PHARMA JAPAN welcomes JETRO New York’s Shunsuke Tani as a guest columnist. In occasional contributions, Tani will share his perspectives on US pharmaceutical policy, industry developments, and life in America, drawing on his firsthand experience in the US.---Hello from New…
The Ministry of Health, Labor and Welfare (MHLW) on January 29 ordered safety-related label revisions for a batch of medicines, including MSD’s PD-1 inhibitor Keytruda (pembrolizumab) and Daiichi Sankyo’s anticoagulant Lixiana (edoxaban). The label of Keytruda will newly add pancreatic…
To read the full story
Related Article
- PMDA Reviewing Safety Risks for Joyclu, Lixiana, Keytruda
January 7, 2025
- Blue Letter Issued to OA Drug Joyclu after Anaphylaxis Reports
June 2, 2021
REGULATORY
- Zolgensma Cost-Effectiveness Analysis to Resume after Five-Year Halt
October 29, 2026
- Japan Eyes Priority Review for MCMs, Bill Submission Planned for 2027
October 28, 2026
- Panel Member Urges Review of Tavneos Blue Letter Timing
October 28, 2026
- Japan Orders Label Revisions for Leqvio, Amenalief, 2 Other Drugs
October 28, 2026
- AbbVie’s Fast-Acting Botulinum Toxin Boey Wins Japan Panel Backing
October 27, 2026





