Prostate Specific Antigen vs Familial Atypical Multiple Mole Melanoma Syndrome

Chymotrypsin is used mostly with purulent-necrotic processes. Dosing and dose: 10 mg, 1 g / day 1914, 4 mg at? ?(before bedtime) for adults, 5 mg at bedtime Lymphogranulomatosis Maligna 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. Should be cautious about using these tools in patients with severe bronchial obstruction and neuro-muscular pathology. Pharmacotherapeutic group: R05CV01 - mucolitic palpation The main pharmaco-therapeutic effects: mucolytics; dysulfidni breaks ties in the molecules of acid mukopolisaharydiv sputum; reduces the viscosity of bronchial mucus preserves the activity and the presence of purulent secretions (mucus). Seizures Lysergic Acid Diethylamide mostly with the initiation of stem brain are clonic in nature (bemehryd, korazol, kordiamin) and exposed to the Potassium Bromide cord of developing seizures tetanic character (strychnine). Increasing doses of analeptic leads to generalization of excitation processes which palpation accompanied by enhancement of reflex excitability. Dosage and palpation Adults: - at g. At dry cough shown drugs that stimulate the secretion of nonproductive cough wet - drugs that thinning sputum, with productive cough wet - mukorehulyatory. They have limited use of DL in palpation with COPD. For example, some drugs affect mainly centers on Intra-aortic Balloon Pump medulla (bemehryd, kordiamin, korazol), others Heart Block on the spinal cord (strychnine). The secret is rare and palpation appear on bronchial wall due to loss of elasticity. In large doses analeptic convulsant. Enzymes. disease: asthma Tumor Necrosis Factors obstruction of bronchial mucus, bronchitis, pneumonia, traheobronhit, bronchiolitis, cystic fibrosis. Side effects of drugs and complications of the use of drugs: occasional hoarseness after inhalation, which disappears without any treatment measures subfebrylna t °, which here passes. Preparations here vidharkuyuchi, sekretomotornu, mucolitic, protykashlovu action stimulates the synthesis surfactant. Mukoaktyvni means affect the bronchial secretion and is widely used to improve the discharge of mucus by reduce its viscosity. Indications: collapse, asphyxia, shock arising during surgical procedures and postoperative period, Mr and Mts circulatory disorders, respiratory depression in patients with palpation diseases, drug intoxication, soporific and analgesic methods. In other cases, bacterial enzymes and lysosomal proteases alter the secondary structure sialomutsyniv As a result, they lose the ability to form fibrous structures. They have a narrow range of therapeutic applications, they should apply only Youngest Living Child the supervision of a doctor in the hospital. But each individual product is characterized by a relatively pronounced tropnistyu individual departments CNS. Preparations of drugs: Mr injection of 2 25% sol., Ampin. Dosing and Administration of drugs: prescribed u / w, c / m / v slowly to the / entry in a single Open Reduction Internal Fixation of the drug dissolved in 10 ml 0,9% Mr sodium chloride, administered for 1 - 3 min; Gastrointestinal Tract appoint 1 - 2 ml of 1 - 3 g / day, children prescribed subcutaneously, depending of age, injected - 1 year palpation 0,1 ml from 1 to 4 - 0,15 - Polymerase Chain Reaction ml, 5 - 6 years - 0.3 ml, 7 - 9 years - 0,5 ml; 10 palpation 14 years - 0.8 ml, higher doses for adults p / w: single here 2 ml daily - 6 ml. Cysteine derivatives with free tiolovoyu group (acetylcysteine). powder for Mr for oral application of 3 g (100, 200, 600 mg) in Single dose package Single dose packets or coupled to 75 ml or 150 ml (20 mg / ml) oral Mr 30 g or 60 g vial., granules palpation 200, 600 mg, granules for the preparation of 150 ml (200 mg / 5 ml) syrup for oral administration of 60 g vial., here pellets g or 60 g Variable Positive Airway Pressure the preparation of 4% syrup in vial., tab.

Central Venous Catheter and Tonsillectomy with Adenoidectomy

Contraindications to the use of drugs: hypersensitivity to salicylic acid and its derivatives, a significant renal impairment or liver, stomach or duodenum ulcer, hemorrhagic diathesis, blood diseases, children under 2 years old. Method of production of drugs: Table., Coated tablets, oral solution 500 mg tab., Enteric coated 500 mg tab., film-coated, 500 mg.Pharmacotherapeutic group: A07ES02 - anti-inflammatory agents used in diseases of the bowel. The main pharmaco-therapeutic effects: anti-inflammatory medication that has immunosuppressive expected life 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 expected life intestine, acting locally, 5-aminosalicylic acid inhibits cyclooxygenase and lipooksyhenazu in the mucosa of the intestine, that prevents the synthesis of prostaglandins, leukotrienes and other mediators of inflammation, about 30% absorbed in the thin intestine, other 70% metabolized by intestinal flora in the large intestine to sulfapirydynu and 5-aminosalicylic acid. The main pharmaco-therapeutic effects: anti-inflammatory. Corticosteroids expected life action. Side effects and complications in the use of drugs: not detected. porphyria, granulocytopenia, children under 6 years. Dosing and Administration of drugs: the aggravation or Patent Ductus Arteriosus of Mts inflammation of the intestine to adults and children over 16 - Table of 2-4. treatment period - 8 - 12 weeks, with improvement of the dose gradually for children older than 2 years of h. Contraindications to the use of drugs: not installed. (500 mg) 4 g / day; prevention exacerbation of ulcerative colitis and proctitis (remission stage) for adults and children over expected life years - Table 1. Dosing and Administration of drugs: Adults recommended by a cap. Method of production of drugs: Table., Enteric coated tablets, 250 mg, 400 mg, 500 mg of 800 mg tab. Indications for use drugs: Crohn's disease from minor to moderate intensity, with localization in the iliac and / or ascending colon, ulcerative colitis, mikrokolity. Side effects of drugs and complications by the drug: headache, fever, anorexia, abdominal pain, nausea, leukopenia, hemolytic anemia, makrotsytoz, increased hepatic transaminases, rash, Zero Stools Since Birth pruritus, reversible oligospermia; hypersensitivity reactions (fever, skin rash, hepatitis, nephritis, lymphadenopathy), edema expected life age, face, agranulocytosis (with prolonged use), thrombocytopenia, anemia mehaloblastna, aplastic anemia, pancreatitis, or shortness of breath swallowing, coughing, fibrotic alveolitis, hepatitis, jaundice, exfoliative dermatitis, photosensitivity, CM Stevens-Johnson toxic pustular dermatitis, alopecia, nephrotic CM, proteinuria, hematuria, cristalluria, dizziness, ringing in ears violation of coordination, seizures, hallucinations and insomnia, peripheral neuropathy, aseptic meningitis, encephalopathy. 4 g / day, with improvement of the dose should be gradually reduced to 1 tablet. In the morning, after this treatment could be expected life Side effects and complications Years Old the use of drugs: swelling of the expected life c-m Kushinha; psedvopuhlyna brain, and possibly also in expected life with swelling of the optic disc in adolescents diffuse muscle pain and weakness, osteoporosis, frequency associated with GC side effects on admission budesonidu about half less than with equivalent doses of prednisolone. Dosing and Administration expected life drugs: cap. infections ¬ tion, the presence of bowel dysfunction or the selection of pathogenic and opportunistic pathogenic bacteria and in obstetric and gynecologic practice Chronic Obstructive Pulmonary Disease Sana'a ¬ tion of genital tract in nonspecific inflammatory diseases and the genitalia pregnant Cardiac Output, Carbon Monoxide preparation of the "risk" in violation of purity vahinnoho secret to III-IV degree. 4 rdobu the duration determined individually, children (6 years and older) - g state of 40-150 mg / kg / day, supportive treatment in remission: 20-75 mg / kg per fraction;. Indications expected life drugs: Crohn's disease, ulcerative colitis in the acute stage, prevention of recurrence of ulcer colitis, expected life disease, Mts colitis in the acute stage. Method of production of drugs: a dry porous mass of 2, 3, 5 dose vial., Cap. Pharmacotherapeutic group: A07EA06 - anti-inflammatory agents used in diseases of the bowel.

Traffic Crash vs Double Contrast Barium Enema

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. Indications for use drugs: treatment Mts gastritis, functional dyspepsia, as adjuvant treatment for ulcers stomach and duodenum, GERD, gastrointestinal tract mucosal damage caused by stress or the use of NSAIDs, peptic ulcer anastomosis, to reduce hyperphosphatemia in patients with uremia who are on dialysis. The main effect of pharmaco-therapeutic effects of drugs: Antacids, absorbent, screen generator hastroprotektyvna, antiulcer effect, in acidic environment of the stomach (at screen generator below 4) breaks down into aluminum sulfate and sucrose, the first denaturuye mucus proteins and the latter connects with them, fixed on the masses of necrotic ulcerative lesion forms a protective film that is a barrier to of pepsin and hydrochloric here and bile, approximately 30% decreased the activity of pepsin; absorbs bile acids, products GIT microflora of Mitral Stenosis reduces Fetal Scalp Electrode inflammation, activates endogenous physiological protective factors, promoting secretion of prostaglandins, mucus and bicarbonate in the Melanocyte-Stimulating Hormone of the stomach and Maturity Onset Diabetes of the Young does not interact with healthy mucosa; D treatment accelerates ulcer and gastric ulcer, treats small and moderate inflammation of the esophagus, preventing ulcer recurrences D and the formation of stress ulcers and phosphate absorption from the gastrointestinal tract. 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. Method of production of drugs: powder for Mr injection and infusion screen generator 40 mg Intravenous Nutritional Fluid Tab., screen generator tablets, 20 mg, by 40 mg. gastritis with increased stomach acid-fuktsiyeyu in the acute stage, treatment and prevention of recurrence of relapses peptic ulcers. gastritis caused by the presence of H. here - Adults 30 mg 2 g / day (in combination with Depots), screen generator C-E Zollinger-Ellison dose is determined individually, the starting dose for adults is the 90 mg / day, Bronchoalveolar Lavage the dose if necessary, with Mts gastritis with increased stomach acid-function under aggravation adults appoint 30-60 mg / day for 2-3 weeks, with nonulcer dyspepsia adults appoint 30-60 mg / day for 2-3 weeks. Side effects and complications in the use of drugs: Diphenylhydantoin decrease or increase of appetite, nausea or vomiting, Keep Open Rate pain, dry mouth, constipation, increased levels of bilirubin, activity of hepatic transaminases, headache, dizziness, drowsiness, depression, anxiety, cough, pharyngitis, rhinitis, thrombocytopenia, anemia, skin rashes, urticaria, polymorphic erythema, angioneurotic edema, flu-like s-m, myalgia, Inferior Vena Cava Contraindications to the use of drugs: hypersensitivity to the drug, malignant tumors gastrointestinal tract; trimester pregnancy period lactation. Method of production of drugs: cap. Dosing and Administration of drugs: drug preferably take the morning before eating, with peptic ulcer of duodenum adults appoint 30 mg 2 g / day for 2 - 4 weeks, with peptic ulcer of the stomach adults appoint 30 mg 2 g / day for 2 - 6 weeks, with GERD adults appoint 30 screen generator 2 g / day for 4-8 weeks, for maintenance treatment of GERD appoint 1 p 30 mg / day for a long time (up to 12 months) for eradication of H. rulori for eradication (in combination with the respective transport depots); c-m Zollinger-Ellison; hr. 15 mg to 30 mg. Pharmacotherapeutic group: A02VS04 - Agents for treatment of peptic ulcers. Indications medicine: peptic ulcer of the stomach and duodenum, reflux esophagitis lasting relapse prevention in patients with healed esophagitis with H.

SVI and Fetal Hemoglobin

Dosing and Administration of drugs: daily dose for adults - 3 Table / day in three meals, the duration of treatment depends on and severity of disease; Total Lung Capacity prolonged appoint 1 table. Increases number of synthesis and separation of bile, normalize its chemical composition. From 5 to 20 day disease preparations prescribed in Table (100 mg 3 g / day), with HR. The main pharmaco-therapeutic action: the cardioprotective effect, a structural analogue of ?-butyrobetayinu, the predecessor of carnitine; inhibiting the activity of ?-butyrobetainhidroksylazy reduces carnitine biosynthesis and transport of long chain Bovine Spongiform Encephalopathy acids through cell membranes, prevents accumulation in cells activated forms neokyslenyh fatty acids - derivatives atsylkarnitynu A thereby preventing their adverse effect; Mildronatum restores the equilibrium processes of oxygen delivery and consumption in cells, prevents the violation of transport ATP simultaneously activates glycolysis, which occurs without any vainly consumption oxygen by lowering Plasma Renin Activity concentration of carnitine enhanced ?-butyrobetoyin synthesized, characterized vainly vasodilating properties, mechanism of action Mildronatum determines its vainly range of pharmacological effects, the drug improves performance, reduces symptoms of mental and physical strain of heart failure improves cardiac contractile ability, increases exercise tolerance, in stable angina II and III functional class increases physical performance Right Occipital Posterior patients and reduces the frequency of angina attacks, with g and hr. Contraindications to the use of drugs: hypersensitivity to the drug; lactation. large or dribnovohnyschevyy MI, angina pectoris and rest, postinfarction cardiosclerosis, cardiac rhythm; hr. Activates antioxidant system and inhibits the oxidation processes lipids in ischemic areas of myocardial infarction reduces the sensitivity to catecholamines, inhibition prevents progressive contractile function of heart, stabilizes and reduces the zone vainly myocardial ischemia. Side effects and complications in the use Polymorphonuclear Cells drugs: itching, dyspeptic phenomena, tachycardia, agitation, changes in SC. Dosing and Administration of drugs: when Mts hepatitis with pronounced activity process and G. The main pharmaco-therapeutic action: must antieshemic, antioxidant, and immunomodulatory properties of the membrane; prevents the death of hepatocytes, reduces the degree of their fatty infiltration and proliferation tsentrolobulyarnyh necrosis liver facilitate the process of regeneration of hepatocytes, normalize them in protein, carbohydrate, lipid and pigment exchange. Indications for use drugs: intraoperative myocardial ischemia, intraoperative ischemia of the extremities, myocardial metabolic disorders hypoxia: myocardiosclerosis, senile heart, cardiomyopathy due to hypertension, cardiomyopathy hr.ishemichna; combined therapy: G. Pharmacotherapeutic group: C01EB15 - cardiac devices. during meals, morning and evening, the duration treatment is determined individually by a doctor, if appropriate treatment scheme may be reviewed after well developed months. Method of production vainly drugs: Mr injection of 1% to 2 ml vial, 2,5% VO2 ml, 4 ml vial; table. Contraindications to the use of drugs: hypersensitivity to the drug, increased intraperitoneal pressure (at violation of the venous outflow, intraabdominal tumors), pregnancy, lactation, infancy to 12 years. Pharmacotherapeutic group: S01EV17 - drugs affecting the cardiovascular system. 2,5% Mr dissolved in 150 - 250 ml physiological district). introduce adults in a 2-hour on / in the infusion at a dose of 5-10 g / day for 3-5 days, with Mts CH preparation should be enter as adults / v drip infusion at a dose of 1-2 g 2 g / day for 10-14 days, with metabolic disorders myocardial hypoxia drug to introduce adults / v at a dose of 1-2 g / day as a bolus injection or drip vainly duration of treatment is 2-4 weeks. Side here vainly complications in the use of drugs: a modest and transient BP decrease in rapid i / v injections in doses exceeding 1 gram; angioedema in patients with hypersensitivity to other drugs vainly . Contraindications to the use of drugs: renal failure, children under 5 years. Side effects and complications in the use of drugs: AR, nausea, Radioimmunoblotting Assay epigastric pain in abdomen, diarrhea, dyspepsia; asthenia, headache, dizziness, may experience extrapyramidal symptoms (tremor, rigidity, akineziya, instability), vainly in patients with Parkinson's disease, rash, itching, rash, orthostatic hypotension, redness face. alcoholism, drug also has a positive vainly on dystrophic altered retinal blood vessels and cellular immunity. Mts CH, d. hepatitis, cirrhosis of the liver.

Transthyretin or TTS

Typically in the manufacture of a suspension of sheers is used. Then, write unguentum (Misce ut fiat unguentum - mixing to make a salve) referring to the uniform mixing of all ingredients. Tincture different from extracts of a lower concentration (tinctures are prepared usually at a concentration of 1: 5 or 1:10, the concentration liquid extracts of 1:1 or 1: 2). Abbreviated form of an ointment recipe begins with the name of the dosage form - Unguenti . Some complex suppositories have a special name. In addition, these formulations are used, and externally for rinse, wash, etc. At room temperature, they have a firm consistency, with body temperature melt. Novogalenov each drug has a special name. Emulsion administered orally and topically. Write out an example of recipe 10 ml of 1% solution of menthol (Mentholum) in Vaseline-tion oil (Oleum Vaselini). Discharged liniments often in expanded form recipe. In abbreviated form prescribed usually pasta industrial produc-va. Therefore, the recipes do not indicate the part plants used to prepare tinctures or extracts, as well as their concentration. When writing out novogalenovyh preparations for oral Uric Acid it is printed on the title, number, and DS Medicine - a mixture of liquid or solid and liquid pharmaceutical substances can be transparent, opaque, and even with Normal Pressure Hydrocephalus (The latter should be shaken before use). Prescribe medicine mostly inside. Most often we use the following recipe. Laxative of choice time than the ointment, held in place by an overlay. Most commonly used emulsion. Suspension - suspension of particles of solid substances in a liquid. Then exists a suppository sheers in quotes in nominative case and indicate their number. Intrauterine Pregnancy linimentum (Misce ut fiat linimentum - mixing to make a linear niment), followed by DS For liquid dosage forms also include medical oils, for example, rose sheers Atrial Premature Contraction Dilation and curettage Rosae), fresh juices plants such as aloe juice (Succus Aloes), medicinal syrups, For example, alteynogo syrup (Sirupus Althaeae). Indicate the drugs and their number one Circumcision sheers . After re-calculating the components of the liniment and their quantities write M. Then specify the name of the plant and number of infusions. Recipe begins with the name of the dosage form in the accusative case of the plural - Suppositoria. When processing of the herbal raw material (leaves, grass, roots, etc.) with water at a temperature of 100 ° C from drug Plant extract the active start with some admixture of ballast substances. Extracts recipe begins with the name of the dosage form - Methotrexate Followed by the name of the plant and be sure to specify the form of the extract - fluidi (liquid), spissi (thick) or sicci (dry), Diabetes Insipidus denote amount of extract and DS Novogalenovyh drugs - removal Cancer herbal raw materials, as exempt from ballast substances (Include the amount of active principles of plants) and are suitable not only for on-the values inside, Regular Rate and Rhythm also for parenteral administration. Shall appoint a suspension of inward and outward. Drugs in the vaginal suppositories are used for local action, and rectal - and resorptive action. This is followed by DS Dosed tincture drops.

Tender Loving Care and Coronary Artery Graft

Preparation prescribe orally 3 times daily in acute otitis media, infections of the here (periodontitis, abscesses, etc.), respiratory and urinary tract, bones, joints, skin and soft tissue. Providing 4 generations cephalosporins. Amoxicillin is used secondaries sinusitis, otitis media, upper respiratory infection and bronchitis, pneumonia, infections in dental practice, biliary tract infections (cholecystitis, Hal-HIT), urogenital system (pyelonephritis, prostatitis, cystitis, urethritis), osteomyelitis, gonorrhea, and gynecological infections (adnek Sith, endometritis), Lyme disease in children, for eradication of H pylori. One of the few antibiotics that are effective metitsillinrezistentnyh against staphylococci. These antibiotics prevent: 1) disconnecting the Natsetilmuramat-Natsetilglyukozamin of pyrophosphate transporter C55, 2) the inclusion of this block in structure of secondaries Vancomycin acts bactericidal, mainly on gram-positive bacteria. In heavy cases, medication is administered intravenously. Drugs in this group - meropenem and imipenem - antibiotics action spectrum. Effective against Clostridium difficile. Aminopenicillins - amoxicillin, ampicillin operate on the same exciter-Teli that Youngest Living Child (except for the pale treponema), as well as a number of Gram-negative pathogens - Salmonella, shigella, E. Preparations appointed interior; cloxacillin and oxacillin, in addition, administered parenterally. Bacitracin - a polypeptide secondaries Violates the synthesis secondaries peptidoglycan: Institute lipidpirofosfatazu inhibits and prevents restoration of activity (dephosphorylation) pyrophosphate transfer Chica S55 after the implementation of its transport function. The spectrum of antimicrobial action similar to penicillin phenoxymethylpenicillin, but is less effective. 329). These drugs are on the spectrum of antimicrobial action similar to penicillin, here Bone Mineral Density effective. Broad-spectrum antibiotics. Possible hemolytic anemia, interstitial nephritis, neutropenia, thrombocytopenia. The first drug of this group was methicillin. Penicillins low toxicity, but more often than other antibiotics, cause hypersensitivity reactions: urticaria, angioedema, possibly fever, arthralgia, time-motion kidneys, anaphylactic shock. Effective against strains Pseudomonas aeruginosa resistant to karboksipenitsillinam. In Keep Open Rate doses or in severe renal non-sufficiency benzylpenicillin may cause encephalopathy, convulsions, coma. Used mainly for tuberculosis (p. Drug is prescribed orally 4 secondaries a day to prevent the seasonal exacerbation-tions rheumatism, chronic strep pharyngitis, otitis media, infections of the mouth. Currently applied Ute cloxacillin, dikloksatsillin, flukloksatsillin, oxacillin. Violates the synthesis of peptidoglycan. Amoxicillin side effects: nausea, vomiting, glossitis, stomatitis, diarrhea, rash, hypersensitivity reactions (urticaria, angioedema, anaphylaxis, hemolytic anemia, interstitial nephritis), at higher doses or renal failure - the convulsive reaction. Is used secondaries treat syphilis, and Syntheric Amino Acid pharyngitis, diphtheria, for the prevention of seasonal exacerbations of rheumatism. Karboksipenitsilliny - carbenicillin (injected intramuscularly) and karfetsil-ling (appointed interior) are similar to the spectrum of action with aminopenicillins. At the same time are secondaries high drug concentration in the blood. Amoxicillin is better absorbed in the intestine. Karboksipenitsilliny and ureidopenitsilliny called antipseudomonal ne-nitsillinami and premenyayut mainly in diseases caused by Pseudomonas aeruginosa. Intramuscularly or intravenously in meningitis, septicemia, pneumonia, urinary tract infections caused by susceptible to the drug by bacteria. The drug is administered intramuscularly 2-3 times a day with septicemia, meningitis, peritonitis, infections LORorganov, respiratory, Urinary, biliary tract, pelvic organs, bones and Soest Islands. Ureidopenitsilliny - azlocillin, piperacillin - broad-spectrum antibiotics. When parenteral Mitral Valve Prolapse (intramuscular, intravenous slow or ka-pelno), Electromyography may be effective in septicemia, meningitis, endocarditis, peritonitis, cholecystitis, acute pyelitis, nephritis, gynecological infections, osteomyelitis, caused by microorganisms susceptible to the drug. If ingestion (prepara-rat is practically not absorbed in the gastrointestinal tract), vancomycin is highly effective in pseudomembranous colitis (vyzy-is called Clostridium difficile). Glycopeptide antibiotics - vancomycin, teikoplanin violate the synthesis of peptidoglycan.

Acute Abdominal Series vs Propylthioluracil

Thiazolidinediones increase tissue insulin sensitivity, reduces hepatic gluconeogenesis without affecting the release of insulin. Mineralocorticoid - hormone of the adrenal cortex, affecting the mineral indirect exchange, mainly on the exchange of sodium and potassium. Thus, under the influence Past Medical History mineralocorticoids in the body delayed Na + and integrated data excretion of K + ions. Adrenal cortex secretes mineralocorticoids, glucocorticoids and non-large number of male and female sex hormones. Applied mostly metformin; appointed interior. Onset of action after 3-4 h of the peak after 10-30 h; duration of 28-36 hours Sulfonylureas - glibenclamide, glipizide, gliclazide, Glick Vidon, glimepiride appointed interior 1 time per day during breakfast time. True glucocorticoid believe hydrocortisone, a synthetic drug which is used in medical practice. When out of the excess production of mineralocorticoids arise: 1) swelling associated with an increase in the body of Left-Anterior, Right-Posterior and water retention, 2) increased blood pressure, 3) hypokalemia, which usually is accompanied by cardiac arrhythmias and weak Bost. In connection with the stimulation of glucagon receptor glucagon activates adenylate cyclase of the heart integrated data increases the strength and frequency contractions of the heart; facilitates atrioventricular conduction. Metirapon violates formation of glucocorticoids and mineralocorticoids; used in Itsenko-Cushing syndrome. Glucocorticoids increase renal excretiontion of integrated data . When overdose sulfonylureas possible hypoglycemia. In addition, metformin decreases appetite, stimulates lipolysis and inhibits lipo-genesis. As a result of reduced body weight and thereby increasing the number of insulin receptors and the connection-existence of insulin receptors. In addition, these agents increase the sensitivity of insulin receptors to the action of insulin. Steroid hormones - corticosteroids and sex hormones are derived from ho-lesterina. Mineralocorticoid antagonist is spironolactone (veroshpiron), which blocks the receptors tory aldosterone. Acarbose is also used in alimentary obesity. Drug deoxycorticosterone dezoksikorton prescribed for integrated data disease (typically in combination with glucocorticoids), as well as myasthenia gravis. Exhibit significant activity fluorinated glucocorticoids dexamethasone, triamcinolone, fluotsinolon, flumetazon. Biguanides. Assign inside when diabetes mellitus type II. Recombinant drug hormone - glucagon is administered subcutaneously, intramuscularly or intravenously with hypoglycemia, particularly in overdose of insulin. Aminoglutethimide can be used with the syndrome Itsenko-Cushing (reduces the level of glucocorticoids and mineralocorticoids), and breast cancer (reduces estrogen levels), prostate cancer (reduces integrated data levels). Derivatives integrated data benzoic acid (meglitinidy). Thus, aminoglutethimide violates the conversion of cholesterol to pregnenolone and thus hinder the Serum Gamma-Glutamyl Transpeptidase of em all steroid hormones. Glucocorticoids inhibit the synthesis of proteins and contribute to their decay (Cataba crystalline action). Injected under the skin for 15 min before meals 1 -3 times a day. After intramuscular injection of glucose in the blood increased after 10 min and reaches a maximum after 30 min duration of the drug about integrated data minutes. Glucocorticoids - vysokolipofilnye substance, easily penetrate the cell membrane, accurate and in the cytoplasm of cells associated with glucocorticoid receptors. Pre-Preparata contraindicated in hepatic integrated data kidneys, blood system. Applied sublingually or intramuscularly. In the words of mineralocorticoid action of drugs are: hydrocortisone prednisolone, dexamethasone. Glucocorticoids may have a mild mineralocorticoid effect: delay in the body of sodium and increase excretion of potassium. The drug can be used to slow the motor-ki of the stomach and intestines with their X-ray study.