food and drug administration news

Bristol Myers Squibb Stock In Focus

FDA approves injectable version of Bristol Myers Squibb's cancer drug Opdivo

The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's blockbuster cancer drug, Opdivo. Opdivo is part of a class of drugs called PD-1 inhibitors,

Newsable Asianet News on MSN · 4h

Bristol Myers Squibb Stock In Focus After FDA Approves Cancer Drug: Retail Sentiment Brightens

Shares of Bristol Myers Squibb ($BMY) were in the spotlight on Friday after the U.S. Food and Drug Administration approved an injectable version of the pharmaceutical major’s cancer drug Opdivo. Opdivo is reportedly part of PD-1 inhibitors class of drugs,

Seeking Alpha on MSN · 6h

Bristol-Myers gets FDA okay for injectable Opdivo

The FDA has reportedly approved an injectable formulation of Bristol-Myers Squibb's (NYSE:BMY) oncology drug Opdivo. Previously, the PD-1 inhibitor drug was only available through IV infusion. The injectable formulation,

Reuters on MSN · 9h

US FDA approves injectable form of Bristol Myers' Opdivo

FDA Proposes New Testing Rules

CBS News on MSN · 8h

FDA proposes new tests to detect asbestos in cosmetics and other products containing talc

Manufacturers of baby powder and cosmetic products made with talc will have to test them for asbestos under a proposal announced by the U.S. Food and Drug Administration. The agency's proposal comes at the directive of Congress, which passed legislation ...

The Hindu · 21h

U.S. Food and Drug Administration proposes new testing rules to ensure cosmetics are asbestos-free

New FDA rule requires cosmetic companies to ensure talc products are asbestos-free, amid cancer concerns and lawsuits.

UPI · 11h

FDA proposes rule to target asbestos in talc cosmetic products

The U.S. Food and Drug Administration (FDA) has proposed a new rule to require standardized testing of talc-containing cosmetics for asbestos, a known carcinogen linked to serious illnesses.

Boise State Public Radio2h

FDA goes after mushroom edibles following illnesses and suspected deaths

The Food and Drug Administration is taking aim at a popular category of mushrooms edibles. That comes after a rash of illnesses and even a few suspected deaths earlier this year.

Off-brand versions of Lilly weight loss drug must be pulled off market, could mean higher prices

The United States Food and Drug Administration says the shortage of Eli Lilly’s Zepbound and Mounjaro drugs has been resolved ...

Bill McEwen9h

Robert F. Kennedy Jr. Wants to Ban Drug Ads on TV. It Wouldn’t Be Easy.

Robert F. Kennedy Jr., Trump's pick for health secretary, is a vocal opponent of TV drug ads. Will the industry face stricter ...

phillyvoice.com3d

FDA upgrades its definition of 'healthy' food for first time in 3 decades

Products must adhere to limits on saturated fats, added sugars and sodium while also drawing specific amounts from essential ...

FDA approves weight-loss drug Zepbound to treat sleep apnea

The Food and Drug Administration on Friday approved Eli Lilly’s weight-loss drug Zepbound to treat sleep apnea, a common but ...

2don MSN

Voluntary pet food recall issued after Oregon house cat dies from eating product that tested positive for bird flu

A Portland-based pet food company issued a nationwide voluntary recall after a house cat in Oregon died from eating one of ...

ConsumerAffairs1d

FDA approves generic GLP-1 drug to treat type 2 diabetes

The U.S. Food and Drug Administration has approved the first generic version of Victoza (liraglutide injection), ...

Merck to discontinue drug for bacterial infection

Merck will discontinue its drug for a bacterial infection that can lead to fatal diarrhea, the U.S. Food and Drug ...

WEIS1d

The Food and Drug Administration Said a Recall of Organic Eggs Sold at Costco

CNN The Food and Drug Administration said a recall of organic eggs sold at Costco is now classified at the highest risk level ...

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Bristol Myers Squibb Stock In Focus

FDA Proposes New Testing Rules

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