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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 04/30/2008
Event Type  Injury  
Event Description

Lasik surgery in 2008. Punctal plugs three months later. Dry eyes continue to date, cannot work a full 40 hour work week due to pain and discomfort. Difficulty seeing in low light conditions. Began taking anxiety and depression medicine about 4 days after surgery. Was hospitalized overnight for chest pains. Turned out that it was likely a side effect of the depression meds, but at the time i thought i was having a heart attack.

 
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Brand NameLASIK SURGERY
Type of DeviceNONE
MDR Report Key1157867
Report NumberMW5008271
Device Sequence Number1
Product CodeLZS
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 09/10/2008
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received09/10/2008
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? No

Patient TREATMENT DATA
Date Received: 09/10/2008 Patient Sequence Number: 1
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