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FDA approves use of animal drugs to treat New World Screwworm

The Food and Drug Administration has authorized emergency use of animal drugs to treat and prevent infestations of the New ...

Orland Park family fights FDA over approval of drug to treat rare genetic disease

A little boy in the Chicago area is battling a rare disease and desperately needs a drug treatment for a better life. The ...
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FDA Cleared to Use Animal Drugs to Combat New World Screwworm Threat

WASHINGTON - The Food and Drug Administration was authorized Tuesday to use "animal drugs" on an emergency basis to treat and ...

US FDA declines to approve PTC Therapeutics' oral drug for rare genetic disorder

The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder ...

FDA’s new expert panels are rife with financial conflicts and fringe views

A series of panels convened by the Food and Drug Administration is raising concerns that the agency is skirting federal rules ...

HHS will allow emergency use of animal drugs in New World screwworm fight

The Food and Drug Administration (FDA) became authorized Tuesday to allow the use of animal drugs to treat or prevent ...

Shrimp, salad kits and more: See list of FDA food recalls in 2025 so far

Fresh & Ready Foods, LLC, recalled a few of their ready-to-eat products, including sandwiches and other snack items, over ...

FDA issues warning letters to Supergoop! and other brands over mousse sunscreen

The FDA urged consumers not to use the foam-style products because they may not be effective in protecting the skin from the ...

Stealth resubmits rare disease drug to FDA

The biotech, which cut jobs following the rejection in May of its Barth syndrome therapy, claimed it has addressed the agency ...

First drug to treat bronchiectasis lung condition approved by FDA

The U.S. Food and Drug Administration has approved Insmed's daily bronchiectasis pill, brensocatib, which will be sold under ...
USA Today1y

From vaping to abortion, conservatives are targeting FDA authority

The 5th Circuit ruled on Aug. 16 that it would limit access to mifepristone, finding that the Food and Drug Administration overstepped its authority with a series of actions that made it easier ...