The Food and Drug Administration announced Wednesday its intention to ... that the oral form of the drug is ineffective ...
The Mental Health Watchdog calls for reforms to protect public safety, citing decades of antidepressant, electroshock, and psychedelic drug risks.
In a long-sought move, the Food and Drug Administration on Thursday formally began the process of abandoning oral doses of a ...
Pharmaceuticals announced that the U.S. FDA has approved Revuforj as the first and only menin inhibitor for the treatment of ...
Phenylephrine is a medication that’s been used to relieve nasal congestion caused by colds, allergies, and hay fever, per the ...
The U.S. Food and Drug Administration is taking the first step to remove an ingredient in non-prescription cold medicines ...
(WBRC) - The U.S. Food and Drug Administration (FDA ... and said the agency is yet to answer a decades-old pledge to ...
The FDA has accepted for review the resubmitted BLA for prademagene zamikeracel for recessive dystrophic epidermolysis bullosa.