Nuremberg Code and Covid Vaxx mandates

Emergency Use Authorization

The first thing we need to remember is that all of the COVID-19 “vaccines” available in the United States fall under an Emergency Use Authorization (EUA).

(a) In general
(1) Emergency uses
Notwithstanding any provision of this chapter and section 351 of the Public Health Service Act [42 U.S.C. 262], and subject to the provisions of this section, the Secretary may authorize the introduction into interstate commerce, during the effective period of a declaration under subsection (b), of a drug, device, or biological product intended for use in an actual or potential emergency (referred to in this section as an “emergency use”).

21 U.S.C. §360bbb-3

The idea is simple. In an emergency, the government will allow a drug, device, or biological product to enter the market before completing the regular approval process, which usually takes years. Certain conditions must exist before such an authorization can be legally issued. Let’s take a look at them one by one in relation to COVID-19

(c) Criteria for issuance of authorization
The Secretary may issue an authorization under this section with respect to the emergency use of a product only if, after consultation with the Assistant Secretary for Preparedness and Response, the Director of the National Institutes of Health, and the Director of the Centers for Disease Control and Prevention (to the extent feasible and appropriate given the applicable circumstances described in subsection (b)(1)), the Secretary concludes-
(1) that an agent referred to in a declaration under subsection (b) can cause a serious or life-threatening disease or condition;

21 U.S.C. §360bbb-3

Is COVID-19 a serious or life-threatening disease? There is evidence that the initial variants of the disease could be serious enough to require hospitalization and even cause death. However, in August of 2020, the Centers for Disease Control and Prevention (CDC) issued a report stating that 94% of the COVID deaths they were reporting involved more than just COVID.

Using the data available by January 16, 2022, 94% of deaths certificates listed an average of four additional causes of death. This brings into question, how many of the over 800,000 deaths the CDC is reporting are people who died with COVID, not of it? As of the writing of this article, the CDC is reporting 862,494 total deaths. If less than 6% of those death certificates list only COVID as the cause of deaths, that means we are only sure that about 52,000 were caused by COVID, or about .015% of the U.S. population.

(2) that, based on the totality of scientific evidence available to the Secretary, including data from adequate and well-controlled clinical trials, if available, it is reasonable to believe that-
(A) the product may be effective in diagnosing, treating, or preventing-
(i) such disease or condition; or
(ii) a serious or life-threatening disease or condition caused by a product authorized under this section, approved or cleared under this chapter, or licensed under section 351 of the Public Health Service Act [42 U.S.C. 262], for diagnosing, treating, or preventing such a disease or condition caused by such an agent; and

(B) the known and potential benefits of the product, when used to diagnose, prevent, or treat such disease or condition, outweigh the known and potential risks of the product, taking into consideration the material threat posed by the agent or agents identified in a declaration under subsection (b)(1)(D), if applicable;

21 U.S.C. §360bbb-3

Based on the totality of scientific data, do the COVID “vaccines” diagnose, treat, or prevent the disease? While there was much hype about the effectiveness of these “vaccines” when they were first released, that bubble has well and truly burst. Well-controlled clinical trials, along with other studies, have shown that the effectiveness of these “vaccines” is short-lived at best, ranging between 2-6 months. Studies have shown that those who have received the “vaccine” can not only get COVID, but when they do they can spread it at least as easily as the “unvaccinated”. So not only do the “vaccines” not treat COVID, they neither prevent infection nor transmission. In other words, the “vaccines” are a private health concern, not a public one.

(3) that there is no adequate, approved, and available alternative to the product for diagnosing, preventing, or treating such disease or condition;

The evidence that existing approved medications were capable of treating COVID-19 has been around for more than a year. However, the same government bureaucracy that has been promoting these “vaccines” has conveniently not only failed to approve these products for the treatment of COVID-19, but they have also lied about the evidence for their effectiveness.

(4) in the case of a determination described in subsection (b)(1)(B)(ii), that the request for emergency use is made by the Secretary of Defense; and

(5) that such other criteria as the Secretary may by regulation prescribe are satisfied.

21 U.S.C. §360bbb-3

These last two are not really an issue currently with COVID-19.

So what does this have to do with The Nuremberg Code? As I stated before, all of the “vaccines” currently available in the U.S. are NOT Food and Drug Administration (FDA) approved; they are issued under an EUA. That means, according to the law, they are either unapproved or conditionally approved.

(2) Approval status of product
An authorization under paragraph (1) may authorize an emergency use of a product that-
(A) is not approved, licensed, or cleared for commercial distribution under section 355, 360(k), 360b, or 360e of this title or section 351 of the Public Health Service Act [42 U.S.C. 262] or conditionally approved under section 360ccc of this title (referred to in this section as an “unapproved product”); or
(B) is approved, conditionally approved under section 360ccc of this title, licensed, or cleared under such a provision, but which use is not under such provision an approved, conditionally approved under section 360ccc of this title, licensed, or cleared use of the product (referred to in this section as an “unapproved use of an approved product”).

21 U.S.C. §360bbb-3

It’s not only the “vaccines” that are being distributed under an EUA, because the COVID-19 RT-PCR test is as well. I’m sure some of you are screaming that “The FDA approved the Pfizer vaccine!” Well, yes and no. You see the FDA gave approval for the Comirnaty brand of the Pfizer-BioNTech “vaccine”, but Pfizer has refused to distribute that particular version in the United States. Furthermore, the FDA required, in their approval letter, that BioNTech conduct no less than six additional studies because they could not assess the risks of myocarditis and pericarditis from the data that had already been submitted.

Not only are the COVID-19 “vaccines” only available in the U.S. under an EUA, but both the Pfizer and Moderna products are based on a new technology, mRNA, which has never been tested in humans before, and is not even legally a vaccine.

A preparation of a weakened or killed pathogen, such as a bacterium or virus, or of a portion of the pathogen’s structure, that is administered to prevent or treat infection by the pathogen and that functions by stimulating the production of an immune response.

American Heritage Dictionary

Even a recent article from the National Institutes of Health (NIH) refers to these mRNA “vaccines” as experimental. So even if you haven’t taken a COVID-19 “vaccine”, you are participating in a medical experiment if you’ve had a PCR test.

We’ve looked at the law and The Nuremberg Code, but what does all of this have to do with the Constitution?

RV wrote:While I understand WHY the "Vaccine" was rushed through. The fact that it does more harm than good, the fact that it is different from ANY other Vaccine and the fact that there is so much politics and bias connected with it points to a scam.

It was intended to get President Trump, implement socialism, hysteria, fear, money for big pharma and install the demented in chief. Clearly it worked.