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Common side effects include swelling, feeling tired, abdominal pain, and nausea. [10] Serious side effects may include low blood pressure or heart attack. [10] Whether use is safe during pregnancy or breastfeeding is unclear. [2] [10] When used by people with liver problems, and in elderly individuals, doses should be reduced. [10]
The side-effects profile varies for different patient populations. [51] Overall adverse effects in treatment are similar between men, women, geriatric, pediatric, and racial groups. [5] Lamotrigine has been associated with a decrease in white blood cell count . [54] Lamotrigine does not prolong QT/QTc in TQT studies in healthy subjects. [55]
The United States Pharmacopeia (USP) is a pharmacopeia (compendium of drug information) for the United States published annually by the over 200-year old United States Pharmacopeial Convention (usually also called the USP), a nonprofit organization that owns the trademark and also owns the copyright on the pharmacopeia itself.
[1] [3] It has moderate anabolic effects and weak androgenic effects, which give it a mild side effect profile and make it especially suitable for use in women. [1] The drug has no estrogenic effects. [1] Drostanolone propionate is an androgen ester and a long-lasting prodrug of drostanolone in the body. [1]
Side effects of estradiol valerate include breast tenderness, breast enlargement, nausea, headache, and fluid retention. [15] [13] [14] Estradiol valerate is an estrogen and hence is an agonist of the estrogen receptor, the biological target of estrogens like estradiol. [5] [4] [16] It is an estrogen ester and a prodrug of estradiol in the body.
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Oxandrolone is an androgen and synthetic anabolic steroid (AAS) medication to help promote weight gain in various situations, to help offset protein catabolism caused by long-term corticosteroid therapy, to support recovery from severe burns, to treat bone pain associated with osteoporosis, to aid in the development of girls with Turner syndrome, and for other indications.
The drug is an agonist of the androgen receptor (AR), the biological target of androgens like testosterone and dihydrotestosterone (DHT), and has strong anabolic effects and moderate androgenic effects. [1] It also has moderate estrogenic effects. [1] Metandienone was originally developed in 1955 by CIBA and marketed in Germany and the United ...