
|Articles|May 15, 2012
FDA Concludes Safety Review Of Novartis MS Drug Gilenya
Advertisement
The U.S. Food and Drug Administration Monday said Novartis AG's (NVS, NOVN.VX) multiple- sclerosis drug Gilenya shouldn't be used in patients with a recent history of stroke or some types of heart problems, concluding a safety review of the drug.
The safety review was prompted by a report last November of a 59-year-old patient dying in the U.S. less than 24 hours after taking the first dose of the drug.
Read the full story:
Source: Morningstar
Newsletter
Stay ahead of policy, cost, and value—subscribe to AJMC for expert insights at the intersection of clinical care and health economics.
Advertisement
Latest CME
Advertisement
Advertisement
Trending on AJMC
1
COVID-19 Vaccination Linked to Lower Risk of Long COVID in Adolescents
2
Breast Cancer Dominating Oncology Research, Access Disparities: Gen Li, PhD
3
Nearly All US Youth With BMI-Defined Obesity Have Excess Adiposity
4
Role of MRAs in Heart Failure Treatment
5















































