VAERS 2711226
UNKNOWN MANUFACTURER · MENINGOCOCCAL (NO BRAND NAME) · Charge U7903AC
- Staat
- KY
- Alter
- 4,0
- Geschlecht
- M
- Eingang
- 07.11.2023
- Impfdatum
- 25.10.2023
- Beginn
- 25.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Symptomtext
nurse mentioned that quadracel was meant to be given to the patient but nurse ended up getting and giving the menquadfi with no reported adverse event; Initial information received on 26-Oct-2023 regarding an unsolicited valid non-serious case received from a Nurse. This case involves a 4 years old male patient and nurse reported that diphtheria-15/tetanus/5 Hybrid Ac Pertussis/IPV (Mrc5) Vaccine [Quadracel] was meant to be given to the patient but ended up getting and giving the Meningococcal A-C-Y-W135 (T Conj) Vaccine [Menquadfi] 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), Varicella Zoster Vaccine Live (Oka/Merck) (Proquad); Hepatitis B Vaccine Rhbsag (Yeast) (Recombivax) And Hepatitis A Vaccine Inact (Vaqta) for Prophylactic vaccination. On 25-Oct-2023, the patient received a unknown (dose 1) dose of suspect Meningococcal A-C-Y-W135 (T Conj) Vaccine Solution for injection (strength: standard, frequency: once, lot U7903AC, expiry date: 31-Dec-2025) instead of diphtheria-15/tetanus/5 Hybrid Ac Pertussis/IPV (Mrc5) Vaccine Suspension for injection (strength, lot number, expiry date: unknown)via intramuscular route in the left deltoid as Immunization (wrong product administered) (latency: same day). Information on the batch number was requested. 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 2001/83/EC and Module VI of the Good Pharmacovigilance 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
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PROQUAD; RECOMBIVAX; VAQTA
- Allergien
- -
- Vorherige Impfungen
- -