FDA Adverse Event
Death
Summary report: N
SYNVISC
MDR report key: 16478286
·
Received March 2, 2023
Report
- Report Number
- MW5115407
- Event Type
- Death
- Date Received
- March 2, 2023
- Date of Event
- February 27, 2023
- Report Date
- February 28, 2023
- Manufacturer
- GENZYME CORPORATION
- Product Code
- MOZ
- UDI-DI
- 58468009003
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- AR, US
- Reporter Occupation
- PATIENT FAMILY MEMBER OR FRIEND
- Health Professional
- N
Narratives
Description of Event or Problem · 0
PT'S WIFE REPORTED THAT (B)(6) WAS DECEASED ON (B)(6) 2023, THE CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1871476 | SYNVISC | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION | 58468009003 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 88 YR | Male | Death |