Report #2870641

Received Nov 5, 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: —
Recovered: Recovered
Vaccinated: —
Onset: —
Days to onset: —
Hospital days: —

Vaccines (1)

Type	Name	Manufacturer	Dose	Lot	Route / Site
RSV	RSV (AREXVY)	GLAXOSMITHKLINE BIOLOGICALS	UNK	UNK	—

Symptoms (1)

Cough

Symptom narrative

I have a cough; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of cough in a patient who received RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the patient received Arexvy. On an unknown date, an unknown time after receiving Arexvy, the patient experienced cough (Verbatim: I have a cough). The outcome of the cough was resolved. It was unknown if the reporter considered the cough to be related to Arexvy. It was unknown if the company considered the cough to be related to Arexvy. Additional Information: GSK Receipt Date: 21-OCT-2025 This case was reported by a patient via interactive digital media. Patient had a cough day after getting Arexvy was this a side effect. The batch number was not provided, and unable to contact the reporter.