— Federal health officials are getting new authority to mine prescription drug usage by millions of participants in the Medicare drug program to look for safety problems with medicines and medical devices after they hit the market. The Food and Drug Administration has been under increasing...
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Posted on: Saturday, 24 May 2008, 00:00 CDT By The Associated Press WASHINGTON (AP) - Federal health officials will begin monitoring prescription-drug usage by millions of Medicare participants in an effort to identify potential safety problems. The Food and Drug Administration has been under...
HHS Secretary Mike Leavitt today announced efforts underway at the U.S. Food and Drug Administration (FDA) and the Centers for Medicare & Medicaid Services (CMS) that will complement each other to imp... [WebWire - Friday, May 23, 2008] ... WEBWIRE – Friday, May 23, 2008...
Food and Drug Administration (FDA) and Medicare will cooperate on launching a new program, which will help in monitoring safety problems of drugs and medical devices that are already in the U.S. prescription drug market. ... Medicare and FDA are going to provide their...
The two agencies will share access to a database containing comprehensive information about the safety and side effects of prescription drugs. ... By Anna Edney CongressDaily May 23, 2008 The Centers for Medicare and Medicaid Services cleared the way Thursday for a...
Washington - U.S. health officials on Thursday announced plans for a new computer tracking system designed to help them identify dangers from prescription drugs and medical devices already on the market. The system would enable the Food and Drug Administration to search various databases for...
HHS on Thursday announced the creation of a new program that will allow FDA, state agencies and academic researchers to use medical record data to ensure drugs and medical devices are safe for consumers after they enter the market, the Washington Post reports (Stein, Washington Post, 5/23). The...
Posted on: Friday, 23 May 2008, 12:00 CDT U.S. health officials said a new program to analyze medical records should mean quicker identification of safety issues with drugs and medical devices. The Food and Drug Administration's Sentinel Initiative will allow the FDA and other agencies to analyze...
FDA seeks to cut deadly side effects NEW YORK TIMES NEWS SERVICE and ASSOCIATED PRESS WASHINGTON – Chastened by repeated instances in which popular medicines proved deadly, federal health officials announced a major effort yesterday to use information on Medicare claims to assess the risks of...
WASHINGTON, May 23 (UPI) -- U.S. health officials said a new program to analyze medical records should mean quicker identification of safety issues with drugs and medical devices. The Food and Drug Administration's Sentinel Initiative will allow the FDA and other agencies to analyze databases...
WASHINGTON, May 23 (UPI) -- U.S. health officials said a new program to analyze medical records should mean quicker identification of safety issues with drugs and medical devices. The Food and Drug Administration's Sentinel Initiative will allow the FDA and other agencies to analyze databases...