VAERS 2531821
SANOFI PASTEUR · HIB (ACTHIB) · Charge U7178AA
- Staat
- IL
- Alter
- 1,3
- Geschlecht
- M
- Eingang
- 15.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Symptomtext
Medical assistant administered ACTHIB to 15-month-old patient and the diluent was expired with no reported adverse event; Medical assistant administered ACTHIB to 15-month-old patient and the diluent was expired with no reported adverse event; Initial information received on 12-Dec-2022 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 15 months old male patient and it was reported medical assistant administered acthib to 15-month-old patient and the diluent was expired with no reported adverse event after receiving HIB (PRP/T) vaccine [ACT-HIB]. The patient's past medical history, medical treatment(s), vaccination(s), concomitants and family history were not provided. Concomitant medications included diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (Daptacel) for immunisation; influenza vaccine inact split 4V (Fluzone quadrivalent) for immunisation; and diphtheria vaccine toxoid, HIB vaccine conj (tet tox), pertussis vaccine acellular 5-component, polio vaccine inact 3V (MRC 5), tetanus vaccine toxoid (Pentacel) for immunisation. On 09-Dec-2022, the patient received 0.5 ml of suspect HIB (PRP/T) vaccine powder and solvent for solution for injection (lot number- U7178AA and expiry date- 30-Nov-2022; strength, formulation: unknown) via unknown route in unknown administration site for immunization. On an unknown date, it was reported that medical assistant administered ACTHIB to 15-month-old patient and the diluent was expired with no reported adverse event (expired medical agent used) (vaccine preparation error) (latency: unknown) following the administration of HIB (PRP/T) vaccine. Action taken: Not applicable. It was not reported if the patient received a corrective treatment for the event. 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
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