The Ministry of Health, Labor and Welfare (MHLW) on October 6 ordered package insert revisions for Takeda Pharmaceutical’s proton pump inhibitor (PPI) Takecab (vonoprazan) and two other drugs - Nippon Shinyaku’s cancer drug Cylocide (cytarabine) and Taiho Pharmaceutical’s antibiotic Zosyn…
To read the full story
Related Article
- PMDA Reviewing Safety Risks for Takecab, 2 Other Drugs
September 7, 2020
REGULATORY
- Update: Tavneos Slapped with Blue Letter Action in Japan over Liver Injury Risk
May 22, 2026
- Blister Pack Supplies Seen Returning to Normal: Health Minister
May 22, 2026
- LDP “Eto” Study Group Submits Honebuto Proposal to Health Minister
May 22, 2026
- Oncolys’ Telomelysin Wins Backing from Japan Panel
May 22, 2026
- MHLW Moves Toward Immunization Act Revision for RSV Antibody Drugs
May 21, 2026
In the complex landscape of the Japanese pharmaceutical market, the “status quo” is often the safest harbor. But for leaders like Kennet Brysting, former president of Gilead Japan, the status quo is the most dangerous place to stay.Innovation in Japan…





