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FDA to Reconsider Removal of Lilly's Obesity Drug

Eli Lilly's tirzepatide is off the FDA's shortage list: What it means for patients

Eli Lilly's weight-loss drug is no longer on the Food and Drug Administration's drug shortage list. Compounding pharmacies say this will limit patient access.

WPTV-TV · 13h

FDA is reconsidering its decision to take tirzepatide off its drug shortage list

Pharmacists can continue making compounded versions of generic tirzepatide, the active ingredient in popular medications Mounjaro and Zepbound, the FDA said in a recent court filing.

The Hill on MSN · 1d

FDA will reconsider decision barring copycat versions of Lilly weight loss drug

The Food and Drug Administration (FDA) said it will reconsider its decision to remove Eli Lilly’s blockbuster weight loss and diabetes drug from its official shortage list and allow compounding

FDA, Novocure and Cancer Treatment

UPI News on MSN · 4d

FDA approves first once-weekly drug treatment regimen for hemophilia

Patients suffering from hemophilia received a "meaningful" advancement on Friday when federal regulators approved the first once-weekly treatment for the disease.

MarketWatch · 12h

Novocure Shares Rise After FDA Approves Optune Lua Cancer Treatment

Shares of Novocure were trading higher in Tuesday's late session after the company said that the Food and Drug Administration had approved Optune Lua, its wearable treatment for certain types of lung cancer.

Investor's Business Daily on MSN · 11h

Novocure Shoots Skyward, Reversing Setbacks, After FDA Approves Lung Cancer Treatment

Novocure stock rocketed late Tuesday after the FDA signed off on its treatment for patients with metastatic lung cancer.

19h

FDA Says Compounding Pharmacies Can Keep Making Weight-Loss Med Tirzepatide, for Now

TUESDAY, Oct. 15, 2024 (HealthDay News) -- Pharmacists may continue making compounded versions of the weight-loss medication ...

fingerlakes11m

FDA partners with URMC to develop digital tools for Huntington’s disease

The project, which will be conducted by URMC’s Center for Health + Technology, seeks to create objective, digital tools that can provide a clearer picture of how Huntington’s disease advances, ...

17hon MSN

US FDA clears CMR Surgical's robotic device to assist gall bladder removal

UK-based medical device maker CMR Surgical said on Tuesday that the U.S. Food and Drug Administration has cleared the ...

FDA upgrades recall of eggs linked to salmonella to 'serious' health risks. Are there IN cases?

The recall was originally announced Sept. 6 by the Centers for Disease Control and Prevention. It was upgraded Sept. 30 to ...

Medscape14h

FDA Approves Fifth Ustekinumab Biosimilar

The drug is approved for multiple inflammatory conditions and is expected to launch in the first half of 2025.

12h

Delta suspends meal service on over 200 flights following FDA inspection

UNDATED (WKRC) - More than 200 Delta Air Lines flights were denied meal service after a routine check found an issue.

The Motley Fool10h

Should Eli Lilly Investors Worry About This Unexpected FDA Move?

The FDA earlier this month recognized Lilly’s progress in increasing supply and took the drug off the agency’s shortage ...

22hon MSN

Maine shooting survivors claim Army negligence and FDA's weight-loss drug decision: Morning Rundown

Detroit, TCF Center, 2024 election, Harris in Pennsylvania, Lewiston Maine shooting, Trump rally shooting survivors, giant ...

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