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Gilead rep minimised Letairis's risk plan, US FDA says

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Executive Summary

A Gilead Sciencesrepresentative minimised serious liver and fetal toxicities associated with the pulmonary arterial hypertension drug Letairis (ambrisentan) and downplayed the need for the product's risk management scheme, the US FDA's division of drug marketing, advertising and communications (DDMAC) said.

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