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Ezetrol 10 mg uk. Or 5 qid. Travopride 20 mg/d. Other Hormone Therapy: (for all patients). If a patient cannot or will not take this medication on a regular basis or if the total daily doses of testosterone esters, ethinyl estradiol, and progestins exceed 10 or more mg, the patient should be referred for evaluation and treatment of medical conditions associated with anemia or hyperprolactinemia, including hypothyroidism, hypopituitarism, and hyperprolactinemia that may be associated with the use of drugs. If anemia or hyperprolactinemia appears to be the result of a tumor or suppressor, decision about whether to treat the tumor or start hormone therapy in the tumor should be made on a case-by-case basis after full evaluation with a knowledgeable urologist in consultation with the patient's physician. Patients who have undergone breast cancer treatment may experience side effects or discontinuation of the drug that may be more difficult to manage than any side effect from the surgery. For patients who have undergone breast cancer surgery, the patient and treating endocrinologist should decide on the dose and frequency of medications needed to manage hormone replacement therapy (HRT) during and after breast cancer treatment. As with any treatment, HRT side effects and discontinuation symptoms require careful observation. Treatment with estradiol gel may cause vaginal irritation, increased bleeding, and bleeding at the injection site, particularly in patients with a history of vaginal hemorrhage or other irritation of the vagina. Patients on oral estrogens must be cautious about self-medicating with the herbals by taking more than recommended doses. Estrogens given orally for treatment are known to be absorbed more quickly than those given by injection. Hormone replacement therapy should not interfere with an existing disease condition that is being treated with an estrogen-based medication, such as oophorectomy or other types of tubal surgery or prostate-specific antigen (PSA) screening. In patients requiring PSA testing, a level of 0.25 ng/mL does not always predict prostate cancer. If an abnormal PSA level is found, the physician may wish to test the possibility of prostate cancer, if not, the patient may elect to undergo further treatment with estrogens by injection or via transurethral resection. Adverse Events Adverse events associated with the use of testosterone include, but are not limited to, the following: Decreases in the size of penis and/or swelling. Increased hair growth. Reduced semen quality. Unsatisfied with quality of sexual intercourse, diminished libido, decreased desire or responsiveness. Decreases in libido. Anxiety and/or irritability. Loss of bone mineral density (BMD). Decreases in body fat (especially lean mass). Homozygosity (an increase in the degree of genetic homogeneity within a population as opposed to genetic differentiation within a population). Impotence, reduced sexual arousal. Decreased interest or satisfaction with sexual intercourse. Decreased satisfaction with erectile function. Decreased sperm concentration or motility. In a review conducted following the FDA approval of a testosterone gel in November 2000, and continuing after the FDA approval of this product as an over-.

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