Sodium adenosintriphosphate-Vial (Solution) Instructions for Use
Marketing Authorization Holder
Vial, LLC (Russia)
Manufactured By
NORTH CHINA PHARMACEUTICAL GROUP FORMULATION, Co., Ltd. (China)
ATC Code
C01EB10 (Adenosine)
Active Substance
Triphosadenine (DCF accepted for use in France)
Dosage Form
| Sodium adenosintriphosphate-Vial | Solution for intravenous administration 10 mg/1 ml: amp. 5 pcs. |
Dosage Form, Packaging, and Composition
| Solution for intravenous administration | 1 amp. |
| Triphosadenine (sodium adenosinetriphosphate) | 10 mg |
1 ml – ampoules (10) – cardboard packs.
Clinical-Pharmacological Group
Drug improving metabolism of the myocardium, used for paroxysmal supraventricular tachyarrhythmias
Pharmacotherapeutic Group
Metabolic agent
Pharmacological Action
A means of improving metabolism and energy supply to tissues. ATP is a natural component of body tissues and is involved in many metabolic processes.
When ATP breaks down into ADP and inorganic phosphate, energy is released, which is necessary for muscle contraction and various biochemical processes.
ATP is involved in the transmission of excitation in adrenergic and cholinergic synapses and facilitates the transmission of excitation from the vagus nerve to the heart.
Apparently, ATP is one of the mediators that excite adenosine receptors. It enhances cerebral and coronary circulation and promotes an increase in peripheral circulation.
Triphosadenine is a derivative of adenosine.
Adenosine is an agonist of purinergic receptors, the activation of which leads to the inhibition of depolarization of the processes of conduction of electrical impulses in the sinus and AV nodes.
This effect underlies the antiarrhythmic action of triphosadenine in supraventricular tachycardias. It acts briefly for a few seconds.
Pharmacokinetics
After parenteral administration, it penetrates into the cells of organs, where it is broken down into adenosine and inorganic phosphate with the release of energy. Subsequently, the breakdown products are included in the resynthesis of ATP.
Indications
Relief of paroxysms of supraventricular tachycardia (excluding atrial fibrillation and/or flutter).
ICD codes
| ICD-10 code | Indication |
| I47.1 | Supraventricular tachycardia |
| ICD-11 code | Indication |
| BC81.0 | Ectopic atrial tachycardia |
| BC81.1 | Nodal ectopic tachycardia |
| BC81.20 | CTI [cavotricuspid isthmus]-dependent atrial tachycardia by "macro re-entry" mechanism |
| BC81.21 | Atrial tachycardia by "macro re-entry" mechanism not associated with scar or cavotricuspid isthmus |
| BC81.2Z | Atrial tachycardia by "macro re-entry" mechanism, unspecified |
| BC81.5 | Sinoatrial reentrant tachycardia |
| BC81.7Z | Atrioventricular reentrant tachycardia, unspecified |
| BC81.8 | Atrioventricular nodal reentrant tachycardia |
| BC81.Z | Supraventricular tachyarrhythmia, unspecified |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Administer intravenously as a rapid bolus injection over 1-2 seconds.
For adult patients, use an initial dose of 10 mg (1 ml).
If the first dose is ineffective, administer a second dose of 20 mg (2 ml) after 1-2 minutes.
Do not exceed a single dose of 20 mg.
Inject directly into a large peripheral vein or a rapidly flowing intravenous infusion line.
Follow each injection with a rapid saline flush to ensure delivery to the systemic circulation.
Continuously monitor electrocardiogram (ECG) and blood pressure during and after administration.
Discontinue the drug immediately upon termination of the supraventricular tachycardia.
Use only in a setting with resuscitation equipment and personnel trained in its use.
This drug is not intended for pediatric use or for maintenance therapy.
Adverse Reactions
With intramuscular administration, headache, tachycardia, increased diuresis, hyperuricemia are possible.
With intravenous administration, nausea, facial skin hyperemia, headache, weakness are possible.
Allergic reactions rarely – itching, skin hyperemia.
Contraindications
Acute myocardial infarction, severe arterial hypotension, severe bradycardia, sick sinus syndrome, second- or third-degree AV block (except in patients with an artificial pacemaker), acute and chronic heart failure in the stage of decompensation, COPD, bronchial asthma, long QT syndrome, pregnancy, breastfeeding period, age under 18 years, hypersensitivity to triphosadenine.
With caution
Bradycardia, first-degree AV block, bundle branch block, atrial fibrillation and flutter, arterial hypotension, coronary artery disease, hypovolemia, pericarditis, heart valve stenosis, left-to-right arteriovenous shunt, cerebrovascular insufficiency, conditions after heart transplantation (less than 1 year).
Use in Pregnancy and Lactation
Contraindicated for use during pregnancy and breastfeeding.
Pediatric Use
Contraindicated for use in children and adolescents under 18 years of age.
Geriatric Use
Use with caution in elderly patients.
Special Precautions
Simultaneous use of triphosadenine and cardiac glycosides in high doses is not recommended.
Drug Interactions
With simultaneous use with cardiac glycosides, the risk of side effects (including arrhythmogenic action) increases.
Storage Conditions
Store at 2°C (36°F) to 8°C (46°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical Disclaimer