The FDA announced, in a press release on Tuesday, that the monovalent Pfizer and Moderna mRNA COVID-19 “vaccines” are “no longer authorized for use in the United States.”
The “monovalent” shots are the original experimental COVID-19 vaccines administered to the public for the two-dose primary series.
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.
Most individuals, depending on age, previously vaccinated with a monovalent COVID-19 vaccine who have not yet received a dose of a bivalent vaccine may receive a single dose of a bivalent vaccine.
How many millions of Americans were coerced into getting the shots or fired from their jobs for refusing to get the shots?
How many were severely injured, or killed, from being coerced into taking this experimental drug?
Now, just like that, they’re no longer authorized for use in the United States.
The FDA claims the decision was made in order to simplify the vaccine process, but many people who have already received the monovalent COVID-19 shot are questioning why the FDA is making the decision now.
Elon Musk asked why.
The FDA responded:
This begs the question, if the COVID-19 “emergency” was declared over, then why are any of the shots authorized for “emergency use?”
James O’Keefe also asked for an explanation from the FDA.
“Can someone from the FDA please tell me what’s going on here?” O’Keefe asked.
Other Twitter users commented:
