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Most clinical trials assessing adverse medical events (AMEs) have focused on inpatient care. Now there's a study looking at AMEs in private practice and it shows that the numbers are about the same. Most AMEs are from surgeries, diagnostic testing, and treatment errors. Every year there are about 11,000 paid malpractice suits that represent the tip of the...

Should supplements be regulated by a competent FDA is a legitamate question. There are too many false claims on supplements and regulation is limited by the FDA. There is also a political aspect involving Big Pharma, physicians, and the supplement industry that gets heated. There are about 10,000 hospitalizations caused by use of supplements, but millions from...

  The regulation of supplements is problematic. We clearly need regulation because supplement companies tend to make statements about what they do that is not proven, but at the same time we also need to have access to using them, especially if they are safe. A balanced regulation is what is needed. MD control of supplements is being suggested; yet they...