Received Nov 12, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARZOS | ZOSTER (SHINGRIX) | GLAXOSMITHKLINE BIOLOGICALS | UNK | UNK | — |
Red pain itchy; Red; Pain; This non-serious case was reported by a consumer and described the occurrence of pruritus in a 76-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On 29-OCT-2025, the patient received Shingrix. On 30-OCT-2025, 1 days after receiving Shingrix, the patient experienced pruritus (Verbatim: Red pain itchy), erythema (Verbatim: Red) and pain (Verbatim: Pain). The outcome of the pruritus, erythema and pain were not resolved. It was unknown if the reporter considered the pruritus, erythema and pain to be related to Shingrix. It was unknown if the company considered the pruritus, erythema and pain to be related to Shingrix. Additional Information: GSK Receipt Date: 02-NOV-2025 The symptoms were not treated. Event outcome date was reported as 02-NOV-2025. The batch number was not provided and a request for this information has been made.