Active substanceNitrofuralNitrofural
Similar drugsTo uncover
  • Furacilin
    solution locally externally 
  • Furacilin
    solution locally externally 
    FARMLEND JV, LLC     Republic of Belarus
  • Furacilin
    solution locally externally 
    SAMARAHEDPROM, JSC     Russia
  • Furacilin
    pills locally externally 
    FORP, CJSC     Russia
  • Furacilin
    pills locally externally 
    KVADRAT-S, LLC     Russia
  • Furacilin
    pills locally externally 
    YUZHFARM, LLC     Russia
  • Furacilin
    solution locally externally 
  • Furacilin
    pills locally externally 
    UPDATE OF PFC, CJSC     Russia
  • Furacilin Avexime
    pills locally externally 
    AVEKSIMA, JSC     Russia
  • Furacilin-LekT
    pills locally externally 
  • Furacilin-SF
    solution locally externally 
    Sphera-Pharm, OOO     Russia
  • Furatsilina alcohol solution 1: 1500
    solution externally 
  • IRBITSK HFZ, OJSC     Russia
  • Dosage form: & nbspeffervescent tablets for solution for local and external use
    Composition:

    Composition per one tablet:

    active substance: nitrofural (furacilin) ​​- 20 mg,

    Excipients: tartaric acid 375 mg, sodium hydrogen carbonate 299 mg, sodium carbonate 325 mg, sodium chloride 100 mg, macrogol 20,000 to 65 mg, povidone medium molecular weight 16 mg.

    Description:

    Round, flat-cylindrical tablet form, from light yellow to yellow with interspersed, chamfered on both sides. Roughness of the surface of the tablet is allowed.

    Pharmacotherapeutic group:Antimicrobial agent-nitrofuran
    ATX: & nbsp

    D.08.A.F.01   Nitrofural

    Pharmacodynamics:

    Antimicrobial agent, a derivative of nitrofuran. Bacterial flavoproteins restoring the 5-nitro group form highly reactive amino derivatives, which can cause conformational changes in proteins (including ribosomal) and other macromolecules, leading to the death of bacteria. It is active against Gram-positive and Gram-negative bacteria, incl. Staphylococcus spp., Streptococcus spp., Escherichia coli, Clostridiumperfringens.Sustainability develops slowly and does not reach a high degree.

    Pharmacokinetics:

    With local and external application, the absorption is insignificant.

    Indications:

    As part of complex therapy: topically: acute tonsillitis (tonsillitis), stomatitis, gingivitis, blepharitis, conjunctivitis; externally: purulent wounds, pressure sores, burns II-III degree, minor damage to the skin (including abrasions, scratches, cracks, cuts).

    Contraindications:

    Hypersensitivity to nitrofural, nitrofuran derivatives and / or other components of the drug, bleeding, allergic dermatosis, marked renal dysfunction.

    Pregnancy and lactation:

    Application in pregnancy and during breastfeeding is possible if the intended benefit to the mother exceeds the potential risk to the fetus or child.

    Dosing and Administration:

    Locally, externally in the form of 0.02 % freshly prepared aqueous solution: immediately before use, one tablet (20 mg furatsilina), dissolved in 100 ml of distilled water at room temperature or in warm boiled water.

    With acute tonsillitis (angina), stomatitis, gingivitis - mouth and throat rinsing with a warm 0.02 % solution of 100 ml 2-3 times a day. With blepharitis, conjunctivitis is instillation of 0.02% solution into the conjunctival sac. Outer 0,02% aqueous solution water the wounds and apply moist bandages.

    Duration of treatment - according to the indications depending on the nature and localization of the affected area.

    If symptoms persist, it is recommended that you consult a doctor.

    Side effects:

    Allergic reactions are possible: itching, dermatitis.

    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:

    No cases of overdose have been reported.

    Interaction:

    Not studied.

    Effect on the ability to drive transp. cf. and fur:

    The drug does not affect the ability to drive vehicles or engage in other potentially hazardous activities that require increased concentration and speed of psychomotor reactions.

    Form release / dosage:

    The effervescent tablets are 20 mg.

    Packaging:

    2 tablets per contour non-cellular package (strip) of packaging material combined on a paper basis.

    For 10, 15, 20, 25 or 30 tablets in a plastic tube, sealed with a plastic lid with a desiccant and first opening control.

    For 10, 15, 20, 25 or 30 tablets in a jar of polymer materials made of low density polyethylene, sealed with a plastic lid with a desiccant and first opening control.

    5 contour non-jawed packages (strips) with instructions for medical use are placed in a pack of cardboard.

    1 plastic tube or jar of polymer materials with instructions for medical use are placed in a pack of cardboard.

    Storage conditions:

    Store in a dry, dark place at a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    After expiration date the drug should not be used.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-002980
    Date of registration:29.04.2015 / 25.12.2017
    Expiration Date:29.04.2020
    The owner of the registration certificate:AVEKSIMA, JSC AVEKSIMA, JSC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp20.03.2018
    Illustrated instructions
      Instructions
      Up