Included in the formulation
АТХ:B.06.A.C.01 C1-inhibitor based on plasma
Pharmacodynamics:It blocks the pathway of the complement system by inactivating the enzymatically active components C1s and C1r, forming complexes in a stoichiometric structure of 1: 1. Inhibits the blood coagulation factor XIIa. Also inhibits plasma kallikrein.
Pharmacokinetics:After intravenous administration, the maximum concentration in the blood plasma is reached after 7-10 minutes.
The half-life is 36 hours. In children, the half-life is 33 hours.
Indications:It is used to treat acute attacks with hereditary angioedema edema of types I and II.
III.D80-D89.D84.1 Defect in the complement system
Contraindications:Individual intolerance, children under 2 years old.
Carefully:Propensity to allergic reactions.
Pregnancy and lactation:Recommendations for FDA - Category C. It is used for life indications.
Dosing and Administration:Intravenously slow to 20 IU / kg.
The highest daily dose: 20 IU / kg.
The highest single dose: 20 IU / kg.
Side effects:The cardiovascular system: rarely - tachycardia, hot flashes, hypertension, development of thrombosis.
Allergic reactions.
Overdose:Cases of overdose are not described.
Treatment is symptomatic.
Interaction:Not described.
Special instructions:With the tendency of patients to allergic reactions, it is recommended to premedicate with glucocorticosteroids and antihistamines before administration of the drug.