Reporte zur Charge UJ569AD

Symptomtext

wrong patient- with no reported adverse event; Initial information received on 29-Mar-2022 regarding an unsolicited valid non-serious case received from a other health professional via call center. This case involves a 7 days old female patient who experienced wrong patient- with no reported adverse event while receiving vaccine HIB (PRP/T) Vaccine [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine for Immunisation. On 29-Mar-2022, the patient received 0.5 ml of 1 dose of suspect HIB (PRP/T) vaccine (batch lot : UJ569AD Expiry date :02-Oct-2022)(unknown :strength and formulation)cycle, series:1 via intramuscular route in the right thigh. On 29-Mar-2022 (latency :same day)the patient developed a non-serious event of wrong patient- with no reported adverse event (wrong patient received product) following the administration of HIB (PRP/T) vaccine Action taken : not applicable. At time of reporting, the outcome was Unknown for the event . 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 guidelines. 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.