Received Sep 5, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| MMRV | MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) | MERCK & CO. INC. | UNK | Z003307 | OT |
No adverse reactions reported associated to any of the administrations of either VARIVAX or PROQUAD to any of the patients involved./No additional AE; HCP called to report TE occurring on 6/20/2025 for VARIVAX and PROQUAD that were administered on multiple different dates to multiple patients.; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 14-Aug-2025, the patient was vaccinated with improperly stored Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) solution for injection, 0.5 ml, lot # Z003307, expiration date: 21-Jul-2026 (dose number, route of administration and anatomical location were not reported), for prophylaxis (Product storage error). The vaccine was reconstituted with sterile diluent (Hollister-Stier STERILE DILUENT) solution for injection (expiration date, and lot # were not reported). On 20-Jun-2025, the vaccine underwent a temperature excursion of 10 up to 8 (-4.76) Celsius (C) degrees for 30 minutes. There were no previous excursions. No additional adverse event was reported. The action taken with Measles, Mumps, Rubella and Varicella (Oka-Merck) Virus Vaccine Live (PROQUAD) and sterile diluent (Hollister-Stier STERILE DILUENT) was considered as not applicable. This is one of several reports from the same reporter.; Reporter's Comments: Keywords : MUL
MERCK STERILE DILUENT