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The most common adverse effects from the SURMOUNT trials include: Nausea: 24-33% of participants (dose-dependent) Diarrhea: 18-25% of participants Constipation: 13-17% of participants Vomiting: 8-12% of participants Decreased appetite: 10-15% of participants Most of these effects are mild to moderate and occur primarily during dose escalation periods

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To assess legitimacy and credentials, we evaluate the following: Active state pharmacy licenses Disciplinary history for pharmacies and providers Licensed medical prescribers Real clinical oversight Unresolved BBB complaints or repeated safety concerns Transparency around pharmacy partners We start here for a reason

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