by Rhoda Wilson, Expose News:
I have discovered some extremely concerning findings in the Pfizer Phase I-II-III clinical trial data. The Sepsis death rate in the 21,926 double vaccinated group of the Pfizer Phase III Clinical trial was twenty-one times higher than normal, and the Cardiovascular death rate was two times higher than normal.
This strongly indicates that the Pfizer Covid-19 injection does in fact cause a new form of ‘acquired immunodeficiency syndrome’, as has been suggested by a mountain of data available from the UK Health Security Agency, because sepsis is caused by failure of the immune system.
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Here is the table of Pfizer trial deaths from Dose 1 (July 2020) to un-blinding after 6 months (January 2021) –
Sepsis/Septicemia results from immune system failure to defeat a microbial (viral yeast or bacterial) infection.
Emphysematous cholecystitis is a relatively rare variant of acute cholecystitis with infection by gas-producing organisms. Diagnosis involves the demonstration of gas within the lumen or wall of the gallbladder by ultrasound or CT scan. In contrast to acute cholecystitis, emphysematous cholecystitis occurs more commonly in elderly and diabetic patients, and is frequently associated with perforation and death. – https://pubmed.ncbi.nlm.nih.gov/12768870/
It is the result of an immune system failure to defeat a microbial (viral yeast or bacterial) infection.
Acute Cholecystitis. The most frequent cause of acute cholecystitis is gallstones. Other causes include typhoid fever and a malignant tumour obstructing the biliary tract. The inflammation may be secondary to systemic sepsis. https://medical-dictionary.thefreedictionary.com/emphysematous+cholecystitis
Acute Cholecystitis is a biliary sepsis, a sepsis of the Gall Bladder and bile ducts.
Here are the US deaths in 2020 by cause and the percentages for each cause.
The first thing the jumps out of these figures is that Pfizer trial participants had a death rate of 17/19 per 21,921/6 per 6 months. Whereas the general US population has a death rate of 111.2 per 21,923 per 6 months. So Pfizer trial participants were over 6x less likely to die than the general public.
The age profile of the original selection of participants is advertised to be –
- 12-15 years old: 2260,
- 16-17 years old: 754,
- 18-55 years old: 25,427
- 56+ year old: 17,879
So Pfizer must have done some extremely heavy exclusions of morbidities to get such an absurdly low mortality figure. Their study protocol reveals whom they excluded – https://clinicaltrials.gov/ct2/show/NCT04368728
The next thing is the incredible match between the unvaccinated Covid and cardiovascular death rates (10.5% and 26.3%) and those in the general population for 2020 (10.3% and 25.3%). So even though the numbers of deaths are small. They appear to be a very good representation of the reality in the general public.
Now we turn to the double vaccinated cardiovascular and sepsis rates and we see (52.9% and 23.5% death rates) compared to the general population (and the unvaccinated) who suffer only (26.3% and 1.1% or 25.3% and 0%).
And there is the toxicity of the Pfizer vaccination laid bare. It weakens the immune system to the point where people succumb to microbial infections and die at 21 times the normal rate in the first 6 months after vaccination.
One can argue that the numbers of deaths here are not large enough to draw any valid statistical conclusions. But against that, the unvaccinated numbers are very clearly representative and the numbers of participants in both groups are large enough to draw valid statistical conclusions from.
When you combine these figures with the weekly 5% immune response degradation catalogued by the UKHSA from Weeks 35-41 , you start to see a picture that suggests the vaccinated are developing acquired immunodeficiency syndrome.
However you look at this, the numbers flag up two major concerns which these days have plenty of other statistical, mass media, clinical and anecdotal evidence to support.
These findings absolutely necessitate further investigation specific to immune system degradation and cardiovascular inflammation. But Pfizer un-blinded the placebo group and permitted them to get vaccinated at the end of the 6 month trial period. So it is difficult to see how we can get any more data from Pfizer.
To be frank we are lucky to have the death data they have so far provided. Let us face facts. There are no long-term clinical trials ongoing into the safety of these vaccines. Quite the reverse in fact. For one can argue that the purpose of the Pfizer lobbied vaccine mandates is to eradicate any unvaccinated control group from existence in order to prevent a proper evaluation of vaccine side effects over the medium term.