Active substanceSulfanilamideSulfanilamide
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  • Streptocide Ointment 10%
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  • Dosage form: & nbspPowder for external use.
    Composition:Sulfanilamide (streptocid) - 2.0 g.
    Description:
    White crystalline powder odorless.

    Pharmacotherapeutic group:Antimicrobial agent - sulfonamide.
    ATX: & nbsp

    D.06.B.A   Sulfonamides

    Pharmacodynamics:Streptocide is an antimicrobial bacteriostatic agent. The mechanism of action is due to competitive antagonism with para-aminobenzoic acid (PABA) and inhibition of dihydropteroate synthetase, which leads to a disruption in the synthesis of dihydrofolic and then tetrahydrofolic acid and, as a result, a violation of the 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.
    Pharmacokinetics:When injected into the body streptotsid quickly absorbed. The highest concentration of the drug in the blood is created 1 to 2 hours after administration. After 4 hours, it is found in the cerebrospinal fluid. It is allocated mainly (90 - 95%) kidneys.
    Indications:Streptocide is used in complex therapy for treatment of purulent wounds, infected burns and other purulent-inflammatory processes of soft tissues.
    Contraindications:
    Hypersensitivity to sulfonamides, pregnancy, lactation. Diseases of the hematopoietic system, oppression of bone marrow hematopoiesis, anemia, azotemia, thyrotoxicosis, chronic heart failure, renal failure, porphyria,hepatic insufficiency, congenital deficiency of glucose-6-phosphate dehydrogenase.
    Dosing and Administration:Streptocide is applied to the wound in the form of a thoroughly crushed powder (5-10-15 g), if necessary, simultaneously assigning antimicrobials to the interior.
    Side effects:
    Allergic reactions, headache, dizziness, nausea, vomiting, dyspepsia, cyanosis, leukopenia, agranulocytosis, crystalluria are possible.
    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: intake of fluid inside, 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.
    Effect on the ability to drive transp. cf. and fur:


    Form release / dosage:
    Powder for external use.
    Packaging:
    2 g in heat-sealing bags of the combined material "Buflen" for the packaging of medicines, from a combined material on a paper basis with polyethylene coating, packaging material from a film of polypropylene metallized.
    2, 5, 10, 20, 50, 100, 200, 600 packages, together with an equal number of instructions for use, are placed in a polyethylene hermetically sealed bag (sleeve) from a polyethylene food film, or combined on a paper and cardboard basis, or packing material from polypropylene metallized films.
    Storage conditions:
    List B. In a dry, the dark place at a temperature of no higher than 25 ° C.
    In a place inaccessible to children.
    Shelf life:
    5 years.
    Do not use after expiry date.
    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-008202/09
    Date of registration:16.10.2009
    The owner of the registration certificate:LYUMI, LLC LYUMI, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp29.08.2015
    Illustrated instructions
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