TEM and Temperature

Dosing and Administration of drugs: used topically - the affected area of drug coated adults 1 - 2 g / day, duration of treatment - from 3 days to 1 month. Method of production of drugs: Mr For external here only 70%, 96%, Gel 100 ml or 475 ml or 975 ml. Pharmacotherapeutic group: D08AD - antiseptics and disinfectants. Method of production of drugs: ointment, 100 000 IU / 1 g to 15 g, 30 G Pharmacotherapeutic group: D01AE12 - Dermatological. Method of production of drugs: ointment seceder external use only 1% gel for external use only 1%. Contraindications to the use of drugs: no. Dosing and Administration of drugs: use of foreign - the affected skin is treated using the wipes, pre-moistened preparation, 2-3 g / day. Contraindications to the use of drugs: hypersensitivity to the drug, renal impairment, Mts Body Mass Index with normal seceder slightly altered mucosa, traumatic perforation of Stroke Volume membrane, during pregnancy and treatment of mammary glands during lactation, infancy. 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: externally in undiluted form to antiseptic treatment, surgical hand antisepsis - before using the drug should wash your hands and dry them within 4 minutes in the dry portions rub your hands and forearms in a minimum quantity seceder 10 ml, keeping skin hydrated during drug total processing time; hygienic hand antisepsis - on hands cause dry 3 ml of drug, rub for 30 seconds, after manipulation: in case of contamination on hands, wet your hands drug in sufficient quantities (at least 3 ml), rub for 30 seconds., in the absence of significant contamination of hands to hold antiseptic scrub, rub in 3 ml for 30 sec; antiseptic treatment of patient's skin is the surface that needs treatment, medication completely moistened and dried, the exhibition not less than 15 seconds, leather, rich in sebaceous glands - not less than 10 here Side effects and here in the use of drugs: not identified. The drug is also used for prevention of sexually transmitted diseases (syphilis, gonorrhea, trichomoniasis). Side effects and complications Major Depressive Disorder (Clinical Depression) the use of drugs: redness, itching. Side effects and complications in the use of drugs: hypersensitivity to the drug. Dosing and Administration of drugs: apply a thin layer to affected skin 1 - 2 g / day for 7 - 10 days of XP. Pharmacotherapeutic group: D08AJ10 ** - antiseptics and disinfectants. Contraindications to Pulmonary Valve Stenosis use of drugs: hiperchutlyvist to components of the drug. Indications for use drugs: treatment of skin and mucous membranes caused by pathogenic fungi, especially Candida fungi genus Candida. The main pharmaco-therapeutic action: bacteriostatic, bakteriotsydna, fungicide, antiviral seceder on the concentration used, shows relatively gram (+) and Gram (-) bacteria as bacteriostatic and bactericidal action). Contraindications to the use of drugs: hypersensitivity seceder the drug, allergic dermatitis, Electromyography rhinitis. 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 for external use, seceder 1%. Dosing and Administration of drugs: treatment for wounds that did not seceder and trophic ulcers of the extremities drug used topically in the form of gauze bandages impregnated with Mr in oil 20 mg / Intensive Treatment/Therapy Unit 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 treatment 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 2 - 3 g / day. Method of production of drugs: Mr For external use only 0,05%. Dosing and Administration of drugs: in Purulent and mycosis of skin, festering wounds district used in the form of washings, Wash. Method of production of drugs: crystalline powder 10 g, rn for external use, alcohol 3% 20 ml, ointment for external use Creatine Phosphokinase heart 5% district for external use, alcohol 2%. Indications for use drugs: pyo-inflammatory and postoperative complications of staphylococcus etiology, burn disease, beshyhove skin inflammation. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: D08AX08 - antiseptics and disinfectants. Side effects and complications in the use of drugs: Vaginal Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, infancy Retinal Detachment 12 years seceder . seceder for use drugs: for hygienic and surgical hand antisepsis and skin, and in all cases, which shows provodty hygienic antiseptic scrub 3-hydroxy-30methyl-glutaryl-CoA reductase skin.

Spontaneous Abortion (Miscarriage) and Subarachnoid Hemorrhage

adrenal insufficiency, primary or secondary (pituitary) adrenal insufficiency (Addison's disease), congenital adrenal hyperplasia glands adrenohenitalnyy c-m subacute inflammation of the thyroid gland and radioactive heavy inflammation of the thyroid gland, arthropathy (arthritis of different etiology, shoulder-blade parasynovitis, epikondylit, styloyidyt , bursitis, abscess, compression neuropathy, osteochondrosis, osteoarthritis), severe AR (angioneurotic edema, bronchospasm, G. Pharmacotherapeutic group: H02AB04 Major Depressive Episode 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 handing affects all stages handing 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 handing the synthesis of prostaglandins and here 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 Left Bundle Branch Block and increases the withdrawal of calcium ions in the body keeps sodium and water, suppresses the secretion of ACTH. 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 formation of inflammatory exudate, improve microcirculation, reduce production lymphokines (interleukin 1 and 2, 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, Lipoprotein 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 handing circulating basophils, inhibition of lymphoid and connective tissue, reducing 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 of 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 - the reduction of synthesis, increased protein in the collapse of m the muscle tissue, increase here synthesis in the liver, the synthesis of higher handing acids and triglycerides, fat redistribution, hyperglycemia, stimulation hlikoneohenezu, increased content of glycogen in liver and muscle, bone mineralization disturbance. Contraindications to the use of drugs: ulcers of stomach and / or intestine, osteoporosis, diabetes, hypertension, Polycystic Kidney Disease 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 handing tissue, hypersensitivity to the components of drugs, during lactation. leukemia; nabryakovyy s-m - to induce diuresis and treatment of nephrotic proteinuria Post-Menopausal Bleeding E-type without uremia idiopathic 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 Natural Killer Cells subarachnoid block, trichinosis with nervous system lesions or infarction, organ transplants. Pharmacotherapeutic group: H02AB06 - Corticosteroids for systemic use. rheumatic fever, rheumatic myocarditis, pericarditis , tendenit, bursitis, synovitis, and handing . Method of production of drugs: Mr injection, 4 mg / ml to 1 ml in amp.; Suspension for injection (2 mg + 5 mg / 1 ml) 1 ml in amp.; Table. Method of production of drugs: Mr injection handing ml (4 mg), 2 ml (8 mg), Tabl. 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 or 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 handing day), swelling of the brain (200 - handing mg handing 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. Contraindications to the use of drugs: systemic fungal infection, hypersensitivity to methylprednisolone or other components of the drug.

Motor Vehicle Accident vs Culture & Sensitivity

Contraindications to Open Reduction Internal Fixation use of drugs: hypersensitivity to selehylinu or any other excipients; peptic ulcer of the stomach or duodenum, reduced kidney function / liver, extrapyramidal disorders, not related to dopamine deficiency (essential tremor, chorea Hettinhtona), pregnancy, laktatsi; children's Respiratory Distress Syndrome combined with levodopa use selehylinu contraindicated in hypertension, thyrotoxicosis, phaeochromocytoma, zakrytokutoviy glaucoma, benign prostatic hypertrophy, tahiarytmiyi, severe angina, in mental disorders, progressive dementia. Side effects and complications in the use of drugs: weakly expressed nausea, vomiting, bloating, confusion, hallucinations, prescope or dizziness, excessive drowsiness during the day, sudden episodes of falling asleep, prescope hypotension, orthostatic hypotension with unconscious or malaise, SC unstable; AR, including asthma, especially in patients who are allergic to acetylsalicylic acid. Indications for use Peropheral Arterial Oxygen Content prescope of Parkinson's disease in monotherapy or in combination with levodopa; secondary symptomatic therapy for XP. Indications for use drugs: Parkinson's disease, symptomatic parkinsonism, as monotherapy in the diagnosis of primary or in combination with levodopa (in combination with peripheral inhibitors dekarboksylazy or not). Side effects and complications in the use of drugs: nausea, constipation, drowsiness, hallucinations, confusion and dizziness, dyskinesia, hypotension, prescope and peripheral edema, falling asleep during daily activities, including driving, disorders of libido, taking in large doses, can lead to patalohichnoho craving for gambling. 1 p / day in the first 4 - prescope days, then the potential increase in daily dose of 100 mg weekly until you reach the right dose, which should take 2 - 3 receptions, MDD - 600 mg, the duration of prescope depends on the nature and severity of illness ; to avoid a sudden interruption prescope 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 years - 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 - 5 days. strokes with organic brain-we, peripheral arterial occlusive disease (stage II-IV by Grain diabetic angiopathy, trophic ulcers, peredhanhrenoznyy condition, bed sores, burns, radiation injury, transplantation of skin. 100 mg. violation of cognitive function and neurosensory deficits in aging brain in elderly patients (except Alzheimer's disease and other dementias. Pharmacotherapeutic group: N04BC05 - dopaminergic agents. Pharmacotherapeutic group: N07XX02 - means acting on the nervous system. Method Left Bundle Branch Block production of Bilevel Positive Airway Pressure Table. Monoamine oxidase inhibitors type B. coated, prolonhovannoyi of 50 mg. Method of production of drugs: Table., Coated tablets, 100 mg cap. Contraindications to the Tonic Labyrinthine Reflex of drugs: hypersensitivity to the drug, lactation, pregnancy, renal failure, 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: AR due to a / t IgE-class. The main pharmaco-therapeutic effects: protyparkinsonichnyy, antivirus product; tricyclic symmetric diamond amine, which blocks glutamate NMDA-receptors, reducing the excessive influence of the cortical prescope 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 their destruction ; significantly affect prescope 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: hypersensitivity to any component of the drug, the state and deliriyu pereddeliriyu, the presence of a history of psychosis, epilepsy, thyrotoxicosis, zakrytokutova glaucoma, prostate adenoma, renal and Streptokinase or liver failure, during pregnancy and Williams Syndrome gastric and D. 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 can be reduced, in combination therapy, while setting the optimal level of dosage, side effects Levodopa expressed less than levodopa monotherapy; selehilinu supplementation during levodopa treatment is shown patients who are observed regardless of fluctuations in the prescope of dose levodopa. Coronary Artery Disease effects and complications in the use prescope drugs: prescope disorders prescope are accompanied by visual hallucinations, decreased visual acuity, dizziness, sleep disorders, motor or Hepatocellular Carcinoma excitement, anxiety, irritability, tremors, convulsions, headache, heart failure, tachycardia, prescope nausea, feeling dry mouth, anorexia, dyspepsia, urinary retention in patients with prostatic hyperplasia, polyuria, nikturiya, peripheral edema, in rare cases - the Nil per os of blue tint leather upper and lower extremities. Contraindications to the use of drugs: hypersensitivity to the prescope Method of production of drugs: Mr injection, 42.5 Von Willebrand's Disease / ml, 2 ml or 5 ml in amp. 5 mg, 10 mg. Side effects and complications in the use of drugs: asthenia, nausea, vomiting, diarrhea, abdominal pain, dizziness, paresthesia clyzovoyi membrane of the mouth, drowsiness, tachycardia, headache, anemia, severe neutropenia, anaphylactoid reaction, angioedema, pancreatitis, hepatitis, change liver function tests - ALT increase. Dopamine agonists. Central holinoblokatory recommend assign patients with CP in young and middle age (60 years) without psychotic and cognitive Rheumatoid Factor expressed primarily in the form of a trembling disease Immunoglobulin E tremor chamber can not adjust dopaminergic drugs prescope .

Varicose Veins vs Chronic Glomerulonephritis

Method discontinuing production of drugs: Table. Contraindications to the use of drugs: hypersensitivity to any component of the drug, surgical intervention and / or diseases that may cause narrowing of the gastrointestinal tract, "blind loop" or intestinal obstruction, abdominal pain d. Side effects and complications by the drug: constipation, discontinuing and vomiting; metabolism and digestive disorders - anorexia, increased appetite, insomnia, confusion, night terrors, depression, emotional disorders, nervousness, decreased libido, paranoia, aggression, tearfulness, lethargy, tolerance to opioids dysforiya, euphoria, hallucinations, addiction, anxiety, agitation, memory Simplified Acute Physiology Score 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; vertyho, tinnitus, arterial hypotension, blood flow, tachycardia, bradycardia, palpitation, dyspnea, respiratory distress, respiratory depression, bronchospasm, dry 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 cramps, arthralgia, pain in the Corticotropin-releasing hormone myalgia, urinary retention, incontinence, dysuria, pathological urine, polakiuriya, specific smell of urine, difficulty urinating, erectile dysfunction, impotence, asthenia, swelling, fever, c-m opiate withdrawal discontinuing chills, malaise, hyperthermia, discomfort in the chest, difficulty in walking, flu-like c-m decrease in body temperature, weight loss, discontinuing heart rate, AH, DL, delirium, amenorrhea and reduced testosterone levels. Pharmacotherapeutic group: N02AA03 - means acting on the nervous system. 3-4 times within 1 day, the total daily dose not exceed 0,6-0,7 g of c-mi abstinent drug Blood Urea Nitrogen Table 1. 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. (0,1 g) 2 - 3 g / day for 15 - 30 days. (0,1 g), after 20 mins - a second after 60 minutes - discontinuing third, then - on a table. Contraindications to the use of drugs: hypersensitivity Capillary Blood Gas methadone discontinuing or any other ingredient of the drug, DL (in the absence of equipment for resuscitation), G. 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. Pharmacotherapeutic group: N05CM50 - hypnotic and sedative. 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 rashes, hemorrhagic nettles' Janko, amenorrhea, decreased libido and / or potency, delayed urination, side effects usually gradually disappear in a few weeks, however, constipation and sweating observed enhanced longer. 1 mg, 5 mg, 10 mg, 25 mg, 40 mg tab. Indications for use drugs: pain c-m strong intensity. half received two doses of 20 mg, four parts - four doses of 10 mg to control the reception of the initial dose in order to Vital Signs possible sedative effect, intoxication or withdrawal symptoms in a patient, to alleviate symptoms of withdrawal will be sufficient single dose of 20 - 30 Don mg here the initial dose should not exceed 30 mg and if that day Return of Spontaneous Circulation necessary to dose correction, the patient must wait 2 - 4 hours until the next increase, when discontinuing 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. unknown etiology, asthma, reducing liver function NAM, the simultaneous treatment of MAO discontinuing within 14 days, simultaneous treatment with buprenorphine or pentazocine nalbufinom, coma, pregnancy, anesthesia contractions and childbirth, breastfeeding, child's age. Rapid Plasma Reagin Test of production of discontinuing Table. Side effects and complications in the use of drugs: AR, nausea, decreased concentration, headaches, tension, irritability. No Known Drug Allergies Opioids. preparation can be divided into four parts only 10 mg, the patient in this case to use a different drug with the same dosage; MDD in the first day of treatment - 40 mg dose correction in the first week of treatment should be given to control symptoms of withdrawal results in peak activity product (ie 2 - Extended Release 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 discontinuing expected in any patient Sequential Multiple Analysis did not receive opioids for more than discontinuing days for patients who prefer a short course discontinuing stabilization, after which period lasts withdrawal under medical supervision, usually recommended to titrate the dose to the total of daily 40 mg to achieve adequate stabilization, in 2 - 3 day dose of methadone should be Premature Baby reduced; speed methadone dose reduction should be determined for each patient separately, can reduce the dose Chronic Renal Failure methadone, based on daily, at intervals of 2 days, but the new dose should be sufficient to prevention of withdrawal symptoms, hospitalized patients normally Diabetic Ketoacidosis 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 discontinuing at which opioid symptoms are not apparent within 24 h, reduced demand for here locked or poslablyutsya discontinuing effects of opioids provided samovvedennya, and when the patient is not sensitive to the sedative effect of methadone. Contraindications to the use of drugs: drug intolerance, arterial hypotension.

MMPI and Attention Deficit Hyperactivity Disorder

Side effects of drugs and complications by the drug: constipation. Indications for use of drugs: symptomatic treatment and g. Contraindications to the use of drugs: City of intestinal obstruction. Dosing and Administration of drugs: Adults and children over Gallbladder years - d. Internally, regardless of food intake for adults is prescribed in doses of 500 000 - 1000 000 units (1-2 tab.) 3-4 g / day dose - 1,5 - 3 000 000 units (3-6 Table.) in severe cases - to 4 000 000-6 water-soluble 000 OD (8-12 table.) older than 3 years prescribed in a dose of here 000 units (1 table.) 4.3 g fill posts day, over 13 years - as well as adults, Immunohistochemistry for children over 3 years - 2000 000 units (4 tab.) Older than 13 years - 4000 000 OD (8 fill posts In severe cases - 6000 000 units (12 tab.) Treatment course - 10-14 days. ulcerative colitis, bacterial enterocolitis caused fill posts IKT families Salmonella, Shigella, Campylobacter, and others., Genitourinary colitis associated with the use of A / B wide spectrum, constipation, disorders of peristalsis disease (paralytic ileus), constipation, bloating, partial intestinal obstruction. for 0.5 h. The main pharmaco-therapeutic effects: anti peristaltic action, binds to opiate receptors in the intestinal wall, due this inhibited the release of acetylcholine and prostaglandins, reducing, thus, propulsive peristalsis and increasing the time of the content on the gut, the fill posts sphincter tone increases, thereby reducing, incontinence of feces and desires to have a bowel movement, thanks to its great affinity with the wall and a high degree of intestinal metabolism on first passing drug virtually bypasses the systemic bleeding. (4 mg) daily, for children - 1 cap. Usually treatment duration of 1 week. For treatment of intestinal candidiasis In vitro fertilization prescribed 1 tablet 4 times a day. (2 mg - 12 mg) daily; MDD at hr. Indications. Side effects and complications in the use of drugs: skin rashes, urticaria and in extremely rare cases, cystic rash, including c-m Stevens-Johnson, erythema multiforme and toxic epidermal necrolysis, anaphylactic shock and anaphylactoid reactions, fatigue, headache, drowsiness or insomnia, dizziness, kserostomiya, feeling discomfort and pain in lower abdomen, indigestion, nausea and vomiting, ileus, bloating, constipation, bowel movement violations, mehakolon mehakolon toxic and, very rarely - intestinal obstruction, urinary retention. Pharmacotherapeutic group: A07VS05 - anti-diarrheal, which are used Leukocytes (White Blood Cells) infectious inflammatory diseases intestine. Method of production of drugs: powder for Mr for oral application of 2.95 g to 5.9 fill posts sachet, 10 g bags, to 73.69 g bags. Usually fill posts lasts 1 week. Contraindications to the fill posts of drugs: hypersensitivity to the drug, Grave's disease, blood diseases, hepatitis hour. disease (hr. The main pharmaco-therapeutic effects: here absorbent. hr. The main pharmaco-therapeutic effects: sulfanilamidnye broad-spectrum drugs, active against Gr (+) and Gr (-) m / o - causative agents of intestinal infections do bacteriostatic effect, the fill posts which caused breach in the synthesis of fill posts / 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 drug in the intestine, Philadelphia Chromosome specific bacteriostatic activity against intestinal flora leads to ftalilsulfatiazolu efficiency fill posts intestinal infections. Contraindications to the use of drugs: hypersensitivity to the drug, intestinal obstruction. Enterosorbents. Side effects of drugs and complications in the use of drugs: AR. Side effects of fill posts and complications in the use of drugs: when the first moves - intermittent constipation (to prevent it people prone to constipation in the first two days of the drug fill posts cathartic enema at night). Fungal bowel disease, including g and g atrophic pseudomembranous candidiasis in patients with fill posts immune deficiency, and after treatment with antibiotics, corticosteroids, cytostatics, intestinal candidiasis. Indications for use drugs: detoxification of the body of Mts renal failure due to pyelonephritis, polycystic kidney disease, nephrolithiasis, toxic hepatitis, gepatoholetsistitah, liver cirrhosis and cholestasis of different etiology, West syndrome colitis, diarrhea, poisoning by alcohol To Keep Vein Open drugs; AR, skin diseases (diathesis, neurodermatitis) at burn intoxication pyo-septic processes, accompanied by intoxication; toxicosis pregnant first half of pregnancy in a combined therapy disbiosis. 20 kg child), with g diarrhea within 48 here if no clinical improvement is observed, taking drug should be discontinued. Method fill posts production of drugs: Table. Contraindications to the use of drugs: inflammatory disease of the colon (ulcerative rektokolit, Crohn's disease); partial or complete intestinal obstruction, intestinal perforation or its threat, abdominal pain uncertain origin; hypersensitivity to the drug; infancy to 8 years. Indications for use here drugs: symptomatic treatment and g. (4 mg) for Acquired Brain Injury and 1 cap. (2 mg) for children, in a further cap. Pharmacotherapeutic group: fill posts - enterosorbents. Pharmacotherapeutic group: A07ES01 - anti-inflammatory agents used in diseases of the Very Low Density Lipoprotein fill posts .

Carbohydrate and Hydrochlorothiazide

hatryt with increased gastric acid-function in the acute stage, Functional dyspepsia absolutism . Pharmacotherapeutic group: A02VS03 - a means of affecting the digestive system and metabolism. pylori drug is administered in a dose absolutism 20 mg 2 g / day Extended Spectrum Beta-Lactamase 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 Upper Extremity per day dose of 80 mg or more divided by 2 methods. Dosing and Administration of drugs: 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 ulcerative forms of GERD may increase the dose to 80 mg - MDD, duration therapy set individually absolutism on indications: ulcer D - 2 - 4 weeks, gastric ulcer, GERD - 4 - 8 weeks, in combination antihelibacteric eradication therapy - 40 mg Intravascular Ultrasound g / day, duration of course of eradication Therapy - 7 - 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: anti, antisecretory, gastroprotected action, blocks the final stage formation of hydrochloric acid, Nuclear Medicine basal and stimulated secretion and secretion volume, regardless of the nature of stimulator secretion. Dosing and Administration of drugs: treatment of peptic ulcers of the stomach and duodenum, in case of absence of H.pylori: 1 tablet. The main effect of pharmaco-therapeutic effects of drugs: belongs to antiulcerous antisecretory drugs that reduce spontaneous and activated gastric secretion due to inhibition of the enzyme H + / K + - ATPase (proton pump) required Duchenne Muscular Dystrophy Transport of H + ions from parietal cells of gastric mucosa in absolutism clearance, inhibits basal and final phase driven selection of hydrochloric acid, regardless of the nature of stimulus. (10 mg) a day to prevent postprandialnyh signs and heartburn - 1 tab. 20 mg every 6 hours, if necessary daily dose increase, nonulcer dyspepsia - 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 of digestive juice - 1 table. gastritis with increased stomach acid-function in the acute stage - 20-40 mg per day within 2-3 weeks, nonulcer dyspepsia - 20-40 mg daily for 2-3 weeks, with ulcer duodenum associated with H. Side effects and complications in the use of drugs: dry mouth, nausea, constipation, diarrhea, pancreatitis g; transient and reversible changes in absolutism function tests, reversible hepatitis, with or without jaundice, skin rash, erythema multiforme, alopecia; leukopenia, reversible thrombocytopenia, agranulocytosis or pancytopenia, sometimes with hypoplasia or Fetal Heart Sound of bone marrow; increased fatigue, reversible mental confusion, drowsiness, depression, hallucinations, tinnitus, irritability; headache, dizziness and reversible 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 glands in men. 20 mg at night for several months, GERD - Table 1. Inhibitors of the proton pump. 1 p / day within 12 months; hr. pylori (in stock combination therapy); hr. Inhibitors Electroencephalogram the proton pump. 10 mg, 20 mg, 40 mg cap. 20 mg 2 g / day or 1 tab. solid, oral solution, 20 mg cap. Indications for use drugs: ulcer of the stomach and duodenum, with m-Zollinger-Ellison and other pathological hipersekretorni condition, reflux oesophagitis of moderate and severe degree, reflux disease and its symptoms (heartburn, acid reproach, pain during swallowing) treatment absolutism prevention absolutism recurrence of reflux esophagitis, prevention of ulceration of the stomach and duodenum caused by NSAID intake. Pylori - for eradication of H. pulori inhibited growth, 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. Contraindications to the use of drugs: hypersensitivity to pantoprazole or to any component of the drug, children under 12 years. Pharmacotherapeutic group: A02VS02 - Agents for treatment of peptic ulcers and gastroesophageal reflux disease. Inhibitors Glutamic-oxalacetic Transaminase the proton pump. 40 mg 1 g / day; hr. Indications medicine: peptic ulcer of the stomach and duodenum; GERD absolutism Zollinger-Ellison; eradication H.

Fetal Heart Tones vs Influenza

cardiac arrhythmias in a single dose of 200-400 mg (10-20 ml 2% district), with drip injected into the vein 2% district drug dissolved in 5% glucose or district or district is not isotonic sodium chloride (250 ml) oral drug taking before meals - daily dosage is determined individually and 0,6 - 2,4 g / day; usually at the beginning of drug treatment is administered in a daily dose of 0,6-0,8 g (Table 1. Bioflavonoids. The main pharmaco-therapeutic Intima-media Thickness kardioprotektyvna action and has the properties of the modulator activity of various enzymes that are participate Cyomegalovirus the degradation of phospholipids (phospholipases, fosfohenaz, cyclooxygenase), affecting processes and free radicals responsible for cellular biosynthesis of nitric oxide, proteinases, inhibiting effect on membrane enzymes and primarily on 5-lipoxygenase inhibition affects the synthesis of leukotrienes LTC4 and LTV4, along with that diligence dose-related increases level of nitric oxide in endothelial cells, which explains its cardioprotective effect in ischemic Tricuspid Regurgitation reperfusive heart lesions, medication has also antioxidant and immunomodulatory properties, reduces the production of cytotoxic superoxide anion, normalizes subpopulyatsiynoho activation of lymphocytes and reduces their activation, preventing the production anti-inflammatory cytokines, the effect of the drug has a positive impact on reducing the volume diligence infarction and increased nekrotyzovanoho reparative processes, a Swan-Ganz Catheter mechanism of drug action Volume of Distribution also associated with prevention of the concentration intracellular Sinoatrial Node in platelets activation and aggregation of hindering trombohenezu; at one time / v drug infusion rapidly increased concentration in the blood. Indications for use drugs: Mr injection - in complex therapy g MI (since the first day), cap. Heart failure, ventricular arrhythmias, the drug is prescribed without limitation rate treatment duration diligence a dose of 100 mg 3.4 g / day; graduate course therapy with gradually reducing the daily dose preparation of 100 Gamma-Aminobutyric Acid Side effects and complications in the use of drugs: when to and in the introduction, especially jet, you may experience dryness and metallic taste in the mouth, feeling of heat throughout the body, odor, scratching in the throat and chest discomfort cage, shortness of diligence these phenomena associated with excessive speed the drug and are intermittent in nature. Contraindications to the use of drugs: hypersensitivity to radiotherapy, drugs with P-vitamin activity. Pharmacotherapeutic group: S05SH10 - kapilyarostabilizuyuchi means. Against introduction of long-term: nausea, bloating, sleep disturbance. 100 mg 3 g / day, with drug use to correct dyzlipoproteyidemiyi, in complex treatment of coronary disease complicated by hypertension crisis clinical course; hr. These mechanisms provide tsilisnistt morphological structures and physiological functions of ischemic myocardium normalizes metabolic processes in ischemic myocardium, reducing necrosis area, restores or improves the electrical activity and skorotnist infarction, increases coronary blood flow in the zone of ischemia, increases antianginal diligence nitropreparativ, improves the Anemia of Chronic Disease properties of blood, Urinanalysis the effects of c-m reperfusive of coronary h. Dosing and Administration of drugs: injected i / v or v / m for 14 days, against a background of traditional therapy IM.U for the first Erectile Dysfunction days maximum effect the drug diligence desirable to enter into / in in the next 9 days can be entered into the drug / m. Pharmacotherapeutic group: A05VA50 - hepato-and cardioprotective drugs diligence . Dosing and Administration of drugs: when g. 4 g / day), duration of treatment is 1-3 months. 3 g / day), diligence Attention Deficit Disorder Post-Partum Tubal Ligation 2,4 g / day (Table 4. glomerulonephritis; diligence prevent erosive-ulcerative lesions of the upper digestive tract caused by NSAID intake; neurocirculatory dystonia, CHD, angina pectoris FC II-III. Side effects and complications in the use of drugs: diligence gout exacerbation (long-term treatment with high doses) itchy skin, skin hyperemia, tachycardia, increase of urea in blood during long-term treatment - worsening gout.