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The medicine, start to finish

Finasteride: what it is, what it is licensed for, and what comes with it

A tablet that interrupts one enzyme. The benefit and every warning attached to it come from that single interruption — here is the whole picture, from documents, with no dose and no recommendation.

One section of this page carries two commission links to online consultation services, marked where they sit. Nothing here links to a seller of the medicine — what we take and what we refuse.

In this file

Finasteride is a prescription tablet that blocks an enzyme called 5-alpha-reductase. In men with male pattern hair loss it slows the loss and, in the trials the licence rests on, partly reversed it. It is also the medicine behind a long and unresolved argument about sexual and psychiatric effects, some of which have been reported as continuing after the tablets stop. Both of those things are true at once, and this page holds them together rather than choosing one.

What finasteride is licensed to do

In the United States the lower-strength tablet has been approved since 1997 for male pattern hair loss in men, and only in men. The FDA-approved labelling puts the restriction in capitals — men only — and adds that effectiveness in the receding corners at the temples has not been established, a detail the marketing rarely carries. The higher-strength tablet is a different licence, for an enlarged prostate.

There is no single answer to what finasteride is, because there are three different regulatory objects wearing the name: the tablet, the topical versions, and its close relative dutasteride. They are not one decision.

What is licensed, and where

FDA, EMA and PMDA documents, read 24 September 2026

Licensed

Finasteride tablets

Licensed for hair loss

Approved in the US in 1997 for male pattern hair loss in men, and licensed across the UK and EU. Not for women, not for children.

Unapproved

Topical finasteride

Depends where you are

No approved topical version exists in the US, so what is sold there is compounded and unapproved. A cutaneous spray is authorised in several EU member states.

Off-label

Dutasteride

Off-label for hair loss

In the US, UK and EU it is licensed for an enlarged prostate only; using it for hair loss is off-label and a prescriber's decision. Japan approved it for male pattern hair loss in 2015.

A licence is not a verdict on whether something works for you, and an off-label prescription is not automatically wrong — it means the regulator has not assessed that use, so the prescriber carries the judgement instead of the label.

That grid matters more than it looks. A licensed medicine has been assessed by a regulator for a stated use; a compounded one has not been assessed at all; an off-label prescription means the regulator never examined that use, so the judgement sits entirely with the prescriber. Japan took the further step of approving dutasteride for male pattern hair loss in 2015, which is why you will find confident claims online that it is "approved" — true in Tokyo, not in Washington, London or Brussels.

The one step it works on

Testosterone becomes dihydrotestosterone — DHT — when 5-alpha-reductase acts on it. There are two types of the enzyme, and the label attributes about two-thirds of circulating DHT to type II, the one this drug is built against. Blocking it lowers DHT in blood and in scalp tissue; the label reports a 65% fall in serum DHT within a day of the first tablet.

Why that helps hair is the second half of the mechanism. In balding scalp, the label says, the follicles are miniaturised and the DHT content is higher than in scalp that still grows hair. Take away much of the DHT and the miniaturising pressure eases. What the label will not claim is which of those two reductions — blood or scalp — is doing the work: it says the relative contributions have not been defined. The mechanism has its own page, because almost every argument about side effects is really an argument about what else that enzyme was doing.

What it does to hair, in the trials' own numbers

The licence rests on three twelve-month randomised trials in 1,879 men aged 18 to 41 with mild to moderate loss, with extensions that ran five years. The most legible result is the photograph panel: standardised photographs, rated blind, at year five.

Five years, judged from photographs

FDA label for finasteride, section 14.1

Took finasteride

48%42%10%

Took placebo

6%19%75%
  • More hair than at the start
  • No visible change
  • Less hair than at the start
The panel rated standardised photographs of men who stayed in the studies for five years. Read it as what a blinded rater saw, not as what will happen to you: the men were 18 to 41 with mild to moderate loss, and the ones still being photographed at year five are the ones who did not drop out.

At five years, 48% of the men on finasteride were rated as having more hair than at the start, 42% as unchanged, and 10% as having lost hair. In the placebo group the same panel rated 6% as having more hair, 19% unchanged and 75% as having lost some. Hold those two columns side by side and the honest summary of this drug appears: its commonest outcome over five years was not regrowth but a stalemate, and the stalemate is the point, because the untreated column kept sliding.

Two warnings about reading that. The men rated at year five are the ones who stayed in the study, which flatters any long trial. And the trial population was young, male and early-stage, so it says nothing about a fiftieth birthday, a fully bare crown, or a woman. Whether this counts as regrowth or as holding is worth its own page.

What it can do to you

In year one of the same hair-loss trials, the investigators recorded sexual adverse experiences they judged possibly, probably or definitely drug-related. The figures are small, and the placebo column is not zero — which is the reason both columns are drawn.

Year one, as the investigators recorded it

FDA label for finasteride, section 6.1

Reduced sex drive

Finasteride1.8%
Placebo1.3%

Erectile dysfunction

Finasteride1.3%
Placebo0.7%

Ejaculation disorder

Finasteride1.2%
Placebo0.7%

One or more of the three

Finasteride3.8%
Placebo2.1%
These are the effects the trial investigators judged to be possibly, probably or definitely caused by the drug, in the first year, among men aged 18 to 41. They are not the whole side-effect record: what happens after someone stops, and the psychiatric reports, come from years of post-approval reporting rather than from this table.

Reduced sex drive was recorded in 1.8% of the men on the drug against 1.3% on placebo; erectile dysfunction in 1.3% against 0.7%; an ejaculation disorder in 1.2% against 0.7%. Counting men who reported at least one of the three, the label gives 3.8% against 2.1%, a difference it reports as statistically significant. It adds that the effects resolved in men who stopped and in most of those who carried on, and that the yearly incidence fell to 0.3% or below by year five.

If that were the whole record this would be a mild drug with a small, reversible side effect. It is not the whole record. Everything that makes finasteride controversial sits in a different section of the same label — the post-approval reports, which have no denominator and no placebo group, and which include sexual dysfunction that continued after treatment stopped, male infertility and poor semen quality, male breast cancer, and depression, suicidal ideation and behaviour. The side-effect record separates those two kinds of evidence properly, because conflating them is how both sides of this argument go wrong.

Who it is not for

This is the part of the label with the least ambiguity in it, and the part most often skipped.

  • Women who are or might become pregnant. Use in pregnancy is contraindicated: by blocking the conversion of testosterone to DHT, the drug can affect the development of a male fetus's genitals. The label also tells women who are or may be pregnant not to handle crushed or broken tablets.
  • Women generally, for hair loss. The tablet is not indicated for women, and the one trial in the label — 137 postmenopausal women — could not demonstrate any effect on hair counts or on any of the other measures.
  • Children. Not indicated, and safety and effectiveness have not been established.
  • Anyone whose hair loss has not been diagnosed. Thyroid disease, iron deficiency, alopecia areata, scarring alopecias, telogen effluvium after illness or stress, and reactions to other medicines all look like thinning hair and none of them is treated by this. A diagnosis comes first.

There is also a prostate-testing wrinkle worth carrying to a doctor: the drug lowers PSA, the blood marker used in prostate screening, so a PSA result taken while on it has to be interpreted knowing that. And in a seven-year prevention trial at five times the hair-loss strength, high-grade prostate cancer was found in 1.8% of men on finasteride against 1.1% on placebo — the label says the significance of that for men taking the hair-loss tablet is unknown, which is exactly as far as the evidence goes.

How people actually get a prescription

Four routes exist and they differ in cost, in how much of a clinician you get, and in who carries the risk. The cheapest is not the worst one.

Routes to a prescription, and what each one really gives you
RouteWhat you getWhat to watchPays this site
Your own GPSomeone with your history, who can investigate other causes and follow upIn the UK this is a private prescription: the NHS does not fund the hair-loss tabletNothing
A dermatologistA diagnosis first — the right route when the loss is patchy, scarring, sudden or painfulWaiting lists, or a private fee; ask what examination and tests are includedNothing
An online prescribing serviceA questionnaire reviewed by a prescriber, and delivery, bundled into a subscriptionWhether a real clinician reviews you, what is asked, and how cancellation worksCommission, disclosed below
Buying without a prescriptionNothing anyone should wantUnknown source and contents, no prescriber, no follow-up, no recourseNothing — we link no seller

One fact makes the whole table easier to read: finasteride is long off patent and sold generically, so the tablet itself is rarely where the money goes. What differs between routes is the consultation and the convenience.

What a first appointment is supposed to cover

The regulators have written down what they expect a prescriber to do, which makes it unusually easy to tell whether a consultation — in a room or through a screen — is doing its job. The MHRA's instructions to prescribers, published 11 May 2026, are the clearest statement of it.

  • Your medical record is reviewed, and you are asked directly whether you have a history of depression or suicidal ideation, before anything is prescribed.
  • The risks are explained at the point of prescribing — not buried in a leaflet you find later — including that sexual dysfunction has been reported to persist after treatment has stopped.
  • You are pointed at the patient card and the leaflet that come in UK packs, which exist precisely because these warnings were not reaching people.
  • Follow-up is arranged: the same advice tells prescribers to review patients regularly for psychiatric and sexual side effects, which means somebody has to be there to review you.

A consultation that asks none of that, and a questionnaire with no question about mood, is not meeting the standard its own regulator has published. That is a fair thing to notice about any route, including the paid one below.

What this site will not tell you

It will not tell you a strength, a schedule, or how to split anything. It will not tell you whether to start, because that answer depends on facts about you that no web page has. It will not show you before-and-after photographs, which are the least reliable evidence in this field and the easiest to stage. And it will not rate this medicine out of ten. A score would imply a recommendation, and a recommendation is not ours to make.

Questions people arrive with

Does finasteride work?
For the population the licence was granted on — men aged 18 to 41 with mild to moderate pattern loss — the trials supporting it showed a clear difference against placebo over five years, with 48% of treated men rated as having more hair by a blinded photograph panel and 10% as having less, against 6% and 75% on placebo. Whether it will work for you is a different question, and it depends on a diagnosis nobody can make through a screen.
How long before anything happens?
The label says daily use for three months or more is generally needed before any benefit is seen, that continued use is needed to sustain it, and that benefit should be reassessed periodically. It also says stopping reverses the effect within twelve months. That is a timetable for a conversation with a prescriber, not an instruction from us.
Are the sexual side effects permanent?
The honest answer is that it is contested. The controlled trials found small differences against placebo that resolved on stopping and in most men who carried on. The post-approval sections of the US label and the UK and EU safety reviews describe reports of sexual dysfunction that continued after treatment stopped, and the UK regulator noted in May 2026 that the published literature showed mixed outcomes. Nobody can tell you an incidence for the lasting form, because no regulator has published one.
Is topical finasteride safer than the tablet?
Not established, and in the US it is not even an approved product. The FDA warned in April 2025 that absorption through the skin into the bloodstream is expected, and that the adverse events reported with compounded topical products looked like the ones reported with the oral drug. Treating a cream as though it were a lower-risk version of the tablet is not something the documents support.
Can women take it for hair loss?
The tablet is not indicated for women, and it is contraindicated in pregnancy or possible pregnancy because of the risk to a male fetus. The only trial in women in the US label, in 137 postmenopausal women, could not demonstrate effectiveness. Any use in women is off-label and a specialist's decision.
Why will you not tell me a dose?
Because printing one invites people to skip the prescriber, and the prescriber is the only part of this process that can look at your history, your other medicines and your actual scalp. Strengths differ by country, by formulation and by what the product is licensed to treat. Where a question is really about strength, we explain what the label decides and why, and stop there.