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Report #2831988

Received Mar 18, 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
NY
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

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

Symptoms (2)

Antibody testTherapy non-responder

Symptom narrative

low titers/didn't have a response; This non-serious case was reported by a other health professional via call center representative and described the occurrence of therapy non-responder in a 48-year-old female patient who received MMR (Priorix) for prophylaxis. Concomitant products included aciclovir sodium (Acyclovir). On an unknown date, the patient received Priorix. On an unknown date, an unknown time after receiving Priorix, the patient experienced therapy non-responder (Verbatim: low titers/didn't have a response). The outcome of the therapy non-responder 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-MAR-2025 Reporter stated that a patient who was currently on Acyclovir had gotten a dose of Priorix back in 2020 no exact date shared, and did not have a response, reporter mentioned that this patient had a titer test and showed low titers.

Other medications

ACYCLOVIR