Multizan® Ferrum 12
Composition

Chelated complex of iron bisglycinate (calculated as elemental iron 12 mg).

Pharmaceutical form

Dispersible tablets.

Properties of components

A chelated form of iron bisglycinate in Multizan® Ferrum’s composition is a highly effective and digestible iron as a part of the chelated complex. Due to the chelated form, the mineral more easily penetrates through the intestinal wall and is absorbed without disturbing the mineral and ionic balance of a cell. Iron in the form of a chelated complex is characterized by high bioavailability, excellent tolerance and safety. It does not irritate the gastric mucosa, does not cause constipation and nausea, does not stain tooth enamel, does not cause a metallic taste in the mouth. Iron bisglycinate does not interrupt the absorption of other minerals and nutrients due to an ionically neutral molecule.

No harmful or allergenic excipients are used in Multizan® Ferrum, therefore, it can be used in pediatrics.

Cocoa allergy is an exception, as a natural cocoa flavor is used for dispersible tablets.

Description

Multizan® Ferrum 12 is used as an additional source of iron to maintain the function of the hematopoietic system, immune and nervous systems, in case of deficiency and an increased need for iron. It is recommended as a complex therapy in all cases of iron deficiency: iron deficiency anemia, latent iron deficiency, as well as the primary and secondary prevention of iron deficiency.

Route of administration

For children from 4 to 15 years to cover normal physiological needs for iron: 1 tablet per day orally, chewing or swallowing whole, taking with water or juice.

To correct iron deficiency, the dose and duration of administration are individually determined by a doctor, depending on the severity of anemia.

If you cannot swallow a tablet or prefer a liquid form, you can dissolve the tablet in water.

1. Put Multizan® Ferrum’s dispersible tablet in a teaspoon or tablespoon.

2. Add a few milliliters of water.

3. Shake carefully to dissolve the tablet.

When suspension is obtained, the dose is ready for administration.

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