The U.S. Food and Drug Administration has pulled draft guidance from its website requiring companies to test medicines and ...

Federal regulators have warned a Waco company that its human amniotic products are “unlicensed” and “unapproved,” and that ...

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The U.S. Department of Health and Human Services has paused public communications until Feb. 1 as Trump appointees take control of health agencies.

Hospitals can play a key role in building holistic treatment and support for perinatal mental health disorders during this critical period.

Overall, women with MS have a 26% increased risk of mental illness during pregnancy and a 33% increased risk after giving birth, compared to women without the degenerative nerve disease.

The bill would mandate two in-person visits for abortion pills, which critics say would restrict abortion access.

Judge Matthew Kacsmaryk, a Trump appointee, allowed three states to go forward with a lawsuit that seeks to change how ...

In the following sections, this press release dives into the science behind Mitolyn, shares real-world success stories, and ...

The FDA approved Zepbound (tirzepatide ... which remains the first-line treatment for OSA. “This is the first drug treatment for obstructive sleep apnea, and so that’s exciting, and it ...

Pristiq (desvenlafaxine) and Effexor (venlafaxine) are SNRIs. Pristiq treats depression, while Effexor treats depression and ...

The Food and Drug Administration has said it is banning the use of Red No. In a farewell speech to Justice Department ...