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  • Type II mucopolysaccharidosis (MPSII) , Hunter syndrome

    Idusulfate

    【Product name】Elaprase

    [English common name]Idursulfase

    [Chinese common name]Idusulfate

    [English name]

    [Chinese other name]

    [Indications] Elaprase is suitable for long-term treatment of patients with Hunter syndrome (Mucopolysaccharide storage disease II, MPS II). Heterozygous females were not studied in clinical trials.

    [Usage and Dosage] Use this medicine exactly as the doctor told you. If you are not sure, please consult your doctor.
    This medicine will be given to you under the supervision of a doctor or nurse who specializes in treating Hunter's syndrome or other hereditary metabolic disorders.
    The recommended dose is 0.5 mg (half mg) per kg of infusion. Before use, Elaprase must be diluted in sodium chloride 9 mg / ml (0.9%) for infusion. After dilution, the drug is administered by intravenous (drip). The infusion usually lasts for 1 to 3 hours and is administered weekly. The recommended dose for children and adolescents and adolescents is the same as for adults.
    If you use more Elaprase than you should
    There is no experience with this drug overdose.
    If you forget to use Elaprase
    If you missed the Elaprase infusion, please contact your doctor.
    If you have any questions about using this medicine, please consult your doctor or nurse.

    [Storage] Store in the refrigerator (2 ° C – 8 ° C). Do not freeze.

    [Tips] Some of the information on this site comes from the Internet and is only used internally by pharmacists or medical staff. It is not a substitute for doctors to diagnose face to face. Please consult a professional pharmacist for specific medications. Please refer to the actual product manual or the actual product for the product content.

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