Clinical and pharmacological group: & nbsp

Spasmolytics myotropic

Included in the formulation
  • Spasmomen®
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  • АТХ:

    A.03.A.B.06   Otilonium bromide

    Pharmacodynamics:

    The drug competitively blocks m-holinoretseptory, mainly in the gastrointestinal tract. This leads to a decrease in the tone of the smooth muscles of the internal organs. Ha tetrameric ammonium compound. The drug also blocks Ca2+ channels, which reduces the concentration of Ca2+ in smooth muscles, as a result, the tone of smooth muscles decreases.

    Pharmacokinetics:

    After oral administration, the preparation is absorbed in a very small amount in the intestine. High degree of distribution in the smooth muscles of the rectum. Excreted through the bile ducts (95-97%). Excretion is long.

    Indications:

    - dyskinesia of the gastrointestinal tract;

    - irritable bowel syndrome (mucous colitis), gastritis, gastroduodenitis, enteritis, esophagitis;

    - spastic conditions;

    - preparation of patients for endoscopy of the gastrointestinal tract.

    XI.K20-K31.K20   Esophagitis

    XI.K20-K31.K29   Gastritis and duodenitis

    XI.K50-K52.K52   Other non-infectious gastroenteritis and colitis

    XI.K55-K63.K58   Irritable Bowel Syndrome

    XXI.Z40-Z54.Z51.4   Preparatory procedures for subsequent treatment, not elsewhere classified

    Contraindications:

    hypersensitivity;

    - Children's age up to 3 years.

    Carefully:

    - glaukoma;

    - diseases of the cardiovascular system;

    - thyrotoxicosis;

    - reflux esophagitis;

    - stenosis of the pylorus;

    - kidney disease;

    - Dow diseaseon;

    - central paralysis in children;

    - liver disease;

    - atony of the gastrointestinal tract;

    - hypertrophy of the prostate.

    Pregnancy and lactation:

    Category FDA not determined. During pregnancy and during lactation, the application is possible when the intended benefit exceeds the risk of side effects.

    Dosing and Administration:

    Orally 20-40 mg 2-3 times a day.

    Rectal 20 mg 3 times a day.

    Side effects:

    - allergic reactions;

    - paresis of accommodation;

    - dry mouth;

    - mydriasis;

    - drowsiness.

    Overdose:

    Shakiness of gait, impaired vision, difficulty breathing, dry mucous membranes, dizziness, muscle weakness, fever.

    Treatment: slow intravenous injection of physostigmine - 0.5-2 mg at a rate of not more than 1 mg per minute, not more than 5 mg per day, or neostigmine methylsulfate intramuscularly - 0.5-1 mg every 2-3 hours, intravenously - 0.5-2 mg (repeat if necessary).

    Interaction:

    Antacids antidiarrhoeal drugs (adsorbents) - a decrease in the absorption of otilonium bromide, a decrease in therapeutic effectiveness.

    Ketoconazole - the drug slows the absorption of ketoconazole.

    Medicines with anticholinergic activity - the enhancement of the m-cholinoblocking effect, up to the paralytic ileus.

    When administered simultaneously with potassium chloride - increased severity of damage to the gastrointestinal tract with potassium chloride.

    Special instructions:

    Impact on the ability to drive vehicles and manage mechanisms

    The drug may cause dizziness, drowsiness, apply with caution.

    Instructions
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