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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||UNKNOWN / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Electrocardiogram, Myocardial infarction, Laboratory test
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? Yes
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Other Medications: SIMVASTATIN; DARIFENACIN
Diagnostic Lab Data: Test Name: ECG; Result Unstructured Data: Test Result:unknown result; Test Name: lab; Result Unstructured Data: Test Result:unknown result
CDC 'Split Type': NLPFIZER INC2021342698
Write-up: Myocardial infarct; This is a spontaneous report from a contactable physician downloaded from the Agency Regulatory Authority-WEB, regulatory authority number NL-LRB-00483517. An 89-year-old female patient received first dose of BNT162B2 (COMIRNATY) via an unspecified route of administration on 13Feb2021 as single dose for covid-19 immunisation. The patient medical history was not reported. Patient had no COVID-19 infection previously. The patient has no past drug. Concomitant medications included simvastatin (10mg film-coated tablet); darifenacin (7.5mg modified-release tablet). The patient experienced myocardial infarct 5 days after BNT162B2 administration on 18Feb2021. The patient underwent lab tests and procedures which included examination at the cardiology department with electrocardiogram (ECG), lab (test), etc., with unknown results (undated). The patient died on an unspecified date. It was not reported if an autopsy was performed. The reported cause of death is Myocardial infarct. The outcome of myocardial infarct is fatal. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Myocardial infarct
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