Antiplatelet agents including low-dose aspirin (LDA) or adenosine diphosphate (ADP) receptor antagonists are widely used for the prevention of cardiovascular events. However, antiplatelet agents increase the risk of bleeding associated with mucosal breaks in the gastrointestinal (GI) tract [1,2]. Because GI bleeding is independently associated with mortality and ischemic compilations, and temporary cessation of antiplatelet agents increases the risk of mortality, GI bleeding prevention is important during therapy [2-5]. Concomitant use of a proton pump inhibitor (PPI) is regarded as appropriate in patients with multiple risk factors for GI bleeding who require antiplatelet therapy [6]. Risk factors for GI bleeding include a history of bleeding or other complications of peptic ulcer disease [7,8], advanced age, use of steroids or non-steroidal anti-inflammatory drugs (NSAIDs) [9-15], and concomitant use of 2 antithrombotic agents [i.e. dual antiplatelet therapy (DAPT)] [1,16-19]. Vonoprazan (TAK-438) belongs to a class of acid-inhibitory agents known as potassium-competitive acid blockers (P-CABs), which reversibly inhibit H + , K +-ATPase independently of acid pH