欧米における医薬品の安全性に関するリスクコミュニケーションの取り組み並びにわが国の現状と課題

概要

  In pharmacovigilance, it has been recognized that it is essential to share the information regarding the risk of drugs among stakeholders and to have risk communication (RC) which enables consumers to make their own judgments regarding the risk. In particular, RC between the governmental agencies and consumers is given a high priority. Hence, its provisions and initiatives should be considered thoroughly. I present a brief overview of current proactive approaches for RC to protect the patient's rights, to increase openness and transparency and to share information in the US and EU. Following the Food and Drug Administration Amendment Act (FDAAA), Institute of Medicine of the National Academies (IOM) recommended that FDA makes efforts for RC. The RC Advisory Committee was established and consumers are involved as its members. FDA published “Guidance Drug Safety Information” in 2007 and “Strategic Plan for RC” in 2009. Thus, its framework has been developed. European Medicines Agency (EMA) issued “Work programme 2010” and “EMA Communication on safety related issues”, which indicated its policies and measures. EMA is promoting development of the framework for Patient Involvement (e.g., members of scientific committees). Regarding the direct patient reporting of adverse drug reactions, FDA began that in 2003 and EMA recommends to encourage it for EU Member States, and it has already started in some countries. RC has important roles to take safety measures for drugs and to protect patient's rights, therefore such an approach for it be implemented is expected in Japan.

著者

山本 美智子 鈴鹿医療科学大学薬学部
山本 美智子 鈴鹿医療科学大学 薬学部

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