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Report #2846528

Received Jun 19, 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
MO
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

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

Symptoms (1)

Incorrect route of product administration

Symptom narrative

intramuscular versus subcutaneous administration of PRIORIX.; This non-serious case was reported by a other health professional via call center representative and described the occurrence of subcutaneous injection formulation administered by other route in a female patient who received MMR (Priorix) (batch number 7975C, expiry date 01-MAR-2027) for prophylaxis. On an unknown date, the patient received Priorix (intramuscular use). On an unknown date, an unknown time after receiving Priorix, the patient experienced subcutaneous injection formulation administered by other route (Verbatim: intramuscular versus subcutaneous administration of PRIORIX.). 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: 11-JUN-2025 Bachelor of Science in Nursing called to ask, are there any safety concerns regarding the intramuscular versus subcutaneous administration of Priorix which led to incorrect route of product administration. Vaccine details and patient demographics were obtained in this call. No vaccination was confirmed from the Bachelor of Science in Nursing's end. No further information was obtained in this call. The vaccine administration facility was the same as primary reporter.