The primary objective is to assess the proportion of Non-valvular atrial fibrillation (NVAF) patients receiving the standard dose of 20 mg of rivaroxaban or the reduced dose of 15 mg of rivaroxaban. The secondary objective is to determine if dosing patterns for rivaroxaban may be influenced by baseline chronic kidney disease (CKD) status (as a proxy for measured baseline renal function).
Study Type
OBSERVATIONAL
Enrollment
12,507
As prescribed by treating physicians
Unnamed facility
New York, New York, United States
Number of NVAF patients receiving 20 mg Rivaroxaban
Time frame: At baseline
Number of NVAF patients receiving 15 mg Rivaroxaban
Time frame: At baseline
Baseline renal function
Time frame: At baseline
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