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    KALBITOR

    ECALLANTIDE INJ. (KALBITOR)

    BOXED WARNING:
    ANAPHYLAXIS
    (See full prescribing information for complete boxed warning)
    Anaphylaxis has been reported after administration ofKALBITOR"'. Because ofthe risk of anaphylaxis, KALBITOR should only be administered by a healthcare professional with appropriate medical support to manage anaphylaxis and hereditar angioedema. Healthcare professionals should be aware of the similarity of symptoms between hypersensitivity reactions and hereditar angioedema and patients should be monitored closely. Do not administer KALBITOR to patients with known clinical hypersensitivity to KALBITOR

    HOW MEDICINE IS ADMINISTERED? TOP
    Use this medicine exactly as directed on the label, unless instructed differently by your doctor
    WARNINGS/PRECAUTIONS: TOP
    * Safety of use during pregnancy has not been established. This medicine SHOULD NOT BE USED DURING PREGNANCY unless benefit justifies potential risk to the fetus. CALL YOUR DOCTOR.
    Other Common Side Effects: TOP
    Diarrhea; Fever; Headache; Injection site reaction; Nausea; Nasopharyngitis.
    Other Common Side Effects:
    If symptoms are mild but do not go away or are bothersome, check with your doctor. IF ANY OF THE ABOVE SIDE EFFECTS IS SEVERE, CALL YOUR DOCTOR IMMEDIATELY.
    Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088.
    This leaflet has been developed by CliniDATA Source, Inc. based primarily on labeling information provided by the manufacturer. The information does not cover all possible uses, actions, precautions, side effects, or interactions of this medicine. It is not intended as medical advice for individual patients.



    Copyright © CliniDATA Source, Inc. 03/14. All rights reserved


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