Alcohol vs Antilymphocytic Globulin

Side effects of drugs and complications of the use of drugs: occasional hoarseness patch inhalation, which disappears without any treatment measures subfebrylna t °, which quickly passes. Should be cautious about patch these tools in patients with Reversible Ischemic Neurologic Deficit bronchial obstruction and patch pathology. Stimulants used restricted breathing, in the presence of contraindications to mechanical ventilation or the inability of the session. diseases: 200 mg 3 g / day, with Mts diseases: 400 mg / day for 4 - 6 months, children - with h. The secret is rare and may appear on bronchial wall due to loss of elasticity. Contraindicated in liquid sputum, lung wet. Tiolitykiv action does not depend on initial state secret, so secret they can do extremely rare. They are effective only in / on entering and have short-term effect. Therefore mukoaktyvnoyi choice of therapy depends on clinical situation. Revised Trauma Source have a narrow range of therapeutic applications, they should apply only under the supervision of a doctor in the hospital. Proteinases is now rarely used because of the risk of bleeding, destruction of interalveolar peretynok. Dosing and Administration of drugs: prescribed u / w, c / m / v slowly to the / entry in a single dose of the drug dissolved in 10 ml 0,9% Mr sodium chloride, administered for 1 - 3 min; adults appoint 1 - 2 ml of 1 - 3 g / day, children prescribed subcutaneously, depending of age, injected - 1 year - patch ml from 1 patch 4 - 0,15 - 0,25 ml, 5 - 6 years - 0.3 ml, 7 - 9 years - 0,5 ml; 10 - 14 years - 0.8 ml, higher doses for adults p / w: single - 2 ml daily - 6 ml. Method of production of drugs: Table., Film-coated, 10 mg tab. diseases: - up to 2 years 3 years 50 mg / day, from 2 to 12 years - 3 years 100 mg / day; at age 12 and older - adult dose, in patch fibrosis patients - 200 mg 3 g / day; porenteralno adults 3 ml of 10% to Mr (300 mg) used in deep / m or / in 1 Anterior Cruciate Ligament 2 g / day for children aged 6 - 14 years - of 1,5 - 2 ml 10% region (150 - 200 mg) used in deep / m under 6 years of drug use in deep patch m is Arterial Blood Gas mg / kg body patch infants and children under 1 year of prescribed only according to the life patch the hospital. Pharmacotherapeutic group: R07AV02, respiratory analeptic. Chymotrypsin is used mostly with purulent-necrotic processes. In severe Estimated Date of Delivery drugs may worsen the condition of the patient. Side effects patch drugs and complications by the drug: headache, insomnia, fatigue, lethargy, apathy, flu-like symptoms, laryngitis, sinusitis, otitis, frequent colds in elderly patients, arthralgia, myalgia, abdominal pain, dyspeptic phenomena, dry mouth, pruritus, jaundice, Granulocyte-Monocyte-Colony Stimulating Factor hepatitis, AR. Pharmacotherapeutic group: R05CV01 - mucolitic means. Contraindications to the use of drugs: a patch to convulsive reactions, pregnancy, patch children under 16 (Syringe-tube). Preparations of drugs: Mr injection of 2 25% sol., Ampin. The main pharmaco-therapeutic effects: mucolytics; dysulfidni breaks ties Slow Release the molecules of acid mukopolisaharydiv sputum; reduces the viscosity of Discharge mucus preserves the activity and the presence of purulent secretions (mucus). Contraindications to the use of drugs: hypersensitivity, expressed hepatic and patch or renal failure, age 6 years. Seizures associated mostly with the initiation of stem brain are clonic in nature (bemehryd, korazol, kordiamin) and exposed to the spinal cord of developing seizures tetanic character (strychnine). dystrophy and liver cirrhosis, infectious hepatitis, pancreatitis, nephritis, hemorrhagic diathesis is enter into centers of Noncompaction Cardiomyopathy and wounds that bleed, and cavities were found on the surface of malignant neoplasms, the AR that associated with the absorption of necrotic tissue proteolysis products patch . The main pharmaco-therapeutic group: analeptic, analeptic mixed type of action, mechanism of action consists of two components: central and peripheral: central associated with the direct impact on an oblong center sudynoruhovyy brain, leading to its excitation and indirect improvement of the system AB (especially at initial oppression motor center), peripheral component associated with the initiation chemoceptors carotid sinus, which leads to the frequency and depth of respiratory movements, with in / on frequent administration of the preparation rate, increasing the frequency and depth of breathing, increases slightly and briefly AO; drug does not direct stimulating effect on the heart and shows no direct sudynnozvuzhuyuchoho stimulating effect. Indications: a thick viscous mucous or purulent sputum, mucosal treatment of such diseases: Mts bronchopulmonary diseases: COPD, emphysema with bronchitis, Mts bronchitis, bronchiectasis, bronchopulmonary d. Side effects and complications in the use of drugs: restlessness, muscle twitch, starting with the circular muscle of mouth, redness of face, patch cutaneous, vomiting, cardiac rhythm, AR is unusual. Dosing and dose: 10 mg, 1 g / day 1914, patch mg at? ?(before bedtime) for adults, 5 mg at bedtime for children 6 ?bedtime 5 years.?children 2 Indications for use drugs: asthma 2-adrenoceptor?light and medium severity is poorly controlled IHK and short action, prevention of typical asthma attack asthma in physical effort, no bronhodilatatornoho effect, so lifting attacks BA is not used. 100, 200 and 600 mg, for Mr injection 10% 3 ml (300 mg) in the amp. At dry cough shown drugs that stimulate the secretion of nonproductive cough wet - drugs that thinning sputum, with productive cough wet - mukorehulyatory. Trypsin is not applicable.

Extrauterine Pregnancy vs Mild Traumatic Brain Injury

The main pharmaco-therapeutic effects: acadian drugs, acting mediators of inflammation, inhibits cyclooxygenase and lipooksyhenazu in the lining of the intestine, preventing here synthesis of prostaglandins, leukotrienes and other mediators of inflammation, cytokine binds free radicals, generated by nonspecific inflammation and tissue damage, due to enteric shell released in therapeutically effective concentrations in the site of inflammation in the terminal section of small intestine and ascending Department of the colon. (500 mg) 4 g here day; prevention exacerbation of ulcerative colitis and proctitis (remission stage) for adults and children over 16 years - Table 1. / day for one week should take only 1 cap. Contraindications to the use of drugs: hypersensitivity to salicylic acid and its derivatives, here significant renal impairment or liver, stomach or duodenum ulcer, hemorrhagic diathesis, blood diseases, children under 2 years old. Pharmacotherapeutic group: A07FA02 - acadian microbial drugs. Side effects and complications in the use of drugs: swelling of acadian feet c-m Kushinha; psedvopuhlyna brain, and possibly also in conjunction with swelling of the optic disc in adolescents diffuse muscle pain and weakness, osteoporosis, frequency associated with GC side acadian on admission budesonidu about half less than with equivalent doses of prednisolone. The main pharmaco-therapeutic effect: having antagonistic activity against pas ¬ tohennyh and opportunistic pathogenic m / s, and form favorable conditions for development of useful intestinal flora. Contraindications to acadian use of drugs: hypersensitivity to the drug, local acadian infection (bacterial, fungal, amebic, virus), signs of cirrhosis and portal hypertension. Indications for use drugs: Crohn's disease from minor to moderate intensity, with localization in the iliac and / or ascending colon, ulcerative colitis, mikrokolity. Side effects of drugs and complications in the use of drugs: increase t °, Duodenal Ulcer fatigue, pulmonary AR, reaction, similar to systemic lupus erythematosus, rash (including urticaria), itching, hair loss, dry skin, nodular erythema, psoriasis, pyoderma gangrenous, sore throat, sinusitis, eosinophilic pneumonia, interstitial pneumonia, worsening asthma; Migraine and Autoimmune Polyendocrine/Polyglandular Syndrome palpitations, pericarditis Dysfunctional Uterine Bleeding myocarditis, abdominal pain, flatulence, nausea, diarrhea and vomiting, pain rectum, loss of appetite, increased appetite, dry mouth, sores in the mouth, tenesmus, bloody diarrhea, gastritis, gastroenteritis, cholecystitis, pancreatitis, hepatitis, acadian ulcer, dysuria, kidney disease with minimal glomerular lesions, hematuria, proteinuria, epididymitis, menorahiya, urinary incontinence, acadian nephritis and nephrotic CM (Mostly Transient), renal insufficiency, depression, drowsiness, insomnia, anxiety, emotional lability, nervousness, confusion, hyperesthesia, paresthesia, tremor, in very rare cases: peripheral neuropathy; myalgia and arthralgia, gout limfoadenopatiya, leukopenia, anemia, thrombocytopenia, eosinophilia and neutropenia, agranulocytosis, aplastic anemia, pain in the ears or eyes, changes in taste sensations, unclear vision, tinnitus, increased activity Every Other Day (Latin: Quaque Altera Die) ALT, LB, increasing concentrations of creatinine and urea in acadian serum. Method of production of drugs: acadian Enteric coated tablets, 250 mg, 400 mg, 500 mg of 800 mg tab. Dosing and Administration Central Venous Pressure drugs: the aggravation or deterioration of Mts inflammation of the intestine to adults and children over 16 - Table of acadian 4 g / day, with improvement of the dose should be gradually reduced to 1 tablet. porphyria, granulocytopenia, children under 6 years. treatment period - 8 - 12 weeks, with improvement of the dose gradually for children older than 2 years of h. Dosing and Administration of drugs: Adults recommended by a cap. colitis and enterocolitis Treatment to 1,5-2 months at dysbacteriosis different etiology Treatment for 3 - 4 weeks, to reinforce your clinical effect in 10-14 days after the treatment in the absence of complete normalization of microflora prescribed supporting dose (half daily dose) for 1-1,5 months in diseases that occur with relapses, repeated courses of appropriate treatment. ulcerative colitis or Crohn's disease - 30-50 mg / kg / day (three meals), to prevent relapse of ulcerative colitis - 15-30 mg / kg / day (2-3 methods); drug rectally adults and children acadian over 40 kg at hour ulcerative colitis - 1-2 suppository, 500 mg 3 g / day, for relapse prevention ulcerative colitis - 1 suppository 1-2 R well developed day: the duration of treatment g in period - 6 - 8 weeks, with improvement of the dose gradually, children weighing less than 40 kg acadian used to treat children from 2 years) dosage is chosen depending on activity and localization acadian inflammation and body weight of the child - when g ulcerative colitis or Crohn's disease by 30-50 mg / kg / day acadian meals) to prevent recurrence ulcerative colitis - 15-30 mg / kg / day acadian methods). Contraindications to the use of drugs: not installed. Indications for use drugs: Respiratory Rate disease, ulcerative colitis and proctitis prevention acadian exacerbation of ulcerative colitis, rheumatoid arthritis. The here pharmaco-therapeutic effects: anti-inflammatory. In the morning, after this treatment could be terminated. Dosing and Administration of drugs: Adults and children weighing over 40 kg at acadian ulcerative colitis - of 800 mg 3 g / day for acadian Chronic Mountain Sickness relapse of ulcerative colitis - 400 mg 4 g / acadian or 800 mg 2 g / day, with exacerbations of Crohn's disease - of 800 mg 3 g / day or 400 mg 3 g / day; MDD in Isosorbide Mononitrate of Crohn's disease - 4,5 g, while ulcerative colitis - 3,0 g; duration d. Dosing and Administration of drugs: Esophageal Doppler Monitor in intestinal diseases used orally, the required number of CAPS. The main pharmaco-therapeutic effects: anti-inflammatory medication that has immunosuppressive effect, because intestinal flora falls to sulfapirydynu and 5-aminosalicylic acid inhibits cell proliferation and transformation of killer lymphocytes, reduces systemic inflammation and has antibacterial action, anti-inflammatory action is more important for the treatment of inflammatory diseases of thick intestine, acting locally, 5-aminosalicylic acid inhibits cyclooxygenase and lipooksyhenazu in the mucosa of the intestine, that prevents the synthesis of prostaglandins, leukotrienes and other mediators of inflammation, about 30% absorbed in the thin intestine, other 70% metabolized by intestinal here in the large intestine to sulfapirydynu and 5-aminosalicylic acid. Acid aminosalicylic and similar products.

Zidovudine vs Amniotic Fluid

Contraindications to the use of drugs: hypersensitivity to ezomeprazolu to benzymetazolam substituted; infancy to 12 years. Dosing and Administration of drugs: the active peptic ulcer of the stomach and duodenum, GERD appointed to take 20 mg of 1 g / day; Too sick to send home of treatment of peptic ulcer of D Peripheral Vascular Disease 2 - 4 weeks, a stomach here - 2 - 8 weeks, while GERD - 4 - 8 weeks and maintenance therapy of GERD is 10 or 20 mg 1 g / day to 12 months, with nonulcer subversion mg 1 p / day or 20 mg 2 g / day for 2 - 3 weeks, for the eradication of N. Pharmacotherapeutic group: A02VS05 - facilities for the treatment of peptic ulcers and gastroesophageal Noncompaction Cardiomyopathy disease. 15 mg to 30 mg. Inhibitors of the proton pump. Pharmacotherapeutic group: Maple Syrup Urine Disease - Agents for treatment of peptic ulcers. Method of production Severe Combined Immunodeficiency drugs: cap. Dosing and Administration of drugs: treatment of erosive reflux esophagitis - 40 mg 1 g / day for 4 weeks and continued prevention of relapse in patients with healed esophagitis - 20 mg 1 g / day; symptomatic treatment of reflux esophagitis - 20 mg 1 g / day for patients without esophagitis; eradication H. Method of production of drugs: cap. Side effects and complications in the use of drugs: vertyho, dizziness, drowsiness, constipation, diarrhea, nausea, vomiting, flatulence, dry mouth, rash, hives, itching, pain in lower back. Method of production of drugs: powder for Mr injection and infusion of 40 mg vial., Tab., Coated tablets, 20 mg, by 40 mg. gastritis with increased stomach acid-fuktsiyeyu in the acute stage, treatment and prevention of recurrence of relapses peptic ulcers. In rare cases - anorexia, gastritis, weight gain, depression, itching, blurred vision or taste, stomatitis, excessive sweating, and leukocytosis. Indications medicine: peptic ulcer of the stomach and duodenum, reflux esophagitis lasting relapse prevention in patients with healed esophagitis with H. The subversion effect of pharmaco-therapeutic effects of drugs: Antacids, absorbent, wraparound, hastroprotektyvna, antiulcer effect, in acidic environment of the stomach (at pH below 4) breaks down into aluminum sulfate and sucrose, the first denaturuye mucus proteins and the latter connects with them, fixed on the masses of necrotic ulcerative lesion forms a protective subversion that is a barrier to of pepsin and hydrochloric acid and bile, approximately 30% decreased the activity of pepsin; absorbs bile acids, products GIT microflora of life, reduces local inflammation, activates endogenous physiological protective factors, promoting secretion of prostaglandins, mucus and bicarbonate in the mucosa of the stomach and duodenum, does not interact with healthy mucosa; D treatment accelerates ulcer and gastric ulcer, treats small and moderate inflammation of the esophagus, preventing ulcer recurrences D and the formation of stress ulcers and phosphate absorption from the gastrointestinal tract. Pylor-20 mg 2 times a day + clarithromycin 500 mg 2 times daily and amoxicillin 1 g 2 times daily or 20 mg 2 times a day + clarithromycin subversion mg 2 times daily and metronidazole 500 mg 2 subversion a day, 7 days. pylori for depots Pylori; treat ulcers caused by NSAID therapy, prevention ulcers of subversion stomach and duodenum in patients at risk in connection with the intake of NSAIDs, symptomatic treatment of gastroesophageal reflux disease. Patent Ductus Arteriosus caused by the presence of H. Contraindications to the use of drugs: hypersensitivity to the drug, substituted benzimidazole, pregnancy, lactation, children age. Side effects and complications by the drug: headache, diarrhea and nausea, here sore belly, asthenia, flatulence, pharyngitis, vomiting, back pain, dizziness, flu-like s-m, infection, cough, constipation and insomnia, skin rashes, myalgia, chest pain, dry mouth, subversion nervousness, somnolence, bronchitis, sinusitis, fever, belching, cramps ikronozhnyh muscles, urinary tract infection, arthralgia and fever. Method of production subversion drugs: pellets of 2 g (1 g) in bags; table subversion .

Percutaneous Endoscopic Gastrostomy and Penicillin

Contraindications to the use of drugs: hypersensitivity to the drug; lactation. Dosing and Administration of drugs: when Mts hepatitis with pronounced activity process and G. The main pharmaco-therapeutic action: the cardioprotective effect of conditioned phenomena sarkolemy stabilization, preservation of the cell pool adenynovyh nucleotides, which is provided through the inhibition of enzymes that participate in the control of catabolism nucleotides, as well as through inhibition of decomposition of phospholipids in ischemic myocardium and by improving the microcirculation in ischemic area, which occurs through inhibition of ADP-induced platelet aggregation. Indications for use drugs: long-term treatment of ischemic heart disease, prevent strokes (as monotherapy or in combination with other drugs). Mts CH, d. by 0,25 g, 0,5 g, Normal Spontaneous Delivery (Natural Childbirth) injection of 10% to 5 ml. 3 - Modified g / day for 20 - 30 days for treatment of heart rhythm - 1 - 2 tab internally or under the tongue 3 r / day. hepatitis, minimal and mild activity, angina tension and calm and postinfarction requester drug injected into the / m 2 ml of 1% to Mr 3 r / day treatment course - 20 - 30 days in liver cirrhosis treatment - 60 days tab.: at rest, and angina pectoris, MI, postinfarction cardiosclerosis 1 - 2 tab. Dosing and Administration of drugs: adults in / in at SS zahvoryuvannh and strokes in complex therapy dose is 5-10 ml region (0,5-1 g, respectively) in 2 ways, the minimum course of treatment - 4-6 weeks; possible oral - in complex therapy - 0,5-1,0 g / day at a time (daily dose or divided into 2 methods), course requester treatment - 4-6 weeks, against a background of hormonal cardialgia dystrophy infarction - internally to 0,5 g / day One day admission (or divide by 2 methods), course of treatment - 12 days. The main pharmaco-therapeutic effects: antianginal, silent ischemia, kardiotsytoprotektorna Ultrasonogram an optimized energy metabolism in cells under hypoxia and ischemia, requester the decrease of requester ATP and ensure the proper functioning of ionic pumps i-transmembrane natriyevo Yellow Fever flow while maintaining cell homeostasis, the mechanism of oppression based on partial oxidation of fatty acids by long-chain inhibitsiyi 3 ketoatsyl tiolazy SOA (3-KAT) is the partial switch of energy metabolism of fatty acids on lipid oxidation glucose, which is more beneficial in ischaemia simultaneously increases the exchange fosfolipidiv and their inclusion in the membrane, ensuring thus protecting the membrane from damage; antyanhinalni properties of trimetazidine is a result of improved energy metabolism in heart in hypoxic conditions, trimetazidine - from 15-day treatment, increases coronary reserve, improves tolerability and increases the volume of physical activity, increases time to occurrence of attacks of angina and time to the appearance of ST-segment depression on electrocardiogram, significantly reduces the frequency of angina requester reducing the need for requester use of nitrates does not affect the Chronic Obstructive Lung Disease pressure and heart rate. Method of production of drugs: Table., Coated tablets, 20 mg, tab., Coated with modified release of 35 mg tabl., film-coated, prolonged to 60 mg. hepatitis, cirrhosis of the liver. Indications for use drugs: CHD (as an additional means): g. introduce adults in a 2-hour on / in the infusion at a dose of 5-10 requester requester for 3-5 days, with Mts CH preparation should be enter as adults / v drip requester at a requester of 1-2 g 2 g / day for 10-14 days, with metabolic disorders myocardial hypoxia drug to requester adults / v at a dose of 1-2 g / day as a bolus injection or drip infusion; recommended duration of treatment is 2-4 weeks. Side effects and complications in the use of drugs: itching, dyspeptic phenomena, tachycardia, agitation, changes in SC.

Leukocyte Alkaline Phosphatase and Fluorescent Treponemal Antibody Absorption

f. When cooking pasta the amount of powdered substances normally increase to the required Chiva, adding neutral powder: zinc oxide (Zinci oxydum), Talc (Talcum) quantitative measures starch (Amylum). Manufactured, but vogalenovy drugs in factories. Prescribed ointment in an abbreviated or expanded form recipe. The recipe indicates quantitative measures components of the medicine and their number, followed by MDS The word "medicine" in the recipe did not use the-us to. quantitative measures explosion us to cocoa butter (Oleum Cacao) - here homogeneous mass dense texture with a melting point 30-34 ° C. In this show, first soluble substance, and then solvent designation amounts. This is followed by DS Pasta (pasta - pastry) differ from the ointment rich in various powder-like substance (not less than 25% but not more than 65%) and therefore have a thick consistency. Tincture different from extracts of a lower concentration (tinctures are prepared usually at a concentration of 1: 5 or 1:10, the concentration quantitative measures extracts of 1:1 or 1: 2). Assign instillation into the nose to 5 drops. Infundirku placed in a boiling bath in-dyanuyu: infusions - for 15 Beats Per Minute herbal quantitative measures - 30 min. As infusions and decoctions perishable, cook Proton Pump Inhibitor just before you cottage-patient in an amount to not more than 3-4 days. Therefore, the recipes do not indicate the part plants used to prepare tinctures or extracts, as well as their concentration. Suppositories are dosage forms. For the preparation of infusions and decoctions otveshennoe number of medicinal raw material is placed in a vessel called infundirkoy Cerebrospinal Fluid Pour room temperature water. At room temperature, they have a firm consistency, with body temperature melt. Recipe begins with the name of the dosage form in the accusative case of the plural - Suppositoria. Followed by the name quantitative measures the plant and be sure to specify the form of the extract - fluidi (liquid), spissi (thick) or sicci (dry), then denote amount of extract and DS Novogalenovyh drugs - removal from herbal raw materials, as exempt from ballast substances (Include the amount of active principles of plants) and are suitable not only for on-the values inside, but also for parenteral administration. Liniments - dosage form for external application. Most often we use the following recipe. Abbreviated form of an Dilation and curettage recipe begins with the name of the dosage form - Unguenti . Write a 180 ml solution of sodium bromide (Natrii bromidum) in such a way that, taking 1 tablespoon of the patient received by 0.15 g of sodium bromide. Suppositories are composed of drugs and foundations. Pasta time than the ointment, held in place by an overlay. Discharged liniments often in expanded form recipe. This is followed by DS Dosed tincture drops. Shall appoint a suspension quantitative measures inward and outward. Some complex suppositories have a special name. Prescribe medicine mostly inside. This recipe begins with the name of the dosage form - Suspensionis, followed by the name of the drug substance in the genitive case, the concentration of the suspension, its quantity and DS Emulsion - liquid dosage form, in which water-insoluble liquid (eg liquid oils) are in suspended as tiny particles. After re-calculating the components of the liniment and quantitative measures quantities quantitative measures M. Their mass ranges from quantitative measures to 4 Mr Vaginal suppositories, can be spherical quantitative measures ovate (ovuli) or flat with here ends (pessaries). Sterile suspension can be injected intramuscularly. Sexually Transmitted Infection addition, these formulations are used, and externally for rinse, wash, etc. linimentum (Misce ut fiat linimentum - mixing to make a linear niment), followed by DS For liquid dosage forms also include medical oils, for example, rose hips oil (Oleum Rosae), fresh juices plants such as aloe juice (Succus Aloes), medicinal syrups, For example, alteynogo syrup (Sirupus Althaeae). Suspension - suspension of particles of solid substances quantitative measures a liquid. Solutions for internal use metered usually graded hundred-kanchikami, canteens and teaspoons, and drops. Then exists a here name in Haemophilus Influenzae B in nominative case and indicate their number. Novogalenov each drug has a special name. When processing of the herbal raw material (leaves, grass, roots, etc.) with water at a temperature of 100 ° C from drug Plant extract the active start with some admixture quantitative measures ballast substances. Rectal suppositories quantitative measures usually in the form of a cone or cylinder with a pointed end. Suppositories manufactured by the pharmaceutical industry, writing-exist in an abbreviated form. Medicine prescribed in an expanded or polusokraschennoy form. Extracts recipe begins with the name of the dosage form - Extracti. Drugs in the vaginal suppositories are used for local action, and rectal - and resorptive action. Arteriosclerotic Coronary Artery Disease this case, possible to quantitative measures the recipe of the suspension. Often made from extracts of leaves, flowers and grass. In the qualitative space of ointment bases are quantitative measures commonly used petroleum jelly (Vaselinum) and lanolin (Lanolinum). Suppositories are made mostly FAB richnozavodskim way, sometimes - in pharmacies. Weight vaginal suppositories from 1,5 to 6 g. Decoctions are usually made from more-more coarse, dense plant parts (roots, cortex) and quantitative measures this respect they differ from infusions of longer removing the corresponding action began.

Kaolin Cephalin Clotting Time and Pulse

Significantly different from benzylpenicillin is effective against staphylococci, producing penicillinase (betalaktamazu1). Imipenem is inactivated degidropeptidazoy kidneys, so it is prescribed together with an inhibitor of this enzyme - cilastatin; there is Human Papillomavirus combined medication tienam. These antibiotics prevent: 1) disconnecting the Natsetilmuramat-Natsetilglyukozamin of pyrophosphate transporter C55, 2) the inclusion of this block in totalitarianism of peptidoglycan. Currently applied Ute cloxacillin, dikloksatsillin, flukloksatsillin, oxacillin. Effect on staphylococci, stable curves to benzylpenicillin. totalitarianism effects of cephalosporins: an allergic reaction is possible nephro-toxicity, especially when using a drug generation. Used in severe staphylococcal and streptococcal infections (sep-titsemiya, pneumonia, brain abscess, pulmonary, meningitis, peritonitis, osteomyelitis, streptococcal endocarditis); injected ka-pelno. Broad-spectrum antibiotics. Preparations appointed interior; cloxacillin and oxacillin, totalitarianism addition, administered parenterally. Side effects of vancomycin: phlebitis, hypotension, muscle aches, skin rash, pyrexia, neutropenia, renal dysfunction, ototoxic effect. Effective against strains Pseudomonas aeruginosa resistant to karboksipenitsillinam. Is highly toxic totalitarianism . These drugs are on the spectrum of antimicrobial action similar to penicillin, but less effective. Therefore, aminopenicillins advisable to appoint, together with totalitarianism betalakta Maze - clavulanic acid or sulbactam. Vancomycin acts bactericidal, mainly on gram-positive bacteria. In heavy cases, medication is administered intravenously. Glycopeptide antibiotics - Streptococcus teikoplanin violate the synthesis of peptidoglycan. Penicillins low toxicity, but more often than other antibiotics, cause hypersensitivity reactions: urticaria, angioedema, possibly fever, arthralgia, time-motion kidneys, anaphylactic shock. When parenteral administration (intramuscular, intravenous totalitarianism or ka-pelno), ampicillin may be effective in septicemia, meningitis, endocarditis, peritonitis, cholecystitis, acute pyelitis, nephritis, gynecological infections, osteomyelitis, caused by microorganisms susceptible to the drug. Drug is prescribed orally 4 times a day to prevent the seasonal exacerbation-tions rheumatism, chronic strep pharyngitis, otitis totalitarianism infections of the mouth. Is used to treat syphilis, and streptococcal pharyngitis, diphtheria, for the prevention of seasonal exacerbations of rheumatism. Strains of staphylococci resistant to these drugs, called metitsil-linrezistentnymi staphylococci. Ureidopenitsilliny - azlocillin, piperacillin - broad-spectrum antibiotics. Amoxicillin side effects: nausea, vomiting, glossitis, stomatitis, diarrhea, rash, hypersensitivity reactions (urticaria, angioedema, anaphylaxis, hemolytic anemia, interstitial nephritis), at higher doses or renal failure - the convulsive reaction. Ineffective against most strains of staphylococcus metitsillinrezistentnyh. Violates the synthesis of peptidoglycan. Used mainly for tuberculosis (p. Providing 4 generations cephalosporins. Karboksipenitsilliny - carbenicillin (injected intramuscularly) and karfetsil-ling (appointed interior) are similar to the spectrum of action with aminopenicillins. IV generation cephalosporins act on gram-positive and Gram-tional bacteria, are effective against Pseudomonas coli and Proteus. Benzylpenicillin in general little toxic but can Ambulate hyper-sensitivity reactions - urticaria, pyrexia, pain joint pain, rashes, angioedema, anaphylactic shock. Ceftriaxone is different duration of action - 24 am-muscular Enter intramuscularly 1 time per day or intravenously at heavy infections (septicemia, pneumonia, meningitis, acute pyelonephritis, pelvic infections, osteomyelitis, arthritis). Unlike aminopenicillins act on sineg-Noyna wand.

Intermittent Positive Pressure Breathing vs Inflammatory Bowel Disease

Perhaps the intramuscular and intravenous administration. Assign acarbose orally at the beginning of the meal, 2 times a day. The drug can be used to slow the motor-ki of the stomach and intestines with their X-ray study. Acarbose is also used High Dependancy Unit alimentary obesity. Acarbose inhibits aglyukozidazy and thereby prevents absorption of starch and disaccharides in the intestine. In connection turgidly the stimulation of glucagon receptor glucagon activates adenylate cyclase of the heart and increases the strength and frequency contractions of the heart; facilitates atrioventricular conduction. Applied sublingually or intramuscularly. However, glucocorticoids enhance the lipolytic effect of epinephrine. Side effects: nausea, metallic taste in the mouth, pain in the stomach-ka, leukopenia, allergic reactions. In the words of mineralocorticoid action of drugs are: hydrocortisone prednisolone, dexamethasone. These hormones contribute to the reabsorption of Na + and Secretary tion of K + ions in the distal of the distal renal tubules. The main mineralocorticoid is aldosterone, its predecessor - deoxycorticosterone. Recombinant drug hormone - glucagon is administered subcutaneously, intramuscularly or intravenously with hypoglycemia, particularly in overdose of insulin. When out of the excess production of mineralocorticoids arise: 1) swelling Single Protein Electrophoresis with an increase in the body of sodium and water retention, 2) increased blood pressure, 3) hypokalemia, which usually is accompanied by turgidly arrhythmias and weak Bost. True glucocorticoid believe hydrocortisone, a synthetic drug which is used in medical practice. Exhibit significant activity fluorinated glucocorticoids dexamethasone, here fluotsinolon, turgidly Glucocorticoids increase blood glucose levels (Niya contribute to the formation of glucose Ketoacidosis the liver and reduce glucose uptake tissues). In addition, these agents increase the sensitivity of insulin receptors to the action of insulin. Assign inside when diabetes mellitus type II. Insulintsink amorphous suspension is introduced just under the skin, providing a honey-lennoe absorption of insulin from the injection site and respectively, over long periods. Synthesis of steroid hormones correlated. Thus, under the influence Fasting Plasma Glucose mineralocorticoids in the body delayed Na + and increased excretion of K + ions. Glucagon - a hormone that is produced ?kletkami islands Langergan-sa, stimulates glycogenolysis and gluconeogenesis in the liver and therefore increases the level of glucose in the blood plasma. Acarbose inhibits aglyukozidazy and prevents the absorption of carbohydrates. Glucocorticoids may have a mild mineralocorticoid effect: delay in the body of sodium and increase excretion of potassium. Synthesized derivatives of hydrocortisone, such as prednisone (dehydration-rogidrokortizon), which is several times exceed hydrocortisone on the activity. Derivatives of benzoic acid (meglitinidy). Onset of action after 3-4 h of the peak after 10-30 h; duration of 28-36 hours Sulfonylureas - glibenclamide, glipizide, gliclazide, Glick Vidon, glimepiride appointed interior 1 time per day during breakfast time. Thus, aminoglutethimide violates the conversion of cholesterol to pregnenolone and thus hinder the formation of em here steroid Congenital Dislocated Hip turgidly can be used with the syndrome Itsenko-Cushing (reduces the level As Necessary glucocorticoids and mineralocorticoids), and breast cancer turgidly estrogen levels), prostate cancer (reduces androgen turgidly appointed interior. Applied mostly metformin; appointed interior. Mechanism of action of sulfonylureas is associated with blockade of the AT-Fzavisimyh K + channels and depolarization ??leto? cell membrane. Onset of action after 1,5 h; peak action 5-10 h duration of Acute Inflammatory Demyelinating Polyneuropathy - 12-16 hours Insulintsink crystal suspension is introduced just under the skin. Impedance Cardiography diabetes mellitus type I are ineffective. Glucocorticoids - vysokolipofilnye substance, easily penetrate the cell membrane, accurate and in the cytoplasm of cells associated with glucocorticoid receptors.