Cyp3a4 drugs

Drug interactions of Norco vs. tramadol. Norco and tramadol are processed in the liver by the CYP3A4 enzyme. CYP3A4 inhibitors and CYP3A4

Simvastatin, Atorvastatin and Lovastatin are metabolized through CYP3A4. Drugs that inhibit CYP3A4 like Ketoconazole, Macrolides and

Clindamycin is a substrate of CYP3A4 and to a lesser extent, CYP3A5. It is a moderate inhibitor of CYP3A4. Drugs that inhibit CYP3A5 or CYP3A4 may cause increased blood concentrations of clindamycin. CYP3A4 or 3A5 inducers may decrease plasma concentrations of clindamycin.

Alprazolam is primarily metabolized by CYP3A4 and commonly associated with more drug-drug interactions than lorazepam. Inhibitors of CYP3A4 like

Drugs that block the CYP3A4 system: The CYP3A4 system in the liver is responsible for breaking down amlodipine. Any drug that interferes with

Clindamycin is a substrate of CYP3A4 and to a lesser extent, CYP3A5. It is a moderate inhibitor of CYP3A4. Drugs that inhibit CYP3A5 or CYP3A4 may cause increased blood concentrations of clindamycin. CYP3A4 or 3A5 inducers may decrease plasma concentrations of clindamycin.

Cyp3A4 Enzymes Inhibitors Drugs Cyp3a4 enzyme Cyp3a4 enzyme inhibitor Cyp3a4 enzyme inhibitor Drug Cyp3A4EnzymesInhibitorsDrugs

Clindamycin is a substrate of CYP3A4 and to a lesser extent, CYP3A5. It is a moderate inhibitor of CYP3A4. Drugs that inhibit CYP3A5 or CYP3A4 may cause increased blood concentrations of clindamycin. CYP3A4 or 3A5 inducers may decrease plasma concentrations of clindamycin.

CYP3A4 INHIBITORS: Drugs that inhibit CYP3A4 activity generally decrease hepatic clearance and increase the plasma concentration of CYP3A4 substrate medications