摘要
目的汇总分析盘锦市2007年药品不良反应报告,发挥药品不良反应监测工作的指导作用,保障公众用药安全。方法采用病例回顾性研究方法,对盘锦市2007年1-12月收集到的977例药品不良反应病例报告进行综合分析。结果药品不良反应报告有62.33来源于医疗机构。新的严重的药品不良反应报告占27.94。不良反应累积的主要系统及器官为皮肤及其附件。抗微生物药物占47.08。静脉给药占给药途经的51.79。结论应加强药品不良反应监测工作,提高报告质量和分析评价能力,为保障公众用药健康服务。
Objective To analyze the ADR reports of Panjin in 2007, bring the ADR monitoring into full play in the guarantee of medication safety. Methods 977 ADR cases were analyzed comprehensively and retrospectively. Results The 62.33 % of ADR Reports came from medical institutions, New serious ADR Reports accounted for 27.94 %. Skin and its annex were the major cumulative adverse reaction system and organ. Anti-microbial drugs accounted for 47.08 %. 51.79 % of administration route was vein injection. Conclusion We must strengthen the monitoring of ADR, and improve the quality of reporting and capacity of analysis and evaluation.
出处
《实用药物与临床》
CAS
2008年第6期371-372,共2页
Practical Pharmacy and Clinical Remedies