Clinical trial data in 2020 indicated 80 million adverse events If rolled out to Americans - 4 million life altering and 2 million life threatening - the FDA chose to approve mRNA injections anyway

Note throughout that there are multiple injuries per person.

This table will be familiar to regular readers, it is taken from here:

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

Page 11 of that presentation shows that there were around 21,925 in each of the injected and placebo groups.

Let’s leave aside the fraudulent warping of the trial demographics and the question of how there could possibly be “Related Adverse Events” in the Placebo group. That is, were those injected given the injection with only the mRNA component omitted – so these are adverse events around the lipid nano particle and PEG coating? – to put it bluntly “the Related Adverse Events in the Placebo group should be ZERO”.

Two years on, from here:

COVID-19 vaccine doses administered by manufacturer, United States (ourworldindata.org)

the Pfizer/BioNTech 400 million doses have been administered in the US out of around 670 million in total.

Now, the clinical trial did not test for the impact of boosters, nor did it test for the impact of freezing and thawing of the vials, or the degradation in transit to remote areas, or any other quality control protocols you would expect from a manufacturing process with dozens of contractors contributing to the creation of hundreds of millions of vials and doses from those vials actually shot into vulnerable people’s arms.

Regulatory agencies failed in their tasks of ensuring quality and intentionally allowed poor manufacturing and contaminants to be present throughout the bulk manufacturing process. This means that rather than WYSIWYG of the clinical trials, the actual product shot into arms is NOT the same product tested in clinical trials.

See here for a complete evisceration of the mRNA manufacturing process. Note especially the comment that the spike protein that the mRNA instructs the body to make is 30% bigger than the “natural” spike protein that it is supposed to replicate.

39 minute video I urge you all to learn by heart (sic).

Maria Gutschi - Review of Quality Issues with mRNA Injections 5 Nov 2022 (bitchute.com)

The purpose of this is to work out what the FDA SHOULD HAVE EXPECTED TO HAPPEN BASED ON CLINICAL TRIAL DATA.

CDC COVID Data Tracker: Vaccinations in the US

From the CDC data we can derive these numbers for the numbers that took one, two, old booster and bivalent shots.

The CDC states that 230 million Americans have, at least, completed the “Initial Series”.

Problem is, only around 59 million stuck at just two doses (39 million stuck at one dose) – we can work out that around 119 million took “old” boosters – but not how many took another one or two boosters. We do know that 52.5 million people have taken the new booster.

So, the largest group injected is those 119 million that took boosters – BOOSTERS THAT WERE NEVER T£STED IN ANY TRIAL.

Remember this?

2 Top FDA Officials Resigned Over Biden's Booster Plan: Reports (businessinsider.com)

“The FDA announced the resignations of Marion Gruber and Philip Krause on Tuesday.

The pair lead the FDA office in charge of approving vaccines.

Politico and Endpoints reported they left in frustration over Biden's COVID-19 booster-shot plan.”

Not the original double dose injections – the boosters.

To check out what the FDA KNEW IN ADVANCE would happen if Americans got injected, let’s make a simplifying assumption that, on average, the total doses administered divided by the American population is a good enough proxy – 670 million doses of all kinds divided by 335 million Americans = 2 doses each – which brings us into line with the double dosed clinical trials.

Let’s also assume that Moderna has the same casualty rate as Pfizer and apply that to the number of people that were pre-advised to the FDA would be injured/killed from C19 mRNA injections.

Here is a table of the facts KNOWN IN ADVANCE BY THE FDA, with a comparison to adverse events reported to VAERS.

“Trial” column reflects data from the six month clinical trial that lasted 4 months – the FDA approved the Pfizer mRNA injection two months BEFORE the clinical trials were scheduled to end on 31 January 2021. Just four months, maybe this could be annualized, maybe it can’t.

The VAERS column showing 934,701 injuries and 16,824 deaths, reflects the US only casualties over the last two years or so from here:

VAERS Summary for COVID-19 Vaccines through 2/3/2023 – VAERS Analysis

The figure of 15,279 in the “Ratio” column represents the sampling ratio of the clinical trials relative to the American population.

Extrapolating the clinical trial data to the entire American population, the FDA KNEW IN ADVANCE that there might be 80 million adverse events. As an aside, if this relationship has held true over the last two years, then the one million adverse events reported to VAERS is under-reported by a factor of 80.

For deaths, the 20 deaths indicated in the trial in the injected group indicates deaths of over 300,000 from 670 million total injections –

As with adverse events, this might be for every four months, maybe not – note, this ignores background deaths of 14 in the placebo group.

Out of interest, you can reconcile these numbers to the V-Safe data assessed by VAERSanalysis.info here:

Estimating the Under-Reporting Factor (URF) in VAERS by Way of the Recently Released V-Safe Data – VAERS Analysis

Its geometric mean for under-reporting of adverse events was 61.

The point is: THE FDA KNEW IN ADVANCE THERE WOULD TENS OF MILLIONS OF ADVERSE EVENTS AND DEATHS – AND – THE FDA KNOWS NOW THAT CLINICAL TRIAL PREDICTIONS OF CASUALTIES AND DEATHS HAS BEEN BORNE OUT OVER THE LAST TWO YEARS.

PRE-MEDITATION OF CRIMINAL ASSAULT AND DEATH.

WHO WILL PROSECUTE? THE DOJ? HOUSE AND SENATE?

Onwards!

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