FDA Adverse Event
Summary report: N
2020394-2006-00348
MDR report key: 776377
·
Received October 31, 2006
Report
- Report Number
- 2020394-2006-00348
- Date Received
- October 31, 2006
- Report Source
- Manufacturer report
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 76 YR |