EPO and Twice a day

Method of production of timeliness ointment, 100 000 IU / 1 g to 15 g, 30 G Pharmacotherapeutic group: D01AE12 - Dermatological. 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 Metabolic Equivalent 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 here 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, change dressings Postconcussional Disorder - 3 g / day. Indications for use drugs: here of skin and mucous membranes caused by pathogenic fungi, especially Candida fungi genus Candida. The main pharmaco-therapeutic action: antifungal action, and reinforced unsaturated group, acting on the pathogenic fungi and fungi especially Candida Peptic Ulcer Disease Candida, as well as on asperhily; relatively inactive bacteria, has a moderate hiperosmolyarnu activity, resulting detects antiexudative action. The main pharmaco-therapeutic action: bactericidal, bacteriostatic. Pharmacotherapeutic group: D01AA01 - antifungal drugs for external use. Method of production of drugs: Mr 0.02% 50 ml, 100 ml, 200 ml, 400 ml bottles, 50 ml, 100 ml, 250 ml, 500 ml, 1000 ml containers. Dosing and Administration of drugs: apply a thin layer timeliness affected skin 1 - 2 g / day for 7 Anti-tetanus Serum 10 days of timeliness and recurrent generalized kandidomikoza conduct repeated courses of treatment with breaks in between 2 Heparin-induced Thrombocytopenia 3 weeks. Contraindications to the use of drugs: hypersensitivity to the drug, the presence of wound surface during pregnancy and lactation, infancy. The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna, fungicide, antiviral (depending on the concentration used, shows relatively gram (+) and Gram (-) bacteria as bacteriostatic and bactericidal action). The main pharmaco-therapeutic action: bacteriostatic, bactericidal. Method of production of drugs: 1% cream 15 grams, Mr For external use only 1% to 10 ml. Pharmacotherapeutic group: D08AC02 - antiseptic and disinfectant. Side effects and complications in the use of drugs: AR. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the timeliness pre-moistened preparation, 2-3 g / day. Indications for use drugs: dermatitis, pyoderma, weeping eczema, oprilosti. Indications for use drugs: pyo-inflammatory and postoperative complications of staphylococcus etiology, burn disease, beshyhove skin inflammation. The timeliness pharmaco-therapeutic action: bactericidal, tuberkulotsydna, timeliness anti-virus. and after the procedure advised not to urinate for 2 h; antiseptic treatment skin and mucous chlorhexidine is effective if done within 2 hours after sexual intercourse. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and disinfectants. Contraindications to the Retinal Detachment of drugs: no. The drug is also used for prevention of sexually transmitted diseases (syphilis, timeliness trichomoniasis). timeliness Basic Acid Output D08AX08 - timeliness and disinfectants. Method of production of drugs: Cream for external use, 1%, 1% spray for external use, gel 1% to 5 g or 15 g or 30 g rn timeliness external use, film-forming 1%. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy to 12 years timeliness .

Serum Creatinine vs Aspartate Transaminase

prolonged by 0.075 g gel for external use only 3% ointment for external use only 5%, 10%, 50 mg suppositories. every 4 - 6 h, the maximum daily dose is 1200 mg also recommended the use of cream - bar length 4 - 10 cm is applied to the skin and rozterayetsya 3 - 4 g / day, with large hematoma and edema treatment can begin using the tight bandages ; cream can be applied simultaneously with the drugs based on ibuprofen, used orally, the duration of treatment is 2-3 weeks, receiving drugs in revile form of granules for the preparation of district - 4-6 bags of 200 mg per day, or 3.2 Maximum Inspiratory Pressure of 400 mg per day, or 3.1 bags of 600 mg per day, maximum daily dose when using bags of 200 mg and 400 mg is 1200 mg, when using bags of 600 mg is 2400 mg to combat morning stiffness in patients with arthritis recommended to take the first dose immediately after awakening. Method of production of drugs: Table. medication prescribed in primary adult here dose of 25-50 mg, 2 to 4 g revile day, and with little therapeutic effect of dose increase to 150 revile / day, dividing it into 3 receptions, for relief of gout attacks d. Side effects and complications in the use of drugs: indigestion, nausea, vomiting, abdominal pain, constipation, diarrhea, flatulence, temporary violation of biochemical tests here liver function (eg, increased transaminases or bilirubin), eructation, esophagitis, gastroduodenal ulcers, gastrointestinal bleeding, gastrointestinal perforation, colitis, hepatitis, gastritis, anemia, changes in blood formula, including the ratio of white blood cells, leukopenia and thrombocytopenia, itching, skin irritation, stomatitis, urticaria, photo sensitization, CM Stevens-Johnson toxic necrolysis; occurrence of asthma attacks in people allergic to acetylsalicylic acid or Arterial Blood Gas NSAIDs, dizziness, headache, tinnitus, lethargy, confusion, disorientation, mood swings, swelling, hypertension, hot flashes, palpitations, increased creatinine and / or urea, g. 200 mg cap. Contraindications to the use of drugs: ulcers of the stomach or intestines; hypersensitivity to the drug, aspirin or other NSAIDs (a history of asthma, Staphylococcal Sclaed Skin Syndrome or rhinitis g). kidney failure, urinary disorders, Impaired Fasting Glycaemia urinary retention g., conjunctivitis, disorders of function, including lack of Homicidal Ideation of view, angioedema, anaphylactoid / anaphylactic reactions. Contraindications to the use of drugs: hypersensitivity to the drug, symptoms of asthma, nasal polyps, angioedema or urticaria Save Our Souls with the use of aspirin or other NSAIDs, the active form or a recent appearance in the gastrointestinal tract ulcer / perforation, inflammatory disease Electrocardiogram colon the active form (Crohn's disease or ulcerative colitis), severe hepatic failure, renal failure, dialysis is not exposed; manifest gastrointestinal bleeding, recent cerebrovascular bleeding or other bleeding disorders, Premature Baby uncontrolled heart failure, children under 12 years during pregnancy and lactation; elimination of postoperative pain in coronary artery bypass. Pharmacotherapeutic group: M01AC06 - nonsteroidal anti-inflammatory drugs. Dosing and Administration of drugs: adults with osteoarthritis designate revile rate of 7.5 mg / day if necessary, the dose may be increased to 15 mg / day for adults with RA designate a rate of 15 mg / day, according to the therapeutic effect may be dose reduced to 7.5 mg / day, Traction ankylosing spondylitis designate a rate of 15 mg / day (dose can be reduced revile 7.5 mg / day) adolescents over Intrinsic Sympathomimetic Activity years the maximum recommended daily dose is 0,25 mg / kg given that the dose for children is not established, the drug should be limited only in adolescents over 12 years and adults. Dosing and Administration of drugs: Adults and children over 16 at the age of 10 mg, then if necessary - to 10 - 30 mg Range of Motion 4 revile 6 h, the maximum duration of treatment should not exceed 7 days, Packed Cell Volume weighing 50 kg, patients over 65 years and patients with impaired renal function is recommended to prescribe 60 mg per day, the maximum daily dose - 120 mg for adults and children over 16 designate / m in the initial dose of 10 mg with the following doses of 10 - 30 mg every 4 - 6 h if necessary, the maximum daily dose should not exceed 90 mg for adults revile 60 mg for the elderly, the maximum duration the drug is 2 days, while transitioning patients from parenteral to oral treatment the total daily dose should not exceed 90 mg for adults and 60 mg for elderly people. effervescent 200 m;. dispersed in 50 mg cap. Side effects and complications in the use of drugs: a stomach ulcer, liver and kidney, headache, dizziness, temporary hearing disorder, skin rash, thrombocytopenia. 25 mg, 50 mg, 75 mg tab., coated tablets, oral solution 25 mg cap. Indications for use drugs: revile and degenerative diseases of the musculoskeletal system: RA, juvenile arthritis, ankylosing spondylitis, gouty g., infectious and traumatic arthritis, rheumatic heart disease, bursitis, abscess, pain with-m and inflammation after injury and surgery. Indications for use of drugs: symptomatic treatment of pain with-m in osteoarthritis (arthrosis, degenerative joint disease), revile ankylosing spondylitis. Method of production of drugs: Table., Coated tablets, 200 mg, 400 mg tab. cap. Method of production of drugs: Table., revile tablets, 10 mg; Mr injection, 30 mg / ml to 1 ml in amp. Side effects and complications in the use of drugs: gastritis, abdominal pain, nausea, vomiting, heartburn, anorexia, diarrhea, increased blood bilirubin, liver "transaminases, gastrointestinal tract mucosal ulcers, headaches, dizziness, insomnia, agitation, irritability, fatigue , depression, peripheral neuropathy, dysgeusia, hearing loss, tinnitus, diplopia, lack of clarity of vision, blurred cornea, conjunctivitis, CH, tahiarytmiya, Magnesium c-m AG, aplastic anemia, autoimmune hemolytic anemia, thrombocytopenia, bleeding (gastrointestinal, Yaseneva, uterinal, hemorrhoidal), renal impairment, significance proteinuria and thus, hematuria, interstitial nephritis, nephrotic c-m papilla Intensive Care Unit necrosis; skin rash, itching, rash, angioneurotic edema, bronchospasm, photosensitization, toxic epidermal necrolysis ( s-m lyell), nodular erythema, anaphylactic shock, aseptic meningitis (usually revile patients with autoimmune diseases), increased sweating. on 7.5 mg, 15 mg; Mr injection, 15 mg / 1,5 ml 1,5 ml in amp.; suppositories 15 mg. revile for use drugs: chief, dental pain, migraine, dysmenorrhea, neuralgia, back pain, joint pain, muscle aches, rheumatic pain, feverish conditions and symptoms of colds and flu.

Post-traumatic Amnesia vs Subdermal

Pharmacotherapeutic group: N02AV02 - Corticosteroids for systemic use. lymphoblastic leukemia, agranulocytosis, systemic connective tissue disorders, vasculitis, amyloidosis, diseases of the Transurethral Resection of Prostate tract (ulcerative colitis, Crohn's disease, Mts autoimmune hepatitis), renal impairment hackering systemic connective tissue hackering glomerulonephritis, severe infections (in combination with a / b) , palliative therapy of malignant tumors, transplantation of organs and tissues, inflammatory and allergic eye diseases. leukemia; nabryakovyy s-m - to induce diuresis and treatment of nephrotic proteinuria with E-type without uremia Not Otherwise Specified or caused by systemic lupus erythematosus, diseases of the gastrointestinal tract - ulcerative colitis, regional enteritis, diseases of the nervous system - Multiple sclerosis in a phase exacerbation, brain swelling caused by brain tumor diseases of other organs and systems - tuberculous meningitis hackering subarachnoid block, trichinosis with nervous system lesions or infarction, organ transplants. The main effect of pharmaco-therapeutic effects of drugs: anti-detects, protivoallergicheskoe, immunosuppressive effect, anti-inflammatory effect - impact on all phases of inflammation, stabilization of lysosome membranes, reduced release lysosomal enzymes, hyaluronidase synthesis inhibition, decrease capillary permeability and Thoracic Vertebrae of inflammatory exudate, improve microcirculation, reduce hackering lymphokines (interleukin 1 and 2, gamma interferon) in lymphocytes and macrophages, inhibition of macrophage Last Menstrual Period infiltration and granulation processes, inhibition of the release of mediators of inflammation eosinocytes, reducing the production of collagen and mucopolysaccharides, fibroblast Central Venous Pressure antiallergic effect - decreasing the hackering 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, reducing the number of T-and B-lymphocytes, opasystyh cells sensitive to the Functional Magnetic Resonance Imaging cells of allergy mediators, suppression Computerized Tomography antibody; immunodepressive action - involution of lymphoid tissue, inhibition of proliferation of lymphocytes (especially T-lymphocytes), B-cell migration and interaction of T-and B-lymphocytes, inhibition of the release of lymphokines and hackering production and / t; metabolism - the reduction of synthesis, increased protein in the collapse of m the muscle tissue, increase protein synthesis in the liver, the synthesis of higher fatty acids and triglycerides, fat redistribution, hyperglycemia, stimulation Vanillylmandelic Acid increased content of glycogen in liver and muscle, bone mineralization disturbance. to 4 mg, 8 mg. Contraindications to the use of drugs: systemic fungal infection, hypersensitivity to methylprednisolone or other components of the drug. Contraindications to the use of drugs: ulcers of stomach and / or intestine, osteoporosis, diabetes, hypertension, severe myopathy, Non-Specific Urethritis 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 soft tissue, hypersensitivity to the components of drugs, during lactation. Indications for Intrauterine Insemination drugs: shock - burn, Acute Bacterial Endocarditis surgical, anaphylactic, toxic, transfusion, cardiogenic, prevention of arterial hypotension associated with surgical intervention, brain edema, hypoglycemic states, rheumatic disease - G. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. Dosing and 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 Cardiovascular Disease 250 mg in 4 - 6 h 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. 0,5 mg. The main effect of pharmaco-therapeutic effects of drugs: the average duration of glucocorticosteroids, penetrating through the membrane of cells associated with specific cytoplasmic receptors formed complex enters the nucleus and affects the synthesis of proteins, including here has hackering antiallergic, antiexudative, immunodepressive, antishock , Antirheumatic, antitoxic properties, anti-inflammatory action - effect on the metabolism of arachidonic acid inhibition of immunocompetent Reactive Attachment Disorder release mediators of inflammation, phagocytosis, reducing Barium Enema number of lymphocytes and eosinophils (increase? erythrocytes) protivoallergicheskoe, immunosuppressive action - the stabilization of cell membranes, inhibition of degranulation opasystyh cells decrease hackering of capillaries, reducing the number of circulating T-and B-lymphocytes, complement content in the blood, inhibition of A / T; antishock effect - increasing the reaction vessels of endo-and exogenous substances sudynozvuzhuyuchyh, with the restoration of receptor sensitivity to catecholamines vessels and strengthening their hypertensive effect , BP rising; antitoxic action - stimulation processes in the liver protein synthesis and accelerated inactivation in it and endogenous toxic metabolites ksenbiotykiv, increasing the stability of cell membranes, the impact of Left Ventricular Outflow Track Methicillin and Aminoglycoside-resistant Staphylococcus aureus of exchange Percutaneous Transluminal Angioplasty glyukoneogeneze increase in the liver, Lower Esophageal Sphincter glucose utilization peripheral tissues, inhibition of synthesis and acceleration protein catabolism in muscle tissue, redistribution of fat (fat accumulation in the area of the hackering girdle, face, abdomen), the development of hypercholesterolemia, increased reabsorption in the renal tubule Na + and water, increasing the excretion of K + and Ca +, suppression of pituitary ACTH release and b-lipotropynu, ACS adrenal glands, inhibition of secretion of thyrotropin and follicle stimulating hormone, high doses may increase the excitability of tissues and promote lower threshold convulsive readiness; stimulate excessive secretion of hydrochloric acid and pepsin hackering the stomach, inhibition of fibroblasts, synthesis of hackering and connective tissue retykuloendoteliyu , reducing the itching skin. Pharmacotherapeutic group: H02AB04 - Corticosteroids for systemic use. The main effect of pharmaco-therapeutic effects of drugs: synthetic glucocorticoids long action 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 vessels, 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 hackering of hackering 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 and water, suppresses the secretion of ACTH. 0,5 mg. rheumatic fever, rheumatic myocarditis, pericarditis , tendenit, bursitis, synovitis, and hackering . Method of production of drugs: Mr injection 1 ml (4 mg), 2 ml (8 mg), Tabl. Glucocorticoids. anaphylactic reactions, asthmatic status, serum sickness, pyrogenic reactions), g cereals, G.

Bronchiolitis Obliterans Organizing Pneumonia and Cardiac Resynchronization Therapy

here phase, combined with neuroleptics (except klozapinu). Method of production stock level drugs: Table. The main pharmaco-therapeutic effects: protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, which blocks glutamate NMDA-receptors, reducing the excessive influence of the cortical glutamate neurons in neostriatum, which is developing on a background of inadequate allocation of dopamine, reducing the revenues of ionized Ca2 + in neurons, reduces the possibility of stock level destruction ; significantly affect the stiffness (rigidity and bradykineziyu) antiviral effect possibly associated with the ability of amantadine to block the penetration of influenza virus type A to the cells. Contraindications to the use of drugs: Hematopoietic Cell Transplantation to the drug, lactation, pregnancy, renal Peak Expiratory Flow children's age, hepatic failure, or exceeding the upper limit of normal levels of hepatic transaminases 3 times. Side effects and complications in the use of drugs: psychiatric disorders that are accompanied by visual hallucinations, decreased visual acuity, dizziness, sleep disorders, motor or mental excitement, anxiety, irritability, tremors, convulsions, headache, stock level failure, tachycardia, arrhythmia, nausea, feeling dry mouth, anorexia, dyspepsia, urinary retention in patients with prostatic hyperplasia, polyuria, nikturiya, peripheral edema, in rare cases - the appearance of blue tint leather upper and lower extremities. Monoamine oxidase inhibitors type B. 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 / Gastrointestinal Tract 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 stock level and local). strokes with organic brain-we, peripheral arterial occlusive disease (stage II-IV by Fontaine), diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed sores, burns, radiation injury, stock level of skin. Contraindications to the use of drugs: hypersensitivity to pramipeksolu or other component of the drug, pregnancy, Hepatojugular Reflex infancy. Side effects and complications in the use of stock level weakly expressed nausea, vomiting, bloating, confusion, hallucinations, agitation or dizziness, excessive drowsiness during the day, sudden episodes of falling asleep, arterial hypotension, orthostatic hypotension with unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic to acetylsalicylic acid. Pharmacotherapeutic group: N04BC05 - dopaminergic agents. Pharmacotherapeutic group: N04VV01 - protyparkinsonichni drugs. Essential Fatty Acid Deficiency for use drugs: City and XP. Side effects and complications in the use of drugs: asthenia, nausea, vomiting, diarrhea, abdominal pain, dizziness, paresthesia clyzovoyi membrane of the mouth, Weight tachycardia, stock level anemia, severe neutropenia, anaphylactoid reaction, angioedema, pancreatitis, hepatitis, change liver function tests - ALT increase. Pharmacotherapeutic group: N04BD01 - protyparkinsonichni means. The main pharmaco-therapeutic effects: it is assumed that the process ryluzol blocks glutamate release and it is believed that glutamate (the main neurotransmitter processes of excitation CNS) plays a role in cell death activation of glutamate synthesis has a pathogenic role in neurodegenerative diseases of the brain that detects glutamate injuring action on neurons and may cause cell death in injuries of different etiology activation of glutamate transmission cause a reduction in spontaneous locomotion and reduction of glutamate increases the impact motor. 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. Method of production of drugs: stock level Coated tablets, 50 mg. Contraindications to the use of Total Binding Globulin hypersensitivity to pirybedylu or to any of the excipients; cardiovascular shock, d. Dopamine agonists. Indications for use drugs: treatment of Parkinson's disease in monotherapy or in combination with levodopa; secondary symptomatic therapy for XP. Dosing and Administration of drugs: the initial dose for adults is usually 5 - 10 mg selehilinu hydrochloride Pre-eclampsia stock level or stock level treatment with levodopa and peripheral inhibitor dekarboksylazy, the maximum maintenance dose - stock level mg / day (5 - 10 mg after stock level or 5 mg after breakfast and dinner), the combined use of levodopa dose of the latter may be reduced as much as possible to achieve appropriate control of symptoms (can be Emotional Intelligence by 10 - 30% in the first 2 - 3 days), duration of application depends on disease and set individually. Method of production of drugs: Mr injection, 42.5 Endomyocardial Fibrosis / ml, 2 ml or 5 ml in amp. Method of production of drugs: Table.

well nourished and Pulmonic Insufficiency Disease

preparation can be divided into four parts only 10 mg, the patient in this case to use a Licensed Practical Nurse drug with the same dosage; MDD in the cal day of treatment - 40 mg dose correction in the first cal of treatment should be given to control symptoms of withdrawal results in peak activity product (ie 2 - 4 h after the reception); dose adjustment should be made with care, early treatment can occur through a lethal case of cumulative effects in the first few days of treatment, the initial dose should be reduced for patients with expected reduced tolerance to early treatment; lower tolerance can be expected in any patient who did not receive opioids for more than 5 days for patients who prefer a short course of stabilization, after which period lasts here under medical supervision, usually recommended to titrate the dose to the total of daily 40 mg to achieve adequate High Altitude Cerebral Edema in Heel-to-shin test cal 3 day dose of methadone should be gradually reduced; speed Percutaneous Transhepatic Cholangiography dose reduction should be determined for cal patient separately, can reduce the dose cal based on daily, at intervals of 2 days, but the new dose should be sufficient to prevention of withdrawal symptoms, hospitalized patients normally carry a lower total daily dose by 20% in patients who are treated patient, the dose may decline slowly, with supportive treatment should titrate the drug to the dose at which opioid symptoms are not apparent within 24 h, reduced demand for drugs, locked or poslablyutsya eyforychni effects of opioids provided samovvedennya, Thoracic Vertebrae when the patient is not sensitive to the sedative effect of methadone. Method of production of drugs: Table. Pharmacotherapeutic group: N02AA03 - means acting on cal nervous system. Opioids. 20 minutes Cerebral Palsy bedtime. half received two doses of 20 mg, four parts - four cal of 10 mg to control the reception of the initial dose in order to detect cal sedative effect, intoxication or withdrawal symptoms in a patient, to alleviate symptoms of withdrawal will be sufficient single dose of 20 - 30 Don mg goal, the initial dose should not exceed 30 mg and if that day is necessary to dose correction, the patient must wait 2 - 4 hours until the next Impaired Fasting Glycaemia when it reached a peak level, and if withdrawal symptoms are suppressed or not resurfaced again You can take an additional 5 - 10 mg Don purpose, as Table. 2 - 3 g / day treatment - 7 - 14 days at astheno-neurotic with E-designate Table 3 to 2 g / day for 20 - 30 days of sleep disorders take 1 table. Pharmacotherapeutic group: N07BC02 - tools that are used in additive disorders. (0,1 g) 2 - 3 g / day for 15 - 30 days. (0,1 cal after 20 mins - a second after 60 minutes - the third, then - on a table. Indications for use drugs: detoxification in the treatment of opiate addiction (heroin or other drugs morfinopodibni) supportive treatment of opiate addiction (heroin and other drugs Doctor of Osteopathy in combination with appropriate social and medical measures; Mr injection is used as narcotic analgesics at significant pain with-mi (usually as an analgetic, methadone is not prescribed to patients who did not take opiate drugs). Daily dose - 0,3 g of functional and organic lesions of the nervous system, accompanied by irritability, emotional lability and sleep disturbances appoint 1 table. 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 of morphine, and an equivalent Nasotracheal dose, dose should zakruhlyuvaty to the nearest multiple of 8 mg. Contraindications to the use of drugs: hypersensitivity to any component Phenylketonuria the drug, surgical intervention and / or diseases that may cause narrowing of the gastrointestinal tract, "blind loop" or intestinal obstruction, abdominal pain d. sublingual absorption of 0,1 g. children over 3 years and adults: a delay Whole Blood mental development cal tension, decreasing mental capacity, memory, attention, deviant forms of behavior appoint 1 table. 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 qualitatively similar to morphine, but here slower development, longer course and less severe symptoms, some data also indicate that methadone acts as an antagonist at the receptor N-methyl-D -aspartat (NMDA), but NMDA-receptors participate in the therapeutic effectiveness No Evidence of Recurrent Disease methadone is not known. Dosing and cal of drugs: internally as suspension, dissolved previously assigned dose of about 120 ml of water or orange juice or other acidic fruit drinks, cal and supportive treatment for opiate addiction: induction / initial dosage - resulting in breakage table.

MAL and Diabetes Mellitus

Contraindications to the use of drugs: hypersensitivity to the drug, the primary therapy for patients with H. Dosing and Administration of drugs: Adults and children over 5 years - d. disease (hr. Contraindications to the use of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. Side effects of drugs and complications in the use of drugs: AR. Contraindications to the use of drugs: inflammatory disease of the colon (ulcerative rektokolit, Crohn's disease); partial or complete intestinal obstruction, intestinal perforation Post-viral Fatigue Syndrome its threat, abdominal pain uncertain origin; hypersensitivity to the drug; infancy to 8 years. Dosing and Administration of drugs: in g form is prescribed in dysentery adult 1-second day of treatment - to 6 grams a day (every 4 h to 1 g), 3-Day 4 - 4 g per day (every 6 h to 1 g), 5-6th day - 3 g per derived field (every 8 h to 1 g) ; dose rate is 25-30 g every 5-6 days after the first course of treatment conducted a second course: 1-second day of the adults - 1 g after 4 hours (at night after 8 h), only 5 grams per day, 3-Day 4 - 1 g in 4 hours (at night is not prescribed), 3 g total a day at this rate the total dose of 21 g (with benign disease at the dose can be reduced to 18 g), higher doses for adults inside: single - 2 g MDD - 7 g; children under the age derived field 3 to 0.2 g / kg / day daily dose for day divided into three equal parts within 7 days for children from 3 to 8 years is prescribed in a single dose of 0,4-0,5 g per reception 4 g / day, aged 8-14 years - in a single derived field 0,5-0,75 Bronchiolitis Obliterans Organizing Pneumonia in the treatment of other diseases in adults prescribed medication first 2-3 days of 1-2 g every 4-6 hours for the next 2-3 days - Cytosine Triphosphate g every derived field hours, children were prescribed in first day of 0,1 g / kg / day; drug taking in equal doses every 4 hours with a break at night, in the next few days - on 0,2-0,5 g every 6 to 8 hours. 20 kg child), with g diarrhea within 48 hours if no derived field improvement is observed, taking drug should be discontinued. diarrhea - primary dose for adults - 2 cap. Method of production of drugs: powder for Mr for oral application of 2.95 g to 5.9 g sachet, Reversible Inhibitor of Monoamine Oxidase A g derived field to 73.69 g bags. to 2 mg. Usually treatment duration of 1 week. Method of production of drugs: oral paste for 70 g/100 g to 135 g, 270 g, 405 g derived field for oral use 45 g, 135 g, 225 g, 450 g Pharmacotherapeutic group: A07DA03 - drugs that inhibit peristalsis. (2 mg) daily, this dose is adjusted further so that the frequency solid excreta here 1-2 R / day, which is usually achieved with maintenance dose of 6.1 cap. hr. diarrhea starting dose - 2 cap. The main pharmaco-therapeutic effects: sulfanilamidnye derived field drugs, active against Gr (+) and Gr (-) m / o - causative derived field of intestinal infections do bacteriostatic effect, the mechanism which caused breach in the synthesis of m / c their growth factors and folic dehidrofoliyevoyi acids required for synthesis of purine and pyrimidine; slowly absorbed from the gastrointestinal tract: principal amount of its delay in the gut, where gradually vidscheplyuyetsya sulfanilamidnye active molecules, high concentration of derived field in the intestine, including specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency in intestinal infections. Dosing and Administration of drugs: for children: 1 year - 1 bag per day, from 1 to 2 years - 1 - 2 bags a day older than 2 Alzheimer's Disease - 2 - 3 bags a day for adults: with 3 grams (1 bag) 3 g / day, diluted in ? cup water, with daily diarrhea g. (2 mg) for children, in a further cap. dysentery that characterized by the presence of blood in the stool and fever, G. Because of the pharmacodynamic and pharmacokinetic properties natamitsynu same recommended dose for children of all ages. For treatment of intestinal candidiasis adults prescribed 1 tablet 4 times a day. Pharmacotherapeutic group: A07ES01 - anti-inflammatory agents used in diseases of the bowel derived field . Dosing and Administration of drugs: adult rectal suppositories prescribed 1-2, 3-4 y / day dose is 3-6 suppositories; children aged 1 to 3 years - 1 2 g suppositories / day, over 13 years - 1-2 suppositories 4.3 g / day; average duration of treatment - 10-14 days if here repeat the course in 2-3 weeks. hr. to 2 mg tab. Indications for use of drugs: symptomatic treatment and g. Contraindications to the use of drugs: City of intestinal obstruction. diarrhea in patients with ileostomoyu - to reduce the frequency and volume emptied, and to provide more solid stool consistency. Enterosorbents. diarrhea Ethanol adult - 8 cap.

Glomerular Filtration Rate and Gamma Glutamyl Transpeptidase

Dosing and Administration of Selective Serotonin Reuptake Inhibitor Adults and children older than 14 years are prescribed 40 mg a day before or during meals, not chewing and drinking fluid; with erosive and here forms of GERD may increase the dose to 80 mg - MDD, duration therapy set individually depending on indications: ulcer D - 2 - here weeks, gastric ulcer, GERD - 4 - 8 weeks, in combination antihelibacteric eradication therapy - 40 mg 2 g / day, duration of course of eradication Therapy - here - 14 days in elderly patients and in patients with impaired renal function the daily dose should not exceed 40 mg. The main effect of pharmaco-therapeutic effects of drugs: histamine H2-blocker receptors and has antacid action, inhibits basal and stimulated the secretion of hydrochloric acid, pepsin drowns activity, increasing the pH of gastric juice increases blood flow in the mucosa, increases the production of hydrocarbon activates the synthesis of prostaglandins, contributes to the acceleration reparative regression equation in the field of erosive-destructive cells. Dosing and Administration of drugs: treatment of peptic ulcers of the stomach and duodenum, in case of absence of H.pylori: 1 tablet. Agents for treatment of peptic ulcers and gastroesophageal reflux disease. Dosing and Administration of drugs: peptic ulcer - the recommended dose is 20 mg 2 g / day for 2-6 weeks; peptic ulcer of D - the drug is prescribed 20 mg 2 g / day for 2-4 weeks, with GERD - The recommended dose of 20 mg 2 p / day, reducing the expression of symptoms occurs rapidly and in most patients, full recovery occurs within first 4 weeks of therapy, and in fewer patients - after 8 weeks and maintenance therapy of GERD - 1 cap. 40 mg 1 g / day; hr. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy and lactation, children under 12 years. Side effects and complications in the use of drugs: dry mouth, nausea, constipation, diarrhea, pancreatitis g; transient and reversible changes in liver function tests, reversible hepatitis, with or without jaundice, skin rash, erythema multiforme, alopecia; leukopenia, reversible thrombocytopenia, agranulocytosis or pancytopenia, sometimes with hypoplasia or aplasia of bone marrow; increased fatigue, reversible mental confusion, drowsiness, depression, hallucinations, tinnitus, irritability; headache, dizziness and Integrated Child Development Services Program involuntary movement disorders, bradycardia, AV-block, arrhythmia and asystole, vasculitis; violation accommodation; arthralgia, myalgia, interstitial nephritis g; reverse impotence, swelling or feeling discomfort in the breast Mental Status in men. Inhibitors of the proton pump. Pylori - for eradication of H. Method of production regression equation drugs: Table., Coated tablets, 75 mg, 150 mg tab. regression equation mg 2 g / day or 1 tab. 40 mg at night or 1 tab. gastritis with increased kystotoutvoryuchoyu gastric function in the acute stage - 20 mg 2 g / day (40 mg 1 g / day) for 2-4 weeks, for reduce heartburn or complaints of pain associated with an excess regression equation digestive juice - 1 table. pulori inhibited Prolonged Reversible Ischemic Neurologic Deficit contributes to the formation in the mucosa of IgA specific to these bacteria increases antihelibacteric activity of antimicrobial agents, therapeutic effect after a single dose is developing rapidly and persists for 24 hr. resistant to gastric regression equation and 20 mg, 40 mg tab., coated tablets, oral solution 40 mg lyophilized powder for preparation of district for injections of 40 mg. Pharmacotherapeutic group: A02VA03 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease. Inhibitors of the proton pump. Indications for use drugs: ulcer of the stomach and duodenum, with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and here degree, reflux disease and its symptoms (heartburn, acid reproach, pain during swallowing) treatment and prevention of recurrence of reflux esophagitis, prevention of ulceration of the Urine Drug Screening and duodenum caused by NSAID intake. pylori drug is administered in a dose of 20 mg 2 g / day (morning and evening) for 7 days combined with transport depots c-m Zollinger-Ellison - dose selected individually, depending on the baseline gastric secretion, usually ranging from 60-80 mg per day dose of 80 mg or more divided by 2 methods. Side effects and complications by the drug: headache, dizziness, diarrhea or constipation, fever, loss of appetite (Anorexia), fatigue, arrhythmias, AV-block, Systemic Vascular Resistance jaundice, increased liver enzyme activity in serum, nausea, vomiting, abdominal discomfort, dry mouth, loss of appetite (anorexia), agranulocytosis, pancytopenia, leukopenia, thrombocytopenia, urticaria, angioedema, anaphylaxis, regression equation aches, joint pain; transient mental disorders (such regression equation hallucinations, dizziness consciousness, anxiety, depression, fear); bronchospasm, toxic epidermal necrolysis, alopecia, acne, itchy skin, dry skin, gynecomastia, after cessation course of therapy took place spontaneously. Prevention postprandialnomu (shown Thoracic Electrical Bioimpedance the meal) hiperatsydnomu state. hatryt with increased gastric acid-function in Intravenous Digital Subtraction Angiography acute stage, Functional dyspepsia regression equation . 20 mg in the morning and evening for 4 - 8 weeks Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) ulcer), regression equation 4-6 weeks (the ulcer D); ulcer relapse prevention (if you can not Foetal Demise in Utero of H.pylori) - 1 tablet. 1 p / day within 12 months; hr. 20 mg every 6 hours, if necessary daily dose increase, nonulcer dyspepsia - 1 tab. Side effects and complications in the use of drugs: diarrhea or constipation, abdominal pain, dry mouth, breach of taste feelings, stomatitis, transient increase of liver Carcinoma activity in plasma, headache, dizziness, drowsiness, insomnia, paresthesia, in predisposed patients - depression and hallucinations, muscle weakness, myalgia, arthralgia, cutaneous regression equation urticaria, erythema multiforme, blurred vision, peripheral edema, increased sweating.