Received Jun 24, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | — |
came positive for COVID; My husband took all of them; came positive for COVID; My husband took all of them; This is a spontaneous report received from a Consumer or other non HCP, Program ID. An elderly male 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. Past drug history included: Paxlovid, start date: 2024, stop date: 2024, for COVID-19 treatment. Vaccination history included: Bnt162b2 (some of the vaccines were mixed, Pfizer (Unspecified Vaccine) and Moderna (Unspecified Vaccine)), for Covid-19 Immunization; Moderna (some of the vaccines were mixed, Pfizer (Unspecified Vaccine) and Moderna (Unspecified Vaccine)), for Covid-19 Immunization. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jun2025, outcome "unknown" and all described as "came positive for COVID; My husband took all of them". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Jun2025) Positive. Clinical course: Patient is in his 1st or 2nd day of being sick. The information on the batch/lot number for BNT162b2 omicron (kp.2) will be requested and submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202500126534 same reporter/product/event; different patient; US-PFIZER INC-202500126534 Same reporter, product, and event; different patient;
Test Date: 202506; Test Name: COVID; Test Result: Positive