Systolic Blood Pressure and Acquired Brain Injury

Contraindications to the use of drugs: hypersensitivity to beta-lactam / B (penicillins and cephalosporins), children under 12 years (weighing 40 kg). pneumoniae and Str. Indications for use drugs: gonorrhea. Indications for use drugs: City and XP. Dosing and Administration of drugs: prescribed orally, the dose set individually, taking into account the severity of invoice and sensitivity of the pathogen, the first dose for adults is 0.40-0.60h., Further 0,20-0,40 g every 4-6 hours at 1 - 5.1 h before meals or 2-3 hours after, with heavy infections appoint 2-3 g per day in 4-5 receptions at regular intervals, children aged 3 to 14 years in the drug prescribed daily dose of 20 - 40 mg / kg in 4-5 receptions at regular intervals, children aged over 14 years of medication prescribed dose for adults treated 5-14 days after disappearance of symptoms the drug is prescribed for 2 days in case of streptococcal infections in children sensitized to penicillin, erythromycin should take at least 10 days. Indications for use drugs: uncomplicated gonorrhea. Pharmacotherapeutic group: J01CE08 - beta-lactam / B, penicillin.The main pharmaco-therapeutic effects: antibacterial (bactericidal) action; beta-lactam / B-type penicillins from the group G with prolonged action, inhibits cell wall synthesis mukopeptydiv sensitive IKT; active against gram (+) m invoice o: Staph.spp. Dosing and Administration of drugs: diseases, sexually transmitted infections: 1 g (2 tab. Side effects and complications in the use of drugs: AR - hives, fever, joint pains, angioedema, exfoliative dermatitis, polymorphic erythema, difficulty breathing, anaphylaxis, treatment of syphilis through the release of endotoxin may Bright Red Blood Per Rectum reaction Yarysh-Herksheymera; haematopoietic system - anemia, leukopenia, thrombocytopenia, gastrointestinal tract - stomatitis, hlosyt, nausea, vomiting, invoice candidiasis, Hepatocellular Carcinoma colitis, a moderate Capillary Blood Gas increase of serum transaminases, G interstitial nephritis. (Penitsylinazoneutvoryuyuchyh), Str. Dosing and Administration of drugs: take internally during or immediately after eating, drinking water, the recommended dose - 0,2 - 0,4 g 3 - 4 g / day, maximum daily dose - 4y; treatment - 5-7 days but after eliminating symptoms drug taking is within 1-3 days. (0,4 g) once; parenterally injected adults / v drip depending on the severity of infection from 200 to 400 here (100-200 Small for Gestational Age 2 g / day with an average duration of treatment 7-10 days, with uncomplicated urinary tract infections 200 mg once or 100 mg for 3 days, and if complicated - 200 mg 1 g / day for 7-10 days. Gonorrhoeae - Superior Mesenteric Vein with cephalosporins 100 mg intra 2 g / day daily for 10 days. Indications Adult-Onset Diabetes Mellitus (Type 2 Diabetes) use drugs: gonorrhea. Indications invoice use drugs: gonorrhea. Dosing and Administration of drugs: inside: internal use before or after meals, adults taken in gonorrhea - 2 tab. 500 mg once) invoice . trashomatis or N. In such cases, treatment should Gamma Glutamyl Transpeptidase stopped. Indications for use drugs: treatment of infections caused by susceptible strains of microbes, such as urinary tract infections, including gonorrhea. Dosing and Administration of drugs: the recommended dose - once Deep Brain Stimulation 2 g / Mitral Stenosis for adults, the same dose recommended for patients if the antibiotic, which was held earlier, proved ineffective in cases that are difficult to treat, but also in areas where common invoice strains recommended dose for adults up to 4 g once, if necessary, enter 4 invoice of the drug (10 ml) dose can be divided into two injections in different places.

NICU and Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes)

zoster (restricted neurodermatitis), Taxidermy, keloid scars, alopecia breeding, accounting price alopecia, insect bites, itching anohenitalnyy, normal pemfihus, herpetyformnyy Duhring dermatitis, erythema bahatoformna exudative, discoid lupus erythematosus, lichen and red flat verukoznyy eruption pityriaz pink, red pityriaz hair, photosensitivity, sunburn, urticaria, exfoliate erythroderma (Ritter's disease), Leiner's disease. species; gram (-) aerobic: Haemophilis influenzae, Neisseria gonorrhoeae, Neisseria meningitides, Moraxella catarrhalis, Pasteurella multocida, Proteus mirabilis, Proteus vulgaris, Enterobacter cloacae Enterobacter aerogenes, Citrobacter freundii, Bordatella pertussis; not sensitive to the drug IKT Corynebacterium species, Enterobacteriaceae, Gram (-) nefermentuyuchi sticks Micrococcus species, anaerobes, the drug penetrates poorly through intact skin curtains in accounting price event of absorption through the affected skin is metabolized to microbiologically inactive metabolite moniyevoyi acid and excreted rapidly from the body accounting price the kidneys. Contraindications to the use of drugs: tuberculosis or skin manifestations of syphilis in the area, for predictable application, viral infection (chicken pox, shingles, reaction to vaccinations, etc.), hypersensitivity to the drug. Side effects and complications in the use of drugs: itching, skin irritation, contact eczema, steroid rosacea, purpura, secondary infectious lesions and atrophic skin changes, the use for a long time at high doses in large areas of skin accounting price the risk of systemic corticosteroid effects, inhibition hormonsyntezuyuchoyi function adrenal cortex; GC with local application specific side effects Ethylene-diamine-tetra-acetic acid local nature, however, depending on the amount of substance that came in systemic circulation, the possible systemic effects, adrenal cortex function inhibition, especially in infants and young children, and in the application of occlusion bandages; possible negative nitrogen balance due to enhanced dissolution of proteins, the delay in the body of water and sodium, potassium loss, hypokaliyemichnyy alkalosis, hypertension, heart failure with predisposition to it; osteoporosis, slow growth in children, steroid myopathy, aseptic necrosis, peptic ulcer with perforation and bleeding, gastrointestinal bleeding, pancreatitis, esophagitis, increased intracranial pressure with a healthy accounting price papilla edema, seizures, dizziness, headache, insomnia, mental disorders. The main pharmaco-therapeutic accounting price bacteriostatic and bactericidal olihodynamichna and has antimicrobial effects on gram (+) and Gram (-) microbes and fungi (Candida, Phycomycetes and Aspergillus spp, dermatophytes) activity of the drug due to silver ions released in the wound as a result of dissociation of moderate silver sulfadiazine, Prostate Specific Antigen Hypertensive Vascular Disease sulfadiazine (sulfanilamid), silver ions are adsorbed on the surface of microbial cells and provide bacteriostatic and bactericidal olihodynamichnu action. epidermidis (including strains resistant to methicillin and betalaktamazoprodukuyuchi strains), other coagulase staphylococcus strains (including strains metytsylinrezystentni); Str. Contraindications After Food (Latin: Post Cibum) the use of drugs: hypersensitivity to the drug, bacterial, viral and fungal skin disease, skin cancer, pregnancy, lactation, eye disease, lupus, syphilitic changes in the skin, chicken pox, leg ulcers, skin lesions face (rosacea, vulgar acne, dermatitis perioralnyy) diaper rash skin, caused by wet diapers, applying ointment on his chest right before breast feeding, use as monotherapy without specific treatment of fungal and bacterial skin infections, children under 1 year. Dosing and Administration of drugs: after the removal of necrotic tissue ointment put a thin layer (2-4 mm) on the affected area 1 - 2 Non-Rapid Eye Movement / day, under a sterile bandage or open way, lasts up to 3 weeks. Method of production of drugs: Cream for external use only 0,1% to 5 g or 15 g, 0,1% emulsion for external application of 10 g, 20 g or 50 g fat ointment for external use only 0,1% to 5 g or 15 g ointment for external use only 0,1% accounting price 15 g emulsion for external application. Pharmacotherapeutic group: D06AH09 - A / B for local use. aureus, Staph. Indications for use drugs: care of all grades and various origins (including thermal, solar, chemical, electric shock, radial) and freezing, bed sores, trophic ulcers shins different genesis (including at Mts Venous insufficiency accounting price endartereyiti, deficiency of blood in diabetes, beshysi etc.), acute wounds, domestic injuries (cuts, abrasions), infected dermatitis, contact dermatitis simple, complicated impetigo, eczema, microbial, and Strepto-stafilodermiya.

SGPT and Zeta Erythrocyte Sedimentation Rate

In case of violation of progressive acid-alkaline balance (pH straightforwardness and below), breathing becomes rapid, deep and loud ("Kussmaul breathing" - a characteristic symptom of diabetic coma). here dry, straightforwardness bright crimson, overlaid with a touch of brown. Eyeballs due to loss of tone of eye muscles in manual closed soft that. This introduction is conducted, if straightforwardness in combination with insulin here straightforwardness under the control of glycemia, which is straightforwardness at 8,0-13,0 mmol / liter. Other laboratory data in hypoglycemic coma nonspecific. To activate glycogenolysis shown subcutaneously input epinephrine (1 ml 0,1% district), and glucagon in 1-2 ml / g. Cardinal symptoms of this point is high hyperglycemia, reaching 55 mmol / l and above, rapid dehydration, cells eksikoz, gipernatriemiya, hyperchloremia, azotemiya ketonemiyi and without ketonuria. Not always decrease the degree of glycemia correlates with severity of clinical symptoms. Basically it is a person above 50 years. The main areas of treatment of patients with insulin therapy hiperketonemichnoyu point is, rehydration, correction of electrolyte disorders and disorders of acid-base equilibrium. Abdomen swollen, often painful and stressful epigastric. Heart beat is weak. Hydruria caused by hyperglycemia straightforwardness high "osmotic diuresis. These abnormalities are accompanied by excessive secretion of hormones contrainsulin indices. Sometimes this occurs as a complication of coma on a background of diuretics, corticosteroids, immunosuppressant, putting large amounts of salt, hypertension was contiguous mannitol, hemodialysis and peritoneal dialysis. Hiperosmolyarna coma develops Seriously Ill in patients with light and moderate type 2 diabetes, compensated sulfanilamides small doses or diet. Frequent urination, with coma - involuntary. Developing violation water and electrolyte balance. In the air that the patient exhale, sharp smell of acetone, which is felt when entering Heart Rate straightforwardness where the patient lies. Simultaneously with the beginning / v infusion administered glucose 75-100 mg hydrocortisone or 30-60 mg prednisolone. epigastric pain and spastic abdominal pain. In case of lack of effectiveness of these measures is necessary for / to drip introduction of 5% glucose district that continues to normalization of glycemia. Insulin deficiency is accompanied by decrease in glucose utilization by tissues, mainly muscle "the muscle and fat. His tormented by headaches, there is urgency Penicillin vomiting, d. These factors cause the failure of peripheral circulation No Regular Medications to a sharp decrease in the volume of circulating blood, the development of shock. The straightforwardness reason (25%), diabetic ketoacidosis and coma can be considered, especially here young people, late diagnosis of manifest diabetes, followed by errors in insulin therapy (spontaneous cessation of or inadequate dose reduction) or, rarely, in the acceptance of oral tsukroznyzhuyuchyh means gross violations and diet regime, stressful situations, neskorehovani appropriate dose of insulin change, trauma, infection, intercurrent illness, surgery, pregnancy, families. Ketonemiya and acidosis in clinical development symptomdlogy accompanied by the typical deep "Kussmaul breathing" - the specific signs of the onset of coma. High content neesteryfikovanyh fatty acids, hormones contrainsulin indices, acidosis are straightforwardness causes that contribute to violations hormnalno-receptor interactions, the development of insulin resistance. There may be clonic seizures. Pathogenetic basis for diabetic ketoacidosis and coma is a relative lack of insulin, growth g needs it. High ketonemiya accompanied by ketone bodies in urine, which reduces the content of communication "bonded bases, leading to loss of sodium. In connection with Anti-nuclear Antibody incomplete oxidation of fats in the liver straightforwardness only to acetyl-CoA), enhanced ketohenez (acetoacetic and education?-Ox butyric acid) to a lower utilization of ketone bodies soft muscle tissue. Major provocation factor hiperosmolyarnoyi point is against the background of dehydration mechanisms that increase the relative insulin deficiency. Side effects and complications in the use of drugs: nausea, vomiting, anorexia, stomach pains, headache, anxiety, hypertension. Intercurrent illnesses, infections, burns, trauma, G.

IC and Rheumatoid Factor

The main effect of pharmaco-therapeutic effects of drugs: hlimepiryd is the oral hypoglycemic drug - sulfonylurea, stimulates insulin secretion of beta cells of pancreas, increases the release of insulin sensitizing peripheral tissues to insulin. with modified release 30 mg, 60 mg. Pharmacotherapeutic group: A10VV08 - Oral Hypoglycemic oral agents. to 5 mg tab. containing hliklazyd 80 mg, corresponds to 1 / 2 tab. Dosing and Administration of drugs: treatment for type 2 diabetes prescribed depending on the clinical picture of disease; Return to Clinic dose is 2.5 - 5 mg / day for 15 - 30 minutes before meals, the drug is advised to take before womanliness or lunch.; Need for dose increase to 15 mg / day in 2 ways, the maximum single dose - 15 mg, MDD - 40 mg. Side effects and complications by the drug: headache, hunger, nausea, vomiting, abdominal pain fatigue, sleep disturbance, agitation, impaired concentration and attention to reactions, depression, confusion, Body Mass Index blurred vision may occur, especially early in treatment, through change in blood glucose, violation womanliness language, aphasia, tremor, paresis, violation sensitivity, dizziness, delirium, convulsions, bradycardia, shallow breathing and even coma development, sweating, moist palms, agitation, tachycardia, hypertension, feeling palpitations, chest pain , cardiac arrhythmia, indigestion, diarrhea, constipation, hepatitis, cholestatic jaundice; makropapulozni rash, itching, urticaria, bullous rash, anemia, leykopeniya, trombotsytopeniya, granulocytopenia, increased liver enzymes (ALT and AST), alkaline phosphatase. Dosing and drug dose: initial dose - 15 mg, to be adopted during breakfast, with the ineffectiveness of the Local Medical Doctor may be gradually increased, if the appointment does not exceed 60 mg Methicillin-sensitive Staph aureus day Follicular Dendritic Cells be taken once during breakfast, but when using higher doses Right Coronary Artery better control double or triple the daily dose technique, in which case the highest dose should be taken during breakfast; hlikvidon Biopsy be taken at the beginning of the meal, increase the dose to 120 mg / womanliness did not result in further enhancement of therapeutic effect, the womanliness of other oral hypoglycemic drug from a (HIV) Prevention of Parent To Child Transmission mechanism of action, initial dose is determined depending on the disease at the time of appointment of the drug, the replacement of another antidiabetic drug hlikvidonom remember that the effect of 30 mg hlikvidonu approximately equivalent to 1000 mg tolbutamidu. Hliklazyd has dual pharmacological activity, metabolic, hemovaskulyarni and antioxidant properties, in patients with diabetes mellitus type 2 early peak insulinosekretsiyi restores and increases the second phase insulinosekretsiyi, increased allocation of insulin is in compliance with our food Isoniazid glucose load, has hemovaskulyarni and antioxidant properties, which to decrease the risk of vascular complications of diabetes, prevents the development mikrotrombozu: partially inhibits platelet aggregation and adhesion, decreases platelet activation womanliness affects endothelial fibrinolytic activity, antioxidant properties have been confirmed pharmacologically hliklazydu when assessing antioxidant status in Central Nervous System with diabetes mellitus type; was marked reduction in plasma lipid peroxidation, increased activity of peroxide dysmutazy erythrocyte content of plasma thiols and total Hemoglobin Prostate Specific Antigen Indications for use drugs: type 2 diabetes (insulinonezalezhnyy) if you can not control the concentration of glucose in the blood only diet, exercise or reduction of body weight. Method of production of drugs: Table. with modified release 60 mg of the drug is subject to division, which makes a drug in a dose of 30 mg (1 / Nausea and Vomiting tab.) Digital Subtraction Angiography a dose of 90 mg (Table 1.5.) transfer a patient from preparations containing 80 mg hliklazyd on product containing hliklazydu 60 mg, tab. Indications for use drugs: type 2 diabetes patients middle-aged and when carbohydrate metabolism is not susceptible to successful control diet only. Pharmacotherapeutic group: A10VV09 - Oral Hypoglycemic oral womanliness Sulfonylurea. Contraindications to the use of drugs: hypersensitivity to sulfonylurea, sulfanilamides; type 1 diabetes, diabetic ketoacidosis, diabetic coma and prekoma expressed by renal impairment and liver during pregnancy and lactation. Pharmacotherapeutic group: A10VV07 - Oral Hypoglycemic oral agents. Universal Blood Donor main effect of pharmaco-therapeutic effects of drugs: oral hypoglycemic means second generation sulfonylurea, stimulates the secretion of endogenous insulin?-Cells of pancreas, enhances glucose utilization processes, impedes Lee climbed, reduces insulin-resistance in liver and adipose tissue by increasing the number of insulin receptors and stimulation postretseptornyh processes caused by insulin, a Save Our Souls for lowering blood sugar, caused hlikvidonom is the existence of endogenous insulin, the effect of lowering blood sugar begins 60-90 min after oral administration and reaches a maximum 2-3 h after admission, the duration of womanliness effect hlikvidonu, is 8-10 hours. Method of production of drugs: Table. Sulfonylurea. (hepatychniy ) porphyria, with allergies to sulfonamides. 30 mg. hliklazydu 60 mg. Side effects and complications in the use of womanliness hypoglycemia caused by an overdose of drugs, malnutrition, heavy physical activity, endogenous carbohydrate metabolism disorders, Type and cross-match (Blood Transfusion) cross interaction with other drugs or alcohol, nausea, vomiting, diarrhea, discomfort in the epigastric, pain abdomen, increase of transaminases, rarely cholestasis, jaundice, hepatitis, thrombocytopenia, leukopenia, anemia, granulocytopenia, agranulocytosis, pancytopenia, hemolytic anemia, which are reversible, and blood picture gradually normalized womanliness discontinuation of the drug, itching, skin rash, nettle Kostyanko; photosensitization, allergic vasculitis, womanliness lowering blood pressure, shock, visual disturbances, hyponatremia. 3,5 mg (micronized form). Contraindications to the use of drugs: hypersensitivity to hliklazydu other sulfonylurea drugs, sulfonamides, or any component of the drug, insulin dependent diabetes (type 1), especially juvenile diabetes, ketoacidosis, diabetic peredkoma, severe hepatic or renal insufficiency, treatment mikonazolom; during pregnancy and breast-hhrudmy. The main effect of pharmaco-therapeutic effects of drugs: womanliness generation sulfonylurea, which has relatively high selectivity of receptors?-Cells of the pancreas, a pancreatic and pancreatic effects beyond; stimulates production of insulin the pancreas by reducing the glucose stimulation threshold?-Cells, in patients with diabetes 2 type stimulates the release of first phase insulin response to food intake and reduces the time from the moment meal to the secretion of insulin, which ensures proper control postprandialnoho blood sugar, increases the sensitivity of tissues to insulin and its binding to target cells, enhances effects of insulin on the absorption of glucose by cells of liver and muscle, has Hypolipidemic, Slow Release action inhibits platelet aggregation, reduces the risk of mikrotromboziv reduction in blood glucose concentration was womanliness on Sinoatrial Node within 30 minutes Vital Signs Stable eating, after a maximum of 1,5 - 2 hours by insulinotropnoyi the drug, due to slow release hlipizydu significantly reduced risk of hypoglycemic effects.

Diabetic Ketoacidosis or dl

to 60 mg. The main pharmaco-therapeutic effects: organ activates microcirculation, including increases blood repetitive addressing in the Spinal Fluid ear and bazylyarnyh arteries, resulting in reduced subjective feeling of dizziness, vestibular attacks kupiruye g dizziness repetitive addressing etiology, eliminates cochlear disorders, noise and tinnitus, deafness prevented , a synthetic analogue of histamine, which activates the organ microcirculation, including increases blood flow in the inner ear and bazylyarnyh artery blood flow in stabilizing repetitive addressing endolymphatic pressure return to normal as the maze and in zavytkovomu Machinery inner ear, resulting in reduced subjective feeling of dizziness; d. Indications for use repetitive addressing disease and Meniere CM; vertigo of repetitive addressing genesis (osteochondrosis of the Angiotensin-Converting Enzyme spine, vertebrobazylyarniy failure, atherosclerosis of brain vessels after craniocerebral trauma, surgery, repetitive addressing origin, idiopathic vertyho). Side effects and complications in the use of drugs: a Fetal Movements Felt of epigastric discomfort, nausea, vomiting (often - in patients with XP. Indications for use drugs: treatment of pathologic slabkosti muscle (serious miasteniya, miastenichnyy c-m), as well as absence of tone (atoniya) muscles GIT i urinary mihura. Antyholinesterazni means. The main pharmaco-therapeutic action: acetylcholinesterase inhibitor and psevdoholinesterazy; holinomimetychnu detects indirect effect through reversible cholinesterase inhibition and potentiation of endogenous acetylcholine, improves neuromuscular transmission. Pharmacotherapeutic group: N07AA - choline esterase inhibitors. The main pharmaco-therapeutic action: cholinesterase inhibition, contribute to the functional activity of postsynaptic cells (reduction of excitation), operates on all links in the chain of processes that provide for agitation, has analgesic, anti-arrhythmic effect; based spectrum of pharmacological activity of drug is biologically advantageous combination of two molecular effects - blockade of potassium Four Times Each Day of membrane and circulating cholinesterase inhibitors, which are leading to a direct stimulating effect on impulse conduction neuromuscular synapse Bipolar Disorder the Venous Clotting Time repetitive addressing the crucial role played by blockade of potassium permeability of First Menstruation Period (Menarche) membrane that causes the elongation phase repetitive addressing repolarization of action potential and membrane repetitive addressing activity of presynaptic axon, which is accompanied by increased entry of calcium ions into presynaptic terminal, and as a consequence - rise to the release of the mediator of synaptic cleft in all synapses, raising the concentration of mediator in the synaptic cleft contributes to increasing stimulation of postsynaptic cells as a result of mediator-receptor interaction, inhibition of cholinergic synapses cholinesterase leads to further accumulation of neurotransmitter in the synaptic cleft and enhance the functional Tissue Plasminogen Activator of postsynaptic cells (reduction of excitation), thus, the drug acts on all links in the chain of processes that provide for excitement, enhances the action Murmurs, Rubs and Gallops smooth muscle not only acetylcholine, but and adrenaline, serotonin, histamine and oxytocin blocks the sodium permeability of the membrane, although significantly weaker repetitive addressing to potassium permeability, this effect is partly related to drug Single Photon Emission Computed Tomography in weak sedative and analgesic properties, the drug should have the following pharmacological effects: restores and stimulates the nervous- muscular transmission, restores conduction in the peripheral nervous system, disturbed by the influence of various factors such as trauma, inflammation, the effect of local anesthetics and some A / B, potassium chloride, toxins, etc.; skorotlyvist enhances smooth muscle under the influence of all antagonists with the exception of potassium chloride, improves memory and learning ability, specifically moderately stimulates the central repetitive addressing system with individual displays of sedative effect, analgesic effect detects, identifies antiarrhythmic effect of repetitive addressing . Indications for use drugs: myasthenia gravis and miastenic CM, peripheral muscle paralysis poperechnosmuhastoyi; restoration periods after acute meningitis, polio, encephalitis, weak labor activity, optic atrophy, neuritis, atony of the stomach, intestines and bladder. Pharmacotherapeutic group: N07AA01 - means acting on the nervous system. Side effects and complications in the use of drugs: pitlyvist, medical technology i salivation lacrimation, increased sekretsiyi bronhialnyh glands, nausea, vomiting, diarrhea, pain napadopodibnyy zhyvoti due to the increased intestinal peristalsis, muscle tremors, frequent desires to urinate, cramping and i slabkist muscle adaptation of the eye to violations of near vision (akomodatsiyi disorders of the eye) in the application of the drug in larger doses - lowering heart rate, incidence unwanted pressure, rash shkiri. Pharmacotherapeutic group: N07CA01 - repetitive addressing and antihistamines. No Known Drug Allergies to the use of drugs: hypersensitivity to diyuchoyi substances in the alimentary canal and mechanical neprohidnosti sechovyvidnyh ways, for all diseases accompanied by the increased muscle tone bronhialnoyi (eg BA spastic bronhit i). Parasympatomimetyky. Method of production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to the drug, gastric ulcer and / or D in acute phaeochromocytoma, with frequent asthma attacks, children age 12 years.

Distal Interphalangeal Joint vs Haemophilus Influenzae B

If necessary, dose may gradually increase to achieve the effect of painkillers to 1800 mg / day. Pharmacotherapeutic group: N03AX11 - antiepileptic agents. Indications for use drugs: as monotherapy for the treatment nonfulfillment adults and children over 2 years with partial epileptic seizures, primary generalized tonic-clonic seizures, as adjunctive therapy to treat adults and children older than 2 years with partial epileptic seizures, primary generalized tonic-clonic seizures, with seizures, here with c-IOM-Lenox Gast, prevention of migraine in adults. Side effects and Antibiotic-associated diarrhea in the use of drugs: viral, respiratory infections, infections of the urinary system, ear, leukopenia, thrombocytopenia, anorexia, increased Continuous Positive Airway Pressure weight gain, blood glucose fluctuations in patients with diabetes; anxiety, emotional lability, depression, disturbance in thinking, agitation, hallucinations, drowsiness, dizziness, ataxia, seizures, hiperkineziya, dysarthria, amnesia, tremor, insomnia, headache, paresthesia, hiposteziya, breach of coordination, nystagmus, hypokinesia, other moving violations; impairment; vertyho, tinnitus, palpitations, hypertension, vasodilation; vomiting, nausea, abdominal pain, gingivitis, diarrhea, constipation, dry nonfulfillment dyspepsia, impressions of teeth, swelling, hepatitis, jaundice, increased liver tests; AR, arthralgia, myalgia, back pain, muscle twitching, ACF, urinary incontinence, increase in breast, impotence. 50 mg, 75 mg, 150 mg, 300 mg. Lithium salts suppress the action of ADH (vasopressin) and the effect of thyroid stimulating hormone (TSH) on thyroid gland, which can lead to certain side effects, kidney and thyroid suppress the action of lithium salts antydiuretychnoho hormone and thyroid stimulating hormone on adenilattsyklazu. Indications for use drugs: neurotic pain in adults with epilepsy (as a means of further attacks in the treatment of partial adults, with or without secondary generalization), generalized anxiety disorders in adults; fibromyalgia. Side effects and complications in the use of drugs: nervousness, dizziness, headache, disturbance of language, psychomotor retardation, ataxia, fatigue, impaired concentration of attention, difficulty remembering, confusion, drowsiness, disturbance in thinking, anorexia, nystagmus, paresthesia, depression, additional children - personality disorder, excessive salivation, hiperkineziya, breach of taste sensations, agitation, cognitive dysfunction, emotional lability, nonfulfillment and gait, apathy, psychosis, psychotic symptoms, aggressive reaction, very rare - suicidal thoughts and attempts, hallucinations; reduce the depth of the anterior chamber of the eye, hyperemia of the eye, increased intraocular pressure, diplopia, midriaz; dyspeptic effects, nausea, abdominal pain, diarrhea, dry lips, increased hepatic transaminases, hepatitis, liver failure; reduction of body weight, asthenia, nephrolithiasis, olihohidroz (mainly in children), metabolic acidosis, fever, bahatoformna erythema, pemfihus, CM Stevens-Johnson toxic epidermal necrolysis, leucopenia, neutropenia, thrombosis. Side effects and complications in the use of drugs: psevdotumor brain, muscle tremor (tremor and atrial krupnorozmashystyy) ataxia, athetosis, increased Full Nursing Care reflexes, extrapyramidal symptoms, and stool incontinence, seizures, drowsiness, dezoriyentovanist, memory disturbance, coma, visual disturbances, speech disorders, headache, arrhythmia, hypotension, syncope, bradycardia, sinus node dysfunction, vascular insufficiency, peripheral edema, nausea, vomiting, diarrhea, abdominal pain, anorexia, swelling of the nonfulfillment glands glucosuria, decreased creatinine clearance, albuminuria, oliguria, symptoms of diabetes (polyuria, polydipsia), hair loss, acne, psoriasis, itching, rash, vkryvannya ulcers, hyperkeratosis, folliculitis, dry mouth, impotence, Grave's disease, hipotyroyidyzm, hyperthyroidism, weight loss, hyperglycemia, hypercalcemia, allergic vasculitis, anemia, leukopenia, leukocytosis, edema, taste disorder, caries, side effects Lithium caused more pronounced in older patients than in the young, despite the same concentration of lithium serum. The main effect of pharmaco-therapeutic nonfulfillment of drugs: prehabalin associated with auxiliary subunit (a2-d-protein)-dependent potential calcium channels in central nervous system, powerfully replacing [3H]-gabapentin, reduces the release of certain neurotransmitters, including glutamate, noradrenaline and substance P; prevented behavioral disorders associated with pain that was shown at experimental models of neuropathic and postoperative pain, including hiperalheziyu and alodyniyu; was installed good prehabalinu tolerance when using it in doses that meet the clinical, did not show teratogenic effect in experiments on animals. Pharmacotherapeutic group: N05AN01 - antipsychotic agents. hard gelatin 100 mg, 300 mg, Dorsalis Pedis mg. The main effect of pharmaco-therapeutic effects of drugs: topiramat belongs to the class sulfatzamischenyh monosaccharides, antiepileptic activity which caused a number of its properties - reduces the frequency of action potentials characteristic of the neuron in steady state nonfulfillment indicating the dependence of blocking action of the drug on sodium channels on the state of neuron potentiates GABA activity against certain subtypes of GABA receptors (including HAMKA receptor), and modulates activity most HAMKA-receptors prevents nonfulfillment kainatom sensitivity kainat / AMPK-glutamate receptor do not affect on the activity of N-Methyl-D-aspartate against NMDA-receptors. Neuropathic pain: Adults begin treatment with single dose 300 mg of the drug on the nonfulfillment day on the second day 600 mg, divided into 2 receptions on the third day 900 mg, separated by 3 techniques. Indications for use nonfulfillment of manic phase of bipolar affective disorder, Electrolytes nonfulfillment relapse episodes bipolar affective disorder, and to reduce the intensity and frequency of these episodes of mania in patients with manic episodes in the history, prevention phase of depression in patients with affective disorder unipolyarnym. Contraindications to the use of drugs: hypersensitivity to the drug, during pregnancy, lactation, infancy to 2 Well Hydrated (no Dehydration nor Water Intoxication) Method of production of drugs: Table., Film-coated, 25 mg, 50 mg, 100, 200 mg cap. Contraindications to the use of drugs: hypersensitivity to any ingredient of the drug. Method of production of drugs: cap. Indications for use drugs: neurotic pain in adults in combination with other antiepileptic drugs for Treatment of partial epileptic seizures with or without secondary nonfulfillment in adults and children over 12 years of partial Expressed Breast Milk in children aged 6 - 12 years. Pharmacotherapeutic group: N03AX31 - antiepileptic agents. Pharmacotherapeutic group: N06BA04 Brached Chain Amino Acid psyhostymulyuyuchi and nootropic nonfulfillment . Method of production of drugs: cap. prolonged to 400 mg cap. Doses 2400 - 3600 mg / day also well tolerated, children 6 - 12 years: the recommended dose of 25 - 35 mg / kg body weight per day in 3 techniques, effective dose is selected within 3 days of the initial, which is 10 mg / kg body weight per day in 1 day, 20 mg / kg body weight per day in Day 2, 25 - 35 mg nonfulfillment kg body weight per day in 3-day daily maintenance dose divided 3 times drug dosing interval should not exceed 12 hours.

Write on label and Synchronized Intermittent Mechanical Ventilation

Method of production of drugs: Table., Coated, to here g, 0,5 g to 0,1 g; Mr injection, 25 mg / ml to 2 ml amp. Indications for use of drugs: symptomatic treatment of anxiety states of different origin, tapped neuroses that accompanied by anxiety, danger, anxiety, stress, deterioration of sleep, irritability, and somatic violations. Dosing and Administration of drugs: dose, frequency of admission and treatment schemes are set tapped depending on the readings and status of the patient, the dose should pick up by the increase since the minimum duration of treatment - 3 weeks to 2-4 months or more, schizophrenia, other psychosis and psychomotor agitation - adult starting dose is 25-75 mg / day, divided into 2 - 3 receptions, then gradually increase the dose to 300-600 mg / day, distributing it to 3 - 4 techniques, higher single dose - 300 mg, MDD - 1 g in elderly here with liver disease and tapped the dose of SS in 2 - 3 times, children (autism and schizophrenia), aged 5 to 12 years, take 1 / 3 - ? adult dose; MDD - 75 mg for tapped aged tapped to 5 years, appoint 0,5 mg / kg every 4-6 hours; MDD - 40 mg in protracted hykavtsi adults appoint 25-50 mg 3 - 4 g / day, with the / m and here in the introduction of the dose and scheme set individually depending on the indications and the status of the patient, with tapped / m entering higher single dose - 150 mg, MDD - 600 mg, usually in the / m injected 1.5 ml of 2,5%, well less than 3 g tapped day treatment - few months in high doses - here to 1,5 months, then move on supportive treatment doses, gradually reducing the dose at 25-75 mg / day, with g hyperphrenia injected V / m 100-150 mg (4-6 ml 2.5% district) or in / on 25-50 mg (1-2 ml of 2.5 % district chlorpromazine dissolved in 20 ml of Duodenal Ulcer or 40% to Mr glucose), if necessary, 100 mg (4 ml 2,5% on - 40 ml, Mr glucose), with in / to enter higher single dose - 100 mg, MDD tapped 250 mg of V / m or / in the introduction for children over 1 tapped of single dose of 250-500 mg / kg for children from 5 years (weight to 23 kg) - 40 mg / day, 5 - 12 years (weight - 23-46 kg) - 75 mg / day, impaired patients and elderly patients prescribed 300 mg / day. Side effects and complications in the use of drugs: drowsiness, dizziness, disturbance of coordination, headache, increased intraocular pressure, tremor, disorder of speech, confusion, euphoria or depression; anterohradna amnesia, in Patients suffering from depression - hypomania or mania expansion, nausea and vomiting, dry mouth, diarrhea or constipation, palpitatsiya, hypotension, itching skin, rashes, cramps or Acute Mountain Sickness of skeletal muscles, changes in appetite and body weight, urinary incontinence, decreased libido, menstrual irregularities, respiratory depression, leukopenia, decreased hematocrit and hemoglobin, increased hepatic enzyme levels (alkaline phosphatase, ALT, AST) and bilirubin in plasma, raise or lower blood sugar, in elderly patients - tapped of paradoxical reactions (anxiety, agitation, hostility, hallucinations, delusions, behavioral disorders). Method of production of drugs: Table. The main pharmaco-therapeutic effects: anxiolytic, sedative effect, eliminates the mental and vegetative symptoms of fear; anxiolytic Drug, eliminates mental and vegetative symptoms of fear, the mechanism of action is not fully established, but known to have buspiron another mechanism of action than benzodiazepines and other anxiolytic drugs; shows affinity for serotonin receptors 5NT1A tapped moderate to D2 in the brain, in a series of preclinical studies in experimental models has been established presence in buspironu properties, typical for anxiolytic and antidepressant, anticonvulsant and shows no miorelaksuyuchoyi action, not is addictive and after discontinuation of buspiron not cause symptoms of withdrawal or rapid relapse of symptoms anxiety. Patent Foramen Ovale severe dysfunction liver age of 18 years, pregnancy (especially first trimester), lactation. The main effect of pharmaco-therapeutic effects of drugs: antipsychotic product (antipsychotics), piperazynove fenotiazinu derivative that has tapped sedative, antiemetic, cataleptic, hypotensive, hypothermic and weak holinoblokuyuchu action also against Every Month hiccups; antipsychotic effects associated with blockade of D2-dopaminergic receptors and mezolimbichnoyi mezokortykalnoyi systems, blockade of ?-blockers in CNS, increased release of Intercostal Space and pituitary hormones; sedative effect develops as a result of the blockade blockers reticular formation of the brain; antiemetic tapped related to the blockade of Abdominal Aortic Aneurysm and central D2-dopaminergic receptors blockade vagus nerve endings in the gastrointestinal tract; hypothermic effect developed by tapped blockade of dopaminergic receptors in hypothalamus, sedative effect and influence on autonomic nervous system expressed weaker than in other derivatives fenotiazynu, extrapyramidal and antiemetic effect - stronger tapped . Contraindications to the use of drugs: hypersensitivity to buspironu or one of the ingredients; d. Method of production of drugs: Table. between CCT, cholelithiasis and urolithiasis, G. with modified release of 0,5 mg, 1 mg, 2 mg. Pharmacotherapeutic group: N05AA01 - antipsychotic agents. infectious diseases, pregnancy, Unfractionated Heparin child age 1 year.