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...meat and milk from cloned animals. Their verdict: that these food products are no different from those derived from conventionally bred animals, and are therefore safe to eat. But don't expect your local butcher to be selling hams or rib eyes from cloned animals any time soon. The FDA's report is now available to the public and open for a 90-day comment period. Only after this time will the agency make a final decision on the safety of food products made from cloned animals, a process that may take until the end of next year. Until then...

Author: /time Magazine | Title: Key Questions: Cloned Food at the Supermarket | 12/29/2006 | See Source »

...farmers and breeders voluntarily agreed not to sell any meat or milk from cloned animals to the public. They were willing to wait until the FDA could determine whether these foods were safe for human consumption, and wouldn't pose any health risks to people. This FDA report does not change that moratorium...

Author: /time Magazine | Title: Key Questions: Cloned Food at the Supermarket | 12/29/2006 | See Source »

...bottom line isn't the only culprit. It does take on average more than 13 years and often several hundred million dollars for a company to research and test a major new drug before it's presented to the FDA for approval. Only about one of every 10,000 chemical compounds that are first tested end up as medicine cleared by the feds. Converting basic scientific research into effective medicines to treat complex diseases like cancer has also become more difficult the past several years with more expensive and longer drug trials, as well as higher failure rates. There...

Author: /time Magazine | Title: Too Little Bang for the Buck in Drug Research? | 12/27/2006 | See Source »

...time when basic science is bursting with new breakthroughs in fields like human genome decoding, which in turn have raised hopes for breakthrough cures and treatments of serious illnesses. But the numbers show otherwise. The GAO reviewed all 1,264 of the new drug applications submitted for FDA approval from 1993-2004 and found that 60% of them were actually for what industry analysts call "me too" drugs-variations of medications already out on the market. Only 12% of the applications were for what the FDA classified as "priority" new drugs-that is, medications with new chemical ingredients that will...

Author: /time Magazine | Title: Too Little Bang for the Buck in Drug Research? | 12/27/2006 | See Source »

...most part, Tylenol and acetaminophen products are safe - that's why there are offered over-the-counter and without a doctor's prescription. But the FDA wants to alert people that like any drug, taking too much - more than your liver can handle - can be dangerous. And with more people taking more medications at a younger age, being aware of potential interactions among drugs, as well as potential overdoses, is critical. These over-the-counter drugs just have to be used with an eye toward the total dose per day, and amount being used over a period of days, says...

Author: /time Magazine | Title: The FDA's Painkiller Warning: How to Avoid Taking Too Much | 12/20/2006 | See Source »

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