Dietary supplements are the most commonly used of all integrative, complementary, and alternative therapies Overview of Integrative, Complementary, and Alternative Medicine Integrative medicine and health (IMH) and complementary and alternative medicine (CAM) include healing approaches and therapies that historically have not been included in conventional, mainstream... read more , primarily because they are widely available, relatively inexpensive, and can be bought without consulting a health care practitioner.
The US Food and Drug Administration (FDA) regulates dietary supplements differently from drugs. The FDA regulates quality control and good manufacturing processes but does not ensure standardization of the active ingredients or efficacy.
The Dietary Supplement Health and Education Act (DSHEA) of 1994 defines a dietary supplement as
Any product (except tobacco)—in pill, capsule, tablet, or liquid form—containing a vitamin, mineral, herb or other plant product, amino acid, or other known dietary substance that is intended as a supplement to the normal diet
In addition, certain hormones, such as dehydroepiandrosterone Dehydroepiandrosterone (DHEA) Dehydroepiandrosterone (DHEA) is a steroid produced by the adrenal gland and is a precursor of estrogens and androgens. Effects on the body are similar to those of testosterone. DHEA can also... read more (DHEA, a precursor to androgens and estrogens) and melatonin Melatonin Melatonin, a hormone produced by the pineal gland, regulates circadian rhythms. It can be derived from animals, but most melatonin is manufactured synthetically. In some countries, melatonin... read more , are regulated as dietary supplements and not as prescription drugs.
The DSHEA requires that the product label identify the product as a dietary supplement and notify the consumer that the claims for the supplement have not been evaluated by the FDA. The label must also list each ingredient by name, quantity, and total weight and identify plant parts from which ingredients are derived.
Manufacturers are permitted to make claims about the product’s structure and function (eg, good for urinary tract health) but cannot make or imply claims for the product as a drug or therapy (eg, treats urinary tract infections). Expiration dates may be included on the standardized product labels if this information is supported by valid data demonstrating that it is not false or misleading.
Safety and Efficacy
The FDA does not require manufacturers of dietary supplements to prove safety or efficacy, although supplements must have a history of safety. Manufacturers and distributors of supplements must report serious adverse events to the FDA through the MedWatch system, a medical product safety reporting program.
Most people who use dietary supplements assume that they are good for health generally, are safe and effective for treating and/or preventing specific conditions, or both. People may think this because dietary supplements are natural (ie, derived from plants or animals) and because some are supported by centuries of use in traditional systems of medicine.
Although more and more clinically based studies are now being done, most supplements have not been rigorously studied. Information about studies being done is available from the NIH National Center for Complementary and Integrative Health (NCCIH).
For most dietary supplements, evidence suggesting safety or efficacy comes from
In vitro studies
Certain case reports
Purity and Standardization
Lack of regulation and government monitoring also means that supplements are not monitored to ensure that they contain the ingredients or amount of active ingredient the manufacturer claims they contain. The supplement may have unlisted ingredients, which may be inert or harmful (eg, natural toxins, bacteria, pesticides, lead or other heavy metals, unapproved dyes), or it may contain variable amounts of active ingredients, especially when whole herbs are ground or made into extracts. Consumers are at risk of getting less, more, or, in some cases, none of the active ingredient, if the active ingredient(s) is even known. Most herbal products are mixtures of several substances, and which ingredient is the most active is not always known.
The lack of standardization means not only that products from different manufacturers may vary, but also that separate batches produced by the same manufacturer may differ. This product variability is a particular source of difficulty in conducting rigorous clinical trials and comparing the results among different trials. However, some supplements have been standardized and may include a designation of standardization on the label.
New regulations governing supplement production in the US include rules for Good Manufacturing Practices (GMPs). These rules strengthen standards for keeping manufacturing facilities and equipment clean and raw materials pure and uncontaminated. GMPs also ensure proper labeling, packaging, and storage of the finished product.
Additional areas of concern include
Use of dietary supplements instead of conventional drugs
Stability of supplements (especially herbal products) once manufactured
Interactions between supplements and drugs or disease states
Contribution to incorrect diagnosis
Most information about these concerns comes from sporadic individual reports (see table ) and some research studies.
Despite these concerns, many patients strongly believe in the benefits of supplements and continue to use them with or without a physician’s involvement. Patients may not think to disclose or may wish to conceal their use of dietary supplements. For this reason, the outpatient history should periodically include explicit questions about past and new use of integrative, complementary, and alternative therapies, including dietary supplements. Many physicians incorporate some supplement use into their practice; their reasons include proven benefit of the supplement, a desire to ensure that supplements are used safely by patients who will use supplements anyway, and the physician’s belief that the supplements are safe and effective.
Common concerns about the use of supplements include the following:
Placebo effects can simulate true efficacy, particularly if the patient and/or physician strongly believes in the supplement.
Therapeutic responses to supplements, placebo-mediated or otherwise, could be mistaken as evidence that confirms a particular, possibly incorrect, diagnosis.
There are few data to guide patient counseling regarding supplement safety. But some experts believe that the overall number of problems due to dietary supplements is rare compared with the overall number of doses taken and that the supplement, if correctly manufactured, is likely to be safe. As a result, these experts advise purchase of supplements from a well-known manufacturer, and many recommend buying supplements made in Germany because there they are regulated as drugs and thus oversight is stricter than in the US.
The supplements discussed in The Manuals are ones that are most popular, are effective, or have some questions about their safety. More complete information is available through the NIH National Center for Complementary and Integrative Health.
The following English-language resources may be useful. Please note that THE MANUAL is not responsible for the content of these resources.
U.S. Food & Drug Administration (FDA), Dietary Supplements: General information about the FDA's regulation of finished dietary supplement products and dietary ingredients
U.S. Food & Drug Administration (FDA), MedWatch: Access to the FDA’s medical product safety reporting program for health professionals, patients and consumers
National Institutes of Health (NIH), National Center for Complementary and Integrative Health: General information on research and information about complementary health products and practices
National Institutes of Health (NIH), Office of Dietary Supplements: Dietary Supplement Health And Education Act of 1994 (DSHEA)
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