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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PROCEDURE BY BOOTHE EYE CARE

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PROCEDURE BY BOOTHE EYE CARE Back to Search Results
Event Date 12/01/2004
Event Type  Injury  
Event Description

Developed dry-eye syndrome requiring ongoing use of restasis eye drops. Eyes are extremely sensitive to make-up. Distance vision is blurry when my eyes get dry.

 
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Brand NamePROCEDURE BY BOOTHE EYE CARE
Type of DeviceUNKNOWN
MDR Report Key1595185
Report NumberMW5014620
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 Health Professional
Is The Reporter A Health Professional? No

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