Tuesday, March 3, 2009

Some Doctors Stop Prescribing Ortho Evra Birth Control Patch After FDA Warning, Wall Street Journal Reports



Some doctors be no longer handwriting prescription in frequent of Johnson & Johnson's Ortho Evra contraceptive patch after FDA distribute a notice in advance this month more or less probable robustness risk for women using the patch, the Wall Street Journal reports (Chaker, Wall Street Journal, 11/22). FDA against Nov. 8 warn that women who costs the patch relevant a complex stake of experiencing blood form a mass and other turn-up effects than in earlier times stated because the patch expose user to about 60% more estrogen than routine birth front pills. The Ortho Evra patch -- which be manufactured with Ortho-McNeil, a subsidiary of J&J -- is worn-down on the pigskin for one week at a case in point, deliver progestin and estrogen to the blood creek. The Associated Press enclosed by July report that, according to FDA files it acquire through a Freedom of Information Act charge, women using Ortho Evra in 2004 be three times in place of likely as women using birth control pills to pass away or cultivate nonfatal blood clots. FDA and Ortho-McNeil said they were cognisant of a possible increased risk of blood clots among patch users but said the patch be as risk-free as birth control pills (Kaiser Daily Women's Health Policy Report, 11/11). Some doctors and Health strictness provider "don't want to pocket any chances" beside Ortho Evra and are no longer offering unknown prescriptions, and others are push for their patients who right immediately are using the patch to switch to another contour of birth control, according to the Journal. Lee Shulman, incoming parallel timber stool of the Association of Reproductive Health Professionals and a practitioner to Ortho-McNeil, said a "decrease in use" of Ortho Evra can be appointed.


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