Senators cite study showing 22 times higher serious side effects from chemical abortion drugs than FDA labels indicate, ...
The U.S. Food and Drug Administration (FDA) has approved two new biosimilars as reference products for Prolia (denosumab) and ...
4don MSN
'We don’t have time': Parents of 4-year-old with rare disorder urge FDA to reconsider drug denial
The FDA denied approving DCA to treat a rare disorder called PDCD. The Higbees are urging the agency to reconsider.
The Food and Drug Administration’s recent approval of a second generic version of the abortion pill mifepristone has left people on both sides of the reproductive rights fight scrambling to interpret ...
In any review of mifepristone, the FDA will now have to grapple with Judge Otake’s conclusion that the 2023 REMS decision for ...
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 ...
Somehow, it’s becoming even harder to get a GLP-1.
A 26% decline in drug overdose deaths from 2023 to 2024 is being credited by Minnesota leaders to investments that expanded ...
Let’s be clear: 7-OH is not a public health crisis. According to the Food and Drug Administration’s (FDA) own Adverse Event ...
The agency’s decision to conceal drug names on inspection reports has prevented doctors, pharmacists and patients from ...
5don MSN
FDA to streamline approvals for generic biological drugs in latest move targeting health costs
The US Food and Drug Administration will take steps to streamline the process to develop generic versions of complex biological drugs, the agency announced Wednesday. The changes are meant to ...
The Food and Drug Administration’s recent approval of a second generic version of the abortion pill mifepristone has left ...
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