Received Feb 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARZOS | ZOSTER (SHINGRIX) | GLAXOSMITHKLINE BIOLOGICALS | 3 | 93kk4 | — |
administration of a 3rd dose of Shingrix; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of extra dose administered in a 66-year-old female patient who received Herpes zoster (Shingrix) (batch number 93kk4, expiry date 31-JAN-2027) for prophylaxis. Previously administered products included Shingrix (1st dose received on 10th Oct 2024) and Shingrix (2nd dose received on 11th Dec 2024). On 17-FEB-2025, the patient received the 3rd dose of Shingrix. On 17-FEB-2025, an unknown time after receiving Shingrix, the patient experienced extra dose administered (Verbatim: administration of a 3rd dose of Shingrix). The outcome of the extra dose administered was not applicable. Additional Information: GSK Receipt Date: 17-FEB-2025 The reporter called to request safety information as the immunocompetent patient received 3rd dose of Shingrix, which led to extra dose administered. The vaccine administration facility was the same as primary reporter.