Negro R D
Department of Lung Clinical Pathophysiology, Bussolengo General Hospital, Verona, Italy.
Clin Pharmacokinet. 1998 Aug;35(2):135-50. doi: 10.2165/00003088-199835020-00003.
The safety profile of any pharmacological agent is defined on the basis of its toxicity, tolerability and potential for pharmacokinetic and/or pharmacodynamic interactions with other compounds, which may belong to the same or to a different pharmacological class. Drug-drug interactions are important in clinical practice because short and long term therapeutic regimens frequently require coadministration of different drugs. The pharmacological treatment of gastric and duodenal ulcers (and of related syndromes) includes older and newer compounds, which have different mechanisms of action and exert different therapeutic effects. These compounds are widely prescribed in combination with other drugs being given for the treatment of concomitant diseases. This article reviews pharmacokinetic interactions with anti-ulcer drugs, paying particular attention to those which have clinically relevant adverse effects. Drugs mentioned in the literature as causing any pharmacokinetic interaction with anti-ulcer compounds are considered in this article.
任何药物的安全性概况都是基于其毒性、耐受性以及与其他化合物(可能属于同一或不同药理类别)发生药代动力学和/或药效学相互作用的可能性来定义的。药物相互作用在临床实践中很重要,因为短期和长期治疗方案常常需要联合使用不同药物。胃溃疡和十二指肠溃疡(以及相关综合征)的药物治疗包括作用机制不同、疗效各异的新旧化合物。这些化合物常与用于治疗伴发疾病的其他药物联合使用。本文综述了与抗溃疡药物的药代动力学相互作用,特别关注那些具有临床相关不良反应的相互作用。本文考虑了文献中提到的与抗溃疡化合物存在任何药代动力学相互作用的药物。