FDA Adverse Event Injury Summary report: N

UTERINE ARTERY EMBOLIZATION

MDR report key: 1981189 · Received February 2, 2011

Report

Report Number
MW5019275
Event Type
Injury
Date Received
February 2, 2011
Date of Event
April 15, 2010
Report Date
February 2, 2011
Product Code
NAJ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PROBLEMS WITH BOWEL FUNCTION SINCE UNDERGOING UAE.

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