Reporte zur Charge UJ581AAB

Symptomtext

a temperature excursion due to unknown reasons Temperature reached 1.7C for 6 minutes with no reported adverse event; Initial information received on 14-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a patient with unknown demographics who had a temperature excursion due to unknown reasons temperature reached 1.7c for 6 minutes with no reported adverse event while receiving vaccines[ACT-HIB]. 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 dose of suspect HIB (PRP/T) VACCINE with unknown dose lot UJ581AAB via unknown route in unknown administration site. On an unknown date, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE with unknown dose lot C5788BA via unknown route in unknown administration site. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE with unknown dose lot C5829BA via unknown route in unknown administration site. On an unknown date, the patient received a dose of suspect MENINGOCOCCAL A-C-Y-W135 (D CONJ) VACCINE lot U7191AA via unknown route in unknown administration site. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE with unknown dose lot UJ776AA ,UT7347MA via unknown route in unknown administration site. On an unknown date the patient had a temperature excursion due to unknown reasons temperature reached 1.7c for 6 minutes with no reported adverse event (product storage error) (unknown latency) following the administration of HIB. Action taken not applicable. It was not reported if the patient received a corrective treatment for the event (a temperature excursion due to unknown reasons Temperature reached 1.7C for 6 minutes with no reported adverse event). At time of reporting, the outcome was Unknown for the event a temperature excursion due to unknown reasons temperature reached 1.7c for 6 minutes with no reported adverse 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 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.