Facebook’s fake fact-checkers censor medical journal article on alleged safety issues with Pfizer Covid-19 vaccine study

This is a dangerous time, indeed, when self-proclaimed fact checkers and curators are permitted to control information in the name of what they claim is the public good.

This trend was relatively unheard of prior to 2016. Until that time, the shaping and censoring was largely done in an invisible way. Nobody admitted to it because the public wouldn’t have stood for it.

But a successful propaganda campaign I’ve described in my books The Smear and Slanted aimed to convince many in the public to accept third parties telling us what we can cannot know or see.

Obviously, corporate and political interests are behind the efforts, using them to keep the public from seeing or hearing information that is contrary to their paid interests.

This helps explain a lot about Facebook’s indefensible censorship of a factual investigation published in the prestigious British Medical Journal.

The article by Paul Thacker exposed alleged poor practices and quality control issues during Pfizer’s Covid-19 vaccine studies based on whistleblower documentation.

According to the article:

A regional director who was employed at the research organisation Ventavia Research Group has told The BMJ that the company falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events reported in Pfizer’s pivotal phase III trial. Staff who conducted quality control checks were overwhelmed by the volume of problems they were finding. After repeatedly notifying Ventavia of these problems, the regional director, Brook Jackson, emailed a complaint to the US Food and Drug Administration (FDA). Ventavia fired her later the same day. Jackson has provided The BMJ with dozens of internal company documents, photos, audio recordings, and emails.

Paul Thacker, British Medical Journal

Of course this bombshell information is not what vaccine industry interests and their supporters in government and media wanted to be seen. (Pfizer has always denied any wrongdoing. Pfizer, the FDA and CDC all say all vaccines in use in the U.S. are safe and effective.)

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Pfizer documents reveal variety of vaccine side effects

Documents released by the Food and Drug Administration (FDA) reveal that drugmaker Pfizer recorded nearly 160,000 adverse reactions to its Covid-19 vaccine in the initial months of its rollout.

The documents were obtained by a group of doctors, professors, and journalists calling themselves Public Health and Medical Professionals for Transparency, who filed a Freedom of Information Act (FOIA) request with the FDA for their release.

The first tranche of documents reveal that, as of February 2021, when Pfizer’s shot was being rolled out worldwide on an emergency basis, the drugmaker had compiled more than 42,000 case reports detailing nearly 160,000 adverse reactions to the jab.

These reactions ranged from the mild to the severe, and 1,223 were fatal. The majority of these case reports involved people aged between 31 and 50 in the United States.

More than 25,000 nervous system disorders were reported, along with 17,000 musculoskeletal and connective tissue disorders and 14,000 gastrointestinal disorders. A range of different autoimmune conditions were reported, along with some peculiar maladies, including 270 “spontaneous abortions,” and incidences of herpes, epilepsy, heart failure and strokes, among thousands of others.

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Court Orders FDA To Comply With FOIA and Release Information On Pfizer Vaccine – First Batch of Documents Shows Over 1,200 Vaccine Deaths WITHIN FIRST 90 DAYS

The Food and Drug Administration (FDA) released the first batch of documents related to Pfizer’s Covid-19 vaccine after a federal judge ordered that they must comply with a massive Freedom of Information Act (FOIA) request that was filed by a government accountability group called Public Health and Medical Professionals for Transparency.

The esteemed group of more than 30 professors and scientists asked the federal government to share any and all data that factored into the agency’s hasty decision to grant Pfizer’s experimental mRNA vaccine an emergency use authorization (EUA) – which amounts to a trove of over 329,000 documents.

In a shameless effort to bury the information, the FDA challenged the FOIA request in court. After the agency was told that it must turn over the documents, Justice Department lawyers representing the FDA asked a federal judge to allow them an unthinkable 55 years to process the request, saying that they would be able to release just 500 pages a month.

In other words, Elon will make it to Mars way before the documents would be fully released – in the year 2076.

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