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Life Threatening? No
Write-up: Subarachnoid hemorrhage; This is a spontaneous report from a contactable Physician. This is a report received from the MHRA. Regulatory authority report number GB-MHRA-WEBCOVID-202101191508083250, Safety Report Unique Identifier GB-MHRA-ADR 24615904 An 83-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: BNT162b2, expiry date not reported), via an unspecified route of administration on 10Jan2021 at single dose for COVID-19 immunization. Medical history included chronic obstructive pulmonary disease from an unknown date and unknown if ongoing. Concomitant medication included aclidinium bromide and salbutamol sulfate (VENTOLIN); both for chronic obstructive pulmonary disease. The patient experienced subarachnoid hemorrhage on 14Jan2021. The patient underwent lab tests and procedures which included computerised tomogram head: results not provided on an unspecified date. The patient died on 17Jan2021. It was not reported if an autopsy was performed. The outcome of the event was fatal. No follow-up attempts possible; information regarding batch/lot cannot be obtained; No further information expected.; Reported Cause(s) of Death: Subarachnoid hemorrhage
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