NuvaRing is the trade name for a combined hormonal contraceptive vaginal ring manufactured by Organon that is available by prescription. It is a flexible plastic (ethylene-vinyl acetate copolymer) ring that releases a low dose of a progestin and an estrogen over 3 weeks. NuvaRing was first approved in The Netherlands on February 14, 2001, then by all 14 other countries then in the European Union on June 12, 2001, and in the United States by the FDA on October 3, 2001.1 NuvaRing was first marketed in the United States in July 20022, followed by several European countries in late 2002.citation needed In March 2007, Organon announced the market launch of NuvaRing in Australia, bringing the total number of countries where NuvaRing is available to 32. NuvaRing is currently used by approximately 1.5 million women worldwide.3
UseThe currently approved NuvaRing regimen specifies insertion of the ring into the vagina for a three-week period, then removal of the ring for one week, during which the user will experience a menstrual period. The break week with NuvaRing is comparable to the placebo week for combined oral contraceptive pills ("the Pill"), and the contraceptive effect is maintained during this period. Extended use regimens (7-week, quarterly, or annual) involving back-to-back use of (2, 4, or 17) rings have been studied in clinical trials, but are not currently approved.456 Insertion of the ring is comparable to insertion of other vaginal rings. The muscles of the vagina keep NuvaRing securely in place, even during exercise or sex. Women can check the contraceptive ring periodically with their finger. In rare instances, NuvaRing may fall out during sexual intercourse, while straining during a bowel movement, or while removing a tampon.78 Contraceptive efficacy is not reduced if the ring is removed or accidentally expelled and is left outside of the vagina for less than three hours. If the ring has been out of the vagina for more than three continuous hours, contraceptive efficacy may be reduced and a backup method of contraception must be used until the ring has been used continuously for a subsequent seven days.78 BenefitsThe benefits of the ring include:
Side effectsIn two large studies, over a one year period, 15.1% of users discontinued NuvaRing because of adverse events. Device-related adverse events (foreign body sensation, coital problem, or expulsion) were the most frequently reported adverse events that resulted in discontinuation (by 2.5% of users). Device-related adverse events were reported at least once during the one year study period by 4.4% of NuvaRing users.10 The most common adverse events reported by 5 to 14% of the 2501 women who used NuvaRing in five clinical trials were: vaginitis (14.1%), headache (9.8%), upper respiratory tract infection (8.0%), leukorrhea (5.8%), sinusitis (5.7%), nausea (5.2%), and weight gain (4.9%).81516 NuvaRing is weight neutral.1718 Additional side effect information is provided in the NuvaRing full prescribing information.816 NuvaRing has the cardiovascular contraindications associated with combined oral contraceptives, such as stroke and heart attack. These risks have been shown to be much greater if combined with other risk factors such as smoking, recent surgery, a history of cardiovascular disease, or old age. Beyond the risks associated with combined oral contraceptives, NuvaRing is contraindicated for a risk of blood clots that is specific to NuvaRing's class of contraceptives. NuvaRing contains the hormone etonogestrel, the active metabolite of the prodrug desogestrel. This makes the NuvaRing a third-generation contraceptive. Epidemiological studies have shown that oral contraceptives that contain desogestrel can increase the risk of blood clots(venous thrombosis) by 1.5 to 2.4 times the risk of second-generation oral contraceptives. 19 Second-generation oral contraceptives do not contain desogestrel. Large scale studies of NuvaRing have not been done to determine if NuvaRing's risk is larger or smaller than oral contraceptives that contain desogestrel. Hormones are released continuously from NuvaRing, thus peak and total estrogen and progestin doses are significantly lower than with combined oral contraceptives, but what effect this has on the risk of blood clots has not been established8 LawsuitIn March 2008, a lawsuit was filed against the manufacturers, distributors, and marketers of NuvaRing. The plaintiff alleges that these companies concealed the health risks associated with using the device, which is claimed to have cause the death of the plaintiff's wife.20 Mechanism of actionLike all combined hormonal contraceptives, NuvaRing works primarily by preventing ovulation. A secondary mechanism of action is inhibition of sperm penetration by changes in the cervical mucus. Hormonal contraceptives also have effects on the endometrium that theoretically could affect implantation, however no scientific evidence indicates that prevention of implantation actually results from their use.21 NuvaRing should not be used if a woman is pregnant. There is however no known harm to the woman, the course of her pregnancy, or the fetus if NuvaRing is accidentally used during pregnancy.22 NuvaRing delivers 120 µg of etonogestrel (a progestin) and 15 µg of ethinyl estradiol (an estrogen) each day of use. References
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