Coenzyme compositum solution for injection in ampoules 2.2 ml No. 5

Instructions for use Coenzyme Compositum solution for injection in ampoules 2.2 ml No. 5

Composition

active substances: 2.2 ml of solution contain: Acidum alpha-ketoglutaricum D8 - 22 mg, Acidum ascorbicum D6 - 22 mg, Acidum cis-aconicum D8 - 22 mg, Acidum citricum D8 - 22 mg, Acidum fumaricum D8 - 22 mg, Acidum malicum D8 - 22 mg, Acidum succinicum D8 - 22 mg, Acidum thiocticum D6 - 22 mg. mg, Nadidum D8 – 22 mg, Natrium diethyloxalaceticum D6 – 22 mg, Natrium pyruvicum D8 – 22 mg, Natrium riboflavinum phosphoricum D6 – 22 mg, Nicotinamidum D6 – 22 mg, Pulsatilla pratensis D6 – 22 mg, Pyridoxinum hydrochloricum D6 – 22 mg, Sulfur D10 – 22 mg, Thiaminum hydrochloricum D6 – 22 mg;

Excipients: sodium chloride, water for injections.

Dosage form

Solution for injection.

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

Pharmacotherapeutic group

A complex homeopathic preparation.

Pharmacological properties

Pharmacodynamics

The drug activates and regulates the enzyme systems of the Krebs cycle, eliminates tissue hypoxia, has a metabolic, antioxidant, detoxification effect, and improves the course of reparative processes. The action of the drug is based on the activation of the body's defenses and the normalization of impaired functions due to substances of plant and mineral origin that are part of the drug.

Indication

In the complex treatment of acute and chronic diseases of any origin and localization; convalescence after infectious diseases; physical and mental exhaustion; impaired absorption of vitamins.

Contraindication

Hypersensitivity to any component of the drug.

Interaction with other medicinal products and other types of interactions

The drug is compatible with other medications.

Application features

If symptoms persist or worsen, consult a doctor. The drug should be administered with caution to patients with hypersensitivity to vitamin B1. Taking into account the course of the disease and the patient's condition, the doctor may change the duration of the course of treatment and the method of administration.

Ability to influence reaction speed when driving vehicles or other mechanisms

Cases of exposure are unknown.

Use during pregnancy or breastfeeding

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: children aged 3 to 6 years - 1 ml, adults and children over 6 years - 2.2 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.

In case of complicated diseases, a single age-appropriate dose should be used for 3 consecutive days and then 2 times a week.

The course of treatment is 2 to 5 weeks.

Children

The drug is recommended for use in children aged 3 years and older.

Overdose

It was not noted.

Adverse reactions

In rare cases, allergic reactions are possible, including skin rashes, 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.

Keep out of reach of children.

Packaging

5 ampoules of 2.2 ml in a cardboard box.

Vacation category

According to the recipe.

Producer

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.