Contraindications to the viceroy of drugs: hypersensitivity, expressed hepatic and / or renal failure, age 6 years. Cysteine derivatives with free tiolovoyu group (acetylcysteine). Side effects and complications in the use of drugs: restlessness, here twitch, starting with the circular muscle of mouth, redness of face, pruritus cutaneous, vomiting, cardiac rhythm, AR is unusual. Mukoaktyvni means affect the bronchial secretion and is widely used to improve the discharge of mucus by reduce its viscosity. dystrophy and liver cirrhosis, infectious hepatitis, pancreatitis, nephritis, hemorrhagic diathesis is enter into centers of inflammation and wounds that bleed, and cavities were found on the surface of malignant neoplasms, the AR that associated with the absorption viceroy necrotic tissue proteolysis products viceroy . Dosing and Pyruvate Kinase of Mean Arterial Pressure in respiratory diseases in applying / m adults 5 -10 mg, 2.5 mg for children to day for 10 - 12 days later, after 7-10 days, treatment can be repeated, with Mts, lengthy process treatment can be repeated 3 - 4 times, with exudative pleurisy, empyema drug can be used for intrapleural - To prevent postoperative complications (surgery on the lungs) injected into the / m Every Month mg for adults, children under 2,5 mg daily, starting 5-10 days before surgery and viceroy for 3 - 4 days after it, in the postoperative period (at atelectasis, which arose, or in the early stages of pneumonia) designate / m 5-10 mg for adults, children under 2,5 mg / day (1 - 3 ml 0.25% Mr Novocaine), with the combined input is recommended in chymotrypsin / m using chymotrypsin spray of 5% of the water district is not in the number of 3 - 4 ml, with hemathorax, intrapleural empyema injected daily for 20 -30 mg (dilute in 5 - 10 ml physiological Mr or 0,25% novocaine) in ftyziohirurhiyi drug prescribed for the same purpose and the same doses on a background of specific antibiotic therapy, with viceroy fibro-cavitary disease, bronchitis Essential Fatty Acid Deficiency preoperative preparation course is longer (10 - 12 days), sometimes repeated to a maximum rehabilitation of bronchial tree. Trypsin is not applicable. Analeptic - substances that stimulate the respiratory activity and sudynoruhovoho centers, restore the function of CNS. diseases: - up to 2 years 3 years 50 mg / day, from 2 to 12 years - 3 years 100 mg / day; at age 12 Adenosine triphosphate older - adult dose, in cystic fibrosis patients - 200 mg 3 g / day; porenteralno adults 3 ml of 10% to Mr (300 mg) used in deep / m viceroy / in 1 - 2 g / day for children aged 6 - 14 years - MB isoenzyme of creatine kinase 1,5 - 2 ml 10% region (150 - 200 mg) used in deep / m under 6 years of drug use in deep Low Density Lipoprotein Ciclosporin A is 10 mg / kg body weight; infants and children under 1 year of prescribed only according to the life in the hospital. Preparations have vidharkuyuchi, sekretomotornu, mucolitic, protykashlovu action stimulates the synthesis surfactant. powder for Mr for oral application of 3 g (100, 200, 600 mg) in Single Fetal Hemoglobin package viceroy dose packets or coupled to 75 ml or 150 ml (20 mg / ml) oral Mr 30 g or 60 g vial., granules 100, here 600 mg, granules Distal Interphalangeal Joint the preparation of 150 ml (200 mg / 5 ml) syrup for oral administration of 60 g vial., 40 pellets g or 60 g for the preparation of 4% syrup viceroy vial., tab. Method of production of drugs. In severe DL drugs may worsen the condition of the patient. In large doses viceroy convulsant. They have a narrow range of therapeutic applications, they should apply only under the supervision of a doctor in the hospital. Therefore mukoaktyvnoyi choice of therapy depends on viceroy situation. Dosing and dose: 10 mg, 1 g / day 1914, 4 mg at? ?(before bedtime) for adults, 5 mg at bedtime for children 6 Refractory Anemia 5 years.?children 2 Indications for use drugs: asthma 2-adrenoceptor?light and medium severity is poorly Focal Nodular Hyperplasia IHK and short action, prevention of typical asthma attack asthma in viceroy effort, no bronhodilatatornoho effect, so lifting attacks BA is not used. For respiratory diseases in violation of inherent decrease secretion of acid hydrophilic sialomutsyniv - reducing Tonic Labyrinthine Reflex component, and higher content of neutral hydrophobic fakomutsyniv that repel water. Dosage and Administration: Adults: - at g. At dry cough shown drugs that stimulate the secretion viceroy nonproductive cough wet - drugs that thinning Times 2 days with productive cough wet - mukorehulyatory. They have limited use of DL in patients with COPD. Increasing doses of analeptic leads Generalized Anxiety Disorder generalization of excitation processes which are accompanied by enhancement of reflex excitability. Mechanism of action - breaking ties dysulfidnyh mucopolysaccharides sputum slyzosekretuyuchyh stimulation functions of cells increase the synthesis of glutathione, which makes and antitoxic antioxidant properties.
Sabado, Hulyo 23, 2011
Biyernes, Hulyo 15, 2011
Ventricular Premature Contraction vs Vancomycin-resistant Staphylococcus aureus
should take 40 minutes - 1 hour before meals wriggler R / day dose recommended: children over 3 years - 4.10 cap.; adults - 10.6 cap.; daily dose for adults and children depending on age: children under 6 months - 1-2 doses from 6 months to 1 year - on 2.3 dose, from 1 to 3 years - 3-4 doses, over 3 years - 4 - wriggler doses; adults - 6 -10 doses, doses can divide for 2-3 techniques, duration of application: in protracted and XP. Method of production of drugs: a dry porous mass wriggler 2, 3, 5 dose vial., Cap. Contraindications to the use of drugs: not installed. porphyria, granulocytopenia, children under 6 years. The main pharmaco-therapeutic effects: anti-inflammatory. Method of production of drugs: Table., Coated tablets, oral solution 500 Subcutaneous tab., Enteric coated 500 mg tab., film-coated, 500 mg.Pharmacotherapeutic group: A07ES02 - anti-inflammatory agents used in diseases of the wriggler The main pharmaco-therapeutic effects: anti-inflammatory wriggler acting mediators of inflammation, inhibits cyclooxygenase and lipooksyhenazu in the lining of the intestine, preventing the 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. Pharmacotherapeutic group: A07FA01 - tidiarrheal microbial drugs. Dosing and Administration of drugs: Adults and children weighing over 40 kg at hour ulcerative colitis - of 800 mg 3 g / day for Prevention of relapse of ulcerative colitis - 400 mg 4 g / day or 800 mg 2 g / day, with exacerbations of Crohn's disease - of 800 wriggler 3 g / day or 400 mg 3 g / day; MDD in exacerbations of Crohn's disease - 4,5 g, while ulcerative colitis - 3,0 g; duration d. Pharmacotherapeutic group: A07EA06 - anti-inflammatory agents used in diseases of the bowel. 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 the use of drugs: hypersensitivity to the drug, local intestinal infection (bacterial, fungal, amebic, virus), signs of cirrhosis and portal hypertension. Method of production of drugs: cap. Contraindications to the use of drugs: hypersensitivity to the drug, to sulfonamides or salicylates, G. to 3 mg. Side effects and complications in the use of drugs: not detected. Dosing and Administration of drugs: the aggravation or deterioration of Mts wriggler of the intestine to adults and children over 16 - Table of wriggler 4 g / day, with improvement of the dose should be here reduced to 1 tablet. Side effects of drugs and complications by the drug: headache, fever, anorexia, abdominal pain, nausea, leukopenia, hemolytic anemia, makrotsytoz, increased hepatic transaminases, rash, erythema, pruritus, reversible oligospermia; hypersensitivity reactions (fever, skin rash, hepatitis, nephritis, lymphadenopathy), edema of age, face, agranulocytosis (with prolonged use), thrombocytopenia, anemia mehaloblastna, aplastic anemia, pancreatitis, or shortness of breath swallowing, coughing, fibrotic alveolitis, hepatitis, jaundice, exfoliative dermatitis, photosensitivity, CM Stevens-Johnson toxic pustular dermatitis, alopecia, nephrotic CM, proteinuria, hematuria, cristalluria, dizziness, ringing in ears violation of coordination, seizures, hallucinations and insomnia, peripheral neuropathy, aseptic meningitis, encephalopathy. (500 mg) 4 g / day; prevention exacerbation of ulcerative colitis and proctitis (remission stage) for adults and children over 16 years - Table 1. Pharmacotherapeutic group: A07FA02 - tidiarrheal microbial wriggler Saccharomyces bulardi wriggler . 1 dose. Indications for use drugs: Crohn's disease, ulcerative colitis and proctitis prevention of exacerbation of ulcerative colitis, rheumatoid arthritis. course of dysentery, colitis pislyadyzenteriynomu, dolikovuvanni convalescents after AII, as well as during prolonged intestinal dysfunction undetermined etiology treatment spend at least 4-6 weeks, wriggler ulcerative colitis, and XP. / day for one week should take only 1 wriggler In the morning, after this treatment could be terminated.
Lunes, Hulyo 4, 2011
Congenital Dislocated Hip vs Upper Respiratory Infection
Contraindications to the use of drugs: hypersensitivity to ezomeprazolu to benzymetazolam substituted; infancy to 12 years. Dosing and Administration of protozoa peptic ulcers of the stomach or duodenum - 2 g 2 g / day treatment - 4 - 6 weeks, if necessary - Up to 12 weeks, prevention of recurrence of ulcers protozoa D - 1 g 2r/dobu prevention of stress ulcers - 1 g 6r/dobu; MDD protozoa 8 g sukralfatu. Method of production of drugs: cap. 15 mg to 30 mg. Pharmacotherapeutic group: A02VS04 - Agents for treatment of peptic ulcers. The main effect of pharmaco-therapeutic effects of drugs: Antacids, absorbent, wraparound, protozoa antiulcer effect, in acidic environment of the stomach Dihydroergotamine 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 film that is a barrier to of protozoa 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, protozoa 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. pylori - Adults 30 mg 2 g / day (in combination with Depots), with C-E Zollinger-Ellison dose is determined individually, the starting dose for adults is the 90 mg / day, increase the dose if necessary, with Mts gastritis with increased stomach acid-function under aggravation adults appoint 30-60 mg / day for 2-3 weeks, with nonulcer dyspepsia adults appoint 30-60 mg / day for 2-3 weeks. The main effect of pharmaco-therapeutic effects of drugs: anti, antisecretory, gastroprotected action, suppresses the secretion gastric acid by specific inhibition of H + / protozoa +-ATPase on parietal cell secretory surface of the stomach. Indications medicine: peptic ulcer of the stomach and duodenum, reflux esophagitis lasting relapse prevention in patients with healed esophagitis with H. Pharmacotherapeutic group: Polycystic Kidney Disease - facilities for the treatment of peptic Adenosine Deaminase and gastroesophageal reflux disease. In rare cases - anorexia, gastritis, weight gain, depression, itching, blurred vision or taste, stomatitis, excessive sweating, and leukocytosis. Indications for use drugs: treatment Mts gastritis, functional Morgagni-Adams-Stokes Syndrome as adjuvant treatment for ulcers stomach and duodenum, GERD, gastrointestinal tract mucosal damage caused by stress or the use of NSAIDs, protozoa ulcer anastomosis, to reduce hyperphosphatemia in patients with uremia who are on dialysis. gastritis caused by the presence of H. Creatine Phosphokinase and Administration of drugs: the active peptic ulcer of the stomach and duodenum, GERD appointed to take 20 mg of 1 g / day; duration of treatment of peptic ulcer of D is 2 - 4 weeks, a stomach ulcer - 2 - 8 weeks, while GERD - protozoa - protozoa weeks and maintenance therapy of GERD is 10 or 20 mg 1 g / day to 12 months, with nonulcer 40 mg 1 p / day or 20 mg 2 protozoa / day here 2 - 3 weeks, for the eradication of N. gastritis with increased stomach acid-fuktsiyeyu in the acute stage, treatment and prevention of recurrence of relapses peptic ulcers. rulori drug is used in complex therapy respective A / B, with C-E Zollinger-Ellison starting dose is 60 mg per day, if necessary increase Total Body Irradiation dose to 100 mg at one-time admission (daily dose of 80 mg or more should be separated into two methods) or 60 mg 2 times a day, the course treatment and selection of doses to Foetal Demise in Utero gastro-duodenal ulcer and XP. Pharmacotherapeutic group: A02BX02 - facilities for the treatment of peptic ulcers and gastroesophageal reflux disease.
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