© Unknown
Quote from Denis Rancourt, IUHM
The present article is a follow-up of
Compelling Evidence That SARS-CoV-2 Was Man-Made published in June 2020, you are encouraged to read it first. The concluding words were as follows:
It's probable that by the end of 2020, like every year, a flu
epidemic will emerge. This virus will, conveniently, be deemed a close
relative to SARS-CoV-2, maybe with 'extra terrifying features'.
But there will be no need to despair because, by this time, the authorities will have prepared a vaccine.
That's one of the reasons why hydroxycholoroquine was lambasted and
banned. If a safe and effective treatment already exists, who is going
to accept a rushed and unknown vaccine? A vaccine that will allegedly
protect people against COVID-20, but will in reality be designed to
'cancel' the beneficial changes induced by the mutated strain of
SARS-CoV-2. [...]
It's probable that the vaccination won't be mandatory. Remember that the
authorities are now "kinder and gentler". Instead of brute force, the
authorities are more likely to use moral blackmail - "Get vaccinated to
protect others!" - combined with social blackmail - "No vaccine = no
job, no shopping, no travel, no socializing!" Basically, you're free to
choose between the vaccine passport or a life sentence in an isolated cell.
Here were are 7 months later. As suspected new variants have appeared, manufactured COVID-19 deaths are piling up, the
vaccine passport has already been adopted by several countries and vaccinations have started all around the world.
In theory, medicines, vaccines included, are approved and used because
their benefits far exceed their risks. In this sense, the ideal medicine
would display zero risks and total effectiveness against an uncured and
deadly disease. We'll see in the present article that the COVID-19
vaccines, particularly the Pfizer vaccine, is pretty much the opposite
of the ideal drug. It is dangerous, ineffective and targets a benign
disease that already has known effective and safe treatments.
Where's The Pandemic?
Case Fatality Rate
According to the WHO, in October 2020 an estimated
750 million people, that is about 10% of the world population, had been infected by SARS-CoV-2 and
one million
people had died of COVID-19. Those figures lead to a case fatality rate
(CFR) of 0,13%, which is the typical CFR exhibited by the
seasonal flu.
When treated properly, like in Marseilles where hydroxychloroquine
protocol and early clinical diagnosis is used, the CFR drops as low as
0.05%.
In Singapore, where the
use of hydroxichloroquine is widespread and
no national lockdown was ever imposed, the CFR of COVID-19 is the same as Marseilles, a mere 0.05% (
29 deaths out of
59,000 cases)
What kind of pandemic exhibits a case fatality rate equal to, or lower than, seasonal flu?
Real COVID deaths
The numbers above are based on the official data published by the WHO.
Those numbers, particularly the total COVID deaths, are grossly inflated
thanks to various deceptions:
1/ comorbidity:
94% of the people who died of COVID-19 had comorbidity factors. A
majority
of them had not one but several comorbidity factors, in particular
hypertension, obesity, chronic lung disease, diabetes and cardiovascular
disease. For example a UK patient who had advanced cancer, kidney
failure and diabetes, and had tested positive within
60 days prior to his death will have his demise automatically attributed to COVID-19. In the UK, at the very least
30% of deaths attributed to COVID-19 are actually due to the comorbidity.
2/ false positives:
A lot of deaths were attributed to COVID-19 merely because of a positive PCR test. In the
words of its inventor Kary Mullis, Nobel Prize in Chemistry 1993:
[the PCR tests] cannot detect free infectious viruses at all [...] The tests can detect genetic sequences of viruses, but not viruses themselves
Therefore, the obvious questions are: how many other viruses, display
viral sequences similar to SARS-CoV-2 and then get detected and are
wrongly labeled SARS-CoV-2? How many non-pathogenic, non-transmissible
viral sequences of SARS-CoV-2 lead to a "positive" PCR test.
To add insult to injury, there is a serious problem with the number of
PCR amplification cycles. According to the CDC, it is virtually
impossible to detect any live virus above a threshold of
33 cycles. However, many states conduct
40,
45 even
50 amplification cycles. For illustration, a positive test at 40 cycles has about
43% chance of no longer being positive with a cutoff of 35 and
85% chance with a cutoff of 30.
The antigen test is even worse than the PCR test leading to
63% more false positives! These tests are so unreliable that even the
WHO discourage their use.
3/ ban of effective treatments:
In Marseilles, France, where early diagnosis and proper treatment
including hydroxychloroquine combined with azythromycin are administered
the crude mortality rate is
0.01%. 400 miles from there, in Paris, where there's late diagnosis and the
ban on those two drugs is enforced, the overall mortality rate jumps up to
0.075%. That's a 7.5 fold increase.
Similar to Marseilles,
Belarus and
Iceland
administered proper care and/or conducted early diagnosis and they are
among the countries with the lowest number of COVID-19 deaths with
1,560 (0.016% crude mortality rate) and
29 (0.008% crude mortality rate) respectively as of mid-January 2021. In the same vein, In Vietnam, that
uses hydroxichloroquine,
early diagnosis and implemented
no national lockdown, crude mortality due to COVID-19 is 0.000036% (35 death for
96 million inhabitants)
4/ transfer of flu casualty:
The Southern Hemisphere appears to have simply
skipped
the winter 2020 flu season, where flu deaths showed a 90% drop compared
to previous years. According to mainstream media, this drop in flu
deaths is due to the lockdown. If this is the case however, how do we
explain that France recorded a surprisingly low number of flu deaths
during the flu season 2019-2020 that ended
before the lockdown was imposed on March 17th. Indeed, only
3,680 flu deaths were recorded during winter 2019-2020. That's a 70% drop in flu deaths compared to the last
10-year average mortality.
Another mainstream narrative explains this sharp and unexpected drop in
flu casualties as due to the coronavirus preventing the activity of
other viruses. But viruses have no difficulties in cohabiting. For
example, in Europe alone during the 2019/2020 flu season, there were at
least
six
active flu strains: type A A(H1N1)pdm09, A(H3N2)) A(Unknown),
B/Victoria, B/Yamagata et B/Unknown, and we know that SARS-CoV-2 was on
the continent at least since
December 2nd 2019.
In the Northern hemisphere, France was not the only country to
experience the disappearance of the seasonal flu. The USA and the UK
respectively reported a staggering
98% and
90% decrease in deaths attributed to the seasonal flu.
Starting with the hyper-inflated WHO number of COVID deaths which is 1,7
million as of January 2021, we can deduce the following numbers:
- false positive deaths, patients who didn't even have COVID, represent
at the very least 33% of the total number of deaths attributed to
COVID-19. That's
700,000 out of 1.7 million
- deaths due to comorbidities represent 30% of the total number of deaths attributed to COVID, that's
500,000 out of 1.7 million
- About 90% of the
typical flu death toll was transferred to the COVID tally, that's
300,000 deaths out of 1.7 million.
Depending on the overlaps between those three kinds of non-COVID deaths,
the real number of COVID-19 deaths can be estimated at between 300,000
and 1.1 million.
That range doesn't even take into account the 7-fold reduction in
mortality related to proper early diagnosis and adequate treatment.
Factoring this parameter in, the total mortality due to COVID-19 with
early diagnosis and proper care would drop somewhere between 40,000 and
140,000 casualties worldwide. Notice that the estimates above are very
conservative, we are therefore left to wonder
whether SARS-CoV-2 actually directly caused a significant number of deaths.
What kind of pandemic induces much less total deaths than the seasonal flu?
Excess mortality
The excess mortality includes deaths attributed to COVID-19 along with
the numerous deaths due to the lock-downs. As we will see, it is likely
that lock-downs induced many more deaths than COVID-19.
1/ delayed treatments and diagnosis
Only a third of the excess deaths seen in the care homes and private
residences in England and Wales can be explained by covid-19, the
remaining
two thirds
are due elderly citizens who were denied primary care and "who may well
have lived longer if they had managed to get to hospital". This problem
is particularly accurate for cancer patients for whom the denial of
diagnosis and medical treatment may lead, to
18,000 more UK cancer patient deaths.
2/ psychatric conditions
A meta analysis of the mental heath of the general population was
published in December 2020. As expected, the "pandemic" significantly
exacerbated this situation:
Relatively high rates of symptoms of anxiety (6.33% to 50.9%),
depression (14.6% to 48.3%), post-traumatic stress disorder (7% to
53.8%), psychological distress (34.43% to 38%), and stress (8.1% to
81.9%) are reported in the general population during the COVID-19
pandemic in China, Spain, Italy, Iran, the US, Turkey, Nepal, and
Denmark [...] The COVID-19 pandemic is associated with highly significant levels of psychological distress that, in many cases, would meet the threshold for clinical relevance.
Source
It should be noted that the life expectancy of individuals suffering from mental illness is about
8 years shorter than the general population.
3/ suicide
the definitive numbers about deaths in 2020 have not been compiled
yet. However, the trend is already clear. According to some studies,
suicide increased by
145%. Logically, suicidal tendencies surged along actual suicides with, for example, India experiencing a
67,7% increase in reports of suicidal behavior during lock down. Similarly, in
China the appearance of very frequent suicidal thoughts has been noted while in Canada, a
500% increase in suicide is projected.
4/ alcoholism and drug addictions
Alcohol abuse sharply increased during the "pandemic". In the UK, there was a
500% rise in calls to the
British Liver Trust helpline since lockdown began in March. Similarly,
Alcohol Change recorded a
242%
rise in visits to their advice and support pages on their website
during lockdown. Surveys on alcohol consumption tell a similar tale,
with
21% of individuals stating they were drinking more often during lockdown. The heavy drinkers were the most affected,
38% of those who typically drank heavily during pre-lockdown said they drank even more during lockdown. In the US, a
54% increase in national sales of alcohol was recorded for the week ending March 21, 2020, compared with 1 year before.
Similarly, drug overdoses rose strongly in 2020. For example, in the US, overdoses killed a staggering
81,000 people, a
38% increase in fatal overdoses compared to 2019.
5/ poverty
According to the Worldbank, the "pandemic" could throw about
100 million
additional people into extreme poverty. The life expectancy difference
between an individual in extreme poverty and a wealthy individual is at
least
20 years.
Notice that most of the deaths induced by the surge in extreme poverty
will not happen immediately but in the years, if not decades, following
this manufactured global economic crisis.
Despite the number of deaths due to lockdowns and their consequences
rather than COVID-19, many countries didn't even record an excess
mortality during the so-called pandemic. That is the case in
Germany where
hydroxychloroquine was used and a lot of
early diagnosis was done. Better than that,
Iceland - which implemented one of the most
effective early diagnosis
approaches in the world - shows a mortality rate in 2020 that is lower
than its average yearly mortality. But the cherry on the cake is
China, where about 55 tons of hydroxychloroquine were consumed in 2020 and where
no global lockdown was implemented: as a result, China experienced virtually
zero COVID deaths since April 2020.
© ourworldindata.org
Daily COVID-19 deaths in China
Even France which banned
hydroxychloroquine and
azythromycin and implemented extended lockdowns and curfews, experienced a mortality rate during Spring 2020 that was
lower than during the 2017 flu season and since May 1st, 2020,
no increase in mortality has been noticed.
What kind of pandemic doesn't cause a marked excess in mortality?
Life Expectancy
In France, even before they tested positive for the virus,
80%
of alleged COVID-19 victims had a life expectancy lower than one year,
due to comorbities and advanced age. Overall, COVID-19 victims had a
life expectancy of a mere
3 years and
82% of the victims were more than 70 years old. The average age for a COVID-19 death is
82, that is a few months shorter than the overall
life expectancy.
In several countries, the average age of deaths attributed to COVID-19
is even higher than life expectancy. For example, in the UK, the average
age for COVID-19 death is
82,6 years old while the average life expectancy is
81.2 years. In Sweden, the average age of those who have allegedly died of COVID-19 is
84 years old, two years more than the average age of death which is
82.
As a result of the very advanced age of the people who allegedly died of
COVID-19, many countries didn't experience any drop in life expectancy.
This is the case in China that recorded
4,600 deaths attributed to COVID-19 out of a population of 1.4 billion, or Iceland and its
19 COVID victims out of 400,000 Icelandic citizens.
Even in France, where a lot of elderly citizens were left to die in
nursing homes, where drastic lock-downs were implemented, where
diagnosis and care was delayed for serious conditions and effective
medicines against COVID-19 were banned and toxic drugs like
Rivotril or
Remdesivir were administered instead, life expectancy only decreased by
5 months.
What kind of pandemic doesn't notably decrease life expectancy?
In summary, the typical victim of COVID-19 is an individual in his 80's
who lives in a nursing home and has several comorbidities. Typically,
such a person died because of the despair of social isolation and the
delayed diagnosis and treatment of his serious comorbidities. In many
cases, the patient didn't even have COVID-19. However COVID-19 killed
him, not directly, but through the isolation and denial of care induced
by a well-orchestrated pandemic hysteria.
To recap, we are experiencing a rather
peculiar "pandemic", that
exhibits a case fatality ratio lower than the seasonal flu, kills less
than the usual infectious diseases, didn't trigger marked excess
mortality and didn't really increase life expectancy.
Existing Treatment
Not only is COVID-19 a benign disease, it can be cured by numerous treatments that are safe, effective and cheap:
artemisia, high dose
vitamin C, vitamin D,
copper,
Zinc,
doxycyclin,
fluvoxamine,
bromhexine,
colchicine,
Imervectine,
azythromocine and, of course,
hydroxychloroquine. In addition, the combination of some of those drugs revealed beneficial synergies, in particular
a cocktail
of hydroxychloroquine + azythromycin + zinc. Notice also that the
efficacy of the aforementioned drugs has been published in peer-reviewed
journals months ago.
A case in point is
hydroxychloroquine (HCQ) whose efficacy
against COVID-19 has been tested in no less than 195 published papers.
The conclusion of the statistical meta analysis of those papers could
not be clearer
:
HCQ is effective for COVID-19. The probability that an
ineffective treatment generated results as positive as the 195 studies
to date is estimated to be 1 in 1 quadrillion (p = 0.0000000000000009).
Source
Another way to ascertain the efficacy of
HCQ is simply to check if the research papers received funding from
Gilead - the American-Israeli company, laden with
conflicts of interests - that produces the now infamous
Redemsivir.
When there are conflicts of interest with
Gilead,
73% of the papers claim that
HCQ doesn't work, if there is no conflict of interest,
83% of the papers conclude that
HCQ works. It's that simple.
© IHUM
Chloroquine efficacy against COVID-19 (the papers with conflicts of interest are in red)
Despite its repeatedly tested effectiveness,
HCQ has been banned in a
number of Western countries. In contrast, it took only one bogus
paper, (
debunked soon after), for states to buy and administer
billions of dollars worth of the
toxic and
ineffective Redemsivir.
The reason for the suppression of known treatments is at least two-fold:
- social: denial of treatment to deliberately increase deaths and
therefore fear in the population, leading to the reluctant acceptance of
vaccines.
- legal: the
accelerated FDA approval
of a new drug is only possible when the targeted disease "has no cure".
The suppression of known cures enabled the Pfizer vaccine to be
approved after two months of limited testing and a meagre trial report,
while a proper FDA approval requires about
12 years of extensive trials and a
100,000+ page new drug application.
To recap, COVID-19 is a benign disease with numerous safe and effective
treatments. In this context, the logical approach would be to increase
the early clinical diagnosis and to spread and improve the existing
therapeutic strategies. That's not what the elites decided, especially
in the Western world. Instead they banned effective treatments and among
all kind of dubious vaccines, enforced the worst one, the Pfizer RNA
'vaccine' on which we will focus our attention now.
mRNA Vaccine or Gene Therapy?
Despite its name, the Pfizer 'vaccine' is more akin to gene therapy, the
definition
of which is: "the utilization of the therapeutic delivery of nucleic
acids into a patient's cells". The Pfizer "vaccine" is exactly that, an
artificial RNA sequence delivered via nano lipids into the patient's
cells, to hijack them and direct them to produce the spike protein found
on SARS-CoV-2, or at least on one of its old variants. From there, the
host should react to this protein by producing antibodies. Too many
antibodies and an
immune storm happens, no enough antibodies and the triggered immunity is useless.
Notice that gene therapy was never used on a large scale. It was only used in experimental phase 1
anti-tumoral protocols. The drugs were so toxic that phase 2 trials were never conducted.
RNA "vaccines" against MERS and SARS followed the same failure path.
In 1999, geneticist Alain Fischer, conducted the
first clinical trial with some rare positive results in the world of
gene therapies. The same Alain Fischer was
nominated as a vaccine expert by the French authorities. When asked about the Pfizer "vaccine", Fischer
answered
cautiously, emphasizing that the effects of infectiousness and the
duration of immunity were unknown, side effects were unavoidable and the
fear of the vaccine was understandable. Obviously Fischer's analysis
didn't fit the pro vaccine narrative, since then he no longer enjoys any
media exposure.
Vaccine Useless at Best, Detrimental at Worst?
The history of vaccines is replete with major scandals. Here are a few examples:
1/ the
Salk polio vaccine which caused the worst polio outbreak in history, infecting 200,000 people with live polio, of whom 70,000 became sick
2/ the current
prevalence of poliomyelitis caused by vaccines compared to naturally-occurring poliomyelitis
3/ the Dengue vaccine triggering the production of antibodies that are not detrimental but
beneficial to the Dengue virus, leading to more severe forms of Dengue fever.
4/ And let's not forget Bergamo, Italy where the population experienced a high prevalence of severe forms of COVID-19 among
vaccinated people. There's no mystery there, because for years, the flu vaccine has been known to
favor and worsen coronavirus infections.
Likewise, vaccines against close relatives of SARS-COV-2 like
SARS or
MERS,
that target the spike protein like the Pfizer "vaccine", have also been
tested but quickly canceled, one major adverse effect was the creation
of antibodies that didn't prevent but
favored viral infections.
The vaccines against Dengue fever, influenza, SARS and MERS share the
same fundamental flaw, which is well known by scientists as
antibody-dependent enhancement,
where the vaccine, instead of providing immunity, increase
vulnerability and the severity of the disease it targets. In this
context, it would not be surprising that the RNA vaccines trigger more
severe forms of COVID-19.
In addition, like most retroviruses, SARS-CoV-2 is very prone to
mutations. The analysis of 10,000 of its genomes revealed a high number
of genetic modifications:
2969 missense mutations, 1965 synonymous mutations, 484 mutations in
the non-coding regions, 142 non-coding deletions, 100 in-frame
deletions, 66 non-coding insertions, 36 stop-gained variants, 11
frameshift deletions and two in-frame insertions.
Source
This substantial number of genomic variation has let to the emergence of, at least
14 distinct variants, including the 'English variant' which displays
23 detectable mutations,
70% of them being located on its spike protein, which is the very target of the Pfizer "vaccine".
© Nextstrain
Some of the SARS-COV-2 variants
Coincidentally, or not, the above mentioned
Remdevisir has been tested on British patients in at least
15 different health centers and widely administered after its bogus
approval.
Redemsivir is now known to trigger mutations in SARS-COV-2, particularly in its
spike protein. Given its mutagenic property and its use in the UK, the obvious question is "Did
remdesivir play a role in the apparition of the English variant?"
In any case, just in Marseilles no less than
33 patients fell sick twice, from the variant called
Marseille 1, then from the variant
Marseille 4. Worse than that, still in Marseilles, one patient got infected
three times with SARS-CoV-2 variants in just nine months.
Reinfection with SARS-COV-2 is widespread enough that scientists do not wonder any more
if it happens, but
how it happens:
the possibility of reinfection with SARS-CoV-2 is not well understood.[...] previous exposure to SARS-CoV-2 does not necessarily translate to guaranteed total immunity. The implications of reinfections could be relevant for vaccine development[...] Genomic analysis of SARS-CoV-2 showed genetically significant differences between each variant associated with each instance of infection.
Source
Those reinfections suggest that natural immunity against COVID-19 could
last just a few months, one reason for this short immunity probably
being the numerous mutations of SARS-CoV-2. If natural immunity doesn't
prevent a quick re-infection, the Pfizer vaccine, which unlike natural
immunity only targets a small part of the virus - namely its spike
protein, which has substantially changed since the design of the vaccine
- should exhibit even poorer results. In conclusion, the
Pfizer vaccine is unlikely to confer lasting immunity, if any, especially against current and future variants.
The above is not just theory as a
growing number of people is getting infected with SARS-COV-2
after being inoculated with the Pfizer "vaccine".
Pfizer Vaccine Methodology
1/ Irrelevant investigation objectives
A stunning bias in the Pfizer trial was its primary objective: evaluate
the frequency of mild to severe forms of COVID-19, 28 days after the
first inoculation.
Casualty rate, infectiousness, duration of
immunity (if any), or even occurrence of mild to severe forms in the
long term were not investigated. But, wait a minute, the whole
pandemic and vaccine hysteria were built on these very fears of death
and contamination, we heard
ad nauseam the media injunctions:
"people are dying in droves", "get vaccinated to avoid contaminating
others", "get vaccinated to be immune to COVID-19", "get vaccinated to
avoid dying of COVID-19" etc.
2/ Tested group bias
Another striking bias is the trial selection, particularly the age
combined with health status. We've shown above that frail elderly are by
far the
most likely to suffer from COVID-19. But only
2%
of the Pfizer trial includes patients over 75 years old and with
pre-existing medical conditions. In addition subjects of any age with
comorbities are grossly under-represented:
In total, only one out of five of the people appear to have an
underlying condition, and for the various individual underlying
conditions, the percentage of people suffering from them is often less than 1%.
Source
Also the limited size of the vaccine group (about 20,000 participants)
does not exhibit all the age/race/sex/disease/treatment/genetic profile
combinations that the general population does.
There is no
safety data whatsoever about children, immune-compromised individuals or
pregnant women because they were excluded from the trial.
Basically Pfizer selected young and healthy subjects for testing
a vaccine that is now administered as a priority to old and sick
individuals. What is the point of studying healthy young individuals, who, vaccinated or not, are barely affected by COVID-19 anyways?
Does this bias minimize side effects and maintain the illusion of a safe "vaccine"?
3/ Placebo instead known effective drugs
A new drug is tested against a placebo when the targeted disease has no
known cure. In the case of COVID-19, there are several known cures to
which Pfizer should have compared its vaccine.
That's was the design of the
Discovery clinical trial that compared
Remdesivir,
HCQ and other drugs. When the
preliminary results started to show that
HCQ was the most effective,
it was quickly removed from the trials. Pfizer didn't make the same mistake of testing its new drug against an effective one.
Instead, they tested their "vaccine" against a placebo.
4/ Unilateral design and treatment of data
No third party was involved in the design of the trial, its monitoring, and the treatment of the results.The whole study was designed, conducted, analyzed, published and paid for by Pfizer itself.
As Dutch neurologist Jan B. Hommel neurologist
said:
"The fact that an independent data and safety committee was able to see
the data doesn't change this, simply because they had no say in the
design of the research, selection of the participants, the statistics
used or the publication. ... I don't need to explain here how such
a construction can lead to biased results of scientific research,
because it has been extensively researched and published about over the
past twenty years."
Benefits
The main marketing argument for the Pfizer "vaccine" is its alleged
95% efficacy. This figure is the sole claim of Pfizer and it should be taken with a grain of salt because of numerous factors:
1/ Pfizer precedent
First we have to understand the background of the company we are dealing with here. Pfizer is the world's
largest pharmaceutical company and it is also the company that has been hit with the
biggest criminal fine in US history for
lying about one of their drugs and bribing doctors. This record fine is only one example. Pfizer has been sentenced numerous times for covering up major side effects of
Protonix, hiding the cancer-inducing properties of
Prempro, lying about the suicidal behavior induced by
Chantix, promoting
Depo-Testosterone as effective and safe while it was ineffective and induces major side effects, conducting illegal clinical trials for
Trovan in Nigeria killing 11 children. The list of crimes committed by Pfizer goes
on and
on.
Let's also keep in mind that Pfizer will cash in
$14 billion a year, more than the
GDP of Nicaragua, from the worldwide sale of its RNA "vaccine".
2/ Relative efficacy VS absolute efficacy
During the
Pfizer clinical trial
8 COVID-19 cases were found in the vaccine group of 20,000 and 86 cases
in the placebo group of 20,000. This means the attack rate for COVID-19
is 0.0004 in the vaccine group and 0.0043 in the placebo group.
Therefore,
the absolute risk reduction for an individual is only about 0.4% (0.0043-0.0004X100).
The Number Needed To Vaccinate (NNTV) = 256 (1/0.0039), which means that
to prevent just 1 Covid-19 case, 256 individuals must get the vaccine;
the other 255 individuals derive no benefit, but are subject to the
numerous adverse effects of the "vaccine" .
3/ Exclusion of suspicious cases
The claimed 95% (relative) efficacy was attained by excluding
3410
total cases of suspected, but unconfirmed COVID-19 cases (probably due
to false negatives). When those 3410 suspected cases are reintegrated
the relative efficacy drops to
19% (which is well below the 50% effectiveness threshold set by
regulators) and the absolute risk reduction drops to a ridiculous 0.08%.
4/ Non-replicated results
The
cornerstone of any scientific work is its replicability. The results of the clinical trial have been
published in a journal
at the end of 2020, but the clinical trials have not been replicated
and there are unlikely to be ever replicated because no pharmaceutical
company will conduct
pricey clinical trials for a molecule patented by a competitor. So all we have are muti-offender Pfizer's words.
In summary, according to Pfizer, the benefit of its vaccine is a
reduction of flu like symptoms in the young healthy population. They
don't know, or rather, they don't want us to know, about what really
matters: symptoms in the frail elederly, mortality, infectiousness or
duration of immunity. We start to know
The irony is that the "vaccine" didn't even reach its primary (and
irrelevant) objective that was the reduction of the severe form of
COVID-19. In the
editorial of the
NEJM issue where the results of the Pfizer clinical trial were published, one can read:
The number of severe cases of COVID-19 (one in the vaccine group and nine in the placebo group) is too small to draw any conclusions about whether the rare cases that occur in vaccinated persons are actually more severe.
Risks of the Pfizer Vaccine
Not much is known about the benefits of the Pfizer vaccine and the
little that is claimed is quite irrelevant. But information about the
risks is slowly coming in, and it's not a pretty picture.
1/ Adverse effects of the vaccine
According the FDA, the Pfizer "vaccine" can cause many serious "adverse
effects", and these are only the known adverse effects induced by
"traditional" vaccines and their usual
adjuvants:
© FDA
Adverse effect of the Pfizer vaccine
The long term effects of vaccines are
known
to be the most devastating ones. So, in addition to the list above,
it's highly probable that numerous additional serious adverse effects
induced by
RNA "vaccines" will be progressively identified, like Lou Gehrig disease, Alzheimer, cancer and multiple sclerosis as suggested by
Judy Mikovitz.
Infertility will probably be another "unexpected" long term side effect since the targeted spike protein is very similar to
sincytin, a protein involved in placental development. When Pfizer tested their "vaccines" on rats, they reported a
50%
drop in reproductive behavior compared to the unvaccinated rats. That's
probably to hide this side effect that Pfizer excluded pregnant women
from its trial.
Conveniently, the adverse vaccine reactions listed above are
increasingly considered by authorities as a consequence of COVID-19.
This is true of
Guillain-Barré Syndrome
(GBS) which, since December 2020 and soon after the beginning of the
vaccination campaign, is said to be caused by COVID-19. Until then, no
causality between the two was claimed, only a
worsening
of COVID-19 symptoms in patients with GBS. The same was done for
Multisystem Inflammatory Syndrome in Children, which is now considered
as being
caused by SARS-COV-2, and for the Kawasaki syndrome, a known
vaccine reaction now blamed on
COVID-19.
To minimize further the potentially devastating effects of the Pfizer "vaccine", a CDC
report labels
anaphylaxis as the cause for a growing number of adverse reactions.
It would all be fine and dandy, except when you calculate the incidence
percentage for these events you get the following numbers:
Dec.14: 3/679 = 0.4%
Dec.15: 50/6,090 = 0.8%
Dec.16: 373/27,823 = 1.3%
Dec.17: 1,476/67,963 = 2.2%
Dec.18: 3,150/112,807 = 2.8%
As you can see the incidence ratio of "anaphylaxis" keeps increasing. It
increased seven-fold from 0.4 to 2.8% over a mere 5 days, which
suggests that the vaccine has delayed adverse effects that can take days
to manifest. The problem is that anaphylaxis is known to manifest
almost
immediately after exposure to the allergenic agent:
Symptoms can start within seconds or minutes of exposure to the food or
substance you are allergic to and usually will progress rapidly. On
rare occasions there may be a delay in the onset of a few hours.
Source
It means that there are probably other (delayed) adverse reactions going on besides (immediate) anaphylaxis.
2/ Negative reactions to the vaccine
On top of the adverse effects we must add the negative reactions. The
table below recapitulates reactions to the Pfizer vaccine (according to
Pfizer solely) at the second inoculation:
© Vox
Reported reactions to the Pfizer vaccine
There's
a caveat though. This table focuses solely on the 18-55 year old
sub-group, basically the young and healthy individuals, who seldom
develop a severe form of COVID-19 let alone die from it.
The frequency of the side effects is high: 59% experience fatigue, 52%
experience headache, 37% muscle pain. Virtually every patient
experienced side effects. The severity of the symptoms is quite appaling
too. For example, 38% of those young and healthy subjects experienced
moderate to severe fatigue and 26% experienced moderate to severe
headache. "
Moderate" meaning interfering with activity and "
severe" meaning preventing daily activity.
In contrast, the general population has a
more than
60% probability of having no symptoms after contracting SARS-COV-2. The relatively young and healthy subpopulation selected by
Pfizer has about an
80% probability of being asymptomatic. So, on one side we have the
Pfizer "vaccine" with its 100% guaranteed side effets , on the other side we have the 80% symptom-free SARS-COV-2.
Is this vaccine causing more symptoms than the disease it is supposed to cure?
Notice in the table above that, just like the table for adverse vaccine
reactions, only negative reactions soon after inoculation are recorded.
The occurrence of negative reactions more than two months after the
first inoculation were simply not investigated.
It means that we have no
idea whatsoever about the medium and long term risks of the "vaccine".
3/ Vaccine deaths
Death was listed in the FDA's list of adverse reactions, and the FDA was
right. Several deaths occurred soon after vaccination. At first, it
seemed like sporadic cases.
One death, then a
second death occurred in Israel soon after inoculation. Around the same time a similar death occurred in
Switzerland. And then a
Florida doctor died soon after receiving the Pfizer vaccine.
The case of Norway is more interesting with
2 vaccine deaths in the beginning of January followed by
23 deaths in one elderly home. That's a total of 25 vaccine deaths while about
20,000
doses have been administered in Norway in the weeks preceding the
"incidents". So,the vaccine fatality rate is about 0,125% which is
comparable to the CFR of COVID-19 mentioned above. And those
vaccine-induced deaths are only the early ones after just one
inoculation.
Even more shocking is the case of Nice nursing homes, with
50 excess deaths on January 15th, only
4 days after the start of vaccinations. During those four days, about
16,000
doses of the Pfizer "vaccine" were administered in the homes. That
gives a preliminary vaccine fatality rate higher than 0.3%, which is
more than double the CFR of COVID-19 and, again, this death toll is
limited to a few days after the very first inoculation.
Norway and Nice are not isolated case. After the first inoculation of Pfizer "vaccine" on
5,847 patients in Gibraltar,
53
of them died within days. That's a vaccine fatality rate of 0.9%. A New
York nursing home which had experienced zero COVID-19 death before
vaccination, reported
24 deaths right after the vaccination of
193 residents. That's a vaccine fatality rate of 12%. The list of vaccine casualties goes
on and on, and it's just after the first dose.
Is the medecine deadlier than the disease it is supposed to cure?
Of course, the authorities deny any link between vaccinations and these
deaths. They blame comorbidities. When a vaccinated individual with
comorbities dies, it's because of the comorbities. When an alleged
SARS-COV-2 positive individual with comorbities dies, it's because of
the SARS-COV-2. Does that make sense?
Conclusion
COVID-19 is a benign disease for which safe and effective treatments
exist. But those treatments are banned or suppressed while a dangerous
and ineffective RNA vaccine is imposed on us through blackmail: no
vaccine = no freedom.
Tens of millions have already been vaccinated, so, if you must take the vaccine, here is an
article describing therapeutic and nutritional approaches to mitigate its side effects.
The elites don't want to protect us, they want to control us. Those self-proclaimed
reality creators, manufactured
an 'obedience' vaccine which, in a royal backfire, transformed into a
'disobedience' mutant. So, they created out of thin air a fake pandemic
in order to impose a vaccine that I believe is designed to cancel the
beneficial effects of the 'disobedience' mutant. In addition, this
vacceine is deadlier and more harmful than the minor disease it is
supposed to cure.
But as we will see in the next instalment, instead of putting on a show
of preventing a fake pandemic, the RNA vaccine might very well recombine
with dormant endoretroviruses and start a very
real pandemic in a second epic backfire. If this comes to pass, it would show again that history has a superb sense of irony.
Notes: Some of the links in this article direct towards videos in French of IHU Lab researchers
like Didier Raoult, Louis Fouché, Michel Drancourt or Philippe Parola.
Outside China, the IHU Laboratory has published the most papers about
SARS-COV-2 to date. These researchers therefore have a unique knowledge
of the "pandemic", unfortunately their video presentations are mostly in
French.