Health-Essentials.info > Health Issues & Alerts > Codex Update: November 2006
Posted November 2, 2006
Codex Alimentarius Update: eBlast from Alliance for Natural Health
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Adapted from an eBlast from Alliance for Natural Health.
Used by permission.
Launch of new Alliance for Natural Health fund-raising site
The ANH is ramping up its fund-raising activities for the final stage of its legal challenge to the Food Supplements Directive (FSD) in the High Court in London. To make it easier for you to donate, they have launched www.anhfund.org.
In the future, you will find all ANH campaigns listed here so that you can direct your donations to specific areas of interest.
On our own, the ANH comprises a small group of experts, passionate and committed, but with no financial means to act — with your help, we become an unstoppable force!
European plans to outlaw therapeutic nutrients
This month's hot topic, as consultation with the European Commission and the UK Food Standards Agency nears its completion, is the issue of maximum permitted levels in food/dietary supplements. This can also be seen as a very clever way of using a misplaced safety argument to ban any nutrient that could be used in place of a drug — without side-effects! Industry has been invited by the European Commission, via each Member State's competent authority, to comment on this crucial issue by September 30, 2006. We summarise below:
_ The ANH has been at the forefront of demonstrating the flawed science behind the risk assessment methods being contemplated by European regulators for use on nutrients. These flawed methods are, in our view, the single biggest threat to our continued ability to use nutrients therapeutically. If we don't change things now, we will effectively be forcing future generations to limit their healthcare options to drugs.
_ Few people seem to have their heads firmly around this intricate issue; and, admittedly, apart from being a lot less emotive than many of the current campaign issues, it is a deeply complex scientific conundrum.
_ Putting this issue in the "too hard basket" is not an option. In a nutshell, the current risk assessment models are based around the precautionary principle, and they massively over-estimate risk for many nutrient forms. They use arbitrary uncertainty factors, and over-emphasise sensitivity. They also cluster diverse nutrient forms into nutrient groups (such as vitamin A, D and E, or zinc, selenium, chromium or iron) so that the maximum level of the most toxic form is imposed on all other forms in the same group.
For example, vitamin D3 (cholecalciferol) is rapidly being recognised as a powerful anticancer pre-hormone when used daily in doses of 2000 IU (50 mcg) and above.
Bear in mind, your body will synthesise 20,000 IU naturally when exposed to an hour or so of summer sunshine, assuming you're in your swim suit or less.
Under the current model of risk assessment, the more toxic form of the group, vitamin D2 (ergocalciferol) is used to set the upper safe limit according to the adverse effects related to D2. To the lay person, this might seem reasonable, but in practice it means that the proposed maximum permitted level for vitamin D3 might end up around 200 IU, the level as set by the German Risk Assessment Institute (BfR), one of the leading European bodies driving risk assessment in Europe. This will seriously reduce the therapeutic range of D3 — and the same problem can be demonstrated for a host of other nutrients.
ANH will be continuing its work in this area via the submission to the European Commission at the end of September, and through Dr Verkerk's contribution to the Electronic Working Group on Risk Assessment for the Codex Alimentarius Commission. Other key developments in this field are also in the works.
But your donations are needed to continue this work.
It's approaching November, and the critically-important annual meeting of the Codex committee on nutrition starts next week. Here, further detail on how international guidelines affecting food and dietary supplement get thrashed out, with the view to these guidelines being adopted by as many member nations as possible, supposedly to ensure that consumers are adequately protected and trade between nations is facilitated. Sound reasonable? Well, it isn't, and find out why below.
Moving from our usual format at the Alliance for Natural Health, we have devoted this entire eBlast exclusively to the whole issue of Codex, in relation to natural health, simply because we feel there are so many different views being expressed and so much confusion on the subject. We have tackled this complex issue in layperson's terms and hope it will be accessible to a wide audience. We do acknowledge that it is longer than normal, but feel it is imperative that you have this information at this time.
From Germany to the Golden Triangle …
After years of meeting in Bonn, Germany — in the country that has defined ultra-precautionary approaches to nutrition (and which is home to some of the world's largest pharmaceutical companies) — this coming Codex committee meeting has been relocated. It will be convened in Chiang Mai — in Northern Thailand — the heart of the so-called Golden Triangle.
With the increased cost of getting to the Thailand meeting, we're expecting to see a significant drop-off in attendance from some of the smaller — particularly the African — nations. This concern was already voiced by a number of delegates at the end of last November's meeting in Bonn, when the new destination for the next meeting was announced.
Let's not forget that some of these smaller nations are becoming more and more interested in nutritional interventions in healthcare, given the high cost of pharmaceuticals, so they have an interest in ensuring that Codex guidelines don't neuter all nutrients, to the point that their dosages are too low to be therapeutic.
We'll be looking closely at the attendance statistics. One would hope this gerrymandering wasn't part of the reason for the relocation of the meeting …
The National Health Federation, the only health freedom interest with delegate status at Codex, is this year sending a three-member, international delegation comprised of Ingrid Franzon (Sweden), Dr Robert Verkerk (of ANH, UK-based) and Dr Wong Ang Peng (Malaysia).
Confused over the relevance of Codex?
Much has been written and said about the significance of Codex guidelines. The FDA in the USA, and a number of major natural health trade associations, uphold that Codex will not have any effects on nutrients sold within the US, and will only affect exports to countries that decide to adopt Codex guidelines, like Europe and many African and Asian countries. This view has been strengthened by a number of US legal opinions that have dealt with the question of whether Codex guidelines are mandatory in the USA.
However, these legal opinions have crucially failed to address the potential political, economic and social effects of Codex. This is probably because lawyers are paid to focus on legal matters, and they inevitably center their opinions on the very specific questions that are asked of them. These past opinions tend to have been confined to addressing the issue of the mandatory — or otherwise — nature of Codex guidelines, as well as the potential effect of a trade dispute brought under the auspices of the World Trade Organization (WTO).
Unraveling Codex — simply
This is not the place to get into the finer details of how Codex or the WTO works or how, in our considered view, Codex presents a huge threat to the continued, long-term availability of therapeutic nutrients to consumers all over the world. But, given the mass of sometimes conflicting information on the internet, we think it's worth looking at some of the simple facts that make up the worrying picture of Codex, in relation to our ability to self-medicate, self-heal and manage our own health, free — if we should so choose — from the control of the pharmaceutical industry:
- Codex guidelines are being applied initially to maximum dosages of vitamins and minerals; but will likely be applied to both ingredients and dosages of other categories of nutrients in the future, just like the EU Food Supplements Directive is in the process of doing across the EU.
- Codex guidelines are controlled by the EU more than any other country, because European member states have agreed that they will vote en bloc behind the unelected European Commission that has been the primary driver of ultra-restrictive legislation in Europe (this way, Europe provides 25 votes, against one, for example, from the United States).
- Codex Guidelines on Vitamin and Mineral Food Supplements bear remarkable similarities with the EU Food Supplements Directive, so that, given the control of the European Commission, Codex guidelines can be seen as a mechanism that serves to export restrictive EU laws on food/dietary supplements to the world stage.
- The Codex Guidelines on Vitamin and Mineral Food Supplements are using "scientific risk assessment" as the means of establishing maximum dosages, that will ultimately define — internationally — what is regarded as the borderline between food and medicinal doses. This is not good news given that we have now demonstrated amply that the form of risk assessment that is being used is deeply flawed, and therefore, in many cases, massively understates maximum safe dosages. Although the some of the natural products industry celebrated the move to "scientific risk assessment" —which they saw as a coup over RDA-based maximum levels — the truth is that this new science has been orientated in such a way to give results that are not very different and, in some cases, less favorable than RDA-based approaches.
- Even if trade sanctions are not imposed following a trade dispute through the WTO, the political, economic and social effects of internationally-developed and recognized Codex guidelines are enough to force, in time, the vast majority of countries to bring their national laws into line with Codex. (The FDA has already stated its firm intention of doing just that. That is one of the main reasons for the on-going effort by the FDA and pharmaceutical companies to strip DSHEA of its safeguards — if not to abolish it outright.) This is not something that will happen tomorrow, or even next year. The vitamin and mineral guidelines will not be complete until around 2012 or 2013, so they are giving us lots of time to adjust to the new regime that will attempt to deprive us of our right to nutrients that have been systematically depleted from our normal food supply.
Islands, harmonization and manipulation
The United States is widely regarded as the research and development center for nutritional medicine. In the eyes of some people, this is an over-generalization; but the importance of the USA's ability to continue to grow and expand its natural products industry, to help, among other things, to fuel more research is hard to deny.
In the best case scenario, as proposed by the FDA and some of the big natural products trade bodies, like the International Alliance for Dietary Supplement Associations (IADSA), the Council for Responsible Nutrition (CRN) and the Natural Products Association (NPA, formerly the National Nutritional Foods Association [NNFA]), US companies are going to have to handle a two tier system, where they trade in higher dose, therapeutically-active natural products within the USA, while they export dumbed-down products to the majority of the rest of the world that has agreed to become Codex compliant. This idea smacks of an "island mentality" — it's all very well if your island can exist self-sufficiently without itself relying on imports — but this is very rarely the case.
In fact, the USA is busy trying to expand its territory for harmonized trade through a number of trade agreements, such as the Central American Free Trade Agreement (CAFTA), the North American Free Trade Agreement (NAFTA) and the "big one": the anticipated 34-country strong Free Trade Agreement of the Americas (FTAA), which would become the most powerful trading bloc in the world.
Trading blocs are being developed for the exclusive purpose of making life easier for big business — to increase bottom lines. Consumer — or even environmental — protection is sometimes cited as a secondary purpose, but you'll find any such claims are nearly always disingenuous. When it comes to the natural products industry — that little sore that continues to grow and irritate the much larger and more powerful pharmaceutical industry — you'll find that consumer protection gets used as the reason to dumb down effective doses and types of natural product to such feeble levels that they are rendered next to useless.
Why is that?
- Because, when lots of countries are involved in a trading bloc, the tendency is to appeal to the lowest common denominator, so those countries that have long disliked higher-dose, therapeutic natural products can't claim they are being forced to accept unsafe products which might harm consumers.
- Simultaneously, trading bloc regulations generally attempt to shift the burden of proof on safety (one of the biggest costs facing the pharmaceutical industry in getting new drugs licensed) from government to industry, making it prohibitively expensive for any but the largest companies to put products on the market.
Can you imagine if Wal-Mart in the US or Tesco in the UK was told to withdraw all fruit and vegetables from sale until such time as they could prove they were safe? Trading blocs effectively force the natural products industry into a pre-market authorization mechanism, giving it a regime that has ever-increasing similarities to the licensing regime of the pharmaceutical industry. And who said drugs are safe?
This is exactly why the EU, a 25-nation strong trading bloc, is currently in the process of trying to dumb-down the previously higher levels of nutrients found in countries like the UK, Sweden, Holland and Ireland, to cope with regulatory mind-sets that have shunned higher dose products for many years; in particular, those in countries like Germany and France. The process is underway, and the USA and other countries are not immune from it!
Trading blocs and vital organs
Let's look at an analogy. In our analogy let's think of big trading blocs like the EU — vital components in our existing globalized economy — as vital organs of the human body, such as the heart, the lungs, the brain, the liver or the kidneys. In fact, you could argue that the proposed FTAA will be more like the cardiovascular system, comprising the heart, lungs and related plumbing, given its size and diversity.
These blocs need to be very well connected to other parts of the world — or, in our analogy, the body — if they are to survive and flourish. The cardiovascular system needs to be connected via the arterial and venous systems, as well as major parts of the central nervous system, and, directly or indirectly, to all other major parts of the body. The USA, even as it currently stands — outside of a trading bloc — is one of the world's most important trading partners. Accordingly, it cannot exist as an island.
Once it expands — if citizens in a supposedly democratic society allow this to happen — this tendency to be part of the rest of the world will be even greater. The USA is not a tonsil or an appendix that can be extricated from the system without any real adverse effects. As the USA builds its place in ever-expanding trading blocs, it becomes ever more important that it places along with WTO, Codex and other rules created by the "globalizers".
We hope that this analogy goes some way toward helping to demonstrate why the economic and political pressures that can be exerted by Codex might be even more important than the legal pressures. These are pressures that the lawyers who have labeled Codex guidelines as "harmless" are simply not talking about. That's because these lawyers inevitably tackle the narrow remit provided to them, never straying from its literal sense, or the question they have been asked to provide an opinion on, which may have been carefully selected or agreed to provide the given opinion.
The typical question asked is "Are Codex guidelines mandatory in the USA?" However, you now might appreciate how a question such as "What are the legal, political or economic risks of Codex guidelines impacting the nature of the US market once the guidelines are finalized?" might reveal a rather different answer!
Media manipulation
But it gets even worse than this. You may have noticed increased press coverage on safety issues relating to natural health products over the last few years. In the UK, even the BBC has furnished us with headlines as disconcerting as " High dose vitamin E death warning", which followed Miller et al's meta-analysis, or "Vitamin pills do not stop cancer", which carried the misrepresented story about synthetic beta-carotene and vitamin A or synthetic vitamin E increasing the risk of premature death by 30% and 10%, respectively.
This anti-supplement press is part of a deliberate campaign by pharmaceutical interests to skew public opinion against natural health products and self-medication, or frighten people away from complementary health practitioners while steering them towards orthodox medicine and pharmaceuticals. Millions are being spent on these campaigns all over the world, and the data being presented is often seriously misrepresented. It seems the general public are wiser than this, as interest in natural health continues to expand, and many are disillusioned with the ethics, results and side effects associated with pharmaceuticals.
Our Executive and Scientific Director, recently gave a presentation entitled " The CAM Gameshow: Whose evidence is it anyway?" which tackled the thorny subject of scientific evidence at the CAM Expo in London last weekend. If you wish to download a copy of his PowerPoint presentation, click here (16.5 Mb, large file warning).
We need your help — NOW!
We have a detailed strategy which tackles many aspects of Codex and related risk assessment issues — and given that we are funded only by donations, we urgently need your help.
It will cost us more than £100,000 (c. US$190,000 or €150,000) this year just to:
- Attend Codex and other scientific meetings
- Compile and submit major submissions. Click here to see our latest submission.
- Develop and publicize in scientific circles the reasons why Codex-style, ultra-precautionary, guidelines and regulations are scientifically irrational and erroneous.
- Help develop and promote new, scientifically-rational models for risk/benefit assessment of nutrients and other natural health products.
- Coordinate activities with other health freedom organizations, including our affiliate partners in the USA, the AAHF / HFF, and the NHF.
- Continue our legal challenge on the EU Food Supplements Directive.
Please DONATE NOW — to help us help you. Without your support we cannot continue this work.
Important note for US citizens: you can make tax deductible donations marked for the "European campaign" to the AAHF / HFF.
In health — as always.
The ANH Team
Working on your behalf to protect and promote natural health worldwide, using good science and good law.
Alliance for Natural Health
The Atrium, Curtis Road
Dorking, Surrey RH4 1XA
United Kingdom
Tel: +44 (0) 1306 646 600
Fax: +44 (0) 1306 646 552
Email: info@anhcampaign.org
Web: www.anhcampaign.org
www.anhfund.org



