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Tolvaptan interactions

Full monograph for TolvaptanCheck it against another medicine

Medicines

208 documented

Medicines documented to interact with Tolvaptan, worst severity first.
MedicineSeverityMechanismEffectSources
ApalutamideMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
CarbamazepineMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
CeritinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
EnzalutamideMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
Esomeprazole + Amoxicillin + ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Fosphenytoin SodiumMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
ItraconazoleMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
KetoconazoleMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Ketoconazole + Zinc Pyrithione + AleoveraMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Lansoprazole + Amoxicillin + ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
LeflunomideMajorSynergyThe recent, concomitant, or subsequent use (without the recommended leflunomide washout period or procedure) of other agents known to induce hepatotoxicity may…3 sources — open the full entry
Lopinavir + RitonavirMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
MifepristoneMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Mifepristone + MisoprostolMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
NelfinavirMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Nirmatrelvir + RitonavirMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
PhenobarbitalMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
Phenytoin SodiumMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
PosaconazoleMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
PrimidoneMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
Rabeprazole + Amoxicillin + ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
RifampicinMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
Rifampicin + IsoniazidMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
Rifampicin + Isoniazid + Pyrazinamide + EthambutolMajorMetabolismCoadministration with potent inducers of CYP450 3A4 may significantly decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the…4 sources — open the full entry
TucatinibMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
Vonoprazan + Amoxicillin + ClarithromycinMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
VoriconazoleMajorMetabolismCoadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of vasopressin receptor antagonists conivaptan and…7 sources — open the full entry
AbametapirModerateMetabolismBased on in vitro inhibition data, a single topical application of abametapir lotion may increase plasma concentrations of drugs that are substrates of CYP450…1 sources — open the full entry
Afatinib DimaleateModerateOthersCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the plasma concentrations of afatinib, which is a substrate of the efflux transporter.4 sources — open the full entry
Allium cepa + Heparin + AllantoinModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 sources — open the full entry
AlpelisibModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the oral bioavailability of tolvaptan, which has been shown in vitro to be a substrate…3 sources — open the full entry
Amiodarone HydrochlorideModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the oral bioavailability of tolvaptan, which has been shown in vitro to be a substrate…3 sources — open the full entry
Amlodipine Besilate + Benazepril HydrochlorideModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 sources — open the full entry
Amlodipine Besilate + Olmesartan MedoxomilModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 sources — open the full entry
Amlodipine Besilate + TelmisartanModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 sources — open the full entry
Amlodipine Besilate + ValsartanModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 sources — open the full entry
ApixabanModerateMetabolismCoadministration with inhibitors of CYP450 3A4 and/or P-glycoprotein (P-gp) may increase the plasma concentrations of apixaban, which is a substrate of both…2 sources — open the full entry
AprepitantModerateMetabolismCoadministration with inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of tolvaptan, which is almost exclusively metabolized by…2 sources — open the full entry
ArmodafinilModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the isoenzyme.5 sources — open the full entry
ArtesunateModerateDistributionCoadministration with tolvaptan may increase the plasma concentrations of drugs that are substrates of P-glycoprotein (P-gp). The proposed mechanism is…5 sources — open the full entry
AsciminibModerateMetabolismCoadministration with asciminib may increase the plasma concentrations of drugs that are primarily metabolized by the CYP450 3A4 isoenzyme. The mechanism is…1 sources — open the full entry
Azilsartan MedoxomilModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 documented mechanisms3 sources — open the full entry
Azilsartan Medoxomil + ChlorthalidoneModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium…2 documented mechanisms3 sources — open the full entry
BetrixabanModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the plasma concentrations of betrixaban, which is a substrate of the efflux transporter.4 sources — open the full entry
Bosentan MonohydrateModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the isoenzyme. When…3 sources — open the full entry
BrigatinibModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the oral bioavailability of tolvaptan, which has been shown in vitro to be a substrate…3 sources — open the full entry
CabozantinibModerateAbsorptionCoadministration with inhibitors of P-glycoprotein (P-gp) may increase the oral bioavailability of tolvaptan, which has been shown in vitro to be a substrate…3 sources — open the full entry
Calcium Dobesilate + Lidocaine + DexamethasoneModerateMetabolismCoadministration with inducers of CYP450 3A4 may decrease the plasma concentrations of tolvaptan, which is primarily metabolized by the isoenzyme. When…3 sources — open the full entry
Candesartan CilexetilModerateSynergyCoadministration with tolvaptan can potentiate the risk of hyperkalemia in patients treated with other drugs that are known to increase serum potassium.1 sources — open the full entry

Food & lifestyle

Conditions

Conditions in which Tolvaptan needs care, as documented in this source.