The CHMP identified a number of further questions that it is putting to the marketing authorisation holder, GlaxoSmithKline. The responses to these questions will help the Committee to reach its opinion on whether the marketing authorisations for rosiglitazone-containing medicines should be maintained, changed, suspended or revoked.
The CHMP also discussed the available data on the possible risk of narcolepsy with the influenza vaccine Pandemrix, in order to prepare for its plenary meeting later this month.
After the plenary meeting of 20-23 September, the Agency will publish the Committee’s conclusions.