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If more than 3 days have elapsed since the last SAXENDA dosage, reinitiate SAXENDA at 0.6 mg daily and follow the dosage escalation schedule in Table 1, to reduce the risk of gastrointestinal adverse reactions associated with reinitiation of treatment

Unlike FDA-approved drugs, compounded medications are not reviewed by the FDA for safety, effectiveness, or quality before they are dispensed

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A second important limitation relates to the substantial heterogeneity observed across studies

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