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This is VAERS ID 1732961

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First Appeared on 10/15/2021

VAERS ID: 1732961
VAERS Form:2
Age:
Sex:Female
Location:Foreign
Vaccinated:2021-09-10
Onset:2021-09-10
Submitted:0000-00-00
Entered:2021-09-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2153 / 1 - / -

Administered by: Other      Purchased by: ??
Symptoms: Diarrhoea, Dizziness, Nausea, Adnexa uteri pain, Heavy menstrual bleeding

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': GBPFIZER INC202101196562

Write-up: ovarian pain; Heavy periods; Dizziness; Diarrhea; Nausea; This is a spontaneous report from a contactable consumer, this report is received from the regulatory authority report number is GB-MHRA-WEBCOVID-202109121306132360-TWRQX, and Sender''s (Case) Safety Report Unique Identifier is GB-MHRA-ADR 25929086. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot Number: FF2153), dose 1 via an unspecified route of administration on 10Sep2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient has not had symptoms associated with COVID-19. The patient has not tested positive for COVID-19 since having the vaccine. The patient was not enrolled in clinical trial. It was reported that the patient experienced immediate feeling of nausea after injection and diarrhea on 10Sep2021, dizziness on 11Sep2021, very heavy period two weeks early on 12Sep2021 and strong hormonal reaction pain in ovaries on an unspecified date. Outcome of the event nausea, heavy periods and dizziness was reported as not recovered, outcome of the event diarrhea was reported as recovering, outcome of the event ovarian pain was reported as unknown at this time of the report. No follow-up attempts are possible. No further information is expected.

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