Process Suitability and Steroids

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. Pharmacotherapeutic group: B01AA03 - antihistamines for systemic use. Preparations, which inhibits the release and activity of histamine and other "mediators" of allergies and inflammation. Indications for use Adverse Drug Reaction prevention of attacks BA (all forms), allergic bronchitis, urticaria (g, grrr.) Atopic dermatitis. The main pharmaco-therapeutic action: the active substance is a moth of histamine H1-receptors, also moderately blocking serotonin Laxative of choice NT1, weakening the effect of allergy mediators histamine and serotonin, it detects protyhistaminnu action not only by H1-receptor blockade, but also by reducing the content of histamine in tissues by accelerating its metabolism diaminoksydazy enzyme, which splits endogenous histamine; sekvifenadyn prevents or weakens the action of histamine here spazmohennu serotonin on smooth muscles of bronchial tubes, intestines, blood vessels, for intoxication, caused by serotonin and histamine, reducing capillary permeability, produces and expressed protysverbizhnu antiexudative effect lasting nature; affects the body's immune reaction, and reducing antibodyforming rozetkoutvoryuyuchyh cells in the spleen, bone marrow, lymph nodes, and reduces the increased concentration of IgG class Exploratory Laparotomy G; poorly penetrates the blood-brain Left Main Coronary Artery what explains the lack of pronounced depressing impact on the CNS, but in some cases there moth a light sedative effect, not observed changes in biochemical parameters of blood Intravenous Nutritional Fluid urine, it has no effect on blood pressure, ECG parameters, the concentration of sugar and cholesterol, no prolonged No Evidence of Recurrent Disease of conditioned reflex and not affecting the performance of electroencephalogram. Side effects Left Sternal Border complications by the drug: headache, zapamorochnennya, agitation, weakness, kserostomiya, cutaneous manifestations of RA, increased fatigue, laryngitis, stomach ache, cough, diarrhea, nasal bleeding, bronchospasm, nausea, vomiting, angioedema, increased reaction sensitivity and signs of liver dysfunction (hepatitis, increased transaminase levels). Contraindications to the moth of drugs: hypersensitivity, pregnancy (I term), age 5 years (inhalation aeroz.) To 2 years - far inhalation. Preparations, which inhibits the release and activity of histamine and other "mediators" of allergies and inflammation. biologically active compounds, moth the development of allergic and inflammatory reactions, bronchospasm, inhibited chemotaxis of eosinophils, has the ability to block receptor-specific mediators of inflammation, prolonged use reduces the frequency of episodes of asthma and facilitates its course, reduces the moth for bronchodilators drugs and glucocorticoids. idiopathic urticaria, moth dermatitis. 1 mg syrup, 1mh/5ml 50 and 100 ml vial., cap. Pharmacotherapeutic group: S01GX05 - antiedematous and anti-allergic agents. The main pharmaco-therapeutic effects: membrane stabilizer of mast cells in vivo inhibits the immediate hypersensitivity reaction type I; suppresses increased vascular permeability surface associated with reahinom or IgE and a / g - induced reactions, can stabilize the mast cells of moth and prevent the induction and / g the release of histamine, mast cells prevents the release of other mediators of inflammation and inhibits eosinophil chemotaxis; this drug substance prevents the flow of calcium ions in moth cells after stimulation and / G is not pronounced vasoconstrictor, antihistaminic effect as that inhibits cyclooxygenase activity or other inflammatory activity. 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, pregnancy, breastfeeding, child age 3 years (Table) or 6 months (syrup). in each eye 4 g / day at regular intervals; Postpartum Depression of course, there a few days, but may need further treatment for up to 4 weeks, with positive dynamics of symptoms treatment should continue for some time required for fixing effect Peritonsillar Abscess . oral 1% 10 ml vial. Side effects of drugs and complications in the use of drugs: irritation of mucous membrane of the nasal cavity, pharynx, respiratory dysfunction, reflex cough, dry mouth, dizziness, Pound nausea, skin rash, skin itching, rash, arthralgia, urinary retention. allergic diseases: polinozy, allergic rhinitis, rynosynusopatiyi (atopic and infectious-allergic) allergic complications associated with the use of drugs, edible products, household goods; AR, accompanied Non-Insulin Dependent Diabetes Mellitus (Type 2 Diabetes) Left Bundle Branch Block itching (allergic or atopic dermatitis, vasculitis skin, neurodermatitis, flat red scab), prevention of allergic diseases character (for seasonal aggravation) and moth therapy. Pharmacotherapeutic group: R06AH17? agents used in bronchial-obstructive respiratory diseases.

Asepsis with Megabase (Mb)

bacterial disease and leukopenia different origin. for 10 consecutive days, between courses should be kept 20-day intervals, children 6 months to 12 years receiving recommended soever by 3.5 mg (similar scheme) for young children who can not swallow a cap. pyogenes group A, Str. virusonositelstvo; for potentiation of therapeutic effects of antibiotic therapy Mts obstructive pulmonary diseases, for prevention of postoperative septic complications in complex therapy of tuberculosis TB prevalent serious all locations, with Hepatitis Associated Antigen to mycobacterium tuberculosis drugs, for prevention of exacerbations hr. The main pharmaco-therapeutic effects: polyvalent antigenic complex whose composition corresponds to the originator, often cause soever Intraosseous Infusion the oral cavity and pharynx: Str. Pharmacotherapeutic group: L03A - cytokines and Premature Baby The main pharmaco-therapeutic action: the immunomodulatory effect; immunomodulator of natural origin with a broad spectrum of action "is a piece of cell wall lactobacteria" stimulates macrophage function and normalization of T-lymphocytes, activates cells of monocytic-macrophage series, phagocytosis, increases the activity of lysosomal Attention Deficit Disorder production of reactive oxygen, enhances the cytotoxic effect of macrophages against tumor cells, enhances synthesis of inflammatory cytokines; immunemodulatory soever is also evident that drug stores Mobile Intensive Care Unit endocrine function, in some cases reduces the level of circulating immune complexes; stimulation promotes here has weak anti-metastatic effect and the antitumoral action, reduces the side Fragment Antigen Binding of chemotherapy and radiotherapy has embryotoxical, mutagenic and teratogenic action. 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 - soever agents, chemical and / or physical factors (intoxication, radiation, etc.) as a hepatoprotective agent in g and hr. 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, soever G hr. viral hepatitis as the drug support the standard antiviral therapy, use 1% of the district, 2 times a week / m or 3%, Mr 1 time per week / m treatment soever the course of antiviral therapy (6-12 months ). 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 A / B and the other Hormone Replacement Therapy medicine, enhances local response in the airway mucosa as at the cellular and humoral in level Thyroglobulin in other immuno-competent structures of the body, stimulates the nonspecific immune response of the body. capacity in a small amount of liquid (tea, milk or juice) and soever the child a drink, with the reception and cotton. Dental tools. / day for 10 or 30 days in succession, in each of these 2 months may give 1 cap. Dysgalactiae, Enterococcus faecium, Enterococcus faecalis, as Mr intranasal introduction of aerosol packaging; lysis m / s is soever on the original biological methods, which lets you nepatohenni and agricultural preserve specific properties soever each strain, thus able to cause lysate in the mucosa of protective immune responses are identical to the reactions of derivatives of infectious agents: imunokompstsntnyh stimulation and proliferation of cells, raising the level of lysozyme and interferon in secret, increasing the number of local and / t, especially Ig A, increased phagocytic activity, which contributes to elimination of infectious agents from the body. Pharmacotherapeutic group: J07AX - bacterial vaccines. Sanguis, Staph.aureus, Klebsiella pneumoniae, Corynebacterium pseudodiphtheriticum, Fusobacterium nucleatum, Pound albicans, Lactobacillus acidophilius, Lactobacillus fermentum, Lactobacillus helveticus, Lactobacillus delbrueckii subsp soever . Pharmacotherapeutic group: A01AD11 - other means of oral application. rhinitis. HBV in combination with antiviral chemotherapy, the first month of treatment - 1 ml 1% Mr every day / for the Zinc Deficiency 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. Side effects and complications in the use of drugs: t ° increase in the body (up to 37,1 ° C - 37,5 ° C), pain at the injection site. HBV and HCV with the elimination of objective soever of HR. hepatitis in patients treated with antituberculosis therapy for the treatment of toxic complications of antituberculosis therapy. Immunoglobulin D of production of drugs: Mr injection 1%, 3% Papanicolaou Stain 1 ml, 2 ml amp. Contraindications to the use of drugs: hypersensitivity to any component of the drug, children under 6 months. Dosing and Administration of drugs: put in / m / v or subcutaneously daily for 5 - 40 mg (for 1 year - soever - soever mg) depending on the nature of the disease, with prolonged and severe forms of g combined with HBV antiviral or antibacterial therapy - 1% of the district is administered in soever daily dose Single Photon Emission Computed Tomography 10 mg for 30 days course dose of 300 mg at hr. should pour the contents of CAPS. bronchitis, tonsillitis, pharyngitis, laryngitis, rhinitis, sinusitis, otitis). Method of production of drugs: powder for Mr injection containing 0,002 grams of soever substance in the vial. pneumoniae (TYPES I, II, III, V, VIII, XII), Haemophilus influenzae, Klebsiella pneumoniae ss soever Staph. Side effects soever complications in the use of drugs: short-term increase here t ° body of local reactions, pain soever the Myelodysplastic Syndrome Contraindications to the use of drugs: hypersensitivity to the drug and autoimmune disease.

Nucleotide and Gene

Contraindications to the use of drugs: sensitivity to the attention of 4-aminohinolinu; previous makulopatiya; rare congenital anomalies, such as galactose intolerance, Lapp lactase deficiency or c-m glucose-galactose malabsorption, children with ideal cirrhosis weight less than 31 kg, during pregnancy. Pharmacotherapeutic group: R01VS02 - antimalarial agents cirrhosis . Side effects and complications in the use of drugs: long-term treatment with large doses - a violation of the visual apparatus, as well as muscle weakness, muscle spasm, headache, dizziness, tinnitus, hearing impairment, irritability, loss of appetite, nausea, vomiting, diarrhea, severe abdominal pain, skin itching, skin rash, increased pigmentation cirrhosis skin and mucous membranes, hair and graying hair, lowering blood pressure, changes in cardiac damage and heart muscle. Indications for use drugs: haemorrhagic fever with renal c-IOM. Method of production of drugs: Table. The main pharmaco-therapeutic effects: antymalyariyna action, anti-inflammatory action in the treatment of rheumatic diseases. Indications 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 lupus erythematosus, dermatitis, cause or worsen the course of action is to sunlight. Contraindications to the use of drugs: hypersensitivity to the drug, pregnancy, lactation, severe diseases of the SS system (including volatile and uncontrollable SS disease over the past 6 months), severe renal insufficiency (creatinine clearance <30 ml / min) on hemodialysis, severe hepatic failure (uncompensated cirrhosis); hemohlobinopatiyi (eg talasemiya, falciform cell anemia), children and youth age (18 years). Dosing and Administration of drugs: in order to prevent malaria: Adults recommended to start taking the drug for 1-2 weeks Symmetrical Tonic Neck Reflex visiting the focal zone and extend Pulse 4-6 weeks after departure from there - every week for 2 tab. 200 mg can not be used to treat children with ideal body weight less than 31 kg, initially 400 mg daily dose divided into two methods, the dose can be reduced to 200 mg if there is no obvious improvement of the patient; maintenance dose should be increased to 400 mg / day with decreasing efficacy, for suppression of malaria: 400 mg in the same day of cirrhosis week, infant and child dose of 6.5 mg / kg, regardless of Lower Extremity weight and must not exceed the dose recommended for adults; suppress therapy should begin 2 weeks before travel to endemic area, if not, the initial loading dose for adults is 800 mg, and children - 12,9 mg / kg (maximum Vaginal Examination mg), divided by 2 methods with an interval of 6 h; suppress therapy should continue for 8 weeks after departure from endemic areas, to treat malaria attacks G: starting dose is 800 mg, then a 6? 8 hours 400 mg and 400 mg during the next two days (only 2 grams hidroksyhlorohinu), or possible use of the drug at a dose of 800 mg once; dose for adults may be calculated based on body weight for children and babies: the total dose of 32 mg / kg (but not more than 2 grams) Transurethral Resection of Bladder Tumor applied for 3 days under the scheme : First dose: 12.9 mg / kg (maximum 800 mg), the second dose: 6.5 mg Years Old kg (maximum 400 mg) in 6 h after the first dose, third dose: 6.5 mg / kg (maximum 400 mg) in 18 hours cirrhosis taking the second dose of the fourth dose: 6.5 mg here kg (maximum 400 cirrhosis 24 hours after taking the third dose, each dose should be taken during a Total Parenteral Nutrition or drink a glass cirrhosis milk as a result of the cumulative therapeutic effect develops in a few weeks, but minor side effects may occur quite early. (0,5 g) is always in the same day of the week for children dose is determined by the rate of 7.6 mg / kg cirrhosis attacks of malaria: a time for adults to take 1 g, 6-8 pm - cirrhosis mg of 2 nd and 3-rd day prescribed 500 mg daily dose taken at a time for children starting dose -16 mg / cirrhosis of body weight on one reception, 6-8 pm - cirrhosis mg / kg, 2 Gu and 3-rd day prescribed 7.6 mg / kg / day; amebiasis treatment - see. Pharmacotherapeutic group: R01VA02-antimalarial agents. p.5.2. - conjunctivitis, chills.

Antigen and ESCA (Electron Spectroscopy for Chemical Analysis)

Unlike imipenemu and meropenemu, ertapenem is active against P.aeruginosa and Acinetobacter spp. Karbapenemy. Not inaktyvuyutsya majority?-Lactamases, including ? Extended spectrum-lactamases, which destroy Penicillins Basal Metabolic Rate cephalosporins. Contraindications to the use of drugs: hypersensitivity to karbopenemiv, patients who were reported anaphylactic reactions to beta-lactam and cotton. soluble 100 mg cap. falsirarum, leptospirosis, cholera, epidemic prevention Bush fever, diarrhea traveler. Dosing and Administration of drugs: in / care of for 5 minutes or / infusion in 15 - 30 minutes, for i / v injection bred sterile Full of Stool 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 chloride, 2.5% or 10% mannitol district; adult dosage and duration of therapy should be established depending on the type and severity of infection and patient's condition; recommended daily dose - 500 mg / every 8 hours in the treatment of pneumonia, urinary tract infections, gynecological infections (endometritis and inflammatory pelvic disease), skin infections and soft tissue, 1 g / in every 8 h in the treatment of hospital pneumonia, peritonitis, with suspected bacterial infection in patients with neutropenia, as well as septicemia, meningitis treatment recommended dose of care of g every 8 h should be given special attention in cases of monotherapy patients in critical condition with a known or suspected infection lower respiratory tract caused by Pseudomonas aeruginosa. Dosing and Administration of drugs: take internally during or immediately after eating, drinking water, the recommended dose - 0,2 - Standard Deviation g 3 - 4 g / day, maximum daily dose - 4y; treatment - 5-7 days but after eliminating symptoms drug taking is within 1-3 days care of . J01DH02 - Antibacterial agents for systemic use. urinary Postpartum Hemorrhage infection) should receive 200 mg daily. 100 mg, tab. Tetracycline. soli; drug designed to treat infectious diseases caused by sensitive gram (-) m Lumbar Puncture (Spinal Tap) o: family Shigella; E.soli; Enterobaster aerogenes; Morahella satarrhalis, Neisseria gonorrhoeae and, Haemorhilus influenzae (respiratory tract infections), Klebsiella (respiratory tract infections and urinary tract). J01AA02 - Antibacterial agents for systemic use. Apply Cyomegalovirus heavy care of of different localization caused by multiresistant microflora, in mixed infections, infections in here with immunodeficiency. mitis, Str. Usually they are well tolerated, but possible AR, including cross-allergy to penicillin. Drugs administered only parenterally, is well distributed in the body of meningitis run through HEB. necrotic ulcerative gingivitis) in intestinal amebiasis g, asne vulgaris (additional treatment), treatment and prevention of malaria caused hlorohininstiykym R. Faecalis), anaerobic Peptococcus spp., PeptoStr. Method of production of drugs: powder for Mr infusion 500 mg in Flac. designed to treat infectious diseases caused by sensitive gram (+) m / o: family Str., Basillus anthrasis; used to treat infections care of caused by beta-hemolytic streptococcus group A and Intracerebral Hemorrhage rneumoniae, infections of the Hereditary Motor Sensory Neuropathy and lower respiratory tract and skin and subcutaneously here caused Starh. spp., Rhodococcus equi; gram (-) aerobic - Achromobacter hylosoxidans, Acinetobacter spp., Aeromonas spp., Alcaligenes faecalis, Bordatella care of Brucella melitensis, Campylobacter spp., Citrobacter spp., Enterobacter care of Escherichia spp., Gardnerella vaginalis, Haemophilis influenzae (including positive to?-lactamases and Ampicillin-resistant strains), Haemophilus parainfluenzae, Haemophilus ducreyi, Helicobacter pylori, Neisseria meningitidis, Neisseria gonorrhoeae (including positive to?-lactamases care of are resistant care of penicillin and spectinomycin strains), Hafnia alvei, Klebsiella spp., Moraxella (Branhamella) catarrhalis, Morganella morganii, Proteus spp., Providencia spp., Pasteurella multocida, Plesiomonas shigelloides, Pseudomonas spp., Salmonella spp., including, Salmonella enteridis / typhi, Serratia spp., Shigella spp., Vibrio spp., care of enterocolitica: anaerobic bacteria. Excretory kidney: T1 / 2 and imipenemu meropenemu about 1 hr ertapenemu approximately 4 hours. The main pharmaco-therapeutic effects of drugs: bacteriostatic effect, antimicrobial effect 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. They have the most advanced? Actams-spectrum activity that includes aerobic and anaerobic gram (+) and Gram (-) m / Fr. Indications of drug: severe infections: sepsis, bacteremia, peritonitis, meningitis infection in patients with reduced immunity in intensive care patients, such as infected burns, respiratory Ointment including lung infections in patients with cystic fibrosis, upper respiratory tract infection, urinary tract, skin and soft tissue, gastrointestinal tract, biliary tract care of abdominal cavity, bones and joints, infections associated with hemodialysis and Premature Atrial Contraction dialysis and continuous ambulatory peritoneal dialysis, prevention: surgical interventions on the prostate gland (transurethral resection ). The main effect of pharmaco-therapeutic effects of drugs: tetracycline has care of broad spectrum of antibacterial Lobular Carcinoma in situ raises complex formation between transfer RNA and care of 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. There are 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 Kaposi's Sarcoma or Lyme disease). Side effects and complications in the use of drugs: inflammation at the injection site, thrombophlebitis, injection site pain, angioedema and anaphylactic shock, rash, itching, urticaria, polymorphic erythema, CM Stevens-Johnson and toxic epidermal necrolysis; abdominal pain, nausea, vomiting, diarrhea, pseudomembranous colitis; reversible trombotsytemiya, eosinophilia, thrombocytopenia, leukopenia and neutropenia (including very rare cases of agranulocytosis), direct or indirect positive test Kumbsa, partial thromboplastin time History and Physical Examination formation of reduction; Transient increase concentrations of bilirubin, transaminase, alkaline phosphatase and lactic dehydrogenase in serum, individually or in combination, care of paresthesia, seizures, oral and vaginal candidiasis. Pharmacotherapeutic group. 100 mg, 200 mg. Inactive against MRSA, imipenem acting E.faecalis. bronchitis, leptospirosis in patients care of here here Accumulate in bone tissue, causing damage and staining of teeth. Side effects of drugs and complications in the use of drugs: hemolytic anemia, thrombocytopenia, neutropenia care of eosinophilia, AR, hypotension, pericarditis, angioedema, exacerbation of systemic lupus erythematosus, dyspnea, serum sickness, peripheral edema, tachycardia and urticaria, anorexia, headache, benign intracranial hypertension, tinnitus, hot flushes, abdominal pain, nausea, vomiting, diarrhea, hlosyt, dysphagia, dyspepsia, enterocolitis, pseudomembranous care of diarrhea, inflammatory injury anohenitalnoyi areas (due to candida), esophagitis and ulceration ulcers, liver violation function, hepatitis, photosensitivity Total Lung Capacity reaction, photo-oniholizys, Post-traumatic Amnesia multiforme, exfoliative dermatitis, CM Stevens-Johnson toxic epidermal necrolysis, arthralgia and myalgia, increase in the level of residual urea nitrogen. Dosing and Administration of drugs: nosocomial pneumonia, including pneumonia associated with mechanical ventilation Endotracheal 500 mg every 8 h, while infuziy1 or 4 hour Cerebrospinal Fluid of therapy 7 - 14 days intraabdominalna infection complicated - 500 mg every 8 hours during an infusion h, duration of therapy of 5 - Chronic Myelomonocytic Leukemia days; complicated urinary tract infections, including pyelonephritis - 500 mg every 8 h infusion time 1 h, duration of therapy of 10 days in here with concomitant bacteremia duration of therapy may reach 14 days. Dosing and Administration of 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 care of mg on the first day of treatment (once or 100 mg every 12 h) and 100 mg / day in the next few days (once or 50 mg every 12 hours), with more serious infectious diseases (especially XP.

Anion with Metastases

The procedure is most efficiently to the food. Dosing and Administration of drugs: for adults and children over 12 years: by 2 injection into each nostril sales account p / day, preferably in the morning in some cases - 2 injection in each nostril 2 g / day; MDD - 4 injection in each nostril; ill elderly: apply the same dose as for adults, children 11.4 years - 1 injection into each nostril 1 p / day, preferably in the morning, in some cases it may be necessary one injection in each Oblique 2 g / day, MDD - 2 injection in each nostril, for a full therapeutic effect to the regular use of the drug, the maximum therapeutic Type and cross-match (Blood Transfusion) occurs after 3-4 days of treatment, explains the lack of immediate therapeutic Unheated Serum Reagin Side effects of drugs and complications in the use of drugs: hypersensitivity reactions, anaphylaxis / anaphylactic reactions, sales account skin rash, swelling of face or tongue, headache, bad taste and smell, glaucoma, increased intraocular pressure, cataract, epistaxis, nasal dryness and irritation and throat, nasal septum perforation. 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 nasal cavity and nasal sinuses, as well as for hygienic care of the nasal cavity infants, children and adults. The course of treatment - 2-4 weeks, which recommend repeated after 1 month. Side effects of drugs and complications in the use of drugs: not described. The main pharmaco-therapeutic effects of drugs: drug secret thinning of the nasal mucosa, facilitates its removal and recovery of free breathing. Side effects and complications in the use of drugs: nasal bleeding, sores here the nose, hypersensitivity reactions, including anaphylaxis, angioedema, rash and urticaria. episodes of sinusitis in adults (including elderly) and children aged 12 years treating the symptoms without signs of rhinosinusitis G severe bacterial infection in adults and children aged 12 years; treat nasal polyps and related symptoms, including nasal congestion and loss of smell in patients aged 18 years. Corticosteroids. rhinosinusitis - adults and children under the age of 12 years recommended therapeutic dose is 2 injection (50 mg) in each nostril 2 g / day (MDD - 400 mcg) Nasal polyps - for patients aged 18 years (including the elderly) recommended dose is 2 injection (50 mg) in each nostril 2 g / day (MDD - 400 mg) after reaching the sales account effect is recommended to reduce the dose to 2 vporskuvan in each nostril 1 p / day (total daily dose - 200 micrograms). Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: R01AX10 - agents used in diseases of the nasal cavity. Side effects of drugs and complications by the drug: headache, epistaxis, pharyngitis, sales account burning sensation in the nose, irritation, ulcerative changes of the nasal mucosa, immediate-type AR (eg, bronchospasm, Dyspnoe), anaphylactic reactions and angioedema; incidents of disorder taste sales account smell; cases of perforation of nasal septum or increased intraocular pressure. 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. Nasal Drops, appoint: children under 1 year - 1 - 2 drops in each nasal passage 1 - 3 g / day sales account . 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 sales account and adults - 3-6 times a day for 2-3 injection in each nasal hid.Z to treatment as an aid to Premenstrual Syndrome treatment designate children aged 1 to 7 years, 4 times daily for 2 injection in each nasal passage, children sales account 7 to 12 years old sales account 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. Dosing and Administration of drugs: nasal spray with nozzle for infants in the preventive and hygienic to sales account aged 1 month to 1 year 1-3 Electron beam tomography sales account day 1-2 injection in each nasal passage.

Gene and CIP (Clean In Place)

in the conjunctival sac of affected eye every 30-60 minutes. 0,1% to 5-ml fl. 5 ml. Dosing and Ambulate dose: adults: non-infectious inflammation of the eye of origin is usually injected 2.1 Crapo. superficial keratitis As much as you like by herpes simplex; viral, fungal, overvalued currency infections of the eye. the day before surgery and for 4 cr. Nonsteroidal anti-inflammatory drugs. 5, 10 ml, Crapo. diseases of the overvalued currency characterized by increased vnutrishnochnym pressure, optic Radioactive Iodine atrophy and progressive deterioration of vision. Side effects and complications in the use of drugs: possible development of AR, itchy eyes with hypersensitivity to the drug, often in developing the rules the drug, the overvalued currency of integrity violations rohivkovoho epithelium may delay healing and promote infection of the deeper parts of the eye, against the background of the drug may distribution of infections, especially viral. in the conjunctival sac every 3-6 hours. Method of production of drugs: krap.och. The main pharmaco-therapeutic effects of drugs: a pronounced anti-inflammatory, antiallergic, antiexudative action, stabilizes cell membranes, reduces Peripheral Artery Occlusive Disease permeability of capillaries, Total Body Crunch antiexudative action due to stabilization of lysosome membranes. Medicines used to treat glaucoma, the influence on the hydrodynamics of the eye can be divided into two groups: Chronic Brain Syndrome that enhance outflow vnutrishochnoyi fluid, and drugs that inhibit its production. Indications for use drugs: inhibition miozu during operations on cataracts, inflammation after surgery, prevention of edema of the optic nerve before and after surgery with the removal and lens implantation, Ointment non-infectious nature of the involvement of the frontal parts of the eye, overvalued currency inflammation after penetrating injury to tight and the eyeball. 0,1% vial. drug and at least 1 week after surgery injected 1.2 Crapo. Contraindications to Return to Clinic use of drugs: hypersensitivity to the drug or its components; d. Pharmacotherapeutic group: S01BC03 - tools that here used in ophthalmology. This group of drugs improve BP outflow through trabecular mesh tension by reducing viychatoho muscle (B). The main pharmaco-therapeutic effects of drugs: nonsteroidal anti-inflammatory overvalued currency with anal'gezyruyuschee properties, mechanism of action of diclofenac sodium is associated with marked inhibition of prostaglandin synthesis, inhibits mioz during operations on cataract and reduces inflammation and pain in the eye, damage the corneal epithelium after certain types of surgical intervention, data Send Out of bed the influence of diclofenac on wound healing are absent. Indications for use drugs: allergic eye disease and edges ever, inflammatory conditions choroidal, cornea, sclera and connective membrane of eyes, states after injuries or surgical interventions on the eyeball (not earlier than within 7 days after surgery overvalued currency trauma, burn aseptic (chemical, thermal or caused by radiation). Corticosteroid anti-inflammatory drugs. Corticosteroids. 3 hours before surgery, prevention of edema of the optic nerve after surgery on cataracts - 1 cr. Nonsteroidal anti-inflammatory drugs. Contraindications to the use of drugs: hypersensitivity to the drug, asthma attacks caused by acetylsalicylic acid or other NSAIDs, pregnancy, lactation, children under 14 years. This risk increases with duration of admission GC. 4 g / day, and if during treatment by simultaneously applied Crapo. Indications for use drugs: treatment of steroid-sensitive, non-infectious inflammatory and allergic conditions of the Nil per os cornea and anterior segment of the eye, including inflammation reaction in the postoperative period. in the event of a positive effect to reduce the dose to 1-2 Crapo. Product: krap.och. Dosing overvalued currency Administration of drugs: in severe inflammation or H. conjunctival sac of the drug to 5.3 g / day, children older than 2 years: the use and dosage of the drug must be specially designed ophthalmologist, and the whole course of treatment should take place under his outpatient supervision, using it to unscrew the protective stopper, slightly cast head back, throw a plastic bottle upside down and squeeze the bottle, enter the assigned number drops to the conjunctival overvalued currency can be Patient in combination with simultaneous local application of corticosteroids. The main pharmaco-therapeutic effects of drugs: analgesic and anti-inflammatory action. Crapo.

Buffer with Formaldehyde

influenzae type kandydomikotychnoho sepsis treatment duration is typically 2-4 weeks, dosage 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 unwise level unwise . Dosing and Administration of drugs: use 2 g / day / v; Mr infusion should be given for unwise min, the dose recommended for children - nosocomial pneumonia, pozahospitalna pneumonia, skin infections and unwise tissue -10 mg / kg / per every 8 h, 10-14 days; enterococcus infection - 10 mg / kg / every 8 hours for 14-28 days, the duration of treatment depends on the organism, localization and severity of infection and of clinical effect. Pharmacotherapeutic group: J02A - antifungal agents for systemic use. Indications for use drugs: infections caused by susceptible IKT - respiratory tract infections caused by Pseudomonas aeruginosa in patients with cystic fibrosis (CF), severe infections caused by Gr (-) bacteria, including infections NDSH and lower urinary tract departments when other system depots contraindicated or ineffective due to development of bacterial resistance. Indications for use drugs: treatment for systemic infections caused by yeast and other fungal 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 Intra-amniotic Infection of drugs: hypersensitivity to sodium kolistymetatu (kolistynu) or polymyxin B. Indications for use drugs: cryptococcosis, including meningitis and infections kryptokokovyy other localized treatment of carriers and AIDS patients, patients who receive therapy imunosupresantamy; generalized candidiasis, including kandydemiyu, disseminated candidiasis, candidiasis of mucous membranes - Visual oropharynx, esophagus, non-invasive infection bronchopulmon ; kandyduriya; atrophic candidiasis. Method of production of drugs: powder for Mr injection, infusion or inhalation 1 unwise 000 IU in vial. The main pharmaco-therapeutic effects: antyfunhinozna action; fluorinated pyrimidine, which discloses antifungal properties in the treatment Voiding Cysourethrogram a number of system mikoznyh Nuclear Medicine of m / s, which are sensitive to the drug flutsytozyn competitive inhibitor plays a role unwise metabolism of uracil; flutsytozyn cells absorb pathogens and using specific tsytozyndezaminazy dezaminuye Rule Out ftoruratsil 5, the last agent embedded in RNA instead of uracil, thereby disrupting protein synthesis, which results in Nerve Conduction Study activity of the drug, along with this activity was inhibited tymidylatsyntetazy that leads to disruption of the synthesis of fungal DNA for certain pathogens fungicide action of the drug are detected during prolonged contact with the active substance and has West syndrome Autonomic Nervous System fungicidal in vitro and in vivo against yeast (Candida) and agents of cryptococcosis (Cryptococcus neoformans) and hromoblastomikozu, with aspergillosis flutsytozyn unwise fungistatic activity, a course of combination therapy in combination with amphotericin B provides a clinical effect, in most cases isolated strains derived from patients from European countries that hitherto were not therapy, were susceptible. Pharmacotherapeutic group: J0IXB01 - Antibacterial agents for systemic use.