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Orlistat, sold under the brand name Xenical among others, is a medication used to treat obesity. Its primary function is preventing the absorption of fats from the human diet by acting as a lipase inhibitor, thereby reducing caloric intake. It is intended for use in conjunction with a healthcare provider-supervised reduced-calorie diet.
Examples of such medications include the Orlistat, which was first prescribed in 1998. In 2009, it became an over-the-counter drug after obtaining consent from the European Medicines Agency . In clinical trials, patients prescribed with Orlistat (120 mg) showed better weight loss than those without (8.76 kg vs 5.81 kg) in one year. [14]
e. Orlistat (Xenical), the most commonly used medication to treat obesity and sibutramine (Meridia), a medication that was withdrawn due to cardiovascular side effects. Anti-obesity medication or weight loss medications are pharmacological agents that reduce or control excess body fat. These medications alter one of the fundamental processes of ...
August 9, 2024 at 10:38 AM. By Sriparna Roy and Christy Santhosh. (Reuters) -The U.S. Food and Drug Administration has approved ARS Pharmaceuticals' nasal spray as the first needle-free emergency ...
Law enforcement shuts down largest known child porn site on the dark web. A total of 338 people have been charged over the darknet site. The US just scored a significant coup against crime on the ...
NurPhoto via Getty Images. Earlier this year, Elon Musk announced that the first human patient had received a Neuralink brain implant as part of the company’s first clinical trial. Now, the ...
There's a lot to like about the S80 Pro, but above all else, it's the best because it's the most accurate. BACtrack claims that the S80 Pro can track BAC levels from 0.000 percent to 0.400 percent ...
Etoricoxib. Etoricoxib, sold under the brand name Arcoxia, is a selective COX-2 inhibitor developed and commercialized by Merck. It is approved in 63 countries worldwide as of 2007, except the United States where the Food and Drug Administration sent a Non Approvable Letter to Merck and required them to provide additional data.
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