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Life Threatening? No
Write-up: cardiac arrest; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202103270909463110. A 62-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 26Feb2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Medical history included diabetes, immunodeficiency (Taking other treatments or medicines, not listed above, known to lower the immune response and i...), and hypertension. Patient had not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient had not tested positive for COVID-19 since having the vaccine. The patient''s concomitant medications were not reported. The patient experienced cardiac arrest on an unspecified date. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on 19Mar2021. The patient died on 24Mar2021. It was not reported if an autopsy was performed and the reported cause of death was cardiac arrest. The clinical course was reported as: "Vaccine caused cardiac arrest which caused death. Postmortem samples sent for confirmation" No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Reported Cause(s) of Death: Cardiac arrest
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