Oral Menopausal hormone replacement therapy, Prophylaxis of postmenopausal osteoporosis
Adult: Available preparations:
Continuous combined therapy
Estradiol 0.5 mg and norethisterone 1 mg tab
Estradiol 1 mg and norethisterone 0.5 mg tab
1 tab daily w/o interruption, preferably at the same time each day.
Continuous sequential therapy
Estradiol 1 mg and norethisterone 1 mg tab
Estradiol 2 mg and norethisterone 1 mg tab
1 tab once daily from pack, as directed.
Transdermal Menopausal hormone replacement therapy, Prophylaxis of postmenopausal osteoporosis
Adult: Available preparations:
Estradiol 0.05 mg and norethisterone 0.14 mg per day patch
Estradiol 0.05 mg and norethisterone 0.17 mg per day patch
Estradiol 0.05 mg and norethisterone 0.25 mg per day patch
Continuous combined therapy
1 patch worn continuously and changed twice wkly. Apply patches to the trunk, below the waist. Do not apply on or near the breasts.
Continuous sequential therapy
1 patch for 14 days following a 14-day estradiol-only regimen. Change patches twice wkly. Begin a new cycle w/o break. Apply patches to the trunk, below the waist. Do not apply on or near the breasts.
Suy gan
Contraindicated.
Cách dùng
Should be taken with food.
Chống chỉ định
Known, suspected, or history of breast cancer and oestrogen-dependent malignant tumours (e.g. endometrial cancer), current or history of venous thromboembolism (e.g. DVT, pulmonary embolism), undiagnosed genital bleeding, endometrial hyperplasia, thrombophilic disorders (e.g. protein C, protein S or antithrombin deficiency), active or recent arterial thromboembolic disease (e.g. angina, MI), porphyria. Hepatic impairment. Pregnancy and lactation.
Thận trọng
Patient w/ risk factors for thromboembolic disorders (e.g. major surgery, prolonged immobilization, obesity, postpartum period, cancer) and oestrogen-dependent tumours (e.g. 1st degree heredity for breast cancer); history of cholestatic jaundice, history or current leiomyoma (uterine fibroids) or endometriosis, HTN, liver disorders (e.g. liver adenoma), DM, cholelithiasis, migraine or severe headache, SLE, history of endometrial hyperplasia, epilepsy, asthma, otosclerosis, hereditary angioedema and mastopathy; cardiac dysfunction, hypertriglyceridaemia, hypoparathyroidism. Smokers. Renal impairment. This combination drug is indicated for non-hysterectomised women. Not indicated for prevention of CV disease or dementia.
Tác dụng không mong muốn
Significant: Irregular or breakthrough bleeding, spotting, increased risk of coronary artery disease, ischaemic stroke, probable dementia and gall bladder disease, endometrial hyperplasia, exacerbation of endometriosis, venous thromboembolism, angioedema, fluid retention; increased levels of circulating total thyroid hormone, corticosteroids, and sex steroids and other plasma proteins (e.g. angiotensin or renin substrate, α-1-antitrypsin, ceruloplasmin). Rarely, increased risk of invasive breast cancer, endometrial cancer, ovarian cancer, chloasma, vision abnormalities (e.g. retinal vascular thrombosis); contact sensitisation (transdermal). Nervous: Headache, dizziness, insomnia, depression, nervousness, affect lability, asthenia, malaise. CV: Peripheral oedema, HTN. GI: Nausea, abdominal distension, diarrhoea, dyspepsia, abdominal pain, flatulence. Genitourinary: Dysmenorrhoea, menstrual disorder, menorrhagia, genital discharge, irregular vaginal bleeding, uterine spasms, vaginal infection. Endocrine: Wt gain, libido disorder; breast pain, tenderness, or enlargement. Musculoskeletal: Back pain, pain in extremity, arthralgia, myalgia. Dermatologic: Acne, rash, pruritus, dry skin. Others: Pain, application site reactions (transdermal).
Ensure adequate intake of Ca and vit D when used for prevention of osteoporosis.
Chỉ số theo dõi
Monitor BP, changes in breasts and signs of endometrial cancer, vision abnormalities (e.g. loss of vision, migraine) and of thromboembolic disorders. Perform Papanicolaou smear and mammogram. Assess need for hormonal replacement therapy at 3-6 mth intervals. When used for prophylaxis of postmenopausal osteoporosis, measure bone density.
Quá liều
Symptoms: Breast tenderness, nausea, vomiting and/or metrorrhagia, depressive mood, fatigue, acne and hirsutism. Management: Symptomatic treatment. Consider gastric lavage.
Tương tác
Decreased pharmacological effect and changes in the uterine bleeding profile w/ CYP inducers (e.g. phenytoin, rifampicin, bosentan). May decrease exposure and seizure control of lamotrigine. May decrease folic acid absorption.
Tương tác với thức ăn
Decreased pharmacological effect and changes in the uterine bleeding profile w/ St. John’s Wort. Alcohol increases risk of breast cancer and of osteoporosis. Avoid alcohol.
Ảnh hưởng đến kết quả xét nghiệm
Reduced response to metyrapone test. May interfere w/ tests for coagulation factors, binding proteins, glucose tolerance, lipids.
Tác dụng
Description: Mechanism of Action: Estradiol is a synthetic sex hormone similar to endogenous oestrogen. During menopause, estradiol substitutes for oestrogen production and alleviates its symptoms. Estradiol also prevents bone loss following menopause or ovariectomy. Norethisterone reduces the estradiol-induced risk of endometrial hyperplasia in non-hysterectomised women. Pharmacokinetics: Absorption: Estradiol: Well absorbed from the GI tract and from the skin. Bioavailability: 53% (oral). Time to peak plasma concentration: 5-8 hr (oral); W/in 21 hr (transdermal).
Norethisterone: Well absorbed from the GI tract and from the skin. Bioavailability: 100% (oral). Time to peak plasma concentration: 0.5-1.5 hr (oral); approx 37 hr (transdermal). Distribution: Estradiol: Plasma protein binding: 60-65% to albumin, 35-45% to sex hormone binding globulin (SHBG).
Norethisterone: Plasma protein binding: 61% to albumin, 36% to SHBG. Metabolism: Estradiol: Undergoes extensive first-pass metabolism mainly in the liver and in the gut and other target organs mainly by CYP enzyme system to oestrone, oestriol and several oestrogen glucuronides and sulfates.
Norethisterone: Undergoes first-pass metabolism in the liver mainly by CYP enzyme system to isomers of 5α-dihydro-norethisterone and of tetrahydro-norethisterone. Excretion: Estradiol: Mainly via urine (90-95%, as inactive glucuronide and sulfate conjugates); faeces (5-10%, as unconjugated form). Elimination half-life: 12-14 hr (oral).
Norethisterone: Mainly via urine, as glucuronide and sulfate conjugates; faeces. Elimination half-life: 8-11 hr (oral); approx 15 hr (transdermal).
Đặc tính
Estradiol Source: National Center for Biotechnology Information. PubChem Compound Summary for CID 5757, Estradiol. https://pubchem.ncbi.nlm.nih.gov/compound/Estradiol. Accessed Nov. 23, 2023.
Norethisterone Source: National Center for Biotechnology Information. PubChem Database. Norethindrone, CID=6230, https://pubchem.ncbi.nlm.nih.gov/compound/Norethindrone (accessed on Jan. 22, 2020)
Bảo quản
Tab: Store between 20-25°C.
Wear gloves during receiving, unpacking, and placing in storage.
Amabelz (Lupin Pharmaceuticals, Inc.). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 04/08/2017.Anon. Estradiol and Norethindrone. Lexicomp Online. Hudson, Ohio. Wolters Kluwer Clinical Drug Information, Inc. https://online.lexi.com. Accessed 04/08/2017.CombiPatch 0.05 mg/0.25 mg (Novartis Pharmaceuticals Corp). DailyMed. Source: U.S. National Library of Medicine. https://dailymed.nlm.nih.gov/dailymed/. Accessed 04/08/2017.Joint Formulary Committee. Estradiol with Norethisterone. British National Formulary [online]. London. BMJ Group and Pharmaceutical Press. https://www.medicinescomplete.com. Accessed 04/08/2017.
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