Compound:
active ingredient: polymethylsiloxane xerogel;
1 capsule contains polymethylsiloxane xerogel 0.32 g;
excipients: gelatin, titanium dioxide (E 171).
Dosage form. Capsules for oral use.
Basic physical and chemical properties: hard gelatin capsules, white body and cap. The contents of the capsules are white or almost white powder, odorless.
Pharmacotherapeutic group.
Enterosorbents. Code ATX A07B C
Pharmacological properties.
Pharmacodynamics.
When used internally, it has a detoxifying effect. The drug effectively adsorbs medium-molecular toxic substances, products of incomplete metabolism, from the contents of the intestine and blood (through the capillary membranes of the villi of the intestinal mucosa), and promotes the excretion of incorporated radionuclides. Enterosgel ExtraCaps eliminates the manifestations of toxicosis, improves the function of the intestines, liver, kidneys, and normalizes blood and urine counts. As an effective detoxifier, Enterosgel ExtraCaps helps improve immunity.
Pharmacokinetics.
The drug envelops the mucous membrane of the stomach and intestines, protecting it from erosive processes. Not absorbed from the intestines.
Clinical characteristics.
Indications.
As part of complex detoxification therapy for chronic renal failure, which is caused by pyelonephritis, polycystic kidney disease, nephrolithiasis; for toxic hepatitis, viral hepatitis A and B, hepatocholecystitis, liver cirrhosis and cholestasis of various etiologies, gastritis with low acidity, enterocolitis, colitis, diarrhea; in case of poisoning with alcohol and drugs; allergic reactions, skin diseases (diathesis, neurodermatitis); with burn intoxication; purulent-septic processes, which are accompanied by intoxication; toxicosis of pregnant women in the first half of pregnancy, in complex therapy of intestinal dysbiosis.
Contraindications.
Acute intestinal obstruction.
Individual intolerance to the components of the drug.
Interaction with other drugs and other types of interactions.
Provided that the method of administration is followed (Enterosgel ExtraCaps and medications are taken separately), the drug can be used in complex therapy with other medications and prophylactics, including bacterial preparations (bifidum-, lactobacilli), herbal remedies, adaptogens, and immunomodulators. Concomitant use with drugs belonging to the class of bile acid sequestrants, such as cholestyramine, is not recommended, due to the increased risk of constipation.
The drug should not be used in conjunction with silver preparations.
Features of application.
The drug should be taken in accordance with the recommendations set out in this instruction.
Use during pregnancy or breastfeeding.
The drug is used during pregnancy or breastfeeding. Use should be limited in pregnant women prone to constipation.
The ability to influence the reaction rate when driving vehicles or other mechanisms.
Does not affect.
Method of administration and dose.
Take 1-2 capsules orally 2-3 times a day, 1.5-2 hours before or 2 hours after meals or medications, with a sufficient amount of water. For adults and children over 14 years of age, a single dose of the drug is 1-2 capsules, a daily dose is 6 capsules. For children from 6 to 14 years old, a single dose is 1 capsule, a daily dose is 3 capsules.
The course of treatment is from 7 to 14 days. In severe forms of the disease, a double single dose is used during the first 3 days, and in the chronic course of the disease (chronic renal failure, cirrhosis of the liver), longer use of the drug is possible.
Children.
The drug can be used in children from 6 years of age. To make it easier to swallow, before use, you can first open the capsule (single dose) and mix it with a small amount of liquid.
Overdose.
Exceeding the maximum single dose does not cause adverse reactions.
Adverse reactions.
When you first take the drug, short-term constipation is possible. To prevent it, for people prone to constipation, in the first two days of taking the drug, a cleansing enema at night or taking laxatives (lactulose, sodium picosulfate) is recommended.
Possible manifestations of individual intolerance to the components of the drug.
Best before date. 3 years.
Storage conditions.
In the original packaging at a temperature not exceeding 25 ° C, out of the reach of children.
Package.
7 capsules in a blister. 1, 2 or 4 blisters are placed in a cardboard box.
Vacation category. Over the counter.
Manufacturer.
PrJSC EOF KREOMA-PHARM.
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