Report #2870619

Received Nov 4, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex: Unknown
Age: Age unknown
State: —
Recovered: Unknown
Vaccinated: —
Onset: —
Days to onset: —
Hospital days: —

Vaccines (1)

Type	Name	Manufacturer	Dose	Lot	Route / Site
COVID19	COVID19 (COVID19 (PFIZER-BIONTECH))	PFIZER\BIONTECH	1	—	—

Symptoms (1)

Allergy to vaccine

Symptom narrative

Patient had allergy to COVID 19 vaccine; This is a spontaneous report received from an Other HCP from medical information team and a sales representative. A patient (age and gender not provided) received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 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. The following information was reported: ALLERGY TO VACCINE (non-serious), outcome "unknown", described as "Patient had allergy to COVID 19 vaccine". Additional information: Patient had allergy to COVID 19 vaccine. Provider was prescribing Bactrim 800 mg -160 mg, mupirocin 2:1 topical. Red flag came up stating severe interaction. Provider overrode the flag but would like more information about this red flag.