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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||- / UNK||- / -|
Administered by: Other Purchased by: ??
Symptoms: Diarrhoea, Anal haemorrhage, Haemorrhage, 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: Medical History/Concurrent Conditions: Acid reflux (esophageal); Lactation decreased; Vitamin D deficiency
Diagnostic Lab Data: Test Name: COVID-19 virus test; Test Result: Negative ; Comments: No - Negative COVID-19 test
CDC 'Split Type': GBPFIZER INC2021657556
Write-up: bleeding; Anal bleeding; Diarrhoea; This is a spontaneous report from a contactable consumer received from the Medicines and Healthcare products Regulatory Agency (UK-MHRA). The regulatory authority report number is GB-MHRA-APPCOVID-20210604095402, Safety Report Unique Identifier GB-MHRA-ADR 25418964. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 03Jun2021 (Lot number was not reported), vaccination at 33 years, as unknown, single dose for COVID-19 immunization. Medical history included Lactation decreased, Acid reflux (esophageal) and Vitamin D. Patient has not had symptoms associated with COVID-19. Patient was not enrolled in clinical trial. Patient was not pregnant or currently breastfeeding. The patient''s concomitant medications were not reported. The patient previously took vitamin d [colecalciferol] and folic acid. The patient experienced bleeding on an unspecified date, anal bleeding on 03Jun2021, diarrhoea on 03Jun2021. The patient bleeding a fair amount every time i the toilet (as reported). The patient underwent lab tests and procedures which included COVID-19 virus test: No - Negative COVID-19 test on unspecified date. The outcome of event bleeding was unknown, others was not recovered. This case was reported as not serious. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
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