Inside the FDA Mafia

by Jon Rappoport

I post this piece now and then to show how personal things can get inside a terminally corrupt government agency.

It’s not all about remote decisions made from a great height.

These decisions can come about through the rank intimidation the Mafia exercises with a member who wants to leave the mob and go straight.

As in: “We know where your wife and kids are.”

This article is based on a Truthout interview of a man who did drug reviews for the FDA. He examined applications to approve new medical drugs for public consumption.

Pharmaceutical companies must have their new drugs certified as safe and effective before they can enter the market, before doctors can prescribe them. The FDA does this certification. Thumbs up or thumbs down. The drug is okay or it isn’t.

Here’s the story:

In a stunning interview with Truthout’s Martha Rosenberg, former FDA drug reviewer, Ronald Kavanagh, exposes the FDA as a relentless criminal mafia protecting its client, Big Pharma, with a host of mob strategies.

Kavanagh: “…widespread racketeering, including witness tampering and witness retaliation.”

“I was threatened with prison.”

“One [FDA] manager threatened my children…I was afraid that I could be killed for talking to Congress and criminal investigators.”

Kavanagh reviewed new drug applications made to the FDA by pharmaceutical companies. He was one of the holdouts at the Agency who insisted that the drugs had to be safe and effective before being released to the public.

But honest appraisal wasn’t part of the FDA culture, and Kavanagh swam against the tide, until he realized his life and the life of his children were on the line.

What was his secret task at the FDA? “Drug reviewers were clearly told not to question drug companies and that our job was to approve drugs.” In other words, rubber stamp them. Say the drugs were safe and effective when they were not.

Kavanagh’s revelations are astonishing. He recalls a meeting where a drug-company representative flat-out stated that his company had paid the FDA for a new-drug approval. Paid for it. As in bribe.

He remarks that the drug pyridostigmine, given to US troops to prevent the later effects of nerve gas, “actually increased the lethality” of certain nerve agents.

Kavanagh recalls being given records of safety data on a drug—and then his bosses told him which sections not to read. Obviously, they knew the drug was dangerous and they knew exactly where, in the reports, that fact would be revealed.

We are not dealing with isolated incidents of cheating and lying. We are not dealing with a few isolated bought-off FDA employees. The situation at the FDA isn’t correctable with a few firings. This is an ongoing criminal enterprise, and any government official, serving in any capacity, who has become aware of it and has not taken action, is an accessory to mass poisoning of the population.

Fourteen years ago, the cat was let out of the bag. Dr. Barbara Starfield, writing in the Journal of the American Medical Association, on July 26, 2000, in a review titled, “Is US health really the best in the world,” exposed the fact that FDA-approved medical drugs kill 106,000 Americans per year.

In interviewing her, I discovered that she had never been approached by any federal agency to help remedy this tragedy. Nor had the federal government taken any steps on its own to stop the dying.

Ronald Kavanagh’s story, exposed in Truthout, never jumped the rails and made it into the mainstream press as the explosive revelation it was.

Too hot to handle. Too many bodies buried. Too many media outlets bought off by pharmaceutical advertising money. Too close to bought-off government officials. Too likely to shake the pillars of the medical cartel. Too real.

It was the kind of story that could actually wake people up from their mind-controlled slumber.

It still is.

Related:  Former FDA Reviewer Speaks Out About Intimidation, Retaliation and Marginalizing of Safety

Second-Largest Dutch City Bans Monsanto’s Roundup Herbicide

Natural Society
by Elizabeth Renter

Some cynics write off citizen action including petitions and sign-carrying protestors. They don’t believe such small efforts can make any big difference. But the more than 600,000 people of Dutch city Rotterdam disagree. Their efforts, which began with a petition, have led to a “green initiative” in their city including the banning of Roundup, Monsanto’s flagship product.

The petition campaign was called “Non-toxic Sidewalks for Our Children.” With support from that country’s Green Party, concerned citizens were able to make a significant change for their city and their future.

As we know, Roundup (glyphosate) is a dangerous pesticide that is used all over the world. Though its maker, Monsanto, would have you believe there’s nothing to be afraid of, research says differently. As a matter of fact, glyphosate has been connected to numerous health problems including respiratory distress, cellular damage, and even cancer.  Check out this article which outlines just 7 nasty effects of pesticides. 

 “It is bad stuff and I’m glad we’re giving it up,” says Emile Cammeraat, Green party leader in the council. “The producer Monsanto also provides genetically engineered seeds, Monsanto’s own plants are the only thing RoundUp doesn’t kill. In such a business district as you want to be, no Roundup is simply necessary, as there are organic alternatives.” (Translated by Fritz Kreiss)

 Global consumers are getting wise to the dangers of Roundup and the GMO seeds designed to resist it. They don’t want Monsanto and other GMO-seed giants taking over the global food supply and have started grassroots resistance movements around the world. The problem lies in getting enough people to take actual action against the seed giants and local, state, and federal lawmakers who support them in one way or another.

Collectively, the people of Rotterdam were able to make their voices heard, essentially eliminating glyphosate from their local environment. There’s no reason similar cities in other areas of the world couldn’t do the very same thing.

Comically, the U.S. government has recently decided to increase the allowable amount of glyphosate in U.S. food crops, just as another place bans the substance. The new rule allowing for even greater use of this damaging ingredient would take existing limits on glyphosate and dwarf them with new, higher ones. These limits would truly only work to benefit the interests of one, and it’s not the American people, but Monsanto – the giant corporation who is making millions off of genetically modified crops and the destruction of agriculture and human health.

In addition to the Roundup ban, Rotterdam’s green initiative will provide new parks and play areas, and even get the city involved in planting fruit trees. There will be more flowers and environments to support bees and wildlife, and more places for the urbanites to take in nature without fear of contamination by Monsanto’s evil poster child.

The Chemical Castration of our Children’s Brains

Common Sense Show
by Dave Hodges

Government should not be in the business of mandating personal choices and government should never be allowed to legislate choices which should be reserved for parents with regard to their children’s health and welfare. The parents are sovereign over the welfare of their children, not the state.

In the name of increasing the corporate bottom line, the government watchdog industries of the DEA and FDA, as well as the office of the President, have become the willing lap dogs for Big Pharma and this unholy alliance is serving to endanger our children.

Big Pharma has gone to great lengths to increase sales to the youth of America either through chemically castrating our children’s brains or by producing drugs with very serious side effects which serve to seriously degrade both the brain and the body. Our children are being systematically destroyed by the pharmaceutical industry.

The Ritalin Conspiracy

Let’s make up a brain disorder, which parallels normal restlessness of children and then transform a dangerous drug, methamphetamine, and get as many kids on the drug as possible. It is good work if you can find it and pharmaceutical companies like Merck and Eli Lilly are leading the way in medical fraud and in the name of record corporate profits

The use of Ritalin has become so rampant, that even the DEA has become alarmed by the tremendous increase in the prescribing of these drugs in recent years. Since 1990, prescriptions for methylphenidate have increased by 500%, while prescriptions for amphetamine for the same purpose have increased 400%. The American Pediatric Association claims Ritalin is over prescribed by 600%.

For well over a decade, many scientists have speculated that ADD drugs are dangerous and can cause serious injury and death. Etta Brown, a licensed educational psychologist and author of Learning Disabilities: Understanding the Problem and Managing the Challenges explained in response to her study that drugs like Ritalin actually destroy the neural function in children’s brains. As a result, children who have undergone treatment with Ritalin will actually have a much more difficult time processing information and learning new things. This kind of defeats the purpose of getting children to sit still in school while placed in a zombified state.

Brown further reported that Ritalin is responsible for the development of a permanent tic in the face, neck, and head of many of the children who have taken or are taking it. Ironically, Ritalin is responsible for causing far more serious neurological damage than the problems it is alleged to treat. Meta analyses studies over the years have revealed that while drugs like Ritalin visibly place children into a trance like state, these drugs destroy the vulnerable, delicate and developing nervous systems which can and does permanently cripple their ability to function as normal human beings.

The Gardasil Conspiracy

Last year a bill sponsored by Toni G. Atkins, D-San Diego passed into California state law which places every child in danger in California. Atkins bill begs the question of who has the ultimate authority of the welfare of our children. Is it the state or is it the parents? Well, if you live in California, the nanny state purports to have the final say. The Atkins bill makes it legal for a school district or a doctor to medicate or inoculate a child without parental notification.

In an era when Gardasil has resulted in needless tragedy for over 40,000 children who have been vaccinated by well intentioned doctors who are ignorant of the side effects, we are now witnessing states like California mandating the forced inoculation of young girls with Gardasil.

What the medical establishment is not telling you is that thousands of girls are having adverse reactions to the HPV Vaccines, some have even died -at last count, at least 103 lives have been lost to Gardasil. This is a brilliant strategy being invoked by California. Let’s kill the girls, thus preventing them from having sex, thus, preventing STD’s.

You remember MERCK don’t you? They were the creator of the wonder death drug, Vioxx. This is the same Merck, who only after intense pressure from the medical community and the media decided to pull the dangerous drug, Vioxx, from the market after an estimated 140,000 adverse reactions had already occurred. And the pulling of Vioxx occurred only after a safety trial was stopped because there was an undeniable and increased risk for serious cardiovascular dangers such as heart attacks and strokes from using the drug.

Merck has been no less reckless in their administration of Gardasil as they were with Vioxx. First and foremost, Merck and the Food and Drug Administration’s clinical trials have been called into question for blatant fraud committed during the required FDA testing period. Both the control group and the experimental group, in the clinical trials, were given the aluminum adjuvant contained in the Gardasil. Control group and experimental group comparisons are done to ensure public safety from adverse side effects as much as possible. In this case, it would have be standard practice to provide the control group with a saline solution instead of the aluminum adjuvant in order to determine the risk posed by the adjuvant given to the experimental group. In failing to follow these research norms, Merck and the FDA have endangered the public health.

These research protocols violate every known tenant to proper research; it represents an air of unprofessionalism, not to mention criminal fraud, which clearly demonstrates collusion to commit fraud against the general public on behalf of Merck as sponsored by the FDA. In fact, Judicial Watch was forced to file a lawsuit under the Public Records Act in order to obtain the obfuscated side effect results as the FDA tried to cover up their own complicity in this research fraud by refusing to release the relevant documents.

Gardasil is marketed as a vaccine that prevents cancer, but the drug has not been evaluated for the potential to cause cancer or genotoxicity. Gardasil is a prophylactic, preventative vaccine and is of absolutely no value in the treatment of a pre-existing HPV infection. It is neither a cancer vaccine nor a cure; yet, the public has been led to believe that this is the case. The New England Journal of Medicine found that there remains no conclusive proof that Gardasil altered the course of HPV-16 or HPV-18 infection for which the patient was symptomatic prior to the administration of the first dose. In other words, this is fraud in the first degree.

Gardasil is the most costly vaccine ever to be approved by the FDA. However, its long-term effectiveness is not known and several estimates state that Gardasil’s life as a vaccine could be only two to three years. This opens up the distinct possibility that a Gardasil vaccinated child will require several booster shots which will undoubtedly increase the bottom line for Merck, but the risk for side-effects among the vaccinated could increase exponentially with each successive vaccination.

The VAERS reports show that as many as eighteen people have died after receiving Gardasil. The VAERS reports document identifies 38 reports of Guillain-Barre Syndrome among juvenile females who previously received the Gardasil vaccine. Guillain-Barre Syndrome is a catastrophic illness that attacks the nervous system which can and often does result in paralysis. Ironically, Gardasil is being developed against only four types of HPV. However, there is over 100 strains of HPV, 30 of which are transmitted sexually. Just what could have Governor Brown and Atkins been thinking?

Do you not think that this is the first time that this kind of dangerous medical fraud has been and will be visited upon your children for profit and political career advancement? Think again! The American Academy of Pediatrics recommends that boys of the age of 11 to 12 years should be vaccinated with the vaccine against HPV with the Gardasil vaccination.

Even my doctors are serving the Big Pharma agenda, as evidenced by the fact that my son’s former pediatrician relentlessly tried to give my then 11 year old son the Gardasil injection. When I presented the good doctor with some of the data contained in this report, he replied “your ideas are not contained within the mainstream of medicine.” Since when is scientific research required to reflect the mainstream of the Big Pharma agenda? The moral of this story is to fire your doctor and find a health care provider who is committed to the welfare of their patients.

FDA Expands Irradiation of Food Supply, Harmonizing with Codex Alimentarius

Activist Post
by Brandon Turbeville

Demonstrating the lack of concern held by regulatory agencies for public safety or public opinion as well as the increasing attempts to become compliant with Codex Alimentarius regulations, the FDA has recently expanded the amount of ionized radiation that can be used to treat unrefrigerated raw meat.

As reported by Food Safety News, the two new policies decided upon by the FDA were issued in response to two petitions filed in 1999 by the Food Safety and Inspection Service of the U.S. Department of Agriculture.

While the previous policy was that only refrigerated or frozen meats could be irradiated, the new rule allows for the irradiation of unrefrigerated raw meat. The second rule change allows for increasing the dose of ionizing radiation in poultry from 3.0 kGY to 4.5 kGy.

Although a period for public comment is always set aside for regulatory agency decisions regarding potential changes to policy, the FDA promptly ignored the many comments it received from individuals all over the country as well as consumer advocacy groups which requested the denial of the two FSIS petitions.

The response from the FDA was that all of these comments, made by individuals and by groups such as Public Citizen and the Center for Food Safety, “were of a general nature” and “did not contain any substantive information that could be used in a safety evaluation of irradiated poultry.” This statement was made regarding both the poultry irradiation rule and the passage of a new meat temperature rule.

Predictably, the FDA has defended its decision by circular logic that flies in the face of science and common sense. The agency is claiming that “irradiating unrefrigerated meat was not found to increase meat’s toxicity, change the food’s nutritional properties or increase the likelihood of certain bacteria thriving on meat; therefore FDA has determined that this is a safe application for the process.”

Of course, while the FDA claims that irradiation is not found to increase toxicity or change nutritional properties, the very reason that the FDA has jurisdiction over food irradiation to begin with is because the process of irradiation can do just these very things. Even the FDA admits that, because irradiation “can affect the characteristics of the food,” it is considered a “food additive.” Thus, because food additives fall under the purview of the FDA, irradiation is regulated (or not) by the agency.

By allowing for higher doses of irradiation in food, the FDA is knowingly complicit in covering up unsanitary food production practices by major corporations as well as accepting the inclusion of clearly harmful material (i.e. radiation) into the food supply. Keep in mind, irradiation is mostly used by corporations in order to cover up deplorable manufacturing conditions and dangerous food contamination.

However, much like the FDA’s position on genetically modified food, even the concept of consumer choice is nothing more than a smokescreen.

For instance, while the FDA states that all irradiated foods entering the supply chain must be accompanied by a radura symbol indicating the irradiation process, the fact is that this symbol is only required to be presented to the “first consumer,” not the average person actually buying and eating the food. More often than not, the “first consumer” is actually the high-level distributor of the food. Needless to say, the radura symbol is removed in short order before the goods are shipped to the market and long before they reach the people who purchase them directly.

Indeed, the FDA has made moves to derail consumer knowledge even further with relatively recent attempts to re-label irradiated food as “pasteurized” so as to obscure the real nature of the “treatment” process. In fact, the proposal even states that an “alternate term to ‘irradiation’” may be considered for use with no further suggestion as to what this term may be.

Therefore, one legitimately wonders whether or not, if the proposal should go through, the selected terminology will be even more obfuscating than that of “pasteurization.”

Lastly, it is important to note that the FDA has been making clear strides toward harmonization with Codex Alimentarius guidelines for at least the last ten years. As I discuss in my book Codex Alimentarius – The End of Health Freedom, Codex Alimentarius itself has set the acceptable limit of food irradiation at 10 kGy with loopholes that actually allow for unlimited levels of irradiation.

Indeed, the FDA has also pushed for Codex harmonization with vitamin and mineral supplements, as well as genetically modified foods.

With this in mind, it would be well within reason to expect to see the acceptable levels of food irradiation raised even higher in the very near future.

225,000 American patients die in doctors’ hands: silence of the lambs

Jon Rappoport’s Blog
No More Fake News
by Jon Rappoport

In my previous article, I examined the silence of the lambs (media) concerning the collusion between Monsanto and the FDA.

In the case of medical care in America, that purposeful silence reigns supreme as well.

By the most conservative estimate, researched and published by mainstream medical sources, the US medical system kills 225,000 people each year.

That’s 2.25 MILLION deaths per decade.

You’d think such a mind-boggling fact would rate a relentless series of page-one stories in the press, along with top-story status on the network evening news.

But no. It’s wall-to-wall silence.

Why? We can list the usual reasons, the medical/pharmaceutical advertising dollars spent on television and in newspapers being the most obvious reason.

We have the reality that, of those 225,000 annual deaths, 106,000 occur as a direct effect of pharmaceutical drugs. The FDA is the single government agency tasked with certifying all medicines as safe and effective before they’re released for public use. Any exposure of the medical death statistics would automatically indict the FDA. Major media won’t take on the FDA at that level.

One of the many truths which would come to light in the event that the press did attack the FDA full-on? The FDA spends an inordinate amount of time, energy, and money going after the nutritional supplement industry, which causes virtually no deaths in any year or decade.

The public would of course discover that, by certifying medical drugs as safe and effective, drugs that kill, like clockwork, 106,000 people a year, the FDA is colluding with, and serving, Big Pharma.

You can’t possibly approve so many drugs that wreak so much human destruction through mere incompetence. Apologists for the FDA might like to think so, but they are terribly, terribly wrong. They are whistling in the dark, trusting “science” as our guide.

Since I’ve been reporting these medically-caused death figures—I started 12 years ago—people have told me, “This is impossible. If it were true, the media would be reporting it.”

That argument is upside down. The statistics are real and true. In fact, they are very low estimates. Therefore, the press is colluding to keep them well under the radar.

The mainstream press is built to be able to maintain silence on issues such as this. It’s part of their job. Although many reporters and editors are simply ignorant and clueless, at the highest levels of media we are looking at sheer manipulation. We are looking at the crime of accessory to murder.

I don’t say murder in any non-literal way. It’s murder because, when you know the facts, when you know what a huge government institution (FDA) is doing to the population, and when that institution itself is well aware of its lethal impact on the public and does nothing about it, year after year, decade after decade, it’s FDA murder and it’s media’s accessory to murder.

It’s not merely negligent homicide. There is no negligence here, any more than there would be if you took a loaded gun out into the street and started firing randomly at crowds of people.

Underneath it all, the press maintains silence because they are not permitted to hammer a huge fracture in what is called “the public trust.”

And what is the public trust? It’s the false illusion that basically things are all right. That’s the simplest way to say it. Things are all right.

They’re especially all right when it comes to the medical profession. Doctors are modern priests in white coats.

But the priests are the ones who are prescribing the drugs that are killing people. If the extent of their crimes were made known, trust would evaporate in seconds. And not just trust in the medical profession. Trust, or the lack of it, is contagious. It spreads to other areas quickly.

“Well, if they’re lying abut this, and killing people, then who else is lying and killing?”

“We know that people die in wars. But the doctors are supposed to be saving lives. They’re not supposed to be giving people drugs that kill them at the rate of 106,000 a year, every year.”

The press and the people who own media companies are aware they are guardians of the public trust. However, that has nothing to do with telling the truth. The press is guarding the illusion of truth. That’s how they interpret their mandate.

Nowhere is this perversion more clear than in the medical arena.

As I do every so often, I’m presenting my interview with the late Dr. Barbara Starfield, who for many years was a revered public health authority at the Johns Hopkins School of Public Health. She was the researcher who exposed the truth about medically caused death in America.

Her review, “Is US Health really the best in the world?”, was published in the Journal of the American Medical Association on July 26, 2000.

It presented three key facts. Every year, the US medical system kills 225,000 people. 106,000 die from the direct effects of FDA-approved medical drugs. 119,000 die from the effects of treatment in hospitals.

Soon after her review was published, it gained some media attention. Not headline attention, but the press carried the story. Then, like a report of a car crash or a storm, Starfield’s revelation disappeared, vanished without a trace.

In other articles, I’ve made it clear that Starfield’s journal paper is confirmed by other sources. In fact, on a page of the FDA’s own web site, it is admitted that 100,000 people die every year in America from the effects of pharmaceutical drugs. However, as in the case of every psychotic criminal, the FDA takes no responsibility.

Here are excerpts from my interview with Dr. Barbara Starfield:

What has been the level and tenor of the response to your findings, since 2000?

The American public appears to have been hoodwinked into believing that more interventions lead to better health, and most people that I meet are completely unaware that the US does not have the ‘best health in the world’.

In the medical research community, have your medically-caused mortality statistics been debated, or have these figures been accepted, albeit with some degree of shame?

The findings have been accepted by those who study them. There has been only one detractor, a former medical school dean, who has received a lot of attention for claiming that the US health system is the best there is and we need more of it. He has a vested interest in medical schools and teaching hospitals (they are his constituency).

Have health agencies of the federal government consulted with you on ways to mitigate the [devastating] effects of the US medical system?

NO.

Since the FDA approves every medical drug given to the American people, and certifies it as safe and effective, how can that agency remain calm about the fact that these medicines are causing 106,000 deaths per year?

Even though there will always be adverse events that cannot be anticipated, the fact is that more and more unsafe drugs are being approved for use. Many people attribute that to the fact that the pharmaceutical industry is (for the past ten years or so) required to pay the FDA for reviews [of its new drugs]—which puts the FDA into an untenable position of working for the industry it is regulating. There is a large literature on this.

Aren’t your 2000 findings a severe indictment of the FDA and its standard practices?

They are an indictment of the US health care industry: insurance companies, specialty and disease-oriented medical academia, the pharmaceutical and device manufacturing industries, all of which contribute heavily to re-election campaigns of members of Congress. The problem is that we do not have a government that is free of influence of vested interests. Alas, [it] is a general problem of our society—which clearly unbalances democracy.

Can you offer an opinion about how the FDA can be so mortally wrong about so many drugs?

Yes, it cannot divest itself from vested interests. (Again, [there is] a large literature about this, mostly unrecognized by the people because the industry-supported media give it no attention.)

Would it be correct to say that, when your JAMA study was published in 2000, it caused a momentary stir and was thereafter ignored by the medical community and by pharmaceutical companies?

Are you sure it was a momentary stir? I still get at least one email a day asking for a reprint—ten years later! The problem is that its message is obscured by those that do not want any change in the US health care system.

Are you aware of any systematic efforts, since your 2000 JAMA study was published, to remedy the main categories of medically caused deaths in the US?

No systematic efforts; however, there have been a lot of studies. Most of them indicate higher rates [of death] than I calculated.

What was your personal reaction when you reached the conclusion that the US medical system was the third leading cause of death in the US?

I had previously done studies on international comparisons and knew that there were serious deficits in the US health care system, most notably in lack of universal coverage and a very poor primary care infrastructure. So I wasn’t surprised.

Did your 2000 JAMA study sail through peer review, or was there some opposition to publishing it?

INTERVIEWER COMMENTS:

This interview with Dr. Starfield reveals that, even when an author has unassailable credentials within the medical-research establishment, the findings can result in no changes made to the system.

Many persons and organizations within the medical system contribute to the annual death totals of patients, and media silence and public ignorance are certainly major factors, but the FDA is the assigned gatekeeper, when it comes to the safety of medical drugs.

The buck stops there. If those drugs the FDA is certifying as safe are killing, like clockwork, 106,000 people a year, the Agency must be held accountable. The American people must understand that.

As for the other 119,000 people killed every year as a result of hospital treatment, this horror has to be laid at the doors of those institutions. Further, to the degree that hospitals are regulated and financed by state and federal governments, the relevant health agencies assume culpability.

It is astounding, as well, that the US Department of Justice has failed to weigh in on Starfield’s findings. If 225,000 medically caused deaths per year is not a crime by the Dept. of Justice’s standards, then what is?

To my knowledge, not one person in America has been fired from a job or even censured as result of these medically caused deaths.

Dr. Starfield’s findings have been available for 12 years. She has changed the perception of the medical landscape forever. In a half-sane nation, she would be accorded a degree of recognition that would, by comparison, make the considerable list of her awards pale. And significant and swift action would have been taken to punish the perpetrators of these crimes and reform the system from its foundations.

The pharmaceutical giants stand back and carve up the populace into “promising markets.” They seek new disease labels and new profits from more and more toxic drugs. They do whatever they can—legally or illegally—to influence doctors in their prescribing habits. Many studies which show the drugs are dangerous are buried. FDA panels are filled with doctors who have drug-company ties. Legislators are incessantly lobbied and supported with Pharma campaign monies.

Nutrition, the cornerstone of good health, is ignored or devalued by most physicians. Meanwhile, the FDA continues to attack nutritional supplements, even though the overall safety record of these nutrients is excellent, whereas, once again, the medical drugs the FDA certifies as safe are killing 106,000 Americans per year.

Physicians are trained to pay exclusive homage to peer-reviewed published drug studies. These doctors unfailingly ignore the fact that, if medical drugs are killing a million Americans per decade, the studies on which those drugs are based must be fraudulent. In other words, the whole literature is suspect, unreliable, and impenetrable.

It was rejected by the first journal that I sent it to, on the grounds that ‘it would not be interesting to readers’!

Do the 106,000 deaths from medical drugs only involve drugs prescribed to patients in hospitals, or does this statistic also cover people prescribed drugs who are not in-patients in hospitals?

I tried to include everything in my estimates. Since the commentary was written, many more dangerous drugs have been added to the marketplace.

.

Propecia Causes Permanent Impotence in Some Men: Merck and FDA Knew About It

America First

Big Pharma, Merck in this case, is well aware of the problems some of their “wonder drugs” cause. It’s disturbing how our government approves drugs that regularly ruin the lives of a small minority of those prescribed, yet has declared an all out war on natural products like marijuana and raw milk.

This story also shows how vain Americans have become. What’s more important, a full head of hair, or your sexual function, ambition, and overall happiness?

Kevin Malley was almost 30, and he was starting to lose his hair. He went to his doctor to see if there was a way to keep from going bald, and his doctor prescribed Propecia.

“I looked young for my age, so I wanted to hold off my hair loss for a little bit,” Malley said. “I didn’t plan on taking Propecia for more than a year.”


Malley started taking the drug in May 2011, and by October he was completely impotent and had no sex drive whatsoever. His body changed, even his genitals shrank, and he slipped into a mental fog that he just couldn’t clear. His doctor told him the side effects would go away if he stopped taking the drug, so he did. But nothing changed.


“I kept expecting the side effects to go away, but they did not, they only got worse,” he said.


For 96 percent of the men, the sexual problems lasted for more than a year after they stopped taking the drug.


“Our findings make me suspicious that this drug may have done permanent damage to these men,” said Dr. Michael Irwig, the author of the study. “The chances that they will improve? I think it’s lower and lower the longer they have these side effects.”
http://news.yahoo.com/video#video=29966302

Later in the story we learn that the FDA and Merck knew that some men would face long-term impotence by taking Propecia:

FDA, Merck Know of Drug’s Side Effects


Finasteride works by blocking the conversion of testosterone into a more potent form, called DHT, which contributes to hair loss. It was originally developed in 1992 by drug giant Merck as a treatment for enlarged prostates and sold as the drug Proscar.


Propecia was approved by the U.S. Food and Drug Administration in 1997, and at that time Merck noted that a few men reported sexual side effects during clinical trials of the drug. On its website, the agency said those side effects were resolved when patients stopped taking the drug.
http://gma.yahoo.com/men-propecias-sexual-side-effects-may-long-lasting-215732153–abc-news-wellness.html

The moral of the story? Don’t trust big companies and the FDA with your health. Only take drugs and supplements that are absolutely necessary. Find natural relief and cures when possible.