Received Dec 1, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 4 | FP4554 | IM / LA |
Reported Symptoms: 10029436:NO ADVERSE EFFECT; 10063978:WRONG VACCINE ADMINISTERED; Narrative: 96 patients were seen in the pharmacy drive through vaccination clinic on 10/08/2022 to receive the bivalent Pfizer booster +/- the influenza vaccine; and were inadvertently given the primary series formulation instead as a booster dose. No adverse effects experienced. The primary series lot used was FP4554 exp 10/31/2022. Other Relevant HX: NA Other: primary series formulation given instead of bivalent for COVID Booster; no adverse effects experienced