Long-term safety and effectiveness of vonoprazan for prevention of gastric and duodenal ulcer recurrence in patients on nonsteroidal anti-inflammatory drugs in Japan: a 12-month post-marketing surveillance study

被引:2
作者
Kawai, Takashi [1 ]
Suzuki, Chihiro [2 ]
Honda, Youichirou [2 ]
Fernandez, Jovelle L. [2 ]
机构
[1] Tokyo Med Univ Hosp, Endoscopy Ctr, Tokyo, Japan
[2] Takeda Pharmaceut Co Ltd, Japan Med Off, Tokyo, Japan
关键词
Anti-inflammatory agents; non-steroidal; duodenal ulcer; gastric ulcer; product surveillance; post marketing; Potassium-competitive acid blocker; vonoprazan; COMPETITIVE ACID BLOCKER; PROTON PUMP INHIBITORS; RISK; METAANALYSIS; ASPIRIN; TRENDS;
D O I
10.1080/14740338.2023.2136163
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background This study assessed the safety and effectiveness of vonoprazan for prevention of duodenal and gastric ulcer recurrence in patients on long-term nonsteroidal anti-inflammatory drugs (NSAIDs) in routine clinical practice. Research design and methods This 12-month, prospective, observational study (145 sites, Japan, September 2016-April 2020) analyzed patients with a history of gastric or duodenal ulcer who started once-daily vonoprazan and were receiving NSAIDs for pain or low-dose aspirin for thrombosis/embolism suppression. The primary outcome was the incidence of adverse drug reactions (ADRs). Results Most patients (86.7% [1099/1268]) received vonoprazan for at least 6 months. Most patients (98.6% [1250/1268]) received the 10-mg dose of vonoprazan, 38.3% (486/1268) received cyclooxygenase-2 inhibitors, and 61.7% (782/1268) received other NSAIDs. The overall incidence of ADRs was 0.71% (9/1268). Most commonly reported ADRs were gastrointestinal (0.32%), nervous system (0.16%), and hepatobiliary system (0.16%) disorders. The overall incidence of gastric or duodenal ulcer recurrence was 1.04% (95% CI 0.56-1.78). Conclusions No new safety concerns were reported for vonoprazan for prevention of secondary ulcer or bleeding in patients receiving long-term NSAIDs. Vonoprazan was effective for preventing NSAID-related peptic ulcer recurrence in this real-world study.
引用
收藏
页码:425 / 431
页数:7
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