No More Fake News
by Jon Rappoport
ONE: A bombshell. Alex Berenson, former New York Times reporter, August 6: “Covid vaccine maker Moderna received 300,000 reports of side effects after vaccinations over a three-month period following the launch of its shot, according to an internal report from a company that helps Moderna manage the reports.”
“That figure is far higher than the number of side effect reports about Moderna’s vaccine publicly available in the federal system that tracks such adverse events.”
BOOM. 300,000 vaccine adverse effects NOT reported to VAERS, the federal database.
Berenson: “The 300,000 figure comes from an internal update provided to employees by IQVIA, a little-known but enormous company that helps drugmakers manage clinical trials. Headquartered in North Carolina, IQVIA has 74,000 employees worldwide and had $11 billion in sales last year.”
“Earlier this week, Richard Staub, the president of IQVIA’s Research & Development Solutions division, sent a ‘Q2 2021 update’ which was labeled ‘Confidential – For internal distribution only’.”
“A person with access to the presentation provided screenshots of the relevant slide, which clearly explains the 300,000 side effect reports were received over ‘a three-month span’ – not since the introduction of the vaccine in December…”
TWO: Independent researcher Virginia Stoner has issued a stunning new report on the VAERS numbers, and the effort by mainstream scientists to minimize the destructive effects of the COVID vaccines.…
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.
According to health practitioner and writer Craig Stellpflug in his article ‘Big Pharma: Getting away with murder’(2012), the strategy is to get in quick, design the study to get the result you want, get out fast and make lots of money.
If a study comes up negative for your favorite drug, just don’t publish it! 68 per cent of all drug studies are swept under the carpet to keep those pesky side effects from being reported. Only 32 per cent of studies come up positive and a lot of those studies are ‘shortened’ to limit the long-term findings. Studies cut short were found to overestimate the study drug’s effectiveness and miss dangerous side effects and complications by an average of 30 per cent. This would explain the amazing 85 per cent drug study success rate in the hands of Big Pharma according to the Annals of Internal Medicine.”
Childrens Health Defense
These numbers reflect the latest data available as of Jan. 29 from the CDC’s Vaccine Adverse Event Reporting System website. Of the 501 reported deaths, 453 were from the U.S. The average age of those who died was 77, the youngest was 23.
As of Jan. 29, 501 deaths — a subset of 11,249 total adverse events — had been reported to the Centers for Disease Control and Prevention’s (CDC) Vaccine Adverse Event Reporting System (VAERS) following COVID-19 vaccinations. The numbers reflect reports filed between Dec. 14, 2020, and Jan. 29, 2021.
VAERS is the primary mechanism for reporting adverse vaccine reactions in the U.S. Reports submitted to VAERS require further investigation before confirmation can be made that an adverse event was linked to a vaccine.
As of Jan. 29, about 35 million people in the U.S. had received one or both doses of a COVID vaccine. So far, only the Pfizer and Moderna vaccines have been granted Emergency Use Authorization in the U.S. by the U.S. Food and Drug Administration (FDA). By the FDA’s own definition, the vaccines are still considered experimental until fully licensed.
According to the latest data, 453 of the 501 reported deaths were in the U.S.…
Mint Press News
The most significant scientific discovery since gravity has been hiding in plain sight for nearly a decade and its destructive potential to humanity is so enormous that the biggest war machine on the planet immediately deployed its vast resources to possess and control it, financing its research and development through agencies like the National Institutes of Health (NIH), the Defense Advanced Research Projects Agency (DARPA) and HHS’ BARDA.
The revolutionary breakthrough came to a Canadian scientist named Derek Rossi in 2010 purely by accident. The now-retired Harvard professor claimed in an interview with the National Post that he found a way to “reprogram” the molecules that carry the genetic instructions for cell development in the human body, not to mention all biological lifeforms.
These molecules are called ‘messenger ribonucleic acid’ or mRNA and the newfound ability to rewrite those instructions to produce any kind of cell within a biological organism has radically changed the course of Western medicine and science, even if no one has really noticed yet. As Rossi, himself, puts it: “The real important discovery here was you could now use mRNA, and if you got it into the cells, then you could get the mRNA to express any protein in the cells, and this was the big thing.”…