BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SOLU-MEDROL ACTO-O-VIAL, 40 MG

    MDR report key: 4814962 · Received May 26, 2015

    Report

    Report Number
    MW5042904
    Event Type
    Malfunction
    Date Received
    May 26, 2015
    Date of Event
    May 22, 2015
    Report Date
    May 26, 2015
    Manufacturer
    PHARMACIA & UPJOHN CO
    Product Code
    OOY
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    IA, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    NURSE PUSHED PLUNGER DOWN ON A SOLU-MEDROL ACTO-O-VIAL 40 MG AND THE CIRCULAR BOTTOM OF THE VIAL POPPED AWAY FROM THE REST OF THE VIAL AND CUT THE NURSE. THE NURSE RECEIVED 4 STITCHES ON THE MEDIAL VOLAR ASPECT OF THE THUMB AT IP JOINT (1.5 CM X 2 CM). DOSE: 40 MG; FREQUENCY: BID; ROUTE: INTRAVENOUS. DATES OF USE: (B)(6) 2015. REASON FOR USE: BREATHING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    338886 SOLU-MEDROL ACTO-O-VIAL, 40 MG SOLU-MEDROL ACTO-O-VIAL, 40 MG OOY PHARMACIA & UPJOHN CO LO7461

    Patients

    Seq Age Sex Outcome Treatment
    1 21 YR