儿童和青少年精神病学的标签外处方。为什么,何时,如何?

María Florencia Iveli, Mariano Monti, María Eugenia Benito, Pablo Iveli
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引用次数: 0

摘要

在儿科人群中,特别是在儿童和青少年精神病学领域,标签外适应症是规则而不是例外。当一种药物的病理、年龄、给药途径或治疗时间与产品标签中描述的不同时,就可能发生这种情况。与其他国家不同,阿根廷对标签外处方没有明确的规定。因此,与国家药品、食品和医疗技术管理局(ANMAT)批准的方式不同的药物处方没有关于治疗时必须满足的条件的监管框架。虽然标签外使用不被禁止,但它有额外的风险。为了鼓励儿科研究,诸如食品和药物管理局(FDA)和欧洲药品管理局(EMA)等监管机构已经引入了立法改革。以下文章将回顾与儿科人群相关的监管机构的现行框架,并分析指导医生合理使用超说明书药物治疗的标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Off-label prescriptions in child and adolescent psychiatry. Why, when and how?

In the paediatric population, paticulary in the field of child and adolescent psychiatry, off-label indications are the rule rather than the exception. This may occur when a drug is indicated for a pathology, age, route of administration or treatment length other than those described in the product label. Argentina, unlike other countries, has no explicit regulation on off-label prescribing. Therefore, the prescription of a medicine in a manner different from that approved by the National Administration of Medicines, Food and Medical Technology (ANMAT) does not have a regulatory framework regarding the conditions that must be met at the time of treatment. Although off-label use is not prohibited, it carries an additional risk. In order to encourage research in paediatrics, regulatory agencies such as the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) have introduced legislative reform. The following paper will review the current framework of the regulatory agencies that are relevant to the paediatric population and will analyse criteria to guide physicians in the rational use of off-label pharmacotherapy.

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