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.
Caution - increased level of lisdexamphetamine due to 2D6 inhibition. Monitor for signs of toxicity (ie. tachycardia, agitation, anxiety). 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.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of methadone due to 2D6 inhibition. Titrate with extreme caution due to risk of overdose. If already established on methadone, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - increased level of metoclopramide due to 2D6 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.
Caution - increased level of metoprolol due to 2D6 inhibition. Monitor for signs of toxicity (ie. hypotension, bradycardia, impotence). 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.
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.
No clinically significant drug interactions identified.
Caution - increased level of nortriptyline due to 2D6 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.
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.
Caution - increased level of oxycodone due to 2D6 inhibition. Titrate with extreme caution due to risk of overdose. If already established on oxycodone, may require dose reduction. Consider choosing an alternative agent.
No clinically significant drug interactions identified.
Caution - increased level of paroxetine due to 2D6 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.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - decreased level of abiraterone due to 3A4 induction. Choose an alternative agent.
Avoid combination - decreased level of abiraterone due to 3A4 induction. Choose an alternative agent.
Caution - severe hypoglycemia has been reported when used in combination in patients with pre-existing diabetes. If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - increased level of pravastatin due to OAT1B1 inhibition. Monitor for signs of toxicity (ie. CK). 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.
No clinically significant drug interactions identified.
Caution - increased level of propanolol due to 2D6 inhibition. Monitor for signs of toxicity (ie. hypotension, bradycardia, impotence). 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.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Caution - increased level of repaglinide due to OAT1B1/2C8 inhibition. Monitor for signs of toxicity (ie. hypoglycemia). 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 risperidone due to 2D6 inhibition. Monitor for signs of toxicity (ie. EPS, hyperprolactinemia). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - increased level of rivaroxaban due to potential 3A4 inhibition. 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 rosuvastatin due to OAT1B1 inhibition. Monitor for signs of toxicity (ie. CK). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction.
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.
Caution - increased level of simvastatin due to OAT1B1 inhibition. Monitor for signs of toxicity (ie. CK). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
Avoid combination - increased risk of sub-optimal clinical benefit due to increase in activation of mutant and wild-type androgen receptors in patients receiving abiraterone for treatment of castration-resistant prostate cancer. 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 - increased level of tamsulosin due to 2D6 inhibition. Monitor for signs of toxicity (ie. syncope). 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.
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 - increased level of tramadol due to 2D6 inhibition. Titrate with extreme caution due to risk of overdose. If already established on tramadol, may require dose reduction. Consider choosing an alternative agent.
Caution - increased level of tramadol due to 2D6 inhibition. Titrate with extreme caution due to risk of overdose. If already established on tramadol, 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.
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 vortioxetine due to 2D6 inhibition. Monitor for signs of toxicity (ie. GI upset, agitation). If initiating therapy, titrate slowly. If already established on therapy, may require dose reduction. Consider choosing an alternative agent.
Caution - increased level of warfarin due to 1A2/3A4/2C9/2C19 inhibition. Monitor INR more closely after initiation of abiraterone therapy or dose changes. Titrate warfarin dose to target INR.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.
No clinically significant drug interactions identified.