husband her hands, and he said it looked like she had a glove on. She was trying to stay calm. She told her husband to get back to the car and she had some water so she drank a little bit of water. She sat in the car a little bit and they started to slowly head home and it just continued as far as the arm pain just kept getting worse. It was very painful and had been since the beginning. The pain seemed to get worse every day and went to the neck, back, and shoulder. As far as the redness, that seem like that had gotten better, that had improved. Pins and needles had gotten better. The first week and a half with pins and needles was very bad, but every day, it had started to get a little bit better. She was not having as much, not like it was at all, she was happy about that, that it was improved. The shoulder, neck, back, shoulder blade, it just felt like it was burning. The next day, her husband had to lift her up out of bed, she could not get up. She felt all painful and achy, it was that kind of thing, it came and went. She would say today she had it pretty much on the day of reporting, but she was having a lot of burning in the neck and the back of the shoulder blade, almost like up or down the spine just all over there and the arm and shoulder in the front. She was never even had a flu vaccine but they were vaccinated through childhood for everything but had no real problems with anything. She did not even want to take Tylenol because she did not know what she heard she did not know if she heard they were advising not to take anything like that. She did not visit emergency room and physician office. The outcome of events severe left sided arm pain which radiated to her shoulder blades, neck, upper back under her am, and left breast/ she feels all painful and achy/ she feels all painful and achy/ the whole area was so severe, nauseous was reported as worsened, the shoulder, neck, back, shoulder blade, it just felt like it was burning were not recovered, outcome of events felt pins and needles in her hands, the palms of her hands turned very red, in both hands, that numbing sensation were recovering and outcome of other events were unknown. No follow-up attempts were needed. No further information was expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1412945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: PA
Alter: 69,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 27.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Burning sensation Erythema Flushing Breast pain Hypoaesthesia Movement disorder Musculoskeletal pain Nausea Neck pain Neuralgia Pain in extremity Paraesthesia Pain Physical disability

Symptomtext

was in both hands, that numbing sensation; painful arm, so painful she couldn't even lift it or move it; she could not get up; Nauseous was reported as worsened; the palms of her hands turned very red, it looked like she had a glove on; felt pins and needles in her hands; severe left sided arm pain; arm pain which radiated to her shoulder blades, neck, back under her am/ she feels all painful and achy/ the whole area was so severe; thought the vaccine might have hit a nerve; The shoulder, neck, back, shoulder blade, it just feels like it's burning; severe left sided arm pain which radiated to her shoulder blades; severe left sided arm pain which radiated to her shoulder blades, neck; severe left sided arm pain which radiated to her shoulder blades, neck, back under her am/ upper back; severe left sided arm pain which radiated to her shoulder blades, neck, back under her am, and left breast; This is a spontaneous report from a contactable consumer (patient) reporting herself. A 69-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, lot number EW0169) via an unspecified route of administration, administered in left arm on 27Apr2021 at 14:15-14:30 (age at the time of vaccination was 69-years-old) as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. She did not take any medication. No other products were administered. There were no any history of all previous immunizations with the Pfizer vaccine considered as suspect and no additional vaccines administered on same date of the Pfizer suspect. No prior vaccinations within 4 weeks and no any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No adverse events following prior vaccinations. There was no patient's medical history (including any illness at time of vaccination) and no family medical history relevant to adverse events. No relevant tests. It was reported that, after receiving first dose, the patient has felt pins and needles in her hands. Aside from this, she had severe left sided arm pain which radiated to her shoulder blades, neck, back under her am, and left breast. She was feeling all these stabbing pins and needles in her hands, worse in her left hand. She said this has been going on for 2 weeks now. Nauseous was reported as worsened. She wanted to know if this was a known side effect associated with the Pfizer-BioNTech Covid-19 Vaccine, and if it would go away. Consumer also wanted to know if this might had been caused by the vaccine not being administered properly and did not go into the muscle. She thought the vaccine might have hit a nerve, but she did not that the pins and needles in her hands have already subsided. She stated her hands, the palms of her hands turned very red. She stated it looked like she had a glove on but she experienced such a painful arm, so painful she could not even lift it or move it, it was been severe, it was into her shoulder, neck, shoulder blade, upper back, the whole area was so severe. She stated into the back of her neck, shoulder, her whole back, shoulder blade on left side, under her arm, and into the breast on her left side. She was supposed to go back for another shot, she did not think so. She stated at that point, it was in both hands, that numbing sensation and she was showing to her husband her hands, and he said it looked like she had a glove on. She was trying to stay calm. She told her husband to get back to the car and she had some water so she drank a little bit of water. She sat in the car a little bit and they started to slowly head home and it just continued as far as the arm pain just kept getting worse. It was very painful and had been since the beginning. The pain seemed to get worse every day and went to the neck, back, and shoulder. As far as the redness, that seem like that had gotten better, that had improved. Pins and needles had gotten better. The first week and a half with pins and needles was very bad, but every day, it had started to get a little bit better. She was not having as much, not like it was at all, she was happy about that, that it was improved. The shoulder, neck, back, shoulder blade, it just felt like it was burning. The next day, her husband had to lift her up out of bed, she could not get up. She felt all painful and achy, it was that kind of thing, it came and went. She would say today she had it pretty much on the day of reporting, but she was having a lot of burning in the neck and the back of the shoulder blade, almost like up or down the spine just all over there and the arm and shoulder in the front. She was never even had a flu vaccine but they were vaccinated through childhood for everything but had no real problems with anything. She did not even want to take Tylenol because she did not know what she heard she did not know if she heard they were advising not to take anything like that. She did not visit emergency room and physician office. The outcome of events severe left sided arm pain which radiated to her shoulder blades, neck, upper back under her am, and left breast/ she feels all painful and achy/ she feels all painful and achy/ the whole area was so severe, nauseous was reported as worsened, the shoulder, neck, back, shoulder blade, it just felt like it was burning were not recovered, outcome of events felt pins and needles in her hands, the palms of her hands turned very red, in both hands, that numbing sensation were recovering and outcome of other events were unknown. No follow-up attempts were needed. No further information was expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1395121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 34,0
Geschlecht: F
Eingang: 23.10.2021
Impfdatum: 11.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain Back pain Blood test Chest pain Computerised tomogram Dyspnoea Costochondritis Dizziness Fibrin D dimer increased Headache Hypoaesthesia Loss of personal independence in daily activities Paraesthesia Troponin I Vision blurred

Symptomtext

Shortness of breath with chest pain; Shortness of breath with chest pain; abdominal pain; Shortness of breath with back pain; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0179), via an unspecified route of administration, administered in Left arm on 11May2021 15:15 at the age of 34-years-old as dose 2, single for covid-19 immunisation at Public Health Clinic/facility. Medical history included vertigo from an unknown date and supplements (supplementation therapy) on an unknown date. Concomitant medications included colecalciferol (VITAMIN D [COLECALCIFEROL]) taken as supplement, start and stop date were not reported and iron (IRON) taken as supplement, start and stop date were not reported received within 2 weeks of vaccination. The patient previously took first dose of historical vaccine, bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EW0169), via an unspecified route of administration, administered in Left arm on 20Apr2021 17:00 (at the age of 34-years-old) as single dose for covid-19 immunisation. 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. The patient has not been tested for COVID-19 since the vaccination. Device Date: 19May2021. On 12May2021 at 04:00, the patient experienced Shortness of breath with chest pain, abdominal pain and back pain. Adverse events resulted Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Treatment received for the adverse events included Emergency treatment- medicine prescribed (steroids). The outcome of events was not recovered. Follow-up attempts completed. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Supplementation therapy; Vertigo
Andere Medikamente: VITAMIN D [COLECALCIFEROL]; IRON
Allergien: -
Vorherige Impfungen: -

VAERS 1808594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 30,0
Geschlecht: M
Eingang: 22.10.2021
Impfdatum: 01.05.2021
Beginn: 01.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest pain

Symptomtext

Some mild achy chest pain with exercise and deep breathing x 3 months after second pfizer dose, which has since resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1807462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 48,0
Geschlecht: F
Eingang: 22.10.2021
Impfdatum: 13.08.2021
Beginn: 14.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Asthenia Chest discomfort Dyspnoea Feeling abnormal Headache Illness Laboratory test Musculoskeletal stiffness Myalgia Nausea Nervousness Pain Pain in extremity Pyrexia Respiration abnormal Vaccination site mass Vomiting

Symptomtext

got all of my arm sore/pain in the arm/I had the soreness in that arm; had a large knot in my left arm at the injection site; stiffness in my left part of the injection site; nausea/Horrible nausea; vomiting; body aches/Whole body from head to toe is hurting so bad; had a horrible headache; felt like every joint, every muscle, it just hurt from head to toe; felt like every joint, every muscle, it just hurt from head to toe; weak; no energy; felt sick; nervous; tightness in the chest; wheezing; kind of weird, I felt, it's hard to describe the feeling; breathing was definitely affected; Not being able to breathe; Fever; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EW0169, Expiry Date: Unknown, NDC and UPC number: Unknown), via an unspecified route of administration, administered in the left arm on 13Aug2021 (at the age of 48 years old) as DOSE 1, SINGLE for COVID-19 immunization. The patient medical history included asthma, menstrual cycle (patient had menstrual cycle in Jun2020 and then she had it again in Dec2020 and haven't had one since), preventive Inhaler (I just have a preventive Inhaler (further clarification unknown) as needed) and arthritis. I have had problems with it for years, I just keep the inhaler because sometimes due to the season, I can have seasonal allergies but normally I don't have to take it on a regular basis, arthritis. Concomitant medication(s) included celecoxib (CELEBREX) taken for arthritis, start and stop date were not reported and hydrocodone bitartrate, paracetamol (NORCO) the dose was 7.5-325 (further clarification unknown), took it with the Celebrex in the morning, took both taken for an unspecified indication, start and stop date were not reported, patient stated I do have a vitamin Regimen that I just started. On an unspecified date in 2021 the patient experienced nausea/horrible nausea, vomiting, stiffness in my left part of the injection site, body aches/whole body from head to toe is hurting so bad, had a horrible headache, felt like every joint, every muscle, it just hurt from head to toe, weak, no energy, felt sick, nervous, tightness in the chest, wheezing (and was needing huge amount of my inhaler), kind of weird, I felt, it's hard to describe the feeling, breathing was definitely affected, not being able to breathe, fever. On 14Aug2021 patient had a large knot in my left arm at the injection site, got all my arm sore/pain in the arm/I had the soreness in that arm. The patient underwent lab tests and procedures which included laboratory test resulted came back clear on an unknown date. Reporter stated that I think I did, they were testing, because it's kind of weird when COVID started I could find it weird. When COVID started, I had my menstrual cycle in Jun2020 and then I had it again in Dec2020 and I haven't had one since. So, my doctor then done labs and doing they packed me on Methotriamp and see what's going on, why I stopped having my menstrual cycle (not clarified further). Reporter stated that she had been hearing about people who are developing blood clots regarding the Pfizer COVID-19 Vaccine, and she heard this just through talking to people at work (further clarification unknown). And then she said there was an article that came out on Newsbreak that says Shingles may be a side effect with the Moderna and Pfizer COVID Vaccine (further clarification unknown) and stated, it's scheduled for the 3rd, but I am not going to be able to do it on that day (03Sep2021). The clinical outcome of the events was reported as unknown. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: lab test; Result Unstructured Data: Test Result:came back clear
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Asthma; Inhalation therapy ("I just have a 'preventive' Inhaler (further clarification unknown) as needed.); Menstrual cycle abnormal (I had my menstrual cycle in Jun2020 and then I had it again in Dec2020 and I haven't had one since)
Andere Medikamente: CELEBREX; NORCO
Allergien: -
Vorherige Impfungen: -

VAERS 1804798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 21,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 21.04.2021
Beginn: 01.10.2021
Tage bis Beginn: 163,0
Dosis: 2
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal discomfort Abdominal pain Ageusia Anosmia Asthenia Cough Decreased appetite Dehydration Dry mouth Dyspnoea COVID-19 Cardiac disorder Chest X-ray Chills Condition aggravated Ear pain Fatigue Feeling cold

Symptomtext

I tested positive for COVID-19. I was achy, chilly, cold for hours, had a headache, congestion, sneezing, coughing, tightness, ear pain, fever, and a sore throat. I had bad tachycardia all night long. My lungs were cramping. I had lung pain and wheezing. My heart rate was high. I felt nauseated with no appetite and dehydrated. I had sinus pain and a headache. For a few days my taste was weird then I din have any taste or smell. I felt weak. I had heart complications and muscle spasms. I had a very dry mouth. I had a very heavy period. I was coughing badly. I had abdominal pain and hot flashes and fatigue. Toward the end my heart rate started to get low, and my oxygen was dropping. My migraines and breathing have gotten worse. When my heart rate started going to slow, I had to have some of my medication changed because of that. I went to the ER for extreme fatigue, dehydration, and because of my breathing. My stomach has also felt bad. It has been 20 days since it started.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Chest X-ray- normal COVID-19 test- positive (10/3/2021)
Aktuelle Erkrankungen: Mast Cell activation syndrome POTS Hypermobile EDS Sleep Apnea Obstructive Lung Disease Chronic Migraines
Vorgeschichte: Mast Cell activation syndrome POTS Hypermobile EDS Sleep Apnea Obstructive Lung Disease Chronic Migraines
Andere Medikamente: Cromolyn sodium oral, nebulized, and nasal 4xday (3 different meds) sodium chloride tablet Sodium chloride nebulizer Singulair 1xday Zyrtec 2xday acarbosb 4xday Protonix 2xday Spiriva Respimat 2.5mg 1xday Magnesium Oxide Iron Metformin Me
Allergien: Prednisone
Vorherige Impfungen: Flu shot- mast cell reaction (every year)

VAERS 1804531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 21.10.2021
Impfdatum: 23.04.2021
Beginn: 04.05.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Blood test Insomnia Tremor

Symptomtext

11 days after the 2nd vaccine, I started having tremors, anxiety and insomnia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: Blood work from primary care physician, more blood work, nerve & muscle testing from a neurologist..
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Juice Plus multi vitamin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1801815

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 64,0
Geschlecht: M
Eingang: 20.10.2021
Impfdatum: 30.08.2021
Beginn: 02.09.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Pain Skin warm Supraventricular tachycardia Swelling

Symptomtext

Left shoulder swollen, reddened, warm 48 hours after administration . Soreness and redness lasted for 3 weeks. SVT post vaccine 72 hours for interval of 5 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Supraventricular tachycardia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: NONE
Vorgeschichte: HTN, HLD
Andere Medikamente: Hctz 25mg daily, atenolol 50 mg daily
Allergien: PCN
Vorherige Impfungen: Flu vaccine years ago. Redness swelling, fever.

VAERS 1793071

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 16.10.2021
Impfdatum: 16.04.2021
Beginn: 16.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspnoea Palpitations

Symptomtext

Shortness of breath; Heart palpitations; This is a spontaneous report from a contactable consumer, the patient. A 55-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 16Apr2021 at 10:15 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Medical history included acid reflux. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included pantoprazole (MANUFACTURER UNKNOWN) from an unknown date for an unknown indication and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 16Apr2021 at 19:00, the patient experienced shortness of breath and heart palpitations. Therapeutic measures were 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 shortness of breath and heart palpitations were recovered on an unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acid reflux (esophageal) (Acid reflux)
Andere Medikamente: PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1788205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 14.04.2021
Beginn: 14.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac discomfort Cardiac stress test Chest discomfort Dysgeusia Electrocardiogram normal Heart rate irregular Injected limb mobility decreased Lymph node pain Lymphadenopathy Swelling

Symptomtext

About 15 minutes after getting the shot I got a metallic taste in my mouth. That metallic taste lasted almost 6 weeks. It comes back sporadically, and when it comes back it lasts between one day and a week. The lymph node under my left arm swelled to larger than a softball. I couldn't put my arm down. And that started on 4/21. And it took 2 weeks for the swelling to go down under my arm. And occasionally and sporadically, it'll slightly swell, hurt for a day, and then go away. I had swelling ? of the way across my chest. The swelling was significant. It was approx. 2 inches high. Husband said it looked like I had 3 breasts. That lasted for 2 and a half weeks also. With the swelling came a lot of chest pressure, and I still have chest pressure occasionally now, which caused me to go to my cardiologist. I will say at the time, we had a lot of COVID in my area so I didn't go to the hospital because I was scared to. But it took a while to get into the doctor, so my doctor did not see the complete swelling but there was still some there. When I went to my cardiologist (I go every 6 months) and he does an EKG. This time there was a slight minimal difference in my EKG. A stress test didn't show anything, but there is a slight glitch in my heart beat. My EKG prior to the vaccine was 2 weeks prior, so since the pressure and everything started after the vaccine, that's why I'm relating the heart pressure and everything to the vaccine and the swelling and everything that I had. During all of this, I took aspirin and Benadryl. Since I couldn't get to any doctor. My doctor has told me that her professional advice was not to get the second dose of the vaccine for the risk of anaphylaxis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: EKG - slight difference; Stress test - inconclusive.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lisinopril
Allergien: Tetanus; Bactrim
Vorherige Impfungen: Tetanus - 28/29 years old (1990)

VAERS 1783237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 47,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 27.08.2021
Beginn: 29.08.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest discomfort Chest pain Dizziness Dyspnoea Electrocardiogram Gait disturbance Hyperhidrosis Muscular weakness Musculoskeletal discomfort Pain Pain in extremity Palpitations

Symptomtext

Tightening of the left side of the neck from shoulder to back of the ear. Painful burning and needle prick sensation. Pain extended to the left forearm. Very pain. Rapid back to back heart palpitation, dizziness, sweating, my legs weakened and couldn't walk properly. Went to the ED for this event. In the ED, the event happened again but not as intense. I insisted the check for myocarditis and Pericarditis. I'm not clear if they did or not. Second vaccine dose caused intense pressure and soreness of the sternum and chest. Difficulty breathing and increased BPN of 138-150 for 2 hours. Went to the ED again after the 2nd vaccine. The first event occurred 3 days after the first dose. The second event after the 2nd dose. Then I started getting tightening of the sternum and clavicle. Short ness of breath. Felt sore and tight. Pain shot to my right breast/chest area. Still happens to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Blood work and EKG only performs. All came back normal. I do not smoke, drink caffine or do drugs to increase my heart rate.
Aktuelle Erkrankungen: B12 and iron deficiency symptoms including fatigue, brain fog, heart palpitations.
Vorgeschichte: None
Andere Medikamente: B12 shots, over-the-counter iron supplements, Vitamin C
Allergien: Penicillin as a child. Allergic to certain fruits and raw almonds. Pet dander and seasonal allergies.
Vorherige Impfungen: Yes, adverse event to the first COVID-19 vaccine.

VAERS 1772231

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: AL
Alter: 29,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 27.08.2021
Beginn: 30.08.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Brain natriuretic peptide increased C-reactive protein increased Chest X-ray Chest pain Electrocardiogram normal Pain Red blood cell sedimentation rate normal Troponin increased

Symptomtext

On 08/30/2021 patient experienced chest pain, it lasted 20 minutes was left sided and described as throbbing, the pain did not radiate, denied diaphoresis, dyspnea and palpitations, was not aggravated by exertion. History of pericarditis 11 years ago. VS-BP110/70, HR70, RR17, O2 sat 98%, weight 236, height 6.0ft

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 08/31/2021 - CRP 22, Sed rate 10, Troponin 268, Chest Xray, ECG sinus rhythm within normal limits 09/14/2021 - BNP <5.0 CRP 1, Sed rate 2, Troponin <6
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKA
Vorherige Impfungen: -

VAERS 1771922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 50,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 20.09.2021
Beginn: 07.10.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Cough Decreased appetite Dyspnoea Dyspnoea exertional Nausea Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient received Pfizer vaccination on 8/25/21 & 9/20/21 patient had a 4-day history of progressively worsening cough with dyspnea on exertion, shortness of breath, low-grade fevers, nausea and decreased appetite. He was + 10/4/21. Currently admitted in hospital as of 10/7/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: + 10/4/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1771736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 71,0
Geschlecht: M
Eingang: 08.10.2021
Impfdatum: 07.04.2021
Beginn: 01.04.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Chest pain General physical health deterioration

Symptomtext

Spoke with patient's daughter who states that since he received the Pfizer vaccine in April his health has declined. She states he was fairly healthy before receiving the vaccine and now has been seeing multiple doctors for his issues. States patient now has a neurologist due to having joint pain and shingles like sx without the presence of shingles. States patient is also having chest and back pain that is unexplained. Daughter states he has been hospitalized three times since July and that both his primary physician and neurologist think that his issues can be linked back to the Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Tennis elbow
Vorgeschichte: Heart condition
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1764607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 31.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac monitoring abnormal Heart rate increased Hyperhidrosis Palpitations Ventricular tachycardia

Symptomtext

Within a few days of first dose I went to doctor with heart palpitations, sweating, fast heart rate at rest. It is still ongoing and didn?t put the connection together with vaccine until diagnosis two days ago and research. I presented to doctors office on April 21, 2021 (ironically same day as 2nd dose) with these symptoms and it said in doctors note that I noticed them starting a few weeks earlier which put it at time of first injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Wore heart monitor last few weeks of September. Results showed Ventricular Tachychardia. Never had heart Rhythm issues in my life. Symptoms still ongoing. Going to cardiologist this coming Friday.
Aktuelle Erkrankungen: None
Vorgeschichte: Atherosclerosis, high cholesterol, hypertension, fibromyalgia.
Andere Medikamente: Vitamin D, magnesium, calcium, zinc, aggrenox, losartan potassium, atorvastatin, ropinirole, bupropion, hydroxyzine, Provitalize( turmeric root extract, morning leaf, curry leaf, lecithin, black pepper) hyaluronic acid ,unisom, clarythrimic
Allergien: Shrimp/fish, cat scan dye, adhesive tape, cipro,
Vorherige Impfungen: -

VAERS 1759527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: AZ
Alter: 52,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 22.04.2021
Beginn: 14.09.2021
Tage bis Beginn: 145,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Chest X-ray normal Chest pain Condition aggravated Cough Headache Illness Impaired work ability Influenza like illness Malaise Nasopharyngitis Nausea Oropharyngeal pain Pain in extremity SARS-CoV-2 test negative Vomiting

Symptomtext

When I got the vaccine, I had no real adverse symptoms - just a little pain in my arm (at (left arm). Got sick in September starting on the 14th - on the first day, I thought I was getting a cold, went to work the next day; Thursday, the 16th, I called in - got a pretty severe sore throat during the night. I didn't know if I had the variant or not. Thursday, Friday I stayed home from work. I had various sort of not feeling well symptoms. Friday night, I threw up and had really bad headache. I went to Urgent Care. They gave me shots of medicine - for nausea and for headache. Felt better the next day, headache did come back though. I developed a cough. The work place said to stay home on Monday. After Monday, I went back to work. I didn't have trouble breathing or chest pains at that point and so it felt more like a flu or cold. Just took at-home remedies - cough drops and Acetaminophen. I didn't have chest pain increases during this time. At Urgent Care, the doctor also prescribed me a new kind of medicine for my headaches - very similar to Excedrin - caffeine, Tylenol and a different type of medicine to help with headaches - preventative measure. Note: Chest pain - I had been experiencing that off and on since before I had COVID and the COVID vaccines - had xrays done. It hasn't been too bad - it hasn't been real severe. I would say it a little bit continuing after the x-rays were done in June.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2 COVID tests at home - both came back negative Chest x-rays - in June 2021 (Dr. ordered)-came out clear; no treatment;
Aktuelle Erkrankungen: no
Vorgeschichte: COVID in December 2020 - had some lingering affects - chest pains were being experience even before I had COVID and they said it was anxiety; and then again I noticed the chest pain after having COVID and after COVID vaccines.
Andere Medikamente: Citalopram - 40 mg; Hydroxyzine
Allergien: no
Vorherige Impfungen: -

VAERS 1752035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 01.10.2021
Impfdatum: 16.08.2021
Beginn: 16.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Feeling cold Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

whole left side of my body that is numb and tingly and cold.. even my arm; feet have stronger tingle and pain when she stand; having facial numbness; tingling on left side of face/ feet have stronger tingle and pain; This is a spontaneous report from a contactable consumer (patient). A 34-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EW0169, Expiration date: Not reported), via an unspecified route of administration in left arm on 16Aug2021 at 09:00 (at the age of 34-years-old) as dose 1, single for COVID-19 immunization in a hospital. There was no patient's medical history reported. The patient was healthy and had known allergies to codeine and latex. There were no concomitant medications/any other medications received within 2 weeks of vaccination. The patient was not pregnant at the time of vaccination and 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 since the vaccination, the patient had not been tested for COVID-19. Twenty five minutes after the vaccination, the patient began to have facial numbness and tingling on the left side of the face on 16Aug2021 at 09:25. Two days later on 18Aug2021, the patient's feet have stronger tingle and pain when she standup and currently after 4 weeks in Sep2021, the patient's whole left side of the body was numb, tingly and cold even in her arm. These events resulted in doctor or healthcare professional office/clinic visit and disability or permanent damage. It was unknown if the patient received treatment for these events. The outcome of the events was not recovered at the time of report. 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: Latex allergy; Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient was healthy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1722722

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 06.05.2021
Beginn: 20.09.2021
Tage bis Beginn: 137,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain upper Asymptomatic COVID-19 Cholangiogram normal Cholecystectomy Cholecystitis acute Condition aggravated Essential hypertension Incentive spirometry Laparoscopic surgery Leukocytosis SARS-CoV-2 test positive Sepsis

Symptomtext

Hospitalized (9.20.21-9.21.21); COVID-19 positive (9.20.21); fully vaccinated Discharge Provider: DO Primary Care Provider: None Physician, MD Admission Date: 9/20/2021 Discharge Date: Sep 21, 2021 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Cholecystitis [K81.9] Epigastric pain [R10.13] Essential hypertension [I10] Sepsis, due to unspecified organism, unspecified whether acute organ dysfunction present (HCC) [A41.9] Acute cholecystitis [K81.0] HOSPITAL COURSE: 56-year-old female presented with sepsis secondary to acute cholecystitis and possible choledocholithiasis. Incidentally found was asymptomatic COVID-19 infection. The patient was brought to the operating room where a laparoscopic cholecystectomy with intraoperative cholangiogram was obtained with failure to demonstrate choledocholithiasis. She was admitted to the hospital postoperatively for additional resuscitation and monitoring. She was tolerating a regular diet without difficulty having bowel function. Positive urination. Denies any shortness of breath or other respiratory symptoms. No fevers or chills were noted. She did have of worsening leukocytosis which is likely reactive due to surgery as she is asymptomatic with regards to other sources. She was deemed stable for discharge with close follow-up with laboratory values and strict return to the emergency department instructions. CONSULTS / RECOMMENDATION: Case was discussed with Dr. of Internal Medicine given the asymptomatic COVID 19 infection. He recommended close follow-up as well as incentive spirometer use. Patient was sent home with an incentive spirometer. INPATIENT PROCEDURES: Laparoscopic cholecystectomy with IOC.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: Acute cholecystitis COVID-19 virus infection Sepsis (HCC)
Andere Medikamente: Outpatient Medications hydroCHLOROthiazide (MICROZIDE) 12.5 MG capsule oxyCODONE (ROXICODONE) 5 MG immediate release tablet senna-docusate (PERICOLACE) 8.6-50 MG per tablet
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1722485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: SD
Alter: 37,0
Geschlecht: F
Eingang: 22.09.2021
Impfdatum: 20.09.2021
Beginn: 20.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chills Cough Dizziness Fatigue Feeling abnormal Headache Hyperhidrosis Impaired work ability Lymphadenopathy Migraine Oropharyngeal pain Pain Pain in extremity Pyrexia SARS-CoV-2 test negative Tremor Vision blurred

Symptomtext

Migraine began 15 minutes after shot and lasted 24 hours. Shaking, chills, extreme body aches and fever of 101.5 with Tylenol occurred 16 hours after injection. Cough, chest tightness, had to leave work. Extreme exhaustion, mental fog, diaphoresis, blurry vision, dizziness, swollen lymph nodes, extreme pain I the injected arm, sore throat. Had to leave work and take Tylenol and Motrin to get fever down and pain under control. The next morning work up with continued sweating and mild headache.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Had a Covid 19 test to see if I had Covid and the result was negative.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1718843

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: FL
Alter: 14,0
Geschlecht: M
Eingang: 21.09.2021
Impfdatum: 31.08.2021
Beginn: 02.09.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood test Chest X-ray Chest pain Electrocardiogram

Symptomtext

Two days after admin of dose two of Covid series patient experienced chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: per the family at the ER they did Blood work, Chest X-ray , and EKG
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Reglan
Vorherige Impfungen: -

VAERS 1715394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 36,0
Geschlecht: M
Eingang: 20.09.2021
Impfdatum: 16.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Back pain Depression Dyspnoea Headache Hypoaesthesia Oropharyngeal pain

Symptomtext

Patient reported left arm, 3rd-5th digit numbness, depression, SOB, upset stomach, back pain, headache, and throat pain from day of receiving vaccine to today 9/20/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: COVID-19 a couple weeks before
Vorgeschichte: none
Andere Medikamente: aleve, tylenol, fluticasone
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 1715262

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 20.09.2021
Impfdatum: 20.02.2021
Beginn: 26.08.2021
Tage bis Beginn: 187,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Cough Diarrhoea Fibrin D dimer increased Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

74 yo male patient s/p Pfizer vaccination: dose 1 on 1/30/21, dose 2 on 2/20/21, and booster dose on 8/17/2021. Past medical history significant for living donor renal transplant on immunosuppression with rapamune and cyclosporine, T2DM, HTN, HLD, primary hypothyroidism, gout, anemia, and obesity who presented on 8/26 with 4 days of nausea, vomiting, diarrhea, and dry cough who was found to be positive for COVID-19, despite being fully vaccinated. On admission Infectious Disease was consulted and he received remdesivir for 7 days and dexamethasone for 10 days. He required up to 15L high flow nasal cannula this admission. He had elevated d-dimer measurements this admission and on 9/2/21 CTPE was ordered...

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 12,0
Labordaten: SARS-COV-2 RAPID: Detected (8/26/2021)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1715184

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: SD
Alter: 29,0
Geschlecht: M
Eingang: 20.09.2021
Impfdatum: 14.09.2021
Beginn: 14.09.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood glucose Dizziness Hypotension

Symptomtext

Within 15 minutes of receiving vaccination patient experienced low BP and dizziness. Patient was then transferred over to the ER for further management of symptoms. In the ER patient received normal saline bolus with normalization of BPs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: Random glucose.
Aktuelle Erkrankungen: None
Vorgeschichte: none
Andere Medikamente: Tylenol, ascorbic acid, DM/PE/ acteaminophen/doxylamine, echinacea, multivitamin, zinc
Allergien: Banana, Penicillin
Vorherige Impfungen: -

VAERS 1713849

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 19.09.2021
Impfdatum: 30.07.2021
Beginn: 12.08.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Arthritis Condition aggravated Mobility decreased

Symptomtext

I started to have very painful knees, I went to my Ortho dovtor and am getting injections to see if this helps. I have NEVER had such pain and problems before. it is hard to go up or down steps and I wear a brace on both legs. I will never get a booster that is for sure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: I have arthritis but it never was really that bad until I got the shot. I now have a horrible time with both knees. It is very painful I have never had a problem before this.
Andere Medikamente: norco singular ibuprofen
Allergien: -
Vorherige Impfungen: -

VAERS 1708667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: KS
Alter: 38,0
Geschlecht: F
Eingang: 17.09.2021
Impfdatum: 28.04.2021
Beginn: 28.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Muscle tightness

Symptomtext

Security staff found patient outside on the sidewalk light headed, difficulty breathing, muscle tightness in neck. Vitals were taken: O2 98%, HR 105, BP 106/160 ra taken at 1340; Lungs clear bilaterally; After 5 minutes, patient improved placed supine. Vitals taken at 1346: 02 98%, HR 94, BP 138/92 ra; subjective symptoms improved, patient takes anxiety meds. Vitals taken at 1410: O2 98%, HR 97, BP 142/98 ra.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: -
Vorherige Impfungen: -

VAERS 1704529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 82,0
Geschlecht: F
Eingang: 16.09.2021
Impfdatum: 15.09.2021
Beginn: 16.09.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Tremor

Symptomtext

My hands were shaking uncontrollably (as if I had severe Parkinsons or something) in the middle of the night when I got up to use the bathroom; promptly went back to sleep afraid because of the shaking. The next morning my hands did not seem to be shaking; in the afternoon they shook a bit, but the shaking was mild compared to what happened in the middle of the night. I rested all day (it is currently 2:42 Central Time - I'm still resting and will continue to do so).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None. If this does not resolve, I will contact my primary care physician and the hospital (to let them know). If there are additional complications, I have asked a family member to re-enter information into VAERS.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1704389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TN
Alter: 33,0
Geschlecht: M
Eingang: 16.09.2021
Impfdatum: 17.05.2021
Beginn: 16.09.2021
Tage bis Beginn: 122,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Atelectasis Chest X-ray abnormal Chills Dyspnoea Headache Pain Pleural effusion Sepsis Vomiting

Symptomtext

Ongoing hospitalization. Admitted with headache, vomiting, shortness of breath, chills, body aches. Treatment empirically for sepsis; ceftriaxone and IV fluids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 1,0
Labordaten: Chest x ray: moderate right-sided pleural effusion with adjacent moderate Right lower lobe atelectasis.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Chronic Hepatitis B for 4 years; history of varices; cirrhosis,
Andere Medikamente: Unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1700497

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 15.09.2021
Impfdatum: 08.09.2021
Beginn: 08.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest X-ray Chest pain Electrocardiogram normal Fatigue Full blood count Metabolic function test Sleep disorder Troponin

Symptomtext

23 yo female c/o intermittent left sided chest pain -- in the evening after getting the second Pfizer earlier in the day. Chest pain was positional when she stands or turns from side to side. Had some relief with lying down. Was awakened with chest pain the day after the vaccine, felt chest pain and fatigue with walking. Has hx of Steven's Johnson syndrome from Tylenol. Denies shortness of breath. Chest pain 6-7/10. This patient was referred to the emergency room.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: The ER did cbc, cmp, troponin, CXR, EKG was which normal.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin
Allergien: Tylenol - hx of Steven Johnson Syndrome, hospitalized for 1 month, few yrs ago
Vorherige Impfungen: -

VAERS 1696145

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OK
Alter: 55,0
Geschlecht: F
Eingang: 14.09.2021
Impfdatum: 12.07.2021
Beginn: 02.08.2021
Tage bis Beginn: 21,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Hypoaesthesia Impaired work ability Malaise Muscular weakness Musculoskeletal stiffness Pain in extremity Paraesthesia Vaccination complication X-ray

Symptomtext

I was sick for 6 days, but when I went to bed about 13 hours after the 2nd shot my left hand and arm felt like it was asleep. That never went away thru the night and when I woke up it had gone into my right hand and arm. the next day same thing only when I went to pick up my drinking glass I dropped it because hands were actually numb. each day it it would get worse so went to the emergency room and said it was a side effect from vaccine. gave me steroids that did absolutely nothing. so I went to the doctor and they gave me Gabapentin which has done absolutely nothing as well. very difficult to work. aside from numbness and tingling there as been lots of pain and stiffness in hands , and arms become weak and give out on me. my 2nd shot was given on 08/02/2021 and nothing has changed as of today 09/14/2021. definitely need help on what to do. obviously doctors have know idea what to do. not happy about this situation and want answers!!!!!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood work, and x-rays
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Estradiol
Allergien: codeine
Vorherige Impfungen: -

VAERS 1694457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 61,0
Geschlecht: M
Eingang: 13.09.2021
Impfdatum: 06.05.2021
Beginn: 01.09.2021
Tage bis Beginn: 118,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Dyspnoea Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This case meets vaccine breakthrough criteria. HOME COVID TEST PTA. SXS COUGH, SOB, FEVER FOR LAST 7 DAYS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH HTN, HYPERLIPIDEMIA, DM 2
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1688840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MI
Alter: 49,0
Geschlecht: F
Eingang: 10.09.2021
Impfdatum: 08.09.2021
Beginn: 08.09.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Dyspnoea Throat tightness

Symptomtext

SOB, "like throat tightening" and dizzy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: HTN
Andere Medikamente: norvasc, normodyne,dyazide
Allergien: none
Vorherige Impfungen: -

VAERS 1295069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 09.09.2021
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: ja

Chest discomfort Dyspnoea Electrocardiogram Flushing Palpitations Lip swelling Swelling face Throat tightness Pharyngeal paraesthesia

Symptomtext

15 minutes into her 30 minute wait after receiving the Pfizer vaccine, patient complained of wanting to go to the bathroom but when escorted to bathroom then stated. No I am having a reaction did not want to freak anyone out. Face was flushed complained of heart palpations, BP 145/94 Pulse 89. Was going to give oral Benadryl but complained of chest tightness, throat tingling and shortness of breath. Epi administered and patient brought to the ER EPI given Pepcid given prednisone given, symptoms resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ED treatment on same date EKG done
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1682063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW 0169

moderat

Staat: -
Alter: 39,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 30.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Paraesthesia

Symptomtext

Tingling in fingers of arm that received the injection; This is a spontaneous report from a non-contactable consumer, the patient. A 39-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EW 0169) via an unspecified route of administration in the left arm on 30Aug2021 (at the age of 39-year-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. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications were not reported. On 31Aug2021, the patient experienced tingling in fingers of arm that received the injection. The event did not result in a visit to the doctors or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. It was unknown whether any therapeutic measures were taken for the event. The clinical outcome of the event tingling in fingers of arm that received the injection was not recovered at the time of this report. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1677993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: GA
Alter: 13,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 12.05.2021
Beginn: 12.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Malaise Migraine Myalgia Oropharyngeal pain Pyrexia

Symptomtext

Migraine; Sore throat; General malaise; Muscle aches; Fever; Exhaustion; Bouts of sever chills; This is a spontaneous report from a contactable consumer, the parent. A 13-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 12May2021 at 12:00 (at the age of 13-year-old) as a single dose for COVID-19 immunisation. Medical history included penicillin allergy and COVID-19. The patient did not receive any other medications within two weeks of vaccination. 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. The patient did not receive any medication within two weeks of vaccination. On 12May2021, the patient experienced sore throat, fever, bouts of severe chills, muscle aches, migraine, exhaustion and general malaise. 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 sore throat, fever, bouts of severe chills, muscle aches, migraine, exhaustion and general malaise was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if_covid_prior_vaccination: Yes); Penicillin allergy (known_allergies: Penicillin)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1677901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: -
Alter: 22,0
Geschlecht: M
Eingang: 07.09.2021
Impfdatum: 20.04.2021
Beginn: 20.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Coordination abnormal Fatigue Headache Hyperhidrosis Limb discomfort Nausea Pain in extremity Tremor

Symptomtext

Arm pain; Sweating; Shaky hands; Loss of coordination; Heaviness of limbs; Fatigue; Headache; Nausea; This is a spontaneous report from a non-contactable consumer, the patient. A 22-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 20Apr2021 at 15:45 (at the age of 22-years-old) as a single dose for COVID-19 immunisation. Other medical history was reported as none. The patient had no known allergies to food, medications, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included ibuprofen (MANUFACTURER UNKNOWN) from an unknown date for an unknown indication and unknown if ongoing and testosterone phenylpropionate (TESTOSTERONE) taken for hormone replacement therapy from an unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 20Apr2021 at 15:45, about a minute after the first shot, the patient experienced the following: arm pain, sweating, shaky hands, loss of coordination, heaviness of limbs, fatigue and also experienced a headache and nausea. 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 arm pain, sweating, shaky hands, loss of coordination, heaviness of limbs, fatigue, headache and nausea was unknown at the time of this report. No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: IBUPROFEN; TESTOSTERONE
Allergien: -
Vorherige Impfungen: -

VAERS 1677883

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 07.09.2021
Impfdatum: 18.04.2021
Beginn: 21.04.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Allergy to vaccine Dysphagia Dyspnoea Malaise Mouth breathing Movement disorder Muscle spasms Muscle twitching Nervousness Pharyngeal swelling Sleep apnoea syndrome

Symptomtext

Right Forearm Twitching and Spasming; Right Forearm Twitching and Spasming; problems swallowing; not feeling that great; trouble breathing when she was laying down; feels the same way as her sleep apnea does when she is sitting up; throat feels a little bit swollen and it is restricting her airway from her mouth; she breathes through her nose but breathing through her mouth is hard; it is not as intense as it was; she has allergies; took her two hours to be able to move around; This is a spontaneous report from a contactable consumer (patient) reporting for herself. A 57-year-old female patient received BNT162B2 (Formulation: solution for injection), dose 2 via an unspecified route of administration, administered in left arm on 18Apr2021 at 10:20 (Lot Number: EW0169; NDC and expiry date was unknown) as dose 2, single (at the age of 57 years) for covid-19 immunisation. Medical history included ongoing sleep apnea from an unknown date and unknown if ongoing. Family history included patient father died of Covid in January. The patient's concomitant medications were not reported. Patient historical vaccine includes first dose bnt162b2 (lot number: EP7533) to left arm on 25Mar2021 for Covid-19 immunisation. The patient experienced right forearm twitching and spasming; right forearm twitching and spasming; problems swallowing; not feeling that great; trouble breathing when she was laying down; feels the same way as her sleep apnea does when she is sitting up; throat feels a little bit swollen and it is restricting her airway from her mouth; she breathes through her nose but breathing through her mouth is hard; it is not as intense as it was, she had allergies; took her two hours to be able to move around; all on 21Apr2021 at 09:00. Caller stated that the doctor told to call this number because she was having odd reactions and they think they are from the second Covid dose. Stated she has not seen her yet, she had an appointment this afternoon to see her. She stated that she got the vaccine on Sunday 18Apr2021 and it was her second dose. Stated that the symptoms she is having that she is concerned about started yesterday; her right forearm started twitching and spasming all day and it is still doing it. States she got the shot in her left arm and this is happening in her right forearm. Caller states it was early evening when she started having problems swallowing and then she went to bed early because she was not feeling that great and she started having trouble breathing when she was laying down. States she has sleep apnea, and it feels that way. States usually when she is laying on her side it feels not so bad, it is more when she lays on her back. Caller states it feels the same way as her sleep apnea does when she is sitting up. States her throat feels a little bit swollen and it is restricting her airway from her mouth. States it doesn't feel the same when she breathes through her nose but breathing through her mouth is hard on 21Apr2021. Caller states it has gotten a little better, she took an allergy pill. States she usually takes it at night but she took it in the morning. States it is not as intense as it was this morning. States it took her two hours to be able to move around and feel like she can breathe through her mouth. States she has allergies, and she notices the difference when something is going on with her body. Patient did not got to emergency room she said no, doctor said if harder to breathe should go to the ER, if feels worse or harder time breathing. Physician office visit have appointment today 22Apr2021. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Therapeutic measures were taken as a result of right forearm twitching and spasming, problems swallowing, not feeling that great, feels the same way as her sleep apnea does when she is sitting up, throat feels a little bit swollen and it is restricting her airway from her mouth, she breathes through her nose but breathing through her mouth is hard, it is not as intense as it was, she has allergies, took her two hours to be able to move around and an allergy pill, Cetrzn 10 mg. Outcome of the event Mouth breathing, Nervous, allergy to vaccine, movement disorder was unknown and all other events was recovering. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sleep apnea
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1675589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: IL
Alter: 36,0
Geschlecht: F
Eingang: 06.09.2021
Impfdatum: 01.08.2021
Beginn: 17.08.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood bilirubin increased Blood test abnormal Chest pain Computerised tomogram normal Dizziness Dyspnoea Echocardiogram normal Electrocardiogram normal Hypertension Lymph node pain Lymphadenopathy Migraine Scan with contrast Tremor

Symptomtext

Lymph nodes right arm pit swollen huge and painful 8/17-8/29, went down but still slightly swollen 9/6. 8/29 started having chest pain, high blood pressure, dizziness, shortness of breath, migraines, shaking. Went into the ER 9/1 to make sure my heart was ok.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 09/01/2021 ER: EKG, echocardiogram, CT scan with contrast, blood work. EKG, Echocardiogram, CT scan all showed everything is ok. Blood work shows my bilirubin is high and my blood pressure was high. I normally have no issues with either of those things. Blood pressure is usually 110/70. That day it was all over the place 155/92 to 138/92.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Flu shot in 2019- swollen lymph nodes.

VAERS 1674201

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: UT
Alter: 42,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 07.05.2021
Beginn: 07.05.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Asthenia Blood pressure measurement Cough Dry mouth Dyspnoea Heart rate increased Hypertension Hypoaesthesia Muscle spasms Pain in extremity Paraesthesia Vomiting

Symptomtext

right arm pain; Difficult breathing; fast heartbeat; weakness; tingling; numbness off my upper body and face jaw locking; hands locking stomach painful cramps; numbness off my upper body and face jaw locking, hands locking stomach painful cramps; vomiting; high blood pressure elevated to 190/110; dry mouth follow by thrust develop a mild cough and right arm pain; dry mouth follow by thrust develop a mild cough and right arm pain; This is a spontaneous report from a contactable Consumer. A 42-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: Ew0169), dose 1 via an unspecified route of administration, administered in Arm Left on 07May2021 15:00 (at the age of 42-years-old) as a single dose for covid-19 immunization. Medical history included anaphylactic reaction from 07May2021 to an unknown date and high blood pressure. Concomitant medication(s) in two weeks included hydrochlorothiazide; losartan; iron (FERROUS [IRON]). The patient was not pregnant at the time of vaccination. It was unknown, the patient had any allergies. The patient had no other vaccine within four weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, it was unknown the patient had been tested for COVID-19. On 07May2021 15:15, the patient experienced "difficult breathing fast heartbeat weakness tingling follow by numbness off my upper body and face jaw locking, hands locking stomach painful cramps follow by vomiting high blood pressure elevated to 190/110, dry mouth follow by thrust develop a mild cough and right arm pain". The adverse event resulted in patient to visit emergency room/department or urgent care. The patient was treated with Paramedics help, oxygen given. The patient underwent lab tests and procedures which included blood pressure measurement: 190/110. Outcome of the event was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Blood pressure; Result Unstructured Data: Test Result:190/110
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylaxis; Blood pressure high
Andere Medikamente: HYDROCHLOROTHIAZIDE; LOSARTAN; FERROUS [IRON]
Allergien: -
Vorherige Impfungen: -

VAERS 1670379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: MI
Alter: 20,0
Geschlecht: F
Eingang: 03.09.2021
Impfdatum: 23.04.2021
Beginn: 23.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Abdominal pain upper Alopecia Antinuclear antibody Arthralgia Blood test C-reactive protein Chest X-ray Cough Diarrhoea Dyspnoea Fatigue Fibrin D dimer Hot flush Hyperhidrosis Pyrexia Rash Red blood cell sedimentation rate Retching

Symptomtext

Throat and vocal cord spasms, leading to uncontrollable coughing and gagging and trouble breathing in and out. Excessive sweating and hot flashes. Treatment was nebulized lidocane and epinepherine, along with a number of other nebulized medications, steroids, and anti nausea medication. Active symptoms lasted about 30 hours. For the following 5-10 weeks I had episodes of coughing up watery, pink, foamy liquid, and intense gagging without throwing up. I still have allergic symptoms that began after the vaccine reaction: fatigue, crampy stomach pain with diarrhea, skin rash, hives and swelling, joint pain, hair loss, low grade fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Chest x-ray at time of event. One done at urgent care showed fluid in the lungs (according to the Dr there), one done at the ER was interpreted as normal. Blood tests ordered by Dr months following the reaction, to rule out autoimmune disease. C-reactive protein, D-Dimer, sedimentation rate, ANA screening algorithm were positive or abnormal. Negative for autoimmune-specific antibodies or other indicative things.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prozac 20mg Propranolol 60mg XR
Allergien: None
Vorherige Impfungen: -

VAERS 1666869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: OH
Alter: 28,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 01.09.2021
Beginn: 02.09.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Mobility decreased Pain in extremity

Symptomtext

Received vaccine ~2:10p 9/1 & when I woke up around ~9:30a 9/2 my arm was sore but also my armpit. Hard to raise arm and keep having to ice my armpit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: psoriasis
Andere Medikamente: tremfya, birth control, adderall
Allergien: omnicef
Vorherige Impfungen: -

VAERS 1666671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: NJ
Alter: 44,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 14.05.2021
Beginn: 18.05.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Blood thyroid stimulating hormone abnormal Chest X-ray abnormal Echocardiogram normal Electrocardiogram normal Fibrin D dimer increased Full blood count abnormal Heart rate increased Palpitations Troponin I abnormal

Symptomtext

My heartrate went up to 168 bpm resting and it lasted for about 20 minutes staying within the range of 145-168 (Since I work for a hospital/medical facility they were monitoring me the whole time). The EMS picked me up after 30 from the beginning of the event. I got to the hospital emergency room within 10 minutes. By the time I reach the hospital my heartrate was documented at around 98. They did all type of test and everything except for the EKG came back abnormal. I had a few episodes of palpitation within 1 weeks of the vaccine including a few hours after the 1st dose. I monitor my heartrate at the time and it was at about 125 resting but it went back down to the 90s within a few minutes so I didn't think anything of it. The same happened a few times within the first week of the vaccine except on the 4th day it went up to 168 and didn't go back down within a few minutes. I was discharged from the hospital the same day and told to follow up with a cardiologist which I did and was told everything was ok with my heart.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 5-18-2021 Blood test (D-Dimer, Troponin I, CBC, and TSH), EKG (vent. rate 94BPM, atrial rate 94, P-R interval 188ms, QRS duration 92ms, Q-T interval 378ms, QTC calculation (bazett) 472ms, P axis 55 degrees, R axis 43 degrees, T axis 15 degrees), and Chest x-ray. 8-7-2021 EKG and Echo = negative
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid 75mcg and Nuva-ring
Allergien: -
Vorherige Impfungen: -

VAERS 1665709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: DE
Alter: 51,0
Geschlecht: M
Eingang: 02.09.2021
Impfdatum: 17.08.2021
Beginn: 18.08.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Faeces discoloured Gastric ulcer Gastric ulcer haemorrhage

Symptomtext

He has had a ulcer in his stomach,and he had bleeding inside; and his stomach liner opened up; Black stools; Black stools was reported as worsened.; This is a spontaneous report from a contactable consumer or other non hcp. A 51-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot Number: EW0169; Expiration Date: 31Aug2021) via an unspecified route of administration at arm left on 17Aug2021 (at the age of 51-years-old) as a single dose for COVID-19 immunisation. Medical history included gastric ulcer from an unknown date and unknown if ongoing Verbatim: Stomach ulcer. There were no concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. He got the Pfizer COVID shot on Tuesday 17Aug2021. Then, he noticed the next day his stool was black. He had this before, and he had bleeding inside. His stool is really black. It is really bad now. The dark stools started 18Aug2021. It had worsened. He hasn't seen a doctor or went to the Emergency room. He hasn't had treatment yet. He just went to the bathroom and noticed it was really bad. He just came from the bathroom. He will probably tell his boss today he will need to go get checked out. He has had a ulcer in his stomach, and his stomach liner opened up (gastric disorder). They asked if he had ever had an issue with bleeding before. on 18Aug2021 condition aggravated. Outcome of the events faeces discoloured and condition aggravated was not recovered, gastric ulcer and gastric disorder was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Stomach ulcer (Verbatim: Stomach ulcer)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1662710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 31.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain Chills Condition aggravated Decreased appetite Dizziness Headache Hypoaesthesia Nausea Rheumatoid arthritis Vomiting

Symptomtext

No issues with shot #1 or 2. This was a booster for immunocompromised yesterday (#3). Was fine until around 1900. Because extremely nauseous and vomited. Otherwise ok. Went to bed. Work up at 0530 today (9/1) and it felt like a RA flare. My symptoms have been pretty controlled with meds but today feels like day one. I hurt in every joint and back. Mild headache, dizzy, lack of appetite (I can taste). Chills, mild numbness in hands/feet.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: As of writing this, no additional treatments are been done.
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid Arthritis (sero-negative)- well controlled with meds
Andere Medikamente: Multivitamin, RA medications (Methotrexate, Rinvoq), Ib
Allergien: Compazine, Sulfa
Vorherige Impfungen: -

VAERS 1661634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EW0169

moderat

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 19.04.2021
Beginn: 19.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Nausea Palpitations

Symptomtext

Nausea followed by heart palpitations; Nausea followed by heart palpitations; This is a spontaneous report from a contactable consumer, the patient. A 26-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0169) via an unspecified route of administration in the left arm on 19Apr2021 at 13:00 (at the age of 26-year-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies to medications, food or other products. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any medication within two weeks of vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 19Apr2021 at 01:30 (as reported), the patient experienced nausea followed by heart palpitations. The events did not result 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 reported event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events nausea followed by heart palpitations was recovering at the time of this report. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
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 1658947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge ew0169

moderat

Staat: AL
Alter: 44,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 11.08.2021
Beginn: 11.08.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Migraine Myalgia Pain Pyrexia

Symptomtext

I had uncontrollable chills, shivering, my body hurt, muscles , a low grade fever and an awful migraine headache. I felt like this for about 5 day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: Nexium; Advair; singular
Allergien: Reglan
Vorherige Impfungen: -

VAERS 1658798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Ew0169

moderat

Staat: -
Alter: 48,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 12.08.2021
Beginn: 12.08.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Chills Flushing Heart rate decreased Hypertension Nausea

Symptomtext

During monitoring period post Pfizer COVID-19 vaccine, pt experienced *Hypertension, Slower Heart Rate, Nausea, Facial Flushing and Chills. o Patient declined medications. Water, blanket, distraction techniques and comfort measures initiated. Patient discharged to home with family. Left the clinic in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -