FDA Adverse Event
Summary report: N
8030665-2006-00254
MDR report key: 793595
·
Received November 30, 2006
Report
- Report Number
- 8030665-2006-00254
- Date Received
- November 30, 2006
- Report Source
- Manufacturer report
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |