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After FDA Warning, Depression Diagnosis, Treatment Decline In the wake of a U.S. Food and Drug Administration (FDA) Advisory in 2003 about the increased risk of suicidality for children taking antidepressant medications, diagnosis and treatment of depression in both children and adults has significantly declined from expected rates. The ... ... PsychcentralImpact of U.S. antidepressant warnings still felt CHICAGO (Reuters) - Strong warnings by the U.S. Food and Drug Administration about suicide risks linked to antidepressant use in children and young adults have had a 'spillover effect' on depression care in older adults, researchers said on Monday. ReutersFDA Clears Additional Use For Novartis Bone Drug Novartis, the Basel health-care provider, said the U.S. Food and Drug Administration approved an additional use for its osteoporosis drug Reclast. Topix.netHurdles remain in Obama`s push to revamp health care This year's fast-track timetable on health care calls for leaders of key congressional committees to unveil legislation this ... MedicineNetAcetaminophen needs tougher warnings, FDA says Officials at the U.S. Food and Drug Administration (FDA) say acetaminophen needs tougher standards to protect consumers from liver damage and accidental overdose. Health CentralDevax Receives IDE Approval To Commence DIVERGE II Devax, Inc. announced that the U.S. Food and Drug Administration has conditionally approved an Investigational Device Exemption ('IDE') for its AXXESST Biolimus A9® Eluting Bifurcation Stent System (AXXESS System), allowing the company to initiate a pivotal clinical trial (DIVERGE II) of the device in the United States. Medical News TodayAgendia Supports Genentech`s Citizen`s Petition Urging FDA To Hold In-Vitro Diagnostic Tests To One Set Of Scientific And Regulatory Standards Agendia, a world leader in molecular cancer diagnostics, announced its strong support of Genentech's Citizen's Petition. Filed on December 5, 2008, Docket No. FDA-2008-P-0638-0001/CP petitions that all in vitro diagnostic tests be held to one set of scientific and regulatory standards. In response, on May 28, 2009, Agendia formally submitted a letter of support to the U.S. Food and Drug Administration (FDA). Medical News TodayThis week: TOBACCO ROADBLOCK Expect to see a lot of Sen. Richard Burr on the Senate floor this week. North Carolina's senior senator will be fighting a rearguard action against tobacco regulation by the Food and Drug Administration -- a popular piece of legislation and a battle Burr is likely to lose. The Senate is expected to take up the tobacco bill Tuesday or Wednesday. Sponsored by Sen. Ted Kennedy of Massachusetts, the bill would allow the FDA to impose strict regulations on advertising and the chemical makeup of tobacco products. Join TogetherIt`s wrong to think our brains wear out Sydney - A musical 40 years ago was her first success and Australian playwright Julia Britton is still turning out saleable scripts. I thoroughly enjoy writing, the 95-year-old said. I'm a fast writer with lots of ideas. ... Earth TimesEncouraging Heart Failure Patients To Enjoy Their Food -- Even If It`s Not As Salty As Before The individualised management programme of France's 'Réseau Respecti-coeur' makes quality of life the first objective for heart failure patients, and one of the network's dieticians, Mme Hélène Guibert, explained that the heart-healthy eating recommended in the programme need not be a source of frustration or misery - even for a Frenchman. Medical News Today1 2 |
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