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FDA Boss Sounds Alarm About Future Under Trump and RFK Jr.
FDA commissioner suggests RFK Jr. and Trump might compromise an agency ‘at peak performance’
The agency’s ability to hire and retain skilled employees may be in jeopardy given Trump ally Robert F. Kennedy Jr.’s hostility to civil servants, Califf said. Trump has said he plans to give Kennedy, leader of the “Make America Healthy Again” movement, power over health care policy in his administration.
FDA Boss Sounds the Alarm About Future Under Trump and RFK Jr.
Food and Drug Administration commissioner Robert Califf said he was “disappointed” with the presidential election result and is uncertain about the agency’s future under Donald Trump. “I’m biased, but I feel like the FDA is at peak performance right now and we’ll just see what happens as the new team comes in,
What to know about Trump and RFK Jr.'s "Make America Healthy Again" agenda
Robert F. Kennedy Jr. has vowed to combat "the chronic disease epidemic in this country" in the Trump administration, with the slogan "Make America Healthy Aagain."
FDA recalls nearly 80,000 pounds of Costco butter
Nearly 80,000 pounds of Costco butter recalled for missing 'Contains Milk statement': FDA
Costco customers with dairy allergies may need to check their fridge because 80,000 pounds of the retailer's butter was recalled for packaging that was missing the "Contains Milk statement," according to the U.S. Food and Drug Administration (
FDA
).
FDA recalls nearly 80,000 pounds of Costco butter without 'contains milk' label
The U.S Food and Drug Administration issued a recall for around 80,000 pounds of butter sold at Costco for packaging that was missing the “contains milk" label.
Costco recalls nearly 80,000 pounds of butter due to possible mislabeling
Costco voluntarily recalled 79,200 pounds of two types of its store-brand butter over the past month because their labels may not have said the products contain milk.
FDA to remove ingredient from cold medicines
These Cold and Flu Medicines Contain Phenylephrine, the Ingredient the FDA Plans to Ban
Phenylephrine is a medication that’s been used to relieve nasal congestion caused by colds, allergies, and hay fever, per the U.S. National Library of Medicine.
FDA to remove ingredient from cold medicines after data shows it does not work
The U.S. Food and Drug Administration is taking the first step to remove an ingredient in non-prescription cold medicines after studies showed it does not work.
Which Decongestants Are Effective? Why the FDA Wants to Pull a Popular Medicine Ingredient
Phenylephrine is included in many cold and flu products, but a scientific panel last year found that it doesn't really do its job at "unstuffing" when taken by mouth.
FDA removes clinical hold on Covid-19/flu combo trial
Novavax Gets FDA Approval To Resume Testing Two Vaccines After Clinical Hold
Key Takeaways Novavax said the Food and Drug Administration allowed it to continue testing a combination COVID-19-flu and standalone flu vaccine that had been put on hold.Regulators stopped testing last month as one patient had a serious adverse event after taking the shot.
Novavax to Move Forward With Covid-19-Flu Vaccine After FDA Lifts Clinical Hold -- Update
Novavax can move forward with a trial for its combined Covid-19 and influenza vaccine after regulators lifted a clinical hold. The Gaithersburg, Md., vaccine developer said Monday that the U.S. Food and Drug Administration had removed the clinical hold on its investigational new drug application for its combined vaccine and its standalone flu vaccine candidates.
Novavax: FDA removes clinical hold on Covid-19/flu combo trial
Novavax (NVAX) announced that the U.S. FDA has removed the clinical hold on Novavax’s Investigational New Drug application for its
3h
The FDA is urging these brands of ground cinnamon products to issue voluntary recalls
The products are part of the agency's ongoing public health alert concerning cinnamon with elevated lead levels ...
Hosted on MSN
4h
US FDA declines full approval for Intercept's liver disease drug
Under the accelerated pathway, the
FDA
mandates additional trials that verify the drug's benefits. If the data from the ...
FiercePharma
4h
FDA rejects Intercept's ask for Ocaliva full nod in rare liver disease, but accelerated approval remains
In the wake of an unfavorable advisory committee meeting in September, Intercept Pharmaceuticals’ bid to win full approval ...
10h
FDA extends expiration date for at-home COVID-19 tests: What you need to know
FDA reccommends checking the shelf life of COVID anitigen test close to expiring due to some test with different dates from ...
dvm360
49m
FDA approves renewal for canine chemotherapy-induced diarrhea treatment
Jaguar Health announced that its product, cofelemer delayed-release tablets (Canalevia-CA1; Jaguar Health), received approved ...
Targeted Oncology
22h
Elraglusib Gains FDA Rare Pediatric Disease Designation in Ewing Sarcoma
Elraglusib has been granted rare pediatric disease designation from the
FDA
for the treatment of patients with Ewing ...
Local 12 WKRC Cincinnati
8h
FDA recalls 80,000 pounds of Costco butter for not mentioning it contains milk
UNDATED (WKRC) - Nearly 80,000 pounds of butter were recalled from Costco stores after the
FDA
discovered the packaging did ...
MassDevice
5h
FDA clears AI-powered breast cancer detection tech from iCad
Cad (Nasdaq:ICAD) announced today that the FDA cleared its ProFound Detection version 4.0 for digital breast tomosynthesis ...
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