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After the initial adaptation phase, the second and third months are typically where the momentum becomes undeniable

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Consider lowering the dose of these agents when coadministered with FARXIGA Pooled safety data across 12 placebo-controlled clinical studies of glycemic control in adults with T2D 1 Adverse reactions reported in 2% of adults taking FARXIGA 10 mg (n=1193) vs placebo (n=1393) included female genital mycotic infections (6.9% vs 1.5%), nasopharyngitis (6.3% vs 6.2%), UTIs (4.3% vs 3.7%), back pain (4.2% vs 3.2%), increased urination (3.8% vs 1.7%), male genital mycotic infections (2.7% vs 0.3%), nausea (2.5% vs 2.4%), dyslipidemia (2.5% vs 1.5%), influenza (2.3% vs 2.3%), and discomfort with urination (2.1% vs 0.7%)

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3.3 Evaluation of conformational stability of SR18 Notably, SR18 is an 18-amino acid designer polypeptide, modeled as a helix composed of both coded and NCAAs