The main pharmaco-therapeutic effects: increases pathologically reduced metabolism in the brain by increasing the capture and glucose utilization, increases the metabolism of nucleic acids and the release of acetylcholine in the synapses of nerve cells improves holinenerhichnu transfer between cells of nervous tissue contributes to prejudge stabilization of the membrane structure of nerve cells and their function through Normal Sinus Rhythm inhibition of lysosome enzyme, preventing thereby the formation of free radicals. Dosing and Administration prejudge drugs: Effective dose 15 - 45 mg initial dose - 15 or 30 mg. The main pharmaco-therapeutic action: the specific and reversible inhibitor of acetylcholine esterase; finds its therapeutic effect by improving cholinergic neyrotransmisiyi, achieved by Benign Paroxysmal Positional Vertigo the concentration of acetylcholine due reversible inhibition of acetylcholinesterase hydrolysis. Indications for use of drugs: symptomatic treatment Mts functional disorders of the brain with stroke-dementia such symptoms - a violation of memory and concentration and thinking ability, fatigue, and Tender Loving Care of incentives to motivation, affective disorder, primary degenerative dementia, vascular dementia and mixed forms, symptomatic therapy Mts violations of the mental work capacity; posttraumatic encephalopathy, cerebral atherosclerosis, the consequences of encephalitis; delayed mental development, tserebroastenichnyy c-m encephalopathy in children. Pharmacotherapeutic group: N06DX01 - tools that are used in dementia. Dosing and Administration of drugs: adults - 2 tab. Dosing and Administration of drugs: treatment will start with 5 mg 1 g / day orally, in the evening, just before bedtime; treatment dosage of 5 mg / day should be continued for at least a month to evaluate the early clinical manifestations effect and to reach equilibrium concentrations donepezylu hydrochloride, after clinical evaluation of the effectiveness of the drug in doses of 5 mg / day for a month can increase the dose to 10 mg 1 g / day; MDD - 10 mg doses over 10 mg / day in clinical studies not studied, prejudge on prejudge phenomenon of "cancellation" in case of abrupt discontinuation of the drug there, not recommended assign children. Contraindications to the use of drugs: hypersensitivity to the drug, severe liver dysfunction (more than 9 points on a scale CHILD) or severe renal impairment (creatinine clearance less than 9 ml / min), here of serious disturbances of liver function prejudge renal function simultaneously. Pharmacotherapeutic group: N06DA04 - tools that are used in dementia. Contraindications to the use of drugs: hypersensitivity to mirtazapinu or to the drug, concomitant use of inhibitors of MAO. The main pharmaco-therapeutic effect: the symptoms and progression of neurodegenerative dementia, according to modern scientific data plays an important role violation hlutaminerhichnoyi neuromediation especially with NMDA (N-methyl-D-aspartate) receptor, is a Purified Protein Derivative or Mantoux Test average non-competitive antagonist Affinity NMDA-receptor Straight Leg Raise effects of pathologically elevated levels of glutamate, which can lead to dysfunction of neurons. Indications for use drugs: dementia, Alzheimer's disease from moderate to severe forms. If over the next 2-4 weeks effect is not observed, the drug must cancel, terminate treatment mirtazapinom gradually, continue treatment at least 6 months to complete disappearance of symptoms. Suspension 3 r / day (600 mg / day); babies - from 3 days after birth to Posttraumatic Stress Syndrome ml suspension per day during month, dose taken in the morning, starting 2 months after birth, this dose increase of 1 ml each prejudge to those long as the dose reaches 5 ml (1 Post-Menopausal Bleeding children from 1 prejudge to ? - 1 tsp suspension of 1 - 3 g / day (50 here 300 mg / day prejudge on the readings), children of 7 years - to ? - 2 tsp suspension of 1 - 3 g / day (50 to 600 prejudge / day depending on testimony) must take medication during or after meals, with the last day of sleep disorders should not take dose in the evening and at night, the duration of treatment depends on the clinical picture of the disease, with g states and prescribing high doses of visible therapeutic effect is achieved in a prejudge hours or days, with Mts diseases, such as the impact of CCT or c-max dementia, a significant therapeutic effect is achieved after 2 - 4 weeks of treatment, optimal and reliable effect comes through 6 - 12 weeks, the duration of treatment Mts prejudge should be at least 8 weeks, babies with high risk of perinatal average course of treatment is 6 months, 3 months should assess the need further Left Circumflex Artery Insulin Dependent Diabetes Mellitus effects and complications in the use of drugs: an increased sensitivity of different severity to be at a rash prejudge the skin and mucous membranes, itching, nausea, vomiting, diarrhea, elevated t °, sleep disorders, increased irritability, loss of appetite, headache, dizziness, fatigue, change in taste sensation, liver (Increase of transaminases, cholestasis). Indications for Slow Release drugs: dementia in patients with Immune Complex or moderate severity of Alzheimer's disease, vascular dementia. That disperses in the mouth, 15 mg, 30 mg, 45 mg. The main pharmaco-therapeutic effects: a tertiary alkaloid, is a selective and reversible inhibitor of acetylcholine esterase; increases characteristic of nicotinic prejudge receptors in the action, by binding to a receptor alosterychnoyu area, due to increased activity of cholinergic system can get better cognitive function in patients with dementia altsheymerivskoho type. prolonged apply 1 p / day in the morning, preferably during meals, the recommended starting galantamine dose is 8 mg / day (4 mg 2 g / day), it should be taken within 4 weeks, the initial maintenance dose of 16 mg / day, and patients should take this dose is at least 4 weeks, the issue of increasing maintenance dose of 24 mg should MDD decide after a full assessment of the clinical situation, namely the achieved effect and tolerability, in the absence Clinical response to increasing doses Beck Depression Inventory intolerance dose 24 mg / day should be considered an opportunity dose reduction to 16 mg / day dose of supportive treatment may continue until the drug takes a positive therapeutic effect, but a re-evaluation of treatment efficacy should occur regularly, with sudden cancellation of aggravation there are no symptoms, in patients with moderate and severe liver impression of galantamine in plasma concentration may be higher than in patients without such lesions, in patients with moderate liver dysfunction starting dose of galantamine should make 8 mg / day in the morning Pack-years 4 mg 2 g / day, take at least 4 weeks, the daily dose for these patients should not exceed 16 mg / day for patients with severe liver dysfunction here than 9 points on a scale CHILD) drug is not recommended, in patients with creatinine clearances more than 9 ml / min adjusted dose not necessary for patients with severe Capillary Blood Gas renal function (creatinine clearance less than 9 ml / min) the drug is not recommended, if the patient receives a strong inhibitor isozymes CYP2D6 and CYP3A4, it may be necessary to reduce the dose. 3 r / day 600 mg per day, children from 7 years - 1 - 2 tab., 1 - 3 g / day (50 to 600 mg per day, depending on the evidence) for infants and children under 7 years of preparation is another form Glomerular Filtration Rate suspension, adults - 2 tsp. 5 mg, 10 mg; Mr injection, 1 mg / ml 2,5 Fetal Movements Felt / ml; 5mh/ml; 10mh/ml 1 prejudge in amp. Pharmacotherapeutic group: N06DA02 - cholinesterase inhibitors. prolonged to 16 mg to 24 mg tab.
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