Received Jul 11, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| YF | YELLOW FEVER (YF-VAX) | SANOFI PASTEUR | UNK | — | OT |
2-family members received a booster dos of YF-vax prior to the 10- year interval, with no reported adverse event; Initial information received on 09-Jul-2025 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves Child patient with unknown gender who received a booster dos of Yellow Fever Vaccine - US [YF-VAX] prior to the 10- year interval, with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a Booster dose of suspect Yellow Fever Vaccine - US, Solution for injection (lot number, expiry date and strength not reported) via unknown route in unknown administration site for Immunization and 2-family members received a booster dos of yf-vax prior to the 10- year interval, with no reported adverse event (inappropriate schedule of product administration). Information on the batch number was requested corresponding to the one at time of event occurrence. Reportedly, she was asking if there were any precautions they need to take for this situation. Action taken was not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.; Sender's Comments: US-SA-2025SA194542: