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The U.S. is making it easier for gay and bisexual men to give blood by easing restrictions on groups that traditionally face higher risks of HIV.
The Food and Drug Administration on Monday proposed a simplified approach for future vaccination efforts, allowing most adults and children to get a once-a-year shot to protect against the mutating virus.
U.S. health officials have finalized a rule change that allows women seeking abortion pills to get them through the mail. The update Tuesday by the FDA replaces a long-standing requirement that the medicine be picked up in person.
A massive recall of millions of sleep apnea machines has stoked anger and frustration among patients, and U.S. officials are weighing unprecedented legal action to speed a replacement effort that is set to drag into next year.
The latest government study on teen vaping suggests there's been little progress in keeping e-cigarettes out of the hands of kids.
The Friday announcement from the Food and Drug Administration aims to diversify the nation's highly concentrated formula industry and prevent future shortages.
U.S. health officials are warning against overuse of the lone drug available to treat monkeypox, saying that even a small mutation in the virus could render the pills ineffective.
A panel of federal health advisers voted Wednesday to recommend approval for an experimental drug to treat Lou Gehrig’s disease, a remarkable turnaround for the much-debated medication that was previously rejected by the same group.
The head of the Food and Drug Administration says a government review of prescription opioid medications, including their risks and contribution to the U.S. overdose epidemic, is still underway.
A special House panel looking into the government's coronavirus response says the Trump White House tried to pressure U.S. health experts into reauthorizing the drug hydroxychloroquine that had been discredited as a COVID-19 treatment.
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