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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: LASIK NONE

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LASIK NONE Back to Search Results
Event Date 06/01/2004
Event Type  Injury  
Event Description

Extreme, chronic dry eyes due to lasik surgery. I use restasis, which has had barely any effect on the condition. I have had my tear drainage ducts permanently cauderized, which also had no effect on the dry eye problem. I wear onion goggles to work and live in misery with dry eyes. I cannot go in public places without living in extreme, miserable discomfort due to dry eyes. Prior to the lasik procedure, i had perfectly normal, moist eyes with no problems associated with dryness. Dates of use: 2004. Diagnosis or reason for use: refractive surgery.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1578327
Report NumberMW5014317
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 01/11/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/11/2010
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Health Professional
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 01/11/2010 Patient Sequence Number: 1
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