Clinical and pharmacological group: & nbsp

Antiemetic drugs

Included in the formulation
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    solution w / m in / in 
    ATOLL, LLC     Russia
  • Metoclopramide
    pills inwards 
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    pills inwards 
    UPDATE OF PFC, CJSC     Russia
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    pills inwards 
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    pills inwards 
  • Metoclopramide
    solution w / m in / in 
  • Metoclopramide
    solution w / m in / in 
    ELLARA, LTD.     Russia
  • Metoclopramide
    solution w / m in / in 
    BIOSINTEZ, PAO     Russia
  • Metoclopramide-Acry®
    pills inwards 
    AKRIKHIN HFK, JSC     Russia
  • Metoclopramide-Vial
    solution w / m in / in 
  • Metoclopramide-Promed
    solution w / m in / in 
  • Metoclopramide-ESCOM
    solution w / m in / in 
    ESKOM NPK, OAO     Russia
  • Perinorm
    pills inwards 
  • Perinorm
    solution w / m in / in 
  • Perinorm
    solution inwards 
  • Cerulgan®
    pills inwards 
    BRYNTSALOV-A, CJSC     Russia
  • Cerulgan®
    solution for injections 
    BRYNTSALOV-A, CJSC     Russia
  • Cerucal®
    solution w / m in / in 
  • Cerucal®
    pills inwards 
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    VED

    ONLS

    АТХ:

    A.03.F.A   Motility stimulators GIT

    A.03.F.A.01   Metoclopramide

    Pharmacodynamics:

    It blocks dopamine D2-receptors, serotonin receptors, increases the threshold of chemoreceptors in the trigger zone of the vomiting center. Increases the amplitude of contractions of the antral part of the stomach, accelerates the emptying of the stomach. By increasing the pressure in the gallbladder and bile ducts normalizes the separation of bile. Increases the pressure of the sphincter of the esophagus at rest, preventing gastroesophageal reflux.

    It causes a transient increase in the concentration of circulating aldosterone and stimulates prolactin production, which is accompanied by a short-term fluid retention.

    Pharmacokinetics:

    After oral administration, up to 50-70% is absorbed in the gastrointestinal tract. The maximum concentration in blood plasma is achieved after 1-2 hours. The connection with plasma proteins is 15-30%.

    The therapeutic effect develops 30-60 minutes after ingestion. With intravenous administration begins to act after 1-3 min. The duration of action is 1-2 hours. It penetrates through blood-brain and placental barriers. Metabolism in the liver.

    The half-life is 4-6 hours. Elimination by the kidneys.

    Indications:

    It is used for hiccups, nausea, vomiting, dyskinesia biliary tract, reflux esophagitis, flatulence. Used in complex therapy for exacerbations of peptic ulcer of the stomach and duodenum, as well as to accelerate peristalsis in radiopaque studies of the gastrointestinal tract.

    XI.K20-K31.K21.0   Gastroesophageal reflux with esophagitis

    XI.K20-K31.K26   Duodenal ulcer

    XI.K20-K31.K25   Stomach ulcer

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

    XVIII.R00-R09.R06.6   Hiccups

    XVIII.R10-R19.R11   Nausea and vomiting

    XVIII.R10-R19.R14   Meteorism and related conditions

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

    Contraindications:

    Gastrointestinal bleeding, perforation of the stomach or intestines, mechanical intestinal obstruction, glaucoma, epilepsy, prolactin-dependent tumors, individual intolerance.

    Carefully:

    Bronchial asthma, hepatic and renal insufficiency, arterial hypertension, lactation period, elderly age.

    Pregnancy and lactation:

    Recommendations for FDA - Category B. It is used according to the indications.

    Dosing and Administration:

    Application in children

    6-18 years of 5 mg 1-3 times / day, by mouth, intravenously and intramuscularly. Daily dose: 1 mg / kg.

    Adults

    Inside for 5-10 mg 3-4 times / day, washing down with water. Tablets are swallowed whole.

    Intravenous and intramuscular: 10-20 mg 1-3 times / day.

    The highest daily dose: 60 mg.

    The highest single dose: 20 mg.

    Side effects:

    Central and peripheral nervous system: drowsiness, dizziness, depression; hyperkinesis, spasmodic torticollis, the phenomenon of parkinsonism.

    The system of hematopoiesis: agranulocytosis.

    Digestive system: diarrhea, constipation, rarely dry mouth.

    Reproductive system: disorders of the menstrual cycle, gynecomastia, galactorrhea.

    Allergic reactions.

    Overdose:

    Symtomas: increased side effects.

    Treatment: cancellation of the drug.

    Interaction:

    Strengthens the action of paracetamol, acetylsalicylic acid, levodopa, ethanol, lithium, ampicillin, tetracycline due to acceleration of absorption due to accelerated evacuation from the stomach.

    Slows the absorption of digoxin, cimetidine.

    Simultaneous use with monoamine oxidase inhibitors can provoke the development of hypertensive crisis.

    Reduces the effects of bromocriptine by increasing the concentration of prolactin in the blood plasma.

    Enhances extrapyramidal side effects with the use of neuroleptics.

    Reduces the effectiveness of levodopa.

    Strengthens the effect of drugs that have a depressant effect on the central nervous system, including ethanol.

    Special instructions:

    Patients who are hypersensitive to procainamide and procaine tend to have an increased sensitivity to metoclopramide.

    The total duration of treatment with metoclopramide should not exceed 12 weeks, due to the increased risk of developing tardive dyskinesia.

    Instructions
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