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. 2016 Jul 11;113(27-28):477–483. doi: 10.3238/arztebl.2016.0477

Table 2. Manufacturers’ information about drug interactions of proton pump inhibitors.

Indication Type of interaction OmeprazoleEsomeprazole Lansoprazole Rabeprazole Pantoprazole
Treating anxiety increased plasma levels Benzodiazepines,e.g. diazepam
Anticoagulation
Vitamin K antagonists

Antiplatelet therapy

increased plasma levels

reduced activation of prodrug

Phenprocoumon Warfarin

Clopidogrel



Clopidogrel



Clopidogrel

Phenprocoumon Warfarin

Clopidogrel
Depression reduced PPI levels

increased plasma levels
St. John’s wort

Citalopram
Clomipramine
Imipramine
St. John’s wort

Fluvoxamine
Diabetes Glibenclamide
Tolbutamide
Epilepsy increased plasma levels Phenytoin
Infectious diseasesHIV


Bacteria

Mycoses

severely reduced plasma levels; thus, PPIs contraindicated


absorption reduced with acid deficiency

azole antifungals inhibit the metabolism of PPIs

Atazanavir
Nelfinavir
Saquinavir

Rifampicin


Itraconazole
Ketoconazole
Posaconazole
Voriconazoel

Atazanavir


Erythromycin
Rifampicin
Itraconazole
Ketoconazole

Atazanavir


Itraconazole
Ketoconazole

Atazanavir


Itraconazole
Ketoconazole
Posaconazole
Immunosuppressants Conflicting data:
increased plasma levels possible
Cyclosporine
Tacrolimus
Tacrolimus
Cardiology 10% higher digoxin levelsalong with increased pH Digoxin Digoxin
Oncology decreased plasma levels questionable increased plasma levels, delayed elimination Erlotinib

Methotrexate in high doses
Erlotinib
Reflux disease reduced absorption of PPIs Antacids
Sucralfate
Antacids

The information presented in this table is derived from the patient information leaflets of the manufacturers of proton pump inhibitors (PPIs) producing PPIs as follow-on and generic products. A different listing of medications in this table does not mean that this interaction has been excluded for the respective PPI. Not all listed drugs are included in the package leaflets of each manufacturer. Less drug interactions are reported for pantoprazole (e15) because of its lower level of interaction with CYP2C19. However, with regard to interactions basically the same drugs are listed.