Gaviscon dual action chewable tablets 24 pieces

Composition

1 tablet contains:

active ingredients: 250 mg sodium alginate, 106.5 mg sodium bicarbonate, 187.5 mg calcium carbonate;

excipients: macrogol 20000, mannitol (E 421), copovidone, acesulfame potassium, aspartame (E 951), mint flavoring J8696, carmoisine (E 122), magnesium stearate, xylitol DC.

Release form

Chewable tablets.

Pharmacodynamics. The drug is a combination of two antacids (calcium carbonate, sodium bicarbonate) and sodium alginate, which has an adsorbing and enveloping effect. After administration, the drug quickly reacts with gastric acid, forming a layer of alginic acid gel, which has an almost neutral pH value and covers the walls of the stomach, effectively preventing the occurrence of reflux. In severe cases, the gel layer, distributed over the surface of the stomach contents, rises into the esophagus and prevents its irritation.

Calcium carbonate neutralizes stomach acid and provides rapid relief from indigestion and heartburn. This effect is enhanced by sodium bicarbonate, which also has a neutralizing effect. The total neutralizing capacity of the product at a minimum dose of 10 ml is about 10 mEq H ^+.

Pharmacokinetics. The mechanism of action of the drug is physical and does not depend on absorption into the systemic bloodstream.

Treatment of reflux symptoms associated with the acidity of stomach contents that flows back into the esophagus, such as acid regurgitation, heartburn, indigestion, for example, after eating or during pregnancy.

Hypersensitivity (allergy) to any component of the drug.

The medicine is intended for oral use.

Gaviscon Double Action, tablets. Tablets should be chewed thoroughly. Adults and children over 12 years of age: 2-4 tablets after meals and at bedtime, up to 4 times a day.

Elderly patients: No dose adjustment is required for this age group.

Gaviscon Double Action, suspension. Adults and children over 12 years of age – 10-20 ml (2-4 teaspoons) after meals and before bedtime, up to 4 times a day. Shake before use. Dose should not be adjusted for elderly patients.

Each 4 tablets of the drug contain 221.5 mg (9.64 mmol) of sodium, and each 10 ml of suspension contains 127.25 mg (5.53 mmol) of sodium. This should be taken into account in patients on a highly controlled salt diet, for example in some cases of congestive heart failure and renal failure.

Each 4 tablets contain 300 mg (7.5 mmol) of calcium, and each 10 ml of suspension contains 130 mg (3.25 mmol) of calcium. The drug should be used with caution in patients with hypercalcemia, nephrocalcinosis and recurrent formation of calcium-containing kidney stones.

Gaviscon Double Action contains aspartame, which is a source of phenylalanine. Therefore, the product may be dangerous for patients with phenylketonuria.

Gaviscon Double Action tablets contain carmoisine (E 122), which may cause allergic reactions.

Gaviscon Double Action, suspension contains methyl parahydroxybenzoate (E 218) and propyl parahydroxybenzoate (E 216), which may cause allergic reactions (possibly delayed).

Gaviscon Double Action tablets contain xylitol, which may have a laxative effect. The energy value of 1 g of xylitol is 2.4 kcal.

If symptoms do not improve after 7 days of treatment, the clinical situation should be reviewed.

Use during pregnancy and breastfeeding. Gaviscon Double Action does not affect the course of pregnancy, intrauterine and postnatal development of the child. The drug can be used during pregnancy and breastfeeding.

Ability to influence the reaction rate when driving vehicles or working with other mechanisms. The drug does not affect the ability to drive vehicles and work with mechanisms.

Children: Not recommended for use in children under 12 years of age.

Overdose is very rare and may manifest as discomfort and a feeling of bloating in the abdomen.

In case of overdose, it is necessary to discontinue use of the drug and conduct symptomatic therapy.

Very rarely (1/10,000) in patients with hypersensitivity to the components of the drug, an allergic reaction may occur in the form of urticaria, bronchospasm, anaphylactic or anaphylactoid reactions.

Taking large amounts of calcium carbonate may lead to alkalosis, hypercalcemia, acid reflux, milk-base syndrome, or constipation. These symptoms usually occur when the recommended dose is exceeded.

Due to the presence of calcium carbonate, which acts as an antacid, it is necessary to maintain a 2-hour interval between taking Gaviscon dual action and other medications, especially H2-histamine receptor blockers, tetracyclines, digoxin, fluoroquinolone, iron salts, ketoconazole, neuroleptics, thyroxine, penicillamine, β-adrenoceptor blockers (atenolol, metoprolol, propranolol), corticosteroids, chloroquine and diphosphonates.

In the original packaging at a temperature not exceeding 30 °C. Do not store the suspension in the refrigerator or freeze.