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我院433例药品不良反应报告分析 被引量:33

Analysis of 433 ADR Reports in Our Hospital
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摘要 目的:探讨我院药品不良反应(ADR)发生的临床特点、规律,为临床合理、安全用药提供参考。方法:对广东省ADR监测中心收录的我院2014年1月-2015年6月的ADR报告进行整理、统计与分析。结果:433例发生ADR的患者中,男性185例(42.73%),女性248例(57.27%),男女比例为1∶1.34。中青年(20~59岁)患者ADR发生率较高(71.59%),且男性明显少于女性(1∶1.37)。ADR给药途径以静脉滴注(48.04%)和口服给药(41.57%)为主。抗感染药物引发ADR的例数最多(167例,38.57%),其中以头孢菌素类为主(64.07%)。ADR累及器官/系统以消化系统损害(262例次,36.19%)和皮肤及其附件损害(237例次,32.73%)为主。严重的ADR主要涉及抗感染药物和抗肿瘤药物。结论:临床医务人员应加强头孢菌素类抗菌药物和抗肿瘤药物的ADR监测,谨慎选择给药途径。 OBJECTIVE:To investigate the clinical characteristics and regularity of adverse drug reaction(ADR),and to provide reference for rational and safe drug use in the clinic. METHODS:ADR reports collected from our hospital by Guangdong ADR Monitoring Center during Jan. 2014 to June. 2015 were summarized and analyzed statistically. RESULTS:Of 433 ADR cases,there were 185 male cases(42.73%)and 248 female cases(57.27%),with ratio of 1∶1.34. The incidence of ADR was in high level(71.59%)in young and middle-aged patients(20-59 year-old);that of male was significantly lower than that of female(1∶1.37).ADR cases caused by intravenous drip(48.04%)and oral administration(41.57%)were most common. The most ADR cases were related with anti-infective drugs(167 cases,38.57%),mainly were related with cephalosporins(64.07%). Organs/systems involved in ADR were main the damages of gastrointestinal system(262 cases,36.19%) and the lesion of skin and appendants(237 cases,32.73%). The serious ADR was mainly induced by anti-infective and anti-tumor drugs. CONCLUSIONS:Clinical medical personnel should strengthen the ADR monitoring of cephalosporin antibiotics and anti-tumor drug,and select route of administration carefully.
出处 《中国药房》 CAS 北大核心 2016年第26期3640-3643,共4页 China Pharmacy
关键词 药品不良反应 分析 合理用药 Adverse drug reaction Analysis Rational drug use
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  • 1Vessal G,Mardani Z,Mollai M.Knowledge,attitudes,and perceptions of pharmacists to ADR reporting in Iran[J].Pharm World Sci,2009,31(2):183.
  • 2陈新谦,金有豫,汤光.新编药物学[M].17版.北京:人民卫生出版社,2011:3465.
  • 3国家药品不良反应中心,国家食品药品监督管理局药品评价中心.WHO药品不良反应术语集[M].北京:中国医药科技出版社,2002:1-172.
  • 4卫生部.药品不良反应报告与监测管理办法[S].2011-07-01.
  • 5Baniasadi S,Habibi M,Haghgoo R,et al.Increasing the number of adverse drug reactions reporting:the role of clinical pharmacy residents[J].Iran J Pharm Res,2014,13(1):291.
  • 6周晶鑫.56例参麦注射液不良反应分析[J].中国药物警戒,2012,9(11):693-695. 被引量:20
  • 7雷招宝.药物不良反应中的性别差异[J].药物不良反应杂志,2000,2(3):177-179. 被引量:44
  • 8李家柱,王杰,程诗思,杨成明.我院292例药品不良反应报告分析[J].中国药房,2014,25(46):4379-4381. 被引量:8
  • 9范峥,刘洋,王宏蕾,郭桂明.某院1484例药物不良反应报告分析[J].中国医院药学杂志,2014,34(20):1776-1779. 被引量:19
  • 10Passarelli MC,Jacob-Filho W,Figueras A.Adverse drug reactions in an elderly hospitalised population:inappropriate prescription is a leading cause[J].Drugs&Aging,2005,22(9):767.

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