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头孢克肟致药品不良反应分析
引用本文:龙敏,张丹,陈蓉.头孢克肟致药品不良反应分析[J].中国药房,2012(6):561-562.
作者姓名:龙敏  张丹  陈蓉
作者单位:[1]成都市第六人民医院,成都610051 [2]成都市妇女儿童中心医院,成都610000 [3]成都市木综厂职工医院,成都610081
摘    要:目的:探讨头孢克肟致药品不良反应(ADR)发生的特点及规律。方法:收集国内医药期刊有关头孢克肟致ADR个案报道10例并汇总3家医院2000-2010年上报的头孢克肟致ADR报告79例,共89例,进行分析、评价。结果:ADR临床表现方面,以皮肤及其附件损害居首位(占41.57%),其次为神经系统损害(占19.10%)及消化系统损害(占15.73%);以≤10岁儿童(48.31%)和序贯用药(46.07%)报道率最高;约38.20%的ADR发生在用药48h后。结论:临床应重视头孢克肟引起的ADR,用药时应加强对患者的观察,以减少严重ADR的发生。

关 键 词:头孢克肟  药品不良反应  分析

Analysis of Adverse Drug Reactions Induced by Cefixime
LONG MinThe Sixth People's Hospital of Chengdu,Chengdu,China ZHANG DanThe Women and Children's Central Hospital of Chengdu,Chengdu,China CHEN Rong.Analysis of Adverse Drug Reactions Induced by Cefixime[J].China Pharmacy,2012(6):561-562.
Authors:LONG MinThe Sixth People's Hospital of Chengdu  Chengdu  China ZHANG DanThe Women and Children's Central Hospital of Chengdu  Chengdu  China CHEN Rong
Institution:LONG Min(The Sixth People's Hospital of Chengdu, Chengdu 610051, China) ZHANG Dan(The Women and Children's Central Hospital of Chengdu, Chengdu 610000, China) CHEN Rong(Staff-worker Hospital of Muzong Factory in Chengdu, Chengdu 610081, China)
Abstract:OBJECTIVE: To investigate the characteristics and regularity of ADR induced by cefixime. METHODS: 10 cefixime-induced ADR case reports were collected from domestic medical journals. 79 cefixime-induced ADR cases reported by 3 hospitals during 2000--2010 were summarized. A total of 89 ADR cases were analyzed and evaluated. RESULTS: Of total 89 cases of ADR, lesion of skin and appendants took up the biggest proportion (accounting for 41.57% ), followed by nervous system injury (accounting for 19.10% ) and digestive system injury (accounting for 15.73% ). 48.31% were occurred in children below 10 years old; 46.07% were in sequential therapy. About 38.20% occurred after 48 hours. CONCLUSION: It is necessary to pay attention to ADR induced by cefixime and strengthen observation during medication in order to reduce the serious ADR.
Keywords:Cefixime  Adverse drug reactions  Analysis
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