VAERS Reports #EN6203

VAERS 2657743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 74,0
Geschlecht: M
Eingang: 18.07.2023
Impfdatum: 27.02.2021
Beginn: 15.01.2022
Tage bis Beginn: 322,0
Dosis: 2
Route/Site: IM / RA

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

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

Symptomtext

Presented to ED w c/o productive cough; home COVID-19 test positive; pt admitted for COVID-19 pna, acute on chronic resp failure; tx w/steroids, remdesivir, zinc, O2; dc'd to home on RA

Weitere VAERSDATA-Felder

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

VAERS 2615462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 26.02.2022
Beginn: 07.04.2022
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / -

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

Deep vein thrombosis Hypotension Pulmonary embolism Stomach mass

Symptomtext

I26.99 ACUTE PULMONARY EMBOLISM 4/13/2022 ACUTE DVT OF RIGHT PERONEAL VEIN I82.451 ACUTE DVT OF RIGHT PERONEAL VEIN 4/13/2022 ACUTE DVT OF RIGHT PERONEAL VEIN I95.9 HYPOTENSION 4/7/2022 ACUTE DVT OF RIGHT PERONEAL VEIN I26.99 ACUTE PULMONARY EMBOLISM 4/13/2022 GASTRIC MASS I82.451 ACUTE DVT OF RIGHT PERONEAL VEIN 4/13/2022 GASTRIC MASS I95.9 HYPOTENSION 4/7/2022 GASTRIC MASS

Weitere VAERSDATA-Felder

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

VAERS 2602391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 84,0
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 15.09.2022
Beginn: 13.12.2022
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Cough Diarrhoea Dyspnoea Fatigue Gait disturbance SARS-CoV-2 test positive

Symptomtext

Patient seen in the ED on 12/12/22 with fatigue, mild shortness of breath, and cough. He reported testing positive for COVID at home earlier that morning. At that time, he was discharged back home with a prescription for Paxlovid. Patient returned to the ED on 12/13/22 with increased weakness, difficulties ambulating, and diarrhea. Repeat COVID PCR test done in the ED also resulted positive. He was admitted 12/13/22 - 12/14/22 with discharge diagnosis of acute hypoxic respiratory failure due to COVID-19 pneumonia. He initially required 2 L of supplemental oxygen, however was able to be weaned off. Patient has been vaccinated for COVID-19.

Weitere VAERSDATA-Felder

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

VAERS 2602384

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 78,0
Geschlecht: F
Eingang: 23.03.2023
Impfdatum: 16.11.2021
Beginn: 13.12.2022
Tage bis Beginn: 392,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Asthenia COVID-19 Cough Dyspnoea exertional Headache Hypoxia Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient seen in the ED on 12/13/22 for 2-3 days of headache, weakness, cough, fever, and shortness of breath with exertion. She reported testing COVID positive at home, and also tested positive for COVID by PCR in the ED. In the ED, patient found to be hypoxic at 86% with ambulation. She was admitted 12/13/22 - 12/15/22. Patient was on O2 but was weaned off completely. Discharge diagnosis included acute hypoxic respiratory failure due to COVID-19, among other diagnoses. She has been vaccinated for COVID-19.

Weitere VAERSDATA-Felder

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

VAERS 2569361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

kritisch

Staat: FL
Alter: -
Geschlecht: U
Eingang: 27.01.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / RA

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

Anticoagulant therapy Chest pain Dyspnoea Pulmonary embolism

Symptomtext

Chest pain, shortness of breath 1/20 Pulmonary embolisms 1/22 ER, 1/23-1/24 hospital stay, on eliquis

Weitere VAERSDATA-Felder

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

VAERS 2566892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 81,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 06.10.2021
Beginn: 11.11.2022
Tage bis Beginn: 401,0
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 Chills Cough Dyspnoea Hypervolaemia Myalgia Positive airway pressure therapy Pyrexia Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient with history of atrial fibrillation, oxygen-dependent COPD, ESRD. Patient brought to the ED by EMS on 11/11 for shortness of breath for the past two days. He uses O2 at baseline, but was at 45% upon EMS arrival. EMS placed the patient on 15L via rebreather mask, sating him to 93%. In the ED, patient also reported fever, chills, myalgias, and cough, and notes he tested positive for COVID on 11/9. Patient was also tested for COVID in the ED on 11/11 and was positive. Ultimately patient admitted 11/11/2022 - 11/14/2022 for acute on chronic hypoxic respiratory failure from COVID-19 pneumonia and possible superimposed bacterial pneumonia, as well as fluid overload from missing HD. He initially required BiPAP and eventually weaned down to 3 liters (baseline). Patient has received the COVID primary vaccine series and one booster.

Weitere VAERSDATA-Felder

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

VAERS 1331309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 20.01.2023
Impfdatum: 18.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Adenovirus test Blood calcium normal Blood chloride normal Blood creatinine increased Blood potassium normal Blood sodium normal Blood urea increased Bordetella test negative Chest pain Investigation Lymphadenopathy Pain Weight Coronavirus test negative Cough Decreased appetite

Symptomtext

she could feel it on left side of chest; Had Lymph node swelling; Had Lymph node swelling and pain there; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 73-year-old female patient received BNT162b2 (BNT162B2), on 18Mar2021 as dose 1, single (Lot number: EN6306) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Lyme infection", start date: 2020 (unspecified if ongoing); "mild stroke", start date: 2020 (unspecified if ongoing); "cellulitis" (unspecified if ongoing); "AFIB" (unspecified if ongoing); "allergic to a lot of antibiotics" (unspecified if ongoing); "cough" (unspecified if ongoing); "sinus" (unspecified if ongoing); "congestion" (unspecified if ongoing). Concomitant medication(s) included: CORICIDIN HBP COUGH AND COLD taken for cough, sinus disorder, nasal congestion; ATENOLOL taken for cerebrovascular accident. The following information was reported: CHEST PAIN (non-serious), outcome "recovering", described as "she could feel it on left side of chest"; LYMPHADENOPATHY (non-serious), outcome "recovered", described as "Had Lymph node swelling"; PAIN (non-serious), outcome "recovered", described as "Had Lymph node swelling and pain there". Relevant laboratory tests and procedures are available in the appropriate section.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Test Name: test; Test Result: Negative ; Comments: They tested her and guessed over a period of 3-4 days. First came back negative, 2nd positive and 3rd negative.; Test Name: test; Test Result: Positive ; Comments: They tested her and guessed over a period of 3-4 days. First came back negative, 2nd positive and 3rd negative.; Test Name: test; Test Result: Negative ; Comments: They tested her and guessed over a period of 3-4 days. First came back negative, 2nd positive and 3rd negative.; Test Name: Weight; Result Unstructured Data: Test Result:150-155 lbs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: AFib; Allergy to antibiotic; Cellulitis; Congestion nasal; Cough; Lyme disease; Sinus disorder; Stroke
Andere Medikamente: CORICIDIN HBP COUGH AND COLD; ATENOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2563511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 93,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 03.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: UN / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chronic obstructive pulmonary disease Confusional state Death Hypoxia Pneumonia Respiratory failure SARS-CoV-2 test positive Superinfection

Symptomtext

Patient brought to the ED on 11/8 for evaluation of confusion. Patient lives independently, and for the past 3 days her son has noticed that she has been confused. Patient was brough in by EMS, and on arrival to the scene she was notably hypoxic to 75-85%. She continued to have hypoxia in the ED and required supplemental oxygen. Patient had a COVID-19 PCR test done in the ED which resulted positive. Ultimately, she was admitted 11/8 with acute hypoxic/hypercapnic respiratory failure, suspected COVID-19 pneumonia with superimposed pneumonia, and chronic COPD with possible acute exacerbation, among other diagnoses. Patient was transitioned to comfort cares, and passed away on 11/11.

Weitere VAERSDATA-Felder

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

VAERS 2526154

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 84,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 19.08.2021
Beginn: 03.12.2022
Tage bis Beginn: 471,0
Dosis: 2
Route/Site: IM / RA

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

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

Symptomtext

**case was admitted to ICU 12/03/2022, tested positive for COVID-19 12/04/2022, died 12/06/2022.** Was not able to interview case or POA.

Weitere VAERSDATA-Felder

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

VAERS 2522074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 71,0
Geschlecht: M
Eingang: 02.12.2022
Impfdatum: 17.08.2022
Beginn: 25.09.2022
Tage bis Beginn: 39,0
Dosis: 2
Route/Site: SYR / LA

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

Acute kidney injury Atrial fibrillation COVID-19 Condition aggravated Death General physical health deterioration Intestinal perforation Lung adenocarcinoma Respiratory failure SARS-CoV-2 test positive Shock Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated 5 times with the Pfizer product, having received vaccine on 02/03/2021, 02/24/2021, 08/27/2021, 03/02/2022, and 08/17/2022. They were hospitalized 09/15/2022-09/23/2022for multiple reasons, including small bowel perforation, shock, hypoxic respiratory failure, multiple metastasized adenocarcinoma of the lung, acute renal failure, and a-Fib. They were transferred to a hospice facility on 09/23/2022. They tested negative for COVID-19 on 09/15/2022 and then positive on 09/25/2022 and 09/26/2022. Their health continued to decline and they died on 10/04/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 19,0
Labordaten: Positive COVID-19 test x2 despite being vaccinated x5.
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic Adenocarcinoma of the Lung, Anemia, Acute Kidney Failure The individual entered into a hospice facility 2 days prior to the adverse event.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 03.05.2022
Beginn: 19.10.2022
Tage bis Beginn: 169,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Atrial fibrillation COVID-19 COVID-19 pneumonia Condition aggravated Decreased appetite Dizziness Dyspnoea Malaise Nausea SARS-CoV-2 test positive

Symptomtext

Over the last few weeks the patient has had decreased appetite, dizziness, and nausea. She tested positive for COVID-19 on 10/16/22 by home test. Patient brought in to the ED by EMS for shortness of breath along with her other symptoms. She was admitted to the hospital 10/19-10/24 for management of acute hypoxic respiratory failure secondary to COVID pneumonia as well as atrial fibrillation with RVR. Patient has received the COVID vaccine and booster series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hx of atrial fibrillation and DVT
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 18.11.2022
Impfdatum: 24.02.2021
Beginn: 02.11.2022
Tage bis Beginn: 616,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Central venous catheterisation Cognitive disorder Condition aggravated Death Delirium Explorative laparotomy Gastrointestinal tube insertion Intestinal adhesion lysis Intestinal anastomosis Malnutrition Medical device change Respiratory disorder Respiratory viral panel SARS-CoV-2 test positive Small intestinal obstruction Small intestinal resection

Symptomtext

Clinical Summary Hospital Course: Patient is a 88 y.o. male patient of MD with a history of small bowel obstruction was transferred to a HCF on 11-2-2022. I saw and evaluated patient in the emergency department and subsequently recommended a laparotomy as he had been dealing with a bowel obstruction for approximately 6 to 7 days. The patient did require open lysis of adhesions and resection of the small intestine with primary anastomosis. Postoperatively the patient was sent to a general medical floor. Nasogastric tube was left in place and he was started on TPN as he had already been n.p.o. for a lengthy period of time. We did keep him on TPN. He did suffer from intermittent episodes of delirium and pulled at lines and drains. His PICC line required replacement as well as the nasogastric tube. The patient had a steady decline from a respiratory as well as to cognitive standpoint. He began having bowel function on approximately 11-8-2022. Due to his respiratory concerns a respiratory panel, viral, was checked and he was found to be positive for COVID. Patient was placed in isolation. After long discussion with the family they opted to transition the patient to comfort care as they felt that he would not want to continue with aggressive measures. The patient passed on 11-11-2022. Discharge Diagnoses: Small bowel obstruction COVID-19 pneumonia Protein calorie malnutrition 11/2/22 EXPLORATORY LAPAROTOMY, POSSIBLE BOWEL RESECTION, POSSIBLE OSTOMY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2510753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NC
Alter: 55,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 04.03.2021
Beginn: 23.12.2021
Tage bis Beginn: 294,0
Dosis: 1
Route/Site: SYR / AR

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

Biopsy skin abnormal Chemotherapy Cutaneous T-cell lymphoma Death

Symptomtext

He was diagnosed with mycosis fungoides in 12/2021 and died in mid-2022 after unhelpful chemotherapy treatments.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Skin biopsy done 12/2021 confirming mycosis fungoides (T-cell lymphoma)
Aktuelle Erkrankungen: hyperlipidemia, diabetes type 2, hypertension, depression
Vorgeschichte: as above
Andere Medikamente: atorvastatin 20mg qHS, Farxiga 10mg qd, glimepiride 2mg qd-bid, lisinopril 5m qd, metformin 500g 4 qd, sertraline 50mg 75mg qd
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2494081

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

kritisch

Staat: MN
Alter: 79,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 11.04.2022
Beginn: 29.10.2022
Tage bis Beginn: 201,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Patient expired 10/29/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Lung cancer
Andere Medikamente: Unknown
Allergien: Chlorhexidine, Levofloxacin, Sulfa antibiotics
Vorherige Impfungen: -

VAERS 2493613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 30.10.2022
Impfdatum: 02.07.2022
Beginn: 10.09.2022
Tage bis Beginn: 70,0
Dosis: 1
Route/Site: IM / AR

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

Angiogram cerebral abnormal Cardiac pacemaker evaluation Cerebrovascular accident Hemiparesis Thromboembolectomy Thrombosis Thrombotic stroke

Symptomtext

R MCA THROMBOTIC STROKE REQUIRING COIL EMBOLECTOMY. WAS ON FULL ANTICOAGULATION FOR AFIB BUT THE MONIOR AND THE PACEMAKER SHOWED NO EVIDENCE OF AFIB AROUND THE TIME OF THE STROKE. INTERVENTIONAL RADIOLOGY REMARKED TO THE PATIENT THAT IT WAS A VERY LONG AND LARGE THROMBUS. PATIENT WITH RESIDUAL MILD LEFT HEMIPARESIS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: HEAD CT ANGIOGRAPHY, INTERVENTIONAL RADIOLOGY, HOSPITAL
Aktuelle Erkrankungen: coronary arteriosclerosis paroxysmal atrial fibrillation atypical atrial flutter essential hypertension cardiac pacemaker in situ sick sinus syndrome familial cardiomyopathy ECG: premature ventricular contractions chronic diastolic heart failure essential hypertension hypertensive disorder Check electrocardiogram administration of SARS-CoV-2 vaccine
Vorgeschichte: coronary arteriosclerosis paroxysmal atrial fibrillation atypical atrial flutter essential hypertension cardiac pacemaker in situ sick sinus syndrome familial cardiomyopathy ECG: premature ventricular contractions chronic diastolic heart failure essential hypertension hypertensive disorder Check electrocardiogram administration of SARS-CoV-2 vaccine
Andere Medikamente: Arrange by: Name amLODIPine 5 mg tablet Take 1 tablet twice a day by oral route. atorvastatin 40 mg tablet TAKE 1 TABLET BY MOUTH NIGHTLY Atrovent 42 mcg (0.06 %) nasal spray This medication cannot be associated with an active order
Allergien: ASA CODEINE
Vorherige Impfungen: -

VAERS 2480449

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 17.11.2021
Beginn: 24.04.2022
Tage bis Beginn: 158,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory distress syndrome Acute respiratory failure Anticoagulant therapy Blood gases COVID-19 Cardiac failure Cardiomegaly Cerebral haemorrhage Chest X-ray abnormal Computerised tomogram abnormal Computerised tomogram head abnormal Computerised tomogram thorax abnormal Confusional state Crepitations Death Dysphagia Echocardiogram abnormal Endotracheal intubation

Symptomtext

4/24/2022-Presented to ED, unwitnessed fall states hit head large hematoma on L eye, admitted to drinking alcohol daily. Confused. CT Had, R parafalcine subdural and L frontal/parietal subdural hygroma. CT-sacral fracture and L subtrochanteric femur fx. Covid -test. Baseline 02 use 2L NC. Increased to 3L intermittently desat to mid 80's.Admit intraparenchymal hemorrhage with subdural hematoma s/t to fall. 4/25/2022-Left subtrochanteric hip fracture repair. R occiptal intraparenchymal hemorrhage inceased to 1.5cm L anterior frontal intraparenchymal hemorrhage increased to 5mm. No surgical intervention. BP controlled less then 140/80 currently 104/62, o2 sat 90's on 3L NC. Keppra 750mg BID. ST eval clear liquids, swallowing difficulties. 4/26/2022- R occipital intraparenchymal hemorrhage stable on f/u CT. 4/27/2022-On NRB, sat in mid 70's, o2 changed to 5L sata now 88-92%. 4/28/2022-AM-Mentation decline, desat 70-80 becoming more altered, fine wheezes bilateral and creptation on R side. Placed on NRB 15L. CXR-mod airpace disease/infiltrates LAsix IV and levaquin , CT no evidence of PE. IVC filter placed to prevent PEd/t recent surgery and immobility. PM-Sats in high 90's with NRB, but patient would not keep on, desatting to 70's. 5L NC was placed so suctioning could occur, sats would not maintain over 70%, thick yellow sputum obtained by suction. Became tachy and transfered to ICU and intubated. Acute on chronic hypoxemic resp failure s/t to ARDS d/t pneumonia vs pulm edema in setting of HFrEF and AMS. Current bilevel setting FiO2 60%. 4/29/2022-Bilevel 16 25/10 35%. WBC and h&h stable. On Vanco cefepime and flagyl. 4/30/2022- recent echo showed severe L ventricular dilatation with moderate miral regurg EF 20%. Continue entresto hold toresemide 5/2/2022- Exubated on 2L NC. Continue cefepime and flagyl. 5/3/2022- WBC 15.4 from 13.3 ABG 7.453/31.9/66/22.3/90 cxr-pulmonary vascular congestion and cardiomegaly. Cont digoxin and metoprolol 5/5/2022- Transfered to ICU. Wears bipap at HS. o2 sat on 2L stable. 5/13/2022- Rapid response called Acute RF, hypoxic 80's on sat , tachypneic using resp muscles. BP 154/104 RR 24 ABG 7.45/25/97/18/ on NRB worsening CT chest -pulmonary infiltrates and b/l pleural effusion. Bipap with PEEP 8. Continued distress, intubated and transfered to ICU. Chest Ct consisten with b/l diffuse groundglass opacities/ Covid + test. Ferritin 535.0. Started on steroids, barcitinib, remdesivir, vitamins and heparin. Cefepime and Vanco. 5/15/2022- Vent 12 22/6 60% 5/17/2022-Palliative orders placed d/t severe HF and mitral valve issues, fluid is in lungs and she is at high risk for reintubation if extubation is attempted. Terminally exubated. Morphine increased. WBC 15.5 5/19/2022- Time of death 1003.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ETOH abuse, COPED, Afib, CAD. HLD and post CABG ICD placement
Andere Medikamente: -
Allergien: Aspirin, PCN and adhesive
Vorherige Impfungen: -

VAERS 2468558

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 90,0
Geschlecht: M
Eingang: 04.10.2022
Impfdatum: 26.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 321,0
Dosis: 2
Route/Site: IM / OT

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

COVID-19 pneumonia Death

Symptomtext

This is a hospice admit with COVID pna. Placed on HFNC but could not wean. Placed on comfort care. Expired.

Weitere VAERSDATA-Felder

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

VAERS 2456015

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 74,0
Geschlecht: F
Eingang: 23.09.2022
Impfdatum: 03.03.2021
Beginn: 01.01.2022
Tage bis Beginn: 304,0
Dosis: 2
Route/Site: - / -

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

Asthenia COVID-19 COVID-19 pneumonia Death Dyspnoea Hypertensive heart disease Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

1/20/22 Pt positive for COVID; seen at ED and dc'd the same day; given Levsin and Promethazine; instructions to follow up with Dr. in 2-3 days; 1/28/22 back to ED with SOB, weakness, nausea and vomiting; IVFs given with antiemetic; dc'd to home; 2/2/22 pt DOA to hospital; COD per death certificate shows COVID pneumonia and Hypertensive Cardiac Disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: anxiety, arthritis, cardiac dysrhythmia, GERD, HTN, IBS, NIDDM, kidney disease, osteoporosis, pancreatitis, stroke
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2429667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 06.09.2022
Impfdatum: 16.03.2021
Beginn: 04.09.2022
Tage bis Beginn: 537,0
Dosis: 2
Route/Site: IM / LA

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

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

Symptomtext

SOB, Acute respiratory failure wit hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: positive home covid test 8/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2424066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 78,0
Geschlecht: F
Eingang: 30.08.2022
Impfdatum: 18.03.2021
Beginn: 01.02.2022
Tage bis Beginn: 320,0
Dosis: 2
Route/Site: - / -

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

Ascites COVID-19 Death Dyspnoea General physical health deterioration Hepatic encephalopathy Inappropriate schedule of product administration Mental status changes SARS-CoV-2 test positive Thrombocytopenia

Symptomtext

PFIZER COVID VACCINE #3 GIVEN 9/28/21, LOT #FF2587; 1/27/22 pt had a hospital admission Hospital in from a facility with AMS, hepatic encephalopathy, thrombocytopenia, ascites; functional decline; 2/10/22 tested positive for COVID while in the hospital; required IV morphine for worsening dyspnea; dc'd to Hospice, where she passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DMTW, ETOH CIRRHOSIS, GIP FOR PAIN, BREAST CA, DEPRESSION
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 27.08.2022
Impfdatum: 25.02.2021
Beginn: 27.04.2022
Tage bis Beginn: 426,0
Dosis: 1
Route/Site: IM / LA

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

Acute coronary syndrome Acute kidney injury Acute myocardial infarction COVID-19 Chest pain Death Dyspnoea Electrolyte substitution therapy Endotracheal intubation Haemofiltration Myocarditis Pericarditis Respiratory failure SARS-CoV-2 test positive Troponin increased

Symptomtext

Narrative: Patient received two doses of Pfizer COVID 19 Vaccine and one dose Moderna COVID 19 vaccine on 26 March 2022. The patient tested positive for COVID 19 on 27 April 2022. The patient presented to the ED on 27 April 2022 with chest pain and shortness of breath for one month. The patient was admitted to the hospital with elevated troponins (NSTEMI), acute kidney injury, pericarditis, and myocarditis. The patient was treated with steroids, antibiotics, and electrolyte replacement. The patient was intubated on 28 April 2022 due to respiratory failure and acute coronary syndrome. The patient started CRRT (dialysis) on 2 May 2022. The patent died on 12 May 2022. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2412409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 68,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 24.05.2022
Beginn: 15.07.2022
Tage bis Beginn: 52,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Cough Headache Interchange of vaccine products Pain Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient seen in the ED on 7/15 after testing positive for COVID at home. She reported coughing, headaches, and body aches. COVID-19 PCR swab also done in the ED and was positive. Patient did not feel safe being discharged home, so she was admitted from 7/15-7/18 and diagnosed with acute on chronic hypoxic respiratory failure due to COVID-19. She is vaccinated against COVID-19. This meets criteria for vaccine breakthrough case review.

Weitere VAERSDATA-Felder

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

VAERS 2400433

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CO
Alter: 79,0
Geschlecht: F
Eingang: 03.08.2022
Impfdatum: 23.04.2022
Beginn: 08.07.2022
Tage bis Beginn: 76,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Chest discomfort Chest pain Dyspnoea Electrocardiogram abnormal Fibrin D dimer Full blood count Glycosylated haemoglobin Hepatic enzyme Metabolic function test Myocardial injury Nausea Oropharyngeal pain Productive cough Respiratory tract congestion SARS-CoV-2 test positive Troponin increased

Symptomtext

Patient presented to the Emergency Department with complaints of pressure and non-radiating pain in her chest and shortness of breath. The pain sensation began 3 days after she tested positive for COVID-19. During this time, she experienced nausea with one episode of emesis, sore throat, congestion, and productive cough. On the basis of symptomatology, persistent oxygen requirements, electrocardiographic changes, and elevated troponin levels she was diagnosed with COVID-19 infection with acute hypoxemic respiratory insufficiency and non-ischemic myocardial injury. She was admitted to hospital and received one dose of dexamethasone 6mg intravenously and one dose of IV remdesivir. With symptomatic improvement, she was discharged medically stable with follow-up care plans in place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: Comprehensive Metabolic Panel Complete blood count Troponin Liver enzymes Hemoglobin A1C D dimer
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary heart disease, history of coronary artery bypass grafting Hyperlipidemia Type 2 diabetes Hypertension Osteoarthritis Pseudophakia
Andere Medikamente: Atorvastatin Dapagliflozin Metformin Pioglitazone Pantoprazole Aspirin Metoprolol Isosorbide dinitrate Pregabalin
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2433342

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 61,0
Geschlecht: M
Eingang: 21.07.2022
Impfdatum: 24.02.2021
Beginn: 12.07.2022
Tage bis Beginn: 503,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 Hypervolaemia

Symptomtext

Narrative: Fully vaccinated, admitted for acute hypoxemic respiratory failure 2/2 COVID infection versus volume overload.

Weitere VAERSDATA-Felder

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

VAERS 2364326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 67,0
Geschlecht: F
Eingang: 11.07.2022
Impfdatum: 14.05.2021
Beginn: 03.08.2021
Tage bis Beginn: 81,0
Dosis: 1
Route/Site: IM / RA

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

Burning sensation Hypoaesthesia Magnetic resonance imaging Myocardial infarction Neck pain Paraesthesia Peripheral swelling

Symptomtext

Neuromuscular symptoms: Fingers and toes- swelling, burning, tingling, numbness. Pain going up the right side of my neck. Facial tingling up the right side of face to temple. After about three weeks of this I had a mild heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: 12/2021 MRI 2/2022 MRI
Aktuelle Erkrankungen: none
Vorgeschichte: HCM
Andere Medikamente: levothyrooxine toprol
Allergien: no
Vorherige Impfungen: -

VAERS 2357959

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

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: 2
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 2314090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 09.06.2022
Impfdatum: 03.03.2021
Beginn: 01.08.2021
Tage bis Beginn: 151,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Aspiration pleural cavity COVID-19 Death Endotracheal intubation Haematocrit decreased Haemoglobin decreased Heart rate increased Hypotension Intensive care Pleural effusion Red blood cell transfusion Respiratory disorder SARS-CoV-2 test positive Sepsis Staphylococcal infection

Symptomtext

Pt had a positive COVID test on 8/31/21 and was hospitalized, treated and dc'd; 9/26/21 Pt was brought back to ED from for low BP and increased pulse; presumptive dx of sepsis; given ABX; found to have a low Hgb and HCT; transfused with packed RBCs; pleural effusion; thoracentesis; acute renal failure; did not want dialysis; on 10/3/21 his respiratory status deteriorated; transferred to ICU and was intubated; MRSA infection; status changed to comfort measures and he passed away in the hospital on 10/5/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: CDK stage IV, HTN, chronic diastolic heart failure, paroxysmal A Fib, OSA, GERD, mitral valve insufficiency, anxiety, depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2296381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 74,0
Geschlecht: M
Eingang: 26.05.2022
Impfdatum: 06.03.2021
Beginn: 17.03.2022
Tage bis Beginn: 376,0
Dosis: 2
Route/Site: IM / UN

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chest X-ray abnormal Hypervolaemia SARS-CoV-2 test positive Treatment noncompliance

Symptomtext

Case completed primary Covid vaccine seires in March 2021, then was hospitalized for Covid in March 2022. Hospitalized at: Hospital. Pneumonia due to COVID-19 virus Assessment & Plan Receiving Remdesivir and decadron per protocol; no significant dyspnea/cough observed but he does have a new oxygen need (did not require oxygen his most recent hospitalization); fluid overload on admission CXR possibly obscuring underlying infectious process; continue supportive oxygen; full code confirmed by patient - Positive covid test: 3/17 - 5 days of remdesivir last day 3/21 - 10 days of decadron last day 3/26 Acute respiratory failure with hypoxemia Assessment & Plan Ex-smoker per report. Due to copd noncompliant with chronic or intermittent o2 and due to covid pneumonia plus fluid overload at admission. Resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: Ordered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Ordered Test Codes: Status: Final Accession Number: Specimen Source: SOFT TISSUE SAMPLE Specimen Site: ENTIRE NASOPHARYNX Specimen Collection Date/Time: 2022-03-17 07:23:00.0 * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: DETECTED Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2022-03-17 08:57:55.0 Performing Facility: HOSPITAL Facility ID: (FI) Interpretation: Very abnormal Result Method: LAB DEVICE: CEPHEID GENEXPERT DX SYSTEM Status: Final Test Code: Result Code:
Aktuelle Erkrankungen: Atrial fibrillation ? Chronic kidney disease, stage 4 (severe) ? COPD (chronic obstructive pulmonary disease) ? Diabetic kidney disease ? Diabetic peripheral neuropathy ? ESRD on dialysis ? GERD with esophagitis ? Hyperlipidemia ? Hypertension ? Pacemaker ? Pulmonary hypertension ? Type II diabetes mellitus
Vorgeschichte: Atrial fibrillation ? Chronic kidney disease, stage 4 (severe) ? COPD (chronic obstructive pulmonary disease) ? Diabetic kidney disease ? Diabetic peripheral neuropathy ? ESRD on dialysis ? GERD with esophagitis ? Hyperlipidemia ? Hypertension ? Pacemaker ? Pulmonary hypertension ? Type II diabetes mellitus
Andere Medikamente: ADVAIR DISKUS 250-50 MCG/DOSE diskus inhaler albuterol 90 mcg/puff inhaler albuterol-ipratropium 2.5-0.5 mg/3 mL SOLN amLODIPine (NORVASC) 5 mg tablet aspirin 81 MG tablet atorvaSTATin (LIPITOR) 10 mg tablet be
Allergien: ADhesive tape, Latex
Vorherige Impfungen: -

VAERS 2283106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 75,0
Geschlecht: M
Eingang: 18.05.2022
Impfdatum: 20.02.2021
Beginn: 25.04.2022
Tage bis Beginn: 429,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

HOSPITALIZATION AND DEATH RELATED TO COVID-19 FOLLOWING COMPLETION OF PRIMARY VACCINE SERIES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: COVID-19 VIRUS MOLECULAR TEST POSITIVE 4/25/22
Aktuelle Erkrankungen: NONE KNOWN
Vorgeschichte: HYPERLIPIDEMIA
Andere Medikamente: CIALIS AS NEEDED, FLUTICASONE NASAL SUSPENSION AS NEEDED, MELOXICAM DAILY, IBUPROFEN AS NEEDED, MULTIVITAMIN DAILY, ACETAMINOPHEN AS NEEDED, VITAMIN D DAILY
Allergien: NONE KNOWN
Vorherige Impfungen: -

VAERS 2269002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 63,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 23.02.2021
Beginn: 16.09.2021
Tage bis Beginn: 205,0
Dosis: 2
Route/Site: SYR / RA

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

COVID-19 Cardiogenic shock Computerised tomogram thorax abnormal Death Endotracheal intubation Gastrointestinal haemorrhage Hypoxia Mechanical ventilation Pleural effusion Pulseless electrical activity Respiratory failure 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 02/02/2021 and 02/23/2021. They tested positive for COVID-19 on 09/16/2021 at the nursing home/rehab facility at which they were a resident. They were admitted to hospital on 09/23/2021 with primary complaints of hypoxia and respiratory failure, after not tolerating non-invasive ventilation at the nursing home. They tested positive again for COVID-19 on 09/24/2021. They then had a Pulseless electrical activity arrest for about 15 minutes. They were intubated, and they experienced cardiogenic shock. Bilateral pleural effusions were also discovered on CT scan. The individual remained hospitalized until their death on 09/24/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 1,0
Labordaten: Positive COVID-19 tests x2, on 09/16/2021 and 09/24/2021 despite being vaccinated
Aktuelle Erkrankungen: -
Vorgeschichte: Peripheral Vascular Disease, Coronary artery Disease, Hypertension and End Stage Renal Disease (on hemodialysis), Type II Diabetes, history of GI Bleed (was hospitalized for this for about 2 weeks, they were discharged just a few days before the adverse event) The individual was a resident of the nursing home/rehab facility indicated in the Address portion of this form. This seems to have bee intended as a short-term stay.
Andere Medikamente: -
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2267688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 78,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 13.09.2021
Beginn: 08.05.2022
Tage bis Beginn: 237,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure Angiogram pulmonary abnormal COVID-19 COVID-19 pneumonia Death Dyspnoea General physical health deterioration Inappropriate schedule of product administration Pneumonia Positive airway pressure therapy Productive cough SARS-CoV-2 test positive

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Rec'd Pfizer Vaccines 1/26/2021, 2/20/2021 and 9/13/2021. Prior hospitalization for bilateral community-acquired PNA and acute hypoxic respiratory failure from 4/4/2022 - 4/11/2022 at same facility and was Covid neg. Presented to ED 5/1/2022 with c/o productive cough and SOB, and tested POSITIVE for COVID. Admitted w/acute on chronic hypoxemic resp failure due to Covid PNA, placed on BIPAP. Also found to have a RLL PE on CTA at presentation. Condition deteriorated despite tx w/vanc, dexamethasone, zinc sulfate, and ascorbic acid. Expired on 5/8/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: COVID-19 Posiitve on 5/1/2022 using the BioFIre RP2.1 platform using PCR or Equivalent Nucleic Acid Amplification technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Lymphocytic Leukemia, Prostate Cancer, Reactive Ariway disease, Paroxysmal atrial fibrillation, hypothyroid
Andere Medikamente: Albuterol MDI, Cholecalciferol, Fluticasone MDI, Levothyroxine, Metoprolol XL, Ibrutinib, apixaban
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2248214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: IA
Alter: 90,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 08.03.2021
Beginn: 01.11.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure Asthenia Body temperature increased COVID-19 COVID-19 pneumonia Death Fall Fatigue Inappropriate schedule of product administration Intentional medical device removal by patient SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/12/21 (en6201) Pfizer Dose 2 3/8/21 (EN6203) COVID Positive 11/1/2021 11/1/21: 91-year-old lady presented to the emergency room following a fall at home. A friend helped her from the ground. Reports that she has been very, very weak in the recent days, feeling weak and fatigued. She reports a mechanical fall today and was brought to the emergency room by the EMS. In the emergency room was noted to have a temperature of 100.8. Denies shortness of breath and chest pain. 11/17/21: Patient is 91-year-old female with past medical history of asthma, essential tremors, CKD stage 3, type 2 diabetes, hypothyroidism, hyperlipidemia. She was brought to the emergency room on 11/01/2021 after fall at home. Later, she was found to COVID-19. Her oxygen requirement has been increasing progressively since. Currently she is being managed for acute hypoxic respiratory failure secondary to COVID-19 pneumonia Rule out superimposed bacterial pneumonia and right pneumothorax. Patient was seen examined by the bedside. Her friends by the bedside. Overnight events were noted. Earlier this morning, patient has been removing her OptiFlow. She informed staff and her friends were by the bedside that she wants to be comfortable. I called and talked to patient's daughter and POA who is in agreement with palceing patient on comfort care. Pt passed away at 18:47 PM on 11/17/2021. CPR was not initiated as patient was on comfort care with a DNR code status. Family members notified. Time of death was called at 18:47 PM on 11/17/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: asthma essential tremor CKD DM GERD h/o breast cancer hepatic hemangioma h/o diverticulitis HLD HTN insomnia hypothyroidism mitral valve prolapse RLS paresthesias skin neoplasm
Vorgeschichte: asthma essential tremor CKD DM GERD h/o breast cancer hepatic hemangioma h/o diverticulitis HLD HTN insomnia hypothyroidism mitral valve prolapse RLS paresthesias skin neoplasm
Andere Medikamente: acetaminophen 650 mg PO Q4h PRN aspirin 81 mg PO QD atorvastatin 20 mg PO QD vitamin D 2000 units PO QD docusate 100 mg PO BID docusame-senna 50-8.6 mg PO QD gabapentin 900 mg PO TID ibuprofen 200 mg PO TID PRN levothyroxine 50 mcg PO QD lo
Allergien: codeine - palpitations, SOB novocaine - palpitations, SOB penicillin - redness procaine - unknown quinidine - unknown sulfa drugs - rash
Vorherige Impfungen: -

VAERS 2243728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 09.03.2021
Beginn: 01.09.2021
Tage bis Beginn: 176,0
Dosis: 2
Route/Site: - / -

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

Atrial fibrillation COVID-19 COVID-19 pneumonia Death Diarrhoea Dyspnoea Dyspnoea exertional Endotracheal intubation Fatigue Hypoxia Intensive care Nasopharyngitis Pyrexia Respiratory disorder SARS-CoV-2 test positive

Symptomtext

9/26/21 pt presents to ED after testing positive for COVID on 9/21/21 at the local health department; she has had cold sx, fever, some diarrhea x approximately 1 wk; the last 2 days she's had more fatigue and SOB with exertion; has had a pulse ox of 80% on RA at home; admitted to hosp; COVID PNA with hypoxia; O2 supplementation; transferred to ICU; given dexamethasone, Vitamins C and D, zinc; pt went into A Fib RVR and her respiratory status worsened; she had to be intubated; was made a DNR by husband and eventually transitioned to comfort measures; she passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 03.03.2021
Beginn: 01.10.2021
Tage bis Beginn: 212,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Atrial fibrillation COVID-19 Condition aggravated Death Deep vein thrombosis Dialysis Dysuria Endotracheal intubation Fatigue General physical health deterioration Hypophagia Hypoxia Intensive care Pyrexia Respiratory failure SARS-CoV-2 test positive Septic shock

Symptomtext

9/23/21 pt brought to ED with c/o fever, dysuria, fatigue, decreased oral intake; admitted with UTI; acute renal insufficiency; transferred to ICU due to respiratory failure; intubated; tested positive for COVID on 10/4/21; developed septic shock; acute renal failure and placed on dialysis; developed DVT left upper extremity; hypoxic; hospital stay complicated by A Fib and rapid ventricular response; sputum came back positive for MRSA; ABX given; pt continued to deteriorate; transitioned to comfort measures and passed away in the hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: A Fib and is anticoagulated; DMT2, BPH, HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2241713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 69,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 09.03.2021
Beginn: 16.08.2021
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Death Dyspnoea Electroencephalogram abnormal Epilepsy Pneumonia Respiratory failure SARS-CoV-2 test positive Sepsis Vaccine breakthrough infection White blood cell count increased

Symptomtext

This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Pfizer product on 02/16/2021 and 03/09/2021. They presented to emergency department on 08/16/2021 via ambulance, after being sent over from an urgent care facility with primary complaints of elevated white count and shortness of breath. They were admitted to hospital 08/16/2021 and tested positive for COVID-19 upon admission (on 08/16/2021). They experienced complications of pneumonia, respiratory failure, sepsis, and epileptiform activity on EEG. They remained hospitalized until their death on 09/11/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 26,0
Labordaten: Positive COVID-19 test on 08/16/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Obstructive Sleep Apnea, Chronic Lymphocytic Leukemia, bronchiectasis, Depression, Bipolar Disorder, Borderline Personality Disorder, Hypothyroidism
Andere Medikamente: -
Allergien: Latex (reaction: unknown) Levofloxacin (reaction: nausea and vomiting) Omeprazole (reaction: unknown) Rabeprazole (reaction: unknown)
Vorherige Impfungen: -

VAERS 2241345

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 75,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 26.02.2021
Beginn: 09.03.2022
Tage bis Beginn: 376,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 Death

Symptomtext

Diagnosed and hospitalized and expired with COVID while fully vaccinated

Weitere VAERSDATA-Felder

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

VAERS 2223704

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 62,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 01.11.2021
Beginn: 07.02.2022
Tage bis Beginn: 98,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Cough Death Dyspnoea Inappropriate schedule of product administration Intensive care SARS-CoV-2 test positive Terminal state 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 03/04/2021, 03/30/2021, and 11/01/2021. They presented to emergency department on 02/07/2022 with primary complaints of shortness of breath and cough. They tested positive for COVID-19 and were admitted to hospital (ICU) same day. The individual had stage IV metastatic lung cancer that had spread to the brain (diagnosis approx 4 months earlier) and was on palliative care at the time. They were discharged to a hospice facility on 02/11/2022. An additional COVID-19 test was positive on 02/17/2022. They died on 02/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID-19 tests x2 despite being vaccinated and boosted
Aktuelle Erkrankungen: -
Vorgeschichte: At the time of the adverse event, the individual was terminally ill with stage IV lung cancer that had metastasized to the brain. They were on palliative care at the time of the adverse event. Chart notes medical conditions of: Lung Adenocarcinoma, Brain Metastasis, Neoplasm Causing Mass Effect, Anemia, Acute Hypoxic Respiratory Failure, Mediastinal Adenopathy, Vasogenic Brain Edema, Saddle Pulmonary Embolism, Asthma, Graves Disease, Autoimmune Hepatitis
Andere Medikamente: Radiation therapy for cancer (diagnosis in Oct 2021)
Allergien: Amoxicillin (Reaction: Rash), Clavulanic Acid (Reaction: Rash); Dog Dander (Reaction: Itchy Eyes); Dust Mites (Reaction: Unknown)
Vorherige Impfungen: -

VAERS 2221229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 89,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 27.02.2021
Beginn: 29.03.2022
Tage bis Beginn: 395,0
Dosis: 2
Route/Site: SYR / -

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

COVID-19 Cerebral haemorrhage Death Herpes zoster Laboratory test SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

Per interview with Patient's son, Patient had covid 6 weeks ago (no record in State database),and recovered. On 3/29/22, Patient was found unresponsive in his home, transported via ambulance to hospital, dx'd L-hemi brain bleed. Patient was DNR, discharged to home hospice, then passed away on 3/31/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: 2,0
Labordaten: Routine assessments/tests in hospital, not specified; 3/29/22 Real-Time Reverse Transcriptase PCR COVID-19, (+) test.
Aktuelle Erkrankungen: None recalled or reported.
Vorgeschichte: Patient had heart "several years ago", son/reporter did not specify. Patient began rather severe shingles episode in Nov 2021, son reports Patient only recently began to improve.
Andere Medikamente: Not reported by son during interview.
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2220747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 05.03.2021
Beginn: 01.12.2021
Tage bis Beginn: 271,0
Dosis: 2
Route/Site: - / -

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

Acute kidney injury Acute myocardial infarction Agonal respiration Anaemia COVID-19 Cardiac arrest Cardiac failure congestive Cough Death Decreased appetite Dyspnoea Fatigue Hypercapnia Hypoxia Life support Positive airway pressure therapy SARS-CoV-2 test positive Unresponsive to stimuli

Symptomtext

pt to ED with c/o SOB, cough, decrease in appetite, fatigue; found to be positive for COVID; admitted to hosp; NSTEMI; hypoxemia, anemia, AKI, CHF exacerbation; given remdesivir, dexamethasone, baaricitinib; O2 supplementation; respiratory status worsened; hypercapnia; on BiPAP; pt found by staff with BiPAP pulled off, unresponsive, agonal breathing; code blue called; ACLS protocol x 1 hr with brief recurrence of ROSC; family opted to hold any more resuscitative support and pt passed away

Weitere VAERSDATA-Felder

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

VAERS 2213924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 92,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 19.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death Respiratory failure SARS-CoV-2 test positive

Symptomtext

Dose 1 given 1/29/2022 Pfizer lot # EL9264. Patient had multiple hospitalizations at local Medical Center and died 3/31/2022 from respiratory failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Covid positive 2/25/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, heart disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 24.02.2021
Beginn: 15.04.2021
Tage bis Beginn: 50,0
Dosis: 1
Route/Site: SYR / AR

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

Cerebrovascular accident Laboratory test

Symptomtext

Stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: Many
Aktuelle Erkrankungen: none
Vorgeschichte: Gout High Cholesterol Marginal COPD Hypertension Potential Seizure Thyroid Gerd Potential Congestive Heart Failure
Andere Medikamente: Cyanocobalamin (VIT B12) 1000mcg tab Cholecalciferol (VIT D3) 1000 unit tab Allopurinol 300mg tab Carvedilol 6.25mg tab Levothyroxine NA (Synthroid) .088mg tab Atorvastatin 40mg tab Mometasone Furoate Oral Inhl 60 220mcg Levetiracetam 500mg
Allergien: ENALAPRIL IRBESARTAN LISINOPRIL LOSARTAN
Vorherige Impfungen: -

VAERS 2196245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 64,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 25.03.2021
Beginn: 27.02.2022
Tage bis Beginn: 339,0
Dosis: 1
Route/Site: SYR / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

not known, family did not return interview call

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: RT PCR COVID-19 (+) test on 3/6/2022 is only test known from record; Person passed away on 3/9/2022. Family did not return interview call.
Aktuelle Erkrankungen: not known, family did not return interview call
Vorgeschichte: not known, family did not return interview call
Andere Medikamente: not known, family did not return interview call
Allergien: not known, family did not return interview call
Vorherige Impfungen: -

VAERS 2189482

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 04.03.2021
Beginn: 25.01.2022
Tage bis Beginn: 327,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 Chromaturia Computerised tomogram thorax abnormal Confusional state Cough Death Dementia Fall Pneumonia Respiratory tract congestion Retching SARS-CoV-2 test positive

Symptomtext

Narrative: 75 y/o male with dementia presented to ER on 1/25/22 with weakness, falls, and worsening confusion. Increased cough and congestion. Darker urine and dry heaves but no vomiting earlier in the day. Tested positive for COVID. Treated with remdesivir and dexamethasone. Patient died on 2/3/2022. Cause of death likely due to progression of COVID vs treatment medications. PMH of hypertension, dementia, diabetes, atrial fibrillation on apixaban, aortic dissection, and hyperlipidemia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: COVID positive (1/25/22) CT suspicious for pneumonia (1/25/22)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 77,0
Geschlecht: M
Eingang: 19.03.2022
Impfdatum: 01.02.2021
Beginn: 20.03.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Cardiac murmur Cerebrovascular accident Confusional state Coronary artery disease Echocardiogram Echocardiogram abnormal Ejection fraction Left ventricular hypertrophy Mitral valve disease Mitral valve incompetence Mitral valve replacement Mitral valve thickening Myxomatous mitral valve degeneration Pyrexia

Symptomtext

On March 20 Patient started to have confusion. By March 23 he developed high fever 102.8. He went to his ID and a murmur was noted. He was worked up with a ECHO and had developed a tear in his Mitral Valve to the point of appendages barely holding it. He developed Uncontrolled A-fib and ultimately had Mitral Valve Replacement, extended hospital stay due to stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 20,0
Labordaten: 3/23 - ECHO - Left Ventricle: There is mild concentric left ventricular hypertrophy. ? Left Ventricle: Normal left ventricular systolic function. The EF is visually estimated to be 60-65%. ? Mitral Valve: The valve is myxomatous. The leaflets are thickened. ? Mitral Valve: There is severe regurgitation with an eccentrically directed jet. ? Mitral Valve: Cannot exclude vegetation on the mitral valve. 3/26 - TEE ? Left Ventricle: Normal left ventricular systolic function. The EF is visually estimated to be 60-65%. ? Left Atrium: The pulmonary veins have systolic flow reversal. ? Mitral Valve: There is severe regurgitation with an eccentrically directed jet. ? Mitral Valve: The posterior leaflet is flail. ? Mitral Valve: There is evidence of a posterior leaflet vegetation that is moderately sized and mobile. The vegetation is visualized on the atrial side of the valve. 3/30 -Conclusions: 1. Moderate coronary artery disease 2. Severe MR
Aktuelle Erkrankungen: None
Vorgeschichte: Adenocarcinoma of prostate, Erectile dysfunction, Recurrent UTI, Hypercalcemia, Agatston coronary artery calcium score greater than 400, Obesity (BMI 30-39.9), hyperlipidemia, Abdominal wound dehiscence, Neoplasm of uncertain behavior of bladder, Ileostomy status
Andere Medikamente: gabapentin (NEURONTIN) 300 mg capsule Take 3 capsules (900 mg) by mouth every night at bedtime 270 capsule 3 ? MAGNESIUM PO Take 1 tablet by mouth 2 times a day ? cephalexin (KEFLEX) 500 mg capsule Take one tablet twice a day on Mon, Tu
Allergien: Cipro and soaps
Vorherige Impfungen: -

VAERS 2177171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 80,0
Geschlecht: F
Eingang: 12.03.2022
Impfdatum: 01.03.2021
Beginn: 02.03.2022
Tage bis Beginn: 366,0
Dosis: 2
Route/Site: SYR / -

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

COVID-19 pneumonia Death Dyspnoea Fall Limb injury Pulmonary function test decreased SARS-CoV-2 test positive Vascular resistance systemic

Symptomtext

In early March, in addition to symptoms from chronic conditions, Patient showed fvr, decreased respiratory function, SOB, this last symptom resulted in another admit to hospital from a SNF where Pt was receiving wound care on leg from a fall she suffered sometime in Feb 2022. Case passed away final dx COVID Pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: Real-time Reverse Transcriptase PCR COVID-19 (+) test on 3/2/2022 Pneumonia
Aktuelle Erkrankungen: none recalled
Vorgeschichte: age, CHF, DM, HTN, polymyositis, kidney disease (one kidney)
Andere Medikamente: Rx/medications to treat chronic conditions of CHF, DM, HTN, polymyositis, incl on low dose prednisone
Allergien: NKA
Vorherige Impfungen: -

VAERS 2168051

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: IA
Alter: 92,0
Geschlecht: M
Eingang: 09.03.2022
Impfdatum: 27.02.2021
Beginn: 26.11.2021
Tage bis Beginn: 272,0
Dosis: 2
Route/Site: IM / -

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

Acute kidney injury Acute respiratory failure Asthenia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Death Dehydration General symptom Hypersomnia Laboratory test abnormal Lung infiltration Mobility decreased Oxygen saturation decreased Pulse absent Respiratory arrest Respiratory distress

Symptomtext

COVID Breakthrough Case Pfizer Dose 1 2/6/21 (EL9266) Pfizer Dose 2 2/27/21 (EN6203) COVID Positive 11/28/21 11/28/21: The patient presents with weakness. The onset was 2 days ago and gradual. The course/duration of symptoms is constant and worsening. The character of symptoms is generalized. The degree at present is moderate. Prior episodes: none. Therapy today: none. Associated symptoms: none. Additional history: none Patient states he has been coughing a lot over the past couple of days. Supplemental history provided by a patient's 2 sons and daughter. They states since he was seen here in the hospital 3 days ago he has been sleeping most of the time. They state that they been waking him to feed him but he does not stay up along and then he just goes back to sleep and has hardly moved. They states starting yesterday afternoon patient started coughing, and breathing fast They states that the patient is a DNR per his request. Patient was admitted and respiratory distress with acute hypoxemic respiratory failure secondary to COVID-19 pneumonia. Patient additionally had acute dehydration with acute kidney injury and rhabdomyolysis. Patient presented to the emergency department in moderate respiratory distress with the pulse oximetry only in the 60s. Chest x-ray showed bilateral infiltrates. Laboratory results showed acute kidney injury, severe dehydration and rhabdomyolysis. Family reported patient is a DNR per the patient's instructions. Patient was admitted initially on strict comfort care only patient's daughter who is power of attorney you/power of healthcare requests the patient be put on any medications that might possibly help. Patient was started on remdesivir and dexamethasone and azithromycin and Rocephin. Despite this patient's oxygen saturations did not improve. Patient was somnolent when he arrived and slowly became unresponsive. Patient was assessed and found to be not breathing and without a pulse at 11:20 p.m. and pronounced deceased

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: levothyroxine 50 mcg PO QD
Allergien: NKA
Vorherige Impfungen: -

VAERS 2165411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 83,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 13.03.2021
Beginn: 23.08.2021
Tage bis Beginn: 163,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

per death certificate pt died at home with COVID 19 listed as a condition contributing to death; pt was in hospice ( Medical Center - Hospice) pt had a positive COVID test recorded on 8/23/21; ordering facility (Privacy).

Weitere VAERSDATA-Felder

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

VAERS 2161667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: FL
Alter: 42,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 01.04.2021
Beginn: 16.05.2021
Tage bis Beginn: 45,0
Dosis: 1
Route/Site: SC / RA

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

Asthenia Blood pressure abnormal Blood test Cerebrovascular accident Feeling cold Lumbar puncture Magnetic resonance imaging Muscle twitching Nerve conduction studies Paraesthesia Transient ischaemic attack X-ray

Symptomtext

May 16, 2021: Developed severe facial twitching and weakness. Early June: Experienced what was believed to be a stroke or a TIA, which was ruled-out; extreme tingling throughout my entire body (from head to toe), basically a feeling of getting splashed with ice cold water several times a week. Also, my blood pressure has been a constant roller coaster, ranging from 212/128 as low as 76/53 and everywhere in between while doing nothing. I'm currently on 13 different medications.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: 5 MRIs; 5 CTs; lumbar puncture; nerve conduction tests; several X-Rays; tons of bloodwork.
Aktuelle Erkrankungen: -
Vorgeschichte: Hashimoto's disease, type 2 diabetes
Andere Medikamente: Rosuvastatin, Trulicity, Vitamin D, NP Thyroid
Allergien: Ceclor, Adhesive tape
Vorherige Impfungen: -

VAERS 2134709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 82,0
Geschlecht: F
Eingang: 23.02.2022
Impfdatum: 10.04.2021
Beginn: 09.02.2022
Tage bis Beginn: 305,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Death Inappropriate schedule of product administration Malaise SARS-CoV-2 test positive

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccine on 3/11/21 and 4/10/21. Presented to ED from clinic c/o Covid sxs and COVID+ on 1/27/22. Admitted for acute respiratory failure 2/2 Covid PNA. Tx'd w/steroids and O2. O2 requirements increased, requested DNAR/COT status on 1/30/22. O2 requirements continued to increase. Transitioned to comfort care, expired 2/10/22. Pt was transitioned to comfort care. Treated with decadron,ceftriaxone, piperacilin/tazobactam. Pt expired on 2/09/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: 1/27/22 - This sample has been tested on the platform which detects Sars-COV2 antigen.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hypercholesterolemia
Andere Medikamente: aspirin, vitamin D3, cholestyramine/aspartame, ezetimibe, hydrochlorothiazide, labetalol, olopatadine
Allergien: Simvastatin
Vorherige Impfungen: -

VAERS 2134321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 90,0
Geschlecht: M
Eingang: 23.02.2022
Impfdatum: 25.02.2021
Beginn: 11.02.2022
Tage bis Beginn: 351,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cardiac failure Condition aggravated Death SARS-CoV-2 test positive

Symptomtext

Dose 1 given 2/4/2021 lot # N/A Pfizer Patient died at Medical center on 2/23/2022 from Covid 19, and heart failure

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Praegender Schweregrund: Death
Hospital-Tage: 13,0
Labordaten: Covid 19 + on 2/11/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Heart failure, atrial fibrillation, CKD, hyperlipidemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2128366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CO
Alter: 72,0
Geschlecht: M
Eingang: 19.02.2022
Impfdatum: 25.02.2021
Beginn: 05.08.2021
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Bacteriuria Blood lactic acid Bone marrow transplant Bronchial wall thickening COVID-19 COVID-19 pneumonia Chest X-ray abnormal Hypocalcaemia Intensive care Interstitial lung disease Malaise Oxygen saturation decreased Procalcitonin SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID case: "Admit Date: 8/16/2021 Discharge Date: 8/24/2021 Reason for Hospitalization: 72 y.o. male with history of multiple myeloma on treatment and covid vaccine, admitted for covid 19 pneumonia. Hospital Course by Problem List: #COVID-19 pneumonia #acute hypoxemic respiratory failure ?Likely contracted virus approximately week PTA, COVID VACCINATED ?Recovered in ICU, then transferred to floor ?Started Covid protocol -Decadron, Remdesivir ?Low suspicion at present time for secondary pneumonia ?Pro-Cal, lactate noted -Pulm followed -patient eager to obtain covid booster vaccine -RT eval- 4LPM oxygen #Multiple myeloma ?Status post bone marrow transplant ?Follows with Dr. ?Oncology aware #Bacteruria -without symptoms #Hypocalcemia -replete prn "

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 8,0
Labordaten: "Result Date: 8/16/2021 XR CHEST SINGLE VIEW Indication: Patient reportedly diagnosed with Covid 19 on August 11. Patient is fully vaccinated and started having symptoms a few days before his positive test result. Decreased O2 saturation patient has history of multiple myeloma. History of monoclonal antibody therapy.. sepsis Comparison: Chest x-ray dated March 7, 2013. FINDINGS: Lungs: Normal lung volumes. Diffusely increased reticular interstitial changes in both lungs equally. Mild peribronchial thickening toward lower lung zones bilaterally. Normal pulmonary vascularity. Heart and Mediastinum: Normal heart size and mediastinal contours. Pleura and Chest Wall: There are no pleural effusions or pneumothoraces. Skeleton: Appropriate for age. Other: IMPRESSION: 1. Diffuse bilateral interstitial lung disease, likely chronic and possibly secondary to monoclonal antibody therapy. Other causes of interstitial pneumonitis and pulmonary fibrosis are not excluded. More recent comparisons than 2013 might be helpful. Superimposed Covid pneumonitis is not completely excluded. Report E-Signed By: 8/16/2021 12:34 PM"
Aktuelle Erkrankungen: None
Vorgeschichte: Erectile dysfunction, multiple myeloma, macrocytic anemia, mixed mesenchymal tumor
Andere Medikamente: "B-complex with vitamin C (TOTAL B/C) tablet ferrous sulfate 325 mg (65 mg iron) EC tablet folic acid 400 mcg tablet melatonin 3 mg tablet multivitamins with minerals (CENTRUM SILVER) 0.4-300-250 mg-mcg-mcg Tab tablet tadalafil (CIALIS
Allergien: None
Vorherige Impfungen: -

VAERS 2127882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 02.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Cerebral thrombosis Cerebrovascular accident Investigation Visual impairment

Symptomtext

a blood clot was created which moved to my brain; stroke; It affected my eyesight; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70 year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), administered in arm, administration date 02Mar2021 (Lot number: EN6203) at the age of 70 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing); "Cancer" (unspecified if ongoing). There were no concomitant medications. Patient started, "No, that was given to them at that time." Prior vaccination (within 4 weeks, "No. Vaccination history included: Covid-19 vaccine (1st dose of covid vaccine, Manufacturer unknown, LOT#: patient stated, "For the first dose was EL, I do not know if it is a 4 or 9, 264), administration date: 09Feb2021, when the patient was 70 years old, for COVID-19 immunization. The following information was reported: CEREBRAL THROMBOSIS (medically significant) with onset 2021, outcome "unknown", described as "a blood clot was created which moved to my brain"; CEREBROVASCULAR ACCIDENT (medically significant) with onset 2021, outcome "unknown", described as "stroke"; VISUAL IMPAIRMENT (non-serious) with onset 2021, outcome "unknown", described as "It affected my eyesight". The patient underwent the following laboratory tests and procedures: investigation: unknown result, notes: Patient started, "I do them all the time. Yes, I think so. Within the last 4 weeks, I do not know about 2 weeks.". Concern: Patient stated, "I got my vaccine last year and after I got the second shot a blood clot was created which moved to my brain and I had a stroke and it was right after I got the second shot. I have been trying to report this twice and nobody could tell me where can I report this." When paraphrased the concern, patient stated, "I had a blood clot, it travelled to my brain and gave me a stroke. Plus, I keep getting things that I am supposed to get my booster and everything else but I am afraid to get it because of what happened before. I do not want to get it." When asked if do not want to get the booster shot: Patient stated, "Right, I might get the other shot."(further clarification unknown). Patient stated, "When we get the shot, why do not they give us any information to report any issues because I went to all my doctors because it affected my eyesight and I could not do much of anything and nobody seemed to know what to do." No follow-up attempts are possible. No further information is expected.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Name: Lab work; Result Unstructured Data: Test Result:Unknown result; Comments: Patient started, "I do them all the time. Yes, I think so. Within the last 4 weeks, I do not know about 2 weeks."
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer; Diabetes
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2116882

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 73,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 10.03.2021
Beginn: 28.08.2021
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 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 and 03/10/2021. They presented to emergency dept on 08/28/2021 for shortness of breath and were admitted to hospital the same day. They also tested positive for COVID-19 via PCR test on 08/28/2021. After several days of treatment, the individual was placed on comfort care due to poor prognosis, due to the significant underlying medical conditions. They remained hospitalized until their death on 09/01/2021.

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Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: Positive COVID-19 test on 08/28/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Metastatic stage IV lung cancer; Acute on chronic systolic CHF exacerbation; Pancytopenia; Diabetes mellitus type 2
Andere Medikamente: Metformin (1,000 mg tablet, twice a day); aspirin; Lipitor; Breztri Aerosphere; cholecalciferol; citalopram ; Coreg; cyanocobalamin; ergocalciferol; folic acid; gabapentin; glipiZIDE; magnesium oxide; mirtazapine; ondansetron ; potassium ch
Allergien: -
Vorherige Impfungen: -

VAERS 2116864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 83,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 26.03.2021
Beginn: 23.11.2021
Tage bis Beginn: 242,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 Chemotherapy Cough Death Diarrhoea Dyspnoea Lung neoplasm malignant Nausea Pyrexia Respiratory failure 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 03/05/2021 and 03/26/2021. They tested positive for COVID-19 on 11/23/2021. A surviving family member reported this individual had a symptom onset of approx 11/24/2021. They were admitted to hospital on 11/23/2021 with cough, shortness of breath, fever, nausea, diarrhea, and respiratory failure. The decision was made to put the individual on palliative care, and transition to comfort care only. They remained hospitalized until their death on 12/02/2021. This individual had significant medical history of COPD, lung cancer, and a past pulmonary embolism. The individual's last infusion of Keytruda was approx 11/04/2021. The individual had made the decision to discontinue chemotherapy for the lung cancer on 11/23/2021, which is the same day they were admitted to hospital for shortness of breath.

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Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: Positive COVID-19 test on 11/23/2021 despite being vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Adenocarcinoma (stage I); Osteoarthritis; COPD; past pulmonary embolism
Andere Medikamente: The individual had been receiving chemotherapy for lung cancer; their last infusion of Keytruda was approx 11/04/2021. The individual had made the decision to discontinue chemotherapy for the lung cancer on 11/23/2021, which is the same day
Allergien: -
Vorherige Impfungen: -

VAERS 2095602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 71,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 25.03.2021
Beginn: 17.01.2022
Tage bis Beginn: 298,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Blood culture positive COVID-19 COVID-19 pneumonia Cardio-respiratory arrest Cryptococcosis Death Dialysis Dyspnoea Hypoxia Metabolic encephalopathy SARS-CoV-2 test positive Sepsis

Symptomtext

Pfizer COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/5/2021 and 3/25/2021. Presented to ED on 1/17/2022 with SOB x3 days. Diagnosed with Covid19 PNA. D/c'd 1/26/2022. Presented back to ED 1/28/2022 from dialysis center with report of hypoxia. Admitted for sepsis with acute hypoxemic resp failure without septic shock, acute metabolic encephalopathy and Covid19. Blood cultures: 2 of 2 bottles positive for cryptococcus neoformans and started on fluconazole. Coded on 2/2/2022 and expired.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: Positive COVID-19 on 1/17/2022 and 1/28/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Colon polyp, depression, DM, Dialysis, GERD, GI Bleed, HTN, Hyperlipidemia, Obesity, Osteoarthritis, Peripheral neuropathy, PVD, Prostate cancer, Renal cancer.
Andere Medikamente: Aspirin, Renaplex-D, VItB12, Folic Acid, Doxazosin, Nifedipine
Allergien: Morphine
Vorherige Impfungen: -

VAERS 2082682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 81,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 27.02.2021
Beginn: 11.01.2022
Tage bis Beginn: 318,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase normal Albumin globulin ratio Angiopathy Aspartate aminotransferase increased Asthenia Atrial fibrillation Bacillus test positive Blood alkaline phosphatase normal Blood bilirubin normal Blood calcium decreased Blood chloride increased Blood creatinine increased Blood lactic acid Blood magnesium normal Blood phosphorus normal Blood potassium normal

Symptomtext

82 Y male with h/o prior covid infection (Dec 2020, no hospitalization) in setting of full vaccination, emphysema, CKD (baseline Cr 1.1), hx tobacco use (quit 1999), preDM (last A1C 5.9% 9/19), HTN, was admitted to the ICU from the ED for COVID PNA. Symptom onset sometime 1/2-1/6, presented to ED w/ progressive dyspnea, dehydration, weakness. Found to have new Afib w/ RVR. Developed AKI on admission in setting of severe sepsis, improved over admission. Admitted to ICU 1/12, initially required Bipap but now intubated. PNA suspected during admission given resp culture with chryseobacterium gleum. Continued to have intubation requirement without ability to be weaned off. Discussed GOC and prognosis with the family, who opted for compassionate extubation on 1/25. Complications: Delirium Acute respiratory failure AFib

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: ED pertinent labs and imaging: Na 146, K 3.7, Cl 112, CO2 20, BUN 46, Cr 1.53, AG 14 Ca 8.4, Mg 2.1, Phosp 3.7 BNP 107 ALT/AST 21/74 ALKP 91 Lipase 32 Tbili 0.4 LA 3.0 WBC 10.2 (77% neut), H/H 16.2/49.2, Plt 218 COVID + Chest xray : Mild vascular congestion.
Aktuelle Erkrankungen: -
Vorgeschichte: /o prior covid infection (Dec 2020, no hospitalization) in setting of full vaccination, emphysema, CKD (baseline Cr 1.1), hx tobacco use (quit 1999), preDM (last A1C 5.9% 9/19), HTN, was admitted to the ICU from the ED for COVID PNA
Andere Medikamente: Sig: Inhale 2 Puffs by mouth every 4 hours as needed for quick relief of asthma symptoms . 100 days supply for asthma is 1 canister Aspirin 81 mg Oral Chew Tab Takes Regularly Sig: daily Ipratropium (Atrovent HFA) 17 mcg/actuation Inhl HFAA
Allergien: nkda
Vorherige Impfungen: -

VAERS 2079311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 05.03.2021
Beginn: 21.08.2021
Tage bis Beginn: 169,0
Dosis: 2
Route/Site: - / -

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

Brain oedema COVID-19 Cardio-respiratory arrest Chest pain Computerised tomogram head abnormal Death Endotracheal intubation Intensive care Life support Syncope

Symptomtext

pt brought to hosp ED via EMS with cardio-pulmonary arrest; ACLS protocol on way to ED; ROSC after code run in the ED; pt intubated; per family pt c/o chest pain prior to collapse; diagnosed 1 wk prior with COVID; PCP treated with steroids and hydroxychloroquine; CT showed cerebral edema; transferred to ICU; condition grim; family declined aggressive measures; withdrew care; pt extubated and died in the hosp

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

VAERS 1069829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NM
Alter: 73,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 24.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Cataract Cerebrovascular accident Feeling drunk Gait disturbance Disorganised speech Ischaemic stroke Laboratory test Mobility decreased Hemiparesis NIH stroke scale abnormal Speech disorder Vertigo Muscular weakness Nervous system disorder Vision blurred Visual field defect Vomiting

Symptomtext

42 hours after his 2nd Pfizer COVID19 vaccine patient had a stroke. This was an NIH level 5 ischemic stroke. The stroke began at about 8:30 am on 2/27/21. Patient was admitted to a local Hospital through the emergency room where he arrived at 2:00pm on 2/27/21. He stayed at the Hospital for 6 days. On 3/4/21 patient was transferred from the Hospital by ambulance to an Inpatient Physical Rehab, where he stayed for 2 weeks. Patient suffered total neural disconnect to his left side, had no use of his left leg or arm and had indecipherable speech. He was discharged from the rehab Hospital on 3/17/21, to home care for continued therapy to recover the use of his limbs, which is ongoing today.

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 19,0
Labordaten: Tests were too numerous to list. Please refer to the Hospital for tests and results 2/27/21-3/4/21, and to the rehab Hospital for 3/4/21-3/17/21.
Aktuelle Erkrankungen: None known.
Vorgeschichte: Underwent Mavyret protocol to eradicate Hepatitis C. Protocol lasted from October-December 2020. Hypertension being treated with Losartan.
Andere Medikamente: Losartan
Allergien: None known.
Vorherige Impfungen: -

VAERS 1069829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NM
Alter: 73,0
Geschlecht: M
Eingang: 26.01.2022
Impfdatum: 24.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Cataract Cerebrovascular accident Feeling drunk Gait disturbance Disorganised speech Ischaemic stroke Laboratory test Mobility decreased Hemiparesis NIH stroke scale abnormal Speech disorder Vertigo Muscular weakness Nervous system disorder Vision blurred Visual field defect Vomiting

Symptomtext

42 hours after his 2nd Pfizer COVID19 vaccine patient had a stroke. This was an NIH level 5 ischemic stroke. The stroke began at about 8:30 am on 2/27/21. Patient was admitted to a local Hospital through the emergency room where he arrived at 2:00pm on 2/27/21. He stayed at the Hospital for 6 days. On 3/4/21 patient was transferred from the Hospital by ambulance to an Inpatient Physical Rehab, where he stayed for 2 weeks. Patient suffered total neural disconnect to his left side, had no use of his left leg or arm and had indecipherable speech. He was discharged from the rehab Hospital on 3/17/21, to home care for continued therapy to recover the use of his limbs, which is ongoing today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 19,0
Labordaten: Tests were too numerous to list. Please refer to the Hospital for tests and results 2/27/21-3/4/21, and to the rehab Hospital for 3/4/21-3/17/21.
Aktuelle Erkrankungen: None known.
Vorgeschichte: Underwent Mavyret protocol to eradicate Hepatitis C. Protocol lasted from October-December 2020. Hypertension being treated with Losartan.
Andere Medikamente: Losartan
Allergien: None known.
Vorherige Impfungen: -

VAERS 2042866

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 86,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 24.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 323,0
Dosis: 2
Route/Site: IM / LA

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

Acute myocardial infarction Acute respiratory failure Asthenia COVID-19 Metabolic encephalopathy SARS-CoV-2 test positive

Symptomtext

Hospitalized COVID 19 positive weakness, metabolic encephalopathy, acute hypoxic respiratory failure, NSTEMI type 2 without chest pain.

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

VAERS 2028088

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 82,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 26.03.2021
Beginn: 05.01.2022
Tage bis Beginn: 285,0
Dosis: 1
Route/Site: IM / -

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

Angiogram pulmonary abnormal Ascites Atelectasis COVID-19 Cardiac arrest Cardiomegaly Coma scale Computerised tomogram abdomen normal Computerised tomogram head normal Death Generalised oedema Hypervolaemia Pleural effusion SARS-CoV-2 test positive Ultrasound abdomen

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/5/2021 and 3/26/2021. Patient presented to emergency department from nursing home after cardiac arrest x 10 minutes. According to nursing home patient was COVID-19 positive. Patient GCS was 13 on arrival with positive FAST exam. Patient expired 1/7/2022 at 0929.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 2,0
Labordaten: 1/5/2022: CT head with no acute intracranial abnormality, CTA Chest revealed Bilateral moderate pleural effusions, moderate volume abdominopelvic ascites, body wall anasarca and cardiomegaly suggest a volume overload state with bibasilar atelectatic changes, and CT abdomen/pelvis revealed no additional findings.
Aktuelle Erkrankungen: -
Vorgeschichte: Dementia, congestive heart failure, coronary artery disease, hyperlipidemia, hypertension, hyperthyroidism, atrial fib, diabetes, Gastroesophageal reflux disease, Benign prostatic hyperplasia without lower urinary tract symptoms
Andere Medikamente: atorvastatin 40 mg daily, cholecalciferol 5000 unit daily, cyanocobalamin 1000 mcg daily, levothyroxine 50 mcg daily, linsinopril-hydrochlorothiazide 10-12.5 mg daily, metformin 500 mg twice daily, multivitamin 1 tablet daily, apixaban
Allergien: unable to assess
Vorherige Impfungen: -

VAERS 2027993

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

kritisch

Staat: MO
Alter: 74,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 22.03.2021
Beginn: 02.01.2022
Tage bis Beginn: 286,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

tested (+) 1/2/2022 via PCR at hospital. Unknown symptoms or course of illness. Admitted 1/2/2022 and passed away 1/10/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: 1/2/2022 PCR (+) Nasopharyngeal swab
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2025716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 54,0
Geschlecht: M
Eingang: 11.01.2022
Impfdatum: 20.10.2021
Beginn: 06.12.2021
Tage bis Beginn: 47,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 Death 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 03/03/2020, 03/24/2021, and 10/20/2021. It is not specifically known if this person experienced symptoms of COVID-19 disease, but they tested positive on 12/06/2021 and 12/08/2021. They were admitted to hospital on 12/12/2021 and remained hospitalized until their death on 12/19/2021.

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Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: Positive COVID019 tests x2 despite being fully vaccinated
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2548645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 96,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 01.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / LA

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

Cardiac arrest Death

Symptomtext

Narrative: Patient was not previously Covid positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. Patient was 94 and was brought to the hospital ER on 3/7/21 after suffering cardiac arrest where he could not be revived. He was on warfarin for a fib and had CKD and CHF. Recently presented to the ED on 2/8/2021 with some chest pain which the attending concluded it was a low concern for an ACS.

Weitere VAERSDATA-Felder

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

VAERS 2531872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 88,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 27.02.2021
Beginn: 30.03.2021
Tage bis Beginn: 31,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac failure congestive Condition aggravated Dairy intolerance Death Dyspnoea General physical health deterioration Hypophagia Pain Thrombosis

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. Note on 3/2/21 shows concern from patient's family that his health is declining as he was not eating, he was in pain, and short of breath despite being on 2L oxygen. His contributing comorbidities include CHF, CKD, COPD, CAD, anemia, AAA, HTN, HLD. On 3/9/21 he was admitted for a CHF exacerbation. They found a blood clot in his arm during his hospital course and his status never improved. On 3/24/21 they discharged him home on hospice, and he passed away on 3/30/21.

Weitere VAERSDATA-Felder

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

VAERS 2541699

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 01.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / RA

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

Death Dyspnoea Fall

Symptomtext

Narrative: Patient was not previously COVID-19 positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. PMh significant for nephrogenic diabetes insipidus, cancer of esophagus, prostate cancer, parkinson's disease, dementia, anemia, obstructive sleep apnea, hyperlipidemia, diabetes mellitus, htn, bipolar. Was seen at ER on 4/9 with cc of SOB x 1 week and discharged. Pt fell on 4/21 but not injured. Pt was 72 years of age and deceased on 5/1/2021. No cause of death noted.

Weitere VAERSDATA-Felder

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

VAERS 1104031

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 01.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / RA

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

Cardiac arrest Chest pain Death

Symptomtext

Narrative: Patient was not previously Covid positive and did not have any predisposing factors(PMH, allergies, etc.) for experiencing an adverse drug event. The ADR did not occur at the time of the administration of the vaccine nor was there an ADR that occurred between the observation period and the date of death. Patient presented to MC on 3/8/21 with chest pain and suffered cardiac arrest. Patient had history of homelessness and substance abuse along with COPD.

Weitere VAERSDATA-Felder

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

VAERS 2500378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 26.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

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

Death

Symptomtext

Narrative: Patient received two doses of covid vaccine. Per notes, patient was on home hospice after cancer reoccurrence. No other details of death reported. Reporting per facility instruction.

Weitere VAERSDATA-Felder

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

VAERS 1989276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 59,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 04.03.2021
Beginn: 27.09.2021
Tage bis Beginn: 207,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Chest X-ray normal Dyspnoea Forced expiratory volume Malaise Respiratory distress SARS-CoV-2 RNA SARS-CoV-2 test positive Total lung capacity normal

Symptomtext

Case was hospitalized for Covid 6 months after completing the primary Pfizer series. At Hospital. Discharging physician: MD. Acute respiratory failure with hypoxia Assessment & Plan In respiratory distress with hypoxia in ED at rest needing 2 L. He had complained of shortness of breath in ER in Polson 6/21 and was started and Advair inhaler PFT from 6/28/21 noted FEV1 3.27 ( 101% of predicted) with normal DLCO and CXR at that time was normal so unlikely that he has underlying lung disease It appears that his sats in MD office on 6-17-21 were 97% on RA Today on the day of discharge sats are 94% on RA COVID-19 virus infection Assessment & Plan Tested + 9/24/21 Sxs present for ~ 7 days prior to admission Got 3 days of and 2 days of remdesivir which was stopped because sats were 94% on RA Vaccinated on 1/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: Ordered Test: SARS coronavirus 2 RNA (SARS-CoV-2, NAA) Ordered Test Codes: (LN LOINC)/(L LOCAL) Status: Final Accession Number: Specimen Source: Specimen Site: Specimen Collection Date/Time: 2021-09-24 11:18:00.0 Patient Status at Specimen Collection: Specimen Details: Respiratory Results: Resulted Test: SARS coronavirus 2 RNA (SARS-CoV-2, NAA) Coded Result: Detected (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Not Detect Reference Range To: Performing Facility Details: Date/Time: 2021-09-26 19:38:31.0 Performing Facility:Lab Facility ID: Interpretation: Abnormal Result Method: Probe.amp.tar Status: Final Test Code: (LN LOINC)/(L LOCAL) Result Code: (SCT/LDTDET (L LOCAL)
Aktuelle Erkrankungen: ? Blindness right eye ? Cataract right eye, reports "a couple months after, I went blind" ? Diabetes mellitus ? Hypertension ? Stroke ? Substance abuse
Vorgeschichte: ? Blindness right eye ? Cataract right eye, reports "a couple months after, I went blind" ? Diabetes mellitus ? Hypertension ? Stroke ? Substance abuse
Andere Medikamente: ACCU-CHEK SOFTCLIX LANCETS MISC USE TO CHECK BLOOD SUGAR TWICE A DAY Alcohol Swabs (ALCOHOL PREP) 70 % PADS 1 each by Does not apply route 2 times daily. amLODIPine (NORVASC) 10 MG tablet TAKE ONE TABLET BY MOUTH EVERY DAY Patient n
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1985282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 78,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 20.10.2021
Beginn: 21.10.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

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

Angiogram Chills Computerised tomogram Cough Death Dyspnoea Heart rate decreased Laboratory test Pain in extremity Pneumonia Pyrexia Skin discolouration Stent placement Thrombectomy Thrombosis

Symptomtext

Oct. 21, started out with chills and fever that went up to 102.7. Fever lasted 5 days. Monday, Oct. 25. we called PCP, He said it was a side affect of booster, it should pass. Monday night Mom started to have a cough and hard time breathing. she could not catch her breath after coughing. she was getting worse. Oct. 26, her left hand and fingers started to turn black and very painful, while getting worse with the breathing and coughing. Took her to ER. she had multifocal pneumonia and very low pulse in left arm and wrist. So then she was transfered to Medical Center OCt. 27, had angiogram done then Life flighted Oct. 28. then died Nov. 2, 2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: ct. scans, labs were done daily, angiogram was done. Surgery to try and remove clots from arm and collarbone area. Stint was placed in Collarbone area. Clot was to big to remove.
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure, fibromalgia , degeberatuve disc disease
Andere Medikamente: Losarten/hctz 100-25MG, Laryca 100mg 3x day. Hydrcodone 7.5mg
Allergien: morphine and novicane
Vorherige Impfungen: -

VAERS 1981343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 26.12.2021
Impfdatum: 24.02.2021
Beginn: 28.07.2021
Tage bis Beginn: 154,0
Dosis: 2
Route/Site: SYR / RA

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

Death

Symptomtext

Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Numbness, lathargic, Tingling
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1975012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 61,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 24.03.2021
Beginn: 07.10.2021
Tage bis Beginn: 197,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angiogram normal C-reactive protein abnormal COVID-19 COVID-19 pneumonia Procalcitonin normal SARS-CoV-2 test positive Sepsis Tachycardia Tachypnoea

Symptomtext

Case completed primary Covid vaccine series in March 2021, then was hospitalized for Covid in October 2021 at Hospital Hospitalist. Pneumonia due to COVID-19 virus Symptoms started about 10/4 based on the patient's history. Tested positive 10/7. He is fully vaccinated. Obesity increases his risk for severe disease. Treated with dexamethasone and remdesivir (he received 3 days of remdesivir while admitted). CRP down trended but had not normalized at discharge. Because he was still requiring supplemental oxygen with activity on the day of discharge and his CRP had not normalized he will complete a course of dexamethasone for the covid infection. Acute respiratory failure with hypoxia Secondary to covid infection. CTA 10/7 without PE. Procalcitonin negative. Presenting symptoms not consistent with asthma exacerbation, but getting steroids regardless. No history of heart failure and he denies orthopnea, edema. Needed 1-2L NC with activity on the day of discharge. Severe sepsis Met severe sepsis criteria on admission with tachycardia and tachypnea with respiratory failure. Secondary to covid infection. Sepsis physiology resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Ordered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Status: Final Specimen Source: SOFT TISSUE SAMPLE Specimen Site: ENTIRE NASOPHARYNX(181200003) Specimen Collection Date/Time: 2021-10-07 13:28:00.0 Results: * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: DETECTED Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2021-10-07 14:52:16.0 Performing Facility: HOSPITAL Interpretation: Very abnormal Result Method: LAB DEVICE: CEPHEID GENEXPERT DX SYSTEM Status: Final
Aktuelle Erkrankungen: ? Asthma ? Cancer 05/2019 squamous cell lung ? COPD (chronic obstructive pulmonary disease) ? Deviated septum ? Environmental allergies ? Kidney stone ? Non-small cell cancer of left lung ? Sleep apnea
Vorgeschichte: ? Asthma ? Cancer 05/2019 squamous cell lung ? COPD (chronic obstructive pulmonary disease) ? Deviated septum ? Environmental allergies ? Kidney stone ? Non-small cell cancer of left lung ? Sleep apnea
Andere Medikamente: ADVAIR DISKUS 500-50 MCG/DOSE diskus inhaler INHALE 1 DOSE BY MOUTH TWICE DAILY. Patient taking differently: Inhale 1 puff into the lungs 2 times daily INHALE 1 DOSE BY MOUTH TWICE DAILY. albuterol (VENTOLIN HFA) 90 mcg/puff inhaler INH
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1974708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 23.02.2021
Beginn: 22.12.2021
Tage bis Beginn: 302,0
Dosis: 2
Route/Site: - / -

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

Cardiac failure acute Death

Symptomtext

Dose 1 given 02/02/2021 Pfizer Lot # EL9264 Patient died of acute heart failure at hospital, on 12/22/2021. This is not a Covid 19 death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ESRD-dialysis, heart failure, diabetes, hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 80,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 25.02.2021
Beginn: 12.12.2021
Tage bis Beginn: 290,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death

Symptomtext

Dose 1 Pfizer 2/4/2021 Lot # EL3302, Booster Pfizer 10/13/2021 Lot # FC3184 Patient died from Covid 19 complications on 12/15/2021 at hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Cardiac disease, Hypertension, Pulmonary hypertension, Chronic kidney disease, CLL, lymphoma-on chemo, immunocompromised
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1954366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CO
Alter: 72,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 19.02.2021
Beginn: 10.09.2021
Tage bis Beginn: 203,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Death Immunodeficiency SARS-CoV-2 test positive

Symptomtext

Pt admitted to hospital 9/10/21 with COVID+ pna. Pt had received 2 doses of Pfizer (1/29/21 & 2/19/21). Pt is immunocompromised on chronic prednisone. Hospitalized 9/10-9/14, then re-admitted 9/20 & passed 9/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1952654

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 79,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 28.02.2021
Beginn: 20.07.2021
Tage bis Beginn: 142,0
Dosis: 1
Route/Site: IM / AR

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

Death Pulmonary embolism Sudden death

Symptomtext

On July 20, 2021 I found my mother deceased in her home. She was not sick and died suddenly and unexpectedly of a cardiopulmonary embolism.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: COPD
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1936517

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SD
Alter: 48,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 30.03.2021
Beginn: 24.10.2021
Tage bis Beginn: 208,0
Dosis: 1
Route/Site: SYR / UN

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

COVID-19 Death Distributive shock Respiratory failure SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

This is an instance of breakthrough COVID-19 disease after which a death occurred. The individual was vaccinated with the Pfizer product on 03/09/2021 and 03/30/2021. The individual became symptomatic on 10/18/2021 and a PCR test on 10/19/2021 was negative. However, an additional test done on 10/24/2021 was positive via PCR. The individual was admitted to the hospital on 10/24/2021 and discharged on 10/30/2021. However, they were re-admitted on 11/11/2021. Another additional PCR test was positive on 11/13/2021. They remained hospitalized until their death on 11/23/2021. Death certificate details are as follows: Part I Cause of Death A: Hypoxemic Respiratory Failure B: COVID 19 Part II Other Significant Conditions: Distributive Shock, Multiple Sclerosis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 18,0
Labordaten: Positive COVID-19 PCR tests x2 despite being fully vaccinated.
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1929265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 31.08.2021
Beginn: 08.11.2021
Tage bis Beginn: 69,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chronic kidney disease Condition aggravated Death Hypoxia Immunoglobulin therapy Mechanical ventilation SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/29/2021, 2/21/2021, and 8/31/2021. Pt. w/PMHx of unifocal langerhands cell histiocytosis, pulmonary fibrosis and emphysema s/p bilateral lung transplantation 1/2019. Hx Covid-19, dx'd on 11/4/21 tx'd w/monoclonal antibodies on 11/6. Admitted on 11/08 tx'd with remdesivir, decadron and IVIG, d/c'd home on 11/14. Admitted 11/20 for acute on chronic respiratory failure with hypoxia secondary to Covid pneumonia and CKD. Tx'd w/azithromcin, meropenem, and methylprednisolone. Underwent prolonged mechanical ventilation x13 days. Expired 12/06/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 16,0
Labordaten: Positive COVID-19 tests on 11/6/2021, 11/9/2021, 11/22/2021, 11/30/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, CKD, GERD, Unifocal Langerhans Cell Histiocytosis s/p lung transplant in 2019, Chronic hypoxemic respiratory failure
Andere Medikamente: Acetaminophen PRN, Azithromycin 250 mg MWF, Oscal BID, Clonazepam 0.5 mg QHS prn Anxiety, Dapsone 100 mg QD, Multivitamin QD, Gabapentin 200 mg BID, Itraconazole 100 mg BID, Lisinopril 20 mg QD, Magnesium oxide 400 mg BID, Metoprolol 75 mg
Allergien: Rivaroxaban, Amlodipine
Vorherige Impfungen: -

VAERS 1923697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: SC
Alter: 80,0
Geschlecht: M
Eingang: 05.12.2021
Impfdatum: 26.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: IM / AR

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

Anticoagulant therapy Blood test Blood testosterone decreased Cardiac pacemaker insertion Cerebrovascular accident Echocardiogram Magnetic resonance imaging Malaise Pneumonia

Symptomtext

One week after receiving my second dose of Pfizer, I had a stroke and was hospitalized. I received my dose 02/26 and had a stroke on 03/03. I now have to take a baby aspirin daily and a treatment for low testosterone. After my stroke I developed pneumonia and became very ill. I now have a pace maker installed as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 13,0
Labordaten: I had blood work done daily, echocardiograms, MR'sI and multiple other tests. I was in an out of it so I cannot remember much.
Aktuelle Erkrankungen: I was not experiencing any illness at the time.
Vorgeschichte: I have high bp (controlled), high cholesterol (controlled), atrial fibrillation. I have now experienced a stroke after my second dose.
Andere Medikamente: I was taking Atorvastatin, Lisinopril, Amlodipine, Hydralazine Chloride, Eliquis, Vitamin D3, Zinc and a Probiotic.
Allergien: I do not have any allergies.
Vorherige Impfungen: -

VAERS 1916744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 65,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 28.02.2021
Beginn: 19.10.2021
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Blood creatinine increased COVID-19 COVID-19 pneumonia Hypovolaemia Malaise SARS-CoV-2 test positive

Symptomtext

Case completed primary Covid vaccine series in Feb 2021, then was hospitalized for Covid in October 2021 * Pneumonia due to COVID-19 virus Assessment & Plan Onset of symptoms 10/11. Tested positive 10/15. Admitted 10/19/ Vaccinated. Was about to get booster but got sick first. Initially on 15L. Worsened, has been on high flow, started on baricitinib. No home O2 requirement prior to this admission. - Date of onset 10/11 - should be OK to come off isolation on Nov 1 - Continues on dexamethasone - 10-day course complete the 28th but will continue as she remains on HFNC - Continues on baricitinib to complete 14-day course - Still needing high-flow oxygen but needs trending down dramatically as of 10/31 - Discussed proning, position changes Acute kidney injury Assessment & Plan Creatinine up to 1.4 on admit from 0.8 at baseline. Losartan and chlorthalidone were held. Renal function recovered. Unclear if due to Covid, hypovolemia, or both. Placed back on home antihypertensives. Subsequently received several doses of furosemide, creatinine increased back to 1.6. Stopped home antihypertensives again, gave 500 cc fluid, stopped lasix. Improved. Acute respiratory failure with hypoxia Assessment & Plan Due to Covid-19. See related problem for treatment. - Continue HFNC - Tried some lasix to see if this helps, caused AKI. -Down to 4 L NC at rest on 11/2, possibly home 11/3 if maintains wellness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: Ordered Test: SARS-CoV-2 (COVID-19) RNA [Presence] in Respiratory specimen by NAA with probe detection Ordered Test Codes: 94500-6 (LN LOINC)/ Status: Final Accession Number: F2021-027153 Specimen Source: Anterior Nasal (AN) Swab Specimen Site: Specimen Collection Date/Time: 2021-10-15 17:00:00.0 Results: * Resulted Test: SARS-CoV-2 (COVID-19) RNA [Presence] in Respiratory specimen by NAA with probe detection Coded Result: Detected Numeric Result: Units: Text Result: Reference Range From: Reference Range To: Performing Facility Details: Date/Time: 2021-10-16 15:17:00.0 Performing Facility:FYR DIAGNOSTICS LABORATORY Interpretation: Result Method: Status: Final Test Code: 94500-6 (LN LOINC)/ Result Code: 260373001 (LN/
Aktuelle Erkrankungen: ? Allergic rhinitis, cause unspecified ? Anemia ? Cataract 2018 ? Depression ? Follicular lymphoma ? GERD (gastroesophageal reflux disease) ? Glaucoma 7/31/2018 Dx 2018 ? Hyperlipidemia low HDL ? Hypertension benign ? Idiopathic hypersomnolence 2005 Ritalin ? Insomnia persistent ? Lymphoma 2008 non-Hodgkins ? Macular edema 2009 labs neg for diabetes ? Menopause 2008 ? Nephrolithiasis 2007 ? Type 2 diabetes mellitus, without long-term current use of insulin (HCC)
Vorgeschichte: ? Allergic rhinitis, cause unspecified ? Anemia ? Cataract 2018 ? Depression ? Follicular lymphoma ? GERD (gastroesophageal reflux disease) ? Glaucoma 7/31/2018 Dx 2018 ? Hyperlipidemia low HDL ? Hypertension benign ? Idiopathic hypersomnolence 2005 Ritalin ? Insomnia persistent ? Lymphoma (HCC) 2008 non-Hodgkins ? Macular edema 2009 labs neg for diabetes ? Menopause 2008 ? Nephrolithiasis 2007 ? Type 2 diabetes mellitus, without long-term current use of insulin (HCC)
Andere Medikamente: armodafinil (NUVIGIL) 250 mg tablet TAKE ONE TABLET BY MOUTH EVERY DAY Patient taking differently: Take 250 mg by mouth Daily . 9/2/21 buPROPion (WELLBUTRIN SR) 150 mg 12 hr tablet 1 tablet by mouth daily for 3 days; increase to 1 tabl
Allergien: ? Codeine Nausea And Vomiting Codeine, Codeine ? Lisinopril cough
Vorherige Impfungen: -

VAERS 1913689

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

kritisch

Staat: MT
Alter: 72,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 08.03.2021
Beginn: 24.10.2021
Tage bis Beginn: 230,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure C-reactive protein increased COVID-19 Chills Cough Diarrhoea Hypoxia Myalgia Nausea Pneumonia viral Pyrexia SARS-CoV-2 test positive Sepsis Systemic inflammatory response syndrome Vomiting

Symptomtext

Case completed covid vaccine series in March 2021 then was hospitalized for Covid in October 221. * Acute hypoxemic respiratory failure due to COVID-19 (HCC) Assessment & Plan Fully vaccinated, tested positive for SARS-CoV-2 October 18. Had N/V/D which have improved. Symptom onset about October 16, fevers chills cough nausea diarrhea myalgias -Hypoxia at home to mid 80s. -On arrival systemic inflammatory syndrome, sepsis secondary to viral pneumonia. CRP up at 24.7 but down to 4.7 on the day of d/c. -Dexamethasone 6 mg and remdesivir started October 24, will continue cecadron for 6 more days. - Continue to wean supplemental oxygen as able. Improved symptoms and o2 supplement down to 1L/min, doing ADLs with mild symptoms. - Encourage self proning as able, IS and ambulation. - Note that is DNR/DNI but is agreeable to HFNC, NIPPV, and ICU transfer if needed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: Ordered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Ordered Test Codes: 94500-6 (LN LOINC)/ Status: Final Specimen Source: SOFT TISSUE SAMPLE Specimen Site: Nasopharynx(Nasopharynx) Specimen Collection Date/Time: 2021-10-18 12:52:00.0 Results: * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: POSITIVE Numeric Result: Units: Text Result: Reference Range From: Negative Reference Range To: Performing Facility Details: Date/Time: 2021-10-18 12:52:00.0 Interpretation: Abnormal Result Method: Status: Final Test Code: 94500-6 (LN LOINC)/
Aktuelle Erkrankungen: ? Acid reflux disease ? Allergic state ? Anxiety ? Arthritis ? Back pain ? BPV (benign positional vertigo) ? Cataract ? Chronic diarrhea ? Cough variant asthma ? Diabetes mellitus (HCC) ? Environmental allergies ? GERD (gastroesophageal reflux disease) ? Heart murmur ? Hyperlipidemia 9/17/2020 ? Hypertension (BP 134/92 on 10/18/2017; 160/94 on 11/29/2017) ? Irritable bowel syndrome ? OSA (obstructive sleep apnea) 10/7/2014 Dr intiated CPAP ? Thyroid disease
Vorgeschichte: ? Acid reflux disease ? Allergic state ? Anxiety ? Arthritis ? Back pain ? BPV (benign positional vertigo) ? Cataract ? Chronic diarrhea ? Cough variant asthma ? Diabetes mellitus (HCC) ? Environmental allergies ? GERD (gastroesophageal reflux disease) ? Heart murmur ? Hyperlipidemia 9/17/2020 ? Hypertension (BP 134/92 on 10/18/2017; 160/94 on 11/29/2017) ? Irritable bowel syndrome ? OSA (obstructive sleep apnea) 10/7/2014 Dr intiated CPAP ? Thyroid disease
Andere Medikamente: ALPRAZolam (XANAX) 0.5 mg tablet TAKE 1/2 TO 1 TABLET BY MOUTH NO MORE THAN 3 TIMES A WEEK AS NEEDED FOR ANXIETY AND FEAR OF FLYING. 8/4/21 atorvaSTATin (LIPITOR) 10 mg tablet Take 1 tablet by mouth nightly. 6/23/21 azithromycin (
Allergien: Dust Mite extract
Vorherige Impfungen: -

VAERS 2571910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 03.03.2021
Beginn: 22.09.2021
Tage bis Beginn: 203,0
Dosis: 2
Route/Site: IM / LA

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

Acute left ventricular failure Acute respiratory failure Angiogram pulmonary abnormal Blood fibrinogen increased Blood lactic acid Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac failure acute Cardiac failure congestive Chest X-ray abnormal Condition aggravated Cough Dyspnoea Fatigue Fibrin D dimer International normalised ratio normal Interstitial lung disease

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/10, Pfizer, dose #1 03/03, Pfizer, dose #2 09/22 cc: dx: Acute hypoxic respiratory failure, COVID Pneumonia in a vaccinated patient, ACUTE DECOMPENSATED SYSTOLIC CHF, improved. LOS: 5 days 09/22 pt cc: cough, fatigue, dyspnea, fever, exposure: unknown 09/22 BinaxNOW COVID-19 Ag: NOT DETECTED 09/22 PT/INR 12.1/1.08 09/22 BNP: 963.3 09/22 FIBRINOGEN: 422 09/22 DDIMER: 1.60 09/22 LACTTIC ACID: 1.42 09/22 FERRITIN: 94.5 09/22 COVID swab, result: detected 09/22 SARS-COV-2 IGG Eval: 6.25 09/22 SARS-COV-2 TOTAL AB, SPIKE result: >2500.0 09/22 CTA PE impression: teral pneumonia. Please correlate with Covid status. 09/23 FIBRINOGEN: 431 09/23 DDIMER: 1.79 09/23 ESR: 35 09/23 TROPONIN I: <0.016 09/24 CXR impression Bila 1. No evidence of pulmonary embolism. 2. Bilateral peribronchial consolidation. Groundglass opacities in the periphery, more than expected for simply interstitial lung disease. This is concerning for pneumonia including COVID-19. Correlate clinically. 3. Findings compatible with UIP pattern interstitial lung disease, worsened since March 2020. teral mixed interstitial and airspace opacities with a lower lung predominance, similar to prior. Otherwise no pneumothorax or large pleural effusion. Stable cardiomediastinal silhouette. Osseous structures grossly stable with partially imaged cervical fusion hardware and vertebral cement. 09/24 FIBRINOGEN: 308 09/24 DDIMER: 1.05 09/24 ESR: 51 09/24 IONIZED: 1.05 09/25 FIBRINOGEN: 292 09/25 DDIMER: 1.00 09/25 ESR: 38 09/26 FIBRINOGEN: 308 09/26 DDIMER: 1.04 09/26 ESR: 18 09/27 COVID swab, result: NOT detected 09/27 FIBRINOGEN: 284 09/27 DDIMER: 0.84 09/27 ESR: 32

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 09/22 BinaxNOW COVID-19 Ag: NOT DETECTED 09/22 PT/INR 12.1/1.08 09/22 BNP: 963.3 09/22 FIBRINOGEN: 422 09/22 DDIMER: 1.60 09/22 LACTTIC ACID: 1.42 09/22 FERRITIN: 94.5 09/22 COVID swab, result: detected 09/22 SARS-COV-2 IGG Eval: 6.25 09/22 SARS-COV-2 TOTAL AB, SPIKE result: >2500.0 09/22 CTA PE impression: teral pneumonia. Please correlate with Covid status. 09/23 FIBRINOGEN: 431 09/23 DDIMER: 1.79 09/23 ESR: 35 09/23 TROPONIN I: <0.016 09/24 CXR impression Bila 1. No evidence of pulmonary embolism. 2. Bilateral peribronchial consolidation. Groundglass opacities in the periphery, more than expected for simply interstitial lung disease. This is concerning for pneumonia including COVID-19. Correlate clinically. 3. Findings compatible with UIP pattern interstitial lung disease, worsened since March 2020. teral mixed interstitial and airspace opacities with a lower lung predominance, similar to prior. Otherwise no pneumothorax or large pleural effusion. Stable cardiomediastinal silhouette. Osseous structures grossly stable with partially imaged cervical fusion hardware and vertebral cement. 09/24 FIBRINOGEN: 308 09/24 DDIMER: 1.05 09/24 ESR: 51 09/24 IONIZED: 1.05 09/25 FIBRINOGEN: 292 09/25 DDIMER: 1.00 09/25 ESR: 38 09/26 FIBRINOGEN: 308 09/26 DDIMER: 1.04 09/26 ESR: 18 09/27 COVID swab, result: NOT detected 09/27 FIBRINOGEN: 284 09/27 DDIMER: 0.84 09/27 ESR: 32
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1920016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 04.03.2021
Beginn: 02.10.2021
Tage bis Beginn: 212,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Blood bicarbonate normal Blood fibrinogen increased Blood pH increased Brain natriuretic peptide normal C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Dyspnoea Fatigue Fibrin D dimer International normalised ratio increased Lung opacity Myalgia Nephrolithiasis

Symptomtext

COVID infection following COVID vaccine series 02/10, Pfizer, dose #1 03/04, Pfizer, dose #2 10/02 Pt cc: dyspnea, cough, myalgias, fatigue, cough, exposure: unknown 10/12 pt admit to medicine cc shortness of breath : dx: ACUTE HYPOXIC RESPIRATORY FAILURE DUE TO COVID-19 PENUMONIA LOS: 10 days 10/21 u/s abdomen impression: 1. New bilateral obstruction or pneumoperitoneum. 10/12 CXR impression: 1. New bilateral airspace opacities could relate to pneumonia, including viral. 10/12 CTA PE impression: 1. Technically suboptimal study. No pulmonary embolus in the large central pulmonary arteries. Limited evaluation of the segmental and subsegmental pulmonary arteries. 2. Nonspecific groundglass densities in the lungs probably represent covid 19 pneumonia. Pleas correlate clinically and follow-up as appropriate. 3. Right Pulmonary nodules measuring up to 1.9 cm as above are again noted. Further evaluation and follow-up will be helpful as clinically appropriate. 4. Mild splenomegaly. 5. Nonobstructing left renal calculus. 10/12 TROPONIN I: <0.016 10/12 PT/INR: 16.7/1.49 10/12 FERRITIN: 1035.7 10/12 CRP: 11.387 10/12 PROCALCITONIN: ,0.05 10/12 BNP: 12.0 10/12 COVID swab, result: detected 10/12 DDIMER: 0.98 10/12 SARS-COV-2 Variant Sequencing result: pending 10/12 ABG i-pH 7.47, i-PCo2 38, i-PO2 61, i-HCO3 27.3 10/13 FIBRINOGEN: 480 10/13 DDIMER: 0.83 10/13 ESR: 44 10/14 FIBRINOGEN: 406 10/14 DDIMER: 0.59 10/14 EST: 25 10/14 ABG: I-pH 7.44, i-PCo2 41, i-PO2 66, i-HCO3 27.8 10/15 FIBRINOGEN: 296 10/15 DDIMER: 0.60 10/15 ESR: 27 10/16 FIBRINOGEN: 300 10/16 DDIMER: 0.72 10/16 ESR: 18 10/17 FIBRINOGEN: 253 10/17 DDIMER: 0.92 10/17 ESR: 18 10/18 F8BR8H9GEH: 240 10/18 DDIMER: 0.93 10/18 ESR: 19 10/19 FIBRINOGEN: 242 10/19 DDIMER: 0.90 10/19 ESR: 13 10/21 FIBRINOGEN: 220 10/21 DDIMER: 0.67 10/21 ESR: 6 08/21 FIBRINOGEN: 197 08/21 DDIMER: 0.83 08/21 ESR: 4

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 10/21 u/s abdomen impression: No evidence for intestinal obstruction or pneumoperitoneum. 10/12 CXR impression: 1. New bilateral airspace opacities could relate to pneumonia, including viral. 10/12 CTA PE impression: 1. Technically suboptimal study. No pulmonary embolus in the large central pulmonary arteries. Limited evaluation of the segmental and subsegmental pulmonary arteries. 2. Nonspecific groundglass densities in the lungs probably represent covid 19 pneumonia. Please correlate clinically and follow-up as appropriate. 3. Right pulmonary nodules measuring up to 1.9 cm as above are again noted. Further evaluation and follow-up will be helpful as clinically appropriate. 4. Mild splenomegaly. 5. Nonobstructing left renal calculus. 10/12 TROPONIN I: <0.016 10/12 PT/INR: 16.7/1.49 10/12 FERRITIN: 1035.7 10/12 CRP: 11.387 10/12 PROCALCITONIN: ,0.05 10/12 BNP: 12.0 10/12 COVID swab, result: detected 10/12 DDIMER: 0.98 10/12 SARS-COV-2 Variant Sequencing result: pending 10/12 ABG i-pH 7.47, i-PCo2 38, i-PO2 61, i-HCO3 27.3 10/13 FIBRINOGEN: 480 10/13 DDIMER: 0.83 10/13 ESR: 44 10/14 FIBRINOGEN: 406 10/14 DDIMER: 0.59 10/14 EST: 25 10/14 ABG: I-pH 7.44, i-PCo2 41, i-PO2 66, i-HCO3 27.8 10/15 FIBRINOGEN: 296 10/15 DDIMER: 0.60 10/15 ESR: 27 10/16 FIBRINOGEN: 300 10/16 DDIMER: 0.72 10/16 ESR: 18 10/17 FIBRINOGEN: 253 10/17 DDIMER: 0.92 10/17 ESR: 18 10/18 F8BR8H9GEH: 240 10/18 DDIMER: 0.93 10/18 ESR: 19 10/19 FIBRINOGEN: 242 10/19 DDIMER: 0.90 10/19 ESR: 13 10/21 FIBRINOGEN: 220 10/21 DDIMER: 0.67 10/21 ESR: 6 08/21 FIBRINOGEN: 197 08/21 DDIMER: 0.83 08/21 ESR: 4
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 88,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 05.04.2021
Beginn: 29.11.2021
Tage bis Beginn: 238,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID on 11/23/2021 and died on 11/29/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1890701

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

kritisch

Staat: MT
Alter: 79,0
Geschlecht: M
Eingang: 22.11.2021
Impfdatum: 05.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 Cough Decreased appetite Encephalopathy Fatigue Hypokalaemia Lethargy SARS-CoV-2 test positive

Symptomtext

Hospitalized for Covid after full vaccination. Acute hypoxemic respiratory failure due to COVID-19 Assessment & Plan Presented with 4 to 5 days of cough and fatigue. Subsequently became encephalopathic and lethargic. Was eating very little prior to admit. Found to be a bit hypoxic with volume contraction and hypokalemia as well. - Symptom onset: 10/25 - Date isolation discontinued 11/14 - Finished 10 day course of dexamethasone - Finished 5-day course of remdesivir - Now on room air - DNR/DNI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 19,0
Labordaten: Ordered Test: SARS-CoV-2 RNA Resp Ql NAA+probe Ordered Test Codes: 94500-6 (LN LOINC)/ Status: Final Accession Number: 213020059LP-198922 Specimen Source: SOFT TISSUE SAMPLE Specimen Site: ENTIRE NASOPHARYNX Specimen Collection Date/Time: 2021-10-29 13:19:00.0 Results: * Resulted Test: SARS-CoV-2 RNA Resp Ql NAA+probe Coded Result: DETECTED Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2021-10-29 14:25:23.0 Performing Facility: HOSPITAL Facility ID:27D0410970 (FI) Interpretation: Very abnormal Result Method: LAB DEVICE: CEPHEID GENEXPERT DX SYSTEM Status: Final Test Code: 94500-6 (LN LOINC)/ Result Code: 260373001 (SCT/
Aktuelle Erkrankungen: ACE-inhibitor cough Axonal neuropathy thought genetic by neurology (see Jan2014 Neurology note) (OV 9/8/14) BPH (benign prostatic hyperplasia) in past used flomax, eventually went to uroxatrol (prior followed by Doctor) Diverticula of colon hyperplastic polyp (1085), last colonoscopy Feb2003; to repeat screening Feb2013 Dyslipidemia Eczema ED (erectile dysfunction) prefers Cialis GERD (gastroesophageal reflux disease) prilosec in past. now controlled with diet w/ occasional use of Tums (OV 9/19/18) Gout Allopurinol Gynecomastia 2006, 2012 (hypogonadism) Hard of hearing Hypertension Hypogonadism male discussed HRT treatment in 2012 but never went on it Immunization due prevnar (2017), Shingrix and, high dose flu recommended (OV 9/19/18); Zostavax recommended (OV 8/5/09) Neck pain Uric acid kidney stone treated gout and stones w/ Allopurinol w/ good results Vertigo, central w/u neurology (2013-14) (OV 9/8/14)
Vorgeschichte: ACE-inhibitor cough Axonal neuropathy thought genetic by neurology (see Jan2014 Neurology note) (OV 9/8/14) BPH (benign prostatic hyperplasia) in past used flomax, eventually went to uroxatrol (prior followed by Dr. guth) Diverticula of colon hyperplastic polyp (1085), last colonoscopy Feb2003; to repeat screening Feb2013 Dyslipidemia Eczema ED (erectile dysfunction) prefers Cialis GERD (gastroesophageal reflux disease) prilosec in past. now controlled with diet w/ occasional use of Tums (OV 9/19/18) Gout Allopurinol Gynecomastia 2006, 2012 (hypogonadism) Hard of hearing Hypertension Hypogonadism male discussed HRT treatment in 2012 but never went on it Immunization due prevnar (2017), Shingrix and, high dose flu recommended (OV 9/19/18); Zostavax recommended (OV 8/5/09) Neck pain Uric acid kidney stone treated gout and stones w/ Allopurinol w/ good results Vertigo, central w/u neurology (2013-14) (OV 9/8/14)
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet Take 2 tablets by mouth every 8 hours as needed for Pain. 2/16/17 allopurinol (ZYLOPRIM) 300 mg tablet Take 1 tablet by mouth Daily. 2/19/21 aspirin 81 mg chewable tablet Take 81 mg by mouth Daily
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1877266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 67,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 23.09.2021
Beginn: 19.10.2021
Tage bis Beginn: 26,0
Dosis: 2
Route/Site: UN / UN

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

Acute kidney injury Anticoagulant therapy Asthenia COVID-19 Chest X-ray abnormal Chest pain Chest tube insertion Cough Death Diarrhoea Endotracheal intubation Hypotension Hypoxia Intensive care Lung opacity Mechanical ventilation Nausea Pneumonia

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/8/2021, 3/29/2021, and 9/23/2021. Patient tested for COVID at clinic on 10/19/2021 which resulted positive. Presented to ED on 10/20/2021 with complaints of cough, nausea, vomiting, diarrhea and weakness for 10 days. Admitted for acute kidney injury and requiring oxygen supplementation 3-4 L nasal cannula. Received: dexamethasone, full anticoagulation, remdesivir, broad spectrum antibiotics, paralytics, pressors, and nitric oxide. Transferred to ICU for chest pain and hypoxia. Developed pneumothorax, chest tube placed and intubated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: COVID positive 10/19/2021 and 10/20/2021; CXR: Patchy bibasilar opacities compatible with edema or pneumonia on 10/20/2021.
Aktuelle Erkrankungen: -
Vorgeschichte: Kidney transplant, allergic rhinitis, anemia, Autonomic nervous system disorder, thrombocytopenia, benign prostatic
Andere Medikamente: atorvastatin Take 1 tablet (20 mg total)by mouth daily,
Allergien: Flomax
Vorherige Impfungen: -

VAERS 1876675

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: KY
Alter: 73,0
Geschlecht: M
Eingang: 17.11.2021
Impfdatum: 20.04.2021
Beginn: 18.09.2021
Tage bis Beginn: 151,0
Dosis: 1
Route/Site: IM / -

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

Death

Symptomtext

Unsure of reason for death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic gout Tinea corpus T2DM
Vorgeschichte: Cardiovascular and Mediastinum HTN (hypertension) White coat hypertension Benign essential hypertension Endocrine DM type 2, goal A1C 7-8 Nervous and Auditory Impacted cerumen Anxiety and Depression Anxiety Other S/P cervical spinal fusion Insomnia Hyperlipidemia, mixed Vitamin D deficiency disease Arthrodesis status Dyspnea Gout Mycosis Neck pain
Andere Medikamente: albuterol (ACCUNEB) 1.25 MG/3ML nebulizer solution albuterol HFA (PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aspirin EC 325 MG tablet carvedilol (COREG) 12.5 MG tablet carvedilol (COREG) 25 MG tablet carvedilol (COREG) 25 MG tablet clo
Allergien: Hydroxyzine Valsartan
Vorherige Impfungen: -

VAERS 1850525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: 73,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 22.02.2021
Beginn: 24.09.2021
Tage bis Beginn: 214,0
Dosis: 2
Route/Site: IM / RA

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

Aspergillus test positive Atelectasis COVID-19 Chest X-ray abnormal Cough Death Dyspnoea exertional Fatigue Haemodialysis Intensive care Lung opacity Malaise Myalgia Oxygen saturation decreased Pyrexia Renal failure Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient tested positive for covid on 9/17and has been symptomatic for 2 weeks with dry cough, myalgias, subjective fevers, fatigue and dyspnea on exertion. Patient was transferred to the ED on 9/24/21 from the infusion center when noted to have O2 sat in the 80s requiring 2-4L NC. Patient was initiated on dexamethasone and remdesivir, however, his oxygen requirements have been escalating from NC to HFNC so he was transferred to the MICU. Patient foudn to have sputum culture positive for aspergillus and was started on posaconazole per ID/ Additional treatment with reeneron was provided. Patient developed renal failure and was started on CVVHD. Acute desaturation event on 10/24 requiring re-paralysis. In the setting of inability to continue with CVVHD and severe refractory respiratory failure, he was made CMO. Patient passed on 11/2/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 37,0
Labordaten: covid positive test on 10/26/21 chest x ray impression on 10/24/21: no significant interval change in left greater than right mid and lower lung peripheral predominant ill-defined airspace opacities. Mild left basilar atelectasis.
Aktuelle Erkrankungen: N/A
Vorgeschichte: NICM s/p OHT, c/c/b late graft rejection, COPD, acute on chronic CKD, anemia, hypothyroidism, HLD, HTN
Andere Medikamente: albuterol, alendronate, aspirin, azathioprine, calcium carbonate, vitamin b12, cyclobenzaprine, dapsone, doxazosin, erythomycin, famotidine, fludrocortisone, folic acid, hydrocodone-acetaminophen, levothyroxine, magnesium, metoprolol succin
Allergien: carvedilol, penicillins
Vorherige Impfungen: -

VAERS 1843372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 89,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 13.03.2021
Beginn: 30.10.2021
Tage bis Beginn: 231,0
Dosis: 1
Route/Site: SYR / LA

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

Acute respiratory failure Adenovirus test Bradycardia Choking Hypoxia Loss of consciousness Mental status changes Mycoplasma test negative Posture abnormal Respiratory viral panel Retching Unresponsive to stimuli

Symptomtext

ED to hospital. Admission: Current 10/30/2021 - present (5 days) in hospital. Acute respiratory failure with hypoxia. Hospitalist attestation: This is 89-year-old female, with past medical history of atrial fibrillation on Eliquis, diabetes mellitus, hypothyroidism, dementia and hypertension presented to ER with altered mental status and hypoxia. Patient was with her daughter last evening, while at the dinner table she slumped over the side of the chair and became unconscious. During that unresponsiveness she also had choking and gagging episode. Patient taken to the nearest fire station. Over there, her oxygen saturation was in 50s. She was bradycardic as well. EMS gave 1mg of atropine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 5,0
Labordaten: 10/30/2021. 2002 Respiratory virus detection panel. Collected: 10/30/21 2002. Final result: Specimen: Swab from nasopharynx. Adenovirus not detected. Mycoplasma pneumoniae not detected.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 18.03.2021
Beginn: 08.09.2021
Tage bis Beginn: 174,0
Dosis: 2
Route/Site: IM / -

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

Acute respiratory failure COVID-19 pneumonia Epistaxis Lactic acidosis Respiratory failure Sepsis

Symptomtext

Narrative: 77-year-old male with past medical history of hypertension, hyperlipidemia, coronary disease status post coronary artery bypass graft x3, non-insulin dependent type II diabetes mellitus, squamous cell carcinoma of the lung status post chemoradiation, and recently COVID-19. Patient was admitted from 8/16-8/29 at a local hospital for COVID-19 and discharged on 2L at rest and 4L with activity. He was admitted at the Facility on 09/08/2021 for severe sepsis and acute on chronic hypoxic respiratory failure secondary to COVID-19 pneumonia. Patient's lactic acidosis responded appropriately to IV fluids. He was treated empirically treated for hospital acquired pneumonia with cefepime, later transitioned to oral levofloxacin. Patient's oxygen requirements waxed and waned throughout admission, at one point he required 10L via high flow nasal cannula. Patient was started on 40mg prednisone, which helped his respiratory status and oxygen requirements. Patient with history of poorly controlled diabetes and blood sugars were further uncontrolled when starting steroids. Sliding scale was initiated, as well as 10U NPH when the patient took his prednisone. Of note, patient experienced epistaxis due to the nasal cannula, which improved and was resolved using nasal spray and mupirocin ointment. He was on 2.5L via nasal cannula at discharge. 6 minute walk test revealed patient requires 2L with rest and 6L with activity. He was discharged home with prednisone taper and insulin. Diabetes education provided to patient and family. Follow-up with PCP regarding insulin requirements going forward. He was discharged home in fair condition.

Weitere VAERSDATA-Felder

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

VAERS 2599936

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 22.03.2021
Beginn: 22.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Angiogram pulmonary abnormal Deep vein thrombosis Pain in extremity Pulmonary embolism

Symptomtext

Narrative: 45 year old male with PMH of bilateral ankle surgeries for deep venous insufficiency, right arm superficial thrombophlebitis, MDD, GERD, and concussions presented to the ED for bilateral lower extremity pain. Patient received both doses of Pfizer. Findings were positive for bilateral DVTs in right calf and left groin. Patient was transfered back to Facility where he was started on therapeutic lovenox, IVF, and got a CTA. CTA was positive for multiple, small right sided PEs in segmental branches. Pt was observed in the hospital for one day.

Weitere VAERSDATA-Felder

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

VAERS 1788377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 17.03.2021
Beginn: 09.08.2021
Tage bis Beginn: 145,0
Dosis: 2
Route/Site: SYR / LA

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

Abdominal pain upper Alopecia Anxiety Blood test normal Body temperature abnormal Depression Diarrhoea Dizziness Dysstasia Feeling of despair Gait disturbance Impaired work ability Insomnia Near death experience Palpitations Peripheral swelling Postural orthostatic tachycardia syndrome Stress

Symptomtext

Noticed hair loss and hand swelling between March-August 2021. On August 9, 2021, I had an overwhelming sensation that I was going to faint while walking, I also had stomach pain and diarrhea. In the following week, I was taken to the Emergency Department 4 times; my heart felt like it was racing, I got extremely lightheaded, I could not walk straight, I needed to hold on to something sturdy within my range to hold myself up, felt like I was dying. Doctors performed EKG, routine blood work and results were normal so they did not know what was wrong with me and would just give me IV fluid and discharge me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: I had blood work done for autoimmune disorders, poison testing, results would come back normal. Finally, in September 2021, a Tilt Table Test was performed on me and I was told I meet the criteria for Post Orthostatic Tachycardia Syndrome. I can't stand or walk for more than a few minutes before I get lightheaded and feel faint. I experience an adrenaline reaction, diarrhea, temperature irregularities, and insomnia. This situation is causing me stress, I am anxious, depressed, feeling hopeless. Prior to this, I was healthy, attending the gym 3 days a week, and did not suffer from any illness. I will be forced to resign from a per diem position as a pharmacy technician because I can't perform the duties (standing/walking, delivering medications throughout the hospital).
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Natures Bounty Biotin, Vitamin D3, cyanocobalamin injection once a month, Ozempic 2mg once a week.
Allergien: Allergic to raw fruits and vegetables (Alder, Birch, Ragweed) No allergies to medications
Vorherige Impfungen: -

VAERS 1788022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 15.10.2021
Impfdatum: 16.03.2021
Beginn: 07.10.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Angiogram pulmonary abnormal Arthralgia Arthritis Blood bicarbonate normal Blood gases Blood lactic acid Blood pH increased Blood potassium decreased Blood sodium decreased Chills Condition aggravated Cough Depression Diarrhoea COVID-19 COVID-19 pneumonia Chest X-ray abnormal

Symptomtext

Last updated: 10/8/2021 6:46 AM Have you tested positive for COVID-19 in the last 90 days? No Please select any symptoms you are experiencing: Fever or Chills Cough Shortness of Breath Fatigue Muscle or body aches Headache Sore throat When did symptoms start? 10/7/2021 10/08/2021 Urgent Care- Chief Complaint Patient presents with ? Sore Throat sore throat, fever, body ache, fatigue, chest tightness/burning upon inspiration x2 days Fatigue, headache, fever, bodyaches, sore throat, chest tightness, SOB, diarrhea COVID test done today Sister sick with similar symptoms COVID - COVID FULLY vaccinated ***ED to Hosp-Admission Discharged 10/10/2021 - 10/14/2021 (4 days) MD Last attending ? Treatment team Acute respiratory failure with hypoxia Principal problem Hospital Problems POA * (Principal) Acute respiratory failure with hypoxia Yes Hyperlipidemia Yes Irritable bowel syndrome, unspecified type Yes GERD (gastroesophageal reflux disease) Yes 2019 novel coronavirus-infected pneumonia (NCIP) Yes Hypokalemia Yes Hyponatremia Yes Lactic acidosis Yes Patient is an 58 y.o. female with past medical history of Hodgkin's lymphoma, OSA, hyperlipidemia, irritable bowel syndrome, neuropathy,and depression who presented to the ED for evaluation of worsening shortness of breath, dry cough, pleuritic chest pain, fatigue, nausea, and occasional vomiting. She tested positive for COVID-19 on 10/8/2021. Plan Chief Complaint Patient presents with ? Shortness of Breath 1 Acute hypoxia respiratory failure:Likely secondary to COVID-19 pneumonia. Noted in the ED SPO2 of 86% on room air.Was placed on oxygen at 4 L SPO2 currently is 94% on 4 L. CTA chest was negative for PE. However, noted infectious/inflammatory process consistent with COVID-19 pneumonia. o Continue oxygen supplementation to keep SPO2 greater than 94%. 2 COVID-19 pneumonia:CTA chest was negative for PE. However,noted infectious/inflammatory process consistent with COVID-19 pneumonia.Normal WBC, no fever, o Will check procalcitonin to determine if antibiotic is warranted. o Trend daily procalcitonin and inflammatory markers o Will initiate investigational therapy with remdesivir and Decadron, o Encourage good pulmonary hygiene with incentive spirometer, mucolytic, o Encourage out of bed to chair if feasible o DVT prophylaxis with Lovenox and GI prophylaxis with PPI. 3 Lactic acidosis, resolved.On initial presentation lactate was 3.0, current lactate is 0.7 4 Hypokalemia potassium is 3.4. o will replenish and follow-up potassium level 5 Hyponatremia, mild sodium is 133 o Encourage oral hydration. Avoid IV fluid due to COVID-19 o Follow-up with sodium level 6 Hyperlipidemia: o Continue Lipitor 20 mg p.o. daily 7 Irritable bowel syndrome: o Continue Bentyl 10 mg p.o. daily and nortriptyline 10 mg p.o. daily, uses nortriptyline off label for irritable bowel syndrome. 7 GERD: Continue PPI 8 Neuropathy: Continue gabapentin 9 Arthritis: Continue Celebrex. 10 Depression: Denies suicidal or homicidal ideations: Continue Celexa 20 mg p.o. daily Hodgkin's lymphoma, states it is in remission OSA. On supplemental oxygen, will offer CPAP if needed 1. Nutrition: Heart healthy diet 2. VTE prophylaxis: SCDs and Lovenox subcu 3. Disposition: Admit to 2 E. 4. Code Status: Full code 5. Family Doctor: withheld 6. Estimated length of stay: 2 to 3 days of hospital stays Patient is an 58 y.o. female with past medical history of Hodgkin's lymphoma, OSA, hyperlipidemia, irritable bowel syndrome, neuropathy,and depression who presented to the ED for evaluation of worsening shortness of breath, dry cough, pleuritic chest pain, fatigue, nausea, and occasional vomiting. She tested positive for COVID-19 on 10/8/2021. Patient stated that on Wednesday she started having dry cough, fever off and on, chills, past 1 day ago, fatigue, arthralgias, nausea, occasional vomiting, and worsening shortness of breath. Her symptoms started 5 or 6 days ago. She was diagnosed with COVID-19 on 10/8/2021 after she was tested for due to her symptoms. Today she states that she had worsening shortness of breath, with dyspneic, pleuritic chest pain, and worsening dry cough, due to precisely worsening dry cough, pleuritic chest pain, progressively worsening shortness of breath, she presented to the ED for evaluation. She states that she checked her pulse oximetry at home and it indicated SPO2 of 86%, her heart rate at that time was 150s. She denies GU symptoms,or lightheadedness, In the ED she was noted to have acute hypoxemic respiratory failure as it was indicated by ABG which noted pH 7.49, PCO2 32, PO2 60, bicarb 24, her SPO2 was 86% and was placed on oxygen supplementation at 4 L via nasal cannula. CTA chest was negative for PE. However, noted infectious/inflammatory process that is consistent with COVID-19. Baseline labs with CBC was unremarkable, CMP indicates sodium of 133, potassium 3.4, initial lactate level was 3.0, repeated lactate level is 0.7. Urinalysis was negative for UTI. ED treatment course. Toradol 15 mg, Solu-Medrol 125 mg and Zofran.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 10/08/2021 1445 COVID-19 (SARS CoV-2,RNA Molecular Amplification) Collected: 10/08/21 1445 | Final result | Specimen: Swab from Nasopharynx COVID-19 SARS-CoV-2 Overall Result Detected Critical 10/08/2021 1445 COVID-19 PCR Collected: 10/08/21 1445 | Final result | Specimen: Swab from Nasopharynx Pertinent Radiology Results: ECG 12-lead: HOSPITAL or TEST FACILITY Once Shortness of breath Result Date: 10/11/2021 Narrative: Test Date: 2021-10-11 Pat Name: WITHHELD Department: ED Patient ID: WITHHELD Room: ED WITHHELD Gender: Female Technician: DOB: WITHHELD Requested By: WITHHELD Order Number: WITHHELD Reading MD: Measurements Intervals Axis Rate: 70 P: 27 PR: 161 QRS: -23 QRSD: 74 T: 19 QT: 385 QTc: 417 Interpretive Statements SINUS RHYTHM BORDERLINE LEFT AXIS DEVIATION [QRS AXIS < -20] LOW QRS VOLTAGE IN PRECORDIAL LEADS [QRS DEFLECTION < 1.0 mV IN CHEST LEADS] VOLTAGE CRITERIA FOR LVH [MEETS CRITERIA IN ONE OF: R(aVL), S(V1), R(V5), R(V5/V6)+S(V1)] When compared with prior ekg: Left ventricular hypertrophy is now present Electronically Signed On 10-11-2021 7:13:26 by physician CT angiogram chest pulmonary embolism with and without contrast Result Date: 10/11/2021 Narrative: PROCEDURE INFORMATION: Exam: CTA Chest With Contrast Exam date and time: 10/10/2021 11:24 PM Age: 58 years old Clinical indication: Shortness of breath; Prior surgery; Surgery date: 6+ months; Surgery type: Breast reduction; Patient HX: HX of lymphoma with chemo and rad. Tx; Additional info: Covid SOB TECHNIQUE: Imaging protocol: Computed tomographic angiography of the chest with contrast. 3D rendering (Not supervised by radiologist): MIP and/or 3D reconstructed images were created by the technologist. Total images: 704 Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. Contrast material: OMNIPAQUE 350; Contrast volume: 100 ml; Contrast route: INTRAVENOUS (IV); COMPARISON: CR XR CHEST 2 VW 10/10/2020 2:05 AM FINDINGS: Pulmonary arteries: Pulmonary artery evaluation of good technical quality with no pulmonary artery embolism identified. Aorta: No evidence of acute injury. Lungs: Mild mosaic attenuation of the pulmonary parenchyma, suggesting mild small airway infectious/inflammatory process. Pleural spaces: Unremarkable. No pneumothorax. No pleural effusion. Heart: Unremarkable. No cardiomegaly. No pericardial effusion. Lymph nodes: Unremarkable. No enlarged lymph nodes. Bones/joints: Moderate degenerative changes of the left shoulder are noted. Thoracic spondylosis is present. Soft tissues: Unremarkable. IMPRESSION: 1. No pulmonary artery embolism identified. 2. Mild mosaic attenuation of the pulmonary parenchyma, suggesting mild small airway infectious/inflammatory process. THIS DOCUMENT HAS BEEN ELECTRONICALLY SIGNED BY MD
Aktuelle Erkrankungen: -
Vorgeschichte: Rectal pain RLQ abdominal pain Other chest pain Radiculitis, lumbosacral Iliotibial band syndrome of right side Greater trochanteric bursitis, right Carpal tunnel syndrome, left Posterior vitreous detachment Respiratory Obstructive sleep apnea of adult Acute respiratory failure with hypoxia 2019 novel coronavirus-infected pneumonia (NCIP) Circulatory Thrombosed external hemorrhoid Digestive GERD (gastroesophageal reflux disease) Irritable bowel syndrome, unspecified type Musculoskeletal Ganglion of foot, left Spondylosis, lumbosacral Primary osteoarthritis of first carpometacarpal joint of left hand Primary osteoarthritis of left shoulder Endocrine/Metabolic Hyperlipidemia Thyroid nodule Hypokalemia Hyponatremia Lactic acidosis Other Depression Postop check S/P laparoscopy Family hx colonic polyps Family history of colon cancer Special screening for malignant neoplasms, colon Family history of colonic polyps Anxiety Dry eyes Fatigue Status post surgery
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler atorvastatin (LIPITOR) 20 mg tablet calcium carbonate-vitamin D3 1250 mg, 500 mg calcium,-5 mcg (HI-CAL PLUS VIT D) 1250 mg (500 mg calcium
Allergien: Adhesive Tape-siliconesOther (document details in comments) ErythromycinDiarrhea VancomycinOther (document details in comments)
Vorherige Impfungen: -

VAERS 1786670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 68,0
Geschlecht: F
Eingang: 14.10.2021
Impfdatum: 11.03.2021
Beginn: 04.10.2021
Tage bis Beginn: 207,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Adenovirus test Asthenia Back pain Blood culture Blood lactic acid Bordetella test negative Chest X-ray normal Chlamydia test negative Constipation Cough Diarrhoea Dyspnoea Electrocardiogram normal Enterovirus test negative Exposure to SARS-CoV-2 Fatigue Haematocrit normal

Symptomtext

ED to Hosp-Admission Discharged 10/10/2021 - 10/13/2021 (3 days) COVID-19 Principal problem Hospital Problems POA * (Principal) COVID-19 Yes Essential hypertension Yes Gastroesophageal reflux disease Yes Hospital Course Per Initial HPI By CRNP: patient is an 69 y.o. female who presented to the emergency department with cough, congestion, body aches, weakness, nausea and shortness of breath. She began with symptoms approximately 5 days ago. Both her mother and stepfather are admitted to the hospital for COVID-19. She had a negative Covid test a few days ago, but had increasing shortness of breath. Hospitalist was consulted for admission. On examination today she was resting comfortably in bed. She states for the last five days she had increased shortness of breath and a dry unproductive cough that is getting worse. Shewas tested on Monday for COVID-19 which was negative. Her mother was evaluated by the primary care provider on Wednesday, tested positive and was admitted to the hospital. She reports having chest pain, but most likely musculoskeletal in nature with the cough. She denies any abdominal pain, has had episodes of nausea without any vomiting. She had diarrhea since Friday, but has not had any bowel movement today. She denies any urinary issues. She is vaccinated for COVID-19. On presentation to the emergency department she underwent a chest x-ray which showed no acute pulmonary, pericardial or vascular process suspected. There is no acute pleural process identified. Initial lab study showed normal WBC 6.0, hemoglobin and hematocrit of 13.7 and 43.1 respectfully, all other lab studies have been within normal limits. The cardiac biomarker was negative and lactate was 1.7. Blood cultures are pending. The EKG showed normal sinus rhythm at a rate of 85 bpm with no acute ST changes. She was treated with IV fluids, IV Zosyn, IV Toradol and started on IV dexamethasone 10 mg daily. The initial systolic blood pressure was 109/70 mmHg with a heart rate of 98 bpm with a pulse oximetry of 96% on room air. On reexamination pulse oximetry dipped to 89% on room air and she was placed on supplemental oxygen at 2 L/minute. The most recent systolic blood pressure was 107/56 mmHg with a heart rate is 70 bpm and a pulse oximetry of 99% on 2 L/minute. She denies any lightheadedness or dizziness. She is resting comfortably, offers no complaints and will be admitted for further evaluation and treatment Hospital Course: During the patient brief facility stay, patient was started on supplemental oxygen, IV remdesivir, she was also started on IV Decadron. Patient shows great improvement and was weaned off supplemental oxygen. Patient's cough was treated with Mucinex and Tessalon as needed. Patient showed great improvement, so much so that she requested to be discharged. Patient upon discharge, patient denies nausea, vomiting, diarrhea, chest pain, shortness of breath, Chills, rigors, fever, hematemesis, hematochezia, difficulty urinating, hematuria, and difficulty breathing.. Patient encouraged to follow-up with PCP, she is also to take Decadron 6 mg by mouth for 7 days, she is to follow-up with the remote monitoring program. She has been asked to come back to the hospital emergency room if she develop any worsening condition including elevated temperature difficulty breathing and chest pain. Patient evaluated for discharge and was considered stable enough for discharge patient discharged in stable condition with discharge instruction including instruction for follow-up. Patient and caregiver verbalizes understanding of discharge instruction all of patient questions were answered satisfactorily. Case discussed with my collaborating physician who agrees with the assessment and discharge plan Discharge Instruction Follow-up with your PCP Resume all your medication as prescribed Take Decadron 6 mg p.o. daily for 7 days Follow all the Covid precautions including high wash, mass, isolation Follow-up with the remote monitoring program If your condition worsen please report to the hospital ED for further evaluation Medical Problems Plan: Acute respiratory failure with hypoxia most likely secondary to COVID-19: Begin dexamethasone 6 mg IV daily for total of 10days first dose 10/10/2021. Begin remdesivir 200 mg IV x1 followed by 100 mg IV x4 days. Medication started 10/10/2021 Add Mucinex 600 mg 1 tablet twice daily Continue nasal cannula oxygen to maintain pulse oximetry greater than 92% Encourage incentive spirometer and self proning Continue isolation precautions Essential hypertension: Controlled continue current home medications Disposition: Follow labs in a.m. Obtain procalcitonin if elevated will consider antibiotic therapy. Leukocytosis normal low-grade fever Continue all current home medication DC IV fluids Out of bed to chair Patient will be admitted inpatient to the medical surgical floor. Expected length of stay 2 to 4 days This admission was discussed with my collaborator VTE prophylaxis: Lovenox Full Code History of Present Illness Chief Complaint Patient presents with ? Nausea ? Headache ? Cough Patient is an 69 y.o. female who presented to the emergency department with cough, congestion, body aches, weakness, nausea and shortness of breath. She began with symptoms approximately 5 days ago. Both her mother and stepfather are admitted to the hospital for COVID-19. She had a negative Covid test a few days ago, but had increasing shortness of breath. Hospitalist was consulted for admission. On examination today she was resting comfortably in bed. She states for the last five days she had increased shortness of breath and a dry unproductive cough that is getting worse. Shewas tested on Monday for COVID-19 which was negative. Her mother was evaluated by the primary care provider on Wednesday, tested positive and was admitted to the hospital. She reports having chest pain, but most likely musculoskeletal in nature with the cough. She denies any abdominal pain, has had episodes of nausea without any vomiting. She had diarrhea since Friday, but has not had any bowel movement today. She denies any urinary issues. She is vaccinated for COVID-19. On presentation to the emergency department she underwent a chest x-ray which showed no acute pulmonary, pericardial or vascular process suspected. There is no acute pleural process identified. Initial lab study showed normal WBC 6.0, hemoglobin and hematocrit of 13.7 and 43.1 respectfully, all other lab studies have been within normal limits. The cardiac biomarker was negative and lactate was 1.7. Blood cultures are pending. The EKG showed normal sinus rhythm at a rate of 85 bpm with no acute ST changes. She was treated with IV fluids, IV Zosyn, IV Toradol and started on IV dexamethasone 10 mg daily. The initial systolic blood pressure was 109/70 mmHg with a heart rate of 98 bpm with a pulse oximetry of 96% on room air. On reexamination pulse oximetry dipped to 89% on room air and she was placed on supplemental oxygen at 2 L/minute. The most recent systolic blood pressure was 107/56 mmHg with a heart rate is 70 bpm and a pulse oximetry of 99% on 2 L/minute. She denies any lightheadedness or dizziness. She is resting comfortably, offers no complaints and will be admitted for further evaluation and treatment. Review of Systems Constitutional: Positive for fatigue. Negative for chills and fever. HENT: Positive for congestion. Negative for trouble swallowing. Respiratory: Positive for cough and shortness of breath. Negative for chest tightness. Cardiovascular: Positive for chest pain. Gastrointestinal: Positive for nausea. Negative for abdominal pain, diarrhea and vomiting. Genitourinary: Negative for difficulty urinating, flank pain and frequency. Musculoskeletal: Positive for back pain. Negative for neck pain. Skin: Negative for rash. Neurological: Negative for dizziness, weakness and light-headedness. Psychiatric/Behavioral: The patient is not nervous/anxious. All other systems reviewed and are negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: 10/10/2021 1215 Respiratory virus detection panel Collected: 10/10/21 1215 | 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 Resulted: 10/10/21 1326 Order Status: Completed Updated: 10/10/21 1326 Narrative: XR CHEST 1 VW PORT IMPRESSION: No acute cardiopulmonary process END OF IMPRESSION: INDICATION: Chest pain. TECHNIQUE: Portable COMPARISON: CXR 10/31/2020 FINDINGS: There is no acute pulmonary, parenchymal, or vascular process suspected. The cardiac size and configuration are unremarkable. No hilar or mediastinal abnormality is suspected. No active pleural process is identified . Osseous structures normal.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Chest pain Respiratory Allergic rhinitis Circulatory Essential hypertension Coronary arteriosclerosis Digestive Gastroesophageal reflux disease Musculoskeletal Osteoarthritis Primary osteoarthritis involving multiple joints Age-related osteoporosis without current pathological fracture Endocrine/Metabolic Hyperlipidemia Dyslipidemia Infectious/Inflammatory COVID-19 Other Abnormal results of cardiovascular function studies Anxiety Premenstrual tension syndrome
Andere Medikamente: alendronate (FOSAMAX) 70 mg tablet aspirin 81 mg tablet dexAMETHasone (DECADRON) 6 mg tablet esomeprazole (NexIUM) 40 mg capsule guaiFENesin (MUCINEX) 600 mg 12 hr tablet latanoprost (XALATAN) 0.005 % ophthalmic solution meloxicam (MO
Allergien: PenicillinsHives / Urticaria, Rash Hydrocodone Bitartrate Other AzithromycinRash NitroglycerinHeadaches OxycodoneNausea and Vomiting Propoxyphene NapsylateNausea and Vomiting Sulfa (Sulfonamide Antibiotics)Rash
Vorherige Impfungen: -

VAERS 1782749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MT
Alter: 76,0
Geschlecht: F
Eingang: 13.10.2021
Impfdatum: 24.02.2021
Beginn: 07.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / LA

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

Atrial fibrillation Biopsy Cardiac function test Cardiac therapeutic procedure Cerebrovascular accident Facial paralysis Grip strength decreased Implantable cardiac monitor insertion Platelet count normal Tachycardia

Symptomtext

It occurred on 03/07/2021, I did not feel like I had any symptoms, but I noticed whenever I picked up anything with my left hand I would drop it quickly. I drove to my sister's. They said my face was droopy. They suggested we go to the hospital. We went and they did a heart test. It showed I had a stroke. I was there overnight and then they dismissed me. From then, I have been going to doctors because I developed tachycardia and I had to have a procedure for that. Then I developed atrial fibrillation. They put on a chip recorder in my chest because they were not sure how the stroke occurred. That has been there since March. They also did a platelets test which was negative, they also did a biopsy, but I do not know the results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 1,0
Labordaten: Heart test, stroke. Platelets test, negative. Biopsy, I do not know the results
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Vitamin D; blood pressure medication
Allergien: MSG; sulfites
Vorherige Impfungen: -

VAERS 1782687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

kritisch

Staat: MO
Alter: 87,0
Geschlecht: M
Eingang: 13.10.2021
Impfdatum: 17.03.2021
Beginn: 13.09.2021
Tage bis Beginn: 180,0
Dosis: 1
Route/Site: IM / AR

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

Death Intensive care

Symptomtext

admitted to Hospital 9/13/2021 directly to ICU. No interview was done. At last communication on 9/23/2021, hospital said he was still in the ICU. Passed away on 9/24/2021

Weitere VAERSDATA-Felder

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

VAERS 1776983

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

kritisch

Staat: MO
Alter: 77,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 13.03.2021
Beginn: 28.09.2021
Tage bis Beginn: 199,0
Dosis: 1
Route/Site: IM / AR

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

COVID-19 Coronary artery bypass Myocardial infarction SARS-CoV-2 test positive

Symptomtext

heart attack 9/28 and admitted to hospital. Tested (+) on 9/28.. Had a coronary artery bypass surgery on 10/09/2021. Still admitted as of 10/11/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1769002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 83,0
Geschlecht: M
Eingang: 07.10.2021
Impfdatum: 06.04.2021
Beginn: 10.09.2021
Tage bis Beginn: 157,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Death Decreased appetite Dyspnoea Hypoxia Inappropriate schedule of product administration Nausea Productive cough Respiratory failure SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/9/2021 and 4/6/2021. Presented to the ED on 9/24/2021 reports that over the past 2 weeks, he has had a productive cough, nausea, loss of appetite, and progressivley worsening SOB leading to EMS call. Pt tested positive for COVID, on arrival. He was satting 92% on 10L NRB; hypoxia progressed and pt was transition to HFNC 50/50. He was admitted and ended up requiring max HF settings, developing respiratory failure. Decision made to transfer to comfort care, patient expired on 10/3/2021

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Positive COVID-19 test on 9/24/2021 using the Cepheid GeneXpert platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Anemia, BPH, Cardiac pacemaker, Carotid artery stenosis, chronic pain, CAD, Hypertension, H/O focal seizure, arthritis, GERD, H/O colon polyps, H/O GI Bleed, H/O nephrolithiasis, H/O rickets, H/O TIA, H/O Vertebral compression fraction, Hyperlipidemia, Lesion of bladder, Paroxysmal atrial fibrillation, peripheral vascular disease.
Andere Medikamente: Alendronate 70 mg QWeek, Atorvastatin 40 mg QD, Calcium carbonate 500 mg BID, Vitamin D3 600 units BID, Clopidogrel 75 mg QD, Diclofenac gel QID, Eliquis 5 mg BID, Fosinopril 10 mg QD, Metoprolol 150 mg QD, Fish Oil QD, Pantoprazole 40 mg Q
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1768407

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: 63,0
Geschlecht: F
Eingang: 07.10.2021
Impfdatum: 20.02.2021
Beginn: 03.08.2021
Tage bis Beginn: 164,0
Dosis: 2
Route/Site: IM / LA

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

Acute respiratory distress syndrome COVID-19 Condition aggravated Death Dyspnoea exertional Endotracheal intubation Enterococcal infection Exposure to SARS-CoV-2 Fungal disease carrier Hypoxia Intensive care Lung assist device therapy Lung transplant rejection Pneumonia pneumococcal Respiratory depression SARS-CoV-2 test positive Sepsis Traumatic lung injury

Symptomtext

63 y.o. female patient with PMHx of COPD s/p bilateral lung transplant (CMV D+/R+, EBV D+/R+, Toxo D-/R-) from an increased risk donor on 6/14/18 who was HCV NAT+/Ab+ as well as HBcAb+ and history of acute transplant rejection who presented to ED for dyspnea on exertion for two days. She was found to have had exposure to close contact with Covid 19 infection. She was previously vaccinated for COVID; admitted 8/1/2021 with confirmed COVID-19. Respiratory status has been worsening, requiring higher oxygen suppor, thus she was transferred to the MICU. At a local hospital, she was started on HFNC and then intubated for increasing/worsening hypoxia. ICU course complicated by need for ECMO cannulation with ARDS, sepsis from E.faecalis UTI and strep pneumoniae PNA ISO aspergillus colonization, and acute bilateral lung transplant rejection. Overall burden of lung injury felt to be not survivable, so her family made the decision for CMO on 9/12/21. VV ECMO support discontinued at 12:35 PM on 9/12/2021 and time of death was 1:05 PM on 9/12/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 42,0
Labordaten: 8/1/21 - COVID+ PCR
Aktuelle Erkrankungen: unknown.
Vorgeschichte: COPD, GERD, seasonal allergies, weight loss, anxiety, renal insufficiency, osteopenia, b/l lung transplant.
Andere Medikamente: mycophenolae, amlodipine, MVI, pepcid, iron, flonase, mag ox, reglan, prednisone, sertraline, simethicone, sodium bicarb, bactrim tacrolimus
Allergien: Benadrul, mold, peanut, apricot, red dye
Vorherige Impfungen: -

VAERS 1764984

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: KY
Alter: 81,0
Geschlecht: F
Eingang: 06.10.2021
Impfdatum: 03.03.2021
Beginn: 21.08.2021
Tage bis Beginn: 171,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory distress syndrome Acute respiratory failure Angiogram pulmonary abnormal Anticoagulant therapy COVID-19 Diarrhoea Dyspnoea Emphysema Endotracheal intubation Intensive care Lung disorder Lung opacity Mechanical ventilation Oxygen saturation decreased SARS-CoV-2 test positive

Symptomtext

81 y.o. female with PAD s/p aortobifem bypass, Atrial fibrillation on xarelto who presents to Medical Center with COVID19. Spoke with patient and daughter briefly at bedside prior to emergent intubation. Patient and daughter report that patient tested positive for COVID19 about 10 days ago. Patient has been at home on nasal cannula. Patient reports that today she felt as though she could not breathe. Daughter reports that saturations had dropped at home. Patient reports that otherwise she has felt ok in the last ten days, has had diarrhea that has been bothering her more in the last few days prior to presentation. Of note patient is vaccinated with Pfizer. In the emergency room, patient was requiring HFNC. CTPE showed no pulmonary embolism and moderate bilateral airspace disease consistent with COVID19. Patient also has advanced emphysema. She has a past medical history of CHF (congestive heart failure), Chronic renal failure, Compression fracture of fourth lumbar vertebra with routine healing (11/2020), COPD (chronic obstructive pulmonary disease), Hyperlipidemia, unspecified, Hypertensive heart disease without congestive heart failure, PAD (peripheral artery disease), and Personal history of other diseases of the digestive system. #Acute Hypoxic Respiratory failure secondary to COVID19 infection - Patient's CTPE negative of PE, did show bilateral GGO c/w COVID and some concern for underlying lung disease. No concern for concurrent bacterial pneumonia. PLAN - DEXA ARDS started 8/23 - a.m. gas was borderline requiring proning- will reevaluate this afternoon - Ongoing ICU level care given hypoxic respiratory failure #Acute Hypoxic Respiratory failure secondary to COVID19 infection- worsened - Required increased PEEP for recruitment, paralytic, and increasing to FiO2 100% overnight. This a.m. remains hypoxic despite being on 100% FiO2. Differential includes PE, pneumonia, progression of COVID19 infection. Initially started antibiotics, however as goals are now to keep the patient alive until family arrives, are minimizing treatment to only what is sustaining her life for the next 24 hours. PLAN - Continue steroids - Not proning due to multiple comorbidity and poor prognosis - Cont vent settings. - Heparin drip for possible PE, will not pursue imaging to confirm Patient was unable to be weaned down on her ventilator settings despite dexamethasone and attempts to optimize patient's fluid status. Patient's family elected to have no escalation of care on 8/28, and ultimately decided on comfort care with terminal extubation on 8/30.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: COVID-19 PCR positive on 08/21/21
Aktuelle Erkrankungen: N/A
Vorgeschichte: PMH includes CHF (congestive heart failure), Chronic renal failure, Compression fracture of fourth lumbar vertebra with routine healing (11/2020), COPD (chronic obstructive pulmonary disease), Hyperlipidemia, unspecified, Hypertensive heart disease without congestive heart failure, PAD (peripheral artery disease), and Personal history of other diseases of the digestive system.
Andere Medikamente: albuterol atorvastatin budesonide-formoterol calcitonin cefadroxil docusate furosemide hydrocodone-acetaminophen levothyroxine loratadine-pseudoephedine metoprolol tartrate pantoprazole rivaroxaban
Allergien: Chlorhexidine Chlorhexidine Itching Medium Allergy 1/29/2018 Oxycodone-acetaminophen Oxycodone-acetaminophen Itching Medium Allergy 1/27/2018 Cephalexin Unknown reaction Low Allergy 3/7/2016 Doxycycline Unknown reaction Low Allergy 3/7/2016 Nafcillin Nafcillin Unknown reaction Low Allergy 3/7/2016
Vorherige Impfungen: -

VAERS 1759146

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 88,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 28.02.2021
Beginn: 19.09.2021
Tage bis Beginn: 203,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal pain Acute respiratory failure Adenovirus test Ageusia Anaemia Anion gap Anosmia Arthralgia Asthma Atrial fibrillation Blood glucose normal Blood lactate dehydrogenase Blood sodium decreased Blood urea nitrogen/creatinine ratio Bordetella test negative C-reactive protein COVID-19 Chest pain

Symptomtext

ED to Hosp-Admission Current 9/19/2021 - present (15 days) Hospital MD Last attending ? Treatment team COVID-19 Principal problem Assessment and Plan Patient is a 89 y.o. female with significant PMHx of paroxysmal atrial fibrillation, aortic stenosis status post TAVR, mitral valve stenosis, coronary artery disease status post PCI of the diagonal 6/2020, essential hypertension, chronic heart failure with preserved ejection fraction, chronic kidney disease stage III, history of TIAs presents to Hospital on 9/19/2021 with complaints of shortness of breath and cough. Medical Problems Hospital Problems POA * (Principal) COVID-19 Yes Atrial fibrillation Yes Acute on chronic respiratory failure Yes COVID 19 Acute on chronic respiratory failure chronically on 2 L with exertion currently on 4 L at rest Mild intermittent asthma o D-dimer, procal, LDH, ferritin and CRP pending o Patient follows with pulmonary outpatient, CT chest in September 2021 showed groundglass nodule o Pulmonary function test revealed mild obstructive airway disease patient was initiated on Breo and albuterol o Patient initiated on dexamethasone, end date 9/29 o Patient she did on remdesivir, and date 9/23 o Plasma ordered after consent was obtained Atrial fibrillation with rapid ventricular response, now rate controlled Chronic paroxysmal atrial fibrillation CHA2DS2-VASc score of 5 o Currently on anticoagulation with Eliquis 2.5 mg twice daily Mild hyponatremia, continue to monitor Aortic stenosis status post TAVR 8/2020 Mitral valve stenosis Coronary artery disease status post PCI of the diagonal 6/2020 o It appears that at some point patient's Plavix was discontinued, and has been resumed at this time. Essential hypertension, continue home antihypertensives with hold parameters Chronic heart failure with preserved ejection fraction, continue Lasix Chronic kidney disease stage III, creatinine currently at baseline History of TIAs, continue Plavix and statin Vitamin D deficiency B12 deficiency o Continue supplementation Nutrition: heart healthy VTE prophylaxis: Eliquis Code Status: Full Code Disposition: pending clinical improvement Patient is a 89 y.o. female with significant PMHx of paroxysmal atrial fibrillation, aortic stenosis status post TAVR, mitral valve stenosis, coronary artery disease status post PCI of the diagonal 6/2020, essential hypertension, chronic heart failure with preserved ejection fraction, chronic kidney disease stage III, history of TIAs presents to Hospital on 9/19/2021 with complaints of shortness of breath and cough. Patient was discharged from the hospital last Wednesday 9/15 for symptomatic anemia. the day after her discharge she was doing well. On 9/17 she started to have episodes of a non-productive coughing that started to get progressively worse. She started to become more short of breath even just moving would make her feel out of breath when normally she is able to walk from one side of the house to the other side without issues. She fevers, chills, headaches, arthalgias/myagias, loss of taste/smell, chest pain, abdominal pain. She has been having nausea but no vomiting. She has had loss of appetite. She is vaccinated. In the Emergency Department, vital signs temperature 36.8, heart rate 138, respiratory rate 20, blood pressure 107/68, SPO2 92% on 4 L oxygen. Lab work was remarkable for an H/H of 8.3/25.8, sodium 132, anion gap 12, BUN/creatinine of 34/1.67, glucose of 161, troponin of 0.11. Respiratory viral panel was positive for COVID-19. Initial EKG showed patient was in atrial fibrillation with rapid ventricular response. She was given metoprolol 5 mg once and a 500 cc bolus of normal saline with improvement in her heart rate. She was also given 1 dose of dexamethasone. Hospitalist team was consulted for admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 15,0
Labordaten: 09/19/21 1506 Respiratory virus detection panel Collected: 09/19/21 1408 | 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
Aktuelle Erkrankungen: -
Vorgeschichte: Non-Hospital Asthma Carotid artery stenosis Chronic constipation Hypercholesterolemia Hypertensive heart disease Ischemic stroke Left ventricular outflow tract obstruction Migraine with aura Nonrheumatic aortic (valve) stenosis Osteoarthritis Osteoporosis Primary localized osteoarthrosis of the knee TIA (transient ischemic attack) Vaginal lump VSD (ventricular septal defect) Shortness of breath Mitral valve stenosis Coronary artery disease involving native heart with angina pectoris Vascular dementia, uncomplicated Leukoariosis Coronary artery disease involving native heart with angina pectoris, unspecified vessel or lesion type Aortic valve stenosis, etiology of cardiac valve disease unspecified V-tach Epistaxis CAD (coronary artery disease) History of recurrent TIAs Pulmonary nodule less than 1 cm in diameter with low risk for malignant neoplasm Ground glass opacity present on imaging of lung
Andere Medikamente: Outpatient Medications albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler apixaban (ELIQUIS) 2.5 mg tablet calcium carbonate (CALCIUM 600 ORAL) cholecalciferol, vitamin D3, (VITAMIN D3 ORAL) colesevelam (WELCHOL) 625 mg tablet
Allergien: Sulfa (Sulfonamide Antibiotics) PenicillinsOther (document details in comments) RamiprilOther (document details in comments)
Vorherige Impfungen: -

VAERS 1752112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 01.10.2021
Impfdatum: 08.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / LA

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

Myocardial infarction SARS-CoV-2 test Transient ischaemic attack

Symptomtext

2 TIA; Heart attack; This is a spontaneous report from a contactable consumer (patient). A 52-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in the left arm on 08Mar2021 at 08:00 AM (Batch/Lot Number: EN6203) (at the age of 52-year-old) as dose 1, single, and via an unspecified route of administration, administered in the left arm on 2021 (Batch/Lot Number: ER8730) ((at the age of 52-year-old) as dose 2, single for COVID-19 immunization. Facility where the most recent COVID-19 vaccine was administered: Other. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no COVID prior to vaccination. Medical history included high blood pressure (BP), high cholesterol, and allergy to bee stings. Concomitant medications included blood pressure medication and cholesterol medication. On an unspecified date in 2021, the patient experienced 2 TIA (transient ischemic attack) heart attack, which resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, and hospitalization. The patient was hospitalized for 2 days. The patient was tested for COVID post vaccination which was a nasal swab with negative result in 2021. Therapeutic measures were taken as a result of the events which included stents, follow up appointments with multiple doctors. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: Test Date: 2021; Test Name: COVID test type post vaccination: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to bee sting (Known allergies: Bee stings); Blood pressure high (High BP); High cholesterol
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1730469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CO
Alter: 66,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 26.02.2021
Beginn: 26.06.2021
Tage bis Beginn: 120,0
Dosis: 2
Route/Site: - / LA

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

Computerised tomogram thorax Pain Pulmonary embolism Ultrasound biliary tract Ultrasound kidney Ultrasound liver Ultrasound spleen

Symptomtext

she had severe pain on the right side under her ribs around that side and up her back; experienced a bilateral pulmonary embolism infarction; This is a spontaneous report from a contactable consumer (patient herself). A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in the left arm on 26Feb2021 at 11:00 (Lot Number: EN6203) as DOSE 2, SINGLE (age at vaccination was 66 years old) for covid-19 immunization. The patient had no medical history. The patient's concomitant medications were not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in the left arm on 05Feb2021 at 11:00 (Lot Number: EN9581) as DOSE 1, SINGLE for covid-19 immunization. She stated she doesn't do vaccines other than childhood and DPT that was 6 years ago with no side effects. No additional vaccines were administered on same date of the Pfizer suspect. No prior vaccinations (within 4 weeks). On 26Jun2021, 4 months after the second vaccine, she had severe pain on the right side under her ribs around that side and up her back and experienced a bilateral pulmonary embolism infarction after the Pfizer Covid vaccine. Patient was taken directly to the ER as she had severe pain on the right side under her ribs around that side and up her back. Patient relays she was hospitalized on 26Jun2021 at 8:30am and released 27Jul2021. She states she was diagnosed on 26Jun2021 and is improving and is on blood thinners, Xarelto 20mg daily orally and she started taking that on 27Jun2021, the day she was released from the hospital. Patient states another important piece of information is while she was in the hospital, her name is withheld and she was linking the vaccine to the blood clot. States she is a hospitalist at withheld and Pfizer has her permission to contact her as needed. She states she is wondering, she starts the process and gets issued a case number to track and follow and see if there is any help with payment for the medication, she is on blood thinners. Patient states she is scheduled for an echocardiogram on 27Sep2021, 2 weeks from the date of this report because they saw an enlargement of her heart. She states they turned her inside out. States she had Ultrasounds of her kidney, liver, spleen, and gallbladder. That it took 9 hours to figure out what this was and put her through the ringer. States she had a CT scan of her lungs which showed the embolism. States all these tests were done on 26Jun2021. The patient underwent lab tests and procedures which included computerised tomogram thorax: showed the embolism on 26Jun2021, ultrasound biliary tract, ultrasound kidney, ultrasound liver and ultrasound spleen, all had unknown results on 26Jun2021. Therapeutic measures were taken as a result for severe pain on the right side under her ribs around that side and up her back (pain) and bilateral pulmonary embolism infarction (pulmonary embolism). The outcome of both the events was resolving at the time of this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: Test Date: 20210626; Test Name: CT scan lungs; Result Unstructured Data: Test Result:showed the embolism; Test Date: 20210626; Test Name: Ultrasound gallbladder; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210626; Test Name: Ultrasound kidney; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210626; Test Name: Ultrasound liver; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210626; Test Name: Ultrasound spleen; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1714282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 81,0
Geschlecht: M
Eingang: 19.09.2021
Impfdatum: 24.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

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

Antibody test Biopsy liver abnormal Bladder cancer Bladder catheter temporary Blood creatine increased Blood test Blood urea increased Chest X-ray abnormal Computerised tomogram abnormal Condition aggravated Cystoscopy normal Death Dyspnoea Fatigue Flank pain Haematuria Haemorrhage urinary tract Hepatic lesion

Symptomtext

Received Pfizer 2/24, 24 hours later buttocks cheeks hurt, flank pain started and within 7 days, urinating blood, general feeling unwell, clots became so large they ultimately blocked urine flow completely. Went to ER 3/8, creatine was elevated, did a cat scan which showed enlarged lymph nodes attributed to vaccine hospital said and otherwise unremarkable. Hospital, through a catheter did and aggressive bladder flush and was put on morphine, flushed for 48 hours then had drops in oxygen and labored breathing, x ray showed fluid in lungs, diagnosed with hospital acquired pneumonia from the flush, once on antibiotics and creatine/ bun stabilized, was released. Clots returned in 3-4 days, went to urologist for scope, unremarkable, no invasion of bladder cancer through the wall, recommends another cat scan (3.5 weeks after previous scan ) scan showed enlarged lymph nodes and some liver lesions, recommend biopsy of liver and lymph nodes and kidney scan, both are scheduled. Blot clots get worse, end up in ER 4/18, elevated creatine and bun, urologist tried to do ureter stents, ureters blocked so bilateral nephrostomy tubes were put in. Liver biopsy done 4/20. Dad was stabilized and released with no biopsy results until 4/27, metastatic bladder cancer diagnosis. Oncologist put dad on Keytruda once every 3 weeks. Dad has been feeling unwell since his 1st vaccine, never got the 2nd due to all of these complications. Dad ends up back in hospital on 6/21 with general unwell feeling, fatigue, cat scan shows further progression and because of an error a resident did a cat scan with dye which then added contrast induced nephropathy to the issues. Dad passed away on Wednesday, July 21st at 6:45pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 6,0
Labordaten: Cat Scan 3/8, 4/2 Kidney scan 4/5 Cat Scan 6/21 Plethora of blood work throughout hospital stays Antibody check from vaccine on 4/6- lower antibody levels compared to spouse
Aktuelle Erkrankungen: -
Vorgeschichte: Coronary artery disease Non invasive low grade bladder cancer (under control for 12 years with regular Turbts and BCG )
Andere Medikamente: plavix
Allergien: penecillin
Vorherige Impfungen: -

VAERS 1708464

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: UT
Alter: 66,0
Geschlecht: M
Eingang: 17.09.2021
Impfdatum: 26.02.2021
Beginn: 16.05.2021
Tage bis Beginn: 79,0
Dosis: 2
Route/Site: SYR / LA

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

Pulmonary embolism

Symptomtext

Submassive Pulmonary Embolism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 4,0
Labordaten: Multiple
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetic, HBP
Andere Medikamente: Metformin, Atorvastatin, Amlodopine, Losartan
Allergien: none
Vorherige Impfungen: -

VAERS 1708406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 47,0
Geschlecht: M
Eingang: 17.09.2021
Impfdatum: 30.03.2021
Beginn: 31.07.2021
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Cough Death

Symptomtext

Patient was fully vaccinated. he PUI says that the only symptom that he has had was a cough. The PUI is currently in the hospital but it is not covid related. Patient died due to COVID-19 on 8/30/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 25,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, Hypertension, Immunosuppressive condition
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1700472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 71,0
Geschlecht: F
Eingang: 15.09.2021
Impfdatum: 05.03.2021
Beginn: 11.09.2021
Tage bis Beginn: 190,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Adenovirus test Asthenia Bone disorder Bordetella test negative Condition aggravated Coronavirus test negative Dyspnoea Enterovirus test negative Haematuria COVID-19 Chest X-ray abnormal Chlamydia test negative Chronic obstructive pulmonary disease Chronic respiratory failure Human metapneumovirus test Human rhinovirus test Hypoxia

Symptomtext

ED to Hosp-Admission Current 9/11/2021 - present (4 days) l DETAILS OF HOSPITAL STAY Presenting Problem/History of Present Illness/Reason for Admission COPD exacerbation (CMS/HCC) [J44.1] COVID-19 virus infection [U07.1] HPI Pt is an 71 y.o. female. with Past medical COPD, chronic respiratory failure on 3 L of oxygen, seizure, A. fib, not anticoagulation due to hematuria, came to emergency room due to generalized weakness and hypoxia. As per patient and daughter over the phone, patient had Covid positive family members visiting on Monday, today when daughter checked patient oxygen it was in low 80s, then patient was on 3 L, oxygen was increased to 4 L, was improvement to low 90s. Given patient significant history of COPD, she was brought to emergency room. Lab work in the emergency room unremarkable, no significant changes from previous values. Urine significant for hematuria, negative procalcitonin. Vital tests positive for COVID-19 Patient seen and examined bedside, in mild respiratory distress. Hospital Course Patient was admitted to med surgical floor with acute on chronic hypoxic respiratory failure secondary to COVID-19 infection. Her oxygen requirement at home is 3 L she was requiring up to 4 L with diffuse wheezing bilaterally. She was started on remdesivir as well as Decadron. Her oxygenation requirement came down to 3 L. She is back to her baseline and will be discharged home today. She has completed 5 doses of remdesivir Discharge instructions Patient strictly follow with her primary care provider in 1 week She will take 5 more days of dexamethasone 6 mg and then she can go back to her prednisone 10 mg daily

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 4,0
Labordaten: 09/11/21 2306 Respiratory virus detection panel Collected: 09/11/21 2124 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory 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 [3302504541] Resulted: 09/12/21 1118 Order Status: Completed Updated: 09/12/21 1118 Narrative: XR CHEST 1 VW PORT IMPRESSION: There are no acute-appearing findings. END OF IMPRESSION: INDICATION: shortness of breath sob. TECHNIQUE: Frontal view of the chest was obtained. COMPARISON: X-ray of August 14, 2021 FINDINGS: Bilateral airspace opacities and a right pleural effusion have resolved. There are no consolidations, pulmonary edema or pleural effusions. The heart size is normal.The patient is rotated. Periaortic calcification is seen. There are overlying leads and wires. There are nonspecific coarse interstitial markings. Deformity of the left humerus is compatible with remote trauma. Osteopenia, spondylosis and degenerative skeletal change are noted.
Aktuelle Erkrankungen: -
Vorgeschichte: Advanced COPD (CMS/HCC) Anemia Congestive heart failure (CMS/HCC) Chronic deep vein thrombosis (DVT) of left lower extremity (CMS/HCC) Chronic obstructive pulmonary disease (CMS/HCC) Depression with anxiety Depression Deep vein thrombosis (DVT) (CMS/HCC) Pulmonary emphysema (CMS/HCC) Generalized idiopathic epilepsy and epileptic syndromes, without status epilepticus, not intractable (CMS/HCC) Obstructive sleep apnea Seizure disorder (CMS/HCC) Sinus tachycardia Presence of artificial hip joint, left Fracture of humeral head, closed, right, with routine healing, subsequent encounter Sepsis secondary to UTI (CMS/HCC) Avascular necrosis of hip, right (CMS/HCC) Closed traumatic nondisplaced fracture of proximal end of left humerus with routine healing Hematuria Acute metabolic encephalopathy Confusion Ureteral calculus
Andere Medikamente: albuterol 2.5 mg /3 mL (0.083 %) nebulizer solution albuterol HFA (PROAIR HFA) 90 mcg/actuation inhaler apixaban (ELIQUIS) 5 mg tablet (Expired) budesonide-formoterol (SYMBICORT) 80-4.5 mcg/actuation inhaler cholecalciferol, vitamin D3,
Allergien: NKA
Vorherige Impfungen: -

VAERS 1696347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 74,0
Geschlecht: M
Eingang: 14.09.2021
Impfdatum: 09.03.2021
Beginn: 21.08.2021
Tage bis Beginn: 165,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Death Exposure to SARS-CoV-2 Gait disturbance Headache Lethargy Respiratory tract congestion Rhinorrhoea Sinus disorder

Symptomtext

Patient is fully vaccinated and died due to COVID related causes. According to patient's wife, he presented to hospital with sinus problem runny nose and congestion headache two days before the 8/21 and on 08/21/21 he became Lethargic and had a unsteady Gait prior to testing. Believe contracted Covid from church. Patient died nine days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular disease, current smoker
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1689846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 25.08.2021
Beginn: 31.08.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Cardiac arrest Death Dizziness Dyspnoea Endotracheal intubation Intensive care Malaise Positive airway pressure therapy Pulseless electrical activity Pyrexia SARS-CoV-2 test positive

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 1/27/2021, 2/21/2021, and 8/25/2021. Presented to ED on 8/31/2021 with malaise, low-grade fever, and feeling lightheaded. His daughter was recently diagnosed with COVID and had been quarantining. Patient admitted for acute hypoxic respiratory failure secondary to COVID PNA. Initially required BiPAP, but able to be weaned off. Patient transferred to ICU 9/4 due to increased work of breathing and increased oxygen requirements. Hospital course complicated by worsening hypoxic respiratory failure requiring emergent intubation 9/8 overnight. Pt with a total of 2 cardiac arrests overnight. PEA Arrest on 9/9/2021 @ 0658. Patient converted to DNAR/COT per family wishes and patient expired at 0750 on 9/9/2021. Patient treated with dexamethasone, remdesivir,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 9,0
Labordaten: Positive COVID Test on 9/1/2021 utilizing the Cepheid GeneXpert Platform using PCR or Equivalent Nucleic Acid Amplification technology.
Aktuelle Erkrankungen: -
Vorgeschichte: Allergic rhinitis, Atrial flutter, Vertigo, Chronic kidney disease, Chronic sinusitis, CAD, hypertension, Focal, segmental glomerulosclerosis, Gout, hyperlipidemia, H/O kidney transplant, osteoarthritis of knee, sensorineural hearing loss, H/O stroke, Type 2 DM.
Andere Medikamente: Acetaminophen PRn, Aspirin 81 mg QD, Atorvastatin 40 mg QD, Azelastine/Fluticasone nasal QD, benzonatate 100 mg TID PRN, Clonidine 0.3 mg BID, Epoetin alfa 20,000 units Q2Weeks, Ergocalciferol 50,000 units QWeek, Erythromycin 200 mg QID, Es
Allergien: Ciprofloxacin (muscle rigidity), Levofloxacin (muscle rigidty)
Vorherige Impfungen: -

VAERS 1689255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 65,0
Geschlecht: M
Eingang: 10.09.2021
Impfdatum: 18.03.2021
Beginn: 23.04.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: IM / UN

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

Computerised tomogram thorax Cough Deep vein thrombosis Oedema Pain in extremity Pulmonary embolism Ultrasound Doppler

Symptomtext

Patient developed cramping in his legs after his first COVID vaccine which was given 2.25.2021. in Hospital. After his second vaccine which was given 3.18.2021, he developed a cough and left leg pain and edema which prompted medical attention about 3 weeks after his second dose. He was diagnosed with a left lower extremity deep vein thrombosis and pulmonary embolism 4.23.2021 and was placed on blood thinenrs, Eliquis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: Duplex Ultrasound and Ct Chest 4.23.2021
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1683498

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 08.04.2021
Beginn: 11.08.2021
Tage bis Beginn: 125,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory distress syndrome Blood culture positive COVID-19 COVID-19 pneumonia Candida test positive Cardio-respiratory arrest Chest X-ray abnormal Culture urine Death Dyspnoea Lung opacity Mechanical ventilation Respiratory failure SARS-CoV-2 test positive

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Pfizer Vaccines on 3/11/2021 and 4/8/2021. Presented to ED on 8/11/2021 with complaints of shortness of breath for last 7 days. Supplemental oxygen was initiated in the ED. Admitted with COVID 19 pneumonia with ARDS and ongoing respiratory failure. On 8/22/2021 patient had cardiorespiratory arrest and required mechanical ventilation. Medications administered during hospitalization include: dexamethasone, cefepime, levofloxacin, micafungin, and remdesivir. Support withdrawn after discussion with family about poor prognosis. Patient expired at on 9/1/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 22,0
Labordaten: COVID Positive on 8/11/2021; CXR showed Pulmonary opacities concerning for multifocal pneumonia on 8/11/2021; Blood culture positive for candida albicans 8/25/2021; urine culture; positive for candida albicans 8/26/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Deceased donor kidney transplant, post-transplant erythrocytosis, thrombocytopenia, asthma, hypertension, depression, hypothyroid, coronary artery disease, degenerative joint disease, hyperlipidemia, sleep apnea, anxiety, kidney transplant failure due to chronic rejection, chronic kidney disease
Andere Medikamente: albuterol 1-2 puffs every 4 hours as needed for wheezing, aspirin 81 mg daily, coreg 12.5 g twice daily, famotidine 20 mg twice daily as needed, fluoxetine 40 mg daily, levothyroxine 175 mcg daily, mycophenolate 540 mg twice daily, predniso
Allergien: Cefdinir, penicillins, valganciclovir, cranberry, grapefruit, pomagranate
Vorherige Impfungen: -

VAERS 1666193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 02.09.2021
Impfdatum: 05.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death Dyspnoea Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient was fully vaccinated. Hospitalized and died due to COVID-19. She presented to the ER "acute onset shortness of breath with apparent hypoxia at home 45% on room air." The reason for admission was "Respiratory failure with hypoxia." Both of these statements were due respiratory distress from Covid-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1658663

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 75,0
Geschlecht: M
Eingang: 31.08.2021
Impfdatum: 03.02.2021
Beginn: 25.07.2021
Tage bis Beginn: 172,0
Dosis: 2
Route/Site: SYR / UN

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

Angiogram abnormal Bilevel positive airway pressure COVID-19 Computerised tomogram thorax abnormal Death Dyspnoea Endotracheal intubation Hypoxia Intensive care Lung opacity Oxygen saturation decreased Pneumonia Pulse absent Renal failure Respiratory failure Respiratory rate decreased SARS-CoV-2 test positive

Symptomtext

fully vaccinated 75-year-old male with past medical history significant for HTN, HLD, obesity, tobacco use, and prior DVTs admitted to Hospital on 07/27/2021 for shortness of breath. Patient was seen at urgent care on 07/25/2021 and found to be COVID-19 positive. CT angiogram performed to assess for pulmonary embolism. Imaging was equivocal but demonstrated bilateral patchy ground-glass opacities suggestive of bilateral pneumonia. Patient was administered and completed azithromycin, ceftriaxone, dexamethasone. Initially on 6L of oxygen by nasal cannula on admission. During his admission, patient's respiratory status worsened and he was placed on humidified high-flow nasal cannula at 60 L and 100% O2. Despite being on high-flow nasal cannula patient desaturated to the 70s and a rapid response was called. Patient was placed on BiPAP with some improvement in his respiratory status and was admitted to the hospital on 08/01/2021. On 8/7, his respiratory status progressively worsened and he was sedated and intubated. On 8/8, code status was changed to DNR. He developed progressively worsening renal failure and increased vasopressor requirements to maintain his blood pressure. 08/01 Rapid response called for patient desaturating in the 70s while on 60L. Transferred to Hospital. 8/07 Intubated and sedated due to worsening respiratory failure. 08/08 Worsening hypoxemia, renal failure, Code status changed to DNR. 08/10 Family elects palliative extubation, withdrawal of care with comfort measures. On 8/10/21 following adequate time to say their goodbyes. Palliative extubation performed by RT at 1823 with Nurse and family at bedside. Loss of palpable pulses appreciated by Nurse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, obesity, tobacco use
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1135371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: -
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Catheterisation cardiac abnormal Chest pain Coronary artery disease Echocardiogram abnormal Autoimmune disorder Catheterisation cardiac Chills Condition aggravated C-reactive protein Catheterisation cardiac normal Cardiac disorder Magnetic resonance imaging Myocardial infarction Ejection fraction Electrocardiogram Magnetic resonance imaging heart Myocarditis

Symptomtext

myocarditis following SARS-CoV-2 vaccination; This is a literature report from the Regulatory Authority. Cardiovascular imaging, 2021, pp 1-2, DOI 10.1016/j.jcmg.2021.06.003, entitled A Series of Patients With Myocarditis Following SARS-CoV-2 Vaccination With mRNA-1279 and BNT162b2. This author reported similar events for five patients. This is the first of five reports. An adult male patient (age reported as 35-40 years) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 2, single and via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient developed Cardiac Magnetic Resonance Imaging (CMR)-proven myocarditis shortly after vaccination on an unspecified date. The patient with no infectious prodrome developed severe chest pain and elevated troponin I, 4 days after second vaccination. The patient did not develop any other complications and was discharged home. Lag between vaccination and presentation was 4 days. There was no fever. The symptoms at presentation included positional and pleuritic chest and neck pain; chills; and myalgias. The patient underwent lab tests and procedures which included ejection fraction: 45 % (normal > 55%), electrocardiogram: sinus rhythm with inferolateral ST elevation, Cardiac Magnetic Resonance Imaging (CMR): revealed patchy midmyocardial increased t2 signal (In each panel, T2-weighted sequences are on the left and late gadolinium (LGE) sequences are on the right. Short-axis and 4-chamber views demonstrating areas of increased T2 signal and LGE in the mid wall of the lateral segments (arrowheads) in a patient who received their second SARS-CoV-2 vaccination 5 days earlier.), nasopharyngeal SARS-CoV-2 PCR testing: negative and troponin I: 5.41 ng/ml. The outcome of the event was unknown. Large clinical trials of both BNT162b2 and mRNA1273 in more than 70,000 individuals showed good safety profiles for both of the mRNA-based vaccines and no reports of myocarditis. However, myocarditis has been described after other vaccinations, such as seasonal influenza and smallpox and regulatory agencies are evaluating the risk of COVID-19 vaccine-associated myocarditis based on post-Emergency Use Authorization reports. Findings in the patient with suspected COVID-19 vaccine-associated myocarditis have not been well described in published reports, and the author's report tried to document some of these changes. Although the clinical presentation, Findings, and temporal association strongly suggest the possibility of vaccine associated myocarditis in the patient, authors cannot conclude definitively that COVID-19 vaccine was causative or that other etiologies for myocarditis can be definitively excluded in the patient. Nevertheless, clinicians should be suspicious of myocarditis in recently vaccinated patients with symptoms consistent with this diagnosis. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected. Sender's Comments: A contributory role of BNT162B2 to the event myocarditis cannot be fully excluded based on temporal relationship and since it is part of the product safety profile. This case will be reassessed if additional information becomes available. Linked Report(s): US-PFIZER INC-202101048345 same article/drug/event, different patients; US-PFIZER INC-202101048365 same article/drug/event, different patients; US-PFIZER INC-202101048389 same article/drug/event, different patients; US-PFIZER INC-202101048410 same article/drug/event, different patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: Test Name: Ejection fraction; Test Result: 45 %; Test Name: Electrocardiogram; Result Unstructured Data: Test Result: Sinus rhythm with inferolateral ST elevation; Comments: Sinus rhythm with inferolateral ST elevation; Test Name: CMR; Result Unstructured Data: Test Result: revealed patchy midmyocardial increased T2 signal; Comments: revealed patchy midmyocardial increased T2 signal with corresponding late gadolinium enhancement consistent with the acute inflammation of myocarditis (Figure 1); Test Name: nasopharyngeal SARS-CoV-2 PCR testing; Test Result: Negative; Test Name: Peak cardiac troponin I; Result Unstructured Data: Test Result:5.41 ng/ml.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1641634

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 92,0
Geschlecht: M
Eingang: 27.08.2021
Impfdatum: 16.03.2021
Beginn: 08.08.2021
Tage bis Beginn: 145,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

Breakthrough COVID infection resulting in hospitalization and death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: Hemodialysis
Vorgeschichte: HD, COVID + confirmed on 8/8/21 hospitalized with COVID patient expired 8/21/21
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1623505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: FL
Alter: 89,0
Geschlecht: M
Eingang: 23.08.2021
Impfdatum: 25.02.2021
Beginn: 10.08.2021
Tage bis Beginn: 166,0
Dosis: 2
Route/Site: IM / -

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

Altered state of consciousness COVID-19 Cardiac arrest Cardio-respiratory arrest Cough Death Dyspnoea Myalgia Oxygen saturation decreased Pulseless electrical activity Resuscitation SARS-CoV-2 test positive

Symptomtext

8/10/21: He developed SOB, cough, and muscle aches, starting 3 days ago. He was referred to ER, where he was admitted on 8/10/21. Tested positive for COVID-19 on 8/10/21. 8/18/21: waxing and waning mentation, requires non-rebreather mask and desaturates quickly. In the afternoon of 8/18/21, he was found in cardiac arrest, PEA and code was called. Family requested to stop resuscitation given his age and poor prognosis. Time of death was called at 1628. Note: He received Pfizer vaccines on 2/3/21 and 2/25/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 8,0
Labordaten: SARS CoV2 PCR COVID19 detected on 8/10/21
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, CAD, Hyperlipidemia, Arrhythmia, Thyroid
Andere Medikamente: acetaminophen, apixaban, vitamin C, aspirin, atorvastatin, bisacodyl, furosemide, levothyroxine, midodrine, niacin, nitroglycerin, fish oil
Allergien: NKA
Vorherige Impfungen: -

VAERS 1591564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TN
Alter: 59,0
Geschlecht: M
Eingang: 20.08.2021
Impfdatum: 04.03.2021
Beginn: 07.08.2021
Tage bis Beginn: 156,0
Dosis: 2
Route/Site: IM / -

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

COVID-19 Death Respiratory distress SARS-CoV-2 test positive

Symptomtext

Case received second covid vaccine on 03/04/2021. Hospital on 8/7/21 with respiratory distress . Positive COVID lab on 8/7/21. Case expired at hospital on 8/18/2021.

Weitere VAERSDATA-Felder

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

VAERS 1587125

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 83,0
Geschlecht: M
Eingang: 19.08.2021
Impfdatum: 24.02.2021
Beginn: 04.08.2021
Tage bis Beginn: 161,0
Dosis: 2
Route/Site: - / -

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

Bilevel positive airway pressure Bradycardia COVID-19 Cardiac arrest Cough Death Fall Fatigue Gait disturbance Mechanical ventilation Oxygen saturation decreased Pulseless electrical activity Respiratory failure SARS-CoV-2 test positive

Symptomtext

Patient tested positive for COVID-19. He was hospitalized due to falling frequency, fatigue, and worsening gait. Patient died.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 9,0
Labordaten: Not requiring oxygen however due to small desaturation he was placed on 2 L at 95%. Hospital was asked to admit the patient for further evaluation and management. Per wife, patient with no hx of COPD, asthma, VTE or OSA. No prior hx of oxygen at home.ff sedation has + cough and gag Off pressors Started on nicardipine this am Current support: Invasive Mechanical Ventilatory: Yes - NIV: No - High flow O2: No CRRT: No Vasoactive Drugs: Yes Other: Yes ASSESSMENT S/p In-hospital PEA arrest (8/10) Secondary to hypoxic resp failure - pt pulled off Bipap mask and became hypoxic and then bradycardic per bedside RN ~ 21 mins
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, aortic stenosis, HTN, Chohn's, GERD, CVA, subdural hemorrhage
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1582658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 62,0
Geschlecht: M
Eingang: 18.08.2021
Impfdatum: 05.03.2021
Beginn: 28.07.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute respiratory failure Arteriosclerosis Arteriosclerosis coronary artery Atypical mycobacterial infection Chronic kidney disease Computerised tomogram Computerised tomogram thorax abnormal Cough Dehydration COVID-19 COVID-19 pneumonia Cardiomegaly Chest X-ray abnormal Chest pain Diarrhoea Dyspnoea Gastrointestinal disorder

Symptomtext

Flu Symptoms Clinical Support 8/6/2021 Urgent Care Medication Infusion Reason for Visit Progress Notes (Registered Nurse) ? ? Encounter Date: 8/6/2021 ? ? Signed 1300 Patient arrived for MAB infusion. SOB after walking to exam room. Pulse ox 88% on RA. Encourged to cough and deep breathe. Move pulse ox to another finger. 1305 pulse ox 85% RA patient states he is SOB. 1308 O2 2L NC applied 1311 Pulse ox 90% on 2L NC 1314 Pulse ox 90-91% on 2L. Less labored breathing. Patient states he is fine if he is just sitting but becomes SOB with any exertion. 1319 Asked patient to lean forward to listen to lungs, started coughing and pulse ox dropped to 89%. 1323 Patient stated he noticed significant labor breathing after showering this am that did resolve after resting. He then became SOB anytime he was out of his chair moving about. 1332 Pulse ox 91%. Patient states he is starting to feel a little better. Removed O2 to see if patient can maintain pulse ox of 90% or better. Explain to patient that if pulse ox drops we will not be able to administer the medication. Patient verbalized understanding. 1338 Pulse ox dropped to 89% on RA. O2 @ 2L NC reapplied. 1345 Pulse ox up to 92-93% on 2L NC. Dicussed the need for the ED. Patient would does not want to go by ambulance. His wife is at home and he has the car. Patient declined ambulance. Removed O2. Patient discharged and instructed to go to ED. 1356 Report given to ED ED to Hosp-Admission Discharged 8/6/2021 - 8/17/2021 (11 days) Hospital 1. Acute hypoxic respiratory failure present on admission secondary to COVID-19 pneumonia in a morbidly obese patient. I will start him on O2 protocol nebulization treatments. 2. COVID-19 pneumonia chest x-ray reviewed we will start the patient on remdesivir IV steroids nebulization treatment O2 protocol. 3. Diarrhea with severe dehydration dry oral mucosa we will start him on normal saline at 100 mL/h diarrhea most likely from COVID-19 GI symptoms. 4. Acute on chronic renal injury present on admission underlying CKD stage III. Secondary to diarrhea and poor oral intake I will hold lisinopril and Lasix. We will start him on normal saline at 100 mL/h repeat BMP in the morning. 5. Hypertension benign fairly controlled we will keep a close eye on his blood pressure we will continue the Coreg but will hold lisinopril because of acute on chronic renal injury and dehydration. 6. Morbid obesity with body mass index 50.92 patient's counseling done in detail. 7. DVT prophylaxis moderate risk subcutaneous heparin bilateral compression devices. 8. Advanced care planning discussion he is full code. Patient will be admitted to intermediate care under hospitalist service medical management was discussed with the patient and his wife in detail at the bedside. Chief Complaint Patient presents with ? Hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 11,0
Labordaten: Contains critical data COVID-19: Positive Infection Onset 8/2/2021 Rule-Out SARS-CoV-2 (related to COVID-19) (Resolved) Specimen information: Swab / Nares Added: 8/2/2021 by COVID-19 PCR (08/02/21) Onset date: 8/2/2021 Resolved: 8/3/2021 (Rule-Out Test Resulted) SARS-CoV-2 (related to COVID-19) Specimen information: Swab / Nasopharynx Added: 8/3/2021 by COVID-19 (SARS CoV-2,RNA Molecular Amplification) (Collected 08/02/21) Last indicated by: Respiratory virus detection panel (Collected 08/06/21) Onset date: 8/2/2021 Resolve Rule-Out COVID-19 and Respiratory Viruses (Resolved) Specimen information: Swab / Nasopharynx Added: 8/6/2021 by Respiratory virus detection panel (08/06/21) Onset date: 8/6/2021 Resolved: 8/6/2021 (Rule-Out Test Resulted) Procedure Component Value Ref Range Date/Time CT chest without contrast Resulted: 08/13/21 1744 Order Status: Completed Updated: 08/13/21 1744 Narrative: CT CHEST WO CONTRAST IMPRESSION: Multilobar moderately prominent groundglass pulmonary opacities are noted approximately 50% of the lungs are involved. Infectious inflammatory changes such as Covid 19 should be considered. Moderate right renal atrophy, indeterminate significance. No hydronephrosis or nephrolithiasis. Commonly reported imaging features of COVID-19 pneumonia are present. Other processes that can cause a similar imaging pattern include but are not limited to: atypical infections (such as influenza virus, adenovirus, or organizing pneumonias) or noninfectious etiologies (such as drug induced lung toxicity or connective tissue disease.) END OF IMPRESSION: INDICATION: Shortness of breath. Covid positive. CT CHEST without IV contrast: Helical CT scan of the chest without contrast was performed from the lung apices to below the diaphragm. 3 mm axial reconstruction with MPR coronal and sagittal images were created. Lack of IV contrast results in limited evaluation of certain structures such as lymph nodes, vascular structures, hilar abnormalities etc. Following findings are noted on the current study. COMPARISON STUDY: Chest x-ray 8/13/2021 THYROID: Unremarkable. MEDIASTINUM/HILA/AXILLA/SUPRACLAVICULAR: No significant lymphadenopathy as per size criteria. Few calcified subcarinal mediastinal lymph nodes, sequelae of old ligamentous disease. PULMONARY ARTERIES: Unremarkable at this noncontrast exam. HEART: Mild cardiomegaly.. Mild coronary artery calcification noted. Moderate mitral annular calcifications are seen. AORTA: No aneurysm . There is mild atherosclerotic plaque noted. LUNG/PLEURAL: Multilobar moderately prominent groundglass pulmonary opacities are noted approximately 50% of the lungs are involved. No definite focal dense consolidation, pneumothorax or pleural effusions. Left lung base small calcified benign granuloma.. UPPER ABDOMEN: Partially visualized structures below the level of the diaphragm demonstrate no acute abnormality. Prior cholecystectomy. Moderate hypertrophic right kidney. No hydronephrosis or nephrolithiasis. BONES: No acute bony findings. No focal aggressive lesions. There are mild degenerative changes of the thoracic spine. SOFT TISSUE: Unremarkable. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view Resulted: 08/13/21 1034 Order Status: Completed Updated: 08/13/21 1034 Narrative: XR CHEST 1 VW PORT IMPRESSION: Persistent multifocal patchy infiltrates. New very small area of consolidation at the left base. END OF IMPRESSION: INDICATION: Dyspnea FU Covid, slow improvement. TECHNIQUE: AP portable erect projection of the chest is acquired. COMPARISON: August 6, 2021 FINDINGS: Patient is rotated to the right. There is no widening or shift of the mediastinum and the heart size is not enlarged. There are persistent diffuse patchy increased markings with a small area of new consolidation at the left base. Right upper lobe area which was the most dense on the initial image is somewhat improved but not resolved. There is no effusion. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. X-ray chest 1 view, Portable Resulted: 08/06/21 1549 Order Status: Completed Updated: 08/06/21 1550 Narrative: XR CHEST 1 VW PORT IMPRESSION: Bilateral multifocal infiltrates. In appropriate clinical setting this is consistent with Covid 19 infection. Follow-up to resolution is recommended because of a larger area of mild consolidation in the right upper lung. END OF IMPRESSION: INDICATION: pt c/o chest pain, SOB, coughing, fever, covid positive. SOB. TECHNIQUE: AP portable erect projection of the chest is acquired. COMPARISON: 12/19/2011 FINDINGS: There are multiple bilateral patchy infiltrates most pronounced in the right upper lobe. In the right upper lobe there is a 4 cm focal rounded area of mildly dense infiltrate. Findings are consistent with Covid 19 infection. There is no effusion. Follow-up is recommended to show resolution of the larger finding in the right upper lobe. There is no widening or shift of the mediastinum and the heart size is not enlarged. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient.
Aktuelle Erkrankungen: -
Vorgeschichte: Circulatory Essential hypertension Prolonged PR interval present on electrocardiography Digestive Morbid obesity Vitamin D deficiency Tubular adenoma of colon Genitourinary Chronic kidney disease, stage III (moderate) Musculoskeletal Tinea pedis Genu varum Endocrine/Metabolic Mixed hyperlipidemia Prediabetes Pure hypercholesterolemia Hematologic Leukocytosis Infectious/Inflammatory COVID-19 Other History of diverticulitis of colon History of anemia Incisional hernia, without obstruction or gangrene Localized edema Hx of total knee arthroplasty, left History of arthroplasty of right knee
Andere Medikamente: Outpatient Medications carvediloL (COREG) 6.25 mg tablet cholecalciferol, vitamin D3, (VITAMIN D3) 5,000 unit tablet cloNIDine (CATAPRES) 0.1 mg tablet codeine-guaiFENesin (ROBITUSSIN-AC) 10-100 mg/5 mL liquid cyanocobalamin (vitamin B-12)
Allergien: NKA
Vorherige Impfungen: -

VAERS 1534048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 76,0
Geschlecht: M
Eingang: 07.08.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Aphasia Blindness Confusional state Dyspnoea Feeling abnormal Hallucination Hand-arm vibration syndrome Memory impairment Near death experience Paralysis Parosmia Scan brain Sensory disturbance Taste disorder Ultrasound scan

Symptomtext

Hallucinations; Feeling I was about to die; Felt my vision closing in; Paralyzed; My brain couldn't follow the tv program; Couldn't remember how to do simple tasks; An electric vibration sensation; Distinct tastes and smells; Distinct tastes and smells; Couldn't breathe; Couldn't speak or communicate; Confused; electric vibration sensation traveling up my left leg, into my arm, then the entering left side of my brain and through it to the right, then seemed to dissipate into my right shoulder.; This is a spontaneous report from a contactable consumer. A 76-year-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Right on 23Feb2021 09:00 (Batch/Lot Number: EN6203) as dose 2, single (at the age of 76 years) for covid-19 immunization. The patient's medical history included hypertension and chronic obstructive pulmonary disease (COPD) on an unknown date. The patient's concomitant medications were not reported. The patient received the first dose of COMIRNATY on 02Feb2021 at 09:00AM in the right arm (lot:EL9265) at the age of 76 years for Covid-19 immunisation. On 23Feb2021 18:00, the patient experienced hallucinations, feeling I was about to die, felt my vision closing in, paralyzed, my brain couldn't follow the tv program, couldn't remember how to do simple tasks, an electric vibration sensation, electric vibration sensation traveling up my left leg, into my arm, then the entering left side of my brain and through it to the right, then seemed to dissipate into my right shoulder, distinct tastes and smells, couldn't breathe, couldn't speak or communicate, and confused. The events were further reported as, around 6 pm the evening of the second dose the first event happened, followed by three more the next day. Patient's brain couldn't follow the tv program. He couldn't remember how to do simple tasks. He was having hallucinations, and couldn't distinguish between them and reality. The next day he had three or four experiences of an electric vibration sensation traveling up his left leg, into his arm, then the entering left side of his brain and through it to the right, then seemed to dissipate into his right shoulder. During that time he experienced several distinct tastes and smells all at once, and had the feeling he was about to die. He couldn't breathe, felt his vision closing in, and was completely paralyzed. He couldn't speak or communicate and was confused all day. Two weeks later, he thought it was going to happen again, and had to sit down suddenly. After this, He saw his doctor and they did scans and couldn't find anything. Patient was put on blood thinners. The patient underwent lab tests and procedures which included brain scan and sonogram in Feb2021 with unknown results. The outcome for all the events was recovered with sequelae in 2021. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, has the patient has not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Near death experience
Hospital-Tage: -
Labordaten: Test Date: 202102; Test Name: Brain scan; Result Unstructured Data: Test Result:Unknown results; Test Date: 202102; Test Name: Sonogram; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COPD; Hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1531540

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 79,0
Geschlecht: M
Eingang: 06.08.2021
Impfdatum: 22.02.2021
Beginn: 26.05.2021
Tage bis Beginn: 93,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Death Dyspnoea Pneumonia

Symptomtext

Pfizer-BioNTECH COVID-19 Vaccine EUA Patient received Pfizer COVID Vaccines on 1/29/2021 and 2/22/2021. Patient presented to ED on 7/16/2021 with worsening shortness of breath for the last few days. Admit diagnosis of Pneumonia due to COVID-19. Patient was treated with remdesivir daily (7/16 - 7/20), IV steroids, and Tocilizumab 800 mg x2 doses (7/20&21). Patient expired on 7/29/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 13,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Hx of sinusitis, Hyperlipidemia, Hx NSCLS, Osteoporosis, Enlarged prostate, obesity, aortic valve sclerosis
Andere Medikamente: Benefiber QD, Lovastatin 20 mg QD, Meloxicam 15 mg QD, MVI,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1519700

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 91,0
Geschlecht: F
Eingang: 02.08.2021
Impfdatum: 20.03.2021
Beginn: 09.07.2021
Tage bis Beginn: 111,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia COVID-19 Confusional state Cough Death Dyspnoea SARS-CoV-2 test positive

Symptomtext

Client fully vaccinated for COVID-19 tested positive for COVID-19 on 7/10/2021. Vaccine Dose #1 given 2/27/2021. Vaccine Dose #2 given 3/20/2021. Client hospitalized on 7/14/2021 for shortness of breath, cough, confusion, and severe generalized weakness. Client died on 7/17/2021.

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Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: Positive COVID-19 on 7/10/2021.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: COPD
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1512863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 80,0
Geschlecht: M
Eingang: 29.07.2021
Impfdatum: 16.02.2021
Beginn: 11.04.2021
Tage bis Beginn: 54,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 Death SARS-CoV-2 test positive

Symptomtext

Patient hospitalized and died of COVID after being vaccinated.

Weitere VAERSDATA-Felder

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

VAERS 1512469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 88,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 25.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / -

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

Asthenia Cerebrovascular accident

Symptomtext

Major, life-debilitating stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 14,0
Labordaten: extensive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1509627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 28.07.2021
Impfdatum: 25.02.2021
Beginn: 20.07.2021
Tage bis Beginn: 145,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Bilevel positive airway pressure COVID-19 COVID-19 pneumonia Diarrhoea Dyspnoea Hyperlipidaemia Nausea SARS-CoV-2 test positive Vomiting

Symptomtext

1 week of nausea, vomiting, and diarrhea and worsening dyspnea. His respiratory status decompensated since admission. He was initially on 2-3 L nasal cannula and then worsened to needing BiPAP at 100% FiO2. Even with that, his SpO2 was between 88-90%. He was transferred to another hospital for further management.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: Coronavirus 2 PCR Detect, V symptomatic POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: Hospital Hyperlipidemia Pneumonia Due To COVID-19 Acute Respiratory Failure With Hypoxia (HCC) Vomiting/diarrhea
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1456646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: -
Geschlecht: M
Eingang: 08.07.2021
Impfdatum: 03.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Antibody test COVID-19 Coombs test Death SARS-CoV-2 antibody test negative

Symptomtext

passed away; The initial case was missing the following minimum criteria: adverse event. Upon receipt of follow-up information on 01Jul2021, this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer (patient) and patient's wife. A 69-years-old male patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6201), via an unspecified route on 10Feb2021 (at the age of 69-years) as dose 1, single and second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EN6203), via an unspecified route on 03Mar2021 (at the age of 69-years) as dose 2, single for covid-19 immunisation. The patient medical history included Hodgkin's disease from 1978 (they took his spleen out, so he was a little immunocompromised and they took out his spleen and appendix after diagnosis) and unknown if ongoing. The patient concomitant medications were not reported. On unspecified date, the patient experienced had 3 antibody tests- one that was a 15minutes finger prick and two others that were all 2-3 weeks apart. Patient stated all 3 tests were negative for antibodies and his doctors don't know why. His doctors said maybe it did not detect antibodies to the vaccine. In 1978, he had Hodgkin's disease and they took his spleen out, so he was a little immunocompromised. However, the infectious disease doctor said since he got both doses he should still be protected. Reporter was concerned that he didn't had great immune system when three negative tests came back, he just want to make sure that everybody thinks he was not okay because he was going out over usual instructions because of them. His primary care physician (PCP) said he talked to another doctor and said if he had the vaccine it should be covered but the test came back negative. Reporter stated that the "last test he had was on 24May2021, it was COVID-19 antibody test, SARS test, COB test 2, AbIG Quantitative. This one was done on maybe 10th (unspecified date in 2021) it was rapid test for SARS, COB-2, IGg antibody. That was done on 07Apr201 and stated if Pfizer want, he can give that also, SARS, COVID, COB-2, IGgAb, AbIGm, they all came back negative". Patient's wife stated her husband passed away and at the time of the vaccination she and her daughter got adverse reactions she would like to fill the form for both her and her daughter. The patient died on unspecified date in 2021 with unknown cause of death and autopsy results was unknown. The outcome of the event was fatal. Follow up needed, further information has been requested.; Reported Cause(s) of Death: passed away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Test Date: 20210407; Test Name: IG; Test Result: Negative ; Comments: AbIG Quantitative; Test Date: 20210524; Test Name: IG; Test Result: Negative ; Comments: IGg; Test Date: 2021; Test Name: IG; Test Result: Negative ; Comments: IGgAb, ABIGm; Test Date: 20210407; Test Name: COB TEST; Test Result: Negative ; Test Date: 20210524; Test Name: COB TEST; Test Result: Negative ; Test Date: 2021; Test Name: COB TEST; Test Result: Negative ; Test Date: 20210407; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20210524; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20210407; Test Name: SARS test; Test Result: Negative ; Test Date: 20210524; Test Name: SARS test; Test Result: Negative ; Test Date: 2021; Test Name: SARS test; Test Result: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hodgkin's disease (and they took his spleen out so he is a little immunocompromised.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1237584

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 77,0
Geschlecht: M
Eingang: 02.07.2021
Impfdatum: 02.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: - / -

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

Death Unevaluable event

Symptomtext

Patient was hospitalized multiple times within 60 days of receiving a COVID vaccine series and later passed away

Weitere VAERSDATA-Felder

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

VAERS 1206305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: WA
Alter: 45,0
Geschlecht: F
Eingang: 02.07.2021
Impfdatum: 23.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: SYR / AR

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

Carotid artery occlusion Carotid artery thrombosis Cerebrovascular accident Computerised tomogram Ear pain Cerebral infarction Headache Sinus disorder Echocardiogram Electrocardiogram Magnetic resonance imaging

Symptomtext

ICA stroke; headache; earache; sinus issue; had sudden onset stroke symptoms while hiking; This is a spontaneous report from a contactable pharmacist. A 45-years-old female patient received bnt162b2 (BNT162B2), dose 2 intramuscular on 23Feb2021 (Batch/Lot number was not reported) at age of 45-year-old as DOSE 2, SINGLE for covid-19 immunisation. Facility where the most recent COVID-19 vaccine was administered was Workplace clinic. The patient was not Pregnant at Time of Vaccination. Medical history included acne, eczema, HPV (had resolved in 2018); anxiety/depression, Known alleries Latex. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received First dose of bnt162b2 on 29Jan2021 at age of 45-year-old for covid-19 immunisation. Patient was with complaints of headache and earache. She was seen by urgent care twice (03Mar2021 and 10Mar2021) thinking it was a sinus issue. She then had sudden onset stroke symptoms while hiking and went to ED on 13Mar2021. she was transferred to a larger hospital and diagnosed with ICA stroke. She had no risk factors for stroke previously and her only prescription medication (norethindrone-EE) was discontinued 03Mar2021 thinking it was causing her headaches. Patient now is still having paralysis and is unable to independently manage ADLs. The adverse events result in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care.The onset date of ICA stroke was unknown, of other events was 03Mar2021. Stroke treatment Received. Duration of Hospitalization was 5 days. The events were assessed serious as Life threatening, Caused/prolonged hospitalization, Disabling/Incapacitating, The outcome of events was Recovering. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Information about batch/Lot number has been requested.; Sender's Comments: Based on available information, particularly prolonged onset latency, it appears unlikely that vaccine BNT162B2 contributed to the reported events. These are probably intercurrent medical conditions. This case will be reassessed upon receipt of the follow-up information. 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: Cerebrovascular accident
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Acne; Anxiety; Depression; Eczema; HPV positive oropharyngeal squamous cell carcinoma (had resolved in 2018); Latex allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1433310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 84,0
Geschlecht: F
Eingang: 29.06.2021
Impfdatum: 04.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Acute kidney injury Acute left ventricular failure Acute respiratory failure Anaemia Chronic left ventricular failure Cough Dysphagia Encephalopathy Exposure to SARS-CoV-2 Mechanical ventilation Quarantine SARS-CoV-2 test Upper respiratory tract infection Viral infection

Symptomtext

Phone visito Visit History for 3/12/2021 Problem List* Health Maintenance* Results/Data* Review Flowsheets* History of Present Illness HPI: 84 yo female pmh: DJD right hip, CAD and chronic anticoagulation was contacted via telephone: states she received her covid 19 vaccine 3 days ago: now having dry (non productive cough)-denied any fever/chills or loss of smell/taste. o Visit History for 3/12/2021 Problem List* Health Maintenance* Results/Data* Review Flowsheets* History of Present Illness HPI: 84 yo female pmh: DJD right hip, CAD and chronic anticoagulation was contacted via telephone: states she received her covid 19 vaccine 3 days ago: now having dry (non productive cough)-denied any fever/chills or loss Issues Addressed/ Plan Diagnosis Plan 1. Viral upper respiratory tract infection (s/p covid 19 vaccine) predniSONE 20 MG Oral tablet albuterol (PROVENTIL HFA) 90 mcg/actuation Inhl inhaler (afebrile) Counseled on supportive measures Has declined covid 19 test Informed: if conditions worsens: present to ED (immediatetly) 3/25 pt's son in the room, updated and answered all questions at this time. 4/2 Pt's husband also inpatient and covid+. Spoke with daughter today and updated r/t quarantine. 2. Nursing Education/Concerns: Care team met with family (husband, son and daughter) on 3/18/21 to discuss care goals/plan of care moving forward. Pt's code status officially updated to DNR only with trial intubation. 3/18/2021 spoke updated pts daughter on phone at 1031. Report given to SNF- they were made aware that she needs the second pfizer vaccine 3. Interdisciplinary involvement Social Work/Case Management: From home with spouse. STR- Referral out. STR reviewing. Will not take patient before her 10 day exposure quarantine is over. 4/9. STR- Bed offer for tomorrow pending insurance auth and negative COVID. sent for auth. Patient aware. Son updated. COVID exposure - exposure to covid positive visitor on 3/26 and 3/29 - discussed with infection control. Will test on 3/31 and if negative will test again on 4/7 (day 9 of quarantine) unless symptoms develop in interm. Acute hypoxic respiratory failure secondary to acute on chronic systolic LV failure requiring prolonged ventilation and SNF placement after discharge. Encephalopathy, dysphagia, anemia, tachy, AKI

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 27,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1431522

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CO
Alter: 74,0
Geschlecht: F
Eingang: 28.06.2021
Impfdatum: 25.02.2021
Beginn: 09.06.2021
Tage bis Beginn: 104,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Death

Symptomtext

Pt's cause of death was due to COIVD -19 illness. No one believes that the vaccine was part of the death. The patient was fully vaccinated with 2 doses of Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1419899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NC
Alter: 65,0
Geschlecht: M
Eingang: 23.06.2021
Impfdatum: 25.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 65,0
Dosis: 2
Route/Site: - / -

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

Balance disorder Biopsy Brain oedema Cerebral haemorrhage Cerebral venous thrombosis Computerised tomogram Condition aggravated General physical health deterioration Generalised tonic-clonic seizure Headache Mental status changes Prostatomegaly

Symptomtext

Cerebral venous thrombosis; bilateral intracerebral hemorrhage in the left, greater than the right; tonic-clonic seizure; brain swelling/cerebral edema; headaches; overall imbalance/having balance problems; he had a decline; kind of getting worse/ had the worst symptoms; His prostate is enlarged; patient's mental status is altered; This is a spontaneous report from a contactable physician. A 65-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 25Feb2021 (Batch/Lot Number: EN6203) as 0.3 ml single for COVID-19 immunisation. Patient age at vaccination was 65 years old. Medical history included hyperlipidemia and high cholesterol. Historical vaccine included 1st dose of BNT162B2 (LOT: EL3247) on 03Feb2021 for COVID-19 immunisation. Concomitant medication included pravastatin (strength: 10 mg) taken for an unspecified indication from an unspecified start date and ongoing. Reporter did not know all of the symptoms that the patient had and cannot get the history, because the patient's mental status was altered (from unknown date in 2021). It was reported that he was having symptoms for at least 2 weeks with some increasing over the last 2 weeks. Knew that he had an overall imbalance and was having headaches, both from unknown date in May2021. He had been having symptoms for weeks and went to his doctor as an outpatient. He had initial imaging that was concerning and he went to the hospital because he had a decline (from unknown date in 2021). He had declined and had a hemorrhagic hemorrhage with cerebral venous thrombosis, both from 04Jun2021. He was admitted to the hospital 04Jun2021, and 05Jun2021 he was transferred to the ICU. He had declined since his initial presentation and had been kind of getting worse over the last couple of weeks. Stated the patient was stoic and does not have a lot of medical problems, but everyone knew he was having symptoms over the last 2 weeks. 02Jun2021 he had the worst symptoms and was basically having balance problems. He was getting concerned and had called to get an appointment with his primary care physician. They had done an outpatient CT scan which found the cerebral venous thrombosis and he went to the hospital and was placed on Heparin. While in the hospital, he had a generalized tonic-clonic seizure and had further decline on 04Jun2021. Repeat imaging showed that he had bilateral intracerebral hemorrhaging, the left greater than the right, and they had expanded a bit. He was still on heparin and now (Jun2021) had some cerebral edema due to it but was not on a ventilator. He was still in the time period where he was continuing to have small declines. He was therapeutic on heparin. He had a central line and was getting hypertonic saline for the brain swelling and cerebral edema. Patient previous health condition was reported as he did not have a real significant past medical history. He maybe carried a diagnosis of hyperlipidemia and high cholesterol. He was pretty healthy; regularly went to the doctor and was otherwise pretty stable. Reporter did not even think his LDL was that high. He had never been on any blood thinners or anything like that. They did a full scan to look for cancer and had no history of blood clots. They did a scan that was negative for any types of masses or any concerns for cancer. His prostate was enlarged (from unknown date in 2021) and they had spoken to the family about it and they said he had been worked up with a biopsy which had been negative. Physician Office? Yes, He was directly admitted to the hospital from primary care. He presented to the clinic because he had these symptoms and headaches. The imaging was done and then he was admitted. He never went through the emergency room. Cerebral venous thrombosis, bilateral intracerebral hemorrhage, overall imbalance/having balance problems, he had a decline, headaches resulted in Physician Office Visit. Outcome of cerebral venous thrombosis, bilateral intracerebral hemorrhage was not resolved; outcome of tonic-clonic seizure, brain swelling/cerebral edema, headache, overall imbalance/having balance problems, he had a decline, kind of getting worse/ had the worst symptoms, enlarged prostate and mental status was altered was unknown. Causality: Cerebral venous thrombosis: Can't say for sure because reporter does not know the timeline but can't find any other reason, he would have cerebral venous thrombosis.; Sender's Comments: Based on the temporal relationship, the association between the events cerebral venous thrombosis, intracerebral hemorrhage, tonic-clonic seizure, and brain swelling with BNT162b2 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: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: Test Name: biopsy; Test Result: Negative ; Comments: His prostate is enlarged and they had spoken to the family about it and they said he had been worked up with a biopsy which had been negative.; Test Date: 20210604; Test Name: CT scan; Result Unstructured Data: Test Result:bilateral intracerebral hemorrhage in the left; Comments: bilateral intracerebral hemorrhaging, the left greater than the right, and they had expanded a bit.; Test Date: 20210604; Test Name: CT scan; Result Unstructured Data: Test Result:cerebral venous thrombosis; Test Date: 2021; Test Name: CT scan; Result Unstructured Data: Test Result:prostate was enlarged
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol; Hyperlipidemia
Andere Medikamente: PRAVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1417294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 22.06.2021
Impfdatum: 21.03.2021
Beginn: 14.04.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cardiac arrest Cardio-respiratory arrest Chest pain Death Hypoxic-ischaemic encephalopathy Myocardial infarction Myocardial necrosis marker increased Pyrexia SARS-CoV-2 test negative SARS-CoV-2 test positive Vaccine breakthrough infection Ventricular fibrillation

Symptomtext

I am the epidemiologist for reporting on behalf of patient who tested positive for COVID-19 via PCR on 4/14/21 after the completion of a full Pfizer vaccine series (Dose 1 on 2/28 and Dose 2 on 3/21). The patient later died on 5/08/21. Cause of Death is listed as ?cardiopulmonary arrest; Anoxic encephalopathy; V. Fib cardiac arrest; Myocardial infaction?. Pre-existing conditions listed as: OTHER CHRONIC DISEASES, CARDIOVASCULAR DISEASE, IMMUNOCOMPROMISED CONDITION Case went to Hospital ER on 4/14 after experiencing chest pains for 2-3 days. Rapid COVID test on 4/14 was negative & PCR test on 4/14 was positive. Case remained in ER for retesting on 4/15 (PCR - negative) so she could be admitted to hospital for cardiac catheterization. Case reports having a mild fever at hospital on evening of 4/15 & morning of 4/16. Hospital Internist DX was mild case of COVID with elevated enzymes that indicated a cardiac event. Case is fully vaccinated (1st dose of Pfizer 2/28 & 2nd dose of Pfizer 3/21). Case has history of lupus & rheumatoid arthritis (immuno-suppressed). She receives PT 2-3x/week & biologic treatment (last infusion of Orencia was 4/13). Advised case to follow-up with her PCP & cardiac specialist. Case agreed to isolation guidelines. Case lives alone but has 2 adult sons who live nearby that will provide food drop-offs at door. Emailing vaccination breakthrough info to Epidemiologist & supervisors.nnn=======================nnApril 15, 2021 at 3:28 PM ET Left SMS/VM.

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: PCR + 4/14
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Pre-Existing Conditions: OTHER CHRONIC DISEASES, CARDIOVASCULAR DISEASE, IMMUNOCOMPROMISED CONDITION
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 1406946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 06.04.2021
Beginn: 07.04.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Cerebral haemorrhage Cerebrovascular accident Condition aggravated Electrocardiogram Gastrointestinal disorder Hypertension Magnetic resonance imaging

Symptomtext

stroke, high blood pressure, gastrointestinal, emergency brain bleed,

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Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: mri, ekg, rehab
Aktuelle Erkrankungen: incontinent issue ,
Vorgeschichte: hbp
Andere Medikamente: Iberzerton, Tylenol, multi vitamins, lorazipam, quanizapm, vitamin
Allergien: penicillin, mold
Vorherige Impfungen: -

VAERS 1375972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

kritisch

Staat: MO
Alter: 81,0
Geschlecht: M
Eingang: 04.06.2021
Impfdatum: 20.02.2021
Beginn: 13.03.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: SYR / AR

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

COVID-19 Cough Death Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Symptom onset began on 4/29/2021. Tested (+) on 4/29/2021. Symptoms included fatigue, congestion, cough. Case was interviewed by public health department on 5/3/2021 and family reported he was in hospital and was admitted on 4/30/2021. Deceased as of 5/14/2021. Unknown if in ICU or mechanically ventilated.

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Praegender Schweregrund: Death
Hospital-Tage: 16,0
Labordaten: 2021-04-29: (test:PCR), (result:POSITIVE), (collected:2021-04-29), LABORATORY), 2021-04-29: (test:PCR), (result:POSITIVE), (collected:2021-04-29), 2021-04-29: (test:ANTIBODY OTHER), (result:POSITIVE), (collected:2021-04-29),
Aktuelle Erkrankungen: chronic lung disease; former smoker
Vorgeschichte: chronic lung disease; former smoker
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1358766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MD
Alter: 27,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 26.03.2021
Beginn: 21.05.2021
Tage bis Beginn: 56,0
Dosis: 2
Route/Site: IM / RA

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

Angiogram retina abnormal Arterial catheterisation abnormal Arterial occlusive disease Cerebral artery thrombosis Cerebrovascular accident Chest X-ray Computerised tomogram Computerised tomogram head Echocardiogram Intensive care Magnetic resonance imaging head abnormal Retinal artery thrombosis Scan with contrast Thrombectomy Ultrasound Doppler Urine analysis

Symptomtext

Stroke - Blood Clot in M2 Brain Artery Friday, May 21, 2021 - Air lifted from Hospital to Hospital Admitted to Neuroradiology Dept and immediate Thrombectomy to remove blood clot behind left eye via angiogram through the groin via catheter. Proceedure was sucessful in removing 100% blocked artery and he was transfered to Resovery, observation and follow-on diagnostic testing in ICU for 4 days. Discharged May 24, 2021

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Measurements, Vital Signs, Hematology, Urinalysis, CT Scan of Head, CT Scan w/ Contrast, Chest Xray, Ultrasound of Heart and legs, MRI of Brain
Aktuelle Erkrankungen: -
Vorgeschichte: Learning Disability
Andere Medikamente: 50mg Fluvoxamine Maleate 1X/day, Multi-Vitamin
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1357990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 82,0
Geschlecht: M
Eingang: 28.05.2021
Impfdatum: 11.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: - / -

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

COVID-19 Death Flank pain

Symptomtext

Patient hospitalized. Patient died after testing positive for COVID-19. Admitted to hospital 4/2/2021 for right flank pain. Tested positive on 4/1/2021. Died 4/29/2021

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Congestive Heart Failure, Chronic Abdominal Abscess
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1343001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

kritisch

Staat: NJ
Alter: -
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 27.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / -

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

Confusional state Death General physical health deterioration Pain Skin discolouration

Symptomtext

Went to er on March 3rd around 2am with discoloration on body with confusion and pain. Was told possible ttp. Condition quickly declined and was transferred to hospital main campus around 12pm. Condition continued to rapidly decline and passed away on March 4th at 11am. There is much more to tell about this. To much to write down. I have called several times no one has called me back.

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Praegender Schweregrund: Death
Hospital-Tage: 2,0
Labordaten: Multiple tests were done. To many to write down. I have a complete medical record of all treatments provided.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1337619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 71,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 21.02.2021
Beginn: 14.05.2021
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: - / -

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

Death Diabetes mellitus End stage renal disease Neuromyopathy

Symptomtext

NA End Stage Kidney disease DM Neuromuscular disease

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

VAERS 1334711

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 34,0
Geschlecht: F
Eingang: 20.05.2021
Impfdatum: 30.01.2021
Beginn: 03.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal discomfort Abdominal pain COVID-19 Computerised tomogram abdomen Condition aggravated Diarrhoea Diverticulitis Diverticulum intestinal Exposure to SARS-CoV-2 Large intestinal stenosis Nausea Neoplasm Pulmonary mass Pyrexia SARS-CoV-2 test positive Scan with contrast abnormal Septic pulmonary embolism Vomiting

Symptomtext

ED to Hosp-Admission Discharged 2/16/2021 - 2/17/2021 (28 hours) Last attending o Treatment teamObesity, morbid, BMI 50 or higher (CMS/HCC) Pulmonary nodules COVID-19 Diverticulitis Diarrhea due to COVID-19 Resolved Hospital Course HPI: is an 34 y.o. female. Complaining of abdominal pain. The pain is primarily left side. She does have a history of diverticulitis in the past. She was diagnosed with Covid about 2 weeks ago and has been having fevers initially and diarrhea which have now subsided and she is changing to abdominal discomfort. She denies any fever but did have nausea and vomiting Saturday. She has not required any supp

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Praegender Schweregrund: Septic pulmonary embolism
Hospital-Tage: 1,0
Labordaten: 03/01/21 1520 COVID-19 External (Non or Non Interfaced Lab) Collected: 02/03/21 0000 | Edited Result - FINAL | Specimen: Swab from Nares COVID-19 Overall Result External
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Pulmonary nodules Asthma Mild intermittent asthma without complication Digestive Maternal morbid obesity
Andere Medikamente: Medications Prior Authorizations albuterol HFA (PROVENTIL;V
Allergien: AmoxicillinHives / Urticaria PenicillinsHives / Urticaria, Itc
Vorherige Impfungen: -

VAERS 1331323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 19.05.2021
Impfdatum: 11.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Acute respiratory failure Adenovirus test Ageusia Anosmia Anticoagulant therapy Asthenia Atrial fibrillation Atrial flutter COVID-19 pneumonia Chest X-ray abnormal Chest discomfort Computerised tomogram thorax abnormal Cough Decreased appetite Diarrhoea Dyspnoea Enterovirus test negative Fatigue

Symptomtext

ED to Hosp-Admission Discharged 3/26/2021 - 4/5/2021 (10 days) Last attending ? Treatment team Sepsis Principal problem Discharge Summary Inpatient Discharge Summary BRIEF OVERVIEW Admitting Provider: Discharge Provider: Admission Date: 3/26/2021 Discharge Date: 4/5/2021 Discharge Diagnosis Severe sepsis COVID-19 pneumonia Acute hypoxic respiratory failure Atrial fibrillation/atrial flutter with RVR DETAILS OF HOSPITAL STAY Presenting Problem/History of Present Illness/Reason for Admission patient is an 70 y.o. female with a past medical history of atrial fibrillation chronically anticoagulated with Xarelto, S/P ablation x3 at the Medical Center, and sinus bradycardia who presented to the ED for evaluation of general malaise, shortness of breath, loss of taste and smell, coughing, and shortness of breath and was found to have sepsis due to COVID-19 pneumonia in the ED. Patient states that over the past week she has been extremely weak, with nausea, diarrhea, but denies vomiting. She also reports that her appetite has decreased and noted that the symptoms has worsened and as a result she presented to the ED for further evaluation.Patient denies abdominal pain, lightheadedness, or chest pain. Upon further evaluation and tests in the ED, she was noted to have severe sepsis as indicated by vital signs and chest x-ray imaging indicating groundglass pneumonia typical of COVID-19 infection. She also had COVID-19 swab which returned positive result. Additionally, patient was noted to be hypoxia with SPO2 of 88% requiring oxygen supplementation. Hospital Course patient was admitted to a Hospital due to shortness of breath, with fatigue and weakness, and was found to have severe sepsis with endorgan damage of acute hypoxic respiratory failure due to COVID-19 pneumonia on admission. Imaging study showed no evidence of PE, but did show evidence of bilateral pulmonary infiltrates. Pulmonary was consulted, she was started on remdesivir with Decadron. She had an increase in oxygen requirement to the maximum of 10 L via specialty nasal cannula during the admission. With the treatment of remdesivir and Decadron she had improvement in her hypoxia, and was ultimately weaned to room air by the time of discharge. She underwent a desaturation study on the day of discharge and determined that she did not need any supplemental oxygen. She completed her entire steroid and remdesivir course during the admission. She had no evidence of superimposed bacterial pneumonia. Her hospitalization was complicated by atrial fibrillation/flutter with RVR, that improved with metoprolol administration. This was thought to be precipitated by her severe hypoxia with acute illness. She was kept on metoprolol 25 mg twice daily on discharge, and will need to follow-up with her cardiologist at Medical Center to determine if she can come off of this again. She will continue to take her Xarelto as previously prescribed. She was medically stable for discharge on 4/5 in stable condition, and will need to follow-up with PCP within 7 days, with cardiology within 2 weeks at the hospital, and pulmonary within 2 weeks as well.

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: 03/26/21 2158 Respiratory virus detection panel Collected: 03/26/21 1936 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected Operative Procedures Performed Ct Chest Without Contrast Result Date: 3/26/2021 Narrative: PROCEDURE INFORMATION: Exam: CT Chest Without Contrast; Diagnostic Exam date and time: 3/26/2021 9:48 PM Age: 70 years old Clinical indication: Cough; Additional info: PT here due to weakness that has been ongoing x 1 week. PT also reports productive cough. PT states she is starting to feel a tightness in her chest. PT states she is unsure of fever. Also reports nausea. Follow-up with the finding of findings chest x-ray TECHNIQUE: Imaging protocol: Diagnostic computed tomography of the chest without contrast. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. COMPARISON: CT CHEST WITHOUT CONTRAST 6/21/2016 7:14 AM FINDINGS: Lungs: Bilateral extensive patchy airspace disease with ground-glass opacity, right greater than left suggestive of a covid-19 pneumonia. Pleural spaces: Unremarkable. No pneumothorax. No pleural effusion. Heart: Unremarkable. No cardiomegaly. No pericardial effusion. Aorta: Unremarkable. No aortic aneurysm. Lymph nodes: Unremarkable. No enlarged lymph nodes. Bones/joints: Unremarkable. No acute fracture. Soft tissues: Unremarkable. IMPRESSION: Bilateral extensive patchy airspace disease with ground-glass opacity, right greater than left suggestive of a covid-19 pneumonia. THIS DOCUMENT HAS BEEN ELECTRONICALLY SIGNED X-ray Chest 1 View, Portable Result Date: 3/31/2021 Narrative: XR CHEST 1 VW PORT INDICATION: covid worsening hypoxia, re-eval. Encounter: Initial. TECHNIQUE: 2 projection of the chest is acquired. COMPARISON: 3/26/2021. FINDINGS: Extensive bilateral pulmonary infiltrates are either unchanged or minimally worse than before. No change in the heart, mediastinum, or bony thorax. END OF IMPRESSION: 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 Result Date: 3/27/2021 Narrative: Single view portable chest INDICATION: Shortness of breath, pneumonia, Covid pneumonia, encounter initial Frontal portable chest film demonstrates bilateral interstitial infiltrates characteristic of Covid 19 infection. No effusion, pneumothorax, cardiomegaly, or acute osseous finding. Further evaluation was obtained with CT. See this report. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous CVA (cerebral vascular accident) Anginal equivalent Abdominal pain, right lower quadrant Stroke (cerebrum) Respiratory DOE (dyspnea on exertion) Circulatory Irregular heart rhythm Paroxysmal atrial fibrillation Palpitations Non-rheumatic mitral regurgitation TIA (transient ischemic attack) PAF (paroxysmal atrial fibrillation) Symptomatic bradycardia Atrial flutter Genitourinary Urinary tract infection without hematuria Musculoskeletal Injury of head Endocrine/Metabolic Disorder of thyroid Immune Psoriasis Other Elevated transaminase level Difficulty with speech Long term (current) use of anticoagulants Encounter for screening colonoscopy Pacemaker
Andere Medikamente: alendronate (FOSAMAX) 70 mg tablet calcium carbonate-vitamin D3 1250 mg, 500 mg calcium,-5 mcg 1250 mg (500 mg calcium)-200 unit per tablet cyanocobalamin 500 mcg tablet metoprolol tartrate (LOPRESSOR) 25 mg tablet(Expired) multiple vitamin
Allergien: TriamcinoloneOther (document details in comments)
Vorherige Impfungen: -

VAERS 1313982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 81,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 13.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure Adenovirus test Asthenia Back pain Bordetella test negative COVID-19 Chlamydia test negative Chronic left ventricular failure Computerised tomogram head normal Cough Dysphagia Enterovirus test negative Essential hypertension Human metapneumovirus test Human rhinovirus test Hyperhidrosis Hypothyroidism Hypoxia

Symptomtext

ED to Hosp-Admission Discharged 4/6/2021 - 4/9/2021 (3 days) Last attending ? Treatment team Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC) Principal problem Discharge Summary Internal Medicine Discharge Summary Hospitalist Medicine Admission Date: 4/6/2021 Length of Stay: 3 Days Discharge Date: 4/9/2021 Admission Diagnosis Hospital Problems POA * (Principal) Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC) Yes Type 2 diabetes mellitus (CMS/HCC) Yes Obesity Yes Hypothyroidism Yes Chronic combined systolic and diastolic heart failure (CMS/HCC) Yes Benign essential hypertension Yes 81-year-old female presented to the hospital with a complaint of fever and cough COVID-19 - now saturating well on room air and Afebrile Complaining of sore throat and difficulty in swallowing- now resolving Back pain improving Episode of diaphoresis and blurry vision -now resolved Home Or Self Care CODE STATUS: DNR (Do Not Resuscitate) Active Issues Requiring Follow-up Follow-up with PCP for further care as outpatient. Test Results Pending at Discharge Pending Labs Order Current Status Blood culture- 2 SETS Preliminary result Blood culture- 2 SETS Preliminary result Hospital Course HPI: See H&P Hospital Course: Patient presented to the hospital with a complaint of fever and cough. She was admitted for COVID-19 with respiratory failure. Since she was saturating below 94%, she was started on remdesivir on admission. Oxygen was given for supportive care. She received albuterol inhaler, Mucinex, Tessalon Perles and Decadron. In addition she complained of some sore throat and received Chloraseptic spray along with lozenges. She had an episode of diaphoresis and change in vision during the hospitalization. There were no events on the monitor and the CT of the head was negative. The symptoms resolved. She also complained of insomnia back pain for which he received melatonin and Lidoderm patch respectively. She is feeling much better and has been saturating well on room air above 95% for the past 2 days. I will continue with the albuterol inhaler, Decadron and Mucinex as outpatient for few more days. She is asked to follow-up with her PCP for further care as outpatient. ED to Hosp-Admission Discharged 4/13/2021 - 4/16/2021 (3 days) Last attending ? Treatment team Weakness Principal problem Discharge Summary (Physician) ? ? Internal Medicine Discharge Summary Hospitalist Medicine Admission Date: 4/13/2021 Length of Stay: 1 Days Discharge Date: 4/16/2021 Admission Diagnosis Hospital Problems POA Type 2 diabetes mellitus (CMS/HCC) Yes Hypothyroidism Yes Hyperlipidemia due to type 2 diabetes mellitus (CMS/HCC) Yes Gastroesophageal reflux disease Yes Problem List Resolved POA Resolved Problems Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC) 4/17/2021 Yes * (Principal) Weakness 4/17/2021 Yes Generalized weakness 4/17/2021 Yes Home Under Care Of Organized Home Health Service CODE STATUS: Prior Active Issues Requiring Follow-up Test Results Pending at Discharge Hospital Course HPI: See H&P admit report. Hospital Course: Patient was admitted secondary to weakness and hypoxia she recently did have a bout of COVID-19 and had been discharged home and has been set up for remote outpatient monitoring as per protocol. She returns for ongoing weakness. Patient was continued on Decadron and was seen by physical therapy and Occupational Therapy. The patient slowly continued to improve and was now back to baseline functioning. She may be discharged home and follow-up with PCP as advised as she is no longer on oxygen. She is to complete the dexamethasone dose as she had previously been taking to complete a course. Home health had been previously set up at her previous admission.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: 04/06/21 2001 Respiratory virus detection panel Collected: 04/06/21 1905 | Final result | Specimen: Swab from Nasopharynx Adenovirus Not Detected Mycoplasma pneumoniae Not Detected Chlamydophila pneumoniae Not Detected Parainfluenza Not Detected COVID-19 SARS-CoV-2 Overall Result DetectedCritical Enterovirus/Rhinovirus Not Detected Coronavirus Not Detected Respiratory Synctial Virus Not Detected Influenza A Not Detected Bordetella pertussis Not Detected Influenza B Not Detected Bordetella parapertussis Not Detected Metapneumovirus Not Detected
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Migraine variants, not intractable Hearing loss Atherosclerotic heart disease of native coronary artery with unstable angina pectoris (CMS/HCC) Post-traumatic headache Respiratory Diaphragmatic hernia Allergic rhinitis Circulatory Varicose veins of lower extremity Paroxysmal supraventricular tachycardia (CMS/HCC) Chronic combined systolic and diastolic heart failure (CMS/HCC) Cardiomyopathy (CMS/HCC) Benign essential hypertension Arteriosclerosis of coronary artery Digestive Vitamin D deficiency Obesity Nonalcoholic fatty liver disease Liver cyst Diverticular disease of colon Gastroesophageal reflux disease Genitourinary Midline cystocele Genital herpes simplex Overactive bladder Musculoskeletal Osteochondropathy Lumbar spondylosis Arthropathy Endocrine/Metabolic Type 2 diabetes mellitus (CMS/HCC) Hypothyroidism Hyperlipidemia due to type 2 diabetes mellitus (CMS/HCC) Hematologic Leukocytosis Chronic lymphocytic leukemia (CLL), B-cell (CMS/HCC) Other Recurrent major depression in full remission (CMS/HCC) Panic disorder with agoraphobia and mild panic attacks Insomnia Generalized anxiety disorder Hernia of anterior abdominal wall Anxiety
Andere Medikamente: ACCU-CHEK GUIDE TEST STRIPS strip acetaminophen (TYLENOL) 500 mg tablet albuterol HFA (PROVENTIL;VENTOLIN) 90 mcg/actuation inhaler ALPRAZolam (XANAX) 0.25 mg tablet ascorbic acid, vitamin C, (VITAMIN C) 500 mg tablet aspirin 81 mg tablet a
Allergien: Amoxicillin LatexOther (document details in comments) Magnesium CitrateSwelling Ampicillin Penicillin PioglitazoneDizziness / Lightheaded
Vorherige Impfungen: -

VAERS 1311970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 59,0
Geschlecht: M
Eingang: 12.05.2021
Impfdatum: 11.02.2021
Beginn: 12.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chills Convalescent plasma transfusion Cough Fatigue Headache Pain SARS-CoV-2 test

Symptomtext

Chills, Generalized Body Aches, Cough, Headache, Fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 6,0
Labordaten: COVID-19: History, Infection Status Resolved 2/26/2021, Probable COVID-19 (Resolved) Specimen information: Swab / Nares, Added: 2/12/2021 by POCT COVID-19 Antigen (Collected 02/12/21), Onset date: 2/12/2021, Resolved: 2/26/2021 (Expired), Rule-Out COVID-19 and Respiratory Viruses (Resolved) ,Specimen information: Swab / Nasopharynx, Added: 2/19/2021 by Respiratory virus detection panel (02/19/21) Onset date: 2/19/2021, Resolved: 2/19/2021 (Rule-Out Test Canceled), ED to Hosp-Admission Discharged ,2/19/2021 - 2/25/2021 (6 days), Hospital, MD, Last attending, Treatment team, Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC), Principal problem, Discharge Summary, MD (Physician) Discharge Summary, Hospitalist Medicine, Patient: Date: 2/25/2021, Admission Date: 2/19/2021, PCP, Length of Stay: 6 Days, Discharging provider: MD, Discharge Date: 2/25/2021, Admission Diagnosis, Hospital Problems, POA, (Principal) Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC),Yes, Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin (CMS/HCC),Yes, Pneumonia due to COVID-19 virus, Yes, Hospital Course, HPI: Please see H&P for details. Hospital Course: 59-year-old gentleman with diabetes was admitted to hospital because of Covid related pneumonia and hypoxic respiratory failure. He was placed on oxygen and given convalescent plasma and course of Remdesivir along with dexamethasone. His symptoms improved throughout the stay and he was weaned off oxygen. On the day of discharge she is on room air and saturating satisfactorily. At this point he is going to be discharged home to be follow-up with PCP. He is also instructed to do pronging and increasing activity at home. Because of his dexamethasone he is going to be also given Novolin pen with sliding scale at home. He is going to have his second vaccination around 10 days to 14 days from the discharge date. These were all explained to the patient and wife in detail.
Aktuelle Erkrankungen: -
Vorgeschichte: Respiratory Acute hypoxemic respiratory failure due to COVID-19 (CMS/HCC) Pneumonia due to COVID-19 virus Endocrine/Metabolic Type 2 diabetes mellitus with hyperglycemia, without long-term current use of insulin (CMS/HCC)
Andere Medikamente: insulin aspart U-100 (NovoLOG) 100 unit/mL (3 mL) insulin pen OZEMPIC 0.25 mg or 0.5 mg(2 mg/1.5 mL) pen injector pen needle, diabetic 30 gauge x 5/16" needle SYNJARDY 5-500 mg tablet
Allergien: NKA
Vorherige Impfungen: -

VAERS 1304160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 10.05.2021
Impfdatum: 15.04.2021
Beginn: 29.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: UN / UN

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

Cerebrovascular accident Seizure

Symptomtext

CEREBROVASCULAR ACCIDENT R56.9 - Seizure (CMS/HCC)

Weitere VAERSDATA-Felder

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

VAERS 1280207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NV
Alter: 71,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 28.02.2021
Beginn: 07.04.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: - / -

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

Blood test Cerebral haemorrhage Chest X-ray Chest discomfort Computerised tomogram head Fatigue Near death experience Pulmonary embolism Computerised tomogram thorax abnormal Dyspnoea Intensive care Nausea Syncope Vomiting

Symptomtext

cerebral hemorrhage; Multiple pulmonary embolism in both lung; He merely died twice; he was still tired; This is a spontaneous report from a contactable consumer (patient's wife). A 72-year-old male patient (patient's husband) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6203), via an unspecified route of administration on 28Feb2021 (at the age of 71-year-old) as a single dose for COVID-19 immunization. The patient's medical history included liver replacement from 29Nov (unspecified year), cold, sore shot. When probed for medical condition, reporter stated no, she could remember that he had a cold when he get the sore shot every year and get pneumonia vaccine. He had liver replacement on 29Nov (unspecified year), no side effects or anything, no blood clot. He walks every day. No diabetic no any other complicated factor. Concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3249) on 07Feb2021 (at the age of 71-year-old) as a single dose for COVID-19 immunization and Pneumonia vaccine. It was reported that, reporter stated, she don't know how she just brief, but she would give the best she could. Reporter's husband has the Pfizer vaccine on 07Feb2021 and for the second does on 28Feb2021. He was 73-year-old now with no complicated factor, no history, and no adverse reaction anything like no allergy. Everything was fine, and on 07Apr2021 approximately five and half week after the second dose. He had to go to the emergency room as he could not breathe and he was diagnosed with multiple pulmonary embolism in both lung on 07Apr2021, no precipitating of event, no logical explanation that the doctors could tell, they put him on Eliquis to recover up the blood clots, 19 days later 26Apr2021 he was back in to ER. He was severe headache, nausea, vomiting. Side effects of the blood thinner. He was diagnosed with cerebral hemorrhage on 26Apr2021. We flight to hospital because we live in a small town no neuro surgeon available to get immediate surgery. The doctor told he was calm down, but they took him off from blood thinners and she don't know what she expect more blood clot, what going next, he feels fine, he still had some headache which doctor said it would leave the month because of the blood in the brain. There was no after explaining and no logical explanation what have happen other than the blood thinner, he could take blood thinner. She don't know why the clots come back, that's why she want to report this because this all way comes on with the Pfizer. He was fine with the other vaccine that have five weeks after later. When probed any question regarding side effects, reporter stated, well she just kind a need to know, what to expect. If this going to be ongoing thing with in and out of ER. What to expect, we don't know. Doctor was following up. He has Hematology appointment on Wednesday to try to figure out the consequences. Reporter stated, she was on hold for 40 minutes and she could not even report this as a serious possible adverse reaction of the vaccine and to the drug. He merely died twice. When probed was patient still experiencing the side effects, reporter stated, well he was still tired. He still have the headache it's not severe. He went to the emergency room. We are watching him on helping here to follow up. He was taking medication of anti-seizure Keppra because body has strains body so that's making him tired. The outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cold; Liver transplant (liver replacement from 29Nov (unspecified year)); Pain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1280207

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NV
Alter: 71,0
Geschlecht: M
Eingang: 08.05.2021
Impfdatum: 28.02.2021
Beginn: 07.04.2021
Tage bis Beginn: 38,0
Dosis: 2
Route/Site: SYR / -

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

Blood test Cerebral haemorrhage Chest X-ray Chest discomfort Computerised tomogram head Fatigue Near death experience Pulmonary embolism Computerised tomogram thorax abnormal Dyspnoea Intensive care Nausea Syncope Vomiting

Symptomtext

cerebral hemorrhage; Multiple pulmonary embolism in both lung; He merely died twice; he was still tired; This is a spontaneous report from a contactable consumer (patient's wife). A 72-year-old male patient (patient's husband) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6203), via an unspecified route of administration on 28Feb2021 (at the age of 71-year-old) as a single dose for COVID-19 immunization. The patient's medical history included liver replacement from 29Nov (unspecified year), cold, sore shot. When probed for medical condition, reporter stated no, she could remember that he had a cold when he get the sore shot every year and get pneumonia vaccine. He had liver replacement on 29Nov (unspecified year), no side effects or anything, no blood clot. He walks every day. No diabetic no any other complicated factor. Concomitant medications were not reported. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3249) on 07Feb2021 (at the age of 71-year-old) as a single dose for COVID-19 immunization and Pneumonia vaccine. It was reported that, reporter stated, she don't know how she just brief, but she would give the best she could. Reporter's husband has the Pfizer vaccine on 07Feb2021 and for the second does on 28Feb2021. He was 73-year-old now with no complicated factor, no history, and no adverse reaction anything like no allergy. Everything was fine, and on 07Apr2021 approximately five and half week after the second dose. He had to go to the emergency room as he could not breathe and he was diagnosed with multiple pulmonary embolism in both lung on 07Apr2021, no precipitating of event, no logical explanation that the doctors could tell, they put him on Eliquis to recover up the blood clots, 19 days later 26Apr2021 he was back in to ER. He was severe headache, nausea, vomiting. Side effects of the blood thinner. He was diagnosed with cerebral hemorrhage on 26Apr2021. We flight to hospital because we live in a small town no neuro surgeon available to get immediate surgery. The doctor told he was calm down, but they took him off from blood thinners and she don't know what she expect more blood clot, what going next, he feels fine, he still had some headache which doctor said it would leave the month because of the blood in the brain. There was no after explaining and no logical explanation what have happen other than the blood thinner, he could take blood thinner. She don't know why the clots come back, that's why she want to report this because this all way comes on with the Pfizer. He was fine with the other vaccine that have five weeks after later. When probed any question regarding side effects, reporter stated, well she just kind a need to know, what to expect. If this going to be ongoing thing with in and out of ER. What to expect, we don't know. Doctor was following up. He has Hematology appointment on Wednesday to try to figure out the consequences. Reporter stated, she was on hold for 40 minutes and she could not even report this as a serious possible adverse reaction of the vaccine and to the drug. He merely died twice. When probed was patient still experiencing the side effects, reporter stated, well he was still tired. He still have the headache it's not severe. He went to the emergency room. We are watching him on helping here to follow up. He was taking medication of anti-seizure Keppra because body has strains body so that's making him tired. The outcome of the events was unknown. Information on Lot/Batch number was available. Additional information has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cold; Liver transplant (liver replacement from 29Nov (unspecified year)); Pain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1282173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: ND
Alter: 60,0
Geschlecht: M
Eingang: 03.05.2021
Impfdatum: 02.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: IM / LA

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

Acute myocardial infarction Dizziness

Symptomtext

Patient presented to the ED with severe dizziness on 3/14/21 and was hospitalized for 43 hours. It was also noted he had NSTEMI. This visit is within 6 weeks of receiving COVID vaccination.

Weitere VAERSDATA-Felder

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

VAERS 1274404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 78,0
Geschlecht: F
Eingang: 30.04.2021
Impfdatum: 19.03.2021
Beginn: 04.04.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Cardiomegaly Chest X-ray abnormal Computerised tomogram thorax abnormal Dyspnoea Lung opacity Pleural effusion Pneumonitis Pulmonary embolism X-ray limb abnormal

Symptomtext

"Pfizer-BioNTech COVID-19 Vaccine" - received first dose 2/26/2021 and second dose 3/19/2021, admitted for acute segmental LLL PE. Pt endorsed subacute progressive DOE x6 months. Admitted to hospital with elevated BP and 2 weeks of progressively worsening SOB (after 3/19/2021, at which time pt received the second dose of vaccine.) EMS reported SaO2 79%. CXR - moderate diffuse edema or pneumonitis in both lungs, small pleural effusions, cardiomegaly CTA of chest - acute PE involving segmental pulmonary arteries to L lower lobe, moderate diffuse ground-glass opacities in both lungs (R>L) -- > possible drug-induced pneumonitis (lower suspicion because pt had been on palbociclib x2 years) or volume overload.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 6,0
Labordaten: See item 18.
Aktuelle Erkrankungen: Malignant neoplasm R breast receiving chemotherapy treatment
Vorgeschichte: BMI = 31.2 (Obesity, Class I, BMI 30-34.9) Anthropathy, lower leg - Bilateral knees, xray with mild effusions L>R Impa
Andere Medikamente: Fulvestrant Q30days (start date 04/2019)
Allergien: NKA
Vorherige Impfungen: -

VAERS 1333017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 29.04.2021
Impfdatum: 26.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 25,0
Dosis: 2
Route/Site: IM / LA

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

Anticoagulant therapy Atrial fibrillation Cardiac failure congestive Deep vein thrombosis Dyspnoea Pulmonary embolism

Symptomtext

PULMONARY EMBOLISM Patient reported to OSH 24 days after second Pfizer COVID-19 Vaccine with SOB--diagnosed with bilateral PE/DVT and remained inpatient for approximately 3 days. Patient also diagnosed with Afib and new onset CHF during admission. Discharged home with anticoagulation.

Weitere VAERSDATA-Felder

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

VAERS 1271757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 88,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 24.02.2021
Beginn: 20.03.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / -

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

Death

Symptomtext

Death within 60 days of vaccination

Weitere VAERSDATA-Felder

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

VAERS 1270988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: 81,0
Geschlecht: F
Eingang: 29.04.2021
Impfdatum: 06.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Chills Death Haemarthrosis Herpes zoster Illness Malaise Pain Pericardial drainage Pericardial effusion Pulmonary thrombosis Pyrexia Vena cava filter insertion

Symptomtext

After 2nd Vaccine on 3/6/21, she became ill on 3/8/21, fever and chills was in bed all day on 3/9/21 with the same symptoms. Woke up on 3/9/21 with shingles, Her PCP was treating her with Famciclovir and Gabapentin for pain. She no longer had the fever or chills but still didn't feel well. On 3/17/21 she was admitted at Medical Center which she was treated for a blood clot in her lung and for pericardial effusion. She was put on blood thinners which then caused a bleed in her hip bone. She had a surgery to put a filter in to stop more blood clots and to drain the fluid from her heart. She died on 3/27/21 around 3:30pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 10,0
Labordaten: I am requesting her medical records from the hospital.
Aktuelle Erkrankungen: None
Vorgeschichte: Afib Congestive Heart Failure Kidney Disease COPD
Andere Medikamente: Synthroid 100mg Amiodarone 100mg Furosemide 40mg & 20mg alternating days Aspirin 81 mg Omeprazole 20mg Forsinopril 5mg Allopurinol 100mg Cyclopento 1% 1 drop left eye daily Predn
Allergien: MetFormin HCI Losartan Patassium Zocor Cipro Lipitor Irbesartan
Vorherige Impfungen: -

VAERS 1269415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 06.04.2021
Beginn: 08.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: UN / UN

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

Abdominal pain upper Abnormal behaviour Acidosis Blood glucose increased Blood potassium decreased Blood pressure abnormal Cardio-respiratory arrest Computerised tomogram abdomen normal Computerised tomogram normal Confusional state Cytokine storm Death Dehydration Delirium Diabetic ketoacidosis Dialysis Diarrhoea Electroencephalogram normal

Symptomtext

? Tuesday, April 6th ? Patient receives the 2nd Pfizer vaccine shot ? Thursday, April 8th ? Patient is sick with vomiting and diarrhea ? Friday, April 9th ? Patient is delirious and still sick with vomiting and diarrhea. She is also has pain in her stomach. An ambulance is called to take her to the hospital. The hospital determines her white blood count is elevated, indicating an infection. Blood sugar is very high ? approximately 400. Covid test is negative. She is restless upon arrival. She tries to climb out of bed continuously. She is restrained. o Saturday, April 10th ? Patient is running a fever and is in pain. She is also confused and doesn?t recognize her oldest sister. Meds are administered to handle both items. (Toradol?). Blood sugar around 200. She continuously counts and calls for Mother and Father. Patient continues to be restless o Sunday, April 11th - at request of family, a CT scan is done of her stomach and abdomen. Nothing is found. Potassium was at 3.2 (normal is 3.5) so she received an IV drip to help with potassium levels. Sugar ? 206. Later drops to 176. Patient calms down some. She is still confused and doesn?t recognize her oldest sister. ? Monday April 12th ? the hospital attempts to do an MRI, but patient panics. This is a closed MRI and her 1st husband died in one. The MRI isn?t done. ? Tuesday, April 13th ? she is asked by the doctor to state her name and wiggle her toes. She complies. Doctor orders speech therapy. She is sedated for an MRI and a CT scan. Both are successfully completed. She sleeps for the rest of the day. Blood sugar ? 274 @ 5:09pm. ? Wednesday, April 14th ? Patient was asleep all day. Most of the day she isn?t responsive when nurses come in and do things like take blood. She normally responds even if she is asleep. Around 5pm she starts to respond and make noises; she briefly opens her eyes then falls asleep. She continues to run a temperature. ? Thursday, April 15th ? Patient is asleep most of the day. She is responsive when nurses do things like take blood. A spinal tap is performed. There was mention of dementia. Hospital is sharing little information, varying from she is retreating into herself vs. something worth isolating is going on. Temp was 102.3 at 7:37, but later dropped to 99.3 without meds. Dr. (neurologist) provides an update to the family. Tests so far are negative. EEG showed sleeping brain (she was asleep during test). MRI showed nothing. Spinal tap negative so far. No infection or anything has shown up. Orders another EEG and MRI ? Friday, April 16th ? Patient tried to open her eyes. ? Saturday, April 17th ? a met code was called on her and she was moved to ICU. A circulation issue was found in right leg. Occlusion was really bad. Initially the doctor was concerned about blood clots. None were found, just swelling. Pressure was relieved. Blood pressure issues. She was put on 2 blood pressure meds, at least. She was dehydrated and acidic. Diabetic ketoacidosis was mentioned. A cytokine storm was expected. ? Sunday, April 18th ? blood pressure not stable. She was put on dialysis. Peripheral circulation was worse. ? Monday, April 19th ? she coded around 5am. Doctors were trying to save her. She passed away about 30 minutes later .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: 11,0
Labordaten: see item 18 for the known tests and laboratory results.
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis (all lymph nodes involved) Causes the sleepiness/?ams? Cannot stop prednisone Diabetes Hypothyroidism High blood pressure High cholesterol Lots of pain in legs Toes curled up Osteoarthritis Polyp - found when doctor tried to do Pap smear/removed 04-01-2013 - taken out later in same year Chronic kidney disease
Andere Medikamente: Acetaminophen, 1,500 mg 2x daily Pravastatin, 40 mg daily Glimepiride, 4 mg, 1/2 tab in am, 1 tab in pm Januvia, 50 mg twice daily *Prednisone, 5 mg, 1 in am, 1/2 in pm Levothyroxine, 0.100 mg daily * Azathioprine, 50 mg 2x daily Lisinopri
Allergien: Pseudoephedrines Demerol Oxycodone Vancomycin
Vorherige Impfungen: -

VAERS 1267477

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NC
Alter: 57,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 25.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / RA

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

Computerised tomogram thorax Deep vein thrombosis Pain in extremity Peripheral swelling Pulmonary embolism Ultrasound Doppler

Symptomtext

Left leg pain and swelling a couple weeks after shot one of Pfizer vaccine. After a few more days of leg not getting any better, saw Doctor who ordered Ultra sound of left leg and CT scan of lungs. Extensive DVT clot found in left leg, low density bi lateral pulmonary embolism in both lower lobes of lungs found from CT scan. Hospital stay for 2 days, Heparin given in hospital and now I'm on eliquis blood thinner. Had gotten my second Pfizer shot 3 days before admittance to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lisinopril10mg,Synthroid150mcg,Amlodipine5mg,Atorvanstatin10mg
Allergien: none
Vorherige Impfungen: -

VAERS 1266069

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 28.04.2021
Impfdatum: 06.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / RA

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

Myocardial infarction

Symptomtext

heart attack; This is a spontaneous report from a contactable consumer (patient herself). This 60-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route of administration in the right arm, on 06Mar2021 at 15:30 (Lot number EN6203) as single dose and the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route of administration in the left arm, on 27Mar2021 at 15:30 (Lot number EP7534) as single dose, for COVID-19 immunisation. Relevant medical history included allergy to nickel and latex). Past drug history included allergy to penicillin. Relevant concomitant medications included ezetimibe, chondroitin sulfate, glucosamine, biotin and vitamin (unspecified). No other vaccine was received in four weeks. The patient had a mild heart attack approximately two weeks after her first dose of the vaccine (untreated) in Mar2021 and a major heart attack 2 weeks to the day after her second dose (11Apr2021, at 02:00). The patient visited the emergency room and she was hospitalized for 5 days. The event was also considered serious as life-threatening. Therapeutic measures taken as result of the event includes angioplasty. The patient was recovering from the event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Latex allergy; Nickel sensitivity
Andere Medikamente: EZETIMIBE; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE;GLUCOSAMINE]; BIOTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1266034

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 28.04.2021
Impfdatum: 19.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / -

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

Blood insulin Cerebrovascular accident Fall Speech disorder

Symptomtext

This is a spontaneous report from a contactable consumer (patient's wife). A 74-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6203), dose 2 via an unspecified route of administration on 19Feb2021 (at the age of 74years) as single dose for COVID-19 immunization. The patient received the first dose of BNT162B2 (lot number: EL9262) on 28Jan2021 (at the age of 74years) for Covid-19 immunization and stated no reactions. Medical history included high blood pressure and diabetes but are all currently under control and feeling some leg pain before the vaccine was administered. It was reported that in the past the doctors thought he experienced TIA (transient ischemic attack) but wasn't sure if that was accurate. Concomitant medications included lisinopril (LISINOPRIL), trazodone (TRAZODONE), insulin (INSULIN), bupropion hydrochloride (WELLBUTRIN), and prednisone (PREDNISONE); all taken for an unspecified indication, start and stop date were not reported. It was reported that on 19Feb2021 the patient received the 2nd dose of Pfizer Covid vaccine and stated he remember feeling some leg pain before the vaccine was administered earlier. On Sunday 21Feb2021, the reporter (patient's wife) began noticing that the patient was showing symptoms of a stroke. The patient's one leg was rapidly kicking, and his speech began to slur. The patient was then rushed to ER (emergency room) and hospitalized. At the hospital it was confirmed that the patient was having a stroke. The patient recovered and was doing rehab for his leg. Few weeks later, the patient had an accident in his home while getting up to go to the bathroom and fell. The patient was rushed to the Trauma center. The patient's wife was upset as she carried their vaccine cards to the trauma center to confirm to staff that the patient did not need another Covid vaccine shot and later found out that the patient was given a 3rd (Moderna Covid vaccine) at the trauma center. The patient stated that he does not think the vaccine was related but was upset that the trauma center did not listen to her to take the info with the complete vaccine card present to avoid 3rd shot from another brand. The patient's insulin levels are under control, but the reporter was concerned when the patient does not eat within a certain timeframe. The outcome of events stroke and speech disorder was recovered on an unspecified date; outcome of event fall was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Name: insulin levels; Result Unstructured Data: Test Result:insulin levels are under control; Comments: levels are under control but concerned when patient does not eat within a certain timeframe.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (high blood pressure and diabetes but are all currently under control); Diabetes (high blood pressure and diabetes but are all currently under control); Leg pain (remember feeling some leg pain before the vaccine was administered); TIA (doctors thought he experienced TIA (transient ischemic attack) but wasn't sure if that was accurate)
Andere Medikamente: LISINOPRIL; TRAZODONE; INSULIN; WELLBUTRIN; PREDNISONE
Allergien: -
Vorherige Impfungen: -

VAERS 1105331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 70,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 05.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Back pain Blood calcium Cardiac stress test Echocardiogram Nerve compression Cardiac stress test normal Catheterisation cardiac Chest X-ray Chest pain Computerised tomogram coronary artery abnormal Disease recurrence Computerised tomogram Echocardiogram normal Electrocardiogram Fatigue Full blood count SARS-CoV-2 test Myocardial infarction

Symptomtext

intense pain in his back that radiated to his chest and left arm; intense pain in his back that radiated to his chest and left arm; intense pain in his back that radiated to his chest and left arm; This is a spontaneous report from a contactable consumer (patient) reported for himself that a 70-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6203) via an unspecified route of administration, administered in Arm Left on 05Mar2021 12:00 as single dose for COVID-19 immunisation. Medical history included heart palpitations, partially blocked cardiac arteries. Patient was allergic to Sulfa and ciprofloxacin hydrochloride (CIPRO). In Nov2020, patient consulted a cardiologist for heart palpitations. The cardiologist recommended patient to receive a calcium score test. Since this showed moderate risk in two arteries, he referred patient for an echocardiogram and a nuclear stress test, both of which were normal. Based on these results, cardiologist felt that patient's condition was stable and recommended against catherization. Concomitant medication included colecalciferol (VITAMIN D 1000 IU). No COVID prior vaccination. No other vaccine in four weeks. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EM9809) administered in Left arm on 12Feb2021 12:00 PM at the age of 70 years for COVID-19 immunisation and experienced sore arm, intense pain in his back that radiated to chest and left arm, patient attributed the pain to his supposed pinched nerve. Patient received his second vaccination on 05Mar2021. He began to experience intense pain in his back that radiated to his chest and left arm about 24 hours later on 06Mar2021 03:00 PM. The adverse events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness. Patient admitted to hospital for 4 days and received treatment: Catherization, insertion of stent. Patient had COVID-19 PCR test post vaccination via nasal swab on 06Mar2021 and revealed negative result. Outcome of the events was recovering.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021423183 same patient and reporter, different dose and event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Test Date: 202011; Test Name: nuclear stress test; Result Unstructured Data: Test Result:normal; Test Date: 202011; Test Name: calcium score test; Result Unstructured Data: Test Result:moderate risk in two arteries; Test Date: 202011; Test Name: echocardiogram; Result Unstructured Data: Test Result:normal; Test Date: 20210306; Test Name: COVID-19 PCR test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coronary artery occlusion; Palpitations; Sulfonamide allergy
Andere Medikamente: VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1105331

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 70,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 05.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Back pain Blood calcium Cardiac stress test Echocardiogram Nerve compression Cardiac stress test normal Catheterisation cardiac Chest X-ray Chest pain Computerised tomogram coronary artery abnormal Disease recurrence Computerised tomogram Echocardiogram normal Electrocardiogram Fatigue Full blood count SARS-CoV-2 test Myocardial infarction

Symptomtext

intense pain in his back that radiated to his chest and left arm; intense pain in his back that radiated to his chest and left arm; intense pain in his back that radiated to his chest and left arm; This is a spontaneous report from a contactable consumer (patient) reported for himself that a 70-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6203) via an unspecified route of administration, administered in Arm Left on 05Mar2021 12:00 as single dose for COVID-19 immunisation. Medical history included heart palpitations, partially blocked cardiac arteries. Patient was allergic to Sulfa and ciprofloxacin hydrochloride (CIPRO). In Nov2020, patient consulted a cardiologist for heart palpitations. The cardiologist recommended patient to receive a calcium score test. Since this showed moderate risk in two arteries, he referred patient for an echocardiogram and a nuclear stress test, both of which were normal. Based on these results, cardiologist felt that patient's condition was stable and recommended against catherization. Concomitant medication included colecalciferol (VITAMIN D 1000 IU). No COVID prior vaccination. No other vaccine in four weeks. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EM9809) administered in Left arm on 12Feb2021 12:00 PM at the age of 70 years for COVID-19 immunisation and experienced sore arm, intense pain in his back that radiated to chest and left arm, patient attributed the pain to his supposed pinched nerve. Patient received his second vaccination on 05Mar2021. He began to experience intense pain in his back that radiated to his chest and left arm about 24 hours later on 06Mar2021 03:00 PM. The adverse events resulted in Emergency room/department or urgent care, Hospitalization, Life threatening illness. Patient admitted to hospital for 4 days and received treatment: Catherization, insertion of stent. Patient had COVID-19 PCR test post vaccination via nasal swab on 06Mar2021 and revealed negative result. Outcome of the events was recovering.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021423183 same patient and reporter, different dose and event

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: Test Date: 202011; Test Name: nuclear stress test; Result Unstructured Data: Test Result:normal; Test Date: 202011; Test Name: calcium score test; Result Unstructured Data: Test Result:moderate risk in two arteries; Test Date: 202011; Test Name: echocardiogram; Result Unstructured Data: Test Result:normal; Test Date: 20210306; Test Name: COVID-19 PCR test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Coronary artery occlusion; Palpitations; Sulfonamide allergy
Andere Medikamente: VITAMIN D [COLECALCIFEROL]
Allergien: -
Vorherige Impfungen: -

VAERS 1238440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NJ
Alter: 76,0
Geschlecht: M
Eingang: 21.04.2021
Impfdatum: 22.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / LA

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

Abscess limb Acute kidney injury Acute respiratory distress syndrome COVID-19 pneumonia Computerised tomogram thorax normal Cough Death Diarrhoea Epistaxis Fatigue Gastrointestinal haemorrhage Metabolic disorder Pyrexia Renal failure Thrombophlebitis superficial Ventricular tachycardia

Symptomtext

Patient presented to ED on 3/15/2021 with fatigue, subjective fevers, dry cough, and diarrhea found to have COVID pneumonia. CT PE negative at that time. Hospitalization complicated by RUE superficial cephalic vein thrombus, epistaxis, GIB, gluteal abscess, and AKI. Patient made DNR. Suspected cause of death: ventricular tachycardia secondary to renal failure and metabolic abnormalities in the setting of COVID ARDS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: CAD with stents, former smoker, COPD, HLD, HTN, GERD
Andere Medikamente: amlodipine 5 mg daily, folic acid 1 mg daily, pantoprazole 40 mg daily, meloxicam 15 mg daily, simvastatin 40 mg daily, aspirin 81 mg daily, Norflex 100 mg BID PRN, Stiolto 2 puffs daily, fluticasone-salmeterol 250-50 BID, betaxolol 10 mg d
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1228481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 58,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 25.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: IM / LA

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

Autopsy Pulmonary embolism Resuscitation Syncope

Symptomtext

The patient had previously been diagnosed with COVID-19 in November 2020, but did no require hospitalization and had recovered. He received his first dose of the Pfizer COVID vaccine on 2/25/2021, and on 3/15/2021, collapsed suddenly at home and was unable to be resuscitated. An autopsy was performed at the request of the family, and a massive pulmonary embolus was found in the main pulmonary artery and extending far into the segmental pulmonary arteries of both lungs.

Weitere VAERSDATA-Felder

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

VAERS 1221456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 16.04.2021
Impfdatum: 22.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: SYR / RA

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

Brain stem haemorrhage Cerebrovascular accident Computerised tomogram head abnormal Craniotomy Nausea Pain Vomiting

Symptomtext

Patient woke up on the 28th complaining of severe pain, nausea and vomiting. Was admitted to healthcare facility and kept for observation overnight. On the 29th a CT was done and found bleeding in brain/stroke. Airlifted to healthcare facility where Craniotomy surgery was done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 21,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, stroke in September 2015.
Andere Medikamente: Unknown - possible high blood pressure medication. Patient is in charge of her own medication and unable to confirm now if that was taken on the day of vaccination.
Allergien: None
Vorherige Impfungen: -

VAERS 1214969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: OH
Alter: 69,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 06.03.2021
Beginn: 05.04.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: IM / AR

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

Computerised tomogram thorax abnormal Echocardiogram normal Pulmonary embolism Ultrasound Doppler normal

Symptomtext

Found to have bilateral pulmonary emboli on CT scan done April 5, 2021. He was asymptomatic. Was a scheduled CT to follow-up on previous pulmonary nodules and the PE's were seen. No other reason for the PE's has been found at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 1,0
Labordaten: CTA Chest - bilateral pulmonary emboli, Echocardiogram - normal heart function, Venous doppler - negative for clot
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hyperlipidemia, Asthma, allergic rhinitis, BPH, hiatal hernia with esophagitis, aortic aneurysm,
Andere Medikamente: Lisinopril, atorvastatin, omeprazole, vitamin C, vitamin D, multivitamin, vitamin B-12, curcumin, glucosamine chondroitin, erythromycin ointment, Breo, Incruse, montelukast, tamsulosin, proscar, Proair
Allergien: Nuts
Vorherige Impfungen: -

VAERS 1112373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: TX
Alter: 58,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 05.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Antiphospholipid antibodies negative Antithrombin III Antithrombin III deficiency Blood immunoglobulin M Cardiolipin antibody Chest pain Computerised tomogram thorax abnormal Dyspnoea Dyspnoea exertional Palpitations Computerised tomogram thorax Pulmonary embolism Paroxysmal nocturnal haemoglobinuria Pleuritic pain Protein S normal Prothrombin index Prothrombin level normal

Symptomtext

shortness of breath, right sided pleuritic chest pain started 4 days after 2nd dose. Patient whom is a MD, initially thought asthma exacerbation possibly from the vaccine, took inhaler and steroids. Symptoms worsened and then diagnosed with bilateral pulmonary embolism (see below).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: 3/18/2021 presents to emergency department for pleuritic chest pain to the right side with radiation to right arm. Of note, she received her second dose of Pfizer COVID-19 vaccine on 3/5/2021. 4 days after that, she noted right-sided pleuritic chest pain and dyspnea. It improved with a course of steroids and bronchodilators. After stopping her steroids, the symptoms recurred. 3/18/2021 CTA chest at hospital: Bilateral segmental and subsegmental pulmonary emboli. No CT evidence of right heart strain or pulmonary infarct. She was started on Rivaroxaban (=Xarelto) and discharged home. Labs drawn on same day included laboratory hypercoagulable work-up. Antithrombin antigen mildly low 60% with normal Antithrombin III activity, protein C and protein S normal, factor V Leiden gene mutation negative, prothrombin gene mutation negative, MTHFR heterozygous for C677T with normal homocysteine, PNH 0.001%, PNH monocytes 0.009%, phospholipid antibody panel remarkable for cardiolipin IgM 21, phosphatidylserine IgM 46; dRVVT was prolonged but lupus anticoagulant was not detected. Psoriatic arthritis takes infliximab (=Remicade) and methotrexate PO weekly. Symptoms uncontrolled. She was taking Estrace for menopausal symptoms. She stopped this at timing of PE. Still with residual DOE with activity and trouble taking a deep inspiration. Palpitations with PVCs/bigeminy.
Aktuelle Erkrankungen: psoriatic arthritis
Vorgeschichte: psoriatic arthritis
Andere Medikamente: Estradiol, Remicade, methotrexate, gabapentin, pantoprazole, valacyclovir, symbicort
Allergien: none
Vorherige Impfungen: -

VAERS 1205103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: 81,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 04.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest discomfort Chest pain Computerised tomogram thorax Malaise Pulmonary embolism Ultrasound scan

Symptomtext

On February 20, 2021 in the early evening my husband began to experience chest pain and pressure, took Tylenol, however did not relay the symptoms to me. About 6:50 AM on February 21, 2021 told me that he did not feel well, had chest pain and pressure in his chest. An ambulance was called and my husband was transported to the Hospital. I was contacted by the treating physician and was told that my husband suffered with a Pulmonary Embolysm (sp?). He was started on Heparin and admitted to the hospital. Later that evening his medication was changed to Eloquis. He was released from hospital the following evening. He has since followed up with his primary care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: All tests and labs were performed on February 21, 2021 at the Hospital. Blood work Chest CT Leg ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type 2 Cholesterol
Andere Medikamente: Simvastatin 10mg daily Metformin 1500mg daily Tolterodine ER CAP 4mg daily Aspirin 81mg daily
Allergien: None
Vorherige Impfungen: -

VAERS 1299439

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 16.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Altered state of consciousness Areflexia Blood gases Chills Coma scale abnormal Dyspnoea Endotracheal intubation Hypoxia Pyrexia Speech disorder Staring

Symptomtext

shortness of breath, hypoxia chills/rigors, febrile Narrative: Patient presented to the ED with 1-day history of rigors and chills after receiving the 2nd dose of his SARS-CoV-2 immunization; he reportedly woke up 03/17 with new dyspnea, was "staring off", and was mumbling non- sensical words and phrases. Patient's girlfriend called EMS and was transferred to the ED. SpO2 reportedly in 80%s en route. On arrival, patient's vital signs were significant for temp 102F and transient hypoxia to the 60%s when transferred to ED bed. Patient was notably altered, non-verbal, and not following commands, with an initial GCS of 10 with intact gag reflex. VBG 7.24/69/75/29. but follow-up GCS was 4 with impaired gag reflex. Respiratory therapy was called for intubation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Coma scale abnormal
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1168793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 01.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Death Iron deficiency anaemia

Symptomtext

Death Narrative: Death on 03/07/2021. 2nd dose administered 6 days before serious event. No data about cause of death available. Pt was dx Iron deficiency anemia and had been scheduled to have a diagnostic colonoscopy. No indication that death was related to the vaccine.

Weitere VAERSDATA-Felder

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

VAERS 1168641

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: FL
Alter: 26,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / AR

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

Death

Symptomtext

Death.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: ADHD
Andere Medikamente: Vyvanse, Adderall, Trazodone, Clonazepam
Allergien: Tdap vaccine
Vorherige Impfungen: -

VAERS 1063316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 04.04.2021
Impfdatum: 28.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Anaphylactic shock Hypersensitivity Dyspnoea Flushing Immediate post-injection reaction Pruritus Swelling face

Symptomtext

Anaphylactic Shock; Allergic reaction; This is a spontaneous report from a contactable consumer (patient). A 41-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot number: EN6203 and expiration date: Not available), via an unspecified route of administration in the right arm on 28Feb2021 at 12:00 PM as a single dose for COVID-19 immunisation. The patient was not pregnant. Medical history reported as None. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. No covid test post vaccination. No other vaccine in four weeks. The patient didn't receive other medication in two weeks. On 28Feb2021 at 12:00 PM, the patient experienced Anaphylactic shock/allergic reaction. The patient received Epinephrine Injection for the events. The events resulted in a visit to emergency room/department or urgent care. The clinical outcome of events was recovered with sequel (with lasting effects). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
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 1063316

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 04.04.2021
Impfdatum: 28.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / UN

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

Anaphylactic shock Hypersensitivity Dyspnoea Flushing Immediate post-injection reaction Pruritus Swelling face

Symptomtext

Anaphylactic Shock; Allergic reaction; This is a spontaneous report from a contactable consumer (patient). A 41-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot number: EN6203 and expiration date: Not available), via an unspecified route of administration in the right arm on 28Feb2021 at 12:00 PM as a single dose for COVID-19 immunisation. The patient was not pregnant. Medical history reported as None. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. No covid test post vaccination. No other vaccine in four weeks. The patient didn't receive other medication in two weeks. On 28Feb2021 at 12:00 PM, the patient experienced Anaphylactic shock/allergic reaction. The patient received Epinephrine Injection for the events. The events resulted in a visit to emergency room/department or urgent care. The clinical outcome of events was recovered with sequel (with lasting effects). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic shock
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 1160304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 73,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 09.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / RA

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

Cerebral haemorrhage Computerised tomogram head abnormal Headache Subdural haematoma

Symptomtext

Patient presented to the ER with a severe headache on 3/30. CT found subdural hematoma as well as intra-axial hemorrhage in the left axial lobe. The patient was life flighted from our facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral haemorrhage
Hospital-Tage: -
Labordaten: CT scan 3/30
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1116377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 91,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 01.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: - / LA

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

Asthenia Death Dysstasia Inflammation Magnetic resonance imaging spinal abnormal Bone cancer metastatic Gait disturbance General physical health deterioration Pain Malignant neoplasm of spinal cord Movement disorder Wheelchair user

Symptomtext

On the fourth day, was taken to hospital and diagnosed with metastatic cancer in the spine; 91 yo father received second dose of vaccine, was very sore on second day and then could not walk by third day; 91 yo father received second dose of vaccine, was very sore on second day and then could not walk by third day; incredibly marked decline in health and rapid deterioration resulting in death; This is a spontaneous report from a contactable consumer. A 91-year-old male patient received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine), second dose via an unspecified route of administration, administered in Arm Left on 01Mar2021 16:30 (Batch/Lot Number: EN6203) as SINGLE DOSE for covid-19 immunisation. Medical history included Chronic heart conditions, chronic obstructive pulmonary disease (COPD) and, asymptomatic cancer was diagnosed in hospital following vaccine; all from an unknown date and unknown if ongoing. The patient was vaccinated at a hospital. No other vaccine in four weeks. The patient had no COVID prior vaccination and not tested post vaccination. The patient had no known allergies. The patient previously took bnt162b2 (Pfizer-Biontech Covid-19 Vaccine) first dose on 08Feb2021 (lot: EN6201) 05:30 PM at the left arm. It was reported that the patient "received second dose of vaccine, was very sore on second day (03Mar2021) and then could not walk by third day (04Mar2021). On the fourth day (05Mar2021), was taken to hospital and diagnosed with metastatic cancer in the spine, which had produced no symptoms prior. The vaccine obviously did not cause cancer, but it did precipitate some event that led to an incredibly marked decline in health and rapid deterioration resulting in death 17 days after vaccine." The patient died on 18Mar2021. It was not reported if an autopsy was performed. The event resulted in Emergency room/department or urgent care and hospitalization for 7 days.; Sender's Comments: Based on the current available information, Bone cancer metastatic is considered unrelated to the suspected drug of bnt162b2. The case will be reassessed if additional information becomes available.; Reported Cause(s) of Death: incredibly marked decline in health and rapid deterioration resulting in death; On the fourth day, was taken to hospital and diagnosed with metastatic cancer in the spine; 91 yo father received second dose of vaccine, was very sore on second day and

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (asymptomatic cancer was diagnosed in hospital following vaccine); COPD; Heart disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1116377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: PA
Alter: 91,0
Geschlecht: M
Eingang: 02.04.2021
Impfdatum: 01.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / AR

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

Asthenia Death Dysstasia Inflammation Magnetic resonance imaging spinal abnormal Bone cancer metastatic Gait disturbance General physical health deterioration Pain Malignant neoplasm of spinal cord Movement disorder Wheelchair user

Symptomtext

On the fourth day, was taken to hospital and diagnosed with metastatic cancer in the spine; 91 yo father received second dose of vaccine, was very sore on second day and then could not walk by third day; 91 yo father received second dose of vaccine, was very sore on second day and then could not walk by third day; incredibly marked decline in health and rapid deterioration resulting in death; This is a spontaneous report from a contactable consumer. A 91-year-old male patient received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine), second dose via an unspecified route of administration, administered in Arm Left on 01Mar2021 16:30 (Batch/Lot Number: EN6203) as SINGLE DOSE for covid-19 immunisation. Medical history included Chronic heart conditions, chronic obstructive pulmonary disease (COPD) and, asymptomatic cancer was diagnosed in hospital following vaccine; all from an unknown date and unknown if ongoing. The patient was vaccinated at a hospital. No other vaccine in four weeks. The patient had no COVID prior vaccination and not tested post vaccination. The patient had no known allergies. The patient previously took bnt162b2 (Pfizer-Biontech Covid-19 Vaccine) first dose on 08Feb2021 (lot: EN6201) 05:30 PM at the left arm. It was reported that the patient "received second dose of vaccine, was very sore on second day (03Mar2021) and then could not walk by third day (04Mar2021). On the fourth day (05Mar2021), was taken to hospital and diagnosed with metastatic cancer in the spine, which had produced no symptoms prior. The vaccine obviously did not cause cancer, but it did precipitate some event that led to an incredibly marked decline in health and rapid deterioration resulting in death 17 days after vaccine." The patient died on 18Mar2021. It was not reported if an autopsy was performed. The event resulted in Emergency room/department or urgent care and hospitalization for 7 days.; Sender's Comments: Based on the current available information, Bone cancer metastatic is considered unrelated to the suspected drug of bnt162b2. The case will be reassessed if additional information becomes available.; Reported Cause(s) of Death: incredibly marked decline in health and rapid deterioration resulting in death; On the fourth day, was taken to hospital and diagnosed with metastatic cancer in the spine; 91 yo father received second dose of vaccine, was very sore on second day and

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer (asymptomatic cancer was diagnosed in hospital following vaccine); COPD; Heart disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1156352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 71,0
Geschlecht: M
Eingang: 01.04.2021
Impfdatum: 11.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Brain death Cerebrovascular accident Death Electroencephalogram abnormal Withdrawal of life support

Symptomtext

Patient's wife returned for second Pfizer CoVid vaccine on 4/1/2021 she told the vaccinator, that her husband, died two days after he received the first Pfizer vaccine. Date of Death - 03/13/2021. Wife states that husband had a "massive stroke." EEG indicated no brain activity and it was decided to remove him from life support.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain death
Hospital-Tage: -
Labordaten: EEG
Aktuelle Erkrankungen: Hypertension, Hypercholesterimia,
Vorgeschichte: h/o MI
Andere Medikamente: On baby aspirin as a blood thinner. Also "high blood pressure" meds ( per wife), "cholesterol meds" per wife.
Allergien: None
Vorherige Impfungen: -

VAERS 1147783

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

kritisch

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 30.03.2021
Impfdatum: 24.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / UN

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

Death

Symptomtext

Had 2nd COVID shot died next day physician advised me to notify.

Weitere VAERSDATA-Felder

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

VAERS 1139491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NY
Alter: 45,0
Geschlecht: F
Eingang: 27.03.2021
Impfdatum: 22.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Chills Computerised tomogram Dyspnoea Electrocardiogram Hyperhidrosis Immune system disorder Pulmonary embolism

Symptomtext

I had my second vaccine on Monday, 3/22, and woke up at 1am on Thursday 3/25 with extreme chest pain, shortness of breath, sweating and chills. I went to the ER, and they discovered two blood clots in my lungs. I've never had pulmonary embolisms before, so this is a very strange coincidence. I am in cancer treatment, so my risk of PEs is higher, but the timing is too close for me not to think that the second vaccine traumatized my immune system, causing the PEs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: EKG, Chest x-ray, blood work and CT scan.
Aktuelle Erkrankungen: Stage 4 breast cancer
Vorgeschichte: Stage 4 breast cancer
Andere Medikamente: Levothyroxine, Vit D, Vit B, Iron supplement, and in my off-week from taking Xeloda for stage 4 breast cancer.
Allergien: none
Vorherige Impfungen: -

VAERS 1132800

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: OH
Alter: 67,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 22.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Death Malaise

Symptomtext

Wife found husband dead two days after2nd dose. This Health Department was made aware of the death by the the Kidney Center. The patient failed to show up for a scheduled dialysis appointment on 03/24/2022. The clinic obtained information of the passing from the wife. The patient received his SECOND dose of COVID-19 vaccine on 3/22/21, reported feeling ill 3/23/21 and then passing on 3/24/21. The clinic called the health department to report the death of the patient on 3/24/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, NIDDM, ESRD, OSA
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1059857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 28.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / UN

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

Brain death Fall Haematemesis Haematuria Platelet count Coagulation test abnormal Coagulopathy Computerised tomogram abnormal Haemorrhage intracranial Head injury Headache Laboratory test Syncope Platelet count decreased Subarachnoid haemorrhage

Symptomtext

Brain Death; found to have mixed spontaneous SAH with subsequent trauma; Coagulopathy with hematemesis; Platelets values 160 historical baseline/130 (on arrival to ER)/80/ 70/Patient death; Patient arrived at hospital after fall (within 12 hours of vaccination); hematuria; This is a spontaneous report from a contactable physician. A 74-years-old male patient received first dose of BNT162B2 (Solution for injection, Lot Number: EN6203, Expiration date: Not provided), administered intramuscularly (Anatomical location: Arm left) on 28Feb2021 15:00 as single dose for COVID-19 immunisation. The patient medical history included benign prostatic hyperplasia (BPH). Concomitant medications included acetylsalicylic acid (BABY ASPIRIN) via unknown route of administration for unspecified indication and finasteride via unknown route of administration for an unspecified indication. It was reported that patient had no prior vaccination and covid was not tested. It was reported that patient arrived at hospital after fall (within 12 hours of vaccination), found to have mixed spontaneous Subarachnoid hemorrhage (SAH) with subsequent trauma, Coagulopathy with hematemesis and hematuria. Platelets values 160 historical baseline less than 130 (on arrival to ER) then to less than 80 less than70 and Patient died . The patient underwent lab tests and procedures on 27Feb2021, which included platelet count of 160 historical baseline/130 (on arrival to ER) less than 80 to less than70. Therapeutic measures were taken as a result of brain death, SAH, hematemesis, Platelets decreased, Fall, Hematuria with Platelets, Fresh Frozen Plasma. The patient died on 28Feb2021, Outcome of all events were fatal. Autopsy was not performed.; Sender's Comments: The events fall, subarachnoid hemorrhage, hematamesis, hematuria and brain death are assessed as possibly related to the suspect drug ( bnt162b2 ) based on strong temporal association, but have to ascertain the onset of these events, as it is mentioned the lab test and procedures were done on 27Feb2021 and the patient took the vaccine ( bnt162b2 ) on 28Feb2021.. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the product is evaluated as part of 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.; Reported Cause(s) of Death: Brain Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain death
Hospital-Tage: 2,0
Labordaten: Test Date: 20210227; Test Name: Platelets; Result Unstructured Data: Test Result:160; Comments: 130 (on arrival to ER) -less than 80 to less than 70
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH (BPH otherwise healthy)
Andere Medikamente: BABY ASPIRIN; FINASTERIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1059857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 28.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Brain death Fall Haematemesis Haematuria Platelet count Coagulation test abnormal Coagulopathy Computerised tomogram abnormal Haemorrhage intracranial Head injury Headache Laboratory test Syncope Platelet count decreased Subarachnoid haemorrhage

Symptomtext

Brain Death; found to have mixed spontaneous SAH with subsequent trauma; Coagulopathy with hematemesis; Platelets values 160 historical baseline/130 (on arrival to ER)/80/ 70/Patient death; Patient arrived at hospital after fall (within 12 hours of vaccination); hematuria; This is a spontaneous report from a contactable physician. A 74-years-old male patient received first dose of BNT162B2 (Solution for injection, Lot Number: EN6203, Expiration date: Not provided), administered intramuscularly (Anatomical location: Arm left) on 28Feb2021 15:00 as single dose for COVID-19 immunisation. The patient medical history included benign prostatic hyperplasia (BPH). Concomitant medications included acetylsalicylic acid (BABY ASPIRIN) via unknown route of administration for unspecified indication and finasteride via unknown route of administration for an unspecified indication. It was reported that patient had no prior vaccination and covid was not tested. It was reported that patient arrived at hospital after fall (within 12 hours of vaccination), found to have mixed spontaneous Subarachnoid hemorrhage (SAH) with subsequent trauma, Coagulopathy with hematemesis and hematuria. Platelets values 160 historical baseline less than 130 (on arrival to ER) then to less than 80 less than70 and Patient died . The patient underwent lab tests and procedures on 27Feb2021, which included platelet count of 160 historical baseline/130 (on arrival to ER) less than 80 to less than70. Therapeutic measures were taken as a result of brain death, SAH, hematemesis, Platelets decreased, Fall, Hematuria with Platelets, Fresh Frozen Plasma. The patient died on 28Feb2021, Outcome of all events were fatal. Autopsy was not performed.; Sender's Comments: The events fall, subarachnoid hemorrhage, hematamesis, hematuria and brain death are assessed as possibly related to the suspect drug ( bnt162b2 ) based on strong temporal association, but have to ascertain the onset of these events, as it is mentioned the lab test and procedures were done on 27Feb2021 and the patient took the vaccine ( bnt162b2 ) on 28Feb2021.. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the product is evaluated as part of 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.; Reported Cause(s) of Death: Brain Death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain death
Hospital-Tage: 2,0
Labordaten: Test Date: 20210227; Test Name: Platelets; Result Unstructured Data: Test Result:160; Comments: 130 (on arrival to ER) -less than 80 to less than 70
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH (BPH otherwise healthy)
Andere Medikamente: BABY ASPIRIN; FINASTERIDE
Allergien: -
Vorherige Impfungen: -

VAERS 1127372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MO
Alter: 86,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / -

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

Asthenia Catheterisation cardiac abnormal Cerebral infarction Colonoscopy abnormal Confusional state Coronary arterial stent insertion Electrocauterisation Endoscopy abnormal Gait inability Gastritis erosive Gastrointestinal haemorrhage Magnetic resonance imaging head abnormal Myocardial infarction Pneumonia Pyrexia

Symptomtext

The background is he was hospitalized for 5 days in November 2020 for coronavirus, admitted with fever, chill, weakness, and inability to walk. Discharged with 3 weeks physical therapy to regain his strength. First vaccine on 2/4/2021 and within 24 hours experienced similar symptoms, profound weakness and fever. Second vaccine on 2/25/2021 and within 12 hours he was unable to walk, with weakness, fever, and confusion. He was taken by ambulance to the hospital on 2/26/2021. I did question his internist and the person at HealthCare facility on whether or not to proceed given prior reactions. During this admission determined to have heart attack with cardiac cath and stent placement. Brain MRI showed new 1cm occipital left infarct and developing pneumonia. Started on anticoagulation with Plavix and ASA 81mg. Readmitted to the hospital on 3/8/2021 with suspected GI bleed. Had colonoscopy and endoscopy with gastric erosion cauterized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: unknown
Vorherige Impfungen: Similar reaction without hospitalization after 1 Pfizer COVID vaccine.

VAERS 1126724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: IL
Alter: 67,0
Geschlecht: M
Eingang: 23.03.2021
Impfdatum: 26.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: IM / AR

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

Death

Symptomtext

Death within 30 days of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Hospitalization 3/3-3/11/21 at Hospital transferred to Medical Center and died on 3/15/2021
Aktuelle Erkrankungen: Multiple Co-morbidities.
Vorgeschichte: Alcoholism, Bilateral AKA; Anxiety; Asthma; Back Pain; Depression; Bronchitis; COPD home oxygen as needed; Dyslipidemia; Falls; Traumatic Brain Injury; Hypertension; Pneumonia; Seizures; Stroke.
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1124604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: IL
Alter: 65,0
Geschlecht: M
Eingang: 22.03.2021
Impfdatum: 09.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / UN

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

Cardio-respiratory arrest Condition aggravated Death Dyspnoea Pain in extremity

Symptomtext

Pt presented SOB several days prior to receiving vaccine. His sister reported he had severe COPD and was getting progressively worse. On the day pt was vaccinated, his sister picked him up for the appointment and pt refused a wheelchair. Pt walked into the clinic on his own and recevied his vaccine. Sister reported pt walked to the car after his vaccine and was winded. She dropped him off at his house and called him later to check up on him. Pt stated he was feeling fine but his arm was sore. Pt's sister called the next morning and reported that he sounded terrible. He was strugging to breathe and was SOB. His sister went over to his house to check on him and wanted to take him to the doctor's office or the hospital. Pt refused at that time. Pt agreed to make a doctor appointment for later in the afternoon. Sister left at noon. She stated her brother had made a doctor appointment for 4:00 at Family Practice. Upon arriving, pt started walking towards the entrance and became SOB. His significant other asked the doctor's office for a wheelchair and was denied. Pt coded in parking lot of Doctor's Office and passed away at 4:31 p.m.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardio-respiratory arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: severe COPD had been worsening prior to vaccine administration
Vorgeschichte: COPD
Andere Medikamente: Two inhalers (unknown)
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1119178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NC
Alter: 89,0
Geschlecht: M
Eingang: 20.03.2021
Impfdatum: 03.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Blood sodium decreased Blood test Cerebrovascular accident Computerised tomogram abnormal Computerised tomogram head Condition aggravated Dysarthria Dysstasia Echocardiogram Electroencephalogram abnormal Gait disturbance Hypertension Lethargy Magnetic resonance imaging head abnormal

Symptomtext

Weakness (Mar 5 evening), not able to stand / walk (March 6) ending up in slurring of voice /lethargic , high BP (morning Mar.7). Called 911 and moved to ER @ Hospital. CT Scan did not show stroke, EEG showed slowness in brain activity, MRI showed minor stroke left side of brain. Low salt (124) at the time of admittance. Released from Hospital on Mar 10.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: CT Scan (Mar 7), EEG (Mar 7), blood test(Mar 7 / 8 / 9 / 10, MRI (Mar 8), ECHO (Mar 10)
Aktuelle Erkrankungen: -
Vorgeschichte: High BP, Diabetes (type II), enlarged prostate, thrombosis stroke (year 2007) left side body weakness.
Andere Medikamente: Losartan(50mg), Clopidogrel tablets USP 75 mg, Alfuzosin hydrochloride 10 mg As extended release tables, Dutasteride 0.5 mg, Miglitol Tablets 25 mg, Piogilitazone Hydrochloride (15mg), Metformin Hydrochloride IP (500mg), Glimepiride USP (2m
Allergien: None known
Vorherige Impfungen: -

VAERS 1262003

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: -
Alter: 79,0
Geschlecht: M
Eingang: 18.03.2021
Impfdatum: 27.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: IM / LA

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

Cerebrovascular accident

Symptomtext

Narrative: 79 yo patient with history of stroke, hypertension, prostate cancer. Hospitalized for acute CVA on 3/2 after receiving first dose of Pfizer vaccine on 2/27.

Weitere VAERSDATA-Felder

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

VAERS 1112779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 26.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Aphasia Blood test Cardiac monitoring Cerebral thrombosis Cerebrovascular accident Computerised tomogram head abnormal Echocardiogram Hemiplegia Magnetic resonance imaging Thrombectomy

Symptomtext

Just 38.5 hours after receiving my 2nd dose of the Pfizer Covid-19 Vaccine I suffered a Cerebral Vascular Accident, a CVA, a Stroke @ 5:05a.m. in our home. My entire right side was paralyzed & unable to speak. My husband alerted #911 & fortunately @ the hosp. I received immediate life saving care. I had a C.T. Scan which revealed #2 blood clots in the left side of my brain. Intravenous T.P.A. was administered & then a thrombectomy was performed. Hospitalized approx. 5:45a.m on Sun., Feb. 28th, 2021 till my discharge on Wed., March 3rd, 2021@ 5:30pm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: What I can recall: #2 C.T. Scans, an M.R.I., an Echo-Cardiogram, multiple daily (blood) labworks, Occup. Therapy, Phys. Therapy, constant neuro checks by a team of Neurologists and upon discharge they had placed on me a 30 day Heart Monitor.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure, Type II Diab./No Insulin, Low Thyroid
Andere Medikamente: Hydralazine 100 mg 1 tab 7a.m. & 7p.m.; Telmisartan 80 mg 1 tab 7a.m.; Furosemide 40 mg 1 tab 7a.m.; Levothyroxine 88 mcg 1 tab 7a.m.; Klor-Con 10 meq. 1 tab 9a.m.; Metformin 500 mg 1 tab 9a.m. & 7p.m.; Metoprolol Succinate ER 100 mg 1 tab
Allergien: Sensitivity to Sulfa Ceam
Vorherige Impfungen: -

VAERS 1111554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MA
Alter: 80,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 27.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: SYR / RA

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

Cerebrovascular accident Computerised tomogram Feeling abnormal Headache Magnetic resonance imaging Thrombosis

Symptomtext

Multiple strokes resulting from blood clots starting 10 days past 2nd shot. Fuzzy headed with headache prior to strokes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 4,0
Labordaten: Catscan 3/10/21, 3/15/21, 3/18/21 MRI 3/11/21, 3/17/21
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Thyroid medication
Allergien: Slightly to apples Seasonal allergies Dermal allergies to some perfumes
Vorherige Impfungen: -

VAERS 1099264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 71,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 06.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Death Myocardial infarction

Symptomtext

Patient found dead in bed at home 3/7/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: no autopsy
Aktuelle Erkrankungen: None
Vorgeschichte: COPD,CKD 3,HTN, high lipids
Andere Medikamente: Nifedipine, hydrochlorothiazide, lisinopril, gabapentine, spirva
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1081063

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CT
Alter: 66,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 03.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / -

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

Angiogram Aphasia Blindness Cerebrovascular accident Computerised tomogram Disorientation Gait inability Intensive care Malaise Vomiting

Symptomtext

Pfizer shot on Sunday am - my father noticed my mother c/o not feeling well and unable to explain why she didn't feel well. She woke up feeling well and then quickly became disoriented and vomited. She was then unable to walk or communicate appropriately. Emergency services was called and she was transported to Emergency room. She was diagnosed with a posterior brain CVA and was treated with tpa and now remains hospitalized in the ICU with expressive aphasia and vision loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: CT scan, CT angiography
Aktuelle Erkrankungen: family history of cardiac disease
Vorgeschichte: hypothyroidism
Andere Medikamente: synthroid
Allergien: none
Vorherige Impfungen: -

VAERS 1076188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: NC
Alter: 65,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Acute kidney injury Cardiac arrest Death Ischaemic hepatitis Respiratory failure Shock

Symptomtext

Out of hospital cardiac arrest and refractory shock, acute kidney injury, shock liver, respiratory failure leading to death

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: Mild kidney impairment, mild hyperkalemia
Vorgeschichte: Mitral valve prolapse, congestive heart failure, atrial fibrillation
Andere Medikamente: Entresto, Coumadin, Carvedilol, Spironolactone, Lanoxin, Calcium, Probiotics
Allergien: None
Vorherige Impfungen: -

VAERS 1063485

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Blood creatine Blood creatine phosphokinase Blood glucose Blood magnesium Blood potassium Blood sodium Blood thyroid stimulating hormone Cardiac arrest Diarrhoea Dizziness Electrocardiogram Haematocrit Haematology test Haemoglobin Headache Heart rate increased Injection site erythema

Symptomtext

First muscle soreness at site of injection, then severe redness at site, cherry electric red and pink, severe muscle aches, severe joint aches, severe headache, diarreah, dizzyness, the extreme rapid heart rate of 205 BPM. SEVERE SVT, SUPREVENTRICULAR TACHYCARDIA lasting from 9 p.m. Friday evening through the a.m. until I was transported from Urgent Care via Paramedics to Emergency Hospital. I was given an IV of a Medicine to restart my heart twice. I felt like I was dying.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: EKG, creatine, glucose level, potassium, sodium, troponin, TSH, CK, Magnesium level, CKD screen, Hematology, Hct, Hgb, MCH, MCHC, MCV, MPV, NRBC, Platelet Count, RBC, RDW, WBC
Aktuelle Erkrankungen: none
Vorgeschichte: Chrohn's disease
Andere Medikamente: tamoxifen
Allergien: orange juice zilactin
Vorherige Impfungen: -

VAERS 1052049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

kritisch

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 24.02.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Death Malaise Pain in extremity Peripheral swelling Syncope

Symptomtext

Patient was into the clinic on the afternoon of 2/23/21 for a COVID-19 vaccine. He had a podiatry clinic visit after his vaccine same day. It was reported by the patients family physician that patient stated he didn't feel well and suddenly collapsed at home at approximately 4:45 pm. Emergency medical personnel were not able to revive him. Patient died at approximately 4:45 pm on 2/23/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None known at the time of the vaccination. However, patient did have a podiatry visit after the vaccination for right foot pain and swelling
Vorgeschichte: None
Andere Medikamente: Multivitamin and Glucosamine. Started on Prednisone after the vaccine was administered
Allergien: None known
Vorherige Impfungen: -

VAERS 2713326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 65,0
Geschlecht: F
Eingang: 13.11.2023
Impfdatum: 23.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Cardiac monitoring normal Echocardiogram Headache Loss of consciousness Magnetic resonance imaging head abnormal Magnetic resonance imaging heart Memory impairment Ultrasound Doppler White matter lesion

Symptomtext

Starting passing out n headaches brain forgetfulness, told doctor sent to heart specialist, still complain n went to another doc. Had dappled of neck n heart, heart monitor, mri of brain, heart is great but now have white matter on brain after shots, but didn't have 2 year before, still just passport, n life is so different

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Blood, mri 2 heart montor, doppler of heart, dappled of neck main arthritis mri of brain
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2624627

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VT
Alter: 76,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 21.02.2021
Beginn: 01.09.2021
Tage bis Beginn: 192,0
Dosis: 2
Route/Site: IM / AR

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

Chills Neurological symptom Pain Pyrexia Scar Seizure

Symptomtext

After receiving the vaccine, I had fever chills and body aches that put me down for about a week. In 09/2021, I was having neurological issues and I was referred to a neurologist. It was determined that I have left frontal lobe scarring that was causing me to have seizures. As of today, I am still having seizures.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Bupropion; Fluoxetine; Amlodipine; Nose Drops
Allergien: N/A
Vorherige Impfungen: -

VAERS 2583941

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 24.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 15,0
Dosis: 2
Route/Site: OT / LA

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

Ischaemic stroke Laboratory test Magnetic resonance imaging Urine analysis

Symptomtext

Ischemic stroke; 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 female patient received BNT162b2 (BNT162B2), on 24Feb2021 as dose 2, single (Lot number: EN6203) at the age of 67 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "High Blood Pressure", start date: 2020 (unspecified if ongoing), notes: Losartan keeps in check since stroke Baby; "High Cholesterol", start date: 2020 (unspecified if ongoing), notes: Atorvastatin, then Profluent after stroke. The patient's family history included: "Stroke" (unspecified if ongoing), notes: Mother had stroke after taking celebrex years ago. The patient's concomitant medications were not reported. Vaccination history included: pfizer/biontech coviD-19 vaccine (DOSE 1, SINGLE, Time: AM, Site and route of injection: Left arm, Route of administration: Intramuscular, Batch/Lot number: EL9264), administration date: 03Feb2021, when the patient was 67-year-old, for COVID-19 immunization, reaction(s): "COVID-19". The following information was reported: ISCHAEMIC STROKE (hospitalization, life threatening) with onset 11Mar2021 at 12:00, outcome "recovered" (12Mar2021 at 12:00), described as "Ischemic stroke". The patient was hospitalized for ischaemic stroke (start date: 11Mar2021, discharge date: 12Mar2021, hospitalization duration: 1 day(s)). The event "ischemic stroke" required emergency room visit. The patient underwent the following laboratory tests and procedures: Battery of tests: (11Mar2021) Ischemic Stroke; Magnetic resonance imaging: (unspecified date) Unknown result; Urine analysis: (unspecified date) Unknown result. Therapeutic measures were taken as a result of ischaemic stroke (Lisinopril, Losartan, Atorvastatin). The clinical course was reported as follows: had ischemic stroke 16 days after second COVID vaccination. At the time I asked view of Withheld doctors if they were reporting to you. They said no, since it wasn't a known side effect.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 1,0
Labordaten: Test Date: 20210311; Test Name: Battery of tests; Result Unstructured Data: Test Result:Ischemic Stroke; Test Name: MRI; Result Unstructured Data: Test Result:Unknown result; Test Name: URC; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high (Losartan keeps in check since stroke Baby); High cholesterol (Atorvastatin, then Profluent after stroke); Stroke (Mother had stroke after taking celebrex years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2579988

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 85,0
Geschlecht: F
Eingang: 11.02.2023
Impfdatum: 06.03.2021
Beginn: 26.08.2021
Tage bis Beginn: 173,0
Dosis: 1
Route/Site: SYR / LA

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

Anticoagulant therapy Computerised tomogram thorax abnormal Dyspnoea Peripheral swelling Pulmonary thrombosis Thrombosis X-ray abnormal

Symptomtext

trouble Breathing Swollen legs. Admitted to hospital for two days. CAT scans & X rays performed. Told i have blood clots in both lungs & legs Eliquis prescribed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 2,0
Labordaten: CAT Scans every 6 months
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Diltiazem Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2546973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

schwer

Staat: IN
Alter: 68,0
Geschlecht: M
Eingang: 30.12.2022
Impfdatum: 02.02.2021
Beginn: 21.05.2021
Tage bis Beginn: 108,0
Dosis: 2
Route/Site: IM / RA

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

Aphasia Brain stem stroke Emotional disorder Impaired driving ability Ischaemic stroke Loss of personal independence in daily activities Magnetic resonance imaging head abnormal Movement disorder

Symptomtext

Brain stem ischemic stroke in PONS area. Seen by a neurologist. 7 speech therapy sessions. Recovery of speech to some extent. Recovery of right side movement. 1 physical therapy session. 4 occupational therapy sessions. Permanent impairment of full singing ability as a semi professional singer. Handicapped driver. Impairment of emotional control.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain stem stroke
Hospital-Tage: 3,0
Labordaten: An MRI confirmed the stroke had occurred.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2530361

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NM
Alter: 78,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 11.12.2022
Beginn: 01.01.1900
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Computerised tomogram head Computerised tomogram spine Dizziness postural Electrocardiogram Eye contusion Fall Full blood count Influenza virus test Loss of consciousness Metabolic function test Myalgia Myocardial necrosis marker Pyrexia Respiratory syncytial virus test SARS-CoV-2 test Skin laceration Wound closure

Symptomtext

I received my booster on Sunday 12/11/22 at 4:30 PM. During the night of 12/11 I had muscle aches throughout my body. I got up at 7:30 AM on 12/12/22. Muscles no longer ached. Went to the bathroom. When I attempted to stand up I was momentarily very dizzy, apparently blacked out (syncope), fell, and was brought back to consciousness by my husband calling me. EMT arrived and while trying to get me onto a stretcher I had another syncope. I was taken to the emergency room at hospital, where I received the tests indicated below. When I fell I apparently whacked my head, resulting in 3 staples in my scalp and a black eye. I have had a fever varying from 99-101.4 since the shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG 12-lead, XR chest, comprehensive metabolic panel, cardiac injury panel, complete blood count, CT head-brain, CT cervical spine, SARS cov-2, flu, RSV, laceration repair
Aktuelle Erkrankungen: none
Vorgeschichte: high cholesterol, Gilbert's Sndrome
Andere Medikamente: baby aspirin, fish oil, magnesium glycinate, multivitamin
Allergien: sulfa, shellfish
Vorherige Impfungen: -

VAERS 2529065

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 78,0
Geschlecht: M
Eingang: 12.12.2022
Impfdatum: 10.03.2021
Beginn: 04.12.2022
Tage bis Beginn: 634,0
Dosis: 1
Route/Site: IM / LA

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

Intensive care

Symptomtext

Unknown **unable to interview case or POA, case was admitted to ICU 12/04/2022.**

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 5,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2501310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 36,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 23.02.2021
Beginn: 01.02.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Blood test Disorientation Dizziness Feeling cold Headache Photophobia Presyncope Sinusitis Toothache Weight

Symptomtext

feeling like he was about to pass out; The vaccine was causing extreme pressure on his head and putting pressure on his sinus cavity/on antibiotics for a toothache; head pain and tooth pain, like a sinus infection.; sensitivity to light; The vaccine was causing extreme pressure on his head and putting pressure on his sinus cavity/on antibiotics for a toothache; dizziness; feeling the extreme coldness; being disoriented; 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 36-year-old male patient received BNT162b2 (BNT162B2), on 23Feb2021 as dose 2, single (Lot number: EN6203) at the age of 36 years for covid-19 immunisation. The patient's relevant medical history included: "long Covid" (unspecified if ongoing); "Suspected food allergies" (unspecified if ongoing), notes: Medical Conditions: Suspected food allergies prior to all of this occurring with vaccine.; "Triglycerides" (unspecified if ongoing), notes: Triglycerides were high one year and had gone down. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE: 1, Lot: EM9810, Anatomical Location: Arm right), administration date: 02Feb2021, when the patient was 36-year-old, for COVID-19 Immunization, reaction(s): "feeling like he was about to pass out", "After 2 Pfizer shots, had to get 2 different root canals on the same tooth", "feeling the extreme coldness", "being disoriented", "sensitivity to light"; BNT162b2 (DOSE: 1, Lot: EM9810, Anatomical Location: Arm right), administration date: 02Feb2021, when the patient was 36-year-old, for Covid-19 immunization, reaction(s): "Dizziness". The following information was reported: TOOTHACHE (medically significant), HEADACHE (non-serious) all with onset Feb2021, outcome "unknown" and all described as "The vaccine was causing extreme pressure on his head and putting pressure on his sinus cavity/on antibiotics for a toothache"; DISORIENTATION (non-serious) with onset Feb2021, outcome "unknown", described as "being disoriented"; DIZZINESS (non-serious) with onset Feb2021, outcome "unknown"; PRESYNCOPE (medically significant) with onset Feb2021, outcome "unknown", described as "feeling like he was about to pass out"; FEELING COLD (non-serious) with onset Feb2021, outcome "unknown", described as "feeling the extreme coldness"; SINUSITIS (medically significant) with onset Feb2021, outcome "unknown", described as "head pain and tooth pain, like a sinus infection."; PHOTOPHOBIA (non-serious) with onset Feb2021, outcome "unknown", described as "sensitivity to light". The events "feeling like he was about to pass out", "the vaccine was causing extreme pressure on his head and putting pressure on his sinus cavity/on antibiotics for a toothache", "head pain and tooth pain, like a sinus infection.", "sensitivity to light", "dizziness", "feeling the extreme coldness" and "being disoriented" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood test: good health, notes: Test results: No. Does blood work every single year and has been in pretty good health. Triglycerides were high one year and had gone down; Weight: 175, notes: Current weight is about 175. When he got the shot, he was like over 200. Therapeutic measures were taken as a result of presyncope, toothache, sinusitis, photophobia, headache, dizziness, feeling cold, disorientation. Clinical course: Has reason to believe he originally had Covid in 2003. It is what he called the OG Covid. Lived in country in 2003. Being on his deathbed and 106 fever for 3 days, though he was going to die. Was in high school in city. Was also working at a high school the last 12 years. When this happened, he started tracking it Dec2019, saying the country was going to shut down and nobody believed him. That is why he got vaccinated. First Dose: 02Feb2021, Second Dose: 23Feb2021, Third Dose: 02Nov2021, Fourth Dose: 28Sep2022. Event details: This started Feb2021. The symptoms are primarily in his head. Before he got the shot, he believes and there is no way to retest but, believes he was one of the early people to get Covid-19 in Feb2020. He worked at a high school and when that happened, it was by the summer of 2020, he started having really crazy symptoms like dizziness and essentially, it was POTS. Had tinnitus, like ringing in his ear. Was telling people, it was like a concussion grenade going off. Was so confused, he would stand up and would almost pass out. Everything would go black and he would almost pass out. Was getting extremely cold, very, very, cold, like blood circulation issues. Was the feeling he would get right before he was about to pass out. Never fully passed out or blocked out. Was cognizant to sit down and brace himself slowly, down to the ground. Occurred to him he was having some neurological symptoms. Chalked it up to long Covid. Clarified this was all prior to getting any of the Covid vaccines. After he got the shots, within usually about 2 weeks, he started having similar symptoms that he experienced before, like dizziness. Clarified this started with the very first vaccine, 02Feb2021. He was instantly impacted and felt like he about to pass out. It was like a huge rush to the head and immediately felt like extreme coldness all over the body. Was like, really disoriented and actually nervous about not being able to drive. Clarified that with every shot, he experiences the dizziness, feeling like he was about to pass out, feeling the extreme coldness and being disoriented. That same sensation happens with every single shot. It was only that severe with the very first and second shot. Outcome: He always stayed put after every single shot, at least 15 to 30 minutes. Thinks they had pretty good system, tracking who was impacted every time and would say that he needed to stay about 30 minutes. Was not going to go anywhere and would get nervous during that time. His blood rushed and had that feeling like it went straight from his arm into his head, like almost immediately. Would have that dizziness and the other symptoms. Now, everything is extremely loud in his head, sounds very loud. His son would be right next to him and he would ask him to whisper because, even talking sounds are loud to him. Sensitivity to light is also painful to him. When he had Covid, that was a good 6 months, he was feeling dizzy, like things were very loud and those kind of symptoms. The reason he is describing this all is because, this exact thing reignites that response. Would say this happens within 2 or 3 weeks after getting the vaccine, he would feel these symptoms. Clarified that the sensitivity to light also occurred within 2 or 3 weeks after getting the shots. Outcome: Would say it used to take longer for these symptoms to show up. Would have to go back and look at his medical records. Has contacted every single doctor he has been to about his medical history over the last year, to connect the dots. On 02Feb2021, got the shot, by 23Feb2021, got the second shot, thinks it was 3 weeks later and was fully vaccinated. Within 2 months of that time, he was on antibiotics for a toothache. The vaccine was causing extreme pressure on his head and putting pressure on his sinus cavity, making it seem like he was having tooth pain. Appeared to the dentist, that he needed to have root canal. That was May2021, that he had the root canal. Is not 100 percent sure when this started but would have been between late Mar2021 and late Apr2021 and had the root canal May2021. They gave him antibiotics because, they said they couldn't operate on the tooth because it was so infected. They needed to get the swelling down. They put him on another round of antibiotics and because he still had the infection after the root canal. Jun2021, was still being impacted to the point where he had to go see a bunch of doctors. Has an appointment to see a neurologist tomorrow. Had to go again because they still thought he needed antibiotics and he was still in pain. Then, he started having appointments with the Ear, nose and throat doctor. Started appointments 16Jun2021. For the last month, he had been complaining about head pain and tooth pain, like a sinus infection. Doctor said he had a very deep sinus infection. They put him on Levaquin, a high grade antibiotic and Prednisone, a steroid. Had follow up 30Jun2021 and they stuck a metal rod up his nose in the nasal cavity and they could see that it was a very deep infection. The infection was so far in there, they would have to do a surgery on the sinus cavity. It was very deep in there. They said to just continue the medication to see if it would go away. They told him, he really needed a CT scan of the sinus cavity and had to go back for a hearing test. Took a month to get the CT scan. On 17Aug2021, had the hearing test, said hearing was fine and his vitals were fine. When they explained CT scan, they said nothing was really showing up and they do still think it was maybe something super deep in there. Right now, the antibiotics have run their course and he is not in as much pain anymore. Everybody was kind of satisfied with it. Was fully vaccinated Feb2021 and have a booster 02Nov2021. Within the end of the month, or sooner, was complaining about the same issues. Was having headaches, dizziness, tooth pain coming. Went back to the dentist 1 month later, 01Dec2021 and again 08Dec2021. They referred him to endodontist because he was complaining about the same tooth. He was looking for antibiotics for the tooth pain. Was having heavy discharge, infection was literally coming out of the nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:good health; Comments: Test results: No. Does blood work every single year and has been in pretty good health. Triglycerides were high one year and had gone down.; Test Name: Weight; Result Unstructured Data: Test Result:175; Comments: Current weight is about 175. When he got the shot, he was like over 200
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Food allergy (Medical Conditions: Suspected food allergies prior to all of this occurring with vaccine.); Long COVID; Triglycerides (Triglycerides were high one year and had gone down.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: SC
Alter: 76,0
Geschlecht: F
Eingang: 29.07.2022
Impfdatum: 23.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Pain in extremity Thrombosis Ultrasound Doppler

Symptomtext

In total she's had five blood clots/ three in her right leg and two in her left leg; had some pain in her toe; The initial safety information received was reporting only non-serious adverse drug reaction(s). Upon receipt of follow-up information on 20Jul2022, this case contains serious adverse reaction(s) and all safety information is processed together. This is a spontaneous report received from contactable reporter(s) (Nurse) from medical information team. The reporter is the patient. A 77-year-old female patient received BNT162b2 (BNT162B2), on 23Feb2021 as dose 2, single (Lot number: EN6203) at the age of 76 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "diabetes" (unspecified if ongoing); "heart attack", start date: 2018 (unspecified if ongoing), notes: Had stents in her heart placed. He put her on plavix, aspirin 81mg and 2 heart pills; "pain" (unspecified if ongoing); "Left mastectomy", start date: 1999 (unspecified if ongoing), notes: done 23 years ago and she had chemo; "Broken hip", start date: 12Aug2018 (unspecified if ongoing), notes: was in the hospital on the 12Aug2018 and was sent to a nursing home on the 15Aug2018.; "Blood thinner" (unspecified if ongoing). Concomitant medication(s) included: CLOPIDOGREL taken for myocardial infarction (ongoing); PLAVIX taken for anticoagulant therapy, start date: 2018; ASPIRIN [ACETYLSALICYLIC ACID] taken for anticoagulant therapy, myocardial infarction, start date: 2018 (ongoing). Vaccination history included: BNT162b2 (Dose 1, Batch/lot number: EL9265, injection right arm), administration date: 01Feb2021, when the patient was 76-year-old, for Covid-19 Immunization. The following information was reported: THROMBOSIS (medically significant, life threatening) with onset 2021, outcome "unknown", described as "In total she's had five blood clots/ three in her right leg and two in her left leg"; PAIN IN EXTREMITY (non-serious) with onset 2021, outcome "unknown", described as "had some pain in her toe". The event "had some pain in her toe" required physician office visit. The patient underwent the following laboratory tests and procedures: Ultrasound Doppler: blood clots, notes: they were able to see she had blood clots. Therapeutic measures were taken as a result of thrombosis. Clinical course: After the second dose she had some pain in her toe, and went to see the doctor because her toe was sore. With the doppler they were able to see she had blood clots. They called the cardiologist and the cardiologist said that they can put some stents in her legs and they put 3 stents in in the right leg in Jul2021. They did some more stents in her left leg in Sep2021 at the heart center. Caller said that her previous cardiologist, (name withheld), did the stents in Jul2021 and Sep2021. She was thinking if she takes the vaccine again she does not want to get another clot. She is nervous about taking it and wants to know if the blood clots are reported side effects.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 vaccine cannot be excluded for the reported events of Thrombosis and Pain in extremity. 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.,Linked Report(s) : US-PFIZER INC-202200993577 same patient, different drug dose, similar event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: doppler; Result Unstructured Data: Test Result:blood clots; Comments: they were able to see she had blood clots
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anticoagulant therapy; Broken hip (was in the hospital on the 12Aug2018 and was sent to a nursing home on the 15Aug2018.); Diabetes; Heart attack (Had stents in her heart placed. He put her on plavix, aspirin 81mg and 2 heart pills); Mastectomy (done 23 years ago and she had chemo); Pain
Andere Medikamente: CLOPIDOGREL; PLAVIX; ASPIRIN [ACETYLSALICYLIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2393202

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: CO
Alter: 70,0
Geschlecht: M
Eingang: 27.07.2022
Impfdatum: 20.02.2021
Beginn: 11.06.2022
Tage bis Beginn: 476,0
Dosis: UNK
Route/Site: IM / LA

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

Bell's palsy Gout

Symptomtext

1. Crippling Gout flare 5/22 2. Bells Palsy. 6/11/22

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: 2,0
Labordaten: Gout: hospitalized 1 night 5/18/22 Bells Palsy: medical doctor analysis 6/20/22
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac, psoriasis
Andere Medikamente: Losarton, hydrclorothiazide, Ilyumya,
Allergien: Gluten, codeine, oxycodone, tramadol
Vorherige Impfungen: -

VAERS 2390957

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 36,0
Geschlecht: M
Eingang: 26.07.2022
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Electrocardiogram Electrocardiogram ambulatory Impaired driving ability Laboratory test Seizure like phenomena Sleep study Swelling face Urinary incontinence

Symptomtext

1st morning after shot I woke up on floor with lump on chin and urinated pants. Same the 2nd morning after vaccination except lump on forehead. 3rd morning after vaccine I became light headed dizzy, had to pull over to store parking lot. 3 state police arrived after I had seizure like episode inside the store. These events have never happened before in my life happened the first 3 mornings after my 1st and only dose. 3 less severe mild but similar incidents since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: Sleep monitors. EKG. Halter monitors, sleep studies and more. More to come.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D supplement
Allergien: None
Vorherige Impfungen: -

VAERS 2319014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IL
Alter: 24,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 23.03.2021
Beginn: 23.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Diarrhoea Electric shock sensation Insomnia Movement disorder Nausea Pain Pyrexia Tremor Vision blurred

Symptomtext

Received first dose at 10 am. By 5 pm, I had severe digestive issues (diarrhea, nausea) that lasted severely for two days and lingered for a week. Accompanied by mild body aches and small fever in the 99s. Received second dose at 10am. By 10:30am I was physically shaking and could not stop. Shaking lasted for the rest of the day. Developed a fever within three hours in the 102s with severe body aches. Fever and body aches lasted for 3 days. Was unable to move or sleep. When fever was at its highest, vision was blurry and brain felt like it was being zapped by electricity. Scared enough to almost go to hospital. Fever lasted through multiple doses of ibuprofen. Severe side effects lasted 3 days, mild body aches lingered.

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Paxil ER 12.5mg
Allergien: Penicillin, Amoxycillin, Zithromax
Vorherige Impfungen: -

VAERS 2287060

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IA
Alter: 93,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 09.03.2021
Beginn: 09.12.2021
Tage bis Beginn: 275,0
Dosis: 2
Route/Site: IM / -

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

Anaemia Anticoagulant therapy Arterial haemorrhage Atrial fibrillation COVID-19 COVID-19 pneumonia Chest pain Computerised tomogram head abnormal Computerised tomogram spine Condition aggravated Device malfunction Fall Haemoglobin decreased Head injury Hypotension Hypoxia Inappropriate schedule of product administration Intensive care

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/12/21 (en6201) Pfizer Dose 2 3/9/21 (EN6203) COVID Positive 12/10/21 12/9/21: Patient is a 93-year-old female with past medical history of AAA, chronic low back pain, history of CVA, chronic anemia, B12 deficiency, hypertension, cystocele, hyperlipidemia, irritable bowel syndrome, lumbosacral spondylosis, peptic ulcer disease, restless legs, uterine prolapse, tremor. She presented to the emergency department on 12/09/2021 after suffering a mechanical fall at home and hit her head. She states that her walker malfunctioned. CT head and CT C-spine were unremarkable for acute changes with the exception of a left parietal scalp hematoma noted. Patient had an x-ray of her lumbar spine that was notable for a T12 compression fracture new from previous scan performed approximately 1 month ago. The patient was also noted to have arterial bleeding from her scalp. ED provider stated that it took some time to repair this due to high ED volumes. Patient is believed to have lost a significant amount of blood. The patient did become mildly tachycardic and hypotensive in the ED. her hemoglobin on arrival was 11.4. The remainder of her labs were otherwise unremarkable. Patient was administered 1 L of fluid in the ED as well as 2 mg of morphine, Zofran, and tetanus shot. She was admitted for further monitoring of her anemia and fluid resuscitation. The patient confirms the story above. She denies any current pain. She also denies fever, chills, sweats, numbness, tingling, confusion, or changes otherwise. She does admit to drinking beer occasionally. She does not use tobacco or illicit drugs. Family history is noncontributory. 12/14/21: 93-year-old female with past medical history of AAA, chronic low back pain, history of CVA, chronic anemia, B12 deficiency, hypertension, cystocele, hyperlipidemia, irritable bowel syndrome, lumbosacral spondylosis, peptic ulcer disease, restless legs, uterine prolapse, tremor. She presented to the emergency department on 12/09/2021 after suffering a mechanical fall at home and hit her head suffering left occipital laceration complicated by significant bleed requiring fluid resuscitation. Patient did not require blood transfusion. Was mildly hypoxic and found to have COVID-19 infection/pneumonia. Was put on low-dose oxygen, received Decadron, received short course of remdesivir, he mental status got worse Decadron was discontinued. Pt had elevated troponin and a complaint of chest pain that was transient at that time she had AFib with RVR, patient was started on heparin drip and amiodarone drip. Transferred to CIU, cardiology were consulted and they recommended stress test however patient was refusing. Upon my evaluation patient was chest pain-free, troponin were down trending. She was normal sinus rhythm. Discussed with Cardiology who recommended to discontinue amiodarone drip and heparin drip and treat the patient medically until seen in the office.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: AAA chronic low back pain h/o CVA chronic anemia B12 deficiency HTN cystocele HLD IBS lumosacral spondylosis peptic ulcer disease RLS uterie prolapse tremor
Vorgeschichte: AAA chronic low back pain h/o CVA chronic anemia B12 deficiency HTN cystocele HLD IBS lumosacral spondylosis peptic ulcer disease RLS uterie prolapse tremor
Andere Medikamente: acetaminophen 500 mg PO Q4h PRN aspirin 81 mg PO QD atorvastatin 40 mg PO QD ferrous uslfate 325 mg PO BID gabapentin 300 mg PO TID lisinopril 20 mg PO QD lorazepam 0.5 mg PO HS PRN melatonin 5 mg PO HS metoprolol tartrate 50 mg PO BID ocul
Allergien: amlodipine - facial swelling, burning amoxicillin - hives ciprofloxacin - tingling conjuugated estrogens topical - hives darvocet-n 100 - hives escitalopram - nausea hydrochlorothiazide - rash, hives losratan - hives naproxen - ulcers neurontin - unknown nitrofurantoin - didn't feel well, upset stomach penicillin - unsure prednisone - GI ulcers, made pt feel weird sulfa drugs - rash tape - itching, rsah tramadol - hives zolpidem tartrate - hallucinations
Vorherige Impfungen: -

VAERS 2278376

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 88,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 24.02.2021
Beginn: 11.05.2022
Tage bis Beginn: 441,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Syncope

Symptomtext

Admitted to hospital with dizziness and fainting on 05/11/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Cardiac disease
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2277738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

schwer

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 14.05.2022
Impfdatum: 28.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray Chest pain Computerised tomogram thorax Drain placement Dyspnoea Echocardiogram Pericarditis Pulmonary pain Surgery

Symptomtext

After each vaccine I received 2/28/2021, 3/21/2021 and 10/23/2021. I experienced severe chest pain in heart area, lung pain in both lungs and dyspnea. It went away after 2 days so I did not seek medical help. After each vaccine the adverse reaction was worse. After the 10/2022 vaccine I experienced repeated symptoms on and off until the beginning of May, 2022 at which time these symptoms did not go away. The became so severe that I went the the ER feeling like I was having a heart attack. I was given IV morphine, had a CT of the chest, a chest x-ray and multiple echocardiograms. Diagnosis - pericarditis. I had surgery on 5/9/2022 at which time a pigtail drain was inserted. This did not resolve the problem. On 5/13/2022 I had surgical subxiphoid pericardial drainage by a cardio vascular surgeon. I have now been hospitalized from 5/8/2022 through today 5/14/2022. I was told I will continue to stay inpatient for 2-3 may 4 more days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CT of the Chest, Chest s-ray, multiple echocardiograms. beginning on 5/8/2022 and they continue as of today 5/14/2022
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2178300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 14.03.2022
Impfdatum: 30.03.2021
Beginn: 26.12.2021
Tage bis Beginn: 271,0
Dosis: 1
Route/Site: IM / LA

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

Chest X-ray abnormal Dyspnoea Pulmonary oedema

Symptomtext

Patient vaccinated with Pfizer on 3/9/21 and 3/30/21. Presented to ED with complaints of worsening shortness of breath. Previous medical history of type 2 diabetes, urinary incontinence, spinal stenosis, emphysema, and RLS. Chest x-ray showed pulmonary edema. Patient admitted for further workup. Admitted 12/26/21, discharged 12/28/21.

Weitere VAERSDATA-Felder

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

VAERS 2173457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 73,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 02.03.2021
Beginn: 30.05.2021
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: SYR / UN

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

Aortic bypass Aortic dissection Aortic stent insertion Aortic valve replacement Hypertension Intensive care

Symptomtext

5/30/21. Hypertension which resulted in Type B aortic dissection. Stent installed and bypass performed. 3/2/22. Type A aortic dissection. Graph installed, valve replaced. At time of filing this report patient is still in ICU at hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 45,0
Labordaten: Hypertension, which has been managed with 25mg Metrpolol daily
Aktuelle Erkrankungen: None
Vorgeschichte: Partial hearing loss. Large hiatal hernia.
Andere Medikamente: Probiotic, and multi vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2154645

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 27.02.2021
Beginn: 01.05.2021
Tage bis Beginn: 63,0
Dosis: 2
Route/Site: IM / AR

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

Angiogram Blood test Chest X-ray Chest discomfort Chest pain Dyspnoea Fatigue Headache Pulmonary thrombosis SARS-CoV-2 test

Symptomtext

Approximately a few months after my vaccination I experienced the following symptoms: Shortness of breath, Chest Pain, Headache, and Fatigue. I took Tylenol (2x/day) for treatment and it did work for the headache but for my chest pain, it did not. It was intermittent and by August it just would not get better and it became constant and that's when I decided to go to the Emergency Room, and they did a COVID-19 test, and a check for my chest pain and they found a blood clot on my right lung. I was hospitalized for 3 days and after being discharged I was still experiencing intermittent chest pain. Up to this day 03/03/2022 I still experience a bit of chest discomfort but the blood clot in my lung is already gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 3,0
Labordaten: COVID Test, Chest X-Ray, Blood work, Angiogram.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, Magnesium
Allergien: None
Vorherige Impfungen: Arm Soreness, Fatigue.

VAERS 2137640

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 24.02.2021
Beginn: 21.08.2021
Tage bis Beginn: 178,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Head injury Syncope

Symptomtext

Around Aug 2021 she fainted and hit her head on the door knob. She had A-Fib. Went to the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: yes
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2119371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: KY
Alter: 89,0
Geschlecht: M
Eingang: 17.02.2022
Impfdatum: 28.03.2021
Beginn: 08.02.2022
Tage bis Beginn: 317,0
Dosis: 2
Route/Site: IM / LA

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

Alanine aminotransferase normal Albumin globulin ratio Angiogram cerebral normal Angiogram pulmonary abnormal Anion gap Aspartate aminotransferase normal Asthenia Bacterial test Basophil count abnormal Basophil percentage decreased Bilirubin urine Blood albumin normal Blood alkaline phosphatase normal Blood bilirubin increased Blood calcium decreased Blood chloride normal Blood creatinine increased Blood glucose normal

Symptomtext

2/8/22 90-year-old male brought in by EMS after his wife found him on the ground next to his bed. She states for the past several weeks he has been having cough productive of mucus. She states that initially discussed with his physician and he was given Mucinex which helped briefly however the cough then returned. He is not typically on supplemental oxygen. Was seen again yesterday and apparently had a negative Covid swab and was given an oral penicillin which she has been taking. He went to bed this evening and then his wife states around midnight he heard him "moaning and groaning in the bedroom" and she found him on the ground next to the bed. The patient is notably an extremely poor historian due to severe The patient is notably an extremely poor historian due to severe hearing loss but denies pain anywhere. It is unclear whether he struck his head. They state he has not had any nausea/vomiting or diarrhea. No report of abdominal pain. The did not know he had a fever. They do report some worsening fatigue, decreased p.o. intake with approximate 8 pound weight loss. REVIEW OF SYSTEMS Review of Systems Constitutional: Positive for fatigue and unexpected weight change. Respiratory: Positive for cough. Gastrointestinal: Negative for diarrhea and vomiting. Musculoskeletal: Negative for neck pain. Psychiatric/Behavioral: Positive for confusion. All other systems reviewed and are negative. CT Chest, Abdomen, & Pelvis Wo IV Con Without Oral Contrast: IMPRESSION: Findings compatible with pneumonia, IMPRESSION: No acute process detected in abdomen or pelvis Hospital Course: Patient is a 90 yr/o male with history of hypertension, dyslipidemia, other medical problems who presented to the emergency room because of altered mental status, fall and fever. Was uncertain whether the patient hit his head. He apparently had been sick with respiratory symptoms few weeks prior to this event and was seen by primary medical doctor the day prior to presentation and was prescribed oral penicillin. Patient will try to emergency room because of worsening symptoms. Evaluation in the emergency room showed BUN of 27 creatinine 1.95, COVID-19 was positive and CT angiogram of the chest showed new consolidative pulmonary infiltrate with predominant involvement of the right lower lobe and a small additional region of consolidation in the right upper lobe consistent with pneumonia. Other findings as reported below. CT of the head was unremarkable. Patient was admitted to intensive care unit on aggressive pulmonary toilet, bronchodilators, systemic corticosteroids, remdesivir, antibiotics. Patient also required IV hydration. Patient also remarkable improvement and is currently saturating at 98% on room air. Renal function has improved with a BUN of 22 and creatinine of 1.14. COVID-19 inflammatory markers, specifically fighting and procalcitonin remain elevated. Discharge plan: Patient will follow up with primary medical doctor 2/17/22 F/u with PCP: Here with wife for hospital follow-up Admitted to hospital from February 8?February 12, 2022 for pneumonia, hypotension and sepsis due to COVID-19. Presented to ER with altered mental status, fever and a fall at home. Admitted to the ICU. EMR review showed BUN 27, creatinine 1.95 CT angiogram chest showed new consolidative pulmonary infiltrate with predominant involvement of the right lower lobe and right upper lobe consistent with pneumonia. CTA head was negative. CT abdomen pelvis showed 2 prominent cysts on mid and lower pole of right kidney. Of note, there is mention of a 6 mm poorly defined soft tissue nodule in the right lower lobe that was measured at 4 mm on a CT chest 20 months prior. Nodule appeared larger on most recent scan. Repeat CT Chest recommended- Patient reports feeling better but still fatigued/weak at times. No shortness of breath, chest pain, fever, chills. Wife reports patient has gotten his appetite back. He was not eating in the hospital, but now she reports he has been eating double portions of meals over the past couple days. Patient has been able to walk around the house, even walking up and down the stairs. Patient denies syncope, dizziness or any falls. Reports he does not feel like he is going to fall but has some orthostatic hypotension when he gets up after sitting for a while. Discussed with wife to hold 1 dose of his carvedilol until his hypotension and fatigue are better. Will see them back in the office in 1 week. Has upcoming follow-up appt with nephrology

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 4,0
Labordaten: 2/8/22 COVID-19 Result Detected Abnormal CBC w/Diff Collection Time: 02/08/22 2:20 AM Result Value Ref Range White Blood Count 10.60 4.5 - 11.0 10*3/uL CBC w/Diff Collection Time: 02/08/22 2:20 AM Result Value Ref Range White Blood Count 10.60 4.5 - 11.0 10*3/uL Red Blood Count 4.06 (L) 4.5 - 5.9 10*6/uL Hemoglobin 12.7 (L) 13.5 - 17.5 g/dL Hematocrit 38.8 (L) 41.0 - 53.0 % Mean Corpuscular Volume 95.6 80.0 - 100.0 fL Mean Corpuscular Hemoglobin 31.3 26.0 - 34.0 pg Mean Corpuscular HGB Conc 32.7 31.0 - 37.0 g/dL Red Cell Distribution Width-CV 11.7 (L) 12.0 - 16.8 % Platelet Count 206 140 - 440 10*3/uL Mean Platelet Volume 10.4 8.4 - 12.4 fL Diff Type Hospital CBC w/AutoDiff (arb'U) Neutrophils % 91.6 (H) 45 - 80 % Lymphocyte % 2.5 (L) 15 - 50 % Monocyte % 4.7 0 - 15 % Eosinophil% 0.1 0 - 7 % BASO% 0.1 0 - 2 % Immature Granulocyte% 1.0 0.0 - 1.0 % Nucleated RBC % 0 0 /100(WBC) Neutrophil Abs 9.70 (H) 2.0 - 8.8 10*3/uL Lymphocyte-Absolute 0.27 (L) 0.7 - 5.5 10*3/uL Monocyte Absolute 0.50 0.0 - 1.7 10*3/uL EOS-Absolute 0.01 0.0 - 0.8 10*3/uL Basophil Abs 0.01 0.0 - 0.2 10*3/uL Immature Granulocyte Abs 0.11 (H) 0.00 - 0.10 10*3/uL Comprehensive Metabolic Panel (CMP) Collection Time: 02/08/22 2:20 AM Result Value Ref Range Sodium 136 136 - 145 mmol/L Potassium 4.3 3.5 - 5.1 mmol/L Chloride 100 98 - 107 mmol/L Carbon Dioxide 24 22 - 29 mmol/L Anion Gap 12 5 - 13 (arb'U) Glucose 139 (H) 74 - 99 mg/dL Blood Urea Nitrogen (BUN) 27 (H) 8 - 26 mg/dL Creatinine-Blood 1.95 (H) 0.73 - 1.18 mg/dL BUN/Creatinine Ratio 13.8 RATIO Estimated GFR 32 (L) >60 /1.73 m2 Estimated GFR if African-American 39 (L) >60 /1.73 m2 Total Protein 6.5 6.2 - 8.0 g/dL Albumin 3.5 2.9 - 4.5 g/dL Globulin 3.0 1.5 - 4.5 g/dL Albumin/Globulin Ratio 1.2 1.1 - 2.5 RATIO Calcium 8.9 8.4 - 10.2 mg/dL Total Bilirubin 1.4 (H) 0.2 - 1.2 mg/dL AST/SGOT 23 5 - 34 U/L ALT/SGPT 11 0 - 55 U/L Alkaline Phosphatase 47 40 - 150 U/L Troponin I Collection Time: 02/08/22 2:20 AM Result Value Ref Range Troponin 0.257 (HH) 0.000 - 0.034 ng/mL B-Type Natriuretic Peptide Collection Time: 02/08/22 2:20 AM Result Value Ref Range B-Type Natriuretic Peptide 115.4 4 - 254 pg/mL Magnesium Collection Time: 02/08/22 2:20 AM Result Value Ref Range Magnesium 1.8 1.6 - 2.6 mg/dL Phosphorus Collection Time: 02/08/22 2:20 AM Result Value Ref Range Phosphorus 1.6 (L) 2.3 - 4.7 mg/dL Urinalysis Collection Time: 02/08/22 2:20 AM Result Value Ref Range Color-Urine Yellow Clarity-Urine Clear Specific Gravity Urine 1.022 (H) 1.005 - 1.030 (arb'U) pH-Urine 6.5 5.0 - 9.0 (pH) Protein-Urine >300 (A) Negative mg/dL Glucose-Urine Negative Negative mg/dL Ketone-Urine TRACE (A) Negative mg/dL Bilirubin-Urine SMALL (A) Negative mg/dL Occult Blood-Urine Moderate (A) Negative (arb'U) Nitrite-Urine Negative Negative (arb'U) Urobilinogen-Urine 4.0 (A) Normal (EhrlichU)/dL Leukocyte Esterase-Urine Negative Negative (arb'U) Source-Urine Urine Midstream Reflex Microscopic? Microscopic performed RBC-Urine 6 (H) 0 - 2 (HPF) WBC-Urine 1 0 - 3 (HPF) Squamous Epithelial-Urine None Seen 0 - 4 (HPF) Bacteria-Urine TRACE (A) None Seen (HPF) Mucus-Urine TRACE (A) None Seen (LPF) Amorphous Sediment-Urine TRACE (A) None Seen (HPF) Hyaline Cast-Urine 1 0 - 5 (LPF) Lactic Acid Collection Time: 02/08/22 2:20 AM Result Value Ref Range Lactic Acid 1.5 0.7 - 2.0 mmol/L
Aktuelle Erkrankungen: -
Vorgeschichte: Benign essential HTN o Hyperlipidemia
Andere Medikamente: allopurinol (ZYLOPRIM) 100 MG tablet Take 2 tablets by mouth o aspirin 81 MG EC tablet Take 1 tablet by mouth every other day. o carvedilol (COREG) 3.125 MG tablet TAKE 1 TABLET BY MOUTH TWICE DAILY WITH MEALS o clopidogrel (PLAVIX) 75
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2108973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 67,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 20.02.2021
Beginn: 29.09.2021
Tage bis Beginn: 221,0
Dosis: 2
Route/Site: OT / LA

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

Electroencephalogram normal Magnetic resonance imaging head Partial seizures

Symptomtext

Developed focal consciousness impairing seizures on 29Sep2021; This is a spontaneous report received from contactable reporter(s) (Physician). A 68 year-old male patient received bnt162b2 (BNT162B2, Solution for injection), intramuscular, administered in arm left, administration date 20Feb2021 (Lot number: EN6203) at the age of 67 years as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1, Date/Time (24hr): 28Jan2021 , Anatomical site of injection: Upper right arm, Route of administration: Intramuscular, Batch/Lot number: EN9581), administration date: 28Jan2021, when the patient was 67 years old, for COVID-19 Immunization. The following information was reported: PARTIAL SEIZURES (medically significant) with onset 29Sep2021, outcome "not recovered", described as "Developed focal consciousness impairing seizures on 29Sep2021". The patient underwent the following laboratory tests and procedures: electroencephalogram normal: normal; magnetic resonance imaging head: showed stable 1.3 cm right temporal cavernous, notes: malformation without edema or recent hemorrhage. Therapeutic measures were taken as a result of partial seizures. The reporter considered "developed focal consciousness impairing seizures on 29sep2021" not related to bnt162b2. Clinical course: Developed focal consciousness impairing seizures on 29Sep2021 (1st witnessed). EEG normal. Brain MRI showed stable 1.3 cm right temporal cavernous malformation without edema or recent hemorrhage. Following that was prescribed medication Levetiracetam to stop seizures. He initially was non compliant and had additional seizures. Subsequently started Levetiracetam and developed side effect of depression and irritability. Subsequently changed to Lamotrigine for seizure prophylaxis which to this date has been helpful in preventing seizures. Reporter did not think patient's seizures are related to his Pfizer covid vaccines that he received 28Jan2021, 20Feb2021 and 01Oct2021. Reporter did not consider Pfizer product had a causal effect to the adverse event.; Sender's Comments: The event focal consciousness impairing seizures is assessed as likely due to the cavernous malformation and assessed as unrelated to BNT162B2 vaccine administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: -
Labordaten: Test Name: EEG; Result Unstructured Data: Test Result:Normal; Test Name: Brain MRI; Result Unstructured Data: Test Result:showed stable 1.3 cm right temporal cavernous; Comments: malformation without edema or recent hemorrhage
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2087990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 43,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Antibody test abnormal Cardiac flutter Chest X-ray Feeling abnormal Hyperhidrosis Hypersensitivity Inappropriate schedule of product administration Interchange of vaccine products Loss of consciousness Palpitations Pyrexia Vaccination complication Vomiting

Symptomtext

03/10/2021 about 5 minutes after my vaccine my heart started to pound, I became sweaty. I started lifting my mask, a police officer asked if I was ok. And he took me to see the paramedics. They said it is not unusual for me to feel like this, but I said I don't feel okay, something is wrong. I said I feel like I need to go outside. My husbands took me home and I threw up a couple of times. and I passed out cold in my bed. I woke up 4 hours later. I had fever, normal side effects from the vaccine. That lasted about a week. My doctor said you should see an allergist. My doctor said you should not get your 2nd dose. The allergist said I had an allergic reaction and said I should get the Johnson and Johnson. I had fluttering in my chest and was not feeling well for a month. In June I got permission from my doctor to get the Johnson and Johnson. The refused to give me another vaccine. I called the department of health and they helped me get the Johnson and Johnson. It took about 5 months to get it. Now I have one dose of Pfizer and one dose of Johnson and Johnson.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: blood work checked my antibodies he said I had a hypo reaction to the vaccine. And he said my antibodies were off the chart chest x-ray
Aktuelle Erkrankungen: no
Vorgeschichte: celiac white blood cells take longer for me to get healthy again - neutropenia
Andere Medikamente: none
Allergien: wheat
Vorherige Impfungen: flu vaccine, I have a bad reaction, 2019

VAERS 2085375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 50,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 25.10.2021
Beginn: 05.11.2021
Tage bis Beginn: 11,0
Dosis: 2
Route/Site: IM / LA

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

C-reactive protein normal Chest discomfort Chest pain Imaging procedure artifact Magnetic resonance imaging heart Myocarditis Renal cyst Troponin increased

Symptomtext

Patient received 3 pfizer covid vaccines on 2/2/21, 2/23/21, and 10/25/21. Patient had cardiology visit on 11/4/21 due to recent episode of chest pain in the setting of an upcoming marathon participation. On 10/28/21, patient experienced a sudden-onset, left-sided, pressure like chest pain of 8/10 in severity and went to the ED. Troponin on 10/28: 32-- >33-> 31 11/4: 32 CRP: 1.7 cardiac mri done on 11/5/21: Normal biventricular function. The pattern of late gadolinium enhancement is most likely secondary to myocarditis. Cardiac sarcoidosis is considered unlikely given the absence of arrhythmia or evidence of extracardiac sarcoidosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: 11/5/21 mri cardiac impression: 1. The left ventricular size and function are normal by visual assessment. Quantitative assessment was not possible due to artifact. There are no regional wall motion abnormalities of the left ventricular wall. 2. There is no resting first pass myocardial perfusion defect. Normal myocardial gadolinium kinetics with appropriate nulling of the blood pool prior to the myocardium. There is small amount of mesocardial late gadolinium enhancement in the mid-inferoseptal wall and inferior RV insertion point. There is no evidence of focal myocardial edema by T2 weighted imaging. Native T1 values are normal: 1146 - 1194 ms (Normal range: 1200 +/- 80 ms on 3T scanner). 3. The right ventricular size is normal. Global right ventricular function is normal. There are no regional wall motion abnormalities of the right ventricular wall. There is no late gadolinium enhancement of the right ventricle. 4. Left atrial size is normal. Right atrial size is normal. 5. Left renal cyst measuring up to 9 mm.
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: amitriptyline, cyclobenzaprine, etodolac, tizanidine
Allergien: oxycodone
Vorherige Impfungen: -

VAERS 2079227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 75,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 18.03.2021
Beginn: 21.01.2022
Tage bis Beginn: 309,0
Dosis: 1
Route/Site: SYR / LA

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

Acute respiratory distress syndrome COVID-19 COVID-19 pneumonia Endotracheal intubation Intensive care SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 2/25, 3/18/21 COVID-19 positive by PCR on 1/21/22 admitted to Hospital on 1/31/22 d/t COVID pneumonia, ARDS currently in ICU, intubated. underlying CAD, HTN

Weitere VAERSDATA-Felder

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

VAERS 2068526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 23.02.2021
Beginn: 12.01.2022
Tage bis Beginn: 323,0
Dosis: UNK
Route/Site: - / -

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

Asthenia Bronchiolitis COVID-19 Chest X-ray abnormal Electrocardiogram abnormal Hyponatraemia Lung opacity Productive cough SARS-CoV-2 test positive Sinus tachycardia Syncope Vaccine breakthrough infection Ventricular extrasystoles

Symptomtext

Breakthrough COVID . First vaccine 2/1/21. Patiet not boostered. Pt is an 84 yo M admitted on 1/12/22 for syncopal episodes and weakness. He also endorsed cough with productive sputum although pt has hx. of pulm fibrosis and said this was normal. ED workup included EKG showing sinus tach w/PVC's, hyponatremia, Chest XR showed mild to moderate bibasilar multifocular reticular opacities likely representing chronic bronchiolisit. He was given IVF and was admitted for cardiac workup. Pt. had + COVID test on 1/20/22 after being screened for SNF placement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: COVID + test on 1/20/22
Aktuelle Erkrankungen: -
Vorgeschichte: Pulmonary fibrosis, hypertension, hyponatremia.
Andere Medikamente: -
Allergien: iodine, pork
Vorherige Impfungen: -

VAERS 2046443

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: KY
Alter: 40,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.04.2021
Beginn: 13.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Abdominal pain Chest pain Dizziness Migraine Presyncope

Symptomtext

Approximately 10 minutes after 3rd COVID vaccine was administered, patient complained of dizziness and felt faint. Patient was given apple juice. BP 129/91. EMS was contacted and patient was transported to the ED after EMS evaluation. Patient does have a history of vasovagal syncope. Patient stated she felt pre syncopal but no true syncope. While in the ED, patient also complained that she had 2-3 days of N/V/D with cramping abdominal pain. While in the ED, patient then began having left side chest pain. No hx of CAD. Chest pain, dizziness, N/V/D have all resolved but it has now triggered a migraine headache which she has a history of. Denies f/c, cp, soa, abdominal pain, urinary symptoms. Patient was given anti-emetic and fluids. Patient and MD discussed that the booster vaccine caused a vasovagal dizziness and presyncope feeling. Patient had symptom relief and was discharged from the ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None listed
Aktuelle Erkrankungen: None
Vorgeschichte: ? Liver disease, unspecified Liver problem ? Other bacterial infections of unspecified site VRE (vancomycin-resistant Enterococci) ? Overweight Over weight ? Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism History of bleeding disorder ? Personal history of malignant neoplasm, unspecified History of malignant neoplasm ? Personal history of other diseases of the circulatory system History of hypertension ? Personal history of other diseases of the musculoskeletal system and connective tissue History of gout ? Personal history of other diseases of the respiratory system History of hyperventilation ? Personal history of other endocrine, nutritional and metabolic disease History of diabetes mellitus ? Personal history of other medical treatment Transfusion history ? Personal history of other mental and behavioral disorders History of depression ? Personal history of thrombophlebitis History of thrombophlebitis ? Renal tubulo-interstitial disease, unspecified Kidney infection ? Unspecified coma Loss of consciousness
Andere Medikamente: None listed
Allergien: Beeswax - anaphylaxis Ondansetron - anaphylaxis Wound dressing adhesive - rash banana - unknown Egg - no reaction listed morphine - no reaction listed
Vorherige Impfungen: -

VAERS 1134665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 27.02.2021
Beginn: 21.03.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: IM / LA

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

Anal incontinence Back pain CSF test normal Diplegia Laboratory test normal CSF culture Computerised tomogram Laboratory test Magnetic resonance imaging Myelitis transverse Magnetic resonance imaging head normal Magnetic resonance imaging spinal abnormal Paraesthesia Spinal cord infarction Paralysis X-ray Urinary incontinence

Symptomtext

Transverse Mylelitis Paralyzed waist down both sides

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paralysis
Hospital-Tage: 35,0
Labordaten: Several MRI, X-ray, cat scan, lab work, spinal fluid drawn. In emergency room Hospital
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamins, calcium
Allergien: None
Vorherige Impfungen: -

VAERS 2035852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 73,0
Geschlecht: M
Eingang: 14.01.2022
Impfdatum: 08.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

COVID-19 COVID-19 pneumonia Respiratory distress SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 2/25, 3/18, 12/8/21 COVID-19 positive by PCR on 12/12/21. Hospitalized 12/12-12/26/21 d/t COVID 19 pneumonia readmitted on 1/10/22 d/t respiratory distress in setting of COVID 19. underlying COPD, HTN, h/o stroke, pulmonary fibrosis, AAA

Weitere VAERSDATA-Felder

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

VAERS 1332693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 86,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 04.03.2021
Beginn: 24.04.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: - / LA

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

Arrhythmia Atrial fibrillation Blood test Deep vein thrombosis Gait inability Muscle spasms Pain in extremity Sciatica Thrombosis Imaging procedure SARS-CoV-2 test positive Ultrasound scan

Symptomtext

A-FiB; Arrhythmia; Deep vein thrombosis; She then got sciatica in her leg and couldn't walk; blood clot/ blood clot left (L) calf; Sciatica; charley horse in the lower leg; soreness in arm/pain in her foot/lower leg/calf still hurt; This is a spontaneous report from a contactable nurse (patient). This 86-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number EN6203, Expiration date: unknown) intramuscular, administered in left deltoid on 04Mar2021 at 13:15 pm (age at vaccination was 86 years) as dose 2, single for COVID-19 immunization. The patient's medical history included atrial fibrillation (A-FiB) (heart disease) from 2008 and ongoing, hypothyroid from 1976 and ongoing, hypertension and hypolipidemia. The patient was not a smoker/former smoker. The patient received some years ago an unspecified pneumonia vaccine and an unspecified tetanus vaccine and after both experienced headache, swollen arm and rash, the patient was taking concomitant medications routinely prior to the event being reported. She didn't react to the flu vaccine. Her body didn't want any more vaccine. No other vaccines were administered on the same date and within four weeks. The patient did not receive any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination. The patient did not have any pre-existing diseases worsened during the SARS-CoV2 infection. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number EN6201, Expiration date: unknown) intramuscular, administered in left deltoid on 11Feb2021 at 18:15 pm (age at vaccination was 86 years) as dose 1, single. On an unspecified date in Mar2021, maybe a week or two after the second vaccination, early to mid-afternoon, the patient had what felt like a charley horse in her lower leg while walking, but didn't pay any attention to it, just put ice on the leg. She then got sciatica in her leg on 24Apr2021 and couldn't walk; that was what sent her to the hospital as it was getting worse, and she went to the hospital because of the pain. She just ignored it for at least a week, but she was still having pain after the second week and could hardly walk due to the sciatica in that leg. At the hospital they found she had a blood clot in the calf of her leg on 28Apr2021. She was hospitalized from 28Apr2021 to 02May2021. The patient was not admitted to an Intensive Care Unit. The doctors in the hospital recommended that she should report her experience even though they didn't know if it was due to the COVID vaccine due to the proximity. The hospital doctors took care of her but her primary care provider knew that she had been in the hospital. The doctors gave her medications in the hospital that helped the pain in her foot and the sciatica but her lower leg/calf still hurt so they decided to do an ultrasound and found a blood clot. The patient still had to give herself injections in the belly for blood thinner to treat the blood clot. The patient also experienced soreness in arm on an unspecified date in 2021. Sciatica required ER visit. Additionally, the patient experienced positive (pos) COVID-19 test (nasal swab came back positive for covid-19) on 28Apr2021 and A-FiB on an unspecified date both required emergency room (ER) visit and reported as serious with hospitalization criterion and duration of stays from 28Apr2021 to 02May2021. No treatment was received due to positive COVID-19 test while diltiazem 120 mg was given due to A-FiB. It was also reported that patient experienced blood clot left (L) calf and sciatica treated with enoxaparin. The patient did not display clinical signs at rest indicative of severe systemic illness. The patient did not require supplemental oxygen (including high flow or ECMO) or receive mechanical ventilation. The event did not require the initiation of new medication or other treatment or procedure. It was unknown whether the patient had SARS-CoV2 antibodies at diagnosis and SARS-CoV2 antibodies at hospital discharge. The doctor said that there was a possibility that the blood clot could be related to the COVID vaccine, but it may not be related at all. The hypoxemia, arrhythmia, hematological, acute respiratory distress syndrome (ARDS) and dermatological was unknown, COVID-pneumonia, respiratory failure, cardiovascular, gastrointestinal/Hepatic, renal and neurological was no and deep vein thrombosis was yes. The patient underwent lab tests and procedure which included blood test with unknown results, ultrasound showed blood clot in calf and COVID-19 RT-PCR test (positive) (nasal swab came back positive for COVID-19), imaging for thrombo-embolic events (e.g., doppler or CT) on 28Apr2021: DVT 75mm occlusive thrombus (Range: Us Doppler lower venous left) on 28Apr2021. There was no multiorgan involvement, no respiratory, no dyspnoea, no tachypnea, no hypoxemia, no COVID-pneumonia, no respiratory failure, no acute respiratory distress syndrome (ARDS), no cardiovascular, no heart failure, no cardiogenic shock, no acute myocardial infarction, no myocarditis, no gastrointestinal, no vomiting, no diarrhoea, no abdominal pain, no jaundice, no acute liver failure, no vascular, no renal, no acute kidney injury, no renal failure, no neurological, no altered consciousness, no convulsions/seizures, no encephalopathy, no meningitis, no cerebrovascular accident, no dermatological, no chilblains and no erythema multiforme. The outcome of the events blood clot/ blood clot left (L) calf and sciatica was recovering. The patient did not receive any additional therapies for COVID-19. The outcome of the events A-FiB was recovered on an unspecified date in 2021. The outcome of the other events was unknown. Follow-up (07Jun2021): New information received from the same contactable nurse (patient) included: new events ("Pos covid 19 test" and "A-FiB"), clinical details, patient's medical history, lab data and suspect drug details (route of administration) were added, outcome of the events ("blood clot/ blood clot left (L) calf"and "sciatica") and suspect drug details (site and time of administration) were updated. Follow-up (24Jun2021): New information received from a contactable other Healthcare professional reported for the patient in response to HCP letter via follow-up letter included: Updated the date of positive (pos) COVID-19 test (28Apr2021) and outcome as resolved, updated drug ineffective to vaccination failure as SARS Cov-2 test was positive on 28Apr2021, medical history, details of multiorgan involvement and clinical course. Follow-up (06Aug2021): New information was received via contactable consumer (receptionist) in response to HCP letter sent to physician via telephonic follow-up activity which included: Added new reporter: consumer (receptionist). Follow up (07Sep2021): This is a follow-up spontaneous report received in response to the mail trail sent regarding the confirmation of a query. The response included: It is cancelled status in CITI. Follow-up (08Nov2021): This is a follow-up spontaneous report received from a contactable physician. This physician reported in response to HCP letter sent that included unknown concomitant medication, lab test and clinical information in narrative. Follow-up attempts are completed. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Split case created for the events reported only after second dose of vaccine.; Sender's Comments: Based on the available information, there is a reasonable possibility of a causal relationship between the suspect vaccine BNT162B2 (COMIRNATY) and reported events Sciatia, thrombosis, Atrial Fibrillation, Deep Vein thrombosis and Gait inability which cannot be fully assessed/excluded. The case will be reassessed if additional information becomes 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: Thrombosis
Hospital-Tage: 4,0
Labordaten: Test Date: 20210428; Test Name: Blood test; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210428; Test Name: Imaging for thrombo-embolic events; Result Unstructured Data: Test Result:DVT 75mm occlusive thrombus; Comments: Us doppler lower venous left Us doppler + lower venous left; Test Date: 20210428; Test Name: RT PCR test; Test Result: Positive ; Comments: Patient's outcome with COVID-19: Recovered; Test Date: 20210428; Test Name: Ultrasound; Result Unstructured Data: Test Result:Blood clot L calf
Aktuelle Erkrankungen: Atrial fibrillation (Heart disease Ongoing); Cold (Turbinectomy septoblasty Oct2003); Hypothyroidism (ongoing)
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia; Hypertension; Non-tobacco user
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1332693

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 86,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 04.03.2021
Beginn: 24.04.2021
Tage bis Beginn: 51,0
Dosis: 2
Route/Site: OT / LA

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

Arrhythmia Atrial fibrillation Blood test Deep vein thrombosis Gait inability Muscle spasms Pain in extremity Sciatica Thrombosis Imaging procedure SARS-CoV-2 test positive Ultrasound scan

Symptomtext

A-FiB; Arrhythmia; Deep vein thrombosis; She then got sciatica in her leg and couldn't walk; blood clot/ blood clot left (L) calf; Sciatica; charley horse in the lower leg; soreness in arm/pain in her foot/lower leg/calf still hurt; This is a spontaneous report from a contactable nurse (patient). This 86-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number EN6203, Expiration date: unknown) intramuscular, administered in left deltoid on 04Mar2021 at 13:15 pm (age at vaccination was 86 years) as dose 2, single for COVID-19 immunization. The patient's medical history included atrial fibrillation (A-FiB) (heart disease) from 2008 and ongoing, hypothyroid from 1976 and ongoing, hypertension and hypolipidemia. The patient was not a smoker/former smoker. The patient received some years ago an unspecified pneumonia vaccine and an unspecified tetanus vaccine and after both experienced headache, swollen arm and rash, the patient was taking concomitant medications routinely prior to the event being reported. She didn't react to the flu vaccine. Her body didn't want any more vaccine. No other vaccines were administered on the same date and within four weeks. The patient did not receive any other vaccines around the time of Pfizer-BioNTech COVID-19 Vaccine vaccination. The patient did not have any pre-existing diseases worsened during the SARS-CoV2 infection. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number EN6201, Expiration date: unknown) intramuscular, administered in left deltoid on 11Feb2021 at 18:15 pm (age at vaccination was 86 years) as dose 1, single. On an unspecified date in Mar2021, maybe a week or two after the second vaccination, early to mid-afternoon, the patient had what felt like a charley horse in her lower leg while walking, but didn't pay any attention to it, just put ice on the leg. She then got sciatica in her leg on 24Apr2021 and couldn't walk; that was what sent her to the hospital as it was getting worse, and she went to the hospital because of the pain. She just ignored it for at least a week, but she was still having pain after the second week and could hardly walk due to the sciatica in that leg. At the hospital they found she had a blood clot in the calf of her leg on 28Apr2021. She was hospitalized from 28Apr2021 to 02May2021. The patient was not admitted to an Intensive Care Unit. The doctors in the hospital recommended that she should report her experience even though they didn't know if it was due to the COVID vaccine due to the proximity. The hospital doctors took care of her but her primary care provider knew that she had been in the hospital. The doctors gave her medications in the hospital that helped the pain in her foot and the sciatica but her lower leg/calf still hurt so they decided to do an ultrasound and found a blood clot. The patient still had to give herself injections in the belly for blood thinner to treat the blood clot. The patient also experienced soreness in arm on an unspecified date in 2021. Sciatica required ER visit. Additionally, the patient experienced positive (pos) COVID-19 test (nasal swab came back positive for covid-19) on 28Apr2021 and A-FiB on an unspecified date both required emergency room (ER) visit and reported as serious with hospitalization criterion and duration of stays from 28Apr2021 to 02May2021. No treatment was received due to positive COVID-19 test while diltiazem 120 mg was given due to A-FiB. It was also reported that patient experienced blood clot left (L) calf and sciatica treated with enoxaparin. The patient did not display clinical signs at rest indicative of severe systemic illness. The patient did not require supplemental oxygen (including high flow or ECMO) or receive mechanical ventilation. The event did not require the initiation of new medication or other treatment or procedure. It was unknown whether the patient had SARS-CoV2 antibodies at diagnosis and SARS-CoV2 antibodies at hospital discharge. The doctor said that there was a possibility that the blood clot could be related to the COVID vaccine, but it may not be related at all. The hypoxemia, arrhythmia, hematological, acute respiratory distress syndrome (ARDS) and dermatological was unknown, COVID-pneumonia, respiratory failure, cardiovascular, gastrointestinal/Hepatic, renal and neurological was no and deep vein thrombosis was yes. The patient underwent lab tests and procedure which included blood test with unknown results, ultrasound showed blood clot in calf and COVID-19 RT-PCR test (positive) (nasal swab came back positive for COVID-19), imaging for thrombo-embolic events (e.g., doppler or CT) on 28Apr2021: DVT 75mm occlusive thrombus (Range: Us Doppler lower venous left) on 28Apr2021. There was no multiorgan involvement, no respiratory, no dyspnoea, no tachypnea, no hypoxemia, no COVID-pneumonia, no respiratory failure, no acute respiratory distress syndrome (ARDS), no cardiovascular, no heart failure, no cardiogenic shock, no acute myocardial infarction, no myocarditis, no gastrointestinal, no vomiting, no diarrhoea, no abdominal pain, no jaundice, no acute liver failure, no vascular, no renal, no acute kidney injury, no renal failure, no neurological, no altered consciousness, no convulsions/seizures, no encephalopathy, no meningitis, no cerebrovascular accident, no dermatological, no chilblains and no erythema multiforme. The outcome of the events blood clot/ blood clot left (L) calf and sciatica was recovering. The patient did not receive any additional therapies for COVID-19. The outcome of the events A-FiB was recovered on an unspecified date in 2021. The outcome of the other events was unknown. Follow-up (07Jun2021): New information received from the same contactable nurse (patient) included: new events ("Pos covid 19 test" and "A-FiB"), clinical details, patient's medical history, lab data and suspect drug details (route of administration) were added, outcome of the events ("blood clot/ blood clot left (L) calf"and "sciatica") and suspect drug details (site and time of administration) were updated. Follow-up (24Jun2021): New information received from a contactable other Healthcare professional reported for the patient in response to HCP letter via follow-up letter included: Updated the date of positive (pos) COVID-19 test (28Apr2021) and outcome as resolved, updated drug ineffective to vaccination failure as SARS Cov-2 test was positive on 28Apr2021, medical history, details of multiorgan involvement and clinical course. Follow-up (06Aug2021): New information was received via contactable consumer (receptionist) in response to HCP letter sent to physician via telephonic follow-up activity which included: Added new reporter: consumer (receptionist). Follow up (07Sep2021): This is a follow-up spontaneous report received in response to the mail trail sent regarding the confirmation of a query. The response included: It is cancelled status in CITI. Follow-up (08Nov2021): This is a follow-up spontaneous report received from a contactable physician. This physician reported in response to HCP letter sent that included unknown concomitant medication, lab test and clinical information in narrative. Follow-up attempts are completed. No further information is expected. Amendment: This follow-up report is being submitted to amend previous information: Split case created for the events reported only after second dose of vaccine.; Sender's Comments: Based on the available information, there is a reasonable possibility of a causal relationship between the suspect vaccine BNT162B2 (COMIRNATY) and reported events Sciatia, thrombosis, Atrial Fibrillation, Deep Vein thrombosis and Gait inability which cannot be fully assessed/excluded. The case will be reassessed if additional information becomes 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: Thrombosis
Hospital-Tage: 4,0
Labordaten: Test Date: 20210428; Test Name: Blood test; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210428; Test Name: Imaging for thrombo-embolic events; Result Unstructured Data: Test Result:DVT 75mm occlusive thrombus; Comments: Us doppler lower venous left Us doppler + lower venous left; Test Date: 20210428; Test Name: RT PCR test; Test Result: Positive ; Comments: Patient's outcome with COVID-19: Recovered; Test Date: 20210428; Test Name: Ultrasound; Result Unstructured Data: Test Result:Blood clot L calf
Aktuelle Erkrankungen: Atrial fibrillation (Heart disease Ongoing); Cold (Turbinectomy septoblasty Oct2003); Hypothyroidism (ongoing)
Vorgeschichte: Medical History/Concurrent Conditions: Hyperlipidemia; Hypertension; Non-tobacco user
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1967440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 21.12.2021
Impfdatum: 05.03.2021
Beginn: 03.12.2021
Tage bis Beginn: 273,0
Dosis: 2
Route/Site: IM / UN

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

Blood sodium normal COVID-19 Cough Diarrhoea Dyspnoea Hyponatraemia Intensive care Nausea Positive airway pressure therapy Respiratory distress SARS-CoV-2 test positive Sputum discoloured Vomiting

Symptomtext

presented to the emergency room a tonight with the 2-3 day history of worsening shortness of breath associated with cough and brownish sputum production. He denies fever or chills. The shortness of breath progressively got was during this time frame. He also gives a 2-3 day history of nausea, vomiting and diarrhea and unable to keep for liquids or solids down. He denies abdominal pain, melena or hematochezia. He presented and respiratory distress on BiPAP support. He received intravenous Lasix 80 mg upon arrival to the emergency department. Subsequently live auricle investigations revealed a profound hyponatremia with a serum sodium of 111 and hence received 500 mL of... Tested positive on 12/03/2021 presented to the emergency room tonight with the 2-3 day history of worsening shortness of breath associated with cough and brownish sputum production. He denies fever or chills. The shortness of breath progressively got was during this time frame. He also gives a 2-3 day history of nausea, vomiting and diarrhea and unable to keep for liquids or solids down. He denies abdominal pain, melena or hematochezia. He presented and respiratory distress on BiPAP support. He received intravenous Lasix 80 mg upon arrival to the emergency department. Subsequently live auricle investigations revealed a profound hyponatremia with a serum sodium of 111 and hence received 500 mL of intravenous sodium chloride fluid challenge. He also received the duo neb. in view of the profound hyponatremia he is being evaluated to be admitted to the intensive care unit for closer monitoring. During his stay in the emergency department he has been weaned off the BiPAP support and currently on 3 L of oxygen via nasal cannula. Incidentally he claims that he was vaccinated for COVID-19, 6 months ago with 2 dose regimen but he is not sure what type of vaccine it was.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, hyperlipidemia, insulin-dependent type 2 diabetes mellitus, history of TIA, morbid obesity, COPD/emphys, hypertension, hyperlipidemia, insulin-dependent type 2 diabetes mellitus, history of TIA, morbid obesity, COPD/emphysema, gout, depression, chronic GERD, peripheral neuropathy, resident of assisted living facility, functional paraplegia following back surgery and nicotine dependence
Andere Medikamente: nystatin topical
Allergien: Tramadol
Vorherige Impfungen: -

VAERS 1142059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 72,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 25.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: - / RA

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

Arthralgia Chills Computerised tomogram abnormal Laboratory test Lymphadenopathy Blood test Computerised tomogram Platelet count decreased Thrombosis Night sweats Pain Platelet count Pain in extremity Pyrexia Rash erythematous

Symptomtext

severe stabbing pains in upper body; low grade fever; Severe night sweats; platelets drop to 39; 2 Blood clots, one in calf, second in groin; enlarged lymph nodes; Red rash over upper body; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 25Feb2021 10:30 (Lot number: EN6203) at the age of 72 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Prior to vaccination, patient was not diagnosed with COVID-19. Concomitant medication(s) included: SIMVASTATIN; ASPRIN; VITAMIN D 3. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: PAIN (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "severe stabbing pains in upper body"; PYREXIA (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "low grade fever"; NIGHT SWEATS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "Severe night sweats"; PLATELET COUNT DECREASED (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "platelets drop to 39"; THROMBOSIS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "2 Blood clots, one in calf, second in groin"; LYMPHADENOPATHY (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "enlarged lymph nodes"; RASH ERYTHEMATOUS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "Red rash over upper body". The events "severe stabbing pains in upper body", "low grade fever", "severe night sweats", "platelets drop to 39", "2 blood clots, one in calf, second in groin", "enlarged lymph nodes" and "red rash over upper body" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: platelet count: (11Mar2021) drop to 39. Since the vaccination, patient had not been tested for COVID-19. Therapeutic measures were taken as a result of pain, pyrexia, night sweats, platelet count decreased, thrombosis, lymphadenopathy, rash erythematous with various treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210311; Test Name: platelets; Result Unstructured Data: Test Result:drop to 39
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: SIMVASTATIN; ASPRIN; VITAMIN D 3
Allergien: -
Vorherige Impfungen: -

VAERS 1142059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 72,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 25.02.2021
Beginn: 11.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Chills Computerised tomogram abnormal Laboratory test Lymphadenopathy Blood test Computerised tomogram Platelet count decreased Thrombosis Night sweats Pain Platelet count Pain in extremity Pyrexia Rash erythematous

Symptomtext

severe stabbing pains in upper body; low grade fever; Severe night sweats; platelets drop to 39; 2 Blood clots, one in calf, second in groin; enlarged lymph nodes; Red rash over upper body; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 72 year-old male patient received bnt162b2 (BNT162B2), administered in arm right, administration date 25Feb2021 10:30 (Lot number: EN6203) at the age of 72 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Prior to vaccination, patient was not diagnosed with COVID-19. Concomitant medication(s) included: SIMVASTATIN; ASPRIN; VITAMIN D 3. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The following information was reported: PAIN (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "severe stabbing pains in upper body"; PYREXIA (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "low grade fever"; NIGHT SWEATS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "Severe night sweats"; PLATELET COUNT DECREASED (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "platelets drop to 39"; THROMBOSIS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "2 Blood clots, one in calf, second in groin"; LYMPHADENOPATHY (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "enlarged lymph nodes"; RASH ERYTHEMATOUS (disability, life threatening) with onset 11Mar2021, outcome "unknown", described as "Red rash over upper body". The events "severe stabbing pains in upper body", "low grade fever", "severe night sweats", "platelets drop to 39", "2 blood clots, one in calf, second in groin", "enlarged lymph nodes" and "red rash over upper body" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: platelet count: (11Mar2021) drop to 39. Since the vaccination, patient had not been tested for COVID-19. Therapeutic measures were taken as a result of pain, pyrexia, night sweats, platelet count decreased, thrombosis, lymphadenopathy, rash erythematous with various treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Date: 20210311; Test Name: platelets; Result Unstructured Data: Test Result:drop to 39
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: SIMVASTATIN; ASPRIN; VITAMIN D 3
Allergien: -
Vorherige Impfungen: -

VAERS 1955713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 15.03.2021
Beginn: 26.11.2021
Tage bis Beginn: 256,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia Brain natriuretic peptide increased C-reactive protein increased COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Decreased appetite Diarrhoea Dyspnoea Intensive care Lung infiltration SARS-CoV-2 test positive Troponin

Symptomtext

Patient admitted to hospital on 12/3/2021 weakness, shortness of breath and decreased appetite Patient tested COVID positive on 11/26/2021 she reported being ill for about 9-10 days Initially she had a cough, then later diarrhea with worsening dyspnea. No fever, chest pain. Admitted to ICU need for heated high flow oxygen. Received remdesivir and dexamethasone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: -
Labordaten: COVID positive on 11/26/2021 12/3/2021 troponin 3511 12/3/2021 BNP 421 12/3/2021 CXR: patchy infiltrates throughout both lungs consistent with atypical pneumonia. COVID19 pneumonia is suspected. 12/4/2021 troponin 4774 12/4/2021 CRP 13.8
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes mellitus Renal transplant recipient HTN Coronary artery disease s/p 3V CABG Bilateral BKA
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 1944313

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MD
Alter: 47,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 24.02.2021
Beginn: 24.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Computerised tomogram Facial paralysis Gait disturbance Hemiplegic migraine Migraine Speech disorder

Symptomtext

A month after vaccination, I had migraines, a hemiplegic migraine, left side paralysis in my face that radiated, and had speech issues and problems walking.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Blood Test, CT Scan 03/24/2021, Stroke Protocol
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: None
Allergien: Reglan, Compazine, Phenergan, Penicillin, Fosamax
Vorherige Impfungen: -

VAERS 1929233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 66,0
Geschlecht: M
Eingang: 07.12.2021
Impfdatum: 22.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Body temperature increased COVID-19 Chills Dyspnoea Feeling cold Incomplete course of vaccination Influenza like illness Oxygen saturation decreased Presyncope SARS-CoV-2 test positive

Symptomtext

The first night I felt fine and had no issues, no temperature, no reaction, no soreness in arm, no bump at vaccine site. Then, about 3-4 days later, I got the feeling that I was catching the flu and my insurance company had sent me a package that had a digital thermometer and prescription of Tamiflu and COVID test and as my temperature began to rise I felt weak and I thought it might be the flu. I called my doctor and he said I should come in and they asked me to come in at 2 PM. She did the nasal and made me wait and 15 minutes later she came and said I have COVID. They checked my oxygen level which was low. They told me to just go home and rest. I left and came home and checked my pulse oxygen level and it was still low but I had no shortness of breath or cough so I just thought I would take a hot shower and breathe in the steam and break whatever it is in my lungs. In the shower I felt like I was going to black out so I got out and took temperature and it was up but it didn't feel accurate. As the evening progressed my temperature continued to climb and I could tell because I was getting the chills. I turned on the heat and still couldn't get warm. Temperature was at 106 and so I called my doctor and they told me to take an ice bath but I didn't have bathtub or an ice maker, so they told me to lie in the snow and I didn't want to because I thought I'd die. I went out and lied in snow and it brought my temperature down 3 degrees. They called back 10-15 minutes later and I talked to the doctor and she told me she was tired of me calling and to go to the hospital so they could deal with me (CO) and hung up. I changed doctors after that. I couldn't get to the hospital because there was a snow storm but the local fire department looked after me and my neighbor who is a heart surgeon looked after me and brought me a 2 liter bottle oxygen and when I called the Dr. she told me to stop taking oxygen so I was done with her, and the heart surgeon neighbor brought me a oxygen concentration which I used for 3 weeks because I did have shortness of breath. I stopped using the oxygen and started exercising and I did go see a pulmonary specialist and they gave me, after an hour of breathing test, albuterol. They wanted a follow up but couldn't go see them because they were with the old office with the first Dr. and not the new Dr. I finally recovered from that and life was good until it was to get the 2nd dose and they asked me about a temperature when I called to confirm 2nd dose appointment and since I did have a temperature I had to wait until I was 10 days fever free.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Oxygen test
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Imitrex shot
Allergien: None
Vorherige Impfungen: -

VAERS 1905741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 03.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chest X-ray abnormal Dyspnoea Laryngitis Pneumonitis Pulmonary oedema Throat tightness

Symptomtext

I had extreme shortness of breath, throat closed up, my voice was strained. I call advice nurse they directed me to go to nearest ER . They had me take my inhaler, claritin. when I got to Er they gave me they gave me a steroid and a breathing treatment. They gave me an IV, I do not remember what was in IV. I still have shortness of breath and I'm seeing a lung specialist. They have switched up my medication

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: -
Labordaten: Chest X-ray- showed pneumonitis, pulmonary edema
Aktuelle Erkrankungen: none
Vorgeschichte: asthma , high blood pressure, cholesterol
Andere Medikamente: Kozar, Maxzide, tenormin, alvesco, zyrtec,
Allergien: percocet
Vorherige Impfungen: -

VAERS 1903742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 91,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 23.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Asthenia Chest X-ray Cough Dyspnoea Feeling abnormal Frustration tolerance decreased Lung disorder Myocarditis Pericarditis Rhinitis SARS-CoV-2 test Sneezing Tidal volume

Symptomtext

Pericarditis; Myocarditis; Very sudden weakness; Cough; Sneezing; Shortness of breath; Brain fog; Nasal infect rate; bilateral pulmonary infusion; In frustration; This is a spontaneous report from a contactable physician (patient). This 91-year-old male patient received the second dose of bnt162b2 (COMIRNATY), via an unspecified route of administration on 23Feb2021 (at the age of 91-year-old; Lot number: EN6203) as DOSE 2, SINGLE for COVID-19 immunization. Medical history included pacemaker. Concomitant medication included apixaban (ELIQUIS) for stroke. The patient previously received the first dose of bnt162b2, on 02Feb2021 (at the age of 91-year-old, Lot number: EN5318) as single dose for COVID-19 immunization, and after the first shot, he experienced stroke, affected his vision, shortness of breath, cough and marked weakness, about half his strength; lesion mass, scar on the base of his heart. The patient is a retired family practice physician. Patient reported being a very healthy person, never had an illness and has had all kinds of health things come up since receiving the vaccine. Patient had no hypertension and no diabetes, basically he had no illness, he was super healthy all his life. He had a pacemaker which he did not consider an illness. He described his adverse events as "all kinds of phenomenon" and had been told by his physicians to "give it more time". Patient stated that he enjoyed excellent health for 91 years. He had never been sick, never been sick in his life and he had received the two doses of Pfizer BioNTech Vaccine and had all kind of health problems ever since, of which, have with most of the doctor that he consultant he was concerned of a long Covid type of reaction. About 3 weeks after the 2nd shot. Patient waken with (in 2021), it was very sudden weakness, cough, shortness of breath, brain fog but no fever and subsequently that, he had been examine by internist and cardiologist and they really don't know, what going on and the cough and shortness of breath had continue ever since more march of this year. Patient would tell the doctors that, he was short of breath and sneezing and coughing and they were just say, would not say anything. They didn't see very concern about that. Anyhow, finally his internist said, patient should say a pulmonologist and he did have a appointment with pulmonologist but she said, it was urgent but he could not receive the pulmonologist until the Feb of next year so, concern, he went to the urgent care, a place here and got a chest X-ray which showed that, he had nasal infect rate and bilateral pulmonary infusion (basilar fluid at the base of his lungs). You know something is going on ever since Feb and he was, you known in frustration. Patient knew following this Covid long, covid symptoms with and side effects and you know recently discovered pericarditis and myocarditis and things, like that, it's on going learning process for doctors you know the vaccine. All the effect also from the virus but effect of vaccine, it's on to on learning process, been a retired physician himself. He just start doing to find out what going on. Patient acknowledged the reports of myocarditis and pericarditis on rare occasions came out after his vaccine doses were administered. Patient stated that he had not basically received any treatment. Lab data included SARS-CoV-2 test (nasal test for the virus): negative in 2021; Blood tidal test: unknown results in 2021. Outcome of events was unknown.; Sender's Comments: As there is limited information in the case provided, the causal association between the given events and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: chest X-ray; Result Unstructured Data: Test Result:nasal infect rate and bilateral pulmonary infusion; Comments: basilar fluid at the base of my lungs; Test Date: 2021; Test Name: SARS-CoV-2 test; Test Result: Negative ; Comments: nasal test for the virus; Test Date: 2021; Test Name: Blood tidal test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pacemaker insertion (cardiac)
Andere Medikamente: ELIQUIS
Allergien: -
Vorherige Impfungen: -

VAERS 1897552

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MT
Alter: 35,0
Geschlecht: M
Eingang: 24.11.2021
Impfdatum: 08.03.2021
Beginn: 01.11.2021
Tage bis Beginn: 238,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Coronavirus test positive General physical health deterioration Intensive care Respiratory failure

Symptomtext

Case was hospitalized for Covid 7 months after completing the Covid vaccine series. In summary, he is an immunocompromise patient on Rituxan, who was recently discharged from the hospital after being admitted for COVID-19 infection, patient was taking dexamethasone and requiring 2 or 3 L of oxygen at home, nonetheless respiratory failure got much worse and despite the fact that he received a couple of vaccines in the previous months he has no antibodies against COVID-19 for which he received monoclonal antibodies on this admission. He was a started on Remdesivir and dexamethasone but quickly deteriorated for which after discussing pros and cons he received one-time dose of Tocilizumab with excellent response to the treatment. Patient was at some point requiring 40 L of oxygen by high flow nasal cannula in the intensive care unit and now is currently on room air saturating between 89 and 92% feeling comfortable. He is going to go home with 5 more days of dexamethasone to complete a bit more of 10 days. He has 1 refill at hand and has been instructed to take it back immediately if he feels that the symptoms get much worse after he runs out of the medication. In addition, respiratory therapist provided him with an oxygen tank in case that he needs it while walking. He should follow-up with PCP and we will try to see him back telemedicine in the infectious disease clinic over the next week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 2,0
Labordaten: Ordered Test: Coronavirus (CoVID-19), NAA Ordered Test Codes: (LN LOINC)/ Status: Corrected Accession Number: Specimen Source: Tissue Specimen Site: Specimen Collection Date/Time: 2021-10-22 07:34:00.0 Results: * Resulted Test: SARS CORONAVIRUS 2 RNA:PRTHR:PT:RESPIRATORY:ORD:PROBE.AMP.TAR Coded Result: Detected (LOCAL) Numeric Result: Units: Text Result: Reference Range From: Not Detected Reference Range To: Performing Facility Details: Date/Time: 2021-10-23 02:58:23.0 Performing Facility: Medical Center Facility ID: (FI) Interpretation: Very abnormal Result Method: Status: Final Test Code: (LN LOINC)/ Result Code: (SCT/Detected (L LOCAL)
Aktuelle Erkrankungen: ? Anxiety ? Follicular lymphoma grade II 10/2/2018 ? Seizures (HCC)
Vorgeschichte: ? Anxiety ? Follicular lymphoma grade II 10/2/2018 ? Seizures (HCC)
Andere Medikamente: benzonatate (TESSALON) 100 mg capsule Take 1 capsule by mouth 3 times daily as needed for Cough. 10/22/21 dexamethasone (DECADRON) 6 MG tablet Take 1 tablet by mouth every 24 hours for 7 doses. 10/30/21 11/6/21 escitalopram (LEXAPRO)
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1872216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IL
Alter: -
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 10.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Chronic obstructive pulmonary disease Disease recurrence Myocarditis

Symptomtext

symptoms of myocarditis; COPD flare ups after each dose; COPD flare ups after each dose; The initial safety information received on 28Sep2021 and 20Oct2021 was reporting only non-serious adverse drug reactions. Upon receipt of follow-up information on 01Nov2021, this case now contains serious adverse reaction. Information processed together. This is a spontaneous report from a contactable consumer (the patient). This consumer provided information for two reports. This is the first of two reports. This currently 65-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) via an intramuscular route of administration on 17Feb2021 (Lot Number: EL9269; Expiration Date: 31May2021) as Dose 1, single for COVID-19 immunisation, and via an intramuscular route of administration on 10Mar2021 (Lot Number: EN6203; Expiration Date: 30Jun2021) as Dose 2, single for COVID-19 immunisation. Medical history included chronic obstructive pulmonary disease (COPD) and ongoing COPD emphysema since 2007, ongoing coronary artery disease since 2014 with open heart surgery cardiac tamponade stent (1st), coronary artery disease from 2018 with Stent in RCA (2nd), weakened immune system, and ongoing hypertension since 2021. Family Medical History Relevant included: heart disease, diabetes, hypertension, and coronary artery disease. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient's concomitant medications were not reported. On an unspecified date in 2021, the patient experienced COPD flare ups after each dose. The flare up lasted 6 months and was treated with oral prednisone for COPD flare ups from an unspecified date in 2021. It took 6 months to get control of COPD after the 1st and 2nd doses. On an unspecified date in 2021, the patient experienced symptoms of myocarditis. As of 01Nov2021, the patient stated, "I believe I have symptoms of myocarditis. I am currently seeking a doctor to give me tests to confirm myocarditis. This is very serious." The clinical outcome of the events "COPD flare up after each dose" was resolved in 2021 while the outcome of the "symptoms of myocarditis" was unknown.; Sender's Comments: Linked Report(s) : PFIZER INC-202101284220 same patient/reporter, different AE/vaccine dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Coronary artery disease (open heart surgery cardiac tamponade stent (1st)); Emphysema; Hypertension
Vorgeschichte: Medical History/Concurrent Conditions: COPD; Coronary artery disease (Stent in RCA (2nd)); Diabetes; Heart disease, unspecified; Immune system disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1868323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 55,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 25.02.2021
Beginn: 14.03.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: UN / LA

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

Aphasia Blepharospasm Blood test normal Computerised tomogram head Computerised tomogram normal Diplegia Disturbance in attention Electronystagmogram Eye disorder Eye pain Facial paralysis Impaired driving ability Impaired work ability Imperception Laboratory test normal Magnetic resonance imaging head Magnetic resonance imaging neck Peroneal nerve palsy

Symptomtext

March 14, 2021, 17 days after my 2nd Covid vaccine, I experienced a very sudden attack of "vertigo". I experienced 3 severe attack during a 8 hour period which my legs felt paralyzed, I had a very sharp pain in my left eye and the sensation of falling as well as room spinning. I went to my GP who thought it was vertigo and I was sent to an ENT. During that visit 2 days later I was advised to go to the ER during the exam to rule out a TIA. I had a drooping left eye, dropped left foot and trouble forming words and concentrating. After a CT scan, brain MRI and carotid US they could not explain what what wrong. I was sent to several different doctors (opthomologist -who thought I had MG) and Neurologist who could not figure out what was wrong with me. I was sent to see an Eye Specialist who said I had Blephospasm (which now moved to my left eye), but could not say why I was having these issues. I spent 8 weeks,twice a week, in Vestibular therapy just so I could walk and move my my head at the same time. I spent thousands of dollars out of pocket and countless doctors all the tell me "they could find nothing to cause these issues". I was out of work for 4 months and finally went back as I did not want to lose a year towards my pension. I used a cane till July and finally was able to start to drive in August. I continued to have vertigo and eye issues. Fast forward 8 months later, I still have Vertigo and perception issues. After months of 24/7 eyelid spasms and trouble focusing my eyes, it has finally seemed to resolve itself. I am now regaining my balance and not having constant tintinus. Again, this started 17 days after my 2nd covid shot. I was a healthy, active woman who worked out almost everyday and did not have any real health issues that could not be helped by medication. No one can tell me why any of this happened since after all the tests, blood work, CT, MRI's..nothing showed up.

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Praegender Schweregrund: Facial paralysis
Hospital-Tage: 1,0
Labordaten: MRI brain 3/19, MRI brain 6/2/21, MRI cervical 6/2. CT brain 3/18. VNG 5/26/21.
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroid, inappropriate tachychardia
Andere Medikamente: Levothyroxine 75 mg, metoprolol 25 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1856788

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 27.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Chills Immunisation Loss of consciousness Nausea

Symptomtext

DOSE 3 (BOOSTER), SINGLE/10Oct2021; Chills and passing out; Very nauseous; Chills and passing out; This is a spontaneous report from a contactable consumer. A 73-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Left on 27Feb2021 13:00 (Batch/Lot Number: EN6203) as DOSE 2, SINGLE, dose 3 via an unspecified route of administration, administered in Arm Left on 10Oct2021 14:00 (Batch/Lot Number: Ff2590) as DOSE 3 (BOOSTER), SINGLE at the age of 73-years-old for covid-19 immunisation. Medical history included none. Concomitant medication(s) included influenza vaccine (FLU) taken for immunisation from 05Sep2021 to 05Sep2021; hydrochlorothiazide taken for an unspecified indication, start and stop date were not reported; olmesartan taken for an unspecified indication, start and stop date were not reported; atorvastatin taken for an unspecified indication, start and stop date were not reported. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 06Feb2021 (lot number: Zn5318, Left arm) for covid-19 immunisation, erythromycin and experienced drug allergies. Approximately 13 hours after 2nd and 3rd vaccine, patient experienced chills and passing out Very nauseous. Also dose 3 (booster), single/10oct2021 was reported. Prior to vaccination, the patient was not diagnosed with COVID-19.Since the vaccination, the patient has not been tested for COVID-19.Outcome of chills and passing out, chills and passing out, very nauseous was recovered in Oct2021, of DOSE 3 (BOOSTER), SINGLE/10Oct2021 was unknown. Therapeutic measures were taken as a result of very nauseous. No follow-up attempts are possible. No further information is expected

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, Comment: Other medical history: No
Andere Medikamente: HYDROCHLOROTHIAZIDE; OLMESARTAN; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1855774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 01.02.2021
Beginn: 07.08.2021
Tage bis Beginn: 187,0
Dosis: 2
Route/Site: SYR / LA

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

Ageusia Areflexia Bell's palsy Blood test normal Borrelia test negative Computerised tomogram normal Corneal reflex decreased Eyelid disorder Facial paresis Hypoaesthesia Hypoaesthesia oral Magnetic resonance imaging normal SARS-CoV-2 test negative

Symptomtext

Bell's palsy on right side of the face. Started with the tongue feeling numb, no sense of taste to part of the tongue, and 2 days later it lead to the right side of face not being able to close eye at same rate as my other eye. During the morning is when it started to feel like I was losing control of my blinking and being able to gargle when brushing teeth. That Monday I went to the ER to get checked, it was 6 months after vaccinated. So then, tests were provided, COVID, MRI, cat scan, blood tests for Lyme, and observation for 9+ hours. I was released after 9 hours in ER. I had a neurologist follow up and over 2.5 weeks, I started to feel my face muscles coming back slowly. Felt 97% after that. There's still some muscle weakness that I only notice 3 months later and some muscle soreness around mid cheek, chin, and when jawning my eye closes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI clear Cat scan clear COVID negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimotos thyroiditis
Andere Medikamente: Levothyroxine Metformin Vit D3
Allergien: Penicillin family Gluten
Vorherige Impfungen: -

VAERS 1837878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 38,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 31.01.2021
Beginn: 21.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: IM / LA

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

Anti factor Xa assay normal Antiphospholipid antibodies Antithrombin III Blood test Cardiolipin antibody Cerebral venous sinus thrombosis Computerised tomogram Gene mutation identification test Headache Heparin-induced thrombocytopenia test Magnetic resonance imaging Protein C Protein S SARS-CoV-2 test negative Venogram

Symptomtext

Diagnosed on March 31, 2021 with (left side) Cerebral Venous Sinus Thrombosis following approximately 1 week of extremely bad headaches on the left side of head, unlike my normal migraines. I have no history of a clot disorder.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebral venous sinus thrombosis
Hospital-Tage: 15,0
Labordaten: MRI, CT, MRV, CTV: March 31, 2021 Acute to Early Subacute dural sinus thrombosis along left transverse sinus, left sigmoid sinus, and left internal jugular vein. No acute infarct. No intracranial bleed. Full blood workup: March 31, 2021 Negative for Anti XA, Protein S, Protein C, Anti Cardiolipin Panel, Factor V, Antithrombin-III, Lupus Anticoagulant, Anti XA Heparin COVID 19 surveillance: negative
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Arthritis (traumatic) Chronic Infection in lower left leg, followed by lower left leg amputation High Blood Pressure
Andere Medikamente: Labetalol 100 mg 2x/day Gabapentin 600 mg 1x/day ibuprofen 200 mg 6xday Nuvaring 4 weeks in, replace Nurtec ODT As Needed
Allergien: None
Vorherige Impfungen: -

VAERS 1833348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 54,0
Geschlecht: F
Eingang: 01.11.2021
Impfdatum: 27.02.2021
Beginn: 19.03.2021
Tage bis Beginn: 20,0
Dosis: 2
Route/Site: SYR / LA

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

Computerised tomogram Lumbar puncture Magnetic resonance imaging Spinal stroke

Symptomtext

Spinal stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Spinal stroke
Hospital-Tage: 7,0
Labordaten: Multi: MRI's , CT's and one spinal tap. March 19 - Hospital
Aktuelle Erkrankungen: No
Vorgeschichte: I have several autoimmune diseases
Andere Medikamente: Hydroxychloroquine 400 mg a day Multivitamin Vitamin D3 Vitamin B12 Pepcid 20 mg
Allergien: Codeine, gabapentin, Benadryl, pumpkin, ginger and pine
Vorherige Impfungen: -

VAERS 1829288

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 70,0
Geschlecht: F
Eingang: 29.10.2021
Impfdatum: 29.01.2021
Beginn: 30.01.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Drooling Facial paralysis Paraesthesia

Symptomtext

Paresthesias in sides of arms , thighs, finger tips and toes. Partial Right Facial droop with drooling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, type 2 diabetes, tracheobronchial malacia, Essential tremors, Restless Leg Syndrome
Andere Medikamente: Ramipril 10mg Vitamins D
Allergien: Levaquin, Avalox
Vorherige Impfungen: -

VAERS 1825267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: UT
Alter: 84,0
Geschlecht: M
Eingang: 28.10.2021
Impfdatum: 03.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Carotid artery stent insertion Carotid artery thrombosis Fatigue Laboratory test

Symptomtext

Patient suffered blood clots in carotid artery, weariness in the head. Surgery was performed to put stint in. Weariness went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Carotid artery thrombosis
Hospital-Tage: 1,0
Labordaten: extracranial study on 7/21/2021
Aktuelle Erkrankungen: NONE
Vorgeschichte: DIFFICULTING READING AND WRITING DUE TO STROKE IN JULY OF 2020
Andere Medikamente: ELIQUIS
Allergien: NONE
Vorherige Impfungen: -

VAERS 1795549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 74,0
Geschlecht: F
Eingang: 18.10.2021
Impfdatum: 22.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / UN

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

Asthenia Chills Confusional state Dizziness Fatigue Loss of consciousness

Symptomtext

3 days after taking the vaccine she had fatigue and chills. She felt out of body. She had confusion, weakness, lightheaded and loss of consciousness.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: depression, bipolar
Andere Medikamente: atorvastatin 20mg, bupropion 200mg, lorazepam .5mg, acuvite , multi vit, one a day for 50+, calcium 1000mcg
Allergien: no
Vorherige Impfungen: -

VAERS 1777304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 73,0
Geschlecht: F
Eingang: 11.10.2021
Impfdatum: 05.02.2021
Beginn: 30.05.2021
Tage bis Beginn: 114,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Deep vein thrombosis Dehydration Renal failure Thrombectomy

Symptomtext

Many, many DVT blood clots in my left leg and groin area. In hospital 3 days. Upon arrival at hospital via ambulance I was in Kidney failure and was dehydrated. Had a procedure to remove all the DVT's they could get to, and am now on Eliquis for the rest of my life at $40 a month. I still have chronic DVT's.

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Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 3,0
Labordaten: Please contact Dr. for detailed information
Aktuelle Erkrankungen: None
Vorgeschichte: Acidic stomach, Stage 3 CKD
Andere Medikamente: Omeprazole 20mg capsule once a day, famotidine 20mg once a day, alprazolam .25mg once at bedtime, Vitamin D, Vitamin B12
Allergien: None known
Vorherige Impfungen: -

VAERS 1777085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 67,0
Geschlecht: M
Eingang: 11.10.2021
Impfdatum: 18.02.2021
Beginn: 29.09.2021
Tage bis Beginn: 223,0
Dosis: 2
Route/Site: IM / LA

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

Acute kidney injury COVID-19 COVID-19 pneumonia Chest X-ray abnormal Hypophagia Lung opacity Oxygen saturation decreased SARS-CoV-2 test positive Syncope

Symptomtext

68 Y male with a h/o COVID+ on 9/23 (vaccinated in February), history of tobacco use (stopped smoking 1 m/ago), and HTN who presents with syncopal episode at home. The patient experienced a syncopal episode on 9/29 overnight after going to the bathroom. No neurologic symptoms or seizing to suggest a neurologic etiology, and patient has no history of cardiac disease with no events noted on tele for 24 hours to suggest a cardiogenic etiology. Most likely orthostatic and vasovagal in etiology in the setting of poor PO intake for the past week. Patient was noted with improved appetite over the course of his admission eventually eating 100% of his meals with no destaurations or dizziness noted on road test. His initial pre-renal AKI improved to baseline with fluids. Patient notably tested positive for COVID on 9/23 now s/p 5 day course of prednisone 40 mg daily starting 9/22 with symptom onset on 9/22. On arrival to the ED, patient was afebrile, hemodynamically stable, and non-hypoxic satting well on room air. On 9/30, patient's O2 desaturated to 92 and 90-92 on road test requiring 2L NC; he was then started on decadron/remdesivir. He was quickly weaned back to room air on 10/1 and discharged on 10/2 with 2 more days of decadron for a 5 day decadron regimen total. Primary Procedures: None Secondary Procedures: None Reason for Hospital Admission (Admitting Diagnosis): COVID pneumonia

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Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: XRAY CHEST ** HISTORY **: 68 years old, known COVID-19 ** TECHNIQUE **: 1 view of the chest acquired. COMPARISON: Radiograph 9/11/2021 ** FINDINGS **: Osseous structures and cardiomediastinal silhouette are unchanged in their appearance. Interval development of right perihilar opacities. Mildly vascular congestion has also developed. No effusion or pneumothorax.
Aktuelle Erkrankungen: Upper respiratory infection
Vorgeschichte: history of tobacco use (stopped smoking 1 m/ago), and HTN
Andere Medikamente: Lisinopril-hydroCHLOROthiazide (PRINZIDE/ZESTORETIC) 20-25 mg Oral Tab Sig: Take 1 tablet by mouth daily
Allergien: nka
Vorherige Impfungen: -

VAERS 1759271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 72,0
Geschlecht: F
Eingang: 04.10.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Anaphylactic reaction Dyspnoea Full blood count

Symptomtext

Anaphylaxis with EpiPen administered at 60 min. after injection to treat sever breathing difficulty.

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Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 3,0
Labordaten: CBC on 02/27/2021
Aktuelle Erkrankungen: None other than chronic listed below
Vorgeschichte: Chronic low thyroid - Hashimotos , arthritis, rapid heart beat
Andere Medikamente: atenlol, leflunomide, fenofibebrate, guafenesin, niacin, levoxyl
Allergien: sulfadrug - with anafelaxix result, statins result in severe muscle pain, gastric sensitivity to onions, peppers
Vorherige Impfungen: -

VAERS 1732073

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 72,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 26.02.2021
Beginn: 08.08.2021
Tage bis Beginn: 163,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia COVID-19 Chills Malaise Nasal congestion SARS-CoV-2 test positive Syncope

Symptomtext

Patient presented with an syncopal episode. During admission, patient stated that he was feeling sick for the past few days with chills, nasal congestion, and generalized weakness. The patient was discharged in good health.

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Praegender Schweregrund: Syncope
Hospital-Tage: 1,0
Labordaten: SARS-CoV-2 PCR test detected 8/8/2021
Aktuelle Erkrankungen: None
Vorgeschichte: CKD stage 3 and Diabetes Mellitus
Andere Medikamente: Acetaminophen, escitalopram, guaifenesin, insulin glargine, metformin, methylprednisolone, and Trulicity
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1731964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 84,0
Geschlecht: M
Eingang: 24.09.2021
Impfdatum: 23.03.2021
Beginn: 19.07.2021
Tage bis Beginn: 118,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Chest X-ray abnormal Pneumonia SARS-CoV-2 test positive Syncope Vomiting

Symptomtext

Presented to emergency department 7/19 w/ syncope, vomiting. Had abnormal chest X-ray and started on antibiotics for pneumonia. Hospitalized for 3 days and discharged in usual state of health on 7/22/2021.

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Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: SARS-CoV-2 PCR positive 7/19/2021
Aktuelle Erkrankungen: none
Vorgeschichte: CKD 3, anxiety, memory loss, pulmonary fibrosis, pulmonary hypertension, impaired glucose tolerance, depression, hypertension, hyperlipidemia
Andere Medikamente: albuterol, aspirin, buproprion, buspirone, fluticasone, guafenesin, Norco, memantine, fish oil, pantoprazole, simvastatin, tolterodine, vitamin D
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1730414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 24.09.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Anaphylactic reaction Dyspnoea Feeling abnormal Feeling hot Pharyngeal swelling Rash macular Swelling face Throat irritation

Symptomtext

Anaphylactic reaction; she felt weird like her throat was itchy; She got blotches above her bra line up to her neck and face; scalp was hot; felt wonky/ felt weird; swelling of the face and throat; swelling of the face and throat; difficulty of breathing; This is a spontaneous report from a contactable consumer. A 52-years-old female patient received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in arm left at the age of 52 years old on 01Mar2021 (Batch/Lot Number: EN6203) as dose 1, single for covid-19 immunisation. Medical history included type 2 diabetes mellitus (diagnosed in early 20's and reports that diabetes is under control), hypertension (reports that hypertension is under control), early ventricular heart beat (considered benign), menopause, had gall bladder out a few years ago, and hysterectomy last summer. Concomitant medications included metformin (METFORMIN) taken for diabetes mellitus from an unspecified start date and ongoing; diltiazem hydrochloride (DILTIAZEM XR) taken for hypertension from an unspecified start date and ongoing; estradiol (ESTRA [ESTRADIOL]) taken for menopause from Aug2020 and ongoing; calcium (CALCIUM) taken for an unspecified indication, start and stop date were not reported; vitamin d [vitamin d nos] (VIT D [VITAMIN D NOS]) taken for an unspecified indication, start and stop date were not reported; methylcellulose (CITRUCEL) taken for supplementation therapy from an unspecified start date and ongoing. The patient previously took flu shot. On 01Mar2021, the patient had an anaphylactic reaction including difficulty breathing and swelling of the face and throat. Within 4 to 5 minutes after she received the shot, she felt weird like her throat was itchy. She got blotches above her bra line up to her neck and face. Her scalp was hot. She did not have any trouble breathing. She felt wonky. She beeped the horn. The person who came over to her car, told her that it was just a like a little reaction and to sit there until she felt better. The patient stated that she sat there for close to an hour. The blotches went away but she still felt strange and her throat was still itchy. She went home and called her sister who told her that it sounded like she had had an anaphylactic reaction. The patient stated that she is not allergic to anything. She took a couple of Benadryl and went to sleep. When she woke up late that night, she felt fine clarified as she has completely recovered from all of her symptoms. The outcome of the events was recovered on 2021.

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Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gallbladder removal; Hypertension (Additional Information for Other Conditions: Reports that hypertension is under control); Hysterectomy (Had hysterectomy last summer); Menopause; Premature ventricular contractions (Additional Information for Other Conditions: This is considered benign though per caller.); Type 2 diabetes mellitus (Additional Information for Other Conditions: Diagnosed in early 20's. Reports that diabetes is under control).
Andere Medikamente: Metformin; Diltiazem XR; Estradiol [Estradiol]; Calcium; Vitamin D [Vitamin D Nos]; Citrucel
Allergien: -
Vorherige Impfungen: -

VAERS 1696162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 27,0
Geschlecht: M
Eingang: 14.09.2021
Impfdatum: 10.03.2021
Beginn: 17.05.2021
Tage bis Beginn: 68,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest X-ray Chest pain Dizziness Electrocardiogram abnormal Hypoaesthesia Magnetic resonance imaging heart Palpitations Pericarditis Troponin T

Symptomtext

On 05/17/2021- my left side of my chest started to hurt near my shoulder at that point I thought I over did it, or a muscle strain and it would go away on its own, but it did not. The pain continued and became worse toward the weekend. I started to feel dizzy, heart racing, my left arms started to feel numb, I thought I might be having a heart attack and I decided to go to the emergency room. On 05/22/2021, I went to the ER. At the hospital: blood work done, EKG- abnormal, chest x-ray, cardio CT scan of the heart-they came back normal. They administer Advil and ibuprofen. Diagnosis: Pericarditis, inflammation outside the heart muscle The EKG pinpointed the pericarditis. I went to the ER at 12:30 AM, 05/22/2021, I was kept for emergency observation till 9:00 PM 05/23/2021. I saw the cardiologist, they sent me to do a cardio function MRI, on 07/14/2021- identified I did not have pericarditis. It identified I had myocarditis. I cannot exercise. I am on restriction. The MRI showed whatever caused the inflammation was no longer there. I just need to wait for the inflammation to go down and let it heal.

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Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: blood work - troponin-t EKG- abnormal - pericarditis chest x-ray cardio CT scan of the heart- normal 07/14/2021- MRI- myocarditis
Aktuelle Erkrankungen: no
Vorgeschichte: asthma
Andere Medikamente: Flovent albuterol
Allergien: no
Vorherige Impfungen: -

VAERS 1673282

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: WA
Alter: 57,0
Geschlecht: F
Eingang: 04.09.2021
Impfdatum: 19.05.2021
Beginn: 20.05.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Ageusia Anosmia Blood test Computerised tomogram Dyspnoea Emotional disorder Headache Heart rate Heart rate decreased Hypersensitivity Hypoaesthesia Joint swelling Loss of consciousness Loss of personal independence in daily activities Lung disorder Nerve injury Nervous system disorder Pain

Symptomtext

Pulse was 58; Her caregiver had to carry her into the bathroom.; can't breathe, it affected her lungs; can't walk; can't breathe, it affected her lungs; the next day at 4:30AM, she had a severe allergic reactions; head was in a vise being squeezed really hard; loss her sense of smell and taste; loss her sense of smell and taste; nerves in her right knee is damaged; it attacked her entire nervous system; it would numb up one spot, and to her back; her feet swelled up that she couldn't walk/ hands swelled up huge; her sciatic nerve inside of both knees that swelled up really big; very emotional; pain; Kept passing out; This is a spontaneous report from a contactable consumer or other non hcp (the patient). A 57-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EN6203), dose 1 via an unspecified route of administration, administered in arm left on 19May2021 at 13:30 (age at vaccination: 57-years-old) as DOSE 1, SINGLE for covid-19 immunization. Medical history included migraines from an unknown date and unknown if ongoing. Concomitant medication were not reported. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available) was reported as N/A; this was the patient's first dose. Additional Vaccines Administered on Same Date of the Pfizer Suspect If applicable, list all vaccines administered on same date with the Pfizer vaccine: None. (She stated she did not usually get vaccines, but she did it because her landlord was 70 and for her parents). Patient had severe allergic reaction after she had Pfizer BioNTech Covid19 Vaccine. Per patient, she had her 1st dose last 19May2021, the next day at 4:30AM, she had a severe allergic reactions, she could not breathe, it affected her lungs and could even walk. According to the patient it attacked her entire nervous system that's why she would never get the 2nd dose. The severe allergic reactions had been going on since the first dose. She also added, the reaction moved to her body, it would numb up one spot, and to her back, and her feet swelled up that she couldn't walk, and went to her sciatic nerve inside of both knees that swelled up really big and could walk, she called the ambulance and went straight to the hospital but they don't know what to do with her either. She wrote down all her symptoms and took pictures and sent it to her doctor, but her doctor did not believe her. Patient was very emotional, she wanted to know why did this happen to her. She wanted to know what were the ingredients of the vaccine. The patient was calling in regards to the Pfizer vaccine for COVID. The patient stated she had a severe adverse reaction to the first vaccine. She got it at 1:30 in the afternoon and at 4:30 in the morning, it started. She stated it was in her lungs and it would not go away. She was healthy until she got this Pfizer vaccine. She had been to the hospital so many times. The doctors did not do anything about it and won't help. The patient stated her doctor of 5 years would not let her come back ever since she told him what she was experiencing with the Pfizer vaccine. The doctor would not talk about it. She had pictures and videos of it attacking her nerves. She stated she needed help. She had been to the hospital by ambulance so many times. No one seemed to know what was going on. She needed to know what was in the vaccine. She could not walk, she could not breathe. She just wanted to be healthy, she needed Pfizer to help her. The patient stated she could not really walk anymore or do anything. She was in really good shape before vaccine. She could not walk, she could not breathe. She clarified her lungs were the last thing to be attacked, she lost her sense of smell. She had not been able to get help for 3 months, Pfizer had to help her. She had so much damage. She clarified she took the vaccine at 1:30 PM and at 4:30 in the morning, it was like her head was in a vise being squeezed really hard, that was where it started. Then, the bottom of her feet swelled up really big and she couldn't walk. Her hands swelled up huge like baseball gloves. She stated she took pictures and videos. Then, it started attacking her nervous system, down her arms and down her legs from her low back sciatic nerve to the middle of her knee. She was in so much pain she was going to shoot herself in the head. It was too much after 3 weeks and she couldn't take it anymore. She was going to shoot herself and her doctor wouldn't help her. Her doctor wouldn't look at the videos and pictures. She got a caregiver for week who took videos and pictures of her nerves being attacked and the muscles were cramping. She stated one could see the nerves and muscles coming out of her skin. She saw and felt it climb through her lower back. It went into her lower back and it grinded and crunched. Her caregiver said it looked like something crawling through her skin. The caregiver stayed a week and took care of her. Her caregiver had to carry her into the bathroom. She couldn't walk, she couldn't keep food down. She kept passing out. The patient's knees swelled up really. really big from inside where they touched. She stated it was just the inside. She couldn't walk. Her nerves in her right knee is damaged and it's not going away. Right now, it was her lungs that's where it is. It's her low back, lungs, and right knee. The patient stated she had a patient portal where she wrote all of this in the portal to her doctor of 5 years. She wrote every symptom to him. She had not been able to breathe good for weeks. She stated they haven't had a falling out or anything, but her doctor won't help. The caller stated she will go in to the ER but they don't know how to help her. She was given stuff for migraines because she gets migraines. They gave her medicine and sent her home but she didn't fill it because she did not want to be medicated. She has two dates of when she went to the hospital via ambulance, the other dates she did not know. The first date, 26May2021, she was taken by ambulance to the Emergency Room. When she got to the hospital, the doctor wouldn't let her receive pain medications. She was told they had never seen symptoms like hers, but her doctor wouldn't allow her to have any pain medicine at all. The doctor told them not to give her anything. She mentions in 2001, she signed a pain contract saying can't have any pain medication but that was 20 years ago and it's no longer in effect. Her doctor wouldn't let the ER give her any pain medicine although her symptoms were very painful. She was having pain for 3 weeks and she was going to shoot herself in the head. She had a gun and would have done it, but she has 5 kids and 1 grandbaby. She wouldn't live. She stated she can't be in pain anymore, her right knee is so bad. The discharge papers from the hospital say it was body aches after the vaccine, nausea, and adverse reaction after the Pfizer COVID-19 vaccine. She confirms she was only seen in the ER when she went 26May2021, she was not admitted to the hospital, she wanted to go home. She stated she can't see. She loss her sense of smell and taste. She has had multiple Covid tests and blood tests, and never had COVID. She did not understand how the Pfizer vaccine gives her every symptom of COVID even though she has never had COVID. She stated it was spreading to her lungs, it had damaged her lungs. The caller stated she was currently not suicidal. She did not have any suicidal thoughts right now. She stated she did not want to die. She is sick. Her doctor said she was drama and couldn't handle it and she couldn't go back. She asked the doctor if shooting herself in the head was too much. She stated she still has a gun, but she was going to wait a little while longer. She did not want to live in this pain. She stated someone needs to call her and try and help. She can't live like this. Pfizer needs to help her. The caller also provides the date 12Aug2021. She had texted her sister to help her and she guesses her sister called an ambulance. The ambulance took her to the emergency room. Her pulse was 58 when they picked her up. When asked if she was admitted to the hospital from the ER , the caller stated they kept her for a long time. They didn't check her lungs though. A CT scan of her brain was done, but her lungs were not checked again. She told them she was going to shoot herself in the head, the ambulance couldn't help her. She was told she can't have that second vaccine because it would kill her. The caller stated no one was helping her. She was told since it was an emergency vaccine, no one knows anything about it, except Pfizer. The reporter seriousness for pulse was 58 was hospitalization on an unknown date in 2021. The patient underwent lab tests and procedures which included pulse: 58 on an unknown date in 2021, CT scan of brain: unknown results, Covid test (sars-cov-2 test): never had covid (negative) and never had COVID, blood test: unknown results on an unknown date. The events resulted in Emergency Room Visit. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: Blood tests; Result Unstructured Data: Test Result:Unknown results; Comments: She has had multiple Covid tests and blood tests; Test Name: CT scan of brain; Result Unstructured Data: Test Result:Unknown results; Test Date: 2021; Test Name: Pulse; Result Unstructured Data: Test Result:58; Test Name: Covid test; Result Unstructured Data: Test Result:Never had COVID; Comments: She has had multiple Covid tests and blood tests, and never had COVID
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Migraine (She was given stuff for migraines because she gets migraines)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1662186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 58,0
Geschlecht: F
Eingang: 01.09.2021
Impfdatum: 24.02.2021
Beginn: 03.08.2021
Tage bis Beginn: 160,0
Dosis: 2
Route/Site: SYR / RA

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

COVID-19 Cough Loss of consciousness Malaise Mobility decreased Oropharyngeal pain Pain in extremity SARS-CoV-2 test positive Sinus congestion

Symptomtext

I had a sore arm. In August I tested COVID. I had a lot of symptoms and got really sick. Fevers for 4 days, sore throat, lingering cough, lost sense of taste. In bed for entire week. I had head congestion in my head.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: COVID PCR test. And it was positive.
Aktuelle Erkrankungen: No
Vorgeschichte: I have high blood pressure; diabetes; migraines
Andere Medikamente: Lisinopril; Gabapentin; Verapamil; Metformin; Atorvastatin; Omeprazole; Amlodipine; Topiramate; Trazadone
Allergien: I have an allergy to cinnamon; corn silk; allergy to antihistamine
Vorherige Impfungen: -

VAERS 1659087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 01.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Burning sensation Electric shock sensation Paraesthesia Spinal X-ray abnormal Spondylitis

Symptomtext

5 days after the shot, the right side of my body felt like it was on fire; it felt like a jolt of electricity was shooting through it. Exactly 4 weeks after the shot, I was admitted to the hospital through the ER with Afib - this was new to me. 21 weeks after the shot, I started feeling 'pins and needles' on my left side (lower back, buttocks, leg and toes. I saw my PCP who ordered a back xray, and nerve test (scheduled for Sept. 16th)

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 2,0
Labordaten: X-ray shows arthritis in my back. The first available appointment for the nerve test was September 16th. It is scheduled with the doctor.
Aktuelle Erkrankungen: none
Vorgeschichte: Scoliosis, high cholesterol, retinal vein occlusion
Andere Medikamente: atorvastatin
Allergien: cefuroxime, codeine, iodine, nitrofurantoin, Elmiron, tetracycline, sulfa antibiotics, peanuts, shellfish, soy protein..
Vorherige Impfungen: -

VAERS 1657852

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 58,0
Geschlecht: F
Eingang: 31.08.2021
Impfdatum: 22.03.2021
Beginn: 03.04.2021
Tage bis Beginn: 12,0
Dosis: 1
Route/Site: - / LA

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

Bundle branch block left Dizziness Loss of consciousness Seizure

Symptomtext

Im now having dizzy spells and passing out and Seizures and I now have a left Bundle Branch Blockage that I know was not the December 31st when I had a hernia surgery. None of these symptoms showed up; Im now having dizzy spells and passing out and Seizures and I now have a left Bundle Branch Blockage that I know was not the December 31st when I had a hernia surgery. None of these symptoms showed up; Im now having dizzy spells and passing out and Seizures and I now have a left Bundle Branch Blockage that I know was not the December 31st when I had a hernia surgery. None of these symptoms showed up; Im now having dizzy spells and passing out and Seizures and I now have a left Bundle Branch Blockage that I know was not the December 31st when I had a hernia surgery. None of these symptoms showed up; This is a spontaneous report from a contactable consumer (patient). A 58-year-old female patient (not pregnant) received the first dose of BNT162B2 via an unspecified route of administration on the left arm on 22Mar2021 at 15:45 (Lot Number: EN6203) at the age of 58-year-old as single dose for COVID-19 immunization. Medical history included anxiety and depression. The patient didn't receive other vaccine in four weeks. The patient didn't COVID prior vaccination. The patient didn't perform COVID test post vaccination. The patient received medications in two weeks. Known allergies was none. Concomitant medication was not reported. On 03Apr2021 at 14:00, the patient had dizzy spells and passing out and Seizures and had a left bundle branch blockage that the patient was not the 31Dec2021 when he had a hernia surgery. None of these symptoms showed up till after the patient received the Pfizer shot. It was about two weeks after the first shot he started passing out. The events resulted in doctor or other healthcare professional office/clinic visit and hospitalization. Treatment included: Monitored heart and blood pressure took nitro. The outcome of events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1656303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 77,0
Geschlecht: F
Eingang: 30.08.2021
Impfdatum: 01.03.2021
Beginn: 29.03.2021
Tage bis Beginn: 28,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Thrombosis

Symptomtext

I developed blood clots 1 on each leg, don't know if the vaccine had anything to do with it. Dr prescribed Eliquis 2.5 MG. So far the one on the left leg is gone, I will be tested again in October.

Weitere VAERSDATA-Felder

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

VAERS 1651642

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 21,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 10.03.2021
Beginn: 09.04.2021
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

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

Anal incontinence Atrioventricular block second degree Blood test Cardiac stress test normal Chest pain Consciousness fluctuating Dizziness Dyspnoea Echocardiogram normal Electrocardiogram ambulatory abnormal Fall Feeling abnormal Hypotension Loss of consciousness Nausea Pain Pericarditis Syncope

Symptomtext

3 days after recieving my second dose I passed out. I became nauseous and tried to go to the bathroom to vomit but instead I fell and I was in and out of conciousness. During that time I defecated myself and began to vomit as well. I went to the ER in an ambulance they ran many test everything came out okay I was diagnosed with syncope,once I was stable they sent me home. I followed up with a doctor at my DR office (my doctor didn't have space to see me for a while) she refered me to a cardiologist because I was still feeling off, I was dizzy and my blood pressure was a little low. The cardiologist ran many test but everything was basically inconclusive. Fast foward to August I still have not felt like myself. On August 4th I was working a normal shift when I started to feel pain in my chest. I finished my shift and went right to the ER where they admitted me with Acute Pericaditis. To this day even with the madication I still have pain and trouble with my breathing.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 2,0
Labordaten: I've had a ton of blood work only one I had that was off was my Triponin and that was why I was admitted to the hospital. My stress test, Echo, 24 hr Holter monitor were all normal. 2 week holter did show one episode of tyle 1 wenckenbach.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, IBS, Major depressive disorder, ADHD
Andere Medikamente: Vyvanse,Zoloft,Estarylla, Wixela
Allergien: Sulfa drugs, Zithromax, Flagyl
Vorherige Impfungen: -

VAERS 1641083

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 44,0
Geschlecht: F
Eingang: 27.08.2021
Impfdatum: 19.02.2021
Beginn: 09.03.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / LA

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

Aphasia Auditory disorder Bladder dysfunction Chills Coccydynia Cognitive disorder Confusional state Electrocardiogram ambulatory Emotional distress Encephalitis Feeling abnormal Gait disturbance Headache Impaired gastric emptying Insomnia Laboratory test Magnetic resonance imaging head Memory impairment

Symptomtext

Cognitive Impairment (Confusion, Brain Fog, Aphasia, memory deficits, tripping and tipping sideways while walking) Severe Vertigo Occipital Headache Severe Insomnia Mental Health Distress bi-lateral jaw pain tailbone pain Full Body Tremors Chills and inability to regulate body temperature Endocrine (Thyroid Failure) Swelling on the Oronasal passages. Panic Attacks (Frequent and Severe) Photophobia (Severe) Altered Auditory/Sensory abilities Encephalitis Myocarditis/Tachycardia lasting approximately 7-8 weeks Gastroparesis (also included nausea, vomiting and frequent diarrhea) Irregular Menstrual Cycle Bladder Function Abnormalities Multiple Providers/Specialties are investigating and testing currently

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 20,0
Labordaten: Brain MRI with and without contrast multiple lab tests holter monitor test
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: levothyroxin, multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1578470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 63,0
Geschlecht: M
Eingang: 17.08.2021
Impfdatum: 25.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Computerised tomogram Diplopia Facial paralysis Magnetic resonance imaging Myasthenia gravis Scan brain

Symptomtext

Double vision and droopy eyelids

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: yes 4 brain scans ct-scan mri and blood test was dx with Myasthenia-Gravis which is a rare autoimmune disease neurologist.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: titus pectin, curcumin, vit d, resveratrol, low dose aspirin and melatonin
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1554120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IA
Alter: 67,0
Geschlecht: F
Eingang: 13.08.2021
Impfdatum: 26.03.2021
Beginn: 04.04.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: SYR / LA

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

Fatigue Feeling abnormal Ischaemic stroke Magnetic resonance imaging head abnormal Pyrexia

Symptomtext

Ischemic stroke 4/4/21 Continued fevers Brain fog Fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 2,0
Labordaten: Stroke MRI
Aktuelle Erkrankungen: Diabetes COPD HTN Microscopic inflammatory colitis
Vorgeschichte: -
Andere Medikamente: Metformun 1000 daily Glyperide ER 10mg BID amitrittyline 75 mg daily Imitrex 100 mg PRN Losartan/HCTZ 11/12.5 daily Cevemeline 30mg TID esccitalopram 10mg daily Esomeprazole magnesium 40mg daily Nifedipine all 30 mg daily Prednisone 5 mg
Allergien: kna
Vorherige Impfungen: -

VAERS 1499506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: AZ
Alter: 32,0
Geschlecht: M
Eingang: 23.07.2021
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Electrocardiogram abnormal Nausea Palpitations Presyncope Sinus bradycardia

Symptomtext

"Patient received his first dose of the Pfizer COVID-19 vaccine. He received this at approximately 2 PM. Approximately 5 minutes after getting the first dose he felt lightheaded and had a racing heart rate and also felt nauseous. This lasted for approximately 30 minutes. All of his symptoms then resolved. He came to the emergency department today for a further work-up and evaluation."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Emergency Department Course and Clinical Decision Making 32-year-old male who denies any chronic medical history presenting to the emergency department today from the COVID vaccine clinic. He is afebrile nontoxic and non-ill-appearing stable vitals. He is mildly bradycardic with a heart rate around 57 however this is likely asymptomatic bradycardia, he has no complaints currently. I did obtain an EKG due to the episode of lightheadedness, this revealed sinus bradycardia with a heart rate of 57. No abnormal ST or T wave changes, no arrhythmias. No STEMI. Patient has been symptom-free, no further work-up indicated. No complaints, normal physical exam. This is likely a vasovagal response. Patient should not get his second vaccine.
Aktuelle Erkrankungen: unknown
Vorgeschichte: none listed in medical record
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 1470283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: ME
Alter: 75,0
Geschlecht: M
Eingang: 14.07.2021
Impfdatum: 25.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Coagulopathy Thrombosis

Symptomtext

Blood clotting. Blood clot try to pass through dialysis machine. Interfere with dialysis. Clotting issues have happen almost every time at Dialysis since since getting first vaccine. Problem is ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: On Dialysis, Heart problems, diabetic
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1466150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 13.07.2021
Impfdatum: 11.05.2021
Beginn: 11.05.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood cholesterol normal Blood triglycerides normal C-reactive protein decreased Cardiac stress test Chest pain Echocardiogram abnormal Electrocardiogram High density lipoprotein normal Low density lipoprotein Pericarditis

Symptomtext

Patient states that didn't feel normal after her second Pfizer vaccine. She was tired in the afternoons and felt like she doesn't breathe properly. In mid June she started to feel occasional chest pain. Around June 30th she had chest pain that she thought she is having a heart attack. She was seen by a cardiologist on July 1st who diagnosed her with Pericarditis acuta and prescribed Azithromycin, Dexamethasone, Omeprazole, Xarelto and Bisocor (BP medicine).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: Consultation with cardiologist on July 1st ECG on July 1st (microvoltage, normogram, sinus rhythm fr. 129/min, PQ 112 ms, otherwise normal Cardiac echo on July 1st showed pericardial effusion Stress test on July 1st, stopped after 5 min due to chest pain, hypotension and tachycardia response Labs: Cholesterol 3.91 mmol/l; HDL: 1.57 mmol/l, LDL 2.17 mmol/l, tryglicerides 0.88 mmol/l, CRP 0.76 mg/l
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1465585

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 44,0
Geschlecht: F
Eingang: 12.07.2021
Impfdatum: 02.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Anxiety Arthralgia Axillary pain Blood test normal Breast pain Burning sensation Echocardiogram Electric shock sensation Electrocardiogram Fatigue Heart rate increased Herpes zoster Insomnia Joint noise Lymphadenopathy Muscle twitching Musculoskeletal chest pain Neck pain

Symptomtext

Had very bad lymph swelling after the initial dose on day 10. Breast pain and lumps under left arm, vaccine side, running down into my ribs and up into my neck. Random migratory pain in joints along with Muscle twitching, headache over right eye, almost felt like a shingles attack. Increased heart rate, fatigue, anxiety, insomnia. Did not seek medical care as was told that those were normal reactions. Symptoms settled day before second shot on March 23. Felt okay for a week then they started back up again but even more pronounced. Have had armpit, breast, back, rib pain that feel like burning and electrical currents, heart palpitations. Random muscle twitching. Joints have been aching and cracking. Had blood work done for lymes disease in April. Negative. In May saw an obgyn who deemed it vaccine related but could offer no treatment after testing negative to RA, Lupus, Lymes. June 14th presented to urgent care as rib and back pain had intensified. They ran an ecg. Ecg was abnormal and was transferred to ER. June 15 Went to hospital where ekg was again abnormal, lengthened qt and st segments which indicate STEMI but clinically I didn?t present any symptoms. Was referred to cardiologist for heart issues. Still suffering back, rib, underarm pain and breast swelling with sensitivity along with random muscle twitching in various areas multiple times a day. Doctors cannot figure out what is cause and say vaccine related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Lymes blood panel 03/23/21 Complete blood panel 04/29/22 RA, lupus, Lymes panel 05/20/21 EKG 06/14/21 EKG 06/15/21 Blood panel for Heart attack 06/15/21 Stress echo & echocardiogram 07/09/20
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec, Flonase, magnesium, quercetin, curcurmin.
Allergien: Crustaceans.
Vorherige Impfungen: -

VAERS 1456710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: -
Geschlecht: F
Eingang: 08.07.2021
Impfdatum: 01.03.2021
Beginn: 01.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / LA

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

Arthralgia Condition aggravated Contusion Dysphagia Facial paralysis Fatigue Glossodynia Headache Malaise Muscle swelling Oropharyngeal pain Swollen tongue Thyroid function test

Symptomtext

I had paralysis in my face; Swelling of muscles; swelling of tongue; Headache; Pain in joints; Tiredness; I have (bruises) of the face; I had soring of the tongue and the throat; I had soring of the tongue and the throat; I just don't feel well, I haven't been the same since I have taken the shot/The energy I use to have I don't have that anymore; My throat is like when I drink something it comes right out because of swelling; I had joint pain and it is getting worse; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection Batch/Lot number: EN6203, Expiration Date was not reported), via intramuscular, administered in left arm on unspecified date in Mar2021 09:00 as dose 2, single for covid-19 immunisation. Patient stated, she thinks it was 03Mar2021 as date of 2nd vaccine (Consumer not sure hence not captured in tab). The patient medical history included hypothyroidism. Concomitant medication included levothyroxine (0.75mcg, once a day) taken for hypothyroidism. The patient historical vaccine included first dose of BNT162B2(Batch/Lot: EM9810) via muscular administered in right arm on 21Feb2021 (at the age of 71-years-old) for COVID-19 immunization. No prior vaccinations received within 4 weeks. It was reported that, the patient concern is she has side effects. On unspecified date in Mar2021 the patient experienced swelling of her tongue, (bruises) of the face, swelling of her muscle and headache pain the joint pain and the tiredness. She can hardly talk; her tongue is swollen her throat is like when she drinks something it comes right out because of swelling. She just doesn't feel well, she hasn't been the same since she has taken the shot, she just gone down feeling like the energy she use to have she don't have that anymore. She can hardly talk because of her tongue. Patient stated she started feeling it almost in a week she was trying to just be waiting to this to go away, but it started intensifying. Patient stated she had 2nd, she had both, think this is 2nd. She doesn't know this is 1st or 2nd. she just has, they only have one date here. When probed for starting date of adverse event, patient stated, this is same week, but I didn't know what was going on, I was trying to look the way out, it happens in the same week, and again it is getting worse, she can hardly talk. The patient states, she tells you the problem then she can get the information. she had side effects and she tried to wait until it goes away and it has not. she had soring of the tongue and the throat. she had paralysis in my face. Dude then she had multi crannies, she had joint pain and it is getting worse and she is very concerned about her health as a result after taking it. She was told it goes away, but it has not. It has gotten worse, so she is asking what she should do. She has not taken treatment because she wanted to contact you first if what Pfizer will do if it was causing the medical cause or going to cause. The patient underwent lab tests and procedures which included thyroid function test: unknown on unspecified date of Apr2021. The outcome of the events was not resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Test Date: 202104; Test Name: Thyroid test; Result Unstructured Data: Test Result:unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 1423090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: WA
Alter: 27,0
Geschlecht: M
Eingang: 24.06.2021
Impfdatum: 07.06.2021
Beginn: 08.06.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / RA

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

Abdominal discomfort Dizziness Syncope

Symptomtext

tummy was weird; fainted; lightheaded; This is a spontaneous report from a contactable consumer (patient). A 27-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: En6203), dose 2 via an unspecified route of administration, administered in arm right on 07Jun2021 15:30 (at the age of 27-year-old) as single dose for COVID-19 immunization. Medical history and concomitant medications were reported as none. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received 1st single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in left arm, on 17May2021 15:45 (lot number: En203) for COVID-19 immunization. On 08Jun2021 05:15, patent experienced fainted morning after vaccine, and was lightheaded, tummy was weird too. Prior to vaccination, the patient did not diagnose with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
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 1422332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 39,0
Geschlecht: M
Eingang: 23.06.2021
Impfdatum: 03.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 21,0
Dosis: 2
Route/Site: SYR / AR

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

Angiogram cerebral Blood test Computerised tomogram head abnormal Gait inability Headache Intensive care Magnetic resonance imaging head Subarachnoid haemorrhage

Symptomtext

Subarachnoid hemorrhage - bleed day 5/24 - rushed to ER and was seen immediately on first CAT scan. Admitted to Neuro ICU for 14 days. Then transferred to rehabilitation hospital and is now going to outpatient PT. Symptoms were extreme headache and then inability to walk. Rushed to ER via ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 24,0
Labordaten: CAT scans, MRIs, angiograms (2 of 3 completed so far), daily bloodwork in ICU.
Aktuelle Erkrankungen: None
Vorgeschichte: Suffered spinal cord injury in 2000 - no health issues resulted
Andere Medikamente: Baclofen
Allergien: None
Vorherige Impfungen: -

VAERS 1422086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 23.06.2021
Impfdatum: 20.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Dizziness Electrocardiogram Electrocardiogram ambulatory normal Myocarditis Palpitations Tachycardia Vertigo

Symptomtext

Dizziness, vertigo, palpitations, tachycardia, weakness. These started after about 10 days after vaccination and lasted for at least a month. Took physical therapy as well. Took physical therapy for vertigo, took rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: -
Labordaten: EKG did not show significant abnormality, but did not get an echo or cardiology check. QT 406ms, HR 56/mimn at the time of EKG. Holter unremarkable. Symptoms consistent with myocarditis with heart rate ~102. Usual for her is around 70.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, hyperlipidemia
Andere Medikamente: Amlodipine 5 mg daily, HCTZ, 12.5mg daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1413374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 41,0
Geschlecht: M
Eingang: 20.06.2021
Impfdatum: 22.03.2021
Beginn: 18.06.2021
Tage bis Beginn: 88,0
Dosis: 1
Route/Site: IM / LA

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

Blood creatine Blood test Chest X-ray Chest discomfort Computerised tomogram thorax Echocardiogram Electrocardiogram Malaise Pericarditis SARS-CoV-2 test negative Troponin

Symptomtext

I don?t know if it?s caused by the vaccine or not as the timing is so apart, but it is crazy to have something rare like pericarditis all of a sudden so I thought it best to submit to VAERS to let you review in case it was related or coincidental. I?ve had multiple covid tests that are negative but the current theory is this was from a virus I caught while traveling 6/14-6/16. Staring feeling ill 6/17, went to hospital with chest discomfort 6/19, admitted and run through a battery of tests to make sure I wasn?t having a heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: From 6/19-6/20, multiple ekgs, Cardiogram, X-rays, ct scan, bloodwork including Triponin and creatine etc.
Aktuelle Erkrankungen: No
Vorgeschichte: Nothing chronic. Sporadic gout (1-2 times per year), low testosterone.
Andere Medikamente: Testosterone cypionate (only prescription drug) Zinc Vitamin d NAC Glutathione Multivitamin Magnesium glycinate Fish oil Vitamin c
Allergien: Hydroxychlroroquine
Vorherige Impfungen: -

VAERS 1392978

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 43,0
Geschlecht: F
Eingang: 11.06.2021
Impfdatum: 19.03.2021
Beginn: 12.04.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: SYR / LA

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

Cardiac stress test abnormal Catheterisation cardiac normal Chest pain Dizziness Electrocardiogram abnormal Myocardial necrosis marker increased Presyncope Visual impairment

Symptomtext

Started with intermittent Chest pain which I didn?t do anything about and ignored at first and then it progressed to more constant chest pain on Or around April 25th which I went to the ER twice and urgent care once in 2 days time between April 29 an April 30

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: 3,0
Labordaten: Three abnormal ECG tests on April 29 and April 30, followed up by an an abnormal stress test on Friday May 14. I made a cardiology appointment to take place on June 22 by then on May 23 my symptoms escalated to a scary level and dizziness occurred along with chest pain and I saw stars and almost passed out around 4:30pm on May 23 after being out in the heat for my sons flag football game. I wad having a great time and had no anxiety so I started to worry that I should not wait until June 22 to see a cardiologist so I called my doctor the next day and the cardiologist arranged an appointment for May 25 at 4 pm but after reviewing my tests they called me back and sent me straight to ER. I was admitted into the hospital from there after another (4th) ECG came back abnormal. My cardiac enzymes were 7 then 11 then 10. So just slightly abnormal in second draw then back down on third draw. They did a cardiac cath and found no blockages in artieries. They did not take a heart biopsy that I?m aware of. They said it is either anxiety or maybe chest wall inflammation or it?s possible myocarditis one doctor said they have seen that after the Pfizer vaccine.
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure MTHFR Homogeneous double copy genetic testing confirmed
Andere Medikamente: Metoprolol XR Levothyroxine Amlodopine Irbestartan/hctz Duloxutine Oxycodone ER 12 hour Gabapentin as needed
Allergien: No
Vorherige Impfungen: -

VAERS 1381110

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 08.06.2021
Impfdatum: 05.03.2021
Beginn: 16.05.2021
Tage bis Beginn: 72,0
Dosis: 2
Route/Site: - / LA

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

Balance disorder Diarrhoea Disorientation Guillain-Barre syndrome Headache Hypoaesthesia Muscle spasms Paraesthesia

Symptomtext

This is a spontaneous report from a contactable consumer (patient). A 55-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6203, expiration date not provided), 2nd dose via an unspecified route of administration, administered in Arm Left on 05Mar2021 at age of 55 years old as a single dose for COVID-19 immunisation; mepivacaine hcl (manufacture unknown), via an unspecified route, date, dose for an unspecified indication. Medical history included Shingles. Concomitant medication included enalapril maleate (VASOTEC) taken for blood pressure. The patient previously took morphine and experienced allergies, BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL9265, expiration date not provided), 1st dose via an unspecified route of administration, administered in Arm Left on 11Feb2021 as a single dose for COVID-19 immunisation. The patient experienced guillane-barre syndrome, tingling and numbness in the legs, arms and lower face, severe headache, imbalance, disorientation, muscle spasms, diarrhea, all on 16May2021. The action taken in response to the events for mepivacaine hcl was unknown. The outcome of the events was not recovered. No treatment received for the events. The patient was not pregnancy at time of vaccination. The patient had not received 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 had not been tested for COVID-19. Pfizer is a marketing authorization holder of [mepivacaine hcl] in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of [mepivacaine hcl] has submitted the same report to the regulatory authorities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Shingles
Andere Medikamente: VASOTEC [ENALAPRIL MALEATE]; MEPIVACAINE HCL
Allergien: -
Vorherige Impfungen: -

VAERS 1378549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 84,0
Geschlecht: M
Eingang: 07.06.2021
Impfdatum: 15.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / UN

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

Dyspnoea Intensive care Palpitations Pneumonia Troponin increased

Symptomtext

Patient presented to the ED with shortness of breath and was subsequently hospitalized for elevated troponin, pneumonia and palpitations. She was in the ICU for 9 hours before being transferred to the cardiology floor.

Weitere VAERSDATA-Felder

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

VAERS 1377466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 29.05.2021
Impfdatum: 05.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: SYR / LA

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

Blood pressure increased Echocardiogram abnormal Electrocardiogram ambulatory Full blood count Palpitations Pericarditis

Symptomtext

HEART PALPITATIONS & increase in blood pressure some time after #1 dose, wore a holter monitor for 2 weeks and had an echo cardigram which showed Pericardites. has put on Plaquinil & metatoprolol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: CBC, holter monitor, echo 3/18/21, 04/03/2021, 04/23/2021
Aktuelle Erkrankungen: none
Vorgeschichte: SPINAL FUSION, CHRONIC PAIN HYPOTHYROID, NEUOPATHY
Andere Medikamente: -
Allergien: PENICILLIN
Vorherige Impfungen: -

VAERS 1347084

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 32,0
Geschlecht: F
Eingang: 25.05.2021
Impfdatum: 26.02.2021
Beginn: 19.05.2021
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: SYR / AR

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

Deep vein thrombosis Pain in extremity Ultrasound Doppler abnormal

Symptomtext

DVT in Peroneal vein in left leg. diagnosed 05/24/2021. Went to ER with pain in left Calf. Pain onset was 5 days prior to ER visit (05/19/2021).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Ext Lower Venous Doppler Unilat US
Aktuelle Erkrankungen: none
Vorgeschichte: Psoriatic Arthritis, Fibromyalgia
Andere Medikamente: Junel Fe 1.5/30, Celecoxib 200mg, Spironolactone 50mg, Cimzia, Otezla,
Allergien: Mild Latex
Vorherige Impfungen: -

VAERS 1276838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 27.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Gastrooesophageal reflux disease Pain in extremity Chest discomfort Chest pain Dizziness Electrocardiogram normal Loss of consciousness

Symptomtext

Since receiving the vaccine I have extreme lightheadedness requiring me to grab things to avoid falling over until it passes. I passed out once. I have chest pain and fullness as well. My doctor told me to drink juice, wear compression socks, eat salty foods and drink more water. I began tracking my BP and my diastolic is in the 40s and 50s when these incidents occur which is often. The chest pain is consistent. I saw a cardiologist who told me to drum more water and eat more salt. EKGs are fine. I?m going to the Clinic on June 2nd since we all know women?s heart issues are dismissed. The pain and fullness in my chest are becoming annoying and distressing. Since taking the vaccine my exercise fell off almost completely except for pickel ball and when I did play I couldn?t play as I had before at all. I?ve now stopped playing and I?m walking as I used to so that I keep moving. I can?t run. :(

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG was fine. No blood work was done.
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis, fibromyalgia, degenerative disc disease
Andere Medikamente: Belsomra, trazadone, topomax, flexaril, wellbutrin
Allergien: Lobster, octopus, contrast dye, bactrim, z-pack
Vorherige Impfungen: -

VAERS 1276838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 24.05.2021
Impfdatum: 27.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Gastrooesophageal reflux disease Pain in extremity Chest discomfort Chest pain Dizziness Electrocardiogram normal Loss of consciousness

Symptomtext

Since receiving the vaccine I have extreme lightheadedness requiring me to grab things to avoid falling over until it passes. I passed out once. I have chest pain and fullness as well. My doctor told me to drink juice, wear compression socks, eat salty foods and drink more water. I began tracking my BP and my diastolic is in the 40s and 50s when these incidents occur which is often. The chest pain is consistent. I saw a cardiologist who told me to drum more water and eat more salt. EKGs are fine. I?m going to the Clinic on June 2nd since we all know women?s heart issues are dismissed. The pain and fullness in my chest are becoming annoying and distressing. Since taking the vaccine my exercise fell off almost completely except for pickel ball and when I did play I couldn?t play as I had before at all. I?ve now stopped playing and I?m walking as I used to so that I keep moving. I can?t run. :(

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: EKG was fine. No blood work was done.
Aktuelle Erkrankungen: None
Vorgeschichte: Ulcerative colitis, fibromyalgia, degenerative disc disease
Andere Medikamente: Belsomra, trazadone, topomax, flexaril, wellbutrin
Allergien: Lobster, octopus, contrast dye, bactrim, z-pack
Vorherige Impfungen: -

VAERS 1340892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 22.05.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Electric shock sensation Lip swelling Muscle tightness Paraesthesia oral Pyrexia

Symptomtext

In an hour time I feelt an electric shock ( Like a live wire) travel up my back into the top roof of my mouth, My mouth muscles tighten down, my lips started to tingle and swell. The fever hit me 20 minutes later. I took allergy pills and ibuprofens for two days straight. I fell asleep right after I took the first set of allergy pills. I would wake off on on for the next three hours to chew on ice for my lips and mouth. These symptom last for two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 Diabetic
Andere Medikamente: Metformin, Atrovastatin, Humulin N Nph , Lisinopril, Humulin R, Latanoprost,
Allergien: Catrs, certain breed of dog, eggs
Vorherige Impfungen: Flu shot 10 years ago

VAERS 1337715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 21.05.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Flushing Hyperhidrosis Respiratory distress Skin warm

Symptomtext

The following is transcribed from a report submitted by Paramedic on a 72 yo female who received 2nd Pfizer COVID vaccine (Lot# EN 6203, exp 6/2021) in right arm at approx 10:45am: "At 10:45am, I observed an elderly female with increased respiratory effort, flushed skin, appearing to be in mild distress, sitting in the 15 min. observation area. I approached patient and asked if she was doing okay, and she stated "yes." Patient's skin was flushed, diaphoretic, and warm. Pupils equal and sluggish. Patient denied any other complaints but claims she felt lightheaded prior to vaccine. Patient was moved to 30 min. observation. Patient was able to stand up and ambulate without assistance. EMTs took vital signs as another patient arrived. 11:05am baseline vital signs obtained: blood pressure 124/80, respiratory rate 16, heart rate 100, alert and oriented to person, time, place, and situation. At 11:12am, patient's vital signs were re-assessed and radial pulse palpated which was strong, regular with occasional PVC's felt. Blood pressure 130/82, respiratory rate 16, heart rate 108, alert and oriented to person, time, place and situation. C/C reassessed and she reported no change. It was advised that due to her physical appearance not improving with skin flushed and diaphoretic, ALS would be contacted to further evaluate; patient obliged. At 11:27am 911 contact made with a 6 minute response time with fire department on scene. Patient turnover report given and care transferred. Patient AMA'd (left against medical advice) with fire department. Patient ambulated with steady gait and without assistance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: asthma, DM2, HTN, hyperlipidemia, depression
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 1314608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 32,0
Geschlecht: F
Eingang: 13.05.2021
Impfdatum: 07.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Allergy to chemicals Allergy to plants Anaphylactic reaction Crying Dyspnoea Food allergy Full blood count Hypoaesthesia Lymphadenopathy Malaise Mobility decreased Obstructive airways disorder Pruritus Urticaria

Symptomtext

5 minutes after vaccination, I felt unwell. I sat with EMS that was onsite. HR was 160's, BP 160's systolic. Right arm went numb in first 5 minutes and my face went numb after 15 minutes post injection. After sitting 45 minutes with EMS my vitals stabilized and no numbness present. I walked to the car, sat in the car for 10 minutes and then I went into anaphylaxis. My airways began to close. My husband got the EMS on site and I was taken by ambulance to the ER. I was given IM Benadryl in the ambulance. In the ER I was given IV Benadryl and IV steroids. After anaphylaxis event I had difficulty breathing for 3 weeks from enlarged lymph nodes. I had extreme shortness of breath for the 2 weeks following injection in that I had to crawl up the flight of stairs to the second level of our home. About the 3rd week after injection, I began having full body itching with no known stimuli. Only benadryl would treat it. I was on allegra or zyrtec daily. I would also develop 1 or 2 hives on my right arm. 4 weeks after injections I was reacting to food and drink. I could not drink alcohol- gin or vodka- it would result in full body itching and a few hives. I did a course of prednisone, and it decreased my allergic reactions and I felt almost normal for several months. On May 8th, 2021 I had be experiencing great stress since February from a family member's cancer diagnosis. I had a crying event and immediately after I had an allergic reaction to gin, which had not occurred since the course of steroids. Today is 5/13 and I have had 2 additional allergic reactions: one involving food and the other flowers. None of which I have ever been allergic to before. I have full body itching and I am now developing hives more often.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: CBC done on 3/8/2021 in ER visit
Aktuelle Erkrankungen: none. Pervious numbness in arms and face after initial vaccination. PCP suggested I still get the second vaccine and I reported it.
Vorgeschichte: -
Andere Medikamente: zyrtec
Allergien: sulfa drugs
Vorherige Impfungen: First dose of Pfizer vaccine

VAERS 1307790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OK
Alter: 68,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 24.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / RA

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

Blood prolactin increased Electroencephalogram normal Magnetic resonance imaging head normal Pain in extremity Seizure like phenomena

Symptomtext

He got first Pfizer COVID shot March 3 with no problem. He got second COVID shot March 24, sore arm at the time, but then early AM March 25 and also early AM March 26 he had what was suspected to be seizure (both times). EEG, MRI are negative, but prolactin level is up, and the episodes were consistent with seizure. He is now on Keppra, not having any more episodes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: Prolactin level 25.48 on March 26. EEG negative April 26. MRI brain negative May 6.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, HTN, GERD, osteoarthritis
Andere Medikamente: aspirin, glipizide, Xalatan, lisinopril, HCTZ, metformin, Aleve, Prilosec, sildenafil, simvastastin, cannabis
Allergien: none
Vorherige Impfungen: -

VAERS 1306677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 72,0
Geschlecht: M
Eingang: 11.05.2021
Impfdatum: 08.03.2021
Beginn: 22.04.2021
Tage bis Beginn: 45,0
Dosis: 1
Route/Site: IM / LA

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

Deep vein thrombosis Ultrasound Doppler normal

Symptomtext

Acute occlusive deep vein thrombosis of the right femoral and popliteal veins.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: doppler ultrasound
Aktuelle Erkrankungen: none
Vorgeschichte: bladder cancer impaired fasting glucose
Andere Medikamente: dutasteride tamsulosin
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1288377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 05.05.2021
Impfdatum: 26.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: - / LA

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

Computerised tomogram Electroencephalogram Investigation Magnetic resonance imaging Seizure

Symptomtext

seizures; This is a spontaneous report from a contactable consumer (Patient's husband). A 70-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at the age of 70-year-old via an unspecified route of administration, administered in Arm Left on 26Feb2021 (Lot Number: EN6203) as single dose, second dose of BNT162B2 via an unspecified route of administration, administered in Arm Left on 19Mar2021 (Lot Number: EN8727) as single dose both for covid-19 immunisation. Medical history included High blood pressure, atrial fibrillation. No family medical history. No prior vaccination within 4 weeks. Ongoing Concomitant medications included rivaroxaban (XARELTO); losartan taken for hypertension; hydrochlorothiazide taken for blood pressure abnormal, fluid imbalance; diltiazem hydrochloride (CARTIA XT) taken for atrial fibrillation; loratadine. After the first shot, about a week and a half later, she started having seizures in Mar2021. Since the second shot, it had gotten worse. The event resulted in Emergency Room visit. She was taken in twice. The first time, she was in the hospital for 4 days. This occurred last month, in Mar2021. After the second dose, she had been hospitalized, the end of March, almost April. They took her twice. The first time, they did a bunch of tests and were questioning seizure or a stroke. At the end, they thought it was a seizure. She then came home and had it worse. They put her on medication. The patient underwent lab tests and procedures which included tests: all were negative, computerised tomogram: unknown results, electroencephalogram: unknown results, magnetic resonance imaging: unknown results all in Mar2021. The events outcome was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 4,0
Labordaten: Test Date: 202103; Test Name: Tests; Result Unstructured Data: Test Result:All were negative; Test Date: 202103; Test Name: CT scans; Result Unstructured Data: Test Result:unknown results; Test Date: 202103; Test Name: EGG scan; Result Unstructured Data: Test Result:unknown results; Test Date: 202103; Test Name: MRI's; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Atrial fibrillation (Verbatim: A-Fib); Blood pressure high (Verbatim: High blood pressure)
Andere Medikamente: XARELTO; LOSARTAN; HYDROCHLOROTHIAZIDE; CARTIA XT; LORATADINE
Allergien: -
Vorherige Impfungen: -

VAERS 1285661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CT
Alter: 64,0
Geschlecht: M
Eingang: 04.05.2021
Impfdatum: 01.03.2021
Beginn: 06.04.2021
Tage bis Beginn: 36,0
Dosis: UNK
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram Laboratory test Magnetic resonance imaging Muscular weakness

Symptomtext

Bell's Palsy Left side of face, no muscle control

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CAT, MRI, Various Blood tests
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes, Hypertension, BPH, Sleep Apnea, Gout, Kidney Stones, Tinnitus
Andere Medikamente: ALLOPURINOL ZYLOPRIM 300mg AM ASPIRIN EC 81mg AM ATORVASTATIN LIPITOR EQ 40mg PM CHOLECALCIF VITAMIN D3 2,000 IU AM / 2,000 IU PM DOCUSATE SODIUM 100mg Oral Cao AM / 100 mg PM EMPAGLIFLOZIN JARDIANCE EQ 25mg AM FELODIPINE PLENDIL EQ 10mg
Allergien: None
Vorherige Impfungen: -

VAERS 1284861

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: NC
Alter: 25,0
Geschlecht: F
Eingang: 04.05.2021
Impfdatum: -
Beginn: 21.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / RA

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

Anaphylactic reaction

Symptomtext

anaphylactic reaction; This is a spontaneous report from a contactable nurse (patient). A 25-year-old female patient received the second dose of bnt162b2 (Lot Number: En6203), via an unspecified route of administration, administered in right arm on an unspecified date (at the age of 25-year-old) as single dose for COVID-19 immunization. The patient is not pregnant. Medical history included COVID prior vaccination on unspecified date. The patient had no known allergies. Concomitant medication included unspecified birth control pills. The patient previously received the first dose of bnt162b2 (Lot Number: En9581) in the right arm on 09Feb2021 at 02:00 PM (at the age of 25-year-old) as single dose for COVID-19 immunization. No other vaccine in four weeks. On 21Mar2021 at 14:00 after her second vaccine the patient had an anaphylactic reaction. It was something she had eaten before so not new to her body. It happened again on 27Apr2021. Still from things she eats normally. Both occurrences happened 30 minutes after eating and came on quickly. The event resulted in Emergency room/department or urgent care, Life threatening illness (immediate risk of death from the event). Therapeutic measures were taken as a result of the event which included Benedryl, steroids, and given an epipen. The patient recovered from the event on unspecified date.; Sender's Comments: Based on the information provided, known drug safety profile and plausible temporal association, the causality between the suspect drug and the event cannot be excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (If covid prior vaccination: Yes)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1278579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 01.05.2021
Impfdatum: 05.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: - / LA

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

Loss of consciousness Nausea SARS-CoV-2 test Presyncope

Symptomtext

like I was going to pass out.; felt nauseous; This is a spontaneous report from a contactable consumer (patient). A 72-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in left arm on 05Mar2021 at 15:30 (Batch/Lot Number: EN6203), at the age of 72 years old, as single dose for Covid-19 immunisation. Medical history included suspected covid-19 from Mar2020 to an unknown date (I believe I had Covid. Had all kinds of symptoms for many months after). The patient has no allergies to medications, food, or other products. The patient is not pregnant. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and no other medications received within 2 weeks of vaccination. The patient's concomitant medications were not reported. On 24Mar2021, 19 days after, the patient felt nauseous and like she was going to pass out. The patient underwent lab test which included Covid-19 test: unknown, in 2021. The patient did not receive any treatment for the events. Outcome of the events was recovering. No follow-up attempts are needed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: Covid 19 test; Result Unstructured Data: Test Result:Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Suspected COVID-19 (I believe I had Covid. Had all kinds of symptoms for many months after.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1266354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IA
Alter: 31,0
Geschlecht: M
Eingang: 28.04.2021
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: ja Erholt: nein

Altered state of consciousness Seizure Vomiting

Symptomtext

Patient received vaccine in clinic around 10:20am. Patient waited around the pharmacy for around 20 min and then left. Patient returned around 11-11:10 am with his mother in which we were notified that he was having a reaction. We brought the patient into the patient care room in which he was vomiting and patient's mother stated that he had a seizure. Patient was conscious but had some altered mental status. Patient denied any falls. 911 was called and EMS took patient to the hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic seizure disorder
Vorgeschichte: chronic seizure disorder
Andere Medikamente: Oxcarbazepine
Allergien: N/A
Vorherige Impfungen: -

VAERS 1180188

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 66,0
Geschlecht: M
Eingang: 25.04.2021
Impfdatum: 09.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 17,0
Dosis: 2
Route/Site: IM / RA

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

Back pain Bell's palsy Blood test normal Chills Computerised tomogram normal Facial paralysis Fatigue Headache Immunoglobulin therapy Magnetic resonance imaging head normal Neck pain Night sweats Red blood cell sedimentation rate increased

Symptomtext

partial facial paralysis (eyes, nose, lips); moving to head pain (30 days, back of neck everywhere, but right side worse, could take pulse from throbbing); Progression of symptoms: back pain; chills; fatigue; night sweats without fever; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 66-year-old, via an unspecified route of administration, administered in left arm on 09Feb2021 12:00 (Lot Number: EM9809) as single dose for COVID-19 immunisation. Medical history included hepatitis C (HCV) - Cured (5-years ago), hypertension, mild cholesterol, benign prostatic hyperplasia (BPH), gastrooesophageal reflux disease (GERD), and occasional fever blister on lips. The patient has no known allergies. The patient has no COVID prior vaccination and not tested for COVID post vaccination. Concomitant medications included alfuzosin, atorvastatin, losartan, and pantoprazole. Progression of symptoms: back pain (5 days then resolved), moving to head pain (30 days, back of neck everywhere, but right side worse, could take pulse from throbbing) controlled with Gabapentin 1x daily and frequent Advil, symptoms included chills, fatigue and night sweats without fever, as these resolved, it moved to partial facial paralysis (eyes, nose, lips), 6 days so far. The patient was given IV Immune Globulin and IV Solumedrol in hospital and then Prednizone 40 mg tabs for 7 days (4 days left) as treatment for the events. All events occurred on 26Feb2021 at 20:00 and resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care, and hospitalization for 1 day. The outcome of the event back pain was recovered on 03Mar2021 20:00, facial paralysis was not recovered, and for the rest of the events was recovered. The patient received the second dose of BNT162B2 (lot number: EN6203) on 02Mar2021, 12:00 PM, administered at the right arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Cholesterol; Fever blister; GERD; Hepatitis C; Hypertension
Andere Medikamente: ALFUZOSIN; ATORVASTATIN; LOSARTAN; PANTOPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 1248715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 60,0
Geschlecht: F
Eingang: 23.04.2021
Impfdatum: 02.04.2021
Beginn: 04.04.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Computerised tomogram normal Diplopia Laboratory test Magnetic resonance imaging Magnetic resonance imaging normal VIth nerve paralysis Visual impairment

Symptomtext

After receiving the 2nd dosage of vaccine, 2 days later I began having problems with my vision, which was on Sunday 4/4/21, I went to bed thinking it would correct itself. I woke up on Monday 4/5/21 and had double vision so I immediately went to the ER at hospital where my BP was 190/95. At the hospital they did a CT Scan and an MRI which both came back normal, I was eventually diagnosed with 6th Nerve Palsy and referred to see a neurologist, I am currently under Dr's care at facility who is a neurologist in the specialty eye clinic. I am currently wearing a patch over my right eye to prevent the double vision which is still present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: VIth nerve paralysis
Hospital-Tage: -
Labordaten: CT Scan, MRI both on 4/4/21 at Medical Center . I'm not certain of all the lab tests which were performed. Doctors also ran numerous tests to see what's going on with my eye and have confirmed the 6th Nerve Palsy is present.
Aktuelle Erkrankungen: RA, Fibromyalgia. PTSD, Depression
Vorgeschichte: RA, Fibromyalgia, PTSD, Depression
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1237965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CT
Alter: 61,0
Geschlecht: F
Eingang: 21.04.2021
Impfdatum: 26.03.2021
Beginn: 26.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Blood sodium decreased Hyperhidrosis Laboratory test Nasopharyngitis Pyrexia Seizure Speech disorder Visual impairment X-ray

Symptomtext

fever of 101.7, cold, then sweat, resulting in a seizure affecting speech and vision all gray. Ambulance to Hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: bloodwork, xrays, provided sodium (sodium was 128)
Aktuelle Erkrankungen: -
Vorgeschichte: epilepsy, chronic bronchiectasis, meningioma tumor remains in frontal lobe of brain
Andere Medikamente: Aptiom, Sodium Chloride, Keppra, Alendronate sodium, sodium chloride inhalation solution, albuterol sulfate inhalation solution, atorvastatin calcium, digestive probiotic, st joseph aspirin, one a day over 50 vitamin, osteo bi-flex triple s
Allergien: none
Vorherige Impfungen: -

VAERS 1235554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 26.03.2021
Beginn: 17.04.2021
Tage bis Beginn: 22,0
Dosis: 1
Route/Site: SYR / RA

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

Facial paralysis Herpes zoster Rash

Symptomtext

Rash on side of head occular droop shingles - herpes zoster shingles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Doctor Visit 4/20/21
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Synthroid, Lexapro, Valsartan
Allergien: none
Vorherige Impfungen: -

VAERS 1235554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 20.04.2021
Impfdatum: 26.03.2021
Beginn: 17.04.2021
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: SYR / RA

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

Facial paralysis Herpes zoster Rash

Symptomtext

Rash on side of head occular droop shingles - herpes zoster shingles

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Doctor Visit 4/20/21
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Synthroid, Lexapro, Valsartan
Allergien: none
Vorherige Impfungen: -

VAERS 1231212

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MN
Alter: 64,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 20.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / RA

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

Balance disorder Blood test Chest X-ray Computerised tomogram Concussion Electrocardiogram Electroencephalogram Head injury Headache Loss of consciousness Memory impairment Swelling Vestibular disorder

Symptomtext

Passed out on Monday hit head and got a concussion.Went to ER had . Headaches caused by optical and vestibular systems does to hitting head. Bump on right side of head that continues to hurt.Balance is off due to vestibular. Some short term memory issues.OT and PT.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: ER - chest xray, EKG, blood test, CAT Scan,all to rule out heart issues and brain bleed.2/22/2021 EEG 3/31/2021 Rule out seizures
Aktuelle Erkrankungen: None
Vorgeschichte: Osteopenia, dry eye, Rosacea
Andere Medikamente: Restastis eye drops, vitamin D,C,Flax seed, calcium,garlic,multi vitamin for women.
Allergien: Tramadol
Vorherige Impfungen: -

VAERS 1230277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 72,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 20.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / -

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

Angiogram cerebral normal Arteriogram carotid normal Condition aggravated Hemiparesis Mental status changes Seizure

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: patient with cerebral amyloid angiopathy, parenchymal microhemorrhages, and seizure disorder with recurrent seizures presents to emergency department with alertered mental status and left-sided weakness immediately following a seizure and two days after vaccination. Admitted to hospital, anti-epileptic medications adjusted, and patient discharged home in good condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: CTA head and neck: no evidence of large territory infarct or hemorrhage; no evidence of large vessel occlusion
Aktuelle Erkrankungen: recurrent seizures, cerebral amyloid angiopathy, parenchymal microhemorrhages
Vorgeschichte: hypertension, seizures
Andere Medikamente: amlodipine, vitamin B12, dorzolamine, timolol, gatifloxacin, Ilevro, irbesartan, levetiracetam, multivitamin, omeprazole, potassium chloride, prednisolone ophthalmic, thiamine, travoprost
Allergien: dexmedetomidine, penicillins
Vorherige Impfungen: -

VAERS 1229505

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 16,0
Geschlecht: F
Eingang: 19.04.2021
Impfdatum: 17.04.2021
Beginn: 17.04.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Electrocardiogram Full blood count Human chorionic gonadotropin Metabolic function test Syncope

Symptomtext

Syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: CBC, BMP, Beta HCG, EKG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Pollen
Vorherige Impfungen: -

VAERS 1224325

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 73,0
Geschlecht: M
Eingang: 18.04.2021
Impfdatum: 26.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: OT / RA

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

Computerised tomogram Foreign body sensation in eyes Headache IIIrd nerve paralysis

Symptomtext

Drooping and closed left eyelid/third nerve ocular palsy paralysis; Headache; Sandy eyes; This is a spontaneous report received from a contactable consumer (Patient) reporting for himself. A 73-year-old patient received second dose of BNT162B2 0.3ml on 26Feb2021 at 12:00 pm (Lot no: EN6203, Expiration date: unknown) via intramuscularly route of administration in right arm as SINGLE DOSE for covid-19 immunization. The patient does not have cardiovascular disease, he just had a blockage at one time. The patient had one stent put in and low dose to preventative for plaque buildup in veins. The patient's concomitant medications included Simvastatin for mild heart attack in 2013. The patient previously vaccinated with first dose of BNT162B2 on 05Feb2021 at 13:00 pm and 5 days later got sandy eye. It was reported that, on 04Mar2021 (3 weeks later of second dose) the patient experienced blurred vision and drooping, closed left eyelid which were diagnosed as third nerve ocular palsy paralysis on 08Mar2021. It was reported that the patient still gets Headaches periodically. The outcome of the events was not recovered. Follow attempts are requested. Further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: IIIrd nerve paralysis
Hospital-Tage: -
Labordaten: Test Date: 20210308; Test Name: emergency CAT scan; Result Unstructured Data: Test Result:It said there was no aneurysm.; Comments: It said there was no aneurysm.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart attack (He had a mild heart attack in 2013 and had a stent placed. He does not have cardiovascular disease, he just had a blockage at one time. Back in 2013); Stent placement
Andere Medikamente: SIMVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 1219007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 43,0
Geschlecht: M
Eingang: 16.04.2021
Impfdatum: 14.04.2021
Beginn: 15.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Loss of consciousness Pyrexia Syncope

Symptomtext

Fainting. It was sudden onset, I felt fine for 24h after the injection (and had no side effects to the first dose), then felt very suddenly dizzy and lightheaded, then passed out for a few seconds. After I came to, I was able to quickly catch my breath and recover with no additional episodes. Beyond this, I had a mild fever but no other serious adverse effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: iodine
Vorherige Impfungen: -

VAERS 1214380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 51,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 26.03.2021
Beginn: 13.04.2021
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: SYR / RA

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

Bell's palsy Facial paralysis Nasopharyngitis

Symptomtext

DEVELOPED BELL?S PALSY - DIAGNOSED 4/14/2021 COLD SYMPTOMS DEVELOPED 8 DAYS AFTER SECOND SHOT (4/3//2021), AND THEN FACIAL PARALYSIS WITH BELL?S DIAGNOSED ON 4/14

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: JUST OBSERVATIONS BY 911 FOLKS AND AT URGENT CARE
Aktuelle Erkrankungen: NONE
Vorgeschichte: MILD HYPERTENSION
Andere Medikamente: LOSARTAN POTASSIUM D3 MAGNESIUM CITRATE COQ10 B12 VITAMIN C
Allergien: SHELL FISH
Vorherige Impfungen: -

VAERS 1213183

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 79,0
Geschlecht: M
Eingang: 15.04.2021
Impfdatum: 03.02.2021
Beginn: 04.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Echocardiogram Electrocardiogram Facial bones fracture Fall Hypertension Hypoaesthesia oral Laboratory test Lip injury Suture insertion Syncope

Symptomtext

Received the vaacine on 2/3/2021 I felt fine that whole day. The following day as I was showering I got lightheaded and fell in the bathroom . I went to the ER and the sent me home because I had no injuries. My blood pressure was high . For a few days I got lightheaded off and on. Then on 2/24/2021 I went for the second dose again i felt fine the whole day. On 2/25/2021 as I was showering I got lightheaded and fainted. My family called the ambulance and I was hospitalized from 2/25/2021 to 2/27/2021. I had facial fractures, fractured septum (nose) and cut upper lip received 10 stitches and teesth and gums were numb and still are a little numb.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: 3,0
Labordaten: Labs, ekg, echocardiogram and niot sure what other tests were done.
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes Type II and High Blood Pressure
Andere Medikamente: Pantoprazole ; Metformin HCL: Glipizide; Lovastatin; Valsartan: Amlodipine Besylate; Aspirin; Atenolol
Allergien: NKA
Vorherige Impfungen: -

VAERS 1209247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 24,0
Geschlecht: F
Eingang: 14.04.2021
Impfdatum: 03.03.2021
Beginn: 12.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

Antinuclear antibody Aphasia Balance disorder Beta-2 glycoprotein antibody Blindness Brain injury C-reactive protein Cardiolipin antibody Computerised tomogram head Double stranded DNA antibody Hypoaesthesia Magnetic resonance imaging head Protein S Red blood cell sedimentation rate Rheumatoid factor Thrombosis Vomiting

Symptomtext

Severe Vascular Thrombosis (vomit, loss of balance, numbness in arms and legs, lost of speech, impaired vision) had to be hospitalized for 4 days, and had some brain damage from the thrombosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: 4,0
Labordaten: Simple skull CT (03.12.2021) Skull MRI (03.12.2021) Anti-dsDNA (03.13.2021) Antinuclear antibody test (03.13.2021) Rheumatoid factor test (03.13.2021) Erythrocyte sedimentation rate (03.13.2021) C-reactive protein test (03.13.2021) S-reactive protein test (03.13.2021) Anticardiolipin test (03.13.2021) beta-2 glycoprotein I (?2GPI) (03.13.2021) MRI skull with and without contrast (04.03.2021)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1206312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 81,0
Geschlecht: M
Eingang: 14.04.2021
Impfdatum: 31.01.2021
Beginn: 04.03.2021
Tage bis Beginn: 32,0
Dosis: 2
Route/Site: SYR / RA

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

Arthralgia Blood test Chest X-ray Computerised tomogram Dyspnoea Lymphadenopathy Pulmonary thrombosis Swelling

Symptomtext

Lung blood clot found after emergency room visit experiencing shortness of breath 03/04. Tennis ball size neck lymph node swelling starting 02/25. Joint pain and swelling starting 2/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 1,0
Labordaten: 3/5 Chest X-ray, cat scan of head, bloodwork in ER. Primary care visit 2/26 for neck swelling.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Baby aspirin, prostate medication
Allergien: None
Vorherige Impfungen: -

VAERS 1200335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 41,0
Geschlecht: M
Eingang: 13.04.2021
Impfdatum: 23.02.2021
Beginn: 20.03.2021
Tage bis Beginn: 25,0
Dosis: UNK
Route/Site: SYR / LA

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

Angiogram Hypertension Thrombosis Ultrasound Doppler

Symptomtext

Blood clot in right hand. Could not feel right thumb pointer and middle fingers and they turned purple. Went to hospital and treated with Heprin. Outcome - still have the blood clot. Put on Eliquis. Also developed high blood pressure from event and put on valsartan

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: CT Angio , arterial studies on both arms, Doppler. Many tests at Valley hospital over 3 days.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Seroquel, tramadol, duloxetine, bupropion, gabapentin
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1199719

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VA
Alter: 45,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 09.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chest discomfort Chills Computerised tomogram thorax normal Deep vein thrombosis Diarrhoea Echocardiogram Electrocardiogram normal Full blood count normal Loss of consciousness Muscle tightness Pain Presyncope Pyrexia Troponin normal Ultrasound Doppler Ultrasound Doppler abnormal

Symptomtext

Patient received second Pfizer dose on 4/9 at 9:15 am. That evening she developed fever of 102.5 F with body aches and chills. On 4/10 at about noon, she developed squeezing chest tightness for about 20-30 minutes. 7/10 with back and neck tightness as well. she developed an urgent need to have diarrhea and had a momentarily loss of consciousness consistent with presyncope. Afterwards,the chest tightness went away and she felt better. All other symptoms resolved. The patient came to the clinic. Vitals: BP 97/63, P90, T36.6C, D-dimer 7140 ng/ml EKG- NSR, rate 83 bpm, no acute ST-T changes, Troponins negative, CBC - normal Chest CT with contrast negative for PE B/L LE Venous ultrasound- Right posterior tibial thrombus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: -
Labordaten: Bilateral Lower extremity Ultrasound- showed Posterior tibial Thrombus- 4/10/21 Chest CT with contrast- normal 4/10/21 Echocardiogram- pending 4/13/21 Carotid ultrasound pending 4/13
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac disease, Adenomyosis
Andere Medikamente: Aviane, Multivitamins
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1199631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 44,0
Geschlecht: F
Eingang: 13.04.2021
Impfdatum: 23.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Thrombosis Ultrasound scan

Symptomtext

Blood clot. Right leg. Treatment Lovenox injections and Pradaxa blood thinner medication. Time on Pradaxa to be determined on resolution of blood clot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Ultrasound to diagnose blood clot in right leg. (3/4/21)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1190586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 10.04.2021
Impfdatum: 08.04.2021
Beginn: 10.04.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: - / -

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

Activated partial thromboplastin time Alanine aminotransferase Anion gap Anion gap decreased Aspartate aminotransferase Base excess Basophil count Basophil percentage Blood albumin Blood alcohol Blood alkaline phosphatase Blood bicarbonate Blood bilirubin Blood calcium Blood calcium normal Blood chloride Blood chloride normal Blood creatinine

Symptomtext

syncope

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Contains abnormal data BLOOD GAS/ELEC/OXIMETRY PROF-VEN (Final result) Component (Lab Inquiry) Collection Time Result Time PH , VEN (POCT) PCO2 , VEN (POCT) PO2 , VEN (POCT) HCO3 , VEN (POCT) TOT CO2 , VEN(POCT) BASE EX , VEN(POCT) O2 SAT , VEN (POCT) HEMATOCRIT-VEN(POCT) Hemoglobin-Ven (Gem - poct) WB NA , VEN (POCT) 04/10/21 09:49:00 04/10/21 09:50:00 7.36 45 27 25 27 -0.4 52 35 11.8Low 136 Collection Time Result Time WB K , VEN (POCT) WB CA++ , VEN(POCT) WB GLUCOSE-VEN (POCT) Wb Chloride Ven (Poct) WB LACTATE-VEN (POCT) Anion Gap - Ven (Gem-poct) O2HB - Ven (Gem - Poct) COHB - Ven (Gem - Poct) Methemoglobin - Ven (Gem - Poct) Deoxyhemoglobin-Ven (Gem-poct) 04/10/21 09:49:00 04/10/21 09:50:00 3.6 1.15 134High 103 0.60 6Low 50.4 1.2 1.0 47.4High Final result ALCOHOL (QUANT) SERUM (Final result) Component (Lab Inquiry) Collection Time Result Time ALCOHOL (QUANT) 04/10/21 09:27:00 04/10/21 10:24:00 <10.0 Final result Contains abnormal data COMPREHENSIVE METABOLIC PANEL (Final result) Component (Lab Inquiry) Collection Time Result Time ALBUMIN, BLD BILIRUBIN TOTAL CALCIUM CHLORIDE-BLD CREATININE GLUCOSE ALK PHOSPHATASE, BLD POTASSIUM Protein Total, Serum SODIUM-BLD 04/10/21 09:27:00 04/10/21 10:25:00 4.0 1.1 8.9 106 0.7 148 Please note: As of 08/...High 72 4.4 6.8 138 Collection Time Result Time AST (SGOT) UREA NITROGEN CO2 TOTAL ALT(SGPT) ANION GAP EST GFR 04/10/21 09:27:00 04/10/21 10:25:00 13 8 24.9 11 7.10 >=60 Effective December 8, ... Final result Contains abnormal data CBC+PLT+DIFF (Final result) Component (Lab Inquiry) Collection Time Result Time WHITE BLOOD CELL RBC BLOOD CELL HEMOGLOBIN HEMATOCRIT MEAN CORP. VOLUME MEAN CORP. HGB MEAN CORP. HGB CONC. RED DISTRIB. WIDTH PLATELET MEAN PLT VOLUME 04/10/21 09:27:00 04/10/21 10:01:00 5.16 3.97Low 12.1 35.4 89.1 30.4 34.2 11.9 175 6.8Low Collection Time Result Time NEUTROPHIL % LYMPHOCYTE % MONOCYTE % EOSINOPHIL % BASOPHIL % NEUTROPHIL # LYMPHOCYTE # MONOCYTE # EOSINOPHIL # BASOPHIL # 04/10/21 09:27:00 04/10/21 10:01:00 75.1 9.8Low 14.2High 0.1 0.8 3.9 0.5Low 0.7 0.0 0.0 Final result LIPASE (Final result) Component (Lab Inquiry) Collection Time Result Time LIPASE 04/10/21 09:27:00 04/10/21 10:24:00 13 Final result PT/INR AND APTT (Final result) Component (Lab Inquiry) Collection Time Result Time PRO TIME INR APTT 04/10/21 09:27:00 04/10/21 10:02:00 14.5 As of July 6, 2016, pl... 1.2 General recommendation... 25.2 General Recommendation... Final result Contains abnormal data ACETAMINOPHEN (Final result) Component (Lab Inquiry) Collection Time Result Time ACETAMINOPHEN 04/10/21 09:27:00 04/10/21 10:49:00 <3Low Final result SALICYLATE-BLD (Final result) Component (Lab Inquiry) Collection Time Result Time SALICYLATE 04/10/21 09:27:00 04/10/21 10:37:00 <5 Final result PREGNANCY TEST-URINE (POCT) (Final result) Component (Lab Inquiry) Collection Time Result Time PREGNANCY TEST-URINE (POCT) 04/10/21 08:58:00 04/10/21 09:04:00 Negative If the specific gravit... Final result Imaging Results CT ANGIO CHEST W CONTRAST (Final result) Result time 04/10/21 13:19:00 Final result (04/10/21 13:19:00) Impression: IMPRESSION: No pulmonary embolism. Clear lungs without acute pulmonary disease. Narrative: QN CTA CHEST WITH CONTRAST CLINICAL HISTORY: EPIC: Reason for Exam?: ?PE (h/o iliac artery thrombosis, p/w syncope; eupoxic) ACRSelect Session ID: ACRSelect Score: 6 - Marginal Dyspnea on exertion : TECHNIQUE: CT angiogram of the chest was performed on a multirow-detector scanner. Coronal and sagittal reformats were generated. Dose reduction techniques were utilized including kVp/mA dose modulation based on patient size and iterative reconstruction. 3-D MIP images were reconstructed from the vascular sequence. Contrast: 60 mL Isovue 370 Radiation dose: 242 mGy-cm COMPARISON: Chest radiograph 4/10/2021 FINDINGS: Pulmonary circulation: No pulmonary emboli. The pulmonary artery is normal in caliber. Aorta: No dissection, pseudoaneurysm, or ulcerated plaque. Common origin of right brachiocephalic and left common carotid arteries. Lungs: Faint bibasilar atelectasis. Otherwise clear. No consolidation or nodule. Lymph nodes: No thoracic lymphadenopathy. Pleura: No effusion. Cardiovascular: Normal heart size. Osseous: No suspicious lesion. Upper abdomen: Normal. ARTIFICIAL INTELLIGENCE (AI) DATA REVIEW: Agreement with AI findings X-RAY CHEST PA AND LATERAL ONLY (Final result) Result time 04/10/21 10:48:00 Final result (04/10/21 10:48:00) Impression: IMPRESSION: No acute pulmonary disease. Narrative: QN CHEST PA AND LEFT LATERAL ONLY CLINICAL HISTORY: Reason for Exam?: syncope OTHER (PLEASE ENTER CHEST X-RAY INDICATION BELOW) : TECHNIQUE: Frontal and lateral radiographs of the chest. COMPARISON: None FINDINGS: Lungs are clear without pleural effusion, consolidation, or pneumothorax. Cardiac silhouette is unremarkable. No acute osseous abnormality. CT HEAD WO CONTRAST (Final result) Result time 04/10/21 10:45:00 Final result (04/10/21 10:45:00) Impression: IMPRESSION: No acute hemorrhage, mass effect, or cortical infarct. Narrative: QN CT HEAD WITHOUT CONTRAST HISTORY: EPIC: Reason for Exam?: syncope + head trauma, ?ICH ACRSelect Session ID: 176257482 ACRSelect Score: 8 - Indicated Altered mental status : TECHNIQUE: CT images of the head are provided in multiple planes. Dose reduction techniques were utilized including kVp/mA dose modulation based on patient size and iterative reconstruction. RADIATION DOSE: 579 mGy-cm COMPARISON: None FINDINGS: Hemorrhage: None. Mass effect: No mass effect, midline shift, or herniation. Infarct: No acute cortical infarct. White Matter: Normal and symmetric. CSF Spaces: No hydrocephalus or atrophy. Clear basal cisterns. Skull: No fracture. Sinuses/mastoids: Clear paranasal sinuses and mastoid air cells. ARTIFICIAL INTELLIGENCE (AI) DATA REVIEW: No AI report available
Aktuelle Erkrankungen: n/a
Vorgeschichte: h/a
Andere Medikamente: ofloxacin eye drops, loteprednol etabonate eye drops, percocet
Allergien: gadollinium
Vorherige Impfungen: -

VAERS 1178266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 49,0
Geschlecht: M
Eingang: 07.04.2021
Impfdatum: 23.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / -

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

Disease recurrence Facial paralysis Feeling abnormal Hypoaesthesia Nerve injury Oral discomfort

Symptomtext

Numbness on side of face and cheek/numbness went from his cheek up on to the temple area and jaw area; Mouth pulls weird; Previous nerve damage in his neck that hadn't been acting up in about a year but it was acting up now; Previous nerve damage in his neck that hadn't been acting up in about a year but it was acting up now; Felt loopy; Some weird palsy going on in his face/mild palsy in the left side of the face/Felt like face was heavy on left side or drooping/left side of his face was sagging; This is a spontaneous report from a contactable consumer reporting for himself. A 49-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EN6203), via an unspecified route of administration on 23Mar2021 14:40 at single dose for COVID-19 immunization. Medical history included he had some previous nerve damage in his neck that had not been acting up in about a year. Concomitant medications were not reported. Historical Vaccine included first dose of BNT162B2 (Lot Number: EL9269) on 02Mar2021 for COVID-19 immunization. On 24Mar2021, patient had some facial numbness and mild palsy in the left side of the face. He stated he had some previous nerve damage in his neck that had not been acting up in about a year, but it was acting up then. He stated it was the feeling like when you go to sleep on something, and it felt heavier. He asked what he should do, if he should seek medical attention and for information on this. After providing information from the Prescribing information, he asked if the Bell's Palsy went away in these individuals in the clinical trials? He stated his wife just said that the left side of his face was sagging. He stated he did not think it was a stroke though because he could move that side of his face and can articulate everything. He felt loopy but did not feel like it was a stroke. Patient reported that basically he felt numbness on the side of his face and cheek. There were reactions when he smiled, it seemed a little bit off. There was a weird feeling and numbness in his face. The numbness went from his cheek up on to the temple area and jaw area, the numbness was primarily on the left side of his face. Patient had nerve damage in his neck already. Patient wanted to know if he should go somewhere with it, was it ok, what was going on with the numbness in his face. Patient thought the numbness in his face and cheek had worsened. Felt like face was heavy on that side or drooping: Caller reported that looking in mirror, the left side of his face did not react the same. Patient's face felt like it was heavy or drooping on the left side, but that it pulls up higher. Patient reported that his face looked ok. Mouth pulls weird: Patient reported that this could be from his prior nerve damage, it was like he had got some weird palsy going on in his face. Patient stated that he just wanted someone to tell him dude wait it out, go to the emergency room, go to the doctor. Patient inquired if the facial numbness was because he had prior nerve condition and if the Covid-19 vaccine had exacerbated his existing nerve condition. The outcome of the events were unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Nerve damage
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1111441

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: GA
Alter: 44,0
Geschlecht: F
Eingang: 07.04.2021
Impfdatum: 17.03.2021
Beginn: 17.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dizziness Feeling hot Immediate post-injection reaction Nausea Asthenia Chills Investigation Loss of consciousness Movement disorder

Symptomtext

weakness; nausea; chills; dizziness; passed out/ LOC; could not move my body; This is a spontaneous report from a contactable consumer (patient). A 44-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not provided) via an unspecified route of administration, administered in left arm on 17Mar2021 15:00 as a single dose for COVID-19 immunisation. Medical history includes Chronic migraines and gastritis. The patient is not pregnant at time of vaccination. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included omeprazole (PROTONIX) and loratadine (CLARITINE). The patient previously took pethidine hydrochloride (DEMEROL) and oxycodone hydrochloride;oxycodone terephthalate;paracetamol (PERCOCET) and experienced allergies. On 17Mar2021 15:15, the patient experienced nausea, dizziness, and chills. Within 10 mins, she passed out. Within 30 mins, she passed out/LOC when came to, she could not move her body and she was in locked state for approximately 1 minute. This occurred two more times the same day (once in ED). It seemed as every time she tried to stand/walk, she would pass out. She was hospitalized on 19Mar2021 for 3 days until 21Mar2021 with similar symptoms. Her lungs, brain, heart scans were all good. She had no previous medical issues to cause such symptoms for in-patient need. On 22Mar2021, she had to use a walker to get around due to weakness and dizziness. She was healthy and active prior to the vaccine. The events resulted in Emergency room/department or urgent care and Hospitalization. Therapeutic measures were taken as a result of the events which included tests that came back clear, and care. The outcome of the events was recovered with sequelae on an unspecified date. The patient has not been tested for COVID-19 post vaccination. Information about lot/batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: Test Name: lungs, brain, heart scan; Result Unstructured Data: Test Result:all good
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gastritis; Migraine
Andere Medikamente: PROTONIX [OMEPRAZOLE]; CLARITINE
Allergien: -
Vorherige Impfungen: -

VAERS 1171418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 86,0
Geschlecht: F
Eingang: 06.04.2021
Impfdatum: 22.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cardiac function test normal Monoclonal antibody immunoconjugate therapy Presyncope SARS-CoV-2 test positive

Symptomtext

Developed COVID after first dose of vaccine. Pt arrived to vaccine clinic on 03/13 for her second dose. Had symptoms consistent with COVID since 3/10- sore throat, fevers, body aches, diarrhea, congested. Tested positive for COVID 3/14. Received bamlanivimab on 3/15. Was referred to ED 2 hours after monoclonal infusion after presyncopal episode. Cardiac workup done and was negative. Admitted for monitoring received IV hydration and supportive care (no supplemental O2)

Weitere VAERSDATA-Felder

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

VAERS 1170300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: AK
Alter: 46,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Facial paralysis Hypoaesthesia Neurological examination normal Paraesthesia

Symptomtext

Mild left sided facial paralysis one hour after receiving vaccine, lasted for approximately 24 hours. Continues to have intermittent numbness and tingling to left side of face since that time, though paralysis has not returned. No other neurological symptoms. Vaccine not performed by this provider or at this clinic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Patient had a medical exam by this provider on 03/10/2021 and 04/05/2021. Normal neurological exam.
Aktuelle Erkrankungen: GERD, asthma
Vorgeschichte: GERD, asthma
Andere Medikamente: ethinyl estradiol-norethindrone 20 mcg-1 mg oral tablet Ventolin HFA 90 mcg/inh inhalation aerosol
Allergien: Penicillin, dogs, cats, dust mites, crustaceans.
Vorherige Impfungen: -

VAERS 1170062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IA
Alter: 24,0
Geschlecht: M
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Seizure Syncope

Symptomtext

Had fainted for few seconds. Started to have seizures. Gave Epipen autoinjector. Called 911. EMS arrived.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Taking seizure med. had taken the morning med on the day of vaccination.
Allergien: -
Vorherige Impfungen: -

VAERS 1170040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IA
Alter: 17,0
Geschlecht: F
Eingang: 05.04.2021
Impfdatum: 05.04.2021
Beginn: 05.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hyperhidrosis Pallor Paraesthesia Syncope Tremor

Symptomtext

Fainted for 2 seconds. Sweating. Pale lips but the color got back on after few minutes. Tingling. Could not lift up her arm (but could feel squeezing thumb). Shaken hands and feet. Lied down on the ground around for 10 minutes and elevated feet. Had her to keep breathing in/out. Kept drinking water and gave orange juice. Called 911. EME arrived and took care of patent. Pt didn?t want to ride on the ambulance and said fine. Was able to walk in the end. Left the scene with her mom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Sat O2 100. Pulse 78-98. Bp 113/45.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Allergy to Penicillin- hives Previously had dizziness to Flu shot
Vorherige Impfungen: Flu shot. Had dizziness/anxiety. Other info unknown.

VAERS 1163312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 64,0
Geschlecht: M
Eingang: 03.04.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Blood test Dizziness Feeling abnormal Palpitations Syncope

Symptomtext

light headed, somewhat faint feeling. Continued intermittently for over 3 weeks. Intermittently get weird feeling/sensation, like a surge and get weak. Intermittent gurgling basically daily since vaccine. Feels sometimes like heart beats stronger or like maybe racing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Bloodwork, emergency room visit.
Aktuelle Erkrankungen: n/a
Vorgeschichte: -
Andere Medikamente: Carlson Super 2 daily
Allergien: third one, stelazine, loxitane
Vorherige Impfungen: -

VAERS 1160578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: SC
Alter: 74,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 05.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Computerised tomogram Electrocardiogram Loss of consciousness Memory impairment Road traffic accident Syncope

Symptomtext

Auto Accident - syncope - Ambulanced to Hospital. Passed out and hit a tree, totaled vehicle with no memory of the event. CT without contrast, blood work, EKG, fluid given IV. Stayed about 3 hours and was released.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: 2/23/2021
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Vitamin B12
Allergien: none
Vorherige Impfungen: -

VAERS 1085444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 02.04.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Adrenal insufficiency Anaphylactic reaction Blood potassium Electrocardiogram Gait disturbance Dysphagia Swollen tongue Injection site haematoma Investigation

Symptomtext

This is a spontaneous report received from a contactable female consumer reported for herself that a 65-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EN6203, Expiration date: unknown) via an intramuscular route on left arm on 08Mar2021 at 13:10 (at the age of 65-year-old) as a single dose for COVID-19 Immunization. The patient medical history included ongoing Autonomic neuropathy (Affected her digestive tract. Lost teeth, part of esophagus, gall bladder, stomach and large part of small intestine), Clostridium difficile, several anaphylactic reactions (immediate anaphylactic reaction with bee sting), malnutrition, walker, hypoglycemic, dermatitis from gloves, Hives for several medication (Reglan, compazine, levaquin, cipro, doxycylcine, zpac, arithromycin, sulfa drugs-macrodantin, chorhexadine, tropomate tramadol, msl4, codeines, hydrocodone, oxycodone, ultracept, Carries 4 epi pens in different locations), allergy: corticosteroids, on J tube 12 years, PICC line for 3 years, stomach had to be taken out (A tiny pouch was made where they connected what was left of her esophagus to small intestine. The pouch is the size of a quarter). The patient concomitant medication included teduglutide (GATTEX, Lot number: 1908G, expiration date: Apr2023) ongoing at a dose of 5ml, daily; dicyclomine (capsule, expiration date: 16Mar2022) ongoing at 10mg (2 capsules 3 minutes before meals and bedtime) from an unknown date in 2002; sucralfate (expiration date: Oct2021) ongoing at 100kg/m3, 4 times a day for help keep food down, colesevelam hydrochloride (expiration date: May2022) ongoing at 625mg, twice a day for help aide digestion, fludrocortisone (tablet, expiration date: 23Jan2022), ondansetron (ZOFRAN, Lot number: ON0820008-A, Expiration date : Jan2024) ongoing at 8mg as needed for nausea; midodrine (Expiration date: 22Oct2021) ongoing from 2018 at a dose of 5mg, thrice a day for orthostatic hypotension; alprazolam (tablet) at a dose of 1 mg; ongoing gabapentin. On 8Mar2021, with 5 minutes after vaccination had an anaphylactic reaction- Was taken by ambulance-Caller couldn't breathe or swallow- tongue was thick, couldn't breathe, Tachycardia, chest hurt and felt bruised afterwards, Nausea, Constipated, Oxygen level was down to 90, legs and arms were flapping, could not swallow, felt like she had brain fog. Nurse watched her carefully and she was sent to sit for 30 minutes. The doctor gave her a shot of Epinephrine and it backfired, so she didn't get it. The other doctor got it and the ambulance was there working on her. Oxygen level was down to 90 and was given Decadron. Her legs and arms were flapping due to her disease, because epinephrine was a vasodilator. It was reported that in ambulance patient Was being asked questions and she couldn't talk on 08Mar2021. The patient was taken to the hospital and was given more benadryl, and more epinephrine. Then she felt better over the next few days. She saw her own physician the next day and was given Solumedrol in her tush, 40 mg prednisone twice a day, for 3 days. The patient felt her cognitive skills were not working well the first few days and could not walk very well, even with her walker on an unknown date in Mar2021and dropped 5 dishes in one day. Caller provided information regarding article from British government stating people with history of anaphylaxis should not take Pfizer vaccine. Article stated FDA is still working with Pfizer on this. The patient states she should never have been given that shot and requests for compensation. The patient reported that she was never been so afraid in life. The patient had hematoma after 3 sticks for IV in ambulance on 08Mar2021 and had warm hot packs on it. The patient Oxygen level was low and was given 2liters nasal cannula, which was bumped up to 4 liters. The patient felt like a robot, did not have good control of legs or arms and flailing like baby when epinephrine was given. The patient took Fludrocortisone for Adrenal insufficiency, With all the steroids, should have felt fabulous but didn't. The patient Clarified Epinephrine junior was given in the thigh and backfired. Was given Epinephrine in her other thigh, Was given Benadryl at Vaccine facility. In emergency room patient received Famotidine IV 20mg/50ml STAT 1 dose, Sodium Chloride 0.9% 1000 ml over one hour STAT for hydration, Another sodium chloride 0.9% 1,000ml, Another sodium chloride 0.9% 1,000ml and discharged from emergency room after 6 hours. The patient stated she could not have second COvid-19 Vaccine that was scheduled for this coming Monday. The patient had undergone laboratory test on08Mar2021 potassium was 2.9, EKG was abnormal (tachycardia) and standard blood work was unknown. The outcome of the events anaphylactic reaction was recovering, tongue was swollen was recovered on an unknown date in Mar2021 while for other events was unknown. Follow-up Information has been requested.; Sender's Comments: Based on known drug safety profile and close temporal association the event of Anaphylactic reaction is assessed as related to the suspect vaccine BNT162B2. As there is limited information in the case provided for gait disturbance, adrenal insufficiency and injection site haematoma, the causal association between the events and the suspect vaccine BNT162B2 cannot be excluded. The case will be reassessed once new information is available. 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: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210308; Test Name: Potassium; Result Unstructured Data: Test Result:2.9; Comments: 2.9; Test Date: 20210308; Test Name: EKG; Result Unstructured Data: Test Result:abnormal; Comments: abnormal; tacchycardia; Test Date: 20210308; Test Name: standard bloodwork; Result Unstructured Data: Test Result:unknown
Aktuelle Erkrankungen: Autonomic neuropathy (Affected her digestive tract. Lost teeth, part of esophagus, gall bladder, stomach and large part of small intestine.)
Vorgeschichte: Medical History/Concurrent Conditions: Anaphylactic reaction (immediate anaphylactic reaction with bee sting); Clostridium difficile infection; Dermatitis; Drug allergy; Feeding tube user; Gastrectomy (A tiny pouch was made where they connected what was left of her esophagus to small intestine. The pouch is the size of a quarter.); Hives (Reglan, compazine, levaquin, cipro, doxycylcine, zpac, arithromycin, sulfa drugs-macrodantin, chorhexadine, tropomate tramadol, msl4, codeines, hydrocodone, oxycodone, ultracept Carries 4 epi pens in different locations); Hypoglycemia (carries glucose tablets (LOT: 79187, Exp: Nov2022)); Malnutrition; Peripherally inserted central catheterisation (for 3 years); Walker user
Andere Medikamente: GATTEX; DICYCLOMINE; SUCRALFATE; COLESEVELAM HYDROCHLORIDE; FLUDROCORTISONE; ZOFRAN [ONDANSETRON]; MIDODRINE; ALPRAZOLAM; GABAPENTIN
Allergien: -
Vorherige Impfungen: -

VAERS 1154026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 01.04.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Abdominal pain Anaphylactic reaction Depressed level of consciousness Dysphonia Dyspnoea Eye pruritus Heart rate Lip swelling Ocular hyperaemia Paraesthesia Respiratory distress Respiratory tract oedema Shock Swollen tongue Tachycardia Throat tightness

Symptomtext

Anaphylactic reaction; Tachycardia/she felt her heart going fast; her throat starting to close/ Sensation of throat closure; Upper airway swelling/Increased use of accessory respiratory muscles; she could not breath/Difficulty breathing (without wheeze or stridor); Respiratory distress; her lips and tongue were big and it was getting worse; her lips and tongue were big and it was getting worse; Hoarse voice; Shock; Decreased level of consciousness; Generalized prickle sensation; Red and itchy eyes; Red and itchy eyes; Abdominal pain; The initial case was missing the following minimum criteria: adverse event (unspecified). Upon receipt of follow-up information on (17Mar2021), this case now contains all required information to be considered valid. This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration administered on arm right on 25Feb2021 08:15 (Batch/Lot Number: EN6203) as SINGLE DOSE for COVID-19 immunization at the hospital. Medical history included asthma. It was reported that the patient was allergic to NSAID, paracetamol (TYLENOL), pollen, cats and dogs; and insect bite/sting. She also had environmental allergies. It was also reported that her sister had breast cancer. Ongoing concomitant medications included spironolactone (SPIRONOLACTONE), vitamin C, cyanocobalamin (VITAMIN B12), calcium (CALCIUM), magnesium (MAGNESIUM), iron (IRON) and zinc (ZINC) all taken for unknown indications since unknown date. She had no other vaccines received around the time of COVID-19 vaccine vaccination. The patient was not pregnant (including at the time of vaccination). The patient received the first dose of PFIZER-BIONTECH COVID-19 VACCINE on 25Feb2021 at 08:15 AM. Thirty minutes after the vaccination (at 08:45), she had an anaphylactic reaction as she felt her heart going fast and was noted to have tachycardia (as an organ involvement), had sensation of throat closure her throat starting to close. She had upper airway swelling with increased use of accessory respiratory muscles, respiratory distress as she could not breath (without wheeze or stridor). Her lips and tongue were big and it was getting worse. She also had the following organ involvements manifested by hoarse voice, shock, decreased level of consciousness, generalized prickle sensation, red and itchy eyes, and abdominal pain. She was administered with diphenhydramine (BENADRYL) IV. She was taken to ER and was also administered with famotidine 20 mg. The events were considered life threatening. The patient recovered from the events on unknown date in 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Test Date: 20210225; Test Name: heart; Result Unstructured Data: Test Result:Fast; Comments: 08:45
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergic reaction to analgesics; Allergy to animal; Asthma; Environmental allergy; Insect sting allergy; Pollen allergy
Andere Medikamente: SPIRONOLACTONE; VITAMIN C [ASCORBIC ACID]; VITAMIN B12 [CYANOCOBALAMIN]; CALCIUM; MAGNESIUM; IRON; ZINC
Allergien: -
Vorherige Impfungen: -

VAERS 1153417

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Body height Body height decreased Dizziness Fall Loss of consciousness Weight

Symptomtext

passed out; dizzy spell; fell down; have gotten shorter/ shrunk; This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6203), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunisation. Medical history included high blood pressure, diabetes, thyroid disorder, and bleeding. The patient stated "I am bleeder. My father had hemophilia and I have the female version which I never remember what it's called but I bleed easily but I didn't bleed at all for when I had the shot, it was fine." Concomitant medication included levothyroxine sodium (SYNTHROID). Patient stated, "Yes, I took my medication that morning. I take thyroid medication, blood pressure medication. I don't remember what I take for blood pressure." The patient reported "Well I am calling I felt just fine right now. I had my first shot by Pfizer on the 24th and I felt great and they watched me and I left and I was driving home and I had a dizzy spell while I was driving. I don't know if I passed out or not, I might have but if I did, it wasn't for very long, they were digging up the road I couldn't stop, couldn't park so I made it home okay and I was fine the rest of the day but then the next day, I had a lot of dizzy spells but I was at home so I didn't worry, I just sat down and I was okay and then the 3rd day I got up for breakfast and I bumped into everything, I dropped everything and then I started to get out of chair and the chair fell down and I fell down and that was just a mess. So, I went to bed and I felt at least if I fall, I fall on bed and that was the day I was dizzy but then it went away and I have been fine ever since. That began on 24th, the 24th was the first day and I did call my doctor and I have been trying to call here and I never think it through but finally today, sat to watch, hang on to the phone and what I am concerned about is getting my second vaccine. Is there anything I should watch for or tell anybody or, because my doctor said you shouldn't get dizzy but I did?" The patient confirmed the vaccine as Pfizer's Covid 19 vaccine. About the lot number, the patient stated, "It looks like EN, I am not sure if it's E and N 6203." The patient further reported, "No, I just went home and the first day I was over with it by the time I got home and I didn't had anymore. The next day I just sat down and rested, I knew it will go away and it did and then 3rd day I went to bed and just thought I would fall and hurt myself and that's everything I did. Well I used to be 5 foot 2 and a quarter but I think I have gotten shorter, I don't know what I really am but little bit shorter than that now and my weight is 100 and lets see, I am going to say 170, I don't think that's exactly right but it's pretty close to that I think, I didn't really weighed myself lately. 5 foot 2 and a quarter that's what I was when I did last but now I shrunk and less than that but I don't remember what I am." The outcome of the events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:5 foot 2 and a quarter; Test Name: weight; Result Unstructured Data: Test Result:170
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bleeding; Blood pressure high; Diabetes; Thyroid disorder
Andere Medikamente: SYNTHROID
Allergien: -
Vorherige Impfungen: -

VAERS 1153367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: UT
Alter: 77,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Body temperature Inappropriate schedule of product administration Off label use Peripheral coldness Thrombosis

Symptomtext

left leg was cold/left foot was 79-82 degrees Celsius; blood clots in his left leg/he had three/first one on 02Mar, second one 13Mar and the third one yesterday; he had the Pfizer vaccine on 15Feb and 26Feb; he had the Pfizer vaccine on 15Feb and 26Feb; This is a spontaneous report from a contactable consumer (patient). A 77-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose via an unspecified route of administration on 26Feb2021 (Batch/Lot Number: EN6203) as single dose for covid-19 immunisation; tafamidis (VYNDAMAX), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient took the first dose of PFIZER-BIONTECH COVID-19 VACCINE on 15Feb2021 at age of 77 years old for covid-19 immunisation. The patient medical history and concomitant medications were not reported. A patient taking Vyndamax medication who stated that he had experienced blood clot in his left leg. Clarified that he had the Pfizer vaccine on 15Feb2021 and 26Feb2021. Clarified that on 02Mar2021 that he had blood clots in his left leg. Stated that he had three. Stated that he had the first one on 02Mar2021, second one 13Mar2021 and the third one yesterday (15Mar2021). Stated that he was told left leg was cold. Stated that he took his temperature with a thermometer and his left foot was 79-82 degrees Celsius. Stated that the right foot is 95-96 degrees Celsius. Stated that he filled it out for the Covid vaccination. Stated that he reported Vyndalink when it asked what other medications that he took. The action taken in response to the events for tafamidis was unknown. The outcome of events was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: Test Name: temperature; Result Unstructured Data: Test Result:his left foot was 79-82 degrees Centigrade; Test Name: temperature; Result Unstructured Data: Test Result:right foot is 95-96 degrees Centigrade
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1152529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 30.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Diplopia Discomfort Dizziness Syncope Tinnitus Visual impairment Vomiting

Symptomtext

Patient had initial dizziness and syncopal episode. Patient reported "vision went dark and felt heavy". Patient vomited x1. Patient given cold pack and water. After 10 minutes patient denies headache, dizziness, double vision, or ringing in ears. No report of difficulty breathing, SOB, numbness or tingling in extremities. Patient successfully discharged from observation at 4:05 pm.

Weitere VAERSDATA-Felder

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

VAERS 1152001

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 51,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 23.02.2021
Beginn: 26.03.2021
Tage bis Beginn: 31,0
Dosis: 2
Route/Site: IM / LA

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

Erythema Lymphadenopathy Pain Peripheral swelling Thrombosis

Symptomtext

Patient received second dose of Pfizer BioNTech COVID Vaccine on 2/23/21. On 2/25 patient called PCP office expressing swollen & painful lymph node to left clavicle/shoulder area . Same arm as injection. Pain 2-3/10. Pt denied any other symptoms. Managed with warm compress, however on 3/26/21 patient went to the emergency room with complaint of continued swelling and redness on left arm. Ultra sound of the upper extremity showed short segment Nonocclusive thrombus in the left proximal subclavian

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: 3/26 3:43pm Upper extremity ultra sound showed short segment Nonocclusive thrombus in the left proximal subclavian
Aktuelle Erkrankungen: hyperlipidemia, hormone migraines, history of COVID 19 infection 09/2020
Vorgeschichte: hyperlipidemia, hormone migraines, history of COVID 19 infection 09/2020
Andere Medikamente: atorvastatin, Junel 1/20, ondansetron
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1151426

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 22.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: - / RA

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

Blood test Fall Generalised tonic-clonic seizure Postictal state SARS-CoV-2 test Scan

Symptomtext

Fell out of bed; tonic clonic seizure; postictal (confusion); This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in right arm on 22Feb2021 10:15 (lot number: EN6203) as single dose for COVID-19 immunisation. The patient's medical history included hypertension. The patient's concomitant medications included losartan and OTC vitamin. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 26Jan2021 03:45PM (lot number: EL9262) for COVID-19 immunisation. On 12Mar2021 06:30, the patient fell out of bed and wife witnessed tonic clonic seizure of 5+ minutes. And when EMS arrived on 12Mar2021 06:30, the patient was postictal (confusion). The events resulted to Emergency Room visit and patient was hospitalized for 3 days. The patient had no COVID prior vaccination and was tested for COVID post vaccination. The patient underwent lab tests and procedures and included blood test and scan, both with unknown results on an unspecified date and nasal swab/NAAT: negative on 12Mar2021. Therapeutic measures were taken as a result of the events and included numerous scans, blood tests and levetiracetam. The vaccination facility type was hospital. The outcome of the events were recovered with sequel.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 3,0
Labordaten: Test Name: Blood Test; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210312; Test Name: Nasal Swab/NAAT; Test Result: Negative ; Test Name: Scan; Result Unstructured Data: Test Result:Unknown result
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension
Andere Medikamente: LOSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 1151373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 32,0
Geschlecht: F
Eingang: 31.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Fatigue Myalgia Presyncope Pyrexia Vision blurred

Symptomtext

Blurry vision almost black out when walking.; Blurry vision almost black out when walking.; Muscle ache; fever; Fatigue; This 32- year-old female patient contactable healthcare professional received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE lot EN6203), via an unspecified route of administration, on 09Mar2021 at 09:00am (at the age of 32-years-old) as a single dose for COVID-19 immunization, in left arm. Patient is not pregnant. She has had no other vaccines on the same day or in the past 4 weeks. The patient did not have COVID-19 prior to the vaccine. Historical vaccine included first dose of BNT162B2 for COVID-19 immunization, on 16Feb2021, (Lot EN6200), in left arm. Relevant medical history included birth control use. Concomitant medications included: Junel birth control. On 09Mar2021 at 10:00 pm, the patient experienced Muscle ache, fever, fatigue, blurry vision - almost black out when walking. The patient received treatment of ibuprofen for the events. The clinical outcome of the events Muscle ache, fever, fatigue, blurry vision - almost black out when walking was recovered. It was reported that since the vaccination, the patient had not been tested for COVID-19. Information about lot/ batch number has been requested.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Birth control
Andere Medikamente: JUNEL
Allergien: -
Vorherige Impfungen: -

VAERS 1150394

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: UT
Alter: 77,0
Geschlecht: M
Eingang: 31.03.2021
Impfdatum: 26.02.2021
Beginn: 03.03.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: - / LA

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

Thrombosis

Symptomtext

Two blood clots in left leg; This is a spontaneous report from a contactable consumer. A 77-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration, administered in left arm on 26Feb2021 (Batch/Lot Number: EN6203) as single dose for COVID-19 immunisation. Medical history included back disorder, ATTR amyloidosis, and allergies: caffeine from an unknown date. Concomitant medication included allopurinol (ELAVIL); meloxicam; tizanidine; tafamidis (VYNDAMAX) all taken for an unspecified indication, start and stop date were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9269), on 05Feb2021, administration time: 06:00 PM, vaccine location: Left arm for COVID-19 immunisation. The patient experienced two blood clots in left leg on 03Mar2021 23:00. Treatment for the event includes Aspirin. The event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient had no COVID-19 prior vaccination. The patient was not tested for COVID-19 post vaccination. The outcome of the event was resolved on an unspecified date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Back disorder; Caffeine allergy; Transthyretin-mediated amyloidosis
Andere Medikamente: ELAVIL [ALLOPURINOL]; MELOXICAM; TIZANIDINE; VYNDAMAX
Allergien: -
Vorherige Impfungen: -

VAERS 1143809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / -

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

Body temperature Chills Fatigue Nausea Poor quality sleep Pyrexia Syncope Vaccination site pain

Symptomtext

feeling sick to my stomach ended up fainting onto bathroom floor; feeling sick to my stomach; arm felt mildly painful as injection went in; severe chills; fever; fatigue; restless sleep; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose at the age of 65-years-old via an unspecified route of administration on 08Mar2021 08:15 (lot number: EN6203) as single dose for covid-19 immunisation. Medical history included covid-19 (covid prior vaccination: yes) from 10Jan2021 to an unknown date. There were no known allergies. Concomitant medication included acetaminophen taken for an unspecified indication, start and stop date were not reported. The patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose at the age of 65-years-old, administered on the left arm on 15Feb2021 08:15 (lot number: EL9264) for covid-19 immunisation and experienced very painful injection site, chills, fever and fatigue. The patient reported that when she had her second vaccine on 08Mar2021, her arm felt mildly painful as injection went in, as though never healed from previous shot. This time, within 3 hours of vaccine, she began to feel fatigue, then began to experience chills and fever. She drank plenty of fluids, and took acetaminophen about 6 hrs after injection. In the evening her temp was up to 101.2 (her normal 97.2) and she took Acetaminophen at bedtime. Had very restless sleep, and at 5 AM on 09Mar2021, she got up feeling sick to her stomach ended up fainting onto bathroom floor. Luckily uninjured, and felt better upon "coming to". She was very fatigued rest of day, then normal next day. The patient underwent lab tests and procedures which included body temperature: 101.2 on 08Mar2021. No treatment was received for the events. The patient recovered from the events on an unspecified date.; Sender's Comments: Linked Report(s) : Same reporter,patient,product/ 2nd dose;US-PFIZER INC-2021269674 Same reporter,patient,product/ 2nd dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20210308; Test Name: temp; Result Unstructured Data: Test Result:101.2
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: SARS-CoV-2 infection
Andere Medikamente: ACETAMINOPHEN
Allergien: -
Vorherige Impfungen: -

VAERS 1142926

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 29.03.2021
Impfdatum: 04.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Blood pressure measurement Body temperature Body temperature decreased Dizziness Fatigue Feeling cold Headache Hypertension Loss of consciousness Nausea

Symptomtext

The second day after injection temperature dropped to 93.7; I was very cold; I was dizzy almost passed out; tired; nausea; headache; almost passed out; Hypertension/BP 155/103; This is a spontaneous report from a contactable consumer (patient). A 46-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: EN6203, expiry date not reported) via an unspecified route of administration, administered in left arm on 04Mar2021 at a single dose for COVID-19 immunisation. Medical history included interstitial cystitis and endometriosis, known allergies to milk and sulfa, have had a complete hysterectomy, and patient was getting hormone injections. The patient was not pregnant at the time of the report and vaccination. The patient had no covid prior to vaccination. Concomitant medications were unspecified; it was reported that patient had other medications in two weeks. The patient previously took ibuprofen and experienced known allergies; and had first dose of bnt162b2 for covid-19 immunisation on an unknown date. The patient had no other vaccine in four weeks. The second day after injection (06Mar2021), temperature dropped to 93.7, BP 155/103, and patient was very cold. Patient was dizzy, almost passed out (Mar2021). Patient temp ran from 97 to 98 and was able to get temp up to 95 (2021) but it's been there and dropping to 94.9 since 06Mar2021. Patient did have hypertension BP but take meds for it (Mar2021). Patient was also very tired, nausea and headache on and off (Mar2021). But all those have been reported. It's not normal for the patient to be cold because patient have had a complete hysterectomy and was getting hormone injections. Therapeutic measures were taken as a result of the event hypertension. No treatment received for the other events reported. The patient was not tested for covid post vaccination. The outcome of the events was not recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Test Date: 20210306; Test Name: BP; Result Unstructured Data: Test Result:155/103; Test Date: 202103; Test Name: BP; Result Unstructured Data: Test Result:hypertension; Comments: hypertension; Test Date: 20210306; Test Name: temperature; Result Unstructured Data: Test Result:93.7; Test Date: 20210306; Test Name: temperature; Result Unstructured Data: Test Result:94.9; Test Date: 2021; Test Name: temperature; Result Unstructured Data: Test Result:97 to 98; Test Date: 2021; Test Name: temperature; Result Unstructured Data: Test Result:95
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cystitis interstitial; Endometriosis; Hormone therapy; Hysterectomy; Milk allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1141687

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 28.03.2021
Impfdatum: 24.02.2021
Beginn: 14.03.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / LA

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

Thrombosis

Symptomtext

Blood clots a few weeks after 2nd dose. Currently being treated with Xarelto. No other changes in patient medical or prescription history. Covid vaccine was the only thing that was new. Patient had no prior history of blood clots.

Weitere VAERSDATA-Felder

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

VAERS 1138131

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

schwer

Staat: CO
Alter: 44,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 18.03.2021
Beginn: 24.03.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: SYR / RA

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

Pyrexia Seizure

Symptomtext

On 3/24/21, almost a week after my second vaccine shot, I had a seizure while sleeping in bed. I hadn?t had a seizure in over 30 years, and then only with a fever (I had febrile seizures as a child). My husband got some of it on video after being unsuccessful waking me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: 3/25/21 - CT scan, urine sample, blood work, and EKG all came back normal Awaiting scheduling for MRI and EEG
Aktuelle Erkrankungen: -
Vorgeschichte: Obesity
Andere Medikamente: Bupropion Topiramate
Allergien: -
Vorherige Impfungen: -

VAERS 1137230

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 03.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / -

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

Computerised tomogram thorax abnormal Deep vein thrombosis Dyspnoea Pain in extremity Peripheral swelling Ultrasound scan abnormal

Symptomtext

3 days after completing vaccine series, pt develop right leg pain and swelling, which progressed later on to shortness of breath after a week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 1,0
Labordaten: CT scan showed PE, US showed DVT
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: amitriptyline
Allergien: -
Vorherige Impfungen: -

VAERS 1136786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 19.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 24,0
Dosis: 1
Route/Site: IM / UN

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

Blood pressure abnormal Body temperature decreased Dizziness Heart rate abnormal Intensive care Laboratory test Lethargy

Symptomtext

The first injection was uneventful. 30 hours after the second injection, respectively, patient suddenly became dizzy. VS assessed. BP 90s/40s, which is abnormal for her, HR 30's which is abnormal, and temperature 95.1 orally. She became lethargic. EMS called and confirmed the same VS. Atropine give three times according to protocol without change in HR. Epinephrine dose given with some improvement in HR, but unable to sustain. Pt transported via EMS to Hospital where she was warmed mechanically, started on an IV epinephrine drip and transported to the cardiac ICU where she was monitored for 2 days. Clinically the patient improved after her body temperature normalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Multiple labs and diagnostics at facility which are unavailable to me at this time.
Aktuelle Erkrankungen: none
Vorgeschichte: Type 2 DM, Diabetic peripheral neuropathy, HTN, CAD, likely PAD, GERD, Vit D deficiency, osteoporosis, CHF
Andere Medikamente: Toujeo, Humalog, Bisoprolol, Losartan, Plavix, Norvasc, Levothyroxine, Nitroglycerin Patch, Protonix, Ranexa, Crestor, Demedex
Allergien: ACE inhibitors, Penicillin, Aspirin, Bee venom
Vorherige Impfungen: -

VAERS 1136786

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 71,0
Geschlecht: F
Eingang: 26.03.2021
Impfdatum: 19.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 24,0
Dosis: 2
Route/Site: IM / UN

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

Blood pressure abnormal Body temperature decreased Dizziness Heart rate abnormal Intensive care Laboratory test Lethargy

Symptomtext

The first injection was uneventful. 30 hours after the second injection, respectively, patient suddenly became dizzy. VS assessed. BP 90s/40s, which is abnormal for her, HR 30's which is abnormal, and temperature 95.1 orally. She became lethargic. EMS called and confirmed the same VS. Atropine give three times according to protocol without change in HR. Epinephrine dose given with some improvement in HR, but unable to sustain. Pt transported via EMS to Hospital where she was warmed mechanically, started on an IV epinephrine drip and transported to the cardiac ICU where she was monitored for 2 days. Clinically the patient improved after her body temperature normalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 3,0
Labordaten: Multiple labs and diagnostics at facility which are unavailable to me at this time.
Aktuelle Erkrankungen: none
Vorgeschichte: Type 2 DM, Diabetic peripheral neuropathy, HTN, CAD, likely PAD, GERD, Vit D deficiency, osteoporosis, CHF
Andere Medikamente: Toujeo, Humalog, Bisoprolol, Losartan, Plavix, Norvasc, Levothyroxine, Nitroglycerin Patch, Protonix, Ranexa, Crestor, Demedex
Allergien: ACE inhibitors, Penicillin, Aspirin, Bee venom
Vorherige Impfungen: -

VAERS 1134526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 19.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / -

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

Anaphylactic reaction Anion gap Basophil percentage decreased Blood chloride normal Blood creatinine normal Blood glucose normal Blood potassium normal Blood sodium normal Blood urea normal Carbon dioxide normal Dysphagia Dyspnoea Electrocardiogram Eosinophil percentage Feeling abnormal Haematocrit normal Haemoglobin normal Headache

Symptomtext

58 Y female here for concern of allergic reaction due to covid vaccine. Received second dose of pfizer vaccine yesterday. Today awoke feeling funny, felt some tightness in throat, trouble swallowing, more sob, palpitations, headache. When she arrived at work this morning, started dry heaving very nauseated and had to go home. Driving home, she saw her face and noticed it was swollen. No prior hx of allergic reactions. No other new meds or foods in that time. No chest pain. 58F with likely allergic reaction anaphlyaxis to pfizer vaccine. No severe facial swelling, tongue swelling, wheezing but symptomatically concerning given throat tightness, subjective facial swelling (I did see some mild periorbital edema but unable to observe other differences but she could). Not on any ace inhibitor. Less likely chf, acs, pna/ ptx, asthma Pt symptomatically improved a lot after epi, benadryl Observed and deemed stable Dc with prednisone and pepcid

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Results for AMIGABLE, (MRN 110010339663) as of 3/25/2021 13:33 3/20/2021 09:23 NA: 140 K: 4.0 CL: 105 CO2: 29 BUN: 19 CREAT: 0.79 ANION GAP4 SERPL: 6 GLUC: 100 Results for AMIGABLE, (MRN 110010339663) as of 3/25/2021 13:33 3/20/2021 10:46 EKG 12 OR MORE LEADS W INT & RPT: Rpt HEART RATE: 72 PR: 183 QRS: 107 Results for AMIGABLE, (MRN 110010339663) as of 3/25/2021 13:33 3/20/2021 09:23 WBC: 7.7 RBC'S: 4.21 HGB: 12.3 HCT: 39.4 MCV: 94 RDW, RBC: 12.0 PLT: 198 IMMAT GRANULO % AUTO: 0 NRBC: 0 NEUTROPHILS % AUTO: 48 ANC: 3.7 LYMPHS % AUTO: 44 MONOS % AUTO: 5 EOS % AUTO: 3 BASO'S % AUTO: 0 QT: 419 QT CORRECTED: 459
Aktuelle Erkrankungen: 2/25/21 - Pt with intermittent nausea after meals, mild upset stomach, fatigue, headache, motion sensation
Vorgeschichte: Cancer Female Breast, Abnl Pap, Asthma
Andere Medikamente: Albuterol Inh, Ciclesonide Inh, Escitalopram, Famotidine, Fluticasone, Simthicone 80mg, Lorazepam, Montelukast, Naloxone Nasal Spray, Pantoprazole, Sodium Bicarb-Sodium Chloride Nasal Rinse,
Allergien: nkda
Vorherige Impfungen: -

VAERS 1133033

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 66,0
Geschlecht: M
Eingang: 25.03.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / LA

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

Chills Contusion Feeling abnormal Loss of consciousness Nausea Pyrexia Skin laceration Taste disorder

Symptomtext

I have never passed out prior; 1 in.laceration above the right eye along; food is less flavorful and does not excite me; Feeling queasy; bruising to my upper arm, leg and back; don't feel right; About 10 hours after the second injection began to have chills and a low grade fever.; About 10 hours after the second injection began to have chills and a low grade fever.; This is a spontaneous report from a contactable consumer (patient). A 66 -year-old male patient received his second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: EN6203), via an unspecified route of administration (on left arm) on 06Mar2021 12:00 (at the age of 66 -years-old), single dose for COVID-19 immunisation. Medical history included Diabetes Type 2 (Doctor stated that I really do not fit either profile. Concomitant medications included pioglitazone, metformin, lisinopril, ascorbic acid, tocopheryl acetate, xantofyl, zeaxanthin, zinc (AREDS). Patient stays away from all Opioids they make him very nauseous. Patient typically gets a low grade fever (100-101) and chills 4 hours after a Flu Vaccine that last almost exactly 24 hours. The patient had the first dose of covid vaccine on 11Feb2021 for covid-19 immunisation and experienced only minor soreness at the injection site with the first dose. Experience only minor soreness at the injection site with the first dose. About 10 hours after the second injection began to have chills and a low grade fever. Sunday morning 07Mar2021 started feeling queasy. Patient thought that if I took a shower that I might feel better. As Patient was getting toward the end of his shower Patient just thought, Patient don't feel right. The next thing Patient remember Patient was picking himself of the floor of the shower. Patient have never passed out prior to this episode. Patient received a 1 in. laceration above the right eye along with bruising to his upper arm, leg and back. Patient basically ate nothing the remainder of Sunday nor Monday. It is as if the food is different. Even though he is a Diabetic and keep his blood sugar under control. Patient knows that this may sound weird, but it is as if the food is less flavorful and does not excite him. As 09Mar2021, he still does not feel together. The outcome of the events was not recovered. No treatment for any adverse event. No Covid prior vaccination, not Covid tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Type 2 diabetes mellitus
Andere Medikamente: PIOGLITAZONE; METFORMIN; LISINOPRIL; AREDS
Allergien: -
Vorherige Impfungen: -

VAERS 1132430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PR
Alter: 86,0
Geschlecht: F
Eingang: 25.03.2021
Impfdatum: 24.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Oedema peripheral Pain in extremity Thrombosis Ultrasound Doppler

Symptomtext

The daughter of the patient stated that her mother is a cardiac patient and has a stent. The patient always has edemas on her legs but the day after the vaccination she observed edema and report pain on the left thigh. The following Monday she visited the MD and he order a venous Doppler. The result was a thrombosis on the right leg . The patient was put on medication (Xarelto)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: A venous Doppler. The result was a thrombosis on the right leg . The patient was put on medication (Xarelto)
Aktuelle Erkrankungen: Non reported
Vorgeschichte: None reported
Andere Medikamente: Losartan, Neurotin, Metoprolol ER, Lipitor,40mg, AT
Allergien: ASA, Iodine
Vorherige Impfungen: -

VAERS 1131105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 68,0
Geschlecht: M
Eingang: 24.03.2021
Impfdatum: 04.02.2021
Beginn: 10.02.2021
Tage bis Beginn: 6,0
Dosis: 2
Route/Site: IM / RA

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

Arthritis Blood test Chest pain Condition aggravated Electric shock sensation Gait disturbance Hypoaesthesia Impaired work ability Muscular weakness Pain Pain in extremity X-ray

Symptomtext

First hands are numb. Then legs are extremely weak and it is hard to walk, they are very unstable. When I cough or sneeze, I have shooting electric type pain through my arms and across my chest. This has been consistent since right after my first shot. Doctors are saying that it is only arthritis. They have run blood work and xrays. But symptoms continue to affect me and I am unable to work due to severity.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Xrays were taken around 3/6 Blood work done on same day
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes and arthritis
Andere Medikamente: Cartia -240 MG once/day; Lisinopril-10 MG 1 tablet, 2 times/day; Invokana 100 mg 1 time/day; Pantoprazole 40 mg 1 time/day; hydrochlorothiazide 1 time/day; Atorvastatin 20mg 1 time/day; Basaglar insulin shot 25 units 1 time/day.
Allergien: None
Vorherige Impfungen: -

VAERS 1118116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 20.03.2021
Impfdatum: 03.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Feeling hot Heart rate increased Hyperhidrosis Malaise Retching Syncope

Symptomtext

Within a few minutes, felt faint, unwell, did faint, came to, hot and sweaty, retching, heartbeat 110.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: Hypothyroid, Emphysema
Andere Medikamente: Armour Thyroid, 60mg; homeopathic: E Coli 200c and Causticum 30c; and supplements: vitamin D-3, 4000iu, NAC 600mg, Seleneium 100mcg, L-Carnitine 500mg, Coenzyme Q10,and Magnesium 250mg
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 1113966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: SC
Alter: 67,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 18.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: OT / RA

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

Acute respiratory distress syndrome Pulmonary fibrosis Respiratory distress

Symptomtext

severe ARDS and pulmonary fibrosis; severe ARDS and pulmonary fibrosis; presented to the hospital on 26Feb with severe resp distress; This is a spontaneous report from a contactable Other healthcare professional (HCP). A 67-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular, administered in Arm Right on 18Feb2021 16:00 (Lot Number: EN6203) (at 67-year-old) as single dose for covid-19 immunisation. The COVID-19 vaccine was administered at Store. Medical history included Malignant neoplasm of sigmoid colon, hypertension (HTN). Concomitant medications included tamsulosin; tipiracil hydrochloride/trifluridine (LONSURF), hydrochlorothiazide/lisinopril (ZESTORETIC), docusate sodium (COLACE), hyoscyamine sulfate (LEVSIN/SL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received first dose of BNT162B2 (Lot number: AL9265) at 27Jan2021 12:30 PM, Intramuscular at right arm for covid-19 immunization. Patient received 2nd vaccine on 18Feb2021 and presented to the hospital on 26Feb2021 with severe respiratory distress. Currently intubated/paralyzed with severe Acute respiratory distress syndrome (ARDS) and pulmonary fibrosis. Unknown if any correlation, Adverse event start date was on 26Feb2021. Adverse event resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization, Life threatening illness (immediate risk of death from the event). Adverse event treatment included: Intubation/paralytics. Prior to vaccination, it was unknown if the patient was diagnosed with COVID-19 and since the vaccination, the patient was not been tested for COVID-19. The outcome of the events was not recovered.; Sender's Comments: A contributory role of BNT162B2 to events respiratory distress, Acute respiratory distress syndrome (ARDS) and pulmonary fibrosis cannot be excluded based on temporal association. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Malignant neoplasm of sigmoid colon
Andere Medikamente: TAMSULOSIN; LONSURF; ZESTORETIC; COLACE; LEVSIN/SL
Allergien: -
Vorherige Impfungen: -

VAERS 1112323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 25.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Computerised tomogram Dysarthria Electrocardiogram Facial paralysis Laboratory test Magnetic resonance imaging Monoplegia Movement disorder Transient ischaemic attack

Symptomtext

TIA approximately 2 days later. PT had unilateral facial paralysis, dysarthria, and arm/leg paralysis. Non-ambulatory, unable to use right arm or right legs. Could not lift. Admitted to hospital. CT scan negative for acute stroke. Pt had complete resolution of all symptoms with 6 hours of admission. Felt to represent TIA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: CT, MRI, EKG, blood draw
Aktuelle Erkrankungen: none
Vorgeschichte: pcos cervical cancer bipolar disorder
Andere Medikamente: buproprion-150XL prozac 20 mg xanex .25 (as needed) methocarbomal (750)
Allergien: sudafed (anaphalaxis) morphine (hives)
Vorherige Impfungen: -

VAERS 1110710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NE
Alter: 67,0
Geschlecht: F
Eingang: 18.03.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Dizziness Fatigue Headache Injection site pain Pain Pyrexia Syncope

Symptomtext

About 12hours after the vaccination I had a 101.3 fever (normally 98.1) Body aches; when I got up about 9am the next morning I was dizzy and then fainted. The fever persisted until mid afternoon that day, as did the body aches, and a headache. I spent the day dozing or sleeping. I did eat some oatmeal and have a cup of black coffee about noon. That helped the headache. That evening I was more tired than usual, but no fever or aches. The next day I was also very tired, but I did go to work. The rest of the week I had no energy, but that was the only other side effect. After the first shot, I had only had an achy arm at the injection site that persisted for 2 or 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypo-thyroid
Andere Medikamente: Synthroid-125mcg, premarin-125 mg, B-complex vitamin, Calcium-magnesium-zinc, melatonin,-5mg, Omega-3 fatty acid, Alpha Lipoic Acid and Acetyl L-Carnitine HCL, Ashwagandha-L-Theanine
Allergien: Sulfa antibiotic, Toradal (anti-non-steroidal anti-inflamatory pain med.), codeine
Vorherige Impfungen: I had had an influenza vaccination in Oct 2020. I felt somewhat fluish. 101.8 temp, aches, chills, for 1 day. Only time I have h

VAERS 1109279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 59,0
Geschlecht: M
Eingang: 17.03.2021
Impfdatum: 23.02.2021
Beginn: 08.03.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: SYR / LA

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

Brain stem stroke Dizziness Electrocardiogram normal Magnetic resonance imaging abnormal

Symptomtext

Dizziness the afternoon after the second shot on 23 Feb 2021 On 8 Mar 2021 experienced extreme dizziness. Call 911. Went to Hospital. Dr treated a brain stem stroke.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Brain stem stroke
Hospital-Tage: 10,0
Labordaten: Stroke tests (MRI, EKG, etc) performed at hospital on 8-9 Mar 2021
Aktuelle Erkrankungen: none
Vorgeschichte: None
Andere Medikamente: Lipitor
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1108339

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VA
Alter: 52,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Chills Dyspnoea Facial paralysis Hypoaesthesia Pain

Symptomtext

5 hours after injection patient experienced numbness on right side of face as well as facial drooping. This lasted about 2 hours. About 7 hours after injection patient experienced labored breathing, chills and body aches; these symptoms lasted for about 36 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Topamine 25mg daily Meloxicam 15mg prn 1 fish oil daily 1 Centrum daily
Allergien: nka
Vorherige Impfungen: -

VAERS 1107771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OK
Alter: 68,0
Geschlecht: F
Eingang: 17.03.2021
Impfdatum: 03.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Computerised tomogram head normal Facial paralysis Laboratory test normal Magnetic resonance imaging head normal Taste disorder

Symptomtext

Got COVID shot March 3, then had some alteration of taste around March 8 or so, then L facial paralysis consistent w Bell Palsy on March 11.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: 1,0
Labordaten: Labs OK. CT and MRI brain normal.
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, hyopthyroidism, obesity, type 2 DM
Andere Medikamente: amitriptyline, vitamin D, fluoxetine, Norco, Basaglar, levothyroxine, lorazepam, losartan, metformin, pantoprazole, rosuvastatin, triam-HCTZ
Allergien: -
Vorherige Impfungen: -

VAERS 1105352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 52,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 11.03.2021
Beginn: 14.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Arteriogram carotid normal Arthralgia Chest pain Dyspnoea Electrocardiogram QT prolonged Electrocardiogram T wave abnormal Electrocardiogram T wave inversion Electrocardiogram abnormal Neck pain Pain Pericarditis Troponin

Symptomtext

Patient woke with severe chest pain and difficult to take deep breaths. Chest pain extended over her shoulder and around her neck. Pain worsened during the day, went to ER, found to have positive troponins and subsequent ecg were abnormal. Echo was negative and angiogram showed no blocked arteries. Cardiologist diagnosed her with pericarditis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 2,0
Labordaten: Troponin 3/14/21 @1445 was 0.255, @ 2008 was 0.218 and 3/15/21 at 0002 was 0.159 EKG - 3/14/21 - low voltage qrs and t wave abnormality EKG - 3/15/21 - prolonged QT interval or TU fusion, Diffuse T Wave Inversions anterior and lateral leads ? Ischemia Cardiologist diagnosed her with pericarditis
Aktuelle Erkrankungen: none
Vorgeschichte: gastroparesis, hoshimoto hypothyroidism, epilepsy
Andere Medikamente: omeprazole, Synthroid, venlafaxine, vitamin
Allergien: Tree fruits
Vorherige Impfungen: -

VAERS 1105164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: GA
Alter: 19,0
Geschlecht: F
Eingang: 16.03.2021
Impfdatum: 16.03.2021
Beginn: 16.03.2021
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

Approximately 5 mins after vaccine administration, patient became lightheaded and fainted. Patient regained consciousness and recovered quickly.

Weitere VAERSDATA-Felder

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

VAERS 1104844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

schwer

Staat: AL
Alter: 20,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / AR

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

Dizziness Syncope

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

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

VAERS 1104680

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 68,0
Geschlecht: M
Eingang: 16.03.2021
Impfdatum: 22.02.2021
Beginn: 12.03.2021
Tage bis Beginn: 18,0
Dosis: 2
Route/Site: IM / RA

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

Blood test Computerised tomogram head Confusional state Electrocardiogram Fall Generalised tonic-clonic seizure Magnetic resonance imaging head Magnetic resonance imaging neck Postictal state Urine analysis

Symptomtext

On 03/12/2021 at 0630 fell out of bed, wife witnessed tonic clonic seizure of 5+ minutes duration, when EMS arrived patient was postictal (confusion).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Generalised tonic-clonic seizure
Hospital-Tage: 3,0
Labordaten: 03/12/2021 CT Head WO Contrast. 03/13/2021 MRA Head W/WO Contrast, MRA Neck W/WO Contrast. 03/13/2021 MRI Brain W/WO Contrast. 03/12/2021 EKG. 03/12, 13, 14/2021 Numerous Blood and Urine Tests
Aktuelle Erkrankungen: Hypertension.
Vorgeschichte: Prosthetic aortic valve.
Andere Medikamente: Losartan 50 mg, once daily, OTC Multivitamin, once daily, OYC Zinc 15mg, once daily.
Allergien: None.
Vorherige Impfungen: -

VAERS 2194023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: -
Geschlecht: U
Eingang: 12.03.2021
Impfdatum: 06.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Hypotension Loss of consciousness Presyncope

Symptomtext

Hypotensive, vasovagal, passed out w/LOL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP 103/62
Aktuelle Erkrankungen: None
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril Prilosec citalopram calnthalidal coreg simvastatin
Allergien: -
Vorherige Impfungen: -

VAERS 1096097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: IL
Alter: 66,0
Geschlecht: F
Eingang: 12.03.2021
Impfdatum: 24.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 8,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Computerised tomogram Electrocardiogram Electroencephalogram Magnetic resonance imaging Seizure Tremor Unresponsive to stimuli

Symptomtext

Had a Seizure and was transported to hospital by Ambulance, was admitted and kept overnite to run test. Shaking and Unreponsive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: 2,0
Labordaten: Blood Tests, C.T. Scan, EEG, EKG, and MRI on March 4th and 5th
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic Kidney Disease, Diabetes, Hypertension, Hypothyroid, Sleep Apnea, Angina
Andere Medikamente: Insulin, blood pressure medications, angina medicine, pepcid, vitamin C, Iron, Vitamin D3
Allergien: ShellFish, Iodine, Tetracycline
Vorherige Impfungen: -

VAERS 1092521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MO
Alter: 78,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 24.02.2021
Beginn: 05.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: SYR / LA

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

Bell's palsy Faecaloma Full blood count Magnetic resonance imaging head

Symptomtext

Bells Palsey, currently impacted, recovering, prednisone, valacyclovir

Weitere VAERSDATA-Felder

Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: MRI Brain-3/5/21 CBC with differential-3/5/21 Saline Lock IV-3/5/21
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes, heart murmur, under active thyroid, kidney disease
Andere Medikamente: Apsirin, bisoprolol-hydrochlorothiazide, fish oil, glucosamine-chondroitin oral, lancets, levothyroxine, lisinopril, metformin, multi-vitamin, omeprazole, sim a statin, trazodone
Allergien: Penicillin, Erythromycin
Vorherige Impfungen: -

VAERS 1091624

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 28.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dyspnoea Respiratory distress Wheezing

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Additional Details: patient states that exactly 5 hours after receiving vaccine she went into respiratory distress, she had an albuterol treatment at home which she used and it relieved her distress..then stated that it happened again 5 days later..she says she sometimes has some breathing problems in the fall but never to the degree that it happened after the vaccine...lots of wheezing and gasping for air, no other adverse effects

Weitere VAERSDATA-Felder

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

VAERS 1086493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: HI
Alter: 51,0
Geschlecht: M
Eingang: 11.03.2021
Impfdatum: 02.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Alanine aminotransferase normal Aspartate aminotransferase increased Blood cholesterol increased Blood triglycerides normal Brain natriuretic peptide increased C-reactive protein increased Chest pain Computerised tomogram thorax normal Dyspnoea Echocardiogram abnormal Myocarditis SARS-CoV-2 test negative Ejection fraction decreased Electrocardiogram PR segment depression Electrocardiogram ST segment elevation Fatigue Headache High density lipoprotein normal

Symptomtext

Case developed Chest Pain, dyspnea 1 day after last dose. Dx: Likely vaccine induced Myocarditis. Admitted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 3,0
Labordaten: 03/05/21 : C-Reactive Pro: 20.94 03/05/21: Troponin I Cardiac: 13.568 03/05/21: SAERS-CoV-2 PCR: (-)
Aktuelle Erkrankungen: Paraparesis (LE's)
Vorgeschichte: Spinal cord injury (T12 FX) 2003 Constipation Recurrent UTI HLD Herpes Zoster Osteopenia/osteoporosis OSA Tinnitus ED
Andere Medikamente: Docusate: 100mg PO BID Sildenafil: 25mg PO PRN Ketoconazole Shampoo 2% topical PRN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1077273

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

schwer

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 11.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Amnesia Dizziness Tachycardia Tremor Anaphylactic reaction Blood test Chest X-ray Computerised tomogram Dyspnoea Flushing Hypersomnia Hypertension Loss of consciousness Palpitations

Symptomtext

I was told that 5-7 minutes after my shot had been administered that I was having trouble breathing. Had an Anaphylaxis reaction. Passed out. 911 was called. Epi pen was given in my left thigh. I woke up and had no clue who I was or what had happened. Paramedics arrived. Body was flush. Blood pressure was high. Heart was racing. Taken to ER at Medical Center. Admitted to hospital. Spent two days in hospital. Came home on Saturday and have been sleeping almost all day, every day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: 2,0
Labordaten: I was told that I had a CT Scan, chest x-rays, lots of blood work and I don't remember what else they did.
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, Irregular Heart Beat, Enlarged Thyroid, GERD, Low Blood Sugar, IBS, POTS, Sleep Apnea
Andere Medikamente: Premarin, Lisinopril, Lexapro, IC Levothyroxine, IC Gabapentin, Singulair tabs, Flovent inhaler, fish oil pill, Vitamin D, Multi-vitamin, Aspirin, Omeprazole
Allergien: Codeine, IV Contrast Dye, Phenergan, Dairy, Guaifenesin, Adhesive
Vorherige Impfungen: -

VAERS 1088606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NM
Alter: 38,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
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 hot Injection site pain Loss of consciousness Myoclonus Pallor Vomiting

Symptomtext

?Pfizer-BioNTech COVID-19 Vaccine EUA" 5 minutes after administration of Pfizer COVID vaccine, patient passed out for less than a minute. Patient was alert, knew where he was and what had just happen. He stated he was not experiencing chest pain, shortness of breath, no rash observed. Patient stated he tends to pass out at the site of needles or when he was blood drawn. 10 minutes after passing patient begin to feel lightheaded, skin tone become very pale and patient stated he was hot. Patient passed out a 2nd time and experience 2 body jerk movements for less than a minute. Epi Pen was administered to the patient. Paramedics were called to the scene. Patient become alert and patient stated he need to vomit. Patient vomited profusely. Vitals were taken: BP 100/60mmhg, O2 stat 97%, Temperature 96.5F. Paramedics arrived at scene. Paramedics spoke with patient let him know his vitals were stable and if he would like to be taken down to the ER. Patient declined stated he was feeling much better. On 3.10 patient was contacted and he stated he was feeling great, just experiencing soreness at the site on Pfizer vaccine and Epi pen administration site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No, illnesses at the time of vaccination and up to one month prior to COVID vaccine.
Vorgeschichte: No, chronic or long-standing health conditions.
Andere Medikamente: Patient was not taking any prescription, OTC, dietary supplements or herbal remedies at the time of vaccination.
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1087780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 19,0
Geschlecht: M
Eingang: 10.03.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Loss of consciousness Nausea Syncope

Symptomtext

After receiving first dose and in the observation room, patient was feeling light headed and nauseated. Patient passed out briefly for 2-3 seconds and slumped in his chair. EMT was with the patient at all times. After syncopy episode, patient was alert and oriented. Patient was brought to tent in the supine position and was stable. Patient was still alert and oriented and given juice. Dr. looked patient over and determined to be vasovagal episode. Patient fine 20 minutes post episode. Patient was monitored until sister came to pick him up. Dr. recommended for patient get vaccine recumbrant in 3 wks for second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NO
Vorherige Impfungen: -

VAERS 1086378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 26,0
Geschlecht: M
Eingang: 09.03.2021
Impfdatum: 04.03.2021
Beginn: 04.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Electrocardiogram abnormal Feeling of body temperature change Flushing Hyperhidrosis Palpitations Syncope Ventricular arrhythmia Vision blurred

Symptomtext

Vision blurring, cold sweat, racing heart rate, flushing and syncope 5 minutes post-injection. EKG showed ventricular arrhythmia which converted to normal sinus rhythm with regaining consciousness approximately 5 minutes later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG - ventricular arrhythmia
Aktuelle Erkrankungen: None
Vorgeschichte: Crohn?s Disease
Andere Medikamente: Humira
Allergien: None
Vorherige Impfungen: -

VAERS 1085646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CO
Alter: 41,0
Geschlecht: F
Eingang: 09.03.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Bell's palsy Cough Hypoaesthesia Paraesthesia

Symptomtext

On my way home from receiving my first vaccination my right side of my face started going numb and tinging (like I had a dental procedure). This continued and progressed into my right arm. About an hour later tried to eat something and started coughing. Called public health and ask a nurse and was told to go to the ED for possible stroke. Was assessed and later discharged. Following up on 2/25/21 with primary care team. Was assessed and diagnosed with Bells Palsy and given steroids prescription to begin on Friday (2/26/21).

Weitere VAERSDATA-Felder

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

VAERS 1085152

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 09.03.2021
Impfdatum: 09.03.2021
Beginn: 09.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Syncope

Symptomtext

Snycopal episode immediately following vaccination, patient was lowered to floor, BP slightly low at 92/40. Patient diaphoretic, brought to cot. Evaluated client after fifteen minutes, sent home via medical transport.

Weitere VAERSDATA-Felder

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

VAERS 1082809

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 32,0
Geschlecht: F
Eingang: 08.03.2021
Impfdatum: 08.03.2021
Beginn: 08.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Feeling hot Flushing Head injury Hot flush Hyperhidrosis Loss of consciousness Palpitations Seizure

Symptomtext

Client seated in observation Client lost consciousness (passed out) and fell out of her chair Client fell onto the floor on the left side hitting the side of her head (left temple area) Witness nearby reports the client had a seizure first prior to falling out of the chair Seizure activity was not witnessed by the nurse Client was assisted into a wheelchair and evaluated further in a private area by EMT EMT was present. EMT assessed client and vitals were taken at 9:36 : O Sat 99%, Pulse 53, BP 112/56 Client was able to report that she felt flushed and hot. Client is visibly sweating Client states that she felt like her heart was racing and that she was dizzy Client reports that she has no history of seizures. Client was offered water Nurse called for an ambulance (EMS) and spoke with dispatch Client drove herself and has no one with her The client?s status given included details regarding client?s vehicle Client voiced concern about the cost of an ambulance but decides that she would like to be taken to hospital which is in network with her insurance At 9:43 Client reports that she feels ?heat inside her head? and is feeling very dizzy A 9:46 EMS arrives on site At 9:49 Client was transported via stretcher

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth control
Allergien: None
Vorherige Impfungen: -

VAERS 1079864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 83,0
Geschlecht: M
Eingang: 07.03.2021
Impfdatum: 23.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 9,0
Dosis: 1
Route/Site: IM / LA

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

CSF protein increased Dyspnoea Guillain-Barre syndrome Magnetic resonance imaging normal Musculoskeletal disorder Respiratory failure

Symptomtext

9 days after receiving vaccine, pt developed rapid onset of ascending paralysis. No use of legs, minimal use of right arm. Limited use of left arm. Repiratory difficulty/failure.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: -
Labordaten: increased protein in CSF. No changes on MRI.
Aktuelle Erkrankungen: Recovering from Guillain-Barre Syndrome triggered by COVID December 2020. Was ambulatory again at the time of vaccination.
Vorgeschichte: h/o CAD. s/p CABG x 5 10 years ago.
Andere Medikamente: None.
Allergien: Abalone.
Vorherige Impfungen: -

VAERS 1078369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: KY
Alter: 26,0
Geschlecht: F
Eingang: 06.03.2021
Impfdatum: 06.03.2021
Beginn: 06.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Syncope

Symptomtext

PATIENT EXPERIENCED SYNCOPE IN OBSERVATION AREA AFTER VACCINATION. WAS TREATED BY EMS ON SITE BUT NOT TRANSPORTED

Weitere VAERSDATA-Felder

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

VAERS 2194040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MT
Alter: 71,0
Geschlecht: F
Eingang: 05.03.2021
Impfdatum: 02.03.2021
Beginn: 04.03.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Facial paralysis

Symptomtext

Right side of face "drooping" 2 days after getting second covid vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes Mellitus Type 2
Andere Medikamente: acyclovir, alendronate, AMLODIPINE, Calcium Carbonate, Chlorhexidine, estradiol
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1076232

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: TX
Alter: 19,0
Geschlecht: M
Eingang: 05.03.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Disorientation Dyskinesia Fall Head injury Headache Loss of consciousness Nausea Pallor Pupillary reflex impaired

Symptomtext

Patient ambulated to general observation, sat in chair and suddenly fell straight back and slammed back of head on floor. Patient was unconscious, pale. Immediately turned onto left side. within a few seconds began having generalized rigid jerking for approx 5 sec, then patient came too, sat straight up, disoriented looking around. Able to recall name. states he was here for covid vaccine. Assisted to w/c by 2 EMT's and taken to private observation area. Patient c/o nausea and head pain. Color pale. Has an almond size swollen area at posterior base of head. Initial VS - BP 90/p; HR 53; O2 91% on room air. Responding to questions, but states he feels disoriented. Bilateral pupils 3cm with right reacting sluggish. Patient states he is a student. EMT attempted to contact patient's father and LVM. Patient's step mother returned called. Informed her that patient is being transported to Hospital downtown FW for further eval. She asked him what did she need to do. Nurse informed that his vehicle will be left at the vaccine location and he will need assistance pending hospital eval. Patient then called his boss to notify him that he will not be at work tonight. Patient states that he had a reaction to his first HPV - states he fainted, but completed the series without further problems. Repeat VS at 1550 BP 90/p; HR 67, O2 98%. Color remains very pale. EMS activated. patient states he needs to lie down. Assisted to stretcher per EMT, elevated legs, cushion under head with ice packs on back of head. 1602 EMS arrived, BP 121/75; HR 69 O2 100% on room air. Transferred to stretcher 1605 Patient transported to Hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: past history of ADH
Andere Medikamente: None
Allergien: Seasonal allergies, NKDA
Vorherige Impfungen: Fainted with first dose of HPV

VAERS 1070965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 73,0
Geschlecht: M
Eingang: 03.03.2021
Impfdatum: 24.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / AR

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

Angiogram cerebral Arteriogram carotid Blindness unilateral Computerised tomogram head Echocardiogram Embolic stroke Magnetic resonance imaging head Retinal artery occlusion Ultrasound Doppler

Symptomtext

right sided embolic stroke, right retinal artery occlusion occurred 8 hours after vaccination, requiring hospitalization for 2 days, he is now left with right eye visual loss as the only sequelae to the stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: 2,0
Labordaten: MRI brain, MRA of brain, CT brain, CT Angio of the head and neck, ECHO, carotid ultrasound, all done on 2/24/21 and 2/25/21
Aktuelle Erkrankungen: HTN, CHOL, Gout
Vorgeschichte: HTN, CHOL, Gout
Andere Medikamente: asa 81 mg daily, crestor 10 mg daily, uloric 40 mg daily, valsartan 80 mg daily
Allergien: none
Vorherige Impfungen: -

VAERS 1069289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MD
Alter: 58,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 03.03.2021
Beginn: 03.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Fatigue Hypotension Lethargy Syncope Unresponsive to stimuli

Symptomtext

Systemic: Exhaustion / Lethargy-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Hypotension-Severe, Systemic: Weakness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1069175

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 44,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Condition aggravated Hypersensitivity Hypertension Neck pain Seizure Tachycardia Tremor Urticaria

Symptomtext

Symptoms were: general allergic reaction with hives followed by a seizure and spontaneous recovery. Pt relates Seizure was consistent with her normal seizures but slightly worse. She had a seizure 1 week ago and has seizures in clusters, this was consistent with the waning period of the current cluster. Vital signs were (abnormal with tachycardia and hypertension on arrival to the ED). Exam was notable for neck pain. Patient was treated with Benadryl on scene and with Toradol and fluids in the ED and symptoms recovered but multiple shaking episodes characterized by patient as seizure. Patient was observed in the emergency department for an extended period.

Weitere VAERSDATA-Felder

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

VAERS 1068919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: DC
Alter: 65,0
Geschlecht: F
Eingang: 03.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Chills Diarrhoea Dizziness Fatigue Hyperhidrosis Injection site pain Loss of consciousness Nausea Sleep deficit Sleep disorder Sneezing

Symptomtext

Pronounced pain at injection site started around 6pm, the day of the shot, 3/2/2021. After 8pm, started going downhill with chills and some sneezing. Managed to get to sleep, but woke up at 1:15 am and could not get back to sleep. Feeling chilled all night. At 5:30 am, got out of bed to take Tylenol and experienced dizziness (briefly blacked-out), sweats, nausea (vomited) and slight diarrhea. After that episode, started to feel a little better, though still a bit woozy and exhausted from lack of sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Zyrtec 10 mg tablet daily Estradiol 0.5 mg tablet daily Bisoprolol HCTZ 2.5-6.25 mg tablet daily Lunesta 3 mg tablet at night
Allergien: None
Vorherige Impfungen: -

VAERS 1067445

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 02.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
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 Dyskinesia Feeling hot Nausea Seizure like phenomena Unresponsive to stimuli

Symptomtext

patient c/o feeling nausea and hot. patient then asked for water. patient then became unresponsive for approximately 30 seconds. seizure like active noted, patient began to have involuntary movement of upper and lower extremities that lasted approximately 10 seconds. Patient accessed for gag reflex and then offered water upon becoming responsive.Patient tolerated water well. Patient offered wet paper towels. Skin noted to be cool and clammy.Vital signs assessed noted to be BP 105/74 and HR 69. Patient alert and oriented x 3,placed in wheelchair for continued observation. Mother stated that syncope activity is normal for patient upon receiving injections or blood draws,seizure like activity is not normal per mother. Patient taken to observation area by paramedic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure like phenomena
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE VOICED
Vorgeschichte: NONE VOICED
Andere Medikamente: EFFEXOR, MOTHER AND PATIENT STATED HE IS CURRENTLY ON ANOTHER ANTI-DEPRESSION BUT THEY ARE UNSURE OF THE NAME
Allergien: NONE FOR PATIENT, BUT MOTHER STATES FAMILY HISTORY OF PCN ALLERGRY
Vorherige Impfungen: mother stated every time patient has injections or blood draws

VAERS 1067214

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 02.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Dysarthria Syncope

Symptomtext

After vaccination, patient had slurred speech and syncopal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Reported history of syncope.
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1066748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
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 Chest pain Dizziness Syncope

Symptomtext

PATIENT RECEIVED FIRST DOSE OF PFIZER VACCINE TODAY. AFTER 30 MINUTES OF OBSERVATION PATIENT COMPLAINED OF FEELING FAINT AND HAD A SYNCOPALL EPISODE. PATIENT WAS ASSISTED TO THE FLOOR ,VITALS SIGNS TAKEN AND MONITORED BY HEALTH CARE PROFESSIONAL. PATIENT COMPLAINED OF CHEST PAIN BUT UNABLE TO RATE PAIN . AED MACHINE APPLIED PATIENT IN SINUS RYTHM WITH BP 130/90,HR 88 ,BLOOD GLUCOSE 102 AND SPO2% 99% ON ROOM AIR. 911 CALLED .PATIENT WAS ALERT AND TRANSPORTED TO MEDICAL CENTER BY EMERGENCY MEDICAL SERVICES

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: admitted to hospital 2 weeks ago for severe allergic reaction to chlorohexidine
Vorgeschichte: hypertension ,panic attack and sleep disorder
Andere Medikamente: hypertensive medication and sleep medications
Allergien: chlorohexidine
Vorherige Impfungen: -

VAERS 1066605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Anaphylactic reaction Lip swelling Urticaria

Symptomtext

Swollen lips, mild anaphylaxis, hives all started 60 minutes after vaccination. We traveled from our home (approx 2 hr drive) & were on road. My husband is a physician & when we noticed symptoms administered Benadryl, Claritin, & famatodine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: Still observing symptoms as had vaccine roughly 4 hours ago. The above actions have helped & my husband who is a physician is observing me at home & we have epipen on standby, if need be.
Aktuelle Erkrankungen: No acute illness
Vorgeschichte: chronic kidney disease
Andere Medikamente: None
Allergien: Sulfa drugs, kiwi, amoxicillin, peanuts, IV contrast dye, aspartame
Vorherige Impfungen: -

VAERS 1066048

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 02.03.2021
Beginn: 02.03.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

Patient had a syncope episode aprox. 30 minutes after administration. She passed out while in observation. Paramedics on scene responded and gathered information. She passed out again and at that point she was put on the stretcher and brought to a nearby hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Lupus, stent placement (past heart attack, unknown date)
Vorgeschichte: Lupus, stent placement (past heart attack, unknown date)
Andere Medikamente: blood thinner (unknown),
Allergien: sulfur
Vorherige Impfungen: -

VAERS 1061658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: UT
Alter: 60,0
Geschlecht: F
Eingang: 02.03.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Arthralgia Fatigue Migraine Myalgia Seizure Syncope

Symptomtext

Seizure: Sunday 2/28 @noon Migraines: 2/28 post seizure & 3/1 & 3/2 Pre-seizure symptoms: 3/1 & 3/2 ExtremeMuscle&Joint pain, fatigue, Ubrelvy 100mg 2/28 & 3/2, Ibuprofen 800mg, alt w/Tylenol 2-500mg, Rest/sleep most of days, warm showers, heating pads

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Sinus infection
Vorgeschichte: Seizures migraines, Depression, ibs-c
Andere Medikamente: Zonegran, Vimpat, Venlaflaxine, Trazadone, Nexium, Magnesium, Vitamin D-3, HCL Pepsin, Vitamin Code, Super Enzymes, Back on Tract, DGL Ultra, Christopher's Lower Bowel, Mag O7
Allergien: IVP dye, Levaquin, CEFDINIR, Trileptal, Depakote, Dilantin, Lexiscan,
Vorherige Impfungen: -

VAERS 1062952

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: PA
Alter: 33,0
Geschlecht: M
Eingang: 01.03.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Syncope

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: After vaccination, the vaccine recipient had a syncopal episode. They were observed by EMS. No further intervention required.

Weitere VAERSDATA-Felder

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

VAERS 1062725

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NJ
Alter: 44,0
Geschlecht: M
Eingang: 01.03.2021
Impfdatum: 28.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Hyperhidrosis Presyncope

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine EUA: During observation, vaccine recipient had a near syncope event. They were diaphoretic. They were monitored by the EMS. No further intervention.

Weitere VAERSDATA-Felder

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

VAERS 1062375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

schwer

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 01.03.2021
Impfdatum: 28.02.2021
Beginn: 28.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Chills Dysphagia Dyspnoea Flushing Hyperhidrosis Hypersensitivity Nausea Tachycardia Throat tightness Tremor

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Allergic: Difficulty Swallowing, Throat Tightness-Mild, Systemic: Chills-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Medium, Systemic: Tachycardia-Medium

Weitere VAERSDATA-Felder

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

VAERS 1061096

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: MA
Alter: 25,0
Geschlecht: F
Eingang: 28.02.2021
Impfdatum: 21.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Seizure

Symptomtext

Seizure after vaccine overnight. Patient has a history of seizures.

Weitere VAERSDATA-Felder

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

VAERS 1059525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 27.02.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Dizziness Fall Head injury Pain in extremity Syncope

Symptomtext

patient that fainted today. She reported on her screening questionnaire of passing out after receiving a injection. She was placed for 30 minute observation. The patient fainted several minutes after being seated. It was observed that she fell over from the chair and hit her head. Patient denied any symptoms other than her right toe being sore.. A + O x 4 medically stable. VS stable. EMS was dispatched due to patient hitting her head and c/o feeling dizzy still...however, patient declined services. She was with her husband and he agreed to drive her home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: none
Allergien: N/A
Vorherige Impfungen: As a child

VAERS 1059016

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: OH
Alter: 59,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Dizziness Dysgeusia Hyperhidrosis Loss of consciousness Paraesthesia

Symptomtext

Patient began to deeply sweat, was lightheaded, dizzy, and was blacking out. It started 3 minutes after she received the vaccine and also started with a weird iron taste in her mouth, and tingling in her hands. She felt like she was going to pass out but got better after 20 minutes. The tingling in her hands continued though and would start and stop periodically.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Tecturna, atenolol, atorvastatin
Allergien: biaxin (mouth/throat closes)
Vorherige Impfungen: -

VAERS 1058909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 26.02.2021
Beginn: 26.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Syncope

Symptomtext

Approximately 4 minutes post vaccine pt fainted in chair during obs. Pt transferred to gurney, RRT called at 0840, they arrived 0846. Denies high BP. Vitals taken (0843)198/95, HR 96 o2 97% T-98.6. Pt comes to and reports hx of fainting with needles and nausea. No medical hx. Currently feels better and refuse to go to ER x3. V/s(0846) 195/95 HR 81 o2 97%. Husband by bedside fans pt. Continues to refuse ED service. (0855) 124/60 HR 81 o2 97% RRT left at 0852. Pt became anxious 0942 BP 173/81 HR 83 o2 97% pt wants to be released home AAO. D/C @ 0945 with husband.

Weitere VAERSDATA-Felder

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

VAERS 1058802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 26.02.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Syncope Visual impairment

Symptomtext

Near syncope on escalator - vision started to go black. BP 114/74, pulse 78, 99% O2.

Weitere VAERSDATA-Felder

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

VAERS 1055665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 70,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blindness transient Dizziness Feeling abnormal Syncope

Symptomtext

Dizziness; faint; feeling of falling off my chair; vision went black.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Anal Cancer; Dry Eyes; Chronic Gastritis; Lactose Intolerance; Arthritis
Andere Medikamente: Aspirin; Vitamin D; Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 1055186

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Craniocerebral injury Dizziness Fall Headache Loss of consciousness Vomiting

Symptomtext

Felt lightheaded getting up in the observation area. Fell struck head lost consciousness times one minute. Complained of mild headache which cleared while being observed. Drank OJ and vomited it. No further nausea. Denies dizziness, neck pain, double vision, amnesia. Recovered fairly quickly while resting. Felt much better. Refused transport. Taken home by husband with instructions to monitor LOC. Follow up with family MD advised.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: BP 118/73, PR 55, PO2 98%.
Aktuelle Erkrankungen: Post pertem depression; Previous neprectomy for reflux and sepsis
Vorgeschichte: As above
Andere Medikamente: Trazadone, Prozac
Allergien: None
Vorherige Impfungen: -

VAERS 1055050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: KS
Alter: 43,0
Geschlecht: F
Eingang: 25.02.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Asthenia Blood pressure abnormal Dizziness Hypotension Respiratory distress Skin discolouration Swollen tongue

Symptomtext

A 43 y.o. female received her first dose of the COVID 19 vaccination. She was given the Pfizer vaccination in the right deltoid muscle. During her 15 minute waiting period after the injection, the patient began to experience lightheadedness and feeling weak. She denied rash, hives, welts, difficulty breathing, difficulty swallowing, wheezing, throat tightness, hoarseness, stridor, itching, facial swelling, lip swelling and tongue swelling. This provider was notified of patient reaction and she was then assessed in the emergency bay area. Monitored patient for severe reaction symptoms, including but not limited to blood pressure abnormality , hypotension, rapid progression of symptoms, respiratory distress, skin changes and tongue swelling. PMH: anxiety and bipolar. Takes Aripiprazole for this. No other medical history reported. ALLERGY REVIEW OF SYSTEMS: Patient complains of dizziness (lightheaded), Patient denies chills, fever, malaise/fatigue, facial swelling, sore throat, frequent throat clearing, eyes itching, cough, chest tightness, shortness of breath, wheezing, rash, hives, eczema, cysts, itching of skin, abdominal pain, joint pain and headaches. Previous Reactions: none. Vitals -- 02/19/21 0350 02/19/21 1610. BP: 131/77 125/77. Pulse: 89 75. Resp: (!) 22 16. SpO2: 100% 100% Physical Exam--Vitals and nursing note reviewed. Constitutional -- General: She is not in acute distress. Appearance -- Normal appearance. She is well-developed. She is not ill-appearing, toxic-appearing or diaphoretic. HENT: Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Comments: Clear oral airway/intact Eyes: Conjunctiva/sclera: Conjunctivae normal. Neck: Thyroid: No thyromegaly. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. No wheezing. Musculoskeletal -- Cervical back: Neck supple. Skin -- General: Skin is warm and dry. Capillary Refill: Capillary refill takes less than 2 seconds. Neurological -- General: No focal deficit present. Mental Status: She is alert and oriented to person, place, and time; Gait: Gait normal. Psychiatric -- Mood and Affect: Mood is anxious; Behavior: Behavior normal; Thought Content: Thought content normal; Judgment: Judgment normal. Assessment/Plan -- Treatment included: water and snacks. Follow up response to treatment: good. Patient discharge: Stable to go home and follow up with PCP; Differential Diagnosis: Vaccine-Related Anxiety (include misc mental health). Pt aware of monitoring symptoms at home. Follow up as needed with pcp. Recommend that she eat a snack and hydrate prior to next vaccine #2 of Pfizer.

Weitere VAERSDATA-Felder

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

VAERS 1048741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VA
Alter: 47,0
Geschlecht: M
Eingang: 25.02.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Hyperhidrosis Pallor Presyncope

Symptomtext

~10 minutes after receiving second dose of Pfizer COVID vaccine while sitting in the waiting area, I started feeling light headed and I thought I was going to pass out. Medical personnel in the waiting area came over, had me lay down and provided cold packs. They stated this was likely a vasovagal like response. When I have donated blood in the past I have had a very similar reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: local medical professionals did take my blood pressure, heart rate and temperature after the event, these were all normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1048741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: VA
Alter: 47,0
Geschlecht: M
Eingang: 25.02.2021
Impfdatum: 22.02.2021
Beginn: 22.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

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

Dizziness Hyperhidrosis Pallor Presyncope

Symptomtext

~10 minutes after receiving second dose of Pfizer COVID vaccine while sitting in the waiting area, I started feeling light headed and I thought I was going to pass out. Medical personnel in the waiting area came over, had me lay down and provided cold packs. They stated this was likely a vasovagal like response. When I have donated blood in the past I have had a very similar reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: local medical professionals did take my blood pressure, heart rate and temperature after the event, these were all normal.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1052596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: -
Alter: 35,0
Geschlecht: F
Eingang: 24.02.2021
Impfdatum: 24.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood pressure increased Confusional state Facial paralysis

Symptomtext

Increased BP, Confusion, Facial Droop

Weitere VAERSDATA-Felder

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

VAERS 1052058

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 56,0
Geschlecht: F
Eingang: 24.02.2021
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anxiety Dyspnoea Immediate post-injection reaction Loss of consciousness Urinary incontinence

Symptomtext

Prior to receiving vaccine, vaccinator stated patient had increased ?anxiety? making statements such as ?I?m going to die! This vaccine is going to kill me!? Immediately after receiving vaccine (less than 3 seconds) patient slumped down in chair, writer to the patient, patient stating ?I can?t breathe, its going dark, I?m going to die! What about my daughter!? Writer and vaccinator attempted to talk patient down, ineffective. Patient V/S 100/60, 66-HR, 98%-O2, 22-Resp. Patient became limp in chair, unresponsive, episode of urinary incontinence, EMS activated. ~90 seconds into episode patient regained consciousness, A&Ox4, stating ?I?m back. I?m back.? Patient reports this last happened to her ?in college?. Patient also states ?my doctor told me not to get the vaccine, to wait until August since I have Lyme Disease.? Patient to ED with EMS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Reports Lyme Disease
Vorgeschichte: Adrenal Gland D/O Hypothyroid
Andere Medikamente: Synthroid Hydrocortisone
Allergien: PCN Epinephrine
Vorherige Impfungen: -

VAERS 1052032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 44,0
Geschlecht: M
Eingang: 24.02.2021
Impfdatum: 19.02.2021
Beginn: 19.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Seizure

Symptomtext

Patient had seizure, provider could not find pulse, administered 2 rounds CPR and applied AED, EMS notified. Patient alert and awake after 2 rounds CPR and was admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cancer
Vorgeschichte: Cancer
Andere Medikamente: Multiple
Allergien: PCN
Vorherige Impfungen: -

VAERS 1048839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

schwer

Staat: MA
Alter: 33,0
Geschlecht: F
Eingang: 23.02.2021
Impfdatum: 21.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Loss of consciousness

Symptomtext

Patient got unconscious. Patient was sent 911. After following up with facility, patient was stable and doing well. Patient was sent home that evening.

Weitere VAERSDATA-Felder

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

VAERS 1048744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: CA
Alter: 21,0
Geschlecht: M
Eingang: 23.02.2021
Impfdatum: 21.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hypotension Syncope

Symptomtext

Systemic: Syncope -Severe, Systemic: Hypotension-Severe, Additional Details: Reported blood pressure after 911 paramedics arrived was 56/59. Patient was transported to facility. Called facility 3 times to follow up, but no response yet from facility director. Will follow up again on 2/23/21 in the AM.

Weitere VAERSDATA-Felder

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

VAERS 1043255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

schwer

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 20.02.2021
Impfdatum: 20.02.2021
Beginn: 20.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Asthenia Blood pressure decreased Dizziness Fatigue Hot flush Loss of consciousness Nausea

Symptomtext

Patient presented for COVID vaccination today, first dose. Prior to receiving dose, she mentioned to RN that she has a history of vasovagal syncope following her shingles vaccine. She routinely has flu vaccines without any adverse reaction. RN requested I standby and observe while patient receives vaccine. Within minutes of receiving vaccine, patient endorses prodromal symptoms lightheadedness, hot flashes, then lost consciousness while seated in the chair. After approximately 1 minute, the patient did regain consciousness. She was given orange juice and crackers and felt well enough to ambulate to a chair in the observation area. Vital signs were WNL and she was monitored closely in the observing area. She continued to complain of "queasiness" often stating that she just feels that she would like to go lay down and nap in her car. Rechecked her blood pressure which dropped to 94/64, patient states she usually runs low but systolic within the low 100's. She was taken to a private hallway where she laid down on a stretcher. Blood sugar checked reading 121. She was given more water but she was uninterested in any more food, as she questions if the orange juice and the crackers were the cause of the queasiness. Blood pressure was rechecked and she was again WNL. Given her persistent fatigue and "queasiness", team lead contacted ED charge nurse to discuss case. The recommendation was to have the patient further evaluated. Discussed with team lead, and it was agreed upon that this was best course of action given her persistent symptoms. EMS was called. Per EMS report, patient's blood pressure did rise which patient attributed to excitement/anxiety surrounding the situation. Patient ultimately declined EMS transfer to ED. Her husband arrived to drive her home. Discussed the importance of monitoring symptoms for the next 48 hours. If she has any worsening "queasiness", weakness, fatigue, nausea/vominting, throat swelling, wheezing, dyspnea then she is to call 911 immediately. Patient verbalizes understanding and is agreeable to emergency services should any of these problems occur.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: denied
Vorgeschichte: denied
Andere Medikamente: n/a
Allergien: no known allergies
Vorherige Impfungen: Shingles

VAERS 2705729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MA
Alter: 80,0
Geschlecht: F
Eingang: 30.10.2023
Impfdatum: 02.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 16,0
Dosis: 2
Route/Site: IM / UN

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

Aspiration joint normal Blood test C-reactive protein abnormal Chills Colitis Colitis ulcerative Colonoscopy abnormal Condition aggravated Diarrhoea Enema administration Erythema Faecal calprotectin Fatigue Gastrointestinal disorder General physical health deterioration Haemorrhage Hypersomnia Hypertension

Symptomtext

She got her vaccine, and that went OK. Then what appeared to her on 3/18/21 she felt a lump on the left side of the back of her neck. Then on 3/20/21 after her shower her face was red and puffy and had diarrhea. On 3/25/21 she called her PCP and told her that her BP was very high. On 3/26/21 she had blood work done and the bump on her neck started to disappear on 3/27/21. She had an apt with her PCP on 3/29/21 and she told them on 3/31/21 the bump had gone. on 4/7/21 she was extremely exhausted, and on 4/8/21 she slept all day. On 4/14/21 she had diarrhea again. Her GI was acting up and she never associated it with the shot and she continued taking the vaccines. Her PCP checked her out and she did not know what was going on with her. She thinks she was given Pepto which did not help. She continued taking her shots. She completed 5 of them, and the last was 11/1/2022. She is lactose intolerant, and she is assuming that she may have had something that she should not have eaten and that's the way she was treating it. When her stomach got so very bad, and knew that things were not going well with her, the doctor said that she needed to see a gastroenterologist. she suffered for a year with her GI symptoms, and then had a colonoscopy on 9/12/22 and that revealed that she had ulcerated pancolitis. Her symptoms were diarrhea, progressed to bleeding, incontinence, chills. She had to have an 4 iron infusion as she had iron deficiency, she had a calprotectin test and it was 962, when the normal is 50 or less, it is now 8000. She was started with budesanine steroids for IBS, then she was given Mudecinine both of them worked for a little while, but not very long. This is the go to drug for this particular disease but it did not work for her. They kept giving her that and she continued to have enemas, and then she was started on Prednisone, which did help and she is on it still. She was at Hospital 2 weeks ago as her condition was getting worse and she was given an IV and that helped her somewhat. She was admitted on 10/17/23, and discharged on 10/21/2023. She had a flex-sigmoidoscopy and showed that it was moderate in the sigmoid and severe chronic colitis in the rectum. She has received 3 infusions of Remicade and the last one was on 10/18/23. She is on a tapering dose of Prednisone now and goes for her next infusion on 11/15/23. Her CRP and her ESR are now in the normal range where they were not. On 3/17/23 she was on Intebio and that worked for her for 3 months and then it stopped working, which was very unfortunate, and she felt like she was normal again with that. 11/14/21 she had a total knee replacement and when she went back to her surgeon for her check up on her knee they checked the inflammation rate and it was high. This was an indicator that something was wrong with her knee. He aspirated them, it was not the knee that had inflammation and this is how this all started to come together. Gastroelternolgist is Dr. Her mother had lupus and her sister had rheumatoid arthritis, and she is thinking that there could have been something in her immune system that she had a tendency for something like this to happen and thinks it was triggered by this vaccine that happened to her. She had never had a problem with anything like this prior to the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 4,0
Labordaten: Many blood works, infusions, colonoscopiles (4 in total).
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension, bilateral mastectomies in 2011 for breast cancer, 2014 thyroid and parathyroid cancer, osteoporosis.
Andere Medikamente: Synthroid, Amlodipine, Vitamin D, Citracal.
Allergien: Citrofloxicine, (GI upset), Latex (itching), gold, Silicone dioxicide, Sulfa (rash), Taxol (rash).
Vorherige Impfungen: Swine flu vaccine, extremely sick.

VAERS 2683628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: GA
Alter: 54,0
Geschlecht: F
Eingang: 19.09.2023
Impfdatum: 10.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Arrhythmia Cardiac monitoring Cardiac stress test Electrocardiogram Heart rate increased Palpitations

Symptomtext

I would like to report a possible adverse effect of Covid 19 because I have never experienced this kind of effect before until after COVID-19. I experienced an abnormal heart palpation or abnormal heart rhythm like no other palpations. I have experienced abnormal palpations before but sporadically. This recent heartbeat was fast and unusual. I was placed on another pill called Bisoprolol which I never had to take before and I am concerned about this effect because it appears I may have to take this medicine forever, and I don't want to take it at all. I want to know why there is a new fast palpation instead of being put on medications and left without any answers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: ECG, heart monitor, stress test
Aktuelle Erkrankungen: HBP
Vorgeschichte: HBP
Andere Medikamente: BP meds
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2680881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 42,0
Geschlecht: M
Eingang: 11.09.2023
Impfdatum: 26.02.2021
Beginn: 27.12.2021
Tage bis Beginn: 304,0
Dosis: 2
Route/Site: IM / RA

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

C-reactive protein COVID-19 pneumonia Chest X-ray abnormal Dyspnoea Pain Serum ferritin increased

Symptomtext

Presented with SOB/body aches x3 days; dx Covid PNA: Labs: CRP 5.31; Ferritin 2113; CXR: R lung pneumonia Tx: Maxipime, Decadron, Heparin, Singulair, Zinc (no remdesivir due to ESRD); Initially on 3 LPM O2; up to 5 LPM and then back to room air at d/c

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2677117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 93,0
Geschlecht: M
Eingang: 28.08.2023
Impfdatum: 23.02.2021
Beginn: 11.02.2022
Tage bis Beginn: 353,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 pneumonia Chronic kidney disease

Symptomtext

Admit for COVID pna dx same day in clinic. Received O2, steroids, vit-c, zinc. No remdesivir due to CKD. Recovered and DC home on RA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2659097

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 77,0
Geschlecht: M
Eingang: 21.07.2023
Impfdatum: 20.02.2021
Beginn: 05.01.2022
Tage bis Beginn: 319,0
Dosis: 2
Route/Site: IM / UN

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

COVID-19 Cough Dyspnoea Pain

Symptomtext

Presented to ED w c/o cough, shortness of breath and body aches for 1 week; reports dx w/COVID 1 wk ago; tx w/abx, steroids, zinc; pt did not require O2; dc'd home

Weitere VAERSDATA-Felder

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

VAERS 2658644

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 90,0
Geschlecht: F
Eingang: 20.07.2023
Impfdatum: 26.02.2021
Beginn: 14.01.2022
Tage bis Beginn: 322,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Hypoxia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Presented to ED with complaints of shortness of breath , cough, chest congestion x2 weeks. Patient was found hypoxic in ED. Tested positive for COVID 19 infection. Tx w/steroids, zinc, O2. Dc'd to SNF.

Weitere VAERSDATA-Felder

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

VAERS 2650915

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 88,0
Geschlecht: M
Eingang: 29.06.2023
Impfdatum: 20.02.2021
Beginn: 03.01.2022
Tage bis Beginn: 317,0
Dosis: 2
Route/Site: IM / UN

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

Asthenia COVID-19 Dehydration Rhabdomyolysis SARS-CoV-2 test positive

Symptomtext

Admitted for severe dehydration & mild rhabdo; profound continued weakness prompted infectious causes and pt COVID+; was treated w/steroids, abx, remdesivir & O2, weaned to RA. Due to weakness, pt dc'd to rehab

Weitere VAERSDATA-Felder

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

VAERS 2624726

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MO
Alter: 85,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 22.10.2022
Beginn: 07.04.2023
Tage bis Beginn: 167,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia COVID-19 pneumonia Fatigue Respiratory tract congestion

Symptomtext

Congestion, fatigue, weakness, COVID pneumonia. Hospitalized 04/07/203.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Cardiac pacemaker/defibrillator, diabetic, kidney disease.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2619903

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MO
Alter: 77,0
Geschlecht: F
Eingang: 24.04.2023
Impfdatum: 12.12.2021
Beginn: 09.04.2023
Tage bis Beginn: 483,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia COVID-19 Condition aggravated Diabetes mellitus Pyrexia SARS-CoV-2 test positive

Symptomtext

Case was hospitalized on 04/09/2023 due to diabetes and weakness. On 04/18/2023 case had a fever and tested positive for COVID. Case was discharged the the following day 04/19/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 10,0
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: diabetes
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2619002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: KY
Alter: 59,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 01.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 61,0
Dosis: 1
Route/Site: IM / LA

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

Cardiac stress test Catheterisation cardiac Computerised tomogram thorax Dyspnoea Dyspnoea exertional Echocardiogram Electrocardiogram Heart rate increased Pulmonary function test Sinus tachycardia

Symptomtext

Inappropriate sinus tachycardia. Heart rate increased withstanding or any activity. Extremely elevated after few minutes of exercise. Shortness of breath with any activity due to elevated heart rate

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Heart cath, ekg, echocardiogram, respiratory function tests, CT scan to check for pulmonary thrombosis, metabolic stress test. All tests feb between June 2021 and November 2021
Aktuelle Erkrankungen: -
Vorgeschichte: Diastolic heart failure Asthma Gerd CVID CKD stage 3
Andere Medikamente: Bystolic, Bumex, Aldactone, Potassium, Singulair, Synthroid, Prilosec, Symbicort, Dupixent ,
Allergien: -
Vorherige Impfungen: -

VAERS 2588562

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 92,0
Geschlecht: M
Eingang: 28.02.2023
Impfdatum: 22.04.2022
Beginn: 06.12.2022
Tage bis Beginn: 228,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia COVID-19 Dyspnoea Fall SARS-CoV-2 test positive Wheelchair user

Symptomtext

Patient brought in by EMS to ED on 12/6/22 for weakness and shortness of breath. To note, patient fell transferring to wheelchair the morning of 12/6. COVID PCR test done in the ED was positive, and he notably tested positive for COVID the day before. Ultimately, patient admitted to the hospital 12/6/22 - 12/8/22 for COVID-19 and generalized weakness attributed to COVID-19 infection, among other problems. Patient has received the COVID primary vaccine series and two boosters.

Weitere VAERSDATA-Felder

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

VAERS 2583555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 17.02.2023
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Arthralgia Feeling abnormal Flushing Heart rate irregular Impaired driving ability Injection site reaction Mobility decreased Musculoskeletal stiffness Pain Pain in extremity Palpitations Weight bearing difficulty

Symptomtext

Flush all over body after about 20 minutes. Head started feeling peculiar. Heart started palpitating and beating in an odd rhythm. I had to pull over on the way home from the vaccination clinic. Within a few hours (3-4 hours), my arm was hurting from the shoulder all the way down to my fingers, aching and stiff. By the next morning, I could not lift my arm higher than parallel to the ground and it caused excruciating pain to attempt to lift it above that / sleep on that side. I could not lift anything of any weight - a couple of pounds at most. Frequently, shooting pains would run the length of my arm from shoulder down to arm, causing crippling pain. These symptoms lasted for 13 months, when they lessened considerably but have never fully gone away. I can still pinpoint the exact spot of the injection site. I would consider there to be permanent damage as I am still bothered by these symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I informed my doctor of these symptoms.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Mild allergy to penicillin and some crab
Vorherige Impfungen: -

VAERS 2546948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 21.03.2021
Beginn: 18.12.2022
Tage bis Beginn: 637,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest X-ray normal Culture urine positive Leukocytosis Mental status changes Pyrexia SARS-CoV-2 test positive Sepsis Tachycardia Urinary tract infection Urine analysis abnormal White blood cell count increased

Symptomtext

In the ER she tested positive for COVID with no hypoxia and no findings of acute infiltrate on CXR. She was also noted to be septic with tachycardia, fever and leukocytosis with a UA showing a UTI. She was admitted on COVID isolation. COVID was treated with daily Remdesivir but no steroids as no hypoxia. She will need COVID isolation through 12/27/22. For her UTI she was treated with IVF and ceftriaxone. Her WBC normalized on 12/19. Fever resolved after admission. Mental status improved daily and for the last several days of hospital stay she was at her baseline MS. Urine culture grew mixed flora but she improved on ceftriaxone so she was changed to Vantin to complete a full course - last day is 12/27/22. PT saw the patient and she was transferred to on 12/22/22. Hospital course otherwise without complication.

Weitere VAERSDATA-Felder

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

VAERS 2501873

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 83,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 28.04.2022
Beginn: 20.07.2022
Tage bis Beginn: 83,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Chronic obstructive pulmonary disease Computerised tomogram thorax abnormal Condition aggravated Pneumonia Respiratory failure SARS-CoV-2 test positive White blood cell count increased

Symptomtext

7/20/2022-Presnts to ED, Admit chronic hypoxic resp failure s/t to severe COPD with recent exacerbation and unresolved pna. Covid + test. Ordered Levaquin, decadron and bebtelovimab. On 3L NC, on baseline oxygen . WBC-27.3 Recent IP stay 7/10-7/14/2022 for PNA had been on ceftriaxone and azithromycin. Chest CT potential R lower lobe infiltrate. 7/22/2022. Improved, continue prednisone taper ad Levaquin. WBC-22.6. D/C home with home health services.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 DM, HTN, COPD, HLD, peptic ulcer disease with hemorrhage, GE junction carcinoma and sepsis
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2452057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 65,0
Geschlecht: F
Eingang: 20.09.2022
Impfdatum: 14.02.2021
Beginn: 14.09.2022
Tage bis Beginn: 577,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Dyspnoea Hypoxia SARS-CoV-2 test positive Wheezing

Symptomtext

SOB, WHEEZING, HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 9/15/22
Aktuelle Erkrankungen: -
Vorgeschichte: ? Asthma diagnosed in her 20s, no disease or treatment for ? Diabetic neuropathy (HCC) ? DM2 (diabetes mellitus, type 2) (HCC) 1995 uncontrolled ? Gout ? HLD (hyperlipidemia) ? HTN (hypertension) ? Incisional hernia ventral ? Mastitis 3-12-09 left breast, ? Morbid obesity (HCC) ? MRSA (methicillin resistant Staphylococcus aureus) 8/20/2012 skin wound, abdomen wall abscess ? Ovarian cyst ? Seroma 8/12/2010 abdominal- drainage system in place ? Stage 3 chronic kidney disease (HCC) 9/15/2017 ? Thalamic stroke (HCC) 4/18/2022 ? Wound infection drainage from previous surgery
Andere Medikamente: nitroGLYCERIN (NITROSTAT) tablet 0.4 mg (0.4 mg Sublingual Given 9/15/22 1838) ALBUTEROL SULFATE 2.5 MG/3 ML (0.083 %) SOLUTION FOR NEBULIZATION (has no administration in time range) furosemide (PF) (LASIX) injection 40 mg (has no administr
Allergien: ? Ampicillin Dermatitis ? Labetalol Hcl ? Normodyne [Labetalol] Rash ? Penicillins Dermatitis, Unknown and Rash ? Soap Rash Scented soaps
Vorherige Impfungen: -

VAERS 2452042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 20.09.2022
Impfdatum: 03.02.2021
Beginn: 13.09.2022
Tage bis Beginn: 587,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Dyspnoea Hypoxia SARS-CoV-2 test positive

Symptomtext

SOB, HYPOXIA,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: POSITIVE COVID TEST 09/15/2022
Aktuelle Erkrankungen: -
Vorgeschichte: Anxiety Arthritis DVT Pulmonary embolism COPD Hypertension Hyperlipidemia Peripheral artery disease Restrictive lung disease
Andere Medikamente: albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler amLODIPine (NORVASC) 5 mg oral tablet atorvastatin (LIPITOR) 40 mg oral tablet bisacodyl (DULCOLAX) 5 mg oral delayed released tablet busPIRone (BUSPAR) 15 mg Oral Tab dia
Allergien: Ciprofloxacin Metronidazole Pcn [Penicillins]
Vorherige Impfungen: -

VAERS 2379328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 76,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 24.02.2021
Beginn: 21.06.2022
Tage bis Beginn: 482,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: POSITIVE COVID TEST 6/21/22
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma Hypertension Pneumonia Chronic lower back pain.
Andere Medikamente: acetaminophen (TYLENOL) 500 mg oral tablet amLODIPine (NORVASC) 10 mg oral tablet aspirin 81 mg oral enteric coated tablet atorvastatin (LIPITOR) 20 mg oral tablet hydroCHLOROthiazide (HYDRODIURIL) 25 mg oral tablet ketorolac 0.5% (ACULAR)
Allergien: -
Vorherige Impfungen: -

VAERS 2344838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: IL
Alter: 87,0
Geschlecht: M
Eingang: 30.06.2022
Impfdatum: 01.03.2021
Beginn: 01.12.2021
Tage bis Beginn: 275,0
Dosis: 2
Route/Site: - / -

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

Anion gap Anticoagulant therapy Aspartate aminotransferase increased Blood chloride decreased Blood creatinine increased Blood glucose increased Blood sodium decreased Blood urea increased COVID-19 COVID-19 pneumonia Computerised tomogram thorax abnormal Dyspnoea Fatigue Haematocrit decreased Haemoglobin decreased Hypoxia Positive airway pressure therapy Pulmonary mass

Symptomtext

Pfizer Dose 1 2/8/21 (EN6201) Pfizer Dose 2 3/1/21 (EN6203) COVID Positive 1/4/22 1/4/22: Patient is an 87-year-old male with past medical history significant for type 2 diabetes, CKD, CAD s/p stent placement, hypertension, B12 deficiency, history of unprovoked PE in 2018 currently anticoagulated on Eliquis, recent COVID-19 infection, melanoma with metastatic disease to lungs. The patient presents to the ED today via EMS from a facility with worsening shortness of breath. Of note, the patient was admitted to the Hospital for 3 weeks due to COVID-19 pneumonia, he was discharged to a facility 1/3/2022 on 8 L of oxygen via nasal cannula. The patient's HPI is difficult to obtain due to his significant hypoxia and fatigue. The patient is not able to answer questions appropriately during examination. Of note, the patient follows with Dr. for the management of his metastatic melanoma. The patient had a CT of his chest completed on 11/30/2021 and reviewed slight enlargement of the pulmonary nodule in the right middle lobe. He was previously being treated with keytruda; however, it has been on hold for 2 months due to worsening performance while on keytruda. Upon arrival to the ED patient's temperature is 99.3?, heart rate 88, respirations 39, pulse ox 91% on 15 L high-flow oxygen, blood pressure 117/58. The patient was subsequently placed on BiPAP at 50% FiO2 to maintain O2 saturations greater than 90%. Patient's laboratory findings are significant for sodium 130, chloride 93, a gap 18, glucose 205, BUN 38, creatinine 1.68, AST 64, WBC 12.71, hemoglobin 11.5, hematocrit 36.1. The patient received 6 mg IV Decadron, DuoNeb x1, Levaquin 750 mg IV, 2 L IV normal saline in ED. 1/6/22: Discontinue routine blood checks Discontinue glucometer and insulin Continue with comfort measures Follow-up with care coordination and hospice team about DC to skilled on hospice Other medications discontinued.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: DM type 2 CKD CAD s/p stent placement HTN B12 deficiency h/o unprovoked PE in 2018 recent COVID infection melanoma with metastatic disease to lungs
Andere Medikamente: APAP 650 mg PO QD albuterol 2 pufffs Q4h PRNalfuzosin 10 mg PO QD allopurinol 300 mg PO QD alprazolam 0.25 mg PO Q8h PRN apixaban 5 mg PO BID atorvastatin 40 mg PO HS cetirizine 10 mg PO QD vitamin D 125 mcg PO QD clopidogrel 75 mg PO QD cl
Allergien: penicillins - rash
Vorherige Impfungen: -

VAERS 2317460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MO
Alter: 82,0
Geschlecht: F
Eingang: 13.06.2022
Impfdatum: 13.03.2021
Beginn: 09.06.2022
Tage bis Beginn: 453,0
Dosis: 1
Route/Site: IM / LA

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

Cough Dyspnoea Fatigue Respiratory tract congestion

Symptomtext

Symptoms began 06/09/2022, cough, SOB, congestion and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: Chronic Lung Disease, Cardiovascular disease and hypertension.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2280908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 03.02.2021
Beginn: 08.05.2022
Tage bis Beginn: 459,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Decreased appetite Diarrhoea Dyspnoea Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

BREATHING PROBLEMS, COUGH, FEVER, FATIGUE, DECREASED APPETITE, SORE THROAT, DIARRHEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: POSITIVE COVID TEST 5/12/22
Aktuelle Erkrankungen: -
Vorgeschichte: Benign prostatic disease Bladder cancer Depression Duodenal ulcer Hypertension Kyphosis Hyperlipidemia Renal disease
Andere Medikamente: aspirin 81 mg oral enteric coated tablet atenolol (TENORMIN) 50 mg oral tablet atorvastatin (LIPITOR) 40 mg oral tablet nitroGLYCERIN (NITROSTAT) 0.4 mg sublingual tablet omeprazole (PRILOSEC) 20 mg oral delay
Allergien: Aspirin Pneumococcal 23-Val Ps Vaccine
Vorherige Impfungen: -

VAERS 2280797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 94,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 25.02.2021
Beginn: 07.05.2022
Tage bis Beginn: 436,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

SOB

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 8,0
Labordaten: POSITIVE COVID TEST 5/6/22
Aktuelle Erkrankungen: HEADACHE - ED VISIT 2/23/21
Vorgeschichte: ? Angina pectoris (HCC) ? Asthma Triggered by infections ? BCC (basal cell carcinoma), face 2007 s/p excision ? Bilateral cataracts ? CAD (coronary artery disease) Abnormal stress 1/08 s/p stent LAD 2/08, PCI LAD and PTCA D3 4/08. Stents patent without new lesions cath 10/2009. ? Cholelithiasis ? Cognitive impairment 05/09/2022 SLUMS 20/30, ? PTA dementia ? COVID-19 virus detected 05/07/2022 ? Diabetes mellitus type II, controlled (HCC) Diet control only ? Diverticulosis of colon on colonoscopy 1999 ? DJD (degenerative joint disease) ? Dyslipidemia ? Hemorrhoid on colonoscopy 1999 ? History of splenectomy 20-25 years ago, secondary to snowmobile accident ? Hyperlipidemia ? Hypertension ? Hypothyroidism ? Onychomycosis 2010 on oral lamisil ? Osteopenia ? PUD (peptic ulcer disease) 10/2009 resolved on f/u EGD ? Pulmonary fibrosis (HCC) Ongoing diagnosis (Oct 2009), workup in progress ? Renal insufficiency 04/09/2008 ? Right bundle branch block ? Stented coronary artery 4/2011; 2010 ? Temporal pain 01/13/2017 RIGHT WITH ELEVATED SEDATION RATE ? Urinary incontinence, stress
Andere Medikamente: ? acetaminophen (TYLENOL) 500 mg oral tablet ? albuterol 90mcg/puff 90 mcg/Actuation Inhl Aero ? amLODIPine (NORVASC) 10 mg oral tablet ? aspirin 81 mg Oral chew tab ? dexAMETHasone (DECADRON) 6 mg oral tablet ? dextromethorphan 10 mg-gu
Allergien: Adenosine (Diagnostic) Grape Perfume (Nic)
Vorherige Impfungen: -

VAERS 2328594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 27.02.2021
Beginn: 06.10.2021
Tage bis Beginn: 221,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Chest pain Cough Dyspnoea Ischaemic cardiomyopathy SARS-CoV-2 test positive

Symptomtext

Narrative: The patient was admitted to the hospital on 6 Oct 2021 with chest pain. The patient was discharged on 8 Oct 2021. The patient was readmitted on 16 Oct 21 with chest pain and coughing. The patient was discharged on 19 Oct 21. The patient presented to the ED with worsening shortness of breath and coughing on 20 Nov 2021 and was admitted to the hospital on 21 Nov 21. The patient was discharged in stable condition on 24 Nov 21. The patient presented to the ED with chest pain and shortness of breath on 1 Jan 2022 and was admitted. The patient was discharged on 6 Jan 2022. The patient was readmitted on 10 Jan 2022 with chest pain and tested positive for COVID 19. The patient was discharged on 11 Jan 2022 in stable condition. The patient was readmitted to the hospital on 23 Feb 2022 with chest pain and shortness of breath. The patient is diagnosed with ischemic cardiomyopathy. Reported per EUA.

Weitere VAERSDATA-Felder

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

VAERS 2263438

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 73,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 26.02.2021
Beginn: 17.09.2021
Tage bis Beginn: 203,0
Dosis: 2
Route/Site: IM / OT

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

COVID-19 Diarrhoea Dyspnoea SARS-CoV-2 test positive

Symptomtext

Presented with SOB, diarrhea; Covid + in ED; admit 9/17 medical with Covid infection Tx with 9/17 steroids started , 9/18 Rocephin, singulair, zinc started; initially on 3 LPM O2; down to RA by d/c

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2259713

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: SD
Alter: 68,0
Geschlecht: F
Eingang: 30.04.2022
Impfdatum: 04.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Arrhythmia Condition aggravated Heart rate irregular Palpitations

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04Mar2021 at 13:30 as dose 2, single (Lot number: EN6203) at the age of 68 years, in left arm for Covid-19 immunisation. The patient's relevant medical history included: "Mild PVCs" (unspecified if ongoing); "Mild PACs" (unspecified if ongoing); "Infrequent SVT" (unspecified if ongoing); "Osteoporosis" (unspecified if ongoing); "Osteopenia" (unspecified if ongoing); "Contrast dye" (unspecified if ongoing). The patient had mild PVCs, PACs and 3 occasions of SVT in the past 30 yrs. so on Acebutolol. Concomitant medication(s) included: ACEBUTOLOL; ALENDRONATE. Other medications in two weeks were Acebutolol, Alendronate. Vaccination history included: BNT162b2 (Dose:1, Dose administration time: 14:30, Vaccine location: Left arm, Lot number: EL9267), administration date: 11Feb2021, when the patient was 68-year-old, for Covid-19 immunization. Facility type vaccine was Pharmacy or Drug Store. The patient did not receive any other vaccine in four weeks. The patient did not have Covid prior vaccination. The patient was not tested for Covid post vaccination. The following information was reported: CONDITION AGGRAVATED (medically significant), HEART RATE IRREGULAR (non-serious) all with onset Mar2021, outcome "recovering" and all described as "About 3 weeks after 2nd dose felt extreme increase in frequency, duration and intensity of arrhythmias"; ARRHYTHMIA (medically significant) with onset Mar2021, outcome "recovering", described as "About 3 weeks. After 2nd dose felt extreme increase in frequency, duration and intensity of arrhythmias"; PALPITATIONS (non-serious) with onset Mar2021, outcome "recovering", described as "Heart thumping kept me awake. Abated some by 6 months when I got 3rd. 15 days later it all started again. Abating some now but still more frequent and intense than before shots." The events "about 3 weeks after 2nd dose felt extreme increase in frequency, duration and intensity of arrhythmias", "about 3 weeks after 2nd dose felt extreme increase in frequency, duration and intensity of arrhythmias" and "heart thumping kept me awake. abated some by 6 months when I got 3rd. 15 days later it all started again. Abating some now but still more frequent and intense than before shots". Required physician office visit. Therapeutic measures were not taken as a result of arrhythmia, condition aggravated, palpitations, and heart rate irregular.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Contrast media allergy; Osteopenia; Osteoporosis; Premature atrial contraction; Premature ventricular contractions; Supraventricular tachycardia
Andere Medikamente: ACEBUTOLOL; ALENDRONATE
Allergien: -
Vorherige Impfungen: -

VAERS 2258072

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MA
Alter: 74,0
Geschlecht: F
Eingang: 29.04.2022
Impfdatum: 01.03.2021
Beginn: 29.05.2021
Tage bis Beginn: 89,0
Dosis: 2
Route/Site: - / LA

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

Anaemia Blood iron Blood iron decreased Haematocrit Haematocrit decreased Hypoxia Red blood cell count Red blood cell count decreased SARS-CoV-2 test Serum ferritin Serum ferritin decreased Tachycardia

Symptomtext

Hypoxia; anemia; tachycardia; decreased red blood cell count; decreased hematocrit; low iron; very low ferritin level; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 74-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Mar2021 as dose 2, single (Lot number: EN6203) at the age of 74 years, in left arm for covid-19 immunization. The patient's relevant medical history included: "Known allergies: sulfa medications" (unspecified if ongoing). Concomitant medication(s) included: PREMARIN; POSTURE D [CALCIUM PHOSPHATE;COLECALCIFEROL;ERGOCALCIFEROL]; D3. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: EL9262, Location of injection: Arm Left), administration date: 08Feb2021, when the patient was 74-year-old, for COVID-19 immunization. The following information was reported: HYPOXIA (medically significant) with onset 29May2021, outcome "recovered with sequelae"; ANAEMIA (non-serious) with onset 29May2021, outcome "recovered with sequelae", described as "anemia"; HAEMATOCRIT DECREASED (non-serious) with onset 29May2021, outcome "recovered with sequelae", described as "decreased hematocrit"; RED BLOOD CELL COUNT DECREASED (non-serious) with onset 29May2021, outcome "recovered with sequelae", described as "decreased red blood cell count"; BLOOD IRON DECREASED (non-serious) with onset 29May2021, outcome "recovered with sequelae", described as "low iron"; TACHYCARDIA (non-serious) with onset 29May2021, outcome "recovered with sequelae"; SERUM FERRITIN DECREASED (non-serious) with onset 29May2021, outcome "recovered with sequelae", described as "very low ferritin level". The events "hypoxia", "anemia", "tachycardia", "decreased red blood cell count", "decreased hematocrit", "low iron" and "very low ferritin level" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood iron: (2021) Low; Haematocrit: (2021) decreased; Red blood cell count: (2021) decreased; SARS-CoV-2 test: (22Dec2021) Negative, notes: Nasal Swab; Serum ferritin: (2021) Very low. Therapeutic measures were taken as a result of hypoxia, anaemia, tachycardia, red blood cell count decreased, haematocrit decreased, blood iron decreased, serum ferritin decreased. Clinical course: Adverse event: Hypoxia, anemia, tachycardia, decreased red blood cell count, decreased hematocrit, low iron, and very low ferritin level. The symptoms, confirmed with blood testing, occurred twice. Once 2.5 months after the second shot, and again 5.5 months after the third shot. In addition, after the third shot there were periodic skin irritations with itching and non-specific patchy dermatoses. Patient received treatment Slow Fe for 45 days on the first episode, No covid prior vaccination.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the hypoxia cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: Test Date: 2021; Test Name: iron; Result Unstructured Data: Test Result:Low; Test Date: 2021; Test Name: hematocrit; Result Unstructured Data: Test Result:decreased; Test Date: 2021; Test Name: red blood cell count; Result Unstructured Data: Test Result:decreased; Test Date: 20211222; Test Name: PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 2021; Test Name: ferritin; Result Unstructured Data: Test Result:Very low
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: PREMARIN; POSTURE D [CALCIUM PHOSPHATE;COLECALCIFEROL;ERGOCALCIFEROL]; D3
Allergien: -
Vorherige Impfungen: -

VAERS 2254797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 24.02.2021
Beginn: 24.02.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Decreased appetite Feeling abnormal Feeling cold Headache Memory impairment Mobility decreased Pain Parosmia Pyrexia Rhinorrhoea Taste disorder Tremor

Symptomtext

Started with a headache then it proceeded to go into body aches then my joints just like COVID-19. I had a fever chills severe joint and body aches and headache was so bad I couldn't even hold it up. I felt like someone was smashing it with a sledge hammer. The chills were very sever my whole bod was shaking I couldn't get warm. I couldn't get out of bed no appetite or anything I just couldn't move. Present day, I still have a lot of mucus and a fogginess in my head when it comes memory and my taste and smell is still off.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diagnosed July 2019 and Cancer surgery Jan 16,2020; Rheumatoid Arthritis
Vorgeschichte: RA
Andere Medikamente: Simvastatin 5mg; Alprazolam 2mg; Methotrexate unsure of dosage; Hydroxychloroquine 200mg; Zolpidem 10mg; Folic Aide 2mg
Allergien: Aspirin; Penicillin; Codeine; Oxycodone
Vorherige Impfungen: -

VAERS 2236077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MO
Alter: 76,0
Geschlecht: M
Eingang: 15.04.2022
Impfdatum: 01.03.2021
Beginn: 09.04.2022
Tage bis Beginn: 404,0
Dosis: 2
Route/Site: SYR / LA

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

COVID-19 Cough Decreased appetite Dyspnoea Fatigue Malaise Myalgia Respiratory tract congestion SARS-CoV-2 test positive Wheezing

Symptomtext

Case developed COVID symptoms on 4/9/2022. Symptoms: Cough, wheezing, shortness of breath, congestion, fatigue, muscle aches, poor appetite. Admitted to hospital on 4/12/2022 and remained there until 4/14/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 2,0
Labordaten: Tested positive for COVID 19 on 4/12/2022
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Cardiovascular disease, Chronic lung condition - occasional Shortness of Breath, Neurological condition - occasional falls, Diabetes.
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2213647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 08.02.2021
Beginn: 29.12.2021
Tage bis Beginn: 324,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Fall SARS-CoV-2 test positive Sepsis

Symptomtext

Narrative: The patient received two doses of Pfizer vaccine in Feb/Mar 2021. The patient tested positive for COVID 19 on 29 December 2021. The patient was admitted to the hospital due to a fall, but discovered the patient with sepsis and COVID pneumonia diagnosed on 31 Dec 21. The patient was treated with dexamethasone and remdesivir. The patient is still in the hospital as of 10 Jan 22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2213629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: -
Alter: 78,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 25.02.2021
Beginn: 05.01.2022
Tage bis Beginn: 314,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Hypoxia Pneumonia SARS-CoV-2 test positive

Symptomtext

Narrative: This patient received two doses of Pfizer COVID 19 Vaccine in Feb/Mar 2021. The patient tested positive for COVID 19 on 5 Jan 2022. The patient was admitted to the hospital on 5 Jan22 with hypoxia and cough and signs of pneumonia. The patient was treated with dexamethasone and remdesivir. The patient was discharged on 10 Jan 22 in stable condition.

Weitere VAERSDATA-Felder

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

VAERS 2204143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

moderat

Staat: NC
Alter: 35,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Arthralgia Joint injection Magnetic resonance imaging abnormal Mobility decreased Periarthritis Shoulder operation

Symptomtext

Shoulder pain begin after the injection and persisted for 2 days. Then shoulder mobility began to decrease and pain returned. I was then diagnosed with frozen shoulder and underwent months of physical therapy and 3 steroid injections. Then I had to get an MRI and shoulder surgery to repair the shoulder and and undergoing recovery now. I had no previous injuries to that shoulder and am right-handed so there's no other way to explain the onset of frozen shoulder and subsequent related woes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2204116

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: AL
Alter: 47,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 24.03.2021
Beginn: 20.04.2021
Tage bis Beginn: 27,0
Dosis: 2
Route/Site: IM / AR

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

Arthralgia Blood cholesterol Cardiac stress test abnormal Chest X-ray normal Chest pain Chills Diarrhoea Dyspnoea Electrocardiogram abnormal Fatigue Hypertension Musculoskeletal pain Nausea Pain Palpitations Pyrexia Skin burning sensation

Symptomtext

Day after Dose 2 vaccination, high temperature radiated pain in shoulder blade the went into chest, nausea and diarrhea. 03/25/2021 teeth chattered and extreme chills and all joints was achy, burning skin sensation, 10am intense midday all symptoms present was present to at bed time of 10:30pm. Next day. Recovered from the signs and symptoms on 03/26/2021. Then in end of April 2021 shortness of breath, pain in chest, radiated pain in shoulder blade that went into chest, center of chest started having pain. I went to a doctor visit 08/18/2021, Internal Medicine Dr. was sent down stairs for chest x ray and EKG. EKG, stress test was abdominal, but chest x-ray was normal. 09/29/2021 was scheduled for a regular stress, was abnormal so I was scheduled for a nuclear stress test on 10/06/2021. The EKG walking treadmill was not normal. Resting EKG was normal for that day. Treadmill was abnormal for the exercise portion abnormal. The pictures was normal. Directives of new blood pressure for high blood new diagnosis , pressure new medication Propranolol 60mg once a day at bedtime. New diagnosis for Cholesterol, Atorvastatin 03/21/2021 Dr. visit 40mg once a night before bed, this an increase from original dose of Atorvastatin 20mg 10/2021. May or June of 2021. Delayed, having a lot of chest pain and heart palpitation. Gastrointestinal, oxygen issue with getting a complete breath, tiredness in chest and pain in bed. Resting abdominal for EKG, stress test was abdominal. Every now and then I chest pains and shortness of breath.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: EKG; Nuclear stress; Regular stress test; Chest x-ray.
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroids and Acid Reflux
Andere Medikamente: Nexium 40mg once morning; Levothyroxine 75 mcg once in morning Vitamin D3 once a day, Vitamin C 1000mg once a day
Allergien: Allergy environmental allergies trees and grass; food -pineapple, Drugs- Penicillin, Doxycycline; Product adhesive tape bandaids - Paper tape is the only exception to use or equate .
Vorherige Impfungen: -

VAERS 2188020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 24.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 5,0
Dosis: 2
Route/Site: SYR / LA

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

Herpes zoster Interchange of vaccine products Mobility decreased Oedema peripheral Pain Rash

Symptomtext

It was 30 to 45 days after my shot. I was experiencing a rash across my stomach. I was in intense pain. I went to the doctor and was diagnosed with Shingles. I was given several medications. It has spread down my entire left side and torso and legs. I cannot remember how long it took to resolve. After my third dose shot, it was Moderna, My under arm swelled up into the size of a golf ball. I could not move my arm for about two weeks. I was in bed for 3 days.

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Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Multiple Vitamins, Albuterol Inhaler
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2184311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: GA
Alter: 62,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 16.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Diarrhoea Hypertension Migraine Pain Respiratory tract congestion

Symptomtext

Extreme body pain Diarrheas High blood pressure Congestion Severe Migraine

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Obstructive Sleep Apnea COPD High blood pressure
Andere Medikamente: None
Allergien: Penicillin Sesame
Vorherige Impfungen: -

VAERS 2181894

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 25.02.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Condition aggravated Hyperacusis Hypoacusis Tinnitus

Symptomtext

I have never had ringing in my ears and when I had this, Its like a bad case of tinnitus; I can't hear; I hear like music very strange; now it's getting worse. In the afternoon I hear a motor, a constant noise in my ear; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 66 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Feb2021 (Lot number: EN5318) as dose 1, single and administered in arm left, administration date 25Feb2021 (Lot number: EN6203) as dose 2, single for covid-19 immunisation. Relevant medical history included: "Blood pressure" (unspecified if ongoing), notes: Patient history: Blood pressure; "Stenosis" (unspecified if ongoing); "back condition" (unspecified if ongoing); "Cholesterol" (unspecified if ongoing); "Pain" (unspecified if ongoing); "antidepressant" (unspecified if ongoing). Concomitant medication(s) included: OXYCODONE taken for back disorder; ENALAPRIL taken for blood pressure abnormal; VENLAFAXINE taken for blood cholesterol; HYDROCODONE taken for pain; BUPROPION taken for antidepressant therapy. The following information was reported: TINNITUS (non-serious), outcome "not recovered", described as "I have never had ringing in my ears and when I had this, Its like a bad case of tinnitus"; HYPOACUSIS (non-serious), outcome "unknown", described as "I cant hear"; HYPERACUSIS (non-serious), outcome "unknown", described as "I hear like music very strange"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "now its getting worse. In the afternoon I hear a motor, a constant noise in my ear". Therapeutic measures were not taken as a result of tinnitus, hypoacusis, hyperacusis, condition aggravated. Additional information: Consumers have a back condition. So, patient took medicine for my back and patient had a blood pressure medicine but other than that healthy, active, walk every day, no problems, no heart condition, no cancer in family. patient very healthy.For my back a pain, one medication was called Oxycodone, patient took Oxycodone 10mg. daily for back, patient had stenosis unfortunately but any case, blood pressure medicine was, well this, its Enalapril 10mg and then lets see, this was another one guess this was for my, Venlafaxine, patient think thats for Cholesterol (Further clarification unknown) so, this was the other one, this one says 150mg. and patient also, this was another pain medication this one patient think was called Hydrocodone for her back, this one was 10-325mg. Yes, patient have a condition called Stenosis. There was another one for an antidepressant and this one called Bupropion and this one was 300mg, once a day." Prior Vaccination (4 Weeks): no vaccinations. Vaccination facility type: Consumer stated, "It was like a big gymnasium. Time of vaccination: afternoon like from 12 to 2 something like that." No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Antidepressant therapy; Back pain; Blood pressure abnormal (Patient history: Blood pressure); Cholesterol; Pain; Stenosis
Andere Medikamente: OXYCODONE; ENALAPRIL; VENLAFAXINE; HYDROCODONE; BUPROPION
Allergien: -
Vorherige Impfungen: -

VAERS 2174038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: AZ
Alter: 44,0
Geschlecht: F
Eingang: 11.03.2022
Impfdatum: 17.02.2021
Beginn: 14.01.2022
Tage bis Beginn: 331,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Cough Diarrhoea Dyspnoea Exposure to SARS-CoV-2 Headache Hypoxia Lung infiltration Nausea Pain SARS-CoV-2 test positive Vomiting

Symptomtext

Hypoxia 2/2 COVID pneumonia Onset date: 1/14/22 test POS, admitted to hospital 1/21 -presented with: N/V/D, HA, body aches, loss of sense of taste and smell, body aches, shortness of breath, and cough -Recent exposures: many family contacts. -CXR with bilateral multifocal infiltrates -Remdesivir and dexamethasone 1/21 -O2 ambulatory challenge: She did not require oxygen at rest or ambulation on the day of discharge -incentive spirometry

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: Covid +
Aktuelle Erkrankungen: N/A
Vorgeschichte: Bipolar disorder Depression HTN HLD Allergies Neuropathic Pain
Andere Medikamente: Venlafaxine ER 75 mg Gabapentin 300 mg Atenolol 25 mgBupropion XL 150 mg Atorvastatin 20 mg
Allergien: NKA
Vorherige Impfungen: -

VAERS 2170965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: SC
Alter: 59,0
Geschlecht: F
Eingang: 10.03.2022
Impfdatum: 23.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / RA

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

Asthenia Condition aggravated Fatigue Fibromyalgia Mental impairment Pain

Symptomtext

I had exhaustion, massive fatigue, felt like energy was zapped out of you. Widespread pain increased with fibromyalgia flare up. Didn?t have any respiratory issues. Basically, the pain and the fatigue. May have messed with my memory too where I couldn?t think as clearly. Lasted for about a month. Had a Vitamin B12 shot, and symptoms were mentioned to my doctor during this appointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia Chronic fatigue & pain Major Depressive Disorder Interstitial cystitis Ulcerative colitis High cholesterol & triglycerides Hx of Thyroid cancer (in 2005) removed (hypothyroidism & goiters, hachimotos) Hx of gallbladder removal Barett's esophagus GERD Achalasia Cognitive impairment Abnormal EKG Heart murmur Neuropathy Mild Asthma Vitamin B12 deficiency Chronic kidney insufficiency Low Vitamin D
Andere Medikamente: Gabapentin 600mg Vitamin D 50iu 2xweekly Synthroid 0.2 mg Namenda 28mg Elavil 100mg Exelon 3mg Klonopin 2mg Ginkgo biloba 120mg Calcium & magnesium Prediagnose Multivitamin Relpex 20mg Ambien 10mg Phenergan 25mg Meclizine PRN 25mg Zanaf
Allergien: Latex Ancef Drinking alcohol
Vorherige Impfungen: Flu vaccinations- flu like symptoms after those vaccines

VAERS 1387587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 06.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Blood test Blood uric acid increased Burning sensation Condition aggravated Erythema Gout Pain in extremity

Symptomtext

About 24 hours later after vaccine, I began to get extreme pain and burning and redness in my right large toe. It increased overnight, I have experienced an attack of Gout 20 years prior to that, so I assumed it was that. My doctor saw me the next day, verified it was indeed gout and I was medicated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work, abnormal uriacitic level.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril 20mg; Vitamin B12; Vitamin D; Biotin
Allergien: Flagyl; Latex
Vorherige Impfungen: -

VAERS 1387587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 06.03.2021
Beginn: 07.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Blood uric acid increased Burning sensation Condition aggravated Erythema Gout Pain in extremity

Symptomtext

About 24 hours later after vaccine, I began to get extreme pain and burning and redness in my right large toe. It increased overnight, I have experienced an attack of Gout 20 years prior to that, so I assumed it was that. My doctor saw me the next day, verified it was indeed gout and I was medicated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work, abnormal uriacitic level.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril 20mg; Vitamin B12; Vitamin D; Biotin
Allergien: Flagyl; Latex
Vorherige Impfungen: -

VAERS 2158343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

moderat

Staat: MA
Alter: 48,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 16.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 13,0
Dosis: 2
Route/Site: IM / LA

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

Anxiety Anxiety disorder Depression Dyspnoea Feeling abnormal Laboratory test normal Palpitations

Symptomtext

Severe anxiety disorder with impending doom. Heart races, sob. I don't feel like I'm the same person after the vaccine. I feel like I'm going to die. If my life is at risk I shouldn't be made to get booster. If could potentially kill me by excessive anxiety and depression.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Al tests are normal.
Aktuelle Erkrankungen: Menopause
Vorgeschichte: Hypotension
Andere Medikamente: None
Allergien: Penicillin ,succinycholine, percocet, l
Vorherige Impfungen: -

VAERS 2154946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 01.03.2021
Beginn: 10.01.2022
Tage bis Beginn: 315,0
Dosis: 2
Route/Site: SYR / LA

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

Atrial fibrillation Blood test COVID-19 COVID-19 pneumonia Chest X-ray abnormal Electrocardiogram abnormal Vaccine breakthrough infection

Symptomtext

Had a breakthrough of COVID virus after being vaccination. Prescription antibiotics. COVID turned into pneumonia. I was in the hospital for 6 days. I also went into AFIB at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 6,0
Labordaten: EKG, Chest X-rays, Breathing Treatment, Bloodwork
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Prescription medication
Allergien: No
Vorherige Impfungen: -

VAERS 2154631

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: OK
Alter: 51,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 24.08.2021
Beginn: 11.09.2021
Tage bis Beginn: 18,0
Dosis: 1
Route/Site: SC / RA

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

Anal incontinence Angiogram cerebral Asthenia Ataxia Atrial fibrillation Bedridden Cognitive disorder Computerised tomogram abdomen Computerised tomogram head Confusional state Gait inability Inappropriate schedule of product administration Laboratory test Magnetic resonance imaging head Orthostatic hypotension Urinary incontinence Visual impairment

Symptomtext

First vaccine given 3/5/2021 second 3/26/2021 booster given 8/24/2021. Early 2021 weakness began then the below new symptoms started in September 2021. No definitive diagnosis given. Ataxia Sudden decrease in vision Orthostatic Hypotension Weakness Unable to walk/bed bound Confusion Cognitive issues Loss of bladder and bowel control A-fib

Weitere VAERSDATA-Felder

Praegender Schweregrund: Orthostatic hypotension
Hospital-Tage: 114,0
Labordaten: Multiple hospitilizations since September 2021 as well as multiple rehabilitiation hospital stays with no improvement. Symptoms are progressively getting worse. MRI Brain MRA Brain CT Brain CT Abdomen Pelvis Multiple Labs MRI Brain/MRI Cervical spine scheduled for 3/10/2022 DaTScan scheduled for 3/10/2022
Aktuelle Erkrankungen: Gastroparesis Type 1 Diabetes
Vorgeschichte: Type 1 Diabetes Gastroparesis Kidney Transplant status
Andere Medikamente: Prograf 2mg twice Myfortic 180mg once Prednisone 5mg once morning Reglan 5mg twice Hydralizine 50mg as needed Amlodipine 5mg once Pravastatin 20mg once at night Sodium bicarbonate 650mg twice Lyrica 50mg three Pepcid 20mg twice Folic Acid
Allergien: Metoprlol Keflex Tegaderm
Vorherige Impfungen: -

VAERS 1074251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 27.02.2021
Beginn: 02.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Diarrhoea Dizziness Dry eye Fatigue Blood test Chest X-ray Chest pain Dyspnoea Dysstasia Illness Nausea Renal pain Vaccination complication Headache Migraine Myalgia Thirst

Symptomtext

I got very sick couldn't stand up nausea dizzy started vomiting had severe kidney pain and also had chest pain that made it difficult to breathe. It went on for several days. After 4 days went into hospital and was told it was a viral infection from vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: Chest X ray Blood Test
Aktuelle Erkrankungen: No
Vorgeschichte: Psoriasis
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 2151818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 26.03.2021
Beginn: 18.02.2022
Tage bis Beginn: 329,0
Dosis: 1
Route/Site: SYR / -

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

Ageusia Anosmia COVID-19 Chills Chronic obstructive pulmonary disease Condition aggravated Cough Dyspnoea Fatigue Gastric disorder Headache Pyrexia Rectal haemorrhage Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Fever, chills, congestion, cough, SOB, fatigue, headache, loss of smell/taste, gastric sxs, (+) COVID, worsening COPD, rectal bleeding after mAb treatment

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 6,0
Labordaten: 2/22: Reatl-Time Reverse Transcriptase PCR (+) COVID 2/25: Polymerase Chain reaction (PCR), (+) COVID
Aktuelle Erkrankungen: COPD
Vorgeschichte: COPD
Andere Medikamente: None reported
Allergien: NKA
Vorherige Impfungen: -

VAERS 2149101

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CO
Alter: 69,0
Geschlecht: F
Eingang: 28.02.2022
Impfdatum: 26.02.2021
Beginn: 13.05.2021
Tage bis Beginn: 76,0
Dosis: 2
Route/Site: IM / LA

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

Atrial fibrillation Cardiac stress test Condition aggravated Electrocardiogram Influenza Laboratory test Pyrexia

Symptomtext

I went to the Fairgrounds to get my 2nd shot of Covid. I waited for 15 minutes. I went home and was fine. The next day I had a fever and had the flu symptoms. I recovered from those symptoms. A couple of months later I started having the Afib problems. I went to see my PCP to get it checked. I am on medication currently and still being treated for A-fib. I do not have the A-fib under control with all the medication. I have had more over than 64 episodes of the A-fib.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Lab Work; EKG; Stress Test.
Aktuelle Erkrankungen: None
Vorgeschichte: Graves Disease; High Blood Pressure; Low Oxygen; Sleep Apnea; High Cholesterol; Spinal Stenosis; A-fib
Andere Medikamente: Losartan; Hydrochlorizide; Pravastatin; Methimazole; Metoprolol Succinate ER; Xarelto
Allergien: Iodine; Penicillin
Vorherige Impfungen: -

VAERS 2127543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: -
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 11.03.2021
Beginn: 11.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / -

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

Condition aggravated Fatigue Headache Vomiting

Symptomtext

I have an underlying condition; the first shot that I took made my condition episodes longer and much more intense; I was extremely fatigued; like not getting out of the bed for days; I had very strong headache; vomiting; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63 year-old female patient received bnt162b2 (BNT162B2), administration date 11Mar2021 (Lot number: EN6203, Expiration Date: Jun2021) as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: CONDITION AGGRAVATED (non-serious) with onset 11Mar2021, outcome "unknown", described as "I have an underlying condition; the first shot that I took made my condition episodes longer and much more intense"; FATIGUE (non-serious) with onset 11Mar2021, outcome "unknown", described as "I was extremely fatigued; like not getting out of the bed for days"; HEADACHE (non-serious) with onset 11Mar2021, outcome "unknown", described as "I had very strong headache"; VOMITING (non-serious) with onset 11Mar2021, outcome "unknown", described as "vomiting". No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021523905 same patient/drug, different dose/event

Weitere VAERSDATA-Felder

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

VAERS 2108347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 03.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: - / -

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

Balance disorder Balance test Blood pressure measurement Blood test Circumstance or information capable of leading to medication error Dizziness Ear pain Electrocardiogram Hypertension Magnetic resonance imaging Nausea Ultrasound Doppler Vertigo Ultrasound scan

Symptomtext

The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021; blood pressure went sky high; Dizziness; extreme vertigo; Nausea; Unsteadiness; Slight ear ache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 81 year-old female patient received bnt162b2 (BNT162B2), administration date 03Mar2021 (Lot number: EN6203) at the age of 81 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Thyroid" (unspecified if ongoing), notes: Verbatim: thyroid problem; "Rash" (unspecified if ongoing); "fever" (unspecified if ongoing); "severe Lyme disease", start date: 2006 (unspecified if ongoing); "spinal tap" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE. Past drug history included: Rocephine. The following information was reported: CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (non-serious), outcome "unknown", described as "The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021"; DIZZINESS (non-serious) with onset 19Mar2021, outcome "not recovered", described as "Dizziness"; VERTIGO (non-serious) with onset 19Mar2021, outcome "recovering", described as "extreme vertigo"; NAUSEA (non-serious) with onset 19Mar2021, outcome "recovering", described as "Nausea"; BALANCE DISORDER (non-serious) with onset 19Mar2021, outcome "recovering", described as "Unsteadiness"; EAR PAIN (non-serious) with onset 19Mar2021, outcome "unknown", described as "Slight ear ache"; HYPERTENSION (non-serious), outcome "unknown", described as "blood pressure went sky high". The event "slight ear ache" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The caller was calling about the Pfizer covid vaccine. The caller was perfectly healthy and then just after 2 weeks after the vaccine she was experiencing extreme vertigo, dizziness, nausea, unsteadiness. Is there any medication in the vaccine that could have caused this such as cephalosporins and sulfa? The caller was under the care of a neurologist for the next three weeks. Event: All of this started on 19Mar2021 with a slight ear ache. The caller has been in the emergency room because of this event but was never admitted to the hospital. The caller's blood pressure went sky high for 2 days during all of this. Product: The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021 because it was in the middle of this event. What should the caller do about this, she fears getting the second dose? History: The caller is sensitive to medications but her doctor told her to get the vaccine. Years ago in 2006 the caller had severe Lyme disease and had a spinal tap. The caller was given Rocephin via a picc line. 2 weeks after starting the Rocephin the caller had a rash all over her body and a very high fever, unknown lot or expiration date. Investigations: MRI- ruled out if it was a stroke in the neck, it wasn't that. The caller sees her neurologist on 05May2021 to get the results of these test. Caller also had blood test, transcranial doppler, carotid duplex, balance test vng/vor, and an EKG. However, these results were not specified. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: balance test vng/vor; Result Unstructured Data: Test Result:results were not specified; Test Name: blood test; Result Unstructured Data: Test Result:results were not specified; Test Name: EKG; Result Unstructured Data: Test Result:results were not specified; Test Name: MRI; Result Unstructured Data: Test Result:ruled out if it was a stroke in the neck; Test Name: transcranial doppler; Result Unstructured Data: Test Result:results were not specified; Test Name: carotid duplex; Result Unstructured Data: Test Result:results were not specified; Test Name: blood pressure; Result Unstructured Data: Test Result:High; Comments: went sky high for 2 days
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fever; Lyme disease; Rash; Spinal tap; Thyroid pain (Verbatim: thyroid problem.)
Andere Medikamente: LEVOTHYROXINE.
Allergien: -
Vorherige Impfungen: -

VAERS 2108347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 19.02.2022
Impfdatum: 03.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 16,0
Dosis: 1
Route/Site: - / LA

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

Balance disorder Balance test Blood pressure measurement Blood test Circumstance or information capable of leading to medication error Dizziness Ear pain Electrocardiogram Hypertension Magnetic resonance imaging Nausea Ultrasound Doppler Vertigo Ultrasound scan

Symptomtext

The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021; blood pressure went sky high; Dizziness; extreme vertigo; Nausea; Unsteadiness; Slight ear ache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 81 year-old female patient received bnt162b2 (BNT162B2), administration date 03Mar2021 (Lot number: EN6203) at the age of 81 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Thyroid" (unspecified if ongoing), notes: Verbatim: thyroid problem; "Rash" (unspecified if ongoing); "fever" (unspecified if ongoing); "severe Lyme disease", start date: 2006 (unspecified if ongoing); "spinal tap" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE. Past drug history included: Rocephine. The following information was reported: CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (non-serious), outcome "unknown", described as "The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021"; DIZZINESS (non-serious) with onset 19Mar2021, outcome "not recovered", described as "Dizziness"; VERTIGO (non-serious) with onset 19Mar2021, outcome "recovering", described as "extreme vertigo"; NAUSEA (non-serious) with onset 19Mar2021, outcome "recovering", described as "Nausea"; BALANCE DISORDER (non-serious) with onset 19Mar2021, outcome "recovering", described as "Unsteadiness"; EAR PAIN (non-serious) with onset 19Mar2021, outcome "unknown", described as "Slight ear ache"; HYPERTENSION (non-serious), outcome "unknown", described as "blood pressure went sky high". The event "slight ear ache" was evaluated at the emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The caller was calling about the Pfizer covid vaccine. The caller was perfectly healthy and then just after 2 weeks after the vaccine she was experiencing extreme vertigo, dizziness, nausea, unsteadiness. Is there any medication in the vaccine that could have caused this such as cephalosporins and sulfa? The caller was under the care of a neurologist for the next three weeks. Event: All of this started on 19Mar2021 with a slight ear ache. The caller has been in the emergency room because of this event but was never admitted to the hospital. The caller's blood pressure went sky high for 2 days during all of this. Product: The caller received her first dose on 03Mar2021. The caller didn't have the second dose on the 25Mar2021 because it was in the middle of this event. What should the caller do about this, she fears getting the second dose? History: The caller is sensitive to medications but her doctor told her to get the vaccine. Years ago in 2006 the caller had severe Lyme disease and had a spinal tap. The caller was given Rocephin via a picc line. 2 weeks after starting the Rocephin the caller had a rash all over her body and a very high fever, unknown lot or expiration date. Investigations: MRI- ruled out if it was a stroke in the neck, it wasn't that. The caller sees her neurologist on 05May2021 to get the results of these test. Caller also had blood test, transcranial doppler, carotid duplex, balance test vng/vor, and an EKG. However, these results were not specified. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Name: balance test vng/vor; Result Unstructured Data: Test Result:results were not specified; Test Name: blood test; Result Unstructured Data: Test Result:results were not specified; Test Name: EKG; Result Unstructured Data: Test Result:results were not specified; Test Name: MRI; Result Unstructured Data: Test Result:ruled out if it was a stroke in the neck; Test Name: transcranial doppler; Result Unstructured Data: Test Result:results were not specified; Test Name: carotid duplex; Result Unstructured Data: Test Result:results were not specified; Test Name: blood pressure; Result Unstructured Data: Test Result:High; Comments: went sky high for 2 days
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Fever; Lyme disease; Rash; Spinal tap; Thyroid pain (Verbatim: thyroid problem.)
Andere Medikamente: LEVOTHYROXINE.
Allergien: -
Vorherige Impfungen: -

VAERS 2108853

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

moderat

Staat: IA
Alter: 74,0
Geschlecht: U
Eingang: 12.02.2022
Impfdatum: 02.03.2021
Beginn: 03.11.2021
Tage bis Beginn: 246,0
Dosis: 2
Route/Site: OT / -

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

Pneumonia

Symptomtext

Pneumonia; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 75 year-old patient received bnt162b2 (BNT162B2), intramuscular, administered in arm, administration date 02Mar2021 (Lot number: En6203) at the age of 74 years as dose 2, single and intramuscular, administered in arm, administration date 09Feb2021 (Lot number: En6201) as dose 1, single for covid-19 immunisation. Relevant medical history included: "known allergies to Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Morphine, reaction(s): "Allergy". The following information was reported: PNEUMONIA (hospitalization, medically significant) with onset 03Nov2021, outcome "recovered" (13Nov2021), described as "Pneumonia". Therapeutic measures taken as a result of pneumonia included IV antibiotics during hospital stay. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2107395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CT
Alter: -
Geschlecht: U
Eingang: 12.02.2022
Impfdatum: 21.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Chest pain Injection site pain Physical examination Tachycardia

Symptomtext

heart beat sky rocketed/Rapid heart rate; had chest pains (1st two hours after the shot); pain in the shot site; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) for a Pfizer sponsored program. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 21Mar2021 13:00 (Lot number: EN6203) as dose 1, single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: TYLENOL, start date: 21Mar2021, stop date: 23Apr2021. The following information was reported: TACHYCARDIA (non-serious) with onset 21Mar2021 13:20, outcome "recovered" (2021), described as "heart beat sky rocketed/Rapid heart rate"; CHEST PAIN (non-serious) with onset 21Mar2021, outcome "unknown", described as "had chest pains (1st two hours after the shot)"; INJECTION SITE PAIN (non-serious) with onset 21Mar2021, outcome "unknown", described as "pain in the shot site". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of tachycardia. Additional information: Patient know that there was a site where patient can provide feedback regarding COVID shot. Patient just cant seem to find it. Patient wanted to report that after the first shot heart beat sky rocketed and had chest pains (1st two hours after the shot) and pain in the shot site (typical response). Patient was an athlete and workout daily. It kept patient awake for the 1st two weeks because it hurt. Relevant test was none (everything was normal at last physical). Rapid heart rate (about 3-5min after shot Rapid heart rate remained escalated for at least 2 hours. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Physical; Result Unstructured Data: Test Result:Everything normal
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1168406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 20.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Deafness neurosensory Decreased appetite Ear discomfort Head discomfort Dry eye Feeling hot Hyperacusis Paraesthesia Hot flush Nausea Tinnitus Photophobia

Symptomtext

New onset tinnitus/High pitched "screech" feeling/sounding/Lower frequency tones of varying frequency in both ears, although louder in the right; pressure in both ears and in the head; Some paresthesia running through the head with heat waves at various times.; Increased sensitivity to light and sound, dryer eyes.; Increased sensitivity to light and sound, dryer eyes.; Increased sensitivity to light and sound, dryer eyes.; Some paresthesia running through the head with heat waves at various times; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Mar2021 15:00 (Lot number: EN6203) at the age of 59 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Peripheral ulcerative keratitis (eye)" (unspecified if ongoing), notes: other medical history: Peripheral ulcerative keratitis (eye); "known allergies: tree pollens" (unspecified if ongoing); "known allergies: dust" (unspecified if ongoing); "known allergies: Mold" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: TINNITUS (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "New onset tinnitus/High pitched "screech" feeling/sounding/Lower frequency tones of varying frequency in both ears, although louder in the right"; HEAD DISCOMFORT (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "pressure in both ears and in the head"; PARAESTHESIA (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "Some paresthesia running through the head with heat waves at various times."; PHOTOPHOBIA (non-serious), HYPERACUSIS (non-serious), DRY EYE (non-serious) all with onset 21Mar2021 07:00, outcome "not recovered" and all described as "Increased sensitivity to light and sound, dryer eyes."; FEELING HOT (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "Some paresthesia running through the head with heat waves at various times". The events "new onset tinnitus/high pitched "screech" feeling/sounding/lower frequency tones of varying frequency in both ears, although louder in the right", "pressure in both ears and in the head", "some paresthesia running through the head with heat waves at various times.", "increased sensitivity to light and sound, dryer eyes.", "increased sensitivity to light and sound, dryer eyes.", "increased sensitivity to light and sound, dryer eyes." and "some paresthesia running through the head with heat waves at various times" were evaluated at the physician office visit. Therapeutic measures were taken as a result of tinnitus, head discomfort, paraesthesia, photophobia, hyperacusis, dry eye, feeling hot. Additional information: The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient received Multivitamins within 2 weeks of vaccination. Therapeutic measures were taken with Sound therapy, acupuncture. Prior to vaccination, the patient was not diagnosed with COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to molds; Dust allergy; Pollen allergy; Ulcerative keratitis (other medical history: Peripheral ulcerative keratitis (eye))
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1168406

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 20.03.2021
Beginn: 21.03.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Condition aggravated Deafness neurosensory Decreased appetite Ear discomfort Head discomfort Dry eye Feeling hot Hyperacusis Paraesthesia Hot flush Nausea Tinnitus Photophobia

Symptomtext

New onset tinnitus/High pitched "screech" feeling/sounding/Lower frequency tones of varying frequency in both ears, although louder in the right; pressure in both ears and in the head; Some paresthesia running through the head with heat waves at various times.; Increased sensitivity to light and sound, dryer eyes.; Increased sensitivity to light and sound, dryer eyes.; Increased sensitivity to light and sound, dryer eyes.; Some paresthesia running through the head with heat waves at various times; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 20Mar2021 15:00 (Lot number: EN6203) at the age of 59 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "Peripheral ulcerative keratitis (eye)" (unspecified if ongoing), notes: other medical history: Peripheral ulcerative keratitis (eye); "known allergies: tree pollens" (unspecified if ongoing); "known allergies: dust" (unspecified if ongoing); "known allergies: Mold" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: TINNITUS (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "New onset tinnitus/High pitched "screech" feeling/sounding/Lower frequency tones of varying frequency in both ears, although louder in the right"; HEAD DISCOMFORT (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "pressure in both ears and in the head"; PARAESTHESIA (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "Some paresthesia running through the head with heat waves at various times."; PHOTOPHOBIA (non-serious), HYPERACUSIS (non-serious), DRY EYE (non-serious) all with onset 21Mar2021 07:00, outcome "not recovered" and all described as "Increased sensitivity to light and sound, dryer eyes."; FEELING HOT (non-serious) with onset 21Mar2021 07:00, outcome "not recovered", described as "Some paresthesia running through the head with heat waves at various times". The events "new onset tinnitus/high pitched "screech" feeling/sounding/lower frequency tones of varying frequency in both ears, although louder in the right", "pressure in both ears and in the head", "some paresthesia running through the head with heat waves at various times.", "increased sensitivity to light and sound, dryer eyes.", "increased sensitivity to light and sound, dryer eyes.", "increased sensitivity to light and sound, dryer eyes." and "some paresthesia running through the head with heat waves at various times" were evaluated at the physician office visit. Therapeutic measures were taken as a result of tinnitus, head discomfort, paraesthesia, photophobia, hyperacusis, dry eye, feeling hot. Additional information: The patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient received Multivitamins within 2 weeks of vaccination. Therapeutic measures were taken with Sound therapy, acupuncture. Prior to vaccination, the patient was not diagnosed with COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to molds; Dust allergy; Pollen allergy; Ulcerative keratitis (other medical history: Peripheral ulcerative keratitis (eye))
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2088249

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: IA
Alter: 94,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 08.03.2021
Beginn: 13.09.2021
Tage bis Beginn: 189,0
Dosis: 2
Route/Site: IM / -

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

Acute kidney injury Anaemia Asthenia COVID-19 COVID-19 pneumonia Chest X-ray normal Chills Chronic kidney disease Clostridium test negative Cough Crepitations Diarrhoea Dyspnoea Hypoxia Inappropriate schedule of product administration Laboratory test abnormal Metabolic function test normal Pyrexia

Symptomtext

COVID Vaccine Breakthrough Case Pfizer Dose 1 2/12/21 (EN6201) Pfizer Dose 2 3/8/21 (EN6203) COVID Positive 9/13/21 9/23/21: The patient was diagnosed with COVID-19 infection more than a week, referred to our hospital due to generalized weakness with episodes of fever and chills and episodes of dry cough with shortness of breath, decline orthopnea or chest pain or productive cough or nausea or vomiting or diarrhea. At emergency, she was mildly dyspneic and hypoxic 86% on room air required 2 L of oxygen. Her labs show CKD, stable anemia. 9/27/21: The patient presented to the hospital from assisting living facility complaining from worsen generalized weakness with cough, she was dyspneic and hypoxic requiring 3-4 L of oxygen initially at the ED, had wheezing and crepitation her chest exam, chest x-ray unremarkable for acute anomalies, her labs show moderate stable anemia, her CMP unremarkable, she was diagnosed with moderate COVID-19 pneumonia and she was started on dexamethasone IV with vitamins, initially had worsen renal function/AKI on CKD require IV fluid then her renal function improved and the patient started on Remdesivir with improvement in her symptoms. We have been able to wean her of oxygen and clinically improved. She had episodes of severe diarrhea require dedication management system and her C diff is negative. Patient tolerated her diet and improved clinically. Discussed with the patient, will discharge to her assisting living facility with VNA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: htn chronic renal insufficiency seizure breast cancer anemia osteoarthritis gout osteoporosis
Vorgeschichte: htn chronic renal insufficiency seizure breast cancer anemia osteoarthritis gout osteoporosis
Andere Medikamente: acetaminophen 650 mg PO Q4h PRN ascorbic acid 500 mg PO BID aspirin 81 mg PO QD atorvastatin 80 mg PO QD benzonatate 100 mg PO TID PRN bisacodyl 10 mg PR PRN cholecalciferol 25 mcg PO QD iron 325 mg PO 3x per week furosemide 20 mg PO QD mag
Allergien: nitrofurantoin - unknown sulfa drugs - unknown
Vorherige Impfungen: -

VAERS 2215743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 91,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 16.03.2021
Beginn: 12.08.2021
Tage bis Beginn: 149,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Atrial fibrillation COVID-19 Decreased appetite Dyspnoea SARS-CoV-2 test positive

Symptomtext

Narrative: Patient completed COVID series in March 2021. Hospitalized with COVID-19 8/12/21 after presenting with shortness of breath, weakness, and decreased ap/petite, as well as Afib with RVR. Treated with remdesivir (8/12-17) and dexamethasone Discharged to nursing home 8/27/21

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Tested positive for COVID 8/12/21
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: DC
Alter: 60,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 09.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Anxiety Arthralgia Dyspnoea Erythema Joint swelling Peripheral swelling Pruritus Swelling

Symptomtext

First dose - swelling and redness around the knees. Soreness in the knee joints. Went to see the nurse and she wasn't sure what was causing the redness and swelling. Second dose -swelling and redness around knees again. Soreness in knee joints. Did not go to the doctor. Booster - swelling around knees, swelling and redness on forearms, swelling and itching on back, a treated ganglion cyst on wrist was huge and swollen. Had difficulty breathing but could have been due to anxiety about my body swelling up all over. Went to the emergency room and was given benedryl. The ganglion cyst immediately went down and back to normal. Have been taking Zyrtec which seems to help. Still have occasional soreness in the joints of my knees and right elbow.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ?
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Blood pressure medication
Allergien: Quinine Sulfa based drugs
Vorherige Impfungen: -

VAERS 2071251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 08.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: - / LA

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

Alopecia Condition aggravated

Symptomtext

Hair loss; Hair loss was reported as worsened.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 08Mar2021 (Lot number: EN6203) at the age of 70 years as dose 2, single for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE, First Covid vaccine: 15Feb2021, Lot Number / Expiry Date: EN5319 , Route, Anatomical Location: left arm, No. of Previous Doses: NA), administration date: 15Feb2021, when the patient was 69 years old, for COVID-19 immunization. The following information was reported: ALOPECIA (non-serious), outcome "not recovered", described as "Hair loss"; CONDITION AGGRAVATED (non-serious), outcome "not recovered", described as "Hair loss was reported as worsened." Additional information: Patient states her hair was falling out. She used to have a full head of hair, like a rug, and now her hair was thin, like a sheet of paper, or like a sheet on her bed. She was mad, as she used to have a full head of hair and it was now a crappy color and falling out. No other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Patient's Medical History: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2070074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 75,0
Geschlecht: M
Eingang: 27.01.2022
Impfdatum: 24.02.2021
Beginn: 25.01.2022
Tage bis Beginn: 335,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Chest X-ray normal Chronic obstructive pulmonary disease Condition aggravated Decreased appetite Productive cough Respiratory tract congestion SARS-CoV-2 test positive Sputum discoloured Vaccine breakthrough infection Wheezing

Symptomtext

Breakthrough COVID Hospital. Pt vaccinated on 2/5/21 and 2/24/21, did not receive a booster. Patient arrived to ED on 1/25/22 with c/o cough with green sputum, wheezing, chest congestion and decreased appetite. Denies other symptoms. ED workup included normal chest XR, positive COVID test, IV steroids and inhalers. Admitted for COPD exacerbation and covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Covid + test on 1/25/22
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, Parkinson's, diabetes, active smoker
Andere Medikamente: -
Allergien: Amoxicillin, contrast dye, phenobarbital, iodine topical
Vorherige Impfungen: -

VAERS 2062499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: MO
Alter: 88,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 25.03.2021
Beginn: 21.01.2022
Tage bis Beginn: 302,0
Dosis: 1
Route/Site: IM / RA

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

Cough Dyspnoea Fatigue Pyrexia Respiratory tract congestion Rhinorrhoea

Symptomtext

fever, cough, shortness of breath, fatigue, congestion, runny nose admitted to hospital on 1/22 and currently still there

Weitere VAERSDATA-Felder

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

VAERS 2061834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: -
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 21.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: - / -

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

Chills Fatigue Lymphadenopathy Mobility decreased Pain Pain in extremity

Symptomtext

really tired; off-the-chart aches and chills; off-the-chart aches and chills; couldn't move or touch his arm it hurt so much; couldn't move or touch his arm it hurt so much; could tell the exact location of every lymph node in his body; This is a spontaneous report received from non-contactable consumer from a sales representative. The reporter is the patient. A male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), administration date 21Mar2021 (Lot number: EN6203) 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 (non-serious), CHILLS (non-serious) all with onset Mar2021, outcome "not recovered" and all described as "off-the-chart aches and chills"; PAIN IN EXTREMITY (non-serious), MOBILITY DECREASED (non-serious) all with onset Mar2021, outcome "unknown" and all described as "couldn't move or touch his arm it hurt so much"; LYMPHADENOPATHY (non-serious) with onset Mar2021, outcome "unknown", described as "could tell the exact location of every lymph node in his body"; FATIGUE (non-serious) with onset 22Mar2021, outcome "unknown", described as "really tired". Additional information: The patient's age was reported as 62 (unit unspecified). The patient stated that he still a little chilled and moderately achy (although, no fever). No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2058909

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 23.02.2021
Beginn: 22.08.2021
Tage bis Beginn: 180,0
Dosis: 2
Route/Site: UN / UN

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

COVID-19 COVID-19 pneumonia Malaise SARS-CoV-2 test positive Walking distance test abnormal

Symptomtext

Presents with worsening covid symptoms, tested positive 1 week ago. Admitted for Covid PNA. Treated with O2, abx, zinc. The patient was admitted to the hospital, treated with IV dexamethasone, IV antibiotics,iv Remdesivir,the patient's breathing progressively, underwent 6 minutes walk study, was needing supplemental oxygen which was prescribed to have and the patient discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 17,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2057895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: KY
Alter: 65,0
Geschlecht: F
Eingang: 23.01.2022
Impfdatum: 26.02.2021
Beginn: 12.01.2022
Tage bis Beginn: 320,0
Dosis: 1
Route/Site: IM / RA

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

Cough Dyspnoea Dysuria Exposure to SARS-CoV-2 Feeling abnormal Malaise Pyrexia

Symptomtext

Presents to the emergency room with complaints of dysuria and increasing shortness of breath. Says she began to have symptoms of COVID on Wednesday 1/12. Husband also positive. She has gotten progressively more short of breath and feeling poorly. Some fevers at home. Some cough. She has turned up her oxygen and remains short of breath. In the emergency room she is currently 92% on 5 L.

Weitere VAERSDATA-Felder

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

VAERS 2056694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6203

moderat

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 22.01.2022
Impfdatum: 26.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Mobility decreased Neck pain Pain Spinal pain

Symptomtext

The pain continued to get worse and spread to the point where my neck was very painful; pain on the side of my spine on the same side as the injection; pain grew much worse and spread to the other side of my spine; where my neck was very painful neck pain ,difficult to move; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 38 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm left, administration date 26Feb2021 14:30 (Lot number: En6203) at the age of 38 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "pernicious anaemia" (unspecified if ongoing); "iron deficiency anaemia" (unspecified if ongoing). Concomitant medication(s) included: IBUPROFEN. The following information was reported: NECK PAIN (non-serious) with onset 27Feb2021 08:00, outcome "recovering", described as "The pain continued to get worse and spread to the point where my neck was very painful"; SPINAL PAIN (non-serious) with onset 27Feb2021 08:00, outcome "recovering", described as "pain on the side of my spine on the same side as the injection"; PAIN (non-serious) with onset 27Feb2021 08:00, outcome "recovering", described as "pain grew much worse and spread to the other side of my spine"; MOBILITY DECREASED (non-serious) with onset 27Feb2021 08:00, outcome "recovering", described as "where my neck was very painful neck pain ,difficult to move". Therapeutic measures were not taken as a result of neck pain, spinal pain, pain, mobility decreased. Additional information: It was reported that, the morning after the vaccine she work up with neck and pain on the side of her spine on the same side as the injection. Over the course of the morning this pain grew much worse and spread to the other side of her spine. The pain continued to get worse and spread to the point where her neck was very painful and difficult to move. This gradually got better over the week but she continued to have mild soreness after. Patient took vaccine at public health clinic/veterans administration facility. Patient took Ibuprofen after the vaccine. Patient had no known allergies. Patient had no other vaccine in four weeks. The patient was not tested positive for covid 19 prior to vaccination and had not been tested post vaccination. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Iron deficiency anaemia; Pernicious anaemia.
Andere Medikamente: IBUPROFEN.
Allergien: -
Vorherige Impfungen: -

VAERS 2050400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 20.01.2022
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Headache Migraine Nausea

Symptomtext

headaches; migraine; nausea; 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 74 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 05Mar2021 (Lot number: EN6203) at the age of 74 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "diabetes" (unspecified if ongoing), notes: diagnosed about 5-10 years ago; "Congestive heart failure", start date: 2003 (unspecified if ongoing), notes: diagnosed in 2003 and hospitalized for a month. The patient's concomitant medications were not reported. The following information was reported: MIGRAINE (non-serious) with onset 05Mar2021, outcome "recovered" (07Mar2021), described as "migraine"; NAUSEA (non-serious) with onset 05Mar2021, outcome "recovered" (07Mar2021), described as "nausea"; HEADACHE (non-serious) with onset 11Mar2021, outcome "not recovered", described as "headaches". Additional information: It was reported that patient had the first dose of the shot on 05Mar2021 and stated later on that day and the next day had a severe migraine with nausea and was resolved by 07Mar2021. Patient then stated that for two days she did not have anything, and then she started having intermittent headaches on 11Mar2021 and since then. She stated they were not as bad as the migraine but they come and go. Patient wanted to know if these headaches could still be related to the vaccination. 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: Congestive heart failure (diagnosed in 2003 and hospitalized for a month); Diabetes (diagnosed about 5-10 years ago)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2047833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NJ
Alter: 81,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 05.03.2021
Beginn: 17.01.2022
Tage bis Beginn: 318,0
Dosis: 2
Route/Site: - / -

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

Alanine aminotransferase increased Angiogram pulmonary normal Aspartate aminotransferase increased Asthenia Atrial fibrillation Blood lactic acid COVID-19 Computerised tomogram thorax abnormal Condition aggravated Cough Decreased appetite Fatigue Fibrin D dimer increased Hypophagia Lung infiltration Platelet count decreased Pyrexia SARS-CoV-2 antibody test

Symptomtext

This is a 82 year old male with a PMH/PSH as noted below. The patient states he was Covid+ about 2 weeks ago and had been at home. He had been weak, tired with cough. Denied SOB. Had poor appetite and intake at home. Stated he had a fever at home. Today he was feeling weaker and tired prompting him to come to the ED for further work up. In the ED, patient was found to have bilateral infiltrates confirmed by CT scan of chest. Labs noted elevated AST/ALT, WBC was 1.9 with platelet 74, DD 451 with negative CTA for PE, LA 2.23. HR was 109 afib BP stable and saturation 96% on 3l/m. Patient was vaccinated.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 3,0
Labordaten: 01/17/2022 - SARS-CoV-2 Antigen (-) and IgM 0.02 101/18/2022 - SARS_CoV-2 PCR (++)
Aktuelle Erkrankungen: -
Vorgeschichte: Dyslipidemia, HTN; Addt'l Med History CLL Afib/flutter AV block mitral regurg. Significant Surg Hx As Listed Addt'l Surgical History R-total knee replacement. Smoking Status Former Smoker
Andere Medikamente: atorvastatin 10 mg Tablet Directions: 1 tablet oral daily (Active) dronedarone (Multaq) 400 mg Tablet Directions: 1 tablet oral twice a day (Active) lisinopril 5 mg Tablet Directions: 1 tablet oral daily (Active) rivaroxaban (Xarelt
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2043682

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CO
Alter: 71,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 21.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 326,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 pneumonia Chest X-ray abnormal

Symptomtext

Per ED physician note (1/13/2022): Signs and symptoms seem most consistent with likely COVID-pneumonia. Patient appeared to be an excellent candidate for home O2 therapy and ongoing dexamethasone. While the chest x-ray showed streaky opacities, this is consistent with her COVID-19 diagnosis and does not appear to be a clear indication for admission at this time. Patient was observed for more than an hour on her home oxygen without increased work of breathing, change in her respiratory status or desaturation events. Unfortunately, monoclonal antibody therapy has not shown to be effective with Omicron and is no longer accessible for patient. We discussed the above findings as well as ongoing management of COVID-19 symptoms and home oxygen use. There does not appear to be any other indication for admission at this time. Patient appeared safe for discharge. We reviewed strict return precautions and follow-up options. At this point, we will plan for discharge home.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Tamiflu, Keflex
Vorherige Impfungen: -

VAERS 2038277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Axillary pain Bacille Calmette-Guerin scar reactivation Chills Condition aggravated Erythema Nausea Pain in extremity Pyrexia Rash

Symptomtext

1)Red mild rash on the forehead and between breasts that appeared in the same place 72 hrs after first dose, 28hrs after second dose and 20 hrs after third dose. Rash was not raised, warm and tingling. Rash didn't go away after taking antihistamine medication. Rash had the same shape after each dose (Pfizer and Moderna caused the same rash). 2) Reactivation of BCG scar 24 hours after each dose. Scar appeared red and redness lasted for 48 hours along with extreme arm pain. 3) Arm pain, armpit pain, nausea, fever and chills.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: I visited allergist, who confirm that it is very likely that rash on the face is related to allergy to one of the component of vaccine. She was unable to confirm so, due to lack of the test for mRNA vaccine.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control Pill, Velivet
Allergien: None
Vorherige Impfungen: -

VAERS 2035377

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: NY
Alter: 73,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 25.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Blood test Dyspnoea Headache Pain Pyrexia Vaccination complication Vomiting X-ray

Symptomtext

1/2 hour after shot experienced Shortness of Breath, spike in fever (102), vomiting aches and pains and severe headaches. Taken to Emergency room. Admitted and spent 3 or 4 days. Treated with IV meds and told DX adverse reaction to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Blood work, xrays 02/25/2021 to 02/28/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: Bladder control . Gall bladder (removed)
Andere Medikamente: sertraline hcl 100mg
Allergien: None
Vorherige Impfungen: -

VAERS 2035049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: KY
Alter: 66,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 26.02.2021
Beginn: 13.01.2022
Tage bis Beginn: 321,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia Cough Diarrhoea Dyspnoea Dyspnoea exertional Exposure to SARS-CoV-2 Hypophagia Nausea Pyrexia SARS-CoV-2 test negative

Symptomtext

67 y.o. female admitted 1/13/2022 with a past medical history significant for CAD, hypertension, HLD, follicular lymphoma on chemotherapy, and GERD. She present today with complaints of progressively worsening SOB going on for the past 8 days. Dyspnea worse with exertion. There is associated non productive cough, generalized weakness, decreased PO intake, nausea without vomiting, diarrhea, and subjective fever. She is fully vaccinated for COVID-19 with a booster. Patient was initially evaluated by PCP at onset of symptoms wherein she reportedly tested negative for COVID-19. She was subsequently started on tamiflu prophylactically without improvement. She called PCP today who subsequently directed her to ED for further evaluation and treatment. Patient report that she and her daughter were exposed to Covid at a new years eve party. She states he daughter had covid after this event but quickly recovered. There are no complaints of chest pain, syncope, or lower extremity pain or swelling. No abdominal pain, dysuria, or flank pain. No headache or focal weakness/parathedias. Will admit to inpatient to hospitalist service and consult nephrology and ID in the AM.

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

VAERS 2028808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TN
Alter: 79,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 03.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 36,0
Dosis: 2
Route/Site: SYR / LA

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

Anticoagulant therapy Arrhythmia Atrial fibrillation Cardioversion Echocardiogram Electrocardiogram

Symptomtext

Atrial Fibrillation Cardioversion (shock treatment) 07/27/2021 xarelto 20 mg 04/19/2021 Amiodarone 200 mg 04/19/2021 Cardioversion brought heart back in to rhythm but after about 3 months heart rhythm became erratic, and still is out of rhythm.

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Electrocardiogram 04/08/2021 (EKG has been done at each Cardiologist visit) Ultrasonic (Echocradiogram) examination of heart 04/29/2021
Aktuelle Erkrankungen: none
Vorgeschichte: cholelesterol
Andere Medikamente: simvastatin
Allergien: none
Vorherige Impfungen: -

VAERS 2028314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 79,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 24.02.2021
Beginn: 08.01.2022
Tage bis Beginn: 318,0
Dosis: 1
Route/Site: - / -

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

Cough Dyspnoea Headache Oropharyngeal pain Pain

Symptomtext

sore throat, headache, cough, shortness of breath, body aches. starting 1/8/22

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Mild HTN (mild LVH on echo 11/1999). BPH. CKD III. Gout. Micorhematuria. ASCVD s/p bare metal stent to RCA 9/9/13. Prostate cancer.
Andere Medikamente: ?Aspirin 81 MG Tablet Delayed Release 1 tablet Orally Once a day ?Atorvastatin Calcium 20 MG Tablet 1 tablet Orally Once a day ?Losartan Potassium 25 MG Tablet 1 tablet Orally Once a day ?Metoprolol Succinate ER 50 MG Tablet Extend
Allergien: none
Vorherige Impfungen: -

VAERS 2019696

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MA
Alter: 32,0
Geschlecht: M
Eingang: 09.01.2022
Impfdatum: 12.03.2021
Beginn: 16.03.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Adverse reaction Blister Blood test normal Dyspnoea Electrocardiogram normal Erythema Pain Pain in extremity Palpitations Pruritus Rash

Symptomtext

Covid vaccine 1: rash, blisters, redness, itchy and painful toes 4 days post vaccine. These lasted 2.5 weeks. Treatment: steroid cream prescription, hydrocortisone cream, NSAIDS. No relief. Went away on its own. Heart palpitations: 1 day post vaccine. No treatment. Went away on their own after a few weeks. Covid vaccine 2: same symptoms as above. Covid toes last 3.5 weeks, non receptive to medications. Much worse adverse reaction than first vaccine. Heart palpitations persisted for 2-3 months. Covid booster: same reactions as above. Onsight of covid toes started within 24 hours and are present today 1/9/2022 (booster on 12/10/2021) with no signs of relief an are worse than previous times. Heart palpitations are re-occurring every 2-3 days that take my breathe away. Palpitations are more frequent and tracked manually when occurred due to consistency and pain.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: EKG for palpitations, blood panel pre-vaccine (1/2021) and post vaccine 1 and 2 and booster done 1/2022. Unremarkable. Normal blood work/panel.
Aktuelle Erkrankungen: NA
Vorgeschichte: NA.
Andere Medikamente: NA - no medications, vitamins, supplements etc.
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2005897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NJ
Alter: 60,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 04.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 14,0
Dosis: 1
Route/Site: IM / AR

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

Anti-cyclic citrullinated peptide antibody negative Antibody test negative Antinuclear antibody negative Asthenia Back pain Biopsy skin abnormal Blood creatinine normal Blood thyroid stimulating hormone normal Condition aggravated Double stranded DNA antibody Electromyogram normal Electrophoresis protein Full blood count normal Glucose tolerance test abnormal Glycosylated haemoglobin Headache Low density lipoprotein increased Magnetic resonance imaging head normal

Symptomtext

severely painful paresthesias in the upper and lower extremities, head and trunk, neck and back pain, headache, and feelings of weakness that began 2 weeks after first vaccination, significantly worsened after second dose. EMG/NCS essentially normal. Skin biopsies consistent with small fiber neuropathy. She has a painful small fiber neuropathy, most likely a post-vaccine complication

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EMG/NCS essentially normal. Skin biopsies consistent with small fiber neuropathy. Labs 2021: HgbA1c 6.1, SPEP no M protein, Cr 0.72, LDL 147, vitamin D 16.2, abnormal GTT, TSH normal, CBC normal, ANA negative, CCP ab negative, RF normal, dsDNA negative, SSA and SSB negative, Smith ab negative. MRI brain WO June 2021: No intracranial abnormality or evidence of metastatic lesions
Aktuelle Erkrankungen: none
Vorgeschichte: Prediabetes GERD NASH Splenic lesion, possible low grade lymphoma found 2019 Breast cancer in situ 2014 - lumpectomy and XRT Hyperlipidemia
Andere Medikamente: -
Allergien: amoxicllin
Vorherige Impfungen: -

VAERS 2529664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 03.03.2021
Beginn: 04.05.2021
Tage bis Beginn: 62,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chills Cough Diarrhoea Dizziness Dry throat Dyspnoea Exposure to SARS-CoV-2 Fatigue Musculoskeletal chest pain Myalgia Nausea Oropharyngeal pain Respiratory tract congestion Retching Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

Narrative: COVID POSITIVE AFTR COVID VACCINATION SERIES 02/10 COVID vaccine dose #1 03/03 COVID vaccine dose #2 04/28 symptoms started with sneezing and allergy symptoms, 1 day of dizziness (4/29) that resolved same day 05/04 COVID screening positive due to report of myalgia, rhinorrhea, dizziness, sore throat and close exposure to known positive 05/05 c/o continued runny nose, myalgia, congestion 05/06 c/o ongoing myalgia, rhinorrhea (nearly resolved) 05/07 c/o chills, moderate/dry/scratchy throat, diarrhea x4, ongoing fatigue, nausea, rhinorrhea, dry heaves, no fever, O2 sat WNL; rx'd tessalon perles and robittussin DM 05/08 c/o continued cough and diarrhea, ongoing rib pain from coughin, dyspnea when coughing 05/09 c/o continued dry cough improved with robitussin, diarrhea, fatigue, myalgia (rib pain due to coughing); no dyspnea or vomiting 05/10 states dry cough is improving, quarantine ended

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 05/04 COVID POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1955544

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 01.01.2022
Impfdatum: 02.04.2021
Beginn: 31.10.2021
Tage bis Beginn: 212,0
Dosis: 2
Route/Site: - / LA

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

Computerised tomogram head Migraine Tinnitus Headache

Symptomtext

severe ringing in the ears (level 7 on a scale of 1-10) followed by a severe headache; severe ringing in the ears (level 7 on a scale of 1-10) followed by a severe headache; 4 migraine headaches (of the optic nerve, on the same day and several days later); This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 76 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 02Apr2021 (Lot number: EN6203) at the age of 76 years as dose 2, single for covid-19 immunisation. Relevant medical history included: "enlarged prostate" (unspecified if ongoing); "Drug allergy" (unspecified if ongoing), notes: To codeine; "Heartbeats irregular" (unspecified if ongoing), notes: Rapid; "migraine headache" (unspecified if ongoing), notes: spaced at least 6 months apart. Concomitant medication(s) included: SIMVASTATIN; BUSPAR; METOPROLOL. Vaccination history included: Bnt162b2 (Dose 1, Batch/Lot ER8732, in arm left, at 03:45 AM), administration date: 09Mar2021, when the patient was 76 years old, for Covid-19 Immunization. The following information was reported: TINNITUS (non-serious) with onset 31Oct2021 04:00, outcome "not recovered", HEADACHE (non-serious) with onset 31Oct2021, outcome "not recovered" and all described as "severe ringing in the ears (level 7 on a scale of 1-10) followed by a severe headache"; MIGRAINE (non-serious) with onset 31Oct2021, outcome "not recovered", described as "4 migraine headaches (of the optic nerve, on the same day and several days later)". The events "severe ringing in the ears (level 7 on a scale of 1-10) followed by a severe headache", "severe ringing in the ears (level 7 on a scale of 1-10) followed by a severe headache" and "4 migraine headaches (of the optic nerve, on the same day and several days later)" were evaluated at the emergency room visit. Therapeutic measures were not taken as a result of tinnitus, headache, migraine. Additional information: the patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Drug allergy (To codeine); Enlarged prostate; Heartbeats irregular (Rapid); Migraine headache (spaced at least 6 months apart)
Andere Medikamente: SIMVASTATIN; BUSPAR; METOPROLOL
Allergien: -
Vorherige Impfungen: -

VAERS 1995367

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 27.02.2021
Beginn: 10.03.2021
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: - / LA

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

Blood pressure measurement Blood test Colonoscopy Echocardiogram Electrocardiogram Hypertension Urine analysis

Symptomtext

high blood pressure/blood pressure went to 220 after the Pfizer and it stayed 193, 185; it stayed for months/blood pressure went over the roof; This is a spontaneous report received from contactable reporter (consumer) from Medical Information team. The reporter is the patient. A 70 year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), administered in arm left, administration date 27Feb2021 around midday (Lot number: EN6203, Expiration Date: Jun2021) at the age of 70 years as dose 1, single for COVID-19 immunization. The vaccine was not administered at facility. The patient had no relevant medical history. There were no concomitant medications. The patient had no prior vaccinations (within 4 weeks). The patient had no family medical history relevant to the adverse event (AE). The following information was reported: HYPERTENSION (medically significant) with onset 10Mar2021, outcome "unknown," described as "high blood pressure/blood pressure went to 220 after the Pfizer and it stayed 193, 185; it stayed for months/blood pressure went over the roof." The event was evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood pressure: (10Mar2021) 220, 193, and 185, notes: high; (2021) 179 and 175, notes: doctor prescribed Losartan and the blood pressure was still high like 179, 175; (2021) 150, 160, and 140, notes: during the day, blood pressure was much lower it was like 150, 160, 140; (2021) 180 and 195, notes: at night if she woke up, it still could be 180, 195; blood tests: (2021) normal; colonoscopy: (10Mar2021) unknown; echocardiogram: (2021) unknown; electrocardiogram (EKG): (2021) normal; urine tests: (2021) normal. Therapeutic measures were taken as a result of hypertension, which included losartan and hydrochlorothiazide (HCTZ). The patient relayed that since having the two primary doses, she had experienced high blood pressure since Mar2021. She did not have high blood pressure prior to receiving the vaccine. She stated that the nurse should have taken her blood pressure before the shot and after to see if it went up. She had seen a cardiologist and had an EKG and an echocardiogram done. She had been placed on high blood pressure medications and 'water pills.' She stated her blood pressure would go up to 220, 198, and 183. She had read a study that the vaccine causes high blood pressure. She relayed that the doctors didn't know and that they deny the high blood pressure was related to the vaccine, but that she was sure it is. She would like Pfizer to know that this was a side effect. The patient expressed concern that she currently had to take medications to treat her blood pressure, but that they would have negative effects on her kidneys and liver over time. She stated that she did not feel bad or have any physical symptoms of the high blood pressure. The patient was asking what ingredient was causing the high blood pressure. She stated that myocarditis and pericarditis were known side effects with the vaccine and wanted to know how she would know if she had inflammation in the heart. It was relayed to the patient that elevated blood pressure was not a side effect that was reported during clinical trials and because of this, there was no data for it and was referred to speak with healthcare professional (HCP) if she was concerned for this condition or had further questions. The patient did not know if she should receive the booster dose of the vaccine or if it would just make her blood pressure higher and her doctors did not know. The patient was asking if she could have the Moderna booster dose instead. The patient was again referred to speak with HCP regarding fruther questions. It was further reported that she was due to get the booster and she had concerns, but nobody could answer her questions. She suffered from side effects, clarified that ''her blood pressure went over the roof after she had the first and second dose of the Pfizer COVID-19 vaccine. Her blood pressure went up to 220. They did not check her blood pressure during the COVID-19 vaccination, but she had an appointment for a colonoscopy on 10Mar2021, wherein they woke her up and was shaking her like she was so angry, she was told her blood pressure was 220 and then 193 and then 185. They called all the doctors and made such a big fuss and did an EKG. Her blood pressure was high at night, but she took medication in the morning during the day so its lower during the day. All the time she went through all the tests, she was asking herself why she had high blood pressure; she thought it was connected to the colonoscopy, since this was the first time she knew about her blood pressure being elevated. She knew and read research that a lot of patients that took the Pfizer COVID-19 vaccine had blood pressure increased. She was asking what ingredient in the vaccine could be causing the blood pressure increase. She was a 100% healthy person before the Pfizer COVID-19 vaccine. She read it causes myocarditis and was asking if the booster would make her blood pressure worse. The patient reported that for 5 months, she refused to take medication, she thought maybe the side effects would disappear if it was from the vaccine and she was drinking beets and celery to lower the blood pressure. She wanted to know why she had the blood pressure increased, so she went to the cardiologist and had tests. Even during the colonoscopy, the doctors rejected it, clarified the doctor stated that her increased blood pressure had nothing to do with vaccine. When she asked her primary doctor if she should take the booster, she was told according to CDC the benefit outweighed the danger. The blood pressure went through the roof was discovered during the colonoscopy on 10Mar2021. The patient further reported that she was looking online for the booster. She had two Pfizer shots. First one on 27Feb2021 and the second one on 20Mar2021 and she had terrible side effects. The doctors were saying it's not possible. The patient was trying to get the tests from the doctor's what was causing the high blood pressure and they didn't know. The EKG was normal, the blood tests were normal, the urine tests were normal, and they were saying they didn't know, but she should take medication for the high blood pressure, but she refused the medication, because she was a senior citizen and was in excellent health. The patient didn't have any problems till of the Pfizer her blood pressure went over the roof and she started to be very concerned and so she didn't take any high blood pressure medication, because she didn't want more side effects, but her blood pressure stayed in April, in May, in June, in July. Then her doctor told her that she could drop dead anytime from high blood pressure and she had to start the medication. So, she started the medication like two or three months prior reporting. The doctor prescribed losartan and the blood pressure was still high like 179, 175. So, they told her that she should take a water pill, so, that's a long name for that medication. She didn't remember the name, but it's a water pill. So she was taking those two medications and they increased losartan to two pills, so she was taking 1 in the morning, 1 in the evening, and in the middle of the day, she was taking the water pills. So, during the day, her blood pressure was much lower, it was like 150, 160, 140, but at night if she woke up, since she didn't take medication, it still could be 180, 195. The (withheld), they did research and they found the side effects of Pfizer, the heart inflammation, the muscles or in the chamber or on the outside. So, she had this concern because, she spoke to the doctor about the booster. She was afraid to take Pfizer booster, because it might increase to the problem with her heart and they said, CDC, they commented that the benefits outweighed the side effects. So, the patient didn't know if she should take the Pfizer booster and she was worried, because there were restrictions for people who didn't take the booster that like if she wanted to travel if she didn't show that she had the booster, maybe they would decline her travel. So, she wanted to report that because she didn't make it up, it had really happened to her and she was sure it happened to other people and she visited the cardiologist, who didn't know what was causing the high blood pressure. The patient wanted Pfizer to give her answers if she should take the booster, because she didn't want to have heart problems, didn't want to be paralyzed or have a heart attack.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: Test Date: 20210310; Test Name: blood pressure; Result Unstructured Data: Test Result:220; Comments: high; Test Date: 20210310; Test Name: blood pressure; Result Unstructured Data: Test Result:193; Comments: high; Test Date: 20210310; Test Name: blood pressure; Result Unstructured Data: Test Result:185; Comments: high; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:179; Comments: doctor prescribed Losartan and the blood pressure was still high like 179, 175; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:175; Comments: doctor prescribed Losartan and the blood pressure was still high like 179, 175; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:150; Comments: during the day, blood pressure was much lower it was like 150, 160, 140; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:160; Comments: during the day, blood pressure was much lower it was like 150, 160, 140; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:140; Comments: during the day, blood pressure was much lower it was like 150, 160, 140; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:180; Comments: at night if wake up, it still can be 180, 195; Test Date: 2021; Test Name: blood pressure; Result Unstructured Data: Test Result:195; Comments: at night if wake up, it still can be 180, 195; Test Date: 2021; Test Name: blood tests; Result Unstructured Data: Test Result:normal; Test Date: 20210310; Test Name: colonoscopy; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: Echocardiogram; Result Unstructured Data: Test Result:Unknown; Test Date: 2021; Test Name: EKG; Result Unstructured Data: Test Result:normal; Test Date: 2021; Test Name: urine tests; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 74,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 11.02.2021
Beginn: 21.12.2021
Tage bis Beginn: 313,0
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 12/28/2021
Aktuelle Erkrankungen: -
Vorgeschichte: Aortic valve regurgitation Ascending aortic aneurysm Hypertension Chronic atrial fibrillation NSTEMI DVT/PE Hypothyroidism
Andere Medikamente: ADVAIR HFA 115-21 mcg/actuation Inhl HFAA inhaler albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler allopurinol (ZYLOPRIM) 100 mg oral tablet doxazosin (CARDURA) 8 mg oral tablet furosemide (LASIX) 20 mg oral tablet gabap
Allergien: Amlodipine NSAIDs (Non-Steroidal Anti-Inflammatory Drug) Oxycodone Thiazides
Vorherige Impfungen: -

VAERS 2523892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 05.03.2021
Beginn: 21.11.2021
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: IM / LA

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

Asthma COVID-19 Condition aggravated Cough Dyspnoea Gravitational oedema Positive airway pressure therapy SARS-CoV-2 test positive Sick relative Somnolence Urine output decreased

Symptomtext

Narrative: Patient is an 85 yo who presents to the ED due to NOV 21, 2021 Subjective/Chief Complaint: Cough x 1 week. Objective: Significant bilateral dependent edema, which pt states is worsened. States home-use hospital bed is broken and cannot elevate feet as he normally does. Reports compliance with diuretic medication regimen, but greatly decreased urine production x 1 week. He has been covid vaccinated x 2 (no booster). Patient with history of asthma on chronic prednisone, presents with 1 week of dry cough he denies any fever or chills no chest pain. States that he gets a little short of breath when he is a coughing fit however otherwise does not have any shortness of breath. Has been using his inhaler more often than usual. Did have some ill family members in the home before all this started. HOSPITAL COURSE: slow but good progress have been encouraging greater in room activity, movement, States has been trying to use bedside incentive spirometry, but coughing at times has made it difficult. Flutter valve added. Typically somnolent in a.m. CPAP use in place. Patient has improved to point where he is off oxygen and appears closer to baseline. Discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: COVID-19 + ASTHMA EXACERBATION, O2 SATS 86%,
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1987605

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CO
Alter: 72,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 20.02.2021
Beginn: 27.11.2021
Tage bis Beginn: 280,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Chills Dyspnoea Hypoxia Myalgia Pyrexia Vaccine breakthrough infection

Symptomtext

Breakthrough COVID-19 case requiring hospitalization: Patient is a 73-year-old male presents with shortness of breath, fevers and chills and myalgias. Diagnosed with Covid on 11/29, underwent ab infusion outpatient. Still progressing and came to the emergency department with hypoxia. Patient was vaccinated in February 2021 but did not get his booster. He was found to have Covid pneumonia as well as possible concurrent bacterial pneumonia as well as significant hypoxia. Patient started on supportive care, IV antibiotics, steroids and remdesivir. He completed a course of antibiotics as well as remdesivir. He had slow improvement of his oxygen status and was requiring 2 L at time of discharge. He will discharge on 2 L home oxygen as well as complete a course of steroids. He is given follow-up for pulmonology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 8,0
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hyperlipidemia, Hypotension, Obesity, Unspecified vitamin D deficiency, Type 2 diabetes mellitus without complication, without long-term current use of insulin (HC code), Tubular adenoma of colon, Diverticulosis, Esophageal reflux, Erectile dysfunction, Hyponatremia, Neoplasm of uncertain behavior of skin, Primary malignant neoplasm of skin of trunk, History of malignant neoplasm of skin, Depression, Nontraumatic rupture of quadriceps tendon, Tenosynovitis of foot and ankle, Plantar fascial fibromatosis, Acquired equinus deformity of foot, Primary localized osteoarthrosis of hand, Gout, Primary osteoarthritis of left knee, Primary osteoarthritis of right knee, Hereditary and idiopathic peripheral neuropathy, Benign essential tremor
Andere Medikamente: albuterol HFA 90 mcg/actuation inhaler, amlodipine-olmesartan (AZOR) 5-20 mg per tablet, ascorbic acid (VITAMIN C PO), Aspirin 81 mg Tab, cholecalciferol, vitamin D3, (VITAMIN D3 PO), desloratadine (CLARINEX) 5 mg tablet, DULoxetine (CYMBAL
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1985162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: SC
Alter: 67,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 15.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / RA

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

Body temperature decreased COVID-19 Cough Eye irritation Eye pruritus Fatigue Hypertension Laryngitis Oropharyngeal pain SARS-CoV-2 test negative SARS-CoV-2 test positive Sinus congestion

Symptomtext

Started 12/20/2021 (week after booster)-Sore throat; itchy, burning eyes; cough; sinus congestion; high blood pressure(140?s/80?s), below normal temp, o2 stats 98, hr 75; fatigue 12/28/2021-still sore throat, laryngitis, below normal temp, bp is normal(120/76); o2-96; fatigue ED 12/23/2021- *Regen-Cov infusion-12/23/2021 600 mg of casirivimab with 600 mg of imdevimab

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: PCR-3/15/2021-negative PCR-12/21/2021-negative Molecular Rapid-12/22/2021-positive
Aktuelle Erkrankungen: None
Vorgeschichte: Abdominal Separation (Diastasis Recti) Sleep Apnea Osteoarthritis-CMC Rt thumb; rt hip Scoliosis-neck and back L1 fracture; L4 fracture-repaired Osteoporosis Psoriatic Arthritis Spondyloarthritis; entheses
Andere Medikamente: Nexium- 40 mg Temazepam-30mg Proscar-5mg Requip-2mg Rapaflo-8mg Relpax-Eletriptan-20mg-pen HCTZ-25mg Levothyroxine-100mcg Liothyronine (Cytomel)-5mcg 2xday Provigil (Modafinil)-200mg 1x day Astilin spray-0.1% Vitamin D-50,000 units, 1 x wk
Allergien: Sulfa, adhesives
Vorherige Impfungen: -

VAERS 1954886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 12.02.2021
Beginn: 30.11.2021
Tage bis Beginn: 291,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Cough Diarrhoea Dyspnoea Nausea SARS-CoV-2 test positive

Symptomtext

SOB., NAUSEA, MILD COUGH, INTERMITTENT DIARRHEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID DETECTED 12/14
Aktuelle Erkrankungen: -
Vorgeschichte: CAD involving native coronary artery of native heart without angina pectoris Colon polyps Diabetes mellitus type 2 DJD Dysphagia Esophageal ulcer Essential hypertension GERD HOH Hydronephrosis Hyperlipidemia Motion sickness Presbyesophagus Sarcoma of left thigh Tobacco abuse in remission SBO Diverticulosis Vertigo Renal colic Vitamin D deficiency Lumbar herniated disc Leukocytosis Primary osteoarthritis of right knee DDD, lumbar
Andere Medikamente: amLODIPine (NORVASC) 5 mg oral tablet aspirin 81 mg oral enteric coated tablet atorvastatin (LIPITOR) 10 mg oral tablet Cholecalciferol, Vitamin D3, 5,000 unit (125 mcg) oral tablet dulaglutide (TRULICITY) 1.5
Allergien: Naproxen-Pseudoephedrine Aleve [Naproxen Sodium] Triamterene
Vorherige Impfungen: -

VAERS 1948413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 20.02.2021
Beginn: 21.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Asthma Condition aggravated SARS-CoV-2 test

Symptomtext

I had a 3 day ongoing asthma attack that I was unable to get under control. I went to the doctor on the 3rd day and my asthma medication be increased and I had to purchase a humidifier to get it under control. It took about a week to get the issue to completely resolve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Rapid COVID test
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac Disease, Asthma
Andere Medikamente: Multivitamin, Zyrtec, Advair, Albuterol, Benadryl
Allergien: Gluten, Peaches, Curry Spice, Soy
Vorherige Impfungen: -

VAERS 1947615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: FL
Alter: 58,0
Geschlecht: F
Eingang: 14.12.2021
Impfdatum: 29.10.2021
Beginn: 12.12.2021
Tage bis Beginn: 44,0
Dosis: 1
Route/Site: IM / -

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

Angiogram abnormal Blood creatinine increased COVID-19 Chest X-ray normal Dyspnoea Fibrin D dimer increased Malaise Pleural effusion Serology abnormal Tachypnoea

Symptomtext

9/6/21: The patient is a very pleasant 58 year-old female who presents to the ED with worsening shortness of breath after recent diagnosis of acute COVID-19 infection. Patient developed symptoms on Tuesday and received antibody infusion on Wednesday. She later developed severe shortness of breath yesterday and sought medical attention in the ED. Upon initial evaluation patient was tachypneic with SpO2 on room air of 90%. Serologic analysis was fairly benign only notable for elevated creatinine 1.22. Chest x-ray showed no acute cardiopulmonary findings. Due to high D-dimer a CT angio chest was done ruling out acute embolism but showing right pleural effusion. Patient received first dose Pfizer vaccine on 2/24/2021 Lot # EN6203, the second dose on 3/18/2021 Lot # EN6200 and the booster shot on 10/29/2021 Lot# FH8028

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN, HLD, GERD, gastritis, RA, Hypothyroidism
Andere Medikamente: -
Allergien: Demerol HCI, Oxycontin, Penicillin, Sulfa drugs
Vorherige Impfungen: -

VAERS 1943542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 74,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 12.02.2021
Beginn: 09.12.2021
Tage bis Beginn: 300,0
Dosis: 2
Route/Site: - / -

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

Cough Dyspnoea Fatigue Oropharyngeal pain Sinus congestion Sinus operation Sinusitis

Symptomtext

Symptoms starting 12/9/21: fatigue, sinus congestion, nasal drainage, cough, sore throat; reports frequent sinus infections and last two antibiotics only seem to take the edge off and it comes right back; also needing her inhaler more often essentially 2-3 times per day, dating back to September and questions if needs to try something else.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hypertension. Hyperlipidemia. Osteoporosis. Anxiety. Gastroesophageal reflux disease. Allergic Rhinitis. Chest pain, previous nuclear medicine stress testing negative by report. Urinary frequency. History of squamous cell carcinoma excision. History of basal cell carcinoma excision.
Andere Medikamente: ?Cranberry 1000 MG Capsule as directed Orally , Notes: cranberry 8400 mg, vitamin C 40 mg, vitamin E 2.7 mg - 1 capsule orally once a day ?Citalopram Hydrobromide 10 MG Tablet 1 tablet Orally Once a day ?Simvastatin 40 MG Tablet 1 tab
Allergien: Sulfa: diarrhea,rash - Allergy Demerol: vomiting - Allergy Shell fish: anaphylaxis - Allergy Ivp: anaphylaxis - Allergy Novocain: shock - Allergy Alendronate Sodium: GI upset - Side Effects Augmentin: Diarrhea - Side Effects Latex: Hives - Side Effects
Vorherige Impfungen: -

VAERS 1939603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN 6203

moderat

Staat: -
Alter: 72,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 04.03.2021
Beginn: 05.12.2021
Tage bis Beginn: 276,0
Dosis: UNK
Route/Site: - / -

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

Asthenia Band neutrophil percentage increased Biliary dyskinesia Biliary obstruction Blood alkaline phosphatase Blood creatinine increased COVID-19 Cholecystitis Constipation Haemoglobin decreased Hypertension Peripheral coldness Platelet count decreased Pyrexia Renal impairment SARS-CoV-2 test positive Tachycardia Tachypnoea

Symptomtext

Breakthrough COVID / History of COVID in August 2021 72-year-old female with PMH of diabetes, HTN, hypothyroidism and COVID-19. recently admitted to the hospital on Septr 30, 2021 due to constipation and found to have cholecystitis vs common bile duct obstruction, severe gallbladder dyskinesia and renal dysfunction. She was evaluated by general surgery and gastroenterologist. Gen Surg recommended elective cholecystectomy. she returned to the hospital due to generalized weakness, cold extremities and inability to urinate. VS includes tachycardia 120s, tachypnea RR 37, hypertension, fever 102. Her WBC was 7.54, hemoglobin 10.7, 24% bands, platelet 111,000, creatinine 1.8, increased from 1.3 2 months ago, alk-phos 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: COVID PCR ICU + 12/6/2021
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, diabetes
Andere Medikamente: -
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 1938579

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 15.03.2021
Beginn: 15.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Blood creatine phosphokinase Chest X-ray Chest discomfort Computerised tomogram head Dizziness Fibrin D dimer Full blood count Headache Hypertension Incomplete course of vaccination Laboratory test Paraesthesia oral Pulmonary function test SARS-CoV-2 test Tachycardia Tremor

Symptomtext

I waited at the vaccine site for 15 min as instructed. Apx 5 min after leaving I began to feel lip tingling and light headed. I continued to drive home. Upon artiving at my home my symptoms worsened. Lightheaded, chest heaviness, violent tremor, mild headache began. I called y md and was instructed to call EMS & go to ER.. I was evaluated by EMS and told I was tachcardic and hypertensive. I was taken to ER. And arrived apx 2 hours after I had received vaccine . I was given IV steroids snd benedryl and valium for shaking. I was tested for and ruled out for stroke, MI , pulmonary embolism. I improved, but continued to have episodes of symptoms. I was kept for 2 days of observation testing and treatment. I was discharged on medrol pack and xanax for shaking. I was instructed not to receive 2nd covid shot. After discharge I experienced symptoms for over 3 months. I was seen by my md , cardiology, pulmonology and allergy after discharge . They all agreed that I should not take additional covid vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 2,0
Labordaten: Cat scan head , chest x ray, d dimer, cbc, cmet, cpks, covid test, 3/15, 3/16/2021. Pul function test 9/2021 Labs 8/2021
Aktuelle Erkrankungen: None
Vorgeschichte: Herniated discs with radiculopathy cervical and lumbar spine.
Andere Medikamente: Gabapentin, Duexis, Vit D, Flonase
Allergien: PCN, Sulfa
Vorherige Impfungen: -

VAERS 1932192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PR
Alter: 63,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 24.03.2021
Beginn: 24.03.2021
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 Dizziness Dyspnoea Feeling abnormal

Symptomtext

Patient started feeling bad. Had trouble breathing and was dizzy. Hospital where she received the vaccine sent her down to the ER. Had blood work, suero.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Zyrtec
Allergien: Penicillin, seasonal allergies
Vorherige Impfungen: -

VAERS 1172795

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PA
Alter: -
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 17.03.2021
Beginn: 01.03.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Abdominal discomfort Asthenia Chills Diarrhoea Dysgeusia Blood test Eating disorder Feeling hot Insomnia Feeling abnormal Hypoaesthesia Nausea Pain Malaise Menstrual disorder Mobility decreased Muscular weakness Pain in extremity

Symptomtext

Severe arm pain; Major limitation of arm movement; Temporary paresthesia; Significantly diminished menstrual cycle; Feeling of weakness and warmth in hands and arms; Feeling of weakness and warmth in hands and arms; feeling so unwell; Couldn't eat; Brain zaps/vertigo; Losing the ability to fall asleep or stay asleep; GI problems; Developed tinnitus-ringing and humming in the ears; Insomnia; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42 year-old female patient received bnt162b2 (BNT162B2), administration date 17Mar2021 (Batch/Lot number: unknown) as dose 2, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose: 1), when the patient was 42 years old, for COVID-19 Immunization. The following information was reported: EATING DISORDER (non-serious) with onset Mar2021, outcome "unknown", described as "Couldn't eat"; VERTIGO (non-serious) with onset Mar2021, outcome "recovered" (2021), described as "Brain zaps/vertigo"; SLEEP DISORDER (non-serious) with onset Mar2021, outcome "not recovered", described as "Losing the ability to fall asleep or stay asleep"; ABDOMINAL DISCOMFORT (non-serious) with onset Mar2021, outcome "recovered" (2021), described as "GI problems"; TINNITUS (non-serious) with onset Mar2021, outcome "unknown", described as "Developed tinnitus-ringing and humming in the ears"; INSOMNIA (non-serious) with onset Mar2021, outcome "not recovered", described as "Insomnia"; PAIN IN EXTREMITY (non-serious) with onset 18Mar2021, outcome "not recovered", described as "Severe arm pain"; MOBILITY DECREASED (non-serious) with onset 18Mar2021, outcome "not recovered", described as "Major limitation of arm movement"; PARAESTHESIA (non-serious) with onset Mar2021, outcome "unknown", described as "Temporary paresthesia"; MENSTRUAL DISORDER (non-serious) with onset Mar2021, outcome "not recovered", described as "Significantly diminished menstrual cycle"; MUSCULAR WEAKNESS (non-serious), FEELING HOT (non-serious) all with onset Mar2021, outcome "recovered" (2021) and all described as "Feeling of weakness and warmth in hands and arms"; MALAISE (non-serious) with onset Mar2021, outcome "unknown", described as "feeling so unwell". The events "losing the ability to fall asleep or stay asleep" and "insomnia" were evaluated at the physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: After the dose 2, The patient had a typical reaction the following day and felt better for two days after that. However, by Sun, she couldn't eat and developed brain zaps/vertigo like feeling/sensory disturbances which lasted for 5 days. During that time she also started losing the ability to fall asleep or stay asleep. (I also had GI problems for about 3-4 weeks - she never had GI problems, ever). Her brain felt like it was on fire and was so hyper aroused. she had NEVER experienced anything like it, she slept like a baby her whole life until this second vaccine. The patient saw pcp three times in March as well as the chief of sleep neurology at withheld in withheld in May and a sleep psychologist in May. All determined these side effects to be due to vaccine. The hyper arousal was so severe and she missed quite a bit of work due to feeling horrifically sick and exhausted. That has been a traumatizing situation for her. . Additionally she had severe arm pain lasting several days with major limitation of arm movement, temporary paresthesia (feeling of weakness and warmth in hands and arms for several weeks) and significantly diminished menstrual cycle immediately following vaccine #2. Her menstrual cycle was now less than half of what is was previously, it is been about 8 cycles since the shot. Unrelated to hormones or auto-immune as ruled out by my GYN via extensive bloodwork. She was a fit and healthy 42-year-old with zero co-morbid conditions, 5.2 inch and 118 pounds. The lot number for bnt162b2 was not provided and will be requested during follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Name: Blood work; Result Unstructured Data: Test Result:unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2565371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 26.02.2021
Beginn: 15.07.2021
Tage bis Beginn: 139,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia COVID-19 Confusional state Cough Dyspnoea Dyspnoea exertional Fatigue Foreign travel Hypertransaminasaemia Hypotension Hypoxia Liver function test abnormal Malaise Rash SARS-CoV-2 test positive Suicidal ideation Treponema test

Symptomtext

Narrative: COVID infection after completion of COVID vaccine series: 01/05/2021 COVID vaccine dose #1 02/26/2021 COVID vaccine dose #2 07/15/2021 Pt presented to ED c/o 8-day h/o general fatigue/weakness, dyspnea on exertion, and atypical rash covering face, chest, back, and legs. Pt stated he had returned from another country yesterday evening from a mission trip and that he had been off his MH med X 2 weeks. 07/15/2021 COVID positive per nasopharyngeal swab 07/15/2021 Pt admitted to facility given sx and needing 4LPM O2 via NC. Overnight pt became hypotensive and required bolus of NS and methylprednisolone therapy. 07/16/2021 MD attending note reported continued/worsened confusion (AOX2). Continuation of supplemental O2 PRN 2LNC and solumedrol. Pt not candidate for remdesivir at moment due to transaminitis. 07/17/2021 MD attending note reported that pt alert and oriented. Denied any concerns including cough, SOB, CP, or abdominal pain. Continuation of supplemental O2 PRN 2LNC and solumedrol. 07/18/2021 MD attending note reported pt having non-productive cough and mild SOB. Remdesivir started since LFTs normalized and pt hypoxic. Continuation of supplemental O2 and solumedrol. Pt resumed modafinil therapy. 07/19/2021 MD attending note reported pt feeling about the same/fatigued. Continuation of remdesivir and solumedrol. 07/20/2021 MD attending note reported pt not feeling well, slow progression of condition. Continuation of remdesivir and solumedrol. Unclear etiology of rash and labs still pending. Tentative d/c of 07/26/2021. 07/21/2021 MD attending note reported no change in pt condition. Continuation of remdesivir and solumedrol. 07/22/2021 MD attending note reported no clinical improvement. Continuation of remdesivir and solumedrol. Rash resolved, but etiology unclear as syphilis/RPR panel results mixed. 07/23/2021 MD attending note reported pt not feeling well and requested DNR/DNI. Continuation of therapy. 07/23/2021 Pt had elevated NEWS due to low BP and supplemental O2 at 3LNC 07/24/2021 MD attending note reported no clinical improvement. Pt transferred to SDU. Continuation of therapy. 07/26/2021 Pt told chaplain that he was suicidal and planned to OD on antidepressants. RN and MD notified. 07/26/2021 MD attending note reported no clinical improvement. Pt informed likely need SNF. Continuation of remdesivir. End solumedrol and initiated prednisone and vitamin D. 07/27/2021 MD attending note reported pt in better mood and disposition. Last day of remdesivir. Pt on room air. Continuation of prednisone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07/15/2021 COVID positive (nasopharyngeal swab)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2564258

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 03.03.2021
Beginn: 20.07.2021
Tage bis Beginn: 139,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Back pain COVID-19 Chest X-ray abnormal Cough Dyspnoea Hypertension Lung opacity Musculoskeletal chest pain Painful respiration Pulmonary mass Pyrexia SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infections following completion of COVID vaccine series 02/10/21 COVID vaccine dose #1 03/03/21 COVID vaccine dose #2 03/19/21 Pt reports lower back pain and right knee pain 07/20/21 Pt seen in ED for shortness of breath for 1 week, pain in right ribs when he takes a deep breath, nonproductive cough, and high BP; reports fever in the last 14 days but no chest pain; treated with dexamethasone and discharged home with prednisone, albuterol, vitamin D melatonin, and lisinopril hydrochlorothiazide; CXR done; Discharged with rx for albuterol, cholecalciferol, HCTZ/lisinopril, prednisone; COVID POSITIVE 07/21/21 Pt denies any symptoms and states his last known fever was 1.5 weeks ago 07/22/21 Pt reports cough is nearly resolved, does not endorse SOB, CP, discomfort; quarantine completed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 07/20/21 COVID POSITIVE; VARIANT SEQUENCING PENDING 07/20/21 Chest Single View: More conspicuous nodular opacities are noted projecting over the lower lung zones bilaterally
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1920837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: MN
Alter: 80,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 18.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 244,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

. This case meets criteria for vaccine breakthrough review. SxS started 11/17, tested positive 11/22 (unknown where). Cough, SOB.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH/Chronic conditions include HTN, DM, asthma.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 02.03.2021
Beginn: 20.07.2021
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: IM / LA

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

Ageusia Anosmia Asthenia Bronchitis COVID-19 Chest X-ray normal Decreased appetite Diarrhoea Dyspnoea exertional Epistaxis Fatigue Mucosal discolouration Productive cough SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infections following completion of COVID vaccine series 02/09/21 COVID vaccine dose #1 03/02/21 COVID vaccine dose #2 03/26/21 Pt presents to PCP and reports coughing up brown mucus with streaks of blood; given rx for azithromycin; CXR wnl 07/14/21 Pt reports presenting to ED on 07/10 for bronchitis 07/26/21 Pt reports he was admitted to hospital 07/20 for acute bronchitis and was diagnosed with COVID; states he is feeling better and declines COVID calls 07/29/21 Pt reports slowly getting slowly better; weak, tired, diarrhea 3-5 times a day, decreased appetite, no fever, and using inhalers for breathing 07/30/21 Pt reports diarrhea slowing down, fatigue improving, loss of taste/smell returning, and shortness of breath upon exertion 08/02/21 Pt reports improving shortness of breath 08/03/21 Pt is clinically resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: 07/02/21 COVID POSITIVE
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2572877

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 25.02.2021
Beginn: 14.10.2021
Tage bis Beginn: 231,0
Dosis: 1
Route/Site: IM / LA

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

COVID-19 COVID-19 pneumonia Hypokalaemia Hyponatraemia Post-acute COVID-19 syndrome Respiratory failure SARS-CoV-2 test positive Sepsis

Symptomtext

Narrative: Patient received three doses of COVID 19 vaccine (Feb/Mar 21 and Sep 21). The patient tested positive for COVID 19 on 14 October 2021 and was admitted with COVID pneumonia, sepsis, hyponatremia, hypokalemia, and respiratory failure. The patient was discharged on 23 Oct with some improvement, but was readmitted on 31 Oct 21 for long COVID pneumonia. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 26.02.2021
Beginn: 19.10.2021
Tage bis Beginn: 235,0
Dosis: 1
Route/Site: IM / LA

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

Asthenia COVID-19 COVID-19 pneumonia Chills Diarrhoea Hyperhidrosis Pyrexia SARS-CoV-2 test positive

Symptomtext

Narrative: Patient received two doses of Pfizer vaccine in March 2021. The patient tested positive for COVID 19 on 19 Oct 21 and was hospitalized with fever, chills, sweats, weakness, diarrhea, and COVID pneumonia. The patient was treated and discharged in stable condition on 23 Oct 21. Reported per EUA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1909837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: MA
Alter: 59,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 01.03.2021
Beginn: 01.11.2021
Tage bis Beginn: 245,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chest X-ray normal Cough Dyspnoea Inflammatory marker increased Procalcitonin increased Productive cough Pyrexia SARS-CoV-2 test positive Sputum discoloured

Symptomtext

60 y/o man with a PMH of ESRD on HD (TThSat; previously on PD), CAD s/p 3V CABG, iCM (LVEF 20% -- > 45-50%), AFL s/p DCCV in 2/2020, diabetes, hypertension, hyperlipidemia, and colon cancer s/p sigmoid resection (2015) who p/w 2 weeks SOB and dry cough, found to be COVID+ despite 3 doses vaccine. # COVID Full vaccinated with Pfizer, including booster (3rd dose) ~ 1 month prior to admission. SOB x 2-3 weeks with cough productive of green phlegm. S/p outpt CAP tx with azithromycin w/o improvement followed by levo w some improvement, but still had some SOB and persistent dry cough. 11/1/21 Rapid COVID positive as outpatient; child at home also tested positive for COVID. On admission, COVID PCR on admission also positive; cycle threshold 28.6. eRVP negative. In ED, febrile to 100.7F, and satting 90% on RA, so placed on 2L O2. Inflammatory markers elevated. Procal 0.35, but ISO ESRD. CXR without GGOs or consolidations. Given 1x dose remdesivir (11/2/21) before discontinuation given ESRD and suspicion for being late in COVID Course. Given O2 requirement, started on dexamethasone (11/2-3/21). Quickly weaned off O2; ambulatory sats 88% and higher. No indication for antibiotics. Supportive care with APAP, Tessalon perles, and Robitussin. Pt eager to get home on 11/3/21, so reviewed return to hospital precautions and discharged with isolation instructions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: COVID + 11/1/2021
Aktuelle Erkrankungen: Unknown.
Vorgeschichte: ? Adverse effect of anesthetic delayed emergence per patient. ? Anxiety Not on medication and patient reports anxiety not taking medication. ? Arrhythmia PAF atrial flutter (s/p DCCV in 2/2020, Patient remains on Coumadin Followed AMS ? Arthritis R knee aches and pains limited mobility and exercise. ? Chronic kidney disease (CKD) ESRD related to DM. Followed Nephrologist. HD since 2018- PD was not working and R IJ Dialysis cathete placed 2/20. HD scheduled on 12/28/20 day prior to surgery ( usually Tues,Thurs,Sat ) ? Chronic pain Bilateral foot pain -Takes medication. ? Colon cancer 2015 treated with sigmoid resection no chemotherapy .Since surgery has loose stool and takes Immodium prn . ? Congestive heart failure Recent admission 02/9-2/23/20. Medical mangement ? Coronary artery disease diagnostic cardiac cath, which demonstrated severe multivessel disease. Patient denies chest pain. Reports fatigue and no energy and SOB with exertion. ? Hyperlipidemia statin ? Hypertensive disorder On medication ? Obesity ? Shortness of breath SOB with activity ? Type 2 diabetes mellitus Denies and not on medication. Weight loss and patient reports resolved. A 1 C was 6.2 on 2/11/20 Past Surgical History: Procedure Laterality Date ? CARDIOVERSION 02/20/2020 ? CATARACT EXTRACTION, BILATERAL ? FOOT SURGERY Bone Spur Removal- R foot ? LAPAROSCOPIC INSERTION PERITONEAL CATHETER Left 03/14/2018 ? Peritoneal Catheter 2018 Now removed ? SUBTOTAL COLECTOMY 12/2015
Andere Medikamente: acetaminophen, amitriptylini, amlodipine, aspirin, benzonatate, corge, d3, clonazepam, B12, gabapentin, loperamide, pravastatin, sacubitril-valsartan, sevelamer, warfarin
Allergien: ? Sulfa (Sulfonamide Antibiotics) Hives ? Keflex [Cephalexin]
Vorherige Impfungen: -

VAERS 1903948

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: CT
Alter: 35,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 09.03.2021
Beginn: 08.04.2021
Tage bis Beginn: 30,0
Dosis: 2
Route/Site: - / LA

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

Atrial fibrillation Palpitations

Symptomtext

Developed frequent heart palpitations beginning approximately 24 hours after my second dose (received second dose March 9, 2021). Developed an episode of atrial fibrillation on Thursday April 8 , which lasted for approximately 3 hours. My heart rate was in the 110s-120s for approximately 20 minutes, and then decreased to the 80s-100s for the duration of the episode. I am a physician and was able to self-diagnose. My wife is also a physician who confirmed that I was in atrial fibrillation and monitored me during the episode. Given that I did not have additional symptoms to suggest decreased cardiac output during the event, I did not seek medical care at the time of the event. In addition, since I had recently had a normal echocardiogram, I did not pursue additional testing. The frequency of my palpitations decreased over the subsequent months and I had an apparent return to baseline cardiac function in July 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro 10 mg daily
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 1377143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PA
Alter: -
Geschlecht: U
Eingang: 19.11.2021
Impfdatum: 01.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / LA

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

Atelectasis Blood creatine phosphokinase Blood test C-reactive protein increased Chest X-ray abnormal Chest pain Chills Diarrhoea Fall Full blood count Headache Urticaria Hiatus hernia Laboratory test normal Metabolic function test Nausea Neck pain Pain in extremity

Symptomtext

hives; diarrhea; bad headache.; This is a spontaneous report from a contactable consumer or other non hcp (patient) forwarded as an adverse event. A patient of unspecified age and gender received bnt162b2 (COMIRNATY, formulation: solution for injection, lot number and expiration date were not reported) via an unspecified route of administration, administered on Apr2021 as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection), via an unspecified route of administration on unspecified date (Lot Number and expiry date was not reported) as single dose for COVID-19 immunization. On an unspecified date, the patient experienced hives, diarrhea and bad headache. Customer reported that patient got his/her second Pfizer COVID vaccine shot in April. Patient had horrible problems ever since. Patient had many unpaid days off work. Currently patient had hives, diarrhea and a bad headache. It was reported that Pfizer made billions off this vaccine. Patient reported that his/her life was ruined. Patient was starting to think his/her life was too had to live. The outcome of the events was unknown. No follow up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 1876991

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: KY
Alter: 61,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 30.03.2021
Beginn: 17.11.2021
Tage bis Beginn: 232,0
Dosis: 2
Route/Site: IM / LA

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

Chest pain Condition aggravated Coronary artery bypass Coronary artery disease Dyspnoea exertional Electrocardiogram abnormal Positron emission tomogram abnormal Road traffic accident

Symptomtext

Patient is a 61 yr/o female who presents today for cardiac evaluation for chest pain, abnormal EKG and prior history of coronary artery disease. Conference for discussion of abnormal PET scan imaging and recommendationsShe has chest pain and shortness of breath on exertion cardiac cath on 6/29/2016 showed the left main 30 to 40% stenosis distally LAD 40 to 60% segmental stenosis and normal LV function at that time. 61 yo woman previously evaluated in office for CAD, who was involved in a MVA. She was seen and cleared by NS to have CABG. She has not been in a neck brace since initial visit. Patient denies any issues or changes since last visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cardiovascular and Mediastinum Hypertension Coronary artery disease involving native coronary artery of native heart without angina pectoris Coronary artery disease involving native coronary artery of native heart with angina pectoris CAD in native artery PAF (paroxysmal atrial fibrillation) Respiratory Acute respiratory failure Endocrine Type 2 diabetes mellitus with complication, without long-term current use of insulin Secondary diabetes mellitus without complications Musculoskeletal and Integument Patellofemoral arthritis Genitourinary Pyelonephritis Renal insufficiency Other Renal colic Chest pain Abnormal stress test Dyslipidemia Morbid obesity with BMI of 40.0-44.9, adult Hernia of abdominal wall Abnormal nuclear stress test
Andere Medikamente: Outpatient Medications albuterol HFA 108 (90 Base) MCG/ACT inhaler atorvastatin (LIPITOR) 40 MG tablet blood glucometer system carBAMazepine (TEGRETOL XR) 100 MG 12 hr tablet DULoxetine (CYMBALTA) 60 MG capsule gabapentin (NEURONTIN)
Allergien: MorphineAnaphylaxis Vitamin CNausea And Vomiting Citric Acid-potassium Citrate [Potassium Citrate]Nausea And Vomiting Orange Juice [Orange Oil] Pcn [Penicillins]
Vorherige Impfungen: -

VAERS 1873392

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 75,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 31.03.2021
Beginn: 06.11.2021
Tage bis Beginn: 220,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Chills Cough Dyspnoea Exposure to SARS-CoV-2 Headache Pyrexia Vaccine breakthrough infection

Symptomtext

This case meets criteria for vaccine breakthrough review. SxS include SOB, headaches, fevers, chills, weakness, and cough after known COVID exposure from multiple family members.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PMH/Chronic conditions include ESRD s/p renal transplant, HTN, HLD.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1872332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 65,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 26.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: - / LA

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

Migraine Sinus headache

Symptomtext

Continued severe migraine/sinus headaches; Continued severe migraine/sinus headaches; This is a spontaneous report from a contactable nurse (patient) reported for herself. A 65-years-old female patient (patient was not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EN6203, Expiration date: unknown) via an unspecified route of administration, administered in left arm on 26Feb2021 at 03:00 am (age at vaccination was 65 years) as dose 1, single for COVID-19 immunization. The patient's medical history included HTN (hypertension), GERD (Gastrooesophageal reflux disease), ongoing migraines and known allergy to CT (Computed tomography) dye. Concomitant medication or other medication the patient received in two weeks included galcanezumab gnlm (EMGALITY) injection taken for migraines. The patient previously took compazine [prochlorperazine edisylate], omnicef [cefdinir] and reglan [metoclopramide] and experienced known allergies to it. The facility where the most recent COVID-19 vaccine was administered was Other. 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 not been tested for COVID-19. On 27Feb2021, the patient experienced continued severe migraine/sinus headaches. The patient took migraine and sinus meds for the events. The outcome of the events was not resolved.No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraine.
Vorgeschichte: Medical History/Concurrent Conditions: Contrast media allergy (known allergies: CT dye); GERD; Hypertension.
Andere Medikamente: EMGALITY.
Allergien: -
Vorherige Impfungen: -

VAERS 1872255

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 24.02.2021
Beginn: 25.02.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: - / LA

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

Hyperaesthesia Hypoaesthesia Muscular weakness Pain in extremity Paraesthesia

Symptomtext

Weakness in left arm 18 hours after vaccine administration; Also tingling pain and numbness with excessive sensitivity in left hand; Also tingling pain and numbness with excessive sensitivity in left hand; Also tingling pain and numbness with excessive sensitivity in left hand; Also tingling pain and numbness with excessive sensitivity in left hand; This is a spontaneous report from a contactable consumer. This 67-year-old male consumer (patient) received 2nd dose of BNT162B2 (Lot # EN6203), on 24Feb2021 09:30 AM, vaccine location in Left arm for covid-19 immunization (at the age of 66 years old). Medical history included osteoarthritis, osteoporosis, prostate cancer, cancer in remission. No other vaccine in four weeks. No covid prior vaccination. No covid tested post vaccination. Historical vaccine was 1st dose of BNT162B2 (LOT # EL9264), on 03Feb2021 12:00 PM, vaccine location in Left arm for covid-19 immunization. Patient experienced Weakness in left arm 18 hours after vaccine administration. Also tingling pain and numbness with excessive sensitivity in left hand which has not subsided from 25Feb2021. AE resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Disability or permanent damage. Outcome of the event was Not recovered. No follow-up attempts possible. No further information expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cancer in remission; Osteoarthritis (Other medical history: osteoarthritis, osteoporosis, prostate, cancer in remission); Osteoporosis; Prostate cancer
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1867315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 13.11.2021
Impfdatum: 03.03.2021
Beginn: 01.04.2021
Tage bis Beginn: 29,0
Dosis: 1
Route/Site: - / -

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

Condition aggravated Parkinsonism

Symptomtext

increased symptoms in 7 months which was not horrible but was progressing; diagnosed with Tentative Parkinson's Syndrome; This is a spontaneous report from a contactable consumer (patient) or other non healthcare professional. A 69-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection with Lot Number: EN6203), via an unspecified route of administration on 03Mar2021 as DOSE 1, SINGLE (age at the vaccination was 69-year-old) and the patient received second dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection with Lot Number: ER2613) via an unspecified route of administration on 24Mar2021 as DOSE 2, SINGLE for COVID-19 immunisation. The patient had no medical history and there were no concomitant medications. The patient was not if the reaction was to the first or second, but it started 2 weeks after the second. The patient stated that he started to develop what he thought was Parkinson's syndrome. The patient had the vaccine in Mar2021 and was diagnosed with tentative Parkinson's Syndrome on an unknown date Apr2021. The patient had an appointment with a respected hospital. The patient saw his primary care physician, a neurologist, and a rheumatologist. His question to everyone, some of the appointments were on an unknown dated June or July, was when the booster was available is it recommended to get the booster with the tentative Parkinson's Diagnosis in on an unknown dated Apr2021 It had gotten worse. It has progressed over the 7 months. The patient was in a high-risk category. The patient was 7 months past the second shot. The patient doesn't want to stay hibernated in his house. The patient would like to be able to see his children. The patient stated that he had seen doctors over the last 7 months and had been in contact with them through email and asked them specifically about his condition as he had increased symptoms in 7 months which was not horrible but was progressing. The patient wanted to know if this was a reported side effect with the vaccine and how it progresses as his doctors had no data and referred him to call Pfizer. The events outcome was reported as not recovered. These adverse reactions have been identified during post authorization use of Pfizer-BioNTech COVID-19 Vaccine. Because these reactions are reported voluntarily, it was not always possible to reliably estimate their frequency or establish a causal relationship to vaccine exposure.

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

VAERS 1865458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 84,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 03.02.2021
Beginn: 07.11.2021
Tage bis Beginn: 277,0
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

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: POSITIVE COVID TEST 11/10/21
Aktuelle Erkrankungen: -
Vorgeschichte: Cancer, left lung COPD Hypertension Hyperlipidemia Pulmonary nodule, right Postprocedural pneumothorax Pneumonia Ureteral stone Basal cell carcinoma of anal skin Perianal lesion Nephrolithiasis Hydronephrosis with urinary obstruction due to ureteral calculus
Andere Medikamente: acetaminophen (TYLENOL) 500 mg oral tablet albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler amLODIPine (NORVASC) 10 mg oral tablet atorvastatin (LIPITOR) 20 mg oral tablet fluticasone 200 mcg-
Allergien: -
Vorherige Impfungen: -

VAERS 1865195

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 83,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 24.02.2021
Beginn: 25.10.2021
Tage bis Beginn: 243,0
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 11/8/2021
Aktuelle Erkrankungen: -
Vorgeschichte: COPD (chronic obstructive pulmonary disease) Diabetes mellitus Diabetic neuropathy BPH Hyperlipidemia Lung disease Pain in neck Insomnia Low back pain Pulmonary infiltrates Pulmonary fibrosis
Andere Medikamente: albuterol HFA (PROVENTIL;VENTOLIN HFA) 90 mcg/actuation Inhl inhaler ascorbic acid, vitamin C, 500 mg oral tablet carisoprodol (SOMA) 350 mg Oral Tab HYDROcodone-acetaminophen (NORCO) 5-325 mg oral tablet metFORM
Allergien: Dairy Products (Nic)
Vorherige Impfungen: -

VAERS 1864322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 01.02.2021
Beginn: 01.03.2021
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: - / LA

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

Arthralgia Dizziness Paraesthesia

Symptomtext

Dizziness; Pain in right wrist, Pins and needles right arm/hand, then left arm hand. Now, pins and needles in feet and face. Dizziness; Pins and needles right arm/hand, then left arm hand. Now, pins and needles in feet and face.; This is a spontaneous report from a contactable consumer, the patient. A 42-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6203) via an unspecified route of administration in the left arm on an unknown date in Feb2021 (at the age of 42-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient had no known allergies. Concomitant medications included ibuprofen (ADVIL) from an unknown date for an unspecified indication. 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 vaccines within four weeks prior to the vaccination. On 01Mar2021 the patient experienced pain in right wrist, pins and needles right arm/hand, then left arm hand. Now, pins and needles in feet and face. Dizziness. Patient received treatment for the events which included antibiotic. The events resulted in doctor or other healthcare professional office/clinic visit. Clinical outcome of dizziness, wrist pain, pins and needles were not recovered. The patient also received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP7534) via an unspecified route of administration in the left arm on 16Mar2021 at 16:15 (at the age of 42-years-old) as a single dose for COVID-19 immunisation. No follow-up attempts are needed. No further information is expected. Amendment: This follow-up report is being submitted to amend previously reported information: updated narrative.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: ADVIL [IBUPROFEN]
Allergien: -
Vorherige Impfungen: -

VAERS 1860802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: TX
Alter: 70,0
Geschlecht: M
Eingang: 11.11.2021
Impfdatum: 12.03.2021
Beginn: 18.06.2021
Tage bis Beginn: 98,0
Dosis: 2
Route/Site: IM / LA

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

Blindness Electrocardiogram Ventricular tachycardia

Symptomtext

Lost sight while sitting- vision went white screen, 2 - 3 seconds later felt surge of blood in head and vision returned to normal. Sat several minutes to access situation- no SOB, no palpitations, normal pulse, normal respiratory rate. Followed up with Electrophysiologist (submitted pacemaker trace- identified approx 4 hour Afib that transitioned into Ventricular tachycardia with 195bpm rate and heart stopping for 4 seconds unable to maintain rate. Cardiologist, whom I had follow-up appt with said Pacemaker restarted heart and he and new Electrophysiologist- placed me on Flecainide Acetate 50mg bid on 6/25 and all issues resolved.

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Praegender Schweregrund: Ventricular tachycardia
Hospital-Tage: -
Labordaten: Pacemaker trace 6/18; EKG 6/25
Aktuelle Erkrankungen: N/A
Vorgeschichte: A-Fib corrected w/MAZE intracardiac ablation 12/2019; Mitral Valve Rpl 12/2019; Pacemaker post MAZE 12/2019
Andere Medikamente: Atenolol 25mg bid; Eliquis 5mg bid; Vit B Super Complex; Biotin 10000mg; Omega-3 690mg; Melatonin 12mg; Citracal 12.5mcg x2; Tylenol 500mg x 4; Ester C 500mg x 2
Allergien: N/A
Vorherige Impfungen: -

VAERS 1857779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: IL
Alter: 85,0
Geschlecht: M
Eingang: 10.11.2021
Impfdatum: 17.02.2021
Beginn: 09.11.2021
Tage bis Beginn: 265,0
Dosis: 2
Route/Site: IM / -

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

Cough Dyspnoea Fatigue Pneumonia Pyrexia Respiratory disorder

Symptomtext

presents to the ED with respiratory issues. Patient reports 4 days of subjective fevers, cough, SOB, and fatigue. States it has been worsening. Patient reports using inhalers with minimal relief. Denies any other alleviating or aggravating factors

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: PNEUMONIA
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, RENAL, HTN, CARDIAC
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1851628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 74,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 30.01.2021
Beginn: 22.10.2021
Tage bis Beginn: 265,0
Dosis: 2
Route/Site: - / -

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

Ageusia Anosmia Chills Cough Dyspnoea Headache Oropharyngeal pain Respiratory tract congestion

Symptomtext

SOB, cough, congestion, headache, sore throat, loss of taste, loss of smell, chills. Patient denies diarrhea, body aches, fever. starting around 10/22/21

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Hypercholesterolemia. Tubular Adenoma--recheck 7/2019. Previous colostomy bag (due to perforated colon during lap hysterectomy 9/2016). History of obesity, status post gastric bypass. Depression, unspecified depression type. Anxiety. Insomnia. osteoporosis (Fosamax started 12/2019).
Andere Medikamente: ?Womens Multi Gummies - Tablet Chewable as directed Orally ?Sertraline HCl 100 MG Tablet 2 tablets Orally Once a day ?Gabapentin 100 MG Capsule 1 tablet Orally Three times a day ?Zolpidem Tartrate 10 MG Tablet 1 tablet at bedtime
Allergien: none
Vorherige Impfungen: -

VAERS 1850844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: KY
Alter: 79,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 26.02.2021
Beginn: 02.11.2021
Tage bis Beginn: 249,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Cough Dyspnoea Productive cough Respiratory tract congestion

Symptomtext

Admitted with progressive SOA/Cough/congestion//weakness. Clear/white sputum only. Weak. No change in taste/smell/appetite.

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

VAERS 2579499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 03.03.2021
Beginn: 20.08.2021
Tage bis Beginn: 170,0
Dosis: 2
Route/Site: IM / LA

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

COVID-19 Chills Cough Diarrhoea Dyspnoea Fatigue Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/10, Pfizer, dose #1 03/03, Pfizer, dose #2 08/23 COVID swab, result: detected 08/03 pt cc: chills, cough, dirrhea, fatigue, rhinorrhea, dyspena exposure: unknown

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

VAERS 1846357

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge en6203

moderat

Staat: MN
Alter: 51,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 02.04.2021
Beginn: 04.11.2021
Tage bis Beginn: 216,0
Dosis: 2
Route/Site: IM / RA

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

Chest pain Dyspnoea Vaccine breakthrough infection

Symptomtext

This case meets criteria for vaccine breakthrough review. SxS include SOB, chest pain.

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

VAERS 1846053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 82,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 17.03.2021
Beginn: 02.11.2021
Tage bis Beginn: 230,0
Dosis: 1
Route/Site: IM / LA

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

Cough Dyspnoea Fatigue Oropharyngeal pain Pain Pyrexia

Symptomtext

This case meets criteria for vaccine breakthrough review. Symptoms include cough, body aches, fatigue, fever, sore throat and SOB.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: A-fib, asthma, HLD, CKD, DVT
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1842277

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: NY
Alter: 80,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 05.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Condition aggravated Feeling abnormal Headache Neck pain Pain in jaw Tongue discomfort

Symptomtext

This is a spontaneous report from a contactable consumer or other non-HCP. An 80-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# EN6203, expiration date: unknown), at the vaccination age of 80, via an unspecified route of administration, in left arm, on Mar 5, 2021, single dose, for COVID-19 immunization. The patient's medical history included neck pain; pain in the back of her neck, head, forehead and jaw. She reported she had mild pain in these areas before the vaccine. No concomitant medications reported. On Mar 5, 2021 (30 minutes) after receiving the vaccine, patient experienced pain in the back of her neck; pain in back of jaw, head and forehead. The pain got worse after the vaccine and lasted for a few hours. She felt bad. Patient mentioned she had mild pain in these areas before, but just did not pay attention at first. Then the pain got worse and lasted a few hours. Then stopped and went away completely. It did not occur to her it was from the shot as she had no side effects from shots before. She cannot take pain medicine. The outcome of had pain in the back of neck, jaw, head and forehead; had mild pain in these areas before the vaccine; pain got worse after the vaccine and lasted for a few hours; and felt bad recovered on Mar 5, 2021. No follow-up attempts possible. No further information expected.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Forehead headache (back of forehead); headache (back of head); jaw pain (pain in back of jaw); neck pain (pain in the back of neck).
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1840576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: MN
Alter: 69,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 20.02.2021
Beginn: 01.11.2021
Tage bis Beginn: 254,0
Dosis: 2
Route/Site: SYR / UN

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

COVID-19 Hypertension Pneumonia SARS-CoV-2 test positive Type 2 diabetes mellitus

Symptomtext

Received Pfizer vaccines on 1/30, 2/20/21 Tested positive for COVID by PCR on 11/1/21 admitted to hospital on 11/2/21 w/ pneumonia. underlying DM Type 2, HTN

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

VAERS 1840286

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PA
Alter: 70,0
Geschlecht: F
Eingang: 03.11.2021
Impfdatum: 03.03.2021
Beginn: 16.10.2021
Tage bis Beginn: 227,0
Dosis: 1
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Cough, mild SOB, rhinnorhea Registered Nurse Specialty: Emergency Medicine Progress Notes Signed Encounter Date: 10/21/2021 Patient is here for MAB Infusion O2 sats > or = 90% Signs of potential reaction reviewed with patient. Tolerated IV start and MAB infusion without complication. Pt has access to pulse oximeter and thermometer for home monitoring Discharge instructions reviewed. Patient denies any questions

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Probable COVID-19 (Resolved) Specimen information: Swab / Nares Added: 10/19/21 by POCT COVID-19 Antigen (Collected 10/19/21) Onset date: 10/19/21 Resolved: 11/02/21 (Expired) Add Rule-Out COVID-19 and Respiratory Viruses Add SARS-CoV-2 (related to COVID-19) Add Rule-Out SARS-CoV-2 (related to COVID-19) Add Probable COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Polyneuropathy Respiratory Obstructive sleep apnea syndrome Circulatory Atrial fibrillation Chronic systolic heart failure Essential hypertension Digestive Adenocarcinoma of cecum Female proctocele without uterine prolapse Genitourinary Midline cystocele Female stress incontinence Musculoskeletal Rosacea Other H/O rotator cuff surgery History of colon cancer
Andere Medikamente: Outpatient Medications ascorbic acid, vitamin C, (ascorbic acid with rose hips) 500 mg tablet b complex vitamins tablet calcium carb-mag oxide-vit D3 (CALCIUM MAGNESIUM + D) 400-167-133 mg-mg-unit tablet cinnamon bark (CINNAMON) 500 mg
Allergien: Ceftriaxone SodiumRash, Dermatitis, Other (document details in comments)
Vorherige Impfungen: -

VAERS 1839881

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: PA
Alter: 67,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 03.03.2021
Beginn: 15.10.2021
Tage bis Beginn: 226,0
Dosis: 1
Route/Site: IM / RA

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

Adenovirus test Angiogram pulmonary abnormal Aortic arteriosclerosis Blood bicarbonate increased Blood creatinine normal Blood urea normal Bordetella test negative Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Chlamydia test negative Computerised tomogram thorax abnormal Condition aggravated Coronavirus test negative Cough

Symptomtext

ED to Hosp-Admission Discharged 10/18/2021 - 10/22/2021 (4 days) Hospital MD Last attending ? Treatment team Acute on chronic congestive heart failure, unspecified heart failure type Hospital Problems POA * (Principal) Acute on chronic congestive heart failure, unspecified heart failure type Yes Covid pneumonia, Paroxysmal A. Fib, Morbid obesity, Nocturnal hypoxia Presenting Problem/History of Present Illness/Reason for Admission Hypoxia [R09.02] Acute on chronic congestive heart failure, unspecified heart failure type [I50.9] Acute COVID-19 [U07.1] Hospital Course Symptoms started approximately October 15 or 14 with cough with white sputum and exertional shortness of breath as well as shortness of breath lying flat. BNP was a little higher than usual and he was started on IV diuretics but his Covid was also positive. His lungs sounded like Covid in the CT look like Covid. Therefore we diuresed him but on the second day in the hospital I did start him on remdesivir he had been started on steroids upon admission. He certainly improved on a daily basis. On the day of discharge he is feeling well really denying any shortness of breath his edema is better his lungs are clear he is back to his normal diuretic dose and he is not hypoxic with exertion. He got 4 days of remdesivir because he is doing so well we can discharge him before the fifth day but he will complete 10 days of Decadron. LFTs remain normal as always is got a little bit of a hypochloremia with 91 bicarb is mildly elevated at 35 but his BUN and creatinine are stable CBC unremarkable. Rest and exercise oximetry revealed no hypoxia Operative Procedures Performed Treatments: IV Decadron IV diuretics remdesivir Procedures: None Consults: PT OT Pertinent Test Results: CTA of chest consistent with Covid pneumonia

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 4,0
Labordaten: 10/18/2021 1144 Respiratory virus detection panel Collected: 10/18/21 1144 | 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 Resulted: 10/18/21 1700 Order Status: Completed Updated: 10/18/21 1700 Narrative: XR CHEST 1 VW PORT IMPRESSION: 1. Left upper and left lower lobe opacities. Recommend enhanced CT correlation. 2. Cardiomegaly. 3. Underlying chronic interstitial disease and bilateral atelectasis. 4. Old granulomatous disease. END OF IMPRESSION: INDICATION: Pt states that he has been having coughing fits in the morning when he gets out of bed. SOB. TECHNIQUE: Frontal view of the chest was obtained. COMPARISON: X-ray of December 14, 2018 FINDINGS: A confluent left upper lobe and left lower lobe airspace opacities are seen. There are no consolidations, pulmonary edema or pleural effusions. The heart is enlarged..The mediastinum is widened.There is a stable calcified right upper lobe nodule. Overlying leads and wires are identified. Biapical pleural thickening is seen. Underlying chronic interstitial disease and bibasilar atelectasis are visualized. Arthritic change is noted in the right AC joint. There is spondylosis. This report was created using Voice Recognition software. Thank you for allowing us to participate in the care of your patient. CT chest without contrast Resulted: 10/18/21 1637 Order Status: Completed Updated: 10/18/21 1637 Narrative: PROCEDURE INFORMATION: Exam: CT Chest Without Contrast; Diagnostic Exam date and time: 10/18/2021 3:11 PM Age: 67 years old Clinical indication: Shortness of breath; Additional info: Covid-pos. Increasing SOB. Dyspnea TECHNIQUE: Imaging protocol: Diagnostic computed tomography of the chest without contrast. Radiation optimization: All CT scans at this facility use at least one of these dose optimization techniques: automated exposure control; mA and/or kV adjustment per patient size (includes targeted exams where dose is matched to clinical indication); or iterative reconstruction. COMPARISON: CT CHEST WO CONTRAST 2/26/2021 8:02 AM FINDINGS: Lungs: Calcified granuloma right upper lobe. Patchy alveolar airspace consolidation within the apicoposterior segment of the left upper lobe. Likely pneumonic process although recommend follow-up to ensure resolution. Subtle airspace disease left lung base. Pleural spaces: Unremarkable. No pneumothorax. No pleural effusion. Heart: No pericardial effusion. Small amount of fluid within the superior pericardial recess. Aorta: Calcification of the aorta. Lymph nodes: Calcified lymph nodes right hilum Liver: Mild nodularity of the liver is present. Correlate regarding risk factors for hepatocellular disease. Bones/joints: thoracic inlet is unremarkable. Degenerative changes are present within the spine. Soft tissues: Soft tissues of the mediastinum appear unremarkable. IMPRESSION: Patchy alveolar airspace consolidation within the apicoposterior segment of the left upper lobe. Likely pneumonic process although recommend follow-up to ensure resolution. Subtle airspace disease left lung base. Findings consistent with the given history.
Aktuelle Erkrankungen: -
Vorgeschichte: Nervous Lumbar radiculopathy Right leg weakness Greater trochanteric bursitis of left hip Respiratory Allergic rhinitis OSA (obstructive sleep apnea) Circulatory Ascending aortic aneurysm Paroxysmal atrial fibrillation Chronic diastolic CHF (congestive heart failure) Acute on chronic congestive heart failure, unspecified heart failure type Digestive Cholecystitis, chronic Fatty liver disease, nonalcoholic Class 3 severe obesity with serious comorbidity and body mass index (BMI) of 45.0 to 49.9 in adult Gastroesophageal reflux disease Body mass index 50.0-59.9, adult Genitourinary Benign prostatic hypertrophy Chronic renal insufficiency, unspecified stage Musculoskeletal Arthritis Disc degeneration, lumbar Presence of artificial hip joint, right Primary osteoarthritis of left knee Primary osteoarthritis of right knee Primary osteoarthritis of left hip Seborrheic keratosis Muscular deconditioning Endocrine/Metabolic Hypercholesterolemia Infectious/Inflammatory COVID-19 Other Edema Prostate cancer screening Hypertrophy of breast Umbilical hernia Advance care planning Chronic anticoagulation Non-smoker
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet colchicine (MITIGARE) 0.6 mg capsule metOLazone (ZAROXOLYN) 2.5 mg tablet miscellaneous medical supply misc miscellaneous medical supply misc miscellaneous medical supply misc oxygen (02) gas pot
Allergien: NKA
Vorherige Impfungen: -

VAERS 2602962

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 71,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 04.02.2021
Beginn: 27.08.2021
Tage bis Beginn: 204,0
Dosis: 1
Route/Site: IM / RA

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

Aortic dilatation Asthenia Atypical pneumonia COVID-19 COVID-19 pneumonia Cough Dyspnoea Fall Fatigue Hilar lymphadenopathy Lung infiltration Myalgia Pain Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Narrative: Admission Date: AUG 27,2021 Discharge Date: SEP 4,2021 Admit Diagnosis: COVID PNEUMONIA Condition of patient at discharge: Stable 71 yo male presents to Emergency Dept with complaints of fatigue, weakness, myalgias. He reports that he fell earlier due to generalized weakness and just wanted to get checked out. Reports that he tested positive for covid-19 on Sun 08/22 at another urgent care. Reports that he developed a non-productive cough and body aches on Sat 08/21, developed fever and worsening cough on 8/22 which prompted him to seek testing (the first time). He denies fever since 8/22, denies n/v/d/cp/sob/abd pn/back pn/urinary sxs. COVID test positive on admission on 8/27 and CXR with bilateral infiltrates consistent with atypical pneumonia despite being fully vaccinated with Pfizer COVID vaccine on 2/4/2021 and 2/25/2021. Patient completed 10 days of dexamethasone and 10 days of remdesivir while admitted. Patient initially treated for community acquired pneumonia but antibiotics were discontinued shortly after admission due to procal < 0.05. DDimer elevated on admission and patient maintained on therapeutic doses of enoxaparin while admitted. Patient underwent walk test on 9/4 which showed 1L O2 req at rest and 4L O2 req with exertion. At time, he had escalating O2 requirements from 3 to 5L. Patient discharged home on 9/4/2021 with home O2 to isolate until 9/6.

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Praegender Schweregrund: Atypical pneumonia
Hospital-Tage: -
Labordaten: Specimen Collection Date: Aug 27, 2021@01:00 COVID-19_(XPRESS PCR) DETECTED H* Exam Date/Time 08/27/2021 00:55 Procedure Name CHEST-1 VIEW (AP/PA) Reason for Study covid/dyspnea Impression 1. Alveolar and interstitial infiltrates involving the right upper and lower lobes, and the left upper lobe including the lingular segment most likely representing multifocal pneumonia in this Covid-19 positive patient. 2. Probable right hilar adenopathy. 3. No pleural effusion or cardiomegaly. Report Technique: A single portable upright frontal view of the chest was performed. Prior chest x-ray available for comparison dated 11/13/2017. Findings: The cardiac silhouette is diffusely at the upper limits of normal in size with a mild left ventricular configuration. Moderate diffuse ectasia of the thoracic aortic arch. Lung fields are adequately expanded with mild chronic elevation of the right hemidiaphragm with associated mild scalloping. There are diffuse interstitial and alveolar infiltrates within the right upper and lower lobes along with the left midlung zone. No pleural fluid. No pneumothorax.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2601567

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 23.02.2021
Beginn: 07.09.2021
Tage bis Beginn: 196,0
Dosis: 2
Route/Site: IM / RA

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

Blood fibrinogen increased Brain natriuretic peptide increased C-reactive protein COVID-19 Chest X-ray abnormal Fibrin D dimer Hypoxia Lung consolidation Lung disorder Nausea Pneumonia Pulmonary mass Red blood cell sedimentation rate increased SARS-CoV-2 test SARS-CoV-2 test positive Troponin I normal Vomiting

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/02, Pfizer dose #1 02/23, Pfizer, dose #2 09/10 Pt admit to medicine cc: "Nausea and vomiting after covid" dx: COVID-19 complicated with pneumonia and hypoxemia LOS: 3 days 09/10 COVID swab, result: detected 09/10 pt cc: exposure: unknown 09/10 CXR impression: 1. Asymmetric right lung consolidation concerning for pneumonia in the appropriate clinical setting. No significant left lung consolidation. 2. Known right upper lobe nodule reidentified. 09/10 BNP: 153.5 09/10 CRP: 7.551 09/10 DDIMER: 0.36 09/10 SARS-COV-2 Variant Sequencing result: pending 09/11 Eval: negative 09/11 DDMINER: <0.22 09/12 FIBRINOGEN: 459 09/12 DDIMER: 0.37 09/12 ESR: 58 09/13 FIBRINOGEN: 469 09/13 DDIMER: 0.25 09/13 ESR: 43 09/27 Troponin I result: 0.020 09/27 CXR impression: Interval decrease in right mid/lower lung zone airspace disease, but increase in right upper lung zone and new left midlung zone airspace disease, suggestive of multifocal pneumonia.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 09/10 CXR impression: 1. Asymmetric right lung consolidation concerning for pneumonia in the appropriate clinical setting. No significant left lung consolidation. 2. Known right upper lobe nodule reidentified. 09/10 BNP: 153.508/10 CRP: 7.551 09/10 DDIMER: 0.36 09/10 SARS-COV-2 Variant Sequencing result: pending 09/11 Eval: negative 09/11 DDIMER: <0.22 09/12 FIBRINOGEN: 459 09/12 DDIMER: 0.37 09/12 ESR: 58 09/13 FIBRINOGEN: 469 09/13 DDIMER: 0.25 09/13 ESR: 43 09/27 Troponin I result: 0.020 09/27 CXR impression: interval decrease in right mid/lower lung zone airspace disease, but increase in right upper lung zone and new left midlung zone airspace disease, suggestive for multifocal pneumonia.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2595916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 05.02.2021
Beginn: 29.08.2021
Tage bis Beginn: 205,0
Dosis: 1
Route/Site: IM / LA

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

Cough Dyspnoea Fatigue Malaise Nasopharyngitis COVID-19 COVID-19 pneumonia Central venous catheterisation Chest X-ray abnormal Choking sensation Productive cough Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Narrative: Admission Date: AUG 29,2021 Discharge Date: AUG 30,2021 Admit Diagnosis: Covid + 72 yo M w a PMH T2DM, HTN, COPD (not on home O2), CKD on hemodialysis (MWF), CAD, hx substance abuse, prostate cancer (Dx 2017), hep C (treated), who presented with worsening cold-like symptoms of 1 week duration. Patient says that for the past 7 days he has been having worsening fatigue, congestion, mild SOB, and productive cough. He also says that he has been feeling like he's choking . During this time he did not have any subjective fevers, night sweats or chills. Patient also denied any headaches, dizziness, chest pain, nausea, vomiting, bloody bowel movements, hemoptysis, or hematemesis for the past 7 days. When presented to the emergency department, patient was hemodynamically stable, T 98.6, P 75, RR 20, BP 107/66. Covid test was performed which came back positive. Patient previously received two doses of the Pfizer Covid vaccine (2/5/2021 and 2/26/2021). CXR with minimally changed radiographic findings, apart from the new right sided tunneled catheter. Patient was admitted to the Medicine Service for further management. #COVID+ pneumonia/pneumonitis: Patient with covid-like symptoms of 1-week duration. Fatigue, cough, congestion, mild SOB. Has not required supplemental O2 - therefore, dexamaethasone and remdisivir held. Gave Regeneron (8/30) given high risk PMH (COPD, ESRD) and positive test <10 days ago. Discharged on 8/30 in stable condition.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: -
Labordaten: Specimen Collection Date: Aug 29, 2021@15:56 COVID-19_(XPRESS PCR) DETECTED H* Exam Date/Time 08/29/2021 16:45 Procedure Name CHEST-2 VIEWS (PA/AP + LAT) Impression Other than the new right sided tunneled catheter, the radiographic appearance of the chest is minimally changed, as above. Report Comparison: 8/3/2021. Technique: 2 view(s) of the chest provided. Findings: There is now a tunneled right-sided dialysis catheter; tip projects in the region of the upper to mid right atrium. Components of vascular congestion/minor nonspecific interstitial opacity may be present, also seen previously (such as right lower lung field); significant/new airspace opacity is otherwise not appreciated-no significant consolidation. The costophrenic angles are sharp. The remaining findings are relatively stable.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2595911

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 26.02.2021
Beginn: 25.09.2021
Tage bis Beginn: 211,0
Dosis: 1
Route/Site: IM / LA

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

Acquired diaphragmatic eventration Atelectasis Bradycardia COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Hypophagia Hypotension Hypovolaemia Malaise Pleural fibrosis Positive airway pressure therapy SARS-CoV-2 test positive

Symptomtext

Narrative: 83 yo M with COPD on 2-3L home O2, HFrEF (EF 35-40% Jan 2018), Atrial Fibrillation on apixaban presenting with increased O2 requirement and hypotension in the setting of COVID. He was diagnosed with COVID on 9/11 to another hospital in town despite being fully vaccinated with Pfizer's COVID vaccine on 2/5/2021 and 2/26/2021. He was not admitted at that time. Since then he had been staying with one of his daughters (daughter he lives with is also sick with COVID) and has decreased PO intake. He was slightly more SOB than is usual for him, remained on 2.5-3L O2. Used BiPap at night and continued since he has been sick. He received monoclonal antibody infusion 9/16/2021 and at that appointment he was noted to be bradycardic with HR in 40s and hypotensive to 70s/40s so came for further evaluation. He was admitted. Hypotension thought to be due to hypovolemia secondary to PO intake in setting of recent COVID infection. Improved with fluid resuscitation. He was discharged on 9/19/2021.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Specimen Collection Date: Sep 16, 2021@22:35 COVID-19_(XPRESS PCR) DETECTED H* COVID CT VALUE E (CEPHEID) 18.4 COVID CT VALUE N2 (CEPHEID) 20.6 09/16/2021 CHEST-1 VIEW (AP/PA) 1. Interval increased right basilar subsegmental atelectasis. 2. No definite focal pneumonia, pleural effusion, or cardiomegaly. 3. Chronic obstructive pulmonary disease including linear pleural-parenchymal scarring at the right middle lobe. 4. Chronic elevation of the right hemidiaphragm.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2599971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 01.11.2021
Impfdatum: 24.03.2021
Beginn: 02.09.2021
Tage bis Beginn: 162,0
Dosis: UNK
Route/Site: IM / RA

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

Balance disorder Brain fog COVID-19 Cough Dyspnoea Fall Gait disturbance SARS-CoV-2 test positive

Symptomtext

Narrative: 67 yo male with PMH: HTN, OSA, social anxiety disorder, neuroleptic-induced parkinsonism, bipolar, obesity, and arthritis tested positive for covid19 on 9/2/2021. On 9/11/2021, he was admitted due to fogginess, increased falls. In addition, patient had cough and dyspnea on 8/29/2021 and tested positive for covid on 9/2/2021. Family felt that since 8/29/2021, he's had more fogginess and difficulty ambulating and has had 2 falls. During the hospital course, he did not require treatment for covid. It was found that his imbalance was due to polypharmacy (benzo and overuse of OTC robitussin).

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

VAERS 1831912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6203

moderat

Staat: -
Alter: 28,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 10.03.2021
Beginn: 29.10.2021
Tage bis Beginn: 233,0
Dosis: 2
Route/Site: IM / RA

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

COVID-19 Cough Dyspnoea Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Individual symptomatic with HA, cough, congestion, fever, and SOB tested positive on 10/28/21. Quarantine until 11/7/21 or until release by DOH. Individual declined to have antibody testing.

Weitere VAERSDATA-Felder

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