| Literature DB >> 1387011 |
Abstract
In December 1990, the Food and Drug Administration approved Norplant (Wyeth-Ayerst, Radnor, PA) for general US use. This approval comes during a time period when the number of contraceptors relying on sterilization has risen, echoing known dissatisfaction with other reversible methods. During the past year, data have been presented that refute concern that Norplant may be an abortifacient. Continued estradiol production with development of follicles and ovulation in regularly menstruating women was documented. Ovulatory dysfunction among Norplant users, despite follicular development, was also detailed. Changes in carbohydrate metabolism were confirmed to be clinically insignificant. International development of biodegradable and non-biodegradable implants and 1, 3, or 6 months injectables continues. These injectable and implantable contraceptives promise diversity in contraceptive options to match diversity in contraceptive need and life style.Entities:
Keywords: Americas; Behavior; Contraception; Contraception Continuation; Contraceptive Agents; Contraceptive Agents, Female; Contraceptive Agents, Progestin; Contraceptive Implants; Contraceptive Methods; Contraceptive Usage; Depo-provera; Developed Countries; Drug Interactions; Drugs; Economic Factors; Family Planning; Injectables; Levonorgestrel; Literature Review; Medroxyprogesterone Acetate; Norethindrone; Norethindrone Enanthate; North America; Northern America; Psychological Factors; Research And Development; Satisfaction; Technology; Treatment; United States
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Year: 1992 PMID: 1387011
Source DB: PubMed Journal: Curr Opin Obstet Gynecol ISSN: 1040-872X Impact factor: 1.927