REGULATORY
US FDA Begins Review of Risks of Serious Bleeding in Patients Taking Dabigatran
The US FDA issued a notification to medical institutions on December 7 saying it was evaluating post-marketing reports of serious bleeding events in patients taking the novel anticoagulant dabigatran (brand name in Japan: Prazaxa). The FDA said it is currently…
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REGULATORY
- Japan to Cut Drug Prices by 0.86% in FY2026; Central Govt Savings Seen at 105 Billion Yen
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Let’s ditch the stuffy jargon and talk about AI in HR like real humans.One of the biggest myths floating around is that AI is coming to steal our jobs. Newsflash: that’s not happening. Sure, AI can handle the boring stuff…





