Descotes J, Vial T, Delattre D, Evreux J C
Laboratoire de Pharmacologie, Unité INSERM U80-CNRS UA1177-UCBL Faculté de Médecine Alexis Carrel, Lyon, France.
J Antimicrob Chemother. 1988 Jul;22 Suppl B:207-10. doi: 10.1093/jac/22.supplement_b.207.
Spiramycin, a 16-membered lactone ring macrolide, has been in clinical use for the past 15 years with little serious associated toxicity. Gastrointestinal disturbance has usually been mild and no changes in gastrointestinal motility have been noted either experimentally or in humans, in contrast to other macrolides, such as erythromycin. Allergic reactions have been uncommon and mainly restricted to transient skin eruptions. Although liver injury is a possible complication of most macrolide treatments, no conclusive evidence for spiramycin-induced hepatitis is currently available, and, again in contrast to most other macrolides, the lack of drug interactions with spiramycin has been clearly established in biochemical, pharmacokinetic and clinical studies.
螺旋霉素是一种十六元内酯环大环内酯类抗生素,在过去15年中一直用于临床,几乎没有严重的相关毒性。与其他大环内酯类抗生素(如红霉素)不同,胃肠道不适通常较轻,无论是在实验中还是在人体中,均未观察到胃肠动力的变化。过敏反应并不常见,主要表现为短暂的皮疹。虽然肝损伤是大多数大环内酯类药物治疗可能出现的并发症,但目前尚无确凿证据表明螺旋霉素会引起肝炎,而且与大多数其他大环内酯类药物相比,生化、药代动力学和临床研究已明确证实螺旋霉素不存在药物相互作用。