FDA Adverse Event Injury Summary report: N

ENTERYX

MDR report key: 1052163 · Received May 22, 2008

Report

Report Number
MW5007033
Event Type
Injury
Date Received
May 22, 2008
Date of Event
January 14, 2003
Report Date
May 22, 2008
Product Code
LNM
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IMMEDIATELY AFTER SURGERY, I VOMITED FOR ABOUT 12 HOURS. SINCE THEN I HAVE DIFFICULTY SWALLOWING. I CHOKE QUITE OFTEN. I HAVE A CONSTANT LOW GRADE FEVER. I STABBING PAIN ON THE RIGHT SIDE OF MY CHEST, IT FEELS LIKE I HAVE A KNIFE CONSTANTLY STUCK IN ME. SHORTNESS OF BREATH ON THE RIGHT SIDE. IT FEELS LIKE I BREATHE FIRE. I NOW HAVE BAD BREATH. I KEEP GETTING CHEST COLDS THAT LAST FOR 3 WEEKS AND IT TAKES MULTIPLE ANTIBIOTICS TO GO AWAY. I AM ALWAYS TIRED, NO MATTER HOW MUCH I SLEEP, MY ENERGY LEVEL ARE LOW. I HAVE NOT FELT COMPLETELY HEALTHY SINCE THE PROCEDURE. DOSE OR AMOUNT: INJECTED; FREQUENCY: 2003.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENTERYX NONE LNM

Patients

Seq Age Sex Outcome Treatment
1 Other