Lest we forget – Under-reporting in first, the Pfizer Phase 3 Clinical Trial, then the Post Marketing Authorization Report and finally to VAERS – three checks that should have halted the roll-out

The three wise monkeys of the CDC, FDA and NIH – don’t look for facts, certainly don’t speak about their existence or listen to those that speak about them.

Six months ago, CHD published a commentary on an analysis of the under-reporting of adverse events and deaths in the Pfizer Phase 3 clinical trial/study, highlighting deaths that were slow-walked from the injection group compared to fast-walked in the placebo.

How Pfizer Hid Nearly 80% of COVID Vaccine Trial Deaths From Regulators • Children's Health Defense (childrenshealthdefense.org)

“According to an analysis, published this month in the International Journal of Vaccine Theory, Practice, and Research, of Pfizer-BioNTech COVID-19 vaccine clinical trial data, the vaccine makers hid fatality data from regulators in order to qualify for Emergency Use Authorization.”

The abstract is here:

 Forensic Analysis of the 38 Subject Deaths in the 6-Month Interim Report of the Pfizer/BioNTech BNT162b2 mRNA Vaccine Clinical Trial[v1] | Preprints.org

Of particular interest is the population demographic adjusted number of deaths that were expected over the trail/study period of 222 v the several dozen that occurred during the trial period ending on 31 March 2021.

The implication is that the number of deaths that were reported were dramatically understated for both injected and placebo “arms” (sic).

It is not just the obvious sloppy at best or fraudulent at worst clinical trials (where the "at-risk population were not "sampled") - the post-marketing authorisation report also points to the same failings of "lost to follow up" and under-reporting.

From Table 1 on page 7 7 here: reissue_5.3.6-postmarketing-experience.pdf (phmpt.org)

You can see 42,096 adverse events and 1,223 deaths.

Note the "Unknown" outcomes of 9,400 out of that 42,086 - where is the follow-up?

Also, note the diversionary tactic of Pfizer reporting doses "shipped" of 126.2 million on page 6 (previously redacted in the first report for commercial sensitivity, hence the re-issue) rather than doses administered.

The EU and US took the first Pfizer mRNA doses - as at the end of the post-marketing authorization report cut-off on 28 February 2021 (10 weeks after authorization - not three months) the Eu has ADMINISTERED just 29 million Pfizer doses (roll your mouse over to the left to get to the 27 Deb 2021)

COVID-19 vaccine doses administered by manufacturer, European Union (ourworldindata.org)

and the US just 48 million or so

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

For a total of 77 million administered v 126 million shipped. This diversionary tactic between reporting "shipped" and "administered" served to reduce the rate of harm by inflating the denominator.

Now check back to another analysis of the clinical trials conducted in December 2021 and the work of Denis Rancourt estimating a lethality using excess mortality numbers of one death per thousand doses.

Here's the trial analysis.

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

The number of deaths in each arm (sic) needs to be reconciled with the CHD numbers, - but the severe *life altering) and serious (life threatening events ratios are 262 severe events in the injected group receiving around 44,000 doses in the 22,000 in the injected group and 127 serious events for those 44,000 doses.

Let's call it 80 million doses ADMINISTERED up to 28 February 2021, if the clinical trial sampling (amongst the healthy people in the trial v the health workers and unhealthy people prioritize to receive the first doses) you would expect to see 80 million x 262 / 44,000 severe adverse events and  80 million x 127 / 44.000 doses serious adverse events 

That’s over 476,000 serious (life altering) adverse events and 231,000 serious (life threatening) adverse events/

A total of over 700,000 severe and serious adverse events v the 42,086 reported by Pfizer. 

Two other notes - the unblinded clinical trial and the post marketing periods are - arguably the same - just ten weeks or so and secondly, Process 2 was the actual injection not the Process 1 used in the clinical trial. Josh A Guetzkow Senior Lecturer Retsef Levi, Professor, MIT Hebrew University Mt. Scopus, Jerusalem showed that Process 2 was 2-3 times more harmful than Process 1.

Effect of mRNA Vaccine Manufacturing Processes on Efficacy and Safety Still an Open Question | The BMJ

Remember how Pfizer had to recruit a thousand or so extra people just to process the adverse events it reported in its post marketing authorisation report and how the CDC had to pay 30-40 million to General Dynamics IT and Eagle to update VAERS in 2021?

So, whilst the CHD work is great to see, there is another source of evidence that shows the experimental C19 mRNA injections were harmful - and far worse than doing nothing in the healthy population.

I still do not understand how injecting the very "venom" that causes death and injury was ever a solution, rather than an "anti-venom".

Lastly, one death per thousand doses for 80 million doses indicates that 80,000 people were killed by the injections during the 10-week post marketing authorisation reporting period - not 1,224 as reported.

:A quick reminder that applying an under-reporting factor to VAERS of around 40 (Kirsch and Rose) , plus a rule of thumb of one death per thousand doses (Denis Rancourt) and another method devised by Robert Kogon of Ethical Skpetic, the umber of deaths from the experimental C19 mRNA injection of spike venom have resulted I around 700,000 America dead I the three years since roll-out.

Lastly, where is the follow-up on clinical trial participants and those lost to follow-up I the post-marketing authorization report. As I recall, the Pfizer Phase 4 report was due at end February 2024 but was delayed six months in order to follow up on one participant.

Onwards!!!

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