Received Sep 3, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| RAB | RABIES (IMOVAX) | SANOFI PASTEUR | UNK | — | OT |
stated that she then was having some issues with cold sores; Initial information received on 28-Aug-2025 regarding an unsolicited valid non-serious case received from a consumer/non-hcp (non-healthcare professional). This case involves an unknown age female patient who was having some issues with cold sores after receiving Rabies (HDC) Vaccine [Imovax Rabies]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date in Aug-2025, the patient received an unknown dose of suspect Rabies (HDC) Vaccine, Powder and solvent for suspension for injection, (unknown strength and expiry date) lot number not reported via unknown route in unknown administration site for post-exposure prophylaxis vaccines [Immunisation]. Information regarding batch number corresponding to the one at time of event occurrence was requested. On an unknown date in Aug-2025, the patient was having some issues with cold sores (oral herpes) (latency Few days approximately). Reportedly, Reporter freaked out since she took an anti-viral after finishing a vaccine series. Action taken was not applicable. The patient was treated with Valaciclovir Hydrochloride (Valtrex) for Oral herpes. At time of reporting, the outcome was Unknown for the event.