VAERS ID: 2315238

AGE: | SEX: F|STATE: MN

Description

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 01Apr2021 as dose 1, single (Lot number: ER8737), in left arm, on 29Apr2021 as dose 2, single (Lot number: EW0171), in left arm and on 16Nov2021 as dose 3 (booster), single (Lot number: FH8027), in right arm for covid-19 immunisation. The patient's relevant medical history included: "sulpha allergy" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown results, notes: Treatment of COVID-19. Patient received treatment for COVID-19: PF-07321332, ritonavir (PAXLOVID), from 31May2022 (Lot number: GA1513) to 05Jun2022.

Symptoms

COVID-19, SARS-CoV-2 test, Vaccination failure

Vaccines

VAX DATE: 11-16-2021| ONSET DATE: | DAYS TO ONSET:
NameDose #TypeManufacturerLotRouteSite
COVID19 (COVID19 (PFIZER-BIONTECH)) 3 COVID19 PFIZER\BIONTECH FH8027 Unknown RA

RECVDATE:06-10-2022
RPT_DATE:
CAGE_YR:
CAGE_MO:
DIED:U
DATEDIED:
L_THREAT:U
ER_VISIT:U
HOSPITAL:U
HOSPDAYS:
X_STAY:U
DISABLE:U
RECOVD:U
LAB_DATA:Test Name: COVID-19 Test; Result Unstructured Data: Test Result:Unknown results; Comments: Treatment of COVID-19
V_ADMINBY:
OTHER_MEDS:
CUR_ILL:
HISTORY:Medical History/Concurrent Conditions: Sulfonamide allergy
PRIOR_VAX:
SPLTTYPE:USPFIZER INC202200805943
FORM_VERS:2
TODAYS_DATE:06-09-2022
BIRTH_DEFECT:U
OFC_VISIT:U
ER_ED_VISIT:U
ALLERGIES:
V_FUNDBY:

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