Active substanceRifampicinRifampicin
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  • Dosage form: & nbspCapsules.
    Composition:
    1 capsule contains

    Active substances: 150 mg, 300 mg, 450 mg of rifampicin
    Description:
    Hard gelatin capsules of red color with a white "LYKA" imprint, containing a powder of red-brown color.

    Capsule sizes: for capsules 150 mg - № 3, for capsules 300 mg - № 1, for capsules 450 mg - № 0.
    Pharmacotherapeutic group:Antibiotic-rifamycin.
    ATX: & nbsp

    J.04.A.B   Antibiotics

    J.04.A.B.02   Rifampicin

    Pharmacodynamics:
    Rifampicin has a bactericidal action, is a specific inhibitor of RNA synthesis.

    Rifampicin is a broad-spectrum antibiotic with the most pronounced activity against mycobacteria tuberculosis, atypical mycobacteria of various types, gram-positive (especially staphylococci) and gram-negative cocci (meningococci; gonococci); Many non-spore-forming anaerobes are sensitive to it; less active against gram-negative bacteria (E. coli, C. pneumoniae, Salmonella, Shigella, Proteus spp, P.Aeruginosa, etc.) does not affect fungi. Resistance to rifampicin develops rapidly enough. Cross-resistance with other antibacterial drugs has not been identified.
    Pharmacokinetics:Ingestion rifampicin well absorbed from the digestive tract, the maximum concentration in the blood is reached after 2-2.5 hours.At the therapeutic level, the concentration of the drug for ingestion is maintained for 8-12 hours, for highly sensitive pathogens - within 24 hours. Rifampicin well penetrates into tissues and body fluids and is found in therapeutic concentrations in pleural exudate, sputum, cavern contents, bone tissue. The greatest concentration of the drug is created in the tissues of the liver and kidneys. It is excreted from the body with bile and urine.
    Indications:
    The main indication for the use of rifampicin is pulmonary tuberculosis and other organs in combination therapy.

    In addition, the drug is used for various forms of leprosy and for infectious and inflammatory diseases of the lungs and respiratory tract (bronchitis, pneumonia) caused by multidrug-resistant staphylococci, acute and chronic osteomyelitis and other diseases caused by rifampicin-susceptible pathogens in meningococcal transport.
    Contraindications:The use of rifampicin is contraindicated in cases of hypersensitivity to the drug, liver and kidney diseases, accompanied by a pronounced impairment of their function,jaundice (including mechanical), pregnancy and lactation, children under 1 year of age.
    Dosing and Administration:Rifampicin is applied inside on an empty stomach (for 30 minutes - 1 hour before a meal) in a dose of 450 mg. With tuberculosis, the average daily intake for adults inside is 10 mg / kg, but not more than 900 mg and is administered once daily. The average daily dose for children over 3 years is 10 mg / kg (but not more than 450 g per patient per day) and is also prescribed in one session daily. With poor rifampicin tolerance, the daily dose can be divided into 2 doses.

    The total duration of rifampicin for tuberculosis is determined by the effectiveness of the treatment and can reach 6-9 months.

    The monotherapy of tuberculosis with rifampicin is often accompanied by the development of the resistance of the pathogen to the antibiotic, therefore it should be administered in combination with other anti-tuberculosis drugs (streptomycin, pyrazinamide, isoniazid, ethambutol, etc.), to which the sensitivity of mycobacteria of tuberculosis is maintained.

    With leprosy rifampicin used in combination with other antileprosnyh funds inside by the following schemes:

    1. Rifampicin prescribe in a daily dose of 350-450 mg, which is administered in a single dose, with poor tolerance is divided into 2 doses. Duration of treatment with poor tolerance is divided into 2 doses. Duration of the course of treatment is 3-6 months, repeated courses are possible with an interval of 1 month.

    2. Against the background of combined anti-prophylactic therapy rifampicin apply in a daily dose of 450 mg (divided into 3 doses) 2-3 weeks with an interval of 2-3 months for 1-2 years or at a daily dose of 350-450 mg daily or 2-3 times a week for 6 months.

    In infections of non-tuberculous etiology, depending on the localization of the process, the daily dose of rifampicin for adults is 450-900 mg, for children 8-10 mg / kg. The daily dose is divided into 2-3 doses in 7-14 days.
    Side effects:
    In the treatment of rifampicin, disorders of the function of the gastrointestinal tract (decreased appetite, nausea, vomiting, diarrhea) are possible. These phenomena usually pass independently in 2-3 days without drug withdrawal. Rifampicin can have a hepatoxic effect (an increase in the content of transaminases and bilirubin in the serum, jaundice). For the timely detection andprevention of hepatotoxicity, treatment with rifampicin should begin after a study of liver function (determining the level of bilirubin and aminotransferases in the blood, timol test), and in the treatment process carried out monthly. In patients who have had past hepatitis or who suffer from cirrhosis of the liver, these studies should be conducted every 2 weeks. Moderate dysfunctions of the liver usually have a transient nature and can disappear without drug discontinuation in the appointment of allochol, methionine, pyridoxine, vitamin B12. With increasing phenomena of violations of liver function, rifampicin should be discontinued.

    In the treatment of rifampicin may develop leukopenia and thrombocytopenia, allergic reactions. The latter manifest themselves in the form of skin eruptions, eosinophilia, rarely - bronchospasm and Quincke's edema. With intermittent treatment, irregular drug intake, or with the resumption of treatment with rifampicin after a break, severe allergic reactions may occur in the form of urticaria, influenza-like fever, acute renal-hepatic insufficiency, thrombopenic purpura.These complications are sometimes preceded by signs of drug sensitization (rise in temperature after taking the drug, increasing eosinophilia, bronchospasm, interstitial nephritis, induction of porphyria, etc.).

    To prevent these phenomena, the drug should be administered in small doses (150 mg per day). In cases when signs of sensitization to rifampicin have been observed at the previous stage of treatment, it is used under control, temperature changes after taking the drug (within 3 hours at 2-3 day intervals). With good tolerability, the dose of antibiotic can be increased to the usual therapeutic dose.

    When allergic reactions occur rifampicin abolish and conduct desensitizing therapy (antihistamines, calcium preparations, glucocorticosteroid hormones). In cases of severe allergic reactions, it is necessary to administer parenterally large doses of glucocorticosteroid hormones, antihistamines, intravenous haemodes, isotonic sodium chloride solution, diuretics, etc.

    In patients using the drug, urine, tear fluid, sputum becomes orange-red.
    Interaction:
    Rifampicin is the inducer of microsomal enzymes of the cytochrome P-450 system; accelerates the metabolism of many drugs.

    It is not recommended simultaneous reception of rifampicin with indirect anti-coagulants and, in connection with the weakening of their effect.

    With the combined use of rifampicin with oral contraceptives, the reliability of the latter decreases.

    Rifampicin weakens the effect of glucocorticoids.

    Rifampicin lowers plasma concentration and shortens the effect of oral antidiabetics; digitoxin, quinidine, cyclosporine, chloramphenicol, doxycycline, ketoconazole, itraconazole, to a lesser extent - fluconazole.

    Pyrazinamide reduces the concentration of rifampicin in the blood plasma as a result of the effect on the hepatic or renal clearance of the latter.
    Form release / dosage:
    Capsules 150 mg, 300 mg and 450 mg.
    Packaging:
    Labeled blisters (PVC / AL) or strips (AJI / AL) containing 4 or 10 capsules each. By 2.10 or 20 blisters or strips packed in a cardboard box with instructions for use.

    A bottle of high density polyethylene (PVP), containing 100 or 1000 capsules in a polyethylene bag with 1 g or 2 g of silica gel, respectively, and instructions for use.
    Storage conditions:
    Rimpin should be stored in a dry, dark place at a temperature of no higher than 25 ° C. Keep away from children.
    Shelf life:4 years.
    Terms of leave from pharmacies:On prescription
    Registration number:P N013939 / 01-2002
    Date of registration:05.06.2009
    The owner of the registration certificate:Laika Lables LimitedLaika Lables Limited India
    Manufacturer: & nbsp
    Representation: & nbspLAYKA LES LIMITED LAYKA LES LIMITED India
    Information update date: & nbsp16.05.2016
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