VAERS 2387799
SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ472AA
- Staat
- PA
- Alter
- 0,2
- Geschlecht
- M
- Eingang
- 24.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / RL
Symptomtext
a 9 week-old boy received ActHIB vaccine that had expired on 5/21/2022 with no reported adverse event; Initial information received on 18-Jul-2022 regarding an unsolicited valid non-serious case received from a other health professional via call center. This case involves a 9-week-old boy who received HIB (PRP/T) Vaccine [ACT-HIB] vaccine that had expired on 21-May-2022 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 Pneumococcal Vaccine Conj 13V (CRM197) (Prevnar 13) and Rotavirus Vaccine Live Reassort Oral 5V (Rotateq) both for Prophylactic vaccination (Immunization). On 13-Jul-2022, the patient received a 0.5 ml dose once total of suspect HIB (PRP/T) Vaccine (Powder and solvent for solution for injection) (lot: UJ472AA & U6940BA; expiry date: 21-Jul-2022; strength: standard) via intramuscular route in the right thigh for Prophylactic vaccination (Immunization). On 13-Jul-2022, a 9 week-old boy received HIB (PRP/T) vaccine that had expired on 5/21/2022 with no reported adverse event (expired product administered) (latency: same day). It was unknown if there were lab data/results available. Action taken: Not applicable. Outcome: Unknown. 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
- -