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FDA approves VONVENDI for preventing and treating bleeding in von Willebrand Disease patients of all ages.
The FDA has expanded the approval of VONVENDI to include routine prevention of bleeding in adults with von Willebrand Disease (VWD) and on-demand treatment in children with VWD.
VONVENDI is the only recombinant VWF replacement therapy approved for both adults and children.
This approval aids in managing bleeding risks and daily life burdens for VWD patients.
Common side effects include headache, vomiting, nausea, dizziness, and itchy skin.
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La FDA ha aprobado VONVENDI para la prevención y el tratamiento de hemorragias en pacientes de todas las edades con enfermedad de von Willebrand.