Odeston tab. 200mg # 50

Release form, composition and packaging

Tablets from white to white with a yellowish sheen, round, flat-cylindrical, beveled and engraved on one side with the letters Ch".

1 tab.

hymecromone 200 mg

potato starch - 45 mg, gelatin - 3 mg, sodium lauryl sulfate - 1 mg, magnesium stearate - 1 mg.

10 pieces.

- blisters (2) - cardboard packs.

10 pieces.

- blisters (5) - cardboard packs.

10 pieces.

- blisters (10) - cardboard packs.

pharmachologic effect

Choleretic drug.

Increases the formation and secretion of bile.

It has a selective spasmolytic effect on the bile ducts and the sphincter of Oddi.

The drug does not reduce gastrointestinal motility and blood pressure.

Reduces stagnation of bile, prevents the crystallization of cholesterol and thus the development of cholelithiasis.

Pharmacokinetics

Absorption and distribution

After oral administration, it is rapidly absorbed from the gastrointestinal tract.

Cmax in the blood after oral administration is achieved in 2-3 hours. Poorly binds to plasma proteins.

Withdrawal

T1 / 2 is about 1 hour. It is excreted in the urine: about 93% - in the form of glucuronate, 1.4% - in the form of sulfonate, 0.3% - unchanged.

Indications for use

- dyskinesia of the biliary tract and the sphincter of Oddi in the hyperkinetic type

- non-calculous chronic cholecystitis, cholangitis, cholelithiasis

- condition after surgical interventions on the gallbladder and biliary tract

- decreased appetite, nausea, constipation, vomiting (against the background of bile hyposecretion).

Contraindications for use

- obstruction of the biliary tract

- renal failure

- liver failure

- ulcerative colitis

- Crohn's disease

- peptic ulcer of the stomach and duodenum

- hemophilia

- children and adolescents up to 18 years old

- hypersensitivity to drug components.

Dosage regimen

The drug is taken orally 30 minutes before meals.

Adults are prescribed 200-400 mg 3 times / day.

The daily dose is 1200 mg.

The course of treatment is 2 weeks.

If you miss a dose, you should take the drug as soon as possible.

If the next dose is approaching, do not take the missed dose.

Do not take a double dose of the drug to compensate for the missed dose.

Overdose

Currently, no cases of overdose of the drug Odeston have been reported.

Side effect

From the digestive system: diarrhea, flatulence, abdominal pain, ulceration of the gastrointestinal mucosa.

Others: allergic reactions, headache.

Drug interactions

With the simultaneous use of morphine, which causes spasm of the sphincter of Oddi, weakens the effect of Odeston.

With the simultaneous use of Odeston with metoclopramide, a mutual weakening of the action is noted.

Odeston enhances the effects of indirect anticoagulants.

Application during pregnancy and lactation

There is no data on the safety of the use of gimecromone during pregnancy and lactation.

The appointment of Odeston during pregnancy and lactation (breastfeeding) is permissible only in cases where the intended benefit to the mother outweighs the potential risk to the fetus or child.

Special instructions Special precautions for the destruction of unused medicinal product

Medicines should not be disposed of via wastewater or household waste containers.

Ask your pharmacist how to dispose of unused product.

These activities will help protect the environment.

Influence on the ability to drive vehicles and use mechanisms

The drug does not affect the ability to drive vehicles and engage in other potentially hazardous activities that require increased concentration of attention and speed of psychomotor reactions.

Name ENG

ODESTON

Clinical and pharmacological group

A drug with choleretic and antispasmodic action

ATX code

Hymecromone

Dosage

200mg

Structure

1 tablet contains: hymecromone 200 mg.

Excipients: potato starch - 45 mg, gelatin - 3 mg, sodium lauryl sulfate - 1 mg, magnesium stearate - 1 mg.

Storage conditions and periods

At a temperature not higher than 25 degrees.

Expiration date: 3 years

INN / Active ingredient

hymecromone

Specifications

Category

Choleretic

Scope of the drug

Leather

Release form

Tablet

Manufacturer country

Poland

Package quantity, pcs

fifty

Way of introduction

Through the mouth

Vacation conditions

Without recipe

Brand name

PHARMACEUTICAL WORKS POLFA in Pabianice

The amount of the dosage form in the primary package

10 pieces.

Primary packaging type

Blister

Type of consumer packaging

Pack of cardboard

Pharmaco-therapeutic group

Choleretic agent

Anatomical and therapeutic characteristics

A05AX02 Hymecromon

Dosage form

Pills

Dosage (volume) of the substance in the preparation

200 mg

Expiration date in days

1095

Package weight, g

25

Mode of application

:

The drug is taken orally 30 minutes before meals. < br> Adults are prescribed 200-400 mg 3 times / day.

The daily dose is 1200 mg.

The course of treatment is 2 weeks. < br> If you miss a dose, you should take the drug as soon as possible.

If the next dose is approaching, do not take the missed dose.

Do not take a double dose of the drug to compensate for the missed dose.

"