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Some patients taking finasteride or dutasteride may have ongoing sexual problems and depression even after stopping the medication.

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

Men taking 5α-reductase inhibitors for enlarged prostate have a higher chance of experiencing reduced sexual desire and erectile dysfunction.

5α-reductase inhibitors, like finasteride and dutasteride, effectively treat BPH, male baldness, and hirsutism, with potential for acne and prostate cancer prevention.

5α reductase inhibitors treat hair loss but may cause sexual side effects and risks.

Low testosterone and 5α-reductase inhibitors can harm men's metabolic and sexual health; testosterone therapy may help, but discussing 5α-RIs' side effects is important.

The medications 5α-reductase inhibitors and spironolactone are generally safe for breast cancer patients on endocrine therapies and do not significantly increase breast cancer risk.

Compounds from Angelica koreana roots, especially osthenol, could be effective for treating conditions like prostate disease and hair loss.

Special nanoparticles increased skin absorption of hair loss treatments with fewer side effects.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Finasteride effectively treats hair loss and enlarged prostate in men, with mild side effects.

5α-reductase inhibitors can cause serious and possibly lasting sexual and psychological side effects.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

Finasteride effectively reduces hair growth in women with idiopathic hirsutism, but requires careful contraception during treatment.

Finasteride and dutasteride effectively treat hair loss, but may cause side effects like sexual dysfunction and depression.

Long-term finasteride use doesn't change bone density or metabolism.

Finasteride affects urinary steroid profiles and can potentially hide steroid abuse in sports drug testing.

Finasteride temporarily lowers male rat fertility without affecting libido.

Finasteride treats enlarged prostate and baldness, but may cause limited urinary improvement and sex-related side effects.

Avicequinone C, a compound found in the Avicennia marina plant, can reduce hair loss by inhibiting a hormone linked to androgenic alopecia.

Finasteride exposure harms tadpole reproduction and hormone balance.

5α-reductase inhibitors like finasteride may not be effective or safe for transgender individuals, and more research is needed.

Dutasteride may help shrink prostate cancer tumors.

Finasteride exposure in pregnancy causes genital abnormalities in male rats.

Using finasteride or dutasteride may cause long-lasting erectile dysfunction.

High doses of finasteride cause cell growth and tumors in mice.

Finasteride effectively treats male hair loss, improving growth and density.

LY320236 is a strong blocker of two enzymes that change testosterone into dihydrotestosterone and might help treat conditions related to male hormones.

Finasteride causes abnormal growth in male mice cells at high doses.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.