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From the 11/19/2021 release of VAERS data:

This is VAERS ID 1380094

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Case Details

VAERS ID: 1380094 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:2021-03-03
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-06-08
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH ER0866 / 2 - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Ultrasound scan
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: EUTHYROX
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210411; Test Name: Ultrasound; Result Unstructured Data: Test Result:the fetus inside me was seen without pulse
CDC Split Type: ILPFIZER INC2021583731

Write-up: abortion. During 12 week (11Apr2021) test showed that the fetus inside me was seen without pulse; This is a spontaneous report received from a non contactable consumer. A 36-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 03Mar2021 09:45 AM (Lot Number: ER0866) as single dose for covid-19 immunisation. The patient''s medical history was not reported. Concomitant drug included levothyroxine sodium (EUTHYROX, patient received within 2 weeks of vaccination), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient previously received first dose of bnt162b2(lot number: EL7834) on 09Feb2021 for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Allergies to medications, food, or other products reported as no. The patient experienced abortion on an unknown date. During 12 weeks (11Apr2021) ultrasound (US) test showed that the fetus inside the patient was seen without pulse. It seemed that he stopped developing about three weeks before. The patient underwent lab tests and procedures which included ultrasound scan: the fetus inside me was seen without pulse on 11Apr2021. Treatment for the event included misoprostol (CYTOTEC). AE resulted in visit in an office/ clinic of a physician or other medical care provider. The outcome of the event was recovered. No follow-up attempts are possible; No further information is expected.


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