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Side Effects of Oral Finasteride for Hair Loss

Oral finasteride 1 mg daily for male pattern baldness is generally well-tolerated, with sexual side effects (decreased libido, erectile dysfunction, and reduced ejaculate volume) occurring in approximately 2-4% more patients than placebo, and these effects typically resolve upon discontinuation or may even improve during continued treatment. 1

Sexual Side Effects

The most commonly reported adverse effects are sexual in nature:

  • Erectile dysfunction occurs in approximately 2-4% more finasteride users compared to placebo 1. In the large PCPT trial, 67.4% of men on finasteride reported erectile dysfunction versus 61.5% on placebo (relative risk 1.10) 2

  • Decreased libido is reported at similar rates (2-4% above placebo) 1

  • Reduced ejaculate volume affects a small percentage of users 1, 3

  • Important context: The magnitude of sexual dysfunction is relatively small—finasteride's effect represents a mean difference of 3.21 points on sexual function scales, compared to 1.26 points for each year of aging 4, 2. Sexual dysfunction associated with finasteride decreases over time, even with continued treatment 1

Breast-Related Effects

  • Gynecomastia (breast enlargement) occurs in approximately 2-4% of patients taking finasteride versus 0.7-2.8% on placebo 1

  • Male breast cancer has been reported rarely in postmarketing surveillance, though the relationship to finasteride remains unclear 5

Discontinuation Rates

  • Overall discontinuation rates due to adverse events are approximately 6-7% in both finasteride and placebo groups, indicating the drug is generally well-tolerated 1, 4

  • New reports of drug-related sexual adverse events actually decrease with duration of therapy 5

Post-Discontinuation Effects

The FDA label notes that some patients have reported:

  • Persistent sexual dysfunction (erectile dysfunction, decreased libido, ejaculation disorders) that continued after stopping treatment 5

  • Orgasm disorders have been reported in postmarketing experience 5

  • These persistent effects are reported rarely, and their independent relationship to finasteride is uncertain given that most men had comorbid conditions and were taking other medications 5

Other Reported Effects

  • Hypersensitivity reactions including pruritus, urticaria, and angioedema (rare) 5

  • Testicular pain and hematospermia (rare) 5

  • Depression has been reported in postmarketing surveillance 5

  • Male infertility and poor seminal quality reported rarely, with normalization often occurring after discontinuation 5. The 1 mg dose has inconclusive evidence regarding fertility impact 4

Important Clinical Considerations

  • PSA suppression: Finasteride reduces PSA levels by approximately 50% after 12 months of therapy, which must be accounted for when screening for prostate cancer 1, 2

  • Contraindication in pregnancy: Finasteride is absolutely contraindicated in pregnant women due to risk of hypospadias in male fetuses 6

  • Tolerability profile: In phase III studies, only 7.7% of finasteride recipients versus 7.0% of placebo recipients reported treatment-related adverse events 6

Topical Alternative

For patients concerned about systemic side effects, topical finasteride formulations reduce the risk of systemic adverse effects while maintaining efficacy, with side effects localized to the application site (scalp pruritus, burning, irritation) 7

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Finasteride and Testosterone Levels

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Finasteride in the treatment of alopecia.

Expert opinion on pharmacotherapy, 2004

Guideline

Finasteride 1mg and Male Fertility

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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