BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HEPARIN

    MDR report key: 1032529 · Received April 19, 2008

    Report

    Report Number
    MW5006331
    Event Type
    Injury
    Date Received
    April 19, 2008
    Date of Event
    August 7, 2007
    Report Date
    April 19, 2008
    Product Code
    NZW
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IL, US
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEPARIN NZW

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| L| S