Tag: pandemic

US Surgeon General Requests COVID-19 ‘Misinformation’ Data From Big Tech Companies

U.S. Surgeon General Dr. Vivek Murthy issued a request Thursday for information surrounding alleged COVID-19 misinformation from Big Tech companies, community organizations, and healthcare providers.

“Misinformation has had a profound impact on COVID-19 and our response,” Murthy told CNN on Thursday, confirming that he sent a letter to those groups. “Studies have demonstrated that the vast majority of the American public either believes common myths about COVID-19 or thinks those myths might be true. And many of those include myths around the COVID-19 vaccine, so we’ve seen firsthand how misinformation is harming people’s health when it comes to COVID.”

The notice asks the companies to provide “exactly how many users saw or may have been exposed to instances of COVID-19 misinformation,” according to The New York Times. Murthy confirmed the contents of the letter to the news outlet.

The Surgeon General in July 2021 issued an advisory calling COVID-19-related “misinformation” an “urgent threat” in a bid to put public pressure on social media platforms to monitor it.

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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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