第三章:临床回顾、治疗药物监测和药物不良反应管理

G. Taylor, A. Leversha, C. Archer, C. Boland, M. Dooley, P. Fowler, Sharon Gordon-Croal, J. Fitch, S. Marotti, Amy McKenzie, Duncan McKenzie, Natalie Collard, Nicki Burridge, K. O’Leary, C. Randall, A. Roberts, S. Seaton
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引用次数: 2

摘要

临床审查、治疗药物监测(TDM)和药物不良反应(ADR)管理通过确保药物的安全和适当的剂量和给药、提高治疗反应和最大限度地减少药物相关问题,有助于提高药物的使用质量。临床审查、TDM和ADR管理在患者出现或被卫生服务机构收治时开始,并与当前药物管理和其他临床药学活动的评估一起,作为整个护理期间的常规活动继续进行。
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Chapter 3: Clinical Review, Therapeutic Drug Monitoring and Adverse Drug Reaction Management
INTRODUCTION Clinical review, therapeutic drug monitoring (TDM) and adverse drug reaction (ADR) management contribute to the quality use of medicines by ensuring safe and appropriate dosage and administration of medicines, improving response to therapy and minimising medicinesrelated problems. Clinical review, TDM and ADR management commence when a patient presents or is admitted to a health service organisation and continue as routine activities throughout the episode of care in conjunction with assessment of current medication management and other clinical pharmacy activities.
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Issue Information Chapter 1: Medication Reconciliation Chapter 2: Assessment of Current Medication Management Chapter 3: Clinical Review, Therapeutic Drug Monitoring and Adverse Drug Reaction Management Chapter 4: Medication Management Plan
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