Received May 22, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARZOS | ZOSTER (SHINGRIX) | GLAXOSMITHKLINE BIOLOGICALS | UNK | NT357 | — |
swelling at injection site; Redness at injection site; This non-serious case was reported by a consumer and described the occurrence of injection site swelling in a 56-year-old male patient who received Herpes zoster (Shingrix) (batch number NT357) for prophylaxis. On 15-MAY-2026, the patient received Shingrix 50 ug. On 16-MAY-2026, 1 days after receiving Shingrix, the patient experienced injection site swelling (Verbatim: swelling at injection site) and injection site erythema (Verbatim: Redness at injection site). The outcome of the injection site swelling and injection site erythema were not resolved. It was unknown if the reporter considered the injection site swelling and injection site erythema to be related to Shingrix. It was unknown if the company considered the injection site swelling and injection site erythema to be related to Shingrix.