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EU to renew Iran sanctions under defunct nuclear deal: Report

The Cradle | June 29, 2023

European officials recently informed Iran that they plan to renew EU ballistic missile sanctions set to expire in October, according to sources in the know that spoke with Reuters.

The renewal will be conducted under the parameters of the defunct Joint Comprehensive Plan of Action (JCPOA), which officials say Iran “violated” by moving forward with developing its nuclear energy program after the US unilaterally exited the deal in 2018 and reimposed crushing sanctions.

Other reasons the EU is giving for renewing the sanctions are Russia’s use of Iranian drones in Ukraine and “the possibility of Iran transferring ballistic missiles to Moscow.”

“The Iranians have been told quite clearly [of plans to keep the sanctions], and now the question is what, if any, retaliatory steps the Iranians might take and [how] to anticipate that,” a western diplomat told Reuters on condition of anonymity.

The decision to uphold the sanctions would be the first significant instance of the E3 group of nations — France, Germany, and the UK — not abiding by the terms of the nuclear deal.

EU mediator Enrique Mora, who co-ordinates talks to restore the 2015 deal, raised the issue of keeping the sanctions when he met Iranian nuclear negotiator Ali Bagheri Kani in Doha on 21 June, but the latter reportedly refused to discuss the matter, according to an unnamed Iranian official who spoke with Reuters.

“Maintaining sanctions, in any capacity and form, will not hinder Iran’s ongoing advancements,” the Iranian official is quoted as saying. “It serves as a reminder that the west cannot be relied upon and trusted.”

Since 2017, the Islamic Republic has significantly advanced with its ballistic missile and satellite launch programs. The country last month made waves by revealing a hypersonic missile with a potential 2,000-km range.

This progress, on top of Tehran’s enrichment of uranium at 60 percent purity and a China-brokered détente with Saudi Arabia, set off alarms in the west and pushed Washington to begin ‘de-escalation talks‘ with Iran.

June 29, 2023 Posted by | Deception, Economics, Wars for Israel | , , , | Leave a comment

Serious adverse events from Pfizer’s mRNA vaccine are not “rare”

Maryanne Demasi, reports | June 27, 2023

Drug regulators and public health agencies have saturated the airways with claims that serious harms following covid vaccination are “rare.”

But there has been very little scrutiny of that claim by the media, and I could not find an instance where international agencies actually quantified what they meant by the term “rare” or provided a scientific source.

The best evidence so far, has been a study published in one of vaccinology’s most prestigious journals, where independent researchers reanalysed the original trial data for the mRNA vaccines.

The authors, Fraiman et al, found that serious adverse events (SAEs) – i.e. adverse events that require hospitalisation – were elevated in the vaccine arm by an alarming rate – 1 additional SAE for every 556 people vaccinated with Pfizer’s mRNA vaccine.

According to a scale used by drug regulators, SAEs occurring at a rate of 1 in 556 is categorised as “uncommon,” but far more common than what the public has been told.

Therefore, I asked eight drug regulators and public health agencies to answer a simple question: what is the official calculated rate of SAEs believed to be caused by Pfizer’s mRNA vaccine, and what is the evidence?

The agencies were FDATGAMHRAHCPEICDCECDC and EMA.

The outcome was startling.

What is the official SAE rate?

Not a single agency could cite the SAE rate of Pfizer’s vaccine. Most directed me to pharmacovigilance data, which they all emphasised does not establish causation.

The Australian TGA, for example, referred me to the spontaneous reporting system but warned, “it is not possible to meaningfully use these data to calculate the true incidence of adverse events due to the limitations of spontaneous reporting systems.”

Both the German regulator (PEI) and European CDC referred me to the European Medicines Agency which, according to its own report, saw no increase at all in SAEs. “SAEs occurred at a low frequency in both vaccinated and the placebo group at 0.6%.”

The UK regulator MHRA went so far as to state it “does not make estimations of a serious adverse event (SAE) rate, or a rate for adverse reactions considered to be causally related for any medicinal product.”

The US FDA, on the other hand, did conceded that SAEs after mRNA vaccination have “indeed been higher than that of influenza vaccines,” but suggested it was justified because “the severity and impact of covid-19 on public health have been significantly higher than those of seasonal influenza.

Despite analysing at the same dataset as Fraiman, the FDA said it “disagrees with the conclusions” of the Fraiman analysis. The agency did not give specifics on the areas of disagreement, nor did it provide its own rate of SAEs.

Expert response

In response to the criticism, Joe Fraiman, emergency doctor and lead author on the reanalysis said, “To be honest, I’m not that surprised that agencies have not determined the rate of SAEs. Once these agencies approve a drug there’s no incentive for them to monitor harms.”

Fraiman said it’s hypocritical for health agencies to tell people that serious harms of the covid vaccines are rare, when they have not even determined the SAE rate themselves.

“It’s very dangerous not to be honest with the public,” said Fraiman, who recently called for the mRNA vaccines to be suspended.

“These noble lies may get people vaccinated in the short term but you’re creating decades or generations of distrust when it’s revealed that they have been misleading the public,” added Fraiman.

Dick Bijl, a physician and epidemiologist based in the Netherlands, agreed.  “It goes to show how corrupted these agencies are. There is no transparency, especially since regulators are largely funded by the drug industry.”

Bijl said it’s vital to know the rate of SAEs for the vaccines. “You must be able to do a harm:benefit analysis, to allow people to give fully informed consent, especially in young people at low risk of serious covid or those who have natural immunity.”

Bijl said the mainstream media has allowed these agencies to make false claims about the safety of vaccines without interrogating the facts.

“The rise of alternative media is strongly related to the lies being told by the legacy media, which just repeats government narratives and industry marketing. In the Netherlands, there is a lot of discussion about the distrust in public messaging,” said Bijl.

June 28, 2023 Posted by | Deception, Mainstream Media, Warmongering, Science and Pseudo-Science | , , , , | Leave a comment

Merck Knew Its Popular Asthma Drug Could Lead Kids to Commit Suicide, Lawsuits Allege

By Michael Nevradakis, Ph.D. | The Defender | June 27, 2023

Dozens of patients, including many children, died by suicide or suffered from neuropsychiatric problems after taking Singulair, Merck’s allergy and asthma medication, according to lawsuits that are finally proceeding, after decades of delays and legal challenges, Reuters reported.

Merck is accused of downplaying early evidence of Singulair’s impact on the brain. These claims “later faced intense scrutiny,” leading to “a raft of lawsuits alleging [Merck] knew … that the drug could impact the brain and that it minimized the potential for psychiatric problems in statements to regulators.”

Singulair, also known as montelukast, is available to adults and children as a medication for severe allergies and asthma. The drug “blocks chemicals, called leukotrienes, in the body,” according to Dr. Michelle Perro, a pediatrician. Leukotrienes “can be involved in the precipitation of asthma and can cause respiratory symptoms, as well as inflammation of the airways,” Perro told The Defender.

Numerous public comments about Singulair’s side effects were submitted in 2019, prior to the Sept. 27, 2019, joint meeting of the U.S. Food and Drug Administration’s (FDA) Pediatric and Drug Safety and Risk Management Advisory Committees charged with reviewing the drug’s safety.

Many of the comments were submitted by “vocal parents” of children adversely affected by Singulair.

Rolf Hazlehurst, senior staff attorney with Children’s Health Defense (CHD), told The Defender he “worked closely” with several of these parents.

The public comments, along with thousands of reports submitted over several years to the FDA Adverse Event Reporting System (FAERS) plus a 2015 research study finding that a “substantial amount” of Singulair entered the brain, forced the FDA to take action.

On March 4, 2020, the FDA required Singulair to carry a “black box” label — the FDA’s most serious warning, for “serious mental health side effects,” according to Drugwatch.

Black box warnings list “important side effect information surrounded by a thick black border and bold lettering to warn of permanent, serious or fatal side effects.”

In the case of Singulair, the label links the drug to “suicide, depression, aggression, agitation, suicidal thoughts and sleep disturbances.”

The black box label was at least two decades in coming, according to Hazlehurst, who said it “took over a decade’s worth of work by persistent parents, armed with overwhelming evidence of the serious neuropsychiatric side effects, urging the FDA to take action.”

According to Drugwatch, lawsuits now pending against Merck claim the drugmaker “knew or should have known before it started selling Singulair in 1998 that the drug could cause neuropsychiatric injuries during treatment and even after stopping.”

Dr. Liz Mumper, a pediatrician, said she has been “aware of the potential neuropsychiatric side effects of montelukast for many years,” adding that her patients “are instructed to stop the medicine if they notice a change in their mental health.”

“Over the years, parents have reported personality changes in their children, rapid changes in mood and irritability,” Mumper told The Defender. “Typically, these symptoms resolve once off montelukast.”

Since March 2020, when the FDA applied the black box warning to Singulair, numerous lawsuits have been filed against Merck. The lawsuits allege Merck designed “a defective drug,” in addition to claiming “negligence and failure to warn about the risk of mental problems,” according to Drugwatch.

Reuters investigative report revealed the lawsuits also allege “that the company’s own early research indicated the drug could impact the brain but that Merck downplayed any risks in statements to regulators.”

The Reuters investigation states that plaintiffs faced a legal hurdle commonly used by Big Pharma — known as a “preemption defense” — based on a legal argument that federal law and federal regulations supersede state laws, including state product liability laws that traditionally served as the basis for lawsuits like those against Merck.

As a result, “companies increasingly argue that federally regulated products or services should be immune from lawsuits alleging state-law violations,” and plaintiffs “must often demonstrate that a company failed to disclose safety information to federal regulators — and that the information could have spurred new government restrictions or warnings before the alleged harm occurred.”

This has made it particularly difficult to sue manufacturers of generic versions of Singulair and other drugs, because generic drugmakers simply follow the primary manufacturer’s FDA-approved labeling, while the primary drugmaker can’t be sued by claimants if they or their family members took the generic version.

Perro told The Defender that a combination of an abrogation on the part of federal regulators, a lack of integrity on the part of drugmakers and complex legal maneuvering makes it difficult for doctors to prescribe safe treatments to their patients.

She said:

“A medical practitioner now needs to understand their patient, the illness, any prescribed medications, what Pharma reports about their drug, the real science behind the drug, and unfortunately, the legal doctrine of preemption, which is the principle based on federal law trumping state law.

“It is a dark time in medicine when the physician must question the integrity of what is written on the prescription pad.”

The FDA claims it has “diligently monitored reports of side effects possibly associated with montelukast, as well as communicated findings and taken regulatory action, when appropriate,” and that it “continues to monitor and investigate this important issue.”

Merck’s patent on Singulair expired in 2012, allowing generic drugmakers to begin producing and marketing the drug. Still, according to Reuters, Singulair “has provided Merck with about $50 billion in revenue.”

However, once Merck’s patent expired, “The number of patients prescribed the medicine climbed from about 7 million annually to more than 9 million” — with up to half of recipients age 16 or younger.

At least 82 suicides connected to Singular before FDA added black box warning

The Reuters investigation noted that “in the case of Singulair’s potentially deadly side effects, the FDA waited years, despite thousands of reported psychiatric problems, to require its most serious warning on the drug’s label.”

During this time, dozens of individuals taking Singulair committed suicide or faced other neuropsychiatric problems.

For instance, in 2017, 22-year-old Nicholas England, a Virginia resident, shot himself in the head less than two weeks after starting a generic version of the medication. He had no history of mental health problems — and his family had no legal recourse against Merck due to the preemption defense.

In 2007, a 15-year-old boy in New York committed suicide, 17 days after first taking Singulair. According to Reuters, this incident led Merck to propose — and the FDA to accept — an amendment to the drug’s label to add suicidal thinking and behavior to the product’s listed adverse events.

However, this adverse event “appeared in the middle of a list of more than three dozen side effects,” the Reuters investigation found. “Parent advocates argue the new label was grossly inadequate to warn of such a grave risk.”

“Neuropsychiatric side effects are listed in the documentation of potential side effects, but not always prominently,” Mumper told The Defender. And despite the new label, she said, parents searching for its package insert online will find older versions “without a prominent black box warning.”

According to Drugwatch, the change to Singulair’s label was made in August 2009, when the label was updated to also include other neuropsychiatric events including “postmarket cases of agitation, aggression, anxiousness, dream abnormalities and hallucinations, depression, insomnia, irritability, restlessness … and tremor.”

In 2008, the FDA said it was investigating “a possible association between the use of Singulair and behavior/mood changes, suicidality … and suicide,” Drugwatch reported.

In another example, the 3-year-old son of Jan Gilpin was prescribed Singulair for asthma in 2003. He “soon seemed withdrawn and sullen” and “started talking about death,” according to Reuters.

Gilpin initially did not suspect Singulair — until she discovered online posts by parents stating that their children were exhibiting similar behavior while on this medication. She pulled her son off Singular and soon “noticed he began to skip and laugh,” while his “obsessive thoughts about death disappeared after he quit the medicine.”

Indeed, “reports of related neuropsychiatric episodes piled up on internet forums and in the FDA’s early-warning detection system” starting in 1998, Reuters reported. Yet, by the time of England’s suicide in 2017, the FDA was still “reviewing” this data.

According to Reuters, in 2011, the FDA “rejected a petition from Gilpin and other parents seeking a black box warning, citing what it called insufficient evidence that the drug caused suicidal behavior.”

“Parents who argue Singulair endangered their children view the FDA’s 2020 decision to add a black box warning as vindication, but many still want to sue Merck for not acting sooner,” Reuters also reported.

In 2014, an FDA panel acknowledged that neuropsychiatric side effects among Singulair users were a “known safety issue,” but cited this reason and “feasibility concerns” in its decision not to order new studies, according to Reuters.

Yet, as reports of suicides continued to be filed — with 82 suicides linked to Singulair and its generic versions, including at least 31 involving people age 19 and younger, a new FDA advisory panel was convened in 2019.

According to Reuters, “agency staffers again said there was not enough evidence” to merit this. However, with Merck’s patent having expired, an FDA official told the advisory committee that the company may opt to pull Singulair from the market rather than fund expensive new studies to investigate the product’s safety.

This resulted in the March 2020 decision to add the black box label to Singulair.

‘Substantial amount’ of Singulair enters human brain

In its 2020 decision, the FDA cited independent research conducted in 2015 by cell biologist Julia Marschallinger and other researchers at Austria’s Institute of Molecular Regenerative Medicine.

They found that Singulair’s distribution into the brain was more significant than what was stated on the product label, which described its brain distribution as “minimal.”

Merck had claimed, in documents it submitted to FDA for the drug’s approval in 1998, that “only a trace amount” of the drug could be found in the brain and that its presence “declined over time.” Merck’s public marketing of the product later described side effects as “generally mild” and “similar to a sugar pill.”

However, Marschallinger’s team found that while Singulair’s presence decreased almost everywhere in the body within 24 hours after administration, the opposite was true in the brain, where “a substantial amount” of the drug was identified.

In its 1996 patent application for Singulair, Merck also claimed the drug could be used as a treatment for “cerebral spasms” — indicating “knowledge of the drug’s potential brain impacts.” Lawyers for plaintiffs filing Singulair lawsuits against Merck have cited this argument, as well as Marschallinger’s study.

The FDA has confirmed the study’s findings, acknowledging that claims regarding the declining presence of Singulair in all tissues “did not fully reflect the data.”

However, according to Reuters, the FDA also characterized findings of “a substantial amount” of the drug in the brain “a subjective characterization that is not necessarily incompatible with the ‘minimal’ descriptor in other contexts.”

“The FDA could have asked Merck to repeat the experiment or do it for an even longer period of time,” Marschallinger told Reuters. “It’s not hard to do.”

Perro said, “For those children who have been harmed by this drug,” due to the FDA’s 22-year delay in adding a black box warning, “there will not be any compensation because of pharmaceutical protection by our own government and liability shields.”

The FDA’s inaction has resulted in many deaths, Sue Peters, Ph.D., a CHD science fellow, told The Defender :

“The FDA has placed pharmaceutical profits over the safety and mental health of our children. It’s a never-ending cycle, with increased rates of chronic illness, like asthma, leading to pharmaceutical treatments which have not been properly safety-tested.

“These drugs put young people, with critical brain myelination continuing past 25 years of age, at risk of developing mental health disorders, leading to polypharmacy with psychiatric medications, and contributing to iatrogenic deaths as a leading cause of death in the U.S.

Perro called for an overhaul of the FDA, telling The Defender :

“It is clear who our government — including the judicial system — is protecting. A solution to the lack of action by regulatory agencies? Overhaul.

“In the meantime, there are safer pharmaceutical alternatives for asthma in children. Not to mention, this is yet another reason to examine the root causes as to why so many children now have asthma, and address the real culprits, such as air pollution.”

For Mumper, a new approach to treating ailments such as asthma is needed. “Although montelukast is a valuable medication in my toolbox for treating allergies, the prescription should come after other measures, including working on gut health,” she said.

Similarly, Peters called for a “careful analysis” of the role of drugs in the treatment of common disorders and their role in precipitating mental health disorders and even deaths. She told The Defender :

“The tragic increase in the rate of mental health disorders in children in the United States, requires careful analysis of the role of iatrogenic death.

“Failing to consider the role of pharmaceutical drugs and medical treatments in the development of mental health disorders in children, has led to the loss of valuable research time, wasted research dollars, and ultimately the loss of life. Clearly, our current system is broken.”

Preemption defense lets Big Pharma avoid directly addressing safety claims

According to the Reuters investigative report, most of the Singulair lawsuits pending against Merck are still in their early stages.

Drugwatch reported that, as of May 16, “there have been no scheduled trials or court-approved global settlement in Singulair litigation.” Many of the suits against Merck were filed in New Jersey, where in January 2022, they were consolidated into multicounty litigation in the Superior Court of New Jersey Law Division: Atlantic County.

And in April, U.S. District Judge Timothy S. Hillman in Massachusetts denied Merck’s motion to dismiss a Singulair lawsuit “for lack of personal jurisdiction,” Drugwatch reported. Judge Hillman argued Merck manufactured, marketed and sold the drug in the state and allowed the case to continue.

Two U.S. Supreme Court rulings in 2011 and 2013 strengthened the preemption defense.

In Pliva, Inc. v. Mensing (2011), the Supreme Court held that state law requiring “generic drug manufacturers to provide adequate warning labels was preempted where federal law required manufacturers to use the same labels as their brand-name counterparts.”

And in Mutual Pharmaceutical Co. v. Bartlett (2013), the Supreme Court held that design-defect claims questioning the adequacy of a drug’s warnings under state law are preempted by the Federal Food, Drug, and Cosmetic Act and the Pliva v. Mensing ruling.

According to Reuters, the preemption doctrine rests on the U.S. Constitution’s Supremacy Clause, which states that the Constitution and federal law take precedence over state laws and state constitutions.

As a result, “Preemption defenses often deliver companies a swift procedural win, allowing them to avoid addressing the substance of plaintiffs’ allegations.”

While the defense has been used across multiple industries, it “has had a particularly profound impact in the pharmaceutical industry,” particularly as FDA data cited by Reuters indicates that generic drugs account for 91% of U.S. prescriptions.

Reuters, in its review of 257 U.S. Supreme Court and federal appeals court rulings since 2001, found that “judges ruled two-thirds of the time to weaken or kill lawsuits alleging deaths or injuries caused by corporate negligence or defective products.”

Moreover, “The number of potential lawsuits that were never filed” serves as “Another industry benefit” that “can’t be quantified,” according to Reuters.

Preemption defenses became a centerpiece of the George W. Bush administration — and FDA policy under his presidency, Reuters reports. This was part of the Bush campaign’s promise to address what it described as “frivolous” lawsuits.

Daniel Troy, the FDA’s chief counsel under the Bush administration, “interpreted preemption to mean that courts can’t undermine federal regulators based on alleged state-law violations,” Reuters reported, adding that he “aimed to make that argument in high-profile lawsuits” and briefed drug industry lawyers on the strategy in 2003.

Troy — who is now a pharmaceutical industry lawyer — told Reuters, “If you believe in a strong FDA, we can’t have state courts, especially juries, second-guessing and undercutting the FDA’s judgments.”

Hazlehurst told The Defender Troy’s argument is the same one used by Wyeth (Pfizer) before the Supreme Court in Bruesewitz v. Wyeth (2011). The Supreme Court’s decision in this case prohibited design defect lawsuits against vaccine manufacturers.

The U.S. Department of Health and Human Services, the parent agency of the FDA and the Centers for Disease Control and Prevention, supported Wyeth’s 2011 argument.

Similarly, Mumper told The Defender that pharmaceutical companies “have a history of avoiding liability through various legislative protection,” including the preemption defense and the National Childhood Vaccine Injury Act of 1986.

And in 2006, “The FDA formally changed its view of preemption in a 2006 regulation, stating the agency now believed that FDA labeling approval ‘preempts conflicting or contrary State law,’” Reuters reported.

Hazlehurst told The Defender, “CHD is proud to have played a role in advocating and assisting these parents on the journey to hold Merck accountable,” but “one thing rings loud and clear: the FDA is a captured agency, and this is a fundamental problem.”

Some parents have questioned whether the black box warning for Singulair was enough to save lives, citing the damage already done, continued legal obstacles, and Merck’s strong marketing campaign for the drug.

“Due to tremendous financial conflicts of interest, the pharmaceutical industry has tremendous influence over the FDA,” Hazlehurst said. “As a result, the FDA protects the pharmaceutical industry first and people second — this story is just one example.”

He added: “One must wonder, how many lives could have been spared if the FDA had timely done its job of properly investigating and regulating the pharmaceutical industry?”


Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

June 28, 2023 Posted by | Deception | , | Leave a comment

Pandemic Leaders Were Biodefense Puppets and Profiteers

By Debbie Lerman | Brownstone Institute | June 26, 2023

Scandalous incompetence. Profound stupidity. Astounding errors. This is how many analysts – including Dr. Vinay PrasadDr. Scott Atlas, and popular Substack commentator eugyppius – explain how leading public health experts could prescribe so many terrible pandemic response policies.

And it’s true: the so-called experts certainly have made themselves look foolish over the last three years: Public health leaders like Rochelle Walensky and Anthony Fauci make false claims, or contradict themselves repeatedly, on subjects related to the pandemic response, while leading scientists, like Peter Hotez in the US and Christian Drosten in Germany, are equally susceptible to such flip-flops and lies. Then there are the internationally renowned medical researchers, like Eric Topol, who repeatedly commit obvious errors in interpreting Covid-related research studies. [ref]

All of these figures publicly and aggressively promoted anti-public health policies, including universal masking, social distancing, mass testing and quarantining of healthy people, lockdowns and vaccine mandates.

It seems like an open-and-shut case: Dumb policies, dumb people in charge of those policies.

This might be true in a few individual cases of public health or medical leaders who really are incapable of understanding even high school level science. However, if we look at leading pandemic public health and medical experts as a group – a group consisting of the most powerful, widely published, and well-paid researchers and scientists in the world – that simple explanation sounds much less convincing.

Even if you believe that most medical researchers are shills for pharmaceutical companies and that scientists rarely break new ground anymore, I think you’d be hard-pressed to claim that they lack basic analytical skills or a solid educational background in the areas they’ve studied. Most doctors and scientists with advanced degrees know how to analyze simple scientific documents and understand basic data.

Additionally, those doctors and public health professionals who were deemed experts during the pandemic were also clever enough to have climbed the academic, scientific, and/or government ladders to the highest levels.

They might be unscrupulous, sycophantic, greedy, or power-mongering. You might think they make bad moral or ethical decisions. But it defies logic to say that every single one of them understands simple scientific data less than, say, someone like me or you. In fact, I find that to be a facile, superficial judgment that does not get to the root cause of their seemingly stupid, incompetent behavior.

Returning to some specific examples, I would argue that it is irrational to conclude, as Dr. Prasad did, that someone like Dr. Topol, Founder and Director of the Scripps Research Translational Institute, who has published over 1,300 peer-reviewed articles and is one of the top 10 most cited researchers in medicine [ref] cannot read research papers “at a high level.” And it is equally unlikely that Anthony Fauci, who managed to ascend and remain atop the highest scientific perch in the federal government for many decades, controlling billions of dollars in research grants [ref], was too dumb to know that masks don’t stop viruses.

There must, therefore, be a different reason why all the top pro-lockdown scientists and public health experts – in perfect lockstep – suddenly started (and continue to this day) to misread studies and advocate policies that they had claimed in the past were unnecessary, making themselves look like fools.

Public health experts were messengers for the biodefense response

The most crucial single fact to know and remember when trying to understand the craziness of Covid times is this:

The public health experts were not responsible for pandemic response policy. The military-intelligence-biodefense leadership was in charge.

In previous articles, I examined in great detail the government documents that show how standard tenets of public health pandemic management were abruptly and secretly thrown out during Covid. The most startling switch was the replacement of the public health agencies by the National Security Council and Department of Homeland Security at the helm of pandemic policy and planning.

As part of the secret switch, all communications – defined in every previous pandemic planning document as the responsibility of the CDC – were taken over by the National Security Council under the auspices of the White House Task Force. The CDC was not even allowed to hold its own press conferences!

As a Senate report from December 2022 notes:

From March through June 2020, CDC was not permitted to conduct public briefings, despite multiple requests by the agency and CDC media requests were “rarely cleared.” HHS stated that by early April 2020, “after several attempts to get approvals,” its Office of Assistant Secretary for Public Affairs “stopped asking” the White House “for a while.” (p. 8)

When public health and medical experts blanketed the airwaves and Internet with “recommendations” urging universal masking, mass testing and quarantining of asymptomatic people, vaccine mandates, and other anti-public health policies – or when they promoted obviously flawed studies that supported the quarantine-until-vaccine biodefense agenda – they were not doing so because they were dumb, incompetent, or misguided.

They were performing the role that the leaders of the national security/biodefense response gave them: to be the trusted public face that made people believe quarantine-until-vaccine was a legitimate public health response.

Why did public health leaders go along with the biodefense agenda?

We have to imagine ourselves in the position of public health and medical experts at top government positions when the intelligence-military-biodefense network took over the pandemic response.

What would you do if you were a government employee, or a scientist dependent on government grants, and you were told that the quarantine-until-vaccine policy was actually the only way to deal with this particular engineered potential bioweapon?

How would you behave if an unprecedented event in human history happened on your watch: an engineered virus designed as a potential bioweapon was spreading around the world, and the people who designed it told you that terrifying the entire population into locking down and waiting for a vaccine was the only way to stop it from killing many millions?

More mundanely, if your position and power depended on going along with whatever the powers-that-be in the NSC and DHS told you to do – if your job and livelihood were on the line – would you go against the narrative and risk losing it all?

And, finally, in a more venal vane: what if you stood to gain a lot more money and/or power by advocating for policies that might not be the gold standard of public health, but that you told yourself could bring about major innovations (vaccines/countermeasures) that would save humanity from future pandemics?

We know how the most prominent Covid “experts” answered those questions. Not because they were dumb, but because they had a lot to lose and/or a lot to gain by going along with the biodefense narrative – and they were told millions would die if they failed to do so.

Why understanding the motives of public health leaders during Covid is so important

Paradoxically, deeming public health experts stupid and incompetent actually reinforces the consensus narrative: that lockdowns and vaccines were part of a public health plan. In this reading, the response may have been terrible, or it may have gone awry, but it was still just a stupid public health plan designed by incompetent public health leaders.

Such a conclusion leads to calls for misguided and necessarily ineffectual solutions: Even if we replaced every single HHS employee or defunded the HHS or even the WHO altogether, we would not solve the problem and would be poised to repeat the entire pandemic fiasco all over again.

The only way to avoid such repetition is to recognize the Covid catastrophe for what it was: an international counterterrorism effort focused myopically on lockdowns and vaccines, to the exclusion of all traditional and time-tested public health protocols.

We need to wake up to the fact that, since the terrorist attacks of 9/11 (if not earlier), we have ceded control of the agencies that are supposed to be in charge of public health to an international military-intelligence-pharmaceutical cartel.

This “public-private partnership” of bioterrorism experts and vaccine developers is not interested in public health at all, except as a cover for their very secret and very lucrative biowarfare research and countermeasure development.

Public health was shunted aside during the Covid pandemic, and the public health leaders were used as trusted “experts” to convey biowarfare edicts to the population. Their cooperation does not reflect stupidity or incompetence. Making such claims contributes to the coverup of the much more sinister and dangerous transfer of power that their seemingly foolish behavior was meant to hide.

June 27, 2023 Posted by | Corruption, Deception, Militarism, Timeless or most popular, War Crimes | , , , | Leave a comment

Lethal Drones at the U.S.-Mexico Border?

By Laurie Calhoun | The Libertarian Institute | June 27, 2023

Fentanyl has caused many overdose deaths in recent years, and much of it has entered the United States through Mexico. A number of politicians have thrown their support behind a proposal to officially label narcotics traffickers based in Mexico as “terrorists.” Not all of the Republican lawmakers who support this idea have openly embraced the use of lethal drones to eliminate such persons, but that would be the inevitable policy implication of such labeling, given the wording of anti-terrorist legislation. At least one presidential candidate, Vivek Ramaswamy, has said the quiet part out loud: lethal drones should be deployed at the U.S.-Mexico border. There can be little doubt that the many other politicians declaring “war” on the cartels are well aware that lethal force will be used once the fentanyl producers have been designated terrorists, and the current tool of choice among self-styled smart warriors is the unmanned combat aerial vehicle (UCAV) or lethal drone.

The superficially plausible assumption behind this proposal is that if the flow of fentanyl is stanched, then the overdose deaths will subside. But the prospect of deploying lethal drones at the U.S.-Mexico border is a simplistic plan for addressing a very complicated problem. There are dozens of reasons for opposing this approach, on moral, legal, cultural, and geopolitical grounds. Most of those arguments, however, will fall on deaf ears and certainly not deter politicians from plundering ahead, expanding the domain of the killing machine once again, having been, in at least some cases, sincerely persuaded that they are acting not to enrich death industry profiteers but to defend the people of the United States from foreign enemies. The only way to prevent the deployment of lethal drones at the border from happening will be persuasively to demonstrate that the plan could never succeed, on purely tactical grounds. Two fatal flaws virtually guarantee that, if implemented, the plan would not have the desired effect, as can be seen through a consideration of the origins of the opioid crisis and the cross-border use of lethal drones in the Middle East.

The tragic drug overdoses of hundreds of thousands of people in the United States in recent years have had many causal factors, but the prime mover, which initiated the whole ugly mess, was the promiscuous overprescription of narcotics by doctors. Led by Purdue Pharma, drug industry giants aggressively marketed their opioid products as safe to use by anyone for anything, all blessed by the FDA (Food and Drug Administration), which permitted a package insert to be included in boxes of Oxycontin indicating that the time-release format made the product safe to use without concerns about addiction or abuse. This was a classic case of the commandeering by profiteers of a government agency established in order to protect citizens but used instead to promote the interests of those who come to enrich themselves through decisively shaping government policies. (An even more obvious case has been the capture of the Department of Defense by individuals beholden to companies in military industry, such as former Raytheon board member and current secretary of defense, Lloyd Austin.) Because most members of the populace believe that the FDA is their protector (again, just as they believe in the basic goodness of the Pentagon), many of them were taken in by this pharmaceutical industry scheme.

Doctors, too, were remarkably persuaded to believe that they could and should prescribe narcotics liberally, and patients consequently came to believe that they could and should empty their large amber vials. Preposterous though it may seem in retrospect, the pharmaceutical industry undertook aggressive public media campaigns to persuade politicians and their constituents that the nation was in the throes of a “pain epidemic,” for which narcotics were the solution. When clinicians expressed concern that their patients might be turning into addicts, they were tutored by “experts” tethered to the industry that the observed condition was in fact “pseudo-addiction,” the remedy for which would be even higher doses of narcotic drugs.

Prescription narcotics were oversupplied to perfectly ordinary patients suffering from even minor bouts of acute pain, who eventually discovered that they had become dependent on and were unable to function without the drugs. The opiates to which they found themselves hopelessly addicted were prescribed legally to them by physicians whom they had trusted as having their best interests in mind. In this way, people from all walks of life, including injured high school athletes who had never even been recreational drug users, were transformed into junkies.

Some of the working people who were prescribed narcotics for their various, often minor, ailments lost their jobs and, with them, their health insurance. During the early years of what would become the opioid overdose epidemic, addicts and others supported themselves by selling pills they acquired through “doctor shopping”. As a direct consequence of the pharmaceutical industry-created demand for more and more narcotics, mercenary but board-certified doctors teamed up with unscrupulous business persons to open “pain clinics,” which swiftly became places where addicts convened and collected drugs to be diverted for illegal sales. Massive quantities of narcotics were distributed by the now notorious pain clinics. Many of those drugs were sold on the streets for recreational use, thereby creating even more addicts. (For a concise and compelling summary of the government’s indisputable role in this tragic story, see director Alex Gibney’s two-part HBO series, The Crime of the Century [2021].)

Once the pain clinics were shut down, more and more addicts turned to the streets for supplies of their needed fix of whatever was available: diverted prescription pills, heroin, morphine, and most notoriously of all, fentanyl. Because it is so potent (about fifty times more than comparable drugs) and also cheap to produce, fentanyl was mixed or even used to replace other narcotics by unscrupulous dealers. The increased demand by addicts for opioids and the use by dealers of fentanyl to cut or replace heroin and other less dangerous surrogates has resulted in the deaths of many drug users who simply did not know what they were ingesting. At least some of the fentanyl deaths reported have been of non-addicts whose supplies of other drugs, too, were tainted with the highly concentrated and toxic substance.

Can eliminating supplies of fentanyl coming over the border to the United States from Mexico solve this problem? Will summarily executing suspected producers and distributors of fentanyl help to stem the tide of overdose deaths? Even setting aside concerns about procedural justice, the proposal to assassinate suspected drug dealers fails to take into account the etiology of the opioid crisis and, most importantly of all, the nature of drug dependency and the desperation of junkies to acquire the substances to which they are not only psychologically but physically addicted.

The opioid addiction crisis was not caused but seized upon opportunistically by Mexican drug cartels. The very fact that the fentanyl business has become so lucrative for illicit drug purveyors itself illustrates that there is a strong market demand for narcotics, whether natural or synthetic. If addicts cannot acquire cheap black tar heroin and/or fentanyl from Mexican producers and their network of distributors throughout the United States, then they will seek out and locate other sources of the drugs which their bodies crave. No one denies that the opioid addiction crisis is grave. But whacking drug dealers at the U.S.-Mexico border will simply produce more drug dealers, in different places.

We’ve seen a version of this story before, mutatis mutandis. What, after all, happened when war resisters transformed into jihadists on the ground in Iraq and Afghanistan were targeted by missiles? First, there was the hydra problem: targeting suspected militants often resulted in the deaths of innocent civilians, thus fueling the very anger requisite to the recruitment by Al Qaeda and other groups of new converts to violent retaliation. Other factors, beyond the illegal invasions themselves, contributed to the increased number of radical Islamist fighters as well, including the use of torture by the occupiers, along with a variety of other incompetent policies, which led to a general degradation in the quality of life for the inhabitants of occupied territories.

Second, and directly relevant to the proposed plan to execute suspects at the U.S.-Mexico border, as the ranks of the factional fighters increased, some of them fled to other parts of the Middle East to regroup and avoid being killed by occupying forces. The comportment of the dissidents who fled war zones was entirely rational. They believed that they were right, and they naturally wanted to succeed in their missions to eject the invaders from their lands, so they relocated and strategized about how to defeat what they had come to believe was “the evil enemy.” The lethal drones then followed the factional fighters to Pakistan, Syria, Somalia, Mali, Yemen, and beyond. As a result of this lethal creep, civilians in several different countries are now under constant threat of death by missiles launched by drones.

The Mexican drug cartels are not at this point engaged in a war with the U.S. military, but recalling how and why the “Global War on Terror” spread throughout the Middle East, we must soberly consider what is likely to ensue, should lethal drones be unleashed at the border as a way of curtailing the flow of fentanyl. It is quite plausible, given what happened in the Global War on Terror, that the more missiles which are fired on the U.S.-Mexico border, the fewer people there will be who choose to continue to live there. This should be a matter of common sense even to people ignorant of the details of the disastrous Global War on Terror, and yet the politicians pushing for a new “War on Drugs” somehow have not thought through the likely consequences of their plan, preferring instead to follow their usual “act tough” approach to garner political support for superficially appealing policies. No matter that Plan Colombia, intended to reduce the flow of cocaine to the United States, had the opposite effect and led to the militarization of drug traffickers throughout region, not the renunciation of their business activities. Just as the Global War on Terror has been all but forgotten by politicians keen to “move on” rather than acknowledge their role in creating humanitarian catastrophe throughout the Middle East, Plan Colombia has been memory-holed for the very same reason. Both were abject policy failures. Mistakes were made. Stuff happens. Nothing to see here; time to move on—to Ukraine!

Following the same logic used by both the radical jihadists in Afghanistan, and the cocaine cartels in Colombia, targeted groups at the U.S.-Mexico border who wish to continue to ply their trade, producing and distributing fentanyl and other drugs to the people of the United States, may well set up shop somewhere else, in places where they will be safe from the specter of lethal drones hovering above their heads. If fentanyl is easy to produce in Mexico, it is no less easy to produce wherever the same raw materials can be found. We can expect, then, that if lethal drones are used at the border, fentanyl production and distribution will migrate as a result. Some of the producers will move south, some may relocate to Canada, but it seems far more likely that many of them will opt to use the distribution apparatus they already have in place in the United States to begin or increase synthetic drug production in the very country where fentanyl is being sold.

The illicit drug purveyors may well reason that they will be safer moving their businesses to the United States, rather than further south in Mexico or other parts of Latin America, or up north to Canada. They may find it difficult to believe that the U.S. government would deploy lethal drones in the homeland, thereby directly endangering U.S. citizens. That assumption, however, is false. We already have precedents for such deployments abroad, and even the use of robotic means of homicide within the homeland against U.S. citizens.

The case of Anwar al-Awlaki, a U.S. citizen who was summarily executed by the U.S. government in Yemen without ever having been indicted for a crime, on the basis of evidence never made public to his fellow citizens that he was a “terrorist,” illustrates that the drone killers are ready and willing to inflict capital punishment upon citizens at the executive’s decree. Abdulrahman al-Awlaki, the sixteen-year-old son of Anwar al-Awlaki, was also destroyed, along with a group of his teenage friends, by a missile launched from a drone in Yemen, about two weeks after his father was eliminated, and shortly after the boy had turned sixteen, making him a “military-age male”. To this day, we do not know whether the son was killed because military analysts worried that he would be radicalized by his father’s assassination, for the U.S. government has never explained what happened on October 14, 2011.

It is possible, albeit implausible (given the government’s silence on the matter), that the drone strike which ended Abdulrahman’s life was a mistake, an incredible coincidence that the younger al-Awlaki happened to find himself at the receiving end of a missile intended for somebody else. But the case of U.S. citizen Warren Weinstein, who had been taken prisoner (along with an Italian, Giovanni Lo Porto) by a group of suspected Al Qaeda members, and was also destroyed by a lethal drone, illustrates that, in pursuing their targets, the technokillers are ready and willing to risk harming U.S. citizens not even suspected of criminal activity.

Lest anyone suppose that the U.S. government would draw the line with citizen suspects located abroad, it is important to recognize that the presumption against the use of intentional homicide against citizens has been significantly weakened in the homeland as well, arguably as a result of the U.S. military’s “shoot first, suppress questions later” conduct abroad everywhere on display throughout the Global War on Terror. That homicide should be used to resolve conflict has been normalized in the minds of not only military and political elites but also every random mass shooter who emerges out of nowhere to annihilate a group of people as a way of expressing his discontent. When Micah Xavier Johnson, the Dallas cop killer, was blown up on July 8, 2016, using a robotic device at the behest of David O’Neal Brown, the chief of the Dallas police, nearly no one questioned the wisdom of the decision, though it would have been a simple matter to load the robot with incapacitating sedatives instead. Both of these African American men had been indoctrinated to believe that the way to resolve conflict is to obliterate human beings. Johnson, a military veteran apparently suffering from PTSD, claimed that he felt the need to kill Dallas cops as a way of protesting their killing of innocent black men.

Given these precedents, it seems likely that once lethal drones are deployed in the latest doomed-to-fail War on Drugs, the “War on Fentanyl,” they will be used not only in Mexico, but also in the United States as fentanyl production migrates to the homeland along with those fleeing the missiles being fired near the border. In the face of the overdose epidemic, politicians, goaded by both angry and mourning constituents, feel the need to act, and they will likely be supported by many in the populace in their quest to send out lethal drones—until, that is, innocent family members and neighbors begin to be incinerated in the homeland. At that point, perhaps the nation will finally have its long overdue debate about the policy of summarily executing suspects and the labeling as “collateral damage” of any innocent person unlucky enough to be located within the radius of a missile’s effects. But revisiting the immorality and illegality of killing thousands of unarmed brown-skinned young men in the prime of their lives abroad, on the basis of sketchy evidence which would never hold up in a court of law, while perhaps salubrious for future foreign policy, will have no effect whatsoever on the overdose epidemic.

The only truly effective solution to the opioid crisis, given the manifest failure of both the War on Drugs and the Prohibition, will be to legalize all drugs, making it possible for addicts and recreational drug users alike to buy what they need or want, and to know what they are actually getting. Anyone who wishes to liberate himself from the chains of addiction and return to a semblance of normal life should be assisted in that endeavor. Every addict has a story, and rather than criminalizing all of them, we would do well to take seriously the genesis of the opioid crisis in the United States. Many well-meaning patients, leading perfectly ordinary, noncriminal lives, ended up as junkies because they trusted their doctors who, in turn, trusted the pharma-coopted FDA. To those who worry that legalizing drugs will create even more junkies, there is a ready-made, highly visible anti-narcotics abuse campaign currently underway in every major city in the United States. No rational person would freely choose to wind up in the sorry state of the zombies currently haunting our streets. Rather than pinning up posters of fried eggs captioned “Your brain on drugs,” parents need only to take their children to such scenes to dissuade them from making the mistakes which led to the creation of what appear now to be mere vestiges of human beings.

Unfortunately, instead of viewing the opioid crisis as the humanitarian disaster that it is, some of the very politicians who culpably condoned industry malfeasance for years by refusing to acknowledge its root cause—pharmaceutical industry greed and our captured federal agencies—have decided that the suppliers of fentanyl from Mexico are the latest “bad guys” who must be eradicated from the face of the earth. Stigmatizing drug purveyors as “terrorists” not only will not effectively address the overdose epidemic, but it will further undermine our already crumbling republic. If the use of lethal force against suspected drug dealers is undertaken at the border, it will only be a matter of time before the presumption of innocence in the homeland is inverted into a presumption of guilt, just as occurred in the thousands of drone strikes targeting suspects on the basis of hearsay and circumstantial evidence throughout the Global War on Terror abroad.


Laurie Calhoun is the Senior Fellow for The Libertarian Institute. She is the author of We Kill Because We Can: From Soldiering to Assassination in the Drone AgeWar and Delusion: A Critical ExaminationTheodicy: A Metaphilosophical InvestigationYou Can LeaveLaminated Souls, and Philosophy Unmasked: A Skeptic’s Critique, in addition to many essays and book chapters. Questioning the COVID Company Line: Critical Thinking in Hysterical Times will be published by the Libertarian Institute in 2023.

June 27, 2023 Posted by | Civil Liberties, Deception, Militarism | , , , | Leave a comment

Who Is National Security Adviser Jake Sullivan and Why He Should Debate RFK Jr.

By Rick Sterling | Global Research | June 27, 2023

National Security Adviser Jake Sullivan is one of the key people driving US foreign policy. He was mentored by Hillary Clinton with regime changes in Honduras, Libya and Syria. He was the link between Nuland and Biden during the 2014 coup in Ukraine. As reported by Seymour Hersh, Sullivan led the planning of the Nord Stream pipelines destruction in September 2022. Sullivan guides or makes many large and small foreign policy decisions. This article will describe Jake Sullivan’s background, what he says, what he has been doing, where the US is headed and why this should be debated.

Background

Jake Sullivan was born in November 1976. He describes his formative years like this:

“I was raised in Minnesota in the 1980s, a child of the later Cold War – of Rocky IV, the Miracle on Ice, and ‘Tear down this wall’. The 90s were my high school and college years. The Soviet Union collapsed. The Iron Curtain disappeared. Germany was reunified. An American-led alliance ended a genocide in Bosnia and prevented one in Kosovo. I went to graduate school in England and gave fiery speeches on the floor of the Oxford Union about how the United States was a force for good in the world.”

Sullivan’s education includes Yale (BA), Oxford (MA) and Yale again (JD). He went quickly from academic studies and legal work to political campaigning and government.

Sullivan made important contacts during his college years at elite institutions. For example, he worked with former Deputy Secretary of State and future Brookings Institution president, Strobe Talbott. After a few years clerking for judges, Sullivan transitioned to a law firm in his hometown of Minneapolis. He soon became chief counsel to Senator Amy Klobuchar who connected him to the rising Senator Hillary Clinton.

Mentored by Hillary

Sullivan became a key adviser to Hillary Clinton in her campaign to be Democratic party nominee in 2008. At age 32, Jake Sullivan became deputy chief of staff and director of policy planning when she became secretary of state. He was her constant companion, travelling with her to 112 countries.

The Clinton/Sullivan foreign policy was soon evident. In Honduras, Clinton clashed with progressive Honduras President Manuel Zelaya over whether to re-admit Cuba to the OAS. Seven weeks later, on June 28, Honduran soldiers invaded the president’s home and kidnapped him out of the country, stopping en route at the US Air Base. The coup was so outrageous that even the US ambassador to Honduras denounced it. This was quickly over-ruled as the Clinton/Sullivan team played semantics games to say it was a coup but not a “military coup.” Thus the Honduran coup regime continued to receive US support. They quickly held a dubious election to make the restoration of President Zelaya “moot”. Clinton is proud of this success in her book “Hard Choices.”

Two years later the target was Libya. With Victoria Nuland as State Department spokesperson, the Clinton/Sullivan team promoted sensational claims of a pending massacre and urged intervention in Libya under the “responsibility to protect.”  When the UN Security Council passed a resolution authorizing a no-fly zone to protect civilians, the US, Qatar and other NATO members distorted that and started air attacks on Libyan government forces. Today, 12 years later, Libya is still in chaos and war. The sensational claims of 2011 were later found  to be false.

When the Libyan government was overthrown in Fall 2011, the Clinton/Sullivan State Department and CIA plotted to seize the Libyan weapons arsenal. Weapons were transferred to the Syrian opposition. US Ambassador Stevens and other Americans were killed in an internecine conflict over control of the weapons cache.

Undeterred, Clinton and Sullivan stepped up their attempts to overthrow the Syrian government. They formed a club of western nations and allies called the “Friends of Syria.” The “Friends” divided tasks – who would do what in the campaign to topple the sovereign state.  Former policy planner at the Clinton/Sullivan State Department, Ann Marie Slaughter, called for “foreign military intervention.”  Sullivan knew they were arming violent sectarian fanatics to overthrow the Syrian government. In an email to Hillary released by Wikileaks, Sullivan noted “AQ is on our side in Syria.”

Biden’s adviser during the 2014 Ukraine Coup

After being Clinton’s policy planner, Sullivan  became President Obama’s director of policy planning (Feb 2011 to Feb 2013) then national security adviser to Vice President Biden (Feb 2013 to August 2014).

In his position with Biden, Sullivan had a close-up view of the February 2014 Ukraine coup. He was a key contact between Victoria Nuland, overseeing the coup, and Biden. In the secretly recorded conversation where Nuland and the US Ambassador to Ukraine discuss how to manage the coup, Nuland remarks that Jake Sullivan told her “you need Biden.” Biden gave the “attaboy” and the coup was “midwifed” following a massacre of  police AND protesters on the Maidan plaza.

Sullivan must have observed Biden’s use of the vice president’s position for personal family gain. He would have been aware of  Hunter Biden’s appointment to the board of the Burisima Ukrainian energy company, and the reason Joe Biden demanded that the Ukrainian special prosecutor who was investigating Burisima to be fired. Biden later bragged and joked about this.

In December 2013, at a conference hosted by Chevron Corporation, Victoria Nuland said the US has spent five BILLION dollars to bring “democracy” to Ukraine.

Sullivan helped create Russiagate

Jake Sullivan was a leading member of the 2016 Hillary Clinton team which  promoted Russiagate. The false claim that Trump was secretly contacting Russia was promoted initially to distract from negative news about Hillary Clinton and to smear Trump as a puppet of  Putin. Both the Mueller and Durham investigations officially discredited the main claims of Russiagate. There was no collusion. The accusations were untrue, and the FBI gave them unjustified credence for political reasons.

Sullivan played a major role in the deception as shown by his “Statement from Jake Sullivan on New Report Exposing Trump’s Secret Line of Communication to Russia.”

Sullivan’s misinformation

Jake Sullivan is a good speaker, persuasive and with a dry sense of humor. At the same time, he can be disingenuous. Some of his statements are false. For example, in June 2017 Jake Sullivan was interviewed by Frontline television program about US foreign policy and especially US-Russia relations. Regarding NATO’s overthrow of the Libyan government, Sullivan says, “Putin came to believe that the United States had taken Russia for a ride in the UN Security Council that authorized the use of force in Libya… He thought he was authorizing a purely defensive mission… Now on the actual language of the resolution, it’s plain as day that Putin was wrong about that.” Contrary to what Sullivan claims, the UN Security Council resolution clearly authorizes a no-fly zone for the protection of civilians, no more. It’s plain as day there was NOT authorization for NATO’s offensive attacks and “regime change.”

Planning the Nord Stream Pipeline destruction

The bombing of the Nord Stream pipelines, filled with 50 billion cubic meters of natural gas, was a monstrous environmental disaster. The destruction also caused huge economic damage to Germany and other European countries. It has been a boon for US liquefied natural gas exports which have surged to fill the gap, but at a high price. Many European factories dependent on cheap gas have closed down. Tens of thousands of workers lost their jobs.

Seymour Hersh reported details of How America Took Out the Nord Stream Pipeline. He says, “Biden authorized Jake Sullivan to bring together an interagency group to come up with a plan.” A sabotage plan was prepared and officials in Norway and Denmark included in the plot. The day after the sabotage, Jake Sullivan tweeted

“I spoke to my counterpart Jean-Charles Ellermann-Kingombe of Denmark about the apparent sabotage of Nord Stream pipelines. The U.S. is supporting efforts to investigate and we will continue our work to safeguard Europe’s energy security.”

Ellerman-Kingombe may have been one of the Danes informed in advance of the bombing. He is close to the US military and NATO command.

Since then, the Swedish investigation of Nord Stream bombing has made little progress. Contrary to Sullivan’s promise in the tweet, the US has not supported other efforts to investigate. When Russia proposed an independent international investigation of the Nord Stream sabotage at the UN Security Council, the resolution failed due to lack of support from the US and US allies. Hungary’s foreign minister recently asked,

“How on earth is it possible that someone blows up critical infrastructure on the territory of Europe and no one has a say, no one condemns, no one carries out an investigation?”

Economic Plans devoid of reality  

Ten weeks ago Jake Sullivan delivered a major speech on “Renewing American Economic Leadership” at the Brookings Institution. He explains how the Biden administration is pursuing a “modern industrial and innovation strategy.” They are trying to implement a “foreign policy for the middle class” which better integrates domestic and foreign policies. The substance of their plan is to increase investments in semiconductors, clean energy minerals and manufacturing. However the new strategy is very unlikely to achieve the stated goal to “lift up all of America’s people, communities, and industries.” Sullivan’s speech completely ignores the elephant in the room: the costly US Empire including wars and 800 foreign military bases which consume about 60% of the total discretionary budget. Under Biden and Sullivan’s foreign policy, there is no intention to rein in the extremely costly military industrial complex. It is not even mentioned.

US exceptionalism 2.0

In December 2018 Jake Sullivan wrote an essay titled “American Exceptionalism, Reclaimed.” It shows his foundational beliefs and philosophy. He separates himself from the “arrogant brand of exceptionalism” demonstrated by Dick Cheney.  He also criticizes the “American first” policies of Donald Trump. Sullivan advocates for “a new American exceptionalism” and “American leadership in the 21st Century.”

Sullivan has a shallow Hollywood understanding of history: “The United States stopped Hitler’s Germany, saved Western Europe from economic ruin, stood firm against the Soviet Union, and supported the spread of democracy worldwide.” He believes “The fact that the major powers have not returned to war with one another since 1945 is a remarkable achievement of American statecraft.”

Jake Sullivan is young in age but his ideas are old. The United States is no longer dominant economically or politically. It is certainly not “indispensable.” More and more countries are objecting to US bullying and defying Washington’s demands. Even key allies such as Saudi Arabia and United Arab Emirates are ignoring US requests. The trend toward a multipolar world is escalating. Jake Sullivan is trying to reverse the trend but reality and history are working against him. Over the past four or five decades, the US has gone from being an investment, engineering and manufacturing powerhouse to a deficit spending consumer economy waging perpetual war with a bloated military industrial complex.

Instead of reforming and rebuilding the US, the national security state expends much of its energy and resources trying to destabilize countries deemed to be “adversaries”.

Conclusion

Previous national security advisers Henry Kissinger and Zbignew Brzezinski were very influential.

Kissinger is famous for wooing China and dividing the communist bloc. Jake Sullivan is now wooing India in hopes of dividing that country from China and the BRICS alliance (Brazil,Russia, India, China, South Africa).

Brzezinski is famous for plotting the Afghanistan trap. By destabilizing Afghanistan with foreign terrorists beginning 1978, the US induced the Soviet Union to send troops to Afghanistan at the Afghan government’s request. The result was the collapse of the progressive Afghan government, the rise of the Taliban and Al Qaeda, and 40 years of war and chaos.

On 28 February 2022, just four days after Russian troops entered Ukraine, Jake Sullivan’s mentor, Hillary Clinton, was explicit: “Afghanistan is the model.” It appears the US intentionally escalated the provocations in Ukraine to induce Russia to intervene. The goal is to “weaken Russia.” This explains why the US has spent over $100 billion sending weapons and other support to Ukraine. This explains why the US and UK undermined negotiations which could have ended the conflict early on.

The Americans who oversaw the 2014 coup in Kiev, are the same ones running US foreign policy today: Joe Biden, Victoria Nuland and Jake Sullivan. Prospects for ending the Ukraine war are very poor as long as they are in power.

The Democratic Party constantly emphasizes “democracy” yet there is  no debate or discussion over US foreign policy. What kind of “democracy” is this where crucial matters of life and death are not discussed?

Robert F Kennedy Jr is now running in the Democratic Party primary. He has a well informed and critical perspective on US foreign policy including the never ending wars, the intelligence agencies and the conflict in Ukraine.

Jake Sullivan is a skilled debater. Why doesn’t he debate Democratic Party candidate Robert F Kennedy Jr over US foreign policy and national security?

*

Rick Sterling can be contacted at RSterling1@gmail.com.

June 27, 2023 Posted by | Deception, Militarism | , , , | Leave a comment

Republicans ‘Too Afraid’ to Remove Adam Schiff From Office Over Russiagate Hoax

By Andrei Dergalin – Sputnik – 25.06.2023

Despite being censured in the US Congress, Adam Schiff is in fact doing pretty well for himself and is likely going to “get a promotion for lying to the American people for four years,” says a former Colorado state senator.

The US House of Representatives voted to censure Democratic Rep. Adam Schiff this week for his role in promoting unsubstantiated claims that former US President Donald Trump colluded with Russia.

Former Colorado Senator Ted Harvey (Rep.), however, argued that Schiff deserves worse for essentially lying to the American people while in the capacity of the House Intelligence Committee head.

Despite basically knowing that there was no substance to allegations of Trump colluding with Russia, Schiff told the US public that there was “ample evidence of collusion between the Russian government and the Trump campaign,” Harvey told Sputnik.

“That is everything Schiff said to the American people for four years as the chairman of the intelligence community, he should not just be censured. He should be removed from office,” he said.

Alas, Harvey lamented, the US Republicans are simply “too afraid” to pursue this course of actions and instead managed to make a “martyr” out of Schiff.

“And he is raising money by the boatloads and he is now running for the United States Senate and will get a promotion for lying to the American people for four years,” Harvey mused about Schiff’s prospects. “And instead of being held accountable for that, he’s going to be promoted for that.”

During his tenure as the 45th president of the United States, Donald Trump was hounded by allegations of colluding with Russia in order to be elected in 2016, with said allegations being actively promoted by his political opponents.

Despite the seriousness of the allegations brought against him, an investigation into the alleged Russian election interference led by special counsel Robert Mueller failed to produce conclusive evidence to back claims that Trump campaign members conspired with Russia.

June 26, 2023 Posted by | Deception, Russophobia | | Leave a comment

FLASHBACK: Requiem for the Suicided: David Kelly (2011)

Corbett • 06/24/2023

Watch on Archive / BitChute Odysee / Rokfin Rumble / Substack

FROM 2011: Famed microbiologist and UN weapons inspector Dr. David Kelly became the centre of a dispute between the BBC and the UK government over claims that the government had “sexed up” its dossier on Saddam’s weapons of mass destruction in order to sell the Iraq war to the public. He was found dead on Harrowdown Hill on July 18, 2003. It was ruled a suicide. Today we look at the troubling discrepancies, inconsistencies and questions surrounding that official verdict, and broach the question of what secrets Dr. Kelly may have taken to the grave…

CLICK HERE for mp3 audio and show notes for this video

June 26, 2023 Posted by | Deception, Timeless or most popular, Video, War Crimes | | Leave a comment

Clinical Trial to License RotaTeq, Like Almost All Childhood Vaccines, Did Not Use a Placebo Control

Those attacking RFK are wrong

BY AARON SIRI | INJECTING FREEDOM | JUNE 25, 2023

Robert F. Kennedy, Jr. is on record stating that almost all childhood vaccines were licensed based on clinical trials that did not include a placebo control. He is correct.

Nonetheless, numerous news outlets, such as Stat News in its article titled “Correcting Robert F. Kennedy Jr.’s vaccine ‘facts’”, are stating Mr. Kennedy is wrong because they claim the clinical trial relied upon to license the rotavirus vaccine, RotaTeq, did include a placebo control. They are wrong.

A placebo is defined by the CDC as a “substance or treatment that has no effect on living beings.” This means a saline injection or water drops in mouth.

RotaTeq is administered via oral drops. A “placebo” would have been water drops in the mouth. The control used in the trial, however, included bioactive ingredients including almost all the ingredients in the RotaTeq vaccine itself.

How do I know this? Because in 2018, on behalf of ICAN, we were investigating the control used in each clinical trial relied upon by the FDA to license each childhood vaccine.

In that review, we found that while the package insert for the RotaTeq vaccine says the control in its clinical trial was a “placebo,” when we read the FDA’s clinical trial review for RotaTeq, the ingredients of this so-called “placebo” were redacted:

So, on behalf of ICAN we submitted a Freedom of Information Act Request to the FDA for “Documents sufficient to identify the ingredients of the ‘placebo’ in the prelicensure clinical trials identified in Section 6.1 of the package insert for RotaTeq.”

In a response dated June 14, 2018, the FDA provided the requested documents which clearly show that the control was not a placebo. Rather, it included polysorbate-80, sodium citrate, sodium phosphate, and sucrose.

These same four ingredients are also contained in RotaTeq. The only difference between the vaccine and the control is that RotaTeq also included tissue culture medium and rotavirus reassortments. So, bottom line: the control used in the RotaTeq clinical trial was not a placebo since it included bioactive ingredients.

For example, here is what the NIH explains about sodium phosphate, one of the ingredients in the control:

Sodium Phosphate can cause serious kidney damage and possibly death. In some cases, this damage was permanent, and some people whose kidneys were damaged had to be treated with dialysis (treatment to remove waste from the blood when the kidneys are not working well). Some people developed kidney damage within a few days after their treatment, and others developed kidney damage up to several months after their treatment.

And as these studies and data sheet make clear, polysorbate-80 is far from an inert substance, is bioactive, and can have safety concerns, especially when given to infants.

Bottom line, Robert F. Kennedy, Jr.’s claim that virtually all childhood vaccines were licensed based on clinical trials that did not include a control group that received a placebo is correct. The undisputable evidence for this claim, all from FDA or pharma sources, is detailed on pages 3 to 7 of a response we sent to HHS on December 31, 2018. (In sharp contrast to virtually all other childhood vaccines, the clinical trial relied on to license Pfizer’s Covid-19 vaccine for teenagers 12 to 17 years of age appears to have had a placebo control group, though we are still reviewing that claim.)

Here are copies of the charts from that 2018 response to HHS which show what the control group received in each clinical trial for each childhood vaccine:

It is also why the following claim by Dr. Paul Offit in his article “Should Scientists Debate the Undebatable” is categorically false: “All vaccines are tested in placebo-controlled trials before licensure.”

I would more than welcome a public debate with Dr. Offit on this point and would welcome being proven wrong – would gladly prefer that products injected into babies not have this safety gap. Oh, but wait, Dr. Offit says it is undebatable, which again shows precisely why there must always be complete, uncoerced choice when it comes to any medical product.

What is really incredible about the attacks on Mr. Kennedy is that he has made clear he has no intention of changing anyone’s right to obtain vaccines. Everyone who wants to keep vaccinating will be free to do so. He just wants to assure freedom of choice and help those who are injured by these products.

The media and medical profession’s attack on this position is callous. Just as they care about those injured by infectious disease, as Mr. Kennedy certainly does, they should also care about those injured by vaccines. Mr. Kennedy is clear that we can and should do both. And to his amazing credit, no amount of insult or attack has moved him from his position that we must protect every American, including those injured by these pharma products.

June 25, 2023 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular | | Leave a comment

Re Early Spread, what did President Trump NOT Know

… And why didn’t he know it? Were his advisors concealing key information from him? Here’s what SHOULD have happened ….

BY BILL RICE, JR. | JUNE 24, 2023

A fascinating “what-might-have been” article published by The Brownstone Institute presents evidence that one White House meeting – later cancelled – might have prevented the lockdowns and much of the Covid madness that later ensued.

According to author Eric Hartmann, Stanford scientist Dr. John Ioannidis and a team of other “elite” scientists were set to meet with President Trump. The goal: Let the President know that every scientist didn’t think like Anthony Fauci and Deborah Birx.

(Ioannidis later became famous, or infamous, for showing that, for most citizens, the Infection Fatality Rate for this virus was roughly the same or lower than the death risk of the flu.)

The article’s salient points hinge on my favorite taboo subject – “early spread” – as Ioannidis is among the group who believed many Americans had probably already been infected by this virus by mid-March 2020.

This would mean any lockdowns to slow or stop the spread – or “flatten the curve” – were probably pointless and would cause far more harm than these draconian, unprecedented “mitigation” measures would prevent.

For me, the article also raises this intriguing question: What did certain officials know (about virus origins and spread) … and when did they know this?

Although my formal “science education” ended in 11th grade, my parents and God bestowed me with common sense, which I’m going to employ in today’s thought exercise, which shows what I would have done if I was Donald Trump or if I was the Science King of the World in the first 75 days of 2020.

Something like the events that follow SHOULD have happened in the pivotal, history-changing weeks of early 2020.

The fact something like this did NOT happen provides another giant tell about how corrupt and captured our science establishment has become.

I’m no scientist, but here’s what I would have done ….

The key “known knowable” in the “virus origins” saga is perhaps this nugget of information:

On the last day of December 2019, Chinese officials reported a pneumonia-like illness of “unknown origins” to the World Health Organization.

For the entire global “public health” establishment, this was a Super Bowl-type event.

“Okay, guys, this might be the Big One we’ve all been predicting. Let’s all get hot and prove our expert bonafides and save the world,” etc.

What would I have done when this news hit the Emergency Bat Wire?

First, I would have asked, “Okay, what are the symptoms of this alleged/possible new disease?”

Next, I would have asked: “Is it possible this possible new virus was already infecting people outside of Wuhan?”

Knowing the symptoms of this new disease are almost exactly like Influenza-Like Illnesses (ILI), I would have immediately started looking at all the weekly ILI “Surveillance Reports” produced by all 50 U.S. state health agencies and the CDC.

I would have asked: “Have we had a conspicuous spike of people going to the doctor with similar symptoms? For example, are people getting more flu tests than in previous flu seasons?”

As it turns out, as I showed in a recent article, the answer is/was, “Yes. No doubt.”

The next thing I would have done is told all my public health colleagues: “Guys, we need to develop an antibody assay to test for this new disease ASAP.

After our crack scientists and medical labs had developed a suitable antibody test (China had one by late January 2020), I would have said: “We need to test ‘archived’ blood we already have in storage and see if any Americans had developed antibodies to this virus before, say, Dec. 30, 2019.”

My next Question: “Do we have any stored archived blood we can actually test for Covid antibodies?”

Answer: As it turns out, we do.

The Red Cross (and several other blood-bank organizations) actually collects tens of thousands of pints of blood every single day. One assumes at least some of this blood must be saved for weeks or months.

I would then order that we expedite the testing of every vial of “archived blood” in the country – Blood from California, Washington, New Jersey, Florida, Nebraska, Texas, Alabama  – from all 50 states.

The whole purpose of this exercise would be to provide data and intelligence on how many people may have already been infected by this virus.

As Science King, I’d order that we use our invaluable new antibody-diagnostic tool to test samples collected from October 2019 through February 2020.

This way we could see if more blood donors in January had Covid antibodies than in November. If this was the case, we’d have what some might call “a virus-spread situation.”

Another point I would have made: Why do we have to depend on the Red Cross to provide us blood we can test for antibodies?  We’re the U.S. Government; can’t we start collecting our own blood? Tell people it’s for a good cause – “Science.”

Apparently, the U.S. only had one batch of archived blood that could be tested ….

As  readers of Bill Rice, Jr’s Substack Newsletter surely know by now, the CDC identified ONE tranche of saved Red Cross blood from three states, with that blood having been collected Dec. 13-16, 2019.

But surely this was not the only archived blood that had been saved and could have been tested (given that this was, after all, a “national emergency” – The Mother of All Live Exercises.)

But let’s say this was the only 1,900 vials of blood in the country available for antibody testing.

I would have said: “Okay, let’s at least go ahead and test that blood … but let’s test it as fast as we can …. Before we order the whole country to lock down.”

At some point, these 1,900 pints of Red Cross blood were tested for Covid antibodies, but, to this day, nobody knows WHEN these preserved blood specimens were tested. For all we know, that blood might have been tested by the end of February 2020 (weeks before the lockdowns were ordered) … or in September 2020, nine months after the blood had originally been collected.

All we know is the CDC (itself) published a “study” in late November 2020 telling everyone that at least 39 of those blood donors (2.04 percent of the tested cohort) did test positive for IgG (and/or IgM) antibodies via an ELISA antibody test.

So, to be clear, the dad-blasted virus was here – in at least three U.S. states in November 2019. That’s what the CDC’s own antibody test showed.

And President Trump – and Bill Rice, Jr. – could have known this by March 2020 if the Science officials had just put a “rush job” on the testing project. I mean, how long does it really take to test 1,900 units of blood for antibodies? Probably a couple of days.

I also note that the “Red Cross Antibody Study” results were published AFTER the 2020 presidential election – when the vaccine had already begun to be rolled out.

We also know (I think) President Trump wasn’t told anything like this in the weeks between January and March 2020:

“Mr. President, we’ve got a lot of blood we are currently testing to see if any Americans might have had this virus in November or December 2019. It’s possible, sir, this virus was already spreading pretty widely in America a couple of months ago. If this is the case, lockdowns to slow or stop virus spread probably won’t do much good.”

For what it’s worth, my conjecture is that SOMEONE in our Science/Virus-Fighting Leadership didn’t want the President (and/or the public) to know this non-trivial information. 

Certainly nobody ordered any Red Cross archived blood to be tested as soon as possible.

(Also, just as certainly, no Cracker Jack investigative journalist at The New York Times, Wall Street Journal or “Sixty Minutes” asked any questions like: “Is there any evidence this virus has already been spreading around the world?”)

My main point is that nobody at NIH, NIAID, the HHS, the CDC or any member of the White House’s Covid Leadership Team said, “Let’s hold on here. Let’s see what these blood donor antibody tests tell us.”

When it came to locking down a couple billion people on the planet, why check any antibody test results first?

So what does this basic information tell us?

It tells me “someone” wanted to conceal evidence of early spread in America … that these trusted public health officials didn’t want to “confirm” anything that might stop or “call-off” the lockdowns.

… and, if we didn’t have the lockdowns, we might not have had 250 million Americans lining up to get a rushed, experimental” mRNA “vaccine,” a shot that was mandatory for many Americans if they wanted to keep their jobs or keep attending college.

Eric Hartmann’s article is about a White House meeting that did NOT take place, a meeting that might have changed history for the better if it had taken place. 

Regarding Hartmann’s article, I’d simply highlight the topics that could and should have been brought up at said non-meeting … but weren’t … for some reason.

So what might this reason have been?

My strong hunch is that “someone” (or several people) knew, or at least strongly suspected, that this virus had already spread around the world, including America. 

This prompts one final question: How in the hell could this person or people have known this?

It seems to me they knew what they didn’t want anyone to investigate. They didn’t want anyone to find undeniable evidence of early spread and then publicize said evidence to the entire world. Again, how did these people know or suspect what those investigations would have revealed?

June 24, 2023 Posted by | Deception, Science and Pseudo-Science, Timeless or most popular, War Crimes | , , , , , | Leave a comment

Millions in Taxes & FARA Violations Left Out of Hunter Biden Plea Deal, Critics Say

By Ekaterina Blinova – Sputnik – 24.06.2023

Despite President Joe Biden’s son, Hunter, striking a plea deal with regard to a couple of misdemeanor charges of failing to pay taxes, the scandal haunting the Bidens is not over, according to US legal observers and conservative commentators.

The US’ first son reached a plea agreement with the Department of Justice (DoJ) on Tuesday concerning federal tax and weapon possession charges: Hunter Biden is expected to admit that he withheld $100,000 in taxes in 2017-2018.

However, it’s a far cry from what he really owed to the US government, explained Just the News, an independent media outlet founded by US investigative journalist John Solomon. Citing supervisory IRS agent-turned-whistleblower Gary Shapley, the media outlet pointed out that Hunter has failed to pay about $2.2 million in taxes since 2014.

Earlier this week, Shapley’s bombshell testimony alleging the first son’s tax crimes and the DoJ’s meddling to shield the younger Biden, was made public. The whistleblower insisted that the Hunter’s misdeeds included not only tax evasion but also filing false tax returns since at least 2014: “Altogether it was around $2.2 million,” he told US lawmakers.

However, most of these felonies had been swept under the rug by the DoJ, according to Shapley. The department’s apparent interference in Hunter’s case ranged from refusing to approve search warrants to allowing the statute of limitation to expire in some instances, as per the supervisory IRS agent and his subordinate.

For its part, Hunter’s legal team insists that he had belatedly paid over $2 million in back taxes and penalties, accusing the IRS whistleblowers of a biased approach.

Nonetheless, US legal observers believe that the DoJ’s apparent cover-up of Hunter’s tax affairs and other potential felonies is fraught with the risk of a bigger scandal in the making. In particular, legal scholar Jonathan Turley raised concerns about the “absence of certain charges in the plea deal given to Hunter Biden” in his blog on Saturday.

According to Turley, the DoJ somehow overlooked Hunter acting as a de facto unregistered foreign agent, something that former President Donald Trump’s associate Paul Manafort was promptly accused of. The first son likely violated the Foreign Agents Registration Act (FARA) while striking business deals with foreign entities including in China, Romania and Ukraine during and after his father’s vice presidency, the lawyer pointed out.

What’s more disturbing is that the Justice Department never initiated an investigation into the Bidens’ purported influence-peddling despite allegations of millions of dollars generated from Hunter’s foreign partners, according to Turley. Indeed, the House Oversight Committee has recently unveiled evidence supposedly proving hefty transfers to Biden family members from foreign sources. Still, Attorney General Merrick Garland has so far refused to appoint a special counsel to look into the matter.

The DoJ also appears to be uninterested in investigating bribery allegations involving Hunter Biden and his father as well as a 2017 Whatsapp message with threats from Hunter Biden to one of his Chinese associates, following which the Chinese reportedly sent $5 million to Hunter’s account.

According to Turley, the DoJ, Congressional Democrats and US mainstream media want these stories to disappear. He quoted former Sen. Claire McCaskill (D-Mo.) as saying “Everybody needs to back off!” while addressing GOP investigators and conservative critics.

“Of course, it still remains a challenge to hide an elephant if even one audience member goes looking. Polls show that the public overwhelmingly wants to pull back the curtain and see the elephant,” Turley noted, adding that the simmering scandal will create certain obstacles in the way of Joe Biden’s re-election bid.

June 24, 2023 Posted by | Corruption, Deception | , | Leave a comment

‘Criminal’: Confidential EU Documents Reveal Thousands of Deaths From Pfizer-BioNTech Shots

By Michael Nevradakis, Ph.D. | The Defender | June 23, 2023

Documents released by BioNTech to the European Medicines Agency (EMA) reveal tens of thousands of serious adverse events and thousands of deaths among people who received the Pfizer-BioNTech mRNA COVID-19 vaccine.

The documents, dated Aug. 18, 2022, and marked “confidential,” show that cumulatively, during the clinical trials and post-marketing period up to June 18, 2022, a total of 4,964,106 adverse events were recorded. The documents included an appendix with further details about the specifics about the identified adverse events.

Among children under age 17, 189 deaths and thousands of serious adverse events were reported.

The documents present data collected between Dec. 19, 2021, and June 18, 2022 (the “PSUR #3 period”), in addition to cumulative data on adverse events and deaths that occurred among those who received the vaccine during clinical trials and during the post-marketing period, beginning December 2020 up until June 18, 2022.

During this time, Pfizer-BioNTech said it identified almost no safety signals and claimed the vaccine demonstrated over 91% “efficacy.”

Remarking on the documents, Brian Hooker, Ph.D., P.E., senior director of science and research for Children’s Health Defense, told The Defender :

“These adverse event reports are ‘off the charts,’ with myocarditis reports at over 10,000 and pericarditis reports at over 9,000.

“Historically, we know that this would be an under-ascertainment of the actual numbers. It is criminal for the EMA to keep this vaccine on the market.”

According to an analysis by commentator and author Daniel Horowitz, the percentage of adverse events classified as serious was “well above the standard for safety signals usually pegged at 15%,” and women reported adverse events at three times the rate of men.

Sixty percent of cases were reported with either “outcome unknown” or “not recovered,” suggesting many of the injuries “were not transient,” Horowitz said.

The highest number of cases occurred in the 31-50 age group, of which 92% did not have any comorbidities, making it very likely it was the vaccine causing “such widespread, sudden injury.”

There were 3,280 fatalities among vaccine recipients in the combined cumulative period including the clinical trials and post-marketing, up to July 18, 2022.

According to Horowitz, the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.

The documents are not part of the ongoing court-ordered release of the so-called “Pfizer documents” in the U.S., but according to Horowitz, are pharmacovigilance documents requested by the EMA, the EU’s drug regulator.

The documents were made available to an Austrian science and politics blog, TKP, following “a FOIA [Freedom of Information Act] request from an anonymous reader.” They were subsequently published on March 4. However, once published, no European English-language media outlet appears to have reported on them.

As a result, they remained under the radar until recently, when several independent English-language bloggers discovered and published the documents.

Thousands of pediatric serious adverse events and deaths

The main Pfizer-BioNTech document revealed 9,605 adverse events (3,735 serious) during the PSUR #3 and 25 cases during the clinical trials among children ages 11 and younger. These included 20 fatalities, in children as young as 5 years old.

Causes of these fatalities included dyspnea, cardiac arrest, cardio-respiratory arrest, pyrexia and myocarditis, though “all events were assessed as unrelated” to the vaccine.

In one example listed in the document, an 11-year-old boy died of acute respiratory failure two days after the first dose of the vaccine. In another case, a 6-year-old girl died seven days following her initial dose of complications that included renal impairment, epilepsy, apnea, seizure and “sudden death.”

The document lists another case, that of a 6-year-old boy whose listed causes of death are myocarditis, cardio-respiratory arrest and COVID-19. He died seven days after the first dose of the vaccine, and although autopsy results were “pending,” “the reporter concluded that the death ‘had nothing to do’ with the administration of BNT162b2 [the Pfizer-BioNTech vaccine] and was due to natural causes.”

For children ages 12-17, the document listed 21,945 adverse eventss (19,558 serious) in the post-marketing period and 15 cases during clinical trials. A total of 169 deaths were recorded, with listed causes including dyspnea, pyrexia, cardiac arrest, myocarditis, cardiac failure, seizure and shock.

Nevertheless, the document states “No new significant safety information was identified based on the review of the cases reported in the overall paediatric population.”

‘No safety signals’ despites deaths, injuries of pregnant women and newborns

Pregnant and lactating women also were significantly affected. There were 3,642 post-authorization adverse events and 697 clinical trial adverse events in this population, including spontaneous abortion, fetal death, postpartum hemorrhage, premature separation of the placenta, premature labor or delivery, live birth with congenital anomalies and stillbirths.

Nevertheless, the documentation again states, “There were no safety signals regarding use in pregnant/lactating women that emerged from the review of these cases or the medical literature,” despite two key admissions elsewhere in the documentation.

In one instance, the document stated, “The safety profile of the vaccine in pregnant and/or breastfeeding women was not studied in the pivotal clinical trial and the maternal clinical trial was terminated early due to participant recruitment difficulties.”

And in another instance, Pfizer-BioNTech identified the following as “missing information”:

“Use in pregnancy and while breastfeeding; Use in immunocompromised patients; Use in frail patients with co-morbidities … Use in patients with autoimmune or inflammatory disorders; Interaction with other vaccines; Long term safety data.”

Pfizer-BioNTech stated a “commitment” to track “pregnancy outcome[s] in clinical trials.”

Myocarditis and pericarditis deaths among children, young adults

A notable discrepancy appears in terms of reported cases of myocarditis in the clinical trials as compared to the post-marketing period — one myocarditis case (0.15% of all cases) is listed for the clinical trial period, while 5,422 cases (1.1% of all cases) and 5,458 serious events were reported in the PSUR #3 period.

Of these, 87 cases were fatal and 1,608 were listed as “not resolved.” Among children and young adults, 48 cases were reported for those between the ages of 5 and 11 (two deaths), 366 among 12-15-year-olds (three deaths), 345 among 16-17-year-olds and 968 among 18-24-year-olds (four deaths).

In one instance, an 11-year-old girl developed myocarditis two days after her first dose and subsequently died, with the listed causes of death including myocarditis, respiratory failure, acute cardiac failure and cardio-respiratory arrest.

Separately, a 13-year-old boy developed myocarditis five days after his second dose, and subsequently died of myocarditis, cardiac arrest, multiple organ dysfunction syndromeventricular tachycardia and renal failure.

A 13-year-old girl with no medical history developed myocarditis six days after her first dose and also later died.

In the case of a 19-year-old male who developed myocarditis three days after his third dose and who eventually died, an autopsy “revealed extensive necrosis of the left ventricular myocardium (myocardial necrosis); myocarditis/fulminant myocarditis.”

And a 26-year-old male who also took the flu vaccine developed myocarditis four days after his third dose of the Pfizer-BioNTech COVID-19 vaccine, and subsequently died. The listed causes of death included myocarditis, arrhythmia, inflammation and left ventricular dysfunction. Autopsy results “showed myocarditis.”

Similarly, while no cases of pericarditis were recorded during the clinical trial, 4,156 were recorded during the PSUR #3 period, including 4,164 serious adverse events and 19 fatalities. This included 30 cases among 5-11-year-olds, 118 cases among 12-15-year-olds, 106 cases among 16-17-year-olds, 479 cases among 18-24-year-olds (and one death), and 417 cases among 25-29-year-olds, again including one death.

In one example, a 22-year-old male developed pericarditis 31 days after his second dose and eventually died of pericarditis and other causes, including multiple organ dysfunction syndrome, pericardial masspericardial effusionmalignant pericardial mesothelioma and right ventricular failure.

Numerous other cardiovascular adverse events were recorded, totaling 32,712 cases during the PSUR #3 period (496 fatal) and 27 during the clinical trials (two fatal — with none of the events listed as “related” to vaccination).

Causes of death included in this category include arrhythmia, cardiac failure and acute cardiac failure, cardiogenic shock, coronary artery disease, postural orthostatic tachycardia syndrome (POTS) and tachycardia.

Nevertheless, “No new significant safety information was identified.”

Many ‘very severe and very rare’ adverse events identified

The 393-page confidential Pfizer document shows that Pfizer observed more than 10,000 categories of diagnosis, many “very severe and very rare,” Horowitz wrote.

These include 73,542 cases of 264 categories of vascular disorders from the shots, many of which “are rare conditions,” hundreds of categories of nervous system disorders, totaling 696,508 cases and 61,518 adverse events from well over 100 categories of eye disorders, “which is unusual for a vaccine injury,” according to Horowitz.

In addition, “there were over 47,000 ear disorders, including almost 16,000 cases of tinnitus,” “roughly 225,000 cases of skin and tissue disorders,” “roughly 190,000 cases of respiratory disorders” and “over 178,000 cases of reproductive or breast disorders, including disorders you wouldn’t expect, such as 506 cases of erectile dysfunction.”

“Over 100,000 blood and lymphatic disorders, for both of which there’s a wealth of literature linking them to the spike protein” were indicated, as well as “almost 127,000 cardiac disorders, running the gamut of about 270 categories of heart damage, including many rare disorders, in addition to myocarditis.”

There were also “3,711 cases of tumors — benign and malignant,” and “there were over 77,000 psychiatric disorders observed.”

“What is so jarring is that there are hundreds of very rare neurological disorders that reflect something so systemically wrong with the shots, a reality that was clearly of no concern to the manufacturers and regulators alike,” Horowitz wrote, referencing 68 listed cases of a rare diagnosis, chronic inflammatory demyelinating polyneuropathy.

In another example, the “Pharma Files” Substack identified 3,092 neoplasms, noting that ”malignant neoplasms means cancer.”

Pfizer-BioNTech usually identified ‘no safety signal’ despite thousands of deaths

Numerous deaths and serious adverse events were recorded for a wide range of other conditions:

  • Stroke: 3,091 cases and 3,532 serious adverse events during PSUR #3, including 314 fatalities, and 19 cases during the clinical trial (one death).

The document stated, “Cerebral venous sinus thrombosis … and Cerebrovascular Accident/Stroke were evaluated as signals during the reporting period and were not determined to be risks causally associated with the vaccine … No additional safety signals … have emerged based on the review of these cases.”

  • Respiratory: 2,199 cases and 1,873 serious adverse events during PSUR #3, including 363 fatalities, and 33 cases during the clinical trial (four deaths). Serious adverse events included cardio-respiratory arrest, pneumonia, respiratory failure, acute respiratory failure, hypoxia and acute respiratory distress syndrome. Yet, “No safety signals have emerged based on the review of these cases.”
  • Bell’s palsy: 733 cases were reported during PSUR #3, in addition to 1,428 cases of facial paralysis. Six cases were fatal, with all victims over age 60. One additional case of Bell’s palsy, in a 75-year-old female from the U.S., was recorded in the clinical trial but was deemed “not related” to her vaccination. Again, “No new significant safety information was identified.”
  • Neurological: 5,111 cases and 4,973 serious adverse events during PSUR #3, including 67 fatalities, and 15 cases during the clinical trial. Once more, “No safety signals have emerged based on the review of these cases.”
  • Immune-mediated/autoimmune adverse events: 11,726 cases and 8,445 serious adverse events during PSUR #3, including 133 fatalities, and 19 cases during the clinical trial. Serious adverse events included thrombocytopeniainterstitial lung disease, cerebral hemorrhage, encephalitis, multiple organ dysfunction syndrome, renal failure, pneumonia and pulmonary embolism. Yet, “No new safety signals have emerged.”
  • Multisystem inflammatory syndrome: 207 cases and 210 serious adverse events during PSUR #3, including 56 deaths, with 35 involving the elderly. In addition, 38 cases were reported in children. Nevertheless, “No new safety signals have emerged based on a review of these cases [or] literature.”

Pfizer-BioNTech stated a “commitment” for “closely monitoring multisystem inflammatory syndrome in children and in adults … and reporting of new cases.”

  • Thromboembolic adverse events: 6,102 cases and 6,724 serious adverse events during PSUR #3, including 265 fatalities, and 17 cases during the clinical trial (one death). Serious adverse events included pulmonary embolism, thrombosis and deep vein thrombosis. Again, “No safety signals have emerged based on the review of these cases.”

Elsewhere in the document, the case of a 14-year-old male who died of peripheral swelling after getting the COVID-19 vaccine was mentioned, with no additional details.

In another example, a 67-year-old male “with a history of diabetes and idiopathic thrombocytopenic purpura” suffered chest and gastrointestinal discomfort less than 30 minutes after receiving his third dose of the vaccine. A diagnosis of anaphylaxis was made, while an electrocardiogram showed “signs of a myocardial infarction.” He later sustained cardiac arrest and died 12 days following his vaccination.

Moreover, 204 fatalities (and 24,077 cases) of vaccination failure, 81 deaths from “vaccination stress,” 24 deaths (and 1,402 cases) of suspected vaccination failure, two deaths from glomerulonephritis and nephrotic syndrome, two deaths (1,326 cases) from “medication error” and 166 deaths from “other” adverse events — mostly pyrexia — were recorded.

Pfizer-BioNTech and EMA: ‘nothing to see here’

Pfizer and BioNTech claimed that the overall efficacy of their COVID-19 vaccine for the PSUR #3 period was 91.3% — and 100% for some populations.

Moreover, only one safety signal was definitively identified: hearing loss, with Pfizer-BioNTech committing to perform a “safety evaluation of tinnitus and hearing loss.”

Two other conditions, myocarditis and pericarditis, were determined to be an “important identified risk,” while irritability was determined to be an “identified risk (not important).”

“A statement regarding the reporting rates of myocarditis and pericarditis after primary series and booster doses” was added to their vaccine’s European product label.

Labeling was changed for Guillain-Barré syndrome, but in Japan. The document stated:

“Although not considered by definition a regulatory action taken for safety reasons because it does not significantly impact the benefit risk balance of use of the product in authorised populations, due to the receipt of spontaneous reports of Guillain-Barre syndrome (GBS) after vaccination with mRNA COVID-19 vaccines including BNT162b2 … Japan has required class changes to include GBS in the important precautions section of the Japan package insert.”

Despite the large number of deaths and serious adverse events, Pfizer and BioNTech wrote, “Based on the available safety and efficacy/effectiveness data from the reporting interval for BNT162b2, the overall benefit-risk profile of BNT162b2 remains favorable” and that “no further changes … or additional risk minimization activities are warranted.”

The EMA appears to have agreed with this conclusion. In its “assessment report,” its Pharmacovigilance Risk Assessment Committee (PRAC) wrote that “The benefit-risk balance for the use of Comirnaty in its authorized indication remains unchanged.”

“The PRAC considers that the risk-benefit balance of medicinal products containing tozinameran (Comirnaty) remains unchanged and therefore recommends the maintenance of the marketing authorisation(s),” the PRAC added.

However, Horowitz argues that the documents “show that Pfizer knew about a sickening level of injury early on,” yet continued to distribute its COVID-19 vaccine.

Earlier this month, BioNTech was sued in Germany by a woman alleging injuries from the Pfizer-BioNTech COVID-19 vaccine. The lawsuit demands at least 150,000 euro ($161,500) in damages for bodily harm and unspecified compensation for material damages.


Michael Nevradakis, Ph.D., based in Athens, Greece, is a senior reporter for The Defender and part of the rotation of hosts for CHD.TV’s “Good Morning CHD.”

This article was originally published by The Defender — Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

June 23, 2023 Posted by | Deception, Timeless or most popular, War Crimes | , , | Leave a comment