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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PRK/LASIK NONE

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PRK/LASIK NONE Back to Search Results
Event Date 01/31/2008
Event Type  Other  
Event Description

Pt reports that she was not informed of the side effects of the prk surgery states that five hrs after her surgery, she experiences intense pain. She now has extreme dry eyes, has to close one eye to drive because of halos. Pt states that she has to wear glasses to see, however, the glasses makes her nauseated. The office where she had the surgery promised to send her a pair of glasses and has not as of yet.

 
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Brand NamePRK/LASIK
Type of DeviceNONE
MDR Report Key1052127
Report NumberMW5007008
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Nurse
Type of Report Initial
Report Date 05/28/2008
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received05/28/2008
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator Health Professional
Is The Reporter A Health Professional? Yes

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