This information is for educational purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional.
OTC
Adenocor
3 mg/ml, Roztwór do wstrzykiwań
INN: Adenosinum
Data updated: 2026-04-11
Available in:
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Form
Roztwór do wstrzykiwań
Dosage
3 mg/ml
Route
—
Storage
—
About This Product
User Reviews
Reviews reflect personal experiences and are not medical advice. Always consult your doctor.
Manufacturer
InPharm Sp. z o.o.
ATC Code
C01EB10
Source
URPL
Pharmacotherapeutic group: Other Cardiac Preparations, ATC code: C01EB 10
Endogenous nucleoside with peripheral vasodilator / antiarrhythmic effect
Mechanism of action
Adenosine is a potent vasodilator in most vascular beds, except in renal afferent arterioles and hepatic veins where it produces vasoconstriction. Adenosine exerts its pharmacological effects through activation of purine receptors (cell-surface A
1
and A
2
adenosine receptors). Although the exact mechanism by which adenosine receptor activation relaxes vascular smooth muscle is not known, there is evidence to support both inhibition of the slow inward calcium current reducing calcium uptake, and activation of adenylate cyclase through A
2
receptors in smooth muscle cells. Adenosine may reduce vascular tone by modulating sympathetic neurotransmission. The intracellular uptake of adenosine is mediated by a specific transmembrane nucleoside transport system. Once inside the cell, adenosine is rapidly phosphorylated by adenosine kinase to adenosine monophosphate, or deaminated by adenosine deaminase to inosine. These intracellular metabolites of adenosine are not vasoactive.
Pharmacodynamic effects
Intracoronary Doppler flow catheter studies have demonstrated that intravenous Adenoscan at 140 µg/kg/min produces maximum coronary hyperaemia (relative to intracoronary papaverine) in approximately 90% of cases within 2 – 3 minutes of the onset of the infusion. Coronary blood flow velocity returns to basal levels within 1 – 2 minutes of discontinuing the Adenoscan infusion.
The increase in blood flow caused by Adenoscan in normal coronary arteries is significantly more than that in stenotic arteries. Adenoscan redirects coronary blood flow from the endocardium to the epicardium and may reduce collateral coronary blood flow thereby inducing regional ischaemia.
Continuous infusion of adenosine in man has been shown to produce a mild dose-dependent fall in mean arterial pressure and a dose-related positive chronotropic effect, most likely caused by sympathetic stimulation. The onset of this reflex increase in heart rate occurs later than the negative chronotropic/dromotropic effect. This differential effect is mostly observed after bolus injection thus explaining the potential use of adenosine as a treatment for supraventricular arrhythmias when administered as a bolus or as a coronary vasodilator when administered as an infusion
.
Although Adenoscan affects cardiac conduction, it has been safely and effectively administered in the presence of other cardioactive or vasoactive drugs such as beta-adrenergic blocking agents, calcium channel antagonists, nitrates, ACE inhibitors, diuretics, digitalis or anti-arrhythmics.
Paediatric population
Literature review identified three studies where intravenous adenosine infusion was used in conjunction with radionuclide myocardial perfusion imaging at a dose of 0.14 mg/kg body weight/min for 2 – 4 minutes in paediatric patients aged 1 month to 18 years. The largest study included 47 patients aged 1 month to 18 years of age and reported 87% sensitivity (CI 52 – 97%) and 95% specificity (CI 79 – 99%) for cardiovascular magnetic resonance imaging under pharmacological stress with intravenous adenosine in a dose of 0.14 mg/kg/min for 3 minutes. No adverse events were reported in the study.
However, the currently available data is considered very limited to support the use of adenosine for diagnostic purposes in the paediatric population.
⚠️ Warnings
See section 4.2
The product is for single use only.
The product should be inspected visually for particulate matter and colouration prior to administration. Where the visual appearance of the product may have changed, the vial should be discarded.
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.