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1 These findings support the continued use of direct oral anticoagulants.
3 Sex-specific comparative effectiveness of direct oral anticoagulants among patients with nonvalvul
4 clopidogrel, a vitamin K antagonist (VKA), a direct oral anticoagulant, and combined antithrombotic d
7 %; adjusted OR, 1.87 [95% CI, 1.57-2.24]), a direct oral anticoagulant (cases: 1.0%, controls: 0.6%;
8 k of gastrointestinal bleeding with use of a direct oral anticoagulant compared with warfarin or low-
9 risk of major gastrointestinal bleeding with direct oral anticoagulants compared with warfarin or low
10 risk of major gastrointestinal bleeding with direct oral anticoagulants compared with warfarin or low
12 risk of major gastrointestinal bleeding with direct oral anticoagulants did not differ from that with
16 with venous thromboembolism (VTE) compared a direct oral anticoagulant (DOAC) with vitamin K antagoni
17 ompare causes of death in patients receiving direct oral anticoagulants (DOAC) or warfarin for preven
18 , provided validation for the development of direct oral anticoagulants (DOAC), and currently such in
27 e improvements linked to the introduction of direct oral anticoagulants, more than one third of atria
29 e sex-specific, comparative effectiveness of direct oral anticoagulants (rivaroxaban and dabigatran),
30 data on the relative efficacy and safety of direct oral anticoagulants, such as edoxaban, compared w
31 d the risk of gastrointestinal bleeding with direct oral anticoagulants, warfarin, and low-molecular-
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