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Report #2870594

Received Nov 4, 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
76 yrs
State
IA
Recovered
Unknown
Vaccinated
Oct 21, 2025
Onset
Oct 21, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALS2G347X—

Symptoms (1)

Extra dose administered

Symptom narrative

Second dose; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of extra dose administered in a elderly female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number G347X, expiry date 12-DEC-2026) for prophylaxis. Previously administered products included Arexvy (Received 1st dose of Shingrix vaccine in SEP-2024). On 21-OCT-2025, the patient received the 2nd dose of Arexvy. On 21-OCT-2025, an unknown time after receiving Arexvy, the patient experienced extra dose administered (Verbatim: Second dose). The outcome of the extra dose administered was not applicable. Additional Information: GSK Receipt Date: 21-OCT-2025 A patient got a second shot of Arexvy on 21-OCT-2025. First dose was administered back in September 2024. The reporter knew that is a onetime thing, but was curious about adverse effects.