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Report #2824546

Received Feb 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
Age unknown
State
FL
Recovered
Unknown
Vaccinated
Jan 21, 2025
Onset
Jan 21, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALS2255T2—

Symptoms (1)

Extra dose administered

Symptom narrative

a second dose was administered; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of extra dose administered in a 84-year-old female patient who received RSVPreF3 adjuvanted (Arexvy) (batch number 255T2, expiry date 05-DEC-2025) for prophylaxis. Previously administered products included Arexvy (received 1st dose a year ago). On 21-JAN-2025, the patient received the 2nd dose of Arexvy. On 21-JAN-2025, an unknown time after receiving Arexvy, the patient experienced extra dose administered (Verbatim: a second dose was administered). The outcome of the extra dose administered was unknown. Additional Information: GSK Receipt Date: 22-JAN-2025 The pharmacist reported that a patient received a first dose of Arexvy last year and a second dose was administered which led to extra dose administered. The pharmacist asked for potential adverse effects.