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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||- / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Cerebral haemorrhage
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)? Yes
Hospitalized? Yes, days:
Write-up: Cerebral haemorrhage; This is a spontaneous report from a contactable other hcp received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202104070824399490. A 50-years-old female patient (not pregnant) received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 12Mar202, at SINGLE DOSE for covid-19 immunisation. Medical history included suppressed lactation from an unknown date and unknown if ongoing, cerebral haemorrhage from an unknown date and unknown if ongoing, non-tobacco user from an unknown date and unknown if ongoing. The patient has not had symptoms associated with COVID-19, has not had a COVID-19 test, was not enrolled in a clinical trial, was not pregnant, and was not currently breastfeeding. The patient''s concomitant medications were not reported. The patient was admitted via accident & emergency to the intensive care unit of the hospital on 04Apr2021 with cerebral haemorrhage; however, it was reported that the patient experienced cerebral haemorrhage on 05Apr2021. The seriousness criteria of cerebral haemorrhage were considered to be Results in death and Other medically important condition by the regulatory authority. Caused/prolonged hospitalization was considered as an additional seriousness criteria for cerebral haemorrhage. The reporter confirmed that this report relates to possible blood clots or low platelet counts, that it was unknown whether the platelet count was less than 150 x10e9/L, whether the D-dimer was greater than 4000, and whether the anti-PF4 antibodies were identified. The patient has not tested positive for covid-19 since having the vaccine. She was diagnosed as having cerebral haemorrhage. The patient died on 05Apr2021 due to cerebral haemorrhage. It was not reported if an autopsy was performed. Information on the lot/batch number has been requested.; Reported Cause(s) of Death: Cerebral haemorrhage
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