FDA Adverse Event
Death
Summary report: N
SYNVISC ONE PFS 8MG/ML
MDR report key: 19795282
·
Received July 22, 2024
Report
- Report Number
- MW5157420
- Event Type
- Death
- Date Received
- July 22, 2024
- Report Date
- July 16, 2024
- Manufacturer
- GENZYME CORPORATION
- Product Code
- MOZ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
PT'S PROVIDER'S OFFICE REPORTS THAT PT IS DECEASED. THE SPECIFIC CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1005699 | SYNVISC ONE PFS 8MG/ML | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 92 YR | Female | Death |