Benefit-risk review of Sanofi-Aventis's Multaq underway in EU
This article was originally published in Scrip
"Urgent regulatory action" is needed to help prevent the possible risk of severe liver complications associated with Sanofi-Aventis' anti-arrhythmic Multaq (dronedarone), said the Committee for Medicinal Products for Human use (CHMP) on 21 January. A benefit-risk review of the product is now underway.
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