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Cognitive Disorders In the 1-year controlled trials of QSYMIA in adults, the proportion of patients who experienced one or more cognitive-related adverse reactions was 5.0% for QSYMIA 7.5 mg/46 mg and 7.6% for QSYMIA 15 mg/92 mg, compared to 1.5% for placebo

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10.1016/j.ophtha.2016.09.023 40 DewettD.Lam-KamathK.PoupaultC.KhuranaH.RisterJ

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