(Reader: Bob) The Emergency Use Authorization

Reader Post | By Bob

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 C19.


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 C19 cases and deaths by 1,600%. In addition 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” is working.

In addition to hydroxychloroquine + zinc, there is now the I-MASK+ Prophylaxis & Early Outpatient Treatment Protocol for C19,


www.FLCCC.net (home page for the above link)

and Lysine.

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 C19 [corona]virus infections at a clinic in the Dominican Republic. Astonishingly, symptoms of C19 are reported to have dissipated within hours of this natural treatment.

https://beforeitsnews.com/tea-party/2021/02/virologists-report-poor-mans-amino-acid-cure-for-covid-19-would-abolish-need-for-vaccines-2643136.html (link for above)

There are several other examples of nebulizer treatments as well. (I just have not had time to find the research to include here.)

In addition to this, doctors are also prescribing the antibiotic Azythromicin (Z-pack).

For the record, I am not a doctor, just a data researcher.

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 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 way, eventually, we the people will be sending in the military to remove you and your abusive ways.


How can we cause this to happen in the next few days?

Best regards,


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