Active substanceSulfanilamideSulfanilamide
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  • Dosage form: & nbsp
    Powder for external use.

    Composition:Sulfanilamide (streptocid) - 2 g, 5 g
    Description:White crystalline powder odorless.
    Pharmacotherapeutic group:Antimicrobial agent - sulfonamide.
    ATX: & nbsp

    D.06.B.A   Sulfonamides

    Pharmacodynamics:Streptocid - progivomikrobnoe bacteriostatic agent. The mechanism of action caused by a competitive antagonism with para-aminobenzoic acid (PABA) and inhibition digidrogpteroatsintetazy, which disrupts the synthesis of dihydrofolate and then tetrahydrofolic acid and as a result - to disruption synthesis of nucleic acids of microorganisms. Activity is manifested in gram-positive and gram-negative microorganisms: Escherichia coli, Shigella spp., Vibrio cholerae, Clostridium perfringens, Bacillus anthracis, Corynebacterium diphtheriae, Yersinia pestis, Chlamydia spp., Actinomyces israelii, Toxoplasma gondii.
    Indications:In the combined therapy: purulent wounds, infected burns (I-II v.) And other suppurative inflammation of the skin.
    Contraindications:Hypersensitivity to sulfonamides, hematopoietic system disease, inhibition of bone marrow hematopoiesis, anemia, chronic heart failure, hyperthyroidism, renal / hepatic insufficiency, azotemia, porphyria, congenital deficiency of glucose-6-phosphate dehydrogenase, pregnancy, breast-feeding.
    Carefully:Children up to 3 years.
    Dosing and Administration:External, applied directly to the affected surface (in the form of powder for external use); Dressings are carried out after 1-2 days.Maximum doses for adults: single dose - 5 g, maximum daily dose - 15 g. Children older than 3 years - 300 mg - single dose, daily dose of 300 mg.
    Side effects:
    With hypersensitivity to sulfanilamide drugs, allergic reactions are possible, the development of which requires immediate discontinuation of the drug. In addition, headache, dizziness, nausea, vomiting, dyspepsia, cyanosis, leukopenia, agranulocytosis, and crystallography are possible.
    If any of the side effects listed in the manual are aggravated, or if you notice any other side effects not listed in the instructions, tell your doctor.
    Overdose:Symptoms: nausea, vomiting, intestinal colic, dizziness, headache, drowsiness, depression, fainting, confusion, visual impairment, fever, hematuria, crystalluria; with prolonged overdose - thrombocytopenia, leukopenia, megaloblastic anemia, jaundice.
    Treatment: abundant drinking; with accidental ingestion - gastric lavage.
    Interaction:Myelotoxic drugs increase the manifestation of hematotoxicity of the drug.
    Special instructions:During therapy, an abundant alkaline drink is recommended.If necessary, concomitantly prescribe antimicrobials inwards.
    Effect on the ability to drive transp. cf. and fur:Given the side effects of the drug should be careful when driving vehicles, mechanisms.
    Form release / dosage:
    Powder for external use.
    Packaging:
    By 2 g or 5 g in heat-sealing bags of packaging combined material. 1, 2, 3, 4, 5, 6, 7, 8, 10, 12 or 20 bags are placed in a pack of cardboard together with instructions for use.
    The full text of the instructions for use should be applied to the pack.
    50, 100, 200, 400 packages without a bundle, together with an equal number of instructions for use, are placed in a carton box (for hospitals).
    Storage conditions:In dry, the dark place at a temperature of no higher than 30 ° C. Keep out of the reach of children.
    Shelf life:5 years. Do not use after the expiration date.
    Terms of leave from pharmacies:Without recipe
    Registration number:LP-002847
    Date of registration:29.01.2015
    The owner of the registration certificate:IVANOVSKAYA Pharmaceutical Factory, OAO IVANOVSKAYA Pharmaceutical Factory, OAO Russia
    Manufacturer: & nbsp
    Information update date: & nbsp29.08.2015
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