Bye bye EUA🤗

Before Covid, I thought Emergency Use Authorization (EUA) was given only for experimental drugs to dying cancer patients for whom all FDA-approved medicines were no longer working.

Imagine my surprise 🥴

When an experimental “vaccine”, based on a new mRNA technology that had never received FDA approval in prior attempts by the pharmaceutical companies who made them, received EUA approval. THAT news smelled like rotting fish.

I had known that many steps were required to evaluate the safety and efficacy of a drug before the FDA approved it for widespread consumption. These steps require time, typically 7 to 10 years, and huge financial investments.

https://www.drugs.com/fda-approval-process.html

Apparently, this regulatory framework was waived in order to “save humanity” from the viral scourge - a decision made by the first Trump Administration, then adopted by Biden’s.

GOOGLE Gemini explains recent regulatory changes.

Yes, the U.S. Food and Drug Administration (FDA) recently rescinded the emergency use authorizations (EUAs) for the COVID-19 vaccines for the general population.👏

This action, announced in August 2025, coincided with the FDA approving updated 2025-2026 formulations of the COVID-19 vaccines from Pfizer, Moderna, and Novavax.

Key details of the change:

* EUA Rescinded: The blanket Emergency Use Authorization that made the shots widely and easily available to nearly all Americans has been rescinded.

* Narrower Approvals: The FDA instead issued marketing approvals for the updated vaccines, but with restrictions on who can receive them by default.

* They are approved for all adults 65 and over.

* They are approved for younger adults and children (down to a certain age, which varies by manufacturer) who have at least one underlying condition that puts them at high risk for severe COVID-19.

* Impact on Healthy People: For healthy individuals who do not fall into the approved categories, getting the vaccine may require a more involved process, such as consulting with a physician for what is known as “shared clinical decision-making.”

* Impact on Young Children: The decision means that there is no longer a COVID-19 vaccine authorized for healthy children under 5 years old from one of the major manufacturers.

Something missing

I am not a lawyer, but I do feel that the FDA approval received by the pharmaceutical manufacturers for those Covid “vaccines”, including complete liability protection, was a “crime against humanity” that inflicted consequences much too large to calculate.

Criminal prosecution of those responsible, starting with Anthony Fauci and the CEO’s of Pfizer and Moderna, is an announcement that is missing from this good news story.

Informed Consent.

Imagine if the EUA had been granted for the “vaccines” requiring that every recipient be provided with:

• A complete history of past FDA rejections of the mRNA technology,

• Complete and accurate data on the reasons for approval failures,

• A description of the full range of side effects experienced by past subjects of drug testing trials.

• A true revelation of the extent to which these “vaccines” had been tested prior to EUA approval.

If you were presented with this level of “full disclosure” weeks before agreeing to subject yourself to an experimental shot so that you could discuss it with others and validate the information provided, how likely is it that you would have rolled up your sleeve for the needle?