PatientsLikeMe for Partners Blog

Adverse Event Reporting

To better understand and measure the impact of medications that treat diseases in the real world, PatientsLikeMe has implemented a twice-audited pharmaceutical industry grade drug safety system. This drug safety program is designed to capture and report adverse events associated with approved prescription medications to the U.S. Food and Drug Administration (FDA). Adding this functionality to our data collection capabilities provides potential for reliable signal detection to supplement industry and FDA efforts in pharmacovigilance.