Transipeg - instructions for use, doses, side effects, contraindications

Excipients: sodium chloride 73 mg, sodium sulfate 284 mg, potassium chloride 37.5 mg, sodium hydrogen carbonate 84 mg, aspartame 3.75 mg, acesulfame potassium 3.75 mg, flavoring lemon * 51.5 mg.

Powder for solution for oral administration 5.9 g

1 sachet contains:

Active substance: macrogol 3350 5.9 g.

Excipients: sodium chloride 146 mg, sodium sulfate 568 mg, potassium chloride 75 mg, sodium hydrogen carbonate 168 mg, aspartame 7.5 mg, acesulfame potassium 7.5 mg, flavoring lemon * 103 mg.

* Ingredients of lemon flavor: maltodextrin 37.7%, sucrose 37.7%, lemon flavor 16.54%, acacia gum (E414) 1.4%, lecithin (E322) 0.8%, silicon dioxide (E551) 0, 2%.

Description:

White or almost white powder with yellow impregnations, with the smell of lemon.

Description of the prepared solution: colorless, opalescent solution with the smell of lemon.

Pharmacotherapeutic group:laxative

ATX: & nbsp

A.06.A.D.15 Macrogol

Pharmacodynamics:

The preparation contains macrogol 3350, which is not digested and not absorbed in the gastrointestinal tract. Macrogol 3350 has the ability to retain water, which dilutes stool and facilitates their evacuation, having an indirect effect on peristalsis, without causing an irritating effect.

The onset of action occurs 24-48 hours after admission.

Indications:

Symptomatic treatment of constipation.

Contraindications:

Hypersensitivity to macrogol or any of the excipients of the drug, intestinal obstruction, risk of perforation of the intestinal wall, severe colonic dilatation, severe inflammatory bowel disease (ulcerative colitis, Crohn's disease), abdominal pain of unknown origin, dehydration, chronic heart failure in decompensation, phenylketonuria (contains aspartame), intolerance to glucose, impaired absorption of glucose-galactose, or insufficiency of sucrase-isomaltose.

Pregnancy and lactation:

Given the absence of teratogenic effects in animals and absorption in the gut, during pregnancy and during breastfeeding, the drug may be administered only on the advice of a doctor and only if the potential benefit to the mother exceeds the potential risk to the fetus and the baby.

Dosing and Administration:

Adults: 1-2 bags per day at one time (preferably in the morning). The contents of the sachet are first dissolved: for 5.9 g in 100 ml of water (1/2 cup)

The maximum daily dose of 11.8 g (2 sachets of 5.9 grams).

Children: from 1 to 6 years 1-2 bags per day (preferably in the morning). The contents of the sachet are first dissolved: for 2.95 g and in 50 ml of water.

The maximum daily dose of 5.9 g (2 sachets of 2.95 g).

From 6 to 12 years 1-3 bags per day (preferably in the morning). The contents of the sachet are first dissolved: for 2.95 g in 50 ml of water.

The maximum daily dose of 8.85 g (3 sachets of 2.95 g). Use of the drug in a dose of 3 sachets of 2.95 g per day is possible only after consulting a doctor.

The course of self-treatment should not exceed 14 days. If you need a longer time, you need a doctor's consultation.

Side effects:

When the recommended doses are observed, the drug is well tolerated.

Allergic reactions: rash, skin itching, swelling of the skin and / or subcutaneous tissue;

On the part of the digestive system: abdominal pain, nausea, vomiting, flatulence, diarrhea.

Overdose:

Diarrhea disappearing within 24-48 hours after discontinuation of the drug; then treatment can continue in lower doses.

Interaction:Given the ability of the drug Transipeg® to slow the absorption of concomitantly prescribed drugs, it should be taken 2 hours after taking other drugs.

Special instructions:

If there is constipation, which can not be explained by a sedentary lifestyle, or which is accompanied by pain, fever, or other gastrointestinal symptoms, consult a doctor.

When taking the drug, it is necessary to follow additional measures in the treatment of constipation (including a sufficient intake of liquid, foods rich in vegetable fiber, physical activity, etc.).

The drug should be taken as short as possible, and if there is no improvement within two weeks, consult a doctor.

The preparation contains sodium. In the case of a salt-free diet with a limited intake of sodium, the sodium content should be taken into account (in a bag of 3.49 g contains 145 mg of sodium, in a sachet of 6.98 g contains 290 mg of sodium).

The preparation contains potassium, which should be taken into account when determining daily intake (in a bag of 3.49 g contains 20 mg of potassium, in a sachet of 6.98 g contains 40 mg of potassium).

The preparation contains aspartame, which is a source of phenylalanine.

Effect on the ability to drive transp. cf. and fur:

Does not affect.

Form release / dosage:

Powder for solution for oral administration, 2.95 g and 5.9 g.

Packaging:

3.49 g of the preparation (corresponding to 2.95 g of macrogol) or 6.98 g of the preparation (corresponding to 5.9 g of macrogol) are placed in sachets made of heat-sealable paper with laminated coating / aluminum / polyethylene.

By 2, 6, 10, 12, 20 or 30 bags (sachets), together with instructions for use, are placed in a cardboard pack.

Storage conditions:

At a temperature of no higher than 25 ° C.

Keep out of the reach of children.

Shelf life:

3 years.

Do not use after expiry date.

Terms of leave from pharmacies:Without recipe

Registration number:П N015894 / 01

Date of registration:24.06.2009 / 04.10.2016

Expiration Date:Unlimited

The owner of the registration certificate:BAYER, AO BAYER, AO Russia

Manufacturer: & nbsp

LAMP SAN PROSPERO, S.p.A. Italy

Laboratoires M.RICHARD France

Representation: & nbspBAYER, AOBAYER, AO

Information update date: & nbsp30.12.2016

Illustrated instructions

Instructions

Transipeg® (Transipeg®)