SRA's number for the day: 3,867,243
This article was originally published in SRA
As of 31 December 2012, the EU's EudraVigilance database for collecting, managing and analyzing reports of suspected side effects to medicinal products held a total of 3,867,243 adverse reaction reports, referring to 2,224,670 individual cases1,2.
You may also be interested in...
Takeda, Calliditas and Bayer are set to learn whether the European Medicines Agency will grant their respective products accelerated assessment status when they file for pan-EU marketing approval.
UK health technology assessment body NICE has struck deals with the makers of Enhertu for advanced breast cancer and Kesimpta for relapsing forms of multiple sclerosis.
The developers of eleven new drugs could learn this week whether the European Medicines Agency will set them on course for pan-EU marketing approval.