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From the 1/14/2022 release of VAERS data:

This is VAERS ID 278375

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Case Details

VAERS ID: 278375 (history)  
Form: Version 1.0  
Age: 35.0  
Sex: Female  
Location: Unknown  
Vaccinated:2007-02-28
Onset:2007-02-28
   Days after vaccination:0
Submitted: 2007-05-10
   Days after onset:70
Entered: 2007-05-11
   Days after submission:1
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. - / UNK UN / UN

Administered by: Other       Purchased by: Other
Symptoms: Abortion induced, Drug exposure during pregnancy, Ectopic pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: Unknown
Current Illness:
Preexisting Conditions: Pregnancy termination
Allergies:
Diagnostic Lab Data: Unknown
CDC Split Type: WAES0704USA03486

Write-up: Information has been received through the manufacturer Pregnancy Registry from a certified genetics counselor concerning a 35 year old female, with no pertinent medical history, who on 24-FEB-2007 terminated a pregnancy. On 28-FEB-2007 the patient was vaccinated with Varivax. In March 2007, one month post vaccination, the patient was positive for pregnancy. On 16-APR-2007 an in-office pregnancy test was taken and the pregnancy was confirmed. An ultrasound is due to be completed to determine if the termination of the initial pregnancy had "failed", or whether this is a second pregnancy. Unspecified medical attention was sought. There was no product quality complaint. Follow up information has been received through the manufacturer Pregnancy Registry from a healthcare worker who reported that the patient, who had no previous pertinent medical history, developed an ectopic pregnancy, and was given methotrexate to induce an abortion. The patient was not recovered at the time of reporting. There was no product quality complaint. Additional information has been requested.


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