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 |