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Adverse effects observed in clinical trials include: Gastrointestinal effects: nausea, vomiting, diarrhoea, and constipation particularly during dose escalation

Standard reconstitution produces injectable solution

It is not the active ingredient in any FDA-approved drug product, and there is no United States Pharmacopeia (USP) monograph for either AOD-9604 (free base) or AOD-9604 acetate

Adhering to this protocol transforms the process from a potential liability into a reliable, repeatable scientific technique

Laboratory Tests for B12 Deficiency Lab tests are essential for spotting Vitamin B12 deficiency-induced thrombocytopenia

All treatments require provider evaluation