Cerebrum compositum H solution for injection ampoule 2.2 ml No. 5

Instructions Cerebrum compositum H solution for injection ampoule 2.2 ml No. 5

Composition

active substances: 2.2 ml of solution contain: Acidum phosphoricum D10 - 22 mg, Aconitum napellus D6 - 22 mg, Aesculus hippocastanum D4 - 22 mg, Ambra grisea D10 - 22 mg, Anamirta cocculus D4 - 22 mg, Arnica montana D28 - 22 mg, Bothrops lanceolatus D10 - 22 mg, Cerebrum suis D8 - 22 mg, Cinchona pubescens D4 - 22 mg, Conium maculatum D4 - 22 mg, Embryo totalis suis D10 - 22 mg, Gelsemium sempervirens D4 - 22 mg, Hepar suis D10 - 22 mg, Hyoscyamus niger D6 - 22 mg, Kalium bichromicum D8 - 22 mg, Kalium phosphoricum D6 - 22 mg, Magnesium phosphoricum D10 - 22 mg, Manganum phosphoricum D8 - 22 mg, Medorrhinum Nosode D13 - 22 mg, Placenta totalis suis D10 - 22 mg, Ruta graveolens D4 - 22 mg, Selenium D10 - 22 mg, Semecarpus anacardium D6 - 22 mg, Strychnos ignatii D8 - 22 mg, Sulfur D10 - 22 mg, Thuja occidentalis D6 - 22 mg;

Excipients: sodium chloride, water for injections.

Dosage form

Solution for injection.

Main physicochemical properties: clear, colorless, odorless solution, practically free from particles.

Pharmacotherapeutic group

A complex homeopathic preparation.

Pharmacological properties

Pharmacodynamics

Not determined for homeopathic preparations.

Indication

Comprehensive treatment of diseases of the nervous system of functional and organic origin: increased mental tension, irritability, neurotic reactions, states after physical and mental exhaustion; symptoms of anxiety and motor anxiety; concussion, encephalopathies of various origins; psychoses, withdrawal syndrome and alcoholic delirium; mental and physical development delay in children, neuroses, depressions; neurocirculatory dystonia, post-stroke condition, arteriosclerosis; cerebral palsy, Parkinson's disease, multiple sclerosis, memory disorders, including geriatric changes.

Contraindication

Hypersensitivity to any component of the drug, to plants of the Asteraceae family. Hypersensitivity to quinine.

Interaction with other medicinal products and other types of interactions

Compatible with other medications.

Application features

If symptoms persist or worsen, you should consult a doctor.

Ability to influence reaction speed when driving vehicles or other mechanisms

Does not affect.

Use during pregnancy or breastfeeding

The toxicity of the homeopathically diluted substances included in this medicinal product during pregnancy and breastfeeding has not been established.

No adverse reactions were reported.

The question of the appropriateness of using the drug for pregnant and breastfeeding women is decided by the doctor individually, taking into account the benefit/risk.

Method of administration and doses

Single dose: adults and children over 12 years old - 2.2 ml, children from 3 to 6 years old - 1 ml, from 6 to 12 years old - 1.5 ml. Apply a single dose 1-3 times a week in the form of intramuscular, subcutaneous, intradermal, intravenous (jet) injections, as well as into acupuncture points.

The course of treatment is 3-6 weeks.

Children

The drug is recommended for use in children from 3 years of age.

Overdose

It was not noted.

Adverse reactions

In rare cases, hypersensitivity reactions are possible, including skin rashes, fever, itching, and changes at the injection site.

Expiration date

5 years.

The expiration date determines the use of the drug until the last day of the month.

Storage conditions

Store in the original packaging at a temperature not exceeding 25 °C, out of the reach of children.

Packaging

5 ampoules of 2.2 ml in a cardboard box.

Vacation category

According to the recipe.

Producer

Biological Heilmittel Heel GmbH/Biologische Heilmittel Heel GmbH.

Location of the manufacturer and its business address

Dr. Reckeweg-Str. 2-4, 76532 Baden-Baden, Germany/Dr. Reckeweg-Str. 2-4, 76532 Baden-Baden, Germany.