VAERS Results 01312021

Vaccine
Manufacturer
Event
Category
Age
VAERS
ID
Adverse Event Description
PFIZER\BIONTECH Death 65+ years 964617-1 Death, which I believe is unrelated to vaccination
PFIZER\BIONTECH Death 65+ years 964636-1
PFIZER\BIONTECH Death 65+ years 964653-1
Pt on hospice in facility for severe cardiomyopathy unable to perform interventions received
vaccine without adverse sequelae died 5 days later. Reporting as required. Narrative: Reporting
as required patient death 5 days after immunization with Pfizer vaccine. However, no adverse
sequelae were noted to the vaccine in the 15minute observation period, nor in the days
following the immunization related to the vaccine. The patient denied any prior severe reaction
to this vaccine or its components, and the patient gave verbal consent to receive the vaccine.
Patient had been in the facility on hospice since 11/18/20 for severe decompensated HF and
newly diagnosed cardiomyopathy, unable to perform interventions, also LE ischemic wounds
with very poor potential to heal due to advanced PVD.
loss of consciousness; respiratory distress Narrative: Patient tolerated his 1st dose of the COVID-
19 vaccine well, on 12/16/2020, and received his 2nd dose on 1/6/2021. Patient had some mild
clinical decline the past few days prior to 2nd vaccination, with a decreased appetite and some
increased fatigue per nursing report, but no significant changes. He experienced nausea on the
evening of 1/6/21, which was effectively managed, but by early morning he spiked a fever of
102.9 with a sat of 86.1%. He continued to deteriorate from that point on and died 1/7/21
@13:20. Clinically, the presentation was most consistent with an aspiration pneumonia.
PFIZER\BIONTECH Death 65+ years 964671-1 Death on 1-5-21
PFIZER\BIONTECH Death 65+ years 964724-1 Death 1-15-21
Note: Submitting a report to VAERS does not mean that healthcare personnel or the vaccine caused or contributed to the adverse event (possible side effect).
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Notes:
Caveats:
VAERS accepts reports of adverse events and reactions that occur following vaccination. Healthcare providers, vaccine manufacturers,
and the public can submit reports to VAERS. While very important in monitoring vaccine safety, VAERS reports alone cannot be used to
determine if a vaccine caused or contributed to an adverse event or illness. The reports may contain information that is incomplete,