Active substanceFluconazoleFluconazole
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  • Dosage form: & nbspsolution for infusions
    Composition:
    Composition per 1 bottle (bottle) contains:
    active substance: fluconazole (in terms of 100% substance) - 200 mg; auxiliary substance: sodium chloride - 900 mg, water for injection up to 100 ml.

    Description:
    transparent colorless or almost colorless liquid

    Pharmacotherapeutic group:Antifungal agent.
    ATX: & nbsp

    J.02.A.C   Triazole derivatives

    J.02.A.C.01   Fluconazole

    Pharmacodynamics:
    Fluconazole is a synthetic antifungal agent from the group of triazoles. Has a highly specific effect: inhibiting the activity of enzymes of the cytochrome P450 system of fungal cells, violates the C-14 alpha-dimethylation of lanosterol in ergosterol. As a result, the permeability of the cell membrane increases, the growth and replication of fungal cells is disturbed. FluconazoleBeing a highly selective inhibitor of the enzyme cytochrome P450 fungi, practically does not inhibit these enzymes and processes dimethylation in mammalian and human cells; in comparison with itraconazole, clotrimazole, econazole and ketoconazole to a lesser degree suppresses the oxidation-dependent oxidation processes in liver microsomes, dependent on cytochrome P450. Does not have antiadrogenic activity.
    Fluconazole is active against the following microorganisms (in vitro and in vivo tests): Cryptococcus neoformans, Candida spp. (C. albicans, C.parapsilosis, C.tropicalis, C.lusitaniae et al.), Dermatomitsetami (Epidermophyton spp., Microsporum spp., Trichophyton spp.), Blastomyces dermatitidis, Coccidioides immitis, Histoplasma capsulatum, S.schenckii, P .boydii. Most clinical significance has activity against Candida spp., Dermatomitsetami, Cryptococcus neoformans, Coccidioides immitis.

    Pharmacokinetics:
    . After intravenous administration fluconazole penetrates almost all tissues and body fluids. Concentrations of the drug in the kidneys, sweat fluid, epidermis and dermis, articular fluid, saliva, sputum, lungs, peritoneal fluid, vaginal secretions and vaginal tissues, breast milk are similar to its levels in plasma. In patients with fungal meningitis, the fluconazole content in the cerebrospinal fluid reaches 80% of the corresponding levels in the plasma.
    Concentrations in the plasma are in direct proportion to the dose. When administered at therapeutic doses (200 mg / day in adults), equilibrium concentrations in serum are reached by 4-5 days; when a dose twice daily than usual is used on the first day of therapy, equilibrium concentrations are fixed to day 2-3. The apparent volume of distribution approximates the total volume of water in the body. The degree of binding to blood proteins of fluconazole does not exceed 11-12%. Fluconazole is excreted mainly by the kidneys (80% - unchanged, 11% - in the form of metabolites). Half-life is long (30 hours). The clearance of fluconazole depends on the functional state of the kidneys and is directly proportional to the creatinine clearance.After hemodialysis for 3 hours, the concentration of fluconazole in the plasma is reduced by 50%.
    Indications:
    Cryptococcosis: cryptococcal meningitis, cryptococcal sepsis, cryptococcal infections of the lungs and skin.
    Generalized candidiasis: candidemia, disseminated candidiasis with endocardial damage, abdominal organs, respiratory system organs, eyes, organs of the urinary and reproductive systems.
    Candidiasis of the mucous membranes: oral cavity, nasopharynx, esophagus, non-invasive bronchopulmonary infections, candiduria.
    Vaginal candidiasis (acute or in a chronic recurrent form).
    Deep endemic mycoses (coccidioidosis, histoplasmosis, sporotrichosis) in patients with normal immunity.
    Prevention of fungal infections in patients with malignant neoplasms on the background of chemo- or radiation therapy; prevention of recurrence of oropharyngeal candidiasis in AIDS patients.

    Contraindications:
    Hypersensitivity to Flukomabol® and other drugs from the azole group; pregnancy; lactation. Contraindicated simultaneous reception of Flukomabol® with terfenadine, cisapride or astemizole (against the background of the constant use of Flukombola® at a dose of 400 mg / day and above).

    Carefully:
    hepatic failure, the appearance of rash on the background of fluconazole in patients with superficial fungal infection and invasive / systemic fungal infections, simultaneous reception of terfenadine and fluconazole in a dose of less than 400 mg / day, potentially pro-rhythmogenic states in patients with multiple risk factors (organic heart disease, disorders electrolyte balance, simultaneous intake of drugs that cause arrhythmias), pregnancy.

    Pregnancy and lactation:
    The use of fluconazole during pregnancy is indicated only with severe generalized and potentially life-threatening fungal infections. If it is necessary to prescribe the drug during lactation, breastfeeding should be stopped.

    Dosing and Administration:
    Flukomabol® (fluconazole solution 2 mg / ml) is administered by intravenous (IV) infusion, the infusion rate is 200 mg (1 vial) per hour. Doses and dosage regimens depend on nosology.
    Adults
    To treat disseminated candidiasis, candidiasis pneumonia, chronic generalized (granulomatous) candidiasis, candidal peritonitis, candidemia, the loading dose of Flukomabol® is 400 mg on the first day of therapy, then 200 mg once a day.With insufficient clinical effectiveness, the dose of the drug can be increased to 400 mg / day. The duration of therapy depends on clinical effectiveness.
    For the treatment of cryptococcosis of different locations, the loading dose of Flukomabol® on the first day of therapy is 400 mg; in the following days 200 mg once a day, with insufficient clinical efficacy - 400 mg once a day. The duration of therapy for cryptococcal meningitis is at least 6-8 weeks, until a negative culture culture of the cerebrospinal fluid is obtained. To prevent the recurrence of cryptococcal meningitis in AIDS patients, after completing the full course of primary treatment, Flukomabol® is prescribed at a dose of 200 mg / day for a long period of time.
    With deep endemic mycoses: histoplasmosis, coccidioidosis, sporotrichosis, the loading dose of Flukomabol® on the first day of therapy is 400 mg; in the following days 200 mg once a day. The duration of therapy is determined individually; it can be 11-24 months with coccidiomycosis; 2-17 months with paracoccidiomycosis; 1-16 months with sporotrichosis; 3-17 months with histoplasmosis; Considering the need for long-term use of Flukomabol® in these infections (up to 2 years), stepwise therapy is preferable.
    For the prevention of candidiasis against the background of immunodeficiency, incl. in patients who need bone marrow transplantation, the recommended dose of Flukomabol® is 50-400 mg 1 time / day, depending on the degree of risk of fungal infection. If there is a high risk of generalized infection, for example, in patients with expected severe or persistent neutropenia, the recommended dose is 400 mg 1 time / day. Flukomabol® is prescribed several days before the expected appearance of neutropenia; after increasing the number of neutrophils more than 1000 / mm3 treatment is continued for another 7 days.
    With vaginal candidiasis - 150 mg once. To reduce the relapse rate, once a month, 150 mg every 4-12 months, sometimes more frequent use may be required.
    For other candidiasis of mucous membranes (except for genital candidiasis), 50-100 mg 1 time / day for 14-30 days.
    Children aged 1 month. under 12 years old
    In children, as with similar infections in adults, the duration of treatment depends on the clinical and mycological effect. The drug is administered as an intravenous infusion once a day, the daily dose should not exceed 600 mg / day.
    For the treatment of generalized candidiasis (candidemia, disseminated candidiasis, chronic generalized (granulomatous) candidiasis), the loading dose on the first day of treatment is 12 mg / kg / day, in the following days, 6 mg / kg / day is administered.
    In case of cryptococcal infection, including cryptococcal meningitis, the loading dose on the first day of treatment is 12 mg / kg / day, in the following days it is administered at the rate of 6 mg / kg / day. Depending on the severity of the clinical effect, the dose can be increased to 12 mg / kg / day. The duration of therapy is 8-12 weeks.
    Patients with severe oropharyngeal candidiasis, candida esophagitis and the inability to take oral forms of Flucomabol® are administered at a rate of 6 mg / kg on the first day of therapy, on subsequent days 3 mg / kg / day. Duration of treatment with oropharyngeal candidiasis - 2 weeks; with candidal esophagitis - 3 weeks, after the relief of the symptoms of infection continue to take Flukomabol ® for 2 more weeks.
    For the prevention of fungal lesions in children who are at risk for infection due to induced neutropenia (patients undergoing bone marrow transplantation,against the background of treatment with cytostatics and radiation therapy of malignant neoplasms), Flucomabol® doses are 3-12 mg / kg / day, depending on the severity and duration of neutropenia preservation. It is mandatory to monitor the picture of peripheral blood.
    Newborns under 4 weeks of age
    Flukomabol ® is used in the same doses as in older children, but increase the interval between administration of the drug: at the age of 0 to 2 weeks, life is injected every 72 hours, from 2 to 4 weeks of life - every 48 hours.
    Elderly patients
    In the absence of violations of the kidneys should follow the usual dosage regimen. If renal function is impaired (creatinine clearance less than 50 ml / min), dosage adjustment is necessary in accordance with the creatinine clearance rates (see table).
    The use of Flukomabol® in case of impaired renal function
    At course treatment the first (shock) dose is from 50 to 400 mg; in children - the calculation is made per kg of body weight. Then the dose of the drug or the frequency of administration (interdose interval) should be changed depending on the creatinine clearance, namely (see table):

    Creatinine clearance, ml / min

    Dosage

    >50


    The dose of the drug does not change

    11-50


    every 48 hours the usual daily dose or every 24 hours half the usual daily dose

    When regularly conducted hemodialysis

    the usual daily dose after each procedure


    Do not use Flucomabol ® solution as an infusion medium for the administration of other medications.

    Side effects:
    Fluconazole is usually well tolerated. It was noted that the incidence of adverse drug reactions is significantly higher in the AIDS patient population.
    From the nervous system: headache, dizziness, convulsions.
    On the part of the digestive system: change in taste, nausea, vomiting, diarrhea, flatulence, abdominal pain, impaired liver function (increased activity of alkaline phosphatase, bilirubin, serum aminotransferase, hepatitis, hepatocellular necrosis, including fatal).
    On the part of the cardiovascular system: an increase in the duration of the Q-T interval, fibrillation / flutter of the ventricles.
    On the part of the organs of hematopoiesis: thrombocytopenia, leukopenia, neutropenia, agranulocytosis.
    On the part of the urinary system, kidney failure.
    Allergic reactions: skin rash, Stevens-Johnson syndrome, toxic epidermal necrolysis, anaphylactoid reactions.
    Other: impaired renal function, alopecia, hypercholesterolemia,
    hypertriglyceridemia, hypokalemia.

    Overdose:
    Symptoms: transient disturbances of the psyche - hallucinations, psychotic reactions (paranoid behavior); neurologic disorders - ptosis, lacrimation, hypersalivation, convulsions, spontaneous urination, dyspnea.
    Treatment: overdose shows hemodialysis; for a 3-hour procedure of hemodialysis, it is possible to reduce the serum concentrations of fluconazole by 50%.

    Interaction:
    Fluconazole potentiates the effect of coumarinic anticoagulants, possibly an increase in prothrombin time. Promotes the prolongation of prothrombin time in patients receiving warfarin. Assigning fluconazole in combination with anticoagulants, it is necessary to monitor the prothrombin index.
    With simultaneous administration with fluconazole, the concentration of derivatives of sulfonylurea - chlorpropamide, glibenclamide, glipizide and tolbutamide, increases, which potentiates the risk of developing uncontrolled hypoglycemia.Periodically monitor the level of glycemia and, if necessary, correct the dose of hypoglycemic agents (the risk of hypoglycemia!).
    Thiazide diuretics: a possible increase in the level of fluconazole in plasma.
    Phenytoin: simultaneous administration with fluconazole leads to an increase in the concentration of phenytoin in the plasma to a clinically significant extent (with the use of monitoring the concentration of phenytoin in plasma).
    Rifampicin reduces the following pharmacokinetic parameters of fluconazole: T1 / 2 by 20% and AUC by 25%. The faster removal of fluconazole from the blood plasma (by 20%) requires an increase in its dose.
    Cyclosporine: with simultaneous administration with fluconazole, an increase in the concentration of cyclosporine is possible, which requires monitoring of its concentration and dose adjustment.
    Theophylline: with simultaneous administration with fluconazole, an increase in the concentration of theophylline in the blood may be possible due to an increase in its half-life (risk of intoxication). A dynamic clinical control over the concentration of theophylline with possible dose adjustment is necessary.
    Terfenadine and cisapride: with simultaneous administration with fluconazole, their concentrationsin the plasma, which is accompanied by an elongation of the Q-T interval and potentiates the risk of ventricular arrhythmias, including paroxysmal ventricular tachycardia (torsade de pointe).
    Zidovudine: with simultaneous administration with fluconazole, an increase in the concentration of zidovudine in plasma is possible.
    Rifabutin: with simultaneous reception with fluconazole, rifabutin levels in the plasma may increase, in some cases - development of uveitis.
    Astemizole: simultaneous administration of astemizole and fluconazole, medications in the metabolism of which involve enzymes of the cytochrome P450 system, can be accompanied by an increase in their concentrations in the plasma.
    Tacrolimus: with simultaneous admission with fluconazole, the risk of developing nephrotoxicity increases.
    At simultaneous reception fluconazole increases the concentration in the plasma of benzodiazepines of short action, which in some cases requires correction of their doses.
    Fluconazole solution for intravenous administration is compatible with 0.9% sodium chloride solution, 5-10% dextrose solution, Ringer's solution, potassium chloride solution in glucose, Hartman solution.

    Special instructions:
    Treatment should continue to clinical, and in patients with immunodeficiency - also hematologic remission. Premature termination of treatment leads to relapse.In the course of treatment, it is necessary to monitor blood counts, kidney and liver function. If there are severe violations of kidney and liver function, stop taking the drug. The hepatotoxic effect of fluconazole is usually reversible, the symptoms disappear after discontinuation of therapy. When skin rashes occur in patients with immunosuppression, careful observation is necessary, and in the case of progression of the skin reaction, treatment should be discontinued (the risk of development of Stevens-Johnson syndrome, Lyell syndrome). It is necessary to control the prothrombin index while using the coumarinic anticoagulants simultaneously. It is recommended to carry out a dynamic control of the concentrations of cyclosporin in the blood in patients after transplantation of organs simultaneously receiving fluconazole, t. taking fluconazole at a dose of 200 mg / day leads to a slow increase in the concentration of cyclosporine, which can lead to toxic effects.
    Acceptance of certain azoles, including fluconazole, may be accompanied by an elongation of the Q-T interval, so the appointment of fluconazole to patients at risk of arrhythmias, especially severe patients,having an organic lesion of the myocardium and conduction of the heart pathways, electrolyte imbalance and / or receiving supportive cardiotropic therapy, should be strictly justified and carried out under close medical supervision and monitoring of the electrocardiogram.
    Parenteral therapy with fluconazole in preterm infants should be performed under close medical supervision.
    Given the violation of kidney function in elderly (> 65 years) patients, when choosing a dose and mode of administration, it is recommended to take into account biochemical tests characterizing the function of the kidneys, as well as conduct their dynamic monitoring.
    In view of the likely pharmacological incompatibility, do not add or mix fluoxazole solution with other medicines!
    When appointing a patient several medications administered IV, the sequence of the injections should be followed, or fluconazole through a separate intravenous catheter or a system for intravenous infusion.

    Form release / dosage:
    Solution for infusion, 2 mg / ml.

    Packaging:
    100 ml in bottles or bottles of glass with a capacity of 100 ml.
    1 bottle (bottle) with instruction for use is placed in a pack of cardboard.

    Storage conditions:
    List B. In a dry, the dark place at a temperature of no higher than 25 ° C. Keep out of the reach of children. Do not freeze.

    Shelf life:
    2 years.
    Do not use after the expiry date printed on the package.

    Terms of leave from pharmacies:On prescription
    Registration number:LSR-005040/09
    Date of registration:25.06.2009
    The owner of the registration certificate:PREBAND PFC, LLCPREBAND PFC, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp15.10.2015
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