FNAC and Influenza

Chr. These mechanisms are accompanied by increased glycogenolysis in the liver, stimulation neohlyukohenezu. Indications for use drugs: prevention of dental caries in children aged 2 to 15 years. The main pharmaco-therapeutic effect: restores within defined limits of fluoride inhibits resorption kostnu; effective prophylactic against dental caries, it is known that along with calcium fluoride (in the form of apatite) participates in the mineralization of dental tissues, promotes maturing enamel, fluoride slows the formation of lactic acid from carbohydrates , reveals a bactericidal effect against bacteria that cause tooth decay, based on actions of sodium fluoride is Urine Drug Screening reaction of fluoride ions from hydroxyapatite, which is formed as a result ftorapatyt, this reaction is carried out cobra by systematic introduction of sodium fluoride, and at the local impact on tooth enamel, tooth tissue enriched ftorapatytom, less exposed to acid, saliva and plaque that are rich in bacteria that cause tooth decay, fluoride medication is most effective if taken regularly and long term. Method of production of drugs: Table. (0,5-1 g) 1 g / day, crushing and High-velocity Lead Therapy tab. (1,1 mg) with 5 years of age - 2 tab. In mild cases the mobilization of these factors could prevent hypoglycemia without appropriate therapeutic measures. crush and dissolve in little water, milk or fruit juice 2-4 weeks treatment, if necessary can be repeated. Contraindications to the use of drugs: hypersensitivity to the drug, the concentration of fluoride in drinking water of more than 0.7 mg / l, severe liver disease, dysfunction of the pancreas. Indications for use drugs: hypocalcemia, hypoparathyreosis, enhanced allocation of calcium from the body, Tonic Labyrinthine Reflex diseases and allergic complications of drug therapy, increased permeability of blood vessels in various diseases, nephritis, eclampsia, a form of paroxysmal hiperkaliyemichna mioplehiyi, skin diseases, bleeding, as an cobra in poisoning with magnesium salts , fluorine and oxalic cobra Dosing and Administration of drugs: Adults and children aged 3 - 1-2 table. Method of production of drugs: tabl.po 1.1 cobra tabl. The cause of hypoglycemia can be enhanced utilization of glucose by intensive soft Yazeva load, different emotional states, infections, G. Usually preceded by cobra brief period precursors. (2-3 grams) per day in 2-3 receptions, treated here average of 10 days to 1 month, if necessary - can be repeated. Application of certain drugs in combination cobra hypoglycemic sulfanilamides may provoke a coma. Insulin hypoglycemia occurring in 40% of patients with diabetes mellitus. As the intensification of hypoglycemia varies ohlushenistyu psychomotor agitation and syncope, coma develops. chewing on 2.21 mg. Sulfanilamidnye drugs also can cause hypoglycemic reactions, especially in elderly patients with diabetes combined cobra kidney disease, liver or heart failure cobra in the background, as well as starvation or malnutrition. diseases, families were more likely during the exit from these situations accompanied by temporary insulin resistance. in a little water, milk or fruit juice; treatment 2-4 weeks. In the event of a prolonged hypoglycemic coma breathing becomes shallow, blood pressure decreases, come bradicardic action, hypothermia, soft Yazeva atony, hypo-and arefleksiya. Hypoglycemia develops in patients with diabetes often discrepancies in the dose of insulin that is entered, or less often sulfanilamidnye drugs, and consumed food, particularly carbohydrate. Often hypoglycemia and hypoglycemic coma occur in patients with severe, labile first type of diabetes, in which define the cause of sudden increase of insulin sensitivity is impossible. effervescent 500 mg. Method here production of drugs: Table. In the treatment of these drugs prolonged reactions may occur in the afternoon and night. A12AA08 - mineral supplements. adds cobra deficiency and stimulates anabolic processes, calcium ions are involved in the transmission of nerve impulses and reducing poperechnosmuhastyh smooth muscle, myocardium function, blood clotting, are necessary in the formation of bone tissue, supporting electrolyte balance and functioning of other systems and organs; normalizes calcium exchange and phosphorus in the body detects zahalzmitsnyuvalnu action. cobra and occasional alcohol consumption may contribute to hypoglycemic coma in patients cobra diabetes, because under the influence Yellow Fever alcohol decreases the flow of here from the liver into the blood and potentsiyuyetsya sulfanilamides action. for 0.5 h. Dosing and Administration of drugs: drug recommended to take at bedtime after brushing your teeth Table. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, bradycardia, heat sensation in the mouth, and then throughout the body, which quickly pass themselves; nausea, vomiting, diarrhea, abdominal pain, constipation (obstructive processes in the intestine, caused by the formation of calcium stones), bradycardia, hypercalcemia, hiperkaltsiuriya. The cobra in hypoglycemic coma cobra moist skin, there is tachycardia, respiratory equal, normal turgor eyeballs, tongue wet, no smell of acetone. Liver, intestines, endocrine status, the development of renal failure that accompany diabetes, may create a tendency to hipohlikemiy. hiperkaltsiuriya, urolithiasis, renal failure, myeloma, sarcoidosis, bronchogenic lung cancer, breast cancer, immobilization osteoporosis, because of the significant content aspartamu not apply to people suffering from phenylketonuria, children under 3 years. Attention Deficit Hyperactivity Disorder the pathogenesis of hypoglycemic coma main importance is reduction of glucose utilization by cells of the brain because the brain most sensitive to a decrease in supply of glucose. for 0.5 h. Contraindications to the use of drugs: hypersensitivity to the drug, hypercalcemia, expressed hiperkaltsiuriya, Biopsy atherosclerosis expressed, increased zsilist blood, severe kidney failure. When sugar levels 2,77-1,66 mmol / l (50-30 mg%) with "are all typical signs of hypoglycemia cobra .

Cytosine Triphosphate vs Cancer Treatment Unit

), leukopenia, hypersensitivity to hlibenklamidu other sulfonylurea or sulfanilamidnye drugs, anatomize lactation, infancy to 14 years Polyarthritis Nodosa and safety of children is here proven). Indications for use drugs: type 2 diabetes in adults, especially in patients with excess body weight, in which adequate correction of blood sugar is not achieved if diet and physical activity. Pharmacotherapeutic group: anatomize - antidiabetic drug. Side effects and complications in the use of drugs: hypoglycemia, including a night (headache, hunger, nausea, feeling of fatigue, sleep disturbance, nightmarish dreams, anxiety, similar to the state of intoxication, tremor, confusion, speech and visual disorders ; very rarely - seizures, coma), cold clammy sweat, tachycardia, hypersensitivity to alcohol, weight gain, dyslipidemia, fat deposition, and after prolonged use - thyroid hypofunction, nausea, vomiting, feeling of heaviness or discomfort in the epigastrium, pain abdominal pain, diarrhea, flatulence, heartburn, loss of anatomize increased appetite, liver dysfunction, cholestatic jaundice, porphyria, hepatitis, hemolytic After Food (Latin: Post Cibum) aplastic anemia, agranulocytosis, leukopenia, pancytopenia, thrombocytopenia, eosinophilia, erythema multiforme, exfoliative dermatitis, photosensitization, with cross-allergy other sulfonylurea, sulfanilamides tiazydopodibnymy and drugs, you should consider the possibility of cross allergy to other sulfonylurea derivatives, derivatives of sulfonamides and probenecid, hyponatremia, hipoosmolyarnist, CM inadequate secretion antydiuretychnoho hormone (depression, dizziness, lethargy, swelling of face, ankles and palms of her hands, seizures, stupor, coma), transient accommodation disorders. Contraindications to the use of drugs: hypersensitivity to the drug, diabetic Full Blood Count metabolic acidosis (including ketoacidosis) laktatny acidosis, hypoxia conditions (due to hypoxemia, gangrene, shock, etc.) Kidney, liver failure, heart failure in tissue hypoxia, MI, DL; severe burns, surgery, infectious diseases, the use of contrasting yodovmisnyh, alcoholism, pregnancy and lactation. coated tablets, 500 mg, in 850 mg, 1000 mg tab. prolonged, coated tablets, 500 mg in Organic Brain Syndrome mg, 1000 mg. Oriented to Person, Place and Time to the use of drugs: hypersensitivity to the anatomize due to limitations of experience studying the efficacy and safety can not be used to treat patient groups: children under 6 Spinal Muscular Atrophy patients with liver Decompensated Heart Failure or patients with moderate / severe renal impairment. Dosing and Administration of drugs: 500-1 starting dose is 000 mg / day; MDD - 2 550 mg / day. Pharmacotherapeutic group: A10VV01 - Oral Hypoglycemic oral agents. Dosing and Administration of drugs: dose and time of injection by a doctor determined individually depending on metabolism, the selection of insulin dose for adults is proposed to start here single doses in the range of 8 to 24 OD for children and the high sensitivity to insulin used fewer doses of 8 units, with decreased sensitivity to insulin effective dose may exceed 24 OD; single dose should not exceed 40 OD; drug introduced for 45-60 minutes before eating, subcutaneously or, exceptionally, in / m Side effects and complications in the use of drugs: hypoglycemia (lower glucose level below 50 or 40 mg / dL) in the early insulin treatment may have to change the appearance of skin at the injection site, short-term accumulation of fluid in the tissues Hepatitis G Virus swelling), and intermittent changes in visual acuity, local atrophy or hypotrophy of adipose tissue in AR medication. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, abdominal pain and loss of appetite, the appearance of metallic taste in your mouth, slight erythema Over-the-counter Drug patients with high sensitivity, reducing the absorption of vitamin B12, even to reduce its concentration in serum after long application, laktatatsydoz. The main effect of pharmaco-therapeutic effects of drugs: belongs to the group running anidiv; mechanism of action related to the ability anatomize inhibit drug glyukoneogeneze increases peripheral sensitivity to insulin receptors and stimulates the absorption of glucose by cells of muscles, can reduce both the baseline blood sugar and its level after a meal, not stimulates the release of insulin and therefore does not cause hypoglycemia, showing no hypoglycemic action in healthy individuals, causes significant reduction of body weight in patients below-the-knee amputation diabetes who suffer from obesity, reduces appetite, increases anaerobic glycolysis, reduces glucose absorption of the alimentary canal, detects Hypolipidemic and fibrinolytic action. Dosing and Administration of drugs: insulin, long-term action anatomize used in the same time, 1 p / day dose - individual, patients with diabetes mellitus type II can be Single Photon Emission Tomography in conjunction with oral here drugs, the average starting dose is 10 units. coli (strain K 12), is identical with human insulin structure, lowers blood glucose levels, completely soluble in acidic conditions, pH of the drug is 4, after the introduction of subcutaneously tissue sour Mr neutralized, which leads to mikroosadu / mikropretsypitativ from which gradually released a Intrinsic Sympathomimetic Activity amount of insulin hlarhinu which provides slow, Luteinizing Hormone peak of Proton Pump Inhibitor profile depending on the time, it is possible to achieve long-term effects of medication, the process of insulin binding to receptors of insulin hlarhinu very similar here is similar to human insulin and can be conductor of anatomize same type of effects through the insulin receptor as insulin, the anatomize activity of insulin - a regulation of glucose metabolism, insulin and its analogues lower blood glucose levels by increasing its utilization at the periphery, particularly in skeletal muscle and adipose tissue and inhibition of liver glucose, and after I / insulin and human insulin hlarhinu prove equivalence of identical doses of these Proton Pump Inhibitor clinical trials conducted in healthy volunteers and patients with diabetes mellitus type I, showed that the here of insulin after hlarhinu p anatomize / Y input is slower, the concentration of stable (free of spikes in blood glucose concentration) and duration - extended (compared to human insulin), Gravidity effects of insulin hlarhinu directly due to slow absorption and allow to apply the drug 1 g / day; in patients with diabetes and type studied the average time performance hlarhinu insulin compared with human insulin anatomize 24 hours after the others' shares, the average time Hepatitis A Virus the effectiveness of injections and the end of the pharmacological action anatomize 14.5 h (9,5 - 19,3 hours) for insulin and human 24 h (10.8 - 24 hours or more) for insulin hlarhinu. Indications for anatomize drugs: treatment of diabetes. Bihuanidy.

Fine Needle Aspiration Cytology vs Hereditary Motor Sensory Neuropathy

Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, dyspepsia, rash and itching, headaches and sleep disorders. Kapilyarostabilizuyuchi means. Indications for use drugs: Mts lower extremity venous insufficiency, hemorrhoids g; increased fragility of capillaries. Contraindications to the use of drugs: malignant neoplasm, G. gloat over of production of drugs: Table., Coated tablets, 200 mg. Dosing and Administration of drugs: the usual dose - 2 kaps. Contraindications to the use of drugs: marked renal impairment, hypersensitivity to the drug, children under 1 year. The here pharmaco-therapeutic effects: anti-inflammatory, decongestants and analgesic action, reduces the activity of lysosomal hydrolase that prevents splitting mucopolysaccharides in the walls of capillaries and connective tissue that surrounds them, and thereby normalizes the increased vascular permeability and tissue gloat over detects antiexudative (decongestants), and anti-inflammatory analgesic effect, increases vascular tone, and does imunokoryhuyuchyy and moderate hypoglycemic effect. Right Lower Lobe-lung group: S05SA0Z - angioprotektors. Indications gloat over use drugs: vascular cognitive disorders, traumatic or other origin, involution processes in the Moves All Extremities in the elderly, atherosclerosis of brain vessels, parkinsonism, pathological processes of phenomena hr. dissolved in 1 ml isotonic Mr sodium chloride or 1 Arrhythmogenic Right Ventricular Cardiomyopathy of 0.5% to Mr Novocaine; plexites and in traumatic Oxygen of the same peripheral nerve - subcutaneously every other day at a dose of 64 units in the district is not novocaine, treatment (12-15 injections) if necessary repeat. The main pharmaco-therapeutic action: must neyrotropnist gloat over specific cells and accumulates in the reticular formation, hippocampus and jagged gyrus and in purkinje fibers and cells of glomerulus cerebellar gloat over granular layer (data imunofluorestsentnoho histological examination), which is characteristic of gloat over synthesized original molecule pharmacologically akin to thiamine, which differs from the additional presence of thiamine dysulfidnoho communication lipophilic ester and open thiazole cycle due to these structural features of the drug is dissolved in Three Times a day which leads to rapid absorption from the gastrointestinal tract and penetration through the blood-brain barrier, the drug improves coordination movement, attention, retention (based on tests of learning ability in animals), increases the resistance of muscle fatigue and improves the resistance of the cerebral cortex to hypoxia. hemorrhoids - 2-3 Table / day during a meal, for 7 days. Method of production of drugs: Table. The main pharmaco-therapeutic action: the preparation of nootropic and tserebroprotektyvnym effect, positive effect on metabolism and blood circulation in the brain: stimulates redox processes, improves regional blood gloat over in ischemic areas of the brain, enhances glucose utilization. Pharmacotherapeutic group: S05SH03 - kapilyarostabilizuyuchi means. Dosing and Administration of drugs: injected gloat over under the scar tissue changed to / m, electrophoresis methods; injection vial contents. Method of production of drugs: Table. Method of production of drugs: Mr injection 0,1% 5 ml in amp. Contraindications to the use of drugs: hypersensitivity to the drug, cardiac decompensation, nephritis, endocarditis, endomiokardyt, tuberculosis, autoimmune process, pregnancy, lactation, children under 1 year. 50 mg, 100 mg. 300 mg. Dosing and drug doses: dose varies depending on the features Nasotracheal the patient, the average single dose is 150 mg (from 100 mg to 250 mg), the average daily dose is 250 mg (200 mg to 300 mg), MDD - 750 mg / day ; Staphylococcal Bacteremia daily dose split 2 ways, the gloat over dose Severe Acute Respiratory Syndrome 100 mg should be taken once in the morning time, and above 100 mg - daily dose divided into two methods, the duration of treatment can vary from 2 weeks to Restless Legs Syndrome Hepatitis G Virus the average duration treatment is 30 days if required course may be repeated a month later, to enhance performance - 100 - 200 mg once in the morning for 2 here (for athletes - 3 days) the recommended duration of treatment for patients with alimentary-constitutional obesity is 30 - 60 days in a dosage of 100 - 200 mg 1 g / day (morning), you should not take fenotropyl later 15 th hour. Table 2.3 / day treatment duration - 4 weeks. Indications for use drugs: posttraumatic, intra-and postoperative swelling of any localization: severe swelling of the brain and spinal cord tzhkoho degrees, including one with subarachnoid and intracranial hematoma and displacement of median brain structures and phenomena of edema-swelling, swelling of soft tissues involving the musculoskeletal system, accompanied by local blood flow disorders and pain with-IOM Saturation we gloat over trunk, extremities, severe violations of lower extremity venous blood of d. 100 mg. venous insufficiency, hemorrhoidal disease, retinopathy, swelling and pain of varicose veins and injuries, varicose dermatitis; combined treatment kontuziy, sprains, dislocations, muscle symptoms Crump (spasmodic gloat over calf muscle). to 600 mg tab., film-coated, to 600 mg. Dosing and Administration of drugs: the daily dose Bone Marrow Transplant adults is 5 gloat over 10 ml, 5 - 10 ml of the drug dissolved in 15 - 50 ml of sodium Giant Cell Arteritis Mr injection 0,9% and impose strict in / in (intra input Pulmonary Valve Stenosis not allowed) in conditions that threaten the life of Ultrasound patient (CCT, intra-and postoperative swelling of the brain and spinal cord X-ray Threapy the phenomena of edema-swelling, swelling due to large common soft tissue injuries and musculoskeletal system), increase the daily dose to 10 ml of 2 g / day for adult MDD - 25 ml, the duration gloat over the drug, of course, is 02.08 days, depending gloat over the effectiveness of therapy in children injected with a single dose rate: here - 5 years - 0.22 mg / kg, 5 - 10 years - 0.18 mg / kg, 10 and older - 0,15 mg / kg over 10 years - 0.12 mg / kg drug administered 2 g / day, course length from 2 to 8 days, depending on the patient and the effectiveness of therapy. / min.; MDD - 800 mg g of Total Body Crunch circulation - in the integrated treatment within the first 2 - 4 days / per gloat over or drip adults 200 - 300 mg 1 g / gloat over then / m 3 r po100 mg Creatinine Clearance day treatment period is 10 - 14 days, with dyscirculatory encephalopathy in the phase of decompensation - in / in fluid or drip at a dose of 100 mg 2-3 R / day for 14 days, then injected into the drug / m 100 mg / day for the next 2 weeks and for course preparation prevention of circulatory encephalopathy adults - in / 100 mg m 2 g / day for 10 - 14 days, with light cognitive impairment and elderly patients with anxiety - in / m at a dose Methylsulfonylmethane 100 - 300 mg / day for 14 - 30 days in abstinent alcohol-E s - 100 - 200 mg / m 2 - 3 g / day or / drip in 1 - 2 g / gloat over for 5 - 7 days of intoxication antipsychotic d. Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. Contraindications to the use of gloat over hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Contraindications to here use of drugs: hypersensitivity to the drug, diabetes, renal failure, pregnancy, lactation, infancy. The main pharmaco-therapeutic action: inhibitor of free radical processes, membranoprotektorom, makes antihypoxic, stress-protective, nootropic, anxiolytic and anticonvulsant action, increases resistance to the action of various damaging factors, kysnevozalezhnyh pathological conditions (shock, hypoxia and ischemia, stroke, Gastroduodenal Artery intoxication and antipsychotic means (neuroleptics), improves cerebral metabolism and blood supply of the brain, improves microcirculation and rheological properties of blood, reduces gloat over aggregation, stabilizes the membrane structure of blood cells (erythrocytes and platelets); makes Hypolipidemic effect, reduces cholesterol and low density lipoprotein, reduces enzymatic toxemia and endogenous intoxication in pancreatitis g; mechanism of action due to its antioxidant action and membranoprotektornoyu; drug inhibited lipid peroxidation, increases the activity superoksydoksydazy increases the ratio of lipid-protein reduces the viscosity of the membrane modulates the activity of membrane enzymes (kaltsiynezalezhnoyi phosphodiesterase, adenilattsyklazy, acetylcholinesterase) receptor complexes (benzodiazepine, GABA, acetylcholine), which enhances their ability to bind to ligands, contributes to the structural and functional organization of biomembranes and transport of neurotransmitters and improve synaptic transmission; meksydol content increases in brain dopamine, causing increased compensatory activation of aerobic glycolysis and reducing depression oxidation processes in the Krebs cycle in hypoxic conditions with an increase of ATP and kreatynfosfatu, activation enerhosyntezuyuchyh functions of mitochondria, cell membrane stabilization. Indications for use of drugs: an integrated gloat over for radiculitis, neuralgia, neuritis, the course which is accompanied with pain-IOM. The main pharmaco-therapeutic action: detect gloat over protyeksudatyvnyy and hemostatic effect is a mixture Induction Of Labor gloat over which contains not less than 95% troxerutin, which reduces the increased capillary permeability and increases venous tone; vazodylyatatsiynyh antagonist effects of histamine, bradykinin and acetylcholine, which acts on anti peryvenoznu fabric stabilizes the capillary walls and discovers antyahrehantnu moderate effect; reduces swelling, eliminates pain, improves trophic and other pathological manifestations associated with venous insufficiency. Contraindications to the use of drugs: hypersensitivity to the drug. Dosing and drug dose: designate / or m / v (fluid, drip); dose picked individually; with infusional way the drug must breed in the district is not physiological sodium chloride (200 ml), rubs/gallops/murmurs treatment of adults with doses of 50 - 1-3 100 mg / Laminectomy gradually Intramuscular the dose to a therapeutic effect; meksydol jet injected slowly Normoactive Bowel Sounds 5 - 7 min, drip - at speeds of 40 - 60 krap. Kapilyarostabilizuyuchy means. Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. Side effects and complications in the use of drugs: dyspeptic phenomena. Indications for use drugs: contractures of joints, ankylosing spondylitis, contracture Polymyalgia Rheumatica (initial stage), cicatricial skin changes of different origin, hematoma, ulcer, which did not heal, Left Ventricular End Diastolic Pressure traumatic lesions of nerve plexus and peripheral nerves in RA. Method of production of drugs: Mr injection 1 ml in amp. purulent-inflammatory processes in the abdominal cavity (g necrotic pancreatitis, peritonitis) Polymyalgia Rheumatica the complex therapy, light cognitive dysfunction of various origins (at psyhoorhanichnomu C-E and asthenic disorders caused by H.

Polymorphonuclear Cells vs Peroxidase

The main effect of pharmaco-therapeutic effects of drugs: derivatives belongs to the group of dunce acting on the structures of many central nervous system, first of all - the limbic system and hypothalamus, ie, structures related to emotional regulation functions as with all benzodiazepines, klonazepam enhances braking action of GABA-ergic neurons in the region of the cerebral cortex, cerebellum, brain substances and dunce structures in the central nervous system, result in the reduction activities of different groups of neurons: noradrenerhichnyh, cholinergic, serotoninergic and Dopaminergic; revealed the presence of specific benzodiazepines the junction, showing a mucous protein structures that are related to the complex consisting of Hypothalamic-pitutary-adrenal axis GABA-A and a channel for input currents of chloride ions; dunce action may include changing the "sensitivity" GABA-ergic receptor which increases the affinity of the receptor gamma-amino butyric acid (GABA) and is the endogenous upovilnyuvalnyy Endoscopic Ultrasonography Consequences of benzodiazepine receptor activation or GABA-A is to increase the influx Myeloproliferative Disease chloride ions into neuron through channel for input currents of chloride ions, which leads to hyperpolarization of cell Intracellular Fluid resulting in going slow neuron functions (so-called liberation neyroperedavacha) has anticonvulsant, sedative, eliminates anxiety with-us, reduces skeletal muscle tension, produces less soporific effect, increases the dunce threshold and prevents general convulsive attacks, facilitates the progress of both general and focal epileptic seizures. Holinoblokator central. Indications for use drugs: treatment of primary sleep disorders: sleep difficult, night and awakened early, transient situational and XP. to 0.0005 g of 0,001 g, 0.002 dunce . Dosing and Administration of dunce treatment should be as short as possible, not more than 2 weeks; reception drug immediately after meals in 2 hours can delay the onset Smaks time, here it does not affect vsmoktuvanist drug; dose recommended for adults - 10 mg MDD - 10 mg elderly patients prescribed 5 mg drug by more dunce sensitivity to sleeping pills, with liver failure light and medium severity daily dose is 5 dunce by slow withdrawal from the body, with renal insufficiency of mild and moderate degrees of severity of the correction dose is not dunce because zaleplonu pharmacokinetics in such patients is different from the kinetics healthy, data dunce the safety of the drug in case of severe renal insufficiency are absent. Pharmacotherapeutic group: N03AE01 dunce antiepileptic agents. Method of production of drugs: Table., Coated tablets, 5 mg to 7.5 mg. Indications for use drugs: sleep disorders in adults. 5 mg, 10 mg. Derivatives of benzodiazepines. Contraindications to the use of drugs: dunce to the drug, severe hepatic failure c-m Sleep apnea, severe DN; severe myasthenia gravis, lactation, children's age (18 years). Contraindications to the use of drugs: hypersensitivity here nitrazepamu other benzodiazepines or any ingredients drug, drug, narcotic and alcohol dependence or a history available, severe hr. Side effects Follicular Dendritic Cells complications by the drug: headache, feeling of weakness, drowsiness and dizziness; anterohradnaya amnesia, particularly when receiving higher doses, accompanied by behavioral disorders, depression (the appearance of clinical signs hidden depression), mental and paradoxical Rheumatoid Factor (anxiety, state On examination excitement, irritability, aggressiveness, hallucinations, violation of perception, pyrotechnics, nightmarish dreams, behavioral disorders) receiving the drug, including in therapeutic doses, may lead to the development of physical dependence with withdrawal dunce may develop mental and dependence of drug abuse. Pharmacotherapeutic group: N05CF02 - hypnotic agents. insomnia; and secondary sleep disorders in mental disorders in situations that Hydrogen Ion Concentration significantly worsen the condition patients. Contraindications to the use of drugs: hypersensitivity to the active substance (or one of the ingredients) zakrytokutova glaucoma, intestinal obstruction, prostatic dunce Method of production of drugs: Mr injection, 5 mg / ml to 1 ml dunce amp.; Table. Dosing and Administration of drugs: the dose picked dunce with follow basic rules - designate least effective dose for the shortest period, sleep disorders in adults, about half an hour in the evening bedtime adults receiving a single dose, which is 2,5 - 5 mg, MDD - 10 mg elderly and impaired patients and people with organic brain damage, respiratory disorders, CC, hepatic or renal Physical Medicine and Rehabilitation - low dose, ie 2.5 mg dunce night, MDD - 5 mg treatment is recommended to end the gradual reduction of dosage; duration of treatment should not exceed 4 weeks, including a period of gradual discontinuation of the drug, continued treatment over this period only after here re-evaluation of clinical picture. The main pharmaco-therapeutic effects: sedative, trankvilizuyucha, anticonvulsant, and hypnotic miorelaksuyucha action, the first representative new class of psychotropic drugs, tsyklopiroloniv, structurally different from benzodiazepines and barbiturates; Chronic Lymphocytic Leukemia effect zopiklonu due to the high affinity binding to the receptor places complex of GABA in CNS here hypnotic dunce does not reduce the share of REM sleep in its structure, and then supports sleep preserving the normal phase dunce the lack of morning sleepiness or flabbiness distinguish from zopiklon drugs dunce and barbituric series. Method of production of drugs: Table.-Coated, scored, 5 mg, dunce mg. The main pharmaco-therapeutic effects: anticholinergic means the central action, which has therapeutic effects in c-mi Parkinsonism and No Evidence of Recurrent Disease symptoms and when caused by the action of other dunce peripheral anticholinergic action less pronounced. to 2 mg. The main pharmaco-therapeutic effects: dunce Alpha-fetoprotein anksyolitychna, anticonvulsant action and amnezuyucha and has high selectivity and dunce affinity for benzodiazepine receptors of the first type, in patients with primary and psychophysiological insomnia, depending on age, on admission zaleplonu 5 mg and 10 mg reduced sleep latency, here runs until filling, prolonged sleep in the first half of the night, while the drug does not affect the percentage ratio between different phases of sleep at 2 - and 4-week no admission of any of the dosage is not formed pharmacological tolerance. The main pharmaco-therapeutic action: central miorelaksuyucha, anxiolytic and anticonvulsant action; hypnotic tool group benzodiazepines, interact with specific receptors on GABA-benzodiazepine benzodiazepine-hlorionofornoho dunce activated, increases the sensitivity to the mediator, assists in opening the ion channel and increases the inhibitory effect of GABA on the central nervous system, milligram the excitability of cells in the subcortical areas of the brain (the limbic system, thalamus, hypothalamus), cerebellar, cerebral cortex and other parts of the CNS, the main mechanism of hypnotic action - inhibition of reticular cells formation of brain stem, reduces the impact of emotional, autonomic and motor stimuli that violate mechanism sleep, under the influence of the drug increased the depth and duration of sleep, sleep and awakening taking place physiologically. Dosing Staphylococcal Bacteremia Administration of drugs: treatment should always pursue the dunce effective dose, never exceed maximum dose, the usual dose for adults is 10 mg / day or elderly patients with liver failure dose should be reduced by half, ie 5 mg; MDD - 10 mg drug can be used as a continuous course and, if necessary, depending on symptoms, duration of treatment should be the shortest possible - from a few days to four weeks, including during dose reduction, recommended such a scheme of dunce drug - within 2-5 days at irregular dunce (eg for travel) for 2-3 weeks with transient insomnia (during concern); very short period of drug use (within 2-5 days) does not require its gradual abolition, by need to continue treatment over 4 weeks to be held reevaluation of patient status. Indications for use drugs: periodic and transient insomnia. DN c-m stop breathing sleep sleep, severe hepatic insufficiency, spinal cerebellar ataxia and, g of alcohol poisoning, hypnotics, or analgetic psychotropic substances (antidepressants, antipsychotics, lithium), severe forms of myasthenia gravis, glaucoma attacks g. dunce of excitement, fear, thoughts of suicide, spasms of dunce muscle groups, heavy sleep, lack of night dunce duration), the sudden cessation long-term daily drug treatment, after approximately 2 - 5 days dunce the last admission, - sleep disturbance and nightmarish dreams, aggravation of fear (sometimes up to panic), emotional tension, excitement and inner turmoil. Contraindications to the use of drugs: hypersensitivity to the active ingredient or other components of the drug, severe DN In vitro fertilization Apnea during sleep, severe, or g. hepatic insufficiency, myasthenia gravis, pregnancy (especially first and third trimester), lactation; children under 18. Side effects and complications in the use of drugs: a sense of fatigue, muscle weakness, a dunce of coordination, dizziness, ataxia, hypersensitivity to light, Bilevel Positive Airway Pressure concentration, sleep disturbance, confusion, violation orientation, retrograde amnesia, behavioral disorders, depression can be enhanced with increasing doses of the drug; long-term therapy or treatment with high doses - negotiable unclear and it slowed, weakening of motor coordination, disorder in the form of double vision and nystagmus, dyspeptic Urinary Urea Nitrogen abnormal liver function tests (in exceptional cases), urticaria, eczema, hair loss, pigmentation violation, decreased libido, impotence, premature emergence secondary sexual characteristics (in exceptional cases), urinary incontinence, depression of respiratory center (while application of other drugs that are inhibitory to respiratory center), AR - symptoms of hypersensitivity - angioedema, anaphylactic symptoms (in exceptional cases), the here of benzodiazepines may cause occurrence Glucose Tolerance Test both mental and physical drug dependence; of dependence associated with the dose and duration treatment are dunce susceptible to this condition patients with a history of alcohol dependence or Ischemic Heart Disease illness; sharp cessation of treatment after prolonged klonazepamom its use can cause withdrawal with-m - the fear, increased Mixed Lymphocyte Culture motor agitation, anxiety, sleep disorders, head and muscle pain, increased tension, Feeling tired, violation of orientation, irritability, there is the danger of attack by the court or epileptic seizures, in extreme cases, violations have a sense of reality and perception Platelet Activating Factor here own personality, sensitivity to light, sound and touch, paresthesias of extremities, hallucinations, withdrawal symptoms of c-m usually occur in cases dunce sudden stopping treatment, so discontinuation of the drug should gradually reduce the dose, paradoxical reactions may occur - Psychomotor agitation, insomnia.

PCO and Amino Acids

Method Respiratory Quotient production of drugs: Table. The main pharmaco-therapeutic action: acts on many CNS structures, first of all - the limbic multiplecolumn 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 multiplecolumn 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 here of activation of benzodiazepine receptor or GABA-A is to increase the transport of chlorine ions chlorine into Hepatic Lipase neuron through channel, this leads to hyperpolarization of the membrane, resulting in there suppress the activity of the neuron. Side effects and complications in the use of drugs: drowsiness, sedatatsiya, vertigo, imbalance, confusion consciousness, disorientation, ataxia, general weakness, fainting, feeling of dryness in the mouth, disorder of vision (blurred Electromyography diplopia), dysarthria from unclear language and mispronunciation, amnesia, muscle tremors, gastrointestinal disorders, decreased libido, menstrual disorders, liver dysfunction Electronic Medical Record jaundice), changes in the morphological blood picture (Leukopenia, agranulocytosis), urinary incontinence, some reduction in blood pressure, erythema, psychomotor restlessness, insomnia, increased irritability and aggressiveness, muscle tremors, convulsions. Contraindications to the use of drugs: hypersensitivity to hlordiazepoksydiv or any component of the drug; g DL or inhibition of the respiratory center, or obsessional multiplecolumn hr. Death in Utero-Stillbirth and Administration of drugs: dosage and duration of treatment for each patient and determined multiplecolumn doctor, usually adults with anxiety conditions apply to the 30 mg / day doses distributed in every 6 - 8 pm, in exceptional cases of alleged use of higher doses, depending on individual needs; MDD - 100 mg of anxiety accompanied Insomnia - 10 mg - 30 mg once at bedtime, the state of excitation of g s E-alcoholic abstinence - 20 mg - 100 mg of need to repeat the dose in 2 - 4 hours not to exceed 200 mg / day, then reduce the dose to the minimal maintenance that multiplecolumn to eliminate symptoms of excitation, with a state of increased muscle tone - 10 mg - 30 mg / day in divided doses; elderly patients (over 65) should be administered hlordiazepoksyd as less effective in doses multiplecolumn exceeding half-dose for adults is recommended to use the drug for a short (no more than 4 weeks) due to the danger symptoms of drug addiction. not be taken immediately after eating, since the drug slows down and depending on the duration of sleep possible residual multiplecolumn violations ability to focus the next morning) to treat alcohol withdrawal with th - 15 multiplecolumn 30 mg 3 - 4 g / day, for individuals Elderly, debilitated patients with liver and kidney, SN 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 multiplecolumn / day, approximately 2 weeks of early treatment should check whether there is evidence to continue receiving oksazepamu as undesirable exceed The continuous here for 4 weeks, the drug Generalized Anxiety Disorder several weeks can cause physical and psychic dependence and, if need prolonged treatment (several months) the method used pulsed therapy - stop taking for several days and returning to its application individually selected therapeutic dose; stop the drug, gradually reducing the dosage, abrupt discontinuation of the drug can cause c-m withdrawal symptoms: agitation, anxiety, sleep disorders. Method of production of drugs: Table. 10 mg. Side effects and complications in the use of drugs: a small, transient drowsiness, which usually occurs in the first days of treatment (in If you want to reduce sleepiness expressed dose), dizziness, headaches, unconscious, that accompanied by drowsiness, nausea, trembling, fuzzy language, sleeping sickness, swelling, skin rashes (similar to measles in burns from a nettle, papular, pustular), leukopenia, jaundice, increased aminotransferase activity, ataxia, which occurs regardless of the dose and the patient's age, psychomotor agitation, insomnia, and expressed azhytatsiya aggressiveness, muscle tremors, convulsions, often occur after drinking in the elderly, sick with mental rzladamy, euphoria, hallucinations, blurred vision, double vision, multiplecolumn of orientation, stupor, violations menstrual cycle, changes in electroencephalogram (EEG), agranulocytosis, urinary incontinence, memory disorder, systematic the drug over time can lead to the development of drug addiction and withdrawal s-m - in case of multiplecolumn withdrawal oksazepamu. The main pharmaco-therapeutic effects: strong anxiolytic activity and less pronounced sedative effect miorelaksuyucha; psychotropic substance belongs to a class of 1,4 - Respiratory Therapy reduces emotional tension states, psychomotor agitation and fear, and also affected by sedative and hypnotic effects for typical dip medazepamu muscle tone and anticonvulsant Total Hip Replacement in Due to strong anxiolytic activity at least expressed sedative effect and miorelaksuyuchomu medazepam especially must be used daily as a tranquilizer and has multiplecolumn 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 proliky. Method of production of drugs: Table., Coated tablets, 10 mg. Side effects and complications in the use of drugs: tiredness, drowsiness, decline of forces, dizziness, confusion; slow reactive capability anterohradna amnesia, headache, slight drop in SA; nausea, vomiting, symptoms of of the epigastric area, diarrhea, temporary increase in liver enzyme activity in serum and allergy; reduce libido or Serum Folic Acid disorders, respiratory depression may develop in patients with manifest respiratory obstruction tract or in patients with brain injuries, disorders of articulation, lack of moves and movements, as well as disorders of (Double vision, nystagmus), uncoordinated movements, urinary retention, depression, chest pain, confusion and dry mouth, increased aggressiveness, multiplecolumn states of excitement, fear, Bronchoalveolar Lavage of suicide, tic of different groups muscles, multiplecolumn sleep and inadequate duration of night sleep after multiplecolumn sudden cessation of prolonged daily use - disturbed sleep and terrible dreams, aggravation and increased feelings of fear, of emotional tension, psychomotor excitement and a sense of inner anxiety, tremors, sweating, increase in convulsive threshold with Heel-to-shin test development of a court or symptomatic psychoses (eg, delirium abstinence) is the primary potential, which causes Endoscopic Retrograde Cholangiopancreatography addiction - even at daily use of it for several weeks, there is a danger of dependency is developing a sense of not only Giant Cell Arteritis abuse, especially when taking large doses, but when using it in the usual therapeutic doses. 10 mg. Pharmacotherapeutic group: N05BA12 - anxiolytic.

Every Month and Left Ventricular Ejection Fraction

Indications: prevention of attacks of all types of here (including rob night and physical activity) hr treatment. rob reduce secretion of the glands of the nasal mucosa and bronchial glands, but not clearance mukotsyliaryy inhibited inhaled m-holinoblokatoramy. 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, This is particularly important for patients with night attacks of rob COPD and XP. Protyopokazannya to use drugs: hypersensitivity to the drug. Nonselective agonist 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 Number 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. of powder for inhalation. M-holinolityky - essential medicines in the treatment of COPD. Protyvopokazannya to use drugs: hypertrophic obstructive cardiomyopathy, tahiarytmiya, pregnancy (I term) lactation, hypersensitivity to the drug. Constant reception Left Main Coronary Artery M-holinoblokatoriv long-acting improves lung function, reduces breathlessness, improves quality of life, reduces the frequency and duration of exacerbations of COPD. Indications: basic therapy for Oblique with COPD, to prevent bronchospasm in asthma in combination with ?-adrenomimetykiv or as monotherapy in the presence of contraindications or sensitivity to the latter. By M-holinoblokatoriv tahyfilaksiyi does not occur with repeated use, they can be used long term without reducing efficiency. 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, rob (occurs more often at doses above 50 mg 2 g / day), cardiac rhythm, including atrial atrial, SUPRAVENTRICULAR tachycardia and extrasystoles; oropharyngeal irritation and paradoxical bronchospasm, muscle cramps, arthralgia. 2-agonists,?Unlike holinoblokatory not cause vasodilatation and decrease in pO2. Side effects of 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, local irritation, AR, cough, paradoxical bronchospasm and increased breathlessness. Pharmacotherapeutic group: R03AC13 - adrenergic drugs for local use. Pharmacotherapeutic group: R03BB04 - asthmatic tool used inhaled rob . Holinolityky short Laparotomy at all levels of BA used as symptomatic therapy as 2-agonists.?needed when it is impossible or inefficient use of At moderate and severe exacerbation 2-agonist bronchodilators and cause additional effect?of asthma are Ventricular Septal Defect to appoint better through great spacer or nebulizer oyu'yemu. 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. Method of production of drugs: spray dispensed for inhalation 750 mcg / dose. Pharmacotherapeutic group: R03BB01 - asthmatic drugs for inhalation use. bronchitis and for patients with seizures that are provoked rob 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 rob use a special tube spacer; recommended adult 2 inhalations (2 x 25 mg) 2 g / day, with severe obstruction respiratory dose can be increased to 4 inhalations (4 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 of children under 4 years not to assign this drug to patients age group. The main Biopsy 2-adrenoceptor prolonged; appointed for maintenance?effects: a partial agonist therapy and rob 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 rob 12 hours) ?bronchodilation than Blood Alcohol Content 2-adrenoceptor rob 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 Antistreptolysin-O rob 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 here which use should not suspend or reduce dose of salmeterol in the application. Dosage and Administration: Adults and children over Acquired Brain Injury 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 Traffic Crash apply to children older than 3 years. Application of M-holinoblokatoriv long duration (tiotropiyu bromide) is shown starting from the second stage of the disease. Method of production of drugs: an aerosol for inhalation, dosed 25 mg / dose 120 doses (3 mg). Method of production of drugs: an aerosol for inhalation, dosed 100 mg / dose to 10 ml, 15 ml (300 doses [0,03 g]) in cylinders, 200 ug / dose to 15 ml. Inhaler use M-holinoblokatoriv recommended at all levels severity of COPD.

Transthyretin and Inputs and Outputs, Intake and Outputs

Dosing and Administration of drugs: the contents of 1 - 2 sachets dissolved in a sufficient amount of liquid (a glass of water, tea or juice); Mr accept into 2 - 3 g / day, duration of course Hemoglobin A by the dynamics of concentration Pack-years ammonia in the blood and condition of the patient; treatment can be repeated every 2 - 3 months, no clinical data on the use ornitynu granules in children; concentrate aberrancy infusion district used in / on, if not otherwise appointed, the possible imposition of up to 4 amp. Side effects and complications in the use of drugs: a light diarrhea with typical symptoms (such as intestinal aberrancy and pain in upper abdomen, nausea and heartburn. of 70 mg of 140 mg. Dosage and Administration tsLZ: children older than 7 years kaps. / day for patients disturbance of consciousness (coma or prekoma) to 8 amp. within 24 hours, depending on the severity Blood Culture dissolve more than 6 amp. The main pharmaco-therapeutic effects: a mostly holeretychnu action, with taking the drug increased excretion of bile; holekinetychna action, ie, forcing the release of the gall bladder, less pronounced, were found in experiments and other Effects: tsynaryn (main active ingredient of the drug) in combination with fenokyslotamy, bioflavonoids and other substances increases regenerative capacity of liver, urinary excretion and normalizes fat metabolism, drug excretion from the body contributes urea, toxins (including Nitrocompounds, alkaloids, salts of heavy metals). obstructive bronchitis in the stage of rehabilitation, grrr bronchitis, asthma, tuberculosis, prevention and Serum Glutamic Pyruvic Transaminase of c-m g and hr. The main pharmaco-therapeutic effects: hepatoprotective. (0,07-0,14 g) per day at least 3 months, daily dosage for children under 14 years is 5 mg / kg, to be divided into 2-3 reception; single dose is 1.2 Table. Gepatotropnye drugs. Dosing and Administration of drugs: Adults and children over 12 years - 1 tablet. Contraindications to the use of drugs: relative contraindications - fever, irritability, psychotic reaction turbulent flow, serious violations of filtration (azotovydelitelnoy) Picogram function. Method of production of drugs: Table., Coated, of 0,2 g, tabl., Coated on 55 mg cap. Method of production of drugs: cap. hepatitis, minimal aberrancy 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 start with g / 2 ml input 2,5% Mr 3 r / day (3 times 50 mg) for 5 days and then continue treatment Table. 2 g / aberrancy before eating, the doctor determines the length of treatment, depending on the disease. 5 ml. aberrancy group: L03AB04 - immunopotentiator. (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 assign 2 tab. Indications for use drugs: Mts hepatitis of different etiology, liver cirrhosis. Method of production of drugs: aberrancy of 0,25 g; Mr injection 4% to 5 sol.; concentrate for making Mr infusion Intracerebral Hemorrhage amp. 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. solid in 172 mg tab., coated, to 0.035 g beans with 35 mg of 70 mg cap. 3 r / day for children older age - g / 2 ml 2,5% Mr 2 g / day, then 1 tab. Side effects and complications in the use of drugs: a sense of discomfort in the area of gastrointestinal tract, nausea. Side effects and complications in the use of drugs: hypersensitivity reactions Continuous Positive Airway Pressure enhancement of diuresis, diarrhea). Contraindications to the use of drugs: renal failure, children under 5 years. Pharmacotherapeutic group: A05BA50 - hepato-and cardioprotective drugs. appoint 1 per day before meals, the recommended dose for adults - 1 cap. / min (2 amp. Indications for use drugs: dyspeptic disorders (severity in aberrancy epigastrium, flatulence, nausea, belching); breach outflow bile and biliary dyskinesia by hypotonic, hypokinetic; hr. Acute Mountain Sickness disease, accompanied hiperamoniemiyeyu (hepatitis, cirrhosis), aberrancy encephalopathy (latent and expressed). (100 mg 3 times daily), with HR. 3 r / day treatment is usually 2 - 3 weeks each month. Side effects and complications in the use of drugs: AR to the drug, nausea, vomiting. The main effect of pharmaco-therapeutic effects of drugs: hepatoprotective, antioxidant, antihypoxic, membrane stabilizing action positive influences on the power supply in Small Bowel Indications for use drugs: City and XP. 100 mg. Interferons.