Scandal Behind the FDA Fake Approval of Pfizer Jab

30 August 2021 — Origin: New Eastern Outlook

Author: F. William Engdahl

The US Government regulator for drugs, the Food and Drug Administration, has just announced that it has voted full approval for the mRNA genetic vaccine of Pfizer and BioNTech, or did they? This supposed new status is being used by the Biden Administration and many states and companies to impose mandatory vaccinations. The notoriously conflicted Biden covid adviser, Tony Fauci of the NIAID, using that ruling, is calling for national mandatory vaccination for the country. What is not being revealed is the cesspool of corruption and conflicts of interest between the FDA and the major drug companies, including Pfizer, that stand behind the rushed approval. And it’s not full approval for Pfizer’s jab, only for BioNTech’s legally different vaccine.

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Vaccine Billionaires and Human Guinea Pigs

2 July 2021 — Global Research

By Colin Todhunter

How do you make a potentially dangerous and ineffective drug appear like a miracle of modern science? You could, for instance, enrol only certain people in clinical trials and exclude others or bring the study to a close as soon as you see a spike in the data that implies evidence of effectiveness.

There are many ways to do it.

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COVID-19 ‘Vaccines’ Are Gene Therapy

15 March 2021 — Mercola

Analysis by Dr. Joseph Mercola Fact Checked

Story at-a-glance

  • mRNA “vaccines” created by Moderna and Pfizer are gene therapies. They fulfill all the definitions of gene therapy and none of the definitions for a vaccine. This matters, as you cannot mandate a gene therapy against COVID-19 any more than you can force entire populations to undergo gene therapy for a cancer they do not have and may never be at risk for
  • mRNA contain genetic instructions for making various proteins. mRNA “vaccines” deliver a synthetic version of mRNA into your cells that carry the instruction to produce the SARS-CoV-2 spike protein, the antigen, that then activates your immune system to produce antibodies
  • The only one benefiting from an mRNA “vaccine” is the vaccinated individual, since all they are designed to do is lessen clinical symptoms associated with the S-1 spike protein. Since you’re the only one who will reap a benefit, it makes no sense to demand you accept the risks of the therapy “for the greater good” of your community
  • Since mRNA “vaccines” do not meet the medical and/or legal definition of a vaccine, marketing them as such is a deceptive practice that violates the law that governs advertising of medical practices
  • SARS-CoV-2 has not even been proven to be the cause of COVID-19. So, a gene therapy that instructs your body to produce a SARS-CoV-2 antigen — the viral spike protein — cannot be said to be preventive against COVID-19, as the two have not been shown to be causally linked

U.S. And Its Five Eye Partners Use ‘Persuasion’, Sabotage And Disinformation To Gain Vaccine Supremacy

15 March 2021 — Moon of Alabama

The U.S. and some of its allies are engaged in efforts to malign the Russian Sputink V vaccine and to promote the more expensive mRNA vaccines produced by ‘western’ companies.

Back in November we warned that the vaccine competition would be ruthless:
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COVID Vaccine Injury Reports Grow in Number, But Trends Remain Consistent

6 March 2021 — The Defender

Data released today by the CDC confirm several ongoing trends, including that 47% of deaths occurred in people who reported becoming sick within 48 hours of receiving a COVID vaccine, and 20% of vaccine injuries were cardiac-related.

Megan Redshaw 

According to data released today by the Centers for Disease Control and Prevention (CDC), the number of injuries and deaths reported to the Vaccine Adverse Event Reporting System (VAERS) following COVID vaccines continues to climb.

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Dr. Wodarg and Dr. Yeadon File Application for Suspension of All SARS CoV-2 Vaccine Studies and Call for Co-signing the Petition

28 February 2021 — Global Research

First published on December 25, 2020

On December 1, 2020, the ex-Pfizer head of respiratory research Dr. Michael Yeadon and the lung specialist and former head of the public health department Dr. Wolfgang Wodarg filed an application with the EMA, the European Medicine Agency responsible for EU-wide drug approval, for the immediate suspension of all SARS CoV 2 vaccine studies, in particular the BioNtech/Pfizer study on BNT162b (EudraCT number 2020-002641-42).

Dr. Wodarg and Dr. Yeadon demand that the studies – for the protection of the life and health of the volunteers – should not be continued until a study design is available that is suitable to address the significant safety concerns expressed by an increasing number of renowned scientists against the vaccine and the study design.

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Immunologist: Pfizer, Moderna Vaccines Could Cause Long-Term Chronic Illness

9 February 2021 — The Defender

In new research published in Microbiology & Infectious Diseases, immunologist J. Bart Classen warns the mRNA technology used in the Pfizer and Moderna COVID vaccines could create “new potential mechanisms” of adverse events that may take years to come to light.

Hacked emails allegedly detail how EU drug regulator was pressured to approve Pfizer jab despite ‘problems’ with the vaccine

18 January, 2021 — RT

Hacked emails allegedly detail how EU drug regulator was pressured to approve Pfizer jab despite ‘problems’ with the vaccine

A health worker prepares an injection with a dose of the Pfizer/BioNTech COVID-19 ©  REUTERS/Jose Luis Gonzalez

An alleged cache of email exchanges between EU officials and the European Medicines Agency show that the drug regulator was uncomfortable about fast-tracking approval for the Pfizer and Moderna Covid jabs, Le Monde has reported.

China Calls to Suspend Pfizer mRNA Vaccine

16 January 2021 — 21st Century Wire

Chinese health experts have now called on Norway & other countries to suspend the use of the controversial mRNA-based COVID-19 vaccine produced by companies such as Pfizer – due to safety uncertainties following the deaths of 23 elderly Norwegian people.

Watch and help us share this important video report from Friday’s edition of UK Column News

Peter Doshi: Pfizer and Moderna’s ‘95% Effective’ Vaccines — Let’s Be Cautious and First See the Full Data

13 January 2021 — The Defender

Only full transparency and rigorous scrutiny of the data will allow for informed decision making.

In the United States, all eyes are on Pfizer and Moderna. The topline efficacy results from their experimental covid-19 vaccine trials are astounding at first glance. Pfizer says it recorded 170 covid-19 cases (in 44,000 volunteers), with a remarkable split: 162 in the placebo group versus 8 in the vaccine group. Meanwhile Moderna says 95 of 30,000 volunteers in its ongoing trial got covid-19: 90 on placebo versus 5 receiving the vaccine, leading both companies to claim around 95% efficacy.

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Pfizer COVID Vaccine Trial Shows Alarming Evidence of Pathogenic Priming in Older Adults

10 December 2020 — Children’s Health Defense

The Vaccines and Related Biological Products Advisory Committee Briefing Document on the Pfizer-BioNTech COVID-19 vaccine contains disturbing indications that might be a safety signal on pathogenic priming, especially in older adults.

By

James Lyons-Weiler, PhD

Robert F. Kennedy, Jr.

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