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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: Arteriosclerosis coronary artery, Cardiomegaly, Myocardial fibrosis
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 INC202101033741
Write-up: Arteriosclerosis coronary artery; Cardiomegaly; Myocardial fibrosis; This is a spontaneous report from a contactable other health professional via the Regulatory Authority. Regulatory authority report number is 598170. An 89-year-old male patient received BNT162B2 (COMIRNATY), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for Covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced Arteriosclerosis coronary artery; Cardiomegaly; Myocardial fibrosis, all on 23APR2021. The patient died on an unspecified date. It was not reported if an autopsy was performed. The outcome of the events was Fatal. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reported Cause(s) of Death: Arteriosclerosis coronary artery; Cardiomegaly; Myocardial fibrosis
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