Received Mar 10, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
This is the fourth time I've had COVID; This is the fourth time I've had COVID; This is the fourth time I've had COVID; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 64-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE), for Covid-19 immunization; Bnt162b2 (DOSE 2, SINGLE), for Covid-19 immunization; Bnt162b2 (DOSE NUMBER UNKNOWN (BOOSTER), SINGLE), for Covid-19 immunization; Bnt162b2;bnt162b2 omi ba.4-5 (DOSE NUMBER UNKNOWN (BOOSTER), SINGLE), for Covid-19 immunization; Comirnaty (2023-2024 formula) (DOSE 1, SINGLE), for Covid-19 immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), DISEASE RECURRENCE (medically significant), outcome "unknown" and all described as "This is the fourth time I've had COVID". She did not remember it was the 4th or 5th time (as reported). She had all of the Pfizer vaccines. Therapeutic measures were taken as a result of drug ineffective, covid-19, disease recurrence, included Pfizer medication for COVID. On another occasion, they gave the patient Pfizer medication for COVID. The patient said that she did not remember the name of medication for COVID, but on one of those occasions, she got sick with COVID, and they gave her COVID medication. The patient stated that this would be the second time she took COVID medicine. The information on the batch/lot number for BNT162B2 OMICRON (KP.2) will be requested and submitted if and when received.