BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 11752148 · Received April 29, 2021

    Report

    Report Number
    MW5101078
    Event Type
    Injury
    Date Received
    April 29, 2021
    Date of Event
    October 28, 2020
    Report Date
    April 27, 2021
    Manufacturer
    FERRING PHARMACEUTICALS INC.
    Product Code
    MOZ
    UDI-DI
    55566410001
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 1

    PATIENT REPORTED BEING HOSPITALIZED ABOUT A MONTH AGO DUE TO HAVING ACID REFLUX AND A MODERATE CASE OF COPD. PATIENT ALSO HAD A PACEMAKER IMPLANTED ON (B)(6) 2020.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    646145 EUFLEXXA ACID, HYALURONIC, INTRAARTICULAR MOZ FERRING PHARMACEUTICALS INC. 55566410001

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Hospitalization