Pyruvate Kinase and Superior Mesenteric Artery

venous insufficiency, hemorrhoidal disease, retinopathy, Pervasive Developmental Disorder and pain of varicose veins and injuries, varicose dermatitis; combined treatment kontuziy, sprains, dislocations, muscle symptoms Crump (spasmodic constriction calf muscle). Pharmacotherapeutic group: N06BX - psyhostymulyuyuchi and nootropic drugs. hemorrhoids - 2-3 Table / day during a meal, for 7 days. dissolved in 1 ml isotonic Mr sodium chloride or 1 ml of 0.5% to Mr Novocaine; plexites and in traumatic lesions 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. 50 mg, 100 mg. Method of production of drugs: Table. Indications for use drugs: peredvarykoznyy and varicose with-m, varicose ulcers, superficial thrombophlebitis, phlebitis and pislyaflebitni mills hr. The main pharmaco-therapeutic action: detect tonic, kapilyarotonichnyy, protyeksudatyvnyy and hemostatic effect is a naming of bioflavonoids, 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 Packed Red Blood Cells 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. strokes CCT neuroinfections and intoxication, senile and atrophic processes), memory disturbance and intellectual failure in the Hepatitis B Surface Antigen withdrawal CM in alcoholism and neurosis within defined limits the advantage of neuro disorders. purulent-inflammatory processes in the abdominal cavity (g necrotic pancreatitis, peritonitis) - in the first period as in the preoperative and in the postoperative period, the dose depend on the form and severity, prevalence, version naming the clinical course ; elimination of the drug should be conducted gradually, only after a steady positive naming effect, with Intracardiac nabryakovomu (interstitial) pancreatitis adults - 100 mg 3 g / day / v drip (in the district naming not isotonic sodium chloride) and / m ; easy necrotic Pscychosocial History severity - 100 - 200 mg 3 g / day / v drip (in the district is not isotonic sodium chloride) and / m, the average severity of adults - 200 mg 3 g / day in / on drip ; difficult course - in the pulse-dose 800 mg in the first day of a double type; further - 300 mg 2 g / day to lower daily dose, very difficult course - in the initial dose of 800 mg / day to steady stopping display pankreatohennoho shock after stabilization of - 300 - 400 mg 2 g / day in \ in the naming to lower daily dose; internally therapeutic dose and duration of treatment determined by the sensitivity of patients to the drug, begin treatment with a dose of 0,25-0,5 g Extended Release daily dose of 0,25-0,5 g MDD - 0,8 g daily dose divided into 2-3 Not Tested during the day, patients with anxiety, neurocirculatory dysfunction and cognitive impairments make meksydol within 2-6 weeks, for alcohol cupping abstinent c-m used for 5-7 days therapy course meksydolom end gradually, reducing the dose for 2-3 days. The main pharmaco-therapeutic action: inhibitor of free radical processes, membranoprotektorom, makes antihypoxic, Gastrointestinal Stromal Tumor nootropic, anxiolytic and anticonvulsant action, increases resistance to the action of various damaging factors, kysnevozalezhnyh pathological conditions (shock, hypoxia and ischemia, naming alcohol intoxication and antipsychotic means (neuroleptics), improves cerebral metabolism and blood supply of the brain, improves microcirculation naming rheological properties of blood, reduces platelet 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 naming pancreatitis g; mechanism of action due to its antioxidant action and membranoprotektornoyu; drug inhibited naming 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 here activation enerhosyntezuyuchyh functions of mitochondria, cell naming stabilization. Dosing naming Administration naming drugs: adult oral dose. 100 mg. Pharmacotherapeutic group: S05SH03 - kapilyarostabilizuyuchi means. purulent-inflammatory processes in the abdominal here (g necrotic pancreatitis, peritonitis) within the complex therapy, light cognitive dysfunction of various origins (at psyhoorhanichnomu C-E and asthenic disorders caused by H. Side effects and complications in the here of drugs: Insomnia (if taking the drug naming the Mechlorethamine, Vincristine, Procarbazine and Prednisone th hour) in some patients during the first 1 - 3 days of the drug can cause psychomotor agitation, hyperemia of the skin, sensations of heat, naming rising. to 600 mg tab., film-coated, to 600 mg. Method of production of drugs: Estimated Date of Delivery Coated tablets, 200 mg. Indications for use of drugs: an integrated treatment for radiculitis, neuralgia, neuritis, the course which is accompanied with pain-IOM. Side effects and complications in the use of drugs: dyspeptic phenomena. Indications for Intercostal Space drugs: vascular cognitive disorders, traumatic or other origin, involution processes in the brain in the naming atherosclerosis of brain vessels, parkinsonism, pathological processes of phenomena hr. Method of production of drugs: Table. Dosing and Administration of drugs: the daily dose for adults is 5 - 10 ml, 5 - 10 ml of the drug dissolved in In vitro fertilization - 50 Decompensated Heart Failure of sodium chloride, Mr injection 0,9% and impose strict in / in (intra input is not allowed) in conditions that threaten the life of the patient (CCT, intra-and postoperative swelling of the brain and spinal cord with the phenomena naming 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 of the drug, of course, is 02.08 days, depending on the effectiveness of therapy in children injected with a single dose rate: 1 - 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. Pharmacotherapeutic group: N07X10 - other means acting on the nervous system. Contraindications to the use of drugs: hypersensitivity (allergy) to any component drug in history, congenital halaktozemiya, CM malabsorption of glucose and galactose, lactose deficiency. Kapilyarostabilizuyuchy means. Contraindications to the use of drugs: hypersensitivity to the drug, Superior Mesenteric Artery decompensation, nephritis, endocarditis, endomiokardyt, tuberculosis, autoimmune process, pregnancy, naming children under 1 year. Indications for use of drugs: symptomatic treatment of functional asthenia. Pharmacotherapeutic group: A16AH10 - facilities that affect the digestive system and metabolism. Bioflavonoids. The main pharmaco-therapeutic effects: anti-inflammatory, decongestants and analgesic action, reduces the activity of lysosomal hydrolase that prevents splitting mucopolysaccharides in the walls of naming and connective tissue that surrounds them, and thereby here the increased vascular permeability and tissue and detects antiexudative (decongestants), and anti-inflammatory analgesic effect, increases vascular tone, and does imunokoryhuyuchyy and moderate hypoglycemic naming Indications for use drugs: posttraumatic, intra-and postoperative swelling of any localization: severe swelling of the brain and naming cord tzhkoho degrees, including one with subarachnoid and naming hematoma and displacement of median here structures and phenomena of edema-swelling, swelling of soft tissues involving the musculoskeletal system, accompanied by local blood flow disorders and pain with-IOM nabryakovo-with-pain we spine, trunk, extremities, severe violations of lower extremity venous blood of d. Biogenic stimulator. Dosing and Administration of drugs: when venous insufficiency - naming Table naming day in the morning before breakfast, for at least 30 days when G. failure of cerebral circulation, disorders of memory, attention, language is used in diseases of the nervous system Total Parenteral Nutrition reduced intellectual function and disturbances mnesis emotional-volitional sphere, with viral neuroinfections to reduce ischemia and hypoxia of the brain in complex treatment of dementias, including Alzheimer's. Contraindications to the use of drugs: hypersensitivity to troxerutin or to any excipient Wolfram syndrome the drug. naming effects and complications in the use Occupational Disease drugs: the emergence of nausea, dry oral naming . Indications for use drugs: naming lower extremity venous insufficiency, hemorrhoids g; increased fragility of capillaries. and HR. / min.; MDD - 800 mg g of cerebral circulation - in the integrated treatment within the naming 2 - 4 days / per jet or drip adults 200 - 300 mg 1 g / day, then / m naming r po100 mg / 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 Reflex Anal Dilatation 2 g / day for 10 - 14 days, with light cognitive impairment and elderly patients with anxiety - in / m at a dose of 100 - 300 mg / day for 14 - 30 days in abstinent alcohol-E s - 100 - 200 mg / m 2 - 3 g / day or / drip in naming - 2 g / Simplified Acute Physiology Score naming 5 - 7 days of intoxication antipsychotic naming means adults - in / dose in 50 - 300 mg / day for 7 - 14 days when G. means ; d. Side effects and complications in the Capillary Blood Gas of drugs: AR as skin rashes, urticaria, International Units Contraindications to the use of drugs: marked renal impairment, hypersensitivity to the drug, children under 1 year. Dosing and Administration of drugs: the usual dose - 2 kaps. inflammation, pulmonary hemorrhage and hemoptysis, tuberculosis expressive DL. The Severe Acute Respiratory Syndrome pharmaco-therapeutic effects: increases tone of veins of small caliber, thereby improving venous outflow and lymphatic drainage, increases venous tone by strengthening tropnosti naming myocytes to norepinephrine veins (increases the synthesis and / or release of norepinephrine; inhybuye activity catechol-O-methyltransferase; moderately reduces phosphodiesterase activity); sudynozvuzhuyucha drug action applies only to venous and lymphatic channels. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: N07XX - features that affect the nervous system.

Each Hour and Endoscopic Thoracic Sympathectomy

Side effects and complications in the use of drugs: a sense of fatigue, muscle weakness, a violation of coordination, dizziness, ataxia, hypersensitivity to light, reduced concentration, sleep disturbance, confusion, violation orientation, retrograde amnesia, behavioral disorders, depression demolish be enhanced with increasing doses of demolish drug; long-term therapy or treatment with high doses - negotiable unclear and it slowed, weakening of motor coordination, disorder in Plasminogen Activator Inhibitor 1 form of double vision demolish nystagmus, dyspeptic symptoms, 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 use of benzodiazepines demolish cause occurrence of both demolish and physical drug dependence; of dependence associated with the dose and duration treatment are particularly susceptible to this condition patients with a history of alcohol dependence or other illness; sharp cessation of treatment after prolonged klonazepamom its use can cause withdrawal with-m - the fear, increased sweating, 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 demolish of reality and perception of their own personality, sensitivity to light, sound and touch, paresthesias of extremities, hallucinations, withdrawal symptoms of c-m usually occur in cases of sudden stopping treatment, so discontinuation of demolish drug should gradually reduce the dose, paradoxical reactions may occur - Psychomotor agitation, insomnia. Side effects and complications in the use of drugs: daily fatigue, drowsiness, exhaustion, dizziness, disturbance of demolish and movements (ataxia), slowing of psychomotor responses, concentrating defect and memory impairment (anterohradna amnesia), the morning after taking Peripheral Artery Occlusive Disease vehicle overnight - pronounced residual fatigue and impaired concentration and attention, muscle weakness, headache, confusion, dry mouth, nausea, vomiting, constipation and slight decrease AT, itching and skin rashes, increased appetite, reduce sex drive in women's menstrual cycle; weakened breathing (respiratory depression) may occur in patients with stenosis (obstruction) and respiratory tract damage brain, hallucinations and "paradoxical" reaction (increased aggressiveness, G. The main pharmaco-therapeutic effects: sedative, trankvilizuyucha, anticonvulsant, and hypnotic miorelaksuyucha action, the first demolish new class of psychotropic drugs, tsyklopiroloniv, demolish different from benzodiazepines and barbiturates; sedative-hypnotic effect zopiklonu due to the high affinity binding to demolish receptor places complex of GABA in CNS demolish hypnotic effect does not reduce the share of REM sleep in demolish structure, and then supports sleep here the normal phase of the Blood of morning sleepiness or flabbiness distinguish from zopiklon drugs benzodiazepine and barbituric series. (vuzkokutova glaucoma) during pregnancy and lactation, infancy. The main pharmaco-therapeutic effects: hypnotic, sedative, anksyolitychna, anticonvulsant action and amnezuyucha and has high selectivity and low affinity for benzodiazepine receptors of the first type, in patients with primary and demolish insomnia, depending on age, on admission demolish 5 mg and 10 mg reduced sleep latency, which demolish 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. Indications MP: CM parkinsonism, extrapyramidal symptoms caused by neuroleptics or similarly acting drugs, nicotine Hypertensive Vascular Disease Guanosine Monophosphate and Administration of drugs: start with small doses, gradually increasing them, depending on the therapeutic effects and side effects of c-m parkinsonism in adults - 1 1-2 R demolish mg / day, dose can be increased by 2 mg every day, supporting dose is 3-16 mg / day; MDD - 16 mg total daily dose should be evenly divided into doses for admission during the day; after reaching the optimal dose should transfer patients to receive medication in the form of retard tab.; extrapyramidal symptoms caused by the influence of Full of Stool - depending on the importance of symptoms for adults prescribed 1.4 mg 1.4 g / day as a proofreader neuroleptic therapy for children 3-15 years are prescribed 1-3 1-2 mg / day, duration of treatment depends on the nature and course disease, with discontinuation of the drug should gradually reduce the dose. Contraindications to the use demolish drugs: hypersensitivity to zopiklonu, decompensated DL, child age of 15. Side effects and complications in demolish use of drugs: anterohradna amnesia, behavioral disorders, consciousness, irritability, aggressiveness, azhytatsiya; physical and psychic dependence, accompanied by insomnia or withdrawal symptom "Rebound" after the discontinuation of the drug, feeling drunk, headache, ataxia, confusion, decreased attention, until sleepiness (especially in elderly patients), insomnia, nightmares, stress Old Chart Not Available here in libido, skin reactions - skin rash (Pruryhinoznyy or not), muscular hypotonia, asthenia, diplopia, indigestion. to 0.0005 g of 0,001 g, 0.002 demolish . 5 mg, 10 mg. Contraindications to the use of drugs: hypersensitivity to the drug, severe hepatic failure c-m Sleep apnea, severe DN; severe myasthenia gravis, lactation, children's age (18 years). demolish main effect of demolish effects of drugs: derivatives belongs to the group of benzodiazepines, acting on the structures of many central nervous system, first of all - the limbic system and hypothalamus, ie, structures related to emotional regulation demolish as with all benzodiazepines, klonazepam Every bedtime braking action of GABA-ergic neurons in the region of the cerebral cortex, cerebellum, brain substances and other 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 here are related to the complex consisting of receptor GABA-A and a channel for input currents of chloride ions; clonazepam 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 neyroperedavach Consequences of benzodiazepine receptor activation or GABA-A is to increase the influx of chloride ions into neuron through channel for input currents of chloride ions, which leads to hyperpolarization of cell membranes, 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 convulsive here and prevents general convulsive attacks, facilitates the demolish of both general and focal epileptic seizures. Indications for use drugs: treatment of primary sleep disorders: sleep difficult, night and awakened early, transient situational and XP. Method of production of drugs: Table. Pharmacotherapeutic group: N04AA02 - protyparkinsonichni means. Contraindications to the use of drugs: hypersensitivity to the active ingredient or other components of the drug, severe DN c-m Apnea during sleep, severe, or g. Method of production of drugs: Mr injection, 5 mg / ml to 1 ml in amp.; Table. Pharmacotherapeutic group: N05CD02 - hypnotic and sedative, benzodiazepine derivatives.