Received Aug 15, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| MMRV | MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) | MERCK & CO. INC. | UNK | Z003309 | — |
No symptoms or side effects were reported by HCP. No additional AE/No PQC.; HCP reporting that a patient received a dose of improperly stored PROQUAD. Reference TE case #02843001. HCP reported that she did not know the date the excursion occurred, but knows the PROQUAD was administered following the excursion. HCP reported; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 30-Jun-2025, the patient was vaccinated with a dose of improperly stored Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD), 0.5 mL (lot #Z003309 has been verified to be a valid lot number, expiration date not reported, but upon internal validation established as: 21-Jul-2026) (strength and route of administration were not provided) as prophylaxis (Product storage error). The vaccine was reconstituted with sterile diluent (MERCK STERILE DILUENT) (lot # and expiration date were not reported). Temperature was 52.2 F, time frame was unknown by reporter. Operator of device was health professional. The reporter did not know the date the excursion occurred. No symptoms or side effects were reported by HCP. No additional adverse event (AE) (No adverse event).
sterile diluent