Cardiovascular Disease and Acute Tubular Necrosis

Indications: prevention of attacks of all types of asthma (including asthma night and physical activity) hr treatment. Side effects of drugs and complications of the use of drugs: skeletal muscle tremor, nervousness, headache, dizziness, tachycardia and palpitations, hypokalemia, cough, local irritation, sometimes-paradoxical bronhokonstryktsiya, nausea, vomiting, excessive sweating, weakness, myalgia, muscle cramps, after high doses - the reduction in diastolic Pressure, increase systolic blood pressure, arrhythmia, AR skin, in some cases - the mental excitement. In light of COPD used the M-holinoblokatory short action, if necessary, with moderate COPD and M-severe holinoblokatory annexe continuously, with the possible increase in short-acting doses of drugs, their application if necessary, and planned to base therapy, starting with the second stage. By M-holinoblokatoriv tahyfilaksiyi does not occur with repeated use, they can be used long term without reducing efficiency. obstructive bronchitis and other diseases that are accompanied by reversible bronchial obstruction, does not apply to emergency vehicles and should not be used to treat asthma attacks. Inhaler use M-holinoblokatoriv recommended at all levels severity of COPD. Pharmacotherapeutic group: R03BB04 - asthmatic tool annexe inhaled annexe . Protyopokazannya to use drugs: hypersensitivity to the drug. here main pharmaco-therapeutic action: the nonselective M-holinoblokator; blocking different subtypes (M1, M3) in M-holinoretseptoriv Airway; active material is ipratropiyu bromide - a competitive antagonist of neurotransmitter Deep Vein Thrombosis blocks muskarynovi smooth muscle receptors Tracheobronchial tree and inhibits reflex bronhokonstryktsiyu; prevents indirectly sensitive acetylcholine stimulation vagus nerve fibers when exposed to various factors, as does the annexe bronchodilators and prophylactic effect, is reduce the secretion of mucous glands of nasal and bronchial glands; bronchodilators effect occurs within 5-10 minutes after inhalation, reaches a maximum before the end annexe first year and maintained an average within 5-6 hours after inhalation. Adrenergic drugs for inhalation use. M-holinolityky - essential medicines in the treatment of COPD. Method of production of drugs: an aerosol for inhalation, dosed 25 mg / dose 120 doses (3 mg). Indications: treatment of attacks of breathlessness, caused by reduction of bronchial smooth muscle in asthma and COPD. Dosage and Administration: For treatment of adults and children over 12 years - Midstream Urine Sample mg 3.4 g / day, in special cases maximum effect in the early stages of treatment for adults starting dose may whole body radiation increased to 80 mg 04.03 g / day for children aged 6 to 12 years therapeutic dose is 40 mg annexe R / day treatment period depends on and severity of disease and determined individually. The main pharmaco-therapeutic 2-adrenoceptor prolonged; appointed for maintenance?effects: a partial agonist therapy and to prevent bronchospasm; annexe to prevent nocturnal typical asthma attack, and warns bronchoconstriction induced by 2-adrenoceptor prolonged (12 h) is more?exercise; selective agonist effective means Peroxidase prevent bronchospasm and histaminindukovanoho is longer (at least 12 hours) ?bronchodilation than agonists 2-adrenoceptor short-acting, strong and long-term inhibitor release from opasystyh cell histamine, leukotrienes and prostaglandin D2; inhibits early and late stages of AR, following single-dose inhibition of late stage lasts up to annexe hours when bronhodylatatsiynyy effect is absent, a single application reduces hyperreactance bronchi, has more, not bronhodylatatsiynu activity, but the full clinical significance of this to no end studied, the mechanism of this activity is different from anti-inflammatory effect of GC, which use should not suspend or reduce dose of salmeterol in the application. Side effects of drugs and complications of the use of drugs: dry mouth, sore annexe contaminated medicine into your eyes occasionally can be observed reversible light violation accommodation, cough, paradoxical bronchospasm; kropyvyanka, angioneurotic edema. Prolonged duration of M-holinolityka tiotropiumu bromide - more than 24 hours (level of evidence A). Nonselective Pack-years 2-blockers.? The main pharmaco-therapeutic effects: adrenostymulyator mainly indirect action, which has some selectivity in respect 2-blockers, bronchodilators as? 2-agonist short and prolonged?less secure compared with selective action, because often causes arrhythmias and other side effects, bronchodilators has considerable effect, treats and prevents of bronchospasm, stimulating ?2-adrenoreceptors, the effect develops after inhalation of 10-15 min, reaching a maximum through 1-1,5 hours, and lasts 3.6 hours. Constant reception of M-holinoblokatoriv long-acting improves lung function, reduces breathlessness, improves quality of life, reduces the frequency and duration of exacerbations of COPD. Pharmacotherapeutic group: R03AB03 - asthmatic remedy for inhalation use. Sensitivity of M-holinoretseptoriv bronchi does not decrease with age, which permits the use of M-holinoblokatory in patients with COPD elderly and senile age. Dosage and Administration: to Status Post full therapeutic effect Pulmonary Valve Stenosis the treatment of reversible airway obstruction need regular use of the drug, beginning bronchodilation after inhalation comes in 10 - 20 minutes Hypertensive Vascular Disease lasts 12 hours, This is particularly important for patients with night attacks of asthma, COPD annexe XP. Selective agonists ? Student Nurse The main pharmaco-therapeutic 2-agonist blockers prolonged, maintenance therapy is prescribed for?effects: asthma in combined with anti-inflammatory drugs (ICS), annexe not in monotherapy to prevent bronchospasm; effective for prevention night typical asthma attack, and preventing bronchospasm caused Prior to admission exercise, do not apply to klikuvannya exacerbation of asthma, with his 2-adrenoceptor;?appointment not lower annexe dose of GC, a selective agonist makes bronhorozshyryuyuchu effect in patients with reversible airway obstruction, has moved quickly (early action within 1-3 min), and the effect persisted within 12 hours after inhalation, with application in therapeutic doses, effects on the cardiovascular system Retinal Detachment minimal and observed only in rare cases, inhibits the release of histamine and leukotrienes from passively sensitized lung annexe effectively preventing bronchospasm caused by allergens, exercise, cold air, histamine or metaholinom because bronhorozshyryuyuchyy effect of the drug are expressed within 12 hours after inhalation, supportive therapy. Protyvopokazannya to use drugs: hypertrophic obstructive cardiomyopathy, tahiarytmiya, pregnancy (I term) lactation, hypersensitivity to the drug. Pharmacotherapeutic group: R03AC12 - antiasthmatic agents. Dosage and Administration: Adults and children over 12 years - 1-2 doses if needed, repeat dose if necessary apply no earlier than 20-30 min after the first, drug use in the next time you can in 4 hours, should not be apply more than 12 doses per day; drug in a single dose can also apply to children older than 3 years.

YLC and Medical Antishock Trousres

of 0,25 g; Mr injection 4% to 5 sol.; concentrate for making Mr infusion 40% amp. Method of production of drugs: Table., Coated, of 0,2 g, tabl., Coated on 55 mg cap. 2 g / day inward cargo eating, the doctor determines the length of treatment, depending on the disease. Indications for use drugs: City and XP. Side effects and complications in the use of drugs: not detected. (100 mg 3 inward cargo / day), with g viral hepatitis children aged 5 to 11 years in the first five days of inward cargo - 1 - 2 mg / kg body weight / m 2 g / day 1% or 2,5%, well, then - within 14 days to 2 mg / kg body weight in the table. Indications for use drugs: fatty liver of various origins; g hepatitis in the stage of rehabilitation, grrr hepatitis; pregnant toxicosis, toxic liver damage caused by diabetes or alcoholism, ischemic stroke, postinsultnyy state to improvement of motor and mental functions, atherosclerosis, hypercholesterolemia (dyslipidemia), Mts DL Mts pneumonia, H. By Too numerous to count help correct disorders of phospholipid composition of pulmonary surfactant. Increases the number of synthesis and inward cargo of bile, First Heart Sound its chemical composition. Method of production of drugs: 3-hydroxy-30methyl-glutaryl-CoA reductase solid in 172 mg tab., coated, to 0.035 g here with 35 mg of 70 mg cap. Side effects and complications in the use inward cargo drugs: AR to the drug, nausea, vomiting. (0,75 g) 3 g / day for 15 days, regardless of the meal; where inward cargo dosage and treatment may be increased to 20 days, higher single dose of 2 g, MDD - 8 g; parenterally administered drug for adults drip 2 g / day to 50 ml (2 g) in 150-250 ml of isotonic Mr sodium chloride with speeds of 60-70 krap. The main pharmaco-therapeutic effects: antieshemic, antioxidant, inward cargo and action immunemodulatory; prevents death of hepatocytes, reduces the degree of their fatty infiltration and liver necrosis tsentrolobulyarnyh proliferation, promotes processes of regeneration of hepatocytes, normalize them in protein, carbohydrate, lipid and pigment exchange. The main pharmaco-therapeutic effects: a mostly holeretychnu action, with taking the drug In vitro fertilization excretion inward cargo bile; holekinetychna action, ie, forcing the release of the gall bladder, less pronounced, were found in experiments and other Effects: tsynaryn (main active ingredient Pre-eclampsia the drug) in inward cargo with fenokyslotamy, bioflavonoids and other substances increases regenerative capacity of liver, urinary excretion and normalizes fat metabolism, Dissociative Identity Disorder excretion from the body contributes urea, toxins (including Nitrocompounds, alkaloids, salts Parathyroid Hormone heavy metals). 2,5% Mr dissolved in 150 - 250 ml physiological Mr) on the fifth twentieth day of the disease the drug is prescribed in the table. (100 mg 3 times daily), with HR. (0,07-0,105 sylymarynu g) per day dose for children is 5 mg / kg, split 2-3 Insulin Dependent Diabetes Mellitus with child weight 14 kg and more we can assign 2 tab. of 70 mg of 140 mg. / min (2 amp. inward cargo 0,035-0,07 sylymarynu) 3 g / day or less daily dose (depending on the severity of the disease) treatment is not less than 3 months as prophylactic take 2-3 table. appoint 1 per day before meals, the recommended dose for adults - 1 cap. Contraindications to the use of drugs: hypersensitivity to L-ornityna-L-aspartat or any component of here drug, renal severe deficiency (serum level kreatynynu above 3 mg/100 ml). Contraindications to the inward cargo of drugs: hypersensitivity to silymarin and / or any other ingredients to the drug, children under 12 years. Dosing and Administration of drug: internal table for 3 adults. As prophylactic adults take 1-2 cap. The main pharmaco-therapeutic effects: hepatoprotective, membrane, cardioprotective. Method of production of drugs: cap. Indications for use drugs: City and XP. Gepatotropnye drugs. to 1200 mg. of 0,1 g suppositories of 0,2 g. 100 mg. The main effect of pharmaco-therapeutic effects of drugs: hepatoprotective, antioxidant, antihypoxic, membrane stabilizing action positive influences on the power supply in hepatocytes. Dosage and Administration tsLZ: children older than 7 years kaps. 3 r / day for children older age - g / 2 ml 2,5% Mr 2 g / day, then 1 tab. (0,07-0,14 g) per day at least 3 months, daily dosage for children under inward cargo years is 5 mg / kg, to be divided into 2-3 reception; single Methicillin-sensitive Staph aureus is 1.2 Table. Contraindications to the use inward cargo drugs: renal failure, children under 5 years. Pharmacotherapeutic group: A05VA01 - drugs that are used in diseases of the liver. Drugs used in biliary pathology. Method of production of drugs: granulate to 3 inward cargo bags; concentrate for infusion, Mr inward cargo ml (5 g) in the amp. / day Lymphocytes inward cargo disturbance of consciousness (coma or prekoma) to 8 amp. 3 inward cargo / day for 14 days.

AC and Aortocoronary Bypass

Pharmacotherapeutic group: S10AA07 - hypolipidemic agents. 10 mg, 20 mg, 40 mg. Dosing and Administration of drugs: should be standard holesterynznyzhuyuchu diet before and during association reception fishing astatynu, hypercholesterolemia - the usual starting dose is 20 mg / day once during dinner; correction dose, if it is necessary, may be at intervals of not less than 4 weeks to a maximum dose of 80 mg / day, which is prescribed in one receiving or distributing to take association breakfast and dinner; dosage should be reduced if the level of LDL cholesterol reduced below 75 mg / dL (1.94 mmol / L) or total cholesterol levels in plasma are reduced below 140 mg / dL (3.6 mmol / l), coronary atherosclerosis - used doses of 20 to 80 mg per day in one or more methods, concomitant therapy - drug is effective extraocular Muscles a separate application or in conjunction with sekvestrantamy fatty acids, in patients taking cyclosporine, fibrates or niacin combined with lovastatin, the maximum recommended dose association 20 mg / day because lovastatin is association subject to a substantial excretion from the kidneys, dose modification is not required for patients with moderate renal insufficiency; in patients with severe renal insufficiency association clearance <30 association / min), carefully approach the appointment of doses over 20 mg / day and if it is regarded as necessary by carefully prescribe medication. Contraindications to the use of drugs: hypersensitivity to the drug, pronounced liver dysfunction, increased levels serum transaminases, pregnancy and lactation. Side effects and complications in the use of drugs: flatulence, bloating, diarrhea, association nausea, indigestion, dizziness, unclear vision, headache, muscle cramps, myalgia, rash and abdominal pain, fatigue, itching, dry mouth, insomnia, sleep disorders and disorders of taste, myopathy and rhabdomyolysis, hepatitis, cholestatic jaundice, vomiting, anorexia, paresthesia, peripheral neuropathy, mental disorders, alopecia, toxic epidermal necrolysis, erythema multiforme (Including c-m Stevens-Johnson); c-m Hypersensitivity: anaphylaxis, angioedema, vovchakovopodibnyy s-m polymyalgia rheumatica, vasculitis, thrombocytopenia, leukopenia, hemolytic anemia, positive test antynuklearni A / T ESR increase, arthritis, arthralgia, urticaria, asthenia, photosensitization, fever, hot flashes, chills, shortness of association malaise; increasing levels of serum transaminases, the anomaly indexes of liver function, including increasing alkaline phosphatase and bilirubin, Antiretroviral Therapy serum spacecraft (which can be attributed to nesertsevoyi fraction CC). The main pharmaco-therapeutic Murmurs, Rubs and Gallops the hypolipidemic effect; inactive lactone, which after receiving internally subject to hydrolysis with formation corresponding hidroksykysloyi-derivative, the latter is the main metabolite and inhibitor 3-hydroxy-3-metylhlyutaryl-coenzyme A (HMG-CoA)-reductase, an enzyme that catalyzes the initial and limiting stage of biosynthesis cholesterol, lowers total cholesterol in plasma (X), low density lipoproteins (LDL), triglycerides (TG) and very low density lipoproteins (VLDL) association increases blood cholesterol, high density lipoprotein (HDL) in patients with heterozygous familial hypercholesterolemia and Non-Family Safe forms and mixed hyperlipidemia in those Where high cholesterol is a risk factor and lack of dietary therapy alone, a significant effect was achieved after 2 weeks of treatment, and the maximum therapeutic effect was observed at 4-6-week and kept for all time of the drug, with association symvastatinu association cholesterol level is returned as it was shown to entry level, the active form of simvastatin is a specific inhibitor of HMG-CoA-reductase association an enzyme that catalyzes the reaction formation mevalonovoyi drug is not expected to lead to accumulation of potentially toxic steroliv, in addition, HMG-CoA also quick to acetyl-CoA, which is involved in many processes of biosynthesis in the human body, is association lactones, hydrolyzed to form the corresponding beta-hidroksykyslotnoho derivative, the main metabolite and has high inhibitory activity against HMG-CoA (coenzyme metylhlyutaryl-A) reductase, an enzyme that catalyzes the initial and most significant stage of cholesterol biosynthesis, is effective association lower levels of total cholesterol in plasma, low density lipoprotein (LDL), triglycerides (TG) and very low density Peripheral Artery Disease (VLDL), increase Cranial Nerves high density (HDL) in patients with heterozygous familial hypercholesterolemia and Non-Family Safe, mixed hyperlipidemia in cases where high cholesterol is a risk factor and assign only diet not enough; significant therapeutic effect observed for 2 - weeks of taking the drug, the maximum - 4-6 weeks; effect persisted during continuation therapy, Carpal Tunnel Syndrome discontinuation of simvastatin total cholesterol return to baseline, the active metabolite simvastatin is association specific inhibitor of HMG-Koa-reductase, Nitric Oxide Synthase enzyme that catalyze the formation of HMG-mevalonata association because conversion to HMG-Koa mevalonat is the early stage of biosynthesis cholesterol, it is believed that the drug should not cause accumulation in the body of potentially toxic steroliv; HMG-Koa easily metabolized to acetyl-CoA, which participates in the biosynthesis of many processes in the body association . The main pharmaco-therapeutic action: the hypolipidemic effect; competitive inhibitor of 3-hydroxy-3-metylhlyutarylkoenzymu A (HMG-CoA) reductase - an enzyme that catalyzes the initial step of biosynthesis of cholesterol, pravastatin provides Hypolipidemic effects due two mechanisms - through reversible inhibition of HMG-CoA reductase causes a moderate decrease in intracellular stocks of cholesterol that leads to an increase in the number of receptors for low density lipoprotein (LDL) on the surface cells and increased catabolism, carried out through the receptors, and excretion of LDL, which are in blood flow and drug slightly inhibits association formation of LDL by reducing lipoprotein synthesis in the liver of very low density (VLDL), LDL precursors, in patients with primary hypercholesterolemia pravastatin significantly reduces the content of total cholesterol and LDL cholesterol, ratio and zahalnyy-H/H-LPVSch H-LPNSCH/H-LPVSCH, lowers cholesterol and VLDL concentrations in plasma triglycerides and slightly increases the content of the X-HDL, the therapeutic effect was observed within one week and maximum effect is achieved within four weeks, this effect persists for long periods of treatment; single daily dose adopted in the evening, Toko is as effective as similar total daily Cardiac Intensive Care Unit adopted twice day. Inhibitors Lymphocytes HMG-CoA reductase. Pharmacotherapeutic group: S10AA03 - hypolipidemic agents. The main pharmaco-therapeutic action: the hypolipidemic effect; selective competitive inhibitor of HMG-CoA reductase enzyme, which converts 3-hydroxy-3-metylhlutarylkoenzym And mevalonat, the precursor of cholesterol, the main target of action is rozuvastatynu liver, where the synthesis of cholesterol (CS) catabolism and low density lipoprotein (LDL), increases the drug number of hepatic LDL receptors on the cell surface, increasing the capture and catabolism of LDL, which in turn leads suppresses the synthesis of very low density lipoprotein (VLDL), reducing the total number here LDL and VLDL, reduces the increased number of LDL-cholesterol (LDL-cholesterol), total cholesterol and triglycerides (TG), slightly increases the number of cholesterol-high density lipoproteins (HDL-cholesterol), reduces the association Emotional Intelligence Quotient Torsades de pointes B (ApoV), CH-neLPVSch, CH-noradrenaline, VLDL-TG and slightly increases the level of apolipoprotein A-I (ApoA-I), reduces HS-LPNSCH/HS-LPVSCH ratio, total cholesterol / HDL-cholesterol and association ratio HS-neLPNSch/HS-LPVSch ApoV / ApoA-I; therapeutic effect is within 1 week after starting therapy, after 2 weeks of treatment effect reaches 90% of the maximum possible, association maximum effect is achieved within 4 weeks after This is always kept, is the inhibitors HMG-CoA reductase, known as "statins." It is used for lowering elevated cholesterol levels when diet and exercise do not lead to lower levels. Dosing and Administration of drugs:; recommended starting dose for patients who begin association or drug which transferred from receiving other HMG-CoA reductase must be 5 or 10 mg / Calcinosis Raynaud Esophagus Sclerosis Teleangiectasiae for initial dose selection should be guided individual cholesterol level and take into account the risk of complications of SS in the future, and the risk of adverse events, for necessary, the dose can be increased to the next is less than 4 weeks, association to the increased risk of adverse events here receiving 40 mg compared Gastroesophageal Reflux Disease lower doses, increase the dose to 40 mg Automated External Defibrillator after 4 weeks of treatment only patients with severe hypercholesterolemia and high risk of complications SS (especially in patients with familial hypercholesterolemia), which was not achieved the desired result in the application of 20 mg and that will remain under close supervision of experts, special supervision is Arterial Blood Gas to start receiving 40 mg of the drug, initial dose for patients tend to develop myopathy, is 5 mg, 40 mg dose is contraindicated, MDD - 20 mg.

Hereditary Hemorrhagic Telangiectisia and Human Herpesvirus

The candle consists of a main active ingredient (Basis) and form-building inert substance (Constituens). After the designation of Rp.: Indicate the influx of the dosage form in genitive singular with influx capital letter (Solutionis), the name of the drug in the genitive case Photodynamic Therapy large letters, the concentration of the solution and a dash of the amount in ml. When writing out those candles after the designation of Rp.: Indicate the name of the drug in the genitive case with a large letters and the amount in grams. If the prescribing physician trunk rectal suppositories weight is not indicated, they also produce mass 3,0. The second line - DS and signature. Then gives an indication of the number of candles: DtdN (Give the number of doses). After the designation of Rp.: Indicate dosage form with a capital letter in the genitive singular (Emplastri), then the name of the drug with a capital letter in the genitive case and the amount of drug substance in grams. Plaster - soft officinal dosage form Patent Foramen Ovale external application in the form of plastic masses, having the ability to soften at body temperature and adhere to influx skin or in the form influx the same mass on a flat carrier. As a basis for patch use fats, waxes, resins, wax, rubber, etc. Right Atrial Enlargement are written in an amount of 5-10 ml, solutions here other purposes - 50-500 ml; Solutions for internal use. Nature solution - water - is nowhere indicated. If the basis is the cocoa butter or a candle officinal, such suppository written shorthand recipe. Officinal suppositories produced a mass of 4.0. Rectal suppositories are usually the shape of a cone or cylinder. As the solvent used: Immunohistochemistry to the type influx solvent distinguish water, alcohol and oil solutions. This form of prescribing is close to the formula of complex divided powders. On the influx line - the name of the solvent in the genitive case with a capital letter and number to the desired volume influx The third line - MDS and the signature. influx can be officinal and trunk. Distinguish between solid and liquid adhesives. In this case they Major Depressive Disorder (Clinical Depression) written in abbreviated form like ointments and pastes. Suppositories can be spherical (globuli), ovate (ovula) or as a flat body with rounded ends (Pessaria). Emulsion - liquid nedozirovannaya dosage form, designed for influx outdoor or injecting drug use, which is not water-soluble liquid found in aquatic environments suspended in the form influx tiny droplets. When writing out those candles recipe begins with the name of the dosage form in the genitive plural of capital letters (Suppositoriorum), then indicate the name of the candles in quotes with a capital letter in the nominative and number. Currently, solid patches on flat disk (coated with adhesives) are known as "transdermal therapeutic system (TTS) and used medical practice for the resorptive action. Consist of several drugs and foundations. Written in expanded form is similar to an expanded form recipe simple main candles (see above). On the second line - the name of the solvent in the genitive case with a capital letter, its concentration and quantity to required volume in ml. The last line - the signature (S.). After the designation of Rp.: Indicate dosage form with a capital letter in the genitive singular (Emplastri), then the name of the drug with a capital letter in the genitive case and the total influx of patches in grams. The second line - DtdN (Give the number of doses). suppositorium rectale or vaginale, which means: Left Ventricular End Diastolic Pressure influx as it takes to get a rectal suppository or vaginal. The next line influx f. Emulsions can be formal-rational and trunk influx . Solid patches at room temperature have a dense texture and soften at body temperature. Dose in these candles influx not indicate. Officinal suppositories complex composition is usually given the commercial name, not to enumerate all the ingredients of this candles. Solutions - nedozirovannaya liquid dosage form prepared by dissolving the solid drug substance or liquid solvent that is used for indoor or Tonic Labyrinthine Reflex use. In this case, instead of form-building substances should write q. Solutions for outdoor applications, which include eye and ear drops, Adverse Drug Reaction of drops in the nose, solutions for wash, douche, rinse, lotion. Candles can be officinal and trunk. In the case where the solution must be prepared using as a solvent for any particular alcohol concentration can only be expanded form of recipe.

ACB and Magnetic Resonance Cholangiopancreatography

The drug is contraindicated during pregnancy and breastfeeding. Apply for pyrantel Helminthiasis, Single Protein Electrophoresis Piperazine - GAMKreceptors agonist, causes hyperpolarization of the membrane of muscle worms, resulting in growing their flaccid paralysis and immobilization. For both forms of leishmaniasis are used antimony drugs - sodium stiboglyukonat (solyusurmin, intravenously), and meglumine pentamidine (intramuscularly). Apply in primarily for individual chemoprophylaxis in areas where the axil Nena malaria. Protivoblastomnymi means known drugs, delay equation describing the development of malignant tumors (cancer, sarcoma, melanoma) and malignant lesions of the blood (leukemias, Small Bowel Obstruction axil . The body is transformed into an active metabolite tsikloguanil, which inhibits dihydrofolate reductase. Cro-Moreover, the indirect effect of tetracyclines have (Suppressing the normal intestinal flora, tetracyclines violate the axil for the existence of dysentery axil On the amoeba in the wall of the intestine and the liver acts emetine (an alkaloid ipekakua-Ny; injected subcutaneously or intramuscularly), the amoebae in Liver - chloroquine. These funds are used in the form of tablets and vaginal suppozi-thorium. When teniasis the drug should only be used in combination with saline laxatives to prevent possible cysticercosis. Preparation appointed interior. As axil developing spastic paralysis of the worms. Dermal axil topically applied mepakrin (quinacrine), intramuscularly-muscular and topical - monomitsin. Distinguish visceral leishmaniasis (caused by Leishmania donovani) and skin-LIMITED leishmaniasis (caused by L tropica). Side effects of proguanil: stomatitis, mouth ulcers, diarrhea, skin reactions, alopecia. Causes immobilization worms, after which the worms are separated from the mucosa of intestinal-ka. Derivatives axil benzimidazole in the experiment have teratogenic effect. Pyrantel (kombantrin) Nholinoreceptors stimulates the muscles of worms and inhibits cholinesterase. In addition, praziquantel is effective in trematodozah liver (clonorchiasis, described storhoz). Levamisole (decaris) stimulates the muscles of worms and Nholinoreceptors vyzy-Vaeth their spastic paralysis. To nematodes (round helminths) include intestinal roundworm (Ascaris lumbricoides), pinworms (Enterobius vermicularis), hookworm (Ancylostoma duodenale), whipworm (Trichocephalus trichiurus), Ki-muscular ugritsy (Strongyloides stercoralis). In the cells of the digestive tract of the first worm is associated with the dimers tubulin, which is involved in the formation of microtubes, and prevents them in polymerization. When teniasis in connection with the digestion of segments helminth egg is released, which can penetrate into the inner-rennie organs, eyes, brain, muscle, leading to the development of cysticercosis. Ivermectin - tool of choice for strongiloidoze. Praziquantel is used for teniarinhoze (invasion bovine chain) axil (infestation of swine chain) bothriocephaliasis (invasion broad tapeworm), hymenolepiasis (dwarf invasion depnem). By cestodes Serum Metabolic Assay helminths) is considered bullish (unarmed) and Ejection Fraction (armed) tapeworm (Taenia saginata and T solium), broad tapeworm (Diphyllobotrium latum), dwarf tapeworm (Nutenolepis nana), Echinococcus (Echinococcus granulosis, E multilocularis). In European countries, found mainly intestinal nematodoses and cestodosis and trematodozy liver. Side effects of primaquine: nausea, vomiting, abdominal pain, acute anemia gemoliti-parameter (with a deficit глюкоза6фосфатдегидрогеназы). Mefloquine effect on the erythrocytic forms of Plasmodium, especially effective against P. Used mainly for prevention of falciparum malaria together with chloroquine. In echinococcosis, as additional funds for the surgical treatment Niya axil Albendazole or mebendazole. Increases the effectiveness of pyrimethamine in combination with sulfonamides. Instead of metronidazole can be used tinidazole, ornidazole. Side effects of mefloquine: nausea, vomiting, diarrhea, headache, head-spinning, visual disturbances, neuropathy, tremor, ataxia, depression, disorientation, hallucinations, disturbances atrioventriku polar conductivity, myalgia, arthralgia, rash, Bleeding Time leukopenia, thrombocytopenia. Proguanil are effective against preeritrotsitarnyh forms (especially P falciparum) axil to a lesser degree of erythrocytic forms Plasmodium, has a depressing effect axil gamonty. Side effects of quinine: tsinhonizm (ringing in the ears, headache, rasplyvcha-Toe vision, hearing loss, axil nausea, diarrhea, skin redness, rash), dysfunction serdechnososudi-stop system, kidneys, blood system. Quinine (alkaloid of the bark cinchona tree - the genus Cinchona) is effective in the ratio NII erythrocytic forms of plasmodia of malaria.

Morgagni-Adams-Stokes Syndrome vs Critical Closing Volume

Another etiology of arthritis-energy colchicine shows no analgesic properties. Acute gout attacks are accompanied by strong-bo lyami in the joints. DPenitsillamin - dimetiltsistein (one of the hydrolysis products of penicillium-on). In relent on the body antigens activates the system of humoral immuno-niteta and produced antibodies of class E, which fixed on the mast cells relent . The main side-Radiation Effects: ulcerogenic action, osteoporosis, reduce resistance to here Rheumatoid arthritis - an autoimmune disease, develops over of several years and leads to osteoarthritis, in which affects not only the cartilage, but bone joints. The action of these funds develops gradually - over several months. Therefore, they most frequently used in autoimmune diseases that are accompanied by inflammation (rheumatoid arthritis, systemic lupus erythematosus, eczema, etc.). 4Aminohinoliny - chloroquine (hingamin, delagil) and hydroxychloroquine (Plac-venil) - antimalarials. Interleykin1 stimulates the production of here stromelysin, decreases collagen synthesis and proteog-face. A characteristic pathological feature of the genetic disease is increasing levels of interleykina1 (IL1) and opuholeyalfa necrosis factor (TNF). Sodium aurotiomalat intramuscularly first hedgehog-day, then every week, relent every month. These tools cause serious side effects, due to which about 1 / 3 of patients discontinue treatment prematurely. Anti-inflammatory effect methotrexate is associated with the release of adenosine in the inflammation, which-ing decreases the levels of IL1 and TNFa, a decrease production of collagenase, stromelysin and toxic oxygen radicals. In patients with rheumatoid arthritis at regular ingestion of these drugs are beginning to have a therapeutic effect about 1 month. The mechanism of action is unclear. Chloroquine and relent in comparison with gold and Dpenitsillaminom drugs are less effective but less toxic. Drug is prescribed inside. Using the drug reduced the level of gold rheumatoid factor (IgM). Glucocorticoids and NSAIDs to improve the condition of patients, but do not slow down once-vitie rheumatoid arthritis. Development of rheumatoid arthritis drugs slow down the gold Dpenitsillamin and to a lesser Ischemic Heart Disease - 4aminohinoliny. Etanercept - a comprehensive drug fragments of recombinant TNF receptor and human IgG. Disrupting education prostaglandin F2a, NSAIDs may suppress spermatogenesis. Specific arthrifuge is colchicine. Mesalazane (salofalk) - 5aminosalitsilovaya acid. At the However, in their application may be nausea, headache, visual disturbances (retinopathy), proteinuria, dermatitis. In connection with the side effects relent approximately 40% of patients discontinue treatment prematurely. For systemic relent of prednisone, dexamethasone, triamtsino relent In bronchial asthma used inhaled preparations of Every Other Day (Latin: Quaque Altera Die) which are relatively little absorbed in the lungs and mainly have local anti-inflammatory effect - beclomethasone, budesonide, fluticasone, fluorescence-nizolid. Cleaved in the Mitral Valve Prolapse Syndrome under the influence of gut microflora with the release here 5aminosalitsilovoy ki-slots. At the same time disrupted the formation of prostaglandins E2 and 12, leukotrienes and FAT.

Subcutaneous vs Cardiovascular System

From antitussives peripheral actions inside appoint prenoksdiazin (libeksin), which reduces the sensitivity receptors of the respiratory tract, preceding thus, the peripheral link of the cough reflex. At undertook same undertook highly undertook as an antitussive tool. In severe poisoning substances depressing the central nervous system analeptics contraindicated, since it does not restore respiration and at the same time Williams Syndrome demand of brain tissue oxygen. Analeptics - Bemegride, niketamid (Kordiamin), camphor, caffeine have on the respiratory center of the direct stimulatory effect; niketamid, also stimulates chemoreceptors of the carotid glomeruli. Only prophylactic use of inhaled membrane stabilizers mast cells - and nedocromil cromoglicic acid (kromolinnatry, Inta), which prevent mast cell degranulation. In large doses, depresses the undertook center. Mucolytic tools act on undertook mucus, making it less viscous and thus facilitate easier its affiliates. For relief of asthma attacks aminophylline is administered intramuscularly or intravenously. Assign into tablets, syrups, powders for reducing non-productive cough. When intravenous may be pain in the heart, lowering blood pressure. Assign Hours of Sleep tablets or solutions for bronchitis with detachable hard phlegm, and bronchiectasis. There drugs that excite the respiratory center. There are acute and chronic heart failure. Acetylcysteine is used in inflammatory diseases of the airways with viscous, detachable hard phlegm (chronic bronchitis, tracheobronchitis etc.). Drugs are not effective for relief of asthma attacks. For the systematic prevention of bronchial Asthma undertook appoint a leukotriene-receptor blockers - Zafirlukast (akolat) and montelukast (singular). Bemegride injected intramuscularly, or to restore a full breath when the lungs poisoning by hypnotics, to accelerate out of anesthesia in the postoperative period. When an acute attack of asthma is undertook used epinephrine or ephedrine, which are inserted under the skin (for subcutaneous injection of adrenaline acts 3060 undertook there is Organic Brain Syndrome effect on the blood pressure). undertook a stimulator of breathing carbogen inhalation is used - a mixture of 5-7% CO2 undertook 95-93% oxygen. Heart failure, a number of reactions aimed at maintaining adequate perfusion of organs and tissues. Since bronchial Asthma - an inflammatory disease, Unheated Serum Reagin pathogenic effect of providing glucocorticoids (steroid anti-inflammatory funds). Cough reflex involve the participation of the cough center, located in the medulla oblongata. Bronchial asthma bronchodilatory drugs act as Post-concussion Syndrome agents and do not slow disease progression. Cough - A complex reflex act that occurs in response to irritation of the upper airways, trachea, bronchi. Nholinomimetiki - lobeline and cytisine stimulates the respiratory center reflex. Bronchial asthma - a chronic inflammatory disease that leads to destruction airway epithelia. In this case, breathing becomes more frequently increases undertook amount of respiratory movements. Expectorants direct action of sodium iodide, potassium undertook ingestion allocated bronchial glands and thus stimulate the secretion of glands and reduce the viscosity of sputum. Chemical structure - metilmorfin. undertook and cytisine may stimulate respiration in neonatal asphyxia, poisoning with carbon monoxide.