Because of the uncertain nature of various alternative therapies and the wide variety of claims different practitioners make, alternative medicine has been a source of vigorous debate, even over the definition of "alternative medicine". Dietary supplements, their ingredients, safety, and claims, are a continual source of controversy. In some cases, political issues, mainstream medicine and alternative medicine all collide, such as in cases where synthetic drugs are legal but the herbal sources of the same active chemical are banned.
In other cases, controversy over mainstream medicine causes questions about the nature of a treatment, such as water fluoridation. Alternative medicine and mainstream medicine debates can also spill over into freedom of religion discussions, such as the right to decline lifesaving treatment for one's children because of religious beliefs. Government regulators continue to attempt to find a regulatory balance.
Jurisdiction differs concerning which branches of alternative medicine are legal, which are regulated, and which (if any) are provided by a government-controlled health service or reimbursed by a private health medical insurance company. The United Nations Committee on Economic, Social and Cultural Rights - article 34 (Specific legal obligations) of the General Comment No. 14 (2000) on The right to the highest attainable standard of health - states that
Furthermore, obligations to respect include a State's obligation to refrain from prohibiting or impeding traditional preventive care, healing practices and medicines, from marketing unsafe drugs and from applying coercive medical treatments, unless on an exceptional basis for the treatment of mental illness or the prevention and control of communicable diseases.
Specific implementations of this article are left to member states. Two governments, acting under the laws of their respective countries, maintain websites for public information making a distinction between "alternative medicine" and "complementary medicine". In North America, the National Institutes of Health (NIH) (a part of the U.S. Department of Health and Human Services) states:
In the British Isles, the National Health Service (England)'s NHS Choices (owned by the Department of Health) states:
Maps, Directions, and Place Reviews
Evidence and Efficacy
As alternative medicine becomes more available in the Western world, and is increasingly incorporated into conventional healthcare systems, there is a growing demand for science-based evidence to verify the efficacy of these treatments. In the regulation of alternative medicine, policy makers largely rely on biomedical approaches to evidence, such as the randomized clinical trial (RCT), which has been embraced as the 'gold standard' for assessing the effectiveness of all medicine and medical practices. While undoubtedly a useful scientific tool of analysis, the RCT, in its reductionist nature, can present difficulties in assessing those medicines falling outside of the biomedical framework. The RCT, which only measures a small set of symptoms and effects, diminishes the complexity that is involved in the healing systems of some alternative medicines, such as in homeopathy. Additionally, what constitutes as 'evidence' can vary greatly, ranging from the biomedical goal of establishing concrete, statistical results according to scientific criteria to a more holistic approach that examines the effects that a treatment has upon the patient's overall life experience, including social, cultural, and physical factors. In order to gain a more accurate picture of the true efficacy of alternative medicines, it is necessary to challenge the mainstream, biomedical definition of 'evidence' and to move outside of the exclusive use of the RCT in obtaining this evidence. Therefore, it may be useful to consider incorporating other forms of research, such as qualitative and ethnographic studies, in the regulation of alternative medicines. The Formal Case Study (FCS), a systematic, qualitative research technique, has also been suggested as a feasible compromise between biomedical and anthropological approaches in researching alternative medicines.
Alternative Medicin Video
United States
In the United States the Food and Drug Administration's online warnings for consumers about medication health fraud includes a section on Alternative Medicine Fraud, such as a warning that Ayurvedic products generally have not been approved by FDA before marketing.
A number of alternative medicine advocates disagree with the restrictions of government agencies that approve medical treatments. In the United States, for example, critics say that the Food and Drug Administration's criteria for experimental evaluation methods impedes those seeking to bring useful and effective treatments and approaches to the public, and that their contributions and discoveries are unfairly dismissed, overlooked or suppressed. Alternative medicine providers recognize that health fraud occurs, and argue that it should be dealt with appropriately when it does, but that these restrictions should not extend to what they view as legitimate healthcare products.
Texas
In the state of Texas, physicians may be partially protected from charges of unprofessional conduct or failure to practice medicine in an acceptable manner, and thus from disciplinary action, when they prescribe alternative medicine in a complementary manner, if board specific practice requirements are satisfied and the therapies utilized do not present "a safety risk for the patient that is unreasonably greater than the conventional treatment for the patient's medical condition."
New Zealand
In New Zealand, alternative medicine products are classified as food products, so there are no regulations or safety standards in place.
Australia
In Australia, the topic is termed as complementary medicine and the Therapeutic Goods Administration has issued various guidances and standards. Australian regulatory guidelines for complementary medicines (ARGCM) demands that the pesticides, fumigants, toxic metals, microbial toxins, radionuclides, and microbial contaminations present in herbal substances should be monitored, although the guidance does not request for the evidences of these traits. However, for the herbal substances in pharmacopoeial monographes, the detailed information should be supplied to relevant authorities
The production of modern pharmaceuticals is strictly regulated to ensure that medicines contain a standardized quantity of active ingredients and are free from contamination. Alternative medicine products are not subject to the same governmental quality control standards, and consistency between doses can vary. This leads to uncertainty in the chemical content and biological activity of individual doses. This lack of oversight means that alternative health products are vulnerable to adulteration and contamination. This problem is magnified by international commerce, since different countries have different types and degrees of regulation. This can make it difficult for consumers to properly evaluate the risks and qualities of given products.
Denmark
In Denmark, herbal and dietary supplements is the designation of a range of products, which have in common their status as medicine belonging under the Danish Medicines Act. In the Danish Medicines Act there exist four types of herbal and dietary supplements: Herbal medicinal products, Strong vitamin and mineral preparations, Traditional botanical medicinal products and Homeopathic medicinal products. Some dietary supplements fall within a special category of products, which differ from the above in that they are not authorized medicinal products. Dietary supplements are regulated under the Food Act and are registered by the Danish Veterinary and Food Administration.
Alternative therapists
Denmark has a registration system for alternative therapy practitioners, RAB.
Switzerland
The Swiss Federal Constitution prescribes that the Confederation and the Cantons shall, within the scope of their powers, ensure that consideration is given to complementary medicine.
United Kingdom
Safety, quality and efficacy are the only criteria on which United Kingdom legislation is founded to control human medicines. Regulation of medicines and medical devices, to ensure they work and are acceptably safe, is the responsibility of the Medicines and Healthcare products Regulatory Agency. The legal status of medicines is determined under the Medicines Act 1968 and European Council Directive 2001/83/EC which control the sale and supply of medicines. The legal status of medicinal products is part of the marketing authorisation which allows products to be available on a prescription (referred to as Prescription Only Medicines), or in a pharmacy without prescription under the supervision of a pharmacist, or on general sale and saleable in general retail outlets without the supervision of a pharmacist.
There are 12 organisations in the United Kingdom known as health and social care regulators. Each organisation oversees one or more of the health and social care professions by regulating individual professionals across the UK. The General Medical Council is one of these, for medical practitioners who as physicians are registered and licensed to practise under the Medical Act 1983. Councils for other practitioners include the General Chiropractic Council under the Chiropractors Act 1994 and the General Osteopathic Council under the Osteopaths Act 1993.
Source of the article : Wikipedia
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