VAERS 1774869
UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge UJ440AA
- Staat
- NV
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Symptomtext
Patient accidentally received PENTACEL instead of their TDap vaccine in the office with no adverse event; 43 year old patient accidentally received PENTACEL instead of their TDap vaccine, with no adverse event; Initial information received on 04-Oct-2021 regarding an unsolicited valid non-serious case from a physician and consumer/ non-healthcare professional via Media Information (under reference 00796958). This case involves a 43 years old female patient who accidentally received DIPHTHERIA, TETANUS, AC PERTUSSIS, IPV AND HIB VACCINE [PENTACEL (VERO)] instead of their DIPHTHERIA, TETANUS AND NOS PERTUSSIS VACCINE in the office (wrong product administered and product administered to patient of inappropriate age). Patient did not receive other concomitant vaccines. The patient's medical history, past medical treatment(s), past vaccination (s) and family history were not provided. On 04-Oct-2021, the patient received a 0.5 mL dose of suspect PENTACEL (VERO) (Total, lot UJ440AA and expiration date: 29-May-2022) via intramuscular route in the left arm for prophylactic vaccination. It was an actual medication error due to Wrong vaccine administered and Inappropriate age at vaccine administration (same day latency). It was reported "Doctor states that a 43 year old patient accidentally received PENTACEL instead of their TDap vaccine in the office on 04OCT2021 and asked for recommendations on how to proceed. Doctor states that she could not find any information online other than for children that inadvertently received the vaccine. Doctor states that no Adverse Events have occurred and that they will continue to monitor the patient." 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
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -