Free Ephedra Case Evaluation

The safety of ephedra products, like Metabolife, has continued to be debated over the years in addition to whether federal and state lawmakers and regulators are adequately policing the diet industry as a whole. In 1999, the FDA tried to enforce dosage requirements for ephedra supplements like Metabolife, but congressional investigators criticized its use of adverse event reports and the FDA stopped pushing for it. In a 1997 FDA proposal for safety measures to be put into place for ephedrine dietary supplements, the Deputy Commissioner of Food and Drugs, Dr. Michael Friedman, stated that “consumers should be aware that just because a product is labeled ‘natural’ or from an herbal source it is not guaranteed to be safe.” 
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Ephedra is a stimulant that is used as an ingredient in weight loss and appetite suppression pills and over-the-counter nasal decongestants and asthma medications. According to a study commissioned by the Food and Drug Administration (FDA), Ephedra may seriously harm and kill some who use it.

It is also known as Ma Huang, Xenadrine, Metabolife, Desert Tea or Mormon Tea.

Ephedra has been used in products for: Asthma, Common Cold, Weight loss, Hay fever/Allergies, Congestion, Cough , Increased Energy and Weight lifting formulas

Ephedra can produce the following adverse reactions: heart attack, stroke, tachycardia, paranoid psychosis, depression, convulsions, coma, fever, vomiting, palpitations, hypertension, and respiratory depression. The research adds to the long-standing controversy about the dietary supplement, which is also marketed as an energy booster and treatment for respiratory illness.

Ephedra, derived from an Asiatic shrub, contains ephedrine, a stimulant that acts on the central nervous system to relax bronchial tubes. A synthetic form of ephedrine is used in bronchodilators and over-the-counter medications like Sudafed and Actifed, which fall under the FDA's watch.


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