The FDA and manufacturers routinely allow doctors and hospitals to continue using medical devices that could cause serious ...

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The function is not a diagnostic tool, but can tell watch-wearers if they are exhibiting signs of sleep apnea.

The U.S. Food and Drug Administration has declined to approve Vanda Pharmaceuticals' drug to treat stomach paralysis symptoms ...

Federal health officials wrestling with when and how to use artificial intelligence will on Wednesday host an invitation-only ...

The Federal Trade Commission on Friday filed lawsuits against three prescription drug benefit managers or PBMs over concerns ...

Study Reports Safety Data in Children on JAK Inhibitors The most frequently reported adverse events in children on a JAK inhibitor were blood and lymphatic system disorders, in a review of FDA and ...

Biotech Aldeyra Therapeutics has announced that the US Food and Drug Administration (FDA ... which was the most commonly reported adverse event in clinical trials. By diminishing RASP levels ...

A new study, led by Professor John Deanfield from University College London (UCL), reveals that the anti-obesity medication ...

Like clockwork, Apple hosts its iPhone launch event every September. Here's what the company unveiled during its annual Apple ...

Adverse events were generally mild to moderate ... new research suggests. Health News // 15 hours ago FDA expands use of Kisqali to early stage breast cancer patients Women with early stage ...

Unlike rival CDK 4/6 inhibitor abemaciclib, patients don't need to be lymph-node positive to receive ribociclib after surgery ...