PFIZERLEAK REDUX - THE REAL REASON WHY YOUR GOVERNMENT KEEPS THE PFIZER CONTRACTS SECRET FOR 10 YEARS.

(thread)

Deep within the contracts that countries have signed with Pfizer are clauses that put the democracy of these countries under immediate, imminent threat.

#PfizerLeak Image
All democracies have (with some variations) at least three branches: "legislative, executive and judicial... each branch has its own powers and responsibilities."

Here is, for example, the US:
house.gov/the-house-expl… Image
When an executive branch creates laws and/or intervenes in court's decisions, we call that country a totalitarian state.

When a foreign power dictates to another country its laws, we call that country a banana republic, and all banana republics are totalitarian.

#PfizerLeak The phrase banana republic ...
The clauses you are about to read appear, with slight variations, in non-retracted contracts that I have seen so far. The only exception is the EU/EC contract (more on that below).

I will use the Brazilian contract due to its authenticity.
senseofawareness.com/2021/07/31/pfi…

#PfizerLeak
9.4 Waiver of Sovereign Immunity:

"Purchaser also expressly and irrevocably waives the
application of any Law in any jurisdiction that may otherwise limit or cap its obligation to pay damages arising from or in connection with any Indemnified Claims."

#PfizerLeak Image
9.4 (cont)
"...the Person signing this Agreement on its behalf has actual authority to waive such immunity and bind Purchaser and the State of Brazil to the limitations
of liability and liability waivers set forth herein."

#PfizerLeak Image
9.5 Conditions Precedent to Supply:
“Purchaser…will continue to have adequate statutory or regulatory authority and adequate funding…(to) fulfill the indentation obligations and provide adequate protection from liability... in connection with the Vaccine or its use"
#PfizerLeak Image
"a condition precedent to supply… requires that Purchaser shall implement and maintain...such statutory or regulatory requirements…sufficient to meet it obligations … shall maintain such statutory and regulatory requirements… for as long as necessary."

#PfizerLeak Image
"The sufficiency of such statutory or regulatory
requirements or funding appropriation shall be in Suppliers’ sole discretion."

#PfizerLeak ImageImage
"Suppliers’ supply...is in reliance...(that)...Purchaser implementing and maintaining in effect the requirements and funding and other representations and warranties made by Purchaser under this Agreement"

#PfizerLeak Image
END OF QUOTES.

In a democracy, it is the role of the legislative branch to pass laws and budgets, the executive branch executes, and the judiciary has oversight.

If a contract requires legal adjustment, it must pass legislation, and the court must have oversight.

#PfizerLeak
The commitments of the government to Pfizer in sections 9.4 and 9.5 are not only for current laws and regulations but include a commitment "maintaining in effect the requirements" of the "adequate statutory or regulatory authority and adequate funding."

#PfizerLeak ImageImageImage
The commitments in this contract include obligations that supersede the executive branch power as it has legal, monetary, and judiciary implications.

In a democracy such commitment requires legislative changes, as well as oversight of the judiciary.

#PfizerLeak
Even if a parliament voted to approve the contract with Pfizer (and in most countries it didn't), unless the un-retracted version was debated upon, then voted for, there is a path for a judiciary challenge.

Below you can see the long term impact of the contract:

#PfizerLeak
1) The supply agreement is for 2 years, and can supersede the existing government as happened in Israel.

#PfizerLeak
2) The ability of Pfizer to cease any asset or any territory in case of contract breach which would occur beyond the government period is an example of long term obligation.
3) Most countries did not have special rules for vaccine liability protection (source: "COVID-19 Vaccine Cross-Border Liability and Compensation", RAND institute). The parliament in these countries should have voted to change the law.

rand.org/pubs/presentat…

#PfizerLeak Image
4) These clauses include a commitment of the government that "Pfizer decides whether the statutory or regulatory requirements or funding appropriation is correct". There is no time limitation here.

Pfizer becomes the legislator and judge that controls the contract.

#PfizerLeak
5) When a vaccine is defined as "any device, technology, or product used to enhance the use or effect of, such vaccine" (1.57), this contract introduces clauses that can diminish citizen's birthright for bodily autonomy and freedom of movement, against all laws.

#PfizerLeak
TO SUMMARIZE: our governments signed a contract in secrecy, making commitments that diminish the role of the parliament and the judiciary, and might introduce technologies that might have an impact on our fundamental freedoms.

Our democracy is in danger.

#PfizerLeak
Ask yourself:
How can we know what other contracts our governments signed or what contracts would they sign next (in secrecy) which might empty our democracy even further?

Unless we stop it, we will all be living in totalitarian state, in a banana republic.

Ehden

#PfizerLeak Image
This topic first appeared in my blog. There are other topics there as well, you are invited to it and to my telegram channel t.me/eh_den.

Bless you all!

senseofawareness.com/2021/08/07/pfi…
The EC contracts are different and the clauses above are not there, However:
1) This is a form of legislation, which should have been voted in the European Parliament and IT DIDN'T.
2) Indemnification clauses are there.
Totalitarian states comes in different flavors.

#PfizerLeak ImageImage
EU/EC:
In 2017 the European Court of Justice (ECJ) said vaccine injured party can bring "serious, specific and consistent evidence" and it can prevail if it shows vaccine is "the most plausible explanation for the occurrence of the damage".

curia.europa.eu/juris/document…

#PfizerLeak ImageImage
The contract the EC signed on behalf of EU member states is creating a landscape where the member states must indemnify & defend the vaccine manufacturers against their own citizens based on a contract that was signed in secrecy.

This is not how democracy works.

#PfizerLeak
All deals with the devil are based on desire for power; killing democracy gives a government more power.

Governments used a state of emergency regulations (temporary extra power) to sign contracts in secrecy which gives them more power.

This is why they signed it.

#PfizerLeak

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More from @eh_den

May 14
Pediatric Moratorium! Adult Use Restrictions! Veterinary Prohibition!
"Codon Optimization in mRNA Vaccines and Gene Therapies: An Assessment of Protein Misfolding Risks and Regulatory Oversight" submitted to the FDA's Vaccines and Related Biological Products Advisory Committee!
Here's the Executive Summary

Objective: This white paper evaluates the scientific evidence and regulatory oversight related to codon optimization in messenger RNA (mRNA) vaccines and gene therapies for both human and animal applications. Its primary goal is to assess whether the potential risks—specifically protein misfolding, aggregation, and associated diseases like amyloidogenesis and prionogenesis—justify a moratorium on this technology’s use. The analysis aims to inform policy by balancing innovation with safety.

Scope: The assessment covers the principles of codon optimization, the mechanisms of protein folding and misfolding during translation, and the risks of amyloid formation and prion-like propagation. It reviews regulatory frameworks, including the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) Chemistry, Manufacturing, and Controls (CMC) requirements. The scope includes a detailed examination of scientific literature—both foundational and recent—such as studies on tissue-specific codon usage, codon context effects, and structural risks in mRNA vaccines. It also analyzes preclinical and clinical safety data, pharmacovigilance reports, and a case study on COVID-19 mRNA vaccines. Additionally, the paper explores implications for veterinary vaccines and food chain safety, concluding with an updated risk management and policy evaluation.

Key Findings: Codon optimization enhances protein production in mRNA-based vaccines and therapies but introduces risks that challenge its presumed safety. New research shows that changing codons—previously thought to be neutral—affects translation speed and accuracy, potentially leading to protein misfolding and aggregation. For example, the cardiomyocyte PAO model reveals that misfolded proteins can cause delayed, severe damage, such as heart failure, broadening concerns beyond brain-related diseases. Data from TissueCoCoPUTs indicate that generic codon optimization often mismatches the translation needs of specific tissues, increasing misfolding risks. In COVID-19 mRNA vaccines, structural issues like excessive G-quadruplex formation may heighten these dangers.
Regulatory oversight, however, falls short. There are no standard tests to evaluate how codon changes affect protein shape or clumping, and long-term monitoring is insufficient to detect slow-developing issues like neurodegeneration or prion-like diseases. The rapid rollout of COVID-19 mRNA vaccines lacked thorough evaluation of these folding risks. In veterinary applications, the use of codon-optimized therapies in livestock raises unresolved concerns about misfolded proteins entering the food chain and environment, potentially affecting human health.

Conclusion on Moratorium
Given the mounting evidence of risk and gaps in oversight, a tiered moratorium is recommended as the most cautious and effective approach:

· Pediatric Moratorium: Codon-optimized mRNA vaccines and gene therapies should not be used in children under 18 until safer practices are developed. This includes using tissue-specific codon designs, conducting 24-month safety studies in primates, and setting limits on G-quadruplex formation. Children’s developing tissues are especially vulnerable, and long-term data are lacking.

· Adult Use Restrictions: New clinical trials for risky mRNA designs—those with heavy optimization, high clumping potential, or rich GC content—should pause. This halt would last until advanced tests, such as Kinetic Folding Assurance (KFA), hidden gene screening, and cross-seeding checks, are required.

· Veterinary Prohibition: Codon-optimized gene therapies in animals entering the food supply should be banned. Evidence from the PAO model and prion diseases suggests a risk of transmissible misfolded proteins, posing a threat to food safety.

This moratorium should persist until:
· Reliable tests for protein folding and clumping are part of regulatory standards.
· Codon optimization accounts for tissue-specific needs and translation timing.
· Independent research verifies the safety of high-risk designs and pediatric use.
· Better monitoring systems track long-term health effects.

This approach marks a shift in how codon optimization is viewed: it’s not just a tool for efficiency but a process that demands careful study of its effects on protein structure and safety over time. By adopting these measures, we can protect public health while still advancing mRNA and gene therapy innovations.Image
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The whitepaper has just been published in my Sub/I\Stack (Link in my pro/I\file)!
I published my first article on codon optimization risks and the COVID-19 vaccine in August 2021 (#COptiGate) and wrote extensively on the topic. This white paper, submitted to the @US_FDA, is my final attempt to highlight our regulators' complete failure.
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THE GLOBAL IT OUTAGE YOU WITNESSED WAS NOT AN ACCIDENT!
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Before we begin - introduction.
Hi everyone. My name is Ehden Biber. I'm known as the person behind #PfizerLeak, and most of my writing here on X/Twitter has been on ph@rma related topics. HOWEVER, my professional work has been information security and cybersecurity.
My credentials include:
· Head of information security in Metro Bank (UK).
· Merck/MSD Information security office for Europe, Middle East and Africa (EMEA).
· Consultant to insurance and financial institutes.

The opinion you are about to read is based on YEARS of experience.
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"MEDICAL GENETICS…WILL BE THE SOUL OF PERCISION MEDICINE IN EVERY FIELD"
It is time to expose another member of the W.H.O. science council and her views on genomics and gene therapy (mRNA). Introducing Dr Mary-Claire King.

[Thread]
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Doctor Mary-Claire King is a very known geneticist who has discovered in 1990 BRCA1,which was the first gene for a hereditary form of breast cancer. She is a professor of genome sciences in the university of Washington, Seattle, USA.
medgen.uw.edu/people/mary-cl…
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Her later work was focused on the genetics of schizophrenia, she is recognized as a pioneer in the development of DNA sequencing for human rights investigations, and she is also a Senior Associate Core Member of the New York Genome Center.

nygenome.org/news-events/ne…
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THE COUNCIL: INTRODUCING THE W.H.O. SCIENCE COUNCIL THAT IS ABOUT TO CONTROL YOUR LIFE.
As we approach the final stages of the #WHO coup d'état attempt, it is time to expose the group of unelected people who will control your future and their alarming agenda!
#TheCouncil
[Thread] Image
2/
In December 2023 the WHO produced a report that sets the stage to radical changes that soon will be enforced all the citizens of the world: make gene therapy (mRNA) key technology in the fight against infectious diseases, cancer, and combat any resistance to such technologies. Image
3/
It called to develop new gene therapy treatments against pathogens, promote investment in "equitable" development of the technology, use it as THE medical countermeasure mechanism to tackle pandemic threats, and to combat any resistance to the technology ("misinformation").

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Read 43 tweets

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