This bioresorbable standard-size pill can be interrogated via RFID to confirm it has been taken by the patient.
Federal law requires every prescription drug to include a document describing dosing guidelines, contraindications, results from clinical trials and safety considerations. But a spate of recent court ...
Healthcare institutions are currently shifting toward more personalized communication tools to improve patient ...
The FDA has cleared a wearable device for adults with locally advanced pancreatic cancer that delivers low-intensity electric fields through adhesive patches placed on the skin. In the pivotal ...
A patient in an open label extension study of Pfizer’s hemophilia treatment Hympavzi has died, the company and several hemophilia advocacy groups confirmed this week. Pfizer is now working with its ...
Abstract: Diabetes is a chronic metabolic disorder affecting millions of people worldwide, and effective management depends heavily on maintaining stable blood glucose levels through appropriate ...
COPENHAGEN, Nov 21 (Reuters) - Four patients in Denmark, who experienced vision loss after using Novo Nordisk's (NOVOb.CO), opens new tab popular weight-loss and diabetes drugs Wegovy and Ozempic, ...
The FDA has officially limited the label of Sarepta Therapeutics’ Elevidys, putting an end to a whirlwind few months that saw the abrupt departure—and reinstatement—of top agency official Vinay Prasad ...
Add Yahoo as a preferred source to see more of our stories on Google. Black box warnings can influence whether or not clinicians decide to prescribe a drug. SDI Productions/E+ via Getty Images A ...
University of Connecticut provides funding as a member of The Conversation US. A “black box” warning on a health product sounds pretty scary – maybe even more so when it’s suddenly being taken off the ...
(THE CONVERSATION) A “black box” warning on a health product sounds pretty scary – maybe even more so when it’s suddenly being taken off the packaging. Black box warnings – or as the FDA officially ...