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Bunck et al., 2009)

Reconstitution: 2.0 mL per 20 mg vial (~10.0 mg/mL) for accurate unit measurements

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This means that they have not undergone review for safety, efficacy, or quality before being dispensed, and have not been demonstrated to the FDA to be safe or effective. This is transparent, honest, and something many clinics fail to disclose at all

This creates a flatter pharmacokinetic curve with lower peak levels and higher trough levels, potentially reducing the intensity of receptor desensitization at peak concentrations while maintaining more consistent receptor occupancy throughout the week