Howden C W, Tytgat G N
University of South Carolina School of Medicine, Columbia, USA.
Clin Ther. 1996 Jan-Feb;18(1):36-54; discussion 35. doi: 10.1016/s0149-2918(96)80177-9.
Famotidine is a specific, long-acting histamine2-receptor antagonist. It is indicated for the treatment of duodenal ulcer, gastric ulcer, gastroesophageal reflux disease, and Zollinger-Ellison syndrome. Since its introduction for the treatment of acid-related disorders in 1985, an estimated 18.8 million patients worldwide have been treated with famotidine. We present a comprehensive safety profile of oral famotidine, incorporating data from investigational trials, postmarketing studies, and reports of marketed use. The excellent tolerability profile of famotidine observed during investigational trials has remained substantially unchanged during postmarketing experience. Famotidine does not notably bind to cytochrome P-450 or gastric alcohol dehydrogenase and therefore has not been associated with clinically significant drug interactions. It is generally well tolerated in patients with cardiovascular, renal, or hepatic dysfunction or with Zollinger-Ellison syndrome who have tolerated doses up to 800 mg daily.
法莫替丁是一种特异性长效组胺2受体拮抗剂。它适用于治疗十二指肠溃疡、胃溃疡、胃食管反流病和卓-艾综合征。自1985年被用于治疗酸相关疾病以来,全球估计有1880万患者接受了法莫替丁治疗。我们提供了口服法莫替丁的全面安全性概况,纳入了来自试验研究、上市后研究及上市后使用报告的数据。在试验研究中观察到的法莫替丁良好耐受性在上市后应用中基本保持不变。法莫替丁与细胞色素P-450或胃乙醇脱氢酶无明显结合,因此未发现有临床意义的药物相互作用。对于心血管、肾脏或肝功能不全的患者或已耐受每日高达800毫克剂量的卓-艾综合征患者,法莫替丁通常耐受性良好。