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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 12/28/2006
Event Type  Injury  
Event Description

Lasik surgery had complications resulting in keratoconjunctivitis sicca and epithelial cell ingrowth, followed by glaucoma as a result of prednazone forte 1%.

 
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Brand NameLASIK SURGERY
Type of DeviceNONE
MDR Report Key1349475
Report NumberMW5010437
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Type of Report Initial
Report Date 03/22/2009
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/22/2009
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: 03/22/2009 Patient Sequence Number: 1
Treatment
LASIK SURGERY
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