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氨磺必利(索里昂)的安全性:11项临床研究综述

Safety of amisulpride (Solian): a review of 11 clinical studies.

作者信息

Coulouvrat C, Dondey-Nouvel L

机构信息

Drug Under Development Safety Unit, Synthélabo Recherche (LERS), Bagneux, France.

出版信息

Int Clin Psychopharmacol. 1999 Jul;14(4):209-18. doi: 10.1097/00004850-199907000-00002.

Abstract

We assessed the overall safety profile of amisulpride based on the results from 11 clinical studies performed in patients suffering from schizophrenia with predominance of positive or negative symptoms. A total of 1933 patients were randomly assigned to treatment with amisulpride (n = 1247) or haloperidol (n = 309), risperidone (n = 113), flupentixol (n = 62) and placebo (n = 202). Safety data collection was performed using open reporting, UKU scales or specific extrapyramidal side-effect scales; electrocardiogram recording and vital signs examination; laboratory data collection. Amisulpride demonstrated a satisfactory global safety profile in the range of doses usually prescribed. The number of patients having at least one extrapyramidal side-effect was higher in haloperidol patients compared with both amisulpride and risperidone patients (50% versus 30% in the two latter groups). For endocrine events, a similar rate was observed between amisulpride and risperidone groups (4% versus 6%, respectively) versus 1% in the haloperidol group. Electrocardiogram results were satisfactory, confirmed by the absence of cardiovascular events. The overall laboratory safety profile of amisulpride did not show clinically relevant abnormalities in liver function tests nor haematological abnormalities. Our extensive clinical data confirm the satisfactory safety profile of amisulpride which is superior to standard reference compounds.

摘要

我们根据11项针对以阳性或阴性症状为主的精神分裂症患者开展的临床研究结果,评估了氨磺必利的总体安全性。总共1933例患者被随机分配接受氨磺必利治疗(n = 1247)或氟哌啶醇治疗(n = 309)、利培酮治疗(n = 113)、三氟噻吨治疗(n = 62)以及安慰剂治疗(n = 202)。采用开放性报告、UKU量表或特定锥体外系副作用量表进行安全性数据收集;记录心电图并检查生命体征;收集实验室数据。氨磺必利在通常规定的剂量范围内显示出令人满意的总体安全性。与氨磺必利和利培酮组患者相比,氟哌啶醇组出现至少一种锥体外系副作用的患者数量更多(后两组分别为30%,而氟哌啶醇组为50%)。对于内分泌事件,氨磺必利组和利培酮组的发生率相似(分别为4%和6%),而氟哌啶醇组为1%。心电图结果令人满意,未出现心血管事件证实了这一点。氨磺必利的总体实验室安全性在肝功能检查中未显示出临床相关异常,血液学方面也未出现异常。我们广泛的临床数据证实了氨磺必利令人满意的安全性,其安全性优于标准对照化合物。

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