Archive for the ‘vaccines’ Category

Five States Sue Pfizer For False Claims, Report Shows Another COVID Shot Risk Factor & the Uncanny Timing of the Rollout

https://karenkingston.substack.com/p/why-are-5-states-suing-pfizer-and

Why Are 5 STATES SUING PFIZER and NOT Moderna?

Pfizer researched and developed their COVID-19 mRNA injections independent of the Operation Warp Speed program while demanding to maintain ownership and control of their human safety data.

June 18, 2024: Yesterday, Attorney General Kris Kobach broke the news that 4 other states will be joining Kansas in suing Pfizer for willfully concealing, suppressing, and/or omitting material evidence regarding the safety and efficacy of their mRNA injections.

Per the lawsuit, the Big pharma giant conspired with individuals from Health & Human Services, the media, universities, social media platforms, and other businesses and organization in order to manipulate the American people into receiving an injection that they would have otherwise declined if Pfizer had accurately disclosed their COVID-19 mRNA clinical data and adverse events reports to the public and US government.

Why Are 5 U.S. States Suing Pfizer and NOT Moderna?

Per this 4-minute video clip, Kobach addresses the unconscionable acts that Pfizer committed and the reason why he and other state Attorneys General are suing Pfizer first, and not Moderna or J&J.  (See link for article and video)

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**Comment**

In short, Pfizer did not participate in the Operation Warp Speed program.  They remained separate to avoid government oversight and to maintain control (and secrecy) of their data reports.  Our government is still guilty of conspiring with them as well as the media by coughing up $1 Billion to promote the shots. This historical lesson shows that the CIA regularly infiltrates the media, but that now it IS the media.  For decades it has planted news stories.

Again, this is not informed consent.  This is propaganda where people are being paid.

Kingston does a great job explaining the intricacies of contracts and how Pfizer has remained separate from government funding, etc.  She questions if five states suing could spell the end of the mRNA injections.  She also recommends contacting your attorney general and state prosecutor’s office to file a similar suit against Pfizer. Texas Attorney General Ken Paxton filed a similar lawsuit against Pfizer last November.

https://www.reuters.com/legal/kansas-accuses-pfizer-misleading-public-about-covid-vaccine-lawsuit-2024-06-17/

Kansas accuses Pfizer of misleading public about COVID vaccine in lawsuit

Article Excerpts:
June 17 (Reuters) – The U.S. state of Kansas on Monday sued Pfizer (PFE.N), opens new tab, accusing the company of misleading the public about its COVID-19 vaccine by hiding risks while making false claims about its effectiveness.
In a lawsuit, opens new tab filed in the District Court of Thomas County, the state said the New York-based drugmaker’s alleged false statements violated the Kansas Consumer Protection Act. It is seeking unspecified money damages……
The lawsuit claims that, beginning shortly after the vaccine’s rollout in early 2021, Pfizer concealed evidence that the shot was linked to pregnancy complications, including miscarriage, as well as inflammation in and around the heart, known as myocarditis and pericarditis.  (See link for article)
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**Comment**
Pfizer has been in trouble for many crimes throughout history, yet doesn’t pay a dime in taxes.  Its own employees have exposed the company’s misdeeds.
Our corrupt public health agencies protect this company, and it’s taken a court of law to even get Pfizer’s trial data, which should be accessible to everyone.
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BREAKING Publication: COVID-19 Vaccines: A Risk Factor for Cerebral Thrombotic Syndromes

Unacceptable Hazard for Blood Clots to the Brain

I have several patients who have suffered multiple strokes after COVID-19 vaccination. The Spike protein is known to circulate in blood as shown by Brogna et al in half of vaccinated patients for at least six months. Other studies have demonstrated the Spike protein directly damages the wall of the blood vessels and causes blood clots.

Rogers et al use the CDC Vaccine Adverse Event Reporting System to compare rates of cerebral thrombosis among COVID-19 vaccine recipients to the large number of individuals who take an influenza vaccine annually. The vast majority of events reported to VAERS are made by doctors and other healthcare providers who have determined the vaccine is the cause of the problem. Compared to influenza vaccines given over 34 years, COVID-19 vaccines in 36 months of use had over 1000-fold increased risk of most blood clot events, and compared to all vaccines combined administered over 34 years, this risk remained at over 200-times greater with COVID-19 vaccination.

This paper did not capture the level of permanent neurologic devastation and disability suffered by these patients. I can tell you that the rates must be very high given the extensive nature of the blood clots reported. These data among others strongly support removing all COVID-19 vaccines and boosters from the market. No one should be put at risk for a serious stroke with any vaccine.  (See link for article)

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https://www.dossier.today/p/pfizer-pro-quo-more-evidence-emerges?

Pfizer Pro Quo: more evidence emerges that drugmakers cut deal to help Biden win election

Another quid pro quo for quid pro Joe?

Anthony Fauci’s new book has granted the public more detail concerning the truly impeccable timing of Pfizer’s mRNA Covid-19 vaccine trial data rollout.

We already know that Pfizer decided to inexplicably delay publishing the results of their mRNA trial from October 2020 to right after the election….

The original deal with Pfizer was negotiated by the Trump Administration during the days of Operation Warp Speed. It paid the pharma giant $19.50 a dose. The Biden Administration would eventually sign off on a deal to give Pfizer approximately $30.48 per dose, resulting in an astronomical 56+% hike from the deal negotiated by the Trump administration.

At the peak of Covid hysteria, Pfizer was bringing in almost $10 billion in net income per quarter, thanks to a 33% mRNA profit margin in the U.S. market.  (See link for article).  

http://

Comedians Finally Get It.  When Will Everyone Else?

For more: 

The FDA is a Front Organization

**UPDATE**

See: The FDA’s War Against America’s Health

Illustrating the fact the FDA is completely and hopelessly bought out, it is now advocating for a 10th COVID gene therapy injection that doesn’t stop transmission, illness, or death.

When will someone notice the emperor has no clothes on?

https://bailiwicknews.substack.com/p/on-fda-buildings-as-virtual-mailboxes

On FDA buildings as virtual mailboxes to project the public illusion of biological product manufacturing regulation.

Part 9 of series.

 

A Bailiwick reader is doing a deep research dive into pre-1972 statutory and regulatory history of some Public Health Service-Health and Human Services divisions, including National Institutes of Health (NIH) and Food and Drug Administration (FDA).

For context, 1972 is the year that ostensible biologics regulation — which is actually non-regulation — transferred from the NIH Division of Biologics Standards to the FDA Bureau of Biologics.

November 1973 is when FDA published a consolidated set of biological product manufacturing non-regulations in the Federal Register.

Administrative rule-making by FDA since 1973 is relatively easy to locate.

Administrative rule-making by NIH prior to 1973 is more difficult to locate.

One of the questions the reader is trying to answer has to do with whether biological regulation authority was ever statutorily established by Congress, for NIH and its precursor organizations, going back to the late 1800s.

Modern-day NIH and FDA officials present historical accounts of how the biological product and vaccine manufacturing regulatory systems began and developed.

But from her research so far, the reader has concluded that their origin-story claims are not supported by the text of the statutes they cite.  (See link for article)

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Important quote:

Since the advent of electronic filing systems, the application and licensing forms have been filed, transferred and stored electronically, and deleted at regular intervals.

There are no technicians in the buildings, there’s no equipment, no sample testing occurs.

It’s all a front: statutes, regulations, procedures, application forms, buildings, addresses, offices, labs, approved applications and licenses sent by FDA back to the factories, everything.

A handful of people at pharma companies know it.

A handful of people at FDA know it.

Go to top link not only for the full article but for the 8 prior parts.  Watt has done a lot of legwork and it deserves to be shared widely.  Things, once again, are not as they seem.  The FDA like the UN, WHO, and WEF should be disbanded.  These organizations are out of control and do ZERO to protect public health.  They all protect their own vested interests.

For more:

Birx Proposes Weekly Testing For Every Cow in America

https://www.dossier.today/p/deborah-birx-proposes-weekly-testing?

Deborah Birx proposes weekly testing for every cow in America to stop bird flu

What is motivating these truly insane suggestions and demands?

In an interview with CNN this week, Deborah Birx suggested the imposition of a massive testing and surveillance regime to combat the possibility of a bird flu pandemic.

Birx, the former White House Coronavirus Response Coordinator, laid out her battle plan against bird flu for CNN’s Kasie Hunt.

“We should be testing every cow, weekly,” Birx declared, adding, “we could be pool testing every dairy worker.”

The good news for Birx is that she would never let the facts and scientific evidence get in the way of her ill-advised ideas. (See link for article)

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**Comment**

Remember, Birx previously served on the board of the Bill Gates-funded Global Fund.  She and former CDC Director Robert Redfield, both Army medical officers, knowingly falsified scientific data and were charged with data manipulation and misleading data presentation.  Since leaving government work she has already earned MILLIONS in the private sector particularly with Big Pharma. This should tell you everything you need to know. 

A few points:

  • There’s no evidence that birds transmit ‘Bird flu’ to humans.
  • There’s no evidence for human to human transmission of ‘Bird flu’.
  • They now need to push the cow to human angle to create fear and to cull our food source which could create shortages.
    • The USDA Food Safety and Inspection Service tested meat from condemned cows. Late last month the agency announced that 95 of 96 culled cows tested negative for viral particles.
    • The agency also experimented with inoculating meat with high levels of the virus and then cooking it and testing for the virus. The virus was not detected in the meat patties cooked to medium or well-done, and it was “substantially inactivated” in the rare patties.
    • The FDA also tested retail dairy products in 17 states and noted that PCR-positive results “do not necessarily represent live virus that may be a risk to consumers,” so when they found PCR-positive samples, they further tested them through a process called “egg inoculation.”  The agency found many samples with positive PCR tests, but none tested positive for the live virus.
  • Continued reliance upon a faulty PCR test which was never intended to diagnose illness will only raise case counts (similarly to COVID) to further induce fear so people will submit to yet another dangerous injection that doesn’t work.
  • Finland is already offering the ‘vaccine’ to select groups.
  • Evidence suggests that the current ‘bird flu’ in the U.S. is due to ‘gain of function’ research being done at the University of Wisconsin – Madison and in Athens, Georgia.  Remember that Yoshihiro Kawaoka (WI) and Ron Fouchier (Netherlands) have been pushing the virus to infect humans and Wisconsin has already had a safety breach.
  • FDA Commissioner Robert Califf’s pronouncements about a potential bird flu pandemic appears suspect in light of the fact it came right before the vote on the (WHO) pandemic treaty and amendments to the IHR. 
  • Lots of money is involved:
    • The federal government last month announced a new round of funding to reduce the impact of bird flu. The plan appropriated $93 million for the CDC to do virus genomic sequencing, increase monitoring of farmworkers, and improve and expand testing on a national scale for bird flu in animals, wastewater, farmworkers and meat.
    • The FDA also appropriated an additional $8 million to surveil and test the commercial milk supply.
    • Lactating dairy cows must be tested for bird flu before they can cross state lines, per an April 24 Federal Order issued by the USDA.
    • Federal authorities announced in May they would pay farmworkers to get tested and offer incentives to farmers to allow their dairy herds to get tested.  Workers are paid $75 for giving the CDC a blood sample and nasal swab.
All of this is déjà vu. 
We aren’t doing Bird Flu.

Fauci in the Hot-Seat While Other Culprits Go Free

Government bureaucrat Dr. Anthony Fauci has abused his power since beginning his career with NIAID in 1984.  He has directly influenced medicine and health policy world wide yet has never actually treated a patient since his initial four year internship and residency.

Some of his other crimes are:

But, it’s important to remember that while he was certainly complicit and at the very least agreed to and promoted destructive decisions knowing they would yield unprecedented chaos and ruin, along with Francis Collins, Rochelle Walensky, and many, many others, the National Security Council (NSC) was OZ behind the curtain.  This group advises the President on matters of national security – you know, people who advise about war and terrorism.

Ponder this fact for a moment.

War and terrorism.  Not public health.  
This should reframe everything in a quick hurry.

As noted by Debbie Lerman, nobody’s asking the right questions of the right people.  

Regarding the anti-scientific 6ft social distancing rule, it was based on the NSC’s lockdown-until-‘vaccine’ policy, meant to keep everyone terrified and isolated until the application of the miraculous mRNA ‘countermeasures’.

On March 19, 2020 FEMA assumed the lead for the federal response to COVID which was unannounced, unprecedented, and Lerman believes to be illegal. Formerly, and by law, HHS has been designated as Lead Federal Agency for pandemic responses in every document leading up to COVID until FEMA took over, whose parent agency is the Department of Homeland Security (DHS).  

As noted by Lerman, Dr. McCormick in the video below, and so many others, ALL the directives given by talking heads from public health agencies was not based on actual science or public health policy.  

http://  Approx. 6 Min

Dr. McCormick Rips Fauci a New One

June 4, 2024

In the most recent Circus act, I mean Congressional hearings, Representative Rich McCormick, who is a decorated veteran and ER physician who treated COVID patients from beginning to end, had much to say to Dr. Anthony Fauci about his mishandling of the ‘pandemic,’ and the fact it will have have devastating effects far into the future.

“It’s been proven that if you make it difficult for people in their lives, they lose their ideological bull-shit and they get vaccinated.”  ~ Dr. Anthony Fauci

“Everything I was censored on, I was proven to be right.” ~ Dr. McCormick

It is frightening that so many doctors, politicians, and leaders walked in lock-step behind absurd edicts which not only included peddling a brand-new, never used in humans mRNA gene therapy injection, as well as dangerous, ineffective drugs, including drugs used for lethal injection to treat COVID patients by sedating them for mechanical ventilation, both of which proved to be death sentences.

Dr. Mike Yeadon recently stated that 3 years worth of midazolam was used in a matter of weeks in the UK.

Then there’s the unprecedented vilification and cruelty of anyone who refused the clot shots, which is still going on – particularly by WHO Director-General Dr. Tedros Adhanom Ghebreyesus.

Fauci is guilty of many, many things but so are others.

For a well written article on the cruel loss of reason in the medical community: https://www.midwesterndoctor.com/p/the-price-of-truth-vs-deception-in

Go here to listen to Dr. Jay Battacharya professor of health policy at Stanford University, co-author of the Great Barrington Declaration, and a plaintiff in Murthy v. Missouri, a landmark free speech case against the Biden Administration who states that the catastrophic response during COVID will happen again until there’s an explicit repudiation of the doctrine by ‘public health.’

“The International Health Regulations and the WHO treaty are a way to essentially institutionalize this paradigm of how to manage pandemics going forward. You can’t have a Sweden next time that bucks the agenda.”  ~ Dr. Jay Battacharya

And for a bigger picture of why this all matters: https://madisonarealymesupportgroup.com/2024/05/21/rats-jumping-ship-covid-cover-up-uns-secret-plan-schwab-steps-down/

Vaccine Hesitancy in Lyme Borreliosis; Lancet Infectious Diseases

https://www.change.org/p/the-us-senate-calling-for-a-congressional-investigation-of-the-cdc-idsa-and-aldf/u/32649858?

Vaccination hesitancy in Lyme borreliosis; The Lancet Infectious Diseases

Carl Tuttle
Hudson, NH, United States
Jun 2, 2024

Please see the complaint below addressed to the Editor-in-Chief, The Lancet Infectious Diseases…

-Carl Tuttle

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: u.hofer@lancet.com
Cc: marco.deambrogi@lancet.com, saleha.hassan@lancet.com, infectiousdiseases@lancet.com, ombudsperson@lancet.com, weboffice@lancet.com, editorial@lancet.com, cope_assistant@publicationethics.org, raymond_dattwyler@nymc.edu, paul_arnaboldi@nymc.edu
Date: 06/02/2024 12:04 PM EDT
Subject: Challenges to the publishing ethics of the journal—eg, conflicts of interest

The Lancet Infectious Diseases

Vaccination hesistancy in Lyme borreliosis
https://www.thelancet.com/journals/laninf/article/PIIS1473-3099(24)00221-4/abstract

Raymond J Dattwyler, Paul M Arnaboldi

Published:May 31, 2024

“Although most patients respond well to appropriate antibiotic treatment, a subpopulation of individuals has ongoing symptoms after treatment. The cause of this post-treatment syndrome remains undefined.”  – Raymond J Dattwyler

June 2, 2024

The Lancet Group
125 London Wall
London, EC2Y 5AS, UK
Attn: Ursula Hofer, Editor-in-Chief, The Lancet Infectious Diseases

Dear Dr. Hofer,

Dr. Raymond Dattwyler owns 24 patents for Lyme disease that include diagnostic testing and vaccines both live bacteria and oral. How is this not a conflict of interest when publishing on the subject of vaccination in Lyme borreliosis?

Please correct the COI statement on Dattwyler’s publication.

As someone who has published on the subject of “Bacterial longevity” and “Outgrowing antibiotic action,” you may want to ask Dr. Dattwyler why he has not responded to my 2023 inquiry below:

Respectfully submitted,
Carl Tuttle
Independent Researcher
Hudson, NH USA

Cc: Iratxe Puebla, Facilitation and Integrity Officer
Committee on Publication Ethics (COPE)

Inquiry to Dr. Raymond Dattwyler:

———- Original Message ———-
From: CARL TUTTLE <runagain@comcast.net>
To: Raymond_Dattwyler@nymc.edu
Cc: npjvaccines@nature.com, abarrett@utmb.edu, R.W.Titball@exeter.ac.uk, mgomesso@uthsc.edu
Date: 01/06/2023 2:46 PM EST
Subject: The year that shaped the outcome of the OspA vaccine for human Lyme disease

npj Vaccines Jan 2022

The year that shaped the outcome of the OspA vaccine for human Lyme disease
https://www.nature.com/articles/s41541-022-00429-5

Raymond J. Dattwyler & Maria Gomes-Solecki

Department of Microbiology and Immunology
New York Medical College
Valhalla, NY
Raymond J. Dattwyler, Corresponding Author

Dear Dr. Dattwyler,

I read your manuscript with great interest as you call attention to a treatment-resistant Lyme arthritis with “no evidence of DNA” found in the joints of patients after antibiotic treatment.

For some strange reason however, I could not find the following 1995 publication within your paper identifying treatment-resistant neuroborreliosis:

European Neurology 1995

Seronegative Chronic Relapsing Neuroborreliosis
https://www.karger.com/Article/Abstract/117104

Lawrence C., Lipton R.B., Lowy F.D., Coyle P.K.d

Abstract

We report an unusual patient with evidence of Borrelia burgdorferi infection who experienced repeated neurologic relapses despite aggressive antibiotic therapy. Each course of therapy was associated with a Jarisch-Herxheimer-like reaction. Although the patient never had detectable free antibodies to B. burgdorferi in serum or spinal fluid, the CSF was positive on multiple occasions for complexed anti-B. burgdorferi antibodies, B. burgdorferi nucleic acids and free antigen.

In fact, Dr. Dattwyler there seems to be a great deal of “treatment-resistant” evidence published in multiple journals over the past three decades:
 
Peer Reviewed Evidence of Persistence of Lyme Disease Spirochete Borrelia burgdorferi and Tick-Borne Diseases (700 References)
https://www.dropbox.com/s/n09sk90eo6xz7ua/700%20articles%20LYME%20EvidenceofPersistence-V2.pdf?dl=0

So that brings me to the reason for this email…

Question:

Does a chronic relapsing seronegative disease fit the vaccine model? If not, would that, in and of itself, be the hidden reason for denying chronic (treatment-resistant) Lyme disease for almost three decades? In other words, patent royalties and pharmaceutical profits over lifesaving care?
 
A response to this inquiry is requested.

Carl Tuttle
Hudson, NH

Cc: Alan D.T. Barrett, PhD Editor-in-Chief

Rick Titball, PhD, DSc, Deputy Editor

Letter to the Editor of the BMJ published June 2020
https://www.bmj.com/content/369/bmj.m1041/rr-1

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For the latest Lyme disease ‘vaccine’ candidates:  https://www.precisionvaccinations.com/vaccines/lyme-disease-vaccines