AI Article Synopsis

  • In December 2022, Japan's Ministry of Health, Labour and Welfare (MHLW) released new guidelines for assessing how psychotropic drugs affect driving performance, highlighting the importance of these effects on patients' social functioning.
  • The guidelines detail a tiered evaluation process involving both nonclinical and clinical studies, emphasizing the need for specific evaluation methods based on the drug characteristics due to the complex nature of driving.
  • The document reviews the MHLW guidelines in comparison to the FDA's guidelines, aiming to improve drug development strategies related to psychotropic medications and their impact on motor vehicle operation.

Article Abstract

In December 2022, the new guideline for evaluating the effect of psychotropic drugs on the performance to drive a motor vehicle was issued by the Ministry of Health, Labour and Welfare (MHLW) and implemented in Japan. Of the safety information, information on the influence of medications on driving performance is particularly important because it can be relevant to the social functioning of patients. In principle, the package inserts of medications are designed based on evidence and provide precautions regarding the operation of heavy machinery such as automobiles in Japan, the United States, and Europe. The effects of medications on driving performance are generally evaluated in a tiered approach involving nonclinical and clinical studies. Because of the wide variety of functional domains involved in automobile driving, the selection of evaluation methods for a given medication depends on their characteristics, which is a complicated method. Therefore, to evaluate the effects of psychotropic drugs on driving performance efficiently and appropriately, we developed the MHLW guideline that specifically defines the evaluation methods used in pharmacological studies, the neuropsychological tests used in pharmacodynamic studies, and the situations in which driving studies are necessary. Regarding the planning of appropriate drug development strategies, we review the background of the MHLW guideline and its differences from the US Food and Drug Administration (FDA) guideline.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275277PMC
http://dx.doi.org/10.1002/npr2.12339DOI Listing

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