Koichi Masuyama
Tokyo, Japan
Last Updated: 09/26/2026
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Found 10 publications
Drug-drug interactions between sex hormones and analgesics linked to thromboembolic events: an FDA adverse event reporting system analysis.
Journal: Frontiers in pharmacology
Published: January 19, 2026
Differences in Approved Doses and Drug Lag in Drugs Approved between 2012 and 2021: A Comparison between Japan and the U.S.
Journal: Biological & pharmaceutical bulletin
Published: August 27, 2025
Comparative analysis of the characteristics and trends of adverse drug reaction reports from patients in Japan and the Japanese Adverse Drug Event Report database.
Journal: British journal of clinical pharmacology
Published: June 12, 2025
Status of Community Pharmacy Functions and Regional Medical Collaboration System Initiatives in Japan.
Journal: Biological & pharmaceutical bulletin
Published: December 22, 2024
Changes in the trend and quality of adverse drug reaction reports in the Japanese Adverse Drug Event Report database and the impact of COVID-19-related reports.
Journal: The International journal of pharmacy practice
Published: May 03, 2024
Progressive multifocal leukoencephalopathy reports in rheumatoid arthritis concerning different treatment patterns-an exploratory assessment using the food and drug administration adverse event reporting system.
Journal: Frontiers in drug safety and regulation
Published: November 07, 2023
Drug-drug interaction assessment based on a large-scale spontaneous reporting system for hepato- and renal-toxicity, and thrombocytopenia with concomitant low-dose methotrexate and analgesics use.
Journal: BMC pharmacology & toxicology
Published: July 27, 2023
Methotrexate-related adverse events and impact of concomitant treatment with folic acid and tumor necrosis factor-alpha inhibitors: An assessment using the FDA adverse event reporting system.
Journal: Frontiers in pharmacology
Published: August 29, 2022
The association between concerns toward adverse reactions during pre-approval drug reviews and the post-approval addition of clinically significant adverse reactions to package inserts: A retrospective analysis of pre-approval drug review reports and safety updates.
Journal: Pharmacoepidemiology and drug safety
Published: April 22, 2018
Pharmaceuticals and Medical Devices Agency (PMDA)'s new action for Pharmaceutical Affairs Consultation on Research and Development (R&D) Strategy
Journal: Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan
Published: February 02, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026