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FDA Recalls Duloxetine Antidepressant for Cancer Risk
What is Duloxetine? Antidepressant Drug Recalled by FDA
Duloxetine is an antidepressant, with a specific batch having been recalled due to the presence of potentially cancer-causing impurities.
FDA Recalls Duloxetine Antidepressant for Cancer Risk: What to Know
Over 8 million U.S. adults take antidepressants to treat mild to moderate depression, anxiety and, in some cases, chronic pain. A recent Food and Drug Administration (FDA) recall of a commonly prescribed antidepressant,
Antidepressant Duloxetine recalled in the US over cancer risk concerns
Rising Pharmaceuticals has voluntarily recalled over 233,000 bottles of Duloxetine in the US due to potential contamination with N-nitroso-duloxetine, a probable carcinogen. The FDA classified the recall as Class II,
Antidepressant Recall Update As FDA Sets Risk Level
233,003 bottles of duloxetine have been recalled due to potentially containing high levels of cancer-causing impurities.
Recall for antidepressant taken by millions due to cancer chemical
The FDA announced that more than 233,003 bottles of duloxetine were recalled on November 19 after finding the capsules contained high levels of N-nitroso-duloxetine.
FDA may take steps to ban red food dye
Red food dye could soon be banned as FDA reviews petition: ‘Scary stuff’
The U.S. Food and Drug Administration is considering banning an artificial food coloring called Red No. 3 due to potential health risks, including a link to cancer.
Will the FDA ban red dye 3? Controversial food additive used in candy, drinks under scrutiny
While the FDA has claimed that red 3, like other additives the agency has approved, can be safe to consume, advocates have long called for its ban amid concerns that the food dye is linked to cancer and behavioral problems in children.
FDA may finally ban artificial red food dye from beverages, candy and snacks
Is Red No. 3 safe? The FDA may finally move to ban artificial red food dye, the coloring found in beverages, snacks, cereals and candies.
1h
Nano-X Imaging: Expanded FDA Clearance Paves The Path For Deployment
Nano-X Imaging's Nanox.ARC scanner received expanded FDA clearance, potentially boosting sales and deployments. See why I ...
3d
FDA must disclose more COVID-19 vaccine records, US judge rules
A federal judge has ordered the U.S. Food and Drug Administration to publicly disclose more information underpinning its ...
6d
RFK Jr. Says He Wants To Untie Links Between Industry And FDA
It's unclear to what extent RFK Jr would want to disrupt a drug review process that has given the US a comparative advantage, ...
22h
How the FDA allows companies to add secret ingredients to food
It's a U.S. Food and Drug Administration rule that most Americans know little about, yet gives corporations the license to ...
Rutgers University
22h
Why the FDA Should Move Fast to Regulate Nicotine Pouches
In a commentary published in JAMA, experts at the Rutgers Institute for Nicotine & Tobacco Studies have issued a call to ...
4d
FDA adds two more toxic products to supplement recall: Here’s what you need to know
Two more products have been added to a safety alert issued by the Food and Drug Administration (FDA) regarding supplements ...
28m
Theradaptive Obtains FDA IDE Approval to Study OsteoAdaptâ„¢ SP in Additional Spinal Fusion Indications
Theradaptive, a privately held, clinical stage biologics company developing protein therapeutics for spine, orthopedics, soft ...
2d
on MSN
FDA may outlaw food dyes ‘within weeks’: Bombshell move would affect candy, soda and cakes, revolutionize American diets
The Food and Drug Administration will decide on a ban of certain food dyes after receiving a petition to review their safety.
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