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Report #2870336

Received Nov 3, 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
WI
Recovered
Unknown
Vaccinated
Oct 21, 2025
Onset
Oct 21, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNKUNK—

Symptoms (1)

Product preparation issue

Symptom narrative

Maladministration of diluent only; Maladministration of diluent only; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of inappropriate preparation of medication in a 80-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On 21-OCT-2025, the patient received Arexvy. On 21-OCT-2025, an unknown time after receiving Arexvy, the patient experienced inappropriate preparation of medication (Verbatim: Maladministration of diluent only) and inappropriate dose of vaccine administered (Verbatim: Maladministration of diluent only). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date:22-OCT-2025 The pharmacist reported that there was maladministration of only the diluent component for Arexvy on a patient, which led to inappropriate preparation of medication and inappropriate dose of vaccine administered. The Vaccine Administration Facility is the same as Primary Reporter.