by Jon Rappoport
April 17, 2017
The excellent medical reporter, Martha Rosenberg, has written a piece at Salon: “The FDA Now Officially Belongs to Big Pharma.” Here are a few highlights:
It is hard to believe only four senators opposed the confirmation of [the new FDA Commissioner]…[he] received money from 23 drug companies including the giants like Johnson & Johnson, Lilly, Merck, Schering Plough and GSK…”
It would be naive to think that the FDA endeavors to protect the public’s health as its primary focus. Indeed, that would be a conflict of interest, as it serves its master, the pharmaceutical industry. Has the Food and Drug Administration engineered a shortage of intravenous vitamin C as part of an overall attack on natural and non-toxic approaches to healing that compete with prescription drugs? An analysis by Natural Blaze would suggest that the answer is yes.
Natural Blaze claims that a critical shortage of IV bags in general followed an FDA ban on the mass production of intravenous vitamin C. The FDA limited the availability of IV-C and the pharmaceutical industry halted production of injectable vitamins and minerals, after a 60 minute story about the miraculous recovery of a swine flu patient on life support. Because of the shortage of IV-C, doctors called upon compounding pharmacies to produce it. But the FDA began to limit compounding pharmacies after injectable steroids produced by the New England Compounding Center were contaminated with a fungus that caused a deadly outbreak of meningitis. Here is an example of an entire industry being punished for the dubious practices of one compounding pharmacy.
The United States Department of Agriculture’s Food Safety Inspection Service (FSIS) informed Sustainable Pulse on Monday that they will allow multi-ingredient products, which include GMO fed animal products, such as eggs, meat or poultry, to be labeled Non-GMO.
Sustainable Pulse requested further details on the FSIS guidelines published in August, due to ‘confusing’ language regarding which products will be able to be labeled non-GMO.
The U.S. Food and Drug Administration, which is quietly starting to test certain foods for residues of a weed killing chemical linked to cancer, has found the residues in a variety of oat products, including plain and flavored oat cereals for babies.
Source: www.huffingtonpost.com By Carey Gillam
Data compiled by an FDA chemist and presented to other chemists at a meeting in Florida showed residues of the pesticide known as glyphosate in several types of infant oat cereal, including banana strawberry- and banana-flavored varieties. Glyphosate was also detected in “cinnamon spice” instant oatmeal; “maple brown sugar” instant oatmeal and “peach and cream” instant oatmeal products, as well as others. In the sample results shared, the levels ranged from nothing detected in several different organic oat products to 1.67 parts per million, according to the presentation.
Those who support the nationwide legalization of marijuana for therapeutic use, were disappointed by the Food and Drug Administration’s (FDA) recent failure to reclassify marijuana’s status from that of a Schedule I drug to another more appropriate classification.
Since 23 states have now legalized marijuana for medical use, and since numerous studies have confirmed its value as medicine and have proven that it is safe, it seemed the logical next step to begin relaxing the laws at the federal level.
The medicinal value of cannabis cannot be ignored. This healing plant has successfully been used for treatment of pain, insomnia, rheumatoid arthritis, Parkinson’s, multiple sclerosis, seizure disorders, and even cancer.
Despite its long history of medicinal use throughout the world, cannabis has remained an illegal, controlled substance in the US, aggressively pursued by government agents for many decades. The US Drug Enforcement Administration (DEA) gained significant authority over cannabis after the Controlled Substances Act of 1970 was signed into law. Once enacted, the DEA created a scheduling system that classified different substances according to their potential for addiction and abuse. Without any scientific backing, the DEA put cannabis at the top of the list – a schedule one drug with the greatest potential for addiction, with no medicinal value whatsoever.
There are many ways corporations modify food products with chemicals in order to increase sales. They use toxic chemicals to extend shelf life, make food look more attractive, kill bugs in the fields, stave off mold and mildew, kill fungus and bacteria, add flavor back in after chemicals kill the taste, and actually make people depressed and anxious to fuel the chemical medicine industry. Most of it’s nothing new, and has been going on since WWII. GMOs have been in existence for 30 years now, though few people are aware of that.
The cumulative effect of poisons in the body is something you can’t sue one food manufacturer for, or one doctor, or one chemical company. The corporate food industry in America is sinister and insidious. They know they can’t be held accountable for long-term chronic sicknesses from which so many Americans suffer. The FDA could care less about Americans’ health and well-being.
Even though the big revelations about Big Pharma’s science paper research fraud came out years ago, most people are still not aware of this. Here’s the scoop: Drug companies routinely pay P.R. firms to ghostwrite clinical science papers which are published in medical journals and forwarded to the FDA to “prove” the drugs are safe and effective. But it’s all a farce: The papers are pure fiction, dreamed up by what are essentially marketing firms for the sole purpose of getting drugs approved even when they don’t work.
“In 2009, around fourteen thousand women who developed breast cancer while taking Prempro, a hormone replacement therapy (HRT), sued the drug’s manufacturer, Wyeth,” wrote Rupert Sheldrake in an extraordinary book called Science Set Free.
NaturalNews reports; One of the world’s most lucrative industries, spending on cancer drugs reached an all-time high last year, as it was valued at more than $100 billion. Spending on cancer drugs increased 6.5 percent annually over the past five years and is expected to continue growing at a rate of 8 percent each year through 2018, according to figures provided by the IMS Institute for Healthcare Informatics.
That spending is highly concentrated, as the US and five of Europe’s largest countries account for nearly two-thirds of the entire market.
This means that billions and billions of dollars are secured by Americans being diagnosed with cancer.
The former head of the FDA, Margaret Hamburg, used the federal agency to run a massive conspiracy of racketeering and fraud in order to generate millions of dollars in drug company profits for her husband’s hedge fund firm, alleges a damning lawsuit filed in the United States District Court for the District of Columbia.
The lawsuit alleges that while acting as FDA commissioner, Margaret Hamburg engaged in a wide-ranging conspiracy to approve an extremely dangerous drug known to cause severe (and even deadly) side effects, in order to financially benefit her husband’s hedge fund which held very large financial positions in Johnson & Johnson, makers of the drug. “Defendants, each and every one of them, operated a criminal conspiracy at least between the years 2009 to 2015 to fraudulently suppress warnings about the devastating effects of Levaquin,” says the complaint.
Hemp oil extracts containing CBDs (cannibidiols) are such a threat to the pharmaceutical industry that the FDA is now invoking totally insane justifications for outlawing them.
CBDs are non-psychoactive compounds found naturally in hemp plants. They work so well as powerful natural medicine that people everywhere are realizing CBDs work better than pharmaceuticals for treating epilepsy, seizures, neurological disorders and other serious health conditions (including HIV infections).
So the FDA has just launched a massive regulatory assault against CBDs by invoking the most insane logic you’ve ever heard. Here’s how it goes:
(NATURALSOCIETY) Genetically modified mosquitoes designed to limit the spread of the Zika virus will likely soon be unleashed in the southern United States, as the federal government said today it decided to permit a field test in the Florida Keys.
The Food and Drug Administration (FDA) said it had made a preliminary determination that the GM mosquitoes are unlikely to harm humans, animals, or the environment.
The FDA has now officially been completely captured by the pharmaceutical industry. With the confirmation of pharma insider Robert Califf as the new head of the FDA, America can look forward to many years of FDA malfeasance in conspiracy with pharmaceutical manufacturers to cover up the deadly side effects of drugs like Vioxx, all while using the full power of the federal government to intimidate, censor and criminalize natural product companies.
Federal agents subjected a farmer to harassment and warrantless searches simply for producing raw milk, but a county sheriff took the farmer’s side and blocked federal agents from the property – and the sheriff is now speaking out.
The US Food & Drug Administration (FDA) and Department of Justice (DOJ) took the actions four years ago simply because the farmer was providing raw milk to an organic food co-op. The story is receiving renewed coverage because the Indiana sheriff, Elkhart County’s Brad Rogers, wrote a 600-word explanation for a local newspaper as part of his “Ask The Sheriff” series. Off The Grid News previously reported on the dispute.
Just as we predicted, the U.S. Food and Drug Administration (FDA) has brazenly betrayed the public’s trust by approving the world’s first genetically modified (GM) animal in direct defiance of science – a transgenic salmon branded “AquAdvantage” that has never been proven safe for human consumption or the natural environment.
The New York Times (NYT) reports that AquAdvantage, a product of AquaBounty Technologies, has received official FDA approval after years of fierce lobbying by its manufacturer in favor of open approval. Despite repeated warnings from detractors that AquAdvantage poses serious threats to aquatic ecosystems and humans, the FDA has determined that this GM fish is completely safe for everything and everyone on the planet.
The Polonium Conspiracy Goes Far Deeper Than Just Tobacco
SOTN Editor’s Note:
Before the chemical geoengineering phenomenon known as CHEMTRAILS became a daily routine in the skies across America, there was arguably no greater public health disaster than polonium-laced tobacco. According to scientists who have investigated “The Polonium Conspiracy”, the phosphate fertilizers favored by the Tobacco Industry contain alpha-radioactive polonium, the decay product of Radium-226.
How does radioactive material get into a cigarette?
The tobacco leaves used in making cigarettes contain radioactive material, particularly lead-210 and polonium-210. The radionuclide content of tobacco leaves depends heavily on soil conditions and fertilizer use.
Soils that contain elevated radium lead to high radon gas emanations rising into the growing tobacco crop. Radon rapidly decays into a series of solid, highly radioactive metals (radon decay products). These metals cling to dust particles which in turn are collected by the sticky tobacco leaves. The sticky compound that seeps from the trichomes is not water-soluble, so the particles do not wash off in the rain. There they stay, through curing process, cutting, and manufacture into cigarettes.Lead-210 and Polonium-210 can be absorbed into tobacco leaves directly from the soil. But more importantly, fine, sticky hairs (called trichomes) on both sides of tobacco leaves grab airborne radioactive particles.
(Source: EPA — Tobacco Smoke)
Quite curiously, Big Tobacco has known about this predicament since the mid-1950s yet consistently failed to address it in any appropriate way. For this reason tobacco products have always possessed unacceptable levels of highly carcinogenic polonium. It has also been known that the primary cause of lung cancer among smokers is due to both the chemical properties and radioactivity associated with the polonium 210 radionuclides.