Lymphomyosot H solution for injection ampoule 1.1 ml No. 5

Instructions Lymphomyosot H solution for injection ampoule 1.1 ml No. 5

Composition

active ingredients:

1.1 ml of solution contains: Araneus diadematus D6 - 0.55 mg, Calcium phosphoricum D12 - 0.55 mg, Equisetum hiemale D4 - 0.55 mg, Ferrum iodatum D12 - 1.1 mg, Fumaria officinalis D4 - 0.55 mg, Gentiana lutea D5 - 0.55 mg, Geranium robertianum D4 - 1.1 mg, Levothyroxinum D12 - . mg;

Excipients: sodium chloride, water for injections.

Dosage form

Solution for injection.

Main physicochemical properties: transparent, colorless, odorless solution.

Pharmacotherapeutic group

A complex homeopathic preparation.

Pharmacological properties

Pharmacodynamics

The drug has a detoxifying, anti-exudative, immunocorrective, anti-inflammatory effect, which is based on the activation of the body's defenses and the normalization of its functions.

Pharmacokinetics

Not determined for homeopathic preparations.

Indication

Inflammatory and dystrophic processes of various localization (mainly in lymphatic vessels and nodes), allergic diseases.

Contraindication

Hypersensitivity to any component of the drug. The possibility of using the drug for thyroid diseases is determined by the doctor.

Interaction with other medicinal products and other types of interactions

Unknown.

Application features

If symptoms of the disease persist for more than 7 days from the start of treatment or new ones appear, you should stop using the medicine and consult a doctor.

At the beginning of treatment with the drug, a short-term exacerbation of existing symptoms of the disease (primary reaction) is possible. In this case, the drug should be discontinued and a doctor should be consulted.

This medicinal product contains less than 1 mmol (23 mg) sodium/dose, i.e. essentially 'sodium-free'.

Ability to influence reaction speed when driving vehicles or other mechanisms

Unknown.

Use during pregnancy or breastfeeding

Cases of negative effects are unknown. The possibility of use is determined by the doctor if the benefit of using the drug outweighs the potential risk to the fetus/child.

Method of administration and doses

Single dose: adults and children over 6 years old – 1.1 ml. Apply 1–3 times a week as intramuscular, subcutaneous, intravenous injections.

In acute cases – 1 ampoule daily for 3–5 days.

Treatment course: 3–6 weeks.

The possibility of using the drug for more than 7 days depends on the severity and course of the disease and is determined by the doctor individually.

Children

The medicine is recommended for use in children aged 6 years and over.

Overdose

It was not noted.

Adverse reactions

In rare cases, hypersensitivity reactions (or anaphylactic reactions) may occur, as well as changes at the injection site, nausea, dizziness, loss of consciousness, sweating, facial flushing, and general weakness.

In rare cases, skin hypersensitivity reactions may occur, including itching, urticaria, erythema, edema, or dryness.

If any adverse reactions occur, discontinue use of the drug and consult a doctor.

Expiration date

5 years.

Storage conditions

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

Packaging

5 ampoules of 1.1 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.