A Democratic lawmaker is raising new concerns about a Food and Drug Administration program designed to drastically shorten ...
The FDA approved Scancell's phase 3 trial of iSCIB1+ for advanced melanoma, focusing on progression-free survival as a ...
DOJ accuses Louisiana AG, alleged victim of abortion coercion of trying to "short circuit" FDA's review of mifepristone's ...
By Padmanabhan Ananthan Feb 2 (Reuters) - Aquestive Therapeutics said on Monday the U.S. FDA has declined to approve its oral drug for severe allergic reactions due to packaging issues, marking a ...
The FDA approved re-administration of iDose TR for patients with healthy corneas, enhancing treatment flexibility for ...
By Ahmed Aboulenein WASHINGTON, Feb 1 (Reuters) - The U.S. Food and Drug Administration on Sunday began accepting requests to ...
The Food and Drug Administration (FDA) has granted Fast Track designation to QTX-2101, an oral formulation of arsenic trioxide, for the treatment of acute promyelocytic leukemia (APL), an aggressive ...
The US Food and Drug Administration has approved a landmark eye drop that uses a combined dose of medication to restore ...
KLAS Las Vegas on MSN
Las Vegas patients notified after FDA flags mammogram failures at Summerlin Hospital
Patients who received a mammogram at Summerlin Hospital Medical Center over the past two years were informed of a failure, ...
Tens of thousands of cholesterol medication bottles are being recalled nationwide due to manufacturing issues that could reduce drug potency and effectiveness.
The recalled dietary supplements were sold online nationwide and have been linked to dozens of salmonella infections across 28 states.
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