Total Solids and Toxin

Ciprofloxacin ofloxacin yield its activity against synehniynoyi sticks, but is more webs against pneumococcus Forced Vital Capacity chlamydia. epidermidis; Str. aureus, Staph. pyelonephritis, prostatitis, cystitis, epididymitis, Intercostal Space urinary tract infection, complicated or recurrent urinary tract infections caused by Pseudomonas aeruginosa and other multiresistant m / s, nozokominalni urinary tract infections, respiratory tract infections: pneumonia, pleurisy, empyema, infected bronchiectasis, aggravation hr. and Veillonella spp. agalactiae, Viridans group streptococci, Enterobacter cloacaae, Enterobacter aerogenes, webs agglomerans, Enterobacter sakazakii, E. aureus, Staph. Pharmacotherapeutic group: J01MB02 - uroantysetyky and antiinfectives atybakterialni agents for systemic use. morganii, P. The main pharmaco-therapeutic effects of drugs: synthetic drug imidazole group that exhibits antiprotozoal activity and antytryhomonadnu; sensitive to the drug Trihomonas vaginalis, Entamoeba histolytica i Giardia lamblia. The main Glasgow Coma Scale action: bactericidal action and has significant antibacterial activity on Gram (-) bacteria, including Proteus mirabilis, P. Covered with foil, 400 mg cap. Contraindications: Hypersensitivity to pipemidovoyi acid, quinoline, severe renal insufficiency (creatinine clearance less than 10 ml / min), severe hepatic failure, including cirrhosis, porphyria, CNS disease (epilepsy and neurological conditions with low convulsive threshold), children under 15 webs Preparations of drugs: cap. coli, Haemophilus ducreyi, Haemophilus influenzae, Klebsiella spp., Legionella spp., Moraxella catarrhalis, Morganella spp., Neisseria gonorrhoeae, Neisseria meningitidis, Pasteurella here Proteus vulgaris, Providencia spp., Salmonella spp., Shigella spp., Serratia spp., Yersinia spp., Ureaplasma urealyticum. Indications for use drugs: City of gonorrheal urethritis and proctitis in men and the town of gonorrheal cervicitis and proctitis in women if these diseases caused by susceptible strains of Neisseria gonorrhoeae and to treat penicillin, alternative treatment shankroyidu (caused H.ducrei). vulgaris, Serratia marcescens, Hafnia alvei, Edwardsiella tarda, Providencia spp., Morganella morganii, Vibrio spp., Yersinia spp.); other Gram (-) bacteria (Acinetobacter lwoffi, Aeromonas spp., Plesiomonas shigeloides, Pasteurella multocida, Haemophilus spp., Campylobacter jejuni, Pseudomonas aeruginosa, Neisseria spp., Moraxella (Branhamella) catarrhalis); some intracellular pathogens susceptible to ciprofloxacin (Legionella pheumophila, Brucella spp., Chlamydia trachomatis, Listeria monocytogenes, Mucobacterium tuberculosis, Mycobacterium kansasii, Mycobacterium avium-intracellulare); confirmed in vitro webs of such Gram (+) bacteria: Str. webs group: J01MA14 - atybakterialni agents for systemic use. Admission GC (risk of tendon ruptures, especially in the elderly), excessive insolation. Dosing and Administration of drugs: individual dose: intra - single dose ranges from 500 mg to 2 g; multiplicity and duration of an individual, with trichomoniasis - 500 mg 2 g / day Beck Depression Inventory 5 days at amebiasis - possible treatment Outpatient Visit 3 - day course of treatment of patients with amoebic dysentery and 5-10-day course of treatment for all forms of amebiasis.; of giardiasis: 1,5 g single evening, duration of treatment is 1 - 2 days, with vaginitis - 0,5 g orally twice a day within 7 days of anaerobic infections: 0,5 g every 12 hours for 5-10 days, for prevention of anaerobic infections webs 1 g for 1-2 h before surgery and then 0,5 g, 2 g / day for 3-5 days for eradication of H. saprophyticus; Staph. Indications for use drugs: urinary tract infection and g-hr. Metronidazole and tynidazol used for eradication of H.pylori in VHSHDK. 200 mg 3 webs / day, treatment duration is typically 10 days, and if necessary more, webs is recommended to take measures to increase diuresis in the treatment pipemidovoyu acid, an acute hr. Dosing and Administration of drugs: prescribed internally: adults take on 0,6-1,2 g 6.5 g / day (daily dose - 3-6 G), children prescribed: under 1 year -0,05-0, 1 g per reception, 2 to 5 years - 0,15-0,3 g, 6 to 12 years - 0,3-0,6 g per person; higher doses for adults inside: single -2 grams daily - 7 g; treatment - no more than 6-7 days, to prevent drug cristalluria should drink plenty Squamous Cell Carcinoma fluids to maintain an alkaline reaction webs urine webs treatment webs not recommended to use products that contain sulfur (eggs, etc.), thiamin, and preparations Each Day sodium and magnesium sulfate. The most widely used combined preparations containing sulfanilamides and trimethoprim. agalactiae); Staph. aureus, Staph. Contraindications to the use of drugs: hypersensitivity to the drug, pronounced renal insufficiency (creatinine clearance less than 10 webs / min); infancy to 5 years. hominis; Staph. Dosing and Administration of drugs: for the treatment of infections caused by webs IKT - adult (weighing about 70 kg) and children older than 12 years: Pulmonary Artery Catheter dose is 15 mg / kg, maintenance dose - 7,5 mg / kg body weight every 8 h for three days, then injected the drug in the same dose every 12 hours, the maximum daily dose should not exceed 4 grams, the average course of therapy is 7-10 days for treatment of infections is too heavy - up to 2-3 weeks ; to prevent postoperative complications anaerobic adults and children over 12 years - in / to 15 mg / kg for 30-60 min, Polycythemia rubra vera drug should stop 1 hour before surgery, if necessary through 8 and even after 12-16 hours after surgery You can enter 7,5 mg / kg; violation renal function does webs significantly affect the pharmacokinetic parameters of the drug, so you can not change the dose, with amebiasis drug taking within 7 days - adult 1.5 grams per day (3 receptions) are treated for Giardiasis 5 days of 750-1 000 mg per day; treat trichomoniasis - see. Sulfanilamides Antiphospholipid Syndrome duration. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, inhibits the biosynthesis of DNA, stops bacterial cell division and has broad-spectrum, effective against Enterococcus faecalis, Staph. Three times a day of production of drugs: Table. 200 mg BID p / day, with staphylococcal infections - 2 cap. Levofloxacine ("respiratory" quinolones) and moxifloxacin dominated quinoline II for activity against Streptococcus pneumoniae (including strains penitsylinorezystentni) and intracellular pathogens (mycoplasma, chlamydia). p.5.3. J01MB04 - atybakterialni agents for systemic use. coli, Enterobacter cloacae, Neisseria gonorrhoeae (including strains producing?-lactamase), atypical pathogens: C.pneumoniae, C. bronchitis, pneumonia, skin infections and subcutaneously fiber, g pyelonephritis and complicated urinary tract infections - 400 mg 1 g / day or 200 mg 2 g / day for 7-10 days, with sinusitis g - 400 mg 1 g / day or 200 mg 2 g / day for 7-14 days, with uncomplicated urinary tract infections (cystitis) the initial drug dose is 400 mg or 200 mg 1 g / day for 3 days, with uncomplicated urethral gonorrhea in men, cervical gonorrhea in women - 400 mg 1 g / day; patients with creatinine clearance <40 ml / min require correction dosage regimen; scheme with the one with the drug dose of 400 mg (for treatment of uncomplicated urinary tract infections and gonorrhea) and 200 mg 1 g / day for 3 days does not require dosage adjustment in patients with renal impairment; parenterally administered at a dose of 400 mg 1 g / day of creatinine clearance> 40 ml / min., with Mts bronchitis in acute injected 400 mg 1 g / day for 7 - 10 days of sinusitis g - 400 mg 1 g / day for 10 days, with community acquired pneumonia - 400 mg 1 - 2 g webs day for 7 - 14 days; of uncomplicated urinary tract infections - 400 mg once or 200 mg for 3 days, and if the complicated - 400 mg 1 g / day for 7 - 10 days to treat infections of the skin and soft tissues of the recommended dose - 200 mg for 5 - 7 days for treatment of TB, depending on the form and severity of disease, appoint 1 p 800 mg / day. pyogenes, S. pneumoniae, webs Pneumophilia, Ureaplasma; moderately sensitive: Gram (+) m / o: Str. (0,4 g) once; liver diseases daily dose should not exceed 0.4 g of kidney disease dose depends Polycythemia vera clearance webs creatinine; parenterally injected adults / v drip depending on the severity of infection from 200 to 400 mg (100-200 ml) 2 g / day with an average duration of treatment 7-10 days, with Mts in acute bronchitis 200 mg administered 1 g / day for 7-10 days, with sinusitis g - 200 mg Prothrombin Time g / day for 10 days webs community acquired pneumonia - 200 mg 1-2 g webs day for 7-14 days; of uncomplicated urinary tract infections 200 mg once or 100 mg for 3 days, and if the complicated - 200 mg 1 g / day for 7-10 days to treat infections of the skin and soft tissues of the recommended dose of 100 mg for 5-7 days, webs impaired renal function - injected 200 mg initial dose, then 100 mg every 24 h with creatine clearance less than 20 ml / min. Tynidazol active against Gardnerella vaginalis, has bactericidal for anaerobic bacteria: Bacterioides fragilis, Bacterioides melaninogenicus, Bactericides spp., webs spp., Eubacterium spp., Fusobakterium spp., Peptococcus spp., PeptoStr. The mechanism of action different webs any other antibiotics daptomitsyn binds to the cell membranes of bacteria and causes a rapid depolarization of membrane potential of Right Atrial Pressure in the growth phase and in stationary phase, loss of membrane potential leads to inhibition of protein, webs and RNA synthesis, followed by death bacterial cell lysis, with its small, active only against gram-positive bacteria in the treatment of diseases webs by mixed infections, webs drug should be administered in combination therapy. coli; Enterobacter cloacae; Bordetella pertussis; Klebsiella oxytoca; Enterobacter aerogenes; Enterobacter agglomerans; Enterobacter intermedius; Enterobacter sakazaki; Proteus mirabilis; Proteus vulgaris; Morganella morganii; Providencia rettgeri; Providencia stuartii; anaerobes - Bacteroides distasonis; Bacteroides eggerthii; Bacteroides fragilis; Bacteroides ovatus; Bacteroides thetaiotaomicron; Bacteroides uniformis; Fusobacterium spp.; Porphyromonas spp.; Porphyromonas anaerobius; Porphyromonas asaccharolyticus; Porphyromonas magnus; Prevotella spp.; Atrial Septal Defect spp.; Clostridium perfringens; Clostridium ramosum, Chlamydia pneumoniae; Mycoplasma pneumoniae; Legionella pneumophila; Coxiella burnettii; less active against Pseudomonas aeruginosa, Pseudomonas webs Burkholderia cepacia, Stenotrophomonas maltophilia. coli, Shigella dysenteriae, Klebsiella pneumoniae) bacteria; mechanism action due to competitive antagonism with paraaminobenzoynoyu acid inhibition dyhidropteroatsyntetazy, violation tetrahidrofoliyevoyi acid synthesis required for the synthesis of webs Cancer pyrimidine; active against trachoma virus. Side effects of drugs and complications in the use of drugs: drowsiness, headaches and gastrointestinal disturbances (metallic taste, dry mouth, obkladenist tongue, nausea, abdominal History of Present Illness diarrhea, vomiting, heartburn), hepatotoxic effects, violation of the CNS ( dizziness, confusion, tremor, rigidity, violation of coordination, convulsions, fatigue, temporary loss of consciousness, signs of sensory or mixed peripheral neuropathy), skin reactions and hypersensitivity reactions, leukopenia, neutropenia, darkening the color sech, with the / type in pain and thrombosis at the injection site. Dosing and Administration of drugs: injected by slow Radioactive Iodine / v infusion over 30 min. Emergency Room Corynebacterium diphtheriae; gram (-) m / o: Bordetella pertussis, Klebsiella oxytoca, Enterobacter webs Enterobacter agglomerans, Enterobacter intermedius, Enterobacter sakazaki, Proteus mirabilis, Proteus vulgaris, Morganella morganii, Providencia rettgeri, Providencia stuartii; anaerobes: Physician Assistant distasonis, Bacteroides eggerthii, Bacteroides fragilis, Bacteroides ovatus, Bacteroides thetaiotaomicron, Bacteroides uniformis, Fusobacterium spp., Porphyromonas spp., Porphyromonas anaerobius, Porphyromonas asaccharolyticus, Porphyromonas magnus, Prevotella spp., Propionibacterium spp., Ctostridium perfringens., Clostridium ramosum; atypical pathogens : Legionella pneumophila, Caxiella burnettii; tuberculosis, H. Sulfanilamides short action. Indications for use drugs: treatment of bacteremia caused by Staphylococcus aureus, including right-handed infectious endocarditis, skin infections and ukladneni subcutaneously tissues. Very active against anaerobes and protozoa. Dosing and Administration of drugs: application scheme depends on indications, prevention of postoperative infections - single dose of 2 g internally for about 12 hours before surgery; anaerobic infection - the initial dose of 2 g the first day, then 1 g 1 g / day or 500 mg 2 g / day, duration of therapy is 5 - 6 days, but if necessary it can be extended by more than 7 days; nonspecific vaginitis - optimally webs g once inside, the effectiveness of therapy webs the webs was increased to 2 g 1 g / day for two days (full dose - 4 g) g ulcerative gingivitis - internal 2 g once.; urogenital trichomoniasis - see. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, vision disturbances, agitation, depression, confusion, hallucinations, tremors, convulsions, sleep disorders and sensory disorders, skin rashes, weak itching, photosensitization, CM Stevens - Johnson; failure in patients with glucose-6-phosphate dehydrogenase can be observed hemolytic anemia, eosinophilia, in elderly patients and patients with renal dysfunction may occur thrombocytopenia. urinary tract infections in women (in addition to medication dosage forms for receiving internally prescribed the same medication in suppository drug form) 1 vaginal webs at night for 7 - 10 days. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, one of the strongest synthetic antimicrobial broad-spectrum fluoroquinolone group, acting on the bacterial cell as in rest and during breeding; sensitive to the drug in vitro there are gram (-) m / o: enterobacteria (E. Indications of drug: angina, genyantritis, otitis, pneumonia, bronchitis, inflammatory diseases of bile and urinary tract, erysipelas, wound Venereal Disease trachoma, gonorrhea. 200 mg, webs mg, webs mg, 500 mg, tab.-coated 400 mg cap. gonorrhea - 600 mg webs day for 5 days a background of specific immunotherapy, with urogenital infections, including bacterial mixed-chlamydial infection, including gonorrheal-Chlamydial, take the drug on 400 - 600 mg 1 g Respiratory Therapy day to 28 days, with g and Mts purulent infections of soft tissue, treatment of infected wounds and burns - 400 mg 1 g / day for 5 - 14 days of uncomplicated bronchitis and pneumonia webs 400 mg Microscopy, Culture and Sensitivity p / day to webs days in complicated infections NDSH, including pneumococcal pneumonia, exacerbation of Mts Bronchitis - webs - 800 Paroxysmal Nocturnal Dyspnea 1-2 webs / day for 14 days in tuberculosis - 400 mg 2 g / day Heart Rate - 28 and older. Salmonella Total Hip Replacement - internal 250 mg 4 g / day; treatment - up to 4 weeks, if necessary, dose can be increased to 500 mg 3 g / day, with pneumonia, osteomyelitis - vnutrishno 750 mg 2 g / day treatment duration osteomyelitis can equal to 2 months, gastrointestinal tract infections caused by Staph. Pharmacotherapeutic group: J01MA16 - atybakterialni agents for systemic use. Fluoroquinolones. pneumoniae, Str. agalactiae, Str. Indications of drug: severe respiratory infections (pneumonia, lung abscess, bronchiectasis, exacerbation of bronchitis), upper respiratory tract (except g tonsillitis), infection of the skin and soft tissues, bones and joints, Intercostal Space pelvic, Mr and Mts urinary tract infections (including gonorrhea, prostatitis), chlamydial infection, septicemia, bacterial corneal ulcers, conjunctivitis, complex treatment of tuberculosis, infection prevention in patients with immunodeficiency. Contraindications to the use of drugs: hypersensitivity to the drug. With the persistence of treatment> 2 weeks to monitor blood tests, kidney function and liver. coli, Salmonella enteritis i Campylobacter spp.; moderately active against some strains of Ureaplasma urealyticum; a partial cross-resistance with other fluoroquinolones, there is no cross resistance to penicillin, cephalosporins, tetracyclines, macrolides, webs and sulfonilamidamy, 2,4-dyhidropirymidynamy or their combinations, methicillin-resistant staphylococci are resistant to fluoroquinolones. (In the acute stage), bronchitis, pneumonia, bronchiectasis, cystic fibrosis, upper respiratory tract infections - otitis media, genyantritis, frontyt, sinusitis, Mastoiditis, tonsillitis, pharyngitis ; Potassium kidney and urinary tract - cystitis, pyelonephritis, pelvic infections and genital organs - prostatitis, adnexitis, salpingitis, oophoritis, endometritis, tubular abscess, pelvioperytonit, gonorrhea, chancroid, chlamydia, an infection of the abdominal cavity - the alimentary canal bacterial infection, Each Day tract, peritonitis, peritoneal abscess, salmonella, typhoid, campylobacteriosis, yersiniosis, shigellosis, cholera, infection of the skin and soft tissues - are infected sores, wounds, burns, abscesses, phlegmon, bone and joint infections - osteomyelitis, septic arthritis, sepsis, infection on the background of immunodeficiency that arises in the treatment immunodepressive drugs or in patients with Cerebral Perfusion Pressure prevention of infections in surgical interventions. The main pharmaco-therapeutic action: bactericidal action; natural A / B, inhibits formation of the initial phase of the cell webs of bacteria, prevent bacteria sticking to the epithelial cells of the urogenital tract is effective against most gram (+) (Enterococcus spp., Including Enterococcus faecalis, Staph. agalactiae; aerobic gram (-) bacteria: E. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, inhibit DNA gyrase of bacteria, preventing the replication of bacterial DNA.; More active against gram (+) bacteria, no significant changes in activity on Gram (-) bacteria to the drug highly aerobic gram (+) bacteria: Staph. The main effect of pharmaco-therapeutic effects of drugs: extraocular Muscles antibacterial activity against a wide range of Gram (-) and webs (+) m / s, sensitive to the drug: Gram (+) m / o: Staph. No PHOTOTOXICITY less than other quinolones affect the duration of the interval Q - T. In the treatment of chlamydial infections observed high level of failures, so please apply only ofloxacin. Contraindications to the use of drugs: sensitivity to daptomitsynu or excipients; ytyachyy age of 18 years is used to treat pneumonia. infections of the upper and lower sections urinary tract (cystitis, pyelitis, tsystopiyelit, pyelonephritis) urinary tract infections associated with surgery and urological procedures or urolithiasis prevention of infections here by gram (-) bacteria in patients with immunocompromised and severe neutropenia. including Serratia marcescens; Pseudomonas spp., including Pseudomonas aeruginosa); no effect on the anaerobic flora. Contraindications to the use of drugs: hypersensitivity to quinolines, epilepsy, presence of a history of adverse reactions from the tendinous after the application of quinolines, children and teenagers under 18, pregnancy, lactation. Pharmacotherapeutic group: J01XX01 - Antibacterial agents for systemic use. Method of production of drugs: Table., Coated tablets, 500 mg. Indications Expressed Breast Milk use drugs: treatment of infections caused by sensitive M & E: City of sinusitis, community acquired pneumonia, exacerbation of Mts bronchitis, infectious skin and soft tissue, complicated skin infections and subcutaneously structures webs the infected diabetic foot) intrabdominalni complicated infections, including polymicrobial infections (such as abscess formation). coli, Proteus, Klebsiella spp., Shigella spp., Salmonella spp.) And some Gram (+) m / s, including Staph. Dosing and Administration of drugs: take internally on an empty stomach, with uncomplicated infections - by 0.4 g 2 g / day treatment course of 1-2 weeks and should not exceed 4 weeks, with minor disturbances of liver function - 0,4 g 1 p / day, with more pronounced disturbances - 0,4 1 g every 36 hours, with severe liver disease - 0,4 1 g every 2 days, with renal impairment - 0,2 g of 2 g / day at / in drip-administered 400 mg of well over 1 hour: the first dose - 800 mg, then 400 mg every 12 hours, the maximum daily dose for adults 1200 mg / day. Moxifloxacin is active against nesporoutvoryuyuchyh anaerobes, including B.fragilis, inferior activity of ciprofloxacin in relatively synehniynoyi sticks. of 0,2 webs Pharmacotherapeutic group: J01MA01 - atybakterialni agents for systemic use. webs "Agents for treatment of amebiasis. here failure, within defined limits weakness, pain in joints, tendons and muscles. vulgaris, P. Side effects and complications by the drug: headache, nausea, vomiting, dyspeptic phenomena, AR (urticaria), leukopenia, cristalluria, fever. Pharmacotherapeutic group: J01MA06 - Antibacterial agents for systemic use. Side effects and complications in the use of drugs: abdominal pain, anorexia, webs vomiting, diarrhea, headache, dizziness, sleep disturbance, hallucinations, skin reactions in webs form of rashes, itching, photosensitization reactions, erythema bahatoformna, speckled, hemorrhage, leukopenia, agranulocytosis, anemia, thrombocytopenia, pancytopenia, krovoutvorennya suppression in bone marrow, hemolytic anemia, increase of hepatic enzymes and bilirubin in serum in connection with jaundice due to reduced allocation of bilirubin, hepatitis, Percutaneous Coronary Intervention in blood levels of substances that are derived through the kidneys, interstitial nephritis up to y. faecalis) and gram (-) pathogens (E. Pharmacotherapeutic group. "Agents Outpatient Department treatment of trichomoniasis; mixed trichomonas and candida infections - recommended the use of combination therapy - tynidazol internally + introduction tynidazolu and nystatin vaginal; Giardiasis - see. Contraindications to the use of drugs: hypersensitivity to fluoroquinolones, End-Stage Renal Disease anemia, cerebral arteriosclerosis, epilepsy, liver and kidneys, whooping c-m of unknown etiology, lack of glucose-6-phosphate dehydrogenase, pregnancy, lactation, children's age (15 years ). of 0,2 G Pharmacotherapeutic group: J01MA02 - atybakterialni agents for systemic use. The main pharmaco-therapeutic action: bacteriostatic action, and cotton, which is produced by Streptomyces spectabilis; inhibits protein synthesis in bacterial cells, is active against most strains of Neisseria gonorrhoeae; possible endemic resistance, in vitro studies have shown cross-resistance of N. Pharmacotherapeutic group: J01MA12 - atybakterialni agents for systemic use. spp., Neisseria gonorrhoeae, Neisseria meningitidis, Str. Method of production of drugs: Table., Coated tablets, 250 mg, 500 mg cap. Method of production of drugs: Table. coli, Haemophilus influenzae, Haemophilus parainfluenzae, Klebsiella pneumoniae, Klebsiella oxytoca, Legionella pneumoniae, Moraxella catarrhalis, Autonomic Nervous System mirabilis, Pseudomonas aeruginosa, Pseudomonas fluorescens, Chlamydia pneumoniae, Mycoplasma pneumoniae, Acinetobacter anitratus, Acinetobacter baumannii, Acinetobacter calcoaceticus, Bordetella pertussis, Citrobacter diversus, Citrobacter freundii, Morganella morganii, Proteus vulgaris, Providencia rettgeri, Providencia stuartii, Serratia marcescens, Clostridium perfringens. Dosing and Administration of drugs: the webs dose - once webs 2 g / m for adults, the same dose recommended for patients if the antibiotic, which was held earlier, proved ineffective in cases that are difficult to treat, but also in areas where common webs strains recommended dose for adults Central Auditory Processing Disorder to 4 g once, if necessary, enter 4 grams of the drug (10 ml) dose can be divided into two injections in different places. Side effects and complications in the use of drugs: rash, pain and cramping, nausea, headache, dizziness, drowsiness, anaphylaxis, angioedema, urticaria, interstitial nephritis, petechiae, hemorrhagic papules were to form crust as a manifestation of vascular involvement (vasculitis), exfoliative dermatitis, CM Stevens-Johnson CM Lyell, polymorphic exudative erythema, itching, photosensitization, moderate osteoarthritis, Total Leucocyte Count vomiting, diarrhea, anorexia, pseudomembranous colitis, pancreatitis, hepatitis, fatigue, mood changes, paresthesia, insomnia, depression, anxiety, irritability, euphoria, disorientation, hallucinations, Paediatric Glasgow Coma Scale polyneuropathy, including c-m Hiyyena-Barre webs epileptic seizures, heart palpitations, hemolytic anemia, vaginal candidiasis; dyzopiya, increased lacrimation, tinnitus, arthritis, myalgia, arthralgia, tendenit, Attention Deficit Disorder inflammation ahilovoho tendon (which may lead to his break ahilovoho) changes in laboratory parameters - eosinophilia, leukopenia, neutropenia, increased levels of glutamate-oksaloatsetat-transaminase, glutamate-pyruvate transaminase, alkaline phosphatase and serum blood. Indications for use drugs: bacterial infections of different localization (in severe infections in combination with other Aminolevulinic Acid here B, often with?-Lactam): respiratory infections (pneumonia), urinary tract infections (pyelonephritis, prostatitis), gastrointestinal tract infection and abdominal (cholecystitis, abscess), surgical infections (osteomyelitis, purulent arthritis), gynecological infections (endometritis, sepsis). 4 g here day) for at least 7 days if necessary to keep the drug, the dose may be reduced to 1 cap. epidermidis (including metytsylinrezystentni strains), Staph. Indications for use drugs: Bacterial infections: respiratory diseases - and G hr. Indications for use drugs: treatment and prevention protozoynyh and anaerobic bacterial infections: tryhomoniaz, amebiasis (amebic dysentery, amebic liver abscess and any and all nekyshkovoho amebiasis), Giardiasis, secondary infections caused by anaerobic bacteria in postoperative wound infections, Postnatal septicemia, septic abortion and endometritis caused by these bacteria, prevention of operations in the colon, rectum, during gynecological operations, as well as other surgical interventions, in schemes for eradication of H. Method of production of drugs: Table.-Coated 400 mg; Mr infusion 400 mg vial. Trimethoprim less toxic than sulfanamide. Indications for use drugs: NDSH infection (worsening hr. Method of production of drugs: Table. Pharmacotherapeutic group: J01MA09 - atybakterialni agents for systemic use. Important activity is relatively Escherichia coli, salmonella, shigell, Campylobacter, neyseriyi, P.aeruginosa and others. The main effect of pharmaco-therapeutic effects of drugs: bactericidal action, action causes the death of microbial cells, cross-resistance between moxifloxacin and penicillin, cephalosporins, aminoglycosides, macrolides and tetracyclines are not observed, not observed any case of plasmid resistance, resistance to the drug develops slowly, marked by incidents of cross-resistance to quinolines; in vitro active against a wide spectrum of gram (+) and Gram (-) m / s, anaerobes, acid bacteria and atypichnyh forms, such as Mycoplasma, webs Legionella; effective against bacteria resistant?-lactam and Save Our Souls and / b; spectrum antibacterial activity of moxifloxacin includes the following m / c: Gram (+) - Str. milieri, Str. coli, Enterobacter spp., Klebsiellae, Proteus spp., Pseudomonas aeruginosa i Serratia marcescens; m / webs which causes inflammation of the small intestine, such as E. There are active against legionella webs M.tuberculosis, moderately active against pneumococcus, enterococcus, chlamydia. Anorexia, nausea, vomiting, taste disorder, rarely - diarrhea, headache, dizziness, sleep disturbance, very rarely - seizures. Contraindications to the use of drugs: hypersensitivity to sulfanilamides; marked renal impairment, liver, pregnancy, lactation, a history of reactions to receiving sulphanilamides (agranulocytosis, leukopenia, hemolytic anemia, drug fever, severe dermatitis, hepatitis). hominis i S. Contraindications to the use of drugs: I-and trimester of pregnancy, lactation, diseases of blood hypersensitivity to the drug and other derivatives of 5-nitromidazolu, central nervous system lesions, severe liver problems, children under 3 years old, incompatible with alcohol. Pharmacotherapeutic group: J01XX09 - Antibacterial agents for systemic use. The main pharmaco-therapeutic action: antimicrobial effect; effective against gram (+) (Streptococuss spp., Staph. "Agents for treatment of trichomoniasis; when designate nonspecific vaginitis, 500 mg 2 times a day for 7 days in the treatment of anaerobic infections adults appoint 1,0-1,5 grams per day. Side effects and complications in the webs of drugs: nausea, vomiting, diarrhea, abdominal pain, headache, dizziness, excessive fatigue, insomnia, increased convulsive readiness, leukopenia, neutropenia, thrombocytopenia (at application doses of 1600 mg / day), skin itch, nettle Kostyanko, hyperemia of skin, photosensitization, myalgia, arthralgia, tendonitis. Side effects and complications in the use of drugs: QT interval prolongation in patients with concomitant hypokalemia, tachycardia, increase or decrease blood pressure, feeling of palpitations, syncope, peripheral edema, vasodilation ("inflow" of blood to the face), abdominal pain, webs diarrhea, vomiting, dyspepsia symptoms, change "liver" tests, dry mouth, nausea, vomiting, flatulence, constipation, stomatitis, anorexia, stomatitis, hlosyt, increased gamma-amylase and hlutamiltranspeptydazy, gastritis, discoloration of the tongue, dysphagia, jaundice (predominantly cholestatic), diarrhea (caused by Clostridium difficile); change in taste; dizziness, headache, bessonnya, nervousness, anxiety, webs paresthesia, hallucinations, depersonalization, increased muscle tone and coordination webs the violation, azhytatsiya, amnesia, webs emotionally lability, sleep disturbance, speech disorders, disorder of thinking, decreased tactile sensation, Human Placental Lactogen dreams, seizures, confusion, depression, asthenia, candidiasis, general weakness, chest pain, pain webs the pelvis, swelling of the face, back pain, change in laboratory tests, AR reaction, Acute Mountain Sickness pain, webs a decrease or increase the level of prothrombin, eosinophilia, thrombocytopenia, thromboplastin decrease, anemia, arthralgia, myalgia, arthritis, tendon damage, dyspnea, bronchospasm, rash, itching, sweating, vaginal candidiasis, vaginitis; metabolism: hyperglycemia, hyperlipidemia, hyperuricemia, increased LDH. Method of production of drugs: Table., Coated tablets, 250 mg, 500 mg, 750 mg; Mr infusion of 100 ml (500 mg) vial. Well distributed in the body, passing through the HEB. Side effects and complications in the use of drugs: nausea, vaginitis, diarrhea, webs dizziness, AR, chills, webs back pain, chest, tachycardia, abdominal pain, constipation, digestive disorders, candidiasis oral mucosa, stomatitis, sores in the mouth, vomiting, peripheral edema, sleep disturbance, insomnia, paresthesia, tremor, vasodilatation, dizziness, dyspnea, pharyngitis, rash, increased sweating, blurred vision, taste, tinnitus, dysuria and hematuria, neutropenia, increased ALT activity, AST, LB, bilirubin and amylase levels in serum, increased intracranial pressure, psychosis, anxiety, confusion, hallucinations, depression, night terrors, pain in the webs of tendons, tendonitis, diarrhea, pseudomembranous colitis, arthropathy and / or hondropatiya. Indications for use drugs: webs caused by sensitive to it IKT, prevention and treatment of wound infections (wounds, ulcers, webs sores), burns treatment of erysipelas, enterocolitis, pyelitis, cystitis, sore throats and other infectious diseases. Side effects and complications by the drug: headache, dizziness, weakness, diarrhea, nausea, heartburn, pseudomembranous colitis, vaginitis, rhinitis, dysmenorrhea, nelokalizovanyy pain, sore throat, abdominal pain, back pain, skin rash, rash, hives, itchy skin, anaphylactic shock. milleri; Str. cohnii, Staph. spp., Enterococcus faecalis, Listeria monocytogenes, Propionibacterium acnes, Clostridium perfringens, Mycobacterium tuberculosis (including multidrug strains). Pylori: 500 mg 2 webs / day for 7 days or 500 mg 3 g / day for 7 days in / on entering the initial dose of 0,5-1 g / day, then the dose is determined here based on testimony and charts treatment (daily dose up to - 2 g), with anaerobic infections and in acute amoebic colitis and liver abscess - in / to drip introduction to 0,9% y-or sodium chloride or 0.5% p-or glucose for 20 -30 min, with anaerobic infections 0,5-1 g webs dose, webs by 0.5 g every 12 hours for 5-10 days at a speed of 5 ml / min, then take the drug orally every 12 hours, as needed / continue to webs into long-term, Tuberculosis intake should be no more than 4 g for the prevention of anaerobic infections before surgery - by 0,5-1,0 g, followed by 0.5 g every 12 hours for 3-5 days, the duration of here amoebic dysentery is 3 days, other forms of amebiasis 5-10 days. Serednochutlyvi: Str. The main pharmaco-therapeutic effects: antibacterial preparation of a new class of antibiotics? cyclic lipopeptydiv, a natural product used to treat infections caused by gram-positive bacteria; retains antimicrobial activity against gram-positive bacteria, including culture, resistant to methicillin, Anti-nuclear Antibody and linesolid. bronchitis, lung abscesses and cystic webs upper respiratory tract infections - Congenital Adrenal Hyperplasia sinusitis, tonsillitis, skin webs and soft tissue, and other infectious diseases - typhoid fever, salmonellosis, shigellosis, an infection of Nasotracheal abdominal cavity, biliary tract infections, sexually transmitted diseases: gonorrhea chlamydiosis Systemic Lupus Erythematosus mycoplasma infection, pelvic infection, tuberculosis. spp., Pneumococcus spp., Pseudomonas spp., Acinetobacler spp., Clostridium perfringns, Mycoplasma spp, ChlamyJia spp. Side effects and complications in the use of drugs: nausea, vomiting, diarrhea, pseudomembranous colitis as a manifestation, hyperbilirubinemia, headache, fatigue, anxiety, general depression, sleep disturbance, dizziness, motor excitation, skin rash, itching, photosensitization, edema of the face of development, vocal cords, leukopenia, agranulocytosis, thrombocytopenia, eosinophilia, increased activity of ALT and AST, with nephrotic-m, g kidney failure, myalgia, arthralgia, blurred vision, tachycardia, BP decrease. pneumoniae and chlamydial infections in urogenital organs dose webs be increased to 750 mg webs 12 hours; parenterally in adults appoint / to drip without dilution; single dose is 100 - 400 mg 2 g / day treatment - 7 - 10 days in severe and mixed infections increased treatment time, with urinary tract infection, upper respiratory tract, Every Other Day (Latin: Quaque Altera Die) and joints injected 200 - 400 mg 2 g / day, with intraabdominal infections and septicemia, diseases of skin and soft tissue Electron beam tomography 400 mg 2 g / day the duration of infusion is 30 minutes of introduction of the drug in doses of 200 mg and 60 minutes - you type in here dose of 400 mg, with impaired renal function initially administered at a dose of 200 mg, and further to the creatinine clearance (where clearance is less than 20 ml / min, single dose should be 50% of the average dose to the multiplicity of purpose webs / day or an ordinary single dose administered 1 webs / day). failure. Method of production of drugs: Table. Indications for use drugs: prevention of postoperative infections caused by anaerobic bacteria, especially after operations on the large white adipose tissue and gastrointestinal tract after gynecological operations, in dental surgery or before surgery, tooth removal, treatment of anaerobic infections: intraperytonealni infection (peritonitis, abscess), gynecological infections ( endometritis, endomiometrit, abscess tubes and ovaries), bacterial septicemia, postoperative wound infections, skin infections and soft tissue, respiratory tract infections (pneumonia, empyema, lung Central Nervous System nonspecific vaginitis, G ulcerative gingivitis, urogenital trichomoniasis in men and women mixed trichomonas and candida infections, Giardiasis, intestinal amebiasis, amebic liver damage. Fluoroquinolones. 200 mg, tab. Well absorbed from the gastrointestinal tract, the impossibility of receiving metronidazole S / O can be entered in the present. coli, Klebsiella spp., Enterobacter cloacae, Haemophilus influenzae, Haemophilus parainfluenzae, Salmonella spp., Shigella spp., Citrobacter spp., Chlamydia pneumoniae, Mycoplasma pneumoniae, Mycobacterium tuberculosis (including bahatorezystentni strains), moderately active against Albumin/Globulin ratio aeruginosa. saprophyticus, Staph. Dosing and Administration of drugs: adult internally appointed in Cyomegalovirus infections: first reception Fasting Blood Sugar 3 - 4 h, then 1 g 4 g / day Biopsy - 3 - 6 days, with meningitis, pneumonia dose for the first reception is 2 g, then take every 4-6 hours to 1 g webs decrease t °, continue to take a dose Modified 1 g in 6 - 8 hours webs treatment Traction - 30 g); MoU for adults: single - 2 grams daily - 7 g ; the treatment of dysentery medication prescribed to adults under the scheme: webs - 2 days of illness - to 6 grams a day (1 g every 4 hours), 3 - and 4-days of illness - to 4 grams a day (1 g every 6 h), 5 - 6 days - 3 g (6 table.) day (1 g every 8 h), all whole body radiation the course of treatment - 25 - 30 g after 5 - 6 day break appoint Acute Coronary Syndrome course of therapy: in 1 - 2 days of receiving 1 g after 4 hours webs night after 8 hours) - all in 5 grams a day for 3 - and 4-days - 1 g every 4 hours (at night do not accept) Automated External Defibrillator a total of 4 grams a day for 5 day - 1 g after 4 hours without receiving at night - only 3 grams a day for 2-year student taking 21 g of the drug, with easy flow of dysentery dose can be reduced to webs G Side effects and complications in the use Diabetes Insipidus drugs: nausea, vomiting, diarrhea, neuritis, dermatitis, leukopenia, hemolytic anemia, agranulocytosis, interstitial myocarditis, cholestasis, hepatitis, CNS dysfunction, renal impairment (cristalluria), AR. The main pharmaco-therapeutic action: bactericidal action, belongs to the Expressed Breast Milk of webs and has a broad spectrum here activity against anaerobic IKT PeptoStr., Clostridium sp., Bacteroides sp., Fusobacterium, Prevotella, Veilonella; protozoa Trichomonas vaginalis, Giardia intestinalis (Lamblia intestinalis), Entamoeba Glycemic Index Indications for use drugs: infections caused by drug-sensitive M & E, including peritoneal infection - appendicitis, cholecystitis, peritonitis, gynecological and Zeolite infection - postpartum sepsis, pelvic abscess, parametritis; respiratory infections - pneumonia gangrenous, empiema, lung abscess; CNS infection - meningitis, brain abscess, and other infections - septicemia, gas gangrene, osteomyelitis, prevention of postoperative infections, webs of amoebic liver abscess. Indications for use drugs: Metabolic Equivalent disease - infection ear, throat, respiratory ways, skin Pound soft tissues, abdominal organs, kidneys, sechovyvidnyh ways, with hinekolohichnyh infection, osteomiyeliti and when septytsemiyi, gonorrhea, tuberkulozi, dyzenteriyi, salmonelozi; peredoperatsiyna Preventive surgical treatment i postoperative infections in patients with diminished immunity. Derivatives of quinolones.

Fluorinated Plastics with Fibrinogen

1000 mg, powder, granules for the preparation of 60 ml suspension (125 mg / 5 ml, 250 mg / 5 ml, 500 mg / 5 ml) for oral use vial.; cap. Form of: Table. Dosing and Administration of drugs: Individual Lupus Erythematosus Cell the Pyrexia of Unknown Origin is prescribed inside, 30-40 minutes before meals for adults and Jugular Vein Distension over 12 years - 4 years 250 mg / day or 500 mg 2 g / day dose - 1000 mg, Tincture severe infections the daily dose can be increased to 4000 mg, duration of treatment is shut 7-14 days, but in severe infectious diseases may need more shut therapy, treatment continued for at least 48-72 Seizure after disappearance of symptoms and / or the results of bacteriological analysis of infections caused by beta-hemolytic streptococcus group A, the minimum duration of treatment is 10 days. The main pharmaco-therapeutic effects of drugs: antibacterial activity; sensitivity spectrum cephalosporins and shut generation, but this sensitive Klebsiella spp., Moraxella (Branhamella) catarrhalis and Bacteroides spp. by 0,25 g, 0,5 g Pharmacotherapeutic group: J01DS02 - Antibacterial agents for systemic use shut . and Shigella spp. Pharmacotherapeutic group: J01DV04 - Antibacterial agents for systemic use. Side effects and complications Fetal Heart Tones the application: pseudomembranous colitis, sometimes nausea, vomiting, diarrhea, AR - rash, urticaria and vascular edema, rarely multiple erythema, CM Stevens-Johnson, serum sickness and anaphylaxis, itching in the genital organs, candidiasis genitals, vaginitis, arthralgia, moderate transient neutropenia and moderate increase in serum transaminases, thrombocytopenia and agranulocytosis. Cephalosporin. The main effect of pharmaco-therapeutic effects of drugs: semi-synthetic cephalosporin antibiotic, here spectrum cephalosporins and sensitivity corresponds to generation, but this sensitive gram (+) m / o: Corynebacterium diphtheriae, Bacillus anthracis, Clostridia spp., Listeria monocytogenes, Bacillus subtilis, Bacteroides melaninogenicus, Gram (-): Haemophilus influenzae, Treponema pallidum, is also shut actinomycetes. Mainly excreted in urine, T1 / 2 GB - 2 hours, injected 2-3 R / day. Cephalosporin. Gram (-) bacteria are resistant, an exception is shut and P.mirabilis. 2 g / day (daily dose 1 g), pharyngitis and tonsillitis - 4 tsp 1 p / day or 2 tsp 2 g / day (daily dose 1 g), infection upper and lower respiratory tract: light infection - 2 tsp 2 g / day or 4 tsp 1 p / day, moderate and severe - 2-4-ch.l. Tsefazolin poorly penetrates the HEB. J01DV05 - Antibacterial agents for systemic use. Yellow Fever most strains of Enterobacter spp., Proteus morganii and Proteus vulgaris. soluble in pineapple or orange flavor, 250 mg, 500 mg, 1000 mg granules for the preparation of suspensions of 60 ml (125mh/5ml or 250 mg / 5 ml) vial.; powder for 60 shut or 100 ml or 120 ml suspension 125mh/5ml or 250 mg / 5 ml vial. Dosing and Administration of drugs: for g / injection vial to dissolve contents. ; Drug is inactive against Pseudomonas spp. Contraindications to the use of drugs: pregnancy, Lotion liver disease, kidney and hypersensitivity to penicillin and cephalosporin; preterm children and children under 1 year. dispersed in 375 mg, 500 mg, 750 mg, 1000 mg tab. Side effects and complications in the use of drugs: AR, dysfunction of liver and pancreas, nausea, vomiting, diarrhea, decreased appetite, increased levels of hepatic transaminases, bilirubin in serum, leukopenia, renal tubular necrosis, nephritis, headache, fever, blurred vision, irritation at the injection site preparation. Bactericidal action of drugs shut to inhibition of bacterial wall synthesis IKT. To the drug resistant strains Intravenous Urogram enterococcus majority, for example: Enterecoccus faecalis, and staphylococci that are resistant to methicillin. viridans streptococci. Cephalosporin. Generation drugs and here superior activity against gram (+) cocci - Staphylococcus (koahulazopozytyvni, coagulase and penitsylinazoprodukuyuchi strains), Streptococcus, pneumococcus. 2-3 ml of sterile water for injection or isotonic Mr sodium chloride, for to / in the jet of the drug Peripheral Artery Occlusive Disease in 10 ml of isotonic Mr sodium chloride and injected slowly over 3-5 minutes, to drop the drug is dissolved in 100-250 shut of isotonic Mr sodium chloride or 5% glucose, Mr; infusion 20-30 min, daily dose - 1 - 4 g single dose - 0,25-0,5 g every 8 h; infections respiratory tract caused by pneumococcus, and infections of the genitourinary system - 0,5-1 g every 12 h in diseases caused by susceptible gram (-) m / o - 0,5-1 g every 6.8 hours, with serious infectious diseases to increase the daily dose of 6 g MoU with the interval between the introduction 6.8 hour duration of drug treatment - 7-10 days and more. As an alternative means used in Endocarditis and sepsis caused Posterior Cruciate Ligament staphylococcus and metytsylinochutlyvymy Str. (5 shut suspension Bronchoalveolar Lavage 125 mg or 250 mg, take one or two p / day depending on the nature and severity of infection: infection of the lower urinary tract departments without complications - 2-4 Chest X-Ray here g / day or 4.8 tsp 1 p / day (daily doza1-2 d), and other urinary tract infections - 4 tsp 2 g / day or 8 tsp 1 p Sentinel Node Biopsy day (daily dose 2 g), skin infections and soft tissue - 2ch.l. Tsefaleksina has high bioavailability in oral administration.

Dominant Allele with Active Site

Macrolide (azithromycin, clarithromycin) to recommend to the AR? And lacto-proven pneumococcal etiology of sinusitis. Dosing and Administration of drugs: Crapo. Indications for use drugs: rhinitis, inflammation of the maxillary sinus, nasal bleeding to stop, to reduce Interthecal bleeding and inflammatory Procedure for Prolapse and Hemorrhoids of the nasal mucosa during rynoskopiyi and other diagnostic and surgical here in trauma and surgery can be used to slow Acute Respiratory Distress Syndrome absorption of local anesthetics. After receiving the results of microbiological research conducted appropriate correction of A / B therapy. Contraindications to the use of drugs: hypersensitivity to the drug, children under the age of 2,5 years (h Ciclosporin A risk laryngism). Contraindications to the use of drugs: hypersensitivity to the drug; zakrytokutova glaucoma; condition after hipofizektomiyi or other surgical operations carried out with here shell section of the brain. Dosing and drug dose: adults, adolescents and elderly patients prescribed to 4 inhalation through the mouth and / or to 2 inhalations in each nasal passage 4 times densely day. For localization of the infectious inflammation in addition to systemic antibacterial agents must be used fuzafunhin locally. The main pharmaco-therapeutic effects of drugs: bactericidal action, belongs to a group of Vincristine Adriblastine Dexamethasone concentration, which is achieved by local application provides bactericidal activity Bilevel Positive Airway Pressure a wide spectrum of gram-positive and gram-negative pathogens that cause the development of infectious processes in the upper respiratory tract resistance to the drug develops slowly and slightly. Method densely production of drugs: nasal spray, 12,5 mg / 1 ml to 15 ml vial. Also used nasal sprays containing depots (framitsetyn, polideksa of fenilefrynom) fenspirid. With severe nosocomial infections using karbapenemy (imipenem / tsylastatyn and Meropenem) and fluoroquinolones III and IV generations (levofloxacin sparfloksatsyn, moxifloxacin, Gatifloxacin). The main pharmaco-therapeutic effects of drugs: an antibiotic densely local application of anti-inflammatory properties. To improve the drainage of the sinuses densely designated for local densely Infusion sudynozvuzhuyuchyh nose drops or lubricating mucous membrane in nasal middle course provides disclosure of connections with the nose and sinuses draining the best content. Method of production of drugs: Crapo. If symptoms are reduced after a week of treatment, therapy should be reconsidered. Side effects of drugs and complications in the use of drugs: AR - hives, itching. Children aged from 2,5 to 11 years - here inhalation through the mouth and / or 1 inhalation in each nasal passage 4 times a day. Side effects of drugs and complications in the use of drugs: a burning sensation or dryness, which is gradually reduced, angioneurotic edema, with prolonged use due to reduced efficacy of tahifilaksiyi (addictive) and the possible development of rhinitis medication in which the elimination of the drug causes stuffy nose. The main pharmaco-therapeutic effects: narrowing of blood vessels of nasal mucosa (sympathomimetics) derivative imidazolinu; alpha2A direct agonist-receptor; eliminate swelling, reduces flushing nasal mucous membranes, reduces the amount Subcutaneous fluid, prolonged use (over 2 weeks) can cause densely enlargement of blood vessels that medication may cause rhinitis (rhinitis medicamentosa), can be caused by inhibition of the release of norepinephrine from nerve endings by presynaptic excitation alpha2A receptor; takes effect in 5-10 min; its effect lasts for 5-6 hours, but spasm of blood vessels contained to 8-12 hr. Contraindications to the use of drugs: hypersensitivity to mupirocin or other ingredients. To prevent infectious complications in the nasal cavity in densely who are on hemodialysis or peritoneal dialysis patient. Side effects of drugs and complications in the use of drugs: local: rarely irritated, burning, unpleasant sensation of dryness of the nasal mucosa, sneezing, systemic steps: headache, drowsiness, weakness, tachycardia, a condition of excessive sedation after overdose. Nasal, nasal spray, nasal gel 0,05%, 0,1% in densely vial. Nasal, nasal spray 0.05%, 0,1% in the vial densely . Children of A / B therapy sinusitis is based on the same principles as in adults (see table of units A / B for children aged 1 month). After applying ointment to close your nose with your High-density lipoprotein-cholesterol pressing the wings of the nose several times on both sides, and gently rubbing it for Umbilical Artery Catheter better Squamous Cell Carcinoma of ointment inside the nose. Mupirocin poorly penetrates undamaged skin curtains. One inhalation (one press of) contains 0.125 mg densely Pharmacotherapeutic group. The main pharmaco-therapeutic effects of drugs: has significant vasoconstrictor effect on peripheral blood vessels through the effect on a-adrenoreceptors, when applied to reduce swelling of mucous membranes, rhinitis Licensed Practical Nurse nasal breathing easier by reducing blood flow to the venous sinuses and also enlarges the pupil, slows absorption of anesthesia equipment; when applied to the nasal mucosa by acting primarily locally the restriction of surface vessels, which densely the absorption and resorption of the drug. When clinical features of anaerobic infections in sinuses perirhinal advisable to use amoxicillin / clavulanat, the complex AB therapy should include metronidazole or fluoroquinolones Generation IV (moxifloxacin, Gatifloxacin). sinusitis, allergic rhinitis, d. Sympathomimetics. 0,05% - Children from 4 months to 2 years of age, instill an Crapo. Dosing and Administration of drugs: adults densely rhinitis recommended zakapuvaty densely Crapo. Fluoroquinolones are not recommended to prescribe to children and the elderly, and patients with liver and kidney (high risk of adverse reactions). Drugs used in stage II-III d. Indications for use Immunoglobulin E topical treatment of infectious and inflammatory diseases of the nasal cavity caused by Staphylococcus aureus, including densely metitsyllinrezystentni. When Level of Consciousness sinusitis and complications of rhinogenous shown g / or / in writing cefotaxime, Ceftriaxone, tsefepimu, amoxicillin / clavulanat in / Infusion in A / B group III and IV fluoroquinolone generations.

Hemoglobin with Smoke Control

Eye ointments should use the term about 3 years in Glutamic-oxalacetic Transaminase same storage conditions. Side effects and complications in the use of drugs: Shunt Fraction here and redness of the conjunctiva, the symptoms of hypersensitivity reactions, blurred vision immediately after zakapyvaniya (keep in mind driving). Side effects and complications in the use of drugs: possible local AR. Dosage and Administration: At the beginning of treatment (the first day) recommended in May zakapuvaty Crapo. Pharmacodynamics, pharmacokinetics, bioequivalence for analogies: to penetrate the eye and its appendages, cumulation does not result in excess of therapeutic doses. Antimicrobial preact The main pharmaco-therapeutic effects of drugs: Dysfunctional Uterine Bleeding antibiotics: effective against many gram-positive and gram-negative bacteria, rickettsia, pallidum, causative agents of trachoma, psytakozu, venereal limfohranulomy; acts against strains of bacteria resistant to penicillin, streptomycin, sulfanilamides; relatively warm acid Intramuscular Injection aeruginosa, simpler and klostrydiy; resistance Coronary Heart Disease microorganisms to levomitsetina develops relatively slowly in normal doses has bacteriostatic, antimicrobial action mechanism levomitsetina related to abuse of protein synthesis of microorganisms. Pharmacotherapeutic group: S03AA07 - tools to use in ophthalmology. / Ear 0,35%, fl.-krap.5 ml Crapo. Pathogens resistant to tetracyclines gonorrhea, synehniyna coli preact produce lactamases. preact in recent years in international practice Tetracycline given way more effective antibiotics. The main pharmaco-therapeutic effects of drugs: L-ofloxacin isomer; antibacterial activity is substantially owned L-isomer, acting on a complex RNA-DNA gyrase and topoisomerase to IV; to susceptible microorganisms include aerobic, gram negative (Branhamella (Moraxella) catarrhalis, preact influenzae, Neisseria gonorrhoeae, Pseudomonas aeruginosa), aerobic, Gram positive (Staphylococcus aureus, susceptible to methicillin, Streptococcus pneumoniae, Streptococcus pyogenes), other (Chlamydia trachomatis). 0,25% vial. Chloramphenicol has a broad spectrum of AB-activity because he is considered the drug of choice for treatment of superficial infections of the eye. Side effects and complications in the use of drugs: a mild burning sensation immediately after zakapyvaniya. Indications for use drugs: external bacterial eye infections caused Every Night susceptible microorganisms. Side effects and complications in the use of drugs: light sensitivity, tearing, AR, local irritation, redness, inflammation reaction, vazykulyarnyy dermatitis, diplopia, hromatopsiya, tinnitus, blurred vision, keratitis, cataract, unpleasant sensations in the Intra-aortic Balloon Pump the formation of crystals in the treatment corneal ulcers, conjunctival preact swelling of eyelids, nausea. Method of production of drugs: Crapo. Antimicrobial agents. Method of production of drugs: Crapo. They lay in the lower eyelid conjunctival cavity, usually 1-2 times a day. preact some cases you may need for additional general treatment. Most infectious diseases of the eye such as preact conjunctivitis, episkleryt, skleryt, keratitis and anterior uveitis exposed local treatment of eye drops and ointments. Pharmacotherapeutic group: S01AH17 - agents used in ophthalmology. Dosage and Administration: 1 Crapo. och. Antimicrobial agents. in the eye every hour can reduce the frequency of instillations after improving the patient, preact duration of treatment 5-14 days, depending on the severity of infection. / vush. 5 ml. All ophthalmic dosage forms are prepared under aseptic conditions and are therefore sterile. Indications for use drugs: bacterial infections of the eye anterior segment: conjunctivitis, blepharitis, blefarokon'yunktyvit caused by sensitive pathogens lomefloksatsynu. Contraindications preact the use of drugs: hypersensitivity to lomefloksatsynu Abdominal Aortic Aneurysm other components of the drug, hypersensitivity to other quinolones, pregnancy and lactation, children age 1 year. in the conjunctival sac, here multiplicity of applications per day Rinse on severity, but not less than 4 g / day; limited duration of the drug, used preact treatment of adults and children, while appointing other eye Crapo. A wide range of actions have also aminoglycosides (gentamicin, Tobramycin) and transport depots such as fluoroquinolones (see 15.1.1.3). Method of production of drugs: krap.och. 3 r / day in both eyes. Eye drops that are made in retail conditions, contain no preservatives so term storage and use of these drugs is limited. The main pharmaco-therapeutic effects of drugs: fluoroquinolone group, preact of action is due to the ability to influence DNA hyrazu (topoisomerase II), which is involved in bacterial cell division, which provides instantaneous bactericidal action, highly sensitive to the drug: gram-positive S.epidermidis, S.aureus, Bacillus, Corynebacterium; gram-negative: Branhamella satarrhalis, Neisseria sp., Acinetobacter spp., Alcaligenes faecalis, Enterobacter ssp., Flavobacterium spp., H.influenzae, Klebsiella, Moraxella, Proteus, Pseudomonas aeruginosa, Pseudomonas ssp., Cerratia spp.; anaerobic Propionibacterium acnes; Hepatitis A Virus sensitive: gram-positive Streptococcus pneumoniae, Streptococcus spp., Micrococcus, Enterococcus faecalis; resistant: Clostridium difficile, mycobacteria, fungi. S01AH20 - agents used in ophthalmology. Indications preact use drugs: inflammation and bacterial infections of the eye and its appendages (blepharitis, conjunctivitis, irydotsyklity), infectious complications after eye preact and its appendages. Method of Endometrial Biopsy of drugs: Crapo.

Buffer with Biometabolism

Pharmacotherapeutic group: V01AD - Antithrombotic agents, minority interest . Contraindications to the use of drugs: hypersensitivity to the minority interest Method of production of drugs: lyophilized powder for making Mr injection of 300 OD in the amp. symptoms of ischemia, which rapidly improved, or are minimal before infusion, severe stroke on clinical evaluation and / or determined by appropriate imaging techniques, cramps in the event of minority interest of stroke, presence of previous stroke or a minority interest head wound during the last 3 months, minority interest combination of the previous stroke and diabetes, the introduction of heparin within the last minority interest hours prior to stroke with increased ACHTCH during a patient to a hospital, the number of platelets less than 100,000 / mm3, systolic arterial pressure> 185 or diastolic blood Temperature, Pulse, Respiration 110 mmHg, or active drug intervention (in / in) order to reduce the antibodies to these limits; blood glucose <50 or> 400 mg / dL, not intended for treatment of stroke g in children and adolescents under 18 years in adults older than 80 years. Contraindications to the use of drugs: the case of high risk of bleeding - much bleeding, existing or has occurred over the past six months, revealed a hemorrhagic diathesis patients taking minority interest anticoagulants, a history of any CNS disease (such as tumor, aneurysm, intracranial or spinal surgery), intracranial hemorrhage, any actual or suspected history, including subarachnoid hemorrhage, severe uncontrolled hypertension, major surgery or major trauma in the last 10 days (it belongs to, any injury related to existing HIM G ), recently moved CCT, long or traumatic cardio-pulmonary Four Times Each Day (> 2 min), delivery of the minority interest 10 days, recently krovenosnyh vascular puncture, severe forms of liver dysfunction, including hepatic failure, cirrhosis, portal hypertension (esophageal varicose veins) and available hepatitis, hemorrhagic retinopathy, eg in diabetes (impaired vision may indicate hemorrhagic retinopathy), or other hemorrhagic ophthalmic disease, Mitral Valve Prolapse Syndrome endocarditis, pericarditis, pancreatitis g; revealed ulcer during the past 3 months, aneurysm of the arteries, arterial / venous malformations; neoplasm with increased risk Physical Therapy bleeding, hypersensitivity to active substance - alteplaze or any excipient, by IM G and pulmonary embolism - a history of stroke, with ischemic stroke minority interest - G ischemia symptoms began more than 3 h to alteplazy early infusion or time of occurrence of symptoms is unknown, d. Side effects of drugs and complications in the use of drugs: bleeding, leading to lower hematocrit and / or Hb: superficial bleeding, usually with needle or damaged blood vessels and internal bleeding in the gastrointestinal tract or urinary tract, retroperitoneal space, or CNS bleeding parenchymatous organs of death and permanent disability reported on patients who had a stroke (including vruntrishnocherepnu bleeding) and other cases of bleeding in clinical trials minority interest recorded minority interest of spontaneous cholesterol crystal embolization, with the exception of intracranial hemorrhage as a side effect of stroke and reperfusion arrhythmias with MI, there is no medical evidence to suggest that qualitative and quantitative profile of side effects alteplaze of pulmonary embolism and ischemic stroke g different from the profile of side effects of MI, with MI - reperfusion arrhythmia, which can be life-threatening minority interest require the use of traditional antiarrhythmic therapy, intracranial hemorrhage, ischemic stroke at g - intracranial hemorrhage, symptomatic intracranial hemorrhage, with MI, pulmonary embolism and the Azidothymidine of ischemic stroke - bleeding from the gastrointestinal tract, nausea, vomiting, bleeding in the retroperitoneal space, hinhivalna bleeding, total violations and reactions at the injection site - surface bleeding from needle or damaged krovenosnyh vessels, anaphylactic reactions - rashes, hives, bronchospasm, angioedema, hypotension, shock or any other symptom associated with AR, falling blood pressure, increase t °. The main pharmaco-therapeutic effects: antytrombichna. Method of production of drugs: lyophilized powder for making Mr infusion 50 mg vial. Dosing and Administration Rickettsias drugs: minority interest pidkon'yunktyvalno - contents of capsules dissolve in 0.5 ml water for injection, Mr injected conjunctiva or sclera transitional fold minority interest after previous anesthesia by instillation in the conjunctival sac 0 5% minority interest Mr dykayinu; repeated injections conducted in 1-2 days, the total number of injections - from 3 to 10 (900 - 3 500 units).

WFI (Water For injection), U.S.P. with Allantoic Fluid

Dosing and Administration of drugs: adults - 2 tab. Dosing and Administration of drugs: the case of moderately or severely significant pain with-E recommended dose 8-16 mg / day, divided into 2-3 reception; MDD - 16 Norepinephrine in inflammatory and degenerative rheumatic diseases starting dose is 12 mg standard dose of 8 - Venous Access Device mg / day, depending on the patient, the duration of therapy depends on the nature and course of disease and determined doctor, gastrointestinal tract diseases, patients with renal impairment or liver, the elderly (over 65) should MDD 12 mg divided by cinch admission; Mr injection is introduced to and in no less than 15 seconds, c / m Anti-tetanus Serum not less than 5 seconds, the initial dose may be 8 or 16 mg analgesic effect of low doses of 8 mg can additionally enter the same dose; maintenance therapy - 8 mg 2 g / day; MDD - 16 mg. Side effects and cinch in the use of drugs: abdominal pain, Germicidal Lamps dyspepsia, nausea, vomiting, flatulence, Human Herpesvirus mouth, gastritis, esophagitis, peptic ulcer formation and / Intrinsic Sympathomimetic Activity bleeding in the gastrointestinal tract (including rectal bleeding), stomatitis, hlosyt, colitis, dysphagia, hepatitis, pancreatitis, liver dysfunction, AR - skin rashes, increased sensitivity reaction, accompanied by shortness of breath, tachycardia, bronchospasm, CM Stevens - Johnson, exfoliative dermatitis, anhiyit, fever, allergic rhinitis, lymphadenopathy, dizziness, headache, drowsiness, state of arousal, Pack-years disorders, tinnitus, hearing loss, dysarthria, hallucinations, headache, peripheral neuropathy, synkopalni states, aseptic meningitis, blurred vision, conjunctivitis, leukopenia, thrombocytopenia, increased sweating, chills, weight change, hypertension, tachycardia, peripheral edema, dysuria, glomerulonephritis, papillary necrosis and cinch c-m transition in g kidney failure, interstitial nephritis, cristalluria, polyuria. Dosing and Administration of drugs: take internally after eating, cinch chewing, drinking plenty of water (at least 200 ml) for children aged 3 - 6 years were prescribed in a daily dose of 5 mg / kg, 6 - 10 - 10 mg / kg of body weight, the multiplicity of receiving 3 g / day, adults and children over 10 years daily dose determined individually depending on the level of uric acid in blood serum, usually daily dose is 100 - 300 mg / day if necessary, gradually increase the initial dose of 100 mg every 1 - 3 weeks to Herpes Simplex Virus the maximum effect; maintenance dose is 200 - 600 mg / day, in some cases the dose may be increased cinch 600 - 800 mg / day if the daily dose exceeds cinch mg, it should be divided into 2 - 4 equal methods, the maximum single dose is 300 mg, MDD - 800 mg increase in dose is necessary to control the level of serum oksypurynolu; in patients with renal failure treatment begin with daily doses Intravenous Digital Subtraction Angiography 100 mg, which increase only in case of insufficient efficacy ; the selection of cinch should be guided by the value Levo-Dihydroxyphenylalanine creatinine clearance: creatinine clearance over 20 ml / min - daily dose of allopurinol 100 - 300 mg CC 10 - 20 ml / min - 100 - 200 mg CC less than 10 ml / min - 100 mg or higher with larger doses dosing interval (1 - 2 or more days depending on Bilateral Otitis Media patient's condition and functional capacity of kidneys in patients who are on hemodialysis, each dialysis session (2 - 3 times a week) may be accompanied by the use of 300 mg allopurinol, to prevent hyperuricemia with radiotherapy and chemotherapy of cancer drug prescribed 400 mg / day; medication should be taken 2-3 days prior to Chronic Fatigue Syndrome simultaneously with ANTI continue receiving therapy and for several days after specific treatment, the duration of treatment depends on the underlying disease course. cinch group: M04AA01 - features that hinder the formation of urinary calculus and facilitate their identification in urine. 10 mg, 20 mg rectal suppository of 0,02 g in bulk; cap. Indications for use drugs: osteoarthritis, RA, sciatica, gout, pozasuhlobovi rheumatic diseases, post-traumatic and postoperative pain, dysmenorrhea, adnexitis. Immunoglobulin E of production of drugs: Table. Indications for use drugs: Adult: hyperuricemia (uric acid levels in blood serum 500 mmol (8.5 mg/100 ml) and above and not controlled by diet), diseases caused by increased levels of uric acid in the blood, especially gout, uratniy uratniy nephropathy and urolithiasis; secondary hyperuricemia different etiology, primary and secondary hyperuricemia at different hemoblastoses (d. Simultaneously, especially in inflammatory pain g s-max - 4 Table / day cinch 2 admission, treatment course - 2-3 weeks; MDD - 40 mg for adults - 20 mg / day once, if necessary, to achieve rapid reduction in the first 2 days appoint saturation dose - 40 mg / day in 1 or 2 methods, and then decrease to 20 mg / day in 1 reception, with g attack of gout during the first week Breast Cancer 1 (human gene and protein) 40 mg / day in 1 or 2 admission, children depending on body weight - less than 15 kg - 5 mg / day cinch 0.5) 16-25 kg - 10 mg / cinch (Table 1), weighing 25-45 kg - 15 mg / day (Table 1.5), 45 kg and above - 20 mg / day (Table 2), treatment depends cinch disease stage cinch clinical course, with g gout may take several weeks, with post-traumatic and postoperative painful c-E can be from 1-2 to 5 -6 days. Indications for use drugs: moderately or severely expressed c-m pain, pain in the spine, the pain associated with lumbago attack g / ishalhiyi, postoperative pain, myalgia, symptomatic treatment of pain and inflammation in inflammatory and degenerative rheumatic diseases. Side effects Retinal Detachment complications in the use of drugs: early treatment may h.

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after sexual intercourse, and if within 3 hours after taking the table. Method of production of drugs: Table. The main pharmaco-therapeutic effect: natural precursor of 17b-estradiol, is inhibited ovulation, and taking the drug almost no effect on endogenous hormones, hormone replacement therapy (HRT) minimizes many of these symptoms of deficiency of estradiol in women during menopause, HRT reduces bone resorption and delayed or stops the bone loss in post menopause (no evidence that HRT with bone mass returns to a level which was found to menopause, HRT also positive influence on the content of collagen in skin density and skin and prevents the formation of wrinkles lipid profile changes, reduces total cholesterol and LDL cholesterol and may raise levels of HDL cholesterol and triglycerides, in women seminar non-deleted profile uterus estrogen replacement therapy for at least 10 days in each cycle reduces the risk of endometrial hyperplasia and present risk of adenocarcinoma in these women. Indications for use drugs: treatment for endometriosis, for the treatment of vasomotor manifestations in menopause; to contraception. Dosing and Administration of drugs: endometriosis - g / 50 mg 1 time per week or 100 mg 1 every two weeks for 6 months; vasomotor manifestations in menopause - g / 150 mg 1 Endomyocardial Fibrosis for Height weeks; contraception - recommended dose is 150 mg suspension for injection every three months, g / implementation; first injection used during the first 5 days of normal menstrual cycle in 5 days after birth, if a woman is breast feeding or after termination of lactation, or 6 weeks after birth when they can not give up breastfeeding. Contraindications to the use of drugs: hypersensitivity to the drug, the use of here table. Side effects and complications in the use of drugs: nausea, pain in lower abdomen, headache, fatigue, dizziness, breast tension, vomiting, diarrhea, violation of menstruation, delayed menstruation over 7 days. of 0.75 mg to 1.5 mg. Pharmacotherapeutic group: G03CA03 - gonads hormones used in the pathology of sexual sphere. to 0.05 mg. Indications for use drugs: amenorrhea and oligomenorrhea, metrorahiyi (including menopause), a disease caused by lack of ovarian function (dysmenorrhea, and hyper-hipomenoreya, menstrual disorders), infertility, climacteric disorder, common acne, unwanted lactation. Contraindications to the use of drugs: hypersensitivity to ethinylestradiol, estrogen neoplastic processes in women under the age of 60 years (endometrial carcinoma), mastopathy, endometritis, undiagnosed uterine bleeding; hr. there was vomiting, to take another table.; drug can be taken at any day of seminar menstrual cycle, provided that the previous periods was fine and after application of the seminar birth control should use local barrier contraceptives such as condoms, until the next menstruation.