BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ORTHOVISC

    MDR report key: 5088345 · Received September 15, 2015

    Report

    Report Number
    MW5056246
    Event Type
    Injury
    Date Received
    September 15, 2015
    Date of Event
    July 30, 2015
    Report Date
    September 15, 2015
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AZ, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    OTHOVISC SHOTS BILATERAL KNEES. FIRST SHOT 3 DAYS LATER RIGHT FOOT SWELLS AND VERY PAINFUL, WEAR COMPRESSION SOCKS AND 2 MONTHS LATER NO BETTER. WENT TO EMERGENCY ROOM ON 3RD DAY, COULD FIND NO OTHER PROBLEMS OR BLOOD CLOTS. FOLLOWING WEEK RECEIVED 2ND SHOT NEXT DAY VERY SHORT OF BREATH WITH EXERTION. THIRD DAY WHEEZING WITH REST AND SHORT OF BREATH ANOTHER EMERGENCY ROOM VISIT. NO BLOOD CLOTS SENT TO PC. WENT TO CARDIOLOGIST AND PULMONOLOGIST. TEST DONE NOTHING CAME BACK RELATED TO LUNGS OR HEART. ALLERGIES HAVE BEEN HORRIBLE SINCE WITH SORE THROAT AND CONSTANT DRAINAGE. KNEE PAIN IS MUCH WORSE WITH SWELLING OF KNEES. FOOT STILL SWOLLEN AND PAINFUL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    607880 ORTHOVISC ORTHOVISC MOZ

    Patients

    Seq Age Sex Outcome Treatment
    1 55 YR Other