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'Gas station heroin': The drug sold as a dietary supplement that's linked to overdoses and deaths
The US Food and Drug Administration (FDA) has issued an urgent warning about tianeptine—a substance marketed as a dietary ...
Contributor: Here's how to get GLP-1 drugs covered by employer health insurance
Improving access and affordability could be transformative for public health, given that about 88% of Americans are ...
US judge says layoffs at Department of Health and Human Services were likely unlawful and must be halted
A federal judge has ruled that recent mass layoffs at the US Department of Health and Human Services were likely unlawful and ...
US FDA approves Regeneron's blood cancer therapy
Regeneron Pharmaceuticals said on Wednesday the U.S. Food and Drug Administration has approved its drug for a type of blood ...
US FDA to revise ADHD stimulants labels to warn of weight loss risk in children under 6
The U.S. Food and Drug Administration said on Monday it is revising the labeling of all extended-release stimulants used to ...
HIV prevention drug lenacapavir approved by FDA as twice-yearly injection
Clinical trials showed 99.9% of participants who received the drug, called Yeztugo​ from company Gilead Sciences, remained ...
Investopedia9mon
Food and Drug Administration (FDA): What It Is and Does - Investopedia
Food and Drug Administration (FDA) Approvals and the Market . Companies that are focused on the development and sale of new drugs can be left without key products to drive their revenue if their ...
CBS News3mon
Food and Drug Administration news - Today’s latest updates
The Food and Drug Administration has outlined new regulations for COVID-19 booster shots, ... Protests against the Trump administration took place across the U.S. Saturday.
Food and Drug Administration staff cuts may hinder US biomedical innovation
The elimination of 3,500 full-time employees at the FDA risks undermining the very innovation and domestic capacity the ...
Business Wire1y
U.S. Food and Drug Administration Approves ZELSUVMI™ as a First-in-Class Medication for the Treatment of Molluscum Contagiosum - Business Wire
SAN DIEGO--(BUSINESS WIRE)--Ligand Pharmaceuticals Incorporated (NASDAQ: LGND) today announced that the U.S. Food and Drug Administration (FDA) has approved ZELSUVMI™ (berdazimer topical gel, 10 ...
Business Wire3y
argenx Announces U.S. Food and Drug Administration (FDA) Approval of VYVGART™ (efgartigimod alfa-fcab) in Generalized Myasthenia Gravis - Business Wire
You may report side effects to the US Food and Drug Administration at 1-800-FDA-1088. Please see the full Prescribing Information for VYVGART and talk to your doctor.