Universal reference book for medicines
Product name: BELLACEHOL ® (BELLACEHOL)

Active substance: Belladonna, non appropriate

Type: The drug with cholagogue and antispasmodic effect

Manufacturer: ФАРМЦЕНТР ВИЛАР (Russia)
Composition, form of production and packaging
The tablets covered with a cover of
yellow color, biconvex form.

1 tab.

the amount of alkaloids krasavki 150 mcg

tanacecole (containing the sum of flavonoids and phenol carboxylic acids in terms of lutein and dry matter 50%) 50 mg

Excipients: lactose, potato starch, calcium stearate, aerosil A-380.

Sheath composition: sugar, gelatin, aerosil A-380, magnesium hydroxycarbonate, titanium dioxide, tropeolin-O.

10 pieces.
- packings cellular planimetric (3) - packs cardboard.
30 pcs.
- packings of cellular contour (1) - packs cardboard.
30 pcs.
- banks of dark glass (1) - packs of cardboard.
INSTRUCTION FOR THE SPECIALIST.

Description of the drug approved by the manufacturer for the printed edition of 2008.

PHARMACHOLOGIC EFFECT

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.
PHARMACOKINETICS

Data on the pharmacokinetics of Bellacezol preparation are not available.

INDICATIONS

As part of complex therapy:

- exacerbation of chronic gastritis and / or gastroduodenitis (including with frost-ulcerative changes);

- peptic ulcer of the stomach and duodenum, combined with chronic cholecystitis, hypomotor dyskinesia of bile ducts.

DOSING MODE

Inside, 1 tab.
3 times / day, for 20-30 minutes before meals. If necessary and with good tolerability, an increase in the daily dose to 6 tablets is possible. Duration is determined by the doctor individually and, as a rule, is 3-4 weeks.
SIDE EFFECT

Possible: allergic reactions, dry mouth.

When used in high doses: a violation of accommodation, difficulty urinating.

CONTRAINDICATIONS

- glaucoma;

- prostate adenoma;

- Tachyarrhythmia;

- thyrotoxicosis;

- heart failure;

- stenosis of the pylorus;

- cholelithiasis;

- Pregnancy;

- lactation period (breastfeeding);

- children and adolescence under 18;

- Hypersensitivity to the components of the drug.

APPLICATION FOR CHILDREN

Contraindication - children and adolescence under 18 years.

OVERDOSE

Symptoms: dry mouth, thirst, constipation, palpitations, mydriasis, transient visual impairment, photophobia, skin hyperemia, intestinal atony, urinary retention, headache, dizziness, fever;
in rare cases - psychomotor agitation, convulsions.
Treatment: gastric lavage, symptomatic therapy.

DRUG INTERACTION

Weaken the effect of m-cholinomimetics and anticholinesterase drugs.

TERMS OF RELEASE FROM PHARMACY

The drug is released by prescription.

TERMS AND CONDITIONS OF STORAGE

List B. The drug should be stored out of reach of children, dry, protected from light at a temperature of no higher than 25 ° C.
Shelf life - 2 years.
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