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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||EW3143 / 1||- / -|
Administered by: Other Purchased by: ??
Symptoms: Head discomfort, Tinnitus
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
Preexisting Conditions: Medical History/Concurrent Conditions: Lactation decreased
Diagnostic Lab Data:
CDC 'Split Type': GBPFIZER INC2021657821
Write-up: Pulsatile tinnitus; felt pressure in her head; This is a spontaneous report from a contactable consumer (patient) received from the Agency Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202106042223471030-NFDGS. Safety Report Unique Identifier GB-MHRA-ADR 25424544. A 37-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EW3143), via an unspecified route of administration on 04Jun2021 (37-year-old at time of vaccination) as single dose for COVID-19 immunisation. Medical history included lactation decreased. The patient''s concomitant medications were not reported. The patient experienced pulsatile tinnitus on 04Jun2021. The event was assessed as serious with criteria of Other medically important condition. Additional Information: Had her vaccine. Went home to rest. Within one hour she felt pressure in her head, mainly on vaccination side, and pulsatile tinnitus started. Patient has not had symptoms associated with COVID-19. Patient has not tested positive for COVID-19 since having the vaccine. Not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not pregnant. Patient is not currently breastfeeding. The outcome of pulsatile tinnitus was not recovered; outcome of "felt pressure in her head" was unknown. No follow-up attempts are needed. No further information is expected.
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