The Food and Drug Administration decided Thursday that silicone breast implants to remain in the market, after two days of discussions and hearings on the device?s security and aftermath.
When asked about the comments on the implant safety: ?We felt that way before the meeting, and we continue in this way after the presentations and discussions, the feeling in the past two days,? Dr. William Maisel, deputy director of the FDA Center for Devices and Radiological Health, said the New York Times. Despite FDA approval of the surgery for breast enlargement, press critics have expressed concern about the low participation in its follow-up studies on the potential to cause health problems. beginning of June, FDA suggests that replacing women who suffer the knife frequently experience complications after surgery, and sometimes you need another operation to repair it or pointed. He also indicated that silicone implants are not lifetime devices considered as eligible. Studies of two manufacturers, Mentor and Allergan, about 61 percent and 21 percent of the patients and involved, reports the Wall Street Journal. The FDA said it would with the Company, both divisions of Johnson & Johnson are working to get more women to take on the job post-approval studies, said a report thirdage.com.How did you find us on Facebook
By 2006, silicone implants for more than 10 years because of concerns about leaking silicone gel, and the problems that they in the connective tissue caused prohibited. This year?s survey findings have not shown increased risk of cancer or connective tissue disease, but FDA found that a longer duration study is needed to establish more concrete conclusions.
Peter Romer maintains a surgeon for breast implants one patient named Laura at his clinic in Caracas, 5 November 2009. Undeterred by a recession and rampant inflation shows no sign of image-conscious Venezuelans sacrificing facelifts, liposuction and breast enlargements that have good form beauty treatments. Inclusion of 5 November 2009.
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