Finasteride Side Effects: The Actual Clinical Trial Numbers

The internet is filled with dramatic stories about finasteride side effects. But what do the actual clinical trials—controlled studies with placebo groups—show? The numbers are far less alarming than forum posts suggest.

The Clinical Trial Data

In the pivotal trials that led to FDA approval of finasteride (Propecia) for hair loss:

Side EffectFinasteride (1mg)PlaceboDifference
Decreased libido1.8%1.3%+0.5%
Erectile dysfunction1.3%0.7%+0.6%
Ejaculation disorder1.2%0.7%+0.5%
Any sexual side effect3.8%2.1%+1.7%
1.7%The actual excess risk of any sexual side effect vs. placebo

Why the Placebo Rate Matters

Notice that the placebo group also reported side effects—2.1% experienced sexual issues on a sugar pill. This happens because:

The only meaningful number is the difference between drug and placebo—about 1.7%.

Long-Term Data: The Rossi Study

A 10-year follow-up study by Rossi et al. (2011) tracked men on finasteride long-term:

"The majority of men who experience initial side effects either tolerate them, see them resolve with continued use, or discontinue within the first year. Long-term, the dropout rate is extremely low."

Internet vs. Reality

Why do online reports seem so much worse than clinical data?

Clinical trials are controlled, blinded, and include everyone—not just the vocal minority with complaints.

Resolution Upon Stopping

In clinical trials, among the small percentage who experienced side effects:

Putting Risk in Perspective

Compare the finasteride risk to other accepted medications:

MedicationSide EffectRate
SSRIs (antidepressants)Sexual dysfunction30-60%
Beta blockersED~15%
StatinsMuscle pain5-10%
FinasterideSexual side effects~2% above placebo

Finasteride's side effect profile is remarkably mild compared to many commonly prescribed medications.

Make a Data-Driven Decision

Let the evidence guide your choice, not internet horror stories.

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The Bottom Line

Clinical trial data shows that about 2% of men experience sexual side effects beyond what the placebo group experiences. For most, these resolve upon stopping or with continued use. The catastrophic narratives online are not representative of the typical experience.

References