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Dutasterida CAS:164656-23-9

Dutasterida
CAS: 164656-23-9
FM: C27H30F6N2O2
megavatios: 528.53
Ensayo: 99%
Color: polvo blanco

investigación
  • Presupuesto

Dutasterida (nombre de marca Avodart) Es un inhibidor dual de la 5-α reductasa que inhibe la conversión de testosterona en dihidrotestosterona. (DHT). Utilizado para la hiperplasia prostática benigna.; sin embargo, aumenta el riesgo de disfunción eréctil y disminución del deseo sexual.

Dutasterida útil para los síntomas de la hiperplasia prostática benigna (HPB); conocido coloquialmente como “agrandamiento de la próstata”. En aquellos que se someten a pruebas periódicas de detección del inhibidor de la 5-alfa-reductasa (finasteride and dutasteride) reduce the overall risk of being diagnosed with prostate cancer however there is insufficient data to determine if they have an effect on the risk of death and may increase the chance of more serious cases.

This class of medications increases rates of erectile dysfunction (with between 5% y 9% developing problems after starting their use). This is linked to lower quality of life and can cause stress in relationships. There is also an association with lowered sexual desire. It has been reported that these adverse sexual side effects may persist even after discontinuation of the drug. The FDA has added a warning to dutasteride about an increased risk of high-grade prostate cancer.

While the potential for positive, negative or neutral changes to the potential risk of developing prostate cancer with dutasteride has not been established, evidence has suggested it may temporarily reduce the growth and prevalence of benign prostate tumors, but could also mask the early detection of prostate cancer.

The primary area for concern is for patients who may develop prostate cancer whilst taking dutasteride for benign prostatic hyperplasia, which in turn could delay diagnosis and early treatment of the prostate cancer, thereby potentially increasing the risk of these patients developing high-grade prostate cancer.

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