We saw throughout the COVID Plandemic that the pharmaceutical industry took advantage of "Public Health Emergency" designations to get the FDA to issue EUAs (emergency use authorization) to get new, untested vaccines into the market as soon as possible without proper testing, and more importantly for the pharmaceutical companies, no legal liabilities.

With the W.H.O. and the U.S. Government now declaring monkeypox to be a "Public Health Emergency," could the same thing happen with new vaccines and drugs for monkeypox?

The problem in issuing the existing smallpox/monkeypox vaccine an EUA, is that it was already approved by the FDA, even though it has not been tested in the public much beyond the initial trials conducted by the drug company.

According to Dr. Meryl Nass, that may not stop them from figuring out a way to get the FDA to issue them an EUA to avoid legal liability:

Although I don't have the full story yet, I am warning you that the moneypox vaccine Jynneos is a huge scam, in every way, including the supposed shortage.  I will disclose more about that soon.

But since it is actually licensed, the moneypox vaccine (like other licensed drugs and vaccines) has liability attached to it.  You can currently sue government program planners, the doctor who recommended it, the manufacturer, etc. if anything goes wrong.