Rutacid chewable tablets 500 mg, 20 pcs. (Hydrotaltsyt)

Release form

Chewable tablets



packaging 20 pcs

Pharmacological action

Rutacid has an antacid effect.

Pharmacodynamics

Hydrotalcite has a layered network with a low content of aluminum and magnesium. The release of aluminum and magnesium ions occurs gradually depending on the pH of the gastric juice. The drug provides fast and long-term neutralization of hydrochloric acid while maintaining a pH close to normal. It has a protective effect on the gastric mucosa. Reduces the proteolytic activity of pepsin, binds bile acids.

Pharmacokinetics

The release of magnesium and aluminum ions occurs gradually in the stomach, depending on the pH value. Absorption of the drug occurs in the small intestine. After oral administration, the content of magnesium and aluminum ions in the blood plasma temporarily increases, but penetration into the nervous and bone tissue does not occur (with normal renal function). The absorbed portion is excreted by the kidneys.

Indications

acute gastritis, chronic gastritis with increased secretory function in the exacerbation phase

acute and chronic duodenitis

gastric ulcer and duodenal ulcer

reflux esophagitis

relieves pain and relieves alcohol, medication.

Contraindications

Hypersensitivity to hydrotalcite in children (up to 6 years).

Precautions: chronic renal failure, hypophosphatemia.

Use during pregnancy and lactation

There is no confirmed data on the undesirable effects of hydrotalcite during pregnancy and breastfeeding. The use of the drug during pregnancy is possible if the potential benefit to the mother outweighs the potential risk to the fetus. The drug does not pass into breast milk, so breastfeeding women can take the drug.

Composition

1 tablet contains:

Active ingredient: hydrotalcite 500 mg

Excipients: mannitol - 836 mg sodium saccharinate - 0.6 mg carboxymethyl starch sodium - 12 mg talc - 35 mg magnesium stearate - 14 mg mint flavor - 2.4 mg.

Dosage and administration

Inside, chewing thoroughly.

Adults and children over 12 years of age: 1-2 tablets 1 hour after meals 3-4 times a day and at bedtime.

Children from 6 to 12 years: 1 tablet 2 times a day.

Treatment should be continued for 4 weeks.

Side effects

When taking the drug, side effects are rare. Allergic reactions, diarrhea, belching are possible.

Drug Interaction

Rutacid® reduces absorption of tetracycline antibiotics, fluoroquinolocins, cytoproxylacin, cytoproxolacin, cytoproxolacin, cytoproxolacin

Storage Conditions

At a temperature not exceeding 30 ° C.

Deystvuyushtee substance

Gidrotaltsit

Terms and conditions

without prescription

dosage form

lozenges

Possible product names

RUTACID 0.5 N20 ZHEV TABL

Rutatsid 500mg Tab. chewing X20

RUTACID 500MG. No. 20 TAB.ZHEV. / KRKA /

Rutacid chewable 500mg x 20

Rutacid tab chewable 500mg N20

KRKA d.d. New Town AO, Slovenia



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