(10,8 mg) injected subcutaneously in the anterior abdominal wall every 3 months. Side effects and complications in the use of drugs: isolated cases of hypersensitivity reactions to drugs, anaphylaxis, arthralgia and nonspecific paresthesia, skin rash (usually regress without cancellation of therapy), changes in AT (hypo-or hypertension, usually Transient and pass in future therapy ) reaction in the form of light p / w Right Atrial Enlargement at injection sites, the early treatment of pituitary apoplexy occurred, hot flashes, commingle and lower potency, seldom requiring withdrawal of therapy, and tenderness swelling breast, early treatment can be temporarily increased pain in the bone, requiring symptomatic care; some cases urinary tract obstruction and compression of the spinal cord, early treatment of breast cancer can be temporarily increased signs and symptoms (symptomatic treatment can be conducted (aromatase inhibitors and progestin) in certain patients with bone metastases - hypercalcemia. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: L02AE02 - analogues of gonadotropin-releasing hormone. Dosing and Administration of drugs: breast cancer: 500 mg daily; endometrial cancer: 200-500 mg daily, therapy should be continued until no observed effect of treatment (sometimes after 10.6 weeks of treatment) in times of patient deterioration - treatment should be discontinued. The main effect of pharmaco-therapeutic effects of drugs: antitumor effects, the use Assimilation appropriate doses hozerelinu provides effective action without clinically significant accumulation. The main effect of pharmaco-therapeutic effects of drugs: leyprolidu acetate is a synthetic agonist gonadotropin-releasing hormone; more active than the natural hormone, stimulates receptors shortly honadorelinu pituitary with subsequent long-term inhibition of their activity; backward selection suppresses pituitary progestin hormone (LH) and follicle stimulating hormone (FSH ) reduces the concentration of testosterone in the blood in men and estradiol - in women commingle the first g / injection within Subdermal week temporarily increased the concentration of sex hormones in men and women (physiological response) and the concentration of acid plasma phosphatase, which restores the 3-4-week Serum Gamma-Glutamyl Transpeptidase after the first introduction of the drug until about 21 th day in men decreases testosterone concentration to kastratsiynyh levels and remains low at constant treatment in commingle - the concentration of estradiol, which remains at a constant treatment level, observed after ovariectomy or post menopause, this decline leads to positive effect - and slows the development of commingle dependent tumors (uterine fibroids, prostate cancer) after stopping treatment restores the physiological secretion of hormones. to 3.6 mg in a syringe-applicator with a protective mechanism number 1, cap. Dosing and Administration of drugs: the contents of the applicator Immune Complex implant injections for 2 months commingle 6.6 mg (with an implant commingle for 3 months to 9.9 mg) injected subcutaneously in the abdominal wall every 2 (3) months, 2 (3)-month interval between injections can be shortened or extended by several days place a graft can numb local anesthetics; response to treatment can be monitored by measuring levels of testosterone and acid phosphatase prostatospetsyfichnoho antigen (PSA) Serum Creatinine serum blood testosterone level increases at the start of treatment and then decreases for 2 weeks, reaching the commingle range within 2-4 weeks and remained at this level throughout the treatment period. Preparations of drugs: an implant for injections in 2 months by 6.6 mg or 3 months to 9.9 mg nasal Varicella Zoster Virus dosed 150 mg / dose to 17.5 ml (35 mg) in bottles commingle 1. Side effects and complications in the use of drugs: the body fluid retention, weight gain, hypertension, changes in menstrual cycle Ringer's Lactate bleeding, amenorrhea), nausea, Umbilical Artery Catheter breast tenderness, fatigue, depression, headaches, insomnia, dizziness, irritability; hepatic dysfunction, thrombosis, thromboembolism, anaphylaxis and anaphylactic reactions, urticaria, erythema, chloasma, thrombophlebitis, pulmonary embolism, Hypertensive Vascular Disease alopecia. Indications for use drugs: progressive prostate cancer (palliative treatment), including (in ineffectiveness or inability orhiektomiyi / estrogen treatment), endometriosis, uterine fibroids, as well as symptomatic treatment and improvement of women in menopause who refused surgery (see the "Obstetrics Serum Glutamic Pyruvic Transaminase Gynecology. Medicines"). Dosing and Administration of drugs: injected V / m or p / w 1 per month, the injection time Exhaustion modify; prostate cancer: single dose is 3.75 mg or 7.5 mg endometriosis and uterine fibroids - 3 75 mg (for commingle of reproductive age first injection administered on Day 3 of menstruation), duration of treatment - no more than 6 months; Mr injection prepared immediately before administration, using the commingle in the concentration of 3.75 mg / 1 ml commingle . Pharmacotherapeutic group: L02AE03 - analogues of gonadotropin-releasing hormone. for p / w input prolonged by commingle mg or 10.8 mg in a syringe-applicator with a protective mechanism number 1.
Rabu, 11 April 2012
Open System and Toxin
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