Evidence of “a colossal crime against humanity”: This is how the new book “Pfizer Documents Analysis Reports” is described in the foreword. It is a collection of analyzes of the Pfizer documents, the publication of which the FDA originally wanted to delay by 75 years: A team of 3,500 volunteers led by Naomi Wolf and Steve Bannon evaluated the explosive documents and came to a devastating conclusion. Even a freely available summary of only 16 critical results makes it clear: numerous so-called conspiracy theories about the mRNA vaccine can be confirmed by the official documents.
The book, the result of a collaboration between Bannons War Room and Wolfs DailyClout, is available on Amazon. The freely available excerpt contains, among other things, a summary of 16 critical results of the analyzes of the Pfizer documents: In addition to the lack of effectiveness, the safety of the vaccines is particularly targeted. The devastating conclusion:
If Pfizer had a TV spot for this COVID vaccine, it would probably take a speaker more than 80 hours straight to read out the 158,893 adverse events from the first 12 weeks.
Various translations of this summary are available via the Neue-Medien-Portal – you can read the German version below (individual adjustments to the choice of words by Report24):
effectiveness
#1: Less than 50 percent.
Pfizer’s claimed 95 percent effectiveness was based solely on a vanishingly small number of COVID-19 cases in the clinical trials: 170 cases in over 40,000 study participants. Measured vaccine efficacy in such a small sample of COVID-19 cases is too insignificant to generalize and extrapolate to a population of hundreds of millions of people.
Compared to the number of participants with antibody detection showing that they contracted Covid-19 during the study, only 54 percent efficacy was found in terms of protection.
Since there are vaccine recipients who often do not produce viral antibodies despite Covid-19 infection, a large number of vaccinated people who became infected during the study were not counted at all. And the actual effectiveness was far less than 50 percent – yet the FDA issued an Emergency Use Authorization (EUA).
#2: Damage from launch.
Pfizer’s clinical trial data showing high safety and efficacy do not match real-world data submitted to the FDA.
Regarding the 32,760 vaccine recipients with known impairment from the first 12 weeks of vaccine introduction, Pfizer reported:
About 20 percent of the reports related to COVID-19 diseases. COVID-19 was the third most commonly reported adverse event. Over 15 percent of COVID-19 cases were classified as serious. Over 200 people in this post-marketing study died from COVID-19.
Security
#3: Puncture site.
Contrary to public statements by Pfizer and the FDA, both were aware of data showing that vaccine components travel through the bloodstream from the injection site, crossing key blood-organ barriers (including those in the brain, testes, and ovaries). ) and continue to produce harmful spike proteins indefinitely.
#4: Need for additional employees.
Pfizer did not anticipate that there would be more than 158,000 individual adverse event reports during the 12 weeks of vaccine launch. Pfizer had to hire a crew of 2,400 other full-time employees to handle the caseload. Despite these additional employees, Pfizer was not able to definitively determine the vaccine damage in more than 20,000 people.
#5: Tote Babies.
When Pfizer assessed adverse events during the first 12 weeks of vaccine introduction, 270 pregnant women reported vaccine harm. But Pfizer only investigated 32 of those cases, in which 28 of the babies died. That equates to a shocking 87.5 percent fetal death rate.
#6: Breastfeeding moms.
Real data from Pfizer showed a number of side effects of vaccination in breastfeeding mothers, and infantile vomiting, fever, skin inflammation, restlessness, and allergic reactions in infants. In addition, partial paralysis, suppressed lactation, breast pain, migraines and a blue-green discoloration of the breast milk occurred in the breastfeeding mothers.
Notwithstanding these alarming data regarding vaccination during pregnancy and lactation, Pfizer, health officials and numerous medical societies continued to strongly recommend that pregnant and lactating women across the country should receive the mRNA vaccines.
#7: Shedding.
Pfizer’s clinical trial documents suggest that the mRNA component that triggers spike protein production can be transmitted through skin-to-skin contact, through inhalation, through bodily fluids, and through sexual intercourse, so that an unvaccinated person can get the vaccine through “environmental exposure”. In other words, this “shedding” is real and a problem that is explicitly mentioned in Pfizer’s own documents. But as recently as July 2022, the Centers for Disease Control and Prevention (CDC) was reassuring Americans that shedding the COVID-19 mRNA vaccine was a “myth” and “misleading information.”
#8: Male Fertility I
Criteria for including men in the Pfizer study required either total abstinence from sex with women of childbearing potential or use of condoms and other “highly effective” contraceptives, as well as no sperm donation. This suggests that Pfizer suspected that vaccinated men’s ejaculate could affect both women and unborn children conceived during and after the study.
#9: Male Fertility II.
Pfizer did not evaluate the vaccine’s adverse effects on male fertility during clinical trials because the company was pressed for time. They claim that the omission of the reproductive toxicity data was necessary to speed up the development of the vaccine and to meet the alleged urgent public health need. However, Pfizer’s study documents show that the company knew that its vaccine components (lipid nanoparticles, carriers of the mRNA) crossed the blood-testicular barrier; that, according to previous studies, nanoparticles accumulate in the testicles and that they damage reproduction by affecting the quality, quantity, morphology and motility (movement) of sperm.
#10: Male Fertility III.
In the Pfizer study of adverse events during the early 2021 public launch of the vaccine, “anti-sperm antibody positive” was included among the 1,290 reported adverse events of special interest. The presence of anti-sperm antibodies in male ejaculate is an immunological cause of male infertility, as the attachment of antibodies to sperm impairs their motility, making the sperm’s journey to the egg highly difficult or even impossible.
#11: modRNA.
Although mRNA is naturally occurring in the body and is rapidly broken down, Pfizer has modified vaccine RNA (modRNA) so that it (i) continues to produce spike proteins for an untested duration, (ii) produces myriad spike proteins in untested amounts, and (iii) turns off the body’s normal immune responses, which can suppress immunity to other diseases such as viruses and cancer. Despite these significant changes in vaccine mRNA, Pfizer has not conducted any of the usual studies that measure mRNA lifespan, spike protein lifespan, or modRNA-produced doses of spike protein in different individuals.
#12: Myocarditis.
During the launch of the vaccine, in early 2021, Pfizer received reports of cases of myo-pericarditis (inflammation of the lining of the heart and heart muscle) and a month before the juvenile emergency use authorization (EUA) was granted (May 2021), a peer-reviewed study showed that 35 adolescents had suffered myocarditis after the Pfizer vaccination. It was only in August 2021, after millions of teenagers had already received the vaccine, that the FDA, CDC and Pfizer issued the warning about the risk of myocarditis in teenagers.
#13: miRNA.
Pfizer hid that their COVID-19 vaccine contains something called microRNA (miRNA), which is an important natural component of gene expression and regulation and has been linked to many diseases and a person’s immunity. miRNA introduced into the body from outside, such as through Pfizer’s vaccine, alters the delicate balance between the naturally occurring molecules, which can have potentially harmful consequences that Pfizer didn’t even study.
#14: control group.
In Pfizer’s phase 3 human trial, the vaccine group was to be compared to a control group receiving a placebo for two years to measure the safety of the vaccine. However, Pfizer broke the control group after just four months by vaccinating those who received the placebo injection. In doing so, they destroyed the vital ability to measure the extent to which vaccines are causally related to deteriorating health conditions that develop after vaccination.
#15: Manufacturing.
The Pfizer documents raise serious concerns about vaccine manufacturing standards: The FDA found the Kansas manufacturing facility that filled mRNA vaccine components in 2019 and 2020 to have “mold and bacteria” and “release drugs without quality control.” “. And in its most recent inspection, Pfizer again found isolates of bacteria and/or mold in critical zones, according to the FDA.
#16: Comirnaty.
In September 2021, Pfizer and the FDA pulled a bluff by licensing a version of the vaccine called Comirnaty: Comirnaty was then claimed to be “matched” or “equivalent” to Pfizer’s emergency-approved version of the vaccine. The Pfizer documents show, however, that only about 4 percent [von Comirnaty] match this EUA vaccine, which was thus not available to the public at all. Pfizer says: “Certain lots of Pfizer-BioNTech’s COVID-19 vaccine approved for emergency use are compliant [Comirnaty]“ – exactly 9 of a total of 190 batches.
Conclusion
Pfizer’s positive assessment from the clinical studies contradicts reality: there are undesirable effects and a failure in terms of the guaranteed effect. This was documented after the introduction of the COVID vaccine.
final point
If Pfizer had a TV spot for this COVID vaccine, it would probably take a speaker more than 80 hours straight to read out the 158,893 adverse events from the first 12 weeks.