The Pharmaceuticals and Medical Devices Agency (PMDA) said on August 21 that the anti-PD-1 antibody nivolumab (brand name: Opdivo) is now under review for the possible risk of excessive immune reactions, myasthenia gravis, myositis, colitis, and severe diarrhea. The PMDA…
To read the full story
Related Article
- Thrombopenia Added to Clinically Significant ADR List for Daklinza, Sunvepra
October 28, 2015
- Add Myasthenia Gravis, Myositis to Opdivo Label: MHLW
September 17, 2015
REGULATORY
- Japan Formally Joins Project Orbis for Cancer Drug Reviews
September 14, 2026
- Japan Pharma Investment Subgroup to Hold 1st Meeting September 18
September 14, 2026
- MFN Now a Factor in Japan’s Drug Pricing Debate: New Pharma Policy Chief
September 11, 2026
- MHLW to Weigh Survey Data, Past Approach for FY2027 Revision: Official
September 10, 2026
- Chuikyo Reps Back Greater Transparency, but Lean toward Broader CEA Price Cuts
September 10, 2026
We had just gotten off a call with a client in Europe, and we’d received a bit of an earful. “Philip,” the client pressed, “what can this candidate bring to us? We know what he does, but what has he…





