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Obeticholic Acid interactions

Full monograph for Obeticholic AcidCheck it against another medicine

Medicines

58 documented

Medicines documented to interact with Obeticholic Acid, worst severity first.
MedicineSeverityMechanismEffectSources
Tizanidine HydrochlorideMajorMetabolismCoadministration with inhibitors of CYP450 1A2 may significantly increase the plasma concentrations and pharmacologic effects of tizanidine, which is a…8 sources — open the full entry
AminophyllineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Asenapine MaleateModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of asenapine, which is partially metabolized by the isoenzyme.5 sources — open the full entry
Beclomethasone Dipropionate + Chloramphenicol + Clotrimazole + LidocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
BendamustineModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of bendamustine, which has been shown in vitro to be metabolized by the…1 sources — open the full entry
Betamethasone + Phenylephrine + LignocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Bosentan MonohydrateModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Caffeine CitrateModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Calcium Dobesilate + Lidocaine + DexamethasoneModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Chloramphenicol + Lidocaine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Clomipramine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
ClozapineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Cyclobenzaprine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Cyclosporine (Oral)ModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Diclofenac Sodium + Lidocaine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Duloxetine HydrochlorideModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of duloxetine, which is a substrate of the isoenzyme. Theoretically, high…5 sources — open the full entry
FlutamideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
GlibenclamideModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Hydrocortisone + LidocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Imipramine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
KetoconazoleModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Ketoconazole + Zinc Pyrithione + AleoveraModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Lidocaine + AdrenalineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Lidocaine + EpinephrineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Lidocaine + PrilocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Lidocaine HydrochlorideInjectionSprayModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
MirtazapineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Ofloxacin + Clotrimazole + Beclomethasone + LidocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
OlanzapineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Paracetamol + CaffeineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
PentoxifyllineModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of pentoxifylline and its active hydroxy metabolite (M1), both of which…2 sources — open the full entry
PirfenidoneModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of pirfenidone, which is primarily (70% to 80%) metabolized by the…4 sources — open the full entry
PomalidomideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Propranolol HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
RamelteonModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations and pharmacologic effects of ramelteon, which is primarily metabolized by…2 sources — open the full entry
RasagilineModerateMetabolismCoadministration with inhibitors of CYP450 1A2 may increase the plasma concentrations of rasagiline, which is primarily metabolized by the isoenzyme.14 sources — open the full entry
RevefenacinModerateMetabolismCoadministration of revefenacin with inhibitors of organic anion transporting polypeptide (OATP) 1B1 and/or 1B3 may increase systemic exposure to its active…7 sources — open the full entry
RibociclibModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
RifampicinModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Rifampicin + IsoniazidModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
Rifampicin + Isoniazid + Pyrazinamide + EthambutolModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
RiluzoleModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Roflumilast (Cream)ModerateMetabolismCoadministration with CYP450 3A4 inhibitors or dual CYP450 3A4/1A2 inhibitors may increase the systemic exposure (AUC) to roflumilast following topical…2 sources — open the full entry
Roflumilast (Tablet)ModerateMetabolismCoadministration with CYP450 1A2 inhibitors or dual CYP450 1A2/3A4 inhibitors may increase the systemic exposure to roflumilast and its pharmacologically…6 sources — open the full entry
RopiniroleModerateMetabolismCoadministration with drugs that are inhibitors of CYP450 1A2 may increase the plasma concentrations of ropinirole, which is metabolized by the isoenzyme.7 sources — open the full entry
Ropivacaine HydrochlorideModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Sorafenib TosylateModerateOthersCoadministration with inhibitors of the bile salt efflux pump (BSEP) may increase accumulation of conjugated bile salts in the liver, including the glycine and…3 sources — open the full entry
TheophyllineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Tolperisone + LidocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry
Tropicamide + Phenylephrine + LidocaineModerateMetabolismCoadministration with obeticholic acid may increase the plasma concentrations of drugs that are substrates of the CYP450 1A2 isoenzyme. The mechanism is…1 sources — open the full entry

Conditions

Conditions in which Obeticholic Acid needs care, as documented in this source.