October 21, 2014

Senator Durbin to Reintroduce Bill to Restrict Supplements

pin it button Senator Durbin to Reintroduce Bill to Restrict Supplements

deaths in one year due to drugs vs supplements 3 Senator Durbin to Reintroduce Bill to Restrict Supplements

By Dr. Mercola

Make no mistake, there is a well orchestrated campaign underway to take away your rights and access to vitamins and supplements.

You have likely witnessed the recent flurry of articles from doctors with scary headlines like “Don’t Take Your Vitamins” written by Paul Offit.  Senator Dick Durbin has taken a leading role as well.

Senator Durbin was also a sponsor for the SOPA / PIPA act, which would give the government even more power to censor and control the internet. You would think it would be impossible at this point to have MORE control, considering the recent leaks regarding the NSA.

There is no satiating the hunger for more power in our federal government. Politicians will scare you about sugary beverages loaded with caffeine as examples of the dangerous and ‘unregulated’ supplement industry.

Meanwhile, consumers load up at Starbucks and other coffee shops – where they can easily down cups and cups of this ‘dangerous’ substance. You don’t see Durbin beating down the door of Starbucks or Dunkin Donuts, even though coffee is the primary source where most people get their caffeine fix.

When you notice this type of hypocrisy, you can usually bet there is a serious industry influence behind the scenes. There is a campaign push assaulting the supplement industry by those hoping to gain control of it. Essentially, if supplements become regulated like drugs – only the drug companies will be manufacturing them.

By setting new regulations and gaining control of the industry, big pharma can charge higher prices and make higher profits.

Surprisingly, a newly released GAO Dietary Supplements report has recently shown just how safe dietary supplements really are. There are always bad products in every industry, but overall, supplements appear to be one of the safest of all consumable products.

Senator Durbin has been on a mission that appears, at least superficially, to stem from concern over “your health.” However, when scrutinized more closely, Durbin’s proposed legislation would have precisely the opposite effect.

If Senator Durbin is genuinely concerned about “your health,” then his focus should be on making drugs and vaccines safer, which are the real danger — not dietary supplements.

Why Should Supplement Regulation Be More Stringent Than That for Drugs?

Durbin first introduced the Dietary Supplement Labeling Act (S 1310) in 2011, a bill that threatens the supplement industry by granting FDA more power to regulate supplements as if they were drugs, potentially putting supplement companies out of business.

In fact, under this bill, supplement regulation would be even more stringent than for pharmaceutical drugs! The bill specifies the following:

  • Requires regulators to compile a list of dietary supplement ingredients and proprietary blends of ingredients that are judged capable of causing serious adverse reactions
  • Mandates manufacturers to submit a list of all the products they make at a given facility and their ingredients; new products or reformulations would require new registrations

Despite resorting to sneaky tactics and dispersing blatant misinformation to his legislative colleagues in attempts to garner support, Senator Durbin has had a difficult time obtaining any support for his bill.

Therefore, in May 2012, Durbin tried to slide his amendment (No. 2127) through by piggybacking it onto a senate bill that was slated for a vote the very next day (S 3187, the Food and Drug Administration Safety and Innovation Act).

Because the natural health community so quickly and effectively sprung into action, Durbin’s amendment failed. Although his efforts to pass this ridiculous legislation have been unsuccessful thus far, his determination has not waned, misguided though it is. We must continue our efforts to thwart this bill, which if passed into law, could spell disastrous consequences for your health.

The Danger of Food Supplements Is VASTLY Overstated

Durbin and others would have you believe supplements are dangerous and need further regulation. But the truth is that supplements are already FDA-regulated and produce far fewer adverse reactions than either drugs or vaccines. The March 2013 GAO Dietary Supplements report, which Durbin hoped would paint supplements as dangerous, actually showed how incredibly safe they really are—particularly when compared to drugs and vaccines.

Since 2008, the supplement industry has been required to report adverse events to the FDA’s AER system, pursuant to the 2006 Act. Consider the following statistics comparing dietary supplement AERs with drug AERs (from the 2013 GAO report):

  • From 2008 to 2011, FDA received 6,307 AERs for dietary supplements, not including 1,000 AERs that were submitted to poison control centers, rather than the FDA
  • In 2008, 1,080 dietary supplement AERs were reported to FDA
  • In 2008, 526,527 prescription drug AERs were reported
  • In 2008, 26,517 vaccine AERs were reported

When you do the math, there were 488 times as many adverse events reported from prescription drugs as from dietary supplements!

Supplement AERs increased from 400 in 2007 to 1,080 in 2008, but as the Alliance for Natural Health points out, that stems from an increase in the number of supplements on the market and more careful reporting of AERs to the FDA, especially since the implementation of required good manufacturing protocols. The number of AERs is miniscule compared to the hundreds of millions of supplement servings consumed. According to a 2007 National Health Interview Survey, more than half of Americans(157 million individuals) take nutritional supplements.

Senator Durbin and company are trying to claim AERs are underreported. However, according to the 2013 GAO report, there were only 20 AER compliance problems identified during supplement company inspections, suggesting most of these companies are compliant with mandatory AER guidelines. Adverse reactions aren’t being underreported—there just aren’t that many reactions to report. Even the GAO report itself states:

“The greatest challenge for identifying potential safety concerns from AERs is the small number of AERs that FDA receives related to dietary supplements.”

Poison Control Data Supports the Safety of Nutritional Supplements

Data from the U.S. National Poison Data System’s annual report, which tracked data from 57 U.S. poison centers, showed vitamin and mineral supplements caused zero deaths in 2010, whereas pharmaceuticals caused more than 1,100 of the total 1,366 reported fatalities. FDA-approved drugs cause 80 percent of poison control fatalities each year. Poison control centers report 100,000 calls, 56,000 emergency room visits, 2,600 hospitalizations and nearly 500 deaths each year from acetaminophen (Tylenol) alone.

Data from the European Union indicate that pharmaceutical drugs are 62,000 times as likely to kill you as dietary supplements. You’re actually more likely to be struck dead by lightning or drown in your bathtub than have a lethal reaction to a dietary supplement. These figures make it quite clear where the danger lies. If Senator Durbin really cared about your health, his efforts would be centered on doing something to make drugs safer, as they obviously pose a FAR greater risk to your health.

Laws Regulating Supplements Are Already in Place

According to the GAO report:

“FDA officials told us that the current regulatory framework is sufficient to identify and act on safety concerns regarding foods with added dietary ingredients.”

They are referring to the Dietary Supplement Health and Education Act of 1994 (DSHEA). The only deficiency, to the extent it exists, lies in the enforcement of the current law, in terms of ensuring good manufacturing practices and mandatory reporting of adverse events by supplement companies. If the FDA is already well-equipped with legislative authority to do its job, then what is Senator Durbin really trying to accomplish?

The only answer that makes sense is that the ultimate goal of Durbin’s bill is to make sure every supplement is approved by the FDA before it is sold.

The hidden problem with this is that the FDA is heavily biased in favor of drugs, as the agency is primarily funded by the pharmaceutical industry. The FDA sees supplements as competition for drugs, so not many will be approved. Durbin’s bill attempts to get supplements into the clutches of our completely dysfunctional drug approval regime, where they can be subjected to every possible legal obstacle that will keep them off store shelves. Less competition from supplements would also soften the impact of decreased revenues from expiring drug patents.

Forcing Supplement Companies Out of Business Will Not Improve Your Health

If Durbin’s bill were to pass, the FDA would demand very expensive (on the order of hundreds of millions of dollars) supplement trials just like drug trials which would eliminate the vast majority of recent supplements as most manufacturers have revenues that are only a tiny fraction of drug companies and can’t afford these expenses. More importantly, they are simply unnecessary as they provide virtually no benefit to the consumer. The current reported adverse effects are simply too low to justify this unnecessary safety requirement from a nonexistent danger. Remember, supplements don’t kill tens to hundreds of thousands of people every year; drugs do. Supplements don’t kill anyone.

Unlike drugs, supplements generally cannot be patented, so manufacturers will never see the return on investment that pharmaceutical companies see. The cost of complying with the pre-approval process will likely put many supplement companies out of business, and those who survive may do so only by drastically increasing the price of their products, making them cost prohibitive for many… particularly low-income families who need them the most. Durbin’s bill would also impose a significant burden on federal regulators, diverting these resources away from where they should be focused—i.e., on the drug industry.

Crafty Reclassification of Products Allows Manufacturers to Dodge Regulations

There is an additional problem that appears to be completely ignored by Senator Durbin. Dietary supplements are already more rigorously regulated than food products. Taking full advantage of this, some manufacturers are migrating products previously listed as “supplements” over to the “food products” category in order to sidestep regulation. Energy drinks are a prime example. Loren Israelson, executive director of the United Natural Products Alliance, is quoted as saying:

“I think he [Senator Durbin] misunderstands the dynamics of the energy drinks market. There has been a significant shift of brands going from dietary supplement labeling to food labeling. His bill would not capture some of the products he’s concerned about.”

Caffeine—A Ridiculous Case of Selective Regulation

In related news, the FDA is now going after caffeine to protect your and your children’s health, in response to Senator Durbin’s fervent outcries. Back in November 2012, Senators Durbin and Richard Blumenthal (D-Conn.) sent a series of letters to the FDA asking for energy drinks to be reviewed and potentially regulated.

While caffeine can indeed have detrimental health effects, the irony of the situation is that no attention is going toward actual coffee, which clearly would impact major multinational corporations like Starbucks. No, they’re only concerned with supplement, food and beverage makers using caffeine in their products, while the primary source of caffeine is not even part of the discussion. Supplements are just a tiny portion of caffeine consumption, so why not go after coffee?

As reported by Forbes:

“FDA Deputy Commissioner for Foods Michael Taylor spoke out against what he called the ‘unfortunate’ trend [of adding caffeine to processed foods]… Taylor specifically called out gum maker Wrigley on a new product, and stated that while formal regulation might be forthcoming, ‘we hope this can be a turning point for all to prevent the irresponsible addition of caffeine to food and beverages. Together, we should be immediately looking at what voluntary restraint can be used by industry.’

..Mr. Taylor expressed concern over the ‘cumulative amount’ of caffeine available, particularly for children.

…[A]s long as FDA’s actions aren’t tethered to standards or science, they threaten to sweep in products that don’t merit any concern or scrutiny. During FDA’s successful effort to drive some caffeine-infused alcoholic beverages, like Four Loko, off the market, it also sent warning letters to brewers whose product line featured beers brewed with coffee. The amount of caffeine in and serving sizes of the beer paled in comparison to Four Loko, which led the head of a craft-brewing association to feel such letters were ‘inadvertent.’ He did add, however, ‘brewers should be concerned. This could lead the FDA to question beverages that get their caffeine from natural products like coffee, chocolate or tea. Who’s to say where this will end?’”

Call to Action

Dick Durbin will be up for re-election in 2014. You can bet we will be focusing very specifically on this career politician. Durbin and others would have you believe supplements are dangerous and need further regulation. However, supplements have far fewer reported adverse reactions than either drugs or vaccines and are already FDA regulated.

Durbin is reintroducing his supplement bill in hopes of forcing dietary supplement manufacturers to pass regulations that are even stricter than those governing pharmaceutical drugs. Legislative tactics such as this represent part of a master plan by the drug industry, in partnership with its best friend FDA, to eliminate the competition by taking control of the supplement industry.

Durbin’s bill has failed miserably in the past due to lack of support and strong opposition by health-conscious consumers. We can do that again, but your help is needed. Please contact your representatives and urge them to vote NO on S 1310, Dietary Supplement Labeling Act. You can do this by signing the Alliance for Natural Health (ANH) petition.

sign petition Senator Durbin to Reintroduce Bill to Restrict Supplements

If you live in Illinois, as I do, I would encourage you to contact Senator Durbin directly. Tell him (or whomever your representative is) to stop this overreach of power, and that the proposed guidelines fly in the face of the congressional intent of DSHEA. Congress never intended for the FDA to control supplements, and giving them this control jeopardizes your access to the dietary supplements you rely on, as well as further damaging the US economy. Please be courteous and respectful, and thank them for their time. 

Read the full article here: http://articles.mercola.com/sites/articles/archive/2013/06/19/durbin-supplement-bill.aspx

Global Censorship of Health Information
The Politics of Controlling Therapeutic Information to Protect State-Sponsored Drug Monopolies

Global Censorship of Health Information book coversm Senator Durbin to Reintroduce Bill to Restrict Supplements

by Attorney Jonathan Emord
Free Shipping available!

0 commentsback to post

Other articlesgo to homepage

Boston Nurses Speak Out Against Mandatory Flu Shots

Boston Nurses Speak Out Against Mandatory Flu Shots

Pin It

Last month (September 2014) the Massachusetts Nurses Association sued Brigham and Women’s Hospital over a new policy that required nurses to receive the annual flu vaccine as a condition for employment.

The nurses were, of course, criticized by the medical establishment. They were accused of putting their own interests above the needs of patients. Lynn Nicholas, president of the Massachusetts Hospital Association, stated that the nurses were: “putting a pet peeve of theirs above the safety and well-being of the patients they serve, their families, visitors to the hospital, and their colleagues.”

Pet peeve? Really?

When nurses all across the United States and Canada are willing to sacrifice their jobs and careers to avoid the annual flu shot, it is time to sit up and take notice. This is obviously something much more than a “pet peeve.”

Trish Powers, representing Brigham nurses in Boston fired back a comment that The Boston Globe published. It is titled “Brigham nurses know flu vaccine can do harm.”

Obscene Increase In Maternal Mortality Rates In The United States

Obscene Increase In Maternal Mortality Rates In The United States

Pin It

In most of the world, the number of women dying in childbirth is decreasing, but the United States is one of eight countries in the world where the maternal mortality rate is going up, not down, according to the newest figures. In fact, the US is rock bottom of the developing nations of the world in maternal mortality – #60 out of 180 nations included in the statistics. And that is unacceptable.

Will There Be An Ebola Outbreak in America?

Will There Be An Ebola Outbreak in America?

Pin It

So here is what inquiring minds want to know:

Why did U.S. health officials in Atlanta and on the ground in Africa ignore the exploding Ebola epidemic last spring?

Why did U.S. government officials fly American aid workers infected with Ebola to the U.S. rather than treating them with experimental drugs at hospitals in Africa?

Why did the U.S. government press the United Nations to adopt a resolution calling for no restrictions on international travel from Liberia and other Ebola-stricken countries?

Why did the Centers for Disease Control, supposedly the world’s leading infection control agency, fail to immediately assist Texas health officials when the first case of Ebola was diagnosed on US soil to guarantee that, at a minimum, the kind of infection control measures used in most nursing homes in America would be carried out?

Why has the Director of the CDC repeatedly stated that the only way a person can transmit Ebola is if they have a fever and said that people cannot get Ebola unless they have direct contact with the body fluids of an infected person – but that under no circumstances is Ebola airborne – when he knows, or should know, those statements could be false?

And why are experimental Ebola vaccines being fast tracked into human trials and promoted as the final solution rather than ramping up testing and production of the experimental ZMapp drug that has already saved the lives of several Ebola infected Americans?

A logical conclusion is that some people in industry, government and the World Health Organization did not want the Ebola outbreak to be confined to several nations in Africa because that would fail to create a lucrative global market for mandated use of fast tracked Ebola vaccines by every one of the seven billion human beings living on this planet.

Does Playing on Artificial Turf Increase Your Risk of Cancer?

Does Playing on Artificial Turf Increase Your Risk of Cancer?

Pin It

Artificial turf fields are now everywhere in the United States, from high schools to multi-million-dollar athletic complexes. As any parent or player who has been on them can testify, the tiny black rubber crumbs of which the fields are made — chunks of old tires — get everywhere. In players’ uniforms, in their hair, in their cleats.

But for goalkeepers, whose bodies are in constant contact with the turf, it can be far worse. In practices and games, they make hundreds of dives, and each plunge sends a black cloud of tire pellets into the air. The granules get into their cuts and scrapes, and into their mouths. Griffin wondered if those crumbs – which have been known to contain carcinogens and chemicals – were making players sick.

Griffin has compiled a list of 38 American soccer players — 34 of them goalies – who have been diagnosed with cancer. Blood cancers like lymphoma and leukemia dominate the list.

What Can You Do to Prevent/Treat Ebola and Other Viral Infections

What Can You Do to Prevent/Treat Ebola and Other Viral Infections

Pin It

With the Ebola virus in the news, I thought it might be time to comment on what steps you can take to prevent becoming ill. Keep in mind that conventional medicine has no effective treatments for the Ebola virus. Due to a slow international response, Ebola has spread rapidly.

It is a scary infection as the death rate is very high—from 50-90%. Initially, the Ebola infection can mimic the symptoms from the flu or other upper respiratory infection. However, as it progresses, it can lead to very severe muscle aches, liver and kidney failure along with bleeding out of various areas of the body. Needless to say, Ebola is something to be taken very seriously.

As I previously stated, there is no conventional treatment for the Ebola virus. That does not mean that you are powerless to do anything to combat it. There are many effective natural anti-viral therapies that may prove effective against Ebola. It would be nice if the Powers-That-Be would begin testing these therapies. But, that would make common sense. Instead the Powers-That-Be are actively discouraging the use of alternative therapies even though they have nothing to offer. It is a sad situation.

Keep in mind that Ebola, like any viral infection, can only be cured by a strong immune system. We are designed with a powerful immune system that should mount a response to an infectious agent. However, the immune system can only mount a vigorous defense if it has the raw materials available to it. For over 20 years, I have been checking every patient for their nutrient status. Unfortunately, most are deficient in the basic raw materials that the immune system needs to function optimally.

I say, if you become ill with a viral illness, do the basics to help optimize your immune system. I will show you the four most important items you can use to aid your immune system to fight any illness.

read more

Get the news right in your inbox!