No Double Standards For Natural Health Products
Main Category: Complementary Medicine / Alternative MedicineAlso Included In: Public Health; Regulatory Affairs / Drug Approvals
Article Date: 16 Nov 2011 - 0:00 PST
Natural health products and medicinal foods should be subject to the same regulations as pharmaceutical drugs to ensure safety and efficacy, states an editorial in CMAJ (Canadian Medical Association Journal).
While pharmaceutical drugs are subject to rigorous evaluation and must provide significant evidence of their therapeutic effects and that the benefits outweigh risks, natural health products in Canada are not. Many contain active pharmacological substances that can have potent effects and interactions which should have warnings.
"The multibillion-dollar natural health products industry sells the perception that because its products are "natural," they must also be safe, such that comprehensive testing like that required for pharmaceuticals is not required," write guest author Dr. Stuart MacLeod with CMAJ editor Dr. Matthew Stanbrook and colleagues. "However, it is a near-universal truth that any substance that exerts a beneficial effect on a biological system will also have the potential for adverse effects."
Health Canada created the Natural Health Products Directorate 10 years ago, but the regulatory framework that governs it does not protect the consumer.
"All health claims for any product should be subject to a common set of regulations, starting with consistent and easily understood standards of evidence proportional to health risks and benefits," conclude the authors.
"Uniform regulations are the best way to protect consumers while still allowing choice."
Visit our complementary medicine / alternative medicine section for the latest news on this subject.
MLA
23 Feb. 2012. <http://www.medicalnewstoday.com/releases/237669.php>
APA
http://www.medicalnewstoday.com/releases/237669.php.
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Canada Needs to Keep up With Current Research & Opinion!
posted by Dr Alyssa Burns-Hill on 17 Nov 2011 at 1:00 amThis is yet another go at CAM (Complementary & Alternative Medicine), which is under mounting pressure from pharmaceutical giants. Here's a very brief response ...
The BMJ website, Clinical Evidence, was established to examine the evidence for drug treatments to help patients and doctors make better informed decisions about their use of drugs, it reviews 2500 medical treatments. The data reveal that only 13% of treatments were found to be of definite benefit to the patient: 23% may be beneficial; 8% are a trade off between harm and potential benefit; 6% are deemed unlikely to be beneficial, and 4% are likely to be ineffective or harmful. The remaining 46% were assessed to be of unknown effectiveness (BMJ,2009).
Secondly, an expert opinion, that of Dr Allen Roses (worldwide vice-president of genetics at GlaxoSmithKline), which was highly publicised in 2003 - "The vast majority of drugs - more than 90% - only work in 30 or 50% of the people."
Therefore, does the pharmaceutical industry provide significant evidence of drugs' therapeutic effects or that benefits outweigh the risks?
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