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Report #2853050

Received Aug 6, 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
Male
Age
73 yrs
State
KS
Recovered
Unknown
Vaccinated
Aug 1, 2025
Onset
Aug 1, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MMRMEASLES + MUMPS + RUBELLA (PRIORIX)GLAXOSMITHKLINE BIOLOGICALSUNK7975CIM

Symptoms (1)

Incorrect route of product administration

Symptom narrative

Intramuscular administration; This non-serious case was reported by a nurse via call center representative and described the occurrence of subcutaneous injection formulation administered by other route in a 73-year-old male patient who received MMR (Priorix) (batch number 7975C, expiry date 01-MAR-2027) for prophylaxis. On 01-AUG-2025, the patient received Priorix (intramuscular). On 01-AUG-2025, an unknown time after receiving Priorix, the patient experienced subcutaneous injection formulation administered by other route (Verbatim: Intramuscular administration). The outcome of the subcutaneous injection formulation administered by other route 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: 01-AUG-2025 The registered nurse reported that an adult received a Priorix intramuscularly today (date of reporting), which led to Subcutaneous injection formulation administered by other route.