Date: May 4th 2007

This latest news about the FDA bill in the Senate has been reprinted with the permission of writer Byron Richards by Nutritional Health advocate. Courtesy of Health Freedom Resources www.healthfree.com

S1082 - THE VOICE OF THE PEOPLE IS BEING HEARD
By Byron J. Richards, CCN May 4, 2007

There is still time to stop FDA, Inc.

Bill S1082 is a bill that helps fund the FDA with Big Pharma money. It is known all over Capital Hill as Big Pharma-designed legislation. It is running into all sorts of credibility problems. A vote is likely on Monday – delayed due to all the opposition flooding the Senate by “we the people.”

Major Problem #1 – A Fair Price for Drugs.

Realizing that meaningful FDA reform legislation is not likely again for ten years numerous Senators are backing the Dorgan amendment to S1082. The amendment enables U.S. citizens to buy drugs from Canada and other industrialized nations. This will save us at least 50 billion dollars over the next ten years and cut the price of many drugs in half. Those opposing the amendment, which includes most of the major proponents of S1082 and the Bush administration, are the ones clearly on the payroll of Big Pharma. Their excuse for not supporting it is flimsy – that it will cause safety problems. The majority of Senators are not buying this transparent cover-up. Dorgan won Round 1 of the voting on his amendment yesterday (63-28), showing that he has the power to hit Big Pharma where it hurts – in the pocketbook. A final vote on the Dorgan amendment is expected Monday (keep up support for the Dorgan amendment).

Major Problem #2 – A Fake Safety Bill.

Last year’s Institute of Medicine report labeled FDA management as dysfunctional causing FDA reform to pick up momentum. To deflect public outrage S1082 was created by Kennedy and Enzi, in close consultation with the FDA and Big Pharma. As you might expect from such a meeting of the minds, the bill is really a Big Pharma-sponsored con job and it actually increases the power of dysfunctional FDA management.

Unfortunately for Big Pharma and the FDA, Charles Grassley (R-IA), a man concerned with true and meaningful safety reform, has gone through S1082 with a fine tooth comb. He has proposed 11 amendments <http://grassley.senate.gov/index.cfm?FuseAction=PressReleases.Detail&PressRelease_id=5369>; to close the Big Pharma loopholes that Kennedy, Enzi, the FDA, and Big Pharma built into this legislation. Big Pharma and the FDA hate all 11 Grassley amendments and Big Pharma has its legion of lobbyists trying to defeat them as you read this. Support the Grassley amendments for true and meaningful safety reform.

Major Problem #3 – A Sneak Attack on Dietary Supplements.

As I have been reporting for the last week, language relating to the Reagan-Udall Foundation for the FDA creates a new regulatory category and broadens FDA power in a way that can be used to attack dietary supplements. In response to this devious threat, Jonathan Emord, our nations leading health freedom attorney, prepared amendment language to nullify the threat – an amendment we now call The People’s Amendment. Many of you flooded the Senate with your objections – AND YOUR VOICE IS BEING HEARD.

I have obtained an e-mail message from David Taylor, the president of the Natural Products Association, which went out to various heads of nutrition companies – in an effort to get companies not to protest S1082 (dietary supplement trade groups are not the friends of health freedom). It contained an attachment with a transcribed conversation between Hatch, Harkin, Kennedy, and Enzi about all the phone calls you’ve been making. It shows that Hatch and Harkin don’t really understand what the Reagan-Udall foundation is, that Kennedy and Enzi are lying about what it will do, AND THAT WE ARE GETTING THROUGH. Here is the text:

SEN. HATCH: My office has been inundated by calls from people
throughout the country who believe that this legislation,
specifically the provision establishing a Reagan-Udall Institute,
will overturn the Dietary Supplement Health and Education Act of
1994. That has not been my reading of the bill, but I wonder if
other Senators have heard similar concerns?

SEN. HARKIN: Yes, I have received a good many calls as well. And, I
have to say that I would be very concerned, as I know the Senator
from Utah is, if anything in the bill we are considering, S. 1082,
would overturn DSHEA, a law we fought side-by-side to see enacted.

SEN. ENZI: It might be helpful if I explained the provision you are
discussing, as my office has received many calls as well and I
believe the callers are not informed about this matter. Subtitle B
of Title II of S. 1028, establishes the Reagan-Udall Foundation for
the Food and Drug Administration. That simple purpose of that
non-profit Foundation is to lead collaborations among the FDA,
academic research institutions and industry designed to bolster
research and development productivity, provide new tools for
improving safety in regulated product evaluation, and in the
long-term make the development of those products more predictable
and manageable.

SEN. KENNEDY: That is exactly the purpose of the Foundation, which
was included in the drug safety legislation Senator Enzi and I
introduced last year. The Foundation will be financially supported
by industry and philanthropic donated funds. A Chief Scientist at
FDA will promote intramural research and coordinate it with efforts
at the Foundation.

SEN. HATCH.: That explanation is very helpful. What, specifically,
would the role of the Foundation be with respect to dietary
supplements?

SEN. KENNEDY: Let me make absolutely clear that the Reagan-Udall
Foundation will in no way override, overturn or conflict with the
Dietary Supplement Health and Education Act. Nothing in this bill
would have that effect.

SEN. ENZI: Yes, we took great pains to make certain there would be
no conflict with DSHEA. Regarding foods, and dietary supplements are
generally regulated as foods, the general directive of the
Foundation is to identify holes in the evaluation of food safety and
identify ways to address those deficiencies through collaborative
research with industry.

SEN. HARKIN: So, to make this absolutely clear, what you are saying
is that the bill we are debating would in no way interfere with
consumers’ access to dietary supplements?

SEN. HATCH: To add to that point, it seems that the language could,
in fact, help dietary supplement consumers, because it would allow
collaboration between government and industry to conduct research on
issues that might be helpful to supplement consumers?

SEN. KENNEDY: Yes, that is the case.

SEN. ENZI: I agree with Chairman Kennedy’s assessment.

SEN. HATCH: I thank you for those assurances and that clarification.

SEN. HARKIN: This has been a very helpful discussion, because
Senator Hatch and I could never support legislation that would
interfere with DSHEA and we are glad to receive the assurances of
the Chairman and the Ranking Republican on the Committee.

This is a major breakthrough – Kennedy and Enzi are now on record stating this will in no way affect our dietary supplements. And Hatch and Harkin are on record as being concerned. There are still two problems. 1) Kennedy and Enzi are hard to trust, based on all the Big Pharma loopholes built into their bill. 2) The FDA and its lawyers get to interpret what S1082 means once it becomes law. The FDA could care less what Kennedy or Enzi intended to say. Until the language is fixed it is a problem of magnitude.

Major Problem #4 – The Creation of FDA, Inc.

As you can see from the Kennedy and Enzi comments above, they are portraying the Reagan-Udall Foundation for the FDA as a benevolent and friendly group that will facilitate collaboration between the FDA, academia, and private industry – receiving funding from industry and philanthropic donations – and oh yes, let’s not forget the foundation may even help with safety. Do you really think the FDA needs to create a whole organization to do that? And why wouldn’t such duties just be the function of a few people or a department within the FDA?

It is my opinion that the primary reason for bill S1082 is to create FDA, Inc. by using the Reagan-Udall Foundation for the FDA. The FDA wants to be in the drug development and marketing business and is looking for a way to do it. Most of the issues in S1082 are a smokescreen, keeping Senators like Grassley busy fighting all the Big Pharma loopholes. So far Kennedy and Enzi have skillfully created so much diversion that nobody is paying attention to the FDA becoming a drug company.

In a nutshell, Andrew von Eschenbach, M.D, head of the FDA, has a long history of involvement with the cancer-for-profit industry. His resume includes being head of the National Cancer Institute, where he routinely diverted funding from solid cancer science into the pockets of his friends in Big Bio Tech. He was also a lead player in an old boy network called C-Change, a group of the most powerful vested interests in biotechnology and cancer research – which is headed by George Bush Sr. and his wife, Barbara. It is not surprising that the current president backs Big Pharma and Big Biotech as he does – his family wealth depends on it. Drug research and development performed at the Reagan-Udall Foundation will undoubtedly be paid for, in large part, by companies who have grants from the National Cancer Institute (taxpayer funds).

Von Eschenbach took over the helm of the FDA to create his dream of a cancer sickness industry wherein nobody actually gets well – they just live indefinitely in a sick condition on really expensive biotech drugs. This project is called the Critical Path Initiative. The FDA has created highly sophisticated software that can identify protein-molecule changes at the cellular level. The FDA wants to use this computer software to design the entire next generation of powerful biological medicines – making all of private industry use its software technology. The Reagan-Udall foundation is the tool that FDA plans to use for patent protection and licensing arrangements of its technology with private industry – and thus the creation of FDA, Inc. Von Eschenbach is on record as stating that the Critical Path Initiative is the FDA’s top priority (not drug safety or food safety).

The Critical Path Initiative has been repeatedly attacked because it would expose patients to drugs with far less testing for safety and effectiveness compared to drugs already on the market. Furthermore, these biologic drugs will be far more powerful because they throw gene switches in cells – meaning the risk for adverse events skyrockets. Initially, just patients with no other medical hope will be the guinea pigs. The FDA wants to run this technology in all doctor’s offices around the country – which will require your DNA in an FDA-owned government database. This is not science fiction – this is what the FDA is on public record as wanting to do.

Keep Taking Action – Revised letter

Anti S.1082 Food and Drug Revitalization Act

May 5, 2007

The Honorable (Senator First and Last Name)

Address
Address

Dear Senator Last Name;

The issue of drug safety and access to drugs at a fair price is of the utmost importance to myself and all Americans. In general, I am opposed to Senate bill S1082: Food and Drug Administration Revitalization Act, as it does not go far enough to protect myself and my family from the dangers of drugs. If it is to be passed I want all 11 Grassley amendments which are true safety reform added to the bill. I am also in favor of the Dorgan amendment that enables Americans to get a fair price on prescription medication.

As one of the 150 million Americans that rely on dietary supplements to keep myself and my family well, I am especially concerned that this legislation broadens FDA regulatory power to harass functional foods and dietary supplements – which has nothing whatsoever to do with drug safety. While Senator’s Kennedy and Enzi are telling us not to be concerned – we simply don’t trust the FDA and want language that protects dietary supplements in this legislation.

It is vital that the terms “food” and “food ingredients” be removed from this legislation. There must be no confusing the safety of drugs and the safety of food and food ingredients – which are governed by different laws. This bill authorizes the creation of a new regulatory category that enables the FDA and the Reagan-Udall Foundation for the FDA to attack dietary supplements and functional foods. This problem in the wording can be corrected with this simple amendment – so as to be sure this legislation is about drugs and drug safety only.

Amendment to Bill S1082

Purpose of the amendment:
The bill, S1082: The Food and Drug Administration Revitalization Act, is hereby amended to eliminate any reference to the terms food or food ingredients, such that food and food ingredients will not be subject to any jurisdiction or control by the Reagan-Udall Foundation for the Food and Drug Administration.


Intent of amendment:
To eliminate from the bill any possibility that food or food ingredients would be treated like drugs either for safety review purposes or for assessment of their efficacy. It is a fundamental tenet of food and drug law that foods and food ingredients are presumed to be safe and have to be established to be adulterated only if they present a significant or unreasonable risk of illness or injury.

Sincerely,

To get information on contacting your Senators, click: http://www.senate.gov/general/contact_information/senators_cfm.cfm


Byron J. Richards, Founder/Director of Wellness Resources, is a Board-Certified Clinical Nutritionist and nationally-renowned health expert, radio personality, and educator. He is the author of Mastering Leptin, The Leptin Diet, and Fight for Your Health: Exposing the FDA's Betrayal of America.

++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++++

Please act on this information - and help save our freedom to make safe and natural health choices!

Sincerely,
Ron Radstrom
Health Freedom Resources/Southern Botanicals