The primary purpose of this study is to evaluate the risk of major bleeding and stroke/systemic embolism (SE) among novel oral anti-coagulant (OAC) naïve and warfarin naïve Medicare Advantage patients with non-valvular atrial fibrillation (NVAF) treated with apixaban, dabigatran, rivaroxaban, or warfarin.
Study Type
OBSERVATIONAL
Enrollment
36,000
Treatment for NVAF patients
Treatment for NVAF patients
Treatment for NVAF patients
Major bleeding
Time frame: 36 months
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Treatment for NVAF patients