Received Jul 11, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| PPV | PNEUMO (PNEUMOVAX) | MERCK & CO. INC. | UNK | — | — |
| VARCEL | VARICELLA (VARIVAX) | MERCK & CO. INC. | UNK | — | — |
allergy to vaccine; This spontaneous report was received from a Physician and refers to a 58-year-old female patient. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On an unknown date, the patient was vaccinated with a dose of Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) and Pneumococcal Vaccine, Polyvalent (23-valent) (PNEUMOVAX 23) (25MCG/0.5) (strength, dose, dose number, route, lot #, expiration date and anatomical location were not reported) for Prophylaxis. On an unknown date, the patient experienced allergy to those vaccines. At the reporting time, the outcome of allergy to vaccine was unknown. The reporter considered the event of allergy to vaccine to be related to both vaccines. This is one of two reports received from the same patient (2301380).
Sterile diluent