What’s the Difference Between the FDA and the USDA?
Explaining America’s weirdly complicated food inspection system, including who regulates poultry and eggs and how Robert F. Kennedy Jr. is involved ...
FDA warns users of popular weight-loss drugs to watch for counterfeits
Health experts say popular weight-loss drugs like Ozempic and Wegovy are safe, but the FDA warns counterfeits are becoming more widespread.
btimesonline15d
FDA Greenlights Groundbreaking Pain Medication, But Is It Effective Enough?
The U.S. Food and Drug Administration (FDA) has approved Journavx, the first new class of pain medication in more than two decades. Developed by Vertex Pharmaceuticals, the drug-known generically as ...
kffhealthnews15d
FDA Green Lights New, Nonaddictive Pain Pill Journavx — But It’s Pricey
The drug, known as suzetrigine, is the first new painkiller approved in the U.S. since 1998. It can be used to relieve pain after surgery or injury, and some researchers say it might be the start of a ...
The Boston Globe15d
How the Globe’s Green Book project came together
It relates to the Green Book, a travel guide published from ... OPIOID EPIDEMIC: Older Black men in Boston are dying of drug overdoses at alarming rates, suffering in far greater numbers from ...
The American Journal of Managed Care15d
FDA Approves Celltrion’s Tocilizumab-anoh, Biosimilar to Actemra
Phase 3 study confirmed biosimilarity between tocilizumab-anoh and reference tocilizumab, supporting FDA approval. Study results showed comparable efficacy, pharmacokinetics, safety, and ...
LinkedIn15d
FDA green lights new painkiller
The Food and Drug Administration has approved a new type of drug for treating pain, raising hopes for a less-addictive alternative to opioids. The drug, Journavx, is the first new painkiller ...
centerforbiosimilars15d
FDA Approves Celltrion's Avtozma as Third Tocilizumab Biosimilar
The FDA approved Avtozma, a tocilizumab biosimilar developed by Celltrion, for the treatment of several rheumatic conditions. It is the third biosimilar to reference Actemra (tocilizumab) to be ...
thecooldown15d
How worried should you be about Green 3? Here's what experts say
Six more rainbow-colored food dyes, including Green 3, are under scrutiny following the U.S. Food and Drug Administration's Jan. 15 ban on Red 3 because of health fears. While watchdogs are working ...
BusinessMirror16d
Food, drug administration oversight needed to protect child health, nutrition–UNICEF
It is critical that agencies mandated to protect public health, such as the Food and Drug Administration (FDA), maintain their authority to ensure these products meet high safety standards that ...
FierceBiotech18d
Imperative Care claims FDA green light for its largest large-bore stroke catheter
Imperative Care has received a green light from the FDA for its large-bore catheter to help remove stroke-causing blood clots from within the brain. The new 510(k) clearance expands the portfolio ...
Nasdaq19d
Green Leaf Innovations, Inc. Celebrates Landmark U.S. Court of Appeals Ruling on FDA Regulation of Premium Cigars
PEMBROKE PINES, FL / ACCESS Newswire / January 27, 2025 / Green Leaf Innovations ... of Columbia Circuit to uphold the vacatur of the FDA's "deeming rule" for premium cigars.