Abstract
Drug safety information (DSI) aimed at health professionals and patients is crucial for providing appropriate treatment. It is important to evaluate whether the communication of DSI issued by regulatory agencies is adequate. We investigated DSI communicated through the internet by official bodies in Japan and in several Western countries from 2000 to 2006, with regard to medicines recommended by therapeutic guidelines for the long-term management of asthma. Furthermore, if there were differences, we investigated how they arose. In Japan, DSI from the evidence of clinical studies conducted outside the country has a tendency to be issued with a significant time lag when compared with Western countries. However, the Japanese agency tended to provide rapid dissemination of adverse reactions to drugs commonly used in Japan. Although there are several types of official DSI provided in Japan, duplication often results in unnecessary complexity for health professionals, and there is no DSI issued directly to patients. Thus, Japan needs to provide DSI in a form thai is more accessible and comprehensive to both health professionals and consumers.
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