FDA Adverse Event
Death
Summary report: N
EUFLEXXA
MDR report key: 12280536
·
Received August 4, 2021
Report
- Report Number
- MW5103002
- Event Type
- Death
- Date Received
- August 4, 2021
- Date of Event
- June 6, 2021
- Report Date
- August 3, 2021
- Manufacturer
- FERRING PHARMACEUTICALS INC.
- Product Code
- MOZ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- PATIENT FAMILY MEMBER OR FRIEND
Narratives
Description of Event or Problem · 1
PATIENT'S HUSBAND REPORTED THAT PATIENT PASSED AWAY ON (B)(6) 2021.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1169753 | EUFLEXXA | ACID, HYALURONIC, INTRAARTICULAR | MOZ | FERRING PHARMACEUTICALS INC. | NOT REPORTED |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Death |