Use of term “FDA” should always trigger a warning

Use of term “FDA” should always trigger a warning

by Jon Rappoport

June 6, 2016

(To read about Jon’s mega-collection, The Matrix Revealed, click here.)

“In 1957, the FDA burned all the books of dissident physician Wilhelm Reich, M.D., smashed his laboratory equipment with axes, and threw him in jail, where he died.”—Robert Anton Wilson, High Times, March 2001.

Unless you’ve been living in cave on a remote mountain, you know the FDA has been coming down harder on nutritional companies that publish health claims for their products. Such claims trigger investigations and harassment.

But you see, this arrangement is backwards.

The use of the term “FDA” should be the trigger for immediate investigation, whenever it appears. For example, “The FDA has ruled (name of drug) is safe and effective.” Boom. Probe.

Why? Obviously, the FDA is a rogue criminal organization, which is guilty of massive RICO felonies. That’s why.

A news story mentioning the FDA appears in a major newspaper? The paper, if it has an approximation of ethical concern, should print this:

Warning: any action attributed to the FDA should be considered criminal. Accepting an FDA opinion on something more serious than ‘H2O=water’ endangers life and limb. This news outlet accepts no responsibility for the health consequences of any FDA decision.

Now we’d be on the right track.

July 26, 2000, Journal of the American Medical Association, Dr. Barbara Starfield, Johns Hopkins School of Public Health, “Is US health really the best in the world?”: Medical drugs kill 106,000 Americans per year. That’s a million killings per decade.

Every one of the killer drugs is certified as safe and effective by the FDA, the Agency tasked with protecting the health of the American people.

Example: Vioxx was approved for use by the FDA on May 20, 1999. Eventually, it caused 88,000-140,000 cases of heart disease. Conservative death-toll number? 60,000. (An estimated 58,000 American troops died during the Vietnam War.)

Warning: If you accept the FDA’s advice on a health matter, you’re risking death. In case there is any confusion, death means death.

Did you just read a statement from the FDA? Your life is in imminent danger.

Perhaps you recall the original approval of GMO crops and their associated highly toxic Roundup pesticide? No? Let me summarize it for you.

When you cut through the verbiage, you arrive at two key statements. One from Monsanto and one from the FDA, the agency responsible for overseeing, licensing, and certifying new food varieties as safe.

Quoted in the New York Times Magazine (October 25, 1998, “Playing God in the Garden”), Philip Angell, Monsanto’s director of corporate communications, famously stated:

“Monsanto shouldn’t have to vouchsafe the safety of biotech food. Our interest is in selling as much of it as possible. Assuring its safety is the FDA’s job.”

From the Federal Register, Volume 57, No.104, “Statement of [FDA] Policy: Foods Derived from New Plant Varieties,” here is what the FDA had to say on this matter:

“Ultimately, it is the food producer who is responsible for assuring safety.”

The buck-passing, the direct and irreconcilable clash of these two statements, is no accident. It’s not a sign of incompetence or sloppy work or a mistake or a miscommunication. It’s a clear signal the fix was in.

Warning: The relationship of an FDA certification of safety to actual science is coincidental. Run for the hills.

In a stunning interview with Truthout’s Martha Rosenberg, former FDA drug reviewer, Ronald Kavanagh, exposed the FDA as a relentless criminal mafia protecting its client, Big Pharma, with a host of mob strategies (“Former FDA Reviewer Speaks Out About Intimidation, Retaliation and Marginalizing of Safety,” 7/29/2012).

Kavanagh: “…widespread racketeering, including witness tampering and witness retaliation.”

“I was threatened with prison.”

“One [FDA] manager threatened my children…I was afraid that I could be killed for talking to Congress and criminal investigators.”

Kavanagh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted the drugs had to be safe and effective before being released to the public.

But honest appraisal wasn’t part of the FDA culture, and Kavanagh swam against the tide, until he realized his life and the life of his children was on the line.

What was his secret task at the FDA? “Drug reviewers were clearly told not to question drug companies and that our job was to approve drugs.” In other words, rubber stamp them. Say the drugs were safe and effective when they were not.

Veterans of the Armed Forces, take note: Kavanagh remarks that the drug pyridostigmine, given to US troops to prevent the later effects of nerve gas, “actually increased the lethality” of certain nerve agents.

Kavanagh recalls being given records of safety data on a drug—and then his bosses told him which sections not to read. Obviously, they knew the drug was dangerous and they knew exactly where, in the reports, that fact would be revealed.

Warning: the FDA hammers into submission its own employees who are trying to protect your health. These employees submit, resign, or risk their lives and the lives of their families. Have a nice day.

Of course, the US Department of Justice takes no action against the FDA. Why would they?


The Matrix Revealed


In the government lexicon, killer medical drug equals safe and effective, whereas vitamin, mineral, herb equals H-bomb. Didn’t you know that?

Warning: FDA killers resemble ordinary citizens. They appear entirely normal. Their methods have advanced to the point where they can commit their deeds without brandishing visible weapons.

“—Hi, I’m from the FDA. Hey, why are you running away? I’m a public servant doing his job. Gosh o gee, I’m just like you.”

Yes, they can affect an entirely average presence. They internally censor remorse for their crimes. They commit those crimes while pretending to believe they’re carrying out important work. I don’t know why the CIA and DARPA keep researching more advanced forms of mind control. They merely need to study the FDA. That Agency has it down.

Warning: failing to heed warnings about the FDA is a symptom of advanced dementia.

Jon Rappoport

The author of three explosive collections, THE MATRIX REVEALED, EXIT FROM THE MATRIX, and POWER OUTSIDE THE MATRIX, Jon was a candidate for a US Congressional seat in the 29th District of California. He maintains a consulting practice for private clients, the purpose of which is the expansion of personal creative power. Nominated for a Pulitzer Prize, he has worked as an investigative reporter for 30 years, writing articles on politics, medicine, and health for CBS Healthwatch, LA Weekly, Spin Magazine, Stern, and other newspapers and magazines in the US and Europe. Jon has delivered lectures and seminars on global politics, health, logic, and creative power to audiences around the world. You can sign up for his free NoMoreFakeNews emails here or his free OutsideTheRealityMachine emails here.

This entry was posted in FDA.

7 comments on “Use of term “FDA” should always trigger a warning

  1. Tracy Kolenchuk says:

    From the US FDA webpages, ” If a dietary supplement label includes such a claim, it must state in a “disclaimer” that FDA has not evaluated the claim. The disclaimer must also state that the dietary supplement product is not intended to “diagnose, treat, cure or prevent any disease,” because only a drug can legally make such a claim.” http://www.fda.gov/food/ingredientspackaginglabeling/labelingnutrition/ucm2006881.htm

    Even though the FDA clearly acknowledges that scurvy is caused by a deficiency of Vitamin C, it insists that Vitamin C cannot be claimed to diagnose, treat, cure or prevent any disease, stating instead that “the FDA has not evaluated the claim”. They have evaluated the claim, found it to be valid, and then declared it illegal – all on a single web- page.
    to your health, tracy

  2. BreakawayConsciousness says:

    And that’s why they should be labelled the Forceful Drugging Administration.

  3. johnmarkmcguire says:

    Great stuff! It’s about time someone wrote an article on the subject.

    The FDA is nothing more than a group of thugs that have to be paid off in order to access the US markets it controls. Their “approval” means less than nothing.

  4. Chuck says:

    Medicine kills more than 700,000 Americans per year (Null et al.)

  5. Great “summary” post, Jon.

    This one deserves a “burst” on FB.

    Best
    OT

  6. John says:

    According to Federal Law:

    21 CFR 610.15(a), “TITLE 21 – FOOD AND DRUGS
    CHAPTER I – FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
    SUBCHAPTER F – BIOLOGICS
    PART 610 – GENERAL BIOLOGICAL PRODUCTS STANDARDS
    subpart b – GENERAL PROVISIONS
    610.15 – Constituent materials.
    (a) Ingredients, preservatives, diluents, adjuvants. All ingredients used in a licensed product, and any diluent provided as an aid in the administration of the product, shall meet generally accepted standards of purity and quality. Any preservative used shall be sufficiently nontoxic so that the amount present in the recommended dose of the product will not be toxic to the recipient, and in the combination used it shall not denature the specific substances in the product to result in a decrease below the minimum acceptable potency within the dating period when stored at the recommended temperature. Products in multiple-dose containers shall contain a preservative, except that a preservative need not be added to Yellow Fever Vaccine; Poliovirus Vaccine Live Oral; viral vaccines labeled for use with the jet injector; dried vaccines when the accompanying diluent contains a preservative; or to an Allergenic Product in 50 percent or more volume in volume (v/v) glycerin. An adjuvant shall not be introduced into a product unless there is satisfactory evidence that it does not affect adversely the safety or potency of the product. The amount of aluminum in the recommended individual dose of a biological product shall not exceed: (1) 0.85 milligrams if determined by assay; (2) 1.14 milligrams if determined by calculation on the basis of the amount of aluminum compound added; or (3) 1.25 milligrams determined by assay provided that data demonstrating that the amount of aluminum used is safe and necessary to produce the intended effect are submitted to and approved by the Director, Center for Biologics Evaluation and Research or the Director, Center for Drug Evaluation and Research.

    ~~~

    Yet, Nowhere in the FDA’s “regulations” is there a requirement that the preservative must be a compound that is a known, highly toxic bioaccumulative human terratogen (An agent, such as a virus, a drug, or radiation, that causes malformation of an embryo or a fetus), mutagen, carcinogen, and immune system disruptor at injected levels below 1 part per million as Thimerosal (Sodium Ethylmercurithiosalicylate) does.

    According to the EPA, Sodium Ethylmercurithiosalicylate is classified as a Pesticide with possible degradation to Elemental mercury, and was named in the study: “Pesticide Chemical Use Profile for Pentachlorophenol, Sodium Salt of 63003” Prepared for the United States Environmental Protection Agency, Office of Pesticide Programs, Technical Services Division; Nov., 1976, by: Tracor Jitco, Inc, as a moss inhibitor for roofs.

    Since there is also the possibility of degradation to elemental mercury, which the Federal EPA has recognized as a neurological poison. Elemental (metallic) mercury primarily causes health effects when it is breathed as a vapor where it can be absorbed through the lungs. These exposures can occur when elemental mercury is spilled or products that contain elemental mercury break and expose mercury to the air, particularly in warm or poorly-ventilated indoor spaces. The first paragraph on this page lists the factors that determine the severity of the health effects from exposure to mercury. Symptoms include these: tremors; emotional changes (e.g., mood swings, irritability, nervousness, (excessive shyness); insomnia; neuromuscular changes (such as weakness, muscle atrophy, twitching); headaches; disturbances in sensations; changes in nerve responses; performance deficits on tests of cognitive function. At higher exposures there may be kidney effects, respiratory failure and death. People concerned about their exposure to elemental mercury should consult their physician. Note the bold statements. These, I believe, can all be linked in some way to spectrum disorders to some degree. There are, according to the EPA, potable water drinking limits for mercury because of the effects and accumulation of mercury.

    The degradation process for Sodium Ethylmercurithiosalicylate (Thimerosal), is cited in: International Journal of Pharmaceutics Volume 208, Issues 1-2, 4 November 2000, Pages 23-34

    Abstract: The route of formation and identification of the principal degradation products of thimerosal (thiomersal) has been undertaken. The initial oxidation to dithiosalicylic acid is followed by cleavage of the disulphide bond of the dithiosalicylic acid by the ethylmercuric ion to reform 1.5 mol of thimerosal with concurrent oxidation to form 0.5 mol of 2-sulfinobenzoic acid for each mole of dithiosalicylic acid. In the presence of copper ions 2-sulfobenzoic acid was also formed. A mechanism has been proposed which accounts for the stoichiometry of the cleavage reaction observed and the significance of the reaction is discussed. Ethylmercury degrades to Methylmercury. Thiomersal (or sodium ethylmercurithiosalicylate) commonly known in the United States as thimerosal, is an Organomercury compound (approximately 49% mercury). For fetuses, infants, and children, the primary health effect of methylmercury is impaired neurological development. Methylmercury exposure in the womb, which can result from a mother’s consumption of fish and shellfish that contain methylmercury, can adversely affect a baby’s growing brain and nervous system. Impacts on cognitive thinking, memory, attention, language, and fine motor and visual spatial skills have been seen in children exposed to methylmercury in the womb. Recent human biological monitoring by the Centers for Disease Control and Prevention in 1999 and 2000 (PDF) (3 pp., 42 KB, About PDF) shows that most people have blood mercury levels below a level associated with possible health effects. More recent data from the CDC support this general finding.

    Outbreaks of methylmercury poisonings have made it clear that adults, children, and developing fetuses are at risk from ingestion exposure to methylmercury. During these poisoning outbreaks some mothers with no symptoms of nervous system damage gave birth to infants with severe disabilities, it became clear that the developing nervous system of the fetus may be more vulnerable to methylmercury than is the adult nervous system. (Reference: “Pink’sDisease” and other mercury poisoning episodes in world history).

  7. Don says:

    Bioweapons / vaccine defense is a Congressional feeding cartel $50Billion plus not protecting American people because all Bioweapons are designed to be genetic modified to have complete immunity to drugs
    FDA /NIH/CDC all are corrupted for fleecing public
    Hug your kids A pandemic will kill 10 Million So what will gov do

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