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    Diflucan compresse


    Diflucan (fluconazole) is an antifungal drug used in treatment of fungal and yeast infections by inhibiting their growth. This post provides a detailed and evidence based look at medical and natural Diflucan alternatives. Diflucan is also used to prevent fungal infections (1). It is recommended as a prophylaxis in people with compromised immune system (2, 3, 4). The following groups of people fall in the category of immune-compromised individuals: The symptoms of systemic fungal infections tend to be very different depending on the actual causative agent and also depending on the affected tissue (organ). But some of the common symptoms include the following: Diflucan is an antifungal that can be used to treat many different fungal infections. Diflucan is available as oral suspensions or tablets. Diflucan tablets and suspension should be stored at room temperature and away from sunlight. Веро-Флуконозол, Дисорел-Сановель, Дифлазон, Дифлюзол, Майконил, Медофлюкон, Микомакс, Микосист, Микофлюкан, Нофунг, Проканазол, Фангифлю, Флузол, Флукозан, Флукозид, Флукомабол, Флукомицид СЕДИКО, Флуконазол* (Fluconazole*), Флуконорм, Флукорал, Флукорус, Флунол, Флюкорем, Флюкостат, Форкан, Фунголон, Фунзол, Фуцис, Цискан. Почему дешево не означает хорошо Средняя цена онлайн(1 капсула) Дифлюкан 150 мг относится к триазольным противогрибковым средствам нового класса и считается мощным способом борьбы с грибками различной природы. В составе препарата Дифлюкан содержится активный компонент флуконазол, который обладает антибиотическим действием. Подавляя жизненные процессы грибковых микроорганизмов, флуконазол вызывает их неминуемую гибель. Причем препарат никаким образом не влияет гормональный фон женщины. Эффективность действия флуконазола тестировалась на различных моделях грибковых заболеваний. Особую активность препарат показал при оппортунистических микозах, в том числе вызванных Candida spp.

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    CRIPTOCOCCOSI DIFLUCAN fluconazolo è indicato nella terapie delle infezioni micotiche profonde dovute a Cryptococcus neoformans, incluse quelle. Дифлюкан 150 мг относится к триазольным противогрибковым средствам нового класса и считаетсяВ составе препарата Дифлюкан содержится активный компонент флуконазол. Medscape - Candidia infection dosing for Diflucan fluconazole, frequency-based adverse effects, comprehensive interactions, contraindications, pregnancy & lactation schedules, and cost information.

    QT prolongation Torsades de pointes Alopecia Anaphylactic reactions Angioedema Cholestasis Dizziness Dyspnea Hepatic failure Hepatitis Hypertriglyceridemia Hypokalemia Increased alkaline phosphatase Increased ALT/AST Jaundice Leukopenia Pallor Seizures Stevens-Johnson syndrome Taste perversion Thrombocytopenia Toxic epidermal necrolysis Hypersensitivity to other azoles Use caution in proarrhythmic conditions and renal impairment Use extreme caution or avoid in congenital long-QT patients and patients with conditions that increase QT-prolongation risk Fluconazole inhibits CYP2C9, CYP2C19, and CYP3A4 isoenzymes; coadministration with drugs that are substrates if these isoenzymes may be contraindicated or warrant dosage modifications Capsules contain lactose and should not be given to patients with rare hereditary problems of galactose intolerance, Lapp lactase deficiency, or glucose-galactose malabsorption Powder for oral suspension contains sucrose and should not be used in patients with hereditary fructose, glucose/galactose malabsorption or sucrase-isomaltase deficiency Syrup contains glycerol; may cause headache, stomach upset, and diarrhea Hepatotoxicity reported with use; use with caution in patients with hepatic impairment Rare exfoliative skin disorders reported; monitor closely if rash develops and discontinue if it progresses When driving vehicles or operating machines, it should be taken into account that dizziness or seizures may occasionally occur Candida krusei is inherently resistant Convenience and efficacy of single dose oral tablet of fluconazole regimen for the treatment of vaginal yeast infections should be weighed against acceptability of higher incidence of drug related adverse events with fluconazole (26%) versus intravaginal agents (16%) If drug is used during pregnancy or if patient becomes pregnant while taking the drug, patient should be informed of potential hazard to fetus; effective contraceptive measures should be considered in women of child-bearing potential who are being treated with 400 to 800 mg/day and should continue throughout the treatment period and for approximately 1 week (5 to 6 half-lives) after the final dose Highly selective inhibitor of fungal cytochrome P-450-dependent enzyme lanosterol 14-alpha-demethylase Subsequent loss of normal sterols correlates with accumulation of 14 alpha-methyl sterols in fungi and may be responsible for the fungistatic activity of fluconazole Additive: TMP-SMX Y-site: Amphotericin B, amphotericin B cholesteryl sulfate, ampicillin, calcium gluconate, cefotaxime, ceftazidime(? ), ceftriaxone, cefuroxime, chloramphenicol, clindamycin, co-trimoxazole, diazepam, digoxin, erythromycin lactobionate, furosemide, haloperidol, hydroxyzine, imipenem/cilastatin, pentamidine, piperacillin, ticarcillin, TMP-SMX Solution: D5W, LR Additive: Acyclovir, amikacin, amphotericin B, cefazolin, ceftazidime, ciprofloxacin, clindamycin, gentamicin, heparin, meropenem, metronidazole, morphine, piperacillin, potassium chloride, ranitidine with ondansetron, theophylline Y-site: Acyclovir, aldesleukin, allopurinol, amifostine, amikacin, aminophylline, amiodarone, ampicillin-sulbactam, aztreonam, benztropine, bivalirudin, cefazolin, cefepime, cefotetan, cefoxitin, cefpirome, chlorpromazine, cimetidine, cisatracurium, dexamethasone sodium phosphate, dexmedetomidine, diltiazem, diphenhydramine, dobutamine, docetaxel, dopamine, doxorubicin liposomal, droperidol, etoposide PO4, famotidine, fenoldopam, filgrastim, fludarabine, foscarnet, ganciclovir, gatifloxacin, gemcitabine, gentamicin, granisetron, heparin, hetastarch, hydrocortisone, immune globulin, leucovorin, linezolid, lorazepam, melphalan, meperidine, meropenem, metoclopramide, metronidazole, midazolam, morphine, nafcillin, nitroglycerin, ondansetron, oxacillin, paclitaxel, pancuronium, penicillin G, phenytoin, piperacillin-tazobactam, prochlorperazine, promethazine, propofol, quinupristin-dalfopristin, ranitidine, remifentanil, sargramostim, tacrolimus, teniposide, theophylline, thiotepa, ticarcillin-clavulanate, tobramycin, vancomycin, vecuronium, vinorelbine, zidovudine Tablets: Store below 86° F (30° C) Dry powder: Store below 86° F (30° C); reconstituted suspension should be stored between 86° F (30° C) and 41° F (5° C), and unused portion should be discarded after 2 weeks; protect from freezing Injection (glass bottles): Store between 86° F (30° C) and 41° F (5° C); protect from freezing Injection (Viaflex Plus plastic containers): Store between 77° F (25° C) and 41° F (5° C); protect from freezing The above information is provided for general informational and educational purposes only. Individual plans may vary and formulary information changes. Contact the applicable plan provider for the most current information. Действующее вещество Дифлюкана – флуконазол, входит в группу триазолов, обладает противогрибковой активностью, основанной на мощном селективном ингибировании в клетке грибов синтеза стеролов. Флуконазол демонстрировал активность в клинических инфекциях и in vitro к большинству следующих микроорганизмов: Candida albicans, Candida parapsilosis, Candida glabrata (многие штаммы проявляют умеренную чувствительность), Candida tropicalis и Cryptococcus neoformans. Активность флуконазола in vitro была показана в отношении следующих микроорганизмов (клиническое значение неизвестно): Candida dubliniensis, Candida kefyr, Candida guilliermondii, Candida lusitaniae. Как при приеме внутрь, так и при парентеральном (в/в) введении, флуконазол проявлял активность на разных моделях грибковых поражений животных: Высокую специфичность флуконазол проявляет в отношении ферментов грибков, зависимых от CYP450. Применение Дифлюкана в суточной дозе 50 мг в течение 4 недель на плазменную концентрацию тестостерона у мужчин или уровень стероидов у женщин детородного возраста не влияет. Флуконазол в суточной дозе 200–400 мг на уровни эндогенных стероидов, а также их реакцию на стимуляцию АКТГ (адренокортикотропного гормона) у здоровых мужчин-добровольцев клинически значимого влияния не оказывает. Существуют следующие механизмы развития невосприимчивости к флуконазолу: качественная или количественная модификация фермента-мишени для флуконазола – ланостерол 14-α-деметилазы либо уменьшение доступа к ней (возможна комбинация двух механизмов).

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