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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: VISXCUSTOMVUE NONE

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VISXCUSTOMVUE NONE Back to Search Results
Event Date 08/27/2008
Event Type  Other  
Event Description

It has been over a year and i suffer from dry eye and halos from my lasik surgery. I was told that those two issues were no longer a concern and only happened to early pts of the surgery. After the surgery, i feel that my doctor was dismissive of the fact that i had dry eye. I have plugs and am using restasis and still have to use a lot of refresh eye drops as my eyes are still dry. It really has changed my life for the worse.

 
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Brand NameVISXCUSTOMVUE
Type of DeviceNONE
MDR Report Key1474456
Report NumberMW5012717
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 09/13/2009
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received09/13/2009
Is This An Adverse Event Report? No
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? No

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