Posted BY: | NwoReport
In a press release on Tuesday, the FDA declared the monovalent Pfizer and Modena mRNA Covid-19 vaccines are no “longer authorized for use in the United States.”
The decision was made through a recent amendment to the Emergency Use Authorizations of the Moderna and Pfizer Covid-19 bivalent vaccines.
In the amendment, the FDA ruled the bivalent Moderna and Pfizer Covid-19 vaccines will be used for all doses and monovalent doses (targeted original strain) will no longer be authorized.
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 vaccine are questioning why the FDA is making the decision now.
Trending: NYC mother says Alvin Bragg’s office treated her ‘like garbage’ after ‘brutal … slaughter’ of veteran son
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— U.S. FDA (@US_FDA) April 18, 2023
What you need to know. 🧵👇 pic.twitter.com/9394LP1HvR