Our government, which is getting bigger and bigger, is continually trying to take away the rights of us citizens. Being consistent, the government has taken hold of several industries over the last few years to no benefit, and is now set its sights on the supplement industry. The FDA, a sheep in wolves clothing, is claiming they’re interest in taking over the supplement industry is public safety. However, government statistics show that supplements are basically benign, especially when compared to prescription drugs. Not to mention the outstanding natural health benefits associated with supplement intake.
If the government gets their way, they and the pharmaceutical industry know the supplement industry companies won’t be able to afford the FDA’s drug trial process. Most supplement companies will go out of business if supplements, which includes vitamins, are treated as drugs under the new regulations; drug companies like Merk, Pfizer and others will step in and take over.
Drug companies are not in the business of building health. It is in their best interest to have as many unhealthy people as possible. Its so important that big pharma spends more money on ads than it does on research (twice as much). It’s a marketing driven industry, trying to convince people they have an affliction and the drug companies have the answer.
Is it any wonder why there have been so many drug recalls associated with so many deaths. Perhaps if big pharma spent more on research, and the FDA did their job, many people wouldn’t have lost their lives needlessly. And this is who we’re supposed to put our trust in running our supplement industry?
Taken from Mercola.com:
Dietary Supplement Labeling Act of 2011, introduced at the end of June by U.S. Senator Richard Durbin (D-Illinois) is trying to treat vitamins as if they are drugs, allegedly to “improve the safety of dietary supplements,” which implies that supplements must be a major safety hazard to begin with. Durbin’s bill goes hand-in-hand with new FDA regulations that amend the definitions for new dietary ingredients (NDI’s), and together, they can threaten your health and freedom of choice, and further serve to strengthen the fatally flawed paradigm of health and medicine.
An estimated 106,000 hospitalized patients die each year from drugs that, by medical standards, are properly prescribed and administered, and an estimated two million more suffer serious side effects.
How does the safety of supplements compare?
In 2001, 84.6 percent of all substances implicated in fatal poisonings were pharmaceutical drugs, according to that year’s American Association of Poison Control Centers (AAPCC) report. This compares with 0.8 percent for all dietary supplements combined, even including substances such as dinitrophenol, a dangerous (and illegal) substance banned in 1938, as well as the central nervous system stimulant Ma Huang (Ephedra). ONE drug alone, the anti-asthma drug theophylline, which was responsible for 15 deaths that year, amounted to 66 percent more than all the available dietary supplements combined.
According to CDC mortality data for 2005, prescription drugs killed more than 33,500 people that year, second only to car accidents. That same year, the American Association of Poison Control Centers reported 27 deaths that were associated with dietary supplements
Legal DRUGS are killing massive numbers of people, not vitamins and supplements. Unfortunately, one reason for all these drug deaths could be the lax way the FDA “regulates” the drug industry by not requiring that all serious events in a trial be made public:
“When a clinical trial that is undertaken by drug companies shows that a drug has serious side effects, there is no law that says that study has to be published or made public in any way,” Dr. Dean says in her book.
Vioxx is a perfect example of a product that was approved without having published all the clinical studies where serious events that resulted in the deaths of over 60,000 people were discovered.
What’s obvious is that the number of people taking supplements and vitamins is continuously growing. It’s a $60-billion-a-year industry, and the drug industry wants a piece of that pie, as evidenced by drug giant Pfizer, which recently announced that it’s going into the supplement business to counter some of the losses from its blockbusters that are soon going off-patent. The FDA is apparently on-track to protect its client’s vitamin and supplement interests by proposing the new policy it slipped in just before July 4.
What can you do? Go HERE and get involved.
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