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Safety and bleeding profile of continuous levonorgestrel 90 mcg/ethinyl estradiol 20 mcg based on 2 years of clinical trial data in Canada
Affiliation:1. MedStar Franklin Square Medical Center Department of Family Medicine, 9101 Franklin Square Dr. Baltimore, MD 21237;2. Johns Hopkins Bloomberg School of Public Health General Preventive Medicine Residency, 615 N. Wolfe St. Room WB602, Baltimore, MD 21205-1996;3. MedStar Family Choice, 5233 King Ave, Ste. 400, Rosedale, MD 21237;4. MedStar Health Research Institute, 110 Irving St. NW Suite EB-7113, Washington, DC 20010;5. MedStar Washington Hospital Center, 110 Irving St. NW Suite EB-7113, Washington, DC 20010
Abstract:BackgroundThe study was conducted to evaluate bleeding profile and safety of continuous oral contraceptive (OC) containing levonorgestrel (LNG) 90 mcg/ethinyl estradiol (EE) 20 mcg.Study DesignHealthy women who participated at seven Canadian sites in 1-year open-label study of LNG 90 mcg/EE 20 mcg daily were eligible for this second-year extension study. Primary end points included bleeding profile and adverse events.ResultsSeventy-nine women enrolled without interrupting pill taking; 62 (78.5%) completed. Adverse events were comparable to cyclic OC regimens, except unscheduled vaginal bleeding. Amenorrhea and absence of bleeding increased to about 80% and 90%, respectively, by Pill Pack 18. Mean (median) number of bleeding days for the last two 90-day intervals was 1.1 (0) and 0.7 (0) days, respectively.ConclusionsContinuous LNG 90 mcg/EE 20 mcg had a safety profile similar to low-dose cyclic OCs. Short-term safety profile remained excellent, with increasing rates of amenorrhea and decreasing incidence of unscheduled bleeding and/or spotting.
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