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Lilly's Olumiant Resubmission Includes Safety Data From US FDA's Sentinel Network

 
• By Cathy Kelly

Lilly used Reagan-Udall’s IMEDS to tap Sentinel for data on incidence of venous thromboembolism in patients with rheumatoid arthritis. 

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Eli Lilly & Co. resubmitted an application to FDA for the rheumatoid arthritis candidate Olumiant (baracitinib) that includes safety information drawn from US FDA's Sentinel data network for postmarket medical product surveillance.

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