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FDA Recalls Duloxetine Antidepressant for Cancer Risk
Brownie Recall Update as FDA Sets Risk Level
The products were found to contain an undeclared allergen, which could be a risk for those with food allergies.
Duloxetine Recall: FDA Sets Second-Highest Risk Level for Antidepressants Containing Potential Carcinogen
Certain bottles and doses of duloxetine, a common antidepressant, have been recalled due to the presence of potentially cancer-causing chemicals. The recall was initiated on Nov. 19 by manufacturer Rising Pharma,
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,
Corn Salsa Recall as FDA Sets Risk Level
The Food and Drug Administration ( FDA) has set the risk level for a corn salsa at a "class 2 recall," stating that 192 jars of the salsa have been recalled due to having a pH of 4.7.
FDA may take steps to ban red food dye
FDA red food dye ban: When it could happen, and what to know
The FDA is reviewing a petition that could ban an artificial food coloring called Red No. 3. Here’s what to know about the petition and the product.
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.
FDA to consider banning red food dye — an ingredient not allowed in skin products yet ‘a kid can eat it’
The U.S. Food and Drug Administration (FDA) may enact a total ban on red food dye, the artificial coloring that’s not allowed in skin products but “a kid can eat it.” On December 5, the FDA gathered for a health committee meeting with the U.S. Senate to discuss a petition regarding Red No. 3, otherwise referred to as Erythrosine.
13h
on MSN
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 ...
Rutgers University
8h
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 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 ...
3d
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.
5d
on MSN
Senators grill FDA on ultra-processed food, key part of RFK Jr.’s agenda
Senator Bernie Sanders and Kennedy have a common goal: tackling chronic disease by cracking down on ultra-processed food.
18h
on MSN
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.
JD Supra
8h
Stem Cell Litigation Update: FDA Won the Latest Battle, but the Future of HCT/P Enforcement Remains Unclear
On September 27, 2024, the U.S. Court of Appeals for the Ninth Circuit reversed the district court’s decision in U.S. v. California Stem ...
9h
SetPoint’s neurostimulation device for rheumatoid arthritis ready for FDA review
SetPoint Medical’s vagus nerve stimulator offers another treatment option for patients who do not properly respond to ...
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