Received Oct 20, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
I had tested positive for COVID; I had tested positive for COVID; This is a spontaneous report received from a Consumer or other non HCP, Program ID. A 67-year-old female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 11Sep2025 as dose 1, single (Batch/Lot number: unknown) at the age of 67 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (primary immunization series complete; unknown manufacturer), for Covid-19 Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2025, outcome "unknown" and all described as "I had tested positive for COVID". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Oct2025) Positive. Clinical course: On 11Sep of this year (2025), the patient's husband and the patient herself went and had the COVID vaccine, Pfizer COVID vaccine at their local (Withheld) drug store. The patient went to the doctor on Saturday, saying she had tested positive for COVID. The patient was prescribed a five-day, ten-pill prescription. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Test Date: 202510; Test Name: COVID; Test Result: Positive