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    GADAVIST

    GADOBUTROL INJ. (GADAVIST)

    BOXED WARNING: NEPHROGENIC SYSTEMIC FIBROSIS
    Gadolinium-based contrast agents increase the risk for nephrogenic systemic fibrosis (NSF) in patients with:
    • acute or chronic severe renal insufficiency (glomerular filtration rate <30mL/min/1.73m2), or
    • acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.

    In these patients, avoid use of gadolinium-based contrast agents unless the diagnostic information is essential and not available with non-contrast enhanced magnetic resonance imaging (MRI). NSF may result in fatal or
    debilitating systemic fibrosis affecting the skin, muscle and internal organs. Screen all patients for renal dysfunction by obtaining a history and/or laboratory tests. When administering a gadolinium-based contrast agent, do not exceed the recommended dose and allow a sufficient period of time for elimination of the agent from the body prior to any readministration
    BOXED WARNINGS:
    NEPHROGENIC SYSTEMIC FIBROSIS (NSF)
    See full prescribing information for complete boxed warning
    Gadolinium-based contrast agents (GBCAs) increase the risk for NSF among patients with impaired elimination of the drugs. Avoid use of GBCAs in these patients unless the diagnostic information is essential and not available with non-contrasted MRI or other modalities.
    • The risk for NSF appears highest among patients with:
    o Chronic, severe kidney disease (GFR < 30 mL/min/1.73m2), or
    o Acute kidney injury.
    • Screen patients for acute kidney injury and other conditions that may reduce renal function. For patients at risk for chronically reduced renal function (for example, age >60 years, hypertension or diabetes), estimate the glomerular filtration rate (GFR) through laboratory testing

    HOW MEDICINE IS ADMINISTERED? TOP
    Use this medicine exactly as directed on the label, unless instructed differently by your doctor
    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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