Testosterone Replacement Therapy Dosing for a 46-Year-Old Male
For a 46-year-old male on testosterone replacement therapy (TRT), the recommended starting dose is 50-100 mg of testosterone weekly for injectable formulations or 40.5-50 mg daily for transdermal gels, with dose adjustments based on serum testosterone levels targeting the mid-normal range (500-600 ng/dL). 1
Formulation Options and Dosing
Injectable Testosterone
- Testosterone Cypionate/Enanthate:
Transdermal Formulations
Testosterone Gel 1.62%:
Testosterone Gel 1%:
Other Options
Testosterone Patches:
Testosterone Undecanoate (long-acting):
Monitoring and Dose Adjustment
Timing of Monitoring
- Injectable testosterone: Measure levels midway between injections 1
- Transdermal preparations: Can be measured at any time, understanding peak values occur 6-8 hours after application 1
Target Levels and Adjustments
- Target range: 350-600 ng/dL (mid-normal range) 1
- Dose adjustment criteria: 2
750 ng/dL: Decrease dose
- 350-750 ng/dL: Maintain current dose
- <350 ng/dL: Increase dose
Monitoring Schedule
- Test levels 2-3 months after treatment initiation or dose change 1
- Once stable, monitor every 6-12 months 1
- Monitor hematocrit and PSA at baseline and every 6 months 1
Formulation Selection Considerations
Injectable vs. Transdermal
Injectable advantages:
Transdermal advantages:
Safety Considerations
Cardiovascular Risk
- FDA labeling indicates potential increased risk of heart attack and stroke 1
- Injectable testosterone may be associated with greater cardiovascular risk compared to gels due to fluctuating levels 1
- Consider transdermal preparations for patients with cardiovascular risk factors 1
Hematologic Monitoring
- Monitor for erythrocytosis (elevated hematocrit) 1
- Injectable formulations have higher risk of erythrocytosis (43.8%) compared to transdermal preparations (15.4%) 1
- If hematocrit rises above normal range, consider dose reduction, therapeutic phlebotomy, or switching to transdermal preparation 1
Prostate Considerations
- Monitor PSA at baseline and periodically during treatment 1
- No consistent evidence of increased risk of prostate cancer or benign prostatic hyperplasia 1