US FDA approves Eli Lilly's drug for eczema
Eli Lilly said on Friday the U.S. Food and Drug Administration approved its eczema drug for use in adults and children above ...
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FDA Approvals, Fraud Settlements, and Global Health Initiatives: Latest Health News
This health news brief covers significant updates including the FDA's approval of new therapies for multiple sclerosis and ...
FDA advisers unconvinced by Intercept's liver disease drug benefits, safety
Independent advisers to the U.S. Food and Drug Administration voted on Friday against confirmatory trial data for Intercept Pharmaceuticals' liver disease drug, putting into question the treatment's ...
US FDA expands J&J's psoriasis drug for inflammatory bowel disease
The U.S. Food and Drug Administration has allowed the expanded use of Johnson & Johnson's drug, Tremfya, to treat adults with ...
US FDA staff questions confirmatory trial data for Intercept's liver disease drug
Staff reviewers at the U.S. Food and Drug Administration said on Wednesday a confirmatory trial did not show the ...
Following massive recalls and outbreaks, Americans are losing confidence in food safety regulations
A Gallup poll has found that consumers' confidence in food safety has dropped by 23 points between 2006 to 2024 ...
How A Future Harris Administration Could Expand Medicare Drug Pricing Provisions
Harris touts the IRA's drug pricing measures which reduce Medicare beneficiary out-of-pocket costs. If elected her quest to ...
Weight-loss drugs and children: What doctors say about the safety, effectiveness of the medications
Novo Nordisk's liraglutide has been approved for children who are at least 12 years old. However, the drug is now being ...
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Breakthrough Therapy designation for Sanbexin sublingual tablets granted by the United States Food and Drug Administration
The Breakthrough Therapy designation stems from the provisions of 《Food and Drug Administration Safety and Innovation Act》.
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Confusion persists with food traceability rule as compliance date nears
From reporting metrics to how the FDA investigation process works, several major questions are looming for industries impacted by the rule, a new report found.
Senators Target Influencers, Telehealth Firms for Misleading Weight-Loss and Other Drug Promotion
The legislation would allow the FDA to warn and fine companies and individuals who post false information online about medications such as Ozempic and Wegovy.
Elutia Announces First Patient Implant of EluPro™, the World’s First Drug-Eluting BioEnvelope for Cardiac Pacemakers and Neurostimulators
Elutia Inc. (Nasdaq: ELUT) (“Elutia”), a pioneer in drug-eluting biomatrix products, today announced a landmark achievement ...