Who is at high risk for Ephedra injuries?
Products containing ephedrine are contra-indicated in heart disease,
hypertension, thyroid disease, diabetes, enlarged prostate, anxiety
and restlessness, and glaucoma. Ephedra/ephedrine aggravates these
conditions and therefore should not be used except if recommended
by and under the surveillance of a health care professional. It
should also not be used during pregnancy and lactation. Because
of the stimulant and euphoric properties of Ephedra/ephedrine, certain
segments of the population are more likely to abuse these products,
increasing the risk to their health.
What are the side effects of Ephedra use?
Adverse effects of ephedrine can include dizziness, headache, decreased
appetite, anxiety, restlessness or nervousness, gastrointestinal
distress, irregular heartbeat, tachycardia (accelerated heart rate),
insomnia, elevated blood pressure, flushing, hepatitis, chest pain,
sweating, hypertension, stroke, seizures, psychosis, myocardial
infarction and death.
What should I do if I suffered a reaction to Ephedra?
If you have suffered a reaction to an ephedrine product, you should
immediately consult a physician. You should then report the facts
of your adverse reaction to the FDA Consumer Hotline at (800) 532-4440.
The state you live in has a department of health services which
also should be contacted. Then, contact Brown & Crouppen for
legal advice.
What are the treatments for injuries caused by Ephedra?
Fortunately, many of the short-term effects of Ephedra toxicity
disappear when you stop taking the drug. However, the more serious
side effects like stroke, hypertension, or heart damage may require
continued medical care. Check with your doctor.
Why Is Ephedra not federally regulated?
Ephedra is a dietary supplement that stimulates the nervous system
and speeds up metabolism. Contained in hundreds of other herbal
products, despite being linked to more deaths and injuries than
every other type of herbal product combined, a 1994 federal law
allows ephedra to be exempted from federal regulation because it
is classified as a food. Supplements like Metabolife are not subjected
to the same strict clinical testing standards as prescription and
most over-the-counter drugs. The FDA has been criticized for trying
to obtain information on the adverse effects associated to Metabolife
and other ephedra products.
How is Ephedra listed on the ingredients label?
Be sure to check the label of any dietary supplement before use.
Ephedra may be listed under any of the following names: