Adverse drug events are more common in older people with comorbidities, a new study finds. Factors that are independently linked with adverse drug events are being female, taking more drugs daily, ...

Among adults treated for community-acquired pneumonia in the outpatient setting, broad-spectrum antibiotics vs macrolide monotherapy were associated with an increased risk for adverse drug events.

The FDA recently sent a warning letter to Novo Nordisk, raising concerns about the drug company failing to report adverse drug events. The letter, dated March 5, outlines the FDA’s observations at the ...

Adverse drug events can add approximately $3,000 to hospitalization costs, according to research published in the Joint Commission Journal on Quality and Patient Safety. For their study, researchers ...

The FDA announced that adverse event data from the FAERS will now be published daily. HealthDay News — The US Food and Drug Administration is now providing real-time, daily publication updates on ...

CHICAGO -- Adverse event risks varied across biologics used by asthma patients, an analysis of data submitted to the FDA Adverse Event Reporting System (FAERS) showed. In comparing relative number of ...

Lizzy leads STAT’s coverage of the FDA. Her stories explore the relationship between politics and science at the FDA, industry influence, and the agency’s ability to protect and promote public health.

The US Food and Drug Administration (FDA) sent a warning letter on 10 March to Novo Nordisk at its Plainsboro, NJ, site for a raft of postmarketing adverse drug experience (PADE) violations, including ...