FDA Expands Approval to wilate for Prophylaxis in All Types of VWDr

FDA Expands Approval to wilate for Prophylaxis in All Types of VWDr

Octapharma USA’s wilate, von Willebrand factor (VWF)/coagulation factor VIII complex (human) lyophilized power for solution for intravenous injection, has been given expanded approval by the U.S. Food and Drug Administration (FDA) for routine prophylaxis to reduce the frequency of bleeding episodes in adults and children aged 6 and older with any type of von Willebrand disease (VWD).

FDA Approves Wezlana, First Interchangeable Biosimilar to Stelara

FDA Approves Wezlana, First Interchangable Biosimilar to Stelara

The U.S. Food and Drug Administration (FDA) has approved Wezlana (ustekinumab-auub) as a biosimilar to and interchangeable with Stelara for adult patients with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy; active psoriatic arthritis; moderately to severely active Crohn’s disease; and moderately to severely active ulcerative colitis.

Coming Soon: Dried Plasma for Hemorrhagic Trauma in the Prehospital Setting

Dried Plasma for Hemorrhagic Trauma in the Prehospital Setting

It is now well-established that prehospital transfusion of plasma, with its balanced mix of coagulation proteins, counters the hemodilution and progressive derangement of hemostatic mechanisms caused by crystalloid-based resuscitation, improving the changes of survival in severely bleed trauma victims.