Less than three-quarters of medical device-related adverse events are reported on time by their manufacturers.

In patients with CKD, hyperkalemia significantly increases risk for major adverse cardiovascular events and arrhythmia.

BD, Medtronic and Abbott were among the top 10 device companies with the highest number of late reports to the FDA, the study ...

A protocol for transitioning patients with heart failure and a left ventricular assist device to a stepdown unit from the ICU ...

The newly formed panel will compile and analyse data on adverse reactions, forwarding regular reports to the central ...

Sarepta stock may recover sharply as additional information and data reveal that the adverse event reported by the company is ...

Reports on medical device adverse events widely exceed FDA deadlines, according to a recent study published in the BMJ. Read ...

During a live event, James W. Smithy, MD, MHS, and other oncologists discussed how their experience with immune-related ...

Intraoperative floppy iris syndrome is associated with an increased rate of severe intraoperative complications and greater ...

An expert discusses how in the first-line (1L) treatment of advanced unresectable hepatocellular carcinoma (uHCC) with tyrosine kinase inhibitors (TKIs) such as lenvatinib or sorafenib, proactive ...

Patients with LORA and CLD at baseline had lower rates of treatment response and a higher risk for SAEs over 5 years, compared against those without CLD.

Hampton Roads isn’t alone in its overreliance on ADHD diagnoses and psychotropic drugs to handle troublesome schoolchildren, ...