EFFICACY AND SAFETY IN PATIENTS WITH FACTORS THAT INCREASE THE RISK OF BLEEDING WHO WERE DOSE-REDUCED TO LIXIANA® (edoxaban) 30 mg

Once-daily LIXIANA® (edoxaban) demonstrated similar risk reduction in efficacy vs well-managed warfarin in NVAF patients with factors that increase the risk of bleeding who were dose-reduced to LIXIANA® 30 mg qd.1

STROKE/SEE EVENTS (PRIMARY EFFICACY ENDPOINT) IN PATIENTS DOSE-REDUCED AT RANDOMIZATION2

Once-daily LIXIANA® demonstrated consistent efficacy results across a broad range of NVAF patients3

STROKE/SEE EVENTS (PRIMARY EFFICACY ENDPONT) ACROSS MAJOR SUBPOPULATIONS (INTENTION-TO-TREAT POPULATION)1

a Includes patients taking LIXIANA® 60 mg and those dose-reduced to 30 mg.
b Congestive heart failure
c Transient ischemic attack
d Myocardial infarction

Once-daily LIXIANA® (edoxaban) demonstrated consistently favorable safety vs well-managed warfarin in NVAF patients with factors that increase the risk of bleeding who were dose-reduced to LIXIANA® 30 mg qd.1

MAJOR BLEEDING EVENTS (PRIMARY SAFETY ENDPOINT) IN PATIENTS DOSE-REDUCED AT RANDOMIZATION2

a Relative risk reduction.

Once-daily LIXIANA® demonstrated consistent safety results across a broad range of NVAF patients.3

MAJOR BLEEDING EVENTS (PRIMARY SAFETY ENDPOINT) ACROSS MAJOR SUBPOPULATIONS (ON-TREATMENT POPULATION)1

a Includes patients taking LIXIANA® 60 mg and those dose-reduced to 30 mg