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Edoxaban: from data quality to safety in clinical practice
Reduced dosage, high efficacy and greater safety in the anticoagulant treatment of fragile patients
Reduced dosage, high efficacy and greater safety in the anticoagulant treatment of fragile patients
Edoxaban: from data quality to safety in clinical practice
Reduced dosage, high efficacy and greater safety in the anticoagulant treatment of fragile patients
At the 77th SIC national congress, a symposium was held, sponsored by Daiichi-Sankyo, on the characteristics of Edoxaban, the latest addition to the family of NAOs (New Oral Anticoagulants). Strengthened by the results of the Engage AF-TIMI 48 study, which involved over 21 thousand patients, segmented into different subgroups with specific needs, Edoxaban is proposed as an anticoagulant capable of personalising the dosage in non-valvular atrial fibrillation, attesting to high levels of efficacy and safety. Similar results are expected in the treatment of venous thromboembolism, based on the evidence that emerged following extensive in-depth analyses of the Hokusai study.
At the 77th SIC national congress, a symposium was held, sponsored by Daiichi-Sankyo, on the characteristics of Edoxaban, the latest addition to the family of NAOs (New Oral Anticoagulants). Strengthened by the results of the Engage AF-TIMI 48 study, which involved over 21 thousand patients, segmented into different subgroups with specific needs, Edoxaban is proposed as an anticoagulant capable of personalising the dosage in non-valvular atrial fibrillation, attesting to high levels of efficacy and safety. Similar results are expected in the treatment of venous thromboembolism, based on the evidence that emerged following extensive in-depth analyses of the Hokusai study.

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