Received Sep 29, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| COVID19 | COVID19 (COVID19 (PFIZER-BIONTECH)) | PFIZER\BIONTECH | 1 | — | LA |
flush; hives; rash; redness; This is a spontaneous report received from a Consumer or other non HCP. A 71-year-old female patient (not pregnant) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), on 19Sep2025 at 16:00 as dose 1, single (Batch/Lot number: unknown), in left arm for covid-19 immunisation. The patient's relevant medical history included: "allergic to hornets" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Codeine, reaction(s): "Allergy". The following information was reported: FLUSHING (non-serious) with onset 20Sep2025 at 19:00, outcome "recovered" (25Sep2025), described as "flush"; URTICARIA (non-serious) with onset 20Sep2025 at 19:00, outcome "recovered" (25Sep2025), described as "hives"; RASH (non-serious) with onset 20Sep2025 at 19:00, outcome "recovered" (25Sep2025); ERYTHEMA (non-serious) with onset 20Sep2025 at 19:00, outcome "recovered" (25Sep2025), described as "redness". Therapeutic measures were not taken as a result of flushing, urticaria, rash, erythema. Additional information: Reason why batch/lot was unknown: Unable to locate or read the details; facility where vaccine was administered: Doctor's office/urgent care; the patient did not receive any other vaccines on the same date as the vaccine. The patient did not receive any other vaccines within 4 weeks prior to the vaccine. The patient was not taking any other medications within 2 weeks of the event starting. No follow-up attempts are possible. Batch/lot number is not provided, and it cannot be obtained.
Medical History/Concurrent Conditions: Allergy to arthropod sting