Your Health. Your Family. Your Choice.
|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||ET1831 / 1||LA / OT|
Administered by: Other Purchased by: ??
Symptoms: Asthenia, Body temperature, Chest pain, Blood pressure measurement
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Current Illness: Diabetes mellitus insulin-dependent; Hypertension; OA knee (knee arthrosis)
Preexisting Conditions: Medical History/Concurrent Conditions: Weakness; Wheelchair user
Diagnostic Lab Data: Test Date: 20210305; Test Name: blood pressure; Result Unstructured Data: Test Result:140/80 mmHg; Test Date: 20210305; Test Name: body temperature; Result Unstructured Data: Test Result:36.4 Centigrade
CDC 'Split Type': HUPFIZER INC2021354240
Write-up: weakness; chest pain; This is a spontaneous report from a contactable physician downloaded from a regulatory authority- WEB. E2B Authority Number is HU-OGYI-145721. An 81-year-old female patient received her 1st dose of BNT162B2 (COMIRNATY, lot number ET1831, expiry date: unknown) at 0.3 ml single dose intramuscular in left upper arm on 05Mar2021 for COVID-19 immunisation. Medical history included knee arthrosis, hypertension, and diabetes mellitus insulin-dependent, all ongoing. Before vaccination, the patient was already very weak; she could be travelled by wheelchair although her diseases were balanced by her current pharmacotherapy. Based on the vaccinating doctor, there was no contraindication of vaccination, she was cardio-pulmonary compensated, her blood pressure and body temperature were normal (140/80 Hgmm and 36.4 degree C, respectively). Concomitant drug was not provided. During the half-hour observation period, no reaction was observed. On the next day in the afternoon, the patient became weak, later, she experienced chest pain and died at her home. Based on the opinions of the patient''s vaccinating physician and family doctor, the death was not related to the vaccination but could be due to a cardiac event. Autopsy has been done, the result is unknown. Sender Comment: Weakness is an expected adverse event of COMIRNATY, however, the patient was already reported to be weak before vaccination. Time to onset was one day. Causality between the weakness, and resulting death and COMIRNATY is not assessable. The case is serious because the patient has died. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: weakness; chest pain
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