OxandroloneCardiovascular side effects have included edemawith and without congestive heart oxydrrolone. Elderly male patients may experience prostatic enlargement resulting in urinary obstruction. Priapism and excessive stimulation may develop. Female patients may experience virilization including deepening voice, hirsutism legal high sp alive, acneclitomegaly not reversibleand menstrual abnormalities. Oxydrolone side effects of anabolic steroids at signs of mild virilization may oxydrolone side effects irreversible virilization.
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Cardiovascular side effects have included edema , with and without congestive heart failure. Elderly male patients may experience prostatic enlargement resulting in urinary obstruction. Priapism and excessive stimulation may develop. Female patients may experience virilization including deepening voice, hirsutism , acne , clitomegaly not reversible , and menstrual abnormalities. Discontinuation of anabolic steroids at signs of mild virilization may prevent irreversible virilization.
Hepatic side effects have included life-threatening peliosis hepatitis and hepatic abnormalities, such as hepatic neoplasms and hepatocellular carcinomas, following prolonged therapy with high doses of anabolic steroids.
Tumor regression did not occur in all cases following medication withdrawal. Cholestatic hepatitis, jaundice , and abnormal liver function tests can occur at relatively low dosages. Hepatic tumors associated with anabolic steroid use are more vascular than other hepatic tumors and may remain silent until the development of life-threatening abdominal hemorrhage. Peliosis hepatitis may present as mild liver dysfunction, but has resulted in liver failure. Other side effects have included virilization of female patients including deepening voice, hirsutism, acne, clitomegaly not reversible , and menstrual abnormalities.
Discontinuation of anabolic steroids at signs of mild virilization may prevent irreversible virilization [ Ref ]. Musculoskeletal effects have included termination of linear bone growth due to closure of the epiphyseal growth centers. Appropriate monitoring of bone age is recommended during use in prepubertal patients. Endocrine side effects have included inhibition of endogenous testosterone release by means of feedback inhibition of pituitary luteinizing hormone LH.
Large doses of exogenous anabolic steroids may suppress spermatogenesis through inhibition of pituitary follicle stimulating hormone FSH.
The androgenic activity of anabolic steroids may decrease levels of thyroxin-binding globulin and result in decreased total T4 serum levels and increased resin uptake of T3 and T4.
Free thyroid hormone levels remain unchanged and there is no clinical evidence of thyroid dysfunction. Metabolic side effects have included osteolytic-induced hypercalcemia in immobilized patients or those with metastatic breast disease. Anabolic steroids affect electrolyte balance, nitrogen retention, and urinary calcium excretion.
Edema, with and without congestive heart failure, has occurred during anabolic steroid therapy. Decreased glucose tolerance requiring adjustments in hyperglycemic control has been noted in diabetic patients. Renal side effects have included retention of nitrogen, sodium, potassium, chloride, water and phosphorus, and decreased urinary excretion of calcium. Oncologic side effects have included hepatic neoplasms and hepatocellular carcinomas following prolonged therapy with large doses of anabolic steroids.
Gastrointestinal side effects have included nausea , vomiting , and diarrhea. Psychiatric side effects have included habituation, excitation, insomnia , depression , and libido changes. Dermatologic side effects have included acne and changes in skin color. The greatest incidence of occurrence has been in women and prepubertal males.
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