FDA Adverse Event Injury Summary report: N

UTERINE ARTERY EMBOLIZATION

MDR report key: 1840171 · Received September 14, 2010

Report

Report Number
MW5017445
Event Type
Injury
Date Received
September 14, 2010
Date of Event
February 1, 2007
Report Date
September 14, 2010
Product Code
NAJ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

BROKEN BLOOD VESSELS IN THE EYES. FEVER, SWEATS, CONSTIPATION, AND FOUL SMELLING URINE.

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