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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.

Lilly Senior Research Scientist Claudia Salinas discussed the relatively novel use of the data network during the annual Sentinel Public...

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