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From the 7/23/2021 release of VAERS data:

This is VAERS ID 1329537

Case Details

VAERS ID: 1329537 (history)  
Form: Version 2.0  
Sex: Female  
Location: Pennsylvania  
   Days after vaccination:15
Submitted: 0000-00-00
Entered: 2021-05-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Private       Purchased by: ?
Symptoms: Postmenopausal haemorrhage
SMQs:, Haemorrhage terms (excl laboratory terms) (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy to plants (none. Had an adverse reaction to Aloe many years ago.); Menopause
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2021515349

Write-up: I have post menopausal bleeding.; This is a spontaneous report from a non-contactable consumer (patient). A 53-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: ER8733, expiry date not reported), via an unspecified route of administration, administered in left arm on 17Apr2021 as first dose, single for covid-19 immunisation. Medical history included patient had an adverse reaction to aloe many years ago and have not had her period in 2 years. The patient''s concomitant medications were not reported. The first dose of was administered in a doctor''s office/urgent care. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient had no other medications the patient received within 2 weeks of vaccination. The patient had no covid prior to vaccination. Patient had post menopausal bleeding on 02May2021. Patient have not had her period in 2 years and have started a very heavy flow period. Patient have contacted her doctor and have a pelvic ultra sound scheduled. The event resulted in doctor or other healthcare professional office/clinic visit. It was unknown if treatment was received in response to the event. Since the vaccination, the patient has not been tested for COVID-19. Patient was not pregnant at the time of the vaccination and of the report. The event post menopausal bleeding was not recovered. No follow-up attempts are possible. No further information is expected.

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