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(Note: Herbal Ecstasy is a term used to describe a combination
of herbs which are legal, inexpensive, and marketed as a "natural
high." Caffeine and ephedra (also known as ma huang) are the
key ingredients in herbal ecstasy.)
Effects:
- Increased heart rate and blood pressure
- Liver failure
- Seizures
- Heart attacks
- Stroke
- Death
Description:
In its pure form, ephedrine is a white powder, but it is frequently
sold in tablet or capsule form or as loose plant material.
Herbal ecstasy can be found in a capsule or pill form, of various
colors.
9This is the retyped text of a press release from the FDA)
FDA Statement on Street Drugs Containing Botanical Ephedrine
The Food and Drug Administration is warning consumers not to purchase
or consume ephedrine-containing dietary supplements with labels
that often portray the products as apparent alternatives to illegal
street drugs such as "ecstacy," because these products
pose significant health risks to consumers. These products contain
botanical, or so-called "natural," sources of ephedrine.
Ephedrine is an amphetamine-like stimulant that can have potentially
dangerous effects on the nervous system and heart.
These types of products are marketed under a variety of brand names
with labels that claim or imply that they produce such effects as
euphoria, increased sexual sensations, heightened awareness, increased
energy, and other effects.
Possible adverse effects of ephedrine range from clinically significant
effects such as heart attack, stroke, seizures, psychosis and death,
to clinically less significant effects that may indicate the potential
for more serious effects (for example, dizziness, headache, gastrointestinal
distress, irregular heartbeat, and heart palpitations). "Ecstacy"
is the street name for MDMA (4-methyl-2, dimethoxyamphetamine),
which produces euphoria.
Ingredient panels on these products may list ma huang, Chinese
ephedra, ma huang extract, ephedra, Ephedra sinica, ephedra extract,
ephedra herb powder, epitonin or ephedrine. Any one of these ingredients
listed on the label indicate the presence of ephedrine in the product.
Many of these ephedrine-containing products bear labels that appear
to be targeted at adolescents and young adults and that imply the
products can produce a "high." The agency considers this
type of promotion and these claims to violate the Federal Food,
Drug and Cosmetic Act, even as amended by the Dietary Supplement
Health and Education Act of 1994 (DSHEA), which governs the U.S.
marketing of dietary supplement products.
The FDA takes seriously the health risks inherent in these products
and is currently investigating the production and marketing of ephedrine-containing
products marketed as alternatives to illicit street drugs. The agency
is committed to taking whatever action is necessary to remove dangerous
products from the market. However, under recent amendments to the
Federal Food, Drug and Cosmetic Act, the agency has to act product-by-product
and the legal burden is now on the FDA to show that a marketed product
is unsafe, rather than on the company to gain FDA approval by showing
that the product is safe before it is marketed.
Consumers who have been injured or suffered an adverse effect after
taking a dietary supplement or any product containing an ephedrine
alkaloid should call 1-800-FDA-4010. Health professionals who have
treated patients suffering from an adverse event to these products
are urged to report the event to the FDA's MEDWATCH adverse event
and product problem hot line at 1-800-FDA-1088.
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