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Report #2884135

Received Feb 4, 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
Male
Age
68 yrs
State
NC
Recovered
Unknown
Vaccinated
Jan 8, 2026
Onset
Jan 8, 2026
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MMRMEASLES + MUMPS + RUBELLA (PRIORIX)GLAXOSMITHKLINE BIOLOGICALSUNK575P9—

Symptoms (1)

Product preparation issue

Symptom narrative

Inappropriate reconstitution technique/ administered only the sterile water (diluent) component of Priorix to a patient; one of the pharmacists administered only the sterile water (diluent) component of Priorix to a patient; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate preparation of medication in a 68-year-old male patient who received MMR (Priorix) (batch number 575P9, expiry date 07-OCT-2029) for prophylaxis. On 08-JAN-2026, the patient received Priorix. On 08-JAN-2026, an unknown time after receiving Priorix, the patient experienced inappropriate preparation of medication (Verbatim: Inappropriate reconstitution technique/ administered only the sterile water (diluent) component of Priorix to a patient) and inappropriate dose of vaccine administered (Verbatim: one of the pharmacists administered only the sterile water (diluent) component of Priorix to a patient). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were 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: 20-JAN-2026 The reporter wanted to know whether the Priorix components were sold separately.