Drug Interactions between Nuplazid and oliceridine
This report displays the potential drug interactions for the following 2 drugs:
- Nuplazid (pimavanserin)
- oliceridine
Interactions between your drugs
pimavanserin oliceridine
Applies to: Nuplazid (pimavanserin) and oliceridine
Consumer information for this interaction is not currently available.
MONITOR CLOSELY: Oliceridine can cause prolongation of the QT interval. Theoretically, 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. In a single-dose thorough QT study involving healthy subjects, dose-dependent QTc prolongation occurred after peak oliceridine plasma concentration at a therapeutic dose of 3 mg (7 msec [upper 90% confidence interval: 9 msec]) and a supratherapeutic dose of 6 mg (12 msec [upper 90% confidence interval: 14 msec]). In a multi-dose thorough QT study of healthy subjects who received intermittent oliceridine dosing over 24 hours to the maximum daily cumulative dose of 27 mg, the maximum mean increase in QTc was 11.7 msec (two-sided upper 90% confidence interval: 14.7 msec) at 9 hours. Despite continued dosing, QTc did not progressively increase and began to decrease after 12 hours. Daily cumulative doses greater than 27 mg have not been examined in a thorough QT study but may increase the risk for 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, hypocalcemia). Moreover, the extent of drug-induced QT prolongation is dependent on the particular drug(s) involved and dosage(s) of the drug(s).
MANAGEMENT: Caution is recommended if oliceridine is used in combination with other drugs that can prolong the QT interval. The daily cumulative dose of oliceridine should not exceed 27 mg. Patients should be advised to seek prompt medical attention if they experience symptoms that could indicate the occurrence of torsade de pointes such as dizziness, lightheadedness, fainting, palpitation, irregular heart rhythm, shortness of breath, or syncope.
Drug and food interactions
oliceridine food
Applies to: oliceridine
Do not use alcohol or medications that contain alcohol while you are receiving treatment with oliceridine. This may increase nervous system side effects such as drowsiness, dizziness, lightheadedness, difficulty concentrating, and impairment in thinking and judgment. In severe cases, low blood pressure, respiratory distress, fainting, coma, or even death may occur. You should also avoid consuming grapefruit and grapefruit juice, as this may increase the blood levels and effects of oliceridine. Talk to your doctor or pharmacist if you have questions on how to take this or other medications you are prescribed. Do not exceed the dose of oliceridine prescribed for you or use the medication more frequently or for a longer duration than prescribed by your doctor. Also avoid activities requiring mental alertness such as driving or operating hazardous machinery until you know how the medication affects you. It is important to tell your doctor about all other medications you use, including vitamins and herbs. Do not stop using any medication 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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