Received Jul 2, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
I have COVID; I have COVID; This is a spontaneous report received from a Consumer or other non HCP. A 68-year-old female patient received BNT162b2 omicron (kp.2) (COMIRNATY (2024-2025 FORMULA)), on 19May2025 as dose 1, single (Batch/Lot number: unknown) at the age of 68 years for COVID-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: COMIRNATY (primary immunisation series complete), for COVID-19 immunisation: the patient took the vaccine since it's been available, and every 6 months, and it's always been Pfizer. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2025, outcome "unknown" and all described as "I have COVID". Therapeutic measures were taken as a result of vaccination failure, COVID-19: the patient was prescribed PAXLOVID the morning of this report. The patient specified that she had got symptoms pretty major- not major but quite a few symptoms. The patient took the Pfizer COVID vaccine a month prior to this report, and she had been up to date like every 6 months, and she did not understand why she was so sick. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received.