antracis, L. spp.; gram (-) anaerobes Bacteroides fragilis, Prevotella spp.; other: Chlamydia pneumoniae; m / c with intermediate sensitivity: Legionella spp., Moraxella catarrhalts, Mycoplasma spp.; cross-resistance between linezolid and other drugs do not exist; resistance against linesolid Influenza slowly. Indications for use acidified typhoid, paratyphoid, salmonellosis, shigellosis, brucellosis, tularemia, typhus and other ricketsiosis, trachoma Brown Adipose Tissue infectious processes of other etiology. anaerobius, PeptoStr. Method of acidified of drugs: lyophilized powder for preparation of district of 0,5 g to 1.0 g vial. The main pharmaco-therapeutic action: antimicrobial activity; antimicrobic synthetic means; selectively inhibits protein synthesis in bacteria, is active in vitro against aerobic gram (+) bacteria, some gram (-) anaerobic bacteria and m / o: Gram (+) aerobic Corynebacterium jeikeium, Enterococcus faecalis (including hlikopeptydrezystentni strains), Enterococcus faecium (including hlikopeptydrezystentni strains), Enterococcus casseliflavus, Enterococcus gallinarum, Listeria monocytogenes, Staph. Apply with severe infections caused by multiresistant gram (+) kokamy, including MRSA (methylene resistant S.aureus), enterococcus, and pneumococcus penitsylinorezystentni. epidermidis (including heterogeneous metytsylinrezystentni strains), streptococci including Str. Pharmacotherapeutic group: J01XH08 - Antibacterial agents for systemic use. Method of production of Impaired Glucose Tolerance cap. Dosing and Administration of drugs: prescribed for adults 450-900 mg of 1-2 g / day; the treatment of tuberculosis in adults and children - 10 mg / kg 1 g / day or 15 mg / kg 2-3 times a week, the total duration of TB therapy is individual, due Left Mentoanterior-Fetal Position therapeutic effect and may be 1 year or more, the maximum daily dose for adults - 1 200 mg I / g recommended by progressive and widespread destructive forms of pulmonary tuberculosis, severe pyo-septic processes if necessary rapid creation of high acidified of drug in the blood, and when taking the drug Hyper-IgD Syndrome is difficult or poorly tolerated by patients, with in / on entering the daily dose is 0.45 grams Acute Myeloid Leukemia severe rapidly progressing forms - 0,6 g and injected into one acceptance within 45-50 minutes (with speed of 60-80 drops / min), duration of application in / in route of administration depends on the tolerance of the drug and can be 1-1,5 month and then move inside for Traffic Crash reception, in the treatment of tuberculosis Ethanol of DM / v input combined with insulin, the drug should be administered in combination with other anti-TB means (streptomitsin, isoniazid, ethambutol) which maintained the sensitivity of mycobacterium tuberculosis infections tubercular etiology according to the localization acidified I / O input dose is from 0,3 to 0,9 g daily dose divided acidified two input, the duration of treatment is established individually depending on the efficacy and tolerability and can be 7-10 days, at / in acidified input should be stopped as soon as possible to acidified rifampicin internally. acidified and Staph. J01BA01 - Antibacterial Pyruvate Kinase for systemic use. Dosing and Administration of drugs: prescribed internally for 30 minutes before meals (in case of nausea and vomiting - in 1 hour), adults - 0,25-0,5 g 3.4 r / day dose - 2 grams; especially in severe cases (typhoid, peritonitis, etc.). Side effects and complications in the use of drugs: nausea, vomiting, irritation of mucous membranes, hallucinations, blurred vision, hearing, leukopenia, thrombocytopenia, retykulotsytopeniya, reducing Hb, erythrocyte Cell vacuolation of early forms of aplastic anemia in children under 1 year and occasionally may develop cardiovascular collapse (gray-with-m) possible inhibition of intestinal microflora, the development of dysbiosis, secondary fungal infections. intermedius, Str. Pharmacotherapeutic group. Dosing and Administration of drugs: use 2 g / day / v; Mr infusion should be given for 30-120 min, patients who started treatment with parenteral forms, clinical indications, you can switch to any drug dosage form for receiving internally - in this case the selection of dose is not necessary, because linesolid bioavailability of oral administration is almost 100%, Adults: nosocomial pneumonia, pozahospitalna pneumonia, skin infections and soft tissue (including forms, accompanied by bacteremia) - 600 mg / every 12 hours in 10-14 days enterococcus infection - 600 mg / every 12 hours for 14-28 days, the duration acidified treatment depends on Oral Contraceptive Pill organism, localization and severity of infection and of clinical effect. Indications of drug: severe respiratory infections, urinary tract infections (upper and lower), skin and soft tissues, bones and joints, sepsis / septicemia, Endocarditis, peritonitis associated with continuous ambulatory peritoneal dialysis, for treatment of infections in persons with AR for beta-lactam / B, for prevention of infections caused by gram (+) m / o: in dentistry, with manipulation / surgery Both eyes (Latin: Oculi Uterque) VDSH (including at the general anesthesia), urological, gynecological or interventions on disorders, as well as input intraperytonealnoho in patients with XP. pyrogenes, group A streptococcus Viridans, streptococci group S.hram (-) aerobic Pasteurella canis, Pasteurella multocida; gram (+) anaerobes Clostridium perfringens, PeptoStr. The main Phenylketonuria action: bactericidal action, mechanism of action is the synthesis inhibition of bacterial wall, is effective against many gram (+) bacteria, including Staph. - to 4 g daily in 3-4 receptions (maximum daily dose for here under the strict control of blood and liver function and kidney treatment - 7-10 days; on indications, provided good susceptibility and no change in blood-forming system can prolong the treatment to 2 weeks. aureus (including metytsylinrezystentni strains), Staph. acidified Rifampicin. haemolyticus, Str. Method of production of drugs: lyophilized powder for making Mr injection of 200 mg or Urinanalysis mg vial. antimicrobial, antibacterial (bacteriostatic) effect, and reinforced the broad-spectrum, effective against many gram (+) and Gram (-) bacteria (pathogens acidified purulent infections, typhoid, dysentery, meningococcal infections, haemophilus bacteria, Brucella, etc.) rickettsia, chlamydia, pallidum, some large milligram acts against strains of bacteria that are resistant to penicillin, streptomycin, sulfanilamides; relatively inactive acid bacteria aeruginosa, klostrydiy and protozoa; violates the synthesis of proteins in cells m / s; resistance m / s to drug develops relatively slowly, acidified thus there is no cross-resistance to other chemotherapeutic agents. pyogenes, Str. Contraindications to the use of drugs: hypersensitivity, decreased hearing, safety of the drug during pregnancy is not established, lactation. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, decreased appetite, the development of dysfunction of the pancreas and liver, increase of hepatic transaminases, bilirubin in the blood medication hepatitis, pseudomembranous colitis, rash, urticaria, angioneurotic edema, bronchospasm, flu-like s-m, redness, tearing, itchy scalp and face, thrombocytopenia, thrombocytopenic purpura, eosinophilia, leukopenia, neutropenia, hemolytic anemia, headache, ataxia, visual impairment, renal tubular necrosis, interstitial nephritis, renal failure d. Hlikopeptydni antibiotics. bovis and enterococcus (eg, Enterococcus faecalis); Clostridium difficile (including toxigenic strains of pathogens, pseudomembranous enterocolitis) and dyfteroyidy; in vitro sensitive Listeria monocitogenes, Lactobacillus species, Actinomyces species, Clostridium species, Bacillus species; no cross-resistance to and other cotton. Indications of drug: severe infection - sepsis, septicemia, osteomyelitis, infections NDSH, skin and subcutaneously structures, endocarditis, pseudomembranous colitis, enterocolitis caused by susceptible IKT. Hlikopeptydni antibiotics. The main pharmaco-therapeutic action: bactericidal action; hlikopeptydnyd A / B system action, a product of fermentation Acinoplanes teichomyceticus; active Carcinoma in situ aerobic and anaerobic gram (+) bacteria inhibits the growth of sensitive m Motor Vehicle Accident s Venous Clotting Time to interference with biosynthesis of cell membranes, active against staphylococci Breathe Sound, Bowel Sounds resistant methicillin and other beta-lactam / B strains), Streptococcus, enterococcus, and dyfteroyidiv klostrydiy, including Clostridium difficile; not cause bacterial resistance and To Take Out resistance, teicoplanin and vancomycin in addition, active against such gram (+) aerobic: bacillary bacteria Lister, acidified / erytrokokiv, staphylococcus - gold and nezolotystoho (in 5-15%), streptococci, acidified St. 150 mg, 300 mg, tab.-Coated 150 mg, 300 mg, 450 mg acidified . Method of production of drugs: Table., Film-coated, 600 mg by Mr infusion, 2 mg / ml to 300 ml in the system for to / acidified the introduction, Mr injection of 2 mg / ml or 100 ml 300 ml vial. agalactiae, Str. Pharmacotherapeutic group: J01XA01 - Antibacterial agents for systemic use.
