[Mb-civic] codex update
IHHS at aol.com
IHHS at aol.com
Mon Oct 10 08:10:52 PDT 2005
just FYI, b
Codex update
European court cases stall pharmaceutical companies' plans to control
natural supplements.
Dateline: Sunday, October 02, 2005
by Helke Ferrie
What do airplanes, pharmaceutical drugs and Codex Alimentarius have in
common? Answer: a black box. When an airplane crashes, its black box, retrieved
from the wreckage, contains the record of events up to the moment of the crash
and enables analysts to determine the cause of the tragedy. The US Federal
Drug Agency (FDA) "blackboxes" a drug when post-marketing experience shows it
killed a lot of people and frequently produces potentially fatal side effects.
Doctors are informed accordingly in the US and Canada. When consulting the
annually-updated CPS (Compendium of Pharmaceuticals and Specialties), you will
see literally a black box under such drugs with warnings printed inside.
Codex Alimentarius is a black box containing most of what you wish you didn't
have to know about the transformation of medical science into a purely
iatrogenic enterprise. The late Ivan Illich coined the word "iatrogenic" from the
Greek iatros, meaning "physician" and genesis, meaning "creating".
Iatrogenesis refers to physician-caused illness. Codex is the political equivalent of
the current toxicology manuals because it endorses and promotes for
international trade and consumption in the whole wide world everything from pesticides
to irradiation, genetically engineered foods and synthetic analogs for drugs
and nutrients in preference to bio-compatible natural substances.
Codex does have the power to impose regulations that could restrict the
availability of vitamins worldwide.
The Codex black box was opened a crack by the April 5 opinion handed down by
Justice Leendert A Geelhoed, the European Union Advocate General, who
happened to refer to the arbitrary powers of the Codex-supporting EU legislation as
being "about as transparent as a black box". The box was opened wider on July
12th when the European Court of Justice provided a ruling for the EU that
zeroed in on the central problem of the entire Codex exercise, namely the
preference for synthetic over natural medicinal substances. This is key to
understanding Codex, why EU legislation can affect Canada and the US, and what the
current health freedom movement wants to achieve.
Their rulings both came in response to legal challenges launched by Dr Robert
Verkerk, the executive director of the UK Alliance for Natural Health (_ ANH
www.natural-health.org_ (http://www.natural-health.org/) ). His litigation
questioned Codex's supporting EU legislation. Dr Verkerk said in a telephone
interview on September 16: "It is a serious mistake for you in Canada and the
US to believe that whatever happens here in Europe will not happen to you."
By virtue of its mandate from the World Health Organization (WHO) and its
Food and Agricultural Organization (FAO), Codex does have the power to impose
regulations on the world that restrict the dosages of and even the very
availability of vitamins, minerals, phytonutrients, amino acids, enzymes, essential
fatty acids, probiotics as well as traditional Chinese, Aryuvedic and other
old systems of medicine. Codex would have succeeded in doing just that in
Europe in August of this year, if the ANH hadn't gone to court.
In 1990-2000 about 7.8 million victims suffered death from properly
prescribed and implemented medications.
To understand how all this hangs together we need to go back to the beginning
of this process: On November 6, 2001, the European Parliament tabled
Directive 2001/83/EC, which states in section 2 and 3 of its preamble the following:
"The essential aim of any rules governing the production, distribution and
use of medicinal products must be to safeguard public health. However, this
objective must be attained by means which will not hinder the development of
the pharmaceutical industry or trade in medicinal products within the European
Community."
However, since 2001, several factors have shaken the public's faith in
pharmaceuticals. For example, the International Committee of Medical Journal
Editors updated its guidelines in October 2004 and specifically warned against all
the ways that pharmaceutical sponsorship could influence journal articles.
_www.icmje.org/#conflicts_ (http://www.icmje.org/#conflicts)
Dr Carolyn Dean has written, in Death by Modern Medicine that in 1990-2000
about 7.8 million victims suffered death from properly prescribed and
implemented medications. In particular, she stated that "There have been 140,000
fatal or near fatal reactions to Vioxx; one third of the millions of women who
took fen-phen, the weight loss drug, suffered heart and lung damage; heart
disease is caused by Celebrex and all the other non-steroidal anti-inflammatory
drugs; Prozac is causing suicides and homicides as well as heart disease... "
A new book, Selling Sickness, by Ray Moynihan, charges that pharmaceutical
companies are quite deliberately trying to sell drugs to people who aren't
sick at all — these being a much larger market than actual sick people.
Big Pharma has demonstrated that it fully understands that its products do
not work, often kill, and usually harm, as proven by the research they
themselves did to establish the toxicity of their products but then hid from the
regulators (see Let Them Eat Prozac). Big Pharma staff understands the superior
biochemistry of natural substances. Recently, the prestigious British
Institute for Science and Society (ISIS) put the whole puzzle together:
_www.i-sis.org.uk/CFV.php_ (http://www.i-sis.org.uk/CFV.php)
ISIS reports that pharmaceutical corporations have started to buy up vitamin
and mineral companies. Merck has acquired Lamberts, and Wyeth bought Solgar.
Virtually all raw materials for supplements are produced by the big
pharmaceutical companies, such as Bayer and Hoffman-La Roche. "In fact," Sam Burcher
reports on ISIS's website, "drug companies have gained control of food
supplements through pharmaprinting, the result of collaboration between PharmaPrint
Inc and the University of Miami. Pharmaprinting is a technology that isolates
and measures the bioactivity of an active compound of any plant or natural
remedy and replicates it in a laboratory. These compounds are standardized as
pharmaceuticals for government approval [necessary for patenting]. Patents
are currently pending on pharmaceutical versions of some of the most useful
herbal remedies such as St John's Wort (for depression), Echinacea (immune
function) Ginko Biloba (brain function), Saw Palmetto (prostate function) and mi
stletoe (alternative cancer treatment)."
ISIS reports that pharmaceutical corporations have started to buy up vitamin
and mineral companies.
Subsequent clinical trials cost about $ 6.5 million per product and gaining
patent protection costs another half a million dollars. The whole process
takes five years. ISIS observes that, "investors are reluctant to commit unless
market exclusivity is assured. One way of creating an exclusive market is to
ban or remove natural remedies. The existing US health care market is
estimated to be worth US $ 1.5 trillion [which] makes it worth manipulating.
[Therefore] the 'foods as drugs' guidelines laid out by Codex were adopted by
Australia, Denmark, Germany and Norway and many products have been co-opted by
pharmaceutical companies and repacked as drugs. The Health Protection Branch of
Canada has registered 'natural therapeutic' food products as drugs. Fish oil
(for joints), cranberry capsules (urinary problems) and hawthorn berries
(heart) have all been issued DIN numbers (drug identification number)." ISIS
concludes, that "this is a thoroughly disproportionate degree of 'protection'
imposed on what are in effect harmless food items, especially when conventional
drugs kill" so many people every year.
Agricultural and pharmaceutical corporations are trans-national. Sound
business practice requires international harmonization in trade. Because most 171
Codex member states are also World Trade Organization members, the stage is
set for world-wide trade harmonization. Ratified Codex guidelines are enforced
among its members by the WTO court (which operates in secret) as well as by
CAFTA, NAFTA and several more trade treaties involving Europe, Australia and
North America. Each of these treaties has clauses referring explicitly to
Codex for the simple reason that the major players are the pharmaceutical,
agricultural and food producing corporations that want to remove every possible
trade barrier — or, to put it another way: reduce responsibility for quality.
We live in a world in which corporations hope to create designer customers
who are offered one-size-fits-all products to make them into corporate engines
of wealth. Today, the customer is the last resource on earth that is not
totally controlled and exploited. Customers who ask questions concerning quality,
safety and especially sound science are the only formidable barrier
remaining to corporate world control.
The July 12th ruling of the International Court of Justice in Luxembourg
followed the July 4th Rome meeting of Codex when the 85 countries present
ratified these restrictive guidelines for dietary supplements. Canada and the USA
were among them. Objections from China and South Africa were ignored. Just as
in the original 2001 version, the current guidelines, under Article 6 (2) of
the EU Directive, strictly prohibit information about diseases being treatable
by nutrients and call for future supplement dosage restrictions. Conspiracy?
No way! To borrow a phrase by Moynihan and Cassels about Big Pharma's
tactics in general: "This is daylight robbery."
Eight days after the Rome meeting, the International Court of Justice handed
down a ruling that surprised everyone. The judges conceded that EU countries
were free to have a law that regulated production and trade in dietary
supplements, namely the EU Directive, which also forms the basis of the
international Codex guidelines. However, the judges agreed with the Advocate General
Justice Geelhoed who had in April put his finger on a sore spot and observed
that there was a rather odd "preference for the inorganic forms [of vitamins]
which results in unjustifiable and disproportionate exclusion of their natural
forms, which are, nevertheless, common in the normal diet and generally
better tolerated by the body." Justice Geelhoed had also noted that the Directive
requires completely unnecessary toxicity studies: "It would be odd to start
the evaluation procedure [of all supplements according to risk assessment
principles used for toxins and synthetic drugs] from zero again, when it is
clear that the products concerned have already undergone [tests] establishing
safety and bioavailability [which should be used] as the existing evaluations as
a starting point."
2005 was a close call: had the Alliance for Natural Health not appealed to
the EU Advocate and then proceeded to the International Court of Justice,
Europe would have been the first vast area virtually under complete Big Pharma
control. Most vitamins and minerals would have been banned from the European
market on August 1 this year, some to return at exorbitant prices after Big
Pharma had identified and created patented synthetic analogs.
Now, however, the game has shifted. Big Pharma is no longer solely in
control, except in countries that have already adopted these stringent guidelines,
such as Denmark, Australia, and especially Germany. I received an email on
September 6th from Germany informing me that a bottle of 90 vitamin E capsules
now costs 45.50 Euros, which is about $ 70 — manufactured, patented and
marketed by a pharmaceutical company and, in limited amounts, available without
prescription. This price is about seven times higher than in Canada.
Furthermore, the Court dealt a terrific blow to Big Pharma and the corporate
agenda by ruling that this restrictive Directive does not apply to vitamins
and minerals in their "natural forms", but only to those from "synthetic
sources or those derived from a manufacturing process using chemical substances."
Thus, natural substances that have necessarily been part of our diet for the
past several million years cannot be regulated in a restrictive manner, nor
can they be subjected to toxicity studies in the same manner as is necessary
for synthetic chemicals used in drugs. The ANH lawyers who led these two legal
challenges state that "food supplements in the EU [will] not be classified
as drugs and [will be] readily available across the EU."
However, the battle is far from over. The Court did not forbid the scientific
assessment of supplements as part of this international trade harmonization
process. That means, they can still be subjected to corporate-driven phony
science and be sold at very high prices in very low dosages to make more money
from less — which, according to the ANH and Dr Verkerk is exactly what the
industry now wants to achieve. Whose science will be used? Big Pharma's
"tobacco science", or independent science based on actual research, not financed by
any industry? The International Court of Justice clearly orders independent
scientific assessments, but enforcing this is another matter. Dr Verkerk said
that several leading universities in Europe have joined the health freedom
movement in order to establish an assessment process that is truly scientific
and not corporate controlled, to ensure that meaningless low dosages will not
become the standard. Research institutions and medical organizations in the
US are also joining. An international health freedom conference on Codex is
taking place in Minneapolis on October 28 – 30th to hammer out strategy.
Most helpfully, a British filmmaker has produced a documentary on Codex
entitled "We Become Silent". It will be aired in the US late this year and seen
by an estimated 25 million people. On Saturday, November 5th, I will be showing
it for the first time in Canada at OISE in Toronto (12 noon – 4 pm) and I
will report on the results of the Minneapolis conference. The film shows how
Codex may affect Canada, unless we all work to protect natural medicine, which
actually works.
Sources:
M Angell, The Truth About The Drug Companies, Random, 2004 (former editor
New England Journal of Medicine)
C Dean, MD, Death By Modern Medicine, Matrix Verite, 2005
S Ellison, Health Myths Exposed, Author House, 2005 (former drug designer
for Big Pharma)
D Healy, MD, Let Them Eat Prozac, Lorimer, 2003
J Kassirer, MD, On The Take: How Medicines Complicity With Big Business Can
Endanger Your Health, Oxford University Press, 2005 (former editor New
England Journal of Medicine)
R Moynihan & A Cassels, Selling Sickness: How The Worlds Biggest
Pharmaceutical Companies Are Turning Us All Into Patients, Nation Books, 2005 (from the
British Medical Journal and Canada's CBC)
German-born, Helke Ferrie is the owner and director of KOS Publishing
(incorporated in Ontario, Canada, in July 2002). Ferrie's education includes
prehistoric, ancient, Near Eastern and Greek archaeology; Chinese and Buddhist
studies; and she holds a master's degree in physical anthropology. Her areas of
special interest are the evolution of disease and the application of Complexity
Theory to biological evolution.
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