VAERS 2708461
SANOFI PASTEUR · DTAP + IPV + HIB (PENTACEL) · Charge UJ870AA
- Staat
- ME
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 24.10.2023
- Beginn
- 24.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Symptomtext
patient received 2 doses of DTaP-IPV from the PENTACEL vaccine with no reported adverse event; it was not reconstituted with the powder HIB portion with no reported adverse event; Initial information received on 24-Oct-2023 regarding an unsolicited valid non-serious case received via Nurse. This case involves a 4 years old female patient received 2 doses of dtap-ipv from the diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine [Pentacel (VERO)] vaccine with no reported adverse event and it was not reconstituted with the powder hib portion with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s), concomitant(s) nd family history were not provided. On 24-Oct-2023, the patient received a dose 1 of 0.5 ml dose of suspect diphtheria/tetanus/5 hybrid AC pertussis/IPV(VERO)/HIB(PRP/T) vaccine, Suspension for injection (strength: unknown) (lot: UJ870AA, expiry date: 24-Mar-2024) via intramuscular route in the left deltoid for immunization and patient received 2 doses of dtap-ipv from the pentacel vaccine with no reported adverse event (extra dose administered) and it was not reconstituted with the powder hib portion with no reported adverse event (poor quality product administered) (latency: same day) 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 Directive and Regulatory Authority Practices. 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
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -