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Suspected adverse reactions can be reported to the FDA MedWatch program at www.fda.gov/medwatch or by calling 1-800-FDA-1088

In order to test the impact of the uncertainty of cardioprotective effects on the results, a sensitivity analysis which applied no cardiovascular protective effect to GLP-1 RA treatments was conducted

FDA approves Ruxolitinib (Opzelura) for Vitiligo Therapy: A breakthrough in the field of dermatology

User demographics span age 18 to 80+, though the majority of new users fall between ages 30-55, with slightly higher representation among women seeking sustainable weight loss solutions

[1] [2] Its primary therapeutic goal is improved glycaemic control, with weight reduction occurring as a beneficial effect