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FDA backs Vytorin after finishing study review (AP) AP - The Food and Drug Administration said Thursday patients should not stop taking Vytorin or other cholesterol-lowering drugs, based on its just-completed review of a controversial study that hammered Vytorin sales. yahoo.comNew Drug Development Still Takes 8 Years Despite Faster FDA Review While the U.S. Food and Drug Administration Drug has quickened review and approval of new medicines, the complex nature of diseases for which new therapeutics are being developed has resulted in longer clinical development times, according to the Tufts Center for the Study of Drug Development. news-medical.netCorruption among FDA Managers Revealed in Letter to Obama Team Nine FDA scientists have revealed a serious level of corruption among FDA managers in a terse letter written to President Obama's transition team.The letter, written on the FDA Center for Devices and Radiological Health letterhead reads, 'The purpose of this letter is to inform you that the scientific review process for medical devices at the FDA has been corrupted and distorted by current FDA managers, thereby placing the American people at risk.'read more eMaxHealthFDA Says ENHANCE Results Do Not Shake Cholesterol Theory ROCKVILLE, Md. (MedPage Today) -- When it comes to cholesterol, lower is still better and lowest may be the best, according to the FDA, which said today that it has completed its review of data from the ENHANCE trial. Med PageAfter Further Review, Vytorin Gets FDA OK The Food and Drug Administration said patients should not stop taking Vytorin or other cholesterol-lowering drugs, based on its just-completed review of a controversial study that hammered Vytorin sales. CBC.caFDA Backs Cholesterol Drug Vytorin (HealthDay) HealthDay - THURSDAY, Jan. 8 (HealthDay News) -- After nearly a year of review, U.S. health officials said Thursday that they supported the continued use of the controversial cholesterol-lowering drug Vytorin. yahoo.comMore `screen time` linked to poor fitness in girls Title: More 'Screen Time' Linked to Poor Fitness in GirlsCategory: health newscreated: 1/8/2009 2:00:00 AMLast Editorial Review: 1/8/2009 (Source: MedicineNet Osteoporosis General) Med WormIpsen: FDA`s First-Cycle Review Of Reloxin(R) Extended Ipsen (Paris:IPN) announced that the U.S. Food and Drug Administration (FDA) provided notification that the Prescription Drug User Fee Act (PDUFA) action date for ReloxinŽ (botulinum toxin of type A) Biologics License Application (BLA) in aesthetic indications (glabellar lines) has been extended to April 13, 2009. The FDA did not issue any specific request on the occasion of this extension. Medicalnewstoday.comHuman Genomics In China Ten years ago, the Chinese National Human Genome Center at Shanghai (South Center, hereafter) was established in the Zhangjiang HiTech Park of Pudong District in Shanghai. To commemorate this important event, which marks the beginning of the Genomics Era in China, we specially organize a series of mini-reviews for this special issue. TelegrapheHeart Drug May Be a Cancer Fighter Title: Heart Drug May Be a cancer FighterCategory: health newscreated: 1/8/2009 2:00:00 AMLast Editorial Review: 1/8/2009 medicinenet.com1 2 3 |
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