Would the FDA have approved bleach as a C19 treatment if Pfizer and Moderna had called it a C19 mRNA “vaccine”?

“Reminder” post today.

It seems that there is little headway being made in getting out the message of how C19 injections FAILED clinical trials and were only rolled out because of the actions of a criminal racket involving the FDA/CDC/NIH/NIAID/WHO and mRNA manufacturers, Pfizer and Moderna.

(Article by Peter Halligan republished from PeterHalligan.Substack.com)

All the harms suffered as a result of 12.8 billion injections on 5.5 billion of the world’s 8 billion population (that’s right, the world population passed 8 billion a few weeks ago and 5.5 billion people have received at least one injection.

As previously posted, if viral vector injections are as deadly as mRNA injections (anyone seen a comparison?) globalizing the VAERS and EUDRA deaths and injuries and applying a well-tested under-reporting factor of 40, then 20 million people have been killed by the C19 injections and 2.2 billion injuries (multiple per person) have been inflicted.

Out of interest, the 21,920 or so in the injected group of the Pfizer/BioNTech Phase 3 clinical trial are around one/25,000 of those injected globally. So 20 deaths in the injected group DURING THE SIX MONTH CLINICAL TRIAL, translates to around 5 million amongst the 5.5 billion injected with at least one dose. The adverse events – at 24% of those injected – translates to 1.3 billion adverse events. Make of that what you will!

No doubt this genocidal harm is being suppressed by the MSM and social media outlets globally, which is why there are still many who think a murderous criminal racket actually want to help them. The analogy is the thug demanding protection money from you – to protect you from – the thug.

Rhetorical – “tongue in cheek” – question.

What would the FDA have done differently if barely tolerable doses of bleach had been used as a C19 injection trial candidate, rather than the complex, carcinogenic PEG coated, lipid nano-particles instructing the body to produce spike proteins that cripple the bodies passive and active immune system?

Would the FDA have granted emergency use authorization without any verification of substance or outcomes of trials?

The mRNA C19 injections were NOT tasked with preventing or designed to prevent transmission

The mRNA C19 injections were NOT tasked with preventing or designed to prevent hospitalization and death

The mRNA C19 injections WERE intended to prevent symptomatic disease.

Here are the pre-specified clinical trial end-points, set BEFORE the clinical trials commenced.

Any representation of different end-points or intentions is A LIE. Not misinformation, not disinformation, or malinformation, or alternative facts. IT IS A LIE.

The ONLY clinical trial end-point was the “Prevention of symptomatic disease in vaccine recipient”.

There is a virus – SARS-COV2 – that causes a disease – CoVID19. The virus on its own does not make you sick or automatically cause the C19 disease. The viral infection can be treated BEFORE it becomes the disease – the CDC BANNED all treatments like HCQ and IVM protocols. People either recovered from the virus or were hospitalized once it turned into the disease.

The C19 disease has many symptoms. They are called “adverse events”. Adverse events are classified as “Severe” when they impede normal activities or “Serious” when they are life threatening/require urgent medical attention.

The Pfizer/BioNTech Phase 3 clinical trial showed that 24% of those in the C19 injected group of around 21,900 suffered from adverse events – compared to just 6% in the placebo group of the same size.

Of these adverse events, “Severe” events were 75% higher in the injected group and “Serious” events were 10% higher.

ONLY THE NON-“SERIOUS” ADVERSE EVENTS WERE AN ENDPOINT.

In other words, forget the infections, forget the “Serious” adverse events, forget the Deaths.

The only end-point that the C19 injections were tasked to prevent were “adverse events” less “serious events”.

Here is a link to the Canadian Covid Care Alliance analysis of the Pfizer/BioNTech Phase 3 clinical trial.

The COVID-19 Inoculations – More Harm Than Good FINAL Video & Print (canadiancovidcarealliance.org)

https://www.canadiancovidcarealliance.org/wp-content/uploads/2021/12/The-COVID-19-Inoculations-More-Harm-Than-Good-REV-Dec-16-2021.pdf

It is there, in black and white. The Pfizer/BioNTech Phase 3 clinical trial FAILED to meet its only clinical end point and, in fact, caused more damage than doing nothing.

Rather than satisfying the sole end point required of the clinical trials – that of the prevention of symptomatic disease – the clinical trials CLEARLY DEMONSTRATED C19 INJECTIONS CAUSED SYMPTOMATIC DISEASE.

The FDA authorized the Pfizer/BioNTech and Moderna C19 injections for Emergency Use in the full knowledge of the FAILURE of the clinical trials to prevent symptomatic disease and the cause of much more harms.

Pfizer and Moderna knew their clinical trials had FAILED to prevent symptomatic disease and submitted their C19 injections anyway.

In other words, the C19 mRNA injections emergency use authorised by the FDA were known IN ADVANCE by all parties involved.

That is the definition of criminal racketeering and all involved should be prosecuted under RICO laws.

Health authorities and governments around the world, failed to verify the Pfizer/BioNTech clinical trials and simply rubber stamped what should have been a trivial matter to “trust, but verify”. These health authorities and governments around the world failed in their duty of care to protect their people from dangerous experimental injections. They need to be prosecuted for wilful negligence and criminal malfeasance.

Read more at: PeterHalligan.Substack.com