Smecta por d/susp d/orally orange 3 g pack/pack cards x10


Compound

Powder for oral suspension (orange)1 sachet
active substance:
dioctahedral smectite3 g
excipients:
orange flavor - 0.01 g; vanilla flavoring - 0.05 g; dextrose monohydrate - 0.679 g; sodium saccharinate - 0.021 g
Powder for oral suspension (vanilla)1 sachet
active substance:
dioctahedral smectite3 g
excipients:
vanillin - 0.004 g; dextrose monohydrate - 0.749 g; sodium saccharinate - 0.007 g

Pharmacodynamics

The drug is an aluminosilicate of natural origin and has an adsorbing effect. Stabilizes the mucous barrier of the gastrointestinal tract, forms polyvalent bonds with mucus glycoproteins, increases its quantity, improves cytoprotective properties (regarding the negative effects of hydrogen ions of hydrochloric acid, bile salts, microorganisms and their toxins). It has selective sorption properties, which are explained by its discoid-crystalline structure; adsorbs bacteria and viruses located in the lumen of the gastrointestinal tract. In therapeutic doses it does not affect intestinal motility. Diosmectite is radiolucent and does not stain stool. Aluminum in smectite is not absorbed from the gastrointestinal tract, incl. for gastrointestinal diseases accompanied by symptoms of colitis and colonopathy.

Buy Smecta powder for the preparation of oral suspension Vanilla 3g No. 10 in pharmacies

Smecta por. d/susp.internal Vanilla 3g No. 10

Release form, composition and packaging Powder for the preparation of suspension for oral administration (vanilla) from grayish-white to light grayish-yellow color, from a weak non-specific to a weak vanilla odor.

1 pack dioctahedral smectite 3 g Excipients: vanillin - 4 mg, dextrose monohydrate - 749 mg, sodium saccharinate - 7 mg.

3.76 g - laminated paper bags (10) - cardboard packs. 3.76 g - laminated paper bags (30) - cardboard packs. Pharmacological action Antidiarrheal drug, is an aluminosilicate of natural origin. Has an adsorbing effect.

Stabilizes the mucous barrier of the gastrointestinal tract, forms polyvalent bonds with mucus glycoproteins, increases the amount of mucus and improves its cytoprotective properties (with respect to the negative effects of hydrogen ions of hydrochloric acid, bile salts, microorganisms and their toxins).

It has selective sorption properties, which are explained by its discoid-crystalline structure; adsorbs bacteria and viruses located in the lumen of the gastrointestinal tract.

Smecta® in therapeutic doses does not affect intestinal motility.

Diosmectite is radiolucent and does not stain stool.

Aluminum in the composition of diosmectite is not absorbed from the gastrointestinal tract, incl. for gastrointestinal diseases accompanied by symptoms of colitis and colonopathy. Pharmacokinetics Smecta® is not absorbed. It is excreted from the body unchanged. Indications: acute and chronic diarrhea (allergic, drug origin; in violation of the diet and quality of food);

— diarrhea of ​​infectious origin (as part of complex therapy);

- symptomatic treatment of heartburn, bloating and abdominal discomfort and other symptoms of dyspepsia accompanying diseases of the gastrointestinal tract. Dosage regimen Acute diarrhea

Adults are recommended to use 6 sachets per day.

Children under 1 year of age - 2 sachets/day for 3 days, then 1 sachet/day; children over 1 year old - 4 sachets/day for 3 days, then 2 sachets/day.

Other indications

Adults are prescribed 3 sachets/day.

Children under the age of 1 year - 1 sachet/day, at the age of 1-2 years - 1-2 sachets/day; over 2 years - 2-3 sachets/day.

A course of treatment of 3-7 days is recommended.

For esophagitis, Smecta® should be taken orally after meals, for other indications - between meals.

Rules for taking the drug

For adults, dissolve the contents of the sachets in 1/2 cup of water, gradually pouring in the powder and stirring it evenly. The prescribed dose is distributed into 3 doses during the day.

For children, the contents of the sachets are dissolved in a baby bottle (50 ml) and distributed into several doses throughout the day or mixed with some semi-liquid product (porridge, puree, compote, baby food). Side effects From the digestive system: in clinical studies, rarely - constipation (mild, went away after adjusting the dose of the drug).

Allergic reactions: in routine practice, very rarely - urticaria, rash, itching, Quincke's edema. Contraindications for use: intestinal obstruction;

- fructose intolerance, glucose-galactose malabsorption syndrome;

- sucrase-isomaltase deficiency;

- hypersensitivity to the components of the drug. Use during pregnancy and lactation The drug Smecta® is approved for use during pregnancy and lactation according to indications. No dosage adjustment is required. Use in children Use in children is possible according to the dosage regimen. Special instructions Use with caution in patients with a history of severe chronic constipation.

For adults, therapy with Smecta® in combination with rehydration measures is prescribed if necessary.

A set of rehydration measures is prescribed depending on the course of the disease, age and characteristics of the patient.

The interval between taking Smecta and other medications should be 1-2 hours.

Use in pediatrics

In children with acute diarrhea, the drug should be used in conjunction with rehydration measures.

Impact on the ability to drive vehicles and operate machinery

No information available. Overdose Possible severe constipation or bezoar. Drug interactions When used simultaneously, Smecta® may reduce the rate and extent of absorption of other drugs. It is not recommended to take the drug simultaneously with other medications. Conditions and periods of storage The drug should be stored out of the reach of children at a temperature not exceeding 25°C. Shelf life: 3 years. Conditions for dispensing from pharmacies The drug is approved for use as an over-the-counter product.

Directions for use and doses

Inside.

Acute diarrhea

Children, including infants:

up to 1 year - 2 sachets/day for 3 days, then - 1 sachet/day; over 1 year - 4 sachets/day for 3 days, then 2 sachets/day.

Adults:

The recommended dosage regimen is 6 sachets/day.

Other indications

Children, including infants:

up to 1 year - 1 sachet/day; 1–2 years – 1–2 sachets/day; over 2 years - 2-3 sachets/day.

Adults:

3 sachets/day.

A course of treatment of 3–7 days is recommended.

For esophagitis, Smecta® should be taken after meals, for other indications - between meals.

For children, the contents of the sachets are dissolved in a baby bottle (50 ml) and distributed into several doses throughout the day or mixed with some semi-liquid product (porridge, puree, compote, baby food). For adults, dissolve the contents of the sachets in 1/2 cup of water, gradually adding the powder and stirring it evenly. The prescribed dose is distributed into 3 doses during the day.

Smecta por d/susp d/orally orange 3 g pack/pack cards x10

Trade name: Smecta International name: Smectite dioctaedric

Release form: powder for suspension for oral administration 3 g (sachets)

Composition: diosmectite 3 g

Pharmacological group: antidiarrheal agent

Pharmacological group according to ATK: A07BC05 (Diosmectite)

Pharmacological action: absorbent, antidiarrheal, mucus-forming, analgesic. Antidiarrheal drug of natural origin, which has a protective effect on the mucous membrane of the stomach and intestines and has pronounced adsorbent properties. Smecta, being a mucosal barrier stabilizer, forms polyvalent bonds with mucus glycoproteins and increases its lifespan, forming a physical barrier that protects the mucous membrane of the digestive tract from the negative effects of H+ ions, hydrochloric acid, bile salts, microorganisms, their toxins and other irritants. Smecta has selective sorption properties, which are explained by its discoid-crystalline structure. Smecta in therapeutic doses does not affect intestinal motility.

Pharmacodynamics: The drug is of natural origin, has an adsorbing effect. Stabilizes the mucous barrier, forms polyvalent bonds with mucus glycoproteins, increases the amount of mucus, improves its gastroprotective properties (with respect to the negative effects of hydrogen ions HCl, bile salts, microorganisms and their toxins). It has selective sorption properties, which are explained by its discoid-crystalline structure, and adsorbs bacteria and viruses located in the lumen of the gastrointestinal tract. In therapeutic doses it does not affect intestinal motility.

Pharmacokinetics Smecta is not absorbed. It is excreted from the body unchanged.

Indications: – acute and chronic diarrhea in adults and children, – treatment of symptoms associated with esophagitis, gastroduodenitis and colon diseases. Diarrhea (allergic, drug-induced, poor diet and quality of food), gastritis, peptic ulcer of the stomach and duodenum, colitis, diarrhea of ​​infectious origin - as part of complex therapy.

Dosage regimen

Adults are prescribed 3 sachets per day for at least 3 days. For acute diarrhea, at the beginning of treatment the daily dose can be doubled. Before use, dissolve the contents of 1 sachet in half a glass of water. To obtain a homogeneous suspension, gradually pour the powder into the liquid, stirring it evenly. For esophagitis, it is preferable to take the drug after meals, in other cases - between meals. Children under 1 year of age are prescribed 1 sachet per day, from 1 to 2 years - 2 sachets per day, over 2 years - 2-3 sachets per day. The course of treatment is at least 3 days. The contents of the sachet are dissolved in a baby bottle for 50 ml of water and distributed into several doses throughout the day, or thoroughly mixed with some semi-liquid product: soup, porridge, compote, puree, baby food.

Side effect

In some cases: allergic reactions, constipation (as a rule, intestinal function is restored when the dose of the drug is reduced).

Contraindications Hypersensitivity, intestinal obstruction.

Pregnancy and lactation

It is possible to use the drug Smecta during pregnancy and lactation according to indications. Experimental studies have shown that the drug does not have a teratogenic effect.

special instructions

The patient should consult a doctor if symptoms do not improve within 7 days after taking the drug, as well as in cases where abdominal pain is accompanied by fever or vomiting. Smecta should not be prescribed simultaneously with other drugs. It is recommended to take any other medicine 1-2 hours before taking Smecta.

Overdose

Currently, no cases of overdose of Smecta have been reported.

Drug interactions

When used simultaneously, Smecta may reduce the rate and/or extent of absorption of other drugs.

Storage conditions and periods

The drug should be stored at a temperature not exceeding 25°C. Shelf life: 4 years. Conditions for dispensing from pharmacies The drug is approved for use as an over-the-counter product.

special instructions

It is recommended to maintain an interval of 1–2 hours between taking Smecta® and other drugs.

Use with caution in patients with a history of severe chronic constipation.

In children with acute diarrhea, the drug should be used in conjunction with rehydration measures. If necessary, adults can also be prescribed drug therapy in combination with rehydration measures.

A set of rehydration measures is prescribed depending on the course of the disease, age and characteristics of the patient.

Impact on the ability to drive a car and operate machinery.

No information available.

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