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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||- / 2||- / -|
Administered by: Other Purchased by: ??
Symptoms: Dizziness, Motion sickness, Syncope, Illness, SARS-CoV-2 test
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
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC 'Split Type': GBPFIZER INC2021649549
Write-up: Fainting; Sea sickness; started being sick; felt light headed; This is a spontaneous report from a contactable consumer received from the regulatory authority report number is GB-MHRA-WEBCOVID-202106021836060740-BTBAT. Safety Report Unique Identifier GB-MHRA-ADR 25407663. A 41-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 02Jun2021 (Lot number was not reported) as single dose for COVID-19 immunisation. The patient medical history was not reported. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient was not pregnant. The patient''s concomitant medications were not reported. The patient experienced felt light headed on an unspecified date in Jun2021 with outcome of recovering, fainting on 02Jun2021 with outcome of recovering, sea sickness on 02Jun2021 with outcome of recovering, started being sick on an unspecified date in Jun2021 with outcome of unknown, all reported as medically significant. Clinical course reported as follow: Felt light headed, fainted in parked vehicle, started being sick when came round. The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test. Patient has not tested positive for COVID-19 since having the vaccine. No follow-up attempts are possible. No further information is expected.
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