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Vitamins and Minerals: The Health Care Industries Big Deep Secret

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There is no doubt that vitamins and minerals are critical to good health. Vitamins are carbon-containing substances derived from living things. They are used by the body in tiny amounts to build, maintain, and repair tissues. For example, the various compounds dubbed vitamin A are used in eye tissues for vision, and in cell nuclei to aid gene expression, among other functions. Vitamin D is needed for bones to develop properly, and the B vitamin folic acid aids in the digestion of amino acids and plays a role in the metabolism of deoxyribonucleic acids (DNA) and ribonucleic acids (RNA). DNA is genetic material that codes instructions for the production of proteins—the basic building blocks of life; RNA is a molecule that helps carry out those instructions.


Unlike vitamins, minerals are inorganic (not bound to carbon). They come from soil and water, but make their way into the plants and animals people eat. Essential minerals include calcium, phosphorous, magnesium, iron, zinc, iodine, and selenium. These minerals have myriad biological roles. Some work in enzymes, protein “tools” that make possible many critical biological processes. Others enable blood to carry oxygen to the body's tissues; strengthen bones and teeth; help cells grow and repair themselves; or keep the heart beating properly.


The RDAs – Recommended Daily Allowances

Unlike macronutrients—the fats, proteins, and carbohydrates people burn for energy—vitamins and minerals are used by the body in much smaller quantities. How much of these micronutrients do people need? That depends on the nutrient and on the person. However, general guidelines known as Recommended Dietary Allowances, or RDAs, are set by the Food and Nutrition Board of the National Academy of Sciences (NAS), a scientific advisory council for the U.S. government.

Recommended Daily Allowances - RDAs, which are revised about once every five years, are educated guesses about nutrient requirements based on evidence gleaned from studies in large human populations, test-tube experiments, and everything in between. In setting RDAs, scientists account for the body's inability to completely digest or absorb certain vitamins and minerals in foods or pills, and include a margin of safety.


RDAs are, in most cases, designed to prevent nutrient deficiency diseases such as scurvy, caused by a lack of vitamin C, and goiter, resulting from too little iodine. The consequences of such diseases can be serious. In scurvy, the gums become spongy, the teeth loosen, and tiny blood vessels called capillaries bleed into the skin and mucous membranes. Goiter, an enlargement of the thyroid gland at the base of the neck, can lead to a type of mental retardation known as cretinism.


Are Recommended Daily Allowances - RDAs Adequate?

In America, severe micronutrient deficiencies are rare, because most Americans' diets are good enough to prevent them. That does not mean Americans' diets are necessarily good, however. High in fat and low in fruits and vegetables, the typical American diet may be contributing to chronic ailments such as cancer and heart disease. Indeed, many experts believe it is a lack of certain vitamins and minerals in the foods Americans eat that raises their risk of chronic ailments.


In a few cases, the RDA reflects this notion. For instance, the RDA for calcium is set at a level to ward off a disease of weakened bones called osteoporosis that usually shows up in old age. But the RDA for many nutrients may be too low to stave off certain illnesses. Some studies even suggest that truly protective doses far exceed what a person could eat in a day and thus, supplements are necessary.

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The Folic Acid Story

An argument for supplements could certainly be made for folic acid; a B vitamin that recent evidence has shown can prevent certain deadly or paralyzing birth defects and may also ward off heart disease. The RDA for folic acid, also called folate, is 200 micrograms for adult men and 180 micrograms for adult women. (A microgram is one-thousandth of a milligram.) However, many experts now recommend that all women of child-bearing age consume at least 400 micrograms of folate a day to prevent birth defects.


What is the basis for this recommendation? Controlled studies (studies that include control groups) have shown that women who took folic acid supplements when they conceived were far less likely to give birth to infants with neural tube defects such as anencephaly, in which the brain does not develop fully, or spina bifida, when the spinal cord does not completely close. Folic acid, it appears, is critical for the closure of the neural tube, the tissue that encloses a developing embryo's brain and spinal cord.


Folate is also used by the body to break down an amino acid called homocysteine, and that role is critical to its presumed ability to prevent heart disease. In large amounts, homocysteine is thought to scar arteries and cause them to clog, leading to heart attacks. Recent studies have shown that people with high homocysteine levels are at increased risk for heart disease. Other recent work has indicated that people with low blood levels of folic acid are likewise at increased risk. Folate supplements can lower homocysteine levels. However, no one has yet shown that taking folic acid supplements prevents heart attacks and prolongs lives.


Thus, the American Heart Association (AHA) still recommends getting folic acid from foods such as leafy green vegetables, beans, and orange juice instead of supplements, since these foods have other beneficial nutrients as well. But since most Americans do not consume even the RDA for folic acid, women of childbearing age are advised to take supplements, especially since the folic acid in supplements is better absorbed than that in foods. By January 1, 1998, the FDA will require all grain products sold in the United States to be fortified with folic acid.

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The Antioxidant Debate

Scientists have also been turning up evidence suggesting that large doses of vitamins E and C and beta-carotene, a substance the body converts into vitamin A, may prevent chronic illnesses such as heart disease and cancer. These nutrients are thought to “mop up” unstable chemicals in the body known as free radicals that can damage tissues and contribute to disease.


Free radicals are formed all the time—whenever the body uses oxygen or is exposed to a toxin such as cigarette smoke—and can harm cells in a number of ways. They can chemically alter fats in low-density lipoproteins (LDL) (components in the blood that carry cholesterol), making them more likely to clog arteries. Free radicals can also damage DNA, possibly raising the risk of cancer.


Vitamins C and E and beta-carotene are thought to work as antioxidants, molecules that block the formation of free radicals and thus lower the risk of heart disease and cancer. What is the evidence for this theory? Numerous studies have shown that people who eat lots of fruits and vegetables—the major sources of many antioxidant nutrients—have a lower risk of heart disease than those who do not. Similarly, a lot of research indicates that people whose diets are produce-poor have a higher risk of several kinds of cancer.


While those studies strongly support the recommendations of the National Cancer Institute (NCI) to eat at least five servings of fruits and vegetables a day, they do not prove that isolated antioxidants in the form of supplements provide disease protection. Although test tube and animal studies do suggest benefits from antioxidant supplements, the evidence in people has been mixed. Here is a rundown.

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Vitamin E and Heart Disease
Will large doses of vitamin E protect against heart disease? Several lines of research seem to indicate so. In one, scientists examined whether vitamin E supplements caused favorable changes in blood chemistry—such as lowering levels of oxidized LDL. In the February 1995 issue of the journal Arteriosclerosis, Thrombosis, and Vascular Biology, Texas scientists described results from testing the blood of 48 men who had been given various daily doses of vitamin E. They found that doses of 400 International Units (IU) (about 27 times the RDA for men) produced significant protection against the oxidation of LDL particles in their blood.


Such research does not say whether vitamin E can prevent heart disease. That is left up to studies that follow people for years and associate vitamin E intake with heart disease incidence. Three major studies have shown that taking daily vitamin E supplements of at least 100 IU for two years or longer reduced the risk of heart disease by almost half.


But even those studies are not definitive: While they associate vitamin E intake with low disease rates, they do not show cause and effect. That is because people who take vitamins often have other healthy habits—such as exercising and eating a balanced diet—that could explain the lowered disease risk. The best type of evidence is a so-called intervention trial in which participants are given supplements or placebos and followed for a period of many months to many years to determine the incidence of disease in the two groups.


So far, just one small study of this type has examined the effects of vitamin E on heart disease. Published in the March 23, 1996, issue of the British medical journal The Lancet, Cambridge University researchers in England found a more than 75 percent reduction in nonfatal heart attacks among people who took from 400 to 800 IU of vitamin E for a little more than a year. However, the vitamin did not appear to prevent deaths from heart attacks: There was a slight increase in the percentage of patients who had fatal heart attacks, 2.6 percent in those on vitamin E vs. 2.4 percent in those on placebo. Several larger human studies currently underway promise to shed more light on the effects of vitamin E on heart disease.


Beta-Carotene and Cancer

Earlier research showing associations between intake of beta-carotene and reduced cancer incidence have not held up in the latest intervention trials. One of these trials, the Beta Carotene and Retinol Efficacy Trial (CARET), was halted in January 1996 because preliminary results indicated that a combination of beta-carotene and vitamin A was not preventing lung cancer in high-risk men and women and may actually have been harming study participants. Published in the May 2, 1996, New England Journal of Medicine, the study found 28 percent more lung cancers and 17 percent more deaths in participants taking 30 mg of beta-carotene and 25,000 IU of vitamin A.

This result was similar to that found in two other trials. Researchers conducting the Physicians' Health Study reported in the same issue of the New England Journal that they found no benefit or harm from beta-carotene on cancer or heart disease. And the 1994 results of the Alpha-Tocopherol, Beta-Carotene Lung Cancer Prevention Trial, published in the same journal on April 14, showed 18 percent more lung cancers and 8 percent more deaths in smokers who took 20 mg of beta-carotene daily for five to eight years.


Not all of the intervention trials have reported negative results, however. In 1993 a study published in the September 15 Journal of the National Cancer Institute suggested that a combination supplement of beta-carotene, vitamin E, and selenium reduced the stomach cancer mortality rate by 21 percent on average among subjects in Linxian, China.

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Vitamin E: Foods or Supplements?

Many scientists and physicians are excited about the recent results from studies of vitamin E and heart disease and are taking E supplements themselves. However, given the contradictory nature of much of this data, especially the beta-carotene and cancer work, other experts are cautious in recommending antioxidant supplements for the prevention of chronic diseases. A better option, they say, is to get as many of these nutrients as possible from foods. Indeed, that is the official word from the NAS, the AHA, and the NCI.


What might be better about fruits and vegetables? The micronutrients identified so far may not actually be the protective ones or foods may contain other chemicals that magnify a nutrient's protective effect. In some cases, evidence indicates that the form of a nutrient in foods is better absorbed than the form that comes in pills or powders. Calcium in milk and other dairy products, for example, is known to be better absorbed by the body than in pill form.


Potential Dangers

Taking high doses of certain supplements can be dangerous. Although they are not called drugs, vitamins and minerals at high doses act like drugs and can have drug-like side effects. For example, it is known that doses of vitamin A above 25,000 IU can cause, among other things, severe liver damage, bone diseases, and, when taken by pregnant women, birth defects. Recent evidence has shown that doses even as low as 10,000 IU can cause some types of birth defects.

Other vitamins can also be toxic. Taking more than 100 mg per day of vitamin B6—a whopping 50 times the RDA—can harm the nervous system, causing problems with balance and altered sensations. Nevertheless, this vitamin often is sold in capsules containing 100 mg to 500 mg. And niacin, which comes in supplements of 250 mg, 400 mg, and 500 mg, can trigger vomiting, diarrhea, and even liver damage, among other maladies, in doses of 500 mg from slow-release formulations and 750 mg from immediate-release pills.

Toxicity also has been associated with high doses of iron, selenium, and even vitamin C. Folic acid doses above 1 mg can mask symptoms of vitamin B12 deficiency, a rare condition that is most often seen among the elderly and some strict vegetarians. If it goes undetected, vitamin B12 deficiency can lead to irreversible nerve damage. There may be unidentified dangers as well. While doses of vitamin E up to 800 IU appear to be safe for most healthy people, it will take long-term studies of the use of vitamin E, involving thousands of people, to know whether high doses are safe for everyone.

Doses of supplements go largely unregulated because of the 1976 Proxmire Amendment to the Federal Food, Drug, and Cosmetic Act. One provision of this amendment prohibits the FDA from establishing a maximum daily dose unless the agency can prove there is a health hazard.
Herbal Remedies
Unlike vitamins, which consumers use primarily for prevention, herbs are typically used as treatments, for everything from colds to cancer. Unrefined herbs—the leaves, bark, flowers, berries, or roots of plants—are not yet a part of mainstream U.S. medicine. But they are in other countries.

In China, herbal remedies—such as Yin Chiao, an herbal formulation used to treat colds, and stephania, a root used for weight loss—dominate medical practice. European doctors also readily incorporate herbs into their practices. In Germany, a concentrated extract made from the leaves of the ginkgo tree is used as a treatment for headaches and tinnitus (a ringing in the ears), among other maladies. In the South Sea Islands, tea-tree oil, pressed from the leaves of a tropical tree, has been used for centuries as a skin antiseptic.

In the United States, herbal remedies have caught on among the general public, if not physicians. Experts say that herbal remedies or “botanicals” are the fastest growing segment of the supplement market. Their appeal lies largely in the word “natural.” But natural is not a synonym for safe. It does not mean the stuff works, either.


Do Herbs Work?

Some herbs probably are effective. After all, about 25 percent of U.S. prescription drugs are derived from plants. For example, digitalis, the heart-muscle strengthener, is an herb derived from a plant called foxglove, and taxol, a cancer treatment, comes from the Pacific yew tree. To date, the FDA has judged at least 16 herbs as safe and effective, allowing them to be sold over the counter as drugs. These include elm bark, sold as Throat Coat Tea, and the laxatives senna, marketed under the brand name Senokot, and psyllium seeds, sold under the label Metamucil.

That still leaves hundreds of herbs sold in the United States whose effectiveness is unproven. For instance, there is little documentation for the purported ability of a Chinese root called ginseng to build up the body's resistance to stress and disease and to enhance sexual potency. Similarly, garlic's power to strengthen the immune system, prevent cancer, or unstuff sinuses remains highly controversial.

Still, that does not mean that these herbs and others do not do something to the body. In fact, ingredients in some products sold as herbs are similar to over-the-counter drugs. White willow bark, for instance, is a lot like aspirin. Both belong to a class of compounds called salicylates and so have similar effects on the body. And the Chinese herb Ma Huang, derived from an evergreen plant of the genus Ephedra, contains ephedrine, a stimulant used in many over-the-counter and prescription drugs.


Are They Safe?

Because herbs are not required to undergo safety tests, it is difficult to be sure any are completely safe. The safest herbs are those for which no one has reported toxic effects. Examples of such herbs include ginger, milk thistle, and garlic. The absence of negative reports about a substance is not, however, proof of safety, since people do not always associate their symptoms with herbs they are taking. Thus, many adverse effects probably go unnoticed and unreported.

Meanwhile, many herbs known to be toxic remain on the market. One such herb is a desert shrub called chaparral. In the February 8, 1995, Journal of the American Medical Association (JAMA), doctors reported severe liver damage in a 60-year-old woman who had taken capsules of a chaparral extract for 10 months for its supposed antioxidant properties. The woman experienced no symptoms before becoming seriously ill with liver failure; she eventually needed a liver transplant.
Ma Huang is perhaps the best known example of herbal toxicity of late.

Containing ephedrine, a stimulant that can harm the nervous system and heart, Ma Huang is a component in dietary supplements that manufacturers claim will promote weight loss and boost energy. In some cases, it is supposed to produce a natural “high” like that from illegal drugs such as “ecstasy.” Its harmful effects range from dizziness, headaches, and stomachaches to heart attacks, strokes, seizures, and death. So far, more than 600 reports of injuries and 17 deaths linked to ephedrine products have poured into the FDA.

The majority of injuries were reported by women taking weight-loss formulations containing the substance.

Herbs can also pose risks because they are unregulated and thus bear no warning labels mentioning side effects or safe dosages. For instance, consumers are not told on a package of white willow bark that this herb, like aspirin, can upset the stomach, cause bleeding during pregnancy, increase the risk of a stroke, or spawn Reye's syndrome, a serious illness appearing in some feverish children given aspirin.


In addition, herbal products are not subject to careful quality control; thus, undesirable substances can sneak in without anyone knowing. Ayurvedic herbs, made in India and used in traditional Hindu medicine, are boiled in clay or metal pots, which can leave behind traces of toxic substances such as lead, mercury, or arsenic. And sometimes products contain misidentified plant parts. In the early 1990s, 70 women at a clinic in Belgium took an herb for weight loss that clinic administrators thought was stephania. Instead, it was a toxic plant, called aristolochia, that poisoned their kidneys.

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Amino Acids Supplement

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Amino acid supplements are, like herbs, largely unstudied and unregulated; thus, as a group, their safety and efficacy cannot be assured. Still, Americans are downing them for undocumented promises, ranging from building muscles to calming jittery nerves. Last year, amino acid supplement sales rang up about $400 million in the United States, estimates Euromonitor International.

Should anyone be taking amino acid supplements? There is certainly no health reason to do so, according to many experts. The body does need amino acids, which it uses to build proteins and to make other vital molecules including those that send messages in the brain. However, most Americans are highly unlikely to face a shortage. Of the 20 amino acids that make up animal and plant proteins, the body can manufacture all but 9. And all of those 9—histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine—are typically plentiful in the diet in the form of proteins.


Nearly all Americans eat the RDA for protein many times over. Thus, people are not popping amino acid supplements because they are worried about meeting their protein requirement. They are after druglike effects. Some are amateur bodybuilders looking for legal, muscle-building alternatives to steroids (illegal drugs derived from the male hormone testosterone that are believed to increase muscle size and power). Others are less concerned about brawn than brain: They take high-potency supplements of single amino acids to give them more energy, calm them down, or even make them smarter.


Do They Work?

Many of the claims have logic behind them. Amino acids make up proteins and proteins pack muscle, so it is theoretically possible that some amino acid mixtures could help increase muscle mass. However, they certainly will not have that effect in the absence of weight training or other muscle-building exercises. And even when combined with exercise, the evidence that amino acid supplements are beneficial is tenuous at best, top scientists say. A more likely effect of taking such supplements, they add, is nitrogen-rich urine, since amino acids contain nitrogen.


Taking large doses of single amino acids could, in some cases, affect the brain, experts say. Overloading the body with a single amino acid can cause more of that amino acid to enter the brain, where it may be used to make neurotransmitters, chemicals that carry messages between brain cells and influence mood. For instance, the amino acid tryptophan is used to produce the neurotransmitter serotonin, which can have a calming or sleep-inducing effect. And a few studies suggest that tryptophan can have a sedative effect on humans; it may also suppress appetite. But consumers no longer can find this supplement on store shelves. The FDA banned its sale because of the substance's potential toxicity.


Although some amino acids may turn out to be useful drugs, the evidence supporting their purported effects is still slim. And some of those claims are downright fanciful. For instance, experts discount the possibility that any amino acid supplement could influence such a broad-based brain function as intelligence. Even for amino acids such as tryptophan that may indeed alter mood, no one knows what the effective—and safe—doses are.


Are They Safe?

Indeed, the biggest question about amino acid supplements is safety. In humans, short-term studies have shown that high doses of some amino acids are safe—up to a point. To date, however, scientists have not established safe intake levels for any amino acid.


Animal studies have suggested that amino acids may be harmful. In large doses, single amino acids can depress the growth of lab animals, change their brain chemistry, and cause damage to organs such as the pancreas and kidneys. The reason, experts say, is that a particular balance of various amino acids is crucial for the health of many body organs; thus, taking a lot of one amino acid can upset this balance and damage organs from the liver to the brain.


At least two amino acids in dietary supplements have been associated with serious injuries in healthy people, according to the FDA. The use of phenylalanine has been linked to various ailments including scleroderma, a disease in which fibrous connective tissue accumulates in the skin and often internal organs.


But the most famous example of amino acid toxicity is the tryptophan scare of 1989. That is when public health officials tied tryptophan supplements to an outbreak of a rare, painful muscle disease called eosinophilia-myalgia (EMS) that sickened 1500 people and killed 38. Studies later suggested the illness was due to impurities in a particular tryptophan product. However, the FDA has not ruled out tryptophan as the cause.

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Supplements: The Regulatory Picture

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Under current law, such potentially hazardous products can easily wind up on the market. Dietary supplements have never had to stand up to the scrutiny that drugs do, meaning they do not have to be approved—or even evaluated—by the government before they are sold. Recently, with the passage of the Dietary Supplement Health and Education Act (DSHEA) in October 1994, supplement manufacturers received even wider latitude in the claims they can make. The act also expands the definition of dietary supplement to include a greater range of substances within this loosely regulated realm.


Traditionally, dietary supplements were considered to be only vital nutrients such as vitamins and minerals. In 1990 the Nutrition Labeling and Education Act (NLEA), which established rules for ingredient lists and health claims on foods, added “herbs, or similar nutritional substances” to the definition of dietary supplement. DSHEA expanded that definition further to include chemicals such as amino acids, fish oils, enzymes, mixtures of these, and even drugs that were marketed as supplements or food before they were approved as drugs.


How does the FDA ensure that all these products are safe? It does not, for the most part. At times, the FDA has tried to exert tighter control. Twenty years before the tryptophan tragedy, there was a move to ban amino acids from the marketplace. However, that and other efforts of the 1960s and 1970s—including one to regulate high-dose vitamins and minerals as drugs—failed due to red tape, court challenges, and ultimately, the Proxmire Amendment.


Still, for many years, supplements were regulated much like foods. As it can with foods, the FDA could challenge whether there were adequate data to support the safety of a new ingredient in a supplement before it hit the market. Now though, under DSHEA, manufacturers no longer have to provide evidence that a new supplement is safe before it is sold. Just about any sort of supplement can be sold. To take a product off the market, the FDA must prove that the product is unsafe.


The FDA will soon, however, exert some control over the purity and quality of supplements. The agency is now drafting a document that outlines “good manufacturing practices” (GMPs) for the preparation, packing, and storage of supplements. DSHEA granted the FDA the authority to set up GMPs, but the approved rules probably will not be finalized for at least two years.


Labels
Under DSHEA, the FDA still retains some control over what a supplement can say on its label, especially in the area of health claims, which specify a relationship between a substance and a disease. To make a health claim for a supplement, a manufacturer must get approval from the FDA, which will grant it only when there is “significant scientific agreement” that the claim is true. So far, the FDA has authorized only two health claims for supplements: calcium's ability to prevent osteoporosis and folic acid's ability to reduce the risk of neural tube defects.


But “nutritional support statements” are another story. Under this second category of claims, allowed only on dietary supplements, a claim can describe the supplement's effect on the structure and function of the body, the biological mechanism by which the supplement acts, and effects on well-being. It can also describe a benefit relating to a nutrient deficiency disease.


Before DSHEA, structure and function claims would have implied that a product was a drug and would have allowed the FDA to regulate it as such. Now, however, a label can tout, for instance, that a supplement “makes joints feel better” or “helps you sleep”—as long as it does not mention a benefit for a specific ailment such as arthritis or insomnia. Manufacturers must notify the FDA that they are making a nutritional support statement. They are supposed to have data to substantiate it, but do not have to supply this to the FDA. Instead, the FDA must prove that a statement is false or misleading.


Enforcement

Although the FDA still has the authority to crack down on unsafe products or misleading labels, it only has the resources to do so in the most egregious circumstances. That is because taking action requires preparing a legal case and taking it before a judge. Nevertheless, the agency is now marshaling its troops to fight ephedrine.


By the end of 1996 FDA officials plan to institute restrictions on ephedrine formulations. These could range from setting a maximum allowable dose—which would undoubtedly be far below that in supplements such as Herbal Ecstasy—and mandating specific warning labels, to establishing standards for the active ingredient, whose form now varies between products. The FDA could ultimately ban ephedrine, but that would take more regulatory firepower than the FDA has plans to assemble just now.


The Upshot: Buyer Beware

For the many untested pills, capsules, powders, and liquids that remain on the shelves, it pays to be cautious. Here are a few tips for dealing with the supplement conundrum.
*Bone Up: Before taking a supplement, find out what evidence supports its advertised benefits—and dangers. It is a good idea to glean information from a variety of sources, not just one book or magazine article.

*Do Not Overdo It: Learn what scientists know about safe dosages and do not exceed them. In particular, do not use a large variety of herbs on a regular basis. There are no data on the safety of any botanical when combined with another herb or drug.

*Do Not Trust the Label: It can make any number of claims that are not backed by good science or, in some cases, any science at all. Do pay attention to the print that reads: “This statement has not been evaluated by the Food and Drug Administration.”

*Discuss Supplement Use With a Doctor: Inform a doctor about supplement use, including vitamins. Pregnant women and people with genetic defects that impair their ability to metabolize a nutrient should not use any supplements without approval or recommendation from their physicians.

*Consider Food: When possible, it is generally better to get nutrients from food than from supplements. Consumers should learn what foods supply those they need most and include them in their diet.

*Report Adverse Reactions to FDA: Anyone who believes he or she has symptoms related to dietary supplement use should call 1-800-332-1088 or 1-800-332-4010.


Dietary Supplements: What is Safe, What is Risky?

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The use of dietary supplements has skyrocketed in recent years. Increasingly, people are taking herbs and other “natural” substances in addition to vitamins and minerals. Nutritional supplements are not as strictly regulated by the government as drugs, however, and to use them wisely consumers should know about the risks and benefits associated with supplements. A special feature in the October 1996 installment of the Encarta Yearbook explored this issue.

Dietary Supplements: They are billed as “brain power,” immune power,” weight-loss wonders, broccoli in a bottle, muscle-expanding elixirs, and much more. They can be plucked from the shelves of health food stores, drug stores, and supermarkets. They are dietary supplements—a category that used to include just vitamins and minerals but now also encompasses herbs, amino acids, fish oils, hormones, and many other substances.


Not only is the array of supplements dazzling, but also their popularity is soaring. In 1995 sales of vitamins and minerals alone in the United States reached $4.1 billion, up nearly 20 percent over the previous year, according to Euro monitor International, a market research firm. The more exotic substances—herbs such as ginkgo and Echinacea and hormones such as melatonin—have drawn an even more impressive crowd. In 1995 Americans spent $2.7 billion on herbal remedies. That represents a 65 percent increase from 1993, reports Euromonitor.

Why all the hoopla? Americans have always been interested in healthful products, but their eagerness to try vitamins and natural remedies has gotten a lift lately. Part of the reason is rising medical costs, which encourages both prevention and self-care. But in addition, science has lent credence to a handful of the claims made for dietary supplements. Some studies have suggested, for example, that vitamins may help prevent serious illnesses such as heart disease and cancer.

All this has fed a media frenzy regarding the latest research into natural remedies. At the same time, supplements of all kinds have moved from niche retailers such as health food stores into drugstores and supermarkets, making them more widely available and also more appealing to the mainstream public. And the claims are appealing indeed—to everybody from athletes to people with chronic diseases—and they go far beyond what science has shown. Here are some of them:

*For vegetable haters, “Broccoli Extract” and “Vital Veggies” promise the natural disease-fighting potential of produce—without, of course, the taste.
*The mineral chromium picolinate allegedly promotes weight loss, prevents or reverses diabetes, reduces cholesterol, and builds muscle.
*Garlic is supposed to lower cholesterol levels and blood pressure, boost a weakened immune system, unstuff sinuses, and ward off some cancers.
*Dong quai, a root from China, will supposedly relieve menstrual cramping and other “female” ailments.
*Amino acid mixtures suggest a power to produce muscle-bound individuals without barbells or sweat.


While a few of the claims have scientific backing, most do not. And many supplements have unmentioned, but documented, dangers. Even ordinary vitamins such as vitamin A and niacin (a B vitamin) can produce gruesome ailments from birth defects to liver damage at excessive doses. And the recent spate of illnesses and deaths from the stimulant ephedrine, sold in druglike potions under such brand names as Herbal Ecstasy and Ultimate Xphoria, underscores the potential risks from taking herbs that have not been studied for possible side effects.


There are no safeguards or guarantees. Government regulatory agencies do not sanction these pills nor do they evaluate most of what is written on or inside their bottles. Unlike over-the-counter drugs such as aspirin, dietary supplements are only very loosely regulated by the Food and Drug Administration (FDA). In fact, supplement manufacturers have more leeway than food producers and can legally print all manner of unsupported claims on their labels.


Many nutrition scientists are skeptical of these claims, even those supported by sound scientific reasoning and a smattering of studies. Why? Only rarely does a consistent body of research, including large studies in humans, buttress a health claim for a vitamin, mineral, or herb. For instance, chemical analysis shows that dong quai contains compounds known to expand blood vessels (which may help relieve cramps), but no study of its effect on humans supports this claim. The evidence for the benefits of chromium picolinate and garlic is conflicting, and the claims made for vegetable pills and amino acids are little more than wishful thinking, top scientists say.


Some people seem to be helped by supplements that prove ineffective in scientific studies. That is often because of something called the “placebo effect,” in which a substance works only because a person believes it works. The placebo effect is quite real, and because of it, all reliable studies include a control group, a group of people who get dummy pills or sugar syrups instead of the real thing. By comparing the control group to subjects who get the substance under study, scientists can see whether the supplement has a genuine biological effect or is no better than a placebo.

Organo-natural Based Supplement Medicine/Prescription Drugs Guide

Dietary Supplements: What is Safe, What is Risky?

We Reviewed and Recommend: Based on the organic nature of the supplements, they are completely metabolized, utilized and eliminated from the body without any side effects or adverse effect, hence we recommend:
1. Organo-natural Based Supplement Medicine/Prescription Drugs Guide
2. Organic Liver Detoxifying Supplement Base for immunity boosting and suppress ailments, sicknesses and disease
3. Women Friendly Multivitamins food supplement
4. Natural/Organic based pain relieving Agents:


The use of dietary supplements has skyrocketed in recent years. Increasingly, people are taking herbs and other “natural” substances in addition to vitamins and minerals. Nutritional supplements are not as strictly regulated by the government as drugs, however, and to use them wisely consumers should know about the risks and benefits associated with supplements. A special feature in the October 1996 installment of the Encarta Yearbook explored this issue.

Dietary Supplements: They are billed as “brain power,” immune power,” weight-loss wonders, broccoli in a bottle, muscle-expanding elixirs, and much more. They can be plucked from the shelves of health food stores, drug stores, and supermarkets. They are dietary supplements—a category that used to include just vitamins and minerals but now also encompasses herbs, amino acids, fish oils, hormones, and many other substances.


Not only is the array of supplements dazzling, but also their popularity is soaring. In 1995 sales of vitamins and minerals alone in the United States reached $4.1 billion, up nearly 20 percent over the previous year, according to Euro monitor International, a market research firm. The more exotic substances—herbs such as ginkgo and Echinacea and hormones such as melatonin—have drawn an even more impressive crowd. In 1995 Americans spent $2.7 billion on herbal remedies. That represents a 65 percent increase from 1993, reports Euromonitor.

Why all the hoopla? Americans have always been interested in healthful products, but their eagerness to try vitamins and natural remedies has gotten a lift lately. Part of the reason is rising medical costs, which encourages both prevention and self-care. But in addition, science has lent credence to a handful of the claims made for dietary supplements. Some studies have suggested, for example, that vitamins may help prevent serious illnesses such as heart disease and cancer.

All this has fed a media frenzy regarding the latest research into natural remedies. At the same time, supplements of all kinds have moved from niche retailers such as health food stores into drugstores and supermarkets, making them more widely available and also more appealing to the mainstream public. And the claims are appealing indeed—to everybody from athletes to people with chronic diseases—and they go far beyond what science has shown. Here are some of them:

*For vegetable haters, “Broccoli Extract” and “Vital Veggies” promise the natural disease-fighting potential of produce—without, of course, the taste.
*The mineral chromium picolinate allegedly promotes weight loss, prevents or reverses diabetes, reduces cholesterol, and builds muscle.
*Garlic is supposed to lower cholesterol levels and blood pressure, boost a weakened immune system, unstuff sinuses, and ward off some cancers.
*Dong quai, a root from China, will supposedly relieve menstrual cramping and other “female” ailments.
*Amino acid mixtures suggest a power to produce muscle-bound individuals without barbells or sweat.


While a few of the claims have scientific backing, most do not. And many supplements have unmentioned, but documented, dangers. Even ordinary vitamins such as vitamin A and niacin (a B vitamin) can produce gruesome ailments from birth defects to liver damage at excessive doses. And the recent spate of illnesses and deaths from the stimulant ephedrine, sold in druglike potions under such brand names as Herbal Ecstasy and Ultimate Xphoria, underscores the potential risks from taking herbs that have not been studied for possible side effects.


There are no safeguards or guarantees. Government regulatory agencies do not sanction these pills nor do they evaluate most of what is written on or inside their bottles. Unlike over-the-counter drugs such as aspirin, dietary supplements are only very loosely regulated by the Food and Drug Administration (FDA). In fact, supplement manufacturers have more leeway than food producers and can legally print all manner of unsupported claims on their labels.


Many nutrition scientists are skeptical of these claims, even those supported by sound scientific reasoning and a smattering of studies. Why? Only rarely does a consistent body of research, including large studies in humans, buttress a health claim for a vitamin, mineral, or herb. For instance, chemical analysis shows that dong quai contains compounds known to expand blood vessels (which may help relieve cramps), but no study of its effect on humans supports this claim. The evidence for the benefits of chromium picolinate and garlic is conflicting, and the claims made for vegetable pills and amino acids are little more than wishful thinking, top scientists say.


Some people seem to be helped by supplements that prove ineffective in scientific studies. That is often because of something called the “placebo effect,” in which a substance works only because a person believes it works. The placebo effect is quite real, and because of it, all reliable studies include a control group, a group of people who get dummy pills or sugar syrups instead of the real thing. By comparing the control group to subjects who get the substance under study, scientists can see whether the supplement has a genuine biological effect or is no better than a placebo.

We Reviewed and Recommend: Based on the organic nature of the supplements, they are completely metabolized, utilized and eliminated from the body without any side effects or adverse effect, hence we recommend:
1. Organo-natural Based Supplement Medicine/Prescription Drugs Guide
2. Organic Liver Detoxifying Supplement Base for immunity boosting and suppress ailments, sicknesses and disease
3. Women Friendly Multivitamins food supplement
4. Natural/Organic based pain relieving Agents:

Dr Irem Bright Chimezie