The FDA and Ephedra

The U.S. Food and Drug Administration (FDA) is the part of the Department of health and Human Services that is responsible for safety regulations for foods, drugs, vaccines, Bio-medical products, rake products, radiation-emitting Technology, cosmetics, vet products, and dietary supplements. (2) With the FDA having all of these duties it is easy to see how some things whitethorn slip by, but this does not free them of all blame. The FDA has been below the microscope lately due to the E coli and salmonella outbreaks. But one of the big problems it?s had over the past couple years is the generate of dietary supplements and if they should be monitored by the FDA. Ephedrine found supplements caught the eye of the FDA when clan started dying from heart attacks and heat exhaustion due to exulting the supplement. To understand why the FDA chose to proscription this drug one must introductory understand the drug and what it does to the human body. joint fir is a thermog enic and a stimulant, which increases heart rate, constricts blood vessels thus increase blood pressure, stimulates the brain, and makes the bronchial tubes expand which makes breathing easier. The weight leaving properties have it away from the thermogenic characteristics which cause an increase in metabolic process and body temperature.

(5)The first concerns about the ephedra based supplements arose in 1997 when the FDA proposed a ban on supplements containing 8mg or much of ephedrine alkaloids and more detailed labeling on low dose ephedra products. They besides proposed that the health risks be labeled also, including heart attack, stroke, and death. (4) But aft(prenominal) battlin g with the ephedra based supplement companie! s? public relations group, cognise as the Ephedra Education Council, the FDA withdrew its proposal in 2000. That similar year the parvenue England Journal of Medicine discovered cases of heart... If you loss to get a full essay, order it on our website: OrderEssay.net

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