Report #2881585

Received Jan 12, 2026

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: 65 yrs
State: IN
Recovered: Unknown
Vaccinated: Jan 8, 2026
Onset: Jan 8, 2026
Days to onset: 0
Hospital days: —

Vaccines (1)

Type	Name	Manufacturer	Dose	Lot	Route / Site
MMR	MEASLES + MUMPS + RUBELLA (PRIORIX)	GLAXOSMITHKLINE BIOLOGICALS	UNK	7HGA	—

Symptoms (1)

Expired product administered

Symptom narrative

Expired Product Used; This non-serious case was reported by a other health professional via call center representative and described the occurrence of expired vaccine used in a 65-year-old female patient who received MMR (Priorix) (batch number 7HGA, expiry date 01-JAN-2026) for prophylaxis. On 08-JAN-2026, the patient received Priorix. On 08-JAN-2026, an unknown time after receiving Priorix, the patient experienced expired vaccine used (Verbatim: Expired Product Used). The outcome of the expired vaccine used was not applicable. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 08-JAN-2026 The reporter stated they had given an expired vaccine and wanted to know the recommendations on revaccination and the steps that needed to be taken for the patient.