VAERS 2371891
SANOFI PASTEUR · HIB (ACTHIB) · Charge U6998BA
- Staat
- ID
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 16.07.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / RL
Symptomtext
patient received ActHIB with expired diluent with no reported adverse event; Initial information received on 08-Jul-2022 regarding an unsolicited valid non-serious case received from health professional. GMI number: 01182877 This case involves a 1-year-old female patient who experienced patient received HIB (PRP/T) VACCINE [ACT-HIB] with expired diluent with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Measles Vaccine Live (Enders-Edmonston), Mumps Vaccine Live (Jeryl Lynn), Rubella Vaccine Live (Wistar RA 27/3) (Mmrvaxpro) for Prophylactic vaccination; Hepatitis A Vaccine (Hepatitis A) for Prophylactic vaccination; and Pneumococcal Vaccine (Pneumococcal Vaccine) for Prophylactic vaccination. On an unknown date in 2022, the patient received ACT-HIB vaccine ACCINE (lot: UJ524AA, expiry: 11-Jul-2022, lot: U6998BA, expiry: 25-Jun-2022) at unknown dose once intramuscular route in the right thigh for immunization (expired product administered, same day latency). It was reported that "Health care professional (HCP) reports patient received Act-HIB with expired diluent. She said she thought the year was 2025 but that the day was 25." Action taken: Not applicable. At time of reporting, the outcome was 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -