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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: Dizziness, 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
Preexisting Conditions: Comments: Patient has not had symptoms associated with COVID-19 Patient is not enrolled in clinical trial
Diagnostic Lab Data: Test Date: 20210515; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC 'Split Type': GBPFIZER INC2021649245
Write-up: Dizzy spells; dizzy; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Agency. The regulatory authority report number: GB-MHRA-WEBCOVID-202106020823372060-VK2WY. Sender''s (Case) Safety Report Unique Identifier: GB-MHRA-ADR 25403015. A female patient of an unspecified age received BNT162B2 (COVID-19 MRNA VACCINE BIONTECH), dose 1 via an unspecified route of administration on 01Jun2021 (Batch/Lot Number: Not reported) as single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. The patient experienced dizzy spells on 01Jun2021 the day she had the vaccine and dizzy 20 hours after (Jun2021). The events were assessed as serious: medically significant. The patient underwent lab tests and procedures which included COVID-19 virus test: no - negative covid-19 test on 15May2021. Patient has not tested positive for COVID-19 since having the vaccine. No other relevant investigations or tests conducted. The outcome of dizzy spells was recovering while outcome of dizzy was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.
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