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From the 11/26/2021 release of VAERS data:

This is VAERS ID 1086871

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Case Details

VAERS ID: 1086871 (history)  
Form: Version 2.0  
Sex: Female  
Location: Wisconsin  
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-03-10
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Unknown       Purchased by: ?
Symptoms: Abortion spontaneous, Blood test, Exposure during pregnancy, Human chorionic gonadotropin, Sexually transmitted disease test, Ultrasound abdomen, Urine analysis
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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety; Cosmetic allergy (an allergy to an unknown beauty product); Endometriosis; Environmental allergy (environmental allergies); Kidney stone; Paroxysmal supraventricular tachycardia
Diagnostic Lab Data: Test Date: 20210222; Test Name: Blood Test; Result Unstructured Data: Normal test results; Test Date: 20210222; Test Name: HCG; Result Unstructured Data: 21297 (expected to be); Test Date: 20210222; Test Name: HIV/ Chlamydia /gonorrhea; Test Result: Negative ; Result Unstructured Data: HIV/ Chlamydia /gonorrhea; Test Date: 20210222; Test Name: Ultrasound; Result Unstructured Data: no fetal heart beat; Test Date: 20210222; Test Name: Urine; Result Unstructured Data: Tested normal/negative

Write-up: Miscarriage; Vaccine exposure during pregnancy; A spontaneous report was received from a consumer who was also a 41-year old, female patient who received Moderna''s COVID-19 vaccine (mRNA-1273) resulting in the event miscarriage/ abortion spontaneous and vaccine exposure during pregnancy. The patient''s medical history included environmental allergies and an allergy to an unknown beauty product, kidney stone, endometriosis, anxiety, and paroxysmal supraventricular tachycardia. Products known to have been used by the patient, within two weeks prior to the event, included pre-natal vitamins and escitalopram oxalate. The patient received their first of two planned doses of mRNA-1273 (Batch number: 042L20A) intramuscularly on 14 Jan 2021. On 12 Feb 2021, the patient received their second of two planned doses of mRNA-1273 (Batch number: 012M20A) intramuscularly for prophylaxis of COVID-19 infection. On 21 Jan 2020, the patient had a positive pregnancy test. The first day of the patient''s last menstrual period was on 24 Dec 2020. The estimated date of conception was not provided. The due date was estimated as 30 Sep 2021. On 22 Feb 2021, the patient had a miscarriage. There was no fetal heartbeat on the ultrasound. On 24 Feb 2021, the patient underwent a procedure to complete the miscarriage. The patient received both scheduled doses of mRNA-1273; therefore, action taken with the drug in response to the event is not applicable. The outcome of the events was considered recovered.; Reporter''s Comments: This is a case of product exposure during pregnancy with an Adverse event of Spontaneous abortion for this 41-year-old female. Very limited information regarding this event has been provided at this time. Further information has been requested.

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