Qualms on Sunday – C19 injections = snake venom – adverse events - “number needed to vaccinate” from the UK - are the injected walking around with white fiborus blood clots and more!

As you read this, consider that there are individuals within the Federal government, its agencies, administrators, bureaucrats, the MSM and medics that have perpetrated the most egregious crimes against humanity ever perpetrated. Worse than Hitler, Stalin, Pl Pot and Mao combined. The ever-growing death tell is probably closer to 40 million than 20 million and the number of injured ad maimed – in worsening health is in the billions. Individuals are responsible, not the institutions. All checks and balances were subverted by individuals, enable by presidents – including Trump.

Big pharma is complicit to the full extent. What company would keep mass producing a concoction known to cause death and injury in the pursuit of profit – outside a war?

Dr Ardis video here from last year providing the logic behind a clip called “Antidote” in which he explains how the make0ip of boom slang, krait and king cobra venom is identical to the spike protein (hence why I call the experimental C19 mRNA injections spike venom”). He also explains that melatonin naturally protects children and how nicotine is non-addictive, nicotine receptor cells exist in every cell in the body and how nicotine is ten times more effective than even ivermectin inn blocking the effects of the spike venom.

Three-hour video here: the-antidote (thedrardisshow.com) (h/t Joy)

Regular releasers will be familiar with this summary of Pfizer Phase 3 clinical trial data from here:

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

Around 21,900 in the injected and placebo groups.

Note that these outcomes are from “Process 1” – the “safer” process. Josh Guetzkow and Retsef Levi pointed out that the actual “Process 2” was different.

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

Changes of a single molecule can turn a “treatment” into a “poison”. The relative risks were estimated to be 2-3 times worse for Process 2.

There has been no indication of improvement or deterioration in the health of those suffering adverse events. Given the difference in the product delivered against the product trialled AND the contaminants discovered in global vials, these products are “adulterated” AND contaminated – breaching FDA regulations in two critical areas that make the manufacturers guilty of breaking Federal laws.

Clinical trials are due to be completed this year – the Phase 3 clinical trials are just that – a phase. Phase 4 is the last part.

Note the ratios of “severe” and “serious” adverse events to deaths. It can be argued that the number of deaths is not statistically significant compared to the placebo. Keep in mind that the trial was conducted amongst a relatively healthy population – not including the elderly, previously infected, pregnant women or children. Others have estimated that the expected mortality in a similar demographic = amongst the total of around 44,000 trial participants over 6 months  (which should be three months since the trial was unblinded early) numbered in the 100’s in each trial arm, not the few dozen in the trial.

For Process 1, what we have is around a 25% adverse event rate with 1.2% severe (life altering) and 0.6% serious (life threatening) rate of adverse events – mortality is 0.1%.

Process 2, maybe double those numbers.

So, here’s the adverse events reported to VAERS for US manufacturers of the experimental C19 mRNA injections.

 VAERS Summary for COVID-19 Vaccines through 2/23/2024 – VAERS Analysis

A million adverse events for 677 million doses administered INSIDE the US v 634,000 adverse events for around 6 billion doses of Pfizer and Moderna shots administered OUTSIDE the US. The number of adverse events outside the Us would be around 9 million, instead of 523,000 and the total adverse events should be 10 million. Similarly, the number of deaths in total should be 177,000 not 37,000.

Why are adverse events from overseas not being reported to VAERS? How ridiculous does this make the WHO’s VigiSAFE with its 5 million reports of adverse events? How many Pfizer and Moderna adverse events reported to EUDRA, MHRA, TGA et al have not been “cross-walked” to VAERS? This, just for EUDRA:

50,663 DEAD and 5,315,063 Injured Following COVID-19 Vaccines in European Database of Adverse Reactions - Vaccine Impact

Now for a quick look back to some data on “number needed to vaccinate” from the UK here:

Appendix 1: estimation of number needed to vaccinate to prevent a COVID-19 hospitalisation for primary vaccination, booster vaccination (3rd dose), autumn 2022 and spring 2023 booster for those newly in a risk group - GOV.UK (www.gov.uk)

Here’s a few tables:

218,500 people would need to be injected twice, to prevent ONE hospitalisation. The clinical trials for Pfizer Process 1 indicated that 1% of those injected suffered severe or serious – which means that for every ONE hospitalisation prevented 3,184 suffered a serious or severe adverse event.

The above is for people nit in a risk group and represents the number of people that need to be injected to prevent ONE hospitalization. Here are the numbers for “at risk” groups.

For the “at risk” groups in the 40-49 year age group around 500 people (1% of 48,799) would suffer a serious or severe adverse event for every One hospitalization prevented.  

And yet, the UK have continued for another 18 months with the spike venom injections.

Dr John Campbell did a video a while back which, from memory, referred to 600 people would need to be injected to prevent one hospitalization with Pfizer and 900 for Moderna. By this stage AstraZeneca had been withdrawn – its rates of harms were 4-5 times worse.

(100) EUDRA shows 4-5 times more deaths and adverse events reported per million doses for viral vector C19 "vaccines" compared to mRNA C19 "vaccines" - media silence continues (substack.com)

All this has been known for at least 18 months and yet health regulators globally have ignored the safety data. The number of deaths from the injections has been calculated in a number of ways.

Estimates based on excess mortality of between 800 and 1,000 deaths per million doses in 17 Southern hemisphere countries by Denis Rancourt. Estimates based on US under-reporting factors by Kirsch ad Rose of around 38 and by the Ethical Skpetin each approximate around 799,000 deaths caused by injection of spike venom.

A million US adverse events reported to VAERS adjusted for a URF of 38 implies 38 million people have suffered an injury. Globally, the US pro=rata’ed to global of 10 million balloons all the way up to 380 million in total (including the US).

Those umbers are just for Pfizer ad Moderna (plus JnJ ad Novavax)/ U guesstimate that AstraZeneca’s few billion injections caused 10 million deaths in Idia on its own – not that the Indian “authorities” have even noticed.

Side note: the injections neutralize the body’s immune system for the four weeks it takes to become “vaccinated” with two doses and the last two weeks for the “vaccine” to take – meaning that people are more susceptible to infection AND any infections are classified as occurring in the “unvaccinated”. Note also that according to the FDA and CDC there are no adverse events, only C19 disease harms. The WHO’s VigiSAFE system has 5 million? A URF of the odd 100 to 150?

Ok, now for those blood clots.

(100) ICYMI - Blood clots from the dead – four different types – long white fibrous, coffee grounds, grape jelly, and yellow types - does a survey indicate 30% of ALL the dead have one or more of these? (substack.com)

For blood clots to be detected during embalming, unless the embalming process causes them, the deceased must have been carrying around the fibrous clots for some time – for the time it takes to grow from a small white fibrous clot to the monster sizes in some.

I wonder why autopsies did not reveal the presence of these clots. Were they noticed and ignored or not looked for? Is this why the default disposal of the body was by cremation> Have we endured an upgrade from Zyklon B and chimneys to snake venom and chimneys overseen by medics rather than prison guards?

I wonder if anyone has removed such white fibrous blood clots from the living. How ere they detected, how ca they be removed or destroyed? If dissolved somehow or removed, will they grow back because they are a consequence of the spike venom, and the body has instructions to keep producing it?

What are the mechanisms of action for current treatment protocols on these particular white fibrous clots? Hell, maybe there’s a “parasite that eats them and can be excreted!

Lastly, ICYMI, here’s a link to the SubStack post by Meryl Nass exposing Tedros as the lying stool pigeon that he is, after his latest attempt to defend the indefensible.

(100) As Tedros keeps lying, I have to keep correcting him. (substack.com)

Onwards!

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