Valbenazine Tosylate interactions
Checked as Valbenazine in this data source.
Full monograph for Valbenazine TosylateCheck it against another medicine
Medicines
321 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Amiodarone Hydrochloride | Major | Synergy | Class IA (e.g., disopyramide, quinidine, procainamide) and class III (e.g., amiodarone, dofetilide, sotalol) antiarrhythmic agents can cause dose-related… | 45 sources — open the full entry |
| Amisulpride | Major | Synergy | Amisulpride can cause dose- and concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the… | 3 sources — open the full entry |
| Apalutamide | Major | Metabolism | Coadministration of valbenazine with strong CYP450 3A4 inducers may decrease the plasma concentrations and therapeutic effects of valbenazine and its active… | 3 sources — open the full entry |
| Arsenic Trioxide | Major | Synergy | Arsenic trioxide can cause QT interval prolongation and complete atrioventricular block. Theoretically, coadministration with other agents that can prolong the… | 4 sources — open the full entry |
| Artemether + Lumefantrine | Major | Synergy | Artemether-lumefantrine may cause prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may…2 documented mechanisms | 16 sources — open the full entry |
| Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + Lidocaine | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Betamethasone + Clotrimazole | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Betamethasone + Clotrimazole + Gentamicin | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Bupropion Hydrochloride | Major | Metabolism | Coadministration with a strong CYP450 2D6 inhibitor may increase the exposure of (+)-alfa-dihydrotetrabenazine, the active metabolite of valbenazine, which may… | 2 sources — open the full entry |
| Cabozantinib | Major | Synergy | Cabozantinib can cause prolongation of the QT interval. | 7 sources — open the full entry |
| Carbamazepine | Major | Metabolism | Coadministration of valbenazine with strong CYP450 3A4 inducers may decrease the plasma concentrations and therapeutic effects of valbenazine and its active… | 3 sources — open the full entry |
| Ceritinib | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Chloroquine Phosphate | Major | Synergy | Chloroquine and hydroxychloroquine can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong… | 22 sources — open the full entry |
| Citalopram Hydrobromide | Major | Synergy | Citalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 15 sources — open the full entry |
| Clarithromycin | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Clobetasol Propionate + Ofloxacin + Ornidazole + Terbinafine | Major | Metabolism · Synergy | Coadministration with a strong CYP450 2D6 inhibitor may increase the exposure of (+)-alfa-dihydrotetrabenazine, the active metabolite of valbenazine, which may…2 documented mechanisms | 8 sources — open the full entry |
| ClotrimazoleEar dropEye ointmentTopicalVaginal tablet | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Clotrimazole + Hydrocortisone | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Clozapine | Major | Synergy | Clozapine has the potential to prolong QT interval of the electrocardiogram. Theoretically, coadministration with other agents that can cause QT prolongation… | 13 sources — open the full entry |
| Crizotinib | Major | Synergy | Crizotinib can cause concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT… | 6 sources — open the full entry |
| Dacomitinib | Major | Metabolism | Coadministration with a strong CYP450 2D6 inhibitor may increase the exposure of (+)-alfa-dihydrotetrabenazine, the active metabolite of valbenazine, which may… | 2 sources — open the full entry |
| Dextromethorphan + Bupropion | Major | Metabolism · Synergy | Coadministration with a strong CYP450 2D6 inhibitor may increase the exposure of (+)-alfa-dihydrotetrabenazine, the active metabolite of valbenazine, which may…2 documented mechanisms | 46 sources — open the full entry |
| Efavirenz | Major | Metabolism | Efavirenz can cause significant QT interval prolongation in patients with the CYP450 2B6 *6/*6 genotype due to reduced metabolic clearance of the drug stemming… | 6 sources — open the full entry |
| Enzalutamide | Major | Metabolism | Coadministration of valbenazine with strong CYP450 3A4 inducers may decrease the plasma concentrations and therapeutic effects of valbenazine and its active… | 3 sources — open the full entry |
| Escitalopram Oxalate | Major | Synergy | Escitalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 13 sources — open the full entry |
| Esomeprazole + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Fluoxetine Hydrochloride | Major | Metabolism | Coadministration with a strong CYP450 2D6 inhibitor may increase the exposure of (+)-alfa-dihydrotetrabenazine, the active metabolite of valbenazine, which may… | 2 sources — open the full entry |
| Fosphenytoin Sodium | Major | Metabolism | Coadministration of valbenazine with strong CYP450 3A4 inducers may decrease the plasma concentrations and therapeutic effects of valbenazine and its active… | 3 sources — open the full entry |
| Gatifloxacin | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Gatifloxacin + Dexamethasone | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Haloperidol | Major | Synergy | Haloperidol can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 14 sources — open the full entry |
| Hydroxychloroquine Sulphate | Major | Synergy | Chloroquine and hydroxychloroquine can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong… | 22 sources — open the full entry |
| Iloperidone | Major | Synergy | Iloperidone may cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 9 sources — open the full entry |
| Itraconazole | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Ivabradine | Major | Synergy | Due to its bradycardic effects, the risk of QT prolongation and torsade de pointes arrhythmia may be increased when ivabradine is used with drugs that prolong… | 10 sources — open the full entry |
| Ivosidenib | Major | Synergy | Ivosidenib can cause prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may result in additive… | 6 sources — open the full entry |
| Ketoconazole | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Ketoconazole + Zinc Pyrithione + Aleovera | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Lansoprazole + Amoxicillin + Clarithromycin | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Lefamulin Acetate | Major | Synergy | Lefamulin may cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may result… | 6 sources — open the full entry |
| Linezolid | Major | Others | Coadministration of valbenazine with monoamine oxidase inhibitors (MAOIs) may increase the risk of adverse effects such as serotonin syndrome or reduce the… | 21 sources — open the full entry |
| Lopinavir + Ritonavir | Major | Metabolism · Synergy | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT…2 documented mechanisms | 9 sources — open the full entry |
| Loteprednol Etabonate + Gatifloxacin | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Mifepristone | Major | Synergy | Mifepristone may prolong the QTc interval in a dose-related manner. Theoretically, coadministration with other agents that can prolong the QT interval may… | 10 sources — open the full entry |
| Mifepristone + Misoprostol | Major | Synergy | Mifepristone may prolong the QTc interval in a dose-related manner. Theoretically, coadministration with other agents that can prolong the QT interval may… | 10 sources — open the full entry |
| Moxifloxacin HydrochlorideInjectionOphthalmicTablet | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Moxifloxacin Hydrochloride + Dexamethasone | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Moxifloxacin Hydrochloride + Xanthan Gum | Major | Synergy | Certain quinolones, including gatifloxacin and moxifloxacin, may cause dose-related prolongation of the QT interval in some patients. Theoretically… | 28 sources — open the full entry |
| Nelfinavir | Major | Metabolism | Coadministration with a strong CYP450 3A4 inhibitor may increase the systemic exposure and risk of adverse effects of valbenazine, including somnolence and QT… | 4 sources — open the full entry |
| Nilotinib | Major | Synergy | Nilotinib can cause concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval… | 9 sources — open the full entry |
Food & lifestyle
grapefruit juice
MajorMetabolism
Coadministration with grapefruit juice may increase the plasma concentration of valbenazine. The mechanism is inhibition of CYP450 3A4-mediated first-metabolism in the gut wall by certain compounds present in grapefruits.
What to do: Pharmacologic response to valbenazine should be monitored more closely whenever a strong inhibitor of CYP450 3A4 is added to or withdrawn from therapy. Assessment of baseline QT interval and periodic monitoring during therapy may be considered. The manufacturer recommends reducing the dose of valbenazine to 40 mg once daily during concomitant administration with strong CYP450 3A4 inhibitors. 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. In addition, patients receiving CNS-active agents should be warned of this interaction and advised to avoid or limit consumption of alcohol. Ambulatory patients should be counseled to avoid hazardous activities requiring complete mental alertness and motor coordination until they know how these agents affect them, and to notify their physician if they experience excessive or prolonged CNS effects that interfere with their normal activities.
1 source
- "Product Information. Ingrezza (valbenazine)." Neurocrine Biosciences, Inc. (2017):
Conditions
Conditions in which Valbenazine Tosylate needs care, as documented in this source.
Kidney Diseases
MajorThe use of valbenazine is not recommended in patients with severe renal impairment (creatinine clearance <30 mL/min). Dosage adjustment is not necessary for patients with mild to moderate renal impairment (creatinine clearance 30 to 90 mL/min).
1 source
- "Product Information. Ingrezza (valbenazine)." Neurocrine Biosciences, Inc. (2017):
Liver Diseases
MajorValbenazine is extensively metabolized after oral administration by the liver. Dosage adjustment of valbenazine 40 mg once daily is recommended for patients with moderate or severe hepatic impairment (Child-Pugh score 7 to 15). Close monitoring of hepatic function is recommended.
1 source
- "Product Information. Ingrezza (valbenazine)." Neurocrine Biosciences, Inc. (2017):
Long QT Syndrome
MajorValbenazine may prolong the QT interval, although the degree of QT prolongation is not clinically significant at concentrations expected with recommended dosing. The use of valbenazine should be avoided in patients with congenital long QT syndrome or with arrhythmias associated with a prolonged QT interval. For patients at increased risk of a prolonged QT interval, it is recommended to assess the QT interval before increasing the dosage.
1 source
- "Product Information. Ingrezza (valbenazine)." Neurocrine Biosciences, Inc. (2017):
Parkinson Disease
ModerateThe use of vesicular monoamine transporter 2 (VMAT2) inhibitor, such as valbenazine and deutetrabenazine may cause parkinsonism in patients with tardive dyskinesia. These agents should be used with caution in patients with parkinson disease or those presenting with parkinson-like symptoms such as, falls, gait disturbances, tremor, drooling and hypokinesia. It is recommended to reduce the dose or to discontinue treatment in patients who develop clinically significant parkinson-like signs or symptoms while on treatment with these agents.
2 sources
- "Product Information. Ingrezza (valbenazine)." Neurocrine Biosciences, Inc. (2017):
- "Product Information. Austedo (deutetrabenazine)." Teva Pharmaceuticals USA (2017):