News
The FDA has announced its amendment of the emergency use authorisations (EUAs) for the Moderna and Pfizer-BioNTech COVID-19 bivalent mRNA vaccines in an attempt to simplify the vaccination programme.
These amendments mean that:
Peter Marks MD PhD, director of the FDA’s Center for Biologics Evaluation and Research, commented: “At this stage of the pandemic, data support simplifying the use of the authorised mRNA bivalent COVID-19 vaccines and the agency believes that this approach will help encourage further vaccination.
Evidence is now available that most of the US population five years of age and older has antibodies to SARS-CoV-2, the virus that causes COVID-19, either from vaccination or infection that can serve as a foundation for the protection provided by the bivalent vaccines. COVID-19 continues to be a very real risk for many people, and we encourage individuals to consider staying current with vaccination, including with a bivalent COVID-19 vaccine. The available data continue to demonstrate that vaccines prevent the most serious outcomes of COVID-19, which are severe illness, hospitalisation and death.”