GenESA Disease Interactions
There are 3 disease interactions with GenESA (arbutamine).
Dobutamine/arbutamine (applies to GenESA) arrhythmias
Major Potential Hazard, High plausibility. Applicable conditions: Hypertension
Dobutamine and arbutamine produce stimulation of the beta receptors of the heart. The use of these agents has been associated with an increase in heart rate, ventricular ectopy, atrial fibrillation, hypertension, enhanced A-V conduction, and arrhythmias. Therapy with dobutamine or arbutamine should be administered cautiously in patients with cardiac conduction disorders.
Dobutamine/arbutamine (applies to GenESA) hypotension
Major Potential Hazard, High plausibility. Applicable conditions: Dehydration
The use of dobutamine and arbutamine has been infrequently associated with significant hypotension especially in dehydrated patients secondary to beta-2 mediated vasodilation. Hypovolemia should be corrected before administering dobutamine or arbutamine. Blood pressure and ECG should be monitored at regular intervals. Monitoring of cardiac output and pulmonary wedge pressure may also be desired.
Dobutamine/arbutamine (applies to GenESA) IHSS
Major Potential Hazard, High plausibility. Applicable conditions: Hypertrophic Cardiomyopathy
The use of dobutamine or arbutamine is contraindicated in patients with idiopathic hypertrophic subaortic stenosis (IHSS). Dobutamine or arbutamine may increase the pressure gradient within the left ventricle and thereby worsen cardiac output in patients with IHSS.
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GenESA drug interactions
There are 68 drug interactions with GenESA (arbutamine).
GenESA alcohol/food interactions
There is 1 alcohol/food interaction with GenESA (arbutamine).
Drug Interaction Classification
Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. | |
Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. | |
Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. | |
No interaction information available. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.