Evidence of a “colossal crime against humanity”: This is how the new book “Pfizer Documents Analysis Reports” is described in the preface. It is a collection of analyzes of Pfizer documents, the publication of which the FDA originally wanted to delay for 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 mRNA vaccine conspiracy theories can be confirmed by these official documents.
The book, a collaboration between Bannon’s War Room and Wolf’s DailyClout, is available on Amazon. The freely available excerpt contains, among other things, a summary of 16 critical results of the Pfizer document analysis: In addition to the lack of efficacy, vaccine safety is particularly targeted. The devastating conclusion:
If Pfizer had a TV commercial for this COVID vaccine, it would probably take the speaker more than 80 hours straight to read the 158,893 side effects from the first 12 weeks.
Various translations of this summary are available via the Neue-Medien-Portal – you can read the Croatian version below:
effectiveness
#1: Less than 50 percent.
Pfizer’s claim of 95 percent effectiveness was based solely on the erratically small number of COVID-19 cases in clinical trials: 170 cases in more than 40,000 study participants. The measured effectiveness of the vaccine 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 in whom antibody detection showed they had contracted Covid-19 during the study, only 54 percent efficacy in terms of protection was found.
Since there are vaccines that often do not produce viral antibodies despite the Covid-19 infection, a large number of vaccinated people who became infected during the research were not counted at all. And the actual effectiveness was far less than 50 percent—yet the FDA granted Emergency Use Authorization (EUA).
#2: Launch damage.
Pfizer’s clinical trial data showing high safety and efficacy do not match the real-world data submitted to the FDA.
Regarding the 32,760 vaccine recipients with known impairment in the first 12 weeks of vaccine introduction, Pfizer reported:
About 20 percent of the reports were related to COVID-19 diseases.
COVID-19 was the third most frequently reported adverse event.
More than 15 percent of cases of COVID-19 are classified as serious.
More than 200 people died of COVID-19 in this post-marketing study.
Security
#3: Sting 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 reports of adverse events during the 12 weeks of the vaccine’s launch. Pfizer had to hire a team of 2,400 other full-time employees to handle the caseload. Despite these additional employees, Pfizer was unable to definitively determine vaccine harm in more than 20,000 people.
#5: Dead Babies.
When Pfizer evaluated side effects during the first 12 weeks of the vaccine’s introduction, 270 pregnant women reported harm from the vaccine. But Pfizer investigated only 32 of those cases, in which 28 babies died. This equates to a fetal mortality rate of a shocking 87.5 percent.
# 6: Nursing.
The real data from Pfizer showed numerous side effects of vaccination in nursing mothers, and infant vomiting, fever, skin inflammation, restlessness and allergic reactions in infants. In addition, partial paralysis, suppressed lactation, breast pain, migraines and blue-green discoloration of breast milk occurred in nursing mothers.
Despite these alarming data on vaccination during pregnancy and breastfeeding, Pfizer health officials and numerous medical societies continue to strongly recommend that pregnant and lactating women across the country receive the mRNA vaccine.
#7: Shedding.
Pfizer’s clinical trial documents suggest that the mRNA component that triggers production of spike proteins can be transmitted through skin-to-skin contact, inhalation, body fluids and sexual intercourse, so an unvaccinated person can get the vaccine through “environmental exposure”. In other words, this “spill” 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) assured Americans that rejecting the mRNA vaccine against COVID-19 was a “myth” and “misleading information.”
#8: Male fertility I.
The criteria for the inclusion of men in the Pfizer study required either complete abstinence from sex with women of reproductive age or the use of condoms and other “highly effective” contraceptives, as well as no sperm donation. This suggests that Pfizer suspected that the ejaculate of vaccinated men could affect both women and unborn children conceived during and after the study.
#9: Male Fertility II.
Pfizer did not assess the vaccine’s adverse effects on male fertility during clinical trials because the company was pressed for time. They claim that the omission of data on reproductive toxicity was necessary to expedite vaccine development and meet an alleged urgent public health need. However, Pfizer’s study documents show that the company knew that its vaccine components (lipid nanoparticles, mRNA carriers) crossed the blood-testis barrier; that, according to previous studies, nanoparticles accumulate in the testes and that they damage reproduction by affecting the quality, quantity, morphology and mobility (movement) of sperm.
#10: Fertility of men III.
In Pfizer’s study of side effects during the public presentation of the vaccine in early 2021, “positive anti-sperm” was included among 1,290 reported side effects of special interest. The presence of anti-sperm antibodies in the male ejaculate is an immunological cause of male infertility, since the binding of the antibodies to the sperm hinders their motility, making the journey of the sperm to the egg very difficult or even impossible.
#11: modRNA.
Although mRNA occurs naturally in the body and is rapidly degraded, Pfizer has modified the vaccine RNA (modRNA) so that it (i) continues to produce spiked proteins for untested durations, (ii) produces countless spiked proteins in untested quantities, 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 lifetimes, spike protein lifetimes, or modRNA-produced spike protein doses 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 vaccine’s emergency use authorization (EUA) was issued (May 2021), a peer-reviewed study showed that 35 adolescents suffered from myocarditis after vaccination with Pfizer. It was not until August 2021, after millions of teenagers had already received the vaccine, that the FDA, CDC and Pfizer issued a warning about the risk of myocarditis in teenagers.
#13: miRNAs.
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 the outside, like Pfizer’s vaccine, alters the delicate balance between naturally occurring molecules, which can have potentially harmful consequences that Pfizer hasn’t even studied.
#14: control group.
In Pfizer’s Phase 3 human trial, the vaccinated group was to be compared with a placebo control group for two years to measure the vaccine’s safety. However, after just four months, Pfizer beat the control group by vaccinating those who received a placebo injection. In doing so, they have destroyed a vital ability to measure the extent to which vaccines are causally related to worsening health conditions that develop after vaccination.
#15: Production.
Pfizer’s documents raise serious concerns about vaccine manufacturing standards: The FDA found that the Kansas manufacturing facility that filled the components of the 2019 and 2020 mRNA vaccine had “mold and bacteria” and “released 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 bluffed by licensing a version of the vaccine called Comirnaty : then claiming that Comirnaty was “matched” or “equivalent” to Pfizer’s emergency approved version of the vaccine. However, Pfizer documents show that only about 4 percent [of the Comirnaty] agreed to this EUA vaccine, making it unavailable to the public. Pfizer says: “Certain lots of Pfizer-BioNTech COVID-19 vaccine approved for emergency use comply with [Comirnaty]” – exactly 9 out of a total of 190 lots.
Conclusion
Pfizer’s positive evaluation from clinical studies contradicts reality: there are side effects and failure in terms of the guaranteed effect. This has been documented since the introduction of the COVID vaccine.
