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Although VIZZ is, so far, the first and only FDA-approved aceclidine eye drop, it’s one of three prescription eye drops ...
The FDA has broadened the indication for evolocumab (Repatha; Amgen) to include adults at increased risk of major adverse ...
As the HHS and FDA leadership continues to look for ways to boost transparency and reshape the United States' healthcare ...
The FDA Adverse Event Reporting System, which Commissioner Marty Makary called “clunky,” previously published updates on a ...
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Verywell Health on MSNWegovy Is Now the Second FDA-Approved Treatment for MASH Fibrosis
Drugmaker Novo Nordisk received accelerated approval for the drug’s use in people with moderate to advanced liver scarring, ...
The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...
The FDA classifies this recall as Class II, which the agency describes as a situation "in which use of or exposure to a ...
Southwind Foods said it is "voluntarily recalling a limited quantity of frozen shrimp" due to the possible contamination with ...
The Food and Drug Administration has issued warning letters to several companies producing whipped formulas of sunscreen.
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