Tag Archives: Big Pharma

Pharma’s War on Scientists to Mandate Jabs for Life, by Joseph Mercola

A few years back many computer software companies, including Microsoft, went from a one-time purchase model to software as a service, or subscription model. Now big pharma, maybe egged on by Bill Gates, is trying to impose the same model on medicine: deadly jabs as a service for life, perhaps on an annual subscription. From Joseph Mercola at lewrockwell.com:

The more we learn about Dr. Anthony Fauci, the worse he looks. The grandfatherly figurehead has now had two years in the limelight, urging people to “follow the science,” which he has shamelessly equated to his own ever-shifting opinion.

Another cache of emails obtained via a Freedom of Information Act (FOIA) request by the American Institute for Economic Research (AIER) now reveals Fauci and his boss, National Institutes of Health director Francis Collins, colluded behind the scenes to quash dissenting views on the lockdowns.1

Fauci and Collins Conspired to Destroy Dissent

October 4, 2020, three medical professors — Martin Kulldorff from Harvard, Sunetra Gupta from Oxford and Jay Bhattacharya from Stanford — launched the Great Barrington Declaration, a statement anyone could sign onto that called for focused protection of high-risk individuals, such as the elderly, rather than the continuation of blanket lockdowns. AIER sponsored the declaration.

“Current lockdown policies are producing devastating effects on short and long-term public health,” the declaration stated. “Keeping these measures in place until a vaccine is available will cause irreparable damage, with the underprivileged disproportionately harmed.”

As support of the declaration rapidly spread, Fauci and Collins seemingly panicked, and discussed how they could possibly stop the growing call for a sane, science-based approach. In an October 8, 2020, email to Fauci, Collins wrote:2,3,4,5

“The proposal from the three fringe epidemiologists who met with the Secretary seems to be getting a lot of attention … There needs to be a quick and devastating published take down of its premises …”

“Don’t worry, I got this,” Fauci replied. Later, Fauci sent Collins links to newly published articles refuting the focused protection solution, including an op-ed in Wired magazine, and an article in The Nation, titled “Focused Protection, Herd Immunity and Other Deadly Delusions.” “Excellent,” Collins replied.

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Who’s the Real Anthony Fauci? By Joseph Mercola

It’s a sign of how far the mainstream media has sunk that many Americans still think Anthony Fauci is a great guy. From Joseph Mercola at lewrockwell.com:

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We’re facing the greatest battle of our lifetimes, possibly of all time, according to Robert F. Kennedy Jr. in this riveting interview with James Corbett.1 I urge you to set aside 60 minutes to watch it in its entirety, as it succinctly sums up the coalition of sinister forces — intelligence agencies, pharmaceutical companies, social media titans, medical bureaucracies, mainstream media and the military — that are using a health crisis to impose totalitarian control worldwide.

You can find all of the details in Kennedy’s bestselling book, “The Real Anthony Fauci,” which contains more than 2,200 footnotes backing up its data. The truth is, Fauci, the director of the National Institute of Allergy and Infectious Diseases (NIAID) — part of the U.S. National Institutes of Health (NIH) — isn’t acting alone.

But he’s become the prominent face of the medical cartel and medical technocracy that is wrapped up in obliterating constitutional rights globally. And, as an authoritative medical figure and trusted adviser to six presidents, Fauci’s words are treated as gospel, despite the atrocities he’s committed.

Regulatory Agencies Turned Into Pharmaceutical Companies

Because of financial entanglements between pharmaceutical companies and the agencies that regulate them, public health agencies in the U.S. have been turned into veritable pharmaceutical companies. The U.S. Food and Drug Administration, for instance, receives 45% of its annual budget from Big Pharma, Kennedy explains.2

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Big Pharma uses Big Tobacco’s strategy to defeat Ivermectin, by Justus R. Hope, M.D.

Beware of big pharmaceutical companies offering to conduct studies, especially when the studies are of products that compete with their products. From Justus R. Hope, M.D. at thedesertreview.com:

In the 1950’s scientists Richard Doll and Bradford Hill published a study from the UK finding that the risk of lung cancer was related to the number of cigarettes smoked per day, and this risk was 25 times higher in those who smoked more than 25 cigarettes per day.

Other scientists, namely Ernest Wynder and Evarts Graham, found a strong association between bronchogenic carcinoma and smoking. 96.5% of men with bronchogenic carcinoma were heavy chain smokers compared to 73.7% of the general population. Several extensive studies within one year of each other found the same thing, cigarette smoking is strongly related to lung cancer, and the more one smoked, the higher one’s risk.

The big problem was that the cigarette industry was a multibillion-dollar lobby by the mid- 1960s. And they were not about to allow a few renegade scientists to spoil their profits. The Marlboro Man, as Dr. Mukherjee wrote in his Pulitzer Prize-winning book, The Emperor of All Maladies, was the most successful smoking icon by 1955. Dr. Mukherjee describes how the Tobacco Industry fought back by twisting science against the public, first by arguing that an association does not prove cause and effect, and later by offering to perform the studies.

The tobacco scientists argued that lung cancer was caused by genetics: if you were born with cancer genes, you developed cancer, and if you weren’t, you didn’t get it. Cigarettes might be associated with cancer, but they argued that more studies were needed if one were to actually “prove a causal link” between cigarettes and cancer. The actual cause of lung cancer, the tobacco scientists concluded, was faulty genetics and not cigarettes.

To assist with these studies, the generous Big Tobacco even offered to fund the research by founding the Tobacco Industry Research Committee. The TIRC is described further in The Emperor of All Maladies, a book I strongly recommend everyone read. The author writes how this ingenious strategy kept the tobacco companies in business and record-breaking profits for the next 50 years despite causing many millions of lung cancer deaths.

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First Do No Harm, by Nancy Murdoch

Safety and health are not the first priorities of either the pharmaceutical companies or their regulators. Nancy Murdoch did so well with her first guest post, “Follow the Science to Treatment,” that she’s been invited back.

“As to diseases, make a habit of two things to help, or at least, to do no harm.”

Hippocrates

“Most people believe the medicines they take are safe and effective, that they have been tested properly and have passed stringent regulatory scrutiny.  Few people understand the extent to which pharmaceutical promotion undermines these assumptions.”  Thus reads the first sentence in a book recently published called The Illusion of Evidence-based Medicine by Jon Jureidini and Leemon McHenry.

While many books have been written on this subject, this comes at a time when pharmaceutical companies are in the sights of the public, and these authors have inside information that has been relatively unavailable before.  They became privy to much of the information because they served as consultants to a Los Angeles based law firm that often acts as counsel for those suing pharmaceutical companies because of severe or fatal reactions to drugs.  By deposition the authors had access to documents and emails which laid out the serious problems facing the pharmaceutical companies and their plans to cover it up.  Because of the damning nature of the contents, the documents were considered by the court to be important enough to be declassified and made available to the public. 

While the authors intended audience is generally lawyers and doctors due to its technical jargon, the revelations of the corruption should be of interest to the public in general, especially to those who take prescribed medication now or in the future.  After all, the United States is at ground zero for the corruption, with worldwide implications.

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Why You Can’t Trust the FDA, the WHO, the CDC, the AAP, Merck, GlaxoSmithKline, Sanofi or Pfizer, by Gary G. Kohls, MD

All of the institutions in the title have given us ample reason not to trust them. From Gary G. Kohls, MD, at lewrockwell.com:

“The FDA receives 45% of its annual budget from the pharmaceutical industry. The World Health Organization (WHO) gets roughly 50% of its budget from private sources, including Big Pharma and its allied foundations. And the CDC, frankly, is a vaccine company; it owns 56 vaccine patents and buys and (very profitably) distributes $4.6 billion in vaccines annually through the Vaccines for Children program, which represents over 40% of its total budget.” — Robert F. Kennedy, Jr  

“The American Academy of Pediatrics (AAP) derives a majority of its outside contributions – estimated at more than $25 million per year – from pharmaceutical companies that make vaccines. The pediatricians that the AAP represents derive the majority of their annual revenues from the administration of vaccines to their pediatric patients.) — J.B. Handley  

“Perhaps the most infamous example of corruption at the CDC is how the head of the CDC from 2002 to 2009, Julie Gerberding, left her government job to become president of Merck’s $5 billion dollar/year Vaccine Division. Merck’s CEO understandably described Gerberding as an “ideal choice”. She held that position until 2014 and currently holds the Merck job title of “Executive Vice President & Chief Patent Officer, Strategic Communications, Global Public Policy and Population Health”. That is to say, the former CDC director is now in charge of Merck’s propaganda efforts. One might say she’s basically doing the same job now that she did for the CDC, but even more lucratively. Apart from her salary, in 2015, Gerberding sold shares of Merck worth over $2.3 million. While at the CDC Gerberding shepherded Merck’s highly controversial and highly profitable Gardasil vaccine through the regulatory maize” — From www.collective-evolution.com 

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COVID-19: The Emergence of the Pandemic Industrial Complex, by Brian Berletic

The pandemic industrial complex may be even more deleterious than the military-industrial-intelligence complex. From Brian Berletic from activistpost.com:

If official numbers are to be believed, the United States is one of the worst hit countries in terms of COVID-19 infections and deaths. According to the US Center for Disease Control and Prevention (CDC), at the time of writing, there are supposedly 19 million COVID-19 cases with an alleged 300,000+ deaths suggesting between a 1-2% chance of dying from COVID-19 if infected by it. 

However, these numbers are problematic – even before questioning the validity of the statistics themselves leading to them.

For example, asymptomatic cases will likely go both untested and unreported, meaning many more people are actually being infected by COVID-19, exhibiting no symptoms, receiving no treatment, and most certainly not making it into the CDC’s “cases” statistics.

This means that your chances of being infected by COVID-19 and dying are actually much, much less than the often touted claim of 1-2%. Only those who exhibit severe enough symptoms to be tested and/or treated will make it into the statistics of “cases.”

In terms of framing any pandemic, an exaggeration of the lethality of the virus becomes a fundamental issue. If this information by itself is carelessly or dishonestly presented to the public without mention of the many more people likely being infected and exhibiting no symptoms at all, panic can, and clearly has been spread across society and the world, enabling extreme policies to glide through approval, beginning the process of disfigurement society now suffers today.

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Just Trust ‘Em! . . . Because You Can’t Sue ‘Em, by Eric Peters

Why wouldn’t you trust a product from a manufacturer that’s immune from liability? From Eric Peters at ericpetersautos.com:

You can’t walk into a store without wearing the Holy Rag – because someone might get sick. But if you actually get sick as a result of being forced to take the Holy Jab, you can’t sue the company that made the god-knows-what’s-in-it vaccine.

Which is pretty sick when you think about it.

The pharmaceutical mafia can force you – via its enforcer, the government – to take its products; vaccines are already required for kids in many states and if you don’t submit to it the state can take your kids . . . and then walk away from any harm caused because the government protects the pharmaceutical mafia from you.

Thus one-upping the health insurance mafia  . . . which only forces you to buy its product.

The vaccine-pushers are uniquely endowed with government-granted immunity from lawsuits. They can wreck your life – and you get the bill.

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Sausage Making at FDA: How Human Cancer Cells Got Into Vaccines, by Robert F. Kennedy Jr.

But make sure you get your Covid vaccine. From Robert F. Kennedy Jr. at lewrockwell.com:

In a 2012 meeting, the FDA voted to allow the use of human fetal cells and adult human tumor cells in vaccines, despite acknowledging the many risks, including that vaccine recipients might later develop cancer.

“If the American people knew some of the things that went on at the FDA, they’d never take anything but Bayer aspirin.” — Len Lutwalk, FDA scientist

“The FDA, by spinelessly knuckling under to every whim of the drug companies, has thrown away its high reputation, and in doing so, forfeited our trust.” — Drummond Rennie, deputy editor of JAMA

“[The] honest employee fears the dishonest employee. There is also irrefutable evidence that managers at CDER (Center for Drug Evaluation and Research of the FDA) have placed the nation at risk by corrupting the evaluation of drugs and by interfering with our ability to ensure the safety and efficacy of drugs. While I was at FDA, drug reviewers were clearly told not to question drug companies and that our job was to approve drugs … If we asked questions that could delay or prevent a drug’s approval — which of course was our job as drug reviewers — management would reprimand us, reassign us, hold secret meetings about us or worse … When you are able to dig in, if you found issues that would make you turn down a drug, you could be pressured to reverse your decision, or the review would then be handed off to someone who would simply copy and paste whatever claims the company made in the summary document … I believe I also have documentation of falsification of documents, fraud, perjury and widespread racketeering, including witnesses tampering and witness retaliation.” — Ronald Kavanagh, Ph.D., pharmacist who reviewed medications for the FDA from 1998 to 2008

Vaccines and related biological products advisory committee today

Today — Thursday, Dec. 10 — the Vaccines and Related Biological Products Advisory Committee (VRBPAC), which is the U.S. Food and Drug Administration’s (FDA) internal panel that licenses new vaccines as “safe and effective,” will meet to consider Pfizer’s COVID vaccine. VRBAC will meet in one week, Dec. 17, to consider approval of the Moderna vaccine.

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How COVID-19 Vaccine Trials Are Rigged, by Joseph Mercola

It’s a reassuring thought: the trials for the vaccines they’ll be forcing you to submit to may be rigged. It’s kind of like finding out the surgeon who’s about to operate on you cheated her way through med school. From Joseph Mercola at lewrockwell.com:

There’s been a lot of talk lately about whether or not the fast-tracked COVID-19 vaccine will in fact be safe and effective. While vaccine makers insist that any vaccine reaching the market will have undergone rigorous testing, the way trial protocols are designed suggests these vaccines may leave a lot to be desired.

As reported1 by Forbes contributor William Haseltine, a former professor at Harvard Medical School and Harvard School of Public Health, while Moderna, Pfizer, AstraZeneca and Johnson & Johnson have all published their vaccine trial protocols in a rare display of transparency, “close inspection of the protocols raises surprising concerns.”

In a nutshell, the trial designs are such that the vaccines will get a passing grade even if their efficacy is minimal. Of course, we must also consider vaccine side effects and I’ve also written several articles about mounting safety concerns.

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FDA — Captured and Corrupt, by Joseph Mercola

Two important points. The FDA is captured and corrupt, but it is no different than most government agencies. From Joseph Mercola at lewrockwell.com:

If you’re like most people, you probably assume that the U.S. Food and Drug Administration is funded by the U.S. government and therefore isn’t catering to private industries.

The agency itself certainly tries to present itself as independent from the industries it regulates but, in reality, legal loopholes have led to the FDA receiving money from, and being captured and corrupted by, private interests.

While the FDA itself does not accept corporate money, it does receive money funneled via a nonprofit foundation, which in turn receives money from other nonprofits funded by private interests. It’s really all a façade because the end result is the same. Those donating the money ultimately end up with the ability to pull strings, when needed.

The Reagan-Udall Foundation

As explained by NPR1 back in 2012, the Reagan-Udall Foundation is a nonprofit foundation created by Congress in 2007 to support scientific research that is of interest to the FDA. According to NPR:2

“The idea was that this foundation could do things the FDA can’t. It would raise money from private sources, fund research in areas where the FDA lacks expertise, and organize collaborations involving industry, patient groups and academia.”

As explained in a 2008 article3 in the Journal of the National Cancer Institute, the creation of the Reagan-Udall Foundation was part of a larger plan to establish a private-public partnership to facilitate the Critical Path Initiative.

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