No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
Caution - risk of hypothyroidism due to additive effects. Monitor TSH. May require dose increase of levothyroxine.
Avoid combination - decreased level of linagliptin due to 3A4 induction. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of losartan due to 3A4/2C9 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - decreased level of methadone due to 3A4 induction. Also additive risk of QT prolongation. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of mirabegron due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
Caution - decreased level of mirtazepine due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combinaton - decreased level of nifedipine due to 3A4 induction. Choose an alternative agent.
Avoid combinaton - decreased level of niraparib due to induction of BCRP/Pgp. Also potential risk of increased niraparib toxicity (unknown mechanism). Choose an alternative agent.
No clinically significant drug interactions identified.
Caution - potential decreased level of nortriptline due to 3A4/2C19 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation (dose dependent). Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Avoid combinaton - decreased level of olaparib due to 3A4 induction. Choose an alternative agent.
Avoid combinaton - decreased level of omeprazole due to 2C19 induction. Choose an alternative agent.
Caution - only for short courses of therapy. Potential decreased level of ondansetron due to 3A4/Pgp induction. Higher doses of ondansetron than anticipated may be required for efficacy. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combinaton - decreased level of oxycodone due to 3A4 induction. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of phenobarbital due to 3A4/2C19 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
Caution - decreased level of phenytoin due to 2C9/2C19/3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of prednisone due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combinaton - decreased level of quetiapine due to 3A4 induction. Also additive risk of QT prolongation. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of relugolix due to 3A4/P-gp induction. If concurrent use desired, increased dose of relugolix to 240mg once daily recommended. If apalutamide discontinued, reduce to 120mg once daily. Consider choosing an alternative agent.
Caution - decreased level of repaglinide due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Avoid combination - decreased level of risperidone due to 3A4/Pgp induction. Do not use for treatment of schizophrenia or bipolar disorder. For agitation, higher doses than anticipated may be needed for efficacy. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Choose an alternative agent.
Avoid combinaton - decreased level of rivaroxaban due to 3A4 induction and BCRP/P-gp induction. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of rosuvastatin due to 3A4/BCRP/2C9/OAT1B1 induction. Monitor for efficacy - higher doses than anticipated may be required.
Caution - decreased level of saxagliptin due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of sertraline due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
Avoid combination (in pulmonary hypertension) - decreased level of sildenafil due to 3A4 induction. If use for erectile dysfunction, monitor for efficacy - higher doses than anticipated may be required.
No clinically significant drug interactions identified.
Caution - decreased level of simvastatin due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required.
No clinically significant drug interactions identified.
Caution - decreased level of solifenacin due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination (in pulmonary hypertension) - decreased level of tadalafil due to 3A4 induction. If use for erectile dysfunction, monitor for efficacy - higher doses than anticipated may be required.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combinaton - decreased level of ticagrelor due to 3A4 induction. Choose an alternative agent.
Caution - additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - decreased level of tramacet due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing alternative agent
Caution - decreased level of tramacet due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing alternative agent
Avoid combinaton - decreased level of trazodone due to 3A4 induction. Also additive risk of QT prolongation. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - decreased level of vardenafil due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - additive risk of QT prolongation. Baseline EKG if risk factors present (ie. older age, female, electrolyte abnormalities, low HR, cardiac comorbidities, etc). Consider choosing an alternative agent.
Avoid combinaton - decreased level of verapamil due to 3A4 induction. Potential increased apalutamide toxicity due to 3A4 inhibition. Choose an alternative agent.
Avoid combination - decreased level of vortioxetine due to 3A4/2C9/2C19 induction. If concurrent use cannot be avoided, dose increase of vortioxetine recommended. Choose an alternative agent.
Caution - decreased level of warfarin due to 2C9 (major) induction and 2C19/3A4 induction. Monitor INR more closely after initiation of apalutamide therapy or dose changes. Titrate warfarin dose to target INR.
No clinically significant drug interactions identified.
Caution - decreased level of zolpidem due to 3A4 induction. Monitor for efficacy - higher doses than anticipated may be required. Consider choosing an alternative agent.