Clinical and pharmacological group: & nbsp

Other Metabolites

Included in the formulation
  • Sodium adenosine triphosphate
    solution in / in 
  • Sodium adenosine triphosphate
    solution in / in 
    ELLARA, LTD.     Russia
  • VIAL, LLC     Russia
  • АТХ:

    C.01.E.B   Other drugs for the treatment of heart disease

    Pharmacodynamics:

    Suppression of automatism sinoarthriasis and Purkinje fibers (blockade of Ca2+channels and an increase in permeability for K+). Improves metabolism and energy supply of tissues.

    Pharmacokinetics:

    After parenteral administration, it penetrates into the cells of the organs, where it is split into adenosine and inorganic phosphate with energy release.

    Indications:

    Muscular dystrophy and atony, poliomyelitis, multiple sclerosis; pigmentary degeneration of the retina; diseases of peripheral vessels (intermittent claudication, Raynaud's disease, thromboangiitis obliterans); suppression of paroxysms of supraventricular tachycardia, ischemic heart disease; weakness of labor.

    I.A80-A89.A80   Acute poliomyelitis

    VI.G35-G37.G35   Multiple sclerosis

    VI.G70-G73.G71.0   Muscular dystrophy

    VII.H30-H36.H31.1   Degeneration of the choroid

    IX.I20-I25.I20   Angina pectoris [angina pectoris]

    IX.I30-I52.I47.1   Nadzheludochkovaya tachycardia

    IX.I70-I79.I73.0   Raynaud's syndrome

    IX.I70-I79.I73.1   Obliterating thromboangitis [Berger's disease]

    IX.I70-I79.I73.9   Peripheral vascular disease, unspecified

    XV.O60-O75.O62   Violations of labor [of the clan]

    Contraindications:

    Hypersensitivity, acute myocardial infarction, arterial hypotension, inflammatory lung diseases.

    Carefully:

    Joint reception of cardiac glycosides.

    Pregnancy and lactation:

    Adequate and well-controlled studies in humans and animals have not been conducted. There is no information on the penetration into breast milk.

    Category of recommendations for FDA is not defined.

    Dosing and Administration:With supraventricular paroxysmal tachycardia: intramuscular, intravenous or intra-arterial. In the first days of treatment - intramuscularly 10 mg (1 ml of 1% solution) once a day, then in the same dose 2 times a day or 20 mg once a day. The course of treatment is 30-40 injections, a second course in 1-2 months.

    For arresting supraventricular arrhythmias: intravenously 10-20 mg for 5-6 seconds, re-introduction after 2-3 min.

    Side effects:

    With intramuscular injection: headache, tachycardia, an increase in diuresis, hyperuricemia are possible.

    With intravenous administration: nausea, hyperemia of the facial skin, headache, weakness are possible.

    Allergic reactions: rarely - itching, skin hyperemia.

    Overdose:

    Not described.

    Treatment is symptomatic.

    Interaction:

    Cardiac glycosides - increase the risk of side effects (including increase the arrhythmogenic effect).

    Special instructions:

    In comparison with verapamil it quickly restores the normal rhythm in the treatment of supraventricular paroxysmal tachycardia, however, trifosadenin has more side effects (ventricular ectopies and a general feeling of discomfort).

    Compared with adenosine phosphate (6.6 mg trifosadenina equivalent 3.8 mg adenosine phosphate) is also effective and safe in the treatment of paroxysmal supraventricular tachycardia, however adenosine phosphate gives a more stable effect.

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