Greene W L, Self T H, Levinson M J
J Fam Pract. 1983 Jun;16(6):1087-93.
Cimetidine is a widely used antiulcer medication that is also a potent inhibitor of the mixed-function oxidase enzymes in the liver. This effect results in a number of clinically important interactions with other drugs, which are now being appreciated. Other effects of cimetidine, such as raising of gastric pH, alteration of liver blood flow, or alterations in renal secretory mechanisms, may also contribute to or result in clinically significant interactions. Current data document appreciable alterations in the metabolism or excretion of warfarin, theophylline, phenytoin, lidocaine, certain beta-adrenoceptor antagonists, certain benzodiazepines, and probably narcotic analgesics and procainamide. Thus, effects of these drugs and serum levels, where available, should be more closely followed when used in combination with cimetidine. Cimetidine appears to exacerbate the myelosuppressive effects of the nitrosoureas, and may also significantly alter the absorption of ketoconazole. Though other drugs may affect the absorption or elimination of cimetidine, the clinical implication of these effects is uncertain.
西咪替丁是一种广泛使用的抗溃疡药物,也是肝脏中混合功能氧化酶的强效抑制剂。这种作用导致与其他药物产生许多具有临床重要性的相互作用,目前人们已经认识到这一点。西咪替丁的其他作用,如提高胃内pH值、改变肝血流量或改变肾脏分泌机制,也可能促成或导致具有临床意义的相互作用。目前的数据表明,华法林、茶碱、苯妥英、利多卡因、某些β肾上腺素受体拮抗剂、某些苯二氮䓬类药物,可能还有麻醉性镇痛药和普鲁卡因胺的代谢或排泄有明显改变。因此,这些药物与西咪替丁合用时,应更密切地监测其效果以及(若有)血清水平。西咪替丁似乎会加重亚硝基脲类药物的骨髓抑制作用,还可能显著改变酮康唑的吸收。虽然其他药物可能会影响西咪替丁的吸收或消除,但这些作用的临床意义尚不确定。