FDA Adverse Event
Death
Summary report: N
SYNVISC ONE PFS 8 MG/ML
MDR report key: 19658800
·
Received July 1, 2024
Report
- Report Number
- MW5156919
- Event Type
- Death
- Date Received
- July 1, 2024
- Date of Event
- June 28, 2024
- Report Date
- June 28, 2024
- Manufacturer
- GENZYME CORPORATION
- Product Code
- MOZ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- US
- Reporter Occupation
- UNKNOWN
- Health Professional
- *
Narratives
Description of Event or Problem · 0
PT'S HUSBAND REPORTED THAT HIS WIFE PASSED AWAY AND CAUSE OF DEATH UNKNOWN AS PER PT CARE COORDINATOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 786178 | SYNVISC ONE PFS 8 MG/ML | ACID, HYALURONIC, INTRAARTICULAR | MOZ | GENZYME CORPORATION |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 82 YR | Female | Death |