首页> 外国专利> METHOD OF ESTIMATING THE RISK OF EXPRESSION OF ADVERSE DRUG REACTION CAUSED BY THE ADMINISTRATION OF A COMPOUND, WHICH IS EITHER METABLOIZED PER SE BY UGT1A1 OR WHOSE INTERMEDIATE IS METABOLIZED BY THE ENZYME

METHOD OF ESTIMATING THE RISK OF EXPRESSION OF ADVERSE DRUG REACTION CAUSED BY THE ADMINISTRATION OF A COMPOUND, WHICH IS EITHER METABLOIZED PER SE BY UGT1A1 OR WHOSE INTERMEDIATE IS METABOLIZED BY THE ENZYME

机译:估算由化合物的管理引起的不良药物反应的表达风险的方法,其中化合物被UGT1A1本身代谢,或者其中间体被酶代谢

摘要

A method of estimating a risk of the expression of an adverse drug reaction caused by the administration of irinotecan; and a method of reducing the adverse drug reaction caused by the administration of irinotecan. A polymorphism on the basis of a difference in the repeating numbers of TA repetitive sequences in the promoter region of UGT1 gene and two types of polymorphisms (bases at the 211- and 686-positions) on the basis of single nucleotide polymorphisms in the exon 1 are analyzed. Based on the analytical data, the risk of the expression of an adverse drug reaction caused by the administration of irinotecan is estimated. Further, the administration doses of irinotecan is designed for individual patients depending on the risk of the expression of the adverse drug reaction , thereby reducing the adverse drug reaction cased by the administration of irinotecan. IMAGE
机译:一种估计由伊立替康给药引起的药物不良反应表达风险的方法;以及减少由伊立替康给药引起的药物不良反应的方法。基于UGT1基因启动子区域中TA重复序列重复数的差异的多态性和基于外显子1中单核苷酸多态性的两种类型的多态性(基于211和686位碱基)被分析。基于分析数据,估计了由伊立替康给药引起的药物不良反应表达的风险。此外,依立替康的给药剂量是根据药物不良反应表达的风险为个别患者设计的,从而减少了因依立替康的给药而引起的药物不良反应。 <图像>

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号