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Trazodone's potent α 1-adrenergic blockade may cause some side effects like orthostatic hypotension and sedation. Conversely, along with 5-HT 2A and H 1 receptor antagonism, it may contribute to its efficacy as a hypnotic. Trazodone lacks any affinity for the muscarinic acetylcholine receptors, so does not produce anticholinergic side effects.
Bupropion 1: 1 mixture (racemate) Clinical data Pronunciation / b j uː ˈ p r oʊ p i ɒ n / bew- PROH -pee-on am-fa- BEW -teh-moan Trade names Wellbutrin, Zyban, others Other names Amfebutamone; 3-Chloro- N - tert -butyl-β-keto-α-methylphenethylamine; 3-Chloro-N-tert-butyl-β-ketoamphetamine; Bupropion hydrochloride AHFS / Drugs.com Monograph MedlinePlus a695033 License data EU EMA: by INN ...
Ormeloxifene is a selective estrogen receptor modulator (SERM). In some parts of the body, its action is estrogenic (e.g., bones ), in other parts of the body, its action is antiestrogenic (e.g., uterus, breasts ). [13] [14] [15] It causes an asynchrony in the menstrual cycle between ovulation and the development of the uterine lining, although ...
Dapoxetine is a white, powdery, water-insoluble substance. Taken one to three hours before sexual activity, it is rapidly absorbed in the body. Its maximum plasma concentration (C max) is reached one to two hours after oral administration. The C max and AUC (area under the plasma vs. time curve) is dose dependent.
Enclomiphene is a selective estrogen receptor antagonist, antagonizing the estrogen receptors in the pituitary gland, disrupting the negative feedback loop by estrogen towards the hypothalamic-pituitary-gonadal axis, ultimately resulting in an increase in gonadotropin secretion. In men with secondary hypogonadotropic hypogonadism, this improves ...
Hydrocodone 10 mg is equivalent to about 10 mg of morphine by mouth. History and culture. Hydrocodone was patented in 1923, while the long-acting formulation was approved for medical use in the United States in 2013. It is most commonly prescribed in the United States, which consumed 99% of the worldwide supply as of 2010.
Estriol is well-tolerated and produces relatively few adverse effects. Side effects may include breast tenderness, vaginal discomfort and discharge, and endometrial hyperplasia. Estriol is a naturally occurring and bioidentical estrogen, or an agonist of the estrogen receptor, the biological target of estrogens like endogenous estradiol.
Mean number of moderate-to-severe hot flashes per week with placebo and different doses of oral estradiol in a randomized controlled trial of 333 menopausal women. Estrogen and other hormones are given to postmenopausal women in order to prevent osteoporosis as well as treat the symptoms of menopause such as hot flashes, vaginal dryness, urinary stress incontinence, chilly sensations ...