Received Jun 12, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARZOS | ZOSTER (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | UNK | — |
had as serious allergic reaction to the vax; This serious case was reported by a consumer via interactive digital media and described the occurrence of allergic reaction in a patient who received Herpes zoster (Shingles vaccine) solution for injection for prophylaxis. On an unknown date, the patient received Shingles vaccine. On an unknown date, an unknown time after receiving Shingles vaccine, the patient experienced allergic reaction (Verbatim: had as serious allergic reaction to the vax) (serious criteria other: Serious as per reporter). The outcome of the allergic reaction was not reported. The reporter considered the allergic reaction to be related to Shingles vaccine. The company considered the allergic reaction to be unrelated to Shingles vaccine. Additional Information: GSK Receipt Date: 09-JUN-2026 This case was reported by a patient via interactive digital media. The batch number was not provided and we and unable to contact the reporter.; Sender's Comments: A case of Hypersensitivity, unknown time after receiving Shingles vaccine in a patient. Case lacks further information on time to onset, medical history, concurrent conditions and laboratory confirmation. Based on the available information a possible causality that the event was caused by the GSK product cannot be ascertained. Consent for further follow-up has not been received.