The U.S. Food and Drug Administration on Tuesday issued warning letters to three companies, including Amazon, for selling unapproved products for removing moles and skin tags.
Aug 10, 2022
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39
Asthma and allergy drug montelukast—sold as a generic and under the brand name Singulair—will get a "boxed warning" over potential ties to neuropsychiatric effects, the U.S. Food and Drug Administration announced Wednesday.
Mar 6, 2020
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(HealthDay)—Patients should avoid a class of antibiotics called fluoroquinolone due to an increased risk of heart vessel tears associated with their use, the U.S. Food and Drug Administration warned.
Dec 21, 2018
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13
(HealthDay)—The number of American children with attention-deficit/hyperactivity disorder (ADHD) is rising, U.S. government experts say.
Aug 14, 2015
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The Food and Drug Administration just pointed out something about bottles of hand sanitizer people are hoarding during the coronavirus pandemic: They have an expiration date.
Mar 31, 2020
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7
The U.S. Food and Drug Administration has approved Opzelura (ruxolitinib) as the first topical treatment for vitiligo.
Jul 21, 2022
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31
Monoclonal antibodies are laboratory-designed treatments tailor-made to fight specific infections. In early 2021, the U.S. Food & Drug Administration issued emergency use authorization for two monoclonal antibodies (bamlanivimab/etesevimab ...
Aug 29, 2022
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56
Have you ever been exposed to someone with COVID-19, or had the sniffles, and reached for an at-home test in your medicine cabinet—only to notice it's way past the expiration date stamped on the box?
Nov 13, 2023
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30
(HealthDay)—"Fights off tumors and alleviates symptoms of chemotherapy," one vape's advertising claims, while another is touted as an "asthma remedy, ADHD remedy, and dementia treatment."
Dec 10, 2021
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11
Two University of Rochester physicians—one as an investigator and one as a patient—had major roles in a cutting-edge clinical trial using the body's own immune cells to fight late-stage cancer. The striking results, showing ...
Apr 3, 2020
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