The US Food and Drug Administration on Friday approved the first prescription medicine for obstructive sleep apnea: the weight-loss drug Zepbound.
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The FDA granted accelerated approval to repotrectinib (Augtyro) for adults and children aged 12+ with NTRK fusion-positive tumors. The TRIDENT-1 trial showed a 58% ORR in TKI-naïve patients and a 50% ORR in TKI-pretreated patients, highlighting its efficacy and potential.
Colonoscopies are never fun. But they are necessary to help catch colon cancer. The FDA has approved a drug that could make preparation a lot easier.
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Which sunscreens are safe, and why are the rest being reclassified? You may be wondering why the sudden media attention around sunscreens. There are three big reasons. Chemical sunscreens penetrate your skin at problematic rates First, FDA conducted a study which was published in The Journal of American Medical Assoc
Retail food establishments covered under the menu labeling rule must disclose the number of calories contained in standard menu items on menus and menu boards and on signs adjacent to food on display and self-service food (e.g., restaurant-type food available at a salad bar, buffet line, cafeteria line or similar self-service facility, including self-service beverage stations). Covered establishments also must post a "statement of availability," noting that additional nutrition information is available upon request, and a "succinct statement" to help consumers understand the significance of the calorie information in the context of a total daily diet. Our goal is to ensure that consumers who eat out are provided with consistent nutrition information they can use to make informed choices for themselves and their families. This is an example of the use of a single sign to declare calories for multiple items at a self-service salad bar. For more information, visit the FDA's web page Menu Labeling Requirements.
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The U.S. Food and Drug Administration today granted accelerated approval to benznidazole for use in children ages 2 to 12 years old with Chagas disease. It is the first treatment approved in the United States for the treatment of Chagas disease.
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The Lumipulse G β-Amyloid Ratio (1-42/1-40) test is available at clinical laboratories nationwide for adult patients aged 55 years and older who are presenting with cognitive impairment and being evaluated for Alzheimer’s disease and other causes of cognitive decline.
