Gadobutrol在印度的安全性和有效性综合评价。

Magnetic resonance insights Pub Date : 2017-09-11 eCollection Date: 2017-01-01 DOI:10.1177/1178623X17730048
Jan Endrikat, Nicoletta Anzalone
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引用次数: 1

摘要

Gadobutrol是一种基于钆(Gd)的磁共振成像(MRI)造影剂。在印度,gadobutrol被批准用于中枢神经系统(CNS)、肝脏、肾脏、乳房的MRI检查,以及2岁及以上患者的MR血管造影。所有年龄组的标准剂量为每公斤体重0.1毫摩尔。安全性已在42项临床2 - 4期研究(>6800例患者)、7项观察性研究和2900万份应用的药物警戒数据评估中得到证实。此外,对儿童、成人、老年人以及肝肾功能受损患者的研究均未显示不良事件发生率增加。在许多研究和各种适应症中,如中枢神经系统、外周血管和主动脉上血管、肾脏、肝脏和乳房的疾病,都证明了诊断效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Gadobutrol in India-A Comprehensive Review of Safety and Efficacy.

Gadobutrol is a gadolinium (Gd)-based contrast agent for magnetic resonance imaging (MRI). In India, gadobutrol is approved for MRI of the central nervous system (CNS), liver, kidneys, breast and for MR angiography for patients 2 years and older. The standard dose for all age groups is 0.1 mmol/kg body weight. The safety profile has been demonstrated in 42 clinical phase 2 to 4 studies (>6800 patients), 7 observational studies, and by assessing pharmacovigilance data of 29 million applications. Furthermore, studies in children, adults, and elderly and in patients with impaired liver or kidney function did not show any increased adverse event rate. Diagnostic efficacy was demonstrated in numerous studies and various indications, such as diseases of the CNS, peripheral and supra-aortic vessels, kidneys, liver, and breast.

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