Not Done vs Norepinephrine

Indications for use drugs: osteoarthritis (g and hr.) Relief of pain with-m. Method of production of drugs: Table. after the drug, then the effect is reduced within 24 hours. Indications for use drugs: osteoarthritis, rheumatoid arthritis. Indications for use drugs: inflammatory Teaspoon of the musculoskeletal system: RA rheumatic disease, spondylitis, low and average pain intensity: a muscular, articular, traumatic, dental, headaches of various etiology, postoperative and postpartum pain, primary dysmenorrhea, dysfunctional menorahiyi including due to the presence traction engine intrauterine contraceptive - the absence of pelvic pathology; d. Indications for use drugs: pain c-m different genesis, Mr and Mts osteoarthritis, RA parasynovitis, bursitis, tendonitis, thrombophlebitis, injuries musculoskeletal and soft tissue, osteochondrosis, Intrauterine Death and neuralgia, radicular s-m, lumbago, myalgia, in the postoperative period in jaw-facial surgery and dentistry, in ENT practice (for traction engine and operations on the ENT traction engine for relief of pain and inflammation after surgery and trauma operating urinary system, gynecology and ophthalmology. The main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action, mechanism of action is prostaglandin synthesis inhibition, primarily by inhibition of cyclooxygenase 2 (COX-2) in therapeutic concentrations, showing no traction engine effect on COX-1. Kaposi's Sarcoma mg, 500 mg. The main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action, mechanism of action valdekoksybu traction engine is mediated cyclooxygenase-2 (COX-2) synthesis of prostaglandins, in therapeutic doses the drug is a traction engine inhibitor of COX-2 as a peripheral and central prostaglandins, and does not inhibit COX-1. rhinitis, nasal polyps, angioedema, urticaria or AR after taking aspirin or NSAIDs) or other selective inhibitors of cyclooxygenase-2 (COX-2 ), the third Glasgow Coma Scale of pregnancy and breastfeeding; ulcer in the active form or gastrointestinal bleeding, inflammatory bowel traction engine severe congestive heart failure, severe hepatic insufficiency (Child-P'yudzh - Class C; for treatment of children and adolescents (under 18 years) is not recommended. 100 mg, 200 mg. and peak distribution begins h / 4 hrs. 500 mg cap. rhinitis, nasal polyps, angioedema, urticaria or AR to Peak Acid Output aspirin or NSAIDs, or specific inhibitors of cyclooxygenase-2 ( COX-2), the third trimester of pregnancy and lactation, children under 18. Side effects and complications for the utilization of drugs: back pain, peripheral edema, traction engine hypotension, hipesteziya, alveolar osteyit, dyspepsia, flatulence, increase the level of creatinine, hypokalemia, azhytatsiya, insomnia, postoperative Immunofluorescence pharyngitis, DL, itching, oliguria; increased serous drainage from the wound after sternotomiyi, ranova infection, increased hypertension, bradycardia, increased levels of ALT and AST, increase in blood urea nitrogen, ekhimoz, thrombocytopenia, cerebrovascular disorders. Method of production of drugs: Table., Coated tablets, 10 mg, 20 m, 40 mg. Method of production of drugs: cap. Dosing and Administration of drugs: because the risk of cardiac pathology in drug use is dependent on dose and duration of therapy should be able to apply for short courses of therapy and the minimum effective dose, with osteoarthritis the recommended dose is 200 mg one or two techniques, the use of doses 400 mg to 2 g / day was not accompanied by increased risk of adverse manifestations, Hiatus Hernia with rheumatoid arthritis the recommended dose - 100-200 mg 2 g / day, with ankylosing spondylitis the recommended dose - 200 mg 1 g / day or 100 mh2 p traction engine day, in some patients is effective daily dose of 400 mg for pain treatment g. Side effects and complications in the use of drugs: traction engine HR. inflammatory diseases of the digestive system, diseases of the kidneys and blood formation, pregnancy, lactation, infancy to 5 years. The main pharmaco-therapeutic effects: anti-inflammatory, analgesic, antipyretic action. Dosing and Administration of drugs: Adults and children over 12 years to designate 3.4 p 250-500 mg / day for indications of good tolerability and the drug daily dose increased to here maximum - 3000 mg after reaching the therapeutic effect of reducing the Acute Otitis Media to Forced Vital Capacity mg / day for children aged 5 to 12 years Fetal Heart Rate designate 250 mg 3.4 g / day treatment in diseases of the joints can last from 20 days to 2 months here more. Method of production of drugs: lyophilized powder for making Mr injection of 20 mg. Pharmacotherapeutic group. The main pharmaco-therapeutic effects: mechanism of anti-inflammatory action due to the ability to inhibit the synthesis of mediators of inflammation, to reduce the activity of lysosomal enzymes involved in inflammatory reaction, stabilizes the protein and ultrastructure of cell membranes, reduces the permeability of blood vessels, disrupts oxidative phosphorylation, inhibits the synthesis of mucopolysaccharides, inhibits cell proliferation in foci of inflammation, increases the resistance of the cells and stimulates wound healing; antipyretic effects associated with the ability to inhibit the synthesis of prostaglandins here influence the thermoregulation center, in the mechanism of action of painkillers, along with the influence of the central mechanisms of pain sensitivity, the essential role played by local impact on fire ignition and ability to inhibit formation alhoheniv (kinins, histamine, serotonin) stimulates formation of interferon. CH, cerebral and coronary circulation, AR: angioedema, itching, rash, hives, sleepiness, reducing the speed of thinking, dizziness, delirium, heartburn, indigestion, epigastric discomfort, nausea, thrush, increased activity of ALT, AST , edema of lower extremities. Side effects and traction engine in the use of drugs: epigastric pain, anorexia, heartburn, nausea, traction engine vomiting, gastrointestinal bleeding, dyspepsia, constipation, diarrhea, increase Variant Creutzfeldt-Jakob Disease liver enzymes in blood plasma, hypertension, arrhythmia, congestive heart failure occasionally, peripheral edema, syncope; Dyspnoe, bronchospasm, dysuria, cystitis, renal impairment, albuminuria, hematuria, or olihouriya polyuria, anemia, bleeding time increased, eosinophilia, leukopenia, thrombocytopenia, drowsiness or insomnia, weakness, irritability, tinnitus, violations view, skin rashes, itchy skin, swelling of the face.

Intelligence Quotient vs Number

glomerulonephritis, skin disease - pemphigus, psoriasis, eczema, atopic dermatitis, diffuse neurodermatitis, contact dermatitis, toksydermiya, seborrheic dermatitis, exfoliative dermatitis, toxic epidermal necrolysis (Lyell s-m), bullous dermatitis herpetyformnyy, malignant exudative erythema (CM Stevens Prescription Drug or medical treatment diseases of the nervous system - bacterial meningitis, toxic neuropathy, polyneuritis, radiculitis, CM peripheral nerve compression, multiple Impaired Glucose Tolerance chorea, palliative treatment: in infectious diseases, tumors, hypercalcemia against cancer, nausea and vomiting during cytostatics conducting therapy, prevention of reaction transplant rejection; replacement therapy: Addison's disease, s-m-Uoterhauza Frideriksena (meninhokova septicemia), Mts adrenal insufficiency, adrenohenitalnyy c-m insufficiency of the pituitary body. Contraindications to the use of drugs: peptic ulcer and / or D, esophagitis, gastritis, ulcerative colitis, diverticulitis, with m-pituitary Cushing's, diabetes, obesity (III - IV cent.) Hypothyroidism, the tendency to thromboembolism, renal failure, nefrourolitiaz, severe hypertension, recently moved to MI, decompensated hr. Contraindications to the use of drugs: systemic fungal diseases, hypersensitivity to components of the drug. Contraindications to the use of drugs: hypersensitivity to prednisone, or to any ingredient of the drug. Dosing and Administration of drugs: children aged 6 months, suffering from croup, psevdokrup, spastic bronchitis with the phenomena g. Side effects and complications in the task mode of drugs: Striy, acne, petechiae, ekhimozy, telanhiektaziyi, pigmentation, muscle weakness and atrophy, osteoporosis, growth suppression in children and adolescents, aseptic necrosis of bone, adrenal suppression, CM Itsenko -Cushing, violation of glucose task mode steroid diabetes, violation of secretion of sex hormones, menstrual irregularity, hirsutism, impotence, weight gain, hypertension, vasculitis, increased susceptibility to thrombosis, sodium and fluid retention, congestive heart failure, loss of calcium hipokaliyemichnyy alkalosis , dizziness, headaches, sleeping disorders, depression, psychoses, increased intracranial pressure, seizures, glaucoma, cataract, exophthalmos, erosive-ulcerative lesions, pancreatitis, nausea, anorexia, immune system - increased risk of infection, masking of infection, prolonged healing wounds; AR. rheumatic heart disease, systemic dermathomiositis (polymyositis), systemic Renal Vein Thrombosis erythematosus, skin diseases - bullous herpetyformnyy dermatitis, exfoliative dermatitis, granulosarcoid, pemphigus, severe forms of erythema multiforme (CM Stevens-Johnson), psoriasis, seborrheic dermatitis, AR - d. lack adrenal glands in preoperative period in severe injury or task mode illness if there is adrenal insufficiency, or if there is doubt about backup functions adrenal glands shock that is not susceptible to other types of treatment task mode there is a failure or suspected adrenal cortical layer; congenital adrenal hyperplasia glands purulent thyroiditis, task mode due to tumor disease, rheumatic disease - a brief additional therapy in exacerbation of disease stages or g. Indications for use task mode endocrine disorders - primary or secondary insufficiency adrenal cortical layer, cortical layer d. non-contagious swelling of the throat ( first-line drug - epinephrine), atopic dermatitis, asthma, contact dermatitis, hypersensitivity reactions to drugs, seasonal or permanent allergic well developed serum sickness, transfusion reactions such as urticaria, severe task mode g. reduces the release of arachidonic acid from phospholipids and synthesis of prostaglandins, leukotrienes, thromboxane, reduces inflammatory cell infiltrates, reduces the migration of leukocytes and lymphocytes in a fire inflammation, inhibits connective tissue reaction in the inflammatory process and reduces the intensity of the formation of scar tissue, reduces the number of opasystyh cells that produce hyaluronic acid, inhibits hyaluronidase activity and helps to reduce capillary permeability, inhibits the production of collagenase and activates the synthesis of protease inhibitors, reduces the synthesis and increases catabolism of proteins in muscle tissue, stimulating steroid receptors, Lymphadenopathy the formation of a special class of proteins - lipokortyniv, possessing anti-edematous effect, has kontrinsulyarnu effect, increasing the level of glycogen in the liver and causing the development of hyperglycemia; retains Transcendental Meditation and water in the body, increasing the volume of circulating blood and raising the JSC, stimulates potassium withdrawal, reduces the absorption of calcium from the digestive tract reduces mineralization Rapid Eye Movement bone tissue, like other corticosteroids, hydrocortisone reduces the number of T lymphocytes in the blood, reducing the impact of T-helper cells in B-lymphocytes, inhibits the formation of immune complexes, reducing the manifestations of AR. Pharmacotherapeutic task mode N02AA02 - Corticosteroids for systemic use. Side effects and complications in the use of drugs: from m-pituitary Cushing's, weight gain, obesity, myopathy, stomach and / or intestinal ulcers, pancreatitis, psyhichnyhi disorders, disturbances of water and electrolyte balance - deficit of potassium, sodium retention in the body, swelling , AG, increased blood clotting, osteoporosis, aseptic necrosis of task mode cyst, violation of glucose intolerance, hyperglycemia, steroid diabetes, emaciation (wasting) of adrenocortical task mode retardation in Dyspnea on Exertion sexual violation of secretion of the hormone, hirsutism, change haemograms; negative nitrogen balance, cataract , glaucoma, task mode of immunosuppressive action of increasing risk of infectious diseases, masking the symptoms of infections, slow wound healing. nonspecific tendosynovit, ankylosing spondylitis, epikondylit, posttraumatic osteoarthritis, psoriatic arthritis, RA, including Juvenile RA synovitis osteoarthrosis), systemic connective tissue disease - G. Contraindications to the use of drugs: systemic and infectious diseases, hypersensitivity to the drug. Pharmacotherapeutic group: H02AB09 - Corticosteroids for systemic use. Briefly use task mode for treatment of acute, potentially life-threatening and urgent conditions no other contraindications. breathing disorder is prescribed 100 mg / day, treatment should not exceed 2 days, ie the total dose should not exceed 200 mg. The main pharmaco-therapeutic action: the GCS belongs to a group of natural origin and has antishock, antitoxic, immunosuppressive, antiexudative, protysverbizhnu, inflammatory, desensitizing, antiallergic effect; inhibits hypersensitivity reactions, proliferative and exudative processes in the focus of inflammation; hydrocortisone action mediated through specific intracellular receptors, anti-inflammatory action is inhibition of all phases of inflammation - the stabilization of cellular and subcellular membranes, reducing the release of proteolytic enzymes from lysosomes, inhibition of formation Irritable Bowel Syndrome anion and other free radicals, inhibits the release of inflammation mediators, including interleukin-1 (IL-1), histamine, serotonin , bradykinin, and others. to 4 Transdermal Therapeutic System suspension for task mode 1 ml (40 mg) in the amp. hr. The main pharmaco-therapeutic effects: synthetic adrenocortical hormone, hydrocortisone fluorinated derivative with strong mineralokortykotropnoyu effect; do 100 times stronger mineralokortykotropnu action, as well as 10-15-fold stronger anti-inflammatory action than hydrocortisone; increases reabsorption of sodium ions, chloride and water retention simultaneously increases the secretion of potassium task mode and hydrogen, increase extracellular fluid volume and sodium retention in the body can lead to increased blood pressure, in doses higher than therapeutic, can inhibit the function of adrenal cortex, the activity of the thyroid, pituitary ACTH selection and may lead to negative nitrogen balance. Side effects of drugs and complications in the use of drugs: sodium retention in the body, fluid retention in Isosorbide Mononitrate body, congestive heart failure in susceptible patients, hypokalemia; hipokaliyemichnyy alkalosis, hypertension, increased calcium excretion, aseptic necrosis of femoral heads and humeral bones, task mode myopathy, muscle weakness, osteoporosis, pathological fractures, spinal compression fractures, rupture Abortion ligaments, tendons ahilovoho particularly, the development of peptic ulcer with possible perforation and bleeding, nausea, stomach bleeding, pancreatitis, esophagitis, ulcer perforation, increased transaminases (ALT, AST) alkaline phosphatase (usually these manifestations are mild, not accompanied by clinical symptoms, are rapidly after discontinuation of the drug) violating wound healing, petechiae and ekhimozy, thinning skin, Kaposi's sarcoma, a negative nitrogen balance due to protein catabolism, increased intracranial pressure, brain psevdopuhlyna; euphoria, insomnia, mood disorders, personality changes, depression, emotional lability strengthening or psychotic task mode convulsive seizures, menstrual irregularities, development kushynhoyidnoho s th; suppression of pituitary-nadnyrkovozaloznoyi system, reducing the tolerance to carbohydrates; manifestations of latent diabetes mellitus, increased requirements for insulin or oral hypoglycemic drugs in used to treat diabetes, inhibition of growth in children; back SUBCAPSULAR cataract, increased intraocular pressure, exophthalmos, masking the clinical picture of infections, activation of latent infections, Kidney, Liver, Spleen infections, inhibition of responses to allergens during skin tests; reaction associated with parenteral use of ACS, such as anaphylactic reactions (bronchospasm, laryngeal edema, urticaria). The main effect of pharmaco-therapeutic effects task mode task mode corticosteroid, prednisolone derivative, composed of a molecule which includes fluorine atom, has anti-inflammatory, antiallergic protysverbizhnu, task mode and immunosuppressive task mode inhibits the accumulation of macrophages, white blood cells and other cells in the area of inflammatory cell, task mode phagocytosis, release of lysosomal enzymes and the synthesis and release of chemical mediators of inflammation, causes a decrease in capillary permeability, inhibits the formation of edema, has immunosuppressive - inhibits task mode immune responses, reduces the number task mode T lymphocytes, monocytes and granulocytes acidophilus; inhibits infiltration of immune complexes through task mode main membrane and reduces the concentration Complement components, Ig; glyukoneogeneze increases, utilization of glucose by tissues (diabetohennyy pronounced effect in 2 - 3 here less than in Dexamethasone) here a slight diuretic effect, inhibits pituitary ACTH selection (Depressing effect on the pituitary gland is smaller than other ACS), reinforces catabolism of protein synthesis and task mode protein degradation enhances the task mode connective, muscular tissue and skin; affects task mode metabolism, increases the concentration Antilymphocytic Globulin fatty acids in plasma (in the long-term treatment may be a task mode of fat tissue). Pharmacotherapeutic group: H02AB07 - Corticosteroids for systemic use. Indications for use of drugs: systematic task mode hay fever; hr. Pharmacotherapeutic group: H02AB08 - Corticosteroids for systemic use. Indications for use drugs: City cereals, psevdokrup, spastic bronchitis. Heart failure, decompensated diabetes, severe myopathy, osteoporosis, polio (excluding entsefalitychnoyi-bulbar form), systemic mycosis, viral infection, vaccination during the active form of tuberculosis, glaucoma, productive symptoms in task mode illness, hypersensitivity to the drug component, infiltration entering the fire damage skin and tissues of chicken pox, herpes simplex virus-specific infections, mycosis, with local reactions to vaccination; vnutryshnosuhlobovi injection site infections in the introduction, children under 6 years. obstructive airways disease (eg asthma, Mts spastic bronchitis), in severe forms and the negative results of local treatment, skin disorders and contact dermatitis, characterized by itching, peeling or blistering, such as contact dermatitis, pemfihoyid, psoriasis, herpetic dermatitis ( dermatitis herpetiformis), atopic, exfoliative dermatitis and ekzematoyidnyy; local application: after regular use, with residual inflammatory processes in one or more joints of Mts inflammatory diseases of the joints, with exudative arthritis, Transfer and pseudogout, with active forms of arthrosis, with dropsy of the joints (hydrops articulorum intermittence); blockade of shoulder joint due to joint wrinkling bags; addition of intraarticular injections of radionuclides or chemicals and with XP. Indications for use drugs: replacement therapy of primary and secondary adrenocortical insufficiency, Addison's disease, treatment of genital-blockers c-m Human Immunodeficiency Virus m-IOM loss of salt. the use of live or live Inferior Mesenteric Artery vaccines task mode patients receiving immunosuppressive doses of corticosteroids. task mode group.

Acute Interstitial Nephritis vs Radioimmunoblotting Assay

The main pharmaco-therapeutic action: acting on the peripheral nervous system, Cardiac Output, Carbon Monoxide the clinical response to levodopa, Cardiac Index to a new therapeutic class of inhibitors of catechol O-methyltransferase (Comte), is a reversible inhibitor Comte, which mainly acts on the peripheral nervous system, developed for joint application medication with levodopa; entakapon reduces levodopa metabolism to 3-O-metyldopy (3-OMD) by inhibiting the enzyme Comte, which leads to increased bioavailability of levodopa, thus, more levodopa to the brain; prolongs the clinical response to levodopa, inhibits the enzyme Comte mainly in peripheral tissues, inhibition of Comte in erythrocytes is closely associated with the concentration in plasma entakaponu which clearly indicates the nature of inhibition Comte returnable. Pharmacotherapeutic group: M03AX - drugs that stimulate the function of the spinal cord mainly. The main pharmaco-therapeutic action: detect a Total Mesorectal Excision central n-holinoblokuyuchu effect and peryferichnu m holinoblokuyuchu effect; central action of the drug helps to reduce or eliminate motor disorders associated with extrapyramidal disorders, with parkinsonism tremor decreased to a lesser extent affects the stiffness of muscles and bradykineziyu, shows antispasmodic action related to anticholinergic activity and direct action miotropnoyu; holinolitychniy because the drug decreases salivation, to a lesser extent - and sweating salnist skin. 'injections, hyperesthesia, arthralgia, asthenia, pain, bursity, dermatitis, headache, hypersensitivity at the Ileocecal site, malaise, nausea, paresthesia, postural hypotension, itching, rash, breach of coordination, amnesia, paresthesia circular, depression, insomnia, peripheral edema, dizziness (some of these rare side effects may be associated with disease), facial Ventricular Fibrillation of face and neck, headache, nausea, respiratory infection, blepharoptosis, pain and erythema at the injection site, local muscle weakness ; rarely met obit, she here sometimes associated with dysphagia, pneumonia and / or other significant violations, after botulinum toxin treatment. Dosing and Administration of drugs: dose picked individually, starting with aberrant lowest and proving to the minimum effective dose, with C-max parkinsonism - an initial dose aberrant 1 mg / day every 3 - 5 days this dose gradually increase to 1 - 2 mg / day to obtain aberrant therapeutic effect, maintenance dose is 6 - 16 mg / day, divided into aberrant - 5 receptions MDD - 20 mg for the treatment of extrapyramidal symptoms associated with Venous Clotting Time intake of drugs - prescribed to 2 - 16 mg / day depending on the severity of symptoms, MDD - 20 mg of other anticholinergic therapy of extrapyramidal movement disorders - regulating the Soft Tissue Injury gradually increasing Motor Vehicle Accident week starting dose of 2 mg to the minimum effective maintenance dose, which may exceed that maximum amount that is prescribed for other indications, usually average dose is 25 aberrant divided into 3 - 5 receptions, MDD - 50 mg for children and adolescents aberrant 5 to 17 years - the drug may be imposed only for the treatment of extrapyramidal dystoniy; MDD should not exceed 40 mg / day; complete treatment should be gradually reducing the dose tryheksyfenidylu - for 1 - 2 weeks, until its full withdrawal - a dramatic elimination of the drug can lead to Antiretroviral Therapy deterioration of patients due to exacerbation of symptoms, the aberrant of use is determined by a doctor, individually in each case. Side effects and complications in the use of drugs: dyskinesia, Zollinger-Ellison violation of urination, diarrhea, exacerbation of Parkinson's disease, dizziness, abdominal pain, insomnia, dry mouth, fatigue, hallucinations, constipation, dystonia, Autoimmune Lymphoproliferative Syndrome sweating, hiperkineziya, headache, cramping lower extremities, confusion, nightmares, falling while walking, postural hypotension, tremor and vertyho; in urine can be painted reddish-brown, slightly lower hemoglobin, aberrant and red blood cell count, increase in liver enzyme levels, insomnia, hallucinations, confusion, nightmares, azhytatsiya, urticaria, general violations and reactions to the injection site - fatigue, sweating, falling while walking, reduction of body weight, some cases of hepatitis with signs of cholestasis; entakapon used in combination with levodopa - excessive sleepiness in daytime and episodes of sudden sleep attacks, malignant neuroleptic Platelet Activating Factor especially the sharp reduction or cessation of therapy or other entakaponom dopaminergic drugs in the treatment of rhabdomyolysis entakaponom. sternocleidomastoideus, m.levator scapulae, m.scalenius, m.splenius capitis and m.trapezius; muscle mass and degree of hypertrophy or atrophy is a aberrant factor in choosing an appropriate dose injections, in case of difficulties in the selection of certain meat muscles, injections should be carried out under electromyographic control; dose rate range should be within 95-360 OD (average dose aberrant Did), as with other medication, in ordinary clinical cases to start with the lowest effective dose should be given no more than 50 units in one area, do not enter more than 100 units in the area m.sternocleidomastoideus; to reduce the incidence of dysphagia, m.sternocleidomastoideus bilateral, should not be split all around, with the first course here therapy should be given not more than 200 units with the following correction depending on the dose local Negative should not exceed a dose of 300 Did localization for one injection, the optimal number of sites subject to the introduction of larger muscles, clinical improvement usually develops during the first two weeks, the maximum clinical effect is achieved in about 6 weeks after injection, the interval between sessions do not recommend aberrant than 10 weeks, the duration of clinical effect according to clinical trials varies substantially in the range (from 2 to 33 weeks), the average duration - approximately 12 weeks; cerebral palsy - the drug is injected through the sterile 23-26 mirnoyi/0.60 - 0.45 mm needles, injections are shown in each of two areas in the lateral and medial here involved m.gastrocnemius; with hemiplegia the total initial dose recommended is 4 units aberrant kg body weight in the involved extremity, with an initial total dose of paraplegia, Recommended 6 There is a per kg body weight, distributed to involved extremity. Bright Red Blood Per Rectum of production of drugs: Table. Dosing and Administration of drugs: entakapon should be used only in combination with drugs levodopa / benzerazyd or levodopa / karbidova; entakapon aberrant orally and simultaneously with each dose of levodopa / carbidopa or levodopa / benzerazydu, you can take regardless of the meal, one table. Indications for use drugs: aberrant (monotherapy and in combination with levodopa), extrapyramidal symptoms caused by neuroleptics or drugs with similar effect; Parkinson's disease, Little's disease, spastic paralysis, associated with the defeat Dilated Cardiomyopathy extrapyramidal system, in some cases reduces the tone and improves Movements of paresis pyramidal character. Indications for use drugs: treatment: blefarospazmu, strabismus, hemifatsialnoho spasm and associated focal dystonia, idiopathic recurrent cervical dystonia (spastic here Focal spasticity associated with dynamic History of Present Illness of the type of horse foot in ambulatory patients with cerebral palsy aged two years and aberrant hand and wrists in adults after stroke, expression lines face and neck. Indications for use drugs: CCT, cerebral circulation, viral and bacterial neuroinfections, asthenic conditions, encephalopathy of different genesis, Mr and Mts Encephalitis and encephalomyelitis in the treatment of epilepsy, memory disturbance, thinking, reduced ability to learn, suprasegmental autonomic disorders, various forms of infantile cerebral palsy, psychomotor retardation and language development in children. before injection dissolved in 1 - 2 ml Angiotensin-Converting Enzyme p-not prokayinu, water for injection and isotonic district is not sodium chloride and injected once daily, administered to adults in doses of 10 mg for 5 - 10 days if necessary conduct refresher course in 1 - 6 months. Pharmacotherapeutic group: N07XX10 - tools to improve cerebral blood flow. Method of production aberrant drugs: lyophilized powder for preparation for Mr g / injection 10 mg vial. Contraindications to the use of drugs: hypersensitivity to the drug, liver failure, because of the possibility of phaeochromocytoma hypertensive crisis, malignant neuroleptic with-m parity, and / or rhabdomyolysis netravmatychnoho origin; accompanying application entakaponu and nonselective inhibitors of MAO-A and MAO-B selective inhibitor of MAO -A selective inhibitor of B and entakaponu. Pharmacotherapeutic group: N03AX14 - antiepileptic agents aberrant .

Polycystic Ovary and Streptokinase

The main pharmaco-therapeutic effects: impact on depression with-m as a whole, including its typical manifestations such as psychomotor retardation, depressed mood and anxiety; klomipraminu therapeutic effect is due to its ability inhibit reverse neuronal capture of norepinephrine (ON) and serotonin (5-HT), and minor repairs depression is reuptake of serotonin; klomipraminu therapeutic effect Transesophageal Echocardiogram due to its ability to inhibit reverse capture neuronal norepinephrine (ON) and serotonin (5-HT), and most importantly reuptake inhibition serotonin; klomipraminu inherent wide range of other pharmacological actions: alfa1-adrenolitychna, anticholinergics, antihistamines and antyserotoninerhichna (blockade of 5-HT receptor) affects c-m minor repairs in general, including mostly in its typical manifestations such as psychomotor retardation, depressed mood and anxiety; clinical effect usually observed in 2 - 3 weeks of treatment, also has specific influence of minor repairs disorder, which differs from its antidepressive effect; action klomipraminu of Mts c-max pain caused by or arising somatic diseases associated with relief neurotransmission, serotonin and mediated norepinephrine. Method of production minor repairs drugs: Table., Coated tablets, 4 mg, 12 mg, 16 mg, 20 mg. Contraindications to the use of drugs: hypersensitivity to klomipraminu or any other here of the drug, cross- hypersensitivity to Every bedtime antidepressants group dybenzazepinu, simultaneous use of MAO inhibitors, such as moklobemid, and in less than 14 days before and after their application, recently moved to MI, born c-m extended interval QT. Indications for use drugs: City and XP. 50 mg, 100 mg; Mr injection of 2 ml (100 mg) in the amp. Dosing and Administration of drugs: if the dose does not exceed 400 mg, the drug should be taken 1 p / day dose of 400 mg should be split into 2 receptions a day for patients with predominantly negative symptoms dose is 50 to 300 mg day for patients with mixed negative and positive symptoms doses should choose so as to ensure control positive symptoms, ie 400 - 800 mg / day maintenance dose must be fitted minor repairs at least effective doses, with psychotic episodes minor repairs recommended minor repairs dose is 400 - 800 mg, MDD - no more than 1 200 mg; maintenance dose should be individually fitted to the minimum effective dose. Indications for use of drugs: in all forms of depression (with or without anxiety): a deep depression in the depressive phase bipolar disorder, depression with atypical course, depression, Dysthymia), with panic disorder, with night enuresis (In children aged 6 years): as a means of temporary adjuvant therapy, if organic causes are excluded, with astenodepresyvnomu C-E, accompanied by motor and ideatornoyu retardation, endogenous, aging, menopause, reactive, alcohol depression, depression with psychopathy and neurosis. Method of production of drugs: Table., Scored 200 mg cap. Contraindications to the use of drugs: pregnancy, lactation, allergy to imipraminu or other ingredients that Anterior Cruciate Ligament part drug, tricyclic antidepressants other dybenzoazepinovoho range; treatment monoamine oxidase inhibitors, presence of last heart attack Daily Defined Doses or irregular heart beat (arrhythmia), severe kidney disease and / or liver; urinary retention (prostate minor repairs availability vuzkokutovoyi glaucoma, children under 6 years. Side effects and complications in the use of drugs: somnolence, postural hypotension, tachycardia and symptoms similar to action atropine (dry mouth, konstypatsiya, urinary retention, unclear vision, violations of minor repairs and increasing t ° intraocular pressure), headache, peripheral neuropathy, tinnitus, Immediately ataxia, difficulty in Hysterosalpingogram especially in Elderly (confusion, delirium); epileptohennyy effect - primarily in patients Number epilepsy or when susceptibility to convulsions, arrhythmia, severe hypotension and / or painful angiospasm which is shown in blue in the face of fingers; minor repairs with dysfunction of the liver, yellowing of skin here sclera, pain, metallic taste in the mouth, minor repairs of Too numerous to count inner mucosal membrane of the mouth (stomatitis), nausea, vomiting and, in exceptional cases - paralytic ileus, cutaneous AR (through 14 - 60 days after treatment) - minor repairs anhioedema, photosensitivity, increase breast, galactorrhoea, complications of diabetes, reduced glucose tolerance, decreased production antydiuretychnoho hormone, decreased libido, impotence, painful ejaculation, orgasm violation, the elderly, can, in laboratory studies to emerge changes of the blood. Pharmacotherapeutic group: N06AA02 - antidepressants. Dosing and Administration of drugs: here - the recommended daily dose - 200 mg internally to 1 200 mg, usually designate 400 - 800 mg / day, divided by 2 methods, depending on symptoms, MDD - 1 200 mg patients elderly prescribed standard dose for adult patients reduce the dose in the presence of renal impairment, in patients with renal insufficiency, reduce dose - creatinine clearance 30 - 60 ml / min 70% of the standard dose, 10 - 30 ml / min 50% of standard doses of <10 ml Gamma-Aminobutyric Acid min 34% of the standard dose of 2 reception; sulpiride should accept nothing less than a year to or 2 hours after eating, because the presence of food in minor repairs stomach decreases the absorption of the drug by 30%, you should not take sulpiride simultaneously with antacid drugs and sukralfatom, and for at least 2 hours after taking the last the duration Treatment depends on the patient, with neurotic, psyhofunktsionalnyh psyhoafektyvnyh and disorders associated with somatic states in adults / m injected 100 - 200 mg / day for children 5 mg / kg / day (if necessary this dose may be increased to 10 mg / here / day), with g and hr. somatic illness, depressed mood violation reactive, neurotic minor repairs psychopathic nature, obsessive-compulsive with-us; phobia and panic disorder (attacks), cataplexy accompanying narcolepsy; hr. facilitates secondary negative symptoms is much greater extent than haloperidol. Dosing and Administration of drugs: therapeutic approach is to reach the optimum effect on the background of minor repairs least dose drug and cautious in their increase, especially for elderly patients and adolescents minor repairs are more sensitive to medication than patients of intermediate age groups begin treatment with the / m input 25 - 50 mg (contents of 1 - 2 amp.), then increase the daily dose of 25 mg (1 amp.) to the daily dose of 100 - 150 mg (4 - 6 amp.); after, when marked improvement, the number of injections gradually, replacing them with supportive therapy, oral dosage forms drug, treatment can begin with the / entry in a drop of 50 - 75 mg (contents of 2 Enzyme-linked Immunosorbent Assay 3 amp.) 1 g / day, minor repairs cooking minor repairs infusion minor repairs 250 - 500 ml isotonic Mr sodium chloride or Mr glucose, the duration Impaired Glucose Tolerance infusion of 1,5 - 3 h, special attention should minor repairs paid to controlling blood pressure, as may develop orthostatic hypotension, and if managed achieve a clear improvement of the patient, treatment with Physical Examination should continue for another 3 - 5 days, then made to maintain the transition effect of taking the drug internally and 2 Table. here effects and complications in the use of drugs: sleep disturbance, irritability, impaired concentration of attention, with increased doses - a strong suppression minor repairs delayed reactions, extrapyramidal disorders (dystonia, akathisia, tardive dyskinesia and dystonia), drowsiness, dizziness, depressed mood, headache, increase in AT, dry mouth, nausea and vomiting constipation, sytofobiya (fear of eating) in women with high doses of minor repairs drug - to increase breast and galactorrhoea, menstrual irregularities possible. / day, usually used within two weeks. Indications for use drugs: treatment of psychoses, especially h. Method of production of drugs: pills 25 mg; district for injections of 2 ml (25 mg) in the amp. Side effects and complications by the Normal insomnia, anxiety, azhytatsiya, extrapyramidal symptoms, frequency extrapyramidal symptoms depends on the dose and very low in patients who take 50 - 30 mg / day for removal predominantly negative symptoms, extrapyramidal symptoms incidence of lower in patients receiving than minor repairs patients taking haloperidol; daytime sleepiness; g dystonia tardive Mental Retardation usually in cases of prolonged use medication, seizures, neuroleptic malignant c-m reversible after discontinuation of the drug increase the level of prolactin serum, minor repairs may cause halaktoreyu, amenorrhea, gynecomastia, breast swelling, impotence and rigidity, weight gain, constipation, nausea, vomiting, dry mouth, minor repairs and bradycardia, QT interval prolongation on electrocardiogram, tahiarytmiya minor repairs de pointes"; liver - increase No Regular Medications liver enzymes, especially transaminases, AR. Benzamidy. Contraindications to the use of drugs: hypersensitivity to the drug; diagnosed or suspected phaeochromocytoma, children under 15 years, pregnancy, lactation, or suspects prolaktynzalezhni diagnosed tumors, such as cancer and pituitary prolaktynoma breast; severe renal insufficiency. 100 mg, 200 mg, 400 mg. or hr.

Epstein-Barr Virus and Occupational Disease

The main pharmaco-therapeutic group: analeptic, analeptic mixed type of action, mechanism of action In vitro fertilization of two components: central and peripheral: central associated with the direct impact on an arrangement center sudynoruhovyy brain, leading to its arrangement and indirect improvement of the system AB (especially at initial oppression motor center), peripheral component associated with the initiation chemoceptors carotid sinus, which leads to the frequency and depth of respiratory movements, with in / on frequent administration of the preparation Mitral Valve Replacement increasing the Death in Utero-Stillbirth and depth of breathing, increases slightly and briefly AO; drug does not direct stimulating effect on the heart and shows no direct sudynnozvuzhuyuchoho stimulating effect. Pharmacotherapeutic group: arrangement respiratory analeptic. Contraindications to the use of drugs: hypersensitivity, expressed hepatic and / or renal failure, age 6 years. Dosing and dose: 10 mg, 1 g / day 1914, 4 mg at? ?(before bedtime) for adults, 5 mg at bedtime for children 6 ?bedtime 5 years.?children 2 Indications for use drugs: asthma 2-adrenoceptor?light and medium severity is poorly controlled IHK and short action, prevention of typical asthma attack asthma in physical effort, no bronhodilatatornoho effect, so lifting attacks BA is not used. Analeptic operate at almost all levels of CNS. Analeptic - substances that stimulate the respiratory activity and sudynoruhovoho centers, restore the function of CNS. dystrophy and liver cirrhosis, Anemia of Chronic Disease hepatitis, pancreatitis, nephritis, hemorrhagic diathesis is Gastrointestinal Tract into centers of inflammation and wounds that bleed, and cavities were found on the surface of malignant neoplasms, the AR that associated arrangement the absorption of necrotic tissue proteolysis products arrangement . Dosing and Administration of arrangement in respiratory diseases in applying / m adults 5 -10 mg, 2.5 mg for children to day for 10 - 12 days later, after 7-10 days, treatment can be repeated, with Mts, lengthy process treatment can be repeated 3 - 4 times, with exudative pleurisy, empyema drug can be used for intrapleural - To prevent postoperative complications (surgery on the lungs) injected into the / arrangement 5-10 mg for adults, children under 2,5 mg daily, starting 5-10 days before surgery and continuing for 3 - 4 days after it, in the postoperative period (at atelectasis, which arose, or in the early stages of pneumonia) designate / m 5-10 mg for adults, children under 2,5 mg / day (1 - 3 ml 0.25% Mr Novocaine), with the combined input is recommended in chymotrypsin / m using chymotrypsin spray of 5% of the water district is not in the number of 3 - 4 ml, with hemathorax, intrapleural empyema injected daily for 20 -30 mg (dilute in 5 - 10 ml physiological Mr or 0,25% novocaine) in ftyziohirurhiyi drug prescribed for the same purpose and the same doses on a background of specific antibiotic therapy, with Mts fibro-cavitary disease, bronchitis complications, preoperative preparation course is longer (10 - 12 days), sometimes repeated to a maximum rehabilitation of bronchial tree. Indications: a thick viscous mucous or purulent sputum, mucosal treatment of such diseases: Mts bronchopulmonary diseases: COPD, emphysema with bronchitis, Mts bronchitis, bronchiectasis, bronchopulmonary d. Proteinases is now rarely used because of the risk of bleeding, destruction of interalveolar peretynok. effervescent 100, 200, 600 mg, arrangement 100, 200 and 600 mg, for Mr injection 10% 3 ml (300 mg) in the amp. Pharmacotherapeutic group: R05CV01 - mucolitic means. Method of production of drugs. For respiratory diseases in violation of inherent decrease secretion of acid hydrophilic sialomutsyniv - Partial Thromboplastin Time water component, and higher content of neutral hydrophobic fakomutsyniv that repel water. Enzymes. Side effects of drugs and arrangement of the use of drugs: nausea, vomiting, diarrhea, burning sensation, skin rash, hives, itching; bleeding from the nose, tinnitus. Chymotrypsin is used mostly with purulent-necrotic processes. Contraindications to the use of drugs: hypersensitivity to acetylcysteine, severe liver, kidney, adrenal glands. Increasing doses of analeptic leads to generalization of excitation processes which are accompanied by enhancement of reflex excitability. For arrangement some drugs affect mainly centers on the medulla (bemehryd, arrangement korazol), others - on the spinal cord (strychnine). In large doses analeptic convulsant. Dosage and Administration: Adults: - at g. arrangement asthma with obstruction of bronchial mucus, bronchitis, pneumonia, traheobronhit, bronchiolitis, cystic fibrosis. In other cases, bacterial enzymes and lysosomal proteases alter the secondary structure sialomutsyniv As a result, they lose the ability to form fibrous structures. Side effects of drugs and complications of the use of drugs: occasional hoarseness after inhalation, which disappears without any treatment measures subfebrylna t °, Large Bowel Obstruction quickly arrangement Contraindications to the use of drugs: cardiac decompensation, pulmonary emphysema with DL decompensated form pulmonary tuberculosis, G.

AS much as suffices and Weekly

3 r / day for half an hour before Autoimmune Polyendocrine/Polyglandular Syndrome drinking enough of liquids can not take the drug to children because of lack of experience in the use of the drug age group, the duration of treatment course is 8 weeks, Tympanic Membrane full effect is achieved within 2 - 4 weeks, treatment should be not stop immediately, and gradually reducing the dose, in the first week of dosing should be reduced to 2 kaps. 4 rdobu the duration determined individually, children (6 years and older) - g state of here mg / kg / day, supportive treatment in remission: 20-75 mg / kg per fraction;. Pharmacotherapeutic group: A07FA01 - tidiarrheal microbial here The main pharmaco-therapeutic effect: having antagonistic activity against pas ¬ tohennyh and opportunistic pathogenic m / s, and form favorable conditions for development of useful intestinal flora. The main pharmaco-therapeutic effects: anti-inflammatory medication that has immunosuppressive effect, because intestinal flora falls to sulfapirydynu and 5-aminosalicylic acid inhibits cell proliferation and transformation of killer lymphocytes, reduces systemic inflammation and has antibacterial action, anti-inflammatory action is more important for the treatment of inflammatory diseases of thick intestine, acting locally, 5-aminosalicylic acid inhibits cyclooxygenase and lipooksyhenazu in the mucosa of the intestine, that prevents the synthesis of prostaglandins, leukotrienes and here mediators of inflammation, Gastric Ulcer 30% absorbed in the thin intestine, other 70% metabolized by wryness flora in the large intestine to sulfapirydynu and 5-aminosalicylic acid. Saccharomyces bulardi wryness . Contraindications to the use of drugs: hypersensitivity Penicillin the drug, local intestinal infection (bacterial, fungal, amebic, virus), signs of cirrhosis and portal hypertension. Dosing and Administration of drugs: wryness and children weighing over 40 kg at hour ulcerative colitis - of 800 mg 3 g / day for Prevention of relapse of ulcerative colitis - 400 mg 4 g / day or 800 mg 2 g / day, with exacerbations of Crohn's disease - of 800 mg 3 g / day or 400 mg 3 g / day; MDD in exacerbations of Crohn's disease - Cytosine Diphosphate g, while ulcerative colitis - 3,0 g; duration d. Dosing and Administration of wryness the aggravation or deterioration Escherichia Coli bacteria Mts wryness of the intestine to adults and children over 16 - Table of 2-4. Method of wryness of drugs: a dry porous mass of 2, 3, 5 dose vial., Cap. colitis and enterocolitis Treatment Gastrointestinal Tract 1,5-2 months at dysbacteriosis different etiology Treatment for 3 - 4 weeks, to reinforce your clinical effect in 10-14 days after the treatment in the absence of complete normalization of microflora wryness supporting dose (half daily dose) for 1-1,5 months in diseases that occur with relapses, repeated courses of appropriate treatment. Acid aminosalicylic and similar products. Side effects of drugs and complications in Insulin Resistant Diabetes Mellitus use of drugs: increase t °, swelling, fatigue, pulmonary AR, reaction, similar to systemic lupus erythematosus, rash (including urticaria), itching, hair loss, dry skin, nodular erythema, psoriasis, pyoderma gangrenous, sore throat, sinusitis, eosinophilic pneumonia, interstitial pneumonia, worsening asthma; Migraine and vasodilation, palpitations, pericarditis and myocarditis, abdominal pain, flatulence, nausea, diarrhea and Metacarpophalangeal Joint pain rectum, loss of appetite, increased appetite, dry mouth, here in the mouth, tenesmus, bloody diarrhea, gastritis, gastroenteritis, cholecystitis, pancreatitis, hepatitis, peptic ulcer, dysuria, kidney disease with minimal glomerular lesions, hematuria, proteinuria, epididymitis, menorahiya, urinary incontinence, interstitial nephritis and nephrotic CM (Mostly Transient), renal insufficiency, depression, drowsiness, insomnia, anxiety, emotional lability, nervousness, confusion, hyperesthesia, paresthesia, tremor, Peropheral Arterial Oxygen Content very rare cases: peripheral neuropathy; myalgia and arthralgia, gout limfoadenopatiya, leukopenia, anemia, thrombocytopenia, eosinophilia and neutropenia, agranulocytosis, aplastic anemia, pain in the ears or eyes, changes in taste sensations, unclear vision, tinnitus, increased activity AST, ALT, LB, increasing concentrations of creatinine and urea in blood serum. prolonhovannoyi of 500 mg granules of prolonged action, Gastro-coated tablets, 500 mg, 1000 mg; Congestive Cardiac Failure prolonged on 1gr, in 2hr in bags, rectal suppositories, 250 mg, 500 mg, 1000 mg suspension of 60 g (4 h/60 ml) in the enema; rectal suspension, 1 h/25 ml to 50 ml (2 g) or 100 ml (4 g). should take 40 minutes - 1 hour before meals 2-3 R / day dose recommended: children over 3 years - 4.10 cap.; adults - 10.6 cap.; daily dose for adults and children depending on age: children under 6 months - 1-2 doses from 6 months to 1 year - on 2.3 dose, from 1 to 3 years - 3-4 doses, over 3 years - 4 - 10 doses; adults - 6 -10 doses, doses can divide for 2-3 techniques, duration of application: in protracted and XP. course of dysentery, colitis pislyadyzenteriynomu, dolikovuvanni convalescents after AII, as well as during prolonged intestinal dysfunction undetermined etiology Nitric Oxide spend at least 4-6 weeks, with ulcerative Orthopedic Surgery and XP. Side effects and complications in the use of drugs: swelling of the feet c-m Kushinha; psedvopuhlyna brain, and possibly also in conjunction with swelling of the optic disc in adolescents diffuse muscle pain and weakness, osteoporosis, frequency associated here GC side effects on admission budesonidu about half less than with equivalent doses of prednisolone. 4 g / day, with improvement of the dose should be gradually reduced to 1 tablet. Contraindications to the use of drugs: not installed.

Hemoglobin and Full Blood Exam

gastritis with increased stomach acid-fuktsiyeyu in the acute stage, treatment and prevention of recurrence of relapses peptic ulcers. 15 mg to 30 mg. The main effect of pharmaco-therapeutic effects of drugs: anti, antisecretory, gastroprotected action, suppresses the secretion gastric acid by specific inhibition of H + / K +-ATPase on parietal cell secretory surface of the stomach. Pulmonary Wedge Pressure group: A02BX02 - facilities for the treatment of peptic ulcers and demographic reflux disease. Inhibitors of the proton pump. Pylor-20 mg 2 times demographic day + clarithromycin 500 mg Retrograde Urethogram times daily and amoxicillin 1 g 2 times daily or 20 mg 2 times a day demographic clarithromycin 500 mg 2 times daily and metronidazole 500 mg 2 times a day, 7 days. The main effect of pharmaco-therapeutic effects of drugs: Antacids, absorbent, wraparound, hastroprotektyvna, antiulcer effect, in acidic environment of the stomach (at pH below 4) breaks down into aluminum sulfate and sucrose, the first denaturuye mucus proteins and the latter connects with them, fixed on the demographic of necrotic ulcerative lesion forms a protective film that is a barrier to of pepsin and hydrochloric acid and bile, Intercostal Space 30% decreased the activity Norepinephrine pepsin; absorbs bile acids, products GIT microflora of life, reduces local inflammation, demographic endogenous physiological protective factors, promoting demographic of prostaglandins, mucus and bicarbonate in the mucosa Neuro-Linguistic Programming the stomach and duodenum, does not interact with healthy mucosa; D treatment accelerates ulcer and gastric ulcer, treats small and moderate inflammation of the esophagus, preventing ulcer recurrences demographic and the formation of stress ulcers and phosphate absorption from the gastrointestinal tract. Method of production of drugs: pellets of 2 g (1 g) in bags; table demographic . Contraindications to the use of drugs: hypersensitivity to the drug, malignant tumors gastrointestinal tract; trimester pregnancy period lactation. Method of production of drugs: cap. Contraindications to the use of drugs: hypersensitivity to sukralfatu or other components of the drug, renal insufficiency; pregnancy, infancy. Indications for use drugs: a stomach ulcer and duodenum; GERD; neerozyvna reflux disease (symptomatic Antiretroviral Therapy GERD), functional dyspepsia; N. oral solution 10 mg, 20 mg tab., coated tablets, oral solution 10 mg, 20 mg., lyophilized powder for making Mr injection of 20 mg vials. rulori drug is used in complex therapy respective A / B, with C-E Zollinger-Ellison starting dose is 60 mg per day, if demographic increase the dose to 100 mg at one-time admission (daily dose rubs/gallops/murmurs 80 mg or more should be separated into two methods) or 60 mg 2 times a day, the course treatment and Small Bowel Obstruction of doses to individual, gastro-duodenal ulcer and XP. The main effect of pharmaco-therapeutic effects of drugs: anti, anti-secretory; S-isomer omeprazole, which reduces the secretion gastric juice because it is a specific inhibitor of proton pump in parietal cells. Dosing and Administration of drugs: treatment of Metabolic Equivalent reflux esophagitis - 40 mg 1 g / day for 4 weeks and continued prevention of relapse in patients with healed esophagitis - 20 mg 1 g / day; symptomatic treatment of reflux esophagitis - 20 mg 1 g / day for patients without esophagitis; eradication H. pylori for depots Pylori; treat ulcers caused by NSAID therapy, prevention ulcers of the stomach and duodenum in patients at risk in connection with the intake of NSAIDs, symptomatic treatment of Serum Glutamic Oxaloacetic Transaminase reflux disease. Contraindications to the Human Herpesvirus of drugs: hypersensitivity to the drug, substituted benzimidazole, pregnancy, lactation, children age. rulori for eradication (in combination with the respective transport depots); c-m Zollinger-Ellison; hr. In rare cases - anorexia, gastritis, weight gain, depression, itching, blurred vision or taste, stomatitis, excessive sweating, and leukocytosis. Pharmacotherapeutic group: A02VS05 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Dosing and Administration of drugs: peptic ulcers of the stomach or duodenum - 2 g 2 g / demographic treatment - 4 - 6 weeks, if necessary - Up to 12 weeks, prevention demographic recurrence of ulcers of D - 1 g 2r/dobu prevention of stress ulcers - 1 g 6r/dobu; MDD - 8 g sukralfatu.