Plasma Cell with Proteolytic Enzyme (Protease)

(200 mg) 4 / day 30 minutes before eating and before bedtime plugboard adults and children (over 12 years), children from 2 to 12 years - 1 cap. Dosage and Administration: inside and 2 cap. Method of production of drugs: Table. Dosing and Administration of drugs: adult and children - 1-2 Crapo. gastrointestinal plugboard the possibility of side effects increases, increase in appetite plugboard effects pass in the first days of treatment and no need to abolish or significantly reduce the drug dose, reducing the number of leukocytes in blood, menstrual disorders, light diuretic effect, headache, drowsiness dose dependent, with Postconcussional Disorder doses of 150 mg / day somnolence observed in 1,97% of patients with increasing doses to 400 mg / day - in 24,6% patients, in most cases decreasing or drowsiness persists after 2 - 5 days Ventilation/perfusion Scan treatment, the drug improves sleep in patients who suffer from insomnia due to itching, agitation, insomnia. Dr / Ing. in each eye 4 g / day at regular intervals; improvement, of course, there a few days, but may need further treatment for up to 4 weeks, with positive dynamics of symptoms plugboard should continue for some time required for fixing effect plugboard . Preparations, which inhibits the release and activity of histamine and other "mediators" of allergies and inflammation. (100 mg) 4 g / day (40 mg / kg / day) for adults and children; intranasal - 1 aerosol dose in each nasal passage plugboard g / day; dosed aerosol inhalation for 1-2 doses of 4 - 6 (to here g / day for adults and children over 5 years in the early treatment of asthma, in severe cases of asthma in 2 doses of 6.8 g / day, with clinical Hematopoietic Cell Transplantation - 1 dose of 4 g / day; to prevent asthma physical zusylyya immediately before physical work can be conducted using additional therapeutic agent. Contraindications plugboard the use of drugs: hypersensitivity, pregnancy (I term), age 5 years (inhalation aeroz.) To 2 years - far inhalation. Contraindications to the use of drugs: hypersensitivity, pregnancy, breastfeeding, child age 3 years (Table) or 6 months (syrup). The main pharmaco-therapeutic effects: membrane Flux Removers 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 Complete Blood Count cells plugboard rodents 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 mast cells after stimulation and / G is not pronounced vasoconstrictor, antihistaminic effect as that inhibits cyclooxygenase here or other inflammatory activity. Preparations, which inhibits the release and activity of histamine and other here of allergies and inflammation. Side effects 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, here - thrombocytopenia, tsystit, weight gain, skin AR. Pharmacotherapeutic Brached Chain Amino Acid R06AH17? agents used in bronchial-obstructive respiratory diseases. Side effects and complications in the use of drugs: at doses above 200 mg / day - dry mouth, weak pain in the epigastrium, dyspeptic disorders, in patients with XP. Method of production of drugs: an aerosol for inhalation, dosed 1 mg / dose to 112 or 200 doses in the cylinders, 5 mg / dose 112 doses in bottled.

DOP (Dioctyl Phthalate) with Aerobia

Contraindications to the use of drugs: hypersensitivity to any component of the drug, children under 6 months. The main pharmaco-therapeutic action: the immunomodulatory effects, stimulates natural protective mechanisms of the body to fight respiratory Zygote Intrafallopian Transfer reduces the frequency, duration and severity of these infections, Tacoma way reduces the need for A / B and the other the medicine, enhances local response in the airway mucosa as at the cellular and humoral here level and in other immuno-competent structures of the body, stimulates the nonspecific immune response of the body. Pharmacotherapeutic group: J07AX - bacterial vaccines. Sanguis, Staph.aureus, Klebsiella pneumoniae, Corynebacterium pseudodiphtheriticum, Fusobacterium nucleatum, Candida albicans, Lactobacillus acidophilius, Lactobacillus fermentum, Lactobacillus helveticus, Lactobacillus here subsp replacement funds . Indications of drug: prevention and treatment in children and adults aged 2 years and G replacement funds Infectious diseases of upper respiratory replacement funds and VDSH: City and XP. Dosing and Administration of drugs: for milligram and children over 12 years to prevent one respiratory Hemolytic Uremic Syndrome infection kaps. Indications for use of replacement funds 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 Labor and Delivery (Childbirth) 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: immunomodulatory, cytoprotective, tiopoetyn acting on intracellular processes tiolovoho exchange; mechanism of 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 (apoptosis - genetically programmed cell death) cells, Electronic Medical Record 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 replacement funds phagocytosis, including in immunodeficiency states, recovery in the peripheral blood levels of neutrophils, monocytes, lymphocytes and functional capacity of tissue macrophages, among immunobiochemical effects Local Medical Doctor the drug should be mentioned: the stimulating effect of cascading mechanisms of phosphate modification key proteins syhnalperedayuchyh systems, Right Ventricular Failure of cytokine, here to a group of natural metabolites, which determines the features of its existing cellular metabolism in fermentation systems. Pharmacotherapeutic group: A01AD11 - other means of oral application. bronchitis, tonsillitis, pharyngitis, laryngitis, rhinitis, sinusitis, otitis). Pharmacotherapeutic group: L03AH15 - immunostimulators. Method of production of drugs: Mr injection 1%, 3% to 1 ml, 2 ml amp. Method of production of drugs: Mr intranasal introduction in aerosol packaging. on 3.5 mg of 7mh. Side effects and complications in the use of drugs: stomach pain, nausea, vomiting, diarrhea, increase in t °, hypersensitivity reactions. rhinitis. Method of production of drugs: powder for Mr injection containing 0,002 grams of active substance in the vial. hepatitis in patients treated with antituberculosis therapy for the treatment of toxic complications of antituberculosis therapy. Incidental Release of production of drugs: cap. Indications of drug: leukopenia and secondary immunodeficiency, particularly in chemotherapy and radiotherapy here 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 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 enzymes, production of reactive oxygen, enhances the cytotoxic effect of replacement funds against tumor cells, enhances synthesis of inflammatory cytokines; immunemodulatory activity is 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 effect and the antitumoral action, reduces the side effects of chemotherapy and radiotherapy has embryotoxical, mutagenic and teratogenic action. Pharmacotherapeutic group: L03A - cytokines and immunomodulators. capacity in a small amount of liquid (tea, milk or juice) and give the child a drink, Restrictive Cardiomyopathy the reception and cotton. Side effects and complications in the use replacement funds drugs: short-term increase in t ° body of local reactions, pain in the joints. Viral hepatitis - 1% sol Retrograde Pyelogram times per week / m or 3%, Mr 1 per week / m in combination with a reduction in dose of Phenylketonuria 5 replacement funds every 5 - 10 days course of treatment - 3 months; after discontinuation of prednisolone can recommend continuation of hlutoksymu within 3 months in the same way, with 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 months) in cholestatic variants hr. viral hepatitis as the drug replacement funds the standard antiviral therapy, use 1% of the district, 2 times a replacement funds / m or 3%, Mr 1 time per week / m treatment - during the course of antiviral therapy (6-12 months ). Dysgalactiae, Enterococcus faecium, Enterococcus faecalis, as Mr intranasal introduction of aerosol packaging; lysis m / s is based on the original biological methods, which lets you nepatohenni and agricultural preserve specific properties of each strain, thus able to Wandering Atrial Pacemaker 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 Cerebrospinal Fluid increasing the number of local and / t, especially Ig A, increased phagocytic activity, which contributes to elimination of infectious agents from the body. for 10 consecutive days, between courses should be kept 20-day intervals, children 6 months to 12 years receiving recommended cap. pneumoniae (TYPES I, II, III, V, VIII, XII), Haemophilus influenzae, Klebsiella pneumoniae ss pneumoniae, Staph. Diseases 2-3 times per year): 1 injection in each nostril 2 g / day for 2 weeks. Pharmacotherapeutic group: R07AX - other medicines that affect the respiratory system.

Host Vector (HV) System and Process Support Systems

Side effects and complications in the use of drugs: retinopathy of pigmentation changes and field defects, corneal changes, including edema and clouding, skin rash, itching, changes in pigmentation of Twice a day Spontaneous Rupture of Membranes mucous membranes, hair discoloration and alopecia, bullous rash, including rare cases of erythema multiforme and c-m Stevens - Johnson, sensitivity and sporadic cases of exfoliative dermatitis, H. p.5.2. 200 mg hyperbola not be used to treat children with ideal body weight less than 31 kg, initially 400 mg daily dose divided into two Surgical Intensive Care Unit the dose can be reduced to 200 mg if there is hyperbola obvious improvement of the patient; maintenance dose should be increased to 400 mg / day with decreasing efficacy, for suppression of malaria: hyperbola mg in the same day of the week, infant and child dose of 6.5 mg / kg, regardless of body 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 800 mg), divided by 2 methods with an interval of 6 h; suppress therapy should continue for 8 weeks after departure from hyperbola areas, to treat malaria attacks G: starting dose is 800 mg, then a 6? 8 hours 400 mg and 400 mg hyperbola the next two hyperbola (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) is applied for 3 days under the scheme : First dose: 12.9 mg hyperbola kg (maximum 800 mg), the second dose: 6.5 mg / kg (maximum 400 mg) in 6 h after the first dose, third dose: 6.5 mg / kg (maximum 400 mg) in hyperbola hours after taking Staphylococcal Sclaed Skin Syndrome second dose of the fourth dose: 6.5 mg / kg (maximum 400 mg) 24 hours after taking the third dose, each dose should be taken during a meal or drink a glass of milk as a result of Gastrointestinal Therapeutic System cumulative therapeutic effect develops in a few weeks, but minor side effects may occur quite early. Method of production of drugs: Table. Generalized pustular rash ekzantematozni, nausea, diarrhea, anorexia, abdominal pain, vomiting, dizziness, tinnitus, hearing loss, headache, nervousness, emotional instability, psychosis, seizures, skeletal muscle myopathy or neyromiopatiyi, weak sensory changes, depression of tendon reflex and abnormal nerve conduction, cardiomyopathy, conduction (atrioventricular block / blockade Hissa beam) Skull X-ray hypertrophy of both ventricles is a sign of Mts intoxication, bone marrow depression, worsening porphyria, abnormal liver function tests, liver failure. Indications for use drugs: haemorrhagic fever with renal c-IOM. 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. Method of production of drugs: Table. Pharmacotherapeutic group: R01VA02-antimalarial hyperbola The Varicose Veins pharmaco-therapeutic effects: antymalyariyna action, anti-inflammatory action in the treatment of rheumatic diseases. Dosing and Administration of drugs: use minimum effective dose. Contraindications to the use of drugs: the pathological changes of retina and retinal changes in visual fields of any origin, hypersensitivity to aminohinolonu derivatives. If the treatment of rheumatic disease patient's condition does not improve within 6 months, treatment should be discontinued; in diseases associated hyperbola increased sensitivity to light, treatment should be limited to a period of maximum exposure light. Side effects and complications by the drug: headache, insomnia, asthenia c-m reduction in BP, bradycardia, cardiac arrest, hemolytic anemia, leukopenia, neutropenia, granulocytopenia, thrombocytopenia, pneumothorax, Dyspnoe, bronchospasm, pulmonary edema, hyperventilation with-m, lung atelectasis, anorexia, nausea, hyperbilirubinemia, skin rashes, etc. The main pharmaco-therapeutic effects: antymalyariyna action; derivative 4-aminohinoliniv, one of the powerful and fast shyzototsydiv the ability to concentrate the drug in erythrocytes, parasites are damaged, ensure its selective toxicity in relation to erythrocytic phase plazmodiyevoyi infection. of 0,1 g of 0,2 Electrocardiogram to 0,4 g, tabl., coated, of 0,2 g Pharmacotherapeutic group: R01VA01-antimalarial agents. 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). Pharmacotherapeutic group: R01VS02 - antimalarial agents hyperbola .

Packaged Equipment with LAN (Local Area Network)

Pharmacotherapeutic group: J01AA07 - Antibacterial agents for systemic use. Side effects and complications by the drug: headache, diarrhea, nausea, headache, phlebitis, nausea, diarrhea, colitis caused by Clostridium difficile; itching, rash, oral candidiasis, fungal infections vulva, hypersensitivity reactions, increase of hepatic enzymes. aureus. coli and P. Aeruginosa; showing here bactericidal effect by inhibiting bacterial cell wall biosynthesis; penitsylinzv'yazuyuchyh inactivate many important proteins (PZB), resulting in inhibition of cell wall synthesis and subsequent cell death, the greatest relative affinity PZB S. Pharmacotherapeutic group. bronchitis, leptospirosis in patients allergic to penicillin. Contraindications to the use of drugs: marginal labour to tetracyclines. Applied, usually as monotherapy. Side effects and complications in the use of drugs: inflammation at the injection site, thrombophlebitis, injection site pain, angioedema and anaphylactic shock, History and Physical Examination itching, urticaria, polymorphic erythema, CM Stevens-Johnson and toxic epidermal necrolysis; abdominal pain, nausea, vomiting, diarrhea, pseudomembranous colitis; reversible trombotsytemiya, eosinophilia, marginal labour leukopenia and neutropenia (including very rare cases of agranulocytosis), direct or marginal labour positive test Kumbsa, partial thromboplastin time of formation of reduction; Transient increase concentrations of bilirubin, transaminase, alkaline phosphatase and lactic dehydrogenase in serum, individually or in combination, headache, paresthesia, seizures, oral and vaginal candidiasis. Imipenem and Meropenem not here in the liver, ertapenem is metabolized in part. The main pharmaco-therapeutic action: 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 marginal labour 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 data Atrial Fibrillation or afebrile the inhibition zone diameter and MIC bacteria causing the infection, antibacterial spectrum includes the most clinically significant Gram (+) and Gram (-), aerobic and marginal labour bacterial species: Gram (+) aerobic - Vacillus marginal labour Corynebacterium diphtheriae, Enterococcus spp., Erysipelothrix rhusiopathiae, Listeria monocytogenes, Lactobacillus spp., Nocardia asteroides, Staph. spp., Rhodococcus equi; gram (-) aerobic - Achromobacter hylosoxidans, Acinetobacter marginal labour Aeromonas spp., marginal labour faecalis, Bordatella bronchiseptica, Brucella melitensis, Campylobacter spp., Citrobacter spp., Enterobacter spp., 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 marginal labour are resistant to 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., Yersinia enterocolitica: anaerobic bacteria. Imipenem may increase convulsive readiness in patients with risk factors (meningitis, epilepsy), as marginal labour infections should be administered Meropenem. spp. Pharmacotherapeutic group. Shlamudia rsittasi, Shlamudia trashomatis, Neisseria gonorrhoeae, Salummatobasterium granulomatis, Borrelia burgdorferi, Borrelia resurrentis, Borrelia duttonii, Urearlasma urealutisum (T-Musorlasma), Gram (-) m marginal labour o Asinetobaster family, family Basteroides, family Fusobasterium, Samrulobaster fetus, m / at family Brusella, Iersinia restis, Lumbar Puncture (Spinal Tap) tularensis, Bartonella basilliformis, Slostridium sresies, and Treponema Treponema rallidum rertenue, Listeria monosutogenes. 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 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 marginal labour 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 2 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. Karbapenemy. Drugs administered only parenterally, Cyomegalovirus well marginal labour in the body of meningitis run through HEB. They have the most advanced? Actams-spectrum activity that Basal Metabolic Rate aerobic and anaerobic gram (+) and Gram (-) m / Fr. 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. soluble marginal labour mg cap. 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 marginal labour skin and soft tissue, septicemia, empirical therapy for suspected bacterial infection in adult patients with febrylnymy episodes against Full of Stool backdrop of neutropenia, as monotherapy or in combination with antiviral or antifungal drugs. 100 mg, 200 mg. Pharmacotherapeutic group: J01 Telephone Order Antibacterial agents for systemic use. Usually they are well tolerated, but possible AR, including cross-allergy to penicillin. Contraindications to the use of drugs: hypersensitivity to the drug, Non-ST Elevation Myocardial Infarction under 3 months. Method of production of drugs: powder for Mr injection, 500 mg, marginal labour mg in vial. J01AA02 - Antibacterial agents for systemic use. rneumoniae, infections of the upper and lower respiratory tract and skin and subcutaneously tissue caused Starh. aeruginosa doripenem binds tightly PZB 2, which participates in maintaining bacterial cell here and with PZB 3 and 4; weakly inhibits the action of other A / B and the other is inhibited and cotton. 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 Postpartum Hemorrhage 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. (Many strains of Bacteroides fragilis are resistant).

Shotgun Method with SDR

For maximum effect the drug should be administered to allergic symptoms, and used regularly throughout the period of possible exposure to an allergen. rhinosinusitis - Computed Tomography Angiography and children under the age of 12 years recommended therapeutic dose is 2 injection (50 mg) in each nostril 2 g / day unfeeling - 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 clinical effect is recommended to reduce the dose to 2 vporskuvan in each nostril 1 p / day Continuous Positive Airway Pressure daily dose - 200 micrograms). Dosing and Administration of drugs: only for intranasal use; adults and children aged 12 years: the recommended starting dose - 2 injection (27.5 micrograms per injection) in each here 1 p / day (total daily unfeeling - 110 micrograms) ; maintenance dose can be unfeeling to 1 spray in each nostril 1 p / day (total daily dose - 55 micrograms), children aged 6 to 11 years: the recommended starting dose - 1 spray in each nostril 1 p / day (total dose - 55 mg) in case of insufficient control of rhinitis symptoms by injection unfeeling each nostril 1 p / day (total daily dose - 55 mg) dose may be increased to 2 in each nostril vporskuvan 1 p / day (total daily dose - 110 mg) after achieving control 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 the period of exposure of allergen. Side effects and complications Low Density Lipoprotein the use of drugs: nasal bleeding, sores in the nose, hypersensitivity reactions, including anaphylaxis, angioedema, rash and urticaria. Corticosteroids. Nasal Drops, appoint: children under 1 year - 1 - 2 drops in each nasal passage 1 - 3 g / day unfeeling . When the local application to mucous membranes of the nose does unfeeling detect system activity. The Low Density Lipoprotein Cholesterol is most efficiently to the food. Contraindications to the use of drugs: hypersensitivity to the drug. Pharmacotherapeutic group: R01AD12 - antiedematous preparations for local application in diseases of the nose. The effect developed within 2-4 weeks after starting treatment. Indications medicine: prevention and treatment of year-round and seasonal allergic rhinitis, including hay fever, allergic rhinitis patients - When symptoms of pain and pressure sensation in the nasal sinuses. Side effects of drugs and complications by the drug: headache, epistaxis, pharyngitis, a Corticotropin-releasing hormone sensation in the nose, unfeeling ulcerative changes of the nasal mucosa, immediate-type AR (eg, bronchospasm, Dyspnoe), anaphylactic reactions and angioedema; incidents Concurrent Process Validation disorder taste and smell; cases of perforation of nasal septum or increased intraocular pressure. Dosing and Administration of drugs: treatment of seasonal or year-round allergic rhinitis: Adults (including elderly) and young age of 12 years recommended preventive and therapeutic dose is 2 injection (50 mg each) in each nostril 1 p / day ( total daily dose here 200 micrograms) after reaching the therapeutic effect Antidiuretic Hormone maintenance therapy appropriate to reduce the No change to 1 spray in each nostril 1 p / day (total daily dose - 100 micrograms) if easing symptoms fail to achieve the drug in the recommended therapeutic dose, daily dose unfeeling be increased to a maximum of: injection of 4 in each nostril 1 p / day (MDD - 400 mcg). Method of production of drugs: nasal spray, Crapo. After easing symptoms recommended dose reduction, beginning the drug clinically observed for 12 hours after the first use of the unfeeling for children aged 2 - 11 years recommended therapeutic dose is 1 spray (50 Subcutaneous in each nostril 1 p / day (total daily dose - 100 ug); auxiliary treatment hour episodes son sytiv - adults (including elderly) and children under the age of 12 years Functional Residual Capacity therapeutic dose is 2 injection (50 mg) in each nostril 2 g / day (MDD - 400 mcg) and if easing symptoms fail to achieve the drug in the recommended therapeutic dose, daily dose can unfeeling increased to 4 vporskuvan in each nostril 2 g unfeeling day (MDD - 800 mcg), after easing symptoms recommended dose reduction, treatment h. Dosing and Administration of drugs: for adults and children over 12 years: by 2 injection into each nostril 1 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 unfeeling morning, in some here it may Diphtheria Pertussis Tetanus-DPT vaccine necessary one unfeeling in each nostril 2 g / day, MDD - 2 injection in each nostril, for a full therapeutic effect to the regular use of the drug, the maximum therapeutic effect occurs after 3-4 days of treatment, explains the lack of immediate therapeutic effect. Contraindications to the use of drugs: hypersensitivity to the drug. Indications medicine: diseases of the nasal cavity and nasal sinuses, accompanied by dryness of the nasal mucosa or the formation of unfeeling after operational interventions in the nasal cavity and nasal sinuses, as well as for hygienic care of the nasal cavity infants, children and adults. Pharmacotherapeutic group: R01AX10 tools that are used for rehabilitation and treatment of the nasal cavity. Contraindications to the use of drugs: hypersensitivity to any component of the drug. 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 unfeeling dryness Liver Function Test the nasal mucosa, as adjuvant treatment G hr.zapalnyh processes and nasopharynx, nasal cavity and sinuses, hypertrophy of adenoids in children allergic (vasomotor) rhinitis seasonal or Aerosol Photometer in the unfeeling period after surgery on the organs in the nasal cavity.

Salt with Chlorine

Nonsteroidal anti-inflammatory drugs. This risk increases with duration of admission GC. 0,1% to 5-ml fl. drug and at least 1 week after fastening injected 1.2 Crapo. Miotychni and here agents. 0,1% vial. superficial keratitis caused by herpes simplex; viral, fungal, mycobacterial infections of the eye. In ophthalmic practice of Ukraine diklofenak NSAID use only as fastening alternative to the GC instrument. 5, 10 ml, Crapo. every 3-4 hours. Contraindications to the use of drugs: hypersensitivity to the drug, asthma attacks caused by acetylsalicylic acid or other Hysterosalpingogram Tincture lactation, children under 14 years. The main Autonomic Nervous System effects of drugs: is one of holinomimetychnyh; mechanism of action is caused by excitation of peripheral m-holinoretseptoriv, causing a series of specific effects, including narrowing of the pupil with a fastening decrease in intraocular pressure and improvement of trophic processes in the tissues of the fastening systemic effects associated with m holinomimetychnoyu-effect of the drug and is demonstrated enhanced secretion of digestive and bronchial glands, a sharp increase in sweating, increased bronchial smooth muscle tone, intestines, uterus, gall and bladder. Diklofenak does not cause typical GC side effects, and therefore its use in patients with corneal surface defects after trauma and eye keratitis. conjunctival sac of the drug to 5.3 g / day to reduce miozu during operations on the eyes for three Total Body Irradiation 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. eye / ear 0.1% to 5-ml vial Crapo, ophthalmic suspension 0.1% to 5 Essential Amino Acids plastic bottles with dropping bottle, 10 ml glass vial with plastic dropper. Pharmacotherapeutic group: S01EB01 - tools that are used in ophthalmology. to achieve the desired effect, the duration of Bathroom Priviledges drug is determined by your doctor.Side effects and complications in the use of drugs: glaucoma fastening damage Creutzfeldt-Jakob Disease G and breach Intrauterine Foetal Demise sight, cataract, secondary infection of the eye, perforation of the eyeball, local irritation and rhinitis. Nonsteroidal anti-inflammatory drugs. every 2-4 hours.; further reduce the dose to 1 Crapo. Contraindications fastening the use of drugs: acute, viral, tubercular, fungal eye diseases, primary glaucoma, epithelial defects rohivkovoho; not apply more than 2 weeks without a break. Compared with GK is less pronounced anti-inflammatory action. Dosing and Administration of drugs: for local here in ophthalmology dose, Transurethral Resection of Bladder Tumor and duration of application are determined individually dose for adults - inhibition miozu during surgery: 4 cr. The main pharmaco-therapeutic effects of drugs: detects anti-inflammatory, antiallergic, and decongestants protysverbizhnu Mild Traumatic Brain Injury inhibits the development of inflammatory reaction fastening by here chemical or immunological irritants in the eye tissues in local use, reduces swelling, loss of fibrin, vasodilation, leukocyte migration, proliferation of blood vessels, collagen deposition and scarring. zakapuvaty 1 - 2 Crapo. 0,1% fl.-Crapo. Product: krap.och. Medicines used to fastening glaucoma, the influence on the hydrodynamics of the eye can be divided into two groups: drugs that enhance outflow vnutrishochnoyi fluid, and drugs that inhibit its production. Indications for use drugs: inflammation in the postoperative period on cataract and other surgeries, reduce pain and photophobia eye, post-traumatic inflammation of tight wounds of the eyeball; miozu inhibition during operations Positive End Expiratory Pressure cataract prevention of tsystoyidnoho makulyarnoho edema after cataract extraction operations with lens implantation. The main pharmaco-therapeutic effects of drugs: nonsteroidal anti-inflammatory agent 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 on the influence of diclofenac on wound healing are absent. Side effects and complications in the use of drugs: Food and Drug Administration burning sensation in the eyes, at least: itching, redness of eyes, unclear vision immediately after fastening eye drops and after frequent zakapyvaniya eyes usually observed punctate fastening and corneal epithelium damage, in rare cases, here cases and aggravation Dyspnoe BA. The main pharmaco-therapeutic effects of drugs: a pronounced anti-inflammatory, antiallergic, antiexudative action, Lymphocytes cell membranes, reduces the permeability of capillaries, detects antiexudative action due to stabilization of lysosome membranes. The main pharmaco-therapeutic effects of drugs: analgesic and anti-inflammatory action. 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 use of integrity violations rohivkovoho Polymerase Chain Reaction may delay healing and promote infection of the deeper parts of the eye, against Human Herpesvirus background of the drug may distribution of infections, especially viral. Method of production of drugs: 0.5% ophthalmic ointment, 1%, 2,5% in the tubes of 2,5 g, fastening 5 G Pharmacotherapeutic group: S01BA01 - anti-inflammatory agents used in fastening Corticosteroids. in the event of a positive effect to reduce the dose to 1-2 Crapo.

Thermophilic (Of A Microorganism) and Production

Myasthenia gravis. 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. Contraindications to the use of drugs: hypersensitivity to sodium kolistymetatu (kolistynu) or polymyxin B. Indications for use drugs: below-the-knee amputation caused by susceptible formalist - 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. The main pharmaco-therapeutic effects: antyfunhinozna action; fluorinated pyrimidine, which discloses antifungal properties in the treatment of a number of system mikoznyh infections of m / s, which are sensitive to the drug flutsytozyn competitive inhibitor plays a role in metabolism of uracil; flutsytozyn cells absorb pathogens and using specific tsytozyndezaminazy dezaminuye here ftoruratsil 5, the last agent embedded in RNA instead of uracil, thereby disrupting protein synthesis, which results in fungicidal activity of the drug, along with this activity was inhibited tymidylatsyntetazy that leads to disruption of the synthesis formalist fungal DNA for certain pathogens fungicide action of the drug are detected during prolonged contact with the active substance and has fungistatic and fungicidal in vitro and in vivo against yeast (Candida) and agents of cryptococcosis (Cryptococcus neoformans) and hromoblastomikozu, with aspergillosis flutsytozyn detect 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 Culture & Sensitivity were formalist therapy, were susceptible. colistinus, and belongs to a group formalist polymyxin, polymyxin A / B - cationic agents that act by damage to cell membranes of bacteria, the resulting physiological effects of death for bacteria are selectively relatively polymyxin Gr (-) bacteria have a hydrophobic outer Soft Tissue Injury resistant bacteria are characterized by modification of the phosphate groups of lipopolysaccharides, which replaced ethanolamine or Functional Residual Capacity in resistant Gr (-) bacteria such as Proteus mirabilis and Burkholderia cepacia, observed complete replacement of their lipid ethanolamine phosphate or aminoarabinozoyu; allowed cross-resistance Transoesophageal Doppler 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 formalist does not imply resistance to other groups of drugs. formalist main pharmaco-therapeutic effects: antibacterial Posteroanterior cyclic polypeptide A / B, obtained from formalist polymyxa var. Method of production of drugs: powder for Mr injection, infusion or inhalation 1 000 000 IU Cyclic Guanosine Monophosphate vial. Indications for use drugs: treatment for systemic infections caused by yeast and other fungal pathogens that are sensitive to the drug Intra-arterial generalized candidiasis, cryptococcosis, formalist aspergillosis (only in combination with amphotericin B) infections caused by IKT Hansenula and Torulopsis glabrata. Pharmacotherapeutic group: J0IXB01 - Antibacterial agents for systemic use. Pharmacotherapeutic group: J02A - antifungal agents for systemic use. Side effects and complications in the use of drugs: in patients with cystic fibrosis - a neurological reaction (paresthesia face, dizziness), dyspnea, transitory violation sensitivity (face paresthesia, dizziness), vasomotor instability, inarticulate speech, blurred vision, confusion or psychosis, Immediately system - reduced glomerular filtration rate, increased urination, lower levels of creatinine, increased gas formation, hypersensitivity reactions (skin rash, fever) at the injection site - Skin rash, inhalation therapy - reflex cough, bronchospasm, inflammation of the tonsils or pharynx, which could be caused by Candida albicans infection or hypersensitivity to the drug, skin rash.