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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NONE

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Event Date 04/15/2004
Event Type  Injury  
Event Description

I had lasik done 5 years ago, i was a -6. 5 in both eyes with astigmatism in one eye. I had worn contact lens for 33 years. I began having difficulty seeing up close, i thought lasik would help me, so i would only have to use glasses for reading. My dr tried to under correct one eye so i could see up close without glasses. I could not adjust to my vision being off, i went back for a redo and did both eyes again to get me to 20/20. I never could see 20/20. At dusk i cannot see, difficult to drive and see in dim light. Halos around light also. If i had realized or read about these problems from others, i would not have had this procedure. My husband had his eyes done at the same time and he has been pleased. I have 4 other children that are near sighted one with a prescription of -12. 5 and -13. 00. I would never encourage any of my children to have this procedure.

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Type of DeviceNONE
MDR Report Key1595170
Report NumberMW5014616
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 02/01/2010
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received02/01/2010
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator OTHER
Is The Reporter A Health Professional? Yes

Date Received: 02/01/2010 Patient Sequence Number: 1