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It is intended for use in clinical settings where oral administration is not feasible or where higher plasma concentrations are desired, such as in cases of severe deficiency, certain infections, or as adjunctive therapy in specific medical protocols

Use must comply with all applicable laws and regulations.

A missing FDA listing does not prove that a product is safe, effective, or made to drug-quality standards

It is still under pre-clinical and clinical development and has not been approved for therapeutic use or any treatment plan by any government health authority or drug administration agency

Only 11.2% of participants stopped the trial due to side effects, and the discontinuation rate dropped significantly after week 24, suggesting those who make it through the early phase generally tolerate it well long-term