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. |