BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEALONID GV

    MDR report key: 369117 · Received December 27, 2001

    Report

    Report Number
    9610566-2001-00023
    Event Type
    Injury
    Date Received
    December 27, 2001
    Date of Event
    December 1, 2001
    Manufacturer
    PHARMACIA & UPJOHN, FYRISLUND
    Product Code
    LZP
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    CORNEAL DETERIORATION[CORNEAL DISORDER NOS]. VISION DETERIORATION[VISUAL ACUITY REDUCED]. CASE DESCRIPTION: SPONTANEOUS DEVICE REPORT, LOCAL REF. N: 01-3829-S. CROSS REFERENCE WITH 01-3828-S; 01-3830-S; 01-3831-S; 01-3832-S; 01-3833-S; 01-3034-S; 01-3835-S; 01-3836-S; 01-3837-S. A PHARMACIST REPORTED A CASE REGARDING THE SECOND OF A GROUP OF TEN PATIENTS WHO UNDERWENT CATARACT SURGERY IN AN OPHTHALMOLOGY DEPT. IN 2001, THE SURGERY WAS PERFORMED USING HEALON GV (HYALURONATE SODIUM. AT 5-DAY POST SURGERY CHECK, IT WAS NOTICED THAT THE PATIENT HAD DEVELOPED CORNEAL DETERIORATION, CONSISTING OF A DETERIORATION IN THE PATIENT'S VISION AND IN VISION BECOMING MISTY. THE OUTCOME WAS UNKNOWN. THE REPORTING PHARMACIST STATED THAT THE HOSPITAL HAD SUSPENDED ALL FUTURE CATARACT OPERATIONS UNIT THE INVESTIGATION WILL BE COMPLETE. FURTHER INFORMATION IS BEING SOUGHT.

    Description of Event or Problem · 1

    FOLLOW-UP 1/29/2002. THE FOLLOWING NEW INFO HAS BEEN PROVIDED THROUGH A TECHNICAL COMPLAINT INVESTIGATION REPORT: TWO REFERENCE SYRINGES FROM THE REPORTED LOT N WERE SENT TO THE CHEMICAL DEPT FOR PH ANALYSIS. THE RESULT WAS FOUND TO BE WITHIN THE SPECIFICATION LIMITS. LATER ON, FIVE UNOPENED BLISTERPACK SYRINGES, RETURNED FROM CUSTOMER STORAGE, WERE VISUALLY INSPECTED AND THEY DID NOT EXHIBIT ANY CLOUDY SOLUTION OR MFG DEFECTS. THE SYRINGES WERE SENT TO THE CHEMICAL DEPT AND ANALYZED FOR: APPEARNACE, IDENTIFICATION, ZERO SHARE VISCOSITY, PH, MASS AVERAGE, RELATIVE MOLECULAR MASS, ASSAY FOR SODIUM HYALURONATE. THE RESULTS WERE FOUND TO BE WITHIN THE SPECIFICATION REQUIREMENTS/LIMITS. AN ANALYSIS WAS ALSO PERFORMED ON OSMOLAITY. THE RESULT WAS FOUND TO BE WITHIN THE LIMITS OF WHAT IS PHYSIOLOGICALLY ACCPETED BY THE EYE. THE VISUAL INSPECTION OF REFERENCE SAMPLES EXHIBITED NO CLOUDY SOLUTION OR MFG DEFECT. THE BATCH DOCUMENTATION WAS REVIEWED AND NO SIGNIFICANT DEVIATION WAS FOUND. NO EARLIER COMPLALINT HAD BEEN REPORTED IN THE PAST ON THE BATCH UNDER EVAL. IN CONCLUSION, NO DEVIATION WAS FOUND IN THE INVESTIGATION THAT COULD EXPLAIN THE REASON FOR THIS COMPLAINT. FOLLOWUP 1/29/2002 ADDITIONAL INFO DOES NOT WARRANT A CHANGE IN THE CASE COMMENT. SUBMISSION OF A REPORT DOES NOT CONSTITUTIE AN ADMISSION THAT THE MEDICAL PERSONNEL, USER FACILITY, DISTRIBUTOR, MFR, OR PRODUCT CAUSED OR CONTRIBUTED TO THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    58646 HEALONID GV HYALURONATE SODIUM LZP PHARMACIA & UPJOHN, FYRISLUND NA 5000669

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other