Drug Interactions between dobutamine and sulfur hexafluoride
This report displays the potential drug interactions for the following 2 drugs:
- dobutamine
- sulfur hexafluoride
Interactions between your drugs
DOBUTamine sulfur hexafluoride
Applies to: dobutamine and sulfur hexafluoride
MONITOR: Stress echocardiography with dobutamine can mimic an ischemic episode and increase the risk of rare but serious cardiopulmonary reactions associated with the use of sulfur hexafluoride and other ultrasound contrast agents. These reactions typically occur within 30 minutes of contrast administration, and the risk is increased in patients with cardiovascular instability such as recent acute coronary syndrome, unstable ischemia, evolving or ongoing myocardial infarction, angina at rest within last 7 days, recent coronary artery intervention, recent deterioration of ECG or laboratory/clinical findings, acute cardiac failure, Class III/IV cardiac failure, or severe rhythm disorders.
MANAGEMENT: Sulfur hexafluoride may be used during stress echocardiography with dobutamine in patients who are in stable condition verified by the absence of chest pain or ECG modification during the two preceding days. However, vital signs, ECG, and blood pressure monitoring are recommended during and for at least 30 minutes after sulfur hexafluoride administration. Use of sulfur hexafluoride in patients with cardiovascular instability should only be undertaken after careful risk/benefit assessment and with close monitoring. Sulfur hexafluoride should not be used under circumstances where dobutamine is considered contraindicated.
References (2)
- Cerner Multum, Inc. "UK Summary of Product Characteristics."
- MHRA. Medicines and Healthcare Regulatory Agency (2014) SonoVue (sulphur hexafluoride). http://www.mhra.gov.uk/Safetyinformation/Safetywarningsalertsandrecalls/Safetywarningsandmessagesformedicines/Monthlylistsofinformationforhealthcareprofessionalsonthesafetyofmedic
Drug and food interactions
DOBUTamine food
Applies to: dobutamine
MONITOR: Coadministration of two or more sympathomimetic agents may increase the risk of adverse effects such as nervousness, irritability, and increased heart rate. Central nervous system (CNS) stimulants, particularly amphetamines, can potentiate the adrenergic response to vasopressors and other sympathomimetic agents. Additive increases in blood pressure and heart rate may occur due to enhanced peripheral sympathetic activity.
MANAGEMENT: Caution is advised if two or more sympathomimetic agents are coadministered. Pulse and blood pressure should be closely monitored.
References (7)
- Rosenblatt JE, Lake CR, van Kammen DP, Ziegler MG, Bunney WE Jr (1979) "Interactions of amphetamine, pimozide, and lithium on plasma norepineophrine and dopamine-beta-hydroxylase in schizophrenic patients." Psychiatry Res, 1, p. 45-52
- Cavanaugh JH, Griffith JD, Oates JA (1970) "Effect of amphetamine on the pressor response to tyramine: formation of p-hydroxynorephedrine from amphetamine in man." Clin Pharmacol Ther, 11, p. 656
- (2001) "Product Information. Adderall (amphetamine-dextroamphetamine)." Shire Richwood Pharmaceutical Company Inc
- (2001) "Product Information. Tenuate (diethylpropion)." Aventis Pharmaceuticals
- (2001) "Product Information. Sanorex (mazindol)." Novartis Pharmaceuticals
- (2001) "Product Information. Focalin (dexmethylphenidate)." Mikart Inc
- (2002) "Product Information. Strattera (atomoxetine)." Lilly, Eli and Company
Therapeutic duplication warnings
No warnings were found for your selected drugs.
Therapeutic duplication warnings are only returned when drugs within the same group exceed the recommended therapeutic duplication maximum.
See also
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.
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