Latest Post

On July 6, the U.S. Food and Drug Administration (FDA) revised its emergency use authorization (EUA) for the COVID-19 antiviral treatment PaxlovidTM (nirmatrelvir and ritonavir) to allow prescribing by pharmacists for quicker and easier access for patients. Pfizer’s Paxlovid was first granted an EUA in December 2021, meaning that the FDA authorized the product for emergency use, even though it has not been approved for any purpose by the FDA. Paxlovid is used to treat…