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Androcur

Another NameAndro-Diane、SH-80714、cyproterone、acetate、醋酸环丙孕酮、色普龙

IndicationsAndrocur can inhibit the action of androgens and treat diseases caused by excessive androgens.

  • Reg No.11 L 1038/23

  • Inspection No.2670-23

  • dosage form:tablet

    Reference Price:$104

    Specs:50mg*50 tablets

    Indate:24 months

    Warm tips:Please purchase and use the medication under pharmacist guidance as the outer packaging is for reference only and the information is intended for professionals.
    Introduction of Androcur

    Androcur is a prescription drug with multiple indications and uses, mainly used to treat androgen related diseases.

    Androcur produced by Lucius is a tablet with a specification of 50mg*50 tablets.

    Instructions of Androcur

    Androcu is an anti androgen preparation that can inhibit the action of androgens and exhibit the effects of progesterone and anti gonadotropins.

    1.Main components

    Androcur

    2. Adapt to the population

    Patients with abnormally high secretion of androgens.

    3.Medication for special populations

    3.1Pregnant

    Treatment with Androcur is not indicated for use in women.

    3.2Lactation

    Treatment with Androcur is not indicated for use in women.

    3.3Pediatric Use

    Androcur is not recommended for use in children and adolescents below 18 years of age.Androcur must not be given before the conclusion of puberty since an unfavorable influence on longitudinal growth and the still unstabilized axes of endocrine function cannot be ruled out.

    4.Drug overdose

    There have been no reports of fatal overdosage in man with Androcur (cyproterone acetate). There are no specific antidotes and treatment should be symptomatic. If oral overdosage is discovered within two to three hours, gastric lavage can safely be used if indicated.

    5. Drug storage

    Storage at room temperature.

    6.Pharmacokinetics

    The absorption of cyproterone acetate following oral administration is complete. Peak plasma levels are reached 3 to 4 hours after administration. Plasma levels fall rapidly during the first 24 hours as a result of tissue distribution and excretion, and plasma half-life was 38 ± 5 hours.

    from Bayer,2021.05

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