Drug Interactions between fexinidazole and landiolol
This report displays the potential drug interactions for the following 2 drugs:
- fexinidazole
- landiolol
Interactions between your drugs
landiolol fexinidazole
Applies to: landiolol and fexinidazole
Consumer information for this interaction is not currently available.
GENERALLY AVOID: Fexinidazole can cause concentration-dependent prolongation of the QT interval. Coadministration with other agents that can prolong the QT interval may result in additive effects and increased risk of ventricular arrhythmias including torsade de pointes and sudden death. Based on the exposure-response relationship, treatment with fexinidazole is predicted to cause an average increase of 19 msec in the Fridericia-corrected QT interval (QTcF) at the recommended dosing regimen. In addition, drugs that are inducers of hepatic CYP450 enzymes, such as apalutamide and enzalutamide, may significantly increase the plasma concentration of fexinidazole's active metabolites, fexinidazole sulfoxide (M1) and fexinidazole sulfone (M2). The observed increase in QTcF appears to be associated with the sulfone (M2) metabolite of fexinidazole; therefore, an increase in the plasma concentration of the sulfone (M2) metabolite may increase the risk of QT prolongation. In general, the risk of an individual agent or a combination of agents causing ventricular arrhythmia in association with QT prolongation is largely unpredictable but may be increased by certain underlying risk factors such as congenital long QT syndrome, cardiac disease, and electrolyte disturbances (e.g., hypokalemia, hypomagnesemia). In addition, the extent of drug-induced QT prolongation is dependent on the particular drug(s) involved and dosage(s) of the drug(s).
MANAGEMENT: The concurrent use of fexinidazole with other medications that can prolong the QT interval, block cardiac potassium channels, and/or induce bradycardia should generally be avoided. If coadministration is unavoidable, treatment with fexinidazole should not be initiated until the opposing drug is eliminated from the body (allow a washout period of 5 half-lives) or do not initiate treatment with the opposing drug until fexinidazole is eliminated from the body (allow a washout period of 7 days). All QT-prolonging drugs including fexinidazole should be interrupted in patients who develop clinically significant ventricular arrhythmia or a QTcF interval greater than 500 msec confirmed by repeat ECG. Patients should be advised to seek medical attention if they experience symptoms that could indicate the occurrence of torsade de pointes such as dizziness, lightheadedness, fainting, palpitations, irregular heartbeat, shortness of breath, or syncope.
Drug and food interactions
fexinidazole food
Applies to: fexinidazole
Food can enhance the levels of fexinidazole in your body. To ensure maximal oral absorption, fexinidazole should be administered with or immediately after the main meal of the day. This will make it easier for your body to absorb the medication. Use of herbal medicines and supplements during treatment with fexinidazole should be avoided. Grapefruit or grapefruit juice should not be consumed during treatment with fexinidazole. Grapefruit juice can significantly increase the blood levels and effects of fexinidazole, which can increase the risk of an irregular heart rhythm that may be serious and potentially life-threatening, although it is a rare side effect. You may be more susceptible if you have a heart condition called congenital long QT syndrome, other cardiac diseases, conduction abnormalities, or electrolyte disturbances (for example, magnesium or potassium loss due to severe or prolonged diarrhea or vomiting). You should seek immediate medical attention if you develop sudden dizziness, lightheadedness, fainting, shortness of breath, or heart palpitations during treatment with these medications, whether together or alone. Consumption of alcoholic beverages or products containing alcohol or propylene glycol during treatment with fexinidazole may occasionally trigger a reaction in some patients similar to the disulfiram reaction, which includes unpleasant effects such as flushing, throbbing in head and neck, throbbing headache, difficulty breathing, nausea, vomiting, sweating, thirst, chest pain, rapid heartbeat, palpitation, low blood pressure, dizziness, lightheadedness, blurred vision, and confusion. Rarely, more severe reactions may include abnormal heart rhythm, heart attack, heart failure, unconsciousness, convulsions, and even death. Patients treated with fexinidazole should avoid using any products containing alcohol or propylene glycol during and for at least 48 hours after completion of therapy. Talk to your doctor or pharmacist if you have questions on how to take this or other medications you are prescribed. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medications without first talking to your doctor.
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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