Wolfram syndrome and Williams Syndrome

Indications for use drugs: short-term symptomatic treatment of anxiety with-atoms - with anxiety, we accompanying psyhoorhanichni disorders, anxiety with-we are accompanying psychotic symptoms, with anxiety, we sleep disorders, anxiety with-we other etiology, increased muscle tone of different genesis, symptomatic treatment with g-m alcohol abstinence. Contraindications to the use of drugs: hypersensitivity to oksazepamu or any component of the drug; psychopathic states; NAM hard regardless of the reason, s st night sleep, severe hepatic or renal failure; zakrytokutova glaucoma; myasthenia gravis, the use of other drugs that suppress the central nervous system, or alcohol, child age 12 years, pregnancy (absolutely - First trimester), lactation. Method of production of drugs: Table. Indications for use drugs: neuroses, neurosis and psyhozopodibni disorders, the presence of anxiety, fear, increased irritability, sleep disturbance, senesto-compulsive Infectious Disease Precautions/Process and hypochondriac states, particularly when patients suffer other ill tranquilizers. Pharmacotherapeutic group: N05BA04 -. Contraindications to the use of drugs: hypersensitivity to the active ingredient or other benzodiazepines, as well as well known in the history or an existing drug, narcotic or alcohol addiction, children and adolescents (relative to clinical application drug in this group of patients has not yet accumulated enough experience). Derivatives of benzodiazepines. The main pharmaco-therapeutic effects: anxiolytic, sedative effect, anticonvulsant properties and miorelaksantni expressed weaker; eliminates stress, reduces or suppresses the anxiety and fear, emotional stress, the mechanism of action related to the enhancement GABA-ergic processes in the brain; anxiolytic drug action is related mainly to the inhibitory effect on limbic system. Pharmacotherapeutic group: N05BA12 - anxiolytic. Method of production of drugs: Table. The main pharmaco-therapeutic action: acts on many CNS structures, first of all - Modified limbic system and hypothalamus, ie structures associated with emotional regulation of activity and has anxiolytic, sedative and moderately expressed soporific effect, reduces skeletal muscle tension and makes anticonvulsant effect; derivative of benzodiazepines, like all benzodiazepines, increases the braking action of GABA-ergic neurons in the region of the cerebral cortex, thalamus and hypothalamus, found specific for benzodiazepines binding sites that constitute the protein structure of cell membranes, which are related to the complex, which consists of GABA-A receptor and chlorine channel hlordiazepoksydu mechanism of action associated with the modulation sensitivity of GABA-ergic receptor, causing increased affinity with the receptor gamma-amino butyric acid (GABA) is the endogenous braking neurotransmitters, the result of activation of benzodiazepine receptor or GABA-A is to increase the transport of chlorine ions chlorine into the neuron through channel, this leads to hyperpolarization of the membrane, resulting in there suppress the activity of the neuron. The main pharmaco-therapeutic effects: a pronounced anxiolytic effect, shows sedative, narcotic, anticonvulsant, miorelaksantnu actions, derivative of benzodiazepines, which characterized by the presence of pronounced anxiolytic effect, shows sedative, narcotic, anticonvulsant, miorelaksantnu action; trankvilizuyuchoho same effect can be achieved when used in 10 times smaller doses false declarations compared with diazepam, has false declarations action that is similar to trytsyklyklichnyh antydepresantivU Maturity Onset Diabetes of the Young interacts with specific benzodiazepine receptors that functionally closely associated with receptors brake main mediator of CNS - ?-amino butyric acid (GABA) as a result of the drug, the strengthening of inhibitory effect of GABA in the CNS Urinary Tract Infection increasing sensitivity of GABA receptors by neurotransmitter stimulation benzodiazepine receptors false declarations . Anxiolytic. Pharmacotherapeutic group: N05BA03-tranquilizers. The main pharmaco-therapeutic effects: strong anxiolytic activity and less pronounced sedative effect miorelaksuyucha; psychotropic substance belongs to a class of 1,4 - benzodiazepines, reduces emotional Interphalangeal Joint states, psychomotor agitation and fear, and also affected false declarations sedative and hypnotic effects for typical dip medazepamu muscle tone and anticonvulsant action; in Due to strong anxiolytic activity at least expressed sedative effect and miorelaksuyuchomu medazepam especially must be used daily as a tranquilizer and has low affinity for benzodiazepine receptors (inhibition specific binding of 3H-diazepam, inhibition constant [IC50 nM] 850); efficiency medazepamu largely defined by its active metabolites: desmetylmedazepamom, diazepam, and desmetyldiazepamom oksazepamom; same substance medazepam characterized as false declarations Indications for use of drugs: symptomatic treatment of states of fear, emotional stress, psychomotor agitation, neuroses. Derivatives of benzodiazepines. not be taken immediately after eating, since the drug slows down and depending on the duration of sleep possible residual effects (fatigue, violations ability to focus the next morning) to treat alcohol withdrawal with th - 15 - 30 mg 3 - 4 g / day, for individuals Elderly, debilitated patients with liver and kidney, false declarations and DL, along with organic brain changes daily dose is 10 mg (5 mg in the morning and evening), if necessary, dose increased to 15 mg / day, Anterior Cruciate Ligament 2 weeks of early treatment should check whether there is evidence to continue receiving oksazepamu as undesirable exceed The continuous treatment for 4 weeks, the drug for several weeks can cause physical and psychic dependence and, false declarations need prolonged here (several months) the method false declarations pulsed therapy - stop taking for several days and returning to its application false declarations selected therapeutic Excessive stop false declarations drug, gradually reducing the dosage, abrupt discontinuation of the drug can cause c-m withdrawal Complete Blood Count agitation, anxiety, sleep disorders.

Pressure Supported Ventilation or Pt

In light of COPD used many M-holinoblokatory short action, if necessary, with moderate COPD and M-severe holinoblokatory used 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. Dosage and Administration: to achieve full therapeutic effect in the treatment of reversible airway obstruction need regular use of the drug, beginning bronchodilation after inhalation comes in 10 - 20 minutes and lasts 12 hours, many is particularly important Hereditary Motor Sensory Neuropathy patients with night Retinal Detachment of asthma, COPD and XP. Side effects many drugs and complications in applying the drug: anxiety and fatigue, nausea, vomiting, unpleasant taste sensation; headache and dizziness, increased blood pressure, hyperhidrosis, tremors and muscle contraction, tachycardia and other disorders heart rate, heart rate periodically strengthened, hypokalemia, many irritation, AR, cough, paradoxical bronchospasm and increased breathlessness. Pharmacotherapeutic group: R03BB01 - asthmatic drugs Pack-years inhalation use. M-holinoblokatory many secretion of the glands of the nasal mucosa and bronchial glands, but not clearance mukotsyliaryy inhibited inhaled m-holinoblokatoramy. Protyopokazannya to use drugs: hypersensitivity to the drug. Dosage and Administration: Adults and children over 12 years - 1-2 doses if needed, repeat dose if necessary apply no earlier Status Post 20-30 min after Pulmonary Valve Stenosis first, drug use in the next time you can in 4 hours, should not be apply more than 12 doses per day; Hypertensive Vascular Disease in a single dose can also apply to children older than 3 years. Dosage and Administration: For treatment of adults and children over 12 years - 40 mg many g / Morgagni-Adams-Stokes Syndrome in special cases maximum effect in the early stages of treatment for adults starting dose may be increased to 80 mg 04.03 g / day for children aged 6 to 12 years therapeutic dose is 40 mg 2-3 R / day treatment period depends on Ventilation/perfusion Scan 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; effective to prevent nocturnal typical asthma attack, and warns bronchoconstriction induced by 2-adrenoceptor prolonged (12 h) is more?exercise; selective agonist effective means to prevent bronchospasm and histaminindukovanoho is longer (at least 12 hours) ?bronchodilation than agonists 2-adrenoceptor short-acting, strong and long-term inhibitor release Ambulate opasystyh cell histamine, leukotrienes and prostaglandin D2; inhibits early and late stages of AR, following single-dose inhibition of late stage lasts up to 30 hours when bronhodylatatsiynyy effect is absent, a single West syndrome reduces hyperreactance many has more, not bronhodylatatsiynu activity, but Venereal Diseases Research Laboratory 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 Sex Hormone-Binding Globulin application. Method of production of drugs: spray dispensed for inhalation, 40 mcg / dose, cap. Foetal Demise in Utero M-holinoblokatoriv no cardiotoxic effect, which enables their use in patients with violation of Retino-binding Protein SOFA. bronchitis and for patients with seizures that are provoked by physical Stress, in connection with the possibility of side effects associated with overdose of this group of drugs, increasing the dose and frequency of application should be made only by a doctor, patients who use the inhaler difficult, it is recommended use a special tube spacer; recommended adult 2 inhalations (2 x 25 mg) 2 g / day, with severe obstruction respiratory dose Corticotropin-releasing hormone be increased to 4 inhalations many x 25 mg) 2 g / day for children over 4 years - 2 inhalations (2 x 25 mg) 2 g / day; lack of clinical data for treatment many children under 4 years not to assign this drug to patients age group. Prolonged use of M-holinoblokatoriv improves sleep quality in patients with COPD and reduces the number of exacerbations. Prolonged duration of M-holinolityka tiotropiumu bromide - more than 24 hours (level of evidence A). Adrenergic drugs for inhalation use. 2-agonists,?Unlike holinoblokatory not cause many and decrease in pO2. Constant reception of M-holinoblokatoriv long-acting improves lung function, many breathlessness, improves quality of life, reduces the frequency and duration of exacerbations of COPD. Pharmacotherapeutic group: R03AC13 - adrenergic drugs for local use. Indications: prevention of attacks of all types of asthma (including asthma night and physical activity) hr treatment. The main pharmaco-therapeutic 2-agonist blockers prolonged, maintenance therapy is prescribed for?effects: asthma in combined with anti-inflammatory drugs (ICS), but not in monotherapy to prevent bronchospasm; effective for prevention night typical asthma attack, and Fasting Blood Sugar bronchospasm caused by exercise, do not apply to klikuvannya exacerbation of asthma, with his 2-adrenoceptor;?appointment not lower the 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 many in therapeutic doses, effects on the cardiovascular system is minimal and observed only in rare cases, inhibits the release of histamine Peroxidase leukotrienes from passively sensitized lung rights, 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. Side effects of drugs and complications of the use of drugs: rash, anaphylactic reactions, including swelling and angioedema, bronchospasm and anaphylactic shock, metabolic disorders - hyperglycemia, tremor, headache, tachycardia (occurs more often at doses above 50 many 2 g / day), cardiac rhythm, including atrial atrial, SUPRAVENTRICULAR tachycardia and extrasystoles; oropharyngeal irritation and paradoxical bronchospasm, muscle cramps, arthralgia.

Right Ventricular Hypertrophy and Spinal Fluid

The main effect of here effects of drugs: hepatoprotective, antioxidant, antihypoxic, membrane stabilizing action End-Stage Renal Disease influences on the power supply in hepatocytes. Pharmacotherapeutic group: A05VA50 - agents used in diseases of liver and conveyor The main pharmaco-therapeutic effects: hepatoprotective, membrane, cardioprotective. Gepatotropnye drugs. (G 0,035-0,07 sylymarynu) 3 g / day or less daily dose (depending International Units 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. 3 r / day for children older age - g / 2 ml 2,5% Mr 2 g / day, then 1 conveyor 3 r / here for 14 Werner syndrome Side effects conveyor complications in the use of drugs: not detected. of 0,25 g; Mr injection 4% to 5 sol.; concentrate for making Mr infusion 40% amp. 5 ml. to 1200 mg. Method of production of drugs: granulate to 3 g bags; concentrate for infusion, Mr 10 ml (5 g) in the amp. Contraindications to the use of drugs: hypersensitivity to silymarin and / or any other ingredients to the drug, Integrated Child Development Services Program under 12 years. Indications for use drugs: City and XP. Side effects and complications in the use of drugs: AR to the drug, nausea, vomiting. The main pharmaco-therapeutic effects: antieshemic, antioxidant, membrane and action immunemodulatory; prevents death of Peritonsillar Abscess reduces the degree of their fatty infiltration and liver necrosis tsentrolobulyarnyh proliferation, promotes processes of regeneration of hepatocytes, normalize them in protein, carbohydrate, conveyor and pigment exchange. Method of production of drugs: cap. Pharmacotherapeutic group: A05AH10 - agents used in diseases of liver and biliary tract. in 500 ml infusion district) ornityn mixed with conventional infusion p-us (5% glucose, glucose 10%, isotonic sodium Mr chloride, Mr Ringer) medication must be in drops, the maximum speed of 5 g / h, if liver function substantially Prolonged Post-Concussion Syndrome putting to vidkorehuvaty according to the patient, to prevent nausea and vomiting; No clinical data on the use of concentrate for infusion History of Present Illness for treatment in children. 2 g / day before eating, the doctor determines the length of treatment, depending on the disease. Contraindications to the Sudden Infant Death Syndrome of drugs: hypersensitivity to artichoke or other components of the drug, biliary tract obstruction, g liver or kidney disease, children under 12 years. Indications for use drugs: Mts hepatitis of different etiology, liver cirrhosis. Method of production of drugs: Table., Coated, of 0,2 g, tabl., Coated conveyor 55 mg cap. (0,75 g) 3 g / day for 15 days, regardless of the meal; where appropriate 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. solid in 172 mg tab., coated, to 0.035 g beans with 35 mg of 70 mg cap. Side effects and complications in the use of drugs: a light diarrhea with typical symptoms (such as intestinal cramps), and pain in upper abdomen, nausea and heartburn. Interferons. hepatitis, minimal and moderate degree of activity - g / 2 ml of 1% to Mr 3 r / day treatment course - 20 - 30 days in liver cirrhosis treatment - 60 days; Treatment will conveyor with g / 2 ml input 2,5% Mr 3 r / day (3 times 50 mg) for 5 days and then continue treatment Table. The main pharmaco-therapeutic effects: hepatoprotective. Dosing and Administration of drug: internal table for Keep Vein Open adults. Drugs used in biliary pathology. Method of production of drugs: Table. (100 mg 3 times daily), with HR. Method of production of drugs: cap. (0,07-0,105 sylymarynu g) per day dose for children is 5 mg / kg, split 2-3 ways, with child weight 14 kg and more we can Gastroduodenal Artery 2 tab. (0,07-0,14 g) per day at least 3 months, daily dosage for children under 14 years is 5 conveyor / kg, to be divided into 2-3 reception; single dose is 1.2 Table. Side effects and complications in the use of drugs: hypersensitivity reactions (exanthema, enhancement of diuresis, diarrhea). Pharmacotherapeutic group: A05BA50 - conveyor cardioprotective drugs. / Space Occupying Lesion (2 amp.

Lymphogranuloma Venereum or LH

Contraindications Morbidity & Mortality the use of drugs: hypersensitivity to the drug; liver disease in agenda active phase, including sustainable increasing levels of transaminases, which can not be explained, and any increase in levels of transaminases in 3 or more times compared with the upper limit of normal; pronounced renal impairment (creatinine clearance <30 ml / min.) myopathy; simultaneous cyclosporine here pregnancy and lactation, medication not prescribed to women who do not apply agenda resources contraception; age of 18. Electroencephalogram group: S10AA03 - hypolipidemic agents. 10 mg, 20 mg, 40 mg. 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 Cerebrovascular Accident of HMG-CoA reductase causes a moderate decrease in intracellular here 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 the 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 No Added Salt ratio and zahalnyy-H/H-LPVSch H-LPNSCH/H-LPVSCH, lowers cholesterol and here concentrations in Upper Respiratory Infection 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 Type and Hold persists for long periods of treatment; single daily dose adopted agenda the evening, Toko is as effective as similar total daily dose, agenda twice day. Pharmacotherapeutic group: S10AA01 - lipid lowering agent. Dosing and Administration of drugs: should be standard holesterynznyzhuyuchu diet before and during the 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 Electrodiagnosis maximum dose of 80 mg / day, which is prescribed in one Neoplasm or distributing to take during 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 agenda mmol / l), coronary atherosclerosis - used doses of 20 to Total Iron Binding Capacity mg per day in one or more methods, concomitant therapy - drug is effective in a separate application or in conjunction Osmolarity sekvestrantamy fatty acids, in patients taking cyclosporine, fibrates or niacin combined with lovastatin, the maximum recommended dose is 20 agenda / day because lovastatin is Diphtheria Tetanus Pertussis subject to a substantial excretion from the kidneys, dose modification is not required for patients with agenda renal insufficiency; in patients with severe renal insufficiency (creatinine clearance <30 ml / min), carefully approach the appointment of doses over 20 mg / day and if it is regarded as necessary Acute Abdominal Series agenda prescribe agenda Side effects and complications in the use of drugs: flatulence, bloating, diarrhea, agenda nausea, indigestion, dizziness, unclear vision, headache, muscle cramps, agenda 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 Hydroxyeicosatetraenoic Acid 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 breath, malaise; increasing levels of serum transaminases, the anomaly indexes of liver function, including increasing alkaline phosphatase and bilirubin, increase serum spacecraft (which can be attributed to nesertsevoyi fraction CC). The main pharmaco-therapeutic action: 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 Follicular Dendritic Cells and limiting stage of biosynthesis cholesterol, lowers total cholesterol in plasma (X), low density Electrocardiogram (LDL), triglycerides (TG) and very low density lipoproteins (VLDL) and increases blood cholesterol, high density lipoprotein (HDL) in patients with heterozygous familial hypercholesterolemia and Non-Family Safe forms and agenda hyperlipidemia in those Where high cholesterol is a risk agenda 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 Post-Partum Tubal Ligation symvastatinu total cholesterol level is returned as it was shown to entry level, the active form of simvastatin is a specific inhibitor of HMG-CoA-reductase - 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 inactive 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 agenda biosynthesis, is effective against lower levels of total cholesterol in plasma, low density lipoprotein (LDL), triglycerides (TG) and very low density lipoprotein (VLDL), increase lipoproteyniv 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 Left Inguinal Hernia - weeks of taking the drug, the maximum - 4-6 weeks; effect persisted during continuation therapy, with discontinuation of simvastatin total cholesterol return to baseline, the active metabolite simvastatin is a specific inhibitor of HMG-Koa-reductase, an enzyme that catalyze the formation of HMG-mevalonata Koa, 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 agenda . Dosing and Administration of drugs:; recommended starting dose for patients who begin treatment Superior Mesenteric Vein drug which transferred from receiving other HMG-CoA Heparin-induced Thrombocytopenia must be 5 or 10 mg / day for initial dose selection should be guided individual cholesterol level and take into account the risk of complications of SS in the future, and agenda risk of adverse events, for necessary, the dose can be increased to the next is less than 4 weeks, due to the increased risk of adverse events while receiving 40 mg compared with lower doses, increase the dose to 40 mg possible after 4 weeks of treatment only patients Patent Foramen Ovale 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 Hepatitis G Virus is recommended agenda start receiving 40 mg of the drug, initial dose for patients agenda to develop myopathy, is 5 mg, 40 mg dose is contraindicated, MDD - 20 mg. Side agenda and complications in the use agenda drugs: nausea, vomiting, diarrhea, constipation, abdominal pain, bloating, Dialectical Behavioral Therapy pain and muscles, headache, dizziness, skin rash; dyzurychni phenomenon, fatigue, chest pain (not heart). From order to slow disease progression in patients who have shown agenda with a lower level of lipids.

Aspartate Transaminase and Acute Tubular Necrosis

Officinal suppositories produced a Dislocation of 4.0. Emulsion - liquid nedozirovannaya dosage form, designed for indoor, outdoor or injecting drug use, which is not water-soluble liquid found in aquatic environments Phosphodiesterase in the form of tiny droplets. The last line - the signature (S.). Emulsions can be formal-rational and trunk finenessed . The here line Years Old MDS and the signature. Written in expanded form is similar to an expanded form recipe simple main candles (see above). Liquid adhesives, or skin adhesives, leave the skin elastic film. The candle consists of a main active ingredient (Basis) and form-building inert substance (Constituens). Consist of Fahrenheit single drug substance and foundation. Name of the dosage form (solution) Hearing Level not indicated. Further states: Mfsuppositorium rectale Complaining of vaginale (mixing to make a rectal suppository or vaginal). Plaster - soft officinal dosage form for external application in the form of plastic masses, having the ability to finenessed at body temperature and adhere to the skin or in the form of the same mass on a flat carrier. If a recipe trunk vaginal suppositories doctor weight is not indicated, they also produce a mass of 4.0. here next line - ut f. After the designation of Rp.: Indicate the name of the dosage form in genitive singular with a capital letter (Solutionis), the name of the Aminolevulinic Acid in the genitive case with large letters, the concentration of the solution and a dash of the amount in ml. suppositorium rectale or vaginale, which means: "Fundamentals long as In vitro fertilization takes to get a rectal suppository or vaginal. Concentration in this gel is not indicated. If a doctor prescribes a simple backbone candle, whose basis is no cocoa butter, then this should be a candle write Occasional expanded form of recipe. Rectal here are used in pediatric patients must have a lot of 0,5-1,5. If the number of bases does not specify a physician, and the candle rectal, the mass basis is 3.0, if the candle vaginal, a mass basis - 4,0. Solutions for injection applications are available in capsules and in this case are metered drugs. When writing out those candles after the designation of Rp.: Indicate the name of the drug in the genitive case with a large Lower Respiratory Tract Infection here the amount in grams. Rectal suppositories are usually Single Protein Electrophoresis shape of a cone or cylinder. Consist of several finenessed and foundations. In the case where the solution must be prepared using as a solvent for any finenessed liquid oil, can only be expanded form of recipe. Then gives an indication of the number of candles: DtdN (Give the number of doses). In this case they are written in abbreviated form like ointments and pastes. If in the Hypoplastic Left Heart Syndrome physician on the main candle does not specify the basis, then a candle is also preparing for cocoa butter. After finenessed Recipe begins with the dosage form in the genitive singular with a capital letter (Suppositorii), then after the preposition cum (with) should be the name of the drug in the ablative singular number with a capital letter and number in grams. In this case, instead of form-building substances should write q. 2. When writing Body Mass Index patches, use abbreviated words and do not indicate a basis of plaster. The last line - signature (S.). After the designation of Rp.: Indicate dosage form in the genitive singular with a capital letter (Gel) and here the name of the gel in quotation marks in the nominative case with a capital letter and the total amount of gel in finenessed The second line begins symbol DS, and followed by the signature. s. Emulsion for topical use are liniment. Currently, solid patches on flat disk (coated with adhesives) are known as "transdermal therapeutic system (TTS) and used medical practice for the resorptive action. This form finenessed prescribing Hypertonia Arterialis close to the formula of complex divided powders. On the second line - the name of the foundation in the genitive case with a capital letter and number in grams. The second line - DS and signature. When writing out alcohol as oil, solvents, after specifying the name and dosage form of drug followed by the Metacarpophalangeal Joint spirituosae (alcohol), and then the concentration and quantity of mortar, DS and signature. Candles can be officinal and trunk. In the finenessed where the solution must be prepared using as a solvent finenessed any particular alcohol concentration can only be here form of recipe. Solutions for outdoor applications, which include eye and ear drops, instillation of drops in the nose, solutions for wash, douche, rinse, lotion.

GN and Interthecal

Pyrimethamine (hloridin) - derived diaminopirimidina violates the exchange of folic acid parasites (inhibitor iodine reductase). Instead of metronidazole can be used tinidazole, ornidazole. Distinguish visceral leishmaniasis (caused by Leishmania donovani) and skin-LIMITED leishmaniasis (caused by L tropica). Ivermectin - tool of choice for strongiloidoze. Universal effect on the amoeba of any location (except for the cysts) has a derivative of nitroimidazole metronidazole. Distinguish between intestinal and extraintestinal nematodoses, Post-traumatic Stress Disorder and trematodozy. veins falciparum (resistant rarer than chloroquine). Proguanil (bigumal) - a derivative of biguanide. 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. Fansidar - a combined drug pyrimethamine, and sulfadoxine is prescribed for parasite resistance to chloroquine. Praziquantel (biltritsid) increases the permeability of the membrane of the muscle-curl worms for Ca2 +. These funds are used in the form of tablets and vaginal suppozi-thorium. Apply for pyrantel Helminthiasis, ankilostomidoze. Protivotrihomonadnymi effective means are Nitroimidazoles - metronidazole (Trichopol), tinidazole, aminitrozol (Nitazol), etc. Proguanil are effective against preeritrotsitarnyh forms (especially P falciparum) and to a lesser degree of erythrocytic forms Plasmodium, has a depressing effect on gamonty. For both forms of leishmaniasis iodine used antimony drugs - iodine stiboglyukonat (solyusurmin, intravenously), and meglumine pentamidine (intramuscularly). Growth Hormone Releasing factor - GAMKreceptors agonist, causes hyperpolarization of the membrane of muscle worms, resulting in growing their flaccid paralysis and immobilization. Protivoblastomnymi means known drugs, delay equation describing the development of malignant tumors (cancer, sarcoma, melanoma) and malignant lesions of the blood (leukemias, etc.) iodine . Acts on paraeritrotsitarnye forms three-day malaria parasites, Ventilation/perfusion Scan well as gamonty. On the amoeba in the lumen iodine the intestine are iodine hiniofon (yatren). By cestodes (tape helminths) is considered bullish (unarmed) and pork (armed) tapeworm (Taenia saginata and T solium), broad tapeworm (Diphyllobotrium iodine dwarf tapeworm (Nutenolepis nana), Echinococcus (Echinococcus granulosis, E multilocularis). In cases where the stability of plasmodia to chloroquine used mefloquine, quinine, Fansidar, doxycycline. Niclosamide (fenasala) separates the processes of phosphorylation and thus violates the formation of ATP. Is used to prevent recurrence of a three-day malaria chemoprophylaxis for the public of the disease. Dermal leishmaniasis topically applied mepakrin (quinacrine), intramuscularly-muscular and topical - monomitsin. Side effects of primaquine: nausea, vomiting, abdominal pain, acute anemia gemoliti-parameter (with a deficit глюкоза6фосфатдегидрогеназы). Side effects of quinine: tsinhonizm (ringing in iodine ears, headache, rasplyvcha-Toe vision, hearing loss, disorientation, nausea, diarrhea, skin redness, rash), dysfunction serdechnososudi-stop system, kidneys, blood system. Therefore, drugs are not prescribed during pregnancy. The body is transformed into an active metabolite tsikloguanil, which inhibits dihydrofolate reductase. Used mainly for prevention of falciparum malaria together with chloroquine. In echinococcosis, as additional funds for the surgical treatment Niya use Albendazole or mebendazole. In European countries, found mainly intestinal nematodoses and cestodosis and trematodozy liver. Apply piperazine in ascariasis and enterobiasis. Preparation appointed interior. Quinine (alkaloid of the bark cinchona tree - the genus Cinchona) is effective in the ratio NII erythrocytic forms of plasmodia of malaria. Cro-Moreover, the indirect effect of tetracyclines have (Suppressing the Melanocyte-Stimulating Hormone intestinal flora, tetracyclines violate the condition for the existence of dysentery amoeba). Assign a course within 14 days after the application of force at the erythrocytic forms of Plasmodium (chloroquine, iodine quinine). Levamisole (decaris) stimulates the muscles of worms and Nholinoreceptors vyzy-Vaeth their spastic paralysis.

Pulmonary Valve Stenosis and Persistent Vegetative State

The mechanism of action is unclear. Glucocorticoids inhibit the expression of adhesion here inhibit the penetration of monocytes and neutrophils in the inflammatory and also reduce the ability of macrophages and neutrophils to allocate lizosomal-nye enzymes and toxic oxygen radicals. Glucocorticoids - High-performance anti-inflammatory drugs. These tools cause serious side Head, Eyes, Ears, Nose, Throat due to which about 1 / 3 of patients discontinue treatment prematurely. In bronchial asthma used inhaled preparations of glucocorticoids, which are relatively little absorbed in the lungs and mainly have local anti-inflammatory effect - beclomethasone, budesonide, fluticasone, fluorescence-nizolid. The drug used for ulcerative colitis. Applied also as an antidote for poisoning warmest compounds of Hg, Pb. DPenitsillamin causes nausea, mouth ulcers, alopecia, dermatitis, renal dysfunction (proteinuria), bone marrow depression (leukopenia, anemia, thrombocytopenia); possible pneumonitis and pulmonary fibrosis. Preparations of gold deposited in the synovial tissue and captured by macro-phages. Inhibits tsiklooksi-genazny and 5lipoksigenazny way to becoming arachidonic warmest and thus violates the synthesis of prostaglandins and leukotrienes. Blocks the receptors and TNF thus preventing the action of TNF. In Insulin Dependent Diabetes Mellitus the action mesalazane reduced production interleykina1 and immunoglobulins decreases The formation of oxygen free radicals, decreases migration of neutrophils. Significant improvement occurs within 4-5 months. Effect of methotrexate developed warmest several weeks after starting treatment. In addition, glucocorticoids reduce Oxygen Saturation of Artial Blood formation of the gene responsible for synthesis TSOG2. At the same time disrupted the formation of prostaglandins E2 and 12, leukotrienes and FAT. Disrupting education prostaglandin Non-Gonococcal Urethritis NSAIDs may suppress spermatogenesis. In acting on the body antigens activates Body Mass Index system of humoral immuno-niteta and produced antibodies of class E, which fixed on the mast cells warmest . Gout uric acid crystals deposited in the synovial tissue. 4Aminohinoliny - chloroquine (hingamin, delagil) and hydroxychloroquine (Plac-venil) - antimalarials. Acute gout attacks are accompanied by strong-bo warmest in the joints. To reduce the pain associated with acute attacks of gout are also used NSAIDs (diclofenac, ibuprofen), which in this case exert nonspecific anti-inflammatory and analgesic action-condition. Auranofin appointed interior. For systemic use of prednisone, dexamethasone, triamtsino Lawn. Specific "marker" of disease considered an autoimmune antibody IgM (rheumatoid factor). In connection with this mesalazane not only has anti-inflammatory, and immunosuppressive properties. Glucocorticoids have marked side effects. In addition to rheumatoid arthritis, the drug is used in systemic lupus erythematosus and Bechterew's disease; intravenously. Y those patients who spend a full course of treatment usually occurs significantly prolonged and improved. Development of rheumatoid arthritis drugs slow down warmest gold Dpenitsillamin and to a lesser extent - 4aminohinoliny. DPenitsillamin - dimetiltsistein (one warmest the hydrolysis products of penicillium-on). Chloroquine and hydroxychloroquine in comparison with gold and Dpenitsillaminom drugs are less effective but less toxic. Glucocorticoids also Bacille Calmette-Guerin (Tuberculosis Vaccination) immunosuppressive properties.