Showing posts with label Codex. Show all posts
Showing posts with label Codex. Show all posts

Monday, September 13, 2010

Obama Pens US Alignment with CODEX


Executive Order 13544 of June 10, 2010

Establishing the National Prevention, Health Promotion, and
Public Health Council

http://edocket.access.gpo.gov/2010/pdf/2010-14613.pdf

Courtesy: Rense News Network

In regard to herbs and CODEX
NB:  While I do not accept the move to standardization of herbs, because it moves them more into the category of drugs as they become fractionated and may offer more in the form of side effects and reduced efficacy, this is the doctrine of CODEX - 
The German Commission E Monographs contain scientific data regarding the effectiveness of herbs. 

Between 1983 and 1993 this collective data was compiled and the German Commission E based its results entirely on strict scientific investigation, then released Monographs that have been promulgated to be  recognized for scientific standards. To ensure the completely unbiased investigation of the Commission E, the work was financed by the German government.
The German Commission E Monographs are now used for their authoritative description of herbs, their uses and side-effects by herbalists, pharmacies (Apotheken), and medical doctors (mostly in the EU, few in US).
The complete Monographs can be found in the "Bundesanzeiger"(the federal registry of Germany).

The same is done to supplements.  For example, vitamin C is limited to 60 mg, the amount known to prevent scurvy; vitamin E is to be at 7 IU to 14 IU,  but therapeutic levels will not be permitted. Single B vitamins such as B6 will be excluded as it is already under attack by Big PhRMA to be used only as a patented drug in P5P (bioactive) form.

Monday, May 17, 2010

Update on CODEX

UPDATE: 17 May, 2010 - International Advocates for Health Freedom was the first to call the Codex international threat to health freedom in 1996 via an article by John C. Hammell in Life Extension Magazine. More about CODEX

For the most in depth CODEX information and interrelated issues stay up-to-date with IAHF.

Use the search box to find more than two dozen CODEX related articles on Natural Health News
Prepared by Alliance for Natural Health this new Codex flyer is part of our joint efforts to bring credible, up-to-date information to interested consumers and practitioners.

Originally posted 5/19/08 - The Codex Alimentarius Commission is an inter-governmental body with over 170 member countries, established in 1963, within the framework of the Joint FAO/WHO Food Standards Programme established by the Food and Agriculture Organization of the United Nations (FAO) and the World Health Organization (WHO). Its primary stated purpose is “protecting the health of consumers and ensuring fair practices in the food trade.” The Commission also promotes coordination of all food standards work undertaken by international governmental and non-governmental organizations (INGOs). Guidelines and standards are used as a benchmark for regional/national legislation and in World Trade Organization (WTO) disputes. Work is conducted through nearly 30 committees, each dealing with specific areas of food, and decisions are based on consensus voting by member countries. INGOs do not have voting rights, but may influence proceedings. Most INGOs present at Codex meetings represent transnational corporation interests.

Tuesday, April 13, 2010

Supplements Saved

US office of the great Alliance for Natural Health, started years ago by Dr. Robert Verkirk, just announced a victory for US consumers of nutritonal supplements
Supplements Are Exempted From Codex Language in Food Safety Bill
The FDA Food Modernization Act (S. 510), also referred to as the “Food Safety” bill, has been modified to exempt dietary supplements from language that otherwise creates a slippery slope toward U.S. harmonization with Codex Alimentarius. ANH-USA worked to protect the natural health community from this dangerous provision that threatened access to high quality, therapeutic supplement doses by working with key senators to modify the language, now for the second time. Read Complete Article

Wednesday, March 24, 2010

Limits on Supplements

I found it interesting that another blog just recently reported on the issue of imposed limits to be placed on supplements.  It is interesting to me because as a long time health freedom educator I have been engaged in this issue for most of my career, as well as intensely during the past two decades.

There are two international groups that spearheaded this fight to stop the CODEX effort through food directives in the EU, also WHO, and USDA, etc.  In the USDA effort it was widely known that panel members were industry supported.

One group is International Advocates for Health Freedom, NHF, and the UK based Alliance for Natural Health.

In the arena of health freedom, natural health advocacy, and related areas, please rely on the real and accurate sources that have historically been involved.  Shy from those who try to make panic-ridden headlines as if they are the first to report.

Know your sources!

Saturday, June 20, 2009

Electronic Records, Data Mining and Your Health

While it is more likely than not an activity most people don't about, data mining can be a lucrative endeavor.

Along with drug data and prescribing activity used by CVS and other large pharmacy chains, web sites like Reeal Age are known to have been selling your data for profit.
’Data mining’ for drug companies goes to courts

By Associated Press | Saturday, June 20, 2009 | http://www.bostonherald.com | Healthcare
MONTPELIER, Vt. — The prescription drugs you take are on the minds of a lot of people: judges on two federal courts, legislators in several states, countless doctors and, at the center, the companies that make money by figuring out who’s prescribing what.

"Data-mining" firms — which gather electronic information on the drugs prescribers order for their patients, then sell that information to pharmaceutical companies — have sued to block laws restricting their activities in New Hampshire, Maine and Vermont.

At issue is the use by drug company "detailers" — the sales force that deals with doctors and other prescribers and tries to get them to use the company’s products — of the information about doctors’ prescribing habits.

If, for example, a doctor usually uses one company’s antidepressant drug instead of another’s, that can be valuable information for a detailer trying to get the doctor to switch.

In upholding the New Hampshire law, 1st U.S. Circuit Court of Appeals in Boston found the result of the activity is often higher drug costs, because the detailer usually is trying to steer the prescriber toward the newest, most expensive, medicines.

The data mining companies are set to appear Tuesday at the 2nd U.S. Circuit Court of Appeals in New York to ask a three-judge panel to block Vermont’s law from taking effect July 1.

And the U.S. Supreme Court is expected to decide by the end of the month whether to hear the data-mining companies’ appeal of the Boston court’s decision on the New Hampshire law. The Boston court has put a separate Maine case on hold until New Hampshire’s is resolved.

The issue has come up in more than 20 state legislatures, advocates on both sides said.

Randy Frankel, vice president for external affairs at IMS Health, said restricting the ability of his and similar companies to collect doctors’ prescribing data could hurt more than just commercial activity.

The data also are used to help law enforcement track when narcotic drug prescriptions spike; they help academic and government researchers follow drug safety and help aim information at doctors prescribing a drug when new side effects or other issues crop up, Frankel said.

"These data have enormous value to the public good," he said.

Maine state Rep. Sharon Treat, D-Hallowell, head of a national group of lawmakers following drug issues, said the data-mining companies’ "bread and butter" is selling the information to drug companies to bolster their marketing efforts.

The more that doctors are urged to use expensive drugs rather than generics, the less money there is to spread around to deliver the most health care to the most people, Treat said. She argued that’s a bad idea when many states are cutting people from public and subsidized health programs in budget-cutting moves.

The data companies, IMS Health Inc. and SDI, argue that restricting the data collection and use violates their and the drug companies’ First Amendment free speech rights to collect and use the information.

But the Boston court rejected the First Amendment argument, saying the issue was less a matter of speech than of conduct. In both that court and the U.S. District Court in Vermont, judges ruled that commercial speech can be regulated without violating the First Amendment, and that what the data-mining companies were doing fell into that category.

Treat concurred that "this isn’t about speech. They’re trying to change behavior" — the behavior of health providers in deciding which kinds of drugs to prescribe.

"That’s what it’s all about," Treat said. "What it’s not about necessarily is good health care."
___

On the Net:National Legislative Association on Prescription Drug Prices: http://tinyurl.com/mxn8ab

Article URL: http://www.bostonherald.com/jobfind/news/healthcare/view.bg?articleid=1180068

At the same time as data mining companies are suing to get access to this data in states where it is prohibited, Big Pharma is making half-baked back room deals with Baucus and others to try to boost appearances of something real happening in DC on Plan D.
Emerging $80B deal would help fund Medicare drugs

So far an unmentionable on either side of the asile is the idea that freedom of choice in this discussion should be considered.

The preventive and curative nature of vitamins, minerals, and herbal supplements continue to be ignored and, according to the National Health Federation's support of the efforts of www.CodexFund.com. (More factual information on Codex can be found at www.nocodexgenocide.com)

Consider this from CodexFund's FAQ page -
The 2005 Guidelines are in Direct Conflict with Existing US Law - the Proxmire Amendment of 1976.
In 1976, Congress passed the Proxmire Amendments to stop FDA from establishing standards limiting potency of vitamins and minerals in food supplements or regulating them as drugs based solely on potency. (PL-94-278 Section 501 (a)).

Throughout the 1960s and early 1970s, the FDA initiated measures to reclassify vitamins and minerals with a potency of 150% or more of their recommended daily allowance (RDA) be classified as drugs. (Vitamins A and D were to be classified as drugs at 100% of their RDA.) Congress considered these actions as infringements on consumer's freedom of choice and amended the law to forbid the FDA from setting such limits. The law, which became known as the Proxmire Amendment barred the FDA from setting the composition or maximum potency of vitamins, minerals, or combinations thereof, unless they were of a specified type (e.g., toxic, habit-forming, administered by a doctor) or unless they were intended for use by a specified clientele (e.g., by individuals in the treatment of specific diseases or disorders, by children, by pregnant women).


Dave Lindorf writes, "But you cannot achieve the twin goals of reducing health care costs and providing access to health care to 50 million uninsured people, while leaving the profit centers of the current system—doctors, hospitals and the health insurance industry—in charge and in a position to continue to reap profits."

 
Design by Free WordPress Themes | Bloggerized by Lasantha - Premium Blogger Themes | Macys Printable Coupons