FDA Tyranny to become LAW
Mike Adams:

“On July 11, 2007, the U.S. House of Representatives passed HR 2900, blocking debate on the law and preventing the introduction of any amendments that might have provided meaningful drug safety protections for consumers. This action demonstrates that the House of Representatives, much like the Senate, is utterly controlled by Big Pharma and has abandoned any responsibility to defend the interests of the voters. Drug companies now have complete control over the U.S. Congress, and through a campaign of intense lobbying and financial influence, they have managed to easily water down a law that once proposed to end the American monopoly on pharmaceuticals and ban advertising on new drugs.

Instead of placing new restrictions on Big Pharma and the increasingly dangerous power of the FDA, this new law (a combination of HR.2900 and S.1082, when it is hammered out in conference) grants more power to the FDA while deepening the financial ties between the agency and drug companies. The law effectively surrenders America to a system of medical tyranny under which a criminally-operated FDA will continue to promote pharmaceuticals, censor nutritional education and discredit alternatives that threaten drug company profits. Nothing in the new law protects consumers’ access to dietary supplements or natural medicine……”

……Notice, too, that this sellout crosses party lines and involves both Democrats and Republicans. Only one Congressman, Rep. Ron Paul (a Libertarian-leaning Republican), was attempting to introduce meaningful amendments that would protect the interests of the people. His efforts were blocked by Speaker of the House Nancy Pelosi, a Democrat……
The passage of this FDA reform law is merely one more sign of how thoroughly committed the U.S. Congress is to creating a future of death, disease and bankruptcy for the American people. You gotta give ’em kudos on consistency, however. At least the lawmakers are predictable.
Welcome to the United States of Big Pharma.”
Byron Richards

“On Wednesday, July 11, 2007 the House passed HR.2900 without allowing the Ron Paul (R-TX) amendments to protect dietary supplements. Representatives Frank Pallone, Jr. (D-NJ), John Dingell (D-MI), Henry Waxman (D-CA), and others falsely proclaimed that they were doing America a favor by passing this sweeping FDA-supported legislation that grants the rouge agency more power and money, and even transforms it into a quasi drug company.

Both the House and Senate (S.1082) have made the fatally flawed assumption that the reason for so many deaths and injuries from drugs was due to the FDA’s lack of resources. In reality, it is the INTENTION of FDA management that is the problem, combined with the simple fact that multiple drugs are extremely toxic and don’t work as advertised. Giving the FDA more power and money will only cause the agency to speed more drugs onto the market faster with even less safety testing — while abusing its power and actively stamping out competition to drugs.

FDA management is in bed with Big Pharma and this new legislation makes matters significantly worse through the creation of the Reagan-Udall Foundation for the FDA. This new entity places the FDA in charge of drug design, drug patents, drug licenses, and the creation of new marketing entities/companies. Such a relationship with private industry is an unprecedented conflict of interest, totally at odds with drug safety. The current commissioner of the FDA, Andrew von Eschenbach, M.D. is little more than a Big Biotech sales rep with massive industry connections.

The House, like the Senate, will continue to allow direct to consumer advertising of new drugs with unknown risks — a flagrant safety risk that will cost many people their lives. Congressional leaders said they couldn’t prevent this advertisement for fear of violating the first amendment rights of drug companies. What a joke. The FDA routinely squashes the first amendment rights of American citizens to understand natural health options and the science that explains how they can prevent and treat disease. Thus, the first amendment argument is simply a matter of convenience.

The FDA wants to actively suppress information that will help people, yet allow highly risky and misleading promotion of toxic substances often for untested uses. The FDA even wants to prevent citizens from suing drug companies when they are injured, thus protecting Big Pharma. FDA tyranny, based on this type of arbitrary and unrestrained exercise of power, is used to promote and protect the pharmaceutical industry while at the same time undermining the dietary supplement industry…..

….A new tone has been set. A new chart has been plotted. Congress has transformed the FDA into a quasi drug company with unprecedented new regulatory power to control all health options in America. How many deaths and injuries will it take for a comatose and medicinally-overdosed public to wake up?”

I believe it will take fifty years before America fully wakes up and realizes that we have sown the wind as a society and we are about to reap the WHIRLWIND….

Jenny Hatch