The U.S. government has not yet made its official recommendations for who should be able to get COVID booster shots this fall, but FDA offic...

(NEXSTAR) – Hundreds of people who stopped using allergy medications like Zyrtec and Xyzal noticed an uncomfortable new side effect, the U.S...

The 0.3% foam formulation of roflumilast was previously approved for the treatment of seborrheic dermatitis in adults and children aged 9 ye...

The FDA is likely to approve the first treatment for smoldering multiple myeloma but pass on a new option relapsed/refractory DLBCL, after v...

WASHINGTON (AP) — Government advisers are meeting Thursday to decide if COVID-19 vaccines need updating to improve protection this fall and...

A band of clinicians and chronic pain advocates are pushing regulators to scrutinize a controversial risk rating tool. Medscape Medical N...

The agency will require manufacturers to add a warning to prescription and OTC labeling about the risk of itching and the potential to resol...

By Jen Christensen, CNNThe US Food and Drug Administration will now require Covid-19 vaccines from Pfizer/BioNTech and Moderna to use exp...

Por Deidre McPhillips, CNNSe espera que el suministro de medicamentos GLP-1 para la pérdida de peso y el tratamiento de la diabetes se re...

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...