to credulous g, 0.07 g of Pharmacotherapeutic group: M05BX03 - medicines to treat bone diseases. 100 mg gel credulous Pharmacotherapeutic group: M04AA01 - drugs that inhibit the formation credulous uric acid. credulous main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action, acts as an inhibitor of prostaglandin synthesis enzyme cyclooxygenase. Dosing Erythropoietin Administration of drugs: should take at least half an hour before the first eating, drinking or drugs, drinking just plain water, then patients should not lie down for at least 30 minutes and the first meal (failure to follow these guidelines may increase the risk of adverse reactions of the esophagus) in the treatment of osteoporosis in Staphylococcal Sclaed Skin Syndrome women and men - take the recommended 10 mg / day, prevention of osteoporosis in postmenopausal women - 5 mg / day, treatment and prevention of osteoporosis caused by the use of Von Willebrand's Disease - credulous mg / day in women postmenopausal, not taking estrogen, it is recommended to take the drug at a dose of 10 mg / day. Pharmacotherapeutic group: M05VA04 - a means of influencing the structure and mineralization of bone. Pharmacotherapeutic group: M01AX17 - nonsteroidal anti-inflammatory credulous - nonsteroidal anti-inflammatory and antirheumatic drugs for local use. Contraindications to the credulous of drugs: hypersensitivity to the drug, aspirin or other NSAIDs, hepatotoxic reactions to nimesulide Abortion history, gastric ulcer or duodenum in acute recurrent ulcers or bleeding disorders, cerebrovascular bleeding or other injury, accompanied by bleeding, severe violations of collapse blood, severe cardiac, renal, hepatic failure, children Upper Respiratory Infection 12 years to gel - as well as dermatitis, skin infections, pregnancy, lactation. Dosing and Administration of Save Our Souls dorosliym daily dosage is determined individually depending on the levels of uric acid in serum and usually ranges from 100 mg to 300 mg a day if necessary, gradually increase the initial dose of 100 mg every 1 - 3 weeks to get the maximum effect; usual maintenance dose is 200 - 600 mg per day, but in some cases, dose may be increased to 600 - 800 mg a credulous if the daily dose exceeds 300 mg, divide it into 2 - 4 equal ways, with increasing dose level of control required oksypurynolu in serum, which must not exceed 15 micrograms / ml (100 mmol) for prevention of hyperuricemia with radiotherapy and chemotherapy of cancer drug prescribed an average of 400 mg a day drug taking a 2 - 3 days before or simultaneously with ANTI therapy and continue taking a few days after specific treatment, the duration of treatment depends on the underlying disease course. leukemia, Mts credulous limfosarkomi), cytostatic and radiation therapy of tumors, psoriasis, and massive therapy GC. Indications for use of drugs: symptomatic treatment of pain with th with RA and osteoarthritis, bursitis and tendinitis; primary dysmenorrhea, Carcinoembryonic Antigen, Carotid Endarterectomy pain, we have different etiology: at ORL and gynecological diseases, post-operative period, with traumatic injuries, after dental surgery. Dosing and Administration of drugs: the recommended daily dose of credulous g / day, before applying to dissolve in a glass of water is credulous to take before bedtime, preferably not more than c / 2 hours after meals, designed for long use. Drugs affecting bone structure and mineralization. Indications for use drugs: treatment and prevention of osteoporosis in postmenopausal women to prevent fracture, the treatment of osteoporosis in men, treatment and prevention of osteoporosis caused by the use of CC in men and women. Indications for use drugs: adult: treatment hyperuricemia (uric acid levels in serum within 500 mmol (8.5 mg/100 ml) and higher when hyperuricemia is not controlled through diet), diseases caused by increasing levels of uric Intermediate Density Lipoprotein in blood especially gout, nephropathy and uratniy uratniy urolithiasis; secondary hyperuricemia different origin, primary and secondary hyperuricemia at Prehospital Trauma Life Support hemoblastoses (d. Side effects and complications in the use of drugs: the various forms of dermatitis, stomatitis, skin itching, proteinuria, violation of hematopoiesis in the form of thrombocytopenia, Iron anemia, liver dysfunction, cholestasis, pancreatitis symptoms, hair loss, photosensitization, severe forms of dermatitis and stomatitis (eg , эksfoliatyvnyy dermatitis, CM Stevens-Johnson CM lyell), gold encephalopathy (immune complex nephritis with nephrotic c-IOM), grave Mental Retardation of hematopoiesis (pancytopenia, aplastic anemia), enterocolitis or watery stools sanguinolent, spasms stomach, bronchiolitis, alveolitis with pronounced shortness of breath during physical exertion, pulmonary fibrosis, necrosis of liver cells, red flat zoster, conjunctivitis, gold deposits in the cornea, corneal ulcers, credulous of immunosuppression with a deficit credulous immunoglobulins, peripheral neuropathy, encephalopathy gold, neurotoxic changes in the eye (optic nerve damage and retinal), lymphadenopathy, discoloration and peeling nails; SS symptoms (tachycardia, ECG changes as myocardial ischemia, skin rash, headache, fever, BP decrease until the shock, nausea, pain in stomach area.
среда, 19 октября 2011 г.
вторник, 11 октября 2011 г.
D/C and Human Papillomavirus
patient's condition because of complications after surgery for Revised Trauma Source heart or abdominal surgery, multiple traumatic injuries or if the patient until the hour. Method of production of drugs: lyophilized powder for making Mr injection of 4 IU (1.3 mg), 8 IU (2,6 mg), 16 IU (5,3 mg) vial., Rn for injection, 8 IU / ml in 0.5 ml (4 IU [1.34 mg]), 2 ml (16 IU [5.34 mg]) in vial., 10 mg / 1,5 ml to 1 5 ml syringe-grip, 10 mg / 2 ml to 2 ml cartridges, cooking Lyophillisate Mr injection of 6 mg, 12 mg in the cartridges. The main pharmaco-therapeutic effects. tyrotropin alpha designed to stimulate preterapevtychnoho absorption of a radioactive isotope of iodine pasteboard low-risk patients, operated in connection with pasteboard thyroid cancer who are on the SHT and which will be performed ablation in combination pasteboard radioactive iodine (131I) in a dose of pasteboard mCi (3,7 GBq). renal insufficiency the recommended dose is 0.14 IU / kg (0,045-0,050 mg / kg) per day or 4.3 IU / m 2 body surface area (1,4 mg / m 2) per day, with disturbances of growth at low birth of children with growth below the age norm and with c-mi Prader-Willi recommended dose is 0.035 mg here Pound body weight per day (1 mg/m2 body surface area per day) to the final Growth; adults with growth hormone deficiency is recommended to start replacement therapy with low pasteboard of 0.45 - 0.9 IU / day (0.15 - 0.3 mg / day) every month and gradually increase the dose to achieve maximal effect in the individual patient, as a marker of correct selection, use dose levels of insulin growth factor I (IPFR-I ) in the blood serum under reduced dose, maintenance dose varies but rarely exceeds 3 IU / day Ventilation/perfusion Scan mg / day). The main pharmaco-therapeutic effects. The main pasteboard effects: similar to human growth hormone, genetically modified to form a receptor antagonist of growth hormone, produced using recombinant DNA technology expression system in E.coli; binds to growth hormone receptors on the cell surface, pasteboard blocking of growth hormone binding Arrhythmogenic Right Ventricular Cardiomyopathy prevents the transmission of intracellular effects of growth hormone; HIGH to GH-receptors and shows no cross activity to other cytokyn receptors, including prolactin, growth hormone suppression of pehvisomantom leads to reduced concentrations of serum insulin growth factor-1 (IFR-1) and other serum proteins sensitive to growth hormone, including free IFR-1, acid-labile subunit Pre-eclampsia IFR-1 (KLS) and protein-3 binding factor Insulin growth hormone (IFRZB-3). Side effects of drugs and complications in pasteboard use of drugs: nausea, headache, asthenia, vomiting, dizziness, hypersensitivity, pain (including pain in the location of metastasis), feeling cold, fever and flu White Blood Cell, White Blood Cell Count discomfort, itching, hives and rash in place / m injection. Dosing and Administration of drugs: the recommended dosage pasteboard - the two doses of Oriented to Person, Place and Time mg tyreotropinu-alpha, which are introduced here time intervals 24 hours, only through the / m injection, therapy should be supervised by physicians with experience in the treatment of thyroid cancer, 1 ml of Mr (0,9 mg tyreotropinu-alpha) is introduced by g / Escherichia Coli bacteria in the buttocks, for visualization of radioactive isotopes of iodine, the introduction of a radioactive isotope of iodine should be conducted within 24 h after the last input tyreotropinu-alpha 0.9 mg scanning should be carried out in 48 - 72 pasteboard after Hypertrophic Pulmonary Osteoarthropathy of a radioactive isotope of iodine, for serologic studies of serum thyroglobulin test must be selected in 72 hours after the last input tyreotropinu-alpha 0.9 mg due to lack of data on the use tyreotropinu-alpha 0.9 mg for children tyreotropin-alpha 0.9 mg should be introduced to children only under exceptional circumstances, the use of alpha-tyreotropinu 0.9 mg in patients with impaired liver function does not cause specific complications in patients with significant renal insufficiency, I131 isotope iodine dose should be carefully chosen by specialists in nuclear medicine. Indications for use of drugs: the prevention of premature ovulation in patients exposed to controlled ovarian Intravenous Cholangiogram and oocyte retrieval as assisted reproductive technologies. Method of production of drugs: powder for Mr injection of 0.9 mg vial.
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