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Report #2830316

Received Mar 10, 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
26 yrs
State
TX
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MMRMEASLES + MUMPS + RUBELLA (PRIORIX)GLAXOSMITHKLINE BIOLOGICALSUNKXX9N4IM

Symptoms (2)

Incorrect route of product administrationProduct administered to patient of inappropriate age

Symptom narrative

A 26 years old female patient received a dose of Priorix via IM instead of SC.; dose of Priorix via IM instead of SC; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate age at vaccine administration in a 26-year-old female patient who received MMR (Priorix) (batch number XX9N4, expiry date 01-JUN-2026) for prophylaxis. On an unknown date, the patient received Priorix (intramuscular). On an unknown date, an unknown time after receiving Priorix, the patient experienced inappropriate age at vaccine administration (Verbatim: A 26 years old female patient received a dose of Priorix via IM instead of SC.) and subcutaneous injection formulation administered by other route (Verbatim: dose of Priorix via IM instead of SC). The outcome of the inappropriate age at vaccine administration and subcutaneous injection formulation administered by other route 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: 28-FEB-2025 A pharmacist called to report that a 26 years old female patient received a dose of Priorix via intramuscular instead of Subcutaneous which led to Subcutaneous injection formulation administered by other route. Should the patient be revaccinated. The reporter consented to follow up.