BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MEPITEL

    MDR report key: 19558094 · Received June 17, 2024

    Report

    Report Number
    MW5156322
    Event Type
    Malfunction
    Date Received
    June 17, 2024
    Date of Event
    May 10, 2024
    Report Date
    June 14, 2024
    Manufacturer
    UNK
    Product Code
    FRO
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    SP
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    MAY 3RD A SILVER DRESSING WAS USED ON A WOUND ON MY LEG WHICH RAISED MY BLOOD PRESSURE MAY 10TH CHANGED TO MEPITEL BY MAY 12 MY BLOOD PRESSURE WAS 188/90. THIS CONTINUED TO RISE. MAY 22ND SAW A DOCTOR B/P 193/115. TOOK CAPTOPRIL AND DIAZEPAM MY PRESSURE STILL REMAINS AT 160/90. EVEN WITH CAPTOPRIL. I HAVE REACTIONS TO MANY MEDICINES WHICH ARE USUALLY CURED WITH CAPTOPRIL AND DIAZEPAM. I HAVE NOT HAD ANY TESTS JUST SUPPLIED WITH DIAZEPAM AND CAPTOPRIL. IS THERE AN ANTI DOTE TO SILVER INGESTION? "SUPPLIED BY MEDICAL CLINIC IN (B)(6)." REF: MW5156321.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1655673 MEPITEL DRESSING, WOUND, DRUG FRO UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR Female Other CAPTOPRIL | DIAZEPAM| IVY| KELP | PARACETAMOL| THYME