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Cognitive Disorders In the 1-year controlled trials of phentermine and topiramate extended-release in adults, the proportion of patients who experienced one or more cognitive-related adverse reactions was 5% for phentermine and topiramate extended-release 7.5 mg/46 mg and 7.6% for phentermine and topiramate extended-release 15 mg/92 mg, compared to 1.5% for placebo

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95% CI=[-1.56, -0.36]

Enter vial size, bacteriostatic water volume, and target study dose to see the resulting concentration and draw volume on a U-100 insulin syringe