The rate of emergency department visits for adverse events among patients dispensed semaglutide is low, with most visits involving gastrointestinal effects, according to a research letter published ...

Sotatercept-csrk reduced the risk of major morbidity and mortality events in adults with WHO Group 1 PAH FC 3 or 4 at high risk of mortality.

At least 10% of patient safety events stem from poor communication among healthcare workers, patients and caregivers, according to a meta-analysis published April 14 in Annals of Internal Medicine. ...

Brochures generated using ChatGPT had a higher grade level and lower ease score than those generated using Google Gemini. There seems to be no significant difference between artificial intelligence ...

Leqembi — sold through a partnership between Eisai Co. and Cambridge-based Biogen — is one of the first medications approved that promises to slow the speed at which Alzheimer’s erases a person’s ...

This guidance is part of the The purpose of health records section of the Good practice guidelines for GP electronic patient records. Everyone in a health and care organisation is responsible for ...

This showed a 49% reduction in all-cause mortality and a 39% reduction in major adverse cardiovascular events, when compared to high dose statin therapy alone," said the first author of the study ...

The Fortnite Party Up Spring Raid Event is going live soon, which gives you an excuse to hop in-game with friends and earn a few rewards. If you're a fan of Invincible, you will not want to miss ...

Nearly 100 healthcare professionals from across Dorset, Bournemouth and Poole gathered to share ways to improve patient care. Yesterday's event, organised by the Dorset General Practice Alliance ...

Each patient ... (7 and 21 events) (p<0.001 for both), as well as a 3.2-fold increase in MI (3 and 18 events; p=0.063). Results were consistent after sensitivity analyses. Additionally, researchers ...

Nearly a third of medical device adverse events were not submitted to the FDA within a 30-day regulatory window, with most late reports filed more than six months after manufacturer notifications ...