"All the World's a Stage We Pass Through" R. Ayana

Sunday 22 July 2012

Big Pharma criminality no longer a conspiracy theory

Big Pharma criminality no longer a conspiracy theory
Bribery, fraud, price fixing now a matter of public record


by Mike Adams
http://www.naturalnews.com/gallery/dir/Medical/Doctor-Money-Bribe-Pocket.jpgThose of us who have long been describing the pharmaceutical industry as a "criminal racket" have been wholly vindicated by recent news. Drug and vaccine manufacturer Merck was caught red-handed by two of its own scientists faking vaccine efficacy data by spiking blood samples with animal antibodies. GlaxoSmithKline has just been fined a whopping $3 billion for bribing doctors, lying to the FDA, hiding clinical trial data and fraudulent marketing. Pfizer, meanwhile has been sued by the nation's pharmacy retailers for what is alleged as an "overarching anticompetitive scheme" to keep generic cholesterol drugs off the market and thereby boost its own profits.

The picture that's emerging is one of a criminal drug industry that has turned to mafia tactics in the absence of any real science that would prove their products to be safe or effective. The emergence of this extraordinary evidence of bribery, scientific fraud, lying to regulators and monopolistic practices that harm consumers is also making all those doctors and "skeptics" who defended Big Pharma and vaccines eat their words.

To defend Big Pharma today is to defend a cabal of criminal corporations that have proven they will do anything -- absolutely anything -- to keep their profits rolling in. It makes no difference who they have to bribe, what studies they have to falsify, or who has to be threatened into silence. They will stop at nothing to expand their profit base, even if it means harming (or killing) countless innocents.

Let's take a look at recent revelations:

http://www.conspiracyplanet.com/images/drugs.jpg

 

GlaxoSmithKline pleads guilty to bribery, fraud and other crimes

 

It what is now the largest criminal fraud settlement ever to come out of the pharmaceutical industry, GlaxoSmithKline has pleaded guilty and agreed to pay $1 billion in criminal fines and $2 billion in civil fines following a nine-year federal investigation into its activities.

According to U.S. federal investigators, GlaxoSmithKline (http://www.naturalnews.com/036416_GlaxoSmithKline_fraud_criminal_char...):

• Routinely bribed doctors with luxury vacations and paid speaking gigs
• Fabricated drug safety data and lied to the FDA
• Defrauded Medicare and Medicaid out of billions
• Deceived regulators about the effectiveness of its drugs
• Relied on its deceptive practices to earn billions of dollars selling potentially dangerous drugs to unsuspecting consumers and medical patients

And this is just the part they got caught doing. GSK doesn't even deny any of this. The company simply paid the $3 billion fine, apologized to its customers, and continued conducting business as usual.

By the way, in addition to bribing physicians, GSK has plenty of money to spread around bribing celebrities and others who pimps its products. The company reportedly paid $275,000 to the celebrity doctor known as "Dr. Drew," who promoted Glaxo's mind-altering antidepressant drug Wellbutrin (http://naturalsociety.com/top-radio-doctor-paid-by-glaxosmithkline-to...).

As the Wall Street Journal reports:

In June 1999, popular radio personality Dr. Drew Pinsky used the airwaves to extol the virtues of GlaxoSmithKline PLC's antidepressant Wellbutrin, telling listeners he prescribes it and other medications to depressed patients because it "may enhance or at least not suppress sexual arousal" as much as other antidepressants do. But one thing listeners didn't know was that, two months before the program aired, Dr. Pinsky -- who gained fame as "Dr. Drew" during years co-hosting a popular radio sex-advice show "Loveline" -- received the second of two payments from Glaxo totaling $275,000 for "services for Wellbutrin."
(http://online.wsj.com/article/SB1000142405270230393340457750503200685...)

Merck falsified vaccine data, spiked blood samples and more, say former employees

 

According to former Merck virologists Stephen Krahling and Joan Wlochowski, the company: (http://www.naturalnews.com/036328_Merck_mumps_vaccine_False_Claims_Ac...)

• "Falsified test data to fabricate a vaccine efficacy rate of 95 percent or higher."

• Spiked the blood test with animal antibodies in order to artificially inflate the appearance of immune system antibodies.

• Pressured the two virologists to "participate in the fraud and subsequent cover-up."

• Used the falsified trial results to swindle the U.S. government out of "hundreds of millions of dollars for a vaccine that does not provide adequate immunization."

• Intimidated the scientists, threatening them with going to jail unless they stayed silent.

This is all documented in a 2010 False Claims Act which NaturalNews has acquired and posted here:
http://www.naturalnews.com/gallery/documents/Merck-False-Claims-Act.p...

Millions of children put at risk by Merck

 

In that document the two virologists say they, "witnessed firsthand the improper testing and data falsification in which Merck engaged to artificially inflate the vaccine's efficacy findings."

They also claim that because of the faked vaccine results, "the United States has over the last decade paid Merck hundreds of millions of dollars for a vaccine that does not provide adequate immunization... The United States is by far the largest financial victim of Merck's fraud."

They go on to point out that children are the real victims, however:

"But the ultimate victims here are the millions of children who every year are being injected with a mumps vaccine that is not providing them with an adequate level of protection. ...The failure in Merck's vaccine has allowed this disease to linger with significant outbreaks continuing to occur."

Merck's mumps viral strain is 45 years old!

 

According to the complaint, Merck has been using the same mumps strain -- weakened from generations of being "passaged" -- for the last 45 years! The complaint reads:

"For more than thirty years, Merck has had an exclusive license from the FDA to manufacture and sell a mumps vaccine in the U.S. The FDA first approved the vaccine in 1967. It was developed by Dr. Maurice Hilleman, at Merck's West Point research facility, from the mumps virus that infected his five year-old daughter Jeryl Lynn. Merck continues to use this 'Jeryl Lynn' strain of the virus for its vaccine today."

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A complete medical farce

 

This information appears to show Merck's mumps vaccine to be a complete medical farce. Those who blindly backed Merck's vaccines -- the science bloggers, "skeptics," doctors, CDC and even the FDA -- have been shown to be utter fools who have now destroyed their reputations by siding with an industry now known to be dominated by scientific fraud and unbounded criminality.

That's the really hilarious part in all this: After decades of doctors, scientists and government authorities blindly and brainlessly repeating the mantra of "95% effectiveness," it all turns out to be total quackery hogwash. Utterly fabricated. Quackety-quack quack. And all those hundreds of millions of Americans who lined up to be injected with MMR vaccines were all repeatedly and utterly conned into potentially harming themselves while receiving no medical benefit.

Intelligent, informed NaturalNews readers, home school parents, and "awakened" people who said "No!" to vaccines are now emerging as the victors in all this. By refusing to be injected with Merck's vaccines, they avoided being assaulted with a fraudulent cocktail of adjuvant chemicals and all-but-useless mumps strains over four decades old. They protected their time, money and health. Those who refuse to be physically violated by vaccines are, once again, turning out to be the smartest people in society. No wonder they also tend to be healthier than the clueless fools who line up to get vaccinated every year.

Merck fraudulently misrepresented the efficacy of its vaccine and contributed to the spread of infectious disease, says lawsuit

 

The faked vaccine efficacy numbers aren't the only troubles Merck is now facing. Shortly after the above False Claims Act was made public, Chatom Primary Care filed suit against Merck. That document is available from NaturalNews at:
http://www.naturalnews.com/gallery/documents/Chatom-Lawsuit-Merck-Mum...

It alleges that:

• [Merck engaged in] ...a decade-long scheme to falsify and misrepresent the true efficacy of its vaccine.

• Merck fraudulently represented and continues to falsely represent in its labeling and elsewhere that its Mumps Vaccine has an efficacy rate of 95 percent of higher.

• Merck knows and has taken affirmative steps to conceal -- by using improper testing techniques and falsifying test data -- that its Mumps Vaccine is, and has been since at least 1999, far less than 95 percent effective.

• Merck designed a testing methodology that evaluated its vaccine against a less virulent strain of the mumps virus. After the results failed to yield Merck's desired efficacy, Merck abandoned the methodology and concealed the study's findings.

• Merck also engaged in "incorporating the use of animal antibodies to artificially inflate the results... destroying evidence of the falsified data and then lying to an FDA investigator... threatened a virologist in Merck's vaccine division with jail if he reported the fraud to the FDA."

• "Merck designed a testing methodology that evaluated its vaccine against a less virulent strain of the mumps virus. After the results failed to yield Merck's desired efficacy, Merck abandoned the methodology and concealed the study's findings. [Then] Merck designed even more scientifically flawed methodology, this time incorporating the use of animal antibodies to artificially inflate the results, but it too failed to achieve Merck's fabricated efficacy rate. Confronted with two failed methodologies, Merck then falsified the test data to guarantee the results it desired. Having achieved the desired, albeit falsified, efficacy threshold, Merck submitted these fraudulent results to the FDA and European Medicines Agency."

• "Merck took steps to cover up the tracks of its fraudulent testing by destroying evidence of the falsified data and then lying to an FDA investigator... Merck also attempted to buy the silence and cooperation of its staff by offering them financial incentives to follow the direction of Merck personnel overseeing the fraudulent testing process. Merck also threatened... Stephen Krahling, a virologist in Merck's vaccine division from 1999 to 2001, with jail if he reported fraud to the FDA."

• "Merck continued to conceal what it knew about the diminished efficacy of its Mumps Vaccine even after significant mumps outbreaks in 2006 and 2009."

Obama administration has zero interest in actual justice

 

Another interesting note in all this is that under President Obama, the U.S. Dept. of Justice showed no interest whatsoever in investigating Merck over the False Claims Act filed by two of its former virologists. Despite the convincing evidence of fraud described in detail by insider whistleblowers, the Obama Department of Justice, led by gun-running Attorney General Eric Holder who is already facing serious questions over Operation Fast and Furious, simply chose to ignore the False Claims Act complaint.

When evidence of criminal fraud was brought before the U.S. Department of Justice, in other words, the DoJ looked the other way with a wink and a nod to the medical crimes taking place right under their noses. Who cares if tens of millions of children are being injected year after year with a fraudulent mumps vaccine? There's money to be made, after all, and exploiting the bodies of little children for profit is just business as usual in a fascist nation dominated by corporate interests.

Pfizer sued by retailers over anticompetitive scheme

 

Adding to all this, Pfizer has now been sued by five U.S. retailers (pharmacies) who accuse the company of monopolistic market practices. According to the lawsuit, Pfizer conspired to prevent generic versions of its blockbuster cholesterol drug Lipitor from entering the market. This was done to protect billions in profits while making sure patients did not have access to more affordable cholesterol drugs. Pfizer sells nearly $10 billion worth of Lipitor each year.

According to the Reuters report on this lawsuit, Pfizer is being accused of (http://www.reuters.com/article/2012/07/05/us-pfizer-walgreen-lipitor-...):

• Obtaining a fraudulent patent
• Engaging in sham litigation
• Entering a price-fixing agreement to delay cheaper generics
• Entering arrangements with pharmacy benefit managers to force retailers to buy more Lipitor (chemical name is atorvastatin calcium)

No arrests or prosecution of Big Pharma executives

 

One of the most astonishing realizations in all this is that given all the criminal fraud, bribery, misrepresentation, lying to the FDA, price fixing and other crimes that are going on in the pharmaceutical industry, you'd think somebody somewhere might be arrested and charged with a crime, right?

Nope.

To date, not a single pharmaceutical CEO, marketing employee or drug rep has been charged with anything related to all this fraud. In America, drug company employees are "above the law" just like top mafia bosses of a bygone era.

How insane is this, exactly? Consider this:

Imagine if YOU, an individual, went around town bribing doctors, falsifying data, selling a fraudulent product to the government, lying to regulators, engaging in anti-trade price-fixing and threatening your employees into silence. What would happen to you?

You'd probably wind up rotting in prison, the subject of an FBI investigation and a DoJ prosecution.

So why is it okay for a multi-billion-dollar corporation to carry out these same crimes and get away with it? Why are the CEOs of top drug companies given a free pass to commit felony crimes and endless fraud?

I'll tell you why, and you're not gonna like the answer: Because America has become a nation run by crooks for the benefit of crooks. It's one big country club, and as comedian George Carlin used to say, "YOU ain't in it!"

If Big Pharma would falsify data on vaccines, what else would the industry do?

 

I hope you're getting the bigger picture in all this, friends. If these drug companies routinely bribe doctors, falsify data, defraud the government and commit felony crimes without remorse, what else would they be willing to do for profit?

Would they:

• Falsify efficacy data on other prescription drugs?
• Exploit children for deadly vaccine trials?
• Invent fictitious diseases to sell more drugs?
• Unleash bioweapons to cause a profitable pandemic?
• Conspire with the CDC to spread fear to promote vaccinations?
• Silence whistleblowers who try to go public with the truth?
• Give people cancer via stealth viruses in vaccines?
• Destroy the careers of medical scientists who question Big Pharma?
• Force a medical monopoly on the entire U.S. population via socialist health care legislation?

But of course they would. In fact, the industry is doing all those things right now. And if you don't believe me, just remember that five years ago, no one believed me when I said drug companies were engaged in criminal conspiracies to defraud the nation -- something that has now been proven over a nine-year investigation.



Drug giant probed for not disclosing 15,000 patient death reports

Roche under investigation by UK watchdogs after 80,000 'adverse reactions'



One of the world’s biggest drug companies is at the centre of an urgent investigation after failing to disclose reports that 15,000 people died while taking its medicines.

Swiss pharmaceutical giant Roche failed to pass on a further 65,000 reports of suspected side effects that were recorded by patients.

All of the reactions took place in the United States over the past 15 years with medicines used to treat breast cancer, bowel cancer, hepatitis B, and skin and eye conditions.

Roche, one of the world's biggest drug companies, is at the centre of an urgent investigation after failing to report that people died while taking their medication


Roche, one of the world's biggest drug companies, is at the centre of an urgent investigation after failing to report that people died while taking their medication

There is no evidence so far of  any direct link between the problems and the drugs – but medicines watchdogs say they are taking Roche’s failure to disclose possible concerns ‘extremely seriously’.

The drugs involved include Herceptin, given to about 10,000 breast cancer patients in Britain, and Lucentis, which is used to treat about 20,000 UK patients a year with age-related vision loss. The NHS pays Roche millions of pounds for these treatments every year.

The extent of the failings were discovered when the UK medicines watchdog, the Medicines and Healthcare products Regulatory Agency (MHRA), carried out a routine inspection of Roche’s drug safety procedures at its headquarters in Welwyn Garden City, Hertfordshire.

The company has now been ordered by the MHRA and the EU-wide regulator, the European Medicines Agency, to investigate immediately each of the total 80,000 deaths and side effects reported. Both agencies said they were ‘taking action’ over Roche’s failures.

All of the deaths and possible adverse reactions were reported by patients who rang a call centre run by Roche’s US subsidiary Genentech. Staff there failed to pass on the reports to Roche’s drug safety team – but it is not known why 

Professor Sir Kent Woods, chief executive of the MHRA, said: ‘Patients should continue to take their medicines because our investigation has currently found no evidence of a safety risk to patients.

‘Roche’s actions are unacceptable and our investigation has identified that its reporting systems are inadequate. We are taking urgent action to ensure that these are rectified by Roche as a matter of priority. We will take action to ensure that patients are protected now and in the future.’

Roche, which made profits of £6.3billion in 2010, has a legal duty to examine every suspected side effect and report them to regulators around the world so that potential safety concerns can be investigated.

This means that each side effect reported to the patient support call centre should have been immediately sent to the safety team to be assessed.

These must then be sent to regulators – within 15 days for the most serious reactions – even if no link between the drug and the reaction be proved.

Some of the call centre’s records, which date back to 1997, are said to have been noted down on paper and kept in boxes.

The European Medicines Agency, which made the findings public, said: ‘There is at present no evidence of a negative impact for patients and while the investigations and being conducted there is no need for patients or healthcare professionals to take any action.’

A number of drugs are being investigated following the incident
A number of drugs are being investigated following the incident

However, a spokeswoman  added: ‘It’s not often we make statements on such findings, so we do take this incredibly seriously. The numbers are huge but we’re not talking about confirmed reactions.  

‘Some might not be related, and some may have already been reported to the regulators via other mechanisms – for example directly to us by doctors.’ But she added: ‘We cannot rule out that additional safety concerns could be discovered.’

When asked if legal action could be taken against Roche, she said: ‘We are looking at all options. There are penalty regulations and they could be fined.’

Other drugs being examined  include Avastin, used for bowel and breast cancer; lung cancer medication Tarceva; Rituxan, which treats non-Hodgkin’s lymphoma; the stroke drug Alteplase; Actemra for rheumatoid arthritis; Pegasys for hepatitis B; and Raptiva for the skin condition psoriasis.

If any new safety concerns emerge after examining the data, regulators could decide to withdraw the drugs or change their guidance to doctors.

In a statement, Roche said: ‘Patient safety is of paramount importance to Roche. We acknowledge the concerns that can be caused by this issue for people using our medicines.

‘The non-assessment and non-reporting of these adverse events was not intentional and we are taking comprehensive steps necessary to address the findings of the MHRA inspection. We have provided initial estimates of missed adverse events and are in the process of confirming the final number.

‘We expect to complete all activities related to these programmes as soon as possible.’



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