Abstract
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▲ The continuous-use combination oral contraceptive ethinylestradiol/levonorgestrel 20μg/90μg suppresses gonadotropins, and subsequently ovulation and endometrial thickening, and suppresses breakthrough bleeding.
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▲ Amenorrhoea and absence of breakthrough bleeding increase in incidence with extended administration.
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▲ The pregnancy rate attributable to method failure in a large noncomparative trial of healthy, sexually active (aged 18–49 years) women during treatment with ethinylestradiol/levonorgestrel 20μg/90μg for 12 months was 15 per 2134 women (adjusted Pearl Index 1.26 per 100 women-years of use).
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▲ There were no differences in pregnancy rates over 12 months between continuous-use ethinylestradiol/ levonorgestrel 20μg/90μg and cyclical ethinylestradiol/levonorgestrel 20μg/100μg in a smaller, randomised, nonblind trial.
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▲ Adverse menstrual cycle-related symptoms were significantly improved with administration of continuous-use ethinylestradiol/levonorgestrel 20μg/ 90μg in a noncomparative trial.
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▲ In small trials, hormonal and ultrasound changes indicative of reinstated ovulation occurred within a month of discontinuation of the drug, and menstruation began again in most women within 90 days.
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▲ The incidence of adverse effects was similar in continuous-use and cyclical regimens of ethinylestradiol/levonorgestrel (20μg/90μg vs 20μg/100μg).
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References
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Wagstaff, A.J. Continuous-Use Ethinylestradiol/Levonorgestrel 20μg/90μg. Drugs 67, 2475–2479 (2007). https://doi.org/10.2165/00003495-200767160-00009
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DOI: https://doi.org/10.2165/00003495-200767160-00009