Do You Know The Eight Drugs Doctors Would Never Take??? You Should!!!

spoonful of drugsWould doctors take the medications they prescribe to their patients? Not necessarily, as it was reported in a recent article in Men′s Health, June 22, 2008. A number of physicians were asked which drugs they themselves would refuse to take.

And it may surprise you especially if you are currently taking one of these drugs, but here is their list:

  • Asthma drug Advair
  • Diabetes drug Avandia
  • Pain reliever Celebrex (a relative of the infamous Voixx)
  • Antibiotic Ketek
  • Heartburn medication Prilosec
  • Heartburn medication Nexium
  • Eye drops Visine Original
  • Decongestant Pseudoephedrin

The doctors questioned also suggested alternative treatments. Unfortunately, all they could come up with were other drugs! You have to understand that is all they are trained in at medical school…You can find their recommendations in the original article in Men’s Health.

Here is a portion of a commentary by Dr. Mercola on this very subject:

Seemingly positive and helpful articles like these really highlight how pervasive the conventional drug culture is. Although these drugs are exposed as being dangerous and best avoided at all costs, the writer failed miserably in providing ′healthier′ alternatives; in all cases but two, merely citing alternative drug treatments …”

Actually it was the doctors who failed miserably; the writer just quoted the doctors′ recommendations. Mercola then goes on to comment on three of the drugs on this list — the asthma, diabetes and heartburn/acid reflux medications — and suggests non-pharmaceutical alternatives. This would be a good time for me to restrict my own comments to Avandia. But it should be mentioned that there is a reason lawyers are targeting people who have had adverse reactions to this drug.

In May of 2007 the U.S. Food and Drug Administration (FDA) issued a safety alert on Avandia:

“The U.S. Food and Drug Administration (FDA) is aware of a potential safety issue related to Avandia (rosiglitazone), a drug approved to treat type 2 diabetes …”

The agency goes on to say that safety data from some controlled clinical trials showed a potential increase in the risk of heart attacks, but other data provided contradictory evidence. The agency then issues this warning to patients on Avandia:

“Patients who are taking Avandia, especially those who are known to have underlying heart disease or who are at high risk of heart attack should talk to their doctor about this new information as they evaluate the available treatment options for their type 2 diabetes.”

Why didn′t the FDA just mandate the removal of the drug from the market?

“FDA′s analyses are ongoing. FDA has not confirmed the clinical significance of the reported increased risk in the context of other studies. Pending questions include whether the other approved treatment from the same class of drugs, pioglitazone, has less, the same or greater risks. Furthermore, there is inherent risk associated with switching patients with diabetes from one treatment to another even in the absence of specific risks associated with particular treatments. For these reasons, FDA is not asking GlaxoSmithKline, the drug′s sponsor, to take any specific action at this time.”

If changing treatments poses such a significant health risk, why advise patients to talk to their doctors about their available treatment options, i.e. about switching drugs? And exactly what was the information available to the agency that made it so difficult for them to make a decision?

“Recently, the manufacturer of Avandia (GlaxoSmithKline) provided FDA with a pooled analysis (meta analysis) of 42 randomized, controlled clinical trials in which Avandia was compared to either placebo or other anti-diabetic therapies in patients with type 2 diabetes. The pooled analysis suggested that patients receiving short-term (most studies were 6 months duration) treatment with Avandia may have a 30-40 percent greater risk of heart attack and other heart-related adverse events than patients treated with placebo or other anti-diabetic therapy. These data, if confirmed, would be of significant concern since patients with diabetes are already at an increased risk of heart disease.”  FDA approval for Avandia was given May 1999 and this safety alert wasn’t issued by the FDA until May of 2007. My question is-What took so long to issue the Risk Warnings of serious cardiovascular complications after most of these studies that were conducted over a short 6 month period of time? It sure is odd that it took 8 years to issue this safety alert, in my opinion!

Of significant concern? Can you imagine a natural health product remaining on the market with a rap sheet like that. Does the pharmaceutical industry control the FDA, or what?

The sad thing about all of this is that type 2 diabetes is considered a life style disease that is both preventable and reversible. The American Diabetes Association readily admits this:

“People with diabetes have the same nutritional needs as anyone else. Along with exercise and medications (insulin or oral diabetic pills), nutrition is important for good diabetes control. By eating well-balanced meals in the correct amounts, you can keep your blood glucose levels as close to normal (non-diabetic level) as possible.”

Pharmaceutical intervention shouldn′t even be necessary in type 2 diabetes. Yet the drug peddling continues, with the active participation of the medical establishment.

It is a shame that every Healthcare Provider isn’t required by law to learn what Nutraceutical options exist…but we have to remember who has the greatest influence in a medical doctors education and training-it’s not the nutraceutical companies!


The Answer to Alzheimer’s May Be Found in This…

According to the Alzheimer’s Association’s 2011 Alzheimer’s Disease Facts and Figures…In the United States, someone develops Alzheimer’s disease every 69 seconds, and by 2050 this is expected to increase to a new case every 33 seconds.

This disease is currently at epidemic proportions, with 5.4 million Americans—including one in eight people aged 65 and over—living with Alzheimer’s disease.

By 2050, this is expected to jump to 16 million, and in the next 20 years it is projected that Alzheimer’s will affect one in four Americans. If that comes to pass, it would then be more prevalent than obesity and diabetes is today!

Alzheimer’s is a sad, devastating disease that develops slowly and gets worse over time. Worse yet, there is no known cure and very few treatments. Alzheimer’s drugs are often of little to no benefit at all, which underscores the importance of prevention throughout your lifetime.

Alzheimer’s develops over the course of a few decades, so the time to start preventing it is yesterday. Your approach to preventing this terrible disease should be a comprehensive lifestyle approach.

This natural approach may very well be The Answer to the devastating diseases known as Dementia, and Alzheimer’s.

Astaxanthin is a natural pigment with unique properties and many clinical benefits, including some of the most potent antioxidant activity currently known to man. It is the same pigment that makes flamingos pink.

These birds are born with grey feathers—and after consuming their natural diet of astaxanthin-containing algae and crustaceans, they turn pink! It has been found to reduce the accumulation of phospholipid hydroperoxidases (PLOOH)—compounds known to accumulate in the red blood cells of people who suffer from dementia—and scientists now believe astaxanthin could help prevent dementia, including Alzheimer’s.

As a fat-soluble nutrient, astaxanthin readily crosses your blood-brain barrier.

One study found it may help prevent neurodegeneration associated with Oxidative Stress, as well as make a potent natural “brain food.”

The molecules of astaxanthin neutralize free radicals and other oxidants without being destroyed or becoming pro-oxidants themselves in the process. It’s is a unique molecule whose shape allows it to precisely fit into a cell membrane and span its entire width. In this position, astaxanthin can intercept potentially damaging moleculesbefore they can damage your cells.

In fact, astaxanthin is hundreds of times more effective than vitamin E in squelching singlet oxygen free radicals, and far exceeds the free radical scavenging power of vitamin C, CoQ10, beta-carotene, and green tea. According to a recent article in the Alternative Medicine Review.

“Astaxanthin improved cognition in a small clinical trial and boosted proliferation and differentiation of cultured nerve stem cells…   Astaxanthin’s clinical success extends beyond protection against oxidative stress and inflammation, to demonstrable promise for slowing age-related functional decline.”

This supports the findings of a prior 2011 study in the British Journal of Nutrition that showed taking 6 mg or 12 mg of astaxanthin daily for 12 weeks lowered levels of PLOOH by 40 percent and 50 percent, respectively.

It is unlikely you will be able to obtain enough astaxanthin from diet alone… unless you are a flamingo. You can get some astaxanthin by taking krill oil, which is a fantastic omega-3 fat supplement. But you can boost your astaxanthin even MORE by adding a pure astaxanthin supplement to your nutritional regimen.  For optimal absorption, make sure to take krill oil and/or astaxanthin with a fat-containing meal, since both are fat-soluble.

So, if you have a family history of or are developing early signs of either Dementia or Alzheimer’s you may want to do a little more research into this…

FDA Targets Supplement Manufacturers, Falsely Accuses Them of Selling Drugs…

In the eyes of the US Food and Drug Administration (FDA), there is no difference between a legitimate, scientifically-backed health claim, and a phony, made-up claim, as it concerns food and dietary supplements. Only FDA-approved drugs, you see, provide real health benefits, according to the agency. And in its continued assault against health freedom, the FDA has sent warning letters to five different companies that produce natural treatments and cures for sexually-transmitted diseases (STDs) because those companies dared to make unauthorized health claims, many of which are backed by peer-reviewed, journal-published scientific studies.

What is worse, though, is the fact that the FDA has decreed that any food or dietary supplement that provides any sort of health benefit is automatically a “drug.” Ordinary foods like almonds, cherries, or walnuts literally become recategorized as drugs when accompanied by claims that they cure, heal, or prevent disease– and this is currently the law of the land in the US.

Click here to see the full article and to see what Supplement companies the FDA has targeted…

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