1 in 800 die from the COVID jabs. Failure of regulatory agencies

Earlier this month, Marlies Dekkers of De Nieuwe Wereld Podcast interviewed Dr. Robert Malone and Dr. Theo Schetters.

Dr. Malone wrote about the interview and included the video on his substack page, Data doesn’t lie: mRNA-vaccines and correlation to all-cause mortality.

The interview was 1:14:53 long and very informative. I listened to it twice.

Dr. Robert Malone is an internationally recognized scientist/physician and the original inventor of mRNA vaccination as a technology, DNA vaccination, and multiple non-viral DNA and RNA/mRNA platform delivery technologies.

Dr. Theo Schetters developed a vaccine against coccidiosis in chickens (Nobilis® Cox ATM) and a vaccine against Babesia infections in dogs (Nobivac® Piro). He is the inventor of an improved vaccine formulation against diseases associated with Rhipicephalus ticks.

I summarized the salient points in his article.

COVID shots have zero protection

Dr. Schetters: The COVID-19 “vaccine” in the Netherlands has zero protection as of now.

So I always said, it’s like you run with your syringe behind the virus that’s running away from you.

And so, you can never keep up with the mutations. And that is actually that’s what we see now.

Note: Coronaviruses have a high frequency of mutation. Previous attempts to make vaccines against them have been unsuccessful because of the rapid change in the genetic sequences and the development of antibody-dependent enhancement.

Failure of regulatory agencies

Dr. Malone:

The global regulatory community has failed to do its job of insisting on the correct application of the guidance in the international committee on harmonization and the EMA and FDA regs to insist that the pharmaceutical industry does its job.

There was a conscious decision to not force the pharmaceutical companies to do the things that the regulations require, that we’ve all agreed upon over decades…

In the interview, Dr. Malone said that the FDA has different checklists for every product they have to approve.

For the mRNA shots, the FDA investigated them as vaccines instead of gene therapy biologics. That means the FDA did not do the genotoxic, biodistribution, and pharmacokinetics studies that should be done on gene therapy products were not done on the mRNA and vector vaccines.

The FDA allowed Pfizer and Moderna to get away with many things. Listen at 32:00.

1 in 800 who had the COVID-19 jabs die

According to Dr. Shetters, using data from the Netherlands Central Bureau of Statistics and our National Institute of Health,

…there is a good correlation between the number of vaccinations that are given to people and the number of people that die within a week after that.

So let’s say this week, we gave 10,000 vaccinations. Then this week, we have something like 125 excess death in that week (Dr. Malone’s note – that equals 800 deaths per 100,000 or 1/800 in the 60+ cohort).

In the Netherlands, only 60+ years old are given booster shots. The graph below shows the rise in excess mortality following COVID-19 boosters.

Source: Data doesn’t lie: mRNA-vaccines and correlation to all-cause mortality

One death after 800 COVID jabs is significant.

Dr. Robert Malone: The myocarditis incidence now is publicly acknowledged by some governments as 1 in 5,000.

COVID-19 vaccines should be withdrawn

Dr. Malone:

Months ago, we came out with a press conference in a clear, unequivocal statement that one can find at www.globalcovidsummit.org, where we made a clear, unambiguous statement.

In our opinion, as an organization, these vaccines should be withdrawn. They are no longer justified on a risk-benefit ratio.

Early treatment saves lives

Dr. Malone

It’s our opinion (International Association of Physicians and Medical Scientists), that early (multi-drug) treatment saves lives.

That we now have a broad spectrum of early treatment options.

What matters is that these… our elders, our high-risk individuals have immediate access to therapeutics.

Paxlovid doesn’t work

Dr. Malone has several things to say about Paxlovid.

…a recent Science magazine op-ed clearly outlines that this protease inhibitor strategy against the main protease, which is the mechanism of Paxlovid, is highly susceptible to viral evolutionary escape.

Note: Here is the review that talked about the potential resistance of the SARS-CoV-2 to nirmatrelvir (Paxlovid). The Potential resistance of SARS-CoV-2 Main Protease (Mpro) against Protease Inhibitors

Dr. Malone: Protease inhibitors should be used in combination, and we should use them selectively for the people that need the most.

Pfizer, the manufacturer, who halted their clinical trials for Paxlovid in the normal risk individuals because it wasn’t working. It was not effective in people of average risk. Okay?

Link to CNBC News, Pfizer stops enrollment in Covid antiviral trial in standard-risk population.

CNBC: Pfizer said on Tuesday it would halt enrollment in a trial for its Covid-19 antiviral drug, Paxlovid, in standard-risk patients after a study revealed the treatment was not effective in reducing symptoms in that group.

I agree with everything that Dr. Malone and Dr. Schetters said. Governments should halt the COVID-19 state of emergency and stop the COVID-19 vaccination.

Additionally, health agencies should recognize the vaccine injured. And the “vaccine” manufacturers and all who promoted them should be held accountable.

There is more to the interview. Data doesn’t lie: mRNA-vaccines and correlation to all-cause mortality.

Truth heals. Lies kill. Don’t Get Sick!

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