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Report #2877982

Received Dec 15, 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
Unknown
Age
Age unknown
State
UT
Recovered
Unknown
Vaccinated
Nov 1, 2025
Onset
Nov 1, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
MNPMENINGOCOCCAL CONJUGATE (PENMENVY)GLAXOSMITHKLINE BIOLOGICALSUNK449J9—

Symptoms (1)

Product preparation issue

Symptom narrative

Penmenvy liquid portion only administration; Penmenvy liquid portion only administration; This non-serious case was reported by a other health professional via call center representative and described the occurrence of inappropriate dose of vaccine administered in a patient who received Men ABCWY NVS (Penmenvy) (batch number 449J9, expiry date 08-OCT-2026) for prophylaxis. In NOV-2025, the patient received Penmenvy. In NOV-2025, an unknown time after receiving Penmenvy, the patient experienced inappropriate dose of vaccine administered (Verbatim: Penmenvy liquid portion only administration) and inappropriate preparation of medication (Verbatim: Penmenvy liquid portion only administration). The outcome of the inappropriate dose of vaccine administered and inappropriate preparation of medication 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 5-DEC-2025 A healthcare provider wanted to know how to proceed with a patient that received only the liquid portion of Penmenvy. She was not sure if it was given on 21-NOV-2025 or 26-NOV-2025 and also did not know patient's details. The vaccine administration facility was the same as primary reporter.