Lack of Federal Oversight on Supplements Endangers Lives, Wastes Money

The U.S. Food and Drug Administration (FDA) recently announced its intent to hold a meeting in late March to discuss changes in how it regulates over-the-counter drugs. Although this could be a welcome change, it is clear that a lack of federal oversight regarding other supplements continues to endanger lives. The current review system for over-the-counter medications has been in place since 1972. It is painstakingly slow, with many products on the shelves that are still, technically, under FDA review. This process is nowhere near as strict as the guidelines and requirements in place for prescription medications. So-called dietary supplements, including herbal medications, are completely unregulated by the FDA. This can lead to significant problems. Regulation of drugs is important to foremost ensure their safety. It is imperative that additives and fillers used in their manufacture not be harmful to the consumer. As an example, heavy metals like lead or mercury may contaminate some products. Secondly, the active ingredient, the drug that is being paid for, should be of sufficient quality and quantity to have its intended effects. This depends on manufacturing standards. It can be checked with some simple chemistry, but only if someone is willing to do the quality control analysis. This is a key task for the FDA. Moreover, many dietary supplements, herbal medications, vitamins, and innumerable "health products" are available that make claims that have not been substantiat...
Source: About Sleep Disorders - Category: Sleep Medicine Source Type: news