Clinical and pharmacological group: & nbsp

Immunosuppressive drugs

Included in the formulation
АТХ:

L.04.A   Immunosuppressive drugs

Pharmacodynamics:

Assume the inhibition of sulfhydryl enzyme systems.It is believed that gold preparations suppress the immune response, disrupting the maturation and function of macrophages and T-lymphocytes, against their background, the concentrations of immunoglobulins and rheumatoid factor decrease. As a result, the inflammation of the synovium in the active stage of rheumatoid arthritis is suppressed. In vitro inhibition of prostaglandin synthesis.

Pharmacokinetics:

The connection with plasma proteins is high. Biotransformation in the liver has not been studied, the drug does not decompose to elemental gold. Half-life long, depends on the dose and duration of therapy. Elimination of the kidneys 60-90% (slowly), with faeces 10-40%.

Indications:

Rheumatoid arthritis, juvenile rheumatoid arthritis, psoriatic arthritis.

XIII.M05-M14.M06.9   Rheumatoid arthritis, unspecified

XIII.M05-M14.M06.8   Other specified rheumatoid arthritis

XIII.M05-M14.M06.0   Seronegative rheumatoid arthritis

XIII.M05-M14.M06   Other rheumatoid arthritis

XIII.M05-M14.M05.9   Seropositive rheumatoid arthritis, unspecified

XIII.M05-M14.M05.8   Other seropositive rheumatoid arthritis

XIII.M05-M14.M05.3   Rheumatoid arthritis with involvement of other organs and systems

XIII.M05-M14.M05   Seropositive rheumatoid arthritis

XIII.M05-M14.M08.0   Juvenile rheumatoid arthritis

Contraindications:

Hypersensitivity, polyvalent allergy, anemia, pancytopenia, impaired renal function, severe liver damage, active form of pulmonary tuberculosis, collagenosis (systemic lupus erythematosus, nodular periarteritis, scleroderma, dermatomyositis), ulcerative colitis complicated forms of diabetes mellitus, pregnancy, breast-feeding.

Carefully:

Children under 18 years. Elderly age, renal and hepatic insufficiency.

Pregnancy and lactation:

Category of recommendations FDA C.

Qualitative and well-controlled studies on humans have not been conducted. Has a teratogenic effect in animals. Do not apply! Gold penetrates into breast milk. Violations are not registered. Do not apply!

Dosing and Administration:

Deeply intramuscular. Saturation period: 2 injections per week, 1 to 3 injections are administered 10 mg each, from the 4th to the 6th injection 20 mg, from the 7th injection either twice a week 50 mg each, or once a week, 100 mg. This dose should be maintained until the clinical effect is achieved, but not exceeding the total dose of 1600 mg (maximum 2000 mg). The period of maintenance therapy: 100 mg of the drug once a month or 50 mg once every 2 weeks.This treatment can last for months and years. Children are prescribed 0.7-1 mg / kg per week until the saturation phase is reached. In the phase of maintenance therapy, the drug is administered at a dose of 1 mg / kg 1-2 times per month.

Side effects:

In the period of active therapy: tachyarrhythmia, ECG changes in the type of myocardial ischemia, skin rash, headache, fever, decreased blood pressure, nausea, abdominal pain. During maintenance therapy: stomatitis, alopecia, proteinuria (rarely nephrotic syndrome), liver dysfunction, cholestasis, disorders of hemopoiesis (thrombocytopenia, leukopenia, anemia), photosensitivity, dermatitis, skin itching.

Overdose:

Severe side effects.

Treatment is symptomatic. With serious dermatitis, stomatitis, pulmonary and other manifestations - glucocorticoids (10-100 mg / day), dimercaprol.

Interaction:

Penicillamine - an increased risk of developing serious hematologic and renal side effects, joint use is contraindicated.

Means that inhibit hematopoiesis, hepatotoxic and nephrotoxic drugs - enhance the toxic effects of gold preparations.

Special instructions:

It is not recommended to be used in combination with aminoquinolines, d-penicillamine, small immunosuppressants, sulfasalazine.

Instructions
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