FDA Adverse Event
Injury
Summary report: N
MEDTRONIC PAIN PUMP
MDR report key: 112464
·
Received July 18, 1997
Report
- Report Number
- 112464
- Event Type
- Injury
- Date Received
- July 18, 1997
- Date of Event
- June 12, 1997
- Report Date
- July 14, 1997
- Manufacturer
- *
- Product Code
- LKK
- Adverse Event
- Yes
- Report Source
- User Facility report
- Reporter Location
- GA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
BLOOD PRESSURE DROPPED FROM 220/103 TO NON-DETECTABLE. QUICKLY RECOVERED TO 86/24 (A-LINE 37/32).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MEDTRONIC PAIN PUMP Implant | DILAUDID TOXICITY | LKK | * | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 69 YR | Hospitalization |