VAERS Results 01312021

Vaccine
Manufacturer
Event
Category
Age
VAERS
ID
Adverse Event Description
bibasilar infiltrates consistent with COVID pneumonia but bacterial pneumonia could not be
excluded. The patients BP was documented as 97/64. He was treated with Zofran for nausea and
tylenol. He was prescribed a five day course of Azithromycin, an Albuterol inhaler, guaifenessin
with codeine cough syrup, and Zofran. Labs were drawn and he was discharged. His lab results
were reported after his departure and were significant for a white blood cell count of 1.33,
platelet count of 73, 2% myelocytes, 1% metamyelocytes, an absolute neutrophil count of 0.75
K/ul, a creatinine of 1.83, total bilirubin of 1.3, with direct bilirubin of 0.8, alkaline phosphatase
of 294 and AST of 112 with ALT noted to be within normal limit. His COVID nasopharyngeal swab
from the visit was reported as negative and a swab performed at his employment on 13-Jan-21
was also reported to be negative. Patient could not be reached by phone after discharge from
Urgent Care about these labs. On the evening of 16-Jan-21, Police Department received a 911
call about an adult at the patient's address who was found unresponsive. Upon arrival on scene,
the patient was found to be deceased and a decision was made not to attempt to resuscitate.
The death was deemed to be non-suspicious and the patient's body was transported to a funeral
home. On 19-Jan-21, I contacted the State Medical Examiner's Office. They have decided to
perform an autopsy and have recovered the CBC and chemistry specimens obtained for further
testing.
PFIZER\BIONTECH
Death
60-64
years
958322-1 Shaking and then became unresponsive
PFIZER\BIONTECH
Death
60-64
years
961705-1
approximately 3 hours prior to expiring the patient was experiencing forceful emesis. later was
found to have expired, patient was comfort care only.
PFIZER\BIONTECH
Death
60-64
years
962716-1 Patient deceased
PFIZER\BIONTECH
Death
60-64
years
964629-1
Death - Hospice patient with metastatic CA admitted to facility and received vaccine during stay.
No adverse sequelae noted from vaccine administration, but reporting as required because pt
died 7 days later. Narrative: Reporting this event because patient died 7 days after receiving
vaccine in the facility where he was in hospice care for metastatic cancer. Vaccine was
administered by protocol without complications. The patient had been asked and denied any
prior severe reaction to this vaccine or its components and gave permission to receive it. No
vaccine adverse sequelae were documented after the immunization as monitored for 15 minutes