Finasteride in Women Finasteride is a competitive 5-alpha-reductase inhibitor, an enzyme that catalyzes testosterone conversion to dihydrotestosterone (DHT). Although human body has several isotopes of 5-alpha-reductase, finasteride specifically acts on isoenzyme II present in the uterus, endometrium, fallopian tube, prostate, male genitalia, hair follicle root sheath, and liver (Drake et al., 1999). Since finasteride does not inhibit testosterone synthesis directly or interfere with the androgen receptor, its physiological activity is restricted to DHT-dependent tissues. This drug is used to treat individuals with pattern hair loss, prostate cancer, and prostatic hyperplasia because of its inhibiting effect (Oliveira et al., 2013). However, there is a few research regarding its effect on women. Albasher et al., (2020) took the initiative to study the long-term use of finasteride and its effect on women. Hair loss in female or androgenetic alopecia is a common concern in women and is challenging to treat and understand. It entails the reduction in vertex hair density, while the front hairline is not affected (Price, 2003; Messenger and Sinclair, 2006). It is understood that the condition occurs to an estimated 10 percent of pre-menopausal women, and there is a rise of 50-75 percent to menopausal women who are 65 years or older. The primary purpose of the medication is the reduction of the hair loss through limiting the conversion of testosterone to DHT by 5-αreductase type II, in a process that reduces fat tissue that is around the hair follicle, resulting in dehydration of the skin, reduction