China Sentences Ex-head of Chinese FDA to death over drugcompany bribes. American FDA more guilty.

[Guest guest]

Read and see what the public thinks of the FDA. Because aspartame

damages the mitochondria it interacts with virtually all drugs and

vaccines and you know it. Therefore, for anyone using aspartame no

drug is safe. Your crime is greater than the Chinese FDA head

because you are allowing people the world over to die from aspartame

with full knowledge since you originally tried to have the

manufacturer indicted for fraud and revoked the petition for

approval. You allow this with full knowledge and tell people a

deadly addictive excitoneurotoxic carcinogenic drug is safe knowing

you are lying. You are so guilty you refuse to answer the Citizens

petition for ban of aspartame, six years ago, and the imminent health

hazard amendment serving above the law. I'm asking that all that

read this send it to their congressman and senator asking for a full

investigation of the FDA and aspartame.

 

The aspartame documentary on how the world is poisoned with aspartame

and how Rumsfeld got it on the market after FDA revoked the petition

for approval is ably called: Sweet Misery: A Poisoned World,

www.soundandfury.tv The medical text, Aspartame Disease: An Ignored

Epidemic, by H. J. Roberts, M.D., www.sunsentpress.com is as large as

the New York phone directly filled with diseases and horrors and the

guilt of FDA's crime. Other medical texts like Excitotoxins: The

Taste That Kills by neurosurgeon Russell Blaylock, M.D.,

www.russellblaylockmd.com let the public know aspartame

(NutraSweet/Equal/Spoonful/Canderel/E951/) is a killer.

 

Dr. Betty Martini, D.Hum, Founder

Mission Possible International

9270 River Club Parkway

Duluth, Georgia 30097

770 242-2599

www.mpwhi.com, www.dorway.com, www.wnho.net

Aspartame Toxicity Center, www.holisticmed.com/aspartame

 

 

Fri, 30 May 2008 08:23:26 -0400

"John T. Linnell"

 

 

 

 

 

 

China sentences ex-head of Chinese FDA to death over drug company bribes

 

Found on

< http://www.naturalnews.com/021874.html> http://www.naturalnews.com/021874.html

 

NOTE. Health Prevention Canada is little better than the US FDA.

 

The penalty in China is death, in America it's business as usual.

Zheng Xiaoyu, the former head of China's FDA, was sentenced to death

for accepting $832,000 in drug company bribes and for dereliction of

duty. Like China, our country is in the middle of a drug and food

safety crisis. Why is FDA Commissioner Andrew von Eschenbach, M.D.

getting a free pass? Why did the Senate just pass legislation

(S.1082) that gives von Eschenbach significantly more power to do

whatever he pleases? And exactly what is it that von

< http://www.naturalnews.com/Eschenbach.html> Eschenbach is doing?

 

 

 

 

 

 

 

The Next Vioxx

 

On June 6, 2007, Henry Waxman (D-CA), Chairman of the House Committee

on Oversight and Government Reform will haul in

< http://www.naturalnews.com/Andrew_von_Eschenbach.html> Andrew von

Eschenbach to testify on why

< http://www.naturalnews.com/the_FDA.html> the FDA failed to warn

Americans of the extreme cardiovascular danger and increased risk of

death from taking < http://www.naturalnews.com/Avandia.html> Avandia, a

$3 billion-a-year blockbuster diabetes drug made by

< http://www.naturalnews.com/GlaxoSmithKline.html> GlaxoSmithKline.

Statistics that were primarily obtained from GlaxoSmithKline's own

research data predict that 35,000 people needlessly died taking

Avandia last year and the FDA was fully aware of the risks and chose

to ignore them. In fact, the problem only came to public view because

one independent researcher pursued the investigation and published

his findings in the New England Journal of Medicine. This is the

FDA's job, why do we need citizen watchdogs to do the work instead?

 

It is certain that during Von Eschenbach's testimony he will speak

out of both sides of his mouth and cover the FDA's ineptitude and

deceit. He is likely to blame a lack of FDA funding for the problems.

In reality, the FDA is not at all as incompetent and under funded as

they seem. The truth of the matter is that the FDA does exactly what

they want. The FDA spends its time, energy, and money on management's

priorities.

 

It is hard for some to grasp that safety of drugs or safety of the

< http://www.naturalnews.com/food_supply.html> food supply is not the

top FDA management priority. In the case of Avandia Americans are

being needlessly killed as a result of FDA management decisions.

These decisions preserve the profits of

< http://www.naturalnews.com/drug_companies.html> drug companies and

further the myth that drugs are the answer to our health problems. Do

not be misled, FDA actions are intentional.

 

The timing couldn't be worse for the FDA as Waxman is preparing the

House version (HR.1561) of the recently passed Senate

< http://www.naturalnews.com/drug_safety.html> drug safety bill

(S.1082). The Senate version is a fake safety bill paid for by

< http://www.naturalnews.com/Big_Pharma.html> Big Pharma. Will the

House follow along or will they put some real teeth in the

< http://www.naturalnews.com/legislation.html> legislation?

 

 

 

 

 

 

 

How Does One Define Dereliction of Duty?

 

The dictionary defines it as a deliberate neglect of duty or

obligations. Certainly, Avandia is a case in point. However, Avandia

problems are the tip of the FDA iceberg. Anyone caring to look will

find a rabbit hole so deep and so full of stench that it is virtually

impossible to comprehend. The story is so bad that it falls into the

category of not believable. Under the leadership of Andrew von

Eschenbach collusion with the industries the FDA is supposed to

regulate has reached an all time high. This reckless behavior has

resulted in deaths and injuries to hundreds of thousands of

Americans, all for the profit of drug companies at the expense of

human health.

 

A case in point is the antibiotic Ketek, which the

< http://www.naturalnews.com/FDA_approved.html> FDA approved for broad

applications KNOWING it was going to injure children. Von Eschenbach

even threatened < http://www.naturalnews.com/FDA_scientists.html> FDA

scientists who didn't see the Ketek issue his way. Then there is the

case of the atypical antipsychotic Zyprexa, which the FDA approved

for use in adult schizophrenics even though the FDA knew the drug

caused obesity and diabetes. The FDA sits around allowing billions of

dollars of this drug (mostly at taxpayer expense) to be given to

children for mild behavioral issues, an unapproved use that leads to

extremely poor health and disease. Then there is the Trasylol

scandal, a very expensive cardiovascular bypass drug that needlessly

sentences 15,000 Americans per year to premature death within the

next 5 years. When < http://www.naturalnews.com/Bayer.html> Bayer was

caught directly lying to the FDA regarding Trasylol's dangers, von

Eschenbach deflected legal liability for Bayer by doing virtually

nothing and leaving the drug on the market. These are just a few

examples, there are unfortunately many more.

 

The common theme is that FDA management intentionally hides risks of

drugs so that drug companies can turn them into blockbusters,

oftentimes selling them in ways that were never approved in the first

place. As chilling safety problems are reported to the FDA the

organization fails to act, partly so it won't look bad for approving

the drugs in the first place, partly to preserve billions in profit

for various companies, and partly because FDA management employees

are often eyeing high-paying jobs in the industry that is being

regulated. It is not that the FDA is incompetent. In fact, FDA

scientists routinely warn management of the problems. Management

intentionally does not act in a way that protects American consumers.

In virtually all cases the economic situation of drug companies is

placed ahead of human health and safety. In my way of looking at the

world this is dereliction of duty.

 

This is as true of drugs as it is of our massively adulterated food

supply (genetically modified foods, viral cocktails approved as food

additives, chemicals allowed on food, chemicals allowed as flavoring

agents or sweeteners, etc.). The FDA has no way to trace the toxicity

of genetically modified food and actively prevents labels that would

tell consumers they are even eating the garbage, which now permeates

the packaged foods on grocery store shelves. At the same time the FDA

actively works to suppress information about natural ways to improve

health. All of these FDA actions are intentional.

 

China gives the death sentence for dereliction of duty. In

< http://www.naturalnews.com/America.html> America we conduct hearings

(sometimes) and then do nothing. Big Pharma and Big Biotech own the

FDA, the White House, and much of Congress.

 

 

 

 

 

 

 

The FDA's Real Priority

 

Andrew von Eschenbach has never hidden his agenda; it is more an

issue that people simply aren't paying attention. The top priority of

the FDA is now the von Eschenbach dream, which is to bring new

biotech drugs to the market with far less safety or effectiveness

testing and then conduct experiments on individuals as the drugs are

used in clinical practice. This effort is called the Critical Path

Initiative and it will take a giant step forward should the

Reagan-Udall Foundation for the FDA come into existence as proposed

in Senate bill S.1082. Von Eschenbach has stated that this is the

very top priority of the FDA for many years to come (not food or drug safety).

 

Von Eschenbach is an oncologist who wants to create a

< http://www.naturalnews.com/cancer.html> cancer sickness industry

wherein nobody is cured; they are simply managed indefinitely on

super expensive medications. Von Eschenbach has led this effort for

many years as a key figure in the elder Bush's C-Change, a group

facilitating the development of Big Biotech drugs for highly

profitable cancer "treatment."

 

Andrew von Eschenbach took the top job at the

< http://www.naturalnews.com/National_Cancer_Institute.html> National

Cancer Institute to forward this agenda. As its head he diverted

billions of dollars of research funding into C-Change companies and

away from fundamental cancer research, a shocking travesty. Even more

appalling is that Tommy Thompson, then head of the Department of

Health and Human Services, approved a waiver allowing von Eschenbach

to remain on at C-Change while he headed the National Cancer

Institute. This is one of the most dramatic conflicts of interest

imaginable, setting back vital cancer research at least a decade.

 

Tommy Thompson, like so many government officials, has moved on and

now helps Verichip sell implantable RFID chips. In October of 2006

Von Eschenbach was appointed to head the FDA, and for a while he held

all three spots (C-Change, head of NCI, and head of FDA). In the

recent Lame Duck session von Eschenbach was made permanent head of

the FDA. No questions were asked of his extensive connections to the

Biotech industry.

 

It should come as no surprise that von Eschenbach wants to make the

FDA part of the drug development business, including licensing and

marketing rights for the drugs the FDA helps develop with its

sophisticated software. Is it possible to imagine a greater conflict

of interest? We are not talking about a paltry $780,000 worth of

conflict of interest, we are talking tens of billions. Do you think

for a moment the FDA will ever remove one of its own drugs from the

market or paint a clear picture of its true risks?

 

 

 

 

 

 

 

A Time for Action

 

Senate bill S.1082 and House bill HR.1561 will turn into some type of

new and sweeping FDA "reform" before Big Pharma's funding of the FDA

expires on September 30 of this year. The big question is what will

be in the legislation. So far, Big Pharma was able to buy enough

Senator's votes to neutralize any meaningful reform. The Avandia

scandal is likely to make matters worse for the FDA as the House

considers its version of this legislation after the Memorial Day recess.

 

Buried within this legislation is an FDA sneak attack on

< http://www.naturalnews.com/dietary_supplements.html> dietary

supplements. Dietary supplements are routinely targeted by the FDA as

they offer true competition, both safe and effective, to drugs. The

FDA acts as a police-force bully to help stamp out Big Pharma

competition and keep Americans in the dark on natural ways to prevent

and treat disease. Bill S.1082 allows the FDA to apply drug-related

risk benefit analysis to the safety of food and dietary supplements

and remove commonly used products from the market at their whim. This

must be stopped. A take action letter can be found by clicking here.

 

At least one hundred thousand people needlessly die per year at the

hands of Big Pharma drugs. Several million are injured so seriously

they have to go to the

< http://www.naturalnews.com/hospital.html> hospital and unfortunately

many are injured while at the hospital. The FDA actively and

intentionally withholds from doctors and patients the true risk

profile of many drugs despite the desperate warnings of its own

safety scientists and independent experts. There is no question that

FDA top management suffers serious dereliction of duty. Should we

follow the lead of the Chinese? Maybe then drug safety and

< http://www.naturalnews.com/food_safety.html> food safety would improve.

 

 

 

 

 

 

 

About the author

 

Byron J. Richards, Founder/Director of

< http://www.wellnessresources.com/> Wellness Resources, is a

Board-Certified Clinical Nutritionist and nationally-renowned health

expert, radio personality, and educator. He is the author of

< http://www.wellnessresources.com/products/mastering_leptin.php> Mastering

Leptin, < http://www.wellnessresources.com/Books/leptin_diet.php> The

Leptin Diet, and

< http://www.wellnessresources.com/Books/fight_for_your_health.php> Fight

for Your Health: Exposing the FDA's Betrayal of America.

 

You may now read

< http://www.wellnessresources.com/Books/fight_for_your_health.php> Fight

for Your Health free, and/or purchase the book or a PDF download. All

proceeds from the sales go to defend health freedom.

Richards encourages individuals to take charge of their health, stand

up for their health rights, and not blindly succumb to propaganda

from the vested-interests who profit from keeping Americans sick. As

founder of Wellness Resources, Inc. of Minneapolis, MN, an

independently-owned fine-quality

< http://www.naturalnews.com/dietary_supplement.html> dietary

supplement company since 1985, he has personally developed 75 unique

nutraceutical-grade nutritional formulas.

< http://www.wellnessresources.com> www.wellnessresources.com

E-mail: < byron byron

 

 

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