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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: Electrocardiogram, Loss of consciousness, Malaise, Syncope, Vaccination site haemorrhage, Blood pressure measurement, 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
Hospitalized? Yes, days:
Write-up: loss of consciousness; Fainting; felt sick; Bleeding a lot at site of vaccine; This is a spontaneous report from a contactable consumer received from the regulatory authority (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106041836507160-WYVGE, Safety Report Unique Identifier GB-MHRA-ADR 25422972. A 32-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Jun2021 (Lot number was not reported, at age of 32-year-old) as single dose for covid-19 immunisation. The patient medical history was not reported. No medical history. Patient has not had symptoms associated with COVID-19. Patient is not enrolled in clinical trial. The patient''s concomitant medications were not reported. The patient previously took epinephrine adrenaline [ADRENALINE]. Instantly after having the vaccine on 04Jun2021, patient felt sick. Patient was bleeding a lot at site of vaccine too. After the patient went to sit down, within 10 seconds patient passed out. After he came back around instantly again, patient had loss of consciousness again and had to have adrenaline. Patient has not tested positive for COVID-19 since having the vaccine. The patient underwent lab tests included COVID-19 virus test: negative on 19Oct2020 No - Negative COVID-19 test, blood pressure: unknown result on an unspecified date, electrocardiogram (ECG): unknown result on an unspecified date. The outcome of the events was unknown. The seriousness was reported as hospitalization. No follow-up attempts are possible, information about batch number cannot be obtained.
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