$36.00
Manufacturer: Germany
In the treatment of lymphadenitis, a lymphangitis, limfatice; postoperative and post-traumatic edema; allergic disease; consequences of long-term action of endo-and exotoxins (physical factors, chemical agents, biological factors, including tonsillogenic and tuberculosis intoxication).
Description
LIMFOMIOZOT SOLUTION 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 – 0.55 mg, Myosotis arvensis D3 – 0.55 mg, Nasturtium officinale D4 – 1.1 mg, Natrium sulfuricum D4 – 0.55 mg, Pinus sylvestris D4 – 0.55 mg, Scrophularia nodosa D3 – 0.55 mg, Smilax D6 – 0.55 mg, Teucrium scorodonia D3 – 0.55 mg, Veronica officinalis D3 – 0.55 mg
Excipients: sodium chloride, water for injection.
LIMFOMIOZOT SOLUTION DOSAGE FORM
Injection.
LIMFOMIOZOT SOLUTION MAIN PHYSICAL AND CHEMICAL PROPERTIES:
clear, colorless, odorless liquid.
LIMFOMIOZOT SOLUTION PHARMACOLOGICAL GROUP
Complex homeopathic medicine.
PHARMACOLOGICAL PROPERTIES
Pharmacological.
The drug has a detoxification, anti-exudative, immunocorbing, anti-inflammatory effect, which is based on the activation of the body’s defenses and the normalization of its functions.
Pharmacokinetics.
Not defined for homeopathic remedies.
INDICATIONS
Inflammatory and dystrophic processes of various localization (mainly in the lymphatic vessels and nodes), allergic diseases.
CONTRAINDICATIONS
Hypersensitivity to the components of the drug. The possibility of using the drug for diseases of the thyroid gland is decided with the preliminary consultation of a doctor.
INTERACTION WITH OTHER DRUGS AND OTHER INTERACTIONS
Unknown.
FEATURES OF APPLICATION
If symptoms persist or the condition worsens, you should consult your doctor.
APPLICATION DURING PREGNANCY OR BREASTFEEDING
Cases of negative influence are unknown.
ABILITY TO INFLUENCE THE RATE OF REACTION WHEN DRIVING A VEHICLE OR OTHER MECHANISMS
Unknown.
DOSAGE AND APPLICATION
Single dose: adults and children over 6 years old – 1.1 ml. Apply 1-3 times a week in the form of intramuscular, subcutaneous, intradermal and intravenous injections, as well as in acupuncture points or orally (dissolve a single dose in 50 ml of water and drink during the day, holding for a few seconds in the mouth). In acute cases – 1 ampoule daily for 3-5 days.
The course of treatment is 3-6 weeks.
CHILDREN
The drug is recommended for use in children over 6 years of age.
OVERDOSE
Not noted.
ADVERSE REACTIONS
In rare cases, hypersensitivity reactions (or anaphylactic reactions) may occur, as well as changes at the injection site, nausea, dizziness, dizziness, loss of consciousness, sweating, facial flushing, general weakness.In very rare cases, hypersensitivity skin reactions may occur, including pruritus, erythema, edema, or dryness.
SHELF LIFE
5 years.
The expiration date determines the use of the drug until the last day of the month.
STORAGE CONDITIONS
Store in its original packaging at a temperature not exceeding 25 ° C.
Keep out of the reach of children!
INCOMPATIBILITY
Unknown.
PACKAGE
5 (5×1), 10 (5×2), 100 (5×20) ampoules of 1.1 ml in a cardboard box.
HOLIDAY CATEGORY
On prescription.
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