FDA Adverse Event Death Summary report: N

EUFLEXXA 20 MG/2 ML (6=3 SYR)

MDR report key: 22493469 · Received July 14, 2025

Report

Report Number
MW5172541
Event Type
Death
Date Received
July 14, 2025
Date of Event
June 26, 2025
Report Date
July 8, 2025
Manufacturer
FERRING PHARMACEUTICALS INC.
Product Code
MOZ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PHARMACIST
Health Professional
N

Narratives

Description of Event or Problem · 0

CAREGIVER REPORTED THAT THE PT PASSED AWAY ON (B)(6) 2025. FREQ: INJECT 1 SYRINGE INTRA-ARTICULARLY INTO RIGHT KNEE EVERY WEEK FOR 3 WEEKS. PRESCRIBER INFO: (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1046684 EUFLEXXA 20 MG/2 ML (6=3 SYR) ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC. X10511A

Patients

Seq Age Sex Outcome Treatment
1 83 YR Male Death ALBUTEROL AER HFA.| ALPRAZOLAM TAB 0.25MG.| ATORVASTATIN TAB 80MG.| AYR SALINE GEL NASAL .| BENZONATATE CAP 200MG.| CLOPIDOGREL TAB 75MG.| DEXAMETHASON TAB 4 MG.| ENTRESTO TAB 24-26MG.| FLUTICASONE SPR 50MCG.| FOLIC ACID TAB 1MG.