BEUDAMED
    FDA Adverse Event Death Summary report: N

    EUFLEXXA PFS 20 MG/2ML

    MDR report key: 20621923 · Received November 5, 2024

    Report

    Report Number
    MW5162216
    Event Type
    Death
    Date Received
    November 5, 2024
    Date of Event
    August 25, 2024
    Report Date
    November 1, 2024
    Manufacturer
    FERRING PHARMACEUTICALS INC.
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT FAMILY MEMBER OR FRIEND
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    PATIENTS BROTHER (B)(6) CALLING TO REPORT THAT THE PATIENT PASSED AWAY ON (B)(6)2024. THE CAUSE OF DEATH WAS NOT PROVIDED BY THE REPORTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1990670 EUFLEXXA PFS 20 MG/2ML ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Female Death