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From the 10/8/2021 release of VAERS data:

This is VAERS ID 1211907

Case Details

VAERS ID: 1211907 (history)  
Form: Version 2.0  
Sex: Female  
Location: Foreign  
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-04-15
Vaccin­ation / Manu­facturer Lot / Dose Site / Route

Administered by: Other       Purchased by: ?
Symptoms: Angiocardiogram, Myocardial infarction
SMQs:, Myocardial infarction (narrow), Embolic and thrombotic events, arterial (narrow)

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died: 0000-00-00
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: TIA
Diagnostic Lab Data: Test Name: coronary x-ray; Result Unstructured Data: Test Result:UNKNOWN
CDC Split Type: SEPFIZER INC2021380325

Write-up: heart attack/MYOCARDIAL INFARCTION; This is a spontaneous report from a contactable consumer downloaded from a regulatory authority-WEB. Regulatory Authority report number is SE-MPA-2021-021846. A 97-year-old female patient received second dose of bnt162b2 (COMIRNATY), via an unspecified route of administration in Feb2021 (Batch/Lot Number: EL 1484) as SINGLE DOSE for covid-19 immunization. Medical history included TIA (transient ischaemic attack) from 2014. The patient previously received the 1st dose of COMIRNATY (lot:EL 1484) for covid-19 immunization. The patient''s concomitant medications included blood pressure medications (not specified). The reporter stated that the patient was healthy for her age, managed to walk to the vaccinations 1.4 km both times. Four days after her 2nd vaccination (Feb2021), the patient had a heart attack/myocardial infarct and after about a week of hospitalization, the woman had another heart attack and died. The patient underwent lab tests and procedures which included coronary x-ray: with unknown results;it was decided that a pacemaker would be inserted after her second heart attack but patient died. It was reported that patient received a treatment due to the event. It was not reported if an autopsy was performed. The event was assessed as "serious, causing patient''s death". No follow-up attempts possible. No further information expected.; Reported Cause(s) of Death: heart attack/MYOCARDIAL INFARCTION

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