mmx

Hi everyone, We've been building this for a little over a year now and we're interested in getting some feedback. To explain where this data comes from, one of the primary ways that the United States Food and Drug Administration monitors the safety of marketed drugs is the collection and analysis of reported adverse events (Side Effects) through the Adverse Events Reporting System. DrugCite has created a more friendly interface to help sort and explore this data for both doctors and consumers.