Table 3.
Pharmacokinetic Properties of Injectable TU Formulations
| FDA Approval | PharmacoKinetics | Time to Tmax | Bioavailability in AUC0-tlast (ng/h/L) | Metabolism | Starting Dose | Titration | Special Precautions | Significant Adverse Effects | |
|---|---|---|---|---|---|---|---|---|---|
| Aveed | Yes; March 2014 | Ester bond is cleaved to release testosterone + inactive undecanoate; testosterone is then broken down to biologically active dihydrotestosterone (DHT) by 5a reductase | 4 days | 21,385 | Beta oxidation | 3 mL (750 mg) injected IM; then 4 weeks; then every 10 weeks | No titration | None | Acne, injection site reaction, pulmonary microembolism |
| Nebido | No | 7 days | 4051 | 4 mL (1000 mg) injected IM | No titration | None |