Received Feb 4, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| RVX | ROTAVIRUS (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | UNK | — |
itching; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of pruritus in a patient who received RSVPreF3 adjuvanted (RSV vaccine) for prophylaxis. On an unknown date, the patient received RSV vaccine. On an unknown date, an unknown time after receiving RSV vaccine, the patient experienced pruritus (Verbatim: itching). The outcome of the pruritus was not reported. It was unknown if the reporter considered the pruritus to be related to RSV vaccine. It was unknown if the company considered the pruritus to be related to RSV vaccine. Additional Information: GSK Receipt Date: 26-JAN-2026 This case was reported by a patient via interactive digital media. The batch number was not provided, and unable to contact the reporter.