Fox News & Newsmax Took Biden Money To Push Deadly COVID Vaccines To Its Viewers

Two days ago, Chris Pandolfo at Blaze Media revealed that his media organization had filed FOIA requests regarding the Biden Administration’s covert funding of the deadly new vaccines and the American corporate media. What they discovered will certainly shock you — and it’s a crucial story that our corrupt media will work hard to make the least covered and least discussed news story of the year.

What did Chris Pandolfo find? He discovered that nearly the entire corporate media took money from the Biden Administration to push the vaccines to their audiences without disclosing it. More importantly, so-called “conservative” media organizations took money from the Biden Administration to spin positive stories about deadly and ineffective vaccines to their conservative viwers who were right to be suspicious — and did not disclose it.

Fox News took the money and said nothing to its conservative viewers.

Newsmax took the money and said nothing to its conservative viewers.

In response to a FOIA request filed by TheBlaze, HHS revealed that it purchased advertising from major news networks including ABC, CBS, and NBC, as well as cable TV news stations Fox News, CNN, and MSNBC, legacy media publications including the New York Post, the Los Angeles Times, and the Washington Post, digital media companies like BuzzFeed News and Newsmax, and hundreds of local newspapers and TV stations. These outlets were collectively responsible for publishing countless articles and video segments regarding the vaccine that were nearly uniformly positive about the vaccine in terms of both its efficacy and safety.

That is the largest and most comprehensive breach of journalistic ethics that has ever occurred. Almost everybody took the money. Almost everybody lied about the vaccines (knowingly or unknowingly). Almost everybody refused to report anything negative about the vaccines — because they were paid to close their eyes. Almost everybody is implicated.

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Bayer Exec Brags mRNA Shots Are ‘Gene Therapy’ Marketed as ‘Vaccines’

Without help from the global pandemic people may never have been convinced to inject themselves with an experimental mRNA gene therapy, a scientist bragged during a world health conference.

Speaking at the opening of the World Health Summit 2021 last November, Bayer Pharmaceuticals Division President Stefan Oelrich admitted were it not for the pandemic, the experimental injection may have seen an extremely high rejection rate.

“We are really taking that leap [to drive innovation] – us as a company, Bayer – in cell and gene therapies,” Oelrich stated.

“Ultimately, the mRNA vaccines are an example for that cell and gene therapy,” Oelrich admitted.

“I always like to say: if we had surveyed two years ago in the public – ‘would you be willing to take a gene or cell therapy and inject it into your body?’ – we probably would have had a 95% refusal rate,” he said, adding, “I think this pandemic has opened many people’s eyes to innovation.”

Oelrich continued: “Our successes over these 18 months [the duration of the COVID ‘pandemic’] should embolden us to fully focus much more closely on access, innovation and collaboration to unleash health for all, especially as we enter, on top of everything else that is happening, a new era of science – a lot of people talk about the Bio Revolution in this context.”

LifeSite News compared Oelrich’s statements to those of globalist World Economic Forum founder Klaus Schwab’s comments about the “Great Reset.”

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Report of Toddler’s Death Disappears from VAERS and CDC Has No Records as to Why!

On December 16, 2021, ICAN, through its attorneys, issued a Freedom of Information Act request to the CDC seeking any documents reflecting why a certain VAERS report was no longer available in the VAERS database. The report described an extremely disturbing incident wherein a two-year-old boy “began bleeding out of the mouth, eyes, nose and ears within six hours” of his first dose of Pfizer’s COVID-19 vaccine on November 18, 2021, and died later that night. On February 14, 2022, the CDC finally responded to ICAN’s request, stating: “A search of our records failed to reveal any documents pertaining to your request.”

Significantly, the CDC has made repeated assurances that “COVID-19 vaccines are being administered under the most intensive vaccine safety monitoring effort in the United States’ history.” The CDC’s VAERS Standard Operating Procedures for COVID-19 even states that the “CDC will perform clinical reviews” for certain “Adverse Events of Special Interest,” which include death, “especially in children (<18 years of age) and recipients of newly licensed vaccines).”

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Whilst you’ve been distracted by Russia’s Invasion, the UK Gov. released a Report confirming the Fully Vaccinated now account for 9 in every 10 Covid-19 Deaths in England

The latest data published by the UK Health Security Agency confirms deaths are rising dramatically among the triple vaccinated population whilst declining steadily among the not-vaccinated population in England.

With the most recent figures showing the fully vaccinated accounted for 9 in every 10 Covid-19 deaths over the past month; and the triple vaccinated accounted for 4 in every 5 of them.

These are dark days for the citizens of Ukraine, but if you were to watch mainstream news or read a mainstream newspaper you could be forgiven for thinking the plight of the Ukrainians is currently the only event taking place in the world.

The Russian invasion is being aired in an endless 24/7 loop via BBC News and Sky News, with not a word about Covid-19 to be heard, despite airing nothing but propaganda and lies on the pandemic for the past two years.

It’s times like these that you ought to watch what bad news is being quietly published in the background in the hope that it won’t receive much attention, because there’s nothing better than an international crisis to distract the public from what’s going on at home.

With that being said, let’s take a look at what the UK Government have “quietly” published in the past week in regards to the Covid-19 situation in England.

The UK Health Security Agency (UKHSA) publish a weekly Covid-19 Vaccine Surveillance Report, the most recent of which was published Thursday 24th Feb 22, and it can be viewed here.

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Booster Shots Causing More Injuries Than Previously Thought, Israeli Survey Shows

More Israelis are experiencing injuries and reactions following COVID-19 booster shots than the country’s passive reporting system indicates, according to a survey conducted by the Israeli Ministry of Health (MOH).

The MOH conducted an active survey of booster shot recipients to collect data on adverse events associated with booster doses, then compared the survey data to the data available from the country’s passive reporting system. 

The survey concluded Israel’s passive reporting system was grossly underreporting adverse events.

The data from the Israeli survey could provide some insight into the extent of the underreporting occurring in the U.S.

It also could corroborate safety signals the Centers for Disease Control and Prevention (CDC) is ignoring.

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The WHO is working on a global vaccine passport system

The World Health Organization will meet with member states and reps from vaccine certification credentials groups to discuss a global vaccine certification system.

Over the last two years, vaccine passports have become compulsory for international travel in some countries.

However, different regions and countries have different standards when it comes to proof of vaccination, meaning a passport that is verifiable in one country might not be verifiable in the other.

The World Health Organization wants to get involved in pulling it all together under a global system.

The WHO says it wants to create a “trust framework,” which will allow the verification of a vaccine passport anywhere in the world, co-founder of the Vaccination Credential Institute (VCI) Brain Anderson told POLITICO.

VCI is the group behind SMART Health Cards, which have been widely adopted in the US, and have become the de facto vaccine credentials standard.

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Just Released Documents by Pfizer Show BioNTech Paid FDA $2,875,842.00 “Drug User Fee” for COVID-19 Vaccine Approval

As the news cycle continues to focus on the Ukraine situation, the FDA complied with a court order to begin releasing 55,000 pages of Pfizer data per month that was used to authorize their COVID-19 vaccine produced with BioNTech, with the first batch quietly released yesterday, March 1st.

There are 150 documents that the public can now download here.

One of the documents released was the “Prescription Drug User Fee Payment” that BioNTech paid to the FDA on 4/20/2021 for the “COMIRNATY COVID-19 mRNA Vaccine” which the FDA subsequently approved in August of 2021.

That “Prescription Drug User Fee Payment” was $2,875,842.00. (Source.)

Another interesting document I found was the “EXTERNAL DATA MONITORING COMMITTEE” found here.

Here is the stated purpose of this “External Data Monitoring Committee”:

This External Data Monitoring Committee (E-DMC) (hereafter referred to as “the committee”) is a single, external,  independent, expert advisory group established to oversee safety and efficacy data from the BNT162 Vaccine Program. The  primary rationale for establishing the committee is to make certain that appropriate external safeguards are in place to help ensure the safety of subjects and to maintain scientific rigor and study integrity while the trial is on-going.

The committee will review accumulating safety data across all studies, as well as efficacy data in the Phase 2/3 portion of the C4591001 study. The committee will advise Pfizer regarding the safety of current participants and those yet to be recruited, as well as the continuing scientific validity of the trial. In addition to safety review by the committee, qualified Pfizer personnel will review safety data as specified in the safety surveillance review plan and will inform the committee of  significant findings. Efficacy data from the C4591001 study will be available to the committee when there is a planned  interim analysis of efficacy or if this is considered necessary to conduct a risk-benefit assessment.

And to make sure that this Committee is doing their job properly to ensure “the safety of subjects and to maintain scientific rigor,” who at the FDA is responsible to make sure this happens?

Well, that would be no one. Pfizer is the one who was responsible, and BioNTech funded it.

“Pfizer is responsible for conducting this study. BioNTech is the regulatory sponsor of this study.”

The committee members are to be free from “conflicts of interest.”

The committee members will complete a CT22-GSOP-RF01 Independent Oversight Committee Member Conflict of Interest Form. Committee members should be free of apparent significant conflicts of interest. Any potential conflict of interest that develops during a member’s tenure on the committee must be disclosed by the committee member.

And who at the FDA is responsible for assuring that this committee who is overseeing “safety and efficacy data” is free from conflicts of interest?

Well, that would be no one. Again, Pfizer is responsible for that.

“Pfizer will determine if any potential conflict requires termination of committee membership.”

The question that then begs to be answered here is, what role did the FDA play, if any, in the “external” monitoring of the data to ensure integrity and safety of a new vaccine about to be injected into hundreds of millions people in the U.S.?

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