Received Jun 1, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| TD | TD ADSORBED (TENIVAC) | SANOFI PASTEUR | UNK | U8021BA | IM / LA |
administration of expired tenivac with no ae; Initial information received on 21-May-2026 regarding an unsolicited valid non-serious case received from a health care professional (HCP). This case involves a 73-year-old male patient who Had administration of expired diphtheria and tetanus toxoids (TENIVAC). The patient's past medical history, past drugs, vaccination(s), family history, and concomitant medications were not provided. On 21-May-2026, the patient had administration of expired diphtheria and tetanus toxoids (TENIVAC) suspension for injection (strength: standard) as 0.5 mL intramuscular for immunization [(Expired product administered,latency: same day) (batch: U8021BA, expiry date: 16-Mar-2026)]. Action taken: Not applicable 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.
Comments: NONE