News

FDA’s artificial intelligence is supposed to revolutionize drug approvals. It’s making up studies
Insiders tell CNN the FDA’s AI is “hallucinating” studies and can’t access key documents. Agency leaders insist the AI is ...
FDA panel on the use of antidepressants during pregnancy is alarming experts
On Monday morning, the FDA hosted a 10-person expert panel on the use during pregnancy of SSRIs, which include medications like fluoxetine (Prozac), sertraline (Zoloft) and citalopram (Celexa), among ...
FDA Issues Recall in Various States Due to Possible Listeria Contamination
The Food and Drug Administration (FDA) has been busy lately with various recalls. One involved Power Stick deodorant and ...
Sarepta shares slide again as drugmaker bows to FDA pressure to pause gene therapy
Sarepta Therapeutics is pausing shipments of its gene therapy for muscular dystrophy following several patient deaths that ...
Popular Deodorant Recalled, Impacts Thousands of Cases Sold Nationwide, FDA Reports
The FDA and Power Stick recalled thousands of deodorant cases because manufacturing practices did not comply with FDA ...
American Hospital Association14h
Recall issued by FDA for certain craniotomy kits
The Food and Drug Administration has identified a Class I recall of certain lots of Medline Industries Craniotomy ...
FDA to review prescription fluoride supplements for kids at risk for tooth decay
The Trump administration is inching closer to banning fluoride tablets and drops often prescribed to kids who don’t have ...
This woman was prescribed antidepressants. She was in menopause and needed another drug.
Her doctor prescribed an antidepressant, even though the then 36-year-old insisted she wasn’t depressed. She even went to ...
Over 67,000 Cases of Popular Deodorant Recalled Nationwide, FDA Reports
The U.S. Food & Drug Administration announced the ongoing recall of multiple varieties of deodorant. Keep reading to learn the specific deodorant packaging and scents that were recalled, plus other ...
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FDA Panel Votes Against Brexpiprazole Plus Sertraline for PTSD
The Food and Drug Administration’s (FDA) Psychopharmacologic Drugs Advisory Committee (PDAC) voted 10-1 against the approval of brexpiprazole in combination with sertraline for the treatment of adults ...
Recycling Today14h
LYB joint venture receives FDA nonobjection letters for recycled PP, HDPE processes
Genox LyondellBasell New Material Co. Ltd. is using mechanical recycling processes for the material.
FDA Issues Risk Warning for Bread Recall Update
The FDA's assessment of the bread recall has designated it as a Class II risk, which means the product "may cause temporary ...