FDA Adverse Event
Injury
Summary report: N
UTERINE ARTERY EMBOLIZATION
MDR report key: 1162741
·
Received September 15, 2008
Report
- Report Number
- MW5008311
- Event Type
- Injury
- Date Received
- September 15, 2008
- Report Date
- September 15, 2008
- Product Code
- NAJ
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
WASN'T ABLE TO RETURN TO WORK FOR EIGHT WEEKS AFTER UAE SECONDARY TO CRAMPING. MIGRAINE HEADACHES DEVELOPED POST UAE AND LASTED FOR ABOUT TWO YRS. EXPERIENCED CRAMPING SIX YRS POST UAE AND WENT TO ER WHERE THEY SAID THE CRAMPING WAS SECONDARY TO FIBROIDS. SHE HAD AN ELEVATED WHITE BLOOD COUNT AND CURRENTLY HAS A CLEAR VAGINAL DISCHARGE. SHE STATES "I FEEL LIKE A WALKING TIME BOMB..."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UTERINE ARTERY EMBOLIZATION | NONE | NAJ |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |