Received Feb 27, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARZOS | ZOSTER (SHINGRIX) | GLAXOSMITHKLINE BIOLOGICALS | UNK | 334T3 | — |
adjuvant portion of the Shingrix vaccine was administered to a patient; adjuvant portion of the Shingrix vaccine was administered to a patient; This non-serious case was reported by a other health professional via call center representative and described the occurrence of inappropriate preparation of medication in a 55-year-old female patient who received Herpes zoster (Shingrix) (batch number 334T3, expiry date 29-OCT-2026) for prophylaxis. On 23-JAN-2025, the patient received Shingrix. On 23-JAN-2025, an unknown time after receiving Shingrix, the patient experienced inappropriate preparation of medication (Verbatim: adjuvant portion of the Shingrix vaccine was administered to a patient) and inappropriate dose of vaccine administered (Verbatim: adjuvant portion of the Shingrix vaccine was administered to a patient). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 10-FEB-2025 On 10th February 2025, reporter called to report that only the adjuvant portion of the Shingrix vaccine was administered to a patient on 23th January 2025, which led to Inappropriate preparation of medication and Inappropriate dose of vaccine administered.