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Dutasteride is a selective and specific inhibitor of both I and II 5α-reductase isoenzymes, as it inhibits the I isoenzyme 10 0 times greater th an finasteride and respectively the isoenzyme II 3 m ore times th an finasteride, which accounts for decreasing the serum DHT level by 90% and makes dutasteride more potent th an finasteride in decreasing serum and scalp levels of DHT journals viamedica pl forum_dermatologicum article download 96555 73074journals viamedica pl forum_dermatologicum article view 95391The effectiveness of finasteride and dutasteride used for 3 years in women with AGA 120 women with FPHL 16–84 years finasteride 1 25 mg day or dutasteride 0 15 mg day; the experiment period was 3 years improved hair thickness in 81 7% of patients in finasteride group and in 83 3% of patients in dutasteride group;People also ask--- przeglad-urologiczny pl artykul phpinar pl wp-content uploads 2016 01 dutasteride_CFA_2006 pdf INTRODUCTION AND OBJECTIVE Frontal fibrosing alopecia (FFA) is a primary lymphocytic cicatricial alopecia characterised by a typical clinical pattern of progressively receding fronto-temporal hairline, with scarring that is commonly accompanied by loss of eyebrows [1, 2] Roehrborn C, Andriole G, Schalken J, et al Dutasteride , a novel dual 5a-reductase inhibitor, reduces serum DHT to a greater extent versus finasteride and achieves finasteride maximal reduction in a larger proportion of patients Dutasteride versus finasteride (wiki) Finasteride is also approved for the treatment of benign prostatic hyperplasia, or BPH The medications belong to the same class of drugs Dutasteride inhibits two of the three isoforms of 5-alpha reductase, I and II, whereas finasteride only inhibits type II, and has a much shorter half-lifejournals viamedica pl forum_dermatologicum article view 96555Dutasteride Dutasteride is an inhibitor of both isoforms of 5 -reductase (type I and II) and its primary indication (similarly to finasteride) is benign prostatic hyperplasia Phase II and III trials in men with androgenetic alopecia have shown dose-dependent (0 5 mg day and higher) efficacy of the drug assessed at 12 and 24 weeks of treatment dutasteride (Avodart) and finasteride (Proscar) inhibit the growth of the prostate and decrease the size of the gland, improving urinary symptoms in men with BPH OBJECTIVES: To compare the clinical efficacy and cost-effectiveness of using: dutasteride vs placebo dutasteride vs finasteride in patients with benign prostatic hyperplasia (BPH) § § gemini pl poradnik finasteryd-czy-jest-skuteczny-w-lysieniu-androgenowym Switching from topical minoxidil to its systemic form as well as from finasteride to dutasteride may give better results in some patients In general, male pattern hair loss (MPHL) is a chronic disease that may demand Roehrborn C, Andriole G, Schalken J, et al Dutasteride, a novel dual 5a-reductase inhibitor, reduces serum DHT to a greater extent versus finasteride and achieves finasteride maximal reduction in a larger proportion of patients Presented at: XVIII Congress of European Association of Urology; March 12-15, 2003; Madrid, Spain [Poster 635] dutasteride in a dexpanthenol, biotin, and pyridoxine solution 12 sessions in 16 weeks Hair improvement in 62 8% of dutasteride-treated patients versus 17 5% of placebo-treated patients Additional substances in the preparation make it difficult to assess the effectiveness of dutasteride Saceda-Corralo et al [8] 6 patients with androgeneticFinasteryd – działanie Finasteryd jest lekiem stosowanym w problemach z łysieniem typu androgenowego Jest to kompetycyjny inhibitor 5α-reduktazy typu II, czyli enzymu zlokalizowanego w głównej mierze w mieszkach włosowych Finasteryd hamuje przekształcanie testosteronu do DHT, zmniejszając jego ilość nawet o 70% po jednorazowym Dutasteride lowers dihydrotestosterone concentrations by blocking type I and type II 5a-reductase enzymes, unlike finasteride, which only blocks type II enzyme [1–3] Intralesional administration of micro-doses of dutasteride via mesotherapy into the hairy scalp is a new therapeutic method Safety analysis: dutasteride had similar tolerability to placebo dutasteride vs placebo: § § § § finasteride vs dutasteride: dutasteride (Avodart) vs placebo dutasteride (Avodart) vs finasteride Direct comparison Qmax – larger increase in the dutasteride group,: WMD = 0,3 ml s (95% CI: 0,0; 0,7) after 2 years; thetrychologiakosmetyczna pl finasteryd-przeczytaj-zanim-zaczniesz-stosowacMar 23, 2022 · Finasteride is an inhibitor of type II 5α-reductase, while dutasteride inhibits both isoenzymes (I and II) of 5a-reductase, therefore it is more potent Finasteride stops androgenetic alopecia and causes partial regrowth of hair in approx 90% and approx 65% of men, respectively [5] advances umw edu pl en ahead-of-print 157990Finasteryd to chemiczny związek organiczny z grupy steroidów, pozyskiwany w sposób syntetyczny Jest inhibitorem enzymu 5 alfa reduktazy przekształcającego testosteron w jego bardziej aktywną formę – DHT Finasteryd stosowany jest jako lek u mężczyzn z łagodnym rozrostem gruczołu krokowego oraz w leczeniu łysienia androgenowego Can finasteride treat hair loss in women? What is RF-mesotherapy with dutasteride? Aug 22, 2023 · Dutasteride lowers dihydrotestosterone concentrations by blocking type I and type II 5a-reductase enzymes, unlike finasteride , which only blocks type II enzyme [1–3] Intralesional administration of micro-doses of dutasteride via mesotherapy into the hairy scalp is a new therapeutic method Aug 24, 2023 · In men, the diagnosis of androgenetic alopecia is quite simple, and the treatment usually involves incorporating minoxidil and or finasteride Switching from topical minoxidil to its systemic form as well as from finasteride to dutasteride may give better results in some patients Can finasteride be used to treat FPHL in normoandrogenic women? --- termedia pl Lysienie-androgenowe-kobiet-i-mezczyzn-Rekomendacje-diagn rak-prostaty pl viewtopic php
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