Food and Drug Administration
On December 7 and 8, the EPA's National Drinking Water Advisory Council held its annual meeting at their headquarters office on Constitutional Avenue in Washington, DC. After sitting through lengthy discussions all day on December 7 (in which the word "fluoride" was not mentioned once), Bill Hirzy PhD, Ellen Connett and myself (Paul Connett) finally got our chance to speak during the Public Comment period on Friday morning, Dec 8.
Read original article at The Bolen Report
Linus Pauling discovered, and patented, a Vitamin C cure for heart disease – that works.
But the Obama-Nation’s “HOLDOVER FDA” won’t let the Vitamin C Foundation, OR ANYONE ELSE, tell you about it…
EVERYTHING that competes for Big Pharma dollars is blocked…
And THAT is Just Plain WRONG…
We must keep the FDA from turning a vital nutrient over to Big Pharma. Action Alert!
An important study finds that carbidopa, a standard Parkinson’s drug, “irreversibly binds to and permanently deactivates” pyridoxal-5’-phosphate (P5P), a key form of vitamin B6 in the body. The authors describe the essential role P5P plays in the body: “[P5P] is required for the function of over 300 enzymes and proteins. Virtually every major system of the body is impacted directly or indirectly by [it].”
The historic Nov. 2016 ballot initiatives to legalize cannabis brought a resounding win for freedom in several states, with the exception of Arizona. There, voters narrowly rejected decriminalization, in no small part due to a massive anti-pot propaganda campaign funded in-part by Big Pharma.
A new study published in Clinical Rheumatology exposes how vaccine manufacturers used phony placebos in clinical trials to conceal a wide range of devastating risks associated with HPV vaccines.
Instead of using genuine inert placebos and comparing health impacts over a number of years, as is required for most new drug approvals, Merck and GlaxoSmithKline spiked their placebos with a neurotoxic aluminum adjuvant and cut observation periods to a matter of months.
Agency told lab meat manufacturer it hadn’t demonstrated safety of burger’s genetically engineered heme, which has never been in the food supply. Company put product on the market anyway.
The U.S. Food and Drug Administration told the manufacturer of the meat-like Impossible Burger that the company hadn’t demonstrated the safety of the product’s key genetically engineered ingredient, according to internal FDA documents. Despite FDA’s concerns, Impossible Foods put its GMO-derived burger on the market for public consumption.
While more and more Americans are becoming increasingly skeptical of the current vaccination schedule in the United States and the enormous influential power wielded by the pharmaceutical industry, most are still willing to trust the industry with their loved one’s health.
Government lies and lack of profit incentive are both leading to lack of treatment. Action Alert!
A new report published in Pediatrics estimates that the overall number of children with elevated lead levels in the US for the period 1999 to 2010 was 1.2 million—double what the Centers for Disease Control and Prevention previously reported. Even that figure is likely far lower than the reality.
Sen. Charles Schumer is urging federal regulators to look into a "snortable chocolate" powder, saying he's worried that it could prove harmful and is being marketed like a drug.
In a letter Saturday, the New York Democrat asked the Food and Drug Administration to investigate the use of caffeine in inhalable food products such as so-called Coco Loko. It's gotten buzz in recent weeks.
Schumer, the Senate minority leader, says there are too many unanswered questions about a product pitched under the innocent-sounding name of chocolate.