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Important Legal and Regulatory Information: FDA Category 1 Status: As of the 2026 regulatory updates, AOD-9604 is officially classified as an FDA Category 1 Bulk Drug Substance, meaning it is currently permitted for pharmaceutical compounding by licensed facilities for patients with a valid medical prescription

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For patients using Ozempic, diabetic retinopathy complications may occur, particularly in those with pre-existing retinopathy

However, dose increases should follow the FDA-recommended schedule of 2.5 mg increments every four weeks to minimize gastrointestinal adverse effects

The most common side effects associated with GLP-1 drugs are gastrointestinal, such as nausea, vomiting, diarrhea, stomach pain, and constipation

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