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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||EJ1688/V0007 / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Coma, Haemorrhagic stroke, Hypertension
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
Other Medications: WARFARIN
Preexisting Conditions: Medical History/Concurrent Conditions: Multiple sclerosis (Taking medicines for multiple sclerosis); Thrombosis
Diagnostic Lab Data:
CDC 'Split Type': GBPFIZER INC2021391930
Write-up: Hypertension.; coma; Haemorrhagic stroke; This is a spontaneous report from a contactable consumer. This is a report received from the Agency Regulatory Authority. Regulatory authority report number: GB-MHRA-WEBCOVID-202104080925179560, Safety Report Unique Identifier: GB-MHRA-ADR 25101425. An 80-years-old male patient received first dose of BNT162B2, lot no. EJ1688/V0007, via an unspecified route of administration on 23Dec2020 as single dose for COVID-19 immunisation. Medical history included multiple sclerosis (taking medicines for multiple sclerosis) and thrombosis. He has not had symptoms associated with COVID-19, not had a COVID-19 test, and not enrolled in clinical trial. Concomitant medications included warfarin taken for thrombosis and unspecified medicines for multiple sclerosis. The patient experienced haemorrhagic stroke on 04Jan2021 (fatal per HA assessment). Case narrative: Taken to hospital and went into coma. Passed away from incebral haemorage and hypertension. Not unwell before vaccine. No relevant investigations or tests conducted. The patient died on 04Jan2021 due to haemorrhagic stroke and hypertension. The outcome of coma was unknown. It was not reported if an autopsy was performed. Follow-up attempts are completed. No further information is expected.; Reported Cause(s) of Death: Haemorrhagic stroke; Hypertension
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