Bellacceol® (Bellacehol®)

Composition Pharmacodynamics Indications Carefully Contraindications Dosing and Administration Side effects Form release / dosage
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Composition:
Composition per one tablet:
Active substances:
Tanaceol® dry extract - 0.05 g (tansy of ordinary flowers extract dry) (with the content of the sum of flavonoids and phenol carboxylic acids inrecalculated for luteolin and dry matter 50%)
The belladonna the sum of alkaloids is 0.00015 g
(in terms of 100% of the substance)
Excipients (core):
Lactose (milk sugar) - 0.04785 g
Potato starch - 0.02000 g
Calcium stearate -0.00100 g
Silicon dioxide - 0.00100 g of colloid (Aerosil A-380)
The mass of the core of the tablet is 0.12 g
Auxiliary substances (shell):
Refined sugar (sucrose) 0.0909492 g
Gelatin - 0.0003483 g
Silicon dioxide - 0.0011458g
colloid (aerosil A-380)
Magnesium hydroxycarbonate - 0.01662525 g
pentahydrate (magnesium carbonate basic)
Titanium dioxide 0.001145 8 g
Tropeolin 0 - 0.0000254 g
Beeswax - 0.000133 g
Weight of the tablet coated with 0.23 g
shell
Description:Tablets are round, covered with a shell, biconvex form of yellow color.
Pharmacotherapeutic group:Peptic ulcer treatment of plant origin
ATX: & nbsp
  • The sum of alkalolides of belladonna
    • Pharmacodynamics:Combined drug. Has antiulcer action due to vagal blockade of gastric secretion with spasmolytic, analgesic and reparative action. Normalizes the functional activity of the liver - stimulates bile secretion, improves the biochemical composition of bile.
    Indications:Bellaccehol ® is used in the complex therapy of patients with exacerbation of chronic gastritis and / or gastroduodenitis (including erosive and ulcerative changes), peptic ulcer of the stomach and duodenum, combined with chronic cholecystitis, hypomotor dyskinesia of bile ducts.
    Contraindications:Hypersensitivity to the components of the drug. Glaucoma, prostatic hyperplasia, tachyarrhythmia, thyrotoxicosis, heart failure, stenosis of the gatekeeper, cholelithiasis, pregnancy, breastfeeding, lactation period, children under 18.
    Pregnancy and lactation:The use is contraindicated.
    Dosing and Administration:Inside 1-2 tablets 3 times a day for 20-30 minutes before meals. The duration of treatment is determined by the doctor and is, as a rule, 3-4 weeks. Repeated courses of treatment are possible. Higher doses for adults are single - 4 tablets, daily - 12.
    Side effects:Allergic reactions, dry mouth. When used in high doses - a violation of accommodation, difficulty urinating.
    Overdose:
    With hypersensitivity or overdose of the drug, allergic reactions are possible, dry mouth,thirst, constipation, palpitation, dilated pupils, transient visual impairment. Photophobia. Hyperemia of the skin, intestinal atony, urinary retention, headache, dizziness, fever; in rare cases - psychomotor agitation, convulsions.
    First aid: gastric lavage, symptomatic therapy.
    Interaction:Weakens the effect of M-cholinomimetics and anticholinesterase agents.
    Form release / dosage:The tablets covered with a cover.
    Packaging:For 10 or 30 tablets in a planar cell package. 3 contour cell packs No. 10 or 1 contour pack No. 30 together with the instruction for use are placed in a pack of cardboard.
    Storage conditions:
    In a dry, protected from light place at a temperature of no higher than 25 ° C.
    Keep out of the reach of children.
    Shelf life:

    2 years. Do not use after the expiration date.

    Terms of leave from pharmacies:On prescription
    Registration number:LS-001423
    Date of registration:25.08.2009 / 04.04.2012
    Expiration Date:Unlimited
    The owner of the registration certificate:FARMTSENTR VILAR, ZAO FARMTSENTR VILAR, ZAO Russia
    Manufacturer: & nbsp
    Information update date: & nbsp21.01.2017
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