FDA Adverse Event Injury Summary report: N

UTERINE ARTERY EMBOLIZATION

MDR report key: 1293910 · Received January 20, 2009

Report

Report Number
MW5009675
Event Type
Injury
Date Received
January 20, 2009
Report Date
January 20, 2009
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

SINCE UNDERGOING UAE TWO YEARS AGO, SHE CONTINUES TO EXPERIENCE VAGINAL INFECTIONS AND IS STARTING TREATMENT WITH PREMARIN VAGINAL GEL INJECTIONS 2X A WEEK FOR AN INDEFINITE PERIOD OF TIME. SHE IS ALSO EXPERIENCING MENOPAUSAL SYMPTOMS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UTERINE ARTERY EMBOLIZATION NONE NAJ

Patients

Seq Age Sex Outcome Treatment
1 32 YR Other