Clinical and pharmacological group: & nbsp

H1-antihistamines

Included in the formulation
  • Suprastin®
    solution w / m in / in 
  • Suprastin®
    pills inwards 
  • Chloropyramine
    pills inwards 
    ATOLL, LLC     Russia
  • Chloropyramine
    solution w / m in / in 
  • Chloropyramine
    solution w / m in / in 
    GROTEKS, LLC     Russia
  • Chloropyramine
    solution w / m in / in 
  • Chloropyramine
    solution w / m in / in 
    ELLARA, LTD.     Russia
  • Chloropyramine
    solution w / m in / in 
  • Chloropyramine
    solution w / m in / in 
    ATOLL, LLC     Russia
  • Chloropyramine
    solution w / m in / in 
    BIOSINTEZ, PAO     Russia
  • Chloropyramine-Ferein®
    pills inwards 
    BRYNTSALOV-A, CJSC     Russia
  • Chloropyramine-ESCOM
    solution w / m in / in 
    ESKOM NPK, OAO     Russia
  • Included in the list (Order of the Government of the Russian Federation No. 2782-r of 30.12.2014):

    ONLS

    VED

    Minimal chemist's assortment

    АТХ:

    D.04.A.A.09   Chloropyramine

    R.06.A. C.03   Chloropyramine

    Pharmacodynamics:

    The blocker of histamine peripheral H1-receptors of the first generation, penetrates the blood-brain barrier, has a sedative effect.

    Competitively connects H1-receptors of effector cells. Inhibits allergic reactions after the introduction of specific allergens, histamine, with cold urticaria.Reduces histamine-induced bronchoconstriction in bronchial asthma. Prevents allergic reactions, when they occur - facilitates the course of the disease. Reduces exudation and itching. Has a mild anticholinergic effect. Strengthens the effects of ethyl alcohol and other drugs that have a depressing effect on the central nervous system.

    Pharmacokinetics:

    After ingestion, up to 70% is absorbed in the gastrointestinal tract. The maximum concentration in the blood plasma is reached after 2 hours. The connection with plasma proteins is 93%.

    The therapeutic effect develops 15-30 minutes after administration and lasts for 3-6 hours. Penetrates through the blood-brain and placental barrier, is found in breast milk. Metabolism in the liver.

    The half-life is 14 hours. Elimination by the kidneys.

    Indications:

    It is used for the treatment of allergic rhinitis, hay fever, conjunctivitis, Quincke edema, urticaria. Used in the complex therapy of bronchial asthma.

    VII.H10-H13.H10.1   Acute atopic conjunctivitis

    XII.L20-L30.L20   Atopic dermatitis

    X.J30-J39.J30.3   Other allergic rhinitis

    X.J30-J39.J30.2   Other seasonal allergic rhinitis

    X.J30-J39.J30.1   Allergic rhinitis caused by pollen of plants

    XII.L20-L30.L20.8   Other atopic dermatitis

    XII.L20-L30.L23   Allergic contact dermatitis

    XII.L20-L30.L24   Simple irritant contact dermatitis

    XII.L20-L30.L28.0   Simple chronic lichen

    XII.L20-L30.L29   Itching

    XII.L50-L54.L50   Hives

    XIX.T66-T78.T78.3   Angioedema

    XIX.T80-T88.T80.6   Other serum reactions

    XIX.T80-T88.T88.7   Pathological reaction to medication or medicines, unspecified

    Contraindications:

    Severe renal failure, a period of newborns, an acute attack of bronchial asthma, an individual intolerance.

    Carefully:

    Chronic renal and hepatic insufficiency, cardiovascular diseases, closed-angle glaucoma, prostatic hyperplasia, urinary retention, advanced age, hypersensitivity.

    Pregnancy and lactation:

    Recommendations for FDA - Category C. It is used with caution during pregnancy and lactation in cases where the intended benefit exceeds the risk to the fetus and newborn.

    Dosing and Administration:

    Use in children

    Inside, depending on age:

    1-12 months: 1/4 tablets (6.5 mg) 2-3 times a day;

    1-6 years: for ½ tablets (12.5 mg) 2 times a day;

    6-14 years: 1/2 tablet (12.5 mg) 2-3 times a day.

    Adults

    To stop acute allergic reactions intravenously injected or intramuscularly 1-2 ml of a 2% solution.

    Inside for 25 mg 2-3 times a day during meals. As needed the dose rises to 150 mg for 2-3 doses.

    The highest daily dose: 4 mg for parenteral administration, 150 mg for oral administration.

    The highest single dose: 4 mg for parenteral administration, 75 mg for oral administration.

    Side effects:

    Central and peripheral nervous system: dizziness, headache, rarely - depression, increased excitability, tremor, migraine, euphoria.

    Hematopoietic system: rarely - agranulocytosis, leukopenia.

    The cardiovascular system: rarely - arrhythmia, arterial hypotension, tachycardia.

    Digestive system: dry mouth, dyspepsia, gastritis, edema of the tongue.

    Musculoskeletal system: muscle weakness.

    Sense organs: change in taste perception.

    Urinary system: delay urination.

    Dermatological reactions: photosensitization.

    Allergic reactions.

    Overdose:

    Ataxia, anxiety, athetosis, convulsions, hallucinations.

    Children: fever, anxiety, fixed mydriasis, reddening of the face, urinary retention, sinus tachycardia, coma.

    Treatment is symptomatic.

    Interaction:

    Clinically significant interactions are not described.

    Special instructions:

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

    Instructions
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