As part of its advice on safety-related aspects to European Medicines Agency committees stemming from its June 7-10 meetings, the Pharmacovigilance Risk Assessment Committee (PRAC) discussed direct healthcare professional communications (DHPCs) containing important information for Neofordex (dexamethasone) and Xalkori (crizotinib).
This DHPC informs healthcare professionals of the risk of ocular toxicity, severe visual loss and the need for monitoring in pediatric patients with Xalkori, marketed by US pharma giant Pfizer (NYSE: PFE).
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze