Ketoconazole interactions
Full monograph for KetoconazoleCheck it against another medicine
Medicines
618 documented
| Medicine | Severity | Mechanism | Effect | Sources |
|---|---|---|---|---|
| Abemaciclib | Major | Metabolism | Coadministration with ketoconazole may significantly increase the plasma concentrations of abemaciclib and its pharmacologically active metabolites. The… | 2 sources — open the full entry |
| Acalabrutinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of acalabrutinib, which is primarily metabolized by… | 4 sources — open the full entry |
| Alfuzosin Hydrochloride | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of alfuzosin, which is primarily metabolized by the… | 8 sources — open the full entry |
| Alprazolam | Major | Metabolism | Coadministration with itraconazole or ketoconazole may significantly increase the plasma concentrations and pharmacologic effects of benzodiazepines that are… | 28 sources — open the full entry |
| Amiodarone Hydrochloride | Major | Metabolism | Coadministration with azole antifungal agents may significantly increase the plasma concentrations of amiodarone. The proposed mechanism is azole inhibition of… | 8 sources — open the full entry |
| Amisulpride | Major | Synergy | Amisulpride can cause dose- and concentration-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the… | 3 sources — open the full entry |
| Amlodipine Besilate + Atorvastatin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA…2 documented mechanisms | 61 sources — open the full entry |
| Amlodipine Besilate + Benazepril Hydrochloride | Major | Metabolism · Synergy | Use of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury.2 documented mechanisms | 43 sources — open the full entry |
| Amoxicillin + Clavulanic Acid | Major | Synergy | Use of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury. | 3 sources — open the full entry |
| Apixaban | Major | Absorption · Metabolism | Coadministration with potent inhibitors of CYP450 3A4 that can also inhibit P-glycoprotein (P-gp) may significantly increase the plasma concentrations of… | 6 sources — open the full entry |
| Arsenic Trioxide | Major | Synergy | Arsenic trioxide can cause QT interval prolongation and complete atrioventricular block. Theoretically, coadministration with other agents that can prolong the… | 4 sources — open the full entry |
| Artemether + Lumefantrine | Major | Metabolism · Synergy | Coadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations of artemether and lumefantrine, both of which are primarily metabolized…3 documented mechanisms | 13 sources — open the full entry |
| Atorvastatin + Ezetimibe | Major | Metabolism · Unknown | Coadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA…2 documented mechanisms | 21 sources — open the full entry |
| Atorvastatin Calcium | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 including azole antifungal agents may significantly increase the plasma concentrations of HMG-CoA… | 21 sources — open the full entry |
| Avanafil | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of avanafil, which is primarily metabolized by the… | 10 sources — open the full entry |
| Axitinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of axitinib, which is primarily metabolized by the… | 7 sources — open the full entry |
| Azelastine Hydrochloride + Fluticasone Propionate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may increase the systemic exposure to fluticasone following intranasal administration or oral inhalation… | 40 sources — open the full entry |
| Betrixaban | Major | Others | Coadministration with inhibitors of P-glycoprotein (P-gp) may significantly increase the plasma concentrations of betrixaban, which is a substrate of the… | 11 sources — open the full entry |
| Brexpiprazole | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 and/or 2D6 may significantly increase the plasma concentrations of brexpiprazole, which is metabolized by these… | 5 sources — open the full entry |
| Brigatinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of brigatinib, which is partially metabolized by the… | 4 sources — open the full entry |
| Bromocriptine Mesylate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of bromocriptine. Orally administered bromocriptine… | 7 sources — open the full entry |
| BudesonideInhalerNebuliser SuspensionTablet | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive… | 19 sources — open the full entry |
| Budesonide + Formoterol Fumarate | Major | Metabolism · Synergy | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…2 documented mechanisms | 49 sources — open the full entry |
| Budesonide + Glycopyrronium Bromide + Formoterol Fumarate | Major | Absorption · Metabolism · Synergy | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the systemic bioavailability of budesonide, which undergoes extensive…3 documented mechanisms | 50 sources — open the full entry |
| Cabozantinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may increase the plasma concentrations of cabozantinib, which is a substrate of the isoenzyme. High… | 7 sources — open the full entry |
| Capmatinib Hydrochloride | Major | Metabolism | Coadministration of capmatinib with strong CYP450 3A4 inhibitors may increase the risk and severity of capmatinib adverse effects, such as interstitial lung… | 3 sources — open the full entry |
| Cariprazine | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of cariprazine and its major active metabolite… | 5 sources — open the full entry |
| Cefpodoxime Proxetil + Clavulanic Acid | Major | Synergy | Use of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury. | 3 sources — open the full entry |
| Cefuroxime Axetil + Clavulanic Acid | Major | Synergy | Use of hepatotoxic drugs together with ketoconazole or levoketoconazole may potentiate the risk of liver injury. | 3 sources — open the full entry |
| Ceritinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of ceritinib, which is a substrate of the isoenzyme… | 6 sources — open the full entry |
| Chloroquine Phosphate | Major | Synergy | Chloroquine and hydroxychloroquine can cause dose-related prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong… | 22 sources — open the full entry |
| Cilostazol | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 and/or 2C19 may increase the plasma concentrations of cilostazol and or its pharmacologically active… | 12 sources — open the full entry |
| Citalopram Hydrobromide | Major | Synergy | Citalopram can cause dose-dependent prolongation of the QT interval. Theoretically, coadministration with other agents that can prolong the QT interval may… | 15 sources — open the full entry |
| Clindamycin + Tretinoin | Major | Metabolism | Coadministration with azole antifungal agents may increase the plasma concentrations and toxicities of tretinoin. The proposed mechanism is inhibition of…2 documented mechanisms | 15 sources — open the full entry |
| Clozapine | Major | Synergy | Clozapine has the potential to prolong QT interval of the electrocardiogram. Theoretically, coadministration with other agents that can cause QT prolongation… | 13 sources — open the full entry |
| Colchicine | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 such as ketoconazole may significantly increase the serum concentrations of colchicine, which is… | 22 sources — open the full entry |
| Crizotinib | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of crizotinib, which is primarily metabolized by the… | 6 sources — open the full entry |
| Cyclosporine (Oral) | Major | Metabolism | Certain azole antifungal agents such as ketoconazole and itraconazole that are potent inhibitors of CYP450 3A4 may significantly increase the blood levels of… | 26 sources — open the full entry |
| Dabigatran Etexilate Mesylate | Major | Absorption | Coadministration with potent inhibitors of P-glycoprotein such as ketoconazole may significantly increase the bioavailability of dabigatran following oral… | 4 sources — open the full entry |
| Daclatasvir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by… | 4 sources — open the full entry |
| Daclatasvir + Sofosbuvir | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of daclatasvir, which is primarily metabolized by… | 4 sources — open the full entry |
| Darifenacin | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of darifenacin, which is partially metabolized by… | 7 sources — open the full entry |
| Dasatinib | Major | Metabolism | Coadministration with inhibitors of CYP450 3A4 may increase the plasma concentrations and pharmacologic effects of dasatinib, which is primarily metabolized by… | 8 sources — open the full entry |
| Deflazacort | Major | Metabolism | Coadministration with potent or moderate inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of 21-desdeflazacort, the active… | 3 sources — open the full entry |
| Docetaxel Trihydrate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 or dual CYP450 3A4 and P-glycoprotein (P-gp) inhibitors may significantly increase the plasma… | 21 sources — open the full entry |
| Drospirenone | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by… | 9 sources — open the full entry |
| Drospirenone + Estetrol | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by… | 9 sources — open the full entry |
| Drospirenone + Estradiol | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms | 17 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol0.02 mg0.03 mg | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms | 17 sources — open the full entry |
| Drospirenone + Ethinyl Estradiol + Levomefolate | Major | Metabolism | Coadministration with potent inhibitors of CYP450 3A4 may significantly increase the plasma concentrations of drospirenone which is primarily metabolized by…2 documented mechanisms | 17 sources — open the full entry |
Food & lifestyle
alcohol
ModerateSynergy
Excessive use of alcohol or products containing alcohol together with ketoconazole or levoketoconazole may potentiate the risk of liver injury. Serious hepatotoxicity has been reported with levoketoconazole. Fatal hepatotoxicity or requiring liver transplantation have been reported with the use of oral ketoconazole, of which levoketoconazole is an enantiomer.
What to do: Excessive consumption of alcohol should generally be avoided during ketoconazole or levoketoconazole therapy. Patients receiving ketoconazole or levoketoconazole should be instructed to contact their doctor immediately if they experience swelling, skin rash, itching, loss of appetite, fatigue, nausea, vomiting, abdominal pain, dark colored urine, light colored stools, and/or yellowing of the skin or eyes, as these may be signs and symptoms of liver damage.
3 sources
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Ketoconazole (ketoconazole)." Mylan Pharmaceuticals Inc (2019):
- "Product Information. Recorlev (levoketoconazole)." Xeris Pharmaceuticals Inc (2022):
Conditions
Conditions in which Ketoconazole needs care, as documented in this source.
Liver Diseases
MajorSerious hepatotoxicity including cases with a fatal outcome or requiring liver transplant have been reported. Some patients had no obvious risk factors for liver disease. Liver function tests should be performed prior to initiation of therapy and regularly during treatment in patients receiving prolonged therapy with ketoconazole, particularly those with a current or past history of liver disease. Therapy should be withdrawn if persistent elevations or worsening of liver enzyme levels occur, or if the abnormalities are accompanied by symptoms of possible liver injury. Since ketoconazole is primarily metabolized by the liver, empirically reducing the dosage may also be appropriate in patients with existing liver disease. The use of oral ketoconazole tablets is contraindicated in patients with acute or chronic liver disease.
11 sources
- Knight TE, Shikuma CY, Knight J "Ketoconazole-induced fulminant hepatitis necessitating liver transplantation." J Am Acad Dermatol 25 (1991): 398-400
- Duarte PA, Chow CC, Simmons F, Ruskin J "Fatal hepatitis associated with ketoconazole therapy." Arch Intern Med 144 (1984): 1069-70
- Lewis JH, Zimmerman HJ, Benson GD, Ishak KG "Hepatic injury associated with ketoconazole therapy: analysis of 33 cases." Gastroenterology 86 (1984): 503-13
- Bercoff E, Bernuau J, Degott C, et al. "Ketoconazole-induced fulminant hepatitis." Gut 26 (1985): 636-8
- Stricker BH, Blok AP, Bronkhorst FB, et al. "Ketoconazole-associated hepatic injury: a clinicopathological study of 55 cases." J Hepatol 3 (1986): 399-406
- Lake-Bakaar G, Scheuer PJ, Sherlock S "Hepatic reactions associated with ketoconazole in the United Kingdom." Br Med J (Clin Res Ed) 294 (1987): 419-22
- van Parys G, Evenepoel C, van Damme B, Desmet VJ "Ketoconazole-induced hepatitis: a case with a definite cause-effect relationship." Liver 7 (1987): 27-30
- McCance DR, Ritchie CM, Sheridan B, Atkinson AB "Acute hypoadrenalism and hepatotoxicity after treatment with ketoconazole." Lancet Mar (1987): 573
Show all 11 sourcesShow fewer sources
- Gradon JD, Sepkowitz DV "Massive hepatic enlargement with fatty change associated with ketoconazole." Ann Pharmacother 24 (1990): 1175-6
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2002):
- Chien RN, Yang LJ, Lin PY, Liaw YF "Hepatic injury during ketoconazole therapy in patients with onychomycosis: a controlled cohort study." Hepatology 25 (1997): 103-7
Achlorhydria
ModerateNizoral (brand of ketoconazole) tablets require acidity for proper dissolution and absorption. Therefore, the drug may not be effective in patients with achlorhydria. Taking the medication with an acidic beverage such as orange or cranberry juice may help, but an alternative antifungal agent should be considered.
5 sources
- Lake-Bakaar G, Tom W, Lake-Bakaar D, et al. "Gastropathy and ketoconazole malabsorption in the acquired immunodeficiency syndrome (AIDS)." Ann Intern Med 109 (1988): 471-3
- Mannisto PT, Mantyla R, Nykanen S, et al. "Impairing effect of food on ketoconazole absorption." Antimicrob Agents Chemother 21 (1982): 730-3
- Daneshmend TK, Warnock DW, Ene MD, et al. "Influence of food on the pharmacokinetics of ketoconazole." Antimicrob Agents Chemother 25 (1984): 1-3
- Daneshmend TK "Diseases and drugs but not food decrease ketoconazole "bioavailability"." Br J Clin Pharmacol 29 (1990): 783-4
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2002):
Adrenal Insufficiency
ModerateKetoconazole tablets decrease adrenal corticosteroid secretion at doses of 400 mg and higher. Adrenal function should be monitored in patients with adrenal insufficiency or with borderline adrenal function and in patients with prolonged periods of stress due to major surgery, intensive care, etc.
1 source
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2001):
Long QT Syndrome
ModerateSome azole antifungals have been associated with prolongation of the QT interval on the ECG. Rare cases of QT prolongation and torsade de pointes have been reported during postmarketing experience; such reports usually involved seriously ill patients with multiple confounding risk factors, such as structural heart disease, electrolyte abnormalities, and concomitant medications. These drugs should be administered with caution to patients with potentially proarrhythmic conditions. Concomitant use with other medications that have potential to increase the risk of cardiotoxicity should be avoided.
7 sources
- "Product Information. Nizoral (ketoconazole)." Janssen Pharmaceuticals (2001):
- "Product Information. Diflucan (fluconazole)." Roerig Division (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2002):
- "Product Information. Sporanox (itraconazole)." Janssen Pharmaceuticals (2022):
- "Product Information. VFEND (voriconazole)." Pfizer U.S. Pharmaceuticals (2002):
- "Product Information. Noxafil (posaconazole)." Schering-Plough Corporation (2006):
- "Product Information. Tolsura (itraconazole)." Mayne Pharma Inc (2021):