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    Противомикробное средство широкого спектра действия группы фторхинолонов. Подавляет ДНК-гиразу и угнетает синтез бактериальной ДНК. штаммы, продуцирующие и не продуцирующие пенициллиназу, метициллин-резистентные штаммы), некоторых штаммов Enterococcus spp., Campylobacter spp., Legionella spp., Mycoplasma spp., Chlamydia spp., Mycobacterium spp. Инфекционно-воспалительные заболевания, вызванные чувствительными к ципрофлоксацину микроорганизмами, в т.ч. Высокоактивен в отношении большинства грамотрицательных бактерий: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae. Ципрофлоксацин активен в отношении бактерий, продуцирующих бета-лактамазы. Проникает в спинномозговую жидкость: концентрации ципрофлоксацина при невоспаленных мозговых оболочках достигают 10%, при воспаленных - до 37%. заболевания дыхательных путей, брюшной полости и органов малого таза, костей, суставов, кожи; септицемия; тяжелые инфекции ЛОР-органов. Профилактика и лечение инфекций у больных со сниженным иммунитетом. Продолжительность лечения - от 7-10 дней до 4 недель. К ципрофлоксацину резистентны Ureaplasma urealyticum, Clostridium difficile, Nocardia asteroides. Прием пищи незначительно влияет на всасывание ципрофлоксацина. Для местного применения: острые и подострые конъюнктивиты, блефароконъюнктивиты, блефариты, бактериальные язвы роговицы, кератиты, кератоконъюнктивиты, хронические дакриоциститы, мейбомиты. Для в/в введения разовая доза - 200-400 мг, кратность введения - 2 раза/сут; продолжительность лечения - 1-2 недели, при необходимости и более. Действие в отношении Treponema pallidum изучено недостаточно. Инфекционные поражения глаз после травм или попадания инородных тел. Можно вводить в/в струйно, но более предпочтительно капельное введение в течение 30 мин. При местном применении закапывают по 1-2 капли в нижний конъюнктивальный мешок пораженного глаза каждые 1-4 ч. После улучшения состояния интервалы между инстилляциями можно увеличить. Максимальная суточная доза для взрослых при приеме внутрь составляет 1.5 г. can you buy viagra over the counter in phuket Ciprofloxacin Синтетические химиотерапевтические средства, хинолоны и фторхинолоны Концентрат д/инф. 200 мг/100 мл, 100 мг/50 мл Табл., табл., п.о., 250 мг, 500 мг, 750 мг Ципрофлоксацин — производное фторхинолона II поколения. Ингибирует фермент ДНК-гиразу в бактериальной клетке, нарушает функцию ДНК и синтез РНК, препятствует росту и делению клетки. Антибактериальное средство широкого спектра действия. Активно преимущественно в отношении аэробных грамотрицательных бактерий, действует только против некоторых видов грам-положительных микроорганизмов (стафилококков и некоторых стрептококков), эффективно в отношении хламидий, микоплазмы. Большинство анаэробов к ципрофлоксацину малочувствительны или резистентны. Хорошо всасывается при приеме внутрь; абсолютная биодоступность составляет 63—77%. Максимальная концентрация в крови достигается через 1—1,5 ч и при дозах 250, 500 и 750 мг составляет 0,1, 0,2 и 0,4 мг/л соответственно. После 60 мин в/в инфузии в дозах 200 и 400 мг максимум в крови — 2,1 и 4,6 мг/л, концентрация в плазме через 12 ч — 0,1 и 0,2 мкг/мл соответственно. Проникает в ткани, жидкости и клетки, создавая высокие концентрации в почках, желчном пузыре, печени, легких, слизистой бронхов и синусов, женских половых органах, фагоцитирующих клетках (полинуклеарах, макрофагах), моче, мокроте, желчи, жидкости кожного волдыря; обнаруживается в предстательной железе, спинномозговой жидкости (менее 10% уровня в плазме, при менингите — до 45% и более), слюне, коже, жировой ткани, мышцах, костях, хрящах, проходит через плаценту. Т1/2 при приеме внутрь — 3,5—5 ч, при в/в введении — 5—6 ч.

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    Highest Independently Rated Canadian Online Pharmacy. Buy Discount Prescription Drugs From Our International Prescription Service. Ciprofloxacin Price In. can you buy cipro over the counter To the Editor Shigellosis is an uncommon infection in many industrialized countries, and many cases are linked to travel to Shigella spp. Ciprofloxacin hydrochloride is a broad spectrum antibacterial substance and oral administration. It belongs to the group of fluoroquinolones, with which it shares most of its properties and medical.

    In the countries listed below: [ Australia] [ Brazil] [ Canada] [ France] [ Germany] [ India] [ Italy] [ Japan] [ Korea] [ Mexico] [ Puerto Rico] [ Spain] [ Turkey] [ United Kingdom] [ U. A] Given the nature of the pharmaceutical market, some specialties may be unavailable, have been removed from the pharmaceutical market or have changed its name. So that, in no case can take decisions based on the information contained in the page. MEDIZZINE is not responsible for any damage arising from the information provided, which may be incomplete or outdated. Delayed release dosage forms of ciprofloxacin are indicated only in urinary tract infections Medizzine recommends consulting your doctor if you are unsure (or you do not know) why you have been given ciprofloxacin. Besides the active ingredient ciprofloxacin, tablets contain microcrystalline cellulose, corn starch, insoluble povidone, colloidal silicon dioxide, magnesium stearate, hydroxypropylmethylcellulose 2910, macrogol 4000, and titanium dioxide. Do not use ciprofloxacin If you are allergic (hypersensitive) to ciprofloxacin or any of the other ingredients of the medicinal product prescribed to you. Allergy symptoms may include: - Asthma attacks with shortness of breath, audible wheezing or rapid breathing. - More or less sudden swelling of the face, lips, tongue or elsewhere in the body. Ciprofloxacin is a broad-spectrum antimicrobial drug of fluoroquinolone group with bactericidal action. Inhibits DNA gyrase and inhibits the synthesis of bacterial DNA. Highly active against most gram-negative bacteria: Pseudomonas aeruginosa, Haemophilus influenzae, Escherichia coli, Shigella spp., Salmonella spp., Neisseria meningitidis, Neisseria gonorrhoeae.ciprofloxacin is active against Staphylococcus spp., some strains of Enterococcus spp., Campylobacter spp., Legionella spp., Mycoplasma spp., Chlamydia spp., Mycobacterium spp.ciprofloxacin is active against bacteria producing beta-lactamases. Ureaplasma urealyticum, Clostridium difficile, Nocardia asteroides resistant to ciprofloxacin. Infectious-inflammatory diseases caused by microorganisms susceptible to ciprofloxacin, including respiratory diseases, diseases of abdominal and pelvic organs, bones, joints, skin, septicemia; severe infections of ENT organs. Prevention and treatment of infections in patients with reduced immunity. The effect on Treponema pallidum is studied not enough. It penetrates the cerebrospinal fluid: the concentration of ciprofloxacin for not inflamed meninges reach 10% with inflammation - up to 37%. For ciprofloxacin local use: acute and subacute conjunctivitis, blepharoconjunctivitis, blepharitis, bacterial corneal ulcers, keratitis, keratoconjunctivitis, chronic dacryocystitis, meybomity. For oral administration dose of ciprofloxacin is 250-750 mg 2 times / day. For IV administration a single dose is 200-400 mg, the multiplicity of the introduction is 2 times / day, duration of treatment - 1-2 weeks and more if necessary. ciprofloxacin rapidly absorbed from the gastrointestinal tract. Eating has a little effect on the absorption of ciprofloxacin. Infectious lesions in the eyes from injury or contact with foreign bodies. May be IV injected as jet but more preferably a drip for 30 minutes. When ciprofloxacin applied topically instilled 1-2 drops into the lower conjunctival sac of the affected eye every 1-4 hours.

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