Consolidating adverse event databases is a smart move, but without public education, real-time transparency risks becoming ...

Add Yahoo as a preferred source to see more of our stories on Google. The FDA announced it will now update its Adverse Event Reporting System every day, instead of once per quarter. Photo courtesy FDA ...

What specific assessment frameworks can oncology nurses use to heighten clinical suspicion and catch grade one or two toxicities before they become potentially treatment-ending, and how can nursing ...

Although adverse event rates within 30 days after surveillance colonoscopy increase with age, peaking among patients aged 76-85 years, they remain infrequent, occurring in < 1% of procedures.

Adverse reactions to prescription drugs (adverse drug events, or ADEs) are quite common and usually do little harm to patients. But in a small percentage of cases, they can have serious consequences ...

The guide wire felt wrong. My hands, trained over two decades and thousands of procedures, sensed a resistance the navigation screen denied. The system’s three-dimensional reconstruction, a confident ...

It’s out with the old, in with the new at the FDA as the agency is unveiling a new adverse events monitoring system that joins several reporting systems into one unified platform, an effort that’s ...

Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...

Differences in age of diagnosis and survival period for individuals of Asian Indian/Pakistani origin and American Indian/Alaskan natives with multiple myeloma using Surveillance, Epidemiology, and End ...

The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...