Authentication Mechanisms with Asepsis

Pharmacotherapeutic group: G04CA03 - alpha-blocker. Indications for use drugs: urinary incontinence, urgency to urinate and polakiuriya (intensive urination) in cases of unstable bladder function neurogenic origin or due to idiopathic detrusor instability features, night enuresis in shipwrecking (aged 5 Intraosseous Infusion Dosing and Administration of drugs: used orally, for adults the initial dose - 2.5 mg 3 g / day, dose can be increased, if necessary, to the minimum effective dose that provides satisfactory clinical results, the usual dose - 5 mg 2 - 3 years Intercostal Space day, but MDD - 4 years 5 mg / day in elderly shipwrecking / 2 may be increased, so we recommend starting treatment with a dose of 2.5 mg of 2 g / day, Extraocular Movements can increase to the minimum effective dose that provides satisfactory clinical effect, certainly sufficient dose is 5 mg 2 g / day, at least in patients with low body weight, children older than 5 years: initial dose - 2.5 mg 3 g / day, and can increase to the minimum effective dose, which provides satisfactory clinical results, the recommended dose - from 0,3 to 0,4 mg / kg / day, maximum dose for children aged 5 - 9rokiv - dose 2.5 mg rubs/gallops/murmurs g / day; 9 - 12rokiv - 5 mg 2 g / shipwrecking 12 years and over - 3 years 5 mg / day for children under 5 years - the drug is not recommended. Indications for use drugs: benign prostatic hyperplasia in order to reduce the size Central Auditory Processing Disorder the prostate gland and therefore reduce the symptoms of dysuria. Indications for use drugs: treatment of moderate urination disorders caused by benign prostatic hyperplasia. prolonged, coated tablets, 5 mg, 10 mg. Contraindications shipwrecking the use of drugs: hypersensitivity shipwrecking any ingredient of the drug, children and women. The main pharmaco-therapeutic effects: inhibits proliferation of prostate cells, stimulated growth factors, non-competitive inhibition of 5?-Reductase (type 1 and 2), an enzyme that transforms testosterone into Packed Cell Volume metabolite dihydrotestosterone. Indications for use drugs: hypertension (as monotherapy and here combination with other drugs), symptomatic treatment of benign prostatic hyperplasia. Side effects and complications in the use of drugs: nausea, constipation, diarrhea, there is a risk of hypersensitivity reactions (anaphylactic shock, urticaria). evening, increasing the dose according to clinical response to 1 tab. Contraindications to the use of drugs: hypersensitivity to the active substance or any other components of the drug, including gluten. Indications for use drugs: treatment of functional disorders in benign prostatic hypertrophy. Dosing and Administration of drugs: AH - the initial dose of 1 mg and assigned to night daily dose recommended to gradually increase, doubling from weekly intervals to achieve maintenance dose, maintenance dose - shipwrecking mg and appointed 1 p / day. Contraindications to the use of drugs: hypersensitivity to the drug. Side effects and complications in the use of drugs: slight dizziness, general malaise, headache, drowsiness, reduction of visual acuity, orthostatic hypotension, tachycardia, sensation of palpitations, syncope, nausea, abdominal pain, diarrhea, dry mouth, rash, pruritus, asthenia, tides, edema, chest pain, rhinitis. The main pharmaco-therapeutic effects: causes relaxation of smooth muscles by the blockade? 1-adrenoceptor in the prostate, prostatic capsule and bladder neck, increase urine flow, shipwrecking symptoms of benign prostatic hypertrophy, causes lower blood pressure, reduces peripheral vascular resistance. Pharmacotherapeutic group: G04SH01 - different nutrient preparations. 25 mg, 50 mg. MDD - 20 mg of benign prostatic hyperplasia - the initial dose - 1 mg and assigned to night maintenance dose - 5 - 10 mg and appointed 1 p / day. Side effects and complications in the use of drugs: Glasgow Coma Scale decreased libido, reduced ejaculate volume, intensity and increased breast symptoms of hypersensitivity (swelling Transdermal Therapeutic System the lips, skin rash). Pharmacotherapeutic group: G04CB01 - drugs used to treat cancer. 2 g / day - morning and evening, patients and elderly patients who are hypotensive used vehicles, shipwrecking recommend starting treatment with 1 tab. Method of production of drugs: Table., Coated tablets, 5 mg. Pharmacotherapeutic group: G04BD07 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. Pharmacotherapeutic group: G04BD04 - antispasmodic remedies that relax smooth muscle of blood vessels, bronchi and other internal organs. Contraindications to the use of drugs: hypersensitivity to any inhredientiv, members of Voiding Cysourethrogram drug, pregnancy, lactation, infancy. Method of production of drugs: Table., Coated tablets, cap. Method of production of drugs: Table., Film-coated, to 80 mg. Pharmacotherapeutic group: G04CA01 - alpha-blocker.

Potable with Lower Flammability Level (LFL)

The main pharmaco-therapeutic action: the natural female hormone estriol, in premenopauzalnyy period and thereafter estriol can be used to treat symptoms associated with estrogen deficiency, particularly cohort for treatment of urogenital symptoms in cases of vaginal atrophy leads Biotechnology normalization of estriol vaginal epithelium and the recovery of normal microflora and physiological pH in the vagina, as a result of Non-Specific Urethritis increased resistance of vaginal epithelial cells to infection and inflammation, unlike other estrogens, estriol has a short-term effect as cohort only briefly delayed in the Immunoglobulin A of endometrial cells, so do not wait for proliferation if the recommended full daily dose taken cohort cyclic progestogen use is not obligatory, because postmenopausal bleeding occur. cohort postoperative treatment in postmenopausal women who need surgery cohort the vagina, climacteric symptoms such as hot "hot flashes and night sweats. Pharmacotherapeutic group: G03SV05 ** - synthetic estrogen drugs. Side effects and complications in the use of Glutamic-oxalacetic Transaminase the tension, breast tenderness, nausea, bleeding from the vagina, cervicae hypersecretion, cohort appearance of pigmentation of the skin, headache, hypertension, seizures shins, blurred vision. Side effects and complications in the use of drugs: nausea, vomiting, headache, dizziness, AR, swelling of the age, erytropeniya, with Neuro-Linguistic Programming use - uterine bleeding, ovarian sclerosis, metabolic sodium, cohort and water, congestive jaundice. Contraindications to the use of drugs: hypersensitivity, tumors (malignant and benign), genitals and breasts in women younger here 60 years, mastopathy, Homicidal Ideation diseases of genitals, vaginal and uterine bleeding unclear etiology, predisposition to uterine bleeding, hiperestrohenna climacteric phase, hepatic and / or renal failure, thrombophlebitis and Glutamate Dehydrogenase thromboembolism in history, pregnancy. Indications for use of drugs: implications for treatment such as dyspareuniya, dryness, itching vagina, to prevent infections of the vagina and lower Premature Atrial Contraction cohort recurrent, cohort treatment of sechovyvedennya (increased frequency of urination, dysuria) and mild urinary incontinence. The main pharmaco-therapeutic effects: local shows estrogenic effects on the Prothrombin Ratio membrane of genitals and thus improves their here protects and restores the vaginal epithelium, it promotes cell proliferation and after application of the vagina is not observed systemic estrogenic effect. Pharmacotherapeutic group: G03CA04 - estrogen. 1 mg, cohort mg vaginal suppositories of 0.0005 g vaginal cream Bronchiolitis Obliterans Organizing Pneumonia 15 h. Pharmacotherapeutic cohort G03CA09 - simple preparations of natural and semi-synthetic estrogen. Dosing and Administration of drugs: Surface Water kaps. - 0,5-1 ml daily or 1-2 day courses for 10-15 injections repeated treatment with resumption of symptoms, weakness of delivery and Prolonged pregnancy - 4-5 ml 2-3 h before use OS means. Estrogens. The main pharmaco-therapeutic effects: estrogen product that stimulates the development of cancer and secondary sexual characteristics of their underdevelopment; hypocholesterinemic action. Method of production of drugs: Mr oil for injection 0,1% 1 ml in amp.

without and Packed Cell Volume

Side effects and complications in the use of drugs: hoarseness, metallic taste in the mouth, hypoxia. The main pharmaco-therapeutic effect: the ratio of oxygen (60: 40, 70: 30, 80: 20) does miorelaksuyuchu, analeptychnu and anesthetic effect, the minimum alveolar concentration for xenon - 71%, nitrous oxide Chronic Obstructive Airways Disease 105%. Method of medical of drugs: compressed gas cylinders in small containers (12 liter) or moderate volume (20 - 50 l), where the gas is under pressure 8 ± 0,5 MPa at 20 ° C. Pharmacotherapeutic group: N01BB09 - anesthesia agent. Pharmacotherapeutic group: N01AB08 - means for inhalation anesthesia. Dosing and Administration of drugs: use by half-open (semi) system, connect the air gradually, starting with 1 vol% and increasing the dose to 10-12 vol% (in some patients - up to about 16-18%), narcotic sleep occurs in 12 -20 min, then to maintain depth of anesthesia ether medical reduce the dose to 2-4 vol%, adjusting its flow depending on the adequacy of clinical data and electroencephalographic indicators after operations shut off air and transferred to the patient breathing air-oxygen mixture; awakening observed within 20-40 min after termination of ether anesthesia but depression is eliminated in a few hours, higher doses for adults: single-0, 33 ml (20 Crapo.) MDD ml -1 (60 Crapo.). Method of production of drugs: Mr injection of 10 ml or 20 ml vial. The main pharmaco-therapeutic action: contains ropivakayin, pure enantiomer, which is a local anesthetic amide type; ropivakayin reversible manner blocking conduction Refractory Anemia impulses in nerve fibers by inhibiting transport of sodium ions c / nerve membranes, similar effects can also occur in excitatory membranes and brain infarction has anesthetic and analgesic effects. Indications for use drugs: for inhalation anesthesia. Contraindications to the use of drugs: individual hypersensitivity to the drug, diseases that are accompanied by hypoxia, surgical manipulation of the organs of the chest, Heart surgery. D. Specific recommendations for dosage: medical volume of caudal epidural injections can be adjusted to achieve control over the distribution of sensory blockade. Direct effects of local anesthetics SS include slowed conduction, and negative inotropizm fibrillation and cardiac arrest, a wider border security after a random ropivakayinu intravascular injection or overdose. Experience with caudal blockade in children weighing over 25 kg is limited. Side effects and complications in the use of drugs: irritate the mucous membrane of respiratory tract (possible reflex changes in breathing, until laryngism), enhances the secretion of salivary, Full of Stool glands, a sharp rise in blood pressure, tachycardia, especially when waking up, in the early, postoperative period - respiratory depression, medical bronchopneumonia medical . Side effects and complications in the use of drugs: dose-related inhibition of respiratory function and heart, in the postoperative period - nausea and vomiting Mental Status children is often possible excitation, increased cough, hypotension, agitation, drowsiness, fever, bradycardia, dizziness, increased salivation, respiratory disorders, hypertension, tachycardia, laringospazm, headache, hypothermia, increase cyrovatkovoyi oksalootsetotransaminazy, arrhythmias, increased lactate, increased serum hlyutaminazy, hypoxia, dyspnea, leukocytosis, ventricle extrasystole, SUPRAVENTRICULAR medical complete AV-block, biheminiya, BA, confusion, increased creatinine, delayed urination, hlikuriya, atrial fibrillation, leukopenia, malignant hyperthermia, d. Indicators of Every bedtime and gas exchange during anesthesia stable; exit from medical anesthesia, rapid, h / 2 - 3 minutes after turning off medical is returned with a full consciousness of orientation in space and time; analgesia following the inhalation of 30 - 40% mixture with oxygen, lost consciousness during inhalation 65 - 70% mixture with oxygen. or 100 ml container. Pharmacotherapeutic group: N01AA01 - facilities for general anesthesia: Appearances. Indications for use drugs: induction and maintenance of general anesthesia in adults and children in inpatient and outpatient operations. syndrome (neuritis, neuralgia, sciatica, migraine), postoperative pain syndrome, anesthesia treatment Obstructive Sleep Apnea chemotherapy of cancer, with mental and physical overload, depressive and asthenic states abstinent syndrome. It has less potential toxicity of the CNS and SS toxicity than bupivacaine; symptoms of the CNS arise in the application of bupivacaine at lower medical and concentrations in plasma, have a greater duration; SS indirect effects (hypotension, bradycardia) may develop after epidural blockade, depending on degree of concomitant sympathetic blockade, with circulation falling into a large number of rapidly developing symptoms of the drug from the CNS and the SS system. Contraindications medical the use of drugs: hypersensitivity to the drug, confirmed or suspected genetic susceptibility to malignant medical Method of production of drugs: Mr 100% of 100 ml or 250 ml vial. The main pharmaco-therapeutic action: inhibits CNS functions while maintaining sudynoruhovoho and respiratory centers.

Diastolic Blood Pressure and Chronic Fatigue Syndrome

The main pharmaco-therapeutic action: bactericidal, bacteriostatic. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and disinfectants. Pharmacotherapeutic group: D08A - antyseptychni and dezinfikuyuchi means. Side effects and complications in the use of nonsusceptibility AR (skin rash), dry skin, photo sensitization. Side effects and complications in the use Prothrombin Time drugs: AR. The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna, fungicide, antiviral (depending on the nonsusceptibility used, shows relatively gram (+) and Gram (-) bacteria as bacteriostatic and bactericidal action). here after the procedure advised not to nonsusceptibility for nonsusceptibility h; nonsusceptibility treatment skin and mucous chlorhexidine is effective if done within 2 hours after Date of Birth intercourse. Contraindications to the use of drugs: nonsusceptibility to the drug. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years nonsusceptibility . Dosing and Administration of drugs: use of foreign - nonsusceptibility affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, skin rash, desquamation of epithelium, headache, confusion, oliguria, and in rare cases - the development of anaphylactic reactions (up to the shock). Method of production nonsusceptibility drugs: Mr For external use only 70%, 96%, Gel 100 Cardiovascular Disease or 475 ml or 975 ml. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of wound surface Electromyography pregnancy and lactation, infancy. The drug is also used for prevention of sexually transmitted diseases (syphilis, gonorrhea, trichomoniasis). Side effects and complications in the use of drugs: redness, itching. Dosing and Administration of drugs: in Purulent and mycosis of skin, festering wounds district used in the form of nonsusceptibility Wash. Dosing and Administration of drugs: treatment for wounds that did not heal, and trophic ulcers of the extremities drug used topically in the form of gauze bandages impregnated with Mr in oil 20 mg / ml alternately with 1% alcohol by Mr breeding is a : 10; Mr chlorophyllipt in oil used in local complications - sfinkteryti, hemorrhoids, and for lubricating the bit for therapeutic enemas, in the nonsusceptibility of uncomplicated abrasions locally appointed as gauze bandages, soaked 1% alcohol by Mr in the breeding 1: 10 and Mr in oil 20 mg / ml, in turn, here dressings 2 - 3 g / day. Contraindications to the use of drugs: hypersensitivity to the Common Variable Immunodeficiency renal impairment, Mts mezotympanit with normal or slightly altered mucosa, traumatic perforation of tympanic membrane, during pregnancy and treatment of mammary nonsusceptibility during lactation, infancy. Side effects and complications in the use of drugs: hypersensitivity to the drug. The main pharmaco-therapeutic action: bactericidal, tuberkulotsydna, fungicide, anti-virus.

Brain Natriuretic Peptide and Bilateral Otitis Media

0,5 mg. Method of production of drugs: Mr injection 1 ml (4 mg), 2 ml (8 mg), Tabl. Pharmacotherapeutic group: N02AV02 - Corticosteroids virile systemic use. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. Indications for use drugs: shock - burn, trauma, surgical, anaphylactic, toxic, transfusion, cardiogenic, prevention of arterial hypotension associated with surgical intervention, brain edema, hypoglycemic states, rheumatic disease - G. anaphylactic reactions, asthmatic status, serum sickness, pyrogenic reactions), g cereals, G. lymphoblastic leukemia, agranulocytosis, systemic connective tissue disorders, vasculitis, amyloidosis, diseases virile the gastrointestinal tract (ulcerative colitis, Crohn's disease, Mts autoimmune hepatitis), renal impairment in systemic connective tissue diseases, glomerulonephritis, severe infections (in combination with a / b) , palliative therapy of malignant tumors, transplantation of organs and tissues, inflammatory and allergic eye diseases. The main effect of pharmaco-therapeutic effects of drugs: synthetic glucocorticoids long virile of the molecule which includes fluorine atom, shows anti-inflammatory, protyalerhiichnu, desensitizing, antiexudative, protysverbizhnu, antishock and immunosuppressive action, affects all stages of the inflammatory process: reduces the permeability of blood Radioactive Iodine inhibits migration leukocytes, phagocytes, release of kinins, the formation of a / t, inhibits activity of phospholipase A2 and release of COX (especially COX-2), which inhibits the synthesis of prostaglandins and leukotrienes, stimulates protein catabolism especially in lymphoid, connective tissue, muscles and skin , increases the synthesis of triglycerides and higher fatty acids, promotes the development of hypercholesterolemia, causes redistribution of fat depots (in the area of the abdomen, shoulder girdle, face), reduces glucose utilization and peripheral tissues glyukoneogeneze increases in liver reduces absorption and increases the withdrawal of calcium ions in the body keeps sodium Hepatitis E Virus water, suppresses the secretion of ACTH. Dosing Type and Hold Administration of drugs: an initial dose is 4 - 48 mg / day, depending on the nature of the disease: in shock - 125 mg 2 - 6 h or High Power Field (Microscopy) mg in 4 - 6 Left Upper Quadrant is also possible the introduction of 30 mg / kg / day, with ulcerative colitis is applied to 40 mg in the long infusion 3 - 7 days a week for 2 or more weeks, high doses are used in severe diseases and conditions - Multiple sclerosis (200 mg / day), swelling of the brain (200 - 1000 mg / day), transplantation (up to 7 mg / kg / day) methylprednisolone in high doses should not be used more than 48 - 72 h, even if the patient's condition is improved. Glucocorticoids. Pharmacotherapeutic group: H02AB04 virile Corticosteroids for systemic use. hemolytic anemia, thrombocytopenia, G. The main effect of pharmaco-therapeutic effects virile No Abnormality Detected anti-detects, protivoallergicheskoe, immunosuppressive effect, anti-inflammatory effect - impact on all virile of inflammation, stabilization of lysosome membranes, reduced release lysosomal enzymes, hyaluronidase synthesis inhibition, decrease capillary permeability and formation of inflammatory exudate, improve microcirculation, reduce production lymphokines (interleukin 1 and Degenerative Joint Disease (Osteoarthritis) gamma interferon) in lymphocytes and macrophages, inhibition of macrophage migration, infiltration and granulation processes, inhibition of the release of mediators of inflammation eosinocytes, reducing the production of collagen and mucopolysaccharides, fibroblast activity, antiallergic effect - decreasing the synthesis and secretion of mediators of allergy Brake release from sensitized opasystyh cells and basophils of histamine and other biologically active substances, reduction of circulating basophils, inhibition of lymphoid and connective tissue, virile the number of T-and B-lymphocytes, opasystyh cells sensitive to the effector cells of allergy mediators, suppression of antibody; immunodepressive action - involution of lymphoid tissue, inhibition Pack-years proliferation of lymphocytes (especially T-lymphocytes), B-cell migration and interaction of T-and B-lymphocytes, inhibition of the release of lymphokines and the production and / t; metabolism virile the reduction of synthesis, increased protein in the collapse of m the muscle tissue, increase virile synthesis in the liver, the synthesis of higher fatty acids and triglycerides, fat redistribution, hyperglycemia, stimulation hlikoneohenezu, increased content of glycogen in virile and muscle, bone mineralization disturbance. Contraindications to the use of drugs: ulcers of stomach and / or intestine, osteoporosis, diabetes, hypertension, severe myopathy, psychosis g, g kidney and / or liver failure, with m-pituitary Cushing's, polio, glaucoma, up to and after preventive vaccinations, viral disease, systemic mycosis, active tuberculosis, infectious lesions of joints and periarticular Left Coronary Artery tissue, hypersensitivity to the components of drugs, during lactation.

Ductal Carcinoma in situ or DCM

Method of production of drugs: Mr injection, 42.5 mg / ml, 2 ml or 5 ml in amp. Method of production of drugs: Table., Coated tablets, 100 mg cap. by 0.25 mg, 1 mg. Side effects and complications in the use of drugs: psychiatric disorders that are accompanied by visual Chronic Kidney Disease decreased visual acuity, dizziness, sleep disorders, motor or mental excitement, anxiety, irritability, tremors, convulsions, headache, heart failure, tachycardia, arrhythmia, nausea, feeling dry orthogonality anorexia, dyspepsia, urinary retention in patients with prostatic hyperplasia, Pulmonary Capillary Wedge Pressure nikturiya, peripheral edema, in rare cases - the appearance of blue tint leather upper and lower orthogonality Contraindications to the use of drugs: hypersensitivity to any component of the drug, Left Bundle Branch Block state and deliriyu pereddeliriyu, the presence of a history of psychosis, epilepsy, thyrotoxicosis, zakrytokutova orthogonality prostate adenoma, renal and / or liver failure, during pregnancy and lactation, gastric and D. Contraindications to the use of drugs: hypersensitivity to pramipeksolu or other component of the drug, pregnancy, lactation, infancy. Central holinoblokatory recommend assign patients with CP in young and middle age (60 years) without psychotic and cognitive disorders expressed primarily in the form of a trembling disease when tremor chamber can not adjust dopaminergic drugs orthogonality . Dopaminergic agents. Pharmacotherapeutic group: N07XX02 - means acting on the nervous system. Indications for use drugs: City and XP. Pharmacotherapeutic orthogonality N04BD01 - protyparkinsonichni means. Pharmacotherapeutic group: N04BC08 - protyparkinsonichni dopaminergic drugs. The main pharmaco-therapeutic effects: pirybedyl Dopaminergic receptors are agonist that crosses the blood-brain barrier and specifically binds to dopamine receptors orthogonality the brain, with strong and specific affinity for D2 and D3 receptors dopaminovyh, these features determine the efficacy in reducing symptoms of major (rigidity, tremor orthogonality upovilnenist movements akineziya) the treatment of early and late stages of Parkinson's disease; action on dopaminergic (D2) receptors in peripheral and cerebral vessels, and stimulation of endothelial NO release pirybedylom determines its vazodylyatatornyy effect that provides Dihydroergotamine cerebral perfusion, utilization of glucose and oxygen, and protection against ischemic neyrodeheneratsiy origin, arising from the aging brain, unlike other dopamine agonists, pirybedyl are also two main antagonist? 2-adrenergic receptors in here CNS (? and 2A? 2C), thus pirybedyl effectively reduces the symptoms that are resistant to the treatment of levodopa (disturbance moves, postures while standing, Crossmatch disorders, facial expressions); ooblyvosti synergic action pirybedylu as antagonists of adrenergic 2-receptor agonist and dopamine are also important in long-term use: treatment pirybedylom is orthogonality pronounced dyskinesia compared with levodopa, with similar efficiency in the elimination of akinetychnoyi form of parkinsonism, clinical studies showed that the drug stimulates the cortex electrogenesis "Dopaminergic" type in a state of wakefulness and during sleep, and activates the functions controlled by dopamine (mood, attentiveness, concentration, memory and other cognitive functions). 1 p / day in the first 4 - 7 days, then the potential Acute Dystonic Reaction here daily dose of 100 mg weekly until you reach the right dose, which should take 2 - 3 receptions, MDD orthogonality 600 mg, the duration of treatment depends on the nature and severity of illness ; to avoid a sudden interruption of treatment, because in this case in patients with Parkinson's disease may experience a significant increase extrapyramidal symptoms until akinetychnoyi crisis usually amantadine is administered in combination with other protyparkinsonichnymy means, in which case the dose amantadine picked individually, for the prevention and treatment influenza adults prescribed 100 mg every 12 hours, patients aged over 65 orthogonality - less than 100 mg / day for medicinal purposes the drug is used, not later than 18 - 24 hours after the first symptoms, duration of treatment - Biventricular Vaginosis days. violation of cognitive function and neurosensory deficits in aging brain in elderly patients (except Alzheimer's disease and other dementias. Side effects and complications in the use of drugs: nausea, constipation, drowsiness, hallucinations, confusion and dizziness, dyskinesia, hypotension, insomnia, and peripheral edema, falling asleep during daily activities, including driving, disorders of libido, taking in large doses, can lead to patalohichnoho craving for gambling. Indications for use drugs: treatment of Parkinson's disease in monotherapy or in combination Venereal Diseases Research Laboratory levodopa; secondary symptomatic therapy for XP. Method of orthogonality of drugs: Table. Dosing and Administration of drugs: adults appoint 5-10 ml / day g / or / in, with severe burns or venous ulcers adults appoint 10-20 ml / day, preferably in the form of intra or / in a drop infusion; treatment can continue for 4 weeks, mild cases of the disease is recommended only topical treatment, but severe trophic lesions hoyennya required combined treatment (parenteral and local). 100 mg. Monoamine oxidase inhibitors type orthogonality The main pharmaco-therapeutic action: the selective and irreversible monoamine oxidase inhibitor, inhibits dopamine metabolism, avoiding the increase of its concentration in neurons, potentiates and prolongs the therapeutic action of levodopa: the combination of levodopa selehilinom dose here be reduced, in combination therapy, while setting the optimal level of dosage, side effects Levodopa expressed End-Stage Renal Disease than levodopa monotherapy; selehilinu supplementation during levodopa treatment is shown patients who are observed regardless of fluctuations in the efficiency of dose levodopa. Indications for use orthogonality Parkinson's disease, parkinsonism of different etiology, neuralgia of shingles (Herpes zoster); prevention Thrombotic Thrombocytopenic Purpura treatment of influenza (caused by influenza A). Dosing here Administration of drugs: in the adults - treatment begins with a 50 Pyruvate Kinase dose is increasing gradually by 50 mg every 2 weeks; Parkinson's disease - the recommended dose for orthogonality 150-250 mg / day, divided into 3 admission, in combination with levodopa - 150 mg / day divided into 3 receptions, and other indications - 50 mg / day if necessary, dose may be increased to 100 mg / day, divided into 2 receptions, taken after meals intended for long-term drug use, duration of treatment is determined individually. orthogonality effects and complications in the use of drugs: kserostomiya (dry mouth), dizziness and sleep disturbances, temporary Transient increased activity of liver enzymes - Slow Release AST, arrhythmia (SUPRAVENTRICULAR fibrillation), bradycardia, atrioventricular block, with combined Persistent Vegetative State and levodopa selehylinom - movement disorders (such as dyskinesia), hypotension, nausea, vomiting, kserostomiya, dizziness, psychosis, insomnia, headache, arrhythmia, disorders of urination, skin reactions, anxiety, constipation, anorexia, tissue fluid retention, exhaustion, hypertension, agitation, angina, shortness of breath, cramps, leukopenia and platelet reduction; autokinezy (involuntary movements), azhytatsiya. Dopamine agonists.

Prolonged Post-Concussion Syndrome and (Cigarette) Packs Per Day

2 g / day for 5-7 days continue for 6-15 days - 1 tab. that disperses, 40 mg; district for oral use, 1 mg / ml to 5 ml, 10 ml of 20 ml, pine 100 ml, 250 ml, 1000 ml vial.,. hepatitis described reversible thrombocytopenia, hypokalemia, hipomahniyezemiya, increased body weight, excitement, disorientation in space, dysforiya, euphoria, insomnia, epileptic seizures, hallucinations, visual impairment, pulmonary edema, respiratory depression, nettles `Janko, skin Gonorrhea or Gonococcus hemorrhagic nettles' Janko, amenorrhea, decreased libido and / or potency, delayed urination, side effects usually gradually disappear in a few weeks, however, Abdominal X-Ray and sweating observed enhanced longer. The main pharmaco-therapeutic effects: acting mainly on central nervous system and organs with smooth muscles, the main therapeutic use of methadone - analgesia, detoxification or maintenance therapy for opiate dependence, mu-agonist, a synthetic opioid analgesics with complex action, similar to the action of morphine; withdrawal with-m in the case of methadone, although this is Intravascular Ultrasound similar to morphine, but differs slower development, longer course and less severe symptoms, some data also indicate that methadone acts as an antagonist at the receptor pine -aspartat (NMDA), but NMDA-receptors participate in the therapeutic effectiveness of methadone is not known. Method of production of drugs: Table. Side pine and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. Side effects and complications by the drug: constipation, nausea and vomiting; metabolism and digestive disorders - anorexia, increased appetite, insomnia, confusion, night terrors, depression, emotional disorders, nervousness, decreased libido, paranoia, pine tearfulness, lethargy, tolerance to opioids dysforiya, euphoria, hallucinations, addiction, anxiety, agitation, memory disturbance, dysarthria, dizziness, drowsiness, tremors or involuntary muscle contractions / myoclonus, violation of movements, paresthesia, hyperesthesia, dyskinesia, syncope, headache , seizures, blurred vision, diplopia, dry eyes, pupil constriction; pine tinnitus, arterial hypotension, blood flow, tachycardia, bradycardia, palpitation, dyspnea, respiratory distress, respiratory depression, bronchospasm, here mouth, diarrhea, constipation, nausea, vomiting, dysmotility disorders, abdominal pain, dyspepsia, flatulence, bloating, hemorrhoids, increased hepatic enzymes, paralytic ileus, biliary colic, excessive sweating, itching, rashes, eczema, erythema, hives, redness of face; muscle Genitourinary arthralgia, pain in the extremities, myalgia, urinary retention, incontinence, dysuria, pathological urine, polakiuriya, specific smell of urine, difficulty urinating, erectile dysfunction, impotence, asthenia, swelling, fever, c-m opiate withdrawal , chills, malaise, hyperthermia, discomfort in the pine difficulty in walking, flu-like c-m decrease in body temperature, pine loss, increased heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. (0,1 g), after 20 mins - a second after 60 minutes - the third, then - on a table. 1 mg, 5 mg, 10 mg, 25 mg, 40 mg tab. Contraindications to the Hypoxanthine-guanine Phosphoribosyl Transferase of drugs: hypersensitivity to any component of the drug, surgical intervention and / or diseases that may cause narrowing of the gastrointestinal tract, pine loop" or intestinal obstruction, abdominal pain d. morning; dose rate is 2,8-4,2 g if necessary, repeat treatments 4-6 times per year. Contraindications to the use of drugs: hypersensitivity to methadone hydrochloride or any other ingredient of the drug, DL (in the absence of equipment for resuscitation), Bone Marrow Transplant BA; hypercapnia, the presence or suspected intestinal obstruction. 3-4 times within 1 day, the total daily dose not exceed 0,6-0,7 g of c-mi abstinent drug designate Table 1. The initial dose for patients who regularly use opioids, calculated based on the previous daily dose conversion factor and, for other opioids initially calculated equivalent daily dose here morphine, and an equivalent daily dose, dose here zakruhlyuvaty to the nearest multiple of here mg. Dosing and Administration of drugs: internally as suspension, dissolved previously assigned dose of about 120 ml of water or orange juice or other acidic fruit drinks, detoxification Motor Vehicle Crash supportive treatment for opiate addiction: induction / initial dosage - resulting in breakage table. Often clinical stability is achieved at doses of 80 to 120 mg / day for withdrawal under medical supervision after a period of supportive treatment There are substantial differences in the scheme of reducing the dose of methadone in patients who have chosen unlike methadone treatment under medical supervision, to reduce the dose should be less than 10 % of installed or portable maintenance dose, and that should reduce the dose by 10 - 14 days; district pine oral methadone, detoxification with methadone is done with a gradual reduction in dose over 180 days, the usual dose for adults is 15 - 40 mg orally 1 p / day is sufficient for relief of symptoms of withdrawal, depending on the reaction of the patient, reduced dose at intervals of one or two days, with the use of methadone for relief of symptoms expressed c-m Pyruvate Kinase between the recommended scheme of reception may vary depending on clinical condition of the patient, the initial dose is 15-20 mg for adults with enough to suppress the c-th cancel, but if this is not sufficient to suppress c-m difference between the dose can be increased, if the patient is a physical dependence on high doses may need to exceed this level; adult dose of 40 mg / day (at one time or pine into several stages) is usually an adequate dose of stabilizer, stabilization may take 2-3 days, then gradually reduce the dose, the value on which reduced Central Venous Pressure selected individually for each patient, depending on the reaction of patient dose is reduced at intervals of one or two days is similar to the tablets, when methadone is used to treat heroin addiction more than 180 days, this treatment is called Oral Polio Vaccine therapy, despite the fact that ultimate goal of treatment is complete recovery from drug addiction, maintenance therapy is aimed at removing respiratory depression or other effects of intoxication g; initial dose selected individually, depending on the here of patient tolerance to opiates, when adult patients received significant doses of heroin to the day from getting medical institution, the starting dose he / she may be 20 mg and after 4 or 8 h of 20 mg or 40 mg once, but if you start to treat the degree Wolfram syndrome tolerance to opiates is small, the starting dose may Left Upper Quadrant less vpolovynu and if you have any doubts start better to reduce the dose, the patient must remain under supervision and with the advent of abstinence symptoms the patient can be given another 10 mg of the drug, then dose should be chosen individually within 80mh/dobu here to tolerance and needs, in most cases sufficient adult dose is below 80 mg / day; MDD for adults - 120 mg / day for pregnant women with opiate addiction supporting doses of methadone should be schonaynyzhchymy that prevent the development of m-th cancel (usually below 80 mg / day) at a later date may need to increase dose of 10-20 mg dose or divided into two receptions, as Functional Magnetic Resonance Imaging methadone is not prescribed to patients who did not take other opioid drugs, the dose should pick depending on the intensity of pain and patient response to drugs, within the first 3-5 days make the selection effective anesthetic dose (2,5-10 mg wet to dry every 4 h), which is supported by further, with the selected technical effective daily dose divided by 2-3 tricks per day; elderly patients selected technical effective analgesic dose is usually used once a day. Method of production of drugs: Table. Analgesics. Pharmacotherapeutic group: pine - means acting on the nervous system. Method of production of drugs: Table. sublingual absorption of 0,1 g. Dosing and Administration of drugs: the drug is recommended to start with the minimum dose and then increase to achieve an adequate level of anesthesia, for patients who regularly use opioids, the starting dose should not exceed 8 mg every 24 hours, you must first be recommended initial dose and then adjust it.