Big Pharma’s ‘Emergency Use Authorization’ Vaccine Approval Scam
Evil Big Pharma fooled us. We were conned to believe there was ‘crisis’ pandemic. An untested and problematic vaccine was rushed through so the world could be given a jab against our will and at grave risk to our health.
The Emergency Use Authorization (EAU) for the Experimental Gene Therapy (being unlawfully called a vaccine) by Pfizer and Moderna, was issued based on the premise that there was nothing else available to fight Sars-CoV-2 and the resulting disease called CoVID-19. [1]
Since the EUA was issued, The CDC, WHO, and the AMA have all retracted their statements saying that hydroxychloroquine + zinc is either dangerous and/or ineffective. In addition, according to the CDC website they have over estimated their CoVID-19 cases and deaths by 1,600%. Furthermore, as anticipated, they have told the RT-PCR “testing” centers to run the amplification cycle fewer times to reduce the false positive results. Not more than 35 amplifications.
This will make it look like things are getting better because the “vaccine”, social distancing, and masks are working. All this while the RT-PCR is not even a valid way of testing for a virus or an infection or a disease process.
The inventor of the PCR warned us all that this was a huge problem. [2, 3, 4, 5, 6]
In addition to hydroxychloroquine + zinc, there is now the I-MASK+ Prophylaxis & Early Outpatient Treatment Protocol for COVID-19 such that there is no need to push through any mandatory mass vaccination plan as well as Lysine. [7]
Backed by decades of research and safety data for herpes-family viruses, U.S.-based researchers at Bio-Virus Research Inc, Reno, Nevada, report on the successful treatment of the first 30 frontline doctors and nurses and a thousand-plus patients given the amino acid lysine to prevent and even abolish COVID-19 corona virus infections at a clinic in the Dominican Republic.
Astonishingly, symptoms of COVID-19 are reported to have dissipated within hours of this natural treatment. [8]
Another treatment is Ultraviolet Blood Therapy (UBT). In brief, (see the full UBT protocol at https://infectionscured.com/ ) it involves drawing 40 – 60 cc of blood, diluting it 4 – 1 with saline, adding 1,000 units of heparin to prevent coagulation, shining ultraviolet light (UV) through it and re-infusing the treated diluted blood. The UV-C strips the protective covering off some (not all) of the pathogens in that blood so that, after it is re-infused, the immune system can recognize the live pathogen and eradicate it; the UV-A is absorbed bu the red blood cells and enhances the immune system. The body cures itself. The whole procedure takes about 25 minutes.
There are several other treatments involving nebulizers, one of which is Budesonide, an inhaled Corticosteroid. https://budesonideworks.com/
In addition to this, doctors are also prescribing the antibiotic Azythromicin (Z-pack). Based on the premise from the FDA on the EUA,
“Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), the FDA Commissioner may allow unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN threat agents when there are no adequate, approved, and available alternatives.
Section 564 of the FD&C Act was amended by the Project Bioshield Act of 2004 and was further amended by the Pandemic and All-Hazards Preparedness Reauthorization Act of 2013 (PAHPRA), the 21st Century Cures Act of 2016, and Public Law 115-92 of 2017.
Please note: a determination under section 319 of the Public Health Service Act that a public health emergency exists, such as the one issued on January 31, 2020, does not enable FDA to issue EUAs. A separate determination and declaration are needed under section 564 of the Federal Food, Drug and Cosmetic Act to enable FDA to issue EUAs, provided other statutory criteria are met.”
The conditions under which it was approved no longer exist.
As such The EUA is no longer valid and should be revoked, terminated, or abolished immediately.
Failure to revoke the EUA for the Experimental Gene Therapy from Pfizer and Moderna will place you in violation of sections of the Nuremberg code. Those are war crimes and crimes against humanity. If you continue on your current path of war against the people, as in any war, eventually, we the people will be sending in the military to remove you and your abusive ways.
Read more about the Nuremberg code here history.nih.gov and how Lawyers Promise ‘Nuremberg Trials’ Against All Behind COVID Scam as well as tapnewswire.com
References:
[2] https://off-guardian.org/2020/10/05/pcr-inventor-it-doesnt-tell-you-that-you-are-sick/
[5] https://principia-scientific.com/who-finally-admits-covid19-pcr-test-has-a-problem/
[6] [https://www.eclassifie.com/2020/05/what-is-a-pcr-test-kit-by-kary-mullis/
[7] https://covid19criticalcare.com/i-mask-prophylaxis-treatment-protocol/i-mask-protocol-translations/ www.FLCCC.net
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Alan
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It isn’t just the emergency use approval, which is the same in the UK, it is the missing trial data to show the effectiveness of the vaccines. I have only seen a reference to the Pfizer trial which claimed an efficacy of 95%, but this was calculated without considering the number of people on the trial. The true efficacy was less than 1%. Where are the independent randomised control trials? The UK government said it was not helpful to publish the limited results available. Boris treats us as idiots, and it is becaise most people are. Pavlov’s dogs comes to mind.
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Davo Jaeger
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It is up to the people. They’ve shown the paperwork as per their SOP (they must show a way out and the people must exercise their right to stand up), and now the courage to do something lays within the masses and others–not all of us are part of the masses ‘mindset’.
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