Tenoten children's tablets No. 40




Instructions for Tenoten children's tablets No. 40
Composition
active ingredient: 1 tablet contains antibodies to brain-specific protein S-100 affinity purified: a mixture of homeopathic dilutions C12, C30 and C50 – 3 mg;
excipients: lactose monohydrate, microcrystalline cellulose, magnesium stearate.
Dosage form
Pills.
Main physicochemical properties: flat-cylindrical tablets, with a score and a bevel, white to almost white in color. One flat side is scored, the other flat side is marked TENOTEN KID.
Pharmacotherapeutic group
Homeopathic medicine.
Pharmacological properties
The drug exhibits a calming, anti-anxiety (anxiolytic) effect, without causing undesirable hypnogenic and muscle relaxant effects. Improves tolerance to psycho-emotional stress. Has stress-protective, nootropic, anti-amnestic, anti-hypoxic, neuroprotective, anti-asthenic, antidepressant effects.
In conditions of intoxication, hypoxia, and in conditions after acute cerebral circulation disorders, it has a neuroprotective effect, limits the area of damage in the central nervous system (CNS), and improves learning and memory processes.
Inhibits lipid peroxidation processes.
Modifies the functional activity of the S-100 protein, which connects synaptic (informational) and metabolic processes in the brain. Has a GABA-mimetic and neurotrophic effect, increases the activity of stress-limiting systems, and promotes the restoration of neuronal plasticity processes.
Indication
Neurotic and neurosis-like disorders accompanied by increased excitability, irritability, anxiety, behavioral and attention disorders, and autonomic disorders.
Contraindication
Increased individual sensitivity to the components of the drug. Children under 3 years of age.
Interaction with other medicinal products and other types of interactions
No cases of interaction with other drugs have been identified.
Application features
The drug is used in pediatric practice. It is used in children aged 3 years and older. The drug contains lactose, therefore it is not recommended for patients with congenital galactosemia, glucose or galactose malabsorption syndrome, and congenital lactase deficiency.
Due to the presence of an activating component in the preparation, the last dose should be taken no later than 2 hours before bedtime.
Ability to influence reaction speed when driving vehicles or other mechanisms
The drug is used for children.
Use during pregnancy or breastfeeding
The safety of the drug in pregnant and lactating women has not been studied.
The drug is used for children.
Method of administration and doses
The drug is taken orally. Do not take the drug with food.
The dosage and duration of treatment are determined by the doctor individually depending on the nature and course of the disease.
A single dose for children aged 3 and over is 1–2 tablets. Keep the tablet in your mouth (without chewing or swallowing) until it dissolves completely.
If necessary, the tablet can be dissolved in a small amount (1 tablespoon) of boiled water at room temperature.
Take 1 tablet 1–3 times a day for 1–3 months. If necessary, the course of treatment can be extended to 6 months or repeated after 1–2 months.
If there is no sustained improvement in the condition within 3–4 weeks of starting treatment, you should consult a doctor.
Children
The drug is used in children aged 3 to 18 years.
Overdose
In case of accidental overdose, dyspeptic manifestations are possible, due to the excipients included in the preparation.
Adverse reactions
Reactions of increased individual sensitivity to the components of the drug are possible.
Expiration date
3 years.
Do not use the drug after the expiration date indicated on the package.
Storage conditions
Store at a temperature not exceeding 25 °C.
Keep out of reach of children.
Packaging
20 tablets in a blister, 2 blisters in a cardboard box.
Vacation category
Without a prescription.
Producer
Santonica CJSC.
Location of the manufacturer and its business address
St. Waveryu 134B, Kaunas, Kaunas sam., LT-46353, Lithuania.
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