BEUDAMED
    FDA Adverse Event Other Summary report: N

    OLYMPUS

    MDR report key: 245544 · Received October 20, 1999

    Report

    Report Number
    MW1017375
    Event Type
    Other
    Date Received
    October 20, 1999
    Date of Event
    September 17, 1999
    Report Date
    October 20, 1999
    Manufacturer
    OLYMPUS AMERICA INC.
    Product Code
    EOQ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CO, US
    Reporter Occupation
    RESPIRATORY THERAPIST

    Narratives

    Description of Event or Problem · 1

    POST BRONCHOSCOPY PATIENT COMPLAINS OF VOICE BEING HOARSE, AFEBRILE, PRODUCTIVE COUGH, SMALL AMOUNTS OF BROWN SPUTUM FOR 3 DAYS. PRIMARY CARE PHYSICIAN WAS NOTIFIED BY BRONCHOSCOPIST. PATIENT WAS TREATED WITH ORAL ANTIBIOTICS FOR ONE WEEK; SYMPTOMS WERE RESOLVED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OLYMPUS BRONCHOSCOPE EOQ OLYMPUS AMERICA INC. BF20D *

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Other