YUFLYMA® (adalimumab-aaty) is a high-concentration (100mg/mL) and citrate-free formulation of Humira® (adalimumab) biosimilar[1] Celltrion p...

The agency convened a panel to discuss whether the ingredient should be prohibited from foods, medicines, and cosmetics. Medscape Medical...

The FDA is requiring COVID vaccine makers Pfizer and Moderna to update their warnings about the possible risk of myocarditis and pericarditi...

Presented by The Coalition to Strengthen America's Healthcare — The Trump administration on Tuesday said it plans to limit the approval of u...

The agency will require manufacturers to conduct randomized, controlled trials to secure approval for healthy Americans. Medscape Medical...

A doctor draws the Moderna coronavirus disease booster vaccine at a pharmacy in Schwenksville, Pennsylvania, US.— Reuters/FileAdvisers to th...

FDA advisers are set to meet Thursday to decide on updates for this fall's COVID shots.

The U.S. Food and Drug Administration (FDA) will no longer recommend yearly COVID-19 vaccines for kids and most adults.In an editorial a...

“We just want to ensure that the most popular method for abortion in Virginia and beyond is protected no matter who sits at the White House...

Saudi Gazette report RIYADH — The Saudi Food and Drug Authority (SFDA) has launched a digital awareness campaign to educate the public on th...

Stryker's first basivertebral nerve ablation system targets the basivertebral nerve to provide relief from chronic* vertebrogenic low back p...

The approval of the Novavax COVID-19 vaccine by the FDA has sparked significant discussion due to its restrictive usage guidelines. Unlike t...

The recent approval by the FDA of the Lumipulse G pTau217/ß-Amyloid 1-42 Plasma Ratio test represents a significant advancement in the...

The US Food and Drug Administration has given marketing clearance to a blood test to help diagnose Alzheimer’s disease, making the test the...