Avatar Posted by worldpharmanews 299 days ago (http://www.worldpharmanews.com)
Category: Product | Tags: wyeth pristiqs desvenlafaxine
The European Medicines Agency (EMEA) has been formally notified by Wyeth Europa Ltd of its decision to withdraw the application for a centralised marketing authorisation for the medicine Pristiqs (desvenlafaxine) 50mg and 100mg prolonged release tablets. Pristiqs was expected to be used for the treatment of vasomotor symptoms associated with menopause.
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