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Onglyza: Heart Failure Injuries and the FDA Mandated Label Change
Published by Kentucky Justice Association and Nebraska Association of Trial Attorneys



Summary
Please note: this webinar is only available to plaintiff attorneys and their staff. Registration for the webinar certifies that the attendee only does plaintiff work. We reserve the right to determine eligibility for webinar attendance.

The FDA ordered a label change for the diabetes drug, Onglyza, requiring the manufacturer to warn consumers that the drug can cause heart failure. A clinical study shows that Onglyza can cause heart failure resulting in hospitalization. Learn about the current status of the litigation including the MDL in Kentucky and the coordinated proceeding in California state court.

Presenters
Jennifer A. Moore
Jennifer A. Moore represents individuals and families who have been injured as a result of harmful drugs, products and medical devices, medical negligence, nursing home neglect and abuse, and automobile and truck wrecks. She is a founding partner of Grossman & Moore, PLLC in Louisville, Kentucky. She has served as court-appointed liaison counsel in a multi-district litigation involving a defective product and as trial counsel in numerous cases holding wrongdoers accountable, including...More
Program Agenda
5 Minutes - Introduction
60 Minutes - Presentation
10 Minutes - Live Q&A with the Speaker

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