Hansten P D
School of Pharmacy, University of Washington, Seattle, WA 98195.
DICP. 1990 Nov;24(11 Suppl):S38-41.
Reports of adverse drug reactions due to histamine H2-receptor antagonists (H2RAs) are rare considering their wide usage. Cimetidine produces central nervous system and endocrine toxicities more often than other H2RAs. Drug-drug interactions are of potentially greater concern with H2RAs, especially because the critically ill patient routinely receives many drugs. H2RAs may alter the absorption, metabolism, or renal excretion of concurrently administered drugs. Gastrointestinal absorption of drugs, such as ketoconazole, that dissolve poorly in the absence of adequate acid may be reduced. Inhibition of hepatic oxidative drug metabolism of agents such as warfarin, theophylline, and phenytoin, is primarily a problem with cimetidine. Adverse effects will be seen in predisposed individuals and the time course will depend on the pharmacokinetics of the object drug. The other H2RAs are less likely to inhibit drug metabolism and affect renal clearance of procainamide than is cimetidine.
鉴于组胺H2受体拮抗剂(H2RAs)的广泛使用,其药物不良反应报告较为罕见。与其他H2RAs相比,西咪替丁更常产生中枢神经系统和内分泌毒性。H2RAs的药物相互作用可能更值得关注,尤其是因为重症患者通常会同时服用多种药物。H2RAs可能会改变同时服用药物的吸收、代谢或肾排泄。在缺乏足够胃酸的情况下溶解不良的药物,如酮康唑,其胃肠道吸收可能会减少。西咪替丁主要存在抑制华法林、茶碱和苯妥英等药物的肝氧化代谢的问题。在易感个体中会出现不良反应,其时间进程将取决于目标药物的药代动力学。与西咪替丁相比,其他H2RAs抑制药物代谢并影响普鲁卡因胺肾清除率的可能性较小。