Therapeutic ineffectiveness -: Heads or tails?

被引:17
作者
Figueras, A
Pedrós, C
Valsecia, M
Laporte, JR
机构
[1] Univ Autonoma Barcelona, Dept Farmacol Terepeut & Toxicol, Fdn Inst Catala Farmacol, E-08193 Barcelona, Spain
[2] Univ Nacl Nordeste, Dept Farmacol, Reg Pharmacovigilance Ctr NE Argentina, Corrientes, Argentina
关键词
D O I
10.2165/00002018-200225070-00002
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 [公共卫生与预防医学]; 120402 [社会医学与卫生事业管理];
摘要
Reporting of therapeutic ineffectiveness through adverse drug reaction spontaneous reporting systems has been proposed by some authors. In the WHO Adverse Reactions Terminology (WHO-ART) and Medical Dictionary for Regulatory Activities (MedDRA) terminology, the term therapeutic ineffectiveness includes drug interactions, resistance, tolerance and tachyphylaxis, as well as pharmaceutical defects such as substandard, adulterated, and counterfeit drugs. Under certain circumstances, reporting therapeutic ineffectiveness may contribute to identifying pharmaceutical defects. However, the best approach to avoid their occurrence would be implementing good manufacturing practices and strengthening quality control activities. This would prevent the misuse of spontaneous reporting of adverse drug reactions (e.g. when reporting of therapeutic ineffectiveness is 'suggested' by interested parties, especially when a generic product has been substituted for a branded original product).
引用
收藏
页码:485 / 487
页数:3
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