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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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LASIK Back to Search Results
Event Date 04/20/2004
Event Type  Injury  
Event Description

I was told i was a candidate for lasik surgery - did not inform myself well enough - took my doctor's recommendation and had it done. I suffer daily, wake up in the middle of the night - can't hardly open my eyes. Its acutely painful. I go through bottles of artificial tears as drinking water. Many, many regrets. Brand name: systane, optive, restasis, etc.

 
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Type of DeviceLASIK
MDR Report Key1037831
Report NumberMW5006608
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/01/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received05/01/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 05/01/2008 Patient Sequence Number: 1
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