Motherwort extract tablets 14mg, No. 20

• Increased nervous irritability,

• neurasthenia,

• insomnia,

• cardiopsychoneurosis.

Inside. Adults and children over 12 years old take 1 tablet 3-4 times a day. The course of treatment is selected individually, taking into account the course of the disease.

Active ingredient: motherwort herb extract (motherwort extract dry) - 14.0 mg.

Excipients: sucrose (white sugar) - 149.8 mg, potato starch - 29.4 mg, talc - 4.8 mg, calcium stearate - 2.0 mg

• Increased individual sensitivity to the components of the drug,

• hereditary fructose intolerance,

• glucose-galactose malabsorption,

• deficiency of sucrase-isomaltase,

• peptic ulcer of the stomach and duodenum in the acute phase,

• pregnancy,

• breastfeeding period,

• children under 12 years of age.

Trade name: Motherwort extract

Dosage form: tablets

Composition for one tablet.

Active ingredient: motherwort herb extract (motherwort extract dry) - 14.0 mg.

Excipients: sucrose (white sugar) - 149.8 mg, potato starch - 29.4 mg, talc - 4.8 mg, calcium stearate - 2.0 mg

Description: tablets are round, biconvex, light brown, interspersed from almost white to dark brown.

Pharmacotherapeutic group:

Herbal sedative.

ATX code: [N05CM]

Pharmacological properties:

Has a calming effect, reduces the frequency and increases the strength of heart contractions, exhibits hypotensive properties. By the nature of the action, it is close to valerian preparations.

Indications for use

• Increased nervous irritability,

• neurasthenia,

• insomnia,

• cardiopsychoneurosis.

Contraindications

• Increased individual sensitivity to the components of the drug,

• hereditary fructose intolerance,

• glucose-galactose malabsorption,

• deficiency of sucrase-isomaltase,

• peptic ulcer of the stomach and duodenum in the acute phase,

• pregnancy,

• breastfeeding period,

• children under 12 years of age.

Application during pregnancy and during breastfeeding

The use of the drug during pregnancy is contraindicated. If it is necessary to use the drug during lactation, you should stop breastfeeding.

Method of administration and dosage

Inside. Adults and children over 12 years old take 1 tablet 3-4 times a day. The course of treatment is selected individually, taking into account the course of the disease.

Side effects

Allergic reactions, dyspepsia are possible.

Overdose

To date, no cases of overdose have been reported. If the recommended doses are exceeded, dose-dependent side effects may increase. Treatment is symptomatic.

Interaction with other medicinal products

Compatible with other sedative and cardiological drugs; enhances the effect of hypnotics and analgesics.

Influence on the ability to drive vehicles and mechanisms

During the period of treatment, care should be taken when driving vehicles and engaging in other potentially hazardous activities that require increased concentration of attention and speed of psychomotor reactions.

Release form

Tablets of 14 mg. 10 tablets in a blister strip packaging.

3, 4, 5 blister packs, together with instructions for use, are placed in a box made of cardboard box.

Contoured cell packs, together with an equal number of instructions for use, are placed in a group pack.

Contoured cell packs, together with an equal number of instructions for use, are placed in a group pack 'For hospitals'.

Storage conditions

In a dark place at a temperature not exceeding 25 ? C.

Keep out of the reach of children.

Shelf life

2 years. Do not use after the expiration date indicated on the package.

Vacation conditions

Available without a prescription.

Name and address of the manufacturer / organization accepting claims:

JSC 'Pharmstandard-Tomskkhimfarm', 634009, Russia, Tomsk, Lenin Avenue,

d. 211, tel./fax: (3822) 40-28-56, www.pharmstd.ru