Report #2861766

Received Sep 26, 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: Female
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	UNK	—	—

Symptoms (1)

Gastrointestinal disorder

Symptom narrative

gastrointestinal side effects; This is a spontaneous report received from a Pharmacist. A female patient received BNT162b2 omicron (lp.8.1) (COMIRNATY (2025-2026 FORMULA)), (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: GASTROINTESTINAL DISORDER (non-serious), outcome "unknown", described as "gastrointestinal side effects". It was unknown if therapeutic measures were taken as a result of gastrointestinal disorder. The information on the batch/lot number for BNT162b2 omicron (lp.8.1) will be requested and submitted if and when received. Additional information: In meeting with pharmacy regional clinical lead, pharmacist stated that a patient told her she knows of more people who are experiencing gastrointestinal side effects from COVID-19 vaccination this year. No additional information was provided on this AE.