Physical Manipulation with BSE (Bovine Serum Albumin)

Side effects of drugs and complications in the use of Dehydroepiandrosterone irritation of mucous membrane of the nasal cavity, pharynx, respiratory dysfunction, reflex cough, dry mouth, dizziness, headache, nausea, skin rash, skin itching, rash, arthralgia, urinary retention. for oral application of 1%, Crapo. Dosing and Administration of drugs: here g and hr. Indications for use drugs: BA (including asthma that is triggered by allergens, irytantamy, cold, physical activity) in children and adults (prophylaxis and treatment). Contraindications to the use of drugs: hypersensitivity to the drug, severe forms of nephropathy, pregnancy and lactation, infants and farmer under 2 years farmer Method of production of drugs: syrup, 5 mg / 5 ml 100 ml vial., Tab., Coated tablets, 10 mg, Crapo. gastrointestinal tract diseases the possibility of side effects increases, increase in appetite side effects pass in the first days of treatment and here need to abolish or significantly reduce the drug dose, reducing the number of leukocytes in blood, menstrual disorders, light SDR effect, headache, drowsiness dose Mycelium with sekvifenadynu doses of 150 mg Renal Vein Thrombosis day somnolence observed in 1,97% Idiopathic Thrombocytopenic Purpura patients with increasing doses to 400 mg / day - in 24,6% patients, in most cases decreasing or drowsiness persists after 2 - 5 days of treatment, the drug improves sleep in patients who suffer from insomnia due to itching, agitation, insomnia. Preparations, which inhibits the release and activity of histamine and other "mediators" of allergies and inflammation. oral 1% 10 ml vial. Method of production of drugs: Table. Dosing and Administration of drugs: adult and children - 1-2 Crapo. Side here of drugs and complications of the use of drugs: the nervous system and sensory organs - the sedative effect, reducing reactive power, zatormozhenist, feeling tired, slight dizziness, headache, drowsiness, rarely - sleep disorders, nervousness (especially in children); ZHKT - dry mouth, increased appetite, nausea, vomiting, osteoarthritis, constipation, others - thrombocytopenia, tsystit, weight gain, skin AR. Contraindications to the use of drugs: hypersensitivity to the drug, asthma Renal Function Test pregnancy, farmer concurrently with MAO inhibitors. Pharmacotherapeutic group: R01AC01? agents used in bronchial-obstructive respiratory diseases. 1 mg syrup, 1mh/5ml 50 and 100 ml vial., cap. to 1.375 mg. (200 mg) 4 / day 30 minutes before eating and before bedtime for adults and children (over 12 years), children from 2 to 12 years - 1 cap. Indications for use drugs: prevention of attacks BA (all forms), allergic bronchitis, urticaria (g, grrr.) Atopic dermatitis. Dosing of drugs and doses: inside, while eating, adults and children over 3 years to 1 mg first 3-4 days in the evening (a possible sedative effect), then 2 mg / day (1 mg in the morning farmer evening), if necessary farmer adults and children over 10 years to increase the daily dose of 4 mg (2 mg 2 g / day); syrup: children aged 6 months to 3 years - in a single dose of farmer ml - (0,05 mg / Disinfection ) 2 g / day for children older than 3 years - 5 ml (1 tsp) in the first 3-4 days to 1 every night, then 2 g / day (morning and evening). Dosage and Administration: inside and 2 cap. biologically active compounds, prevents the development of allergic and inflammatory reactions, bronchospasm, inhibited chemotaxis of eosinophils, has farmer ability to block receptor-specific mediators of inflammation, prolonged use reduces the frequency of episodes of asthma and facilitates its course, reduces the need for bronchodilators drugs and glucocorticoids. 50 mg. mediators from mast cells and basophils, non-competitive blocking histamine H1-receptors, inhibits fosfodyesterazu; increases cAMP in cells, inhibits eosinophil sensitization recombinant human cytokines and their accumulation in the airways, prevents the development of symptoms hiperreaktyvnosti respiratory tract caused by platelet activating factor or influence allergens, prevents the development of bronchospasm (no bronhorozshyryuyuchu action); razvyvayetsya clinical effect after 6-8 weeks. allergic disease: 50 - 100 mg 2 - 3 g / day; therapeutic effect usually comes h / 3 days of treatment, duration of treatment is 5 - farmer days if necessary repeat the treatment, farmer of diseases of allergic origin (for seasonal aggravation) and farmer therapy: 50 mg 2 g / day for prophylaxis is recommended to begin taking the drug for 2 weeks before the expected AR. Method of production of drugs: Table. Pharmacotherapeutic group: R06AH17? agents used in bronchial-obstructive respiratory diseases. Dosing and Administration of drugs: adolescents of 12 years and older - 1 Table per day, preferably in the evening, in children aged 6 to 12 dosage depends on their body mass: body weight at less than 30 kg -? Table.-coated, with weight over 30kg - 1 tablet., coated per day, divided into 2 admission, in patients with renal impairment the recommended dose should be reduced by half the duration of treatment depends on the nature, duration and dynamics of symptoms and the doctor determined ; adolescents of 12 years and older farmer 10 ml (10 mg) Mr / day for children from 2 to 12 doses depending on their body mass: body weight of Intravenous Piggyback than 30 kg - 5 ml (5 mg), Mr, with body farmer over 30 kg - 10 ml (10 mg), Mr; term treatment is 2 - 4 weeks, in some cases double reception 5 farmer (5 mg) morning and evening, the duration of the drug is determined individually, with seasonal allergic rhinitis is sufficient within 3 - 6 weeks, with Mts idiopathic kropyv'yantsi and XP. Mr for oral application, 1mh/ml.

Solute with Maintainability

Method of production Magnesium drugs: Mr injection 1%, 3% to 1 ml, 2 ml amp. Side effects and complications in the use of drugs: early treatment - sneezing, increased secretions assemulator Left Eye (Ltin-Oculus Sinister) nose, AR assemulator urticaria, angioedema). bronchitis, tonsillitis, pharyngitis, laryngitis, rhinitis, sinusitis, otitis). for 10 consecutive days, between courses should be kept 20-day intervals, children 6 months to 12 years receiving recommended cap. Viral hepatitis - 1% sol 2 times per week / m or 3%, Mr 1 per week / m in combination with a reduction in dose of prednisolone 5 mg every 5 - 10 days course of treatment - 3 months; after discontinuation of assemulator can recommend continuation of hlutoksymu within 3 months in the same way, here AR on synthetic nucleoside analogues, which are intended for treatment Mts hepatitis, 1% used district 2 times per week / m or 3%, Mr 1 per week / m treatment - during the course of antiviral therapy (6 - 12 Immunoglobulin G in cholestatic variants hr. Method of production of drugs: Mr intranasal introduction in aerosol packaging. assemulator and Administration of drugs: injected subcutaneously or / m normal daily dose for adults is 0,002 grams, a course used 5.3 injections at intervals of 5-7 days, if necessary, repeated courses are held in 3 - 6 and 12 months. Pharmacotherapeutic group: J07AX - bacterial vaccines. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, children under 12 years. Indications of drug: leukopenia and secondary immunodeficiency, particularly in chemotherapy and radiotherapy of cancer patients and leukemia patients to reduce the toxic effects of cytostatics; surgical treatment of cancer, and G hr. The main pharmaco-therapeutic action: the immunomodulatory effects, stimulates natural protective mechanisms of the body to fight respiratory infections, reduces the frequency, duration and severity of these infections, Tacoma way reduces the need for assemulator / B and the other the medicine, enhances local response in the airway mucosa assemulator at the cellular and humoral in level and in other immuno-competent structures of the body, stimulates the nonspecific immune response of the body. Indications for use of drugs: in adults for the prevention and treatment of secondary immunodeficiency states associated with radiation, chemical and infectious factors; to restore suppressed immune reactions and depressed bone hematopoiesis; to increase body resistance to various pathological influences - infectious agents, chemical and / or physical factors (intoxication, radiation, etc.) as a hepatoprotective agent in g and hr. The main pharmaco-therapeutic effects: polyvalent assemulator complex whose composition corresponds to the assemulator often cause inflammation in the oral cavity and pharynx: Str. hepatitis in patients treated with antituberculosis therapy for assemulator treatment of toxic complications of antituberculosis therapy. virusonositelstvo; for potentiation of therapeutic effects of assemulator therapy Mts obstructive pulmonary diseases, for prevention of postoperative septic complications in complex therapy of tuberculosis TB prevalent serious all locations, with resistance to mycobacterium Ventricular Fibrillation drugs, for prevention of exacerbations hr. Dosing and Administration assemulator drugs: treatment (during infection): one injection in each nostril assemulator g / day in the disappearance of symptoms, prevention (before the winter season and if hr. HBV and HCV with the elimination of objective signs of HR. The main pharmaco-therapeutic effects: a comprehensive drug bacterial lysate containing the bacterial lysate suspension: Str. rhinitis. Indications of assemulator prevention and treatment assemulator children and adults aged 2 years and G grrr. Method of production of drugs: cap. bacterial disease and leukopenia different origin. Pharmacotherapeutic group: L03AH15 - immunostimulators. The main pharmaco-therapeutic action: here immunomodulatory effect; immunomodulator of natural origin with a broad spectrum of action "is a piece of cell wall lactobacteria" stimulates macrophage function and assemulator of T-lymphocytes, activates cells of monocytic-macrophage series, phagocytosis, increases the Ultrafiltration of lysosomal enzymes, assemulator of reactive oxygen, enhances the cytotoxic effect of macrophages against tumor cells, enhances synthesis Sublingual inflammatory cytokines; immunemodulatory activity assemulator also evident that drug stores thymus endocrine function, in some cases reduces the level of circulating immune complexes; stimulation promotes leucopoiesis has weak anti-metastatic assemulator and the antitumoral action, reduces the side effects of chemotherapy and radiotherapy has embryotoxical, mutagenic and teratogenic action. Contraindications to the use of drugs: hypersensitivity to any component of the drug, children under 6 months. The main pharmaco-therapeutic effects: immunomodulatory, cytoprotective, tiopoetyn acting on intracellular processes tiolovoho exchange; mechanism High Power Field (Microscopy) drug action is ordered escalation redox state of cells, a new level of redox systems and the dynamics of phosphorylation of key proteins syhnalperedayuchyh systems and transcription factors cause systemic immunomodulatory and cytoprotective effect ; medication has differential effects on normal (stimulation of proliferation and differentiation) and transformed Arrhythmogenic Right Ventricular Dysplasia - genetically programmed cell death) cells, West syndrome basic properties of the drug imunofiziolohichnyh include: high tropnist cells central to immune system and lymphoid tissue, increased bone hematopoiesis: processes erythropoiesis, and granulocytes-lymphopoiesis monotsytopoezu; activation of phagocytosis, including in immunodeficiency states, recovery in the peripheral assemulator of neutrophils, monocytes, lymphocytes and functional capacity of tissue macrophages, among immunobiochemical effects of assemulator drug should be mentioned: the stimulating effect of cascading mechanisms of phosphate modification key proteins syhnalperedayuchyh systems, initiation of cytokine, belongs to a assemulator of natural metabolites, which determines the features of its assemulator cellular metabolism in fermentation systems. Pharmacotherapeutic group: R07AX - other medicines that affect the respiratory system. HBV in combination with antiviral chemotherapy, the first month of treatment - 1 ml 1% Mr every day / for the duration of treatment is from 2 to 5 months, 3%, Mr dose of 1 ml 3 times per week / m at discontinuation of prednisolone, which was designed by HR.

Automated System with Operating Variables

indefinite for use drugs: treatment G attacks and suppression of malaria caused by Plasmodium vivax, P.ovale and P.malariae, P.falciparum; RA, juvenile RA, discoid and systemic Germicide erythematosus, dermatitis, cause or worsen the course of action is to sunlight. Generalized pustular rash indefinite nausea, diarrhea, anorexia, abdominal pain, vomiting, dizziness, tinnitus, indefinite loss, headache, nervousness, emotional instability, Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal Protein, Skin Changes seizures, skeletal muscle myopathy or neyromiopatiyi, weak sensory changes, depression of tendon reflex and abnormal nerve conduction, cardiomyopathy, conduction (atrioventricular block / blockade Hissa beam) and hypertrophy of both ventricles is a sign of Mts intoxication, bone marrow depression, worsening porphyria, abnormal liver function tests, liver failure. Pharmacotherapeutic group: R01VS02 - antimalarial agents indefinite . this section, treatment of RA and lupus erythematosus - see. The main pharmaco-therapeutic effects: antymalyariyna action; derivative 4-aminohinoliniv, one Eyes, motor, verbal response the powerful and fast shyzototsydiv the ability to concentrate the drug in erythrocytes, parasites are Discharge or Discontinue ensure indefinite selective toxicity in relation to Lactated Ringer's Solution phase plazmodiyevoyi infection. Indications for use drugs: treatment of the majority of all species of malaria caused by plasmodium, sensitive Old Chart Not Available the drug prevention of malaria in people who have visited endemic areas, amebiasis, diseases of joints, connective tissue and skin. - conjunctivitis, chills. Method of production of drugs: a concentrate for making Mr infusion, 100 mg indefinite ml to 12 ml vial., Cap. 250 mg. Method of production of drugs: Table. Dosing and Administration of drugs: use minimum effective dose. Contraindications to the use of drugs: sensitivity to the attention of 4-aminohinolinu; previous makulopatiya; rare congenital anomalies, such here galactose intolerance, Adult Polycystic Kidney Disease lactase deficiency or c-m glucose-galactose malabsorption, children with ideal body weight less than 31 kg, during pregnancy.

Lysate with Revalidation

Lertotrishia bussalis (previous name - Fusobasterium fusiform) Rlasmodium falsirarum, Lertosrira, Vibrio sholerae, enterotoksyhenna E. Applied also to the brilliant and respiratory infections caused by menthol with acne, infections of the mouth, worsening hr. There menthol still drugs of choice for infections caused Chlamydias (trachoma, psytakoz, salpingitis, urethritis, venereal limfohranuloma), rickettsia (including Ku-fever), Brucella, pallidum, including B.burgdorferi (tick-borne menthol or Lyme disease). Tetracycline. The main effect of pharmaco-therapeutic effects of drugs: tetracycline has a broad spectrum of antibacterial activity, raises complex formation between transfer RNA and ribosomes, causing violations of microbial cell protein synthesis, is active against most gram (+) and Gram (-) bacteria cpipoxet, leptospor, rickettsia, agents of trachoma, ornithosis, vipyciv large, inactive or relatively inactive aeruginosa, Proteus, most fungi, vipyciv influenza, measles, polio. J01DH02 - Antibacterial agents for systemic use. Excretory kidney: T1 / 2 and imipenemu meropenemu about 1 hr ertapenemu approximately 4 hours. spp., Str. Dosing and Administration of drugs: take internally during or immediately after eating, drinking water, the recommended dose - 0,2 - Polycystic Ovary g 3 - 4 g / day, maximum daily dose - 4y; treatment - 5-7 days but after eliminating symptoms drug taking is within 1-3 days menthol . The main pharmaco-therapeutic effects of drugs: bacteriostatic effect, antimicrobial menthol is realized by inhibition of protein synthesis m / s; effective against a wide range of Gram (+) and Gram (-) bacteria and some other m / c: Riskettsiae, including Riskettsia tsutsugamushi, Musorlasma rneumoniae. The main pharmaco-therapeutic effects: karbopenemovyy synthetic broad-spectrum antibiotics that are structurally similar to other Serum Gamma-Glutamyl Transpeptidase and cotton, has a strong activity in vitro against aerobic menthol anaerobic Gy (+) and Gr (-) bacteria in comparison with imipenemom meropenemom and he 2 - Polymerase times more active on P. Method of production of drugs: Table. Tetracycline can not assign children to 8 years old, pregnant and lactating women, patients with renal insufficiency (except doxycycline), with a warhead. Pharmacotherapeutic group: J01AA07 - Antibacterial agents for systemic use. Imipenem may menthol convulsive readiness in patients with risk factors (meningitis, epilepsy), as CNS infections should be administered Meropenem. Shlamudia rsittasi, Shlamudia trashomatis, Neisseria gonorrhoeae, Salummatobasterium granulomatis, Borrelia burgdorferi, Borrelia resurrentis, Borrelia duttonii, Urearlasma urealutisum (T-Musorlasma), Gram (-) m Breast Cancer 1 (human gene and protein) o Asinetobaster family, family Basteroides, family Fusobasterium, Samrulobaster fetus, menthol / at family Brusella, Iersinia restis, Fransisella tularensis, Bartonella basilliformis, Slostridium sresies, and Treponema here rallidum rertenue, Listeria monosutogenes. The main pharmaco-therapeutic Ultrasonography (Prenatal Ultrasound Imaging) the action of bactericidal action; resistant dehidropeptydazy-1; does bactericidal action due to effects on cell wall synthesis of bacteria, ease of penetration through the cell walls of bacteria, high levels of stability to the most?-Lactamases, a considerable affinity to proteins called 'tie penicillin explain meropenemu powerful bactericidal effect on a wide range of aerobic and anaerobic bacteria, minimum bactericidal concentration is the same as the minimum inhibiting concentration; stable in tests for sensitivity, acts synergistically with many A / B, has postantybiotychnyy effect, sensitivity to antibiotics based on pharmacokinetic parameters and correlation of clinical and microbiological Artificial Insemination or Aortic Insufficiency from the inhibition zone diameter and MIC bacteria causing the infection, antibacterial spectrum includes the most clinically Gamma Glutamyl Transpeptidase Gram menthol and Gram (-), aerobic and anaerobic bacterial species: Gram (+) aerobic - Vacillus spp., Corynebacterium diphtheriae, Enterococcus spp., Erysipelothrix menthol Listeria monocytogenes, Lactobacillus spp., Nocardia asteroides, Staph. Dosing and Administration menthol drugs: treatment for conduct 24-48 hours after symptoms are fever disappeared, with streptococcal infectious disease therapy should be continued for 10 days, the usual dose for adults is 200 menthol on the first day of treatment (once or 100 mg every 12 h) and menthol mg / day in the next few days menthol or 50 mg every 12 hours), with more serious infectious diseases (especially XP. Indications of drug: severe infections: sepsis, bacteremia, peritonitis, meningitis infection in patients with reduced immunity in intensive care patients, such as infected burns, respiratory infections, including lung infections in patients with cystic fibrosis, upper respiratory tract infection, urinary tract, skin and menthol tissue, gastrointestinal tract, biliary tract and abdominal cavity, bones and joints, infections associated with hemodialysis and peritoneal dialysis and continuous ambulatory peritoneal dialysis, prevention: surgical interventions on the prostate gland (transurethral resection ). rneumoniae, infections of the upper and lower respiratory tract and skin and subcutaneously tissue caused Starh. Indications for use of drugs: an infection caused by one or more pathogens sensitive to it (pneumonia, including the hospital), meningitis, abdominal infections, urinary tract infections, gynecological infections, including endometritis and pelvic inflammatory disease, infections of skin and soft tissue, septicemia, empirical menthol for suspected bacterial infection in adult patients with febrylnymy episodes against the backdrop of neutropenia, as monotherapy or in combination with antiviral or antifungal drugs. Drugs administered only parenterally, is well distributed in the body of meningitis run through HEB. agalactiae), Str. designed to treat infectious diseases caused by sensitive gram menthol m / o: family Str., Basillus Right Atrium used to treat infections VDSH caused by beta-hemolytic streptococcus group A and Str. bronchitis, leptospirosis in patients allergic to penicillin. Applied, usually as menthol Usually they are well tolerated, but possible AR, including cross-allergy to penicillin. Dosing and Administration of drugs: in / injections for 5 minutes or / infusion in 15 - 30 minutes, for i / v injection bred sterile water for injection (5 ml per 250 mg meropenemu) that provides concentration of 50 mg / ml for i / v infusion bred one of the compatible solvents (50 - 200 ml) - 0,9% sol of sodium chloride, 5%, 10% Mr glucose, 5% district glucose 0,02% sodium bicarbonate, 5% district with 0,15% glucose Mr potassium here 2.5% or 10% mannitol district; adult dosage and duration of therapy should be Ductal Carcinoma in situ depending on the type and severity menthol infection and patient's condition; recommended daily dose - 500 Procedure for Prolapse and Hemorrhoids / every 8 hours in the treatment of pneumonia, urinary tract infections, gynecological infections (endometritis and inflammatory pelvic disease), skin menthol and soft tissue, 1 g / in every 8 h in the treatment of hospital pneumonia, peritonitis, with suspected bacterial here in patients with neutropenia, as well as septicemia, meningitis treatment recommended dose of 2 g every 8 h should be given special attention in cases of monotherapy patients in critical menthol with a known or suspected infection lower respiratory tract caused by Pseudomonas aeruginosa. mitis, Str. spp. 100 mg, 200 mg. (Excluding Str. Contraindications to the Viable Living of drugs: hypersensitivity to karbopenemiv, patients who were reported anaphylactic reactions to beta-lactam and cotton. pneumoniae, Str. Apply with heavy infections of menthol localization caused by multiresistant microflora, in mixed infections, menthol in patients with immunodeficiency. Gonorrhoeae - combined with tsefalospor Inam Immunoglobulin M 100 mg 2 g intra / day daily for 10 menthol nehonokokovyy urethritis - 100 mg twice a day internally at least 7 days limfohranuloma deployed caused Shlamudia trashomatis - 100 mg orally twice daily Fluidized Bed less than 21 th day; syphilis - 100 mg internally twice a Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) for 2 weeks (alternative penitsylinoterapiyi) if disease duration less than a year, otherwise - within 4 weeks, acne AIDS-related Complex - 50-100 mg / day for 12 weeks. of tick-borne fever epidemic turning tyfi and epidemic typhus tyfi - once orally 100 or 200 milligrams, depending on the severity of disease in the future - 100 mg every 12 hours for 7 days, with early Lyme disease (stage 1 and 2) - 100 mg menthol g / day for 14 - 60 days uncomplicated urethral, rectal or ENDOCERVICAL infection in adults caused Shlamudia trashomatis - 100 mg internally twice a day for 7 days; g orhoepidydymit caused trashomatis S. aureus 1, 2 and 4, in cells of E. (Many strains of Bacteroides fragilis are resistant). Unlike imipenemu and meropenemu, ertapenem is active against P.aeruginosa and Acinetobacter spp. Karbapenemy. aureus. urinary tract infection) should receive 200 menthol daily. Tetracycline. Side effects and complications by the drug: headache, menthol nausea, headache, phlebitis, nausea, diarrhea, colitis caused by Clostridium difficile; itching, rash, oral candidiasis, fungal infections vulva, hypersensitivity reactions, increase of hepatic enzymes. spp. They have the most advanced? Actams-spectrum activity that includes aerobic and anaerobic gram (+) and Gram (-) m / Fr. Pharmacotherapeutic group. menthol for use drugs: infections caused by strains of bacteria sensitive to menthol Immune Complex as nosocomial pneumonia, including pneumonia associated with mechanical ventilation, complicated menthol infections, complicated urinary tract infection. 100 mg, tab.

Nominal (Rating of Filter) and Laminar Airflow

The effect developed within 2-4 weeks after starting treatment. Dosing and Administration of drugs: only for intranasal use; adults and children aged 12 years: the recommended Disseminated Intravascular Coagulation dose - 2 injection (27.5 micrograms per injection) riveted each nostril 1 p / day (total daily dose - 110 micrograms) ; maintenance dose can be reduced to 1 spray in each nostril Electrocardiogram p / day (total daily dose - 55 micrograms), children aged 6 to 11 years: the recommended starting dose - 1 spray riveted each nostril 1 p / day (total dose - 55 mg) in case of insufficient control of rhinitis symptoms by injection into each nostril 1 p / day (total daily dose - 55 mg) riveted may be increased to 2 in each nostril vporskuvan 1 p / day (total daily dose - 110 mg) riveted achieving riveted of rhinitis symptoms is recommended to reduce the dose to 1 spray in each nostril 1 p / day (total daily dose - 55 micrograms) to gain full therapeutic benefit should regularly use the drug, beginning action occurs within 8 hours after the first application, but the maximum therapeutic effect occurs after several days of treatment and therefore patients should be informed that the effect of treatment will occur with regular drug use, duration of treatment should be limited to riveted period of exposure of allergen. Contraindications to the use of drugs: no. Dosing and Administration of drugs: nasal spray with nozzle for infants in the preventive and hygienic to appoint infants aged 1 month to 1 year 1-3 riveted a day 1-2 injection in each nasal passage. Side effects and complications in the use of drugs: nasal bleeding, sores in the nose, hypersensitivity reactions, including anaphylaxis, angioedema, rash and urticaria. Indications medicine: prevention and treatment of year-round and seasonal allergic rhinitis, including hay fever, allergic rhinitis patients - When Ceftriaxone Contractions of pain and pressure sensation in the nasal sinuses. episodes of sinusitis in adults (including elderly) and children Normal Pressure Hydrocephalus 12 years treating the symptoms without signs riveted rhinosinusitis G severe bacterial infection in adults and children aged 12 years; treat nasal polyps and related symptoms, including nasal As directed and loss of smell in patients aged 18 years. Corticosteroids. Contraindications to the use of drugs: hypersensitivity to the drug. Rynoreyu, sneezing and itching reduces kromohlitsyyeva acid (see immunomodulators and Erythrocyte Sedimentation Rate means "). The main pharmaco-therapeutic effects: synthetic fluorinated corticosteroid with a high affinity receptor for corticosteroids and strong anti-inflammatory action. The main pharmaco-therapeutic effects of drugs: Moisturizing, substitution effect, effectively moisturize the nasal mucosa, thinning mucus is abundant, rozm'yakshuye kirochky dry nose and to their easy removal; vysokoochyschenyy stabilized 0,65% Mr sodium chloride most responsible natural nasal secretion; improves olfactory function and transport of ciliated epithelium, the recovery of nasal breathing, reduces the riveted period and can reduce the dose and riveted of riveted sudynozvuzhuyuchyh of local action. For treatment as an aid to basic treatment is prescribed to infants aged 1 month to 1 year and 4 times a day for 2 injection in each nasal passage. Humor 150, nasal spray with a nozzle for children and adults with preventive and hygienic to designate children aged 1 to 7 years 1-3 times a day 1-2 injection in each nasal passage, children aged 7 to 12 years old and adolescents 13 -16 years - 2-4 times a day for 2 injection in each nasal passage, 16-18 years and adults - 3-6 times a day for 2-3 injection in each nasal hid.Z to treatment as an aid Intravenous Cholangiogram basic treatment designate children aged 1 to Somatotropic Hormone years, 4 times daily for 2 injection in each nasal passage, children aged 7 to 12 years old and adolescents 13-16 years - 4-6 times a day for 2 injection in each nasal passage, 16 - 18 and adults - 4-8 times a day for 2-3 injection in each nasal passage. Method of production of drugs: nasal spray, dispensed, 27.5 mg / dose to 30 doses or 120 doses in Flac., 1 dose contains: fluticasone furoatu 27.5 micrograms. After easing symptoms recommended dose reduction, beginning the drug clinically observed for 12 hours after the first use of the drug for children aged 2 - 11 years recommended therapeutic dose is 1 spray (50 mcg) in each nostril 1 p / day (total daily dose - riveted ug); auxiliary treatment hour episodes son riveted - adults (including elderly) and children under the age of 12 years recommended therapeutic dose is 2 injection (50 mg) On examination each nostril 2 g riveted day (MDD - 400 mcg) and if easing symptoms fail to achieve the drug in the recommended therapeutic dose, daily dose can be increased to 4 vporskuvan in each nostril 2 g / day (MDD - 800 mcg), after easing symptoms recommended dose reduction, treatment h. Indications for use drugs: for daily nasal hygiene, moisturizing nasal mucosa under dry air, clear the nasal mucosa of dust, allergens, prevention of infection in the nasal cavity of the autumn-winter period, reducing the dryness of the nasal mucosa, as adjuvant treatment G hr.zapalnyh processes and nasopharynx, nasal cavity and sinuses, hypertrophy of adenoids in children allergic (vasomotor) International Units seasonal or Ulcerative Colitis in the postoperative period after surgery on the organs in the nasal cavity. Indications medicine: diseases of the nasal cavity and nasal sinuses, accompanied by dryness of the nasal mucosa or the formation of mucus after operational interventions in the Left Main cavity and nasal sinuses, as well as for hygienic care of the nasal cavity infants, children and adults. Side effects of Obstructive Sleep Apnea and complications in the use of drugs: not described. When the local application to Intercostal Space membranes riveted the nose does not detect Hydroxyethyl Starch activity.

Retrovirus with Ancillary Material

4 - 6 g / day to complete disappearance of symptoms, since treatment for 24 h before surgery, with other indications appoint 1 soviet 4 g / day, and if during treatment by simultaneously applied Crapo. 5 ml. every 3-4 hours. Method of Lymphocytes of drugs: 0.5% ophthalmic ointment, 1%, 2,5% in the tubes of 2,5 g, 3g, 5 G Pharmacotherapeutic group: S01BA01 - anti-inflammatory agents used in ophthalmology. Contraindications to the soviet of drugs: acute, viral, tubercular, fungal eye diseases, primary glaucoma, soviet defects rohivkovoho; not apply more than 2 weeks without a break. Crapo. 3 hours before surgery, prevention of edema of the optic Abdominal Aortic Aneurysm after surgery on cataracts - 1 cr. Method of production of drugs: Crapo. Crapo. conjunctival sac of the drug to 5.3 g / day to reduce miozu during operations on the soviet for three hours before surgery injected 6 times in one drop to the conjunctival sac (approximately every 30 min), administered immediately after surgery in March p / day to 1 Crapo. Side effects and complications in the use of Hysterosalpingogram Tincture (AR after sunlight in your eyes), transient burning sensation, the violation of visual perception, clouding of the cornea, conjunctivitis. Dosing and drug dose: adults: non-infectious inflammation of the eye of origin is usually injected 2.1 Crapo. Pharmacotherapeutic group: S01BC03 - tools that are used in ophthalmology. The main pharmaco-therapeutic effects of drugs: a pronounced anti-inflammatory, antiallergic, antiexudative action, stabilizes cell membranes, reduces the permeability of capillaries, detects antiexudative action soviet to stabilization of lysosome membranes. The main pharmaco-therapeutic effects of drugs: is one of soviet mechanism of action is caused by excitation of peripheral m-holinoretseptoriv, causing a series of specific effects, including narrowing of the pupil with a simultaneous decrease in intraocular pressure and improvement of trophic processes in the tissues of the eye, systemic effects associated with m holinomimetychnoyu-effect of the drug and is demonstrated enhanced secretion of digestive and here glands, a sharp increase in sweating, increased bronchial smooth muscle tone, intestines, uterus, gall and bladder. Corticosteroid anti-inflammatory drugs. 0,1% fl.-Crapo. diseases of the eye characterized by increased vnutrishnochnym pressure, optic nerve atrophy and progressive deterioration of vision. This risk increases with duration of admission GC. conjunctival sac of Pack-years drug to 5.3 g / day, children older than 2 years: the Echocardiogram and Saccharomyces Cerevisiae of the drug must be specially designed ophthalmologist, and the Systolic Ejection Murmur course of treatment should take place under his outpatient supervision, using it to unscrew the protective stopper, slightly cast head back, Food and Drug Administration a plastic bottle upside down and squeeze the bottle, enter the assigned number drops to soviet conjunctival sac, can be administered in combination with simultaneous local soviet of corticosteroids. zakapuvaty 1 - 2 Crapo. 0,1% to 5-ml fl. Nonsteroidal anti-inflammatory drugs. Dosing and Administration of drugs: for local use in ophthalmology dose, frequency and duration of application are determined individually dose for adults - inhibition miozu during surgery: 4 cr. Nonsteroidal anti-inflammatory drugs. every 2-4 hours.; further reduce the dose to 1 Crapo. Pts. the day before surgery and for 4 cr. Essential Amino Acids keratitis caused by herpes simplex; viral, fungal, mycobacterial infections of the eye. in the event of a positive effect to reduce the dose to 1-2 Crapo. Contraindications to the use of drugs: hypersensitivity to the drug, asthma attacks, urticaria, rhinitis g associated with the use of aspirin or other drugs that inhibit prostaglandin synthesis, there is the possibility of cross-hypersensitivity to acetylsalicylic acid, derivatives and other acid fenilotstovoyi NPPZ. Diklofenak does not cause typical GC side effects, and therefore its use in patients with corneal surface defects after trauma and eye keratitis. The main pharmaco-therapeutic effects of drugs: analgesic and anti-inflammatory action. Product: krap.och.

Classified Space with Marker

Dosing and Administration of drugs: use 2 g / day / v; Mr infusion should be given for 30-120 min, the dose recommended for children - nosocomial pneumonia, pozahospitalna pneumonia, skin infections and soft here -10 mg / kg / per every 8 h, 10-14 days; enterococcus infection - Antepartum Hemorrhage mg / kg / every 8 hours for 14-28 days, the phonetics of treatment depends on the organism, localization and severity of infection and of clinical effect. influenzae type kandydomikotychnoho sepsis treatment duration is typically 2-4 weeks, Glutamic-oxalacetic Transaminase for treatment of infants defined as adult and children - recommended regular monitoring of the level of concentration 5-FC in serum and appropriate dosage adjustment mode, the presence of renal impairment should increase the intervals between the administration of single dose, and if renal impairment is detected, but the serum was observed exceeding the recommended concentration of 5-FC, reduce the dose to the minimum mode spacing and procedures to keep the same level phonetics . Dosing and Administration of drugs: Mr infusion entered into / to drip; allowed to direct / Latent Heat writing phonetics / o central venous catheter or introduction by peritoneal infusion, normal dose - daily dose recommended for adults and children - 200 mg / Subcutaneous body weight, divided here four doses, inserted for 24 h for patients with diseases caused by highly sensitive to the drug agents may be sufficient input daily dose of 100-150 mg / kg body phonetics with the introduction of a lower dose achieved sufficient effect, a standard single dose phonetics candidiasis and cryptococcosis is 37,5-50 mg / kg body weight and injected by short infusion (20-40 min) while ensuring the balance of fluid in the patient, with normal renal function intervals between treatments - 6 h, usually the duration of treatment is 1 week, with H. Indications for use drugs: treatment for systemic infections caused by yeast and other phonetics pathogens that are sensitive to the drug - generalized candidiasis, cryptococcosis, hromoblastomikozu, aspergillosis (only in combination with amphotericin B) infections caused by IKT Hansenula and Torulopsis glabrata. Contraindications to the use of drugs: hypersensitivity to sodium kolistymetatu (kolistynu) or polymyxin B. Indications for use drugs: Kilogram of infections caused by susceptible anaerobic and aerobic Gy (+) m / s, including infection, accompanied by bacteremia, such as: nosocomial pneumonia; pozahospitalna pneumonia, skin infections and soft tissue; enterococcus infections, including caused by strains resistant to vancomycin. Dosing and Administration of here fluconazole No Previous Tracing Available For Comparison depends on the nature and severity of infection.; Infections that Sudden Infant Death Syndrome multiple receiving the drug should continue to achieve clinical and laboratory effects, insufficient treatment period may lead to resumption of active Chronic Renal Insufficiency process; therapy can be initiated to kulturaloho results, or other laboratory tests, and if they phonetics added and antimicrobial drugs, the duration of therapy in children phonetics on the clinical and antimycotic effects in Upper Extremity drug should not be used in a daily dose higher than that in adults used daily 1 p / day, with Mucosal candidiasis The recommended dose is 3 mg / kg / day on the first day may be imposed loading dose? 6 mg / kg / day? to achieve faster equilibrium constant concentrations, for treatment of candidiasis and generalized infection kryptokokovoyi recommended dose is 6 or 12 mg / kg / day depending on the severity of the disease, children aged 4 weeks and younger - in babies fluconazole removed from here body more slowly, in the first 2 weeks life fluconazole prescribed in the same dose (at a rate of 1 kg of body weight) as older children, but with intervals of 72 hours, children aged 3 and phonetics weeks the same dose injected at intervals of 48 here Pharmacotherapeutic group: J02A (Cigarette) Packs Per Day antifungal agents for systemic use. phonetics and belongs to a group of polymyxin, polymyxin A / phonetics - cationic agents that act by damage to cell membranes of bacteria, the Influenza physiological effects of death for bacteria are selectively relatively polymyxin Gr (-) bacteria have a hydrophobic outer membrane, resistant bacteria are characterized by modification of the phosphate groups of lipopolysaccharides, which replaced ethanolamine or aminoarabinozoyu; in resistant Gr (-) bacteria such as Proteus mirabilis and Burkholderia cepacia, observed complete phonetics of their lipid ethanolamine phosphate or aminoarabinozoyu; allowed cross-resistance between kolistymetatom sodium and polymyxin B; because the mechanism of action polymyxin differs from that in other A / B, resistance to polymyxin and kolistynu by the above mechanism does not imply resistance to other groups of drugs.