FDA Adverse Event Injury Summary report: N

*

MDR report key: 787047 · Received November 24, 2006

Report

Report Number
MW1041133
Event Type
Injury
Date Received
November 24, 2006
Date of Event
March 15, 2005
Report Date
November 24, 2006
Manufacturer
*
Product Code
HQL
Report Source
Voluntary report
Reporter Location
MN, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I'VE HAD AN INTRAOCULAR LENS IMPLANT AND I WAS VERY VERY PLEASED, BUT THE ONLY PROBLEM I HAVE NOW IS VERY SEVERE BACK PROBLEM, PROBLEM WITH MY SPINE. I TAKE ALEVE FOR THE PAIN, I ALSO HAVE CHEST PAIN BUT I DON'T KNOW IF THE CHEST PAIN RELATED TO THE SURGERY OR THE OTC, ALEVE IS CAUSING IT. I REALLY DO APPRECIATE THE SURGERY BUT I DO NOT APPRECIATE THE BACK PAIN THAT GOES ALONG WITH IT. SOMETIMES THE PAIN IS SO UNCOMFORTABLE I CAN'T SLEEP AT NIGHT. I KNOW THAT DRS TRY TO MAKE LIFE BETTER, BUT I ALSO KNOW THAT THEY SHOULD TELL PEOPLE THE TRUTH ABOUT THE PAIN THAT GOES ALONG WITH IT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 * INTRAOCULAR LENS IMPLANT HQL * * *

Patients

Seq Age Sex Outcome Treatment
1 35 YR Required Intervention| S