BEUDAMED
    FDA Adverse Event Other Summary report: N

    OLYMPUS

    MDR report key: 245618 · Received October 20, 1999

    Report

    Report Number
    MW1017376
    Event Type
    Other
    Date Received
    October 20, 1999
    Date of Event
    October 12, 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

    WHILE RECOVERING IN ENDOSCOPY SUITE POST BRONCHOSCOPY PT COMPLAINED OF INCREASING SHORTNESS OF BREATH; NOTED TO HAVE BILATERAL EXPIRATORY WHEEZES BY AUSCULTATION. WHEEZES NOT RESOLVED AFTER 0.5CC ALBUTEROL W/ UNIT DOSE ATROVENT VIA HAND HELD NEBULIZER. PT ADMITTED OVERNIGHT FOR 23 HR OBSERVATION. DISCHARGED IN THE MORNING W/ NO COMPLAINTS.

    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 87 YR Other