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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 11/01/2000
Event Type  Injury  
Event Description

Lasik surgery in 2000 - experienced starburst effect immediately, along with dry eyes. My vision has recently started to rapidly regress in right eye, a small amount in left eye. Symptoms: difficulty driving at night, worsened starburst effect, trouble focusing when reading, distance vision impairment. I had to purchase glasses recently, which i was told to wear at night and for the computer. Within 2 weeks, i started having blurred vision, trouble focusing so, went back to eye doctor who informed me, my vision had worsened in my right eye in the past 2 weeks. She ordered a new lens for my glasses.

 
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Brand NameLASIK
Type of DeviceNONE
MDR Report Key1353097
Report NumberMW5010505
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 03/27/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/27/2009
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 03/27/2009 Patient Sequence Number: 1
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