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  • Gadobenic Acid
    1 Drug classified under this active ingredient


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    Multihance
    Dexcel
    RX
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    Multihance

    Gadobenic Acid 334 mg/ml.
    VIAL: 5, 10, 15, 20 ml/vial.
    Liver: the recommended dose in adult
    patients is 0.05 mmol/kg body weight.
    This corresponds to 0.1 ml/kg of the 0.5
    M solution. Brain and spine: the
    recommended dose in adult and in
    paediatric patients greater than 2 years
    of age is 0.1 mmol/kg body weight. This
    corresponds to 0.2 ml/kg of the 0.5 M
    solution. MRA: the recommended dose in
    adult patients is 0.1 mmol/kg body
    weight. This corresponds to 0.2 ml/kg of
    the 0.5 M solution. Breast: the
    recommended dose in adult patients is
    0.1 mmol/kg body weight. This
    corresponds to 0.2 ml/kg of the 0.5 M
    solution. For further information see lit.
    Pediatric Population: No dosage
    adjustment is considered necessary. Use
    for MRI of the brain and spine is not
    recommended in children less than 2
    years of age. Use for MRI of the liver, MRI
    of the breast or MRA is not
    recommended in children less than 18
    years of age. Other Special Populations:
    See lit.
    MultiHance is a paramagnetic contrast
    agent for use in diagnostic magnetic
    resonance imaging (MRI) indicated for:
    MRI of the liver for the detection of focal
    liver lesions in patients with known or
    suspected primary liver cancer (eg.
    hepatocellular carcinoma) or metastatic
    disease; MRI of the brain and spine where it
    improves the detection of lesions and
    provides diagnostic information additional
    to that obtained with unenhanced MRI;
    Contrast-enhanced MR- angiography
    where it improves the diagnostic accuracy
    for detecting clinically significant stenoocclusive
    vascular disease in patients with
    suspected or known vascular disease of the
    abdominal or peripheral arteries; MRI of
    the breast, for the detection of malignant
    lesions in patients where breast cancer is
    known or suspected on the basis of
    previous mammography or ultrasound
    results.
    C/I: Patients with hypersensitivity to the
    active substance or to any of the
    ingredients, patients with a history of
    allergic or adverse reactions to other
    gadolinium chelates. see lit.

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