News

Drugmakers are investing more in U.S. manufacturing as President Donald Trump threatens tariffs, but facilities can take ...
FluMist is now approved by the U.S. Food and Drug Administration for use at home, and it can be ordered online. It is the ...
Following discussions with the FDA, it was decided that the NDA resubmission would seek accelerated approval for elamirpretide on the basis of improvement in knee extensor muscle strength.
The drug, Dawnzera, is approved to prevent symptoms of a rare genetic disease called hereditary angioedema (HAE) in adults ...
Attorney General Kris Mayes wants the U.S. Food and Drug Administration to remove restrictions on one of two drugs used in non-surgical abortions.
Ionis Pharmaceuticals won FDA approval for a drug that prevents painful swelling attacks triggered by a rare genetic ...
In 2024, Hurricane Helene triggered a nationwide shortage of the country's intravenous (IV) fluids after damaging a facility in North Carolina. A similar IV fluid shortage was caused when Hurricane ...
A team of researchers from The Tisch Cancer Institute at the Icahn School of Medicine at Mount Sinai has successfully treated a rare and aggressive T-cell lymphoma that developed after CAR T-cell ...
Trading in shares of Ionis Pharmaceuticals is halted Thursday ahead of an expected decision from the U.S. Food and Drug Administration on the company's proposed donidalorsen treatment for hereditary ...
Ionis on Thursday said the FDA green light covers Dawnzera for prophylaxis to prevent attacks of hereditary angioedema in patients 12 years of age and older and makes the drug is the first and only ...
Dawnzera is the third medicine cleared by U.S. regulators this year for the rare genetic condition, and the second wholly owned medicine Ionis has brought to market.
The Food and Drug Administration is cautioning consumers against eating select packages of Great Value raw frozen shrimp sold ...