REGULATORY
Zyprexa under PMDA Review for Risk of Drug-Induced Hypersensitivity Syndrome
The Pharmaceuticals and Medical Devices Agency (PMDA) said on July 15 that it is reviewing the risk of drug-induced hypersensitivity syndrome for the anti-psychotic Zyprexa (olanzapine) - a move that is likely to result in label changes. Drug-induced hypersensitivity syndrome…
To read the full story
Related Article
REGULATORY
- LDP Returnees Set Sights on Social Security, Drug Policy as Special Diet Opens
February 18, 2026
- 10 Firms Win Approval for Bilanoa Generics, 2 Contenders for Fycompa
February 17, 2026
- MHLW to Brand OTC-Like Drug Cost Rule as “Partially Non-Insured Care”
February 17, 2026
- Taiyo Pharma’s Propranolol Designated as Drug for Specific Use
February 17, 2026
- Japan Grants Orphan Tag to Bayer, Incyte Drugs, and 12 Others
February 17, 2026
The Japanese healthcare sector is experiencing rapid growth, demanding a highly skilled and diverse workforce. However, finding and attracting the best talent in this competitive market presents significant challenges.Enter AI. With the rise of AI-powered tools, healthcare organizations can revolutionize…





