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Report #2859953

Received Sep 19, 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
Male
Age
85 yrs
State
MO
Recovered
Unknown
Vaccinated
Aug 18, 2025
Onset
Aug 18, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNK544SDIM / LA

Symptoms (1)

Product preparation issue

Symptom narrative

administered only the adjuvant component of Arexvy to a patient; administered only the adjuvant component of Arexvy to a patient; This non-serious case was reported by a consumer via call center representative and described the occurrence of inappropriate preparation of medication in a 85-year-old male patient who received RSVPreF3 adjuvanted (Arexvy) (batch number 544SD, expiry date 19-NOV-2025) for prophylaxis. On 18-AUG-2025, the patient received Arexvy (intramuscular, left deltoid). On 18-AUG-2025, an unknown time after receiving Arexvy, the patient experienced inappropriate preparation of medication (Verbatim: administered only the adjuvant component of Arexvy to a patient) and inappropriate dose of vaccine administered (Verbatim: administered only the adjuvant component of Arexvy to a patient). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 28-AUG-2025 The pharmacy technician reported that a pharmacist at his retail location administered only the adjuvant component of Arexvy to a patient and did not reconstitute the vaccine, which led to inappropriate preparation of medication and inappropriate dose of vaccine administered