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Norelgestromin/ethinylestradiol
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    Norelgestromin/ethinylestradiol

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    Norelgestromin/ethinylestradiol
    Combination of
    Norelgestromin Progestogen
    Ethinylestradiol Estrogen
    Clinical data
    Trade names Ortho Evra, Xulane, Evra, others
    AHFS/Drugs.com Professional Drug Facts
    MedlinePlus a602006
    License data
    Pregnancy
    category
    • Contraindicated
    Routes of
    administration
    Transdermal (patch)
    ATC code
    Legal status
    Legal status
    Identifiers
    CAS Number
    PubChem CID
    DrugBank
    ChemSpider
    • None
    UNII
    KEGG
    Chemical and physical data
    Formula C41H53NO4
    Molar mass 623.878 g·mol−1
    3D model (JSmol)
    • CCC12CCC3C(C1CCC2(C#C)O)CCC4=CC(=NO)CCC34.CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O
    • InChI=1S/C21H29NO2.C20H24O2/c1-3-20-11-9-17-16-8-6-15(22-24)13-14(16)5-7-18(17)19(20)10-12-21(20,23)4-2;1-3-20(22)11-9-18-17-6-4-13-12-14(21)5-7-15(13)16(17)8-10-19(18,20)2/h2,13,16-19,23-24H,3,5-12H2,1H3;1,5,7,12,16-18,21-22H,4,6,8-11H2,2H3/b22-15-;/t16-,17+,18+,19-,20-,21-;16-,17-,18+,19+,20+/m01/s1
    • Key:KBFRRZPPJPKFHQ-WKXKRCMPSA-N

    Norelgestromin/ethinylestradiol, sold under the brand name Ortho Evra among others, is a contraceptive patch containing the progestin norelgestromin and the estrogen ethinylestradiol.

    The most common side effects include headache, nausea (feeling sick), breast tenderness, and irregular uterine bleeding.

    Norelgestromin/ethinylestradiol is a transdermal patch (a patch that delivers a medicine across the skin). For the first three weeks of the menstrual cycle a new patch should be applied every week, followed by a fourth week, which is patch-free. The patch-free interval must not be longer than seven days; otherwise, additional non-hormonal contraceptive methods must be used, such as condoms. Transdermal patches must always be applied on the same day of the week to the buttock, abdomen (belly), upper arm or upper back. The same area of skin should not be used for two consecutive patches. Norelgestromin/ethinylestradiol may work less well in women weighing 198 pounds (90 kg) or more.

    Norelgestromin/ethinylestradiol was approved for medical use in the United States in November 2001, and in the European Union in August 2002. It is available as a generic medication.

    Medical uses

    In the United States norelgestromin/ethinylestradiol is indicated for the prevention of pregnancy in women with a BMI < 30 kg/m2 for whom a transdermal delivery system is an appropriate method of contraception.

    In the European Union, norelgestromin/ethinylestradiol is indicated for use as female contraception.

    See also

    External links



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