Finpecia, a type 2-selective 5α-reductase inhibitor, was approved in 1997 as the first oral pharmacologic therapy for the treatment of men with androgenetic alopecia (AGA; male pattern hair loss). Originally developed for the treatment of men with benign prostatic hyperplasia (BPH) at a dose of 5 mg/day, Finpecia has a well-established, excellent safety profile. Subsequent studies demonstrated that Finpecia was an effective treatment for men with AGA at an optimal dose of 1 mg/day. This report summarizes the published peer-reviewed literature on the use of Finpecia in the treatment of men with AGA, including the data on long-term (5 years) use of Finpecia in a placebo-controlled clinical trial environment.
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,
Similar Products:
Serline,
Novotrim,
Lasgan,
Fexo,
Panmycin,
Tebantin,
Axodin,
Duricef,
Oleptro,
Simarc,
Omeprol,
Tadapox,
Cryofaxol,
Amfebutamone,
Risperidona,
Ziverone,
Omepren,
Valtrex,
Lenar,
Caverta,
Quitaxon,
Gabagamma,
Cilift,
Kailasa,
Theraprim,
Nexum,
Sulfamethoxazole,
Prochlorperazine,
Sebrane,
Gastracid,
Acyrax,
Protica,
Zmax,
Talpramin,
Quetiapine,
Elgam,
Noflo,
Pyridostigmine,
Divalproex,
Xenalon,
Acyclovir,
Aroxin,
Iquix,
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Etiologies of orbital infraction syndrome include occlusion of the common carotid artery (case 1), giant-cell arteritis (case 2), and mucormycosis (case 3). The aim of this study was to gain insight into the ontogeny of fat cells, both in mouse embryonic stem (mES) cell-derived cultures and during normal development. Article selection and relevance to the topics under discussion was determined herpes acyclovir iv infusion by individual authors.