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FDA Approved Fat Loss
By Shane Ellison M.Sc.
The proposed ban on ephedra has put most Americans into a panic
state. The media pundits are shouting death, medical doctors are
telling patients that one dose of ephedra can cause immediate heart
attack, and personal trainers are recommending the cancer causing
compound chromium poly-picolinate (or other chromium derivatives) to
be used in place of ephedra. And finally, the FDA and other "experts" are pushing Wellbutrin AKA Zyban (bupropion).
Absurdity!
If you or anybody you know is reaching for supposed FDA approved fat
loss drugs such as Wellbutrin, it would be wise to pay full attention to the next few paragraphs.
The recommendation to use bupropion is based on "check book science"
not real science. Reported in Julys Obesity Research, subjects who
completed 26 weeks of use maintained mean losses of 4.6% of baseline
weight for those taking bupropion (SR 300 mg/d) while those on
placebo lost 1.8% of baseline weight. This equates to a whopping
2.8% loss in body weight by those taking bupropion. The study was
paid for by bupropion manufacturer Glaxo SmithKline, who after
completion touted how wonderful it was for weight loss.
Most professionals accepted it without looking at the facts. A 2.8%
loss in body weight is equivalent to a 200 pound woman who is 5'8"
losing 5.6 pounds. This would bring her weight to 195 pounds. Using
a more accurate figure for beneficial weight loss her BMI would have
gone from 30 (classifying her as scientifically obese) to 30! Thus,
Wellbutrin, scientifically and factually has zero benefits for healthy weight loss!
Nonetheless, this FDA approved drug is often touted by experts for
weight loss while the side effects are typically not discussed. For
example, Dr. Richard Atkinson, president of the American Obesity
Association, has declared that with respect to using bupropion for
fat loss ; "This is a drug that people have taken for many years to
treat depression with few problems or side effects."
Liar or just misinformed?
Looking at the actions of the drug, Clinical Pharmacology gave what
seems to be a warning rather than a mechanism of action. "Bupropion
is a novel antidepressant whose mechanism of action must still be
elucidated." And Further, "The mechanism of action of the novel
antidepressant bupropion remains unclear after many years of study."
The Journal of Clinical Psychology states further that "Bupropion is
widely distributed to tissues and extensively metabolized by
oxidation and reduction to at least six metabolites, some of which
may be active. Bupropion does not inhibit monoamine oxidase, exerts
no effect on serotonin uptake, and minimally alters the reuptake of
norepinephrine at presynaptic sites. It does not appear to exert
action leading to postsynaptic beta-adrenergic down-regulation, and
it has minimal inhibitory effects on presynaptic dopamine
uptake."[4]
Wellbutrin was withdrawn in 1986 because of an unacceptable
incidence of seizures. It was released back to the market by the FDA
in 1986 for unknown reasons. According to clinical trials, 6.1% of
users will suffer from withdrawals due to adverse events.
Additionally, it is well known that all Wellbutrin related seizures
occurred in patients who are taking what is considered to be a
therapeutic dose or 450 mg/day or less. However, real life data is
suggesting much higher rates of adverse reactions.
Wellbutrin is the third leading cause of drug related seizures with
cocaine being number one. Health Canada and GlaxoSmithKline received
1127 reports of adverse reactions to Wellbutrin between May 1998 and
May 28, 2001. Among these were 19 deaths and 172 reports of seizures
or convulsions. Worse, the Medicines Control Agency (equivalent to
FDA) of Britain has confirmed 18 deaths and received reports of
3,457 patients complaining of adverse reactions in the last year
(200-2001)! Despite these staggering figures, the number of children
being prescribed Wellbutrin jumped 195% between 1995-1999!
On June 26, 2003, drug manufacturer of Wellbutrin, Glaxo SmithKline
announced that it has received a FDA approval letter for an extended
release formulation of its widely-used antidepressant Wellbutrin.
Considering that the FDA cannot prove a single death attributed to
ephedra use they should be more fearful of bupropion. Of course this
is logic and the FDA has a history of illogical behavior.
See Also:
Bupropion
(Wellbutrin) - its actions and side effects.
References
[1] Obes Res 2002 Jul;10(7):633-641. Obes Res. 2002 Oct;10(10):1049-
56.
[2] Lipman, Larry. Health Policy Journal Health Affairs. July 9th,
2002
[3] Clin Pharm 1983 Nov-Dec;2(6):525-37
[4] J Clin Psychiatry 1983 May;44(5 Pt 2):74-8
[5] J Emerg Med 2002 Apr;22(3):235-9 J
[6] JAMA, April 17, 2002 - Vol 287, No. 15
Shane holds a Masters degree in organic chemistry and has first- hand industry experience with drug research, design and synthesis. He knows Americans want and deserve natural medicine not prescriptions. Visit www.health-fx.net and for his book www.healthmyths.net [Weight Control Infocenter Home] [ Articles on Diet/Weight Management ] [Remedies Home] [ Holisticonline.com] [ Holistic Living Home] [Healthy Recipes Home] [ Nutrition Infocenter] Holisticonline.com is developed and maintained
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