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|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||- / UNK||- / -|
Administered by: Other Purchased by: ??
Symptoms: Chest pain, Cough, Dyspnoea, Groin pain, Malaise, Myocardial infarction, Myocarditis
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Diagnostic Lab Data:
CDC 'Split Type': AUPFIZER INC202101033744
Write-up: Chest pain; Cough; Dyspnoea; Groin pain; Malaise; Myocardial infarction; Myocarditis; This is a spontaneous report from a contactable other health professional via the Regulatory Authority. Regulatory authority report number is 598851. A 52-year-old male patient received BNT162B2 (COMIRNATY), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On 22Jul2021, the patient experienced chest pain, cough, dyspnoea, groin pain, malaise, myocardial infarction, myocarditis. The outcome of the events was fatal. The patient died on an unspecified date. It was not reported if an autopsy was performed. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reported Cause(s) of Death: Chest pain; Cough; Dyspnoea; Groin pain; Malaise; Myocardial infarction; Myocarditis
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