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COVID-19

New book edited by Naomi Wolf exposes Pfizer’s ‘crimes against humanity’

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From LifeSiteNews

By John Leake

‘The Pfizer Papers: Pfizer’s Crimes Against Humanity’ strikes me as one of the most impressive works of investigative scholarship in history. I strongly recommend the book to everyone in the world who is interested in truth and justice.

When I was born, my maternal great grandmother gave me a generous gift of Pfizer stock. She had been impressed by Pfizer’s key role in discovering how to mass produce penicillin during World War II (in which her son was killed in action). Eighteen years later her gift paid for my university education. And then, in 1998, Pfizer received FDA approval to sell Viagra.

Pfizer initially developed the drug to treat high blood pressure and angina pectoris. However, as Pfizer’s researchers discovered in clinical trials, the drug was better at inducing erections than managing angina. And so, the company repurposed the drug for erectile dysfunction and launched a massive, global PR and marketing campaign – including seeking moral approval from Pope John Paul II and contracting the war hero and 1996 presidential candidate Bob Dole to be the brand’s poster gentleman – that succeeded in making Viagra a blockbuster.

So, I learned why pharmaceutical companies seek to develop blockbuster drugs with fanatical zeal. Formulating a safe and effective new medicine to address a large, unmet need is very difficult and expensive. Performing clinical trials and obtaining FDA-approval is an arduous process that normally takes several years. Thus, if an opportunity for a new blockbuster presents itself, a big drug company like Pfizer will go to extreme lengths to seize it.

Three years after the release of Viagra, I learned that Pfizer was not the respectable company my great grandmother had believed it to be. I arrived at this realization through my interest in British spy novels. In 2001 I lived in Vienna, around the corner from the Burgkino (Burg Cinema) which still played the 1949 film noir classic The Third Man on its big screen every weekend. I spent many a dreary winter Sunday afternoon watching the film. Based on the novella and screenplay by Graham Greene, The Third Man is a crime story about Harry Lime – an American running a medical charity in Vienna, who makes a killing selling penicillin on the bombed out, impoverished city’s black market. To increase his profits, he cuts the drug with other substances, thereby destroying its efficacy and causing the patients (including children) to die horribly from their infections.

In the film’s most iconic scene, the good guy (played by Joseph Cotton) meets his old friend Harry Lime (played by Orson Welles) on the Giant Ferris wheel in the Vienna Prater amusement park and tries to appeal to his conscience. At the wheel’s apex, the charismatic Harry opens the door, points down to people walking on the ground below, and says:

Look down there. Would you really feel any pity if one of those dots stopped moving forever? If I offered you twenty thousand pounds for every dot that stopped, would you really, old man, tell me to keep my money, or would you calculate how many dots you could afford to spare? Free of income tax, old man. Free of income tax. … Nobody thinks in terms of human beings. Governments don’t, why should we? They talk about the people and the proletariat; I talk about the suckers and the mugs. It’s the same thing. They have their five-year plans, and so have I.

READ: Study showing ‘high likelihood’ of link between COVID vaccines and death republished in peer-reviewed journal

I sensed that Graham Greene might have based the story on something he’d witnessed or heard about. Doing some research, I learned that Harry Lime was probably based on the British spy Harold “Kim” Philby, with whom Greene worked in British intelligence during World War II. Greene, it seems, discovered that Philby was a Soviet double agent long before he was exposed as such in 1963. Instead of ratting out his friend, he kept it to himself and left the intelligence service in 1944. Several pieces of evidence suggest that when he wrote The Third Man a few years later, he based it on his conflicted friendship with Philby.

John le Carré was also fascinated by Graham Greene and Kim Philby, and his thriller Tinker, Tailor, Soldier, Spy – one of my all-time favorites – was inspired by the Philby story. His novel The Constant Gardener was published in 2001, and I read it with great interest. The story wasn’t set in Cold War Europe, but in Kenya, where a British diplomat’s wife is brutally raped and murdered. Upon closer examination, the diplomat realizes that she was about to reveal a horrifying crime committed by a pharmaceutical company, which murdered her in order to prevent the exposure.

The novel’s plot was reminiscent of a controversial drug trial performed by Pfizer in Kano, Nigeria in 1996 during a meningococcal outbreak. For the trial of its new antibiotic, trovafloxacin, Pfizer gave 100 children this new drug. The control group of 100 other children received the standard anti-meningitis treatment at the time – a drug called ceftriaxone. However, for the control group, Pfizer administered a substantially lower dose of ceftriaxone than the drug’s FDA-approved standard.

In his author’s note, le Carré claimed that nobody and no corporation in the novel was based on an actual person or corporation in the real world.

But I can tell you this. As my journey through the pharmaceutical jungle progressed, I came to realize that, by comparison with the reality, my story was as tame as a holiday postcard.

In 2009, the same year that Pfizer settled with the trovafloxacin plaintiffs, the New York Times reported that a U.S. federal judge assessed Pfizer with the “largest health care fraud settlement and the largest criminal fine of any kind ever” for its illegal marketing of Bextra and three other drugs. The U.S. Department of Justice was unequivocal in characterizing Pfizer’s officers as guilty of grave criminal conduct at the expense of the American public.

As I have long known all of the above, I wasn’t surprised by the gross criminal conduct revealed in The Pfizer Papers: Pfizer’s Crimes Against Humanity, edited by Naomi Wolf with Amy Kelly and a foreword by Stephen K. Bannon. The 366-page hardcover book – beautifully published by War Room Books, an imprint of Skyhorse Publishing – is a meticulous analysis of Pfizer documents the FDA was forced to release as a result of Aaron Siri’s lawsuit.

The book strikes me as one of the most impressive works of investigative scholarship in history. As Dr. Peter McCullough described it in his praise (printed on the book’s first page):

This is a comprehensive, organized, and compelling presentation of vaccine safety data that has accumulated after mass and indiscriminate administration of the Pfizer mRNA COVID-19 vaccines. Sadly, a large group of vaccine recipients have become injured, disabled, and many have died after the ill-advised injections. The data with histopathological evaluation at necropsy and autopsy with expert analysis is presented so you can evaluate it for yourself. Never before has there been a class of products with this wide range and extended duration of injury to the recipient.

On Saturday, November 16, I attended the official launch of this magisterial work of what I believe falls squarely within the true crime genre of literature. It was a great honor for me to attend the gathering with the book’s editors and authors. It seemed to me that I was witnessing history being made.

I strongly recommend the book to everyone in the world who is interested in truth and justice. The book should be required reading by everyone in the legislative and executive branches of the U.S. government, especially President-elect Trump’s staff.

Please purchase your copy today by clicking here. Producing the book was a Herculean effort. Never before have a book’s authors and publisher been so deserving of compensation for their work. I agree with Dr. Peter Breggin’s sentiment that they, as well as editor Naomi Wolf and project director Amy Kelly, “should get the Nobel Prize for medicine and the praises of a grateful humanity.”

Reprinted with permission from Courageous Discourse.

COVID-19

Freedom Convoy leader Tamara Lich says her trial verdict now delayed to unknown date

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From LifeSiteNews

By Anthony Murdoch

Freedom Convoy leader Tamara Lich said she is “disappointed” in the Canadian “justice system” that her and convoy co-leader Chris Barber’s verdict for their mischief trial, which supposed to have been released in two weeks, has now been delayed to an unknown date.

In a X post late Thursday, Lich shared the news with her followers, noting, “We just received news that our March 12th verdict date is unfortunately being postponed.”

“At the end of our criminal (longest) mischief trial last August, when Her Honour set the verdict date, she let us know the court system assigned her a full trial schedule to help clear the backlog from the Covid years,” wrote Lich.

“This is the sad state of the justice system in Canada. While we are disappointed in yet another delay in our case, we know the importance of the upcoming decision not just for us, but for all Canadians.”

Lich said that as soon as she is told when the new verdict date will be, she will let everyone know.

As reported by LifeSiteNews, Lich and Barber’s verdict was supposed to have been announced on March 12.

They both face a possible 10-year prison sentence. LifeSiteNews reported extensively on their trial.

Lich and Barber’s trial concluded back in September of 2024, more than a year after it began. It was only originally scheduled to last 16 days.

Last week, Lich shared a heartwarming letter she received from a child, who told her to “keep fighting” for everyone and that “God will protect” her from the “enemy.”

Lich was arrested on February 17, 2022, in Ottawa. Barber was arrested the same day.

In early 2022, the Freedom Convoy saw thousands of Canadians from coast to coast come to Ottawa to demand an end to COVID mandates in all forms. Despite the peaceful nature of the protest, Prime Minister Justin Trudeau’s government enacted the never-before-used Emergencies Act (EA) on February 14, 2022.

During the clear-out of protesters after the EA was put in place, one protester, an elderly lady, was trampled by a police horse, and one conservative female reporter was beaten by police and shot with a tear gas canister.

Trudeau revoked the EA on February 23.

The EA controversially allowed the government to freeze the bank accounts of protesters, conscript tow truck drivers, and arrest people for participating in assemblies the government deemed illegal.

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COVID-19

RFK Jr. pauses $240 million contract for new ‘oral COVID vaccine’

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From LifeSiteNews

By Doug Mainwaring

For his first major action since taking office just two weeks ago, Department of Health and Human Services (HHS) Secretary Robert F. Kennedy Jr. has issued a 90-day stop-work order to American biotech company Vaxart Inc., which had been contracted during the Biden administration to develop a new “oral COVID-19 vaccine.”  

Kennedy’s order came just as 10,000 individuals were scheduled to begin clinical trials on Monday.   

HHS will utilize the 90-day hiatus to review Vaxart’s initial findings to determine the future of the human trials and continued drug development.   

Approximately $460 million had been allotted to Vaxart by HHS to develop its new COVID-19 “vaccine,” of which $240 million had been authorized for the preliminary study, according to a report by Fox News Digital, which broke the story.    

“While it is crucial that the Department [of] Health and Human Services support pandemic preparedness, four years of the Biden administration’s failed oversight have made it necessary to review agreements for vaccine production, including Vaxart’s,” Kennedy told Fox News Digital.

“I look forward to working with Vaxart and medical experts to ensure this work produces safe, effective, and fiscal-minded vaccine technology,” added Kennedy.  

“If anyone was worried that RFK would not address vaccine damage, this is proof he’s only getting started,” declared the producers of the 2022 Died Suddenly film, which questioned the motives behind the development and mandating of the first round of COVID-19 shots and the startling number of deaths attributed to them. 

There appears to be plenty of justification for pausing and even terminating Vaxart’s continued development of its “oral COVID-19 vaccine”

According to a report by The Defender’s John-Michael Dumais and published by LifeSiteNews in June, “Vaxart’s pill, VXA-CoV2-1, uses an adenovirus vector to infect epithelial cells in the lower small intestine. The vaccine delivers the genetic material to create the spike protein. The company boasts that a special coating allows the oral pill to survive the low pH in the stomach.” 

Johnson & Johnson’s (J&J) and AstraZeneca’s COVID-19 vaccines also used adenovirus vectors,” noted Dumais, who explained:   

The use of J&J’s vaccine was paused in April 2021 due to reports of thrombosis with thrombocytopenia syndrome (TTS), a severe blood clotting disorder. In July 2021, the FDA warned about the risk of Guillain-Barré syndrome with the J&J vaccine after approximately 100 cases were reported among 12.8 million vaccine recipients. With existing doses of the J&J vaccine having expired in May 2023, the vaccine is no longer in use.

AstraZeneca’s COVID-19 vaccine also caused blood clots, resulting in temporary pauses in its use in several countries. With declining demand, it was also removed from the market in May 2023.

Vaxart’s oral COVID-19 development project is part of the Biden administration’s $4.7 billion Project NextGen initiative, launched in 2023 to accelerate the development of new COVID “vaccines.”

Vaxart’s “vaccine” was funded through a contract with the Biomedical Advanced Research and Development Authority (BARDA), which falls under the umbrella of HHS’s Administration for Strategic Preparedness and Response.

The pausing of Vaxart’s COVID-19 “vaccine” development can be seen as Kennedy’s first important move to fulfill his stated mission as HHS secretary. 

Shortly after Robert F. Kennedy Jr. was sworn in as secretary of the Department of Health and Human Services (HHS), President Donald Trump signed an executive order titled Establishing The President’s Make America Healthy Again Commission (MAHA EO) to investigate and address the root causes of America’s escalating health crisis.

Chaired by Kennedy, the commission has four main policy directives to reverse chronic disease: Empower Americans through transparency and open-source data and avoid conflicts of interest in all federally funded health research; prioritize gold-standard research on why Americans are getting sick in all health-related research funded by the federal government; work with farmers to ensure that U.S. food is the healthy, abundant, and affordable; and ensure expanded treatment options and health coverage flexibility for beneficial lifestyle changes and disease prevention.  

The MAHA EO came at a time when many Americans have lost trust in the nation’s healthcare system and are increasingly skeptical as to whether they are receiving honest answers about the causes of the country’s health crisis and how to improve it.

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