The United States Food and Drug Administration (FDA), a federal health agency, has announced emergency use authorisation (EUA) for a monkeypox vaccination method that could expand the availability of doses.Under the order, health care providers can use a dosing technique that allows them to extract more doses of the JYNNEOS vaccine per vial. The FDA released a statement on Tuesday that said the change could increase vaccine availability “by up to five-fold”.“In recent weeks the monkeypox virus has continued to spread at a rate that has made it clear our current vaccine supply will not meet the current demand,” said FDA Commissioner Robert Califf in a statement. “The FDA quickly explored other scientifically appropriate options to facilitate access to the vaccine for all impacted individuals.”
Load More
Load More