The Politics Of Health: Feature ArticleFDA Approves Viral Adulterations of Our Food SupplyThursday, August 24, 2006Byron Richards, CCN On Friday, August 18, 2006, the FDA approved a viral cocktail to be sprayed on foods we eat. This is the first time viruses have been approved for use as food additives. The FDA wants you to believe it will be safe to consume these viruses every day for the rest of your life with no adverse health effects. This is a monumental announcement by the FDA, indicating they are throwing all caution to the wind regarding the safety of our food supply.
Are you willing to stand in line for a virus-laden sandwich? How do you like the idea of buying virus-infested food for your family? The first virally contaminated foods entering our food supply with the blessings of the FDA will be luncheon meat and poultry. Live viruses will be sprayed on foods such as cold cuts, sausages, hot dogs, sliced turkey, and chicken.
The stated goal of the new FDA-approved viruses is to kill a rare bacterium known as Listeria monocytogenes. This bacterium is killed by cooking; however, it poses a problem in meats that are cooked during processing and not cooked again prior to consumption, so it can readily infect foods such as deli meats.
Yes, the FDA plans to use one infectious organism to fight another. The carnage of battle will end up in your digestive tract along with the victorious live viruses, which the FDA assures us will not attack human cells. However, they cannot possibly be certain the viruses will not attack the friendly bacteria that make up the lining of your digestive tract. The FDA approval was based on scant human testing, mostly from unrelated medical experiments. Such safety data is woefully inadequate to determine safe ingestion of a specific product by humans over the course of a lifetime.
The company that produces these biotech viruses is Baltimore-based Intralytix, Inc. The viruses are known as bacteriophages, viruses that kill bacteria, or phages for short. Phages have been around a long time, living as parasites inside many bacteria. Intralytix uses biotechnology to grow viral phages in a culture with Listeria, in theory teaching the viruses to recognize the bacteria. The FDA-approved cocktail contains six different viruses intended to attack one strain of bacteria. This concoction is then sprayed on food. If Listeria is present in the food, the bacteria will ingest the viruses. This results in massive viral replication inside the bacteria, until such point as the bacteria simply bursts. This battle results in significant production of bacterial poisons called “endotoxins”, as the bacteria tries to defend itself. When the bacteria burst, these endotoxins are released. These, along with the victorious live viruses, will now be on the food that will be eaten.
The FDA and Intralytix would like us to believe that these viruses will only attack the specified bacteria they are intended to kill and will be harmless to humans. I’m sorry to burst their bubble, but they can’t possibly guarantee such safety. It is true that the viruses, at least at this time, cannot recognize human cells. However, the virus can potentially recognize normal bacterial cells in the human digestive tract and may be able to adapt to infect one or more of these friendly bacteria.
There is certainly a risk that humans will be exposed to excessive amounts of endotoxin. This could come from the manufacturing of the viral cocktail, the interaction of the viruses with bacteria after being sprayed on food, and/or the interaction of the viruses with bacteria in the digestive tract. The human immune system is highly reactive and sensitive to bacterial endotoxins. They provoke allergy, asthma, autoimmune problems, and elevate cholesterol. They also interfere with the healthy function of cells lining the digestive tract. Researchers have demonstrated that the presence of bacterial endotoxins can start cancer in the colon. Additionally, the human immune system reacts directly to viral phages. Thus, a person who eats a lot of processed deli meat is certain to evoke an immune reaction to the viruses. What will this reaction be? Allergy? Asthma? Autoimmunity? Cancer? How can the FDA approve a food additive that it knows can induce a variety of human immune responses? Phages are so good at disrupting normal immunity that they are being considered for use as part of organ transplant medicine. The ingestion of significant amounts of viral phages into the human digestive tract is a wild card full of unknown outcomes. For example, it is certainly possible that these phages, which constantly mutate in order to survive, are likely to find a way to infect bacteria they were not intended to infect. Since phages are parasites, they could hijack the friendly bacteria of the digestive tract and turn them into viral machines, constantly generating viral particles that are likely to confuse the human immune system, if not directly infect the body. We know from history that these viral phages can turn innocuous bacteria into a killer, which is how cholera occurs. Furthermore, the Listeria bacteria are not going to take the issue lying down. They will develop resistance to the viruses over time, as we have seen with the overuse of antibiotics. Going down this path we are likely to have hundreds of viral food additives in the food we eat, all designed to combat some possible infection coming from poor quality food. Sooner or later we will inadvertently create deadly new super-strains of bacteria and/or parasitically infect the human digestive tract with an untreatable infection. There is also the very real possibility of unintended viral recombination. What happens when a person with viral stomach flu eats food containing a dose of this viral food additive? It is certainly possible for the genetic material of the flu virus to interact with the genetic material of the viral phages, provoking an undesirable new viral infection. Let’s not forget that the FDA won’t tell us which foods in the food supply contain genetically modified organisms (GMO). Seventy percent of the packaged food on grocery shelves already contains GMO adulterated food. These foods have viral promoter genes woven into the DNA of every cell, a technique used to implant a pesticide toxin into every cell of this fake food (see Fight for Your Health, chapter 15). What happens when the viral phages interact with the viral promoter genes in GMO food? What new virus will be encouraged to form? Keep in mind that the FDA wants to conduct this experiment on our food supply to protect a small minority, only about 2500 people, who are made seriously ill by this infection each year. The ill are mostly pregnant women, elderly with compromised immunity, and small children. It would be a lot more to the point if the FDA would simply warn such people that eating these foods, due to their poor quality of production, may be dangerous. What the FDA should really do is improve the quality of our food supply, the true source of the problem. Why expose millions of Americans to an unproven ingestion of live viruses for the benefit of so few?
The FDA has failed miserably for the past century to protect the public from the adulteration of our food supply by vested interests. This is just one more insult added to a long list of injuries.
The company is also seeking FDA approval for viral sprays to treat foods that could be contaminated with E. coli and Salmonella, which means that similar “trained” viruses could end up in a majority of the protein foods in our food supply.
Intralytix sees financial opportunity. They have already licensed their now FDA-approved viral spray to an undisclosed multi-national company for use around the world. When the CEO of Intralytix, John Vazzara, was recently asked about this partner company, he refused to disclose their name. The grand profit-driven biotech experiment on the health and well being of all Americans is now in full swing.
Congress should investigate the financial ties and backroom dealings that would allow this bizarre food additive approval by the FDA.
Of course, we will need new wonder drugs to combat the new bio-tech produced infections. Americans will stay sick and the sickness-driven bio-tech industry will flourish. The bio-tech industry will make people sick on the front end and treat them on the back end. It’s a win-win situation for profit on illness.
It is quite clear that the Bush agenda has been to promote American biotech companies as the new future for American prosperity. Administrative opinions have trumped science in virtually every situation wherein safety conflicts with profit. The FDA acts to foster profits for biotech companies and the growth of the biotech industry. This is a betrayal of the public trust. The leaders of the FDA are personally responsible and need to be held accountable. This means Andrew von Eschenbach, M.D., temporary head of the FDA and his chief science officer, Scott Gottlieb, M.D. These men are not only obsessed with approving risky drugs for the benefits of Big Pharma, it is now clear that they are willing to allow obvious adulteration of the food supply. They seek to control what we eat, and they are tampering with survival of the human race.
The FDA does not truly know how safe viral phages are to consume on a regular basis. They have no idea of the cumulative effect over the course of a lifetime, especially as more of these viral cocktails are added to the food supply. They have no way to measure how this new type of adulteration in the food supply will interact with the poor digestive/immune health of half the American population, in combination with all the other serious adulterations already approved by the FDA. The FDA lacks due diligence in honoring its mandate to protect the American public.
Consumers standing in line to buy a luncheon meat sandwich will have no idea if they are ingesting live viruses as part of their meal. While the FDA will require the ingredient to be listed on packages as “bacteriophage preparation,” most consumers will have no idea that means they are ingesting live viruses. Foods bought at deli counters or prepared in restaurants will not need to warn consumers.
Get connected to the sustainable family farms in your community. Buy meat that is range raised without antibiotics and synthetic growth hormones. Demand that the food you are eating is labeled with a country of origin. Buy American; buy locally-produced food whenever possible. Support those who truly believe in being the stewards of our land and food for our people and for future generations. These good people are being squashed out of existence by multi-national agribusiness, companies that could truly care less about the quality of our food supply or the security and health of Americans. How you spend your money is your most powerful vote. Vote for those who care.
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Senate Attempts Damage Control – House Braces for Onslaught Senators were taken off guard by the public outrage over the passing of bill S.1082 with language that can be used to seriously harass dietary supplements by enabling the FDA to apply drug-related risk analysis to the safety of food and food ingredients (and thus dietary supplements).
The FDA is Acquiring New Powers to Suppress Alternative Health Your right to have free access to safe and highly effective dietary supplements is under an intense multi-pronged FDA attack. On May 14, 2007 the Supreme Court sided with the FDA by deciding not to hear the case of Nutraceutical v FDA, letting stand a federal appeals court ruling that permits the FDA to use drug-related risk/ benefit analysis to determine if a nutrient is safe.
The Senate has sold out the American people. Anyone voting for change in the last election can now plainly see the shenanigans of a Democratic-controlled Senate. Under Republicans no FDA reform ever took place. Big Pharma owns so many Republicans that all meaningful legislation to curtail the deaths and injuries of American citizens at the hands of Big Pharma and the FDA had been completely thwarted for the past six years. Under Democratic control sweeping FDA reform favorable to Big Pharma was proposed and the majority of meaningful reform was blocked or seriously watered down. Which is worse? As Kennedy stated in his opening remarks today, S1082 (the Kennedy/Enzi FDA bill) was an “elaborate scheme.”
For approximately four days Americans lived in a delusional state that they may soon pay drug prices the same as every other country in the civilized world. Euphoria over breaking the Big Pharma monopoly turned to disgust as the chameleon, Senator Edward Kennedy (D-MA), changed sides and lead a contingency of Democrats against fellow Democrats lead by Byron Dorgan (D-ND). By passing the Cochran amendment the Dorgan amendment is poisoned and will no longer be effective. Maybe Democrats are now learning what Republicans have known for some time – you can’t trust Kennedy.
In May of 2006, after months of research and investigation, I published my ominous findings in the book Fight for Your Health: Exposing the FDA’s Betrayal of America. Everything I predicted in this book is on the fast track to becoming reality. A majority of Americans, not informed on current events and unaware of the history involved, are silent. Mainstream media, one of Big Pharma’s largest clients, is silent. Only the power of the internet, which rivals the invention of the printing press in significance, is making it possible for individuals to understand what is going on.
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.”
S1082 Update – Tuesday’s Activity. Fight Erupts on Senate floor: As the Senate continues to debate the Big Pharma-friendly sweeping reform of the FDA a new problem for Big Pharma’s prize Senators has erupted and quickly turned into confrontation on the floor of the Senate. At stake is at least 10 billion dollars per year in exorbitant Big Pharma profits. In one corner is Big Pharma-puppet Orrin Hatch (R-UT), representing the Kennedy/Enzi drug cartel. In the other corner is a majority of Senators lead by Byron Dorgan (D-ND).
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S1082 Update – Monday’s Activity at the bottom of this article. Bill S1082: The Food and Drug Administration Revitalization Act (also called the Prescription Drug User Fee Act of 2007) is one of the greatest scams and con jobs ever foisted on the American public. Current FDA management is grossly incompetent on the subject of drug safety.
A new attack against health freedom, drug safety, and dietary supplements was launched last week by Senator Edward Kennedy (D-MA) with major support from Michael Enzi (R-WY). It is called the Food and Drug Administration Revitalization Act (S1082). This legislation was planned over the past few years working hand-in-glove with the FDA’s dysfunctional management and legal team – meaning this legislation was written for the profits of Big Pharma and Big Biotech AT THE EXPENSE OF SAFETY AND HUMAN HEALTH.
Americans are up in arms that our pets are being injured and killed by a toxin sent to America by a Chinese company. Melamine, a toxic fertilizer used in China, is the suspected culprit behind the deaths and injuries to potentially hundreds of thousands of our pets. The FDA assures us that this toxin has not entered the human food supply – does anyone believe in the competence of the FDA? It is only a matter of time before this type of problem happens to humans, as the inept FDA has no control over imported food intended for humans, let alone pets.
On February 13, 2007 the House Energy and Commerce Committee’s Subcommittee on Oversight and Investigations opened hearings lambasting the FDA regarding the safety of drugs. The opening statement by Chairman John Dingell (D-MI) set the tone, “It is clear … that the FDA is badly broken. I expect that before we finish this investigation, which is just getting underway, we will discover whether the problems we have found are due to the work of scoundrels, irrational penny-pinching, or because the doors to the FDA “hen house” have been thrown open to foxes. It may be a combination of all three.”
Wall Street, international bankers, President Bush, pharmaceutical companies, new biotech companies, the Rockefeller empire, and the FDA have created a new plan for public health. It is a grand vision based on profit. It will use the FDA and, as needed, the Department of Homeland Security as the regulatory police force that ensures compliance in the name of public safety. Legitimate objections may be overpowered in the name of national security.
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