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This is VAERS ID 1720863

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First Appeared on 10/8/2021

VAERS ID: 1720863
VAERS Form:2
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other      Purchased by: ??
Symptoms: Dysmenorrhoea, 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: Comments: Patient has not had symptoms associated with COVID-19 Not had a COVID-19 test Patient is not pregnant,Patient is not currently breastfeeding
Diagnostic Lab Data:
CDC 'Split Type': GBPFIZER INC202101190739

Write-up: Cramps menstrual; Menstrual flooding; This is a spontaneous report from a contactable consumer. This is a report received from the regulatory authority report number is GB-MHRA-WEBCOVID-202109100505290660-I4FIO, Safety Report Unique Identifier GB-MHRA-ADR 25921494. A 29-year-old female patient (non-pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Aug2021 (Batch/Lot number was not reported) as DOSE 2, SINGLE for COVID-19 immunisation. The patient was not pregnant at the time of vaccination. The patient medical history and concomitant medications were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unknown date for covid-19 immunisation. The patient experienced menstrual cramps and menstrual flooding on 10Sep2021. The clinical course was reported as follows, this happened with her first period after the first jab too. Her periods returned to her usual flow with no cramping thereafter. She not had severe menstrual cramps before. She did not have any cramps since she was 13. Patient had not tested positive for COVID-19 since having the vaccine. Patient was not enrolled in clinical trial. The outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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