Urine of postmenopausal women reflects the hypergonadotropic state of menopause levels of follicle stimulating hormone (FSH) and luteinizing hormone (LH) are high and contain a mixture of these gonadotropins. Other protein substances may be present, including small amounts of human chorionic gonadotropin (hCG).

Menotropin preparations are designed for use in selected women where they stimulate the ovaries to mature follicles, thus making them more fertile. They are administered by typically daily injection, intramuscularly or subcutaneously, for about ten days under close supervision to adjust dose and duration of therapy.

They can also be used in hypogonadal men to stimulate sperm production.

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The medication increases the number of satisfying sexual events. Flibanserin was originally developed as an antidepressant, before being repurposed for the treatment of HSDD.

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The primary use of trazodone is the treatment of major depression. Data from open and double blind trials suggest the antidepressant efficacy of trazodone is comparable to that of amitriptyline, doxepin, and mianserin. Also, trazodone showed anxiolytic properties, low cardiotoxicity, and relatively mild side effects.

Low dose trazodone is used off label in the treatment of insomnia.

Other off label and investigational uses are as follows:

• Complex regional pain syndrome
• Obsessive compulsive disorder (OCD)
• Alcohol withdrawal
• Schizophrenia as an adjunct to improve negative symptoms
• Erectile dysfunction
• Female sexual dysfunction

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The primary use of trazodone is the treatment of major depression. Data from open and double blind trials suggest the antidepressant efficacy of trazodone is comparable to that of amitriptyline, doxepin, and mianserin. Also, trazodone showed anxiolytic properties, low cardiotoxicity, and relatively mild side effects.

Low dose trazodone is used off label in the treatment of insomnia.

Other off label and investigational uses are as follows:

• Complex regional pain syndrome
• Obsessive compulsive disorder (OCD)
• Alcohol withdrawal
• Schizophrenia as an adjunct to improve negative symptoms
• Erectile dysfunction
• Female sexual dysfunction

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It has no immediate anxiolytic effects, and hence has a delayed onset of action. Its full clinical effectiveness may require 2 to 4 weeks to manifest itself. The drug has been shown to be similarly effective in the treatment of generalized anxiety disorder (GAD) to benzodiazepines including diazepam, alprazolam, lorazepam, and clorazepate.
Buspirone is not known to be effective in the treatment of other anxiety disorders besides GAD, although there is some limited evidence that it may be useful in the treatment of social phobia as an adjunct to selective serotonin reuptake inhibitors (SSRIs).

There is some evidence that buspirone on its own may be useful in the treatment of hypoactive sexual desire disorder (HSDD) in women.

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It has no immediate anxiolytic effects, and hence has a delayed onset of action. Its full clinical effectiveness may require 2 to 4 weeks to manifest itself. The drug has been shown to be similarly effective in the treatment of generalized anxiety disorder (GAD) to benzodiazepines including diazepam, alprazolam, lorazepam, and clorazepate.
Buspirone is not known to be effective in the treatment of other anxiety disorders besides GAD, although there is some limited evidence that it may be useful in the treatment of social phobia as an adjunct to selective serotonin reuptake inhibitors (SSRIs).

There is some evidence that buspirone on its own may be useful in the treatment of hypoactive sexual desire disorder (HSDD) in women.

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It is a naturally occurring and bioidentical estrogen, or an agonist of the estrogen receptor, the biological target of estrogens like endogenous estradiol. Due to its estrogenic activity, estradiol has antigonadotropic effects and can inhibit fertility and suppress sex hormone production in both women and men.

Estradiol differs from non-bioidentical estrogens like conjugated estrogens and ethinylestradiol in various ways, with implications for tolerability and safety.

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It is also used for treating benign prostatic hyperplasia (BPH), colloquially known as an enlarged prostate.

Dutasteride is approved for the treatment of male androgenetic alopecia in many countries at a dosage of 0.5 mg per day.
It has been found in several studies to induce hair regrowth in men more rapidly and to a greater extent than even the highest approved dosage of finasteride. The superior effectiveness of dutasteride relative to finasteride for this indication is related to the fact that the inhibition of 5 alfa reductase and consequent reduction of DHT production within the hair follicles is more complete with dutasteride.

Dutasteride is also used off label in the treatment of female pattern hair loss.

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It is a non-steroidal fertility medicine. It causes the pituitary gland to release hormones needed to stimulate ovulation (the release of an egg from the ovary). It is sometimes used in the treatment of male hypogonadism as an alternative to testosterone replacement therapy.

Clomifene has been used in the treatment of gynecomastia.

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It is a non-steroidal fertility medicine. It causes the pituitary gland to release hormones needed to stimulate ovulation (the release of an egg from the ovary). It is sometimes used in the treatment of male hypogonadism as an alternative to testosterone replacement therapy.

Clomifene has been used in the treatment of gynecomastia.

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