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