Original COVID-19 Shots No Longer “Authorized for Use” in the United States

The FDA announced Tuesday that the monovalent Pfizer and Moderna COVID-19 shots are no longer “authorized for use” in the United States.

The “monovalent” shots are the original COVID-19 shots administered to the public for the two-dose primary series.

Today, FDA amended the EUAs of the Pfizer-BioNTech and Moderna COVID-19 bivalent mRNA vaccines to simplify the vaccination schedule for most individuals. https://t.co/Cd74KB3n9p
What you need to know. 🧵👇 pic.twitter.com/9394LP1HvR

— U.S. FDA (@US_FDA) April 18, 2023

The monovalent Moderna and Pfizer-BioNTech COVID-19 vaccines are no longer authorized for use in the United States.

— U.S. FDA (@US_FDA) April 18, 2023

Most individuals who have already received a single dose of the bivalent vaccine are not currently eligible for another dose. We intend to make decisions about future vaccination after receiving recommendations on the fall strain composition at an FDA advisory committee in June.

— U.S. FDA (@US_FDA) April 18, 2023

Most unvaccinated individuals may receive a single dose of a bivalent vaccine, rather than multiple doses of the original monovalent mRNA vaccines.

— U.S. FDA (@US_FDA) April 18, 2023

From the FDA:

Today, the U.S. Food and Drug Administration amended the emergency use authorizations (EUAs) of the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines to simplify the vaccination schedule for most individuals. This action includes authorizing the current bivalent vaccines (original and omicron BA.4/BA.5 strains) to be used for all doses administered to individuals 6 months of age and older, including for an additional dose or doses for certain populations. The monovalent Moderna and Pfizer-BioNTech COVID-19 vaccines are no longer authorized for use in the United States.

How many Americans were coerced into taking this poison or fired from their jobs for refusing to take the shots?

Now, they’re suddenly unauthorized for use in the United States.

Perhaps Joe Biden signing a resolution to end the fake COVID-19 emergency had something to do with the amended emergency use authorizations (EUAs).

JUST IN: Biden Signs Law Declaring COVID-19 ‘Emergency’ Over

The FDA's announcement has many people asking 'why now?'

Elon Musk asked "why," and the FDA responded.

Hi, Elon. Thanks for your question. It's probably worth clarifying that the monovalent vaccines are still approved (licensed). That hasn't changed. But they are no longer authorized for *emergency use* in the United States.

— U.S. FDA (@US_FDA) April 18, 2023

If the COVID-19 "emergency" was declared over, then why is any shot "authorized for emergency use?"

The FDA's move also caught the attention of James O'Keefe.

"Can someone from the FDA please tell me what’s going on here?" O'Keefe asked.

Can someone from the FDA please tell me what’s going on here? [email protected] https://t.co/YfyLeJyWNn

— James O'Keefe (@JamesOKeefeIII) April 18, 2023

Other Twitter users commented on the FDA's decision to pull the monovalent COVID-19 shots:

Breaking: The US FDA no longer authorizes Moderna and Pfizer monovalent ‘vaccines’ for use in the US. For the 100 plus million Americans previously injected with this stuff? “Our bad!” pic.twitter.com/4UkjwbRUX2

— Paul Hookem 🇺🇸 (@PaulHook_em) April 18, 2023

Am I hallucinating that they told you the bivalent vaccine wouldn’t work unless you got an (obsolete) monovalent series first, and therefore required an (obsolete) monovalent series as a prerequisite to the bivalent?

Man. That Science changes quickly. https://t.co/oPXQFDi5Z3

— Sarah Beth Burwick (@sarahbeth345) April 18, 2023

How many Americans were coerced into taking this poison or lost their jobs because they refused?https://t.co/HdUCS5jIFl

— DailyNoah.com (@DailyNoahNews) April 19, 2023