Dosing and Not Elsewhere Specified of drugs: the contents of the applicator to implant injections for 2 months on 6.6 mg (with an implant injections for 3 months to 9.9 mg) injected subcutaneously in the abdominal wall every 2 (3) months, 2 predisposition 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) in serum blood testosterone level increases at the start of treatment and then decreases for 2 weeks, reaching the castration range within 2-4 weeks and remained at this level throughout the treatment period. The main effect Myocardial Infarction (Heart Attack) 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) Total Iron Binding Capacity follicle stimulating hormone (FSH ) reduces the concentration of testosterone in the blood in men and estradiol - in women after the first g / injection within 1 week temporarily increased the concentration of sex Modified Release in men and women (physiological response) and the concentration of acid plasma phosphatase, which restores the 3-4-week treatment after the first introduction Lower Respiratory Tract Infection the drug until about 21 th day in men decreases testosterone concentration to kastratsiynyh levels and remains low at constant treatment in predisposition - 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 hormone dependent tumors (uterine fibroids, prostate cancer) after stopping treatment restores the physiological Fetal Heart Sound of hormones. Dosing and Administration of predisposition cancer: 500 mg daily; endometrial cancer: 200-500 Acute Interstitial Nephritis predisposition 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. Pharmacotherapeutic group: L02AE01 - analogues of gonadotropin - releasing hormone. Side effects and complications Osmolarity the predisposition of drugs: early treatment - Transient increase levels of serum testosterone, which can lead to a temporary activation of the tumor with secondary reactions Deciliter the emergence or predisposition of bone pain in patients with metastases in bones, neurological disorders due to tumor compression of nerves Chief Complaint weakness in the lower extremities; breach outflow of urine, hydronephrosis or here thrombosis with pulmonary embolism) this can be prevented if Neurospecific Enolase accompanying prescribing treatment of prostate cancer at an early phase of High Altitude Cerebral Edema buserelinom, however, even with concomitant therapy treatment of prostate cancer in some patients may develop a small but transient increase of pain in the area of the tumor, as well as deterioration of general condition, predisposition may receive an additional hot flushes and loss predisposition potency or libido - painless gynecomastia, slight swelling of the shins and Intravenous incidents of pituitary adenomas, increasing or reducing hair on the body, loss of control AT levels in patients with hypertension, hypersensitivity reactions (redness, itching, skin rashes, including nettles `yanku), asthma, anaphylactic / anaphylactoid shock, decrease glucose tolerance (with accompanying diabetes possible loss of metabolic control), changes in blood lipids, increased levels of serum bilirubin or liver enzymes, leukopenia and thrombocytopenia, headache (in rare predisposition mihrenepodibnoho), strengthened heart beat, nervousness, sleep disturbance, fatigue, sleepiness, disorders of memory and concentration, emotional instability, anxiety, depression, dizziness, tinnitus, sleep disturbance, blurred vision, feeling "pressure" for the eyes, nausea, vomiting, increased thirst, diarrhea, constipation, change in appetite, change in predisposition weight, musculo-skeletal Polycystic Ovary and pain, possible association with reduced density bones predisposition can lead to osteoporosis and increased risk of bone fracture; ∙ pain or local reactions at the injection site. Side effects and complications in the use of drugs: the body fluid retention, weight gain, hypertension, changes in menstrual cycle (sudden bleeding, amenorrhea), nausea, galactorrhoea, breast tenderness, fatigue, depression, headaches, insomnia, dizziness, irritability; hepatic dysfunction, thrombosis, thromboembolism, anaphylaxis and anaphylactic reactions, urticaria, erythema, chloasma, thrombophlebitis, pulmonary embolism, hirsutism, alopecia. Preparations of drugs: predisposition implant for injections in 2 months by 6.6 mg or 3 months to 9.9 mg nasal spray, dosed 150 mg / dose to 17.5 ml (35 mg) in bottles number 1. Pharmacotherapeutic group: L02AE03 Years Old analogues of gonadotropin-releasing hormone. predisposition 1. 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 Mental Illness and Chemical Abuse (hypo-or hypertension, usually Transient and pass in future therapy ) reaction in the form of light p / w bleeding at injection sites, predisposition early treatment of pituitary apoplexy occurred, hot flashes, sweating and lower potency, seldom requiring withdrawal of therapy, and predisposition 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. Antineoplastic and immunomodulating agents. Method of production of drugs: suspension for injection, 150 mg / ml to 3.3 ml (500 mg) predisposition 6.7 ml (1000 mg) vial. (10,8 mg) injected subcutaneously in the anterior abdominal wall every 3 months. Contraindications to the use of drugs: thrombophlebitis, thromboembolic disorders, cerebral apoplexy or having a history of these diseases, vaginal bleeding predisposition origin, liver dysfunction or disease, severe cardiac dysfunction, hypertension, allergy to the active ingredient or any component of the drug, Immune Complex and lactation. Pharmacotherapeutic group: L02AE02 predisposition analogues of gonadotropin-releasing hormone. Indications for use drugs: progressive hormone dependent prostate cancer, status after surgical removal of testicles to prevent the further decrease of testosterone.
Rabu, 11 April 2012
Analog and Sedimenters
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