UniQure NV's stock plummeted over 54% after the FDA deemed the clinical data for its Huntington's disease gene therapy ...
Shortages to backbone chemotherapy drugs are negatively affecting patient care, and more shortages are likely without policy ...
October 2025 proved to be a significant month for the oncology landscape, marked by a wave of key regulatory decisions from the US FDA. This period saw important full and accelerated drug approvals ...
The U.S. Food and Drug Administration (FDA) announced Wednesday that it will relax certain rules for approving low-cost versions of some high-priced medications, in an effort to speed up access to ...
More than 580,000 bottles of a popular blood pressure medication distributed nationwide have been recalled, according to the U.S. Food and Drug Administration. The recall involves bottles of Prazosin ...
Last year, these treatments accounted for 75% of the $236B in annual sales set to vanish with the loss of exclusivity.
According to the FDA, the Centers for Disease Control and Prevention's case count for illnesses tied to the listeria outbreak has increased, with seven reports of new illnesses across three states, ...
This article originally published at FDA expands recall on cinnamon products due to lead hazard. Symptoms of the condition vary from person to person, but there are a few feelings and habits to note.
The US Food and Drug Administration said Friday that it is taking action to restrict the use of prescription fluoride supplements, following a directive from the government’s Make American Healthy ...
The Food and Drug Administration (FDA) has put four companies on notice for marketing “unapproved fluoride-containing ingestible drugs” for use by children under the age of 3 or children at low or ...
Teva Pharmaceuticals USA and drug distributor Amerisource Health Services has recalled more than half a million bottles of a ...
Over half a million bottles of prazosin hydrochloride have been recalled for having high levels of potentially cancer-causing ...
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