Obeticholic Acid interactions
Full monograph for Obeticholic AcidCheck it against another medicine
Medicines
58 documented
Mechanism
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Tizanidine Hydrochloride | Major | Metabolism | Coadministration 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 |
| Aminophylline | Moderate | Metabolism | Coadministration 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 Maleate | Moderate | Metabolism | Coadministration 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 + Lidocaine | Moderate | Metabolism | Coadministration 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 |
| Bendamustine | Moderate | Metabolism | Coadministration 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 + Lignocaine | Moderate | Metabolism | Coadministration 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 Monohydrate | Moderate | Others | Coadministration 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 Citrate | Moderate | Metabolism | Coadministration 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 + Dexamethasone | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 |
| Clozapine | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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) | Moderate | Others | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 |
| Flutamide | Moderate | Metabolism | Coadministration 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 |
| Glibenclamide | Moderate | Others | Coadministration 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 + Lidocaine | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 |
| Ketoconazole | Moderate | Others | Coadministration 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 + Aleovera | Moderate | Others | Coadministration 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 + Adrenaline | Moderate | Metabolism | Coadministration 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 + Epinephrine | Moderate | Metabolism | Coadministration 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 + Prilocaine | Moderate | Metabolism | Coadministration 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 HydrochlorideInjectionSpray | Moderate | Metabolism | Coadministration 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 |
| Mirtazapine | Moderate | Metabolism | Coadministration 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 + Lidocaine | Moderate | Metabolism | Coadministration 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 |
| Olanzapine | Moderate | Metabolism | Coadministration 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 + Caffeine | Moderate | Metabolism | Coadministration 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 |
| Pentoxifylline | Moderate | Metabolism | Coadministration 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 |
| Pirfenidone | Moderate | Metabolism | Coadministration 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 |
| Pomalidomide | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 |
| Ramelteon | Moderate | Metabolism | Coadministration 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 |
| Rasagiline | Moderate | Metabolism | Coadministration 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 |
| Revefenacin | Moderate | Metabolism | Coadministration 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 |
| Ribociclib | Moderate | Others | Coadministration 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 | Moderate | Others | Coadministration 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 | Moderate | Others | Coadministration 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 + Ethambutol | Moderate | Others | Coadministration 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 |
| Riluzole | Moderate | Metabolism | Coadministration 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) | Moderate | Metabolism | Coadministration 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) | Moderate | Metabolism | Coadministration 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 |
| Ropinirole | Moderate | Metabolism | Coadministration 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 Hydrochloride | Moderate | Metabolism | Coadministration 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 Tosylate | Moderate | Others | Coadministration 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 |
| Theophylline | Moderate | Metabolism | Coadministration 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 + Lidocaine | Moderate | Metabolism | Coadministration 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 + Lidocaine | Moderate | Metabolism | Coadministration 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.
Cholestasis
MajorObeticholic acid is contraindicated in patients with complete biliary obstruction.
1 source
- "Product Information. Ocaliva (obeticholic acid)." Intercept Pharmaceuticals, Inc. (2016):
Liver Failure
MajorIn postmarketing reports, hepatic decompensation and failure, in some cases fatal, have been reported in patients with primary biliary cholangitis (PBC) with decompensated cirrhosis or Child-Pugh Class B or C hepatic impairment when obeticholic acid was dosed more frequently than recommended. The recommended starting dosage is 5 mg once weekly for patients with Child-Pugh Class B or C hepatic impairment or a prior hepatic decompensation event. Patients in treatment should be closely monitored for progression of PBC disease, including liver- related complications, with laboratory and clinical assessments. Dosage adjustment, interruption or discontinuation may be required.
1 source
- "Product Information. Ocaliva (obeticholic acid)." Intercept Pharmaceuticals, Inc. (2016):
Hyperlipidemias
ModeratePatients with primary biliary cholangitis generally exhibit hyperlipidemia characterized by a significant elevation in total cholesterol primarily due to increased levels of high-density lipoprotein-cholesterol (HDL-C). Exercise care when using obeticholic acid in patients with lipids disorder. It is recommended to monitor patients for changes in serum lipid levels during treatment with obeticholic acid. For patients who do not respond to treatment after 1 year at the highest recommended dosage that can be tolerated (maximum of 10 mg once daily), and who experience a reduction in HDL-C, weigh the potential risks against the benefits of continuing treatment.
1 source
- "Product Information. Ocaliva (obeticholic acid)." Intercept Pharmaceuticals, Inc. (2016):