Symptomtext
Temperature excursion at a high of 66F for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event; Initial information received on 08-Feb-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves patient with unknown demographics who had temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event while receiving vaccines [ACT-HIB], [IPOL],[ADACEL],[DAPTACEL]. 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 lot UJ579AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE lot C5829BA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect ACTHIB not produced by Sanofi Pasteur lot UJ579AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE lot U7055AA via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date, the patient received a dose of suspect IPV (VERO) lot T1E87 via unknown route in unknown administration site with(unknown dosage form, strength, frequency)for immunization. On an unknown date the patient had temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event (product storage error) (unknown latency) following the administration of DIPHTHERIA-15/TETANUS/5 AC PERTUSSIS VACCINE. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event (Temperature excursion at a high of 66F for 27 minutes due to the refrigerator being accidentally left opened with no reported adverse event). At time of reporting, the outcome was Unknown for the event temperature excursion at a high of 66f for 27 minutes due to the refrigerator being accidentally left opened 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 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.