Active substanceBoviolanuronidase azoximeBoviolanuronidase azoxime
Similar drugsTo uncover
  • Longidase®
    lyophilizate for injections 
  • Longidase®
    suppositories rect. the vagina. 
  • Dosage form: & nbspVaginal and rectal suppositories
    Composition:Composition per suppository:

    Active substance: Boviolaronidase azoxime (Longidase®) - 3000 ME.

    Auxiliary substance: cocoa butter - until a suppository with a mass of 1.3 g.

    Description:Suppositories torpedo-shaped, light yellow color with a weak specific smell of cocoa butter, marble staining is allowed.
    Pharmacotherapeutic group:Enzyme agent
    ATX: & nbsp

    V.03.A.X   Other medications

    Pharmacodynamics:

    Longidase ® has hyaluronidase (enzymatic) activity of prolonged action, chelating, antioxidant, immunomodulating and moderately expressed anti-inflammatory properties.

    The prolongation of the action of the enzyme is achieved by covalent binding of the enzyme with a physiologically active polymeric carrier (azoxime). Longidase ® exhibits antifibrotic properties, weakens the course of the acute phase of inflammation, regulates (increases or decreases depending on the initial level) the synthesis of inflammatory mediators (interleukin-1 and tumor necrosis factor - alpha), increases the humoral immune response and resistance of the body to infection.

    The expressed antifibrotic properties of Longidase are provided by the conjugation of hyaluronidase with the carrier, which significantly increases the enzyme's resistance to denaturing effects and the action of inhibitors: the enzymatic activity of Longidase persists with heating to 37 ° C for 20 days, while the native hyaluronidase in the same conditions, loses its activity during the day. In the preparation of Longidase®, a simultaneous local presence of the hyaluronidase enzyme and a carrier capable of binding the enzyme inhibitors and collagen synthesis stimulants released during the hydrolysis of matrix components (iron ions, copper ions, heparin, etc.) is ensured. Thanks to these properties, Longidase® has not only the ability to depolymerize the matrix of connective tissue in fibro-granulomuliasis formations, but also to inhibit the reverse regulatory reaction directed to the synthesis of connective tissue components.

    The specific substrate of testicular hyaluronidase is glycosaminoglycans (hyaluronic acid, chondroitin, chondroitin-4-sulfate, chondroitin-6-sulphate), which form the basis of the matrix of connective tissue. As a result of depolymerization (disruption of the bond between C1 acetylglucosamine and C4 glucuronic or induronic acids), glycosaminoglycans change their basic properties: viscosity decreases, the ability to bind water, metal ions, temporarily increases the permeability of tissue barriers, facilitates fluid movement in the intercellular space, increases the elasticity of the connective tissue, which manifests itself in reducing swelling of the tissue, flattening of scars, increasing the volume of movement of joints, reducing contractures and preventing their formation, reducing the adhesion process. Biochemical, immunological, histological and electron microscopic studies have shown that Longidase® does not damage normal connective tissue, but causes destruction of the connective tissue that has changed in composition and structure in the field of fibrosis.

    Longidase ® does not have mutagenic, embryotoxic, teratogenic and carcinogenic effects.

    The drug is well tolerated by patients, there are no local and common allergic reactions.

    The use of Longidase at therapeutic doses during or after surgical treatment does not cause a worsening of the course of the postoperative period or the progression of the infectious process; does not slow down the restoration of bone tissue.
    Pharmacokinetics:

    Experimental study of pharmacokinetics made it possible to establish that, when administered rectally, Longidasa® is characterized by a high rate of distribution in the body, it is well absorbed into the systemic bloodstream and reaches a maximum concentration in the blood after 1 hour. The half-distribution period is about 0.5 hours, the half-elimination period is from 42 to 84 hours. It is excreted mainly by the kidneys. The drug penetrates into all organs and tissues, including passes through blood-brain and hemato-ophthalmic barriers. The absence of tissue cumulation was established.

    Bioavailability of the Longidas preparation at rectal administration is high: about 90%.
    Indications:

    Adults and adolescents over 12 years of age in the form of monotherapy and as part of complex therapy of diseases accompanied by hyperplasia of connective tissue, including against the background of the inflammatory process:

    - in urology: chronic prostatitis, interstitial cystitis, strictures of the urethra and ureters, Peyronie's disease, the initial stage of benign prostatic hyperplasia, prevention of scar formation and strictures after surgical interventions on the urethra, bladder, ureters;

    - in gynecology: adhesive process (prevention and treatment) in a small pelvis with chronic inflammatory diseases of the internal genital organs, after gynecological manipulations, including artificial abortions, previous surgical interventions on pelvic organs; intrauterine synechia, tubal peritoneal infertility, chronic endomyometritis;

    - in dermatovenerology: limited scleroderma, prevention of fibrotic complications of sexually transmitted infections;

    - in surgery: prevention and treatment of adhesions after surgical interventions on the abdominal organs; long-term non-healing wounds;

    - in pulmonology and phthisiology: pneumofibrosis, siderosis, tuberculosis (cavernous fibrotic, infiltrative, tuberculoma), interstitial pneumonia, fibrosing alveolitis, pleurisy;

    - to increase bioavailability antibacterial therapy in urology, gynecology, dermatovenereology, surgery, pulmonology, etc.

    Contraindications:

    - Hypersensitivity to drugs based on hyaluronidase;

    - pulmonary hemorrhage and hemoptysis;

    - fresh vitreous hemorrhage;

    - malignant neoplasms;

    acute renal failure;

    - Children under 12 years of age (no clinical trial results);

    - Pregnancy and the period of breastfeeding.

    Carefully:With caution apply not more than 1 time per week in patients with chronic renal failure, pulmonary hemorrhage in history.
    Pregnancy and lactation:Contraindicated in pregnancy and during breastfeeding (clinical experience is not available).

    Dosing and Administration:Longitude suppository 3000 ME recommended for rectal or vaginal Application once a day at night with a course of 10 to 20 introductions.

    To adolescents from 12 to 18 years of age, suppositories are administered only rectally.

    Adults and teenagers over 12 years of age rectally: by 1 suppository 1 once a day after cleansing the intestine.

    Adults vaginally: by 1 suppository 1 once a day (at night) the suppository is inserted into the vagina in the supine position.

    The scheme of administration is adjusted depending on the severity, stage and duration of the disease: Longidase® appointed every other day or with interruptions of 2-3 days. Recommended regimens and doses:

    - in urology: 1 suppository every other day 10 injections, then in 2-3 days 10 injections, general course of 20 suppositories.

    - in gynecology: rectally or vaginally at 1 suppository in 2 days 10 injections, then, if necessary, maintenance therapy is prescribed.

    - in dermatovenerology: 1 suppository every 1-2 days, 10-15 introductions.

    - in surgery: 1 suppository in 2-3 days 10 injections.

    - in pulmonology and phthisiology: 1 suppository in 2-4 days 10-20 introductions. If necessary, a repeated course of Longidase® not earlier than in three months or long maintenance therapy for 1 suppository once in 5-7 days for 3-4 months.

    Side effects:

    The frequency of adverse reactions is presented in the following classification: very frequent ≥ 10%; frequent ≥ 1% and <10%; infrequent ≥ 0.1% and <1%; rare ≥ 0.01% and <0.1%; very rare <0.001%.

    Very rarely: local reactions in the form of redness, swelling, itching of the perianal zone, vaginal itching due to individual sensitivity to the components of the drug.

    Overdose:Symptoms of overdose can be manifested by chills, fever, dizziness, hypotension. The drug is discontinued and symptomatic therapy is prescribed.

    Interaction:

    The drug Longidase ® can be combined with antibiotics, antiviral, antifungal drugs, bronchodilators. When prescribed in combination with other medicines (antibiotics, local anesthetics, diuretics), the possibility of increasing bioavailability and enhancing their action should be taken into account.

    When co-administered with large doses of salicylates, cortisone, adrenocorticotropic hormone (ACTH), estrogen or antihistamines, the enzymatic activity of the Longidase® preparation can be reduced.

    Do not use Longidase ® at the same time as preparations containing furosemide, benzodiazepines, phenytoin.

    Special instructions:

    When taking the drug, follow the instructions in the instructions.

    If you have any questions, contact your doctor or pharmacist for an explanation.

    With the development of an allergic reaction, discontinue the use of Longidase®.

    When applied to the background of acute foci of infection to prevent the spread of infection should be appointed under the cover of antimicrobial agents.

    If side reactions occur, and if there is an adverse reaction that is not mentioned in the medical instructions, you should contact your doctor.

    Do not use the drug in the presence of visual signs of its unfitness (packaging defect, color change of the suppository).

    If you miss the introduction of a regular dose of the drug, then apply it in the usual mode (do not inject twice the dose).

    If it is necessary to stop taking Longidasa ®, cancellation can be done immediately, without a gradual dose reduction.

    Effect on the ability to drive transp. cf. and fur:The use of Longidasa® does not affect the ability to drive vehicles, service mechanisms, and other types of work that require a high concentration of attention and speed of psychomotor reactions.

    Form release / dosage:

    Vaginal and rectal suppositories 3000 ME.

    Packaging:

    5 suppositories in a planar cell packaging from a polyvinyl chloride film.One, two or four contour squares in a pack of cardboard together with instructions for use.

    Storage conditions:

    In dry, dark place at a temperature of 2 to 15 ° C. Keep away from children.

    Shelf life:

    2 years. Do not use after the expiration date stated on the package.

    Terms of leave from pharmacies:Without recipe
    Registration number:LSR-002940/07
    Date of registration:01.10.2007 / 05.08.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:NPO PETROVAKS PHARM, LLC NPO PETROVAKS PHARM, LLC Russia
    Manufacturer: & nbsp
    Information update date: & nbsp17.05.2017
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