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Finar (Finasteride)

Note: Women who are pregnant or may become pregnant should not use Finar or handle the crushed or broken tablets. Finar can cause birth defects in male babies.

Finar is used to treat men with benign prostatic hyperplasia (BPH) and male pattern hair loss, also called androgenetic alopecia. BPH is caused by an enlarged prostate. Men with BPH usually have difficulty urinating, a decreased flow of urination, hesitation at the beginning of urination, and a need to get up at night to urinate. Finar will make these symptoms less severe and reduce the chance that prostate surgery will be needed. It may be used alone or in combination with other medicines such as an alpha-blocker (doxazosin, Cardura) to treat BPH. For men with hair loss, Finar will increase the number of scalp hairs but will not increase the amount of body hair.

Finar blocks the action of an enzyme called 5-alpha-reductase. This enzyme changes testosterone to another hormone that causes the prostate to grow or hair loss in males. It will increase testosterone levels in the body, which decreases prostate size and increases hair growth on the scalp. The effect of Finar on the prostate and scalp will only last as long as the medicine is taken. When it is stopped, the prostate begins to grow again and the hair will be lost.

This medicine is available only with your doctor's prescription.

This product is available in the following dosage forms:

  • Tablet

Other names for this medication:
Finasteride, Androfin, Avertex, Daric, Fenered, Finahair, Finalo, Finalop, Finar, Finara, Finast, Finax, Fincar, Finpecia, Firide, Monast, Prohair, Propecia, Proscalpin, Proscar, Prosteride, Reduprost, Renacidin, Sutrico, Symasteride, Tealep, Tensen,

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In the present study, mouse, rabbit, and human spermatozoa were stained using a modification of the earlier method. However, emerging evidence suggests that the isokinetic muscle strength remains similar when the placebo effect is eliminated. Diagnostic accuracy of urine dipstick for proteinuria in older outpatients. The lack of significant differences of androgenic suppression in both regimens turns up the question if different metabolism at the cellular level may be responsible for that phenomenon.

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The purpose of this study was to examine the relative contributions of sets of descriptive, organic, and psychosocial variables to a prediction of nocturnal penile rigidity among a group of men presenting with significant erectile dysfunction. The changes of substance P-like immunoreactivity (SPLI) were determined in the central nervous system of renal hypertensive rats (produced by application of a constricting clip on the left renal artery), as compared with those of sham-operated controls. Here, we asked at what stage(s) viral infection is blocked in these cells.

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