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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK SURGERY NONE

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LASIK SURGERY NONE Back to Search Results
Event Date 10/14/2003
Event Type  Injury  
Event Description

Lasik surgery to correct vision. The surgery was done. As a result of my surgery, i have severe, chronic dry eyes. I insert lacriserts in both eyes daily; they blur my vision but do offer some relief. I also use restasis eye drops, theratears liquid gel, and i take 2000 mg of flax oil per day. I have lacrimal plugs in both eyes in both punctum. Sometimes the pain is so unbearable that i am forced to wear swimming goggles to protect my eyes from the air. I've seen three ophthalmologists, and they all agreed there is no occular treatment for my condition, and that the condition is permanent. In other words, my eyes are not going to get any better.

 
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Brand NameLASIK SURGERY
Type of DeviceNONE
MDR Report Key1061846
Report NumberMW5007319
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 06/13/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/13/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 06/13/2008 Patient Sequence Number: 1
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