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FDA, AstraZeneca
FDA approves AstraZeneca's Imfinzi for limited-stage small cell lung cancer
The U.S. Food and Drug Administration has approved AstraZeneca blockbuster drug Imfinzi to treat some adults with limited-stage small cell lung cancer, the health regulator said on Wednesday.
AstraZeneca: FDA Approves Imfinzi To Treat Adult Patients With Limited-stage Small Cell Lung Cancer
British drug maker AstraZeneca Plc (AZN.L, AZN) announced Thursday that the U.S. Food and Drug Administration has approved Imfinzi
Merus Gets FDA Approval for Bizengri Treatment
The clinical-stage oncology company on Wednesday said Bizengri is its first approved medicine based on the proprietary Biclonics technology platform. The approval is based on data from the eNRGy trial,
Supreme Court, FDA
Supreme Court wrestles with FDA’s attempt to curb access to flavored vapes
The Supreme Court on Monday pressed the Food and Drug Administration on whether it followed the law in its effort to keep flavored e-cigarettes off shelves, weighing a lawsuit from a multibillion-dollar industry that has come under scrutiny because its products are popular with school-aged children.
Supreme Court didn’t seem convinced FDA was unfair in blocking flavored vapes amid rise in teen use
Supreme Court justices questioned an FDA crackdown that involved rejections on sales of more than a million nicotine products created to taste like fruit and candy.
Supreme Court Weighs Ban on Flavored E-Cigarettes
On Monday, the Supreme Court heard arguments in a pivotal case concerning the regulation of flavored e-cigarettes. The vaping industry, which has brought the case forward, contests the Food and Drug Administration's restrictions on flavored vaping products,
21h
on MSN
Supplement Recall Update: FDA Adds Two More Toxic Products to Safety Alert
A safety alert by the FDA now covers 25 products sold as tejocote but found to contain a toxic plant called yellow oleander.
Medscape
22m
FDA Approves Bizengri for NSCLC and Pancreatic Cancers Harboring NRG1 Gene Fusion
The systemic agent is the first approved by the FDA for patients with NSCLC or pancreatic adenocarcinoma harboring an NRG1 gene fusion.
23h
on MSN
How the FDA allows companies to add secret ingredients to our food
The FDA allows food makers to vouch for the safety of ingredients they add to our food, calling them 'generally recognized as ...
5h
on MSN
Sauce Recall Update as FDA Sets Risk Level
Anyone who thinks they may have suffered a reaction due to undeclared allergens should also "notify the FDA and local health ...
Psychology Today
13h
FDA Under Trump and the Future of Psychedelics
With Trump back in the White House, will FDA policies on psychedelics shift? What's the impact on mental health care and ...
STAT
20h
Compounding pharmacies rebut Novo’s FDA petition
The Alliance for Pharmacy Compounding rebutted Novo's FDA petition to bar compounding pharmacies from copying its weight loss ...
medtechdive
18h
FDA issues final guidance on postmarket updates to AI-enabled devices
By using pre-determined change control plans, manufacturers can update AI-enabled devices without filing an additional FDA ...
21h
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, ...
1d
SCOTUS appears to lean toward FDA in e-cig case
FDA’S DAY AT SCOTUS — Don’t expect the Supreme Court to take a sledgehammer to the FDA’s ability to regulate tobacco.
16h
on MSN
FDA tags Wegovy with new warning for gastrointestinal reactions
Participants in Wegovy clinical trials were more likely to report “severe gastrointestinal adverse reactions,” the FDA's ...
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