Iberogast® (Iberogast®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Dosage form: & nbspdrops for oral administration
Composition:

100 ml of the preparation contain:

Iberians bitter (Iberis amara L., Cruciferae) whole fresh plant extract liquid (extractant ethanol 50%) 1: 1.5-2.5 - 15.0 ml

Angelica officinalis (Angelica archangelica L., Umbelliferae) roots dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 10.0 ml

Chamomile Chamomile (Matricaria chamomilla L., Compositae) flowers dry extract liquid (extractant ethanol 30%) 1: 2.0-4.0 - 20.0 ml

Cumin Common (Carum carvi L., Umbelliferae) fruits dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 10.0 ml

Milk thistle (Silybum marianum (L.) Gaertn., Compositae) fruits dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 10.0 ml

Melissa officinalis (Melissa officinalis L., Labiatae) leaves dry extract liquid (extractant ethanol 30%) 1: 2,5-3,5 - 0,0 ml

Peppermint (Mentha piperita L., Labiatae) leaves dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 5.0 ml

Purity of May (Chelidonium majus L., Papaveraceae) herbs dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 10.0 ml

Licorice is naked (Glycyrrhiza glabra L., Leguminosae) roots of dry extract liquid (extractant ethanol 30%) 1: 2.5-3.5 - 10.0 ml

Ethanol content: about 31% (volumetric ratio).

Description:

From a transparent to slightly cloudy liquid of a dark brown color. During the storage, a slight deposit may form.

Pharmacotherapeutic group:Herbal origin means
ATX: & nbsp
  • Other drugs used in bowel disorders
    • Pharmacodynamics:

    The drug has a pronounced anti-inflammatory effect, as well as normalizes the tone of the smooth muscles of the gastrointestinal tract: it helps to eliminate spasm without affecting normal peristalsis, and with reduced tone and motility has a toning, prokinetic effect. In the experiment in vitro inhibits the growth of 6 subspecies Helicobacter pylori. Iberogast ® reduces the intensity of ulceration of the gastric mucosa, the secretion of hydrochloric acid, reduces the concentration of leukotrienes, enhances the production of mucins, increases the concentration of mucoprotein prostaglandin E2 in the mucous membrane of the stomach.

    Pharmacokinetics:No data available.
    Indications:The drug is used to treat functional disorders of the gastrointestinal tract (including irritable bowel syndrome), manifested by weight in the epigastric region, gastric or intestinal spasms, belching, nausea, flatulence, constipation, diarrhea or alternation, as well as in complex therapy gastritis, gastric ulcer and duodenal ulcer.
    Contraindications:

    Hypersensitivity to the components of the drug, calculous cholecystitis.

    Children under 12 years of age (due to inadequate clinical data).

    Carefully:

    Diseases of the liver, alcoholism, traumatic brain injury, brain disease - due to the content of ethanol in the drug.

    Pregnancy and lactation:

    The drug should not be used during pregnancy, but also during breastfeeding.

    Dosing and Administration:

    Inside, adults and children over 12 years, 20 drops 3 times a day, before or during meals, with a small amount of water.

    The duration of therapy is 4 weeks.

    An increase in the duration and conduct of repeated courses of treatment is possible on the recommendation of a doctor.

    Side effects:Possible allergic skin reactions, dyspnea, as well as nausea, vomiting, diarrhea. If there are side effects, you must cancel the drug and consult a doctor.
    Overdose:So far, no cases of overdose have been reported.
    Interaction:

    Interaction with other drugs is currently unknown. Consideration should be given to the possibility of interacting with drugs metabolized by the cytochrome P450 system (licorice roots, thistle fruits, chamomile flowers may have an inhibitory effect on a number of cytochrome P450 isoenzymes).At the same time, these effects are dose-dependent and are described when individual components are used at concentrations many times exceeding the recommended daily doses of Iberogast®.

    Special instructions:

    If the severity of the symptoms of the disease does not decrease within 7 days of the drug, or if the symptoms worsen, or if new complaints arise, you need to see a doctor.

    The content of the preparation of ethyl alcohol is from 29.5 to 32.6% (by volume). When receiving 1 single dose (20 drops), the patient receives up to 0.24 grams of absolute ethyl alcohol. The maximum daily dose of the drug (60 drops) contains up to 0.72 g of absolute ethyl alcohol, which is lower than the alcohol content of the 200 ml of apple juice and 75 ml of yogurt.

    In spite of this when using the drug should be taken when performing potentially hazardous activities that require high concentration and speed of psychomotor reactions (including the management of vehicles, work with moving parts, the work manager and operator).

    During storage, slight turbidity or precipitation of a slight precipitate is possible,that does not affect the therapeutic effectiveness of the drug.

    Before use, the contents of the vial should be shaken.

    Effect on the ability to drive transp. cf. and fur:Care should be taken when carrying out potentially dangerous activities requiring increased concentration of attention and speed of psychomotor reactions (including driving, working with driving mechanisms, dispatcher and operator work).
    Form release / dosage:Drops for oral administration.
    Packaging:

    To 20, 50 or 100 ml in bottles of dark glass with a dropper and a screw cap with the control of the first autopsy. Each vial with the instruction for use is placed in a cardboard box.

    Storage conditions:

    At a temperature of no higher than 25 ° C.

    Keep out of the reach of children.

    Shelf life:

    2 years.

    Use within 4 weeks after first opening the vial.

    Do not use after the expiration date.

    Terms of leave from pharmacies:Without recipe
    Registration number:LP-000094
    Date of registration:21.12.2010 / 13.01.2016
    Expiration Date:Unlimited
    The owner of the registration certificate:Bayer Konsyumer Kare AGBayer Konsyumer Kare AG Switzerland
    Manufacturer: & nbsp
    Representation: & nbspBAYER, AOBAYER, AO
    Information update date: & nbsp18.10.2017
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