Matching articles for "Balfaxar"

In Brief: Andexanet alfa (Andexxa) Withdrawn

   
The Medical Letter on Drugs and Therapeutics • January 19, 2026;  (Issue 1746)
Andexanet alfa (Andexxa – AstraZeneca), which received accelerated approval from the FDA in 2018 for urgent reversal of the anticoagulant effect of the direct factor Xa inhibitors apixaban (Eliquis) and...
Andexanet alfa (Andexxa – AstraZeneca), which received accelerated approval from the FDA in 2018 for urgent reversal of the anticoagulant effect of the direct factor Xa inhibitors apixaban (Eliquis) and rivaroxaban (Xarelto), has voluntarily been withdrawn from the market. Andexxa was the only drug FDA-approved for this indication in the US.
Med Lett Drugs Ther. 2026 Jan 19;68(1746):16 | Show Full IntroductionHide Full Introduction

Balfaxar: Another Four-Factor PCC for Warfarin Reversal

   
The Medical Letter on Drugs and Therapeutics • February 19, 2024;  (Issue 1696)
Balfaxar (Octapharma), a human plasma-derived four-factor prothrombin complex concentrate (PCC), has been approved by the FDA for rapid reversal of warfarin anticoagulation in adults who require an urgent...
Balfaxar (Octapharma), a human plasma-derived four-factor prothrombin complex concentrate (PCC), has been approved by the FDA for rapid reversal of warfarin anticoagulation in adults who require an urgent surgical/invasive procedure. It is the second four-factor PCC to become available in the US; Kcentra, which has been available since 2013, is approved for the same indication and for urgent reversal of warfarin anticoagulation in adults with acute major bleeding. Balfaxar is marketed in Canada and Europe as Octaplex.
Med Lett Drugs Ther. 2024 Feb 19;66(1696):31-2 | Show Full IntroductionHide Full Introduction