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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK

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Event Date 09/01/2005
Event Type  Injury  
Event Description

Severe dry eye - since undergoing lasik in 2005, i have been afflicted with severe dry eye. The dry eye has ruined my life, and limits me from partaking in many activities that i used to be able to enjoy effortlessly pre-lasik.

 
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Type of DeviceLASIK
MDR Report Key1503667
Report NumberMW5012970
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 10/07/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received10/07/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator HEALTH PROFESSIONAL
Was Device Available For Evaluation? Yes
Is The Reporter A Health Professional? Yes

Patient TREATMENT DATA
Date Received: 10/07/2009 Patient Sequence Number: 1
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