Clinical and pharmacological group: & nbsp

NSAIDs - Propionic acid derivatives

Included in the formulation
  • Novigan®
    pills inwards 
  • АТХ:

    M.01.A.E.51   Ibuprofen in combination with other drugs

    Pharmacodynamics:

    Combined drug.

    Ibuprofen

    Non-selectively suppresses COX1 and COX2, regulating the synthesis of prostaglandins. It indiscriminately suppresses synthetases of prostaglandins. Suppresses the production of anti-inflammatory cytokines. Violates the synthesis of arachidonic acid. Has analgesic, antipyretic and anti-inflammatory effect. Inhibits the aggregation of platelets. With long-term use has a desensitizing effect.

    Pitophenone

    Inhibits phosphodiesterase, resulting in cAMP accumulation and reducing the concentration of calcium ions within the cells, thereby reducing the smooth muscle tone of the vascular walls and internal organs: respiratory, gastrointestinal, genital, urinary system.

    Fentipierinium bromide

    m-holinolitik, relaxes the smooth muscles of internal organs.

    Pharmacokinetics:

    After ingestion fasting all drugs until 90% absorbed in the gastrointestinal tract. The maximum concentration in the blood plasma is achieved in 1-2 hours. The connection with plasma proteins is 99%.

    Therapeutic effect develops after the reception. Metabolism in the liver.

    The elimination half-life is 2 hours. Elimination by the kidneys.

    Indications:

    It is used for relief of mild to moderate pain syndrome with bile, intestinal and renal colic, dyskinesia of bile ducts, headache, migraine. Used for arthralgia, myalgia, sciatica.

    VI.G40-G47.G43   Migraine

    XI.K80-K87.K80   Gallstone disease [cholelithiasis]

    XI.K80-K87.K82.8   Other specified diseases of the gallbladder

    XIII.M20-M25.M25.5   Pain in the joint

    XIII.M50-M54.M54.1   Radiculopathy

    XIII.M50-M54.M54.3   Sciatica

    XIII.M50-M54.M54.4   Lumbago with sciatica

    XIII.M70-M79.M79.1   Myalgia

    XIII.M70-M79.M79.2   Neuralgia and neuritis, unspecified

    XIV.N20-N23.N23   Renal colic, unspecified

    XIV.N80-N98.N94.4   Primary dysmenorrhea

    XIV.N80-N98.N94.5   Secondary dysmenorrhea

    XVIII.R10-R19.R10.4   Other and unspecified abdominal pain

    XVIII.R50-R69.R51   Headache

    XVIII.R50-R69.R52.0   Acute pain

    XVIII.R50-R69.R52.2   Another constant pain

    Contraindications:

    Liver and kidney failure, hemophilia, asthma, gastric ulcer and duodenal ulcers, granulocytopenia, porphyria, lack of glucose-6-phosphate dehydrogenase, intestinal obstruction, angle-closure glaucoma, tachyarrhythmia, age under 16 years, pregnancy and lactation, hypersensitivity.

    Carefully:

    Ischemic heart disease, diabetes, arterial hypertension, peripheral arterial disease, anemia, hyperbilirubinemia, nephrotic syndrome.

    Pregnancy and lactation:

    Recommendations for FDA - Category C. Contraindicated in pregnancy and lactation.

    Dosing and Administration:

    Inside, for 1 hour or 3 hours after eating 1 tablet 3 times a day.

    The highest daily dose: 3 tablets.

    The highest single dose: 1 tablet.

    Side effects:

    Central and peripheral nervous system: dizziness, headache, irritability, increased excitability, confusion, hallucinations.

    Respiratory system: bronchospasm, shortness of breath.

    Hemopoietic system: anemia, agranulocytosis, leukopenia, thrombocytopenia.

    The cardiovascular system: tachycardia, arterial hypertension, heart failure.

    Digestive system: heartburn, gastralgia, aphthous stomatitis, hepatitis, pancreatitis, flatulence, diarrhea.

    Dermatological reactions: hyperhidrosis, rash, Lyell's syndrome.

    Sense organs: ringing in the ears, hearing loss, impaired vision, paresis of accommodation.

    Urinary system: nephrotic syndrome, polyuria, cystitis, proteinuria, staining of urine in red.

    Allergic reactions.

    Overdose:

    Nausea, anorexia, diarrhea, impaired consciousness, bradycardia, respiratory arrest.

    Treatment is symptomatic. Effective hemodialysis.

    Interaction:

    Simultaneous use with other non-steroidal anti-inflammatory drugs leads to increased toxic effects.

    Increases the concentration in the blood plasma of digoxin and probenecid.

    Increases the toxic effects of preparations of gold, colchicine, methotrexate, lithium.

    Strengthens the action of insulin and oral hypoglycemic agents.

    Reduces the effects of diuretics and antihypertensive drugs.
    Special instructions:

    The drug is intended for short-term use, not more than 5 days.

    The drug is not compatible with alcohol.

    During the treatment it is not recommended to drive vehicles and work with moving mechanisms.

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