In the world of vaccines research Dr. Stanley Plotkin is regarded as such a senior name as to be almost regarded as godfather of vaccines research. In a recent paper he co-authored and published in the New England Journal of Medicine titled ‘Post-authorization Vaccine-Safety Science’ he has questioned important aspects of the existing safety system. (Although several studies quoted in this review are in the context of the USA, these obviously have a wider relevance for safety everywhere).
This paper says,
“Post-authorization studies are needed to fully characterize the safety profile of a new vaccine, since pre-licensure clinical trials have limited sample sizes, follow up durations, and population heterogeneity. It is critical to examine adverse events following immunization (AEFIs) that have not been detected in clinical trials to ascertain whether they are casually or coincidentally related to vaccination.”
Screenshot from NEJM
Further this paper states,
“Although the ACIP (Advisory Committee on Immunization Practices) acknowledges the need, there are currently no resources earmarked for post-authorization safety studies beyond annual appropriations, which must be approved by Congress each year.”
This paper admits that progress in vaccine safety science has been slow.
Further this paper states,
“In 234 reviews of various vaccines and health outcomes conducted from 1991 to 2012, the IOM (Institute of Medicine) found inadequate evidence to prove or disprove causation in 179 (76%) of the relationships explored, illustrating the need for more rigorous science.”
In another important revelation a top official of the USA who was involved with the decisions of the crucial early days of COVID-19 has stated that COVID-19 vaccines were in violation of safety norms.
Robert Redfield was the director of the Centers for Disease Control and Prevention in the USA during 2018-2021, including during the crucial early stage of COVID-19.
He was speaking recently in July 2024 at a hearing of the Senate Committee on Homeland Security and Government Affairs on government oversight of taxpayer-funded high risk virus research. He admitted that the spike protein produced by mRNA vaccines is “toxic to the body” and triggers “a very strong pro-inflammatory response.” He admitted that in his own medical practice he doesn’t administer mRNA vaccine.
He added,
“I do think one of the greatest mistakes that we made, of course, was mandating these vaccines. They should have never been mandated. It should have been open to personal choice.”
He admitted that there was not “appropriate transparency from the beginning about the potential side-effects of these vaccines.”
He expressed disappointment in the US Food and Drug Administration’s (FDA’s) handling of vaccine safety information. He stated, “The FDA should release all of the safety data they have. I was very disappointed to hear that they were planning to hold on to that until 2026. That really creates a sense of total lack of trust in our public health agencies towards vaccination.”
At the same hearing, Senator Ron Johnson highlighted worrying data from the Vaccine Adverse Event Reporting System (VAERS), presenting figures showing over 37,000 deaths following COVID-19 vaccinations, with 24% occurring within two days of injection.
Harvey Risch, Professor Emeritus of Epidemiology at the Yale School of Public Health has recently co-authored a book ‘Toxic Shot: Facing the Dangers of the COVID Vaccine’ in which he has called these vaccines ‘a global catastrophe’ and that “they fail to qualify as real vaccines by any measure.”
His co-author Byram Bridle Ph.D. has written chapters explaining why COVID mRNA shots are not real vaccines, the suppression of information relating to vaccine injuries and the likely mechanisms of immune system harm.
The authors of this book have explored the link between the vaccines and 600,000 unexplained excess deaths, a range of serious side effects including impaired fertility and over 2 million newly disabled people in the USA.
This book has also examined the revolving door relationship between the big pharmaceutical companies and the FDA.
The authors find it monstrous that the COVID vaccinations were ordered to the child vaccines schedules and attendance requirements of many colleges.
A Canada based organization Corelation Research in the Public interest has published a 521 page study this year based on the data of 125 countries which says that the major cause of excess deaths during the pandemic was related to the establishment’s COVID response in the form of lockouts, harmful medical interventions and vaccines.
During this year there have been several US Senate round-table discussions on ‘Federal Health Agencies and the COVID Cartel’. In one such discussion Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense, stated, regarding the situation in the USA, stated
“In 1962 children received five vaccine doses. In 1986 the schedule expanded to 25 doses of five different vaccine formulations. Shortly after the passage of the 1986 National Childhood Vaccine Injury Act, the laws amended to erect a liability shield protecting vaccine manufacturers—and the schedule expanded dramatically: By 2023, 73 doses of 16 different vaccine formulations were given to children up to age 18.”
He added that the FDA approved these formulations with minimal and inadequate safety testing and neglect of the cumulative effect of the vaccine schedule on childhood health outcomes. He added that for every one child that is saved from death from COVID-19, there are 30 child deaths associated with COVID-19 vaccines, so that the risk to benefit ratio in terms of mortality is 30 to 1.
Del Bigtree, CEO of Informed Consent Action Network (ICAN) stated,
“None of the 14 routine vaccines in the CDC’s recommended schedule—was ever put through long-term double-blind placebo based safety trials prior to licensure. Since this type of trial is really the only way to establish a pharmaceutical product is safe, it is misinformation to state that the vaccines are safe.”
“In the 1980s when we were giving 11 doses of about 3 vaccines, the chronic illness rate, which includes neurological and autoimmune disease was 12.8%. Once we passed the 1986 Act and we had the gold rush of vaccines explode…the chronic illness rate, neurological and autoimmune disease skyrocketed to 54%.”
(This data may be even worse today, and apart from vaccines a number of other hazards may have contributed to this increase.)
Bigtree called this the greatest decline of public health. He gave a specific example of Hepatitis B Vaccine. He said,
“The warning lists 50 potential side effects, many of them serious, and that is just the first vaccine given to a baby on their first day of life. The safety study for that Hepatitis B vaccine was only four days long and we had no placebo comprador. That’s not science, that’s insanity.”
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Bharat Dogra is Honorary Convener, Campaign to Save the Earth Now. His recent books include Planet in Peril, Protecting Earth for Children, A Day in 2071 and Man over Machine. He is a regular contributor to Global Research.
Featured image is from NaturalNews
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