Symptomtext
vaccines,had emperature excursion with no reported adverse event; vaccines being given post temperature excursion with no reported adverse event; Initial information was received on 06-May-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 6 months old male patient, vaccines being given post temperature excursion with no reported adverse event and vaccines had temperature excursion with no reported adverse event while receiving vaccine diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine [Pentacel]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant Vaccines included: Rotavirus vaccine; Pneumococcal vaccine CONJ 7V (CRM197) (Prevnar) and Hepatitis B vaccine for prophylactic vaccination. On 04-May-2022, the patient received a dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(MRC5)/HIB(PRP/T) vaccine 0.5 ml (Batch number: UJ625AAA, expiration date: 07-Dec-2022) via intramuscular route in the right thigh for prophylactic vaccination. On 04-May-2022, vaccines being given post temperature excursion with no reported adverse event (product administration error) (latency: same day). On an unknown date, vaccines had temperature excursion with no reported adverse event (product storage error) (unknown latency). Action taken: Not applicable. Corrective treatment: Not reported. Outcome: Unknown for the events. 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.