Dietary Supplements Essay

1356 Words 6 Pages
Dietary Supplements have become a major part of the United States way of living. In 2007 nearly eighteen percent of all Americans claimed to use”nonvitamin, nonmineral, natural products”. This may be due to more endorsement and and prescriptions from health officials. This may be because Dietary Supplements are often regarded as “natural” substitutes for drugs. Dietary Supplements are sold in many different forms such as pills, capsules, liquids, extracts, teas,and powders. Many companies sell the same product in different forms, all claiming have the same effect. Since dietary supplements are not as powerful as drugs they are classified as food. However herbal products are classified as supplements rather than drugs or food. Dietary supplements …show more content…
By the late 1990s consumer groups and government agencies persuaded diet companies to make available details about their products cost and services so that dieters may evaluate their progress. Millions of people take dietary supplements to help ensure adequate nutrition, increase energy, reduce stress, or relieve some condition.Dietary supplements can also cause harmful reactions by interacting or interfering chemically with prescription drugs. The government has little oversight when it comes to the thirty-three billion dollar supplement industry. By law, the FDA can exercise very little oversight of herbal and dietary supplements.Vitamin A prescriptions have experienced a increase for both males and females from twenty-seven percent to thirty-five percent from 2007 to 2011. Over a five year period, vitamin E prescriptions decreased from fifty-one percent to fifty-three percent for both females and males. Vitamin D prescriptions took an exponential leap from forty-two to sixty-two percent for both males and females over the five year period. The Vitamin C prescriptions were remained fairly consistent over the five year study …show more content…
The Food and Nutrition Board of the National Academy of sciences, sets the recommended Dietary Allowances(RDAs) for vitamins.The labels on vitamins supplements display a Daily Values(DVs) percentage. The FDA portions are based on 13 life stages, including children ages four to eight and males and females in the following age groups: nine to thirteen, fourteen to eighteen, nineteen to thirty, thirty-one to fifty, fifty-one to seventy, and older than seventy. To remove a supplement from the marketplace the FDA has to prove it to be unsafe. In March 2003, the FDA proposed new regulations that would require vitamin manufacturers to prove accurate labels. Vitamin manufactures, are not required to submit to the FDA the results of clinical, studies proving their products effectiveness and safety. When it comes to supplements, health care experts say, more is not necessarily better. Research suggests that taking excessive amounts of vitamins can increase the risk of health

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