“Given the extensive, well-documented SAEs and unacceptably high harm-to-reward ratio, we urge governments to endorse a global moratorium on the modified mRNA products…” — Cureus, Journal of Medical Science.
No media. No mea culpa. They are on a death march.
Think of all those poor souls who lost their jobs, their college placements, their livelihoods for having the temerity to think.
Cureus, Journal of Medical Science, is a web-based peer-reviewed open access general medical journal using prepublication peer review.
By: Frank Bergman, Slay News, January 26, 2024:
A group of world-renowned researchers has published a groundbreaking new study on soaring sudden death rates and called on governments to ban Covid mRNA shots globally.
In a peer-reviewed paper published on Wednesday, researchers re-analyzed the Pfizer COVID-19 vaccine phase 3 trial data.
However, the researchers uncovered evidence of far more serious adverse events among those in the vaccine group.
This is not what published reports from Pfizer’s phase 3 trials said.
“Many key trial findings were either misreported or omitted entirely from published reports,” the researchers said.
The study was conducted by seven top researchers:
M. Nathaniel Mead
Peter A. McCullough
In the study’s paper, the researchers explained that they set out to re-analyze Pfizer’s trial data because:
our understanding of covid vaccinations and their impact on health and mortality has evolved substantially since the first vaccine rollouts; and, problems with the methods, execution, and reporting of the pivotal phase 3 trials have emerged.
On Wednesday, they published their findings in a peer-reviewed paper titled “Covid-19 mRNA Vaccines: Lessons Learned from the Registrational Trials and Global Vaccination Campaign.”
The paper was published in the renowned Cureus, a journal of medical science.
“Re-analysis of the Pfizer trial data identified statistically significant increases in serious adverse events (SAEs) in the vaccine group,” the researchers wrote.
Adding, “Numerous SAEs were identified following the Emergency Use Authorisation (EUA), including death, cancer, cardiac events, and various autoimmune, hematological, reproductive, and neurological disorders.”
The EUA the researchers are referring to is the authorization granted to Pfizer by the U.S. Food and Drugs Administration (FDA).
As the paper noted, Pfizer’s Covid vaccines never underwent adequate safety and toxicological testing, according to previously established scientific standards.
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