Adding Finasteride 1mg Daily for Male Pattern Baldness
Finasteride 1mg orally once daily is an effective, evidence-based treatment for male pattern baldness that promotes hair growth and prevents further hair loss in the majority of men, with durable benefits maintained over 5 years of continuous use.
Efficacy and Expected Outcomes
Finasteride 1mg daily demonstrates robust clinical efficacy with measurable improvements beginning at 12 weeks and continuing through long-term treatment 1, 2:
- 58-66% of men show improvement in hair growth based on global photographic assessment at 1-2 years 1, 2
- 83% of men have no further hair loss compared to baseline after 2 years, versus only 28% with placebo 3
- Hair count improvements are durable over 5 years of continuous treatment, while placebo leads to progressive hair loss 1
- The vertex (crown) responds best to treatment; anterior scalp and hairline show minimal response 4
Mechanism and Pharmacology
Finasteride works by competitively inhibiting Type II 5α-reductase, blocking conversion of testosterone to dihydrotestosterone (DHT), the androgen responsible for male pattern hair loss 5:
- Reduces serum DHT by approximately 70% with daily 5mg dosing (the 1mg dose for hair loss produces similar but slightly less suppression) 5
- Circulating testosterone increases by 10-20% but remains within physiologic range 5
- Bioavailability is 63% and is not affected by food 5
- Maximum effect occurs 8 hours after dosing with suppression maintained throughout 24-hour interval 5
Safety Profile and Sexual Side Effects
The overall incidence of sexual dysfunction is low but statistically significant compared to placebo 3, 6:
- 3.8% experience sexual side effects (decreased libido, ejaculation disorders, erectile dysfunction) versus 2.1% with placebo 3
- Sexual adverse events reverse upon discontinuation and many resolve even with continued therapy 3, 6
- Breast-related effects occur in 2.3% (gynecomastia, breast tenderness) versus 0.74% on placebo 7
- No new safety concerns emerged during 5-year follow-up studies 1
- Treatment is generally well tolerated with only 7.7% reporting treatment-related adverse events versus 7.0% with placebo 3
Critical Precautions
PSA levels decrease by approximately 50% after 12 months of finasteride therapy, which must be considered when screening for prostate cancer 7, 5:
- Inform patients and their physicians about this PSA-lowering effect
- Double the PSA value when interpreting results in men on finasteride for prostate cancer screening
Finasteride is absolutely contraindicated in pregnant women due to risk of hypospadias in male fetuses 3:
- Women of childbearing potential should not handle crushed or broken tablets
- Pregnant women must avoid exposure to semen from men taking finasteride
Treatment Protocol
Initiate finasteride 1mg orally once daily 2, 6:
- Minimum trial duration: 12 weeks to assess initial response 2
- Optimal assessment timepoint: 48 weeks for full evaluation of efficacy 2
- Long-term maintenance: Continue indefinitely as benefits are maintained only with ongoing treatment 1
- Discontinuation results in return to baseline within approximately 2-3 months 5
Patient Counseling Points
Provide comprehensive informed consent before initiating treatment 6:
- Set realistic expectations: finasteride maintains existing hair and may promote regrowth, but does not eliminate risk of baldness
- Explain that 58-66% will see improvement, while 83% will prevent further loss 1, 3
- Discuss sexual side effects (3.8% incidence) and their reversibility 3, 6
- Emphasize need for continuous treatment to maintain benefits 1
- Inform about PSA-lowering effect for future prostate cancer screening 7
Combination Therapy Considerations
Finasteride can be used as background therapy with other modalities 8:
- Platelet-rich fibrin (PRF) protocols often include finasteride as part of combined therapy for androgenetic alopecia 8
- The evidence suggests complex combined therapy protocols applied early yield best results 8
Common Pitfalls to Avoid
- Do not expect anterior hairline regrowth: The vertex responds best; anterior scalp shows minimal response 4
- Do not discontinue prematurely: Minimum 12 weeks needed to assess response, with optimal evaluation at 48 weeks 2
- Do not forget PSA counseling: Failure to inform patients about PSA-lowering can complicate future prostate cancer screening 7
- Do not prescribe to women of childbearing potential: Absolute contraindication due to teratogenic effects 3