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Conservative Thought, Action: Republicans and the TEA Party

   
           The country's electorate has long been dissatisfied with chosing between Tweedle-dumb and Tweedle-dumber time after time at the voting booth.  The two major parties have been an abject failure and disappointment to thinking Americans since at least January of 1988.  Looking at the Presidents, for example, Bush, the father, infamously reneged upon his biggest promise ("read my lips . . . ").  Clinton, until the "Contract with America" brought him to his senses was a reincarnation of big spending/big guv Jimmy Carter and even then in '98 he passed the version of mortgage-guarantee legislation that put Carter's CRA of 1977 on steroids and led to our sub-prime lending chaos and financial collapse.  Bush, the younger, forgot all about fiscal restraint.  We knew we were in trouble in 2008, when choosing between a progressive Republican and an ex-ACORN attorney who shook-down banks to force them to make bad loans . . . .    

             Much has been written about the dangers of a "third-party" draining conservative votes and assuring the continued dominance of the big spending, virtually-Marxist, Constitution-hating Obama administration and Democratic majority in Congress.  The answer is simple, straightforward and refreshing . . . it's high time the Republican Party returned to the fiscal-conservativism and smaller, efficient and responsive government it once stood for . . . do that and the TEA Party will embrace 85-90% of Republican candidates and virtually all Republican initiatives.

            Whether TEA means "Taxed Enough Already" or "Taken Enough Abuse," Old Rajjpuut, has been encouraged by the Tea Party phenomenon beyond that of any other occurrence in political-activism since at least the days of Ronald Reagan, Martin Luther King, Jr. and Gandhi. Patriotic opposition and even a bit of civil disobedience against corrupt government and corrupt politicians is certainly long overdue in this country.

           The TEA Party, one hopes, will continue to be a vibrant fiscal-conservative backlash against the abuses of both major parties and the federal government and a strong PRO-voice supporting the U.S. Constitution. Just as the original Sons of Liberty which conducted the Boston Tea Party became the Whig Party; and the original abolitionists became outraged at the impotence of their Whig Party and gave birth to the Republican Party in 1854, let’s hope this new movement leads us back to our conservative, freedom-loving roots once again. Fiscal conservativism and social moderation and tolerance are worthy goals.  To those ends here is a  Suggested Unity Platform for the Tea Party:
 
 

Guiding Principles:

I.                     We hold the Declaration of Independence's truths to be self-evident that all men are created politically equal and own the unalienable rights to LIFE, LIBERTY, and the PURSUIT of HAPPINESS.  We believe in equality of opportunity, not forced equality by government theft and re-distribution. Each human life is potentially of great worth and dignity. Diversity of opinion and diversity of support are vital. Patriotism comes in many wonderful packages. We are a party of inclusion not exclusion. We welcome patriotic dissent as well as patriotic agreement. We expect “discussion” to be civil and search for win-win resolutions at all times, but we totally deny the idea of political correctness.

II.                     We believe that political correctness is gutless and dishonest. In its place we search for political integrity and the best possible results for the American people as a whole. We do not support or agree with notions of affirmative action. The family is sacrosanct, but after childhoold, each person stands on his own within the bounds of reason and compassion.

III.                    Because the original Tea Party  consisted of radicals whose attack on the establishment on December 16, 1773 (flinging taxed tea crates into Boston Harbor) was a defiant act of civil disobedience, we embrace peaceful but intelligent and provocative defiance to the present political establishment. We are the people and they govern at our pleasure, they work for us, we do not work for them.  We loathe their current attempts at "Taxation without Representation" and consider our pocketbooks and our persons equally sacrosanct. The methods of Gandhi, Martin Luther King, Thoreau, our own founding fathers and Ronald Reagan provide a guideline for constructive, intelligent and effective actions.

IV.     Patriotism means first of all respect for the U.S. Constitution and the men and women who’ve fought, died and struggled to make this country great.

 

Be it resolved that we hold this type of federal government to be self-evidently preferible to all others.

A.       A Republic  featuring Democratically-elected representatives


B.      A federal government in line with the principles of the Bill of Rights of the U.S. Constitution


C.      The smallest possible federal government possible that can protect the people from aggressions foreign and domestic

D.      The federal government which taxes the least, interferes in daily life the least and keeps it monetary affairs in good order


E.      The federal government that honors the principles of complete separation and balance of executive, legislative and judicial powers


F.      A federal government that will not invoke nor allow ex post facto laws or ex post facto voting or scheduling of voting to fill vacant seats


G.       A federal government which practices a balanced budget except in wartime


H.      A federal government that does NOT feature a central bank nor (except in wartime) allow national debt


I.      A federal government that supports a strong currency

 
J. A federal government that honors and enforces separation of Church and State
 
K.   A federal government which except as necessary (in keeping with the bill of rights) respects and does not interfere with or subvert the state government or the rights of individuals

 

Be it further resolved that the twenty-one principled behaviors and attitudes listed below outline the attributes of a true American statesman or stateswoman. We believe that candidates that adopt at least eighteen of them are worthy of our votes. We resolve to revisit and revise this list not less than once every eighteen months to keep it current, relevant and intelligent . . . .  

 

                                 The Twenty-One Statements

 

     A statesman/stateswoman of integrity that patriotically represents the American people . . .

•1.      Supports strong national defense


•2.      Supports responsible capitalism and minimal government  interference with honest and responsible captitalist endeavor


•3.      Supports minimal taxation


•4.      Supports smaller, more efficient, more effective and less onerous and interfering government


•5.      Opposes socialism, Marxism, communism and social-progressivism in all forms


•6.      Supports reduction of and elimination of the national debt


•7.       Opposes the existence of the federal reserve bank


•8.       Opposes deficits and unbalanced budgets


•9.     
Supports market-based health care reform and is ready and willing to revoke "Obamacare" should it pass as well as all other socialistic laws created by the present congress and president


•10.   Supports full exploration and use of America’s present energy storehouse and potential by the free market, including but not limited to nuclear power; oil-shale development; offshore drilling; drilling in the country itself, especially in the newly discovered huge Baaken Reserve Fields.  Supports green-tech with minima research funds and leaves development of those sources of energy to private businesses and individuals.


•11.    Opposes mandatory unionization and card check; and supports secret balloting everywhere in America including in the jury room and work place


•12.   Opposes cap and trade or other such energy legislation and willing to revoke any such measures should they pass


•13.   Opposes illegal immigration in all its forms


•14.   Supports victory in Iraq and withdrawal within four years


•15.   Supports victory in Afghanistan and re-building that nation’s infrastructure, especially schools and insisting that nation educate its women before eventual withdrawal.  Opposes all terroristic activity.


•16.   Opposes “marriage” by same-sex individuals; but supports civil unions without the right of adoption.


•17.    Opposes public funding of elective health care options such as abortion and unnecessary plastic surgery


•18.   Supports second amendment freedoms; opposes all irresponsible use of weapons of any sort; opposes violent felons ever getting the right to bear arms; opposes fully-automatic military assault type weapons in the hands of civilians; supports a strong National Guard and other military reserve independent of the federal government except in emergency or wartime necessity


•19.   Opposes the irrational and violent governments of North Korea and Iran and supports all measures to stop their nuclear proliferation


•20. Supports all just laws. Supports abortion as the PRESENT law of the land but opposes federal or state funding of abortions. Respects the right of non-violent opposition to abortion and the right to seek a constitutional amendment limiting late-term abortions. Respects the right of peaceful protest and demonstration against all unjust laws and all unjust local, state and federal actions and laws.

•21.   Opposes all government jobs creation.  Outside of its legitimate limited functions, governments cannot create jobs that benefit the greater public; they can only tax and waste our money. Specifically opposes the present green jobs program of President Obama which will, in order to create the desired five million green-tech jobs, cost the country over eleven million^^^ real jobs. Additionally, the jobs created will be temporary in 91% of the instances; be low-paying in 94% of instances and be a sham. To create jobs and especially green tech jobs the Federal government needs to stand aside, lower taxes and enourage research, period. Supports private sector jobs growth by lowering taxes on business and individuals.

Resolved: candidates whose “track record” demonstrates substantial compliance with both the spirit and the letter of these "Twenty-One Statements" is considered a “friend of the Tea Party” and worthy of our full respect and support. Candidates whose “litmus test” results are very close to the seventeen agreement threshhold may also be supported on a lesser of two-evils basis. Candidates who substantially differ from these standards will be opposed by all legitimate means at our disposal. 
 
Ya'all live long, strong and ornery,
 
Rajjpuut
 
^^^ According to a Spanish study of the results of a similar experiment in their country leading to 18.7% unemployment, each government-created job cost the permanent loss of 2.2 real jobs from the wider economy.  Some government created jobs were of extremely short duration, only roughly 9% were permanent and not many paid well.

 

 


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Eliminate the FDA: Angel of Iatrogenic Death #16

A typical large metropolitan hospital averages 50-60 medication mistakes each hour of the day.  The large majority of them are caught pretty quickly.  When someone, due to medical mistakes, dies, is injured or maimed or otherwise incapacitated it’s called an “iatrogenic” incident. The third leading cause of death in the United States is iatrogenic incidents: 250,000 in all. More than two million people are maimed, disabled, sickened or temporarily injured by iatrogenic incidents.  These incidents occur a lot of different ways:  mistakes during surgery, etc., but medication mistakes are high on the list; and drug incidents where NO medication mistakes occurred at all are even more common. 

                 You are more likely, three times more likely, to die from negative effects of correct medicine prescribed for you by a doctor then from an automobile accident 106,000 die that way.  You are ten times more likely to be taken to the hospital from an iatrogenic incident  with correct medicine than from an automobile accident.
 

The Food and Drug Administration is directly responsible for those 106,000 deaths from negative effects of correctly prescribed drugs. They are also indirectly responsible for 7,000 other deaths from mistakenly administered-medications in hospitals and elsewhere.   There is no good reason for medicine, even mistakenly prescribed or administered medicine to kill anyone unless A. They were in a mighty precarious state to begin with or B. An allergic reaction of some sort took place.  IF, IF the FDA were required to abide by the common-sense medical dictate “First Do NO Harm!” at least 95% of those 113,000 would NOT die every year. Instead some FDA drugs have killed over 100,000 people in their history and keep right on killing today; and the legions of maimed and severely injured from some of those drugs climbs into the millions.

The worst aspect about all this, is that a whole lot of the medicines that do the most damage are palliative medicines that do NOT cure or fix anything. There is nothing wrong with easing patients’ symptoms, but that ease should NEVER come at the cost of endangering the patient’s health, which is the case in 100% of the drugs the FDA approves for palliative purposes. When, in actuality, many of these palliatives are no more effective than placebos (sugar pills) and great harm is possible and the medicines are expensive . . . look for the FDA to be behind this travesty. Medicines that actually cure something can kill or injure on sad occasions; but medicines that cannot cure should NEVER cause harm. This is one more reason why the FDA needs to be eliminated.

Ya’all live long, strong and ornery,

Rajjpuut

For those wondering about other iatrogenic deaths: 80,000 die from infections that are encountered while in the hospital; 45,000 from miscellaneous errors; and 12,000 from unnecessary surgeries.

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They’ve done it again! Eliminate the FDA #9

The FDA bastar_s have added another sellout to their resume.

Vioxx and Fosamax are killers and maimers, PERIOD!

                The Ol’ Health Educator is at it again, attacking the FDA. Loyal readers of Rajjpuut’s “A Far Better Health Care Alternative” series and his previous blogs in this Anti-FDA  series realize that the very first of Rajjpuut’s 43 tenets for an affordable health care program that would get Americans healthy, keep them that way and dramatically lower costs is to . . . . eliminate the FDA or fire all it’s employees and start over to make it a crucial part of the health care solutions in America rather than the #1 cause of health care problems in America.

                 The previous  blogs have proven that this “first tenet” is the most crucial step necessary for reforming health care in the United States. The founding principle of the preceding blogs and of this one is the simplest and most important concept in all of medicine: “First Do NO Harm!” When it comes down to osteoporosis and the health

 a. of American bones and

b. of the pocketbooks of big pharmaceutical companies . . .

the FDA has once again sold out to BigPHARMA (with another killer called Fosamax) and severely endangered the health of Americans. This time the sellout is so severe, it’s only minimally better than putting a gun to the head of osteoporosis victims. Vioxx and Fosamax are killers and maimers, PERIOD! Fosamax, if early reports hold up, is poised to eclipse Vioxx as the most dangerous prescription drug since Thalidomide (by the way, the FDA has welcomed Thalidomide back with open arms). Remember that idea of “First Do NO Harm?” Vioxx has over 60,000 deaths on its resume and perhaps two million injuries . . . so Fosamax has a big challenge ahead of them. But Rajjpuut is confident, if anybody can make Vioxx look like Vitamin C and an apple a day, it’s Fosamax.

                 Osteoporosis, is just what it sounds like: their bones (osteo-) get thin, brittle, less dense and more porous as many people reach age 50 and beyond. The problem is especially crucial for women. 80% of osteoporosis victims are female and typically the very worst cases are among women also. Male victims are almost always found among men whose lifestyle works against them: such as heavy smokers, heavy drinkers, drug users and steroid users. For women drug use, smoking and anything beyond ultra-moderate alcohol consumption is just asking for trouble. For both men and women “sodas” are a leading contributing factor: the phosphorus in many colas and other soft drinks needs to be balanced in the body and that’s done by drawing calcium from the bones. Besides leading to easy fracturing of bones, osteoporosis also causes a marked forward stoop often leading to severe back pain and sometimes deformity.

                 An enormous amount of good can be done to turn around or even reverse osteoporosis and even more good can be done to PREVENT this hideous crippling disease. Apparently our doctors and BigPHARMA and the FDA are not interested in any of this, but wisdom says this is the first place to look. The Hippocratic Oath “First Do NO Harm!” immediately tells us what to do first: STOP the lifestyle practices that bring on osteoporosis, what could be simpler? Stop drug and tobacco use; stop or severely moderate alcohol consumption. Avoid steroids and soft drinks especially colas. Very few osteoporosis victims have a healthy lifestyle. They need to immediately take responsibility for adopting that healthier lifestyle right now . . . to start a walking program or something more vigorous; adopt good nutrition; and consider supplementing with the items mentioned below.

                 The Food and Drug Administration has approved several remedies for osteoporosis but the most popular and most profitable ones are bisphosphonate bone drugs such as Fosamax and Vioxx. These drugs don’t even pretend to help nature, they do absolutely nothing to enhance normal, healthy bone growth and development but instead pose immensely grave risks up to and including crippling and death. Three percent of patients taking these concoctions develop atrial fibrillation and half of them develop serious AF leading to long-term hospitalization or death. These statistics alone (but there’s more, there’s more) implicate bisphosphonates in 100,000 to 200,000 serious injuries or deaths for women every year since roughly ten million women are taking these drugs.

                 Abnormal bone growth and “greater brittleness” (in many cases) leading to abnormal fractures and numerous cases of temporary and permanent paralysis caused by this brittleness and abnormal growth and severe back pains are a COMMON side effect of these poisons. And what will the FDA do about all this? Slap the wrist. They will insist upon stronger warning labels on the carton and in the included literature – if past performance is any clue.   So let’s get back to what SHOULD be done to treat and most importantly, to PREVENT osteoporosis by first of all doing NO HARM . . . .

                 Remember, this is a serious disease: potentially it will maim the victim for life. And if you take Vioxx and Fosamax, you’ve added greatly to your risk. But there is risk even without these medicines: hip fractures may impair ability to walk and may cause permanent disability or even death despite hospitalization and major surgery. Spinal or vertebral fractures also have serious consequences, including loss of height, severe back pain, and deformity. Osteoporosis can cause a person to stoop so far forward she'll appear to have a hump on her spine. It’s a crippler. So what’s to be done?

                 As loyal readers realize, beside panning the FDA, Rajjpuut has made a great case for dramatically enhancing the budget of and, just as importantly, the scope of the CDC (Center for Disease Control) from being the mainstay in the battle against communicable infectious disease to also taking on chronic lifestyle-caused problems like: diabetes, cancer, stroke, heart disease and osteoporosis to name only a few. Rajjpuut has said repeatedly that the CDC is by far the most effective health care organization in this country and should be put in charge of health care education via the media and of coordinating health care education in the schools as well as of chronic disease PREVENTION.

                First that health care education should teach PREVENTION, getting rid of the negative lifestyle habits that make men and especially women prone to osteoporosis. Second the CDC would teach PROACTIVITY: what are the positive things one can do to push osteoporosis potential far, far away from your life? Active lifestyle choices like dancing, walking, jogging and running, other aerobics, bounding and bouncing on trampolines or rebounders; yoga, Pilates and similar exercises; good nutrition; and supplementation with magnesium, and fish oil containing EPA and GLA are the sort of practices that will help make people perhaps 3% as likely to get osteoporosis without any dangerous side-effects and far milder osteoporosis if they do get it.

                 None of this is rocket science, but virtually all of it is news to virtually all Americans, so they take the easy way out. They trust their health to doctors who have taken on too many patients and thus can’t keep up with medical research. These doctors are getting their information on junkets sponsored by BigPHARMA and hear no dissenting voices. Their training has them relying from their days as interns upon drugs to cure every ill. Medical training in this country attacks problems primarily in stage 3 or stage 4 of the process when the process is the most complicated, expensive and potentially dangerous. “First Do NO Harm!” advocates attacking the problem long before it is a problem. 

                And remember “First Do NO HARM!” emphasis advocates as a crucial first step: eliminating the FDA, the agency created to protect our health which instead protects the profits of BigPHARMA to the detriment of our health. FDA = “Fouled-up Disaster Accelerants."

Ya’all live long, strong and ornery,

Rajjpuut
 
ps:  this canNOT be over-emphasized:  when it comes to vitamins, minerals and nutrients (none proven to harm you, many proven to help a lot) the FDA can never hear enough evidence that they are not harmful or that they are actually good for the individual . . . but when it comes to looking at prescription medicines the FDA has approved 80,000 deaths is NOT ENOUGH, 500,000 injuries or maiming is NOT enough to get a reversal of an idiotic FDA decision . . . there is never enough harm that can be done to get the FDA to rule against BigPHARMA.
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Eliminate World Laughingstock FDA #12

Attacking nutrient supplements, FDA always claims “not enough evidence they’re safe;” when defending drugs they’ve let wallow onto the shelves “there’s never enough evidence to prove they’re dangerous” . . . regardless of all the deaths they cause.
 
the U.S. Fraud and Drug Administration . . .
 
When's the last time you heard of a vitamin hurting a person . . . ?
 
 

No Drug Too Deadly for Approval

and Continued FDA Backing

            Many Americans find it difficult to believe that the FDA is a corrupt agency. Well “blatantly corrupt” is the mildest term appropriate for the FDA. As Rajjpuut has been saying all along through the eleven earlier anti-FDA rants, we suspect that health care change is coming this autumn . . . if they only make one change let it be wholesale radical elimination or total reform of the Food and Drug Administration. The outrages continue to mount: Ritalin, Celebrex, Avandia . . . Thalidomide is back again approved by the FDA (Rajjpuut does not make these things up) despite the horrendous birth defects it instigated in the 60’s. COX-2 inhibitors are allowed again despite 60,000 deaths according to the British Journal of Medicine evaluating the FDA advisory panels decision. The online website naturalnews.com put it this way:

“The fact that a single COX-2 drug has reportedly killed more Americans than the entire Vietnam War is apparently not sufficient for the FDA to characterize it as unsafe.

“With this decision, a ‘full safety approval’ by the FDA has now become meaningless. If the agency can put its stamp of public safety approval on a drug that has killed tens of thousands of Americans and that was removed from the market by its own manufacturer following the revelation of studies showing alarming increases in heart attack risk, then what, pray tell, could possibly be the FDA's definition of a dangerous drug?

“For the FDA to consider a drug dangerous, it apparently has to kill more than 60,000 Americans. I'm curious what threshold must be reached before the FDA actually does its job and seeks to protect the U.S. public. Do 250,000 people have to die before the FDA calls a drug unsafe? 500,000 people? How about a million people?”

“There can no longer be any doubt whatsoever about the FDA's true purpose. Regardless of what the agency publicly states, when it comes time to make key decisions about the safety of U.S. consumers, the FDA will side with drug companies every time. We've seen it time and time again: with the FDA's reluctance to pull obviously dangerous drugs off the market in a timely fashion (Rezulin, for example), with the FDA's attempts to silence its own drug safety scientists (censorship of Dr. David Graham, for example), and with the FDA's collusion with drug companies in suppressing clinical trials and other forms of evidence that raise safety questions about prescription drugs. Corruption runs deep at the FDA, it seems.

“This decision with Vioxx and other COX-2 inhibitors was a defining moment for the U.S. Fraud and Drug Administration. It was a moment where the agency could have sided with public safety and held fast to a position of responsibility and ethics. Instead, it chose to favor drug company profits and put its stamp of approval on a class of drugs that is arguably the most deadly drugs ever to hit the open market.

“A sane, ethical FDA would have not only banned COX-2 inhibitors outright, it would have put an end to direct-to-consumer advertising that ultimately led to the over-hyping and over-prescribing of these painkillers in the first place.”

Well said, the FDA does not even appear to be even making a pretense of doing the job it was created for. This once proud federal agency created immediately after the outcry following Upton Sinclair’s novel/expose` “The Jungle” outraged the public in 1906 to demand protection from business charlatans in the food and drug industries. The FDA has spit upon the proud purpose that created it over a hundred years ago. For example, Nsaids, as a class are among the most dangerous, least necessary, most expensive and most hyped of any class of drugs and COX-2 inhibitors are easily the most dangerous of the Nsaids.  Attacking nutrient supplements, FDA always claims “ there's not enough evidence they’re safe;” when defending drugs they’ve let wallow onto the shelves “there’s never enough evidence to prove they’re dangerous” . . . regardless of all the deaths they cause.  This is one dozen rants now . . . the story ought to be clear:   Americans, be vigilant in defending yourselves from the protection of the FDA.

If the citizens of America with all the wealth of information about this most corrupt of agencies continue to stand for it, then they deserve the fruits of FDA decadence heaped upon them. Rajjpuut hopes we are a better more alert and informed people and will rise up and contact our elected officials about this most corrupt evil empire in our midst: The FDA.

Ya’all live long, strong and ornery,

Rajjpuut

 

 

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Eliminate the Killer FDA #11

FDA failed to pass deadly warning to the one million Americans already taking Avandia.

Stronger Warning Labels?

Yeah, that Ought to Do It!
 

            There are some environmental extremists who believe devoutly in NPG, Negative Population Growth (npg.org/whatis.html) as the only hope for Planet Earth. Some of the more enthusiastic of them in England have even suggested a “perfect Terrestrial population of four hundred seventy-eight thousand humans. Since the present population of our world is estimated at six and a half billion . . . their best of all possible worlds would require the death of 93.5% of all those presently living. It’s comforting to find out that the NPG group has found a productive outlet for their energies working for the Food and Drug Administration (FDA) in Washington, D.C. The sheer gall of the FDA is only surpassed by its sheer incompetence and they are definitely NPG’s favorite friend doing their part to trim the unnecessary human population right where it stands . . . .

In early August, 2007, in a classic example of stupidity and by a 22-1 vote the FDA refused to ban the dangerous diabetes drug Avandia, despite 80,000 known deaths, a suspected 205,000 heart attacks and strokes, and knowing it would continue to kill thousands more in the future. Today almost two years later, congratulations NPG advocates, you hitched your wagon to the right horse:  the FDA.  Avandia, Actos and the now defunct Rezulin are a class of drugs called TZD’s, oral anti-diabetes drugs developed in the 1990’s.  Rezulin was dropped early on for causing liver damage in a small but significant percentage of the user population.  Avandia and Actos were said to be free of liver damage . . . however, recent data shows that both significantly increase the risk for liver problems and Avandia is on top of that:  a cardio-vascular system nightmare -- dramatically increasing risk for both heart attacks and stroke.

The New England Journal of Medicine came to that conclusion from one of its studies in 2006, but the FDA had already been told that by the drug’s English manufacturer, Glaxo eighteen months earlier. Then, in a greedy reversal of form, Glaxo said, "To hell with decency and honor" and arrived at the 2007 hearing with thousands of pages of studies and information and received the OK for continuation from the FDA despite its horrific record over the ten years it's been sold, “Let’s not throw the baby out with the wash water!” said one Glaxo enthusiast.    Perhaps he should have said, ” “Let’s not throw Rosemary’s Baby out with the wash water?” Since without any medicine at all . . . one of the more common dangerous side effects of diabetes is increased risk of cardio-vascular problems like heart attacks and strokes, Rajjpuut doesn’t think that giving Avandia (with its notorious record of inflicting cardiovascular damage) to diabetics is a good idea unless you’re an NPGer and euthanasia is your contribution to the movement’s goals.  

The FDA's actions in 2007 with Avandia are part and parcel of the agency's absolute unwillingness over the last decade to reverse even the most atrocious decisions. Much like George Armstrong Custer who has been accurately protrayed as totally unwilling to reverse a "Custer decision," the front-line troops (in this case diabetic patients) are the ones who suffer in large numbers. The case against Ritalin and Celebrex is every bit as strong but in all three of these incidents the FDA seemingly is willing to risk more live and more problems by just making a stronger warning label rather than taking dangerous products off the market.   These are just three of roughly a hundred reasons why Rajjpuut says that since health care is very likely going to change this fall, the very first change needs to be the elimination or complete revamping of the FDA, easily the most corrupt and incompetent agency in the federal government. 

Besides its other sins the FDA did not pass on the Glaxco 2005 warning to American Avandia users, at that time over one million strong. What exactly must the FDA do to receive some sort of sanctions from the GAO or other agencies?

Rajjpuut feels strongly that the doctors' "Hippocratic Oath" "First do NO harm" should apply to anyone in the healing business. When you create drugs that don't actually heal anything, (in this case Avandia clearly doesn't heal diabetes) which are basically a lifelong subscription to expensive and dangerous medicines      . . . you're asking for trouble. Some cases may be marginally worth it . . . clearly the data on Ritalin, Celebrex and Avandia show that the FDAs original assessment was wrong and even more clearly its follow-up assessment was wrong too. This is not an group with the best interests of Americans at heart . . . but NPGers around the world will be grateful to the FDA.

Ya’all live long, strong and ornery,

Rajjpuut

 

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Eliminate the Hypocritical FDA #10

“General Mills, You believed our lies? Shame on you! We’ll bust you to private!”

 

Hypocritical FDA Scolds Cheerios

for Cholesterol Assertion

                In this series of rants against the ultra-corrupt FDA (Food and Drug Administration), Rajjpuut’s premise is that since health care change is coming almost certainly this fall or winter . . . if there were only one improvement that could be made in the American health care mess, that would be to eliminate or totally revamp the FDA. Here we see the FDA at their very hypocritical worst . . . .

                The FDA, approver of the poisonous substances Ritalin and Celebrex which has refused to remove either one of those killer drugs from the market after FDA exaggerations of the two drugs' safety proved to be absolutely erroneous, has attacked cereal maker General Mills for revealing their scientific study showing Cheerios reduces cholesterol 4%.   “Only FDA approved drugs are allowed to make such claims,” is the official FDA lie, ‘er line, on the issue. General Mills, You believed our lies? Shame on you! We’ll bust you to private!   Has the FDA killed two million Americans yet?  Well they've certainly contributed to the maiming or killing of ten million.  Brings a sense of disgusted nausea and bile, no?

                Staying true to form, the FDA which is single-handedly most responsible for boosting iatrogenic deaths in America into 4th place among all deaths (iatrogenic deaths are those caused by medicines and medical treatment) in the nation, fails to mention that the simple fact is this: less than 47% of those who die from heart attacks have elevated cholesterol. The 33 year old lie that high cholesterol brings heart attacks makes statins (cholesterol  lowering drugs) the most profitable of all the billion dollar drug bonanzas in American history for the huge pharmaceutical companies and has probably killed, maimed and injured more Americans than all of our war dead from all the wars in our history, while costing individuals and the government hundreds of billions of dollars for these expensive, dangerous drugs that cure nothing and arguably make strokes much more probable.

                The FDA, which has not shown the courage to attack big food or big drug companies for their improprieties; or to stand up to its sister in corruption the USDA, has however a proven track record for attacking health food stores and individual doctors who have the temerity to prescribe vitamins, minerals or other nutrients for some of their patients’ problems and the FDA now is attacking the most popular semi-healthy cereal in the nation. CLAP! CLAP! CLAP! It makes me so proud to be an American.

                In hypocrisy of the highest audacity, the FDA goes on to say, “. . . Companies that make claims about their whole grain foods are supposed to mention that fruits and vegetables are also part of a fiber-rich diet” which Cheerios does not.    Why are they doing this? Imagine if Cheerios improves its product some day and can say confidently after confirmation from say fifteen studies, “Cheerios reduces elevated cholesterol an average of 32% with a nine week period.” If that were to happen and the statement were true, than there would be clinical study information backing the idea that food can make you healthy: a claim that the FDA adamantly (but wrongly) refutes, repeatedly they have officially claimed:   “There has NEVER been a supplement or a food that has been proven to cure any disease" even though they're hypocritically demanding General Mills say what they've declared invalid that food can make you healthy, in this case fruits and vegetables.  What imbeciles!

Now you and I know that if the doctors find after a few days in the hospital that all your horrendous symptoms show that you have scurvy, they’re NOT going to start feeding you 16 oranges and citrus fruits every day. No, they will probably give you about twelve to fifteen times the RDA of Vitamin C tablets . . . but the FDA statement denies that, denies the experiences of Captain Cook and the epithet “limies” given to British sailors;  denies the Nobel Prize of Linus Pauling; and denies the recent Nobel Prize of Louis Ignarro. The FDA protects the food industry and its lies; the FDA protects the drug industry and its lies; the FDA ultra-protects itself and its own lies and ineptitudes . . . the FDA attacks those whose products have never been proven to do anybody any harm when used in proper dosage. The FDA is a major cause of America’s health problems and needs to step out of the way, change or blow themselves up.  The FDA, once a great agency created in response to Upton Sinclair's monumental novel expose` "The Jungle" in 1906 certainly will not protect the American people.

Ya’ll live long, strong and ornery,

Rajjpuut

 

 

 

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Eliminate the Gutless, Toothless FDA #8

The FDA, which makes twenty-man raids of natural foods stores and offices of doctors who dare to prescribe nutrients (vitamins, minerals, etc.), for their patients has uniformly shown itself to be gutless and toothless when dealing with big food companies, big drug companies and the USDA (Agriculture Department). 

FDA Lacks “Rocky Mountain Oysters”

Necessary to Protect the Nation’s Food Supply 

           The FDA is the mighty, giant agency that’s supposed to protect the integrity of our foods?   The points of this now eight-rant series exposing the FDA corruptions and incompetence are these: A. American lives and health are at risk B. American taxpayers are not getting 1% of what they’d should expect from the FDA on the positive side C.  The American people are getting 100,000% of the negatives they should expect from the FDA  D. President Obama is calling for health care reforms and a whole new expensive federal program but has not really shown much interest in the FDA when reforming the FDA is the single most necessary step that needs to be taken if our health care system is to improve.  Additionally, President Obama’s programs have addressed exactly one significant point out of the forty-three raised by the Ol' Health Educator Rajjpuut’s “A Far Better Health Care Alternative” series . . . .

           The FDA which makes twenty-man raids of natural foods stores and offices of doctors who dare to prescribe nutrients (vitamins, minerals, etc.) for their patients has uniformly shown itself to be gutless and toothless when dealing with big food, big drug companies and the USDA (Agriculture Department).  

Well before the recent scandals, four and a half years ago the FDA responded to anonymous and correct information about salmonella in peanut better which ConAgra’s internal testing had noted but which had NOT been reported to the FDA. Unbelievably the agency turned away when told they would only give the documents asked for in response to an FDA written request. 

Specifically, the company officials A. confirmed the test results reported by the anonymous informant but B. refused to turn over the lab reports and incredibly C. the FDA walked away without further ado. Apparently the FDA according to this example and others gleaned by internet sources will almost NEVER serve paperwork requests and even more rarely take a big company to task (make a raid or take them to court or fine them) regardless of the circumstances. They make big showy raids of small organizations and doctors' offices but back away at the merest sign of resistance at big companies.

This is the mighty giant agency that’s supposed to protect the integrity of our foods?

Of greatest concern is the FDA absolute cowardice in the face of the United States Department of Agriculture (USDA). The first noticeable problem is that the jurisdictions of the two agencies overlap in many places (a huge waste of tax-payer money). The second problem is that it appears that the agriculture department might well be every bit as inept and corrupt as the FDA, perhaps moreso (Rajjpuut can’t believe he said that! Is that possible?) but in cases where the FDA has discovered the USDA dropping the ball . . . reportedly, the USDA ignores anything the FDA says. 

This is the mighty giant agency that’s supposed to protect the integrity of our foods?

The huge 143-million pound beef recall announced in February, was apparently foreshadowed by FDA officials telling USDA officials of problems they’d noticed back in November (three months earlier). The USDA officials did nothing until February and then reported the Hallmark/Westland meatpackers had been “skimping upon inspections” and ordered the recall.  Because of the delay in action the USDA admitted at the recall time that most of the beef had surely been already eaten by consumers – including school children who received the beef as part of a school-lunch program. The wonder is that it was discovered at all. Apparently a video of plant personnel abusing fallen cattle, trying to get them to stand up and to walk to the slaughter point had been surreptitiously recorded by a Humane Society member according to an L.A. Times article. By law, non-ambulatory (they can’t walk) cattle canNOT be slaughtered since “Mad-Cow Disease” is much more likely under those conditions.

If the Humane Society had not created this cause-celebre` would the USDA or FDA have done anything or even reported anything (since what they did had NO positive effect)???

This is the mighty giant agency that’s supposed to protect the integrity of our foods?

            ‘Tis to laugh!

Ya’all live long, strong and ornery,

Rajjpuut

 Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success.

 

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Eliminate the FDA #7

Keeping feces out of meat and salmonella out of everything is not rocket science. The highest standards of cleanliness and conscientious care are required, yes, but if the FDA can’t ensure even that, to a level at least 50 times higher than what we’ve seen in the past three years, what the hell good are they?
 


Taylor Appointment,

Just One More Scandal

in the Sad FDA History

           
            President Obama's new health care system (if it comes) is doomed to failure at huge expense, personal-healthwise and economically to the country . . .  as we mentioned in Rants #4 and #5, #6 there were four main reasons why, two of those reasons are germane to this discussion, items C and D:

C.    And mostly because, the President is NOT expected to address FDA re-organization or clean up in his new program: huge mistake, HUGE!

D.    Additionally, as far as is known, the President is expected to address exactly one of the forty-three points brought up by health educator Rajjpuut in his blog series “A Far Better Health Care Alternative.”

          Point C above, is not only true of the “drug side” of the FDA but especially so of the food side. Just a few years back, the FDA created the position of food czar, to oversee cleanliness and safety for the nation’s food supply. To say that move was an unmitigated disaster is to insult unmitigated disaster everywhere. Last Tuesday, the FDA made Monsanto’s Michael Taylor “senior advisor to the commissioner,” basically a new food czar. The once proud FDA has by this appointment of yet another roving bureaucrat underlined the incestuous nature of its dealings with both the food industry and the pharmaceutical companies. The fact that Mr. Taylor is a lawyer shows the utter disdain with which the FDA holds the public well-being. Let us be perfectly clear here:   Keeping feces out of meat and salmonella out of everything is not rocket science. The highest standards of cleanliness and conscientious care are required, yes, but if the FDA can’t ensure even that, to a level at least 50 times higher than what we’ve seen in the past three years, what the hell good are they?

            A revolving doorful of bureaucrats and aparatchiks is never going to clean up our food supply. What the hell does a lawyer-for-hire know about food safety? About manufacturing processes? About the public interest? Why not search within the FDA itself and find somebody who’s blown the whistle on the agencies own corrupt practices and incompetences? Why not go within the FDA itself and find someone who’s nailed unclean companies repeatedly in the past? Why the hell not try common sense for a change.   Why the hell not try integrity for a change.

            As always, the FDA bigwig has switched sides often; Taylor began as a counsel to the FDA; later he moved to a law-firm representing Monsanto, a high-profile biotech company also involved very much in the agricultural industry. In 1991 he returned to the FDA as “Deputy Commissioner for Policy.” The team that issued virtually all the FDA’s industry-friendly decisions on food and approved Monsanto’s growth hormones for cattle and dairy cattle had constant input from Taylor you can bet. His role was questioned by the Government Accounting Office but he was exonerated.

            In ’94  Taylor became adminstrator of Food Safety and Inspection Services. Then he went back to private law practice; then joined Monsanto again and became one of their chief lobbyists dealing with the FDA. There is NO record of Mr. Taylor knowing anything about public health, Rajjpuut doubts the man ever read “The Jungle,” the book that created the scandal that created the FDA back in 1906. Rajjpuut is quite sure that Mr. Taylor was too busy smoozing to have time to learn anything about public health and welfare. Shame, shame shame FDA shame on you.

           What can we expect from Taylor in his latest incarnation with the FDA? He’s a damn lawyer. We can expect him to counsel closely with his bean-counters about “cost-benefit analysis” and come up with an essentially “risk-based” approach because that’s what lawyer’s do. What? You don’t know what a risk based approach or cost-benefit analysis means? Well, let ol’ Rajjpuut clue you in. When the Ford Pinto’s came on the market with a dangerous exploding gas tank and a high probability of high speed collisions crumpling the doors and trapping passengers inside, the worst aspects of their bad design could have been prevented by either a reduction in trunk space to create a tank position immune to the problems; or modifying the plan they finally approved:  by installing an $11 per car fire-prevention system.

           As it turns out, the bean-counters were right in their cost benefit analysis that fewer than a thousand people would burn to death and at $200,000 a head . . . the company would make substantially more money leaving the $11 fire-prevention system off the car. And the lawyers analyzing their recommendations were right it was an “acceptable risk.” Of course when later on the factors behind the decision-making were made public, the public relations nightmare created, to say nothing of the class action law suit that followed, were probably NOT what Ford would have wanted to risk.  Simple integrity, it seems, and making the best product for your customers play no part in lawyers' outlook.

              By the way, the Ford Pinto was considered “Lee’s Car,” meaning that Lee Iacocca designed it. Iacocca later went to Chrysler and got them their first bailout . . . you can see the man has a talent for incompetence on a national scale that’s beyond virtually any man but the designer of the Titanic or George Armstrong Custer. Taylor is such a man: a natural in the hearts of the bureaucrats at FDA.

            NO!  No, we definitely do NOT need cost-benefit analysis and “risk-based” approaches when it comes to our food safety. We need instead the highest standards of cleanliness and conscientious care possible and a man or woman who’ll ensure that is the result.   We need, instead a man or woman who’s whole life has been dedicated to public health who’ll insist that any contamination at all is unacceptable.        

            At the FDA they’ve long forgotten it’s the public health they’re in the business of protecting; and the public they’re supposed to be serving but the President, congress, and the American Public needs to remember that key fact RIGHT NOW!  The first necessary step in any health care change is to UNDO, REDO and UNcorrupt the FDA.

Live long, strong and ornery,
Rajjpuut  

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success.

 

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Eliminate FDA #6

The FDA has issued several statements at various times in their history that "no supplement has ever beenproved to cure any disease or heal any medical condition."  Amazingly  they've never heard of Vitamin C and scurvy; of Linus Pauling's Nobel Prize; or Louis Ignarro's Nobel Prize.
 
 
 
The FDA Goes Out of Its Way

to Protect the Drug Companies

from Healthier Alternatives


            President Obama's new health care system (if it comes) is doomed to failure at huge expense, personal-healthwise and economically to the country . . .  as we mentioned in Rants #4 and #5, there are four main reasons why:

A.    Government spending programs seldom work.

B.     The two earlier programs, Medicare and Medicaid, did not help and only made health and cost trends already in place much worse.  Both are functionally bankrupt.  Medicare now has obligations of $34 TRillion and will be officially bankrupt in 2016.

C.    And mostly because, the President is NOT expected to address FDA re-organization or clean up in his new program: huge mistake, HUGE!

D.    Additionally, as far as is known, the President is not expected to address a single one of the points brought up by health educator Rajjpuut in his blog series “A Far Better Health Care Alternative.”

          As shown clearly in Rant #5, American medical scientists have time and time again concluded research underlining that there is absolutely NO need for new drugs that mask pain but do not help cure the underlying problems. The problem has been made infinitely worse because now drug companies are allowed to legally "bribe"
** the FDA to rush their newest dangerous concoctions right out into the marketplace and FDA philosophy has deteriorated since 1990.  In that year, 58% of the drugs studied were approved; today about83% of studied drugs are approved. 

In 1990 only 5% of the brand new to the world drugs were approved; today 2/3 of these brand new drugs never before used in any other country now receive FDA approval:  an anguishing 1300% rise in approval of untested drugs.  The combination of rapid (bribed) approval; loose overallapproval habits and ultra-loose sanctions on brand-new drugs has made the American health scene a dangerousplace for patients when given an Rx from their doctor.

The FDA seems to go out of its way to protect the drug companies from potentially healthier, lessexpensive, and less dangerous competitors.  Why else would the FDA have issued several statements at various times in their history that "no supplement has ever been proven to cure any disease or heal any medical condition."  Amazing that they've never heard of Vitamin C and scurvy; of Linus Pauling's Nobel Prize; or Louis Ignarro's Nobel Prize.

             Even though there are virtually no instances of medical PROBLEMS caused by nutrients (vitamins,minerals, etc.) when taken in recommended dosages but combined millions of DEATHS, DEFORMITIES, illnesses and INJURIES caused by "proper" dosages of prescription medicines . . . nevertheless, the FDA has attacked natural ingredients and natural nutrients producers and stores with an incredible vehemence especially, it seems, nutrients which have performed very well in scientific studies such as DHEA, DMSO, hydrogen peroxide and food grade hydrogen peroxide.  Natural ingredients being far less expensive, and having no side effects for people not allergic to them are serious rivals to drugs.  The drug companies have no motivation, for their part, to feature any "natural ingredient" because no natural ingredients are patentable.

             The FDA seemingly attacks all enemies or competitors of the big pharmaceutical companies:  vitamin stores; doctors who routinely prescribe vitamin or nutrient regimens; natural whole-grain diet breads and diet cereals; homemade diet soups, etc., etc., much more eagerly than it applies pressure to the drug companies themselves.  Where are the deaths? deformities, illnesses and injuries that justify that kind of scrutiny?  Why don't they do the math  and do their jobs instead and protect Americans from the irresponsible drug companies?  I think the folks who created the FDA in 1906 must be rolling over in their graves seeing the Frankenstein monster their once great agency has degenerated into.  If for no other reason,the number of iatrogenic deaths, deformities, injuries and illnesses today's drugs have visited upon the unsuspecting American public give them sufficient excuse to continue rolling around in those graves for thenext 100 years.

            At the FDA they’ve long forgotten it’s the public health they’re in the business of protecting; and the public they’re supposed to be serving but the President, congress, and the American Public needs to remember that key fact RIGHT NOW!  The first necessary step in any health care change is to UNDO, REDO and UNcorrupt the FDA.

Live long, strong and ornery,
Rajjpuut  

**   the correct term is "bribe" but the FDA calls them "expedited evaluations" or "expedited reviews"

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success.

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Eliminate the FDA #5

The  33-year old high-cholesterol lie is the most profitable charade in the history of medicine, it makes all other quack medicine salesmen ever known look like Honest Abe.

Americans believe health comes in drug bottles and the few in the medical community who know differently (they ALL should but are hypnotized by drug claims) aren’t advertising the truth.

 At the FDA they’ve long forgotten it’s the public they’re supposed to be serving.


Drug Culture Created by the FDA

and Big Pharmaceutical Companies

Costs Government Programs Heavily

 

Obama plans to put a new health care system in place doomed to failure at huge expense, personal-healthwise and economically to the country . . .  as we mentioned in rant #4, there are four main reasons why: 

A.    Government spending programs seldom work. 

B.     The two earlier programs, Medicare and Medicaid, did not help and only made health and cost trends already in place much worse. Medicare has contractual obligations for $34 TRillion in obligations it cannot cover; officially it will be bankrupt in 2016.

C.    And mostly because, the President is NOT expected to address FDA re-organization or clean up in his new program: huge mistake, HUGE!

D.    Additionally, as far as is known, the President is only expected to address exactly one of the forty-threepoints brought up by health educator Rajjpuut in his blog series “A Far Better Health Care Alternative.”

          American medical scientists have time and time again concluded research that underlines the simple fact that there is absolutely NO need for new drugs that mask pain but do not help cure the underlying problems. There are enough old pain medications at large, and the newer ones are just far more expensive and much, much more dangerous. But the drug companies keep cranking them out and despite the best medical advice ever known (First Do No Harm!), the FDA keeps approving them. The pure cost in money; the cost in iatrogenic ailments (problems caused my errors from doctors, nurses or the hospital itself; or by reactions to medicine) in money and lives; and the cost to the U.S. government all demand that the FDA deny approval to about 90-95% of all such drugs.

          However, the FDA in its inanity and corruption (see Rajjpuut’s earlier FDA rants) doesn’t even deny approval to 10% of these dangerous new concoctions. Year after year the list of horrendous side-effects for new medications we hear advertised on TV grows longer and more virulent. 

          Drug companies then go out of their way to see that their dangerous, expensive concoctions become popular:

A.      Nurses are paid by drug companies for using their products when they have that discretionary power

B.      Schools get paid thousands of dollars monthly for every child they help get prescribed for psychiatric drugs like Prozac or Ritalin.

C.      Doctors routinely get visited by drug sales men with huge amounts of literature “pushing” their drugs and even kickback offers and bonus offers if certain “quotas” are

 met

D.      A, B, and C above are clearly abuses that endanger the patients and the government’s coffers. The FDA which has the power to stop A, B, and C above from happening

never does anything . . . never.

The biggest abuse of all, however, is that drug companies routinely pay scientists and doctors on government advisory panels to recommend their drugs. And often the payments even come for recommending their drugs in front of FDA evaluation hearings and the FDA condones the practice.

Drug companies can now legally bribe** the FDA to hasten their drugs onto the market. 

It’s all a huge pack of lies, deceit, shady practices and outright corruption that endangers the public and costs the government immense amounts of money every second of every day. The FDA knows but will not tell you that:

A.      An aspirin a day makes strokes much more likely

B.      Almost all sunscreens cause cancer but don’t do much to prevent skin cancer (since sunscreens have become common, American skin cancer rates have risen dramatically, far worse than people under the tropic sun typically encounter)

C.      Lowering cholesterol does nothing to stop heart attacks.  The 33-year old high-cholesterol lie is the most profitable charade in the history of medicine making all the quack medicine salesmen ever known look like Honest Abe.

D.      Estrogen therapy is an extraordinarily dangerous practice.

E.       Roughly 60% of the most frequently prescribed drugs for the elderly are found on lists of drugs NOT to be given to elderly persons.

F.       Every prescription drug has dangerous side effects, nevertheless 20% of them have NO printed warnings on the packaging.

G.      Average Americans consume fifty pounds worth of prescription, non-prescription, and over the counter drugs every year (400 times more than Rajjpuut does!)

H.      People who don’t need drugs are now going into their doctors and demanding certain drugs they’ve seen advertised on TV.

I.        Iatrogenic disease (caused by medicines and medical treatment is now the 3rd or 4th

 


largest cause of death and dangerous medicines are a prime cause of them. You are ten times more likely to go to the hospital for a prescription drug reaction and four times more likely to die than if you had an automobile accident.

J.        The FDA could IMMEDIATELY stop every one of these sad situations, the FDA does nothing!

            At the FDA they’ve long forgotten it’s the public health they’re in the business of protecting; and the public they’re supposed to be serving but the President, congress, and the American Public needs to remember that key fact RIGHT NOW!

The first necessary step in any health care change is to UNDO, REDO and UNcorrupt the FDA.

Live long, strong and ornery,
Rajjpuut   

**   the correct term is "bribe" but the FDA calls them "expedited evaluations" or "expedited reviews"

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success.

 

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Eliminate the FDA #4

At the FDA they’ve long forgotten it’s the public they’re supposed to be serving NOT the drug industry.

The Hippocratic Oath says, “First Do No Harm” . . . indicating that 97% of the time, doctors could be sued for malpractice for prescribing drugs they know can do enormous harm according to the official list of side effects.


Drug Culture Created by the FDA

and Big Pharmaceutical Companies

Endangers Citizen’s Health

 

            We all know that Obama plans to put a new health care system in place. Most of us know that it’s doomed to failure at huge expense, (personally and economically) to the country . . . here are the reasons why: 

A.    Government spending programs seldom work. In fact Obamacare is a ruse to cover up the fact that Medicare has obligations of $34 TRillion it can’t cover and will be bankrupt officially in 2016. 

B.     The two earlier programs, Medicare and Medicaid, did not help and only made health and cost trends already in place much worse.

C.    And mostly because, the President is NOT expected to address FDA re-organization or FDA clean up in his new program: huge mistake, HUGE!

D.    Additionally, as far as is known, the President is only expected to address exactly one of the forty-three points brought up by health educator Rajjpuut in his blog series “A Far Better Health Care Alternative.”

The Hippocratic Oath, which doctors swear to, says “First Do No Harm” . . . since study after study indicates that 70% of the expensive drugs Americans take actually have “no effect,” and all drugs created, that means 100% of them, have proven and listed side effects: arguably from 90%-100% of instances when a doctor prescribes a drug for a patient, he is at least technically, if not in fact, breaking the Hippocratic Oath. America is a drug culture. People believe health and happiness comes in bottles. The information found in this paragraph is highlighted because of whistle-blowers who in study after study say that internal memos and other documents generated by the drug companies themselves reveal pretty much those same two sad statistics.

            When it’s also considered that a huge percentage of drugs are only designed to mask or alleviate symptoms but NOT or even NEVER to cure any underlying conditions and all these drugs too have annoying, dangerous and/or deadly side effects . . . the magnitude of the problem becomes clear. The FDA, by approving these palliatives and their side effects is making America’s health problems worse. The fact that drug companies now have the option to legally bribe** the FDA to expedite putting the drugs on the market has exacerbated an already horrendous problem. 

            Additionally, consider this . . . the FDA has known for over thirty years that high cholesterol levels are NOT associated with heart attacks and that lowering cholesterol does NOT cure any actual medical condition;  yet they say nothing to the American health care industry, refuse to remove the drugs from circulation and thus continue to help the drug companies rip off the American public.  It's one of their biggest shams because statins (cholesterol lowering drugs) are some of the most dangerous, very expensive and totally unnecessary drugs.  "First Do No Harm!"

            PPIs (proton pump inhibitors) likewise are drugs for no real disease.  So-called “Acid Reflux Disease” is an invention of the drug companies. If you have persistent heart burn, nine times out of ten you have TOOLITTLE stomach acid NOT too much. PPI’s actually make virtually all heartburn problems worse and they have recently been proved addictive. Taken with over-prescribed anti-biotics, PPIs can decimate the healthy stomach biota and create a horrendous and deadly dysenteric condition called “c. dificile” which kills older Americans quite frequently.   And PPIs are strongly suspected of causing serious bronchitis and even pneumonia.   "First Do No Harm!"

Need Rajjpuut mention that statins are the single most profitable drugs of all time and PPIs are very nearly as profitable?????? Of course a more horrendous example of FDA corruption is the conflict of interest that leads to the Celebrex (used for osteoarthritis; rheumatoid arthritis and painful menstruation) disaster in the first place and that same conflict of interest has kept that deadly drug on the market right up to the present moment with extra warnings added to its packaging. “First Do No Harm,” indeed!

            Depending upon who’s doing the study, iatrogenic deaths (death caused by medicines; doctors’ and nurses’ errors; hospital errors; etc.) rank as either the third or fourth greatest killers of Americans: “First Do No Harm” indeed!! And the biggest danger lies in the medicines themselves . . . every single one of them approved by the FDA. You are ten times more likely to enter a hospital and three and a half times more likely to die because of a prescription drug reaction then from an automobile accident. The root of a huge percentage of the American health care mess is 100% linked to the evil we call the FDA.  "First Do No Harm!"

 

            At the FDA they’ve long forgotten it’s the public they’re supposed to be serving and NOT the drug companies . . .  but the President, congress, and the American Public needs to remember that key fact RIGHT NOW!  President Obama, FIRST DO NO HARM:  re-organize and clean up the FDA before making any other health care change!

Live long, strong and ornery,
Rajjpuut   

**   the correct term is "bribe" but the FDA calls them "expedited evaluations" or "expedited reviews"

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success. 

 

 

 

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Follow the money! GE-MSNBC Steps from Obama's Closet

Let’s call spades:   spades . . . racketeering, influence peddling, and journalistic conflict of interest is going on.

                In the most blatant and shameless sell-out in American journalistic history, Barak Obama now “owns” MSNBC journalistic coverage of Himself and scratching the back that scratches his:  General Electric  (GE: MSNBC’s parent company) now “owns” the inside track on all cap-and-trade contracts; global warming contracts; green job contracts; and, oh yes, bailout money for the nearly bankrupt** General Electric during the Obama administration. GE, of course, has already received $139 Billion dollars in federal bailout funds for its financial arm. While it may have been obvious during the presidential campaign that MSNBC news was incapable of mouthing anything less than glowing praise for Barak Obama . . . their closet relationship has come out into the open courtesy of a leaked memo General Electric Vice Chairman John G. Rice wrote in an Aug. 19 e-mail to his colleagues at GE. First a bit of background . . . .

                It appears that this “open scandal” is no surprise to anyone. The other liberal-leaning networks aren’t commenting and only party-pooper conservative channel Fox News is on the scent. It’s so blatant that Barak Obama himself made light of it at the Radio and TV  correspondent’s dinner when he said, he was trying to come up with ideas for his comments at the gathering and couldn't sleep. But suddenly he knew where to go for help.  He just rolled over in bed and asked Brian Williams what he thought.

                If you watch political news at all, it’s no secret that the Fox Network is on Barak Obama’s enemies list; and that MSNBC, owned by GE, is easily the most pro-Obama TV news department in the whole country. In a land of left-leaning antennae, MSNBC could just as well change its name to the “Barak Network” and no would notice. 

There was one instance during the presidential campaign and another in March of 2009 when some of their CNBC financial analysts began criticizing Obama and his proposed programs (“a spending spree” according to one man) the typical government spending boondoggles GSBs liberals are famous for. Virtually immediately GE CEO Jeff Immelt and NBC President Jeff Zucker both dropped in on aforesaid commentators to inform them as to the weather: “Boys, this is how the wind blows around here . . .”  Apparently the “re-orientation chat” worked.  Since that time criticism, even subtle criticism of Obama the candidate or Obama the president has been non-existent. Their bias for Obama had always been outrageous, but today Zucker and Immelt have become Obama’s trick ponies and President Obama is deified at least three times daily on each NBC affiliate company. Other than Obama getting unlimited use of NBC teleprompters during the campaign and later as president, no one could be sure exactly what the tie in was. Up till late August the nature of their “pact” was still anybody’s guess. Let’s look at three examples of the suspicious nature of the relationship: 

 

1.        GE is relying on the Obama administration to come through on a promise that all American health records could by law only be computerized with GE and its supposedly “superior technology” having the inside track for a contract that would bring in billions. When word of this “cozy relationship was first aired in early August, Obama began showing a bit less favoritism at news conferences and even invited ABC in to tour the White House. Instead of a whole slew of government contracts, however, GE might be cruising for a bruising. Fox commentator Bill O’Reilly opined recently that any important contract for GE

“would make Watergate look like a Shirley Temple movie.” If that is the case, then one video clip that will make every highlight reel will be Kareem Dale (Special Asst. to Obama) smiling, At the White House, as we always like to say, we love MSNBC.”

2.      GE appointed former Senator Tom Daschle to its health advisory board. Daschle, President Obama's nominee for secretary of Health and Human Services until a tax scandal derailed him, has strong connections to the Obama White House. So obviously there is a huge potential conflict of interest here. NBC News is in on the take for Obama, even as GE, the parent company, is aiming to corral billions from the federal government. Hard to believe that MSNBC has only run positive spin stories on Obamacare for the last 11 ½ weeks isn’t it? NBC, was once renowned for the high ethical tone of its (liberal) news coverage but now with Zuckerman, Immelt and Daschle running point for the news gatherers, all you can hear is poisonous left-wing fanaticism supporting the president unerringly. Literally, sneezing or partial eye-rolling while reporting an Obama story is now a capital offense at NBC.

3.      GE, the once mighty Dow Jones Smokestack America Industrial giant who’s dividends were all any frugal retiree every needed, is now moving toward penny-stockville. To arrest that slide they have created a whole new strategy arm called “Ecomagination” which is plotting to win a wide array of ecology-themed contracts associated with global warming, green-tech, and cap and trade legislation. It all comes down on the “Obama connection,” will the president come through?

The connections that were assumed are now obvious, the August 19 e-mail memo from GE Vice Chairman Rice made it all official . . . .

"The intersection between GE's interests and government action is clearer than ever," Vice Chairman John G. Rice wrote in his August 19, 2009 e-mail to colleagues. He was calling on all GE people and GE subsidiary people to join GEPAC, the General Electric Political Action Committee. "GEPAC is an important tool that enables GE employees to collectively help support candidates who share the values and goals of GE,” that is, as the e-mail continued sharing the values and goals of GE means “support for policies that profit the company.”

Rice continues by getting specific about climate change, "we were able to work closely with key authors of the Waxman-Markey climate and energy bill, recently passed by the House of Representatives. If this bill is enacted into law it would benefit many GE businesses."

GE has put almost all its eggs into the Waxman-Markey basket. W-M would profit GE Greenhouse Gas Services, which deals in greenhouse gas credits, products that have value only if a cap-and-trade bill like Waxman-Markey passes. That is if W-M fails, GM is up the creek. Rice did not pull any punches, "Our Company is heavily impacted by a number of issues pending in Washington this fall.”

GE spent more on lobbying in the second quarter of this year than did any other company, according to federal lobbying files. Since 1998, GE has been the king of lobbying expenditures, according to the Center for Responsive Politics, outpacing its runner-up by 40 percent. Tying the lobbying and PAC effort together, Rice said, " . . .we must also make sure that candidates who share GE's values and goals get elected to office . . ."

Six House members have received more than $4,000 from GEPAC this cycle -- all Democrats -- Representative John Murtha, D-Pa., faces an extra rough re-election in 2010, courtesy of accusations that he  used his chairmanship on the Defense Appropriations subcommittee to benefit campaign supporters, other donors and patrons. GE is a defense contractor, of course.

The other big recipients are all incumbents in powerful positions, presumably safe for now: House Speaker Nancy Pelosi, Budget Committee Chairman John Spratt, House Majority Whip Steny Hoyer, Ways and Means member Richard Neal, who chairs the subcommittee on Select Revenue Measures, and key appropriator Norm Ducks**. This year two-thirds of GEPAC money has gone to Democrats, but during the 2008 elections, recipients were pretty equally divided. 

Why would GE give $15,000 to every senatorial candidate in the last election. Obviously, it was not because they cared so much who won, but rather because this way they had an “in” with the winner, whoever he/she was. The process is called “Rent-Seeking” which means: Lobbying and contributing to campaign funds so that favorable government legislation or regulation; or defeat of unfavorable legislation or regulation happens precisely in the manner most calculated to generate huge profits for the company which ordinary free market interchanges could never provide.  

It’s a fact of life in Washington, D.C., and GE is playing the game for high stakes with its presidential stooge benefitting from the firm's (via NBC) unfailing support over the airwaves. A $15,000 contribution to both horses in a two-horse contest may cancel each other out, but they work fine if what you’re really paying for is the “ear” of a congressman.   But the stakes look much higher this time.

How crucial is Waxman-Markey to GE, and by extension to, NBC?  Follow the money.  Follow the money.  Follow the money.  Follow the money.  Is $100,000 too much to pay for a congressman to vote for the most evil and anti-American legislation in history?  Count on once mighty GE to ante-up however much it takes . . . .

Ya’all live long, strong and ornery,

Rajjpuut
 
ps:  If you buy GE products or watch NBC in any of its cable or network variations:   you’re supporting the power behind Barak Obama which maybe is NOT what fiscal-conservatives, Libertarians, Republicans and Independents really need to do.
 
** the Townhall program's censor wouldn't let me call him by his right name, sorry
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Eliminate the FDA #3

At the FDA it’s not considered “conflict of interest” if the public doesn’t find out

At more than 90% of evaluation and recommendation meetings at least one member has a conflict of interest

FDA = Frequently Disguised Avarice

American Citizens’ Best Interest

is NO Concern of the FDA

 

               Before a drug is approved for the public the FDA will listen to a presentation by the drug manufacturer and then listen to expert witnesses.   Federal law prohibits the FDA ever use experts with financial stakes riding on the FDA decisions. According to NY Times Best-selling author Kevin Trudeau, however, this is a rule that is quite commonly waived. Trudeau says that the FDA keeps these meetings secret as well as which companies are involved, what the nature of the conflict is, and how much money may be involved. Your tax dollars at work protecting you!  Rajjpuut has heard that waiving the conflict of interest rule might happen nine or ten times a month. Reuters and USA Today has run articles that imply a far greater degree of financial involvement than that, however -- that well over half the experts the FDA calls upon for testimony have a direct financial interest in the drugs or subject matter being evaluated. With stock ownerships, grant money, consulting charges or other incentives involved, Rajjpuut believes that if three times in every hundred instances the “unbiased expert” testified against his own best financial interests that would be very surprising.

               At the FDA what the public doesn’t know, can’t hurt them (“them” being the FDA). According to Trudeau, once the experts have been heard from (and there’s only one side represented in 85% of instances) it’s very rare that the FDA rules against their advice in broad general matters. If a specific drug is the subject of evaluation, the FDA appears far less biased: at these meetings only 30% of the experts on average have financial conflicts.

               Does this “unbiased” FDA evaluation process work? Listen to the extensive list of side effects that get mentioned every time some drug is advertised on the television. And what happens when the side-effects are truly dangerous or even deadly? The FDA very seldom “pulls” a drug from the market. Instead they typically recommend including another warning on the packaging. Before 1990 less than 60% of drugs were approved today it’s over 80%. Before 1990 about 5% of the drugs approved by the FDA were brand new to the world. Since 1998 the FDA has made enormous amounts of fees approving drugs, 2/3 of them first-time drugs on the market. It is now also considered part of doing business normally for the drug company to legally bribe** the FDA to conclude it’s business much faster than unbribed examinations take.

               The Celebrex story is one of the most infamous of FDA approved drug debacles, as Rajjpuut writes this, Celebrex is still on the market despite a horrendous record with deaths and injuries. Despite this when Celebrex was brought back for another review the FDA recommended it stay on the market. According to Kevin Trudeau this was an instance where virtually every advisory panel member profited from the decision to keep it on the market. 

                Statins (cholesterol lowering drugs) are dangerous, expensive and amount to a virtual life-subscription. Guess what? Only 47% of the people who die from heart attacks have elevated cholesterol readings. The FDA was aware of studies showing that cholesterol had no cause-effect relationship with heart attacks back in 1976. For several years the FDA allowed eggs (remember they're the ones in charge of the safety of our FOOD supply as well as drugs) to be attacked as dangerous causes of high cholesterol and to this day allows drug companies to sell dangerous, expensive statins with utter impunity although these risky concoctions don't prevent heart attacks.

               Acid Reflux medicines (proton pump inhibitors or PPIs) are potions without a real disease. 90% of the time when heartburn strikes, the cause is too little acid, not too much. Acid reflux medicine actually makes heartburn worse.

               Rajjpuut wants to puke when he thinks about the FDA and its horrendous corruption, but he’s afraid someone might give him some FDA recommended medicine – oh no!

Live long, strong and ornery,

Rajjpuut  

**   the correct term is "bribe" but the FDA calls them "expedited evaluations" or "expedited reviews"

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA will allow any health care plan, now or in the future, any hope of success.

 

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Eliminate the FDA #2

 Consumers know far more about about free tap water  than expensive bottled water:  a $16 billion industry.

"FDA . . . Foul, Disgusting Agency" doesn't say the half of it. No more corrupt government entity has ever turned upon the citizens of this country.         

           Unlike ordinary free tap water which is monitored by the EPA, the Food and Drug Administration (FDA) monitors bottled water. As usual that's very bad news.

            Some popular brands of bottled water have had their bottles voluntarily recalled three times just since recalls have been monitored . . .  indeed, bottled water has been recalled on over one hundred separate occasions since monitoring began.  But have you personally ever been notified? Ever heard a news story about a recall?   Ever known anyone who turned back even one single bottle? Did you know that next to plastic shopping bags, bottled water containers are one of the very biggest environmental headaches of our time? Did you know that many popular brands are contaminated with phthalates, a chemical used to make plastic softer which unfortunately disrupts the human endocrine system. Did you realize that many bottled waters are less safe than free tap water?  That many of them basically are free tap water, and nothing more?   That despite their claims of health advantages, not one such advantage has ever been proved.

           Looking at one of the biggest issues more closely, phthalates besides being a disaster for the endocrine system in general is a holocaust for male fetuses.  Have you ever been heard that bottled water should NOT be drunk by pregnant or nursing mothers?   Well it shouldn't because malformed reproductive organs, undescended testes and low sperm counts later in life are all suspected results of ptthalates contamination at high levels. The bottles themselves do NOT contain the chemical phthalates, surprisingly enough. The contaminants are suspected of entry into the water during processing at bottling plants or perhaps were present in the original water source. Phthalates has even been  found on occasion contaminating some tap waters.

          The FDA refuses to give oversight to any water which is bottled and sold within a state, including those huge water-cooler jugs you see in every office . . . so 70% of all bottled water has NO FDA oversight. The FDA has less than one full-time person per state monitoring this sixteen billion dollar industry. Many bottling plants are not inspected even yearly.  The manufacturers are not required to let customers know about recalls, and they don't. Mold, crickets, coliform bacteria, microbes and, of course, super high levels of the contaminate phthalates mentioned earlier are all reasons for some of the hundred plus recalls since 1992.    So the FDA which has the resources to make raids on the office's of doctors suspected of prescribing GASP! vitamins, minerals and other nutrients; and also on health food stores . . . has no interest in looking at our bottled water. But, of course, it all makes sense in a perverted sort of FDA way . . . . Cheers, wait . . . make mine vodka!

Live long, strong and ornery,

Rajjpuut     

Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration). That once great organization created in 1906, the very year that Upton Sinclair’s monumental novel/expose` “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake, or better yet, elimination of the FDA will allow any health care plan, now or in the future, any hope of success. 

 

 

 

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Eliminate the FDA #1

No more corrupt government entity has ever turned upon the citizens of this country.               

The Food and Drug Administration, FDA, that once great organization created in 1906, the year that Upton Sinclair’s monumental novel/expose of the meat packing industry “The Jungle” hit the bookstore shelves, has degenerated into the most corrupt federal organization in America. Rajjpuut, health educator he, believes that only a complete top-to-bottom remake of the FDA or its total elimination will allow any health care plan, now or in the future, any hope of success.

A September, 2006 Spanish study puts second hand smoke in a crowded bar as “over 60 times more toxic than traffic fumes."

The state of California, which can be a little bit nuts Rajjpuut admits, backs up the Spaniards with its own conclusion that second-hand smoke (what's breathed out after first going directly into the lungs of a smoker) ranks in toxicity up there with the most toxic automotive or industrial air pollutants and says California parents “who would NOT willingly fill their homes with motor vehicle exhaust, for their children’s sake, should feel the same way about tobacco smoke.”

Strong words but unfortunately accurate words . . . but Rajjpuut is NOT here to turn the screws a notch tighter on the already beleaguered smokers . . . but rather to ask you to consider this about the FDA: what else besides tobacco products in the United States is allowed to be sold and consumed by mouth without a listing of its ingredients on the package? How did that cozy little arrangement come to be? I submit that it’s just one more long-standing sign of the corruption of the FDA: the typically 554 ingredients of a cigarette are never revealed because big tobacco doesn’t want to lose even one customer, especially a young developing smoker who might look at that god-awful list of chemicals and think, “Oh my heavens, this is what I’m doing to my body!” If the single most unhealthy product available for private consumption is not regulated appropriately, you start to get a handle on the full scope of this nightmare agency's ability to pervert its original great purpose and betray American’s health. Gotta love ‘em with all your heart.

Live long, strong and ornery,

Rajjpuut
 
Regular readers of Rajjpuut’s little rants will recognize a strong personal antipathy toward the FDA (Food and Drug Administration).  It's nothing personal, he feels the same way about the old Nazis, the KGB and  typhus.

 

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