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2C-B was synthesized from 2,5-dimethoxybenzaldehyde by American chemist Alexander Shulgin in 1974. It first saw use among the psychiatric community as an aid during therapy, but was abandoned due to gastrointestinal effects and the lack of empathogenic effects.
Mesterolone, sold under the brand name Proviron among others, is an androgen and anabolic steroid (AAS) medication which is used mainly in the treatment of low testosterone levels. [ 2 ] [ 3 ] It has also been used to treat male infertility , although this use is controversial.
2,5-Dichlorophenol (2,5-DCP) is a chlorinated derivative of phenol with the molecular formula Cl 2 C 6 H 3 OH. References. Cited sources. Haynes, William M., ed ...
Methyltestosterone, sold under the brand names Android, Metandren, and Testred among others, is an androgen and anabolic steroid (AAS) medication which is used in the treatment of low testosterone levels in men, delayed puberty in boys, at low doses as a component of menopausal hormone therapy for menopausal symptoms like hot flashes, osteoporosis, and low sexual desire in women, and to treat ...
Metandienone was formerly approved and marketed as a form of androgen replacement therapy for the treatment of hypogonadism in men, but has since been discontinued and withdrawn in most countries, including in the United States. [15] [4] [6] It was given at a dosage of 5 to 10 mg/day in men and 2.5 mg/day in women. [16] [17] [1
Treatment of breast cancer in women, although they are now very rarely used for this purpose due to their marked virilizing side effects. [43] [18] [44] In low doses as a component of hormone therapy for postmenopausal and transgender women, for instance to increase energy, well-being, libido, and quality of life, as well as to reduce hot flashes.
Side effects of trenbolone acetate include symptoms of masculinization like acne, increased body hair growth, scalp hair loss, voice changes, and increased sexual desire. [5] The drug is a synthetic androgen and anabolic steroid [ 6 ] and hence is an agonist of the androgen receptor (AR), the biological target of androgens like testosterone and ...
A 2010 Cochrane review found that men taking finasteride for BPH (with a mean age of 62.4) are at increased risk for impotence, erectile dysfunction (ED), decreased libido, and ejaculation disorder for the first year of treatment. The rates became indistinguishable from placebo after 2–4 years and these side effects usually got better over time.