No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of alprazolam due to 3A4 inhibition. Monitor for signs of toxicity (sedation, lethargy). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Avoid combination - increased level of amiodarone due to 3A4 inhibiton. Also additive risk of QT prolongation. Choose an alternative agent.
Caution - QT prolongation (EKG monitoring required). Consider choosing an alternative agent.
Caution - increased level of amlodipine due to 3A4 inhibition. Monitor for signs of toxicity (hypotension). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of apixaban due to 3A4 inhibition. Monitor for signs of bleeding - dose reduction may be required. Consider choosing an alternative agent.
Caution - QT prolongation (EKG monitoring required). Increased level of aripiprazole due to 3A4 inhibition. Monitor for signs of toxicity. If initiating therapy, titrate slowly. If already established on therapy, dose reduction advised. Consider choosing an alternative agent.
Caution - increased level of atenolol due to OCT1/OCT2 inhibition. Monitor for signs of toxicity (hypotension, bradycardia). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - QT prolongation (EKG monitoring required). Consider choosing an alternative agent.
Caution - increased level of atorvastatin due to 3A4 inhibition. Monitor for signs of toxicity. If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Avoid combination - additive risk of QT prolongation. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - QT prolongation (EKG monitoring required). Increased level of buprenorphine/naloxone due to 3A4 inhibition. Monitor for signs of toxicity (sedation, confusion, dizziness). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - increased level of buspirone due to 3A4 inhibition. Monitor for signs of toxicity (sedation). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. 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 - increased level of carbamazepine due to 3A4 inhibition. Decreased level of ribociclib 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.
No clinically significant drug interactions identified.
Avoid combination - additive risk of QT prolongation. Choose an alternative agent.
Avoid combination - increased level of citalopram due to 3A4 inhibition. Also additive risk of QT prolongation. Choose an alternative agent.
Avoid combination - increased level of both agents due to 3A4 inhibition. Also additive risk of QT prolongation. Choose an alternative agent.
Caution - increased level of clindamycin due to 3A4 inhibition. Monitor for signs of toxicity (diarrhea). Use the lowest dose and shortest duration clinically indicated. Consider choosing an alternative agent.
Caution - increased level of clonazepam due to 3A4 inhibition. Monitor for signs of toxicity (sedation, lethargy). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of codeine due to 3A4 inhibition. Monitor for signs of toxicity (sedation, confusion, dizziness). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - increased level of colchicine due to 3A4 inhibition. Dose reduction is required. AVOID use in patients with renal and/or hepatic impairment. AVOID use of extended release colchicine. Monitor for signs of toxicity, including increased bloodwork monitoring. Choose an alternative agent when possible.
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 - increased level of dexamethasone due to 3A4 inhibition. Monitor for signs of toxicity. If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - increased level of diazepam due to 3A4 inhibition. Monitor for signs of toxicity (sedation, lethargy). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - increased level of both agents due to 3A4 inhibition. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - increased level of domperidone due to 3A4 inhibiton. Also additive risk of QT prolongation. Choose an alternative agent.
Avoid combination - 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.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - increased level of eletriptan due to 3A4 inhibition. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - 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.
No clinically significant drug interactions identified.
Caution - QT prolongation (EKG monitoring required). Increased level of ribociclib due to 3A4 inhibition. Use lowest dose and shortest duration as clinically indicated. One-time dose low risk of clinically significant interaction; <1 week course of fluconazole may be considered with increased monitoring; >1 week course of fluconazole not advised. Monitor for signs of ribociclib toxicity. Consider choosing an alternative agent.
Caution - QT prolongation (EKG monitoring 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 - increased level of gabapentin due to OCT2 inhibition. Monitor for signs of toxicity (sedation, lethargy). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - QT prolongation (EKG monitoring required). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of guanfacine due to 3A4/OCT1/OCT2 inhibition. Monitor for signs of toxicity (hypotension, bradycardia, sedation). If initiating therapy, titrate slowly. If already established on therapy, 50% dose reduction advised. 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 - additive risk of QT prolongation. Choose an alternative agent.
Caution - QT prolongation (EKG monitoring required). Consider choosing 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.
Avoid combination - increased level of both agents due to 3A4 inhibition. Choose an alternative agent.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - QT prolongation (EKG monitoring required). Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Avoid combination - 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.