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This is VAERS ID 955838

History of Changes from the VAERS Wayback Machine

First Appeared on 5/28/2021

VAERS ID: 955838
VAERS Form:2
Age:83.0
Sex:Female
Location:Foreign
Vaccinated:2021-01-06
Onset:2021-01-06
Submitted:0000-00-00
Entered:2021-01-19
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ6795 / 1 RA / OT

Administered by: Other      Purchased by: ??
Symptoms: Sudden death

Life Threatening? No
Birth Defect? No
Died? Yes
   Date died:2021-01-06
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness: Dementia; Multimorbidity; Pneumonia
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': NOPFIZER INC2021027016

Write-up: Sudden death; This is a spontaneous report from two contactable physicians downloaded from the Regulatory Authority-WEB NO-NOMAADVRE-FHI-2021-UDMAY, Safety Report Unique Identifier NO-NOMAADVRE-E2B_00013809. An 83-year-old female patient received the first dose of bnt162b2 (COMIRNATY, batch/lot number EJ6795) intramuscular in the right arm on 06Jan2021 10:57 at single for covid-19 immunisation. Medical history included dementia, pneumonia, multimorbidity, all ongoing. The patient''s concomitant medications included treatment for pneumonia. The patient experienced sudden death on 06Jan2021. It was not reported if an autopsy was performed. The causality between the suspect product(s) and the event(s) were assessed as possible by the Regional Pharmacovigilance Center. Case narrative: According to reporter, it is doubtful that there is a causal link between vaccination and death, but it cannot be ruled out that vaccination may have helped to speed up death for other reasons. The patient was an elderly demented multi-morbid female who was considered terminal shortly before death. Was at the time undergoing treatment for a suspected pneumonia. Treatment was apparently successful and it was considered that the patient should receive the vaccine. Vaccination was administered approximately 6 hours before the patient was found dead in her own bed. She was observed, without any remarks, by nursing staff 1 hour before she was found dead. Sender''s comments (Health Authority comments): Thank you for reporting a suspected side effect after vaccination. The information is registered in the national adverse reaction register (the Norwegian Medicines Agency), and then forwarded to international adverse reaction databases. In this way, your message becomes part of an important international collaboration that is continuously ongoing to monitor and maintain safe vaccination worldwide. It is stated in the report that the patient had underlying diseases before vaccination. When vaccinating marginal patients who are ill with many underlying diseases, some serious events, including death, may occur shortly after vaccination without any connection to vaccination. As the incident is described, it is more likely that these diseases are behind the incident. However, it cannot be ruled out that the vaccine has contributed to any of the symptoms. It is also conceivable that the incident had a completely different cause that only happened by chance after the vaccination. No follow-up attempts are possible. No further information is expected.; Reported Cause(s) of Death: Sudden death

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