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chinese methods we should consider

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  • Dick Eastman
    China sentences ex-head of Chinese FDA to death over drug company bribes Found on
    Message 1 of 1 , Jun 1, 2008
      China sentences ex-head of Chinese FDA to death over drug company bribes

      Found on

      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?
      From: "Dr. Betty Martini,D.Hum." <bettym19@...>
      Subject: China Sentences Ex-head of Chinese FDA to death over drug company bribes. American FDA more guilty.
      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

      Date: Fri, 30 May 2008 08:23:26 -0400
      From: "John T. Linnell"

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

      Found on

      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
      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

      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

      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 <
      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
      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
      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
      Leptin, <
      Leptin Diet, and
      for Your Health: Exposing the FDA's Betrayal of America.

      You may now read
      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
      supplement company since 1985, he has personally developed 75 unique
      nutraceutical-grade nutritional formulas.
      E-mail: <mailto:byron@...>byron@...

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