Co-administration w/ inducers (eg, rifampicin) or inhibitors (eg, fluconazole) of CYP 2C9. Potentiated blood sugar-lowering effect w/ insulin & other oral antidiabetics, ACE inhibitors, allopurinol, anabolic steroids & male sex hormones, chloramphenicol, coumarin derivatives, cyclophosphamide, disopyramide, fenfluramine, fenyramidol, fibrates, fluoxetine, guanethidine, ifosfamide, MAOIs, miconazole, fluconazole, p-aminosalicylic acid, pentoxifylline (high dose parenteral), phenylbutazone, azapropazone, oxyphenbutazone, probenecid, quinolones, salicylates, sulfinpyrazone, clarithromycin, sulfonamides, tetracyclines, tritoqualine, trofosfamide. Weakened blood sugar-lowering effect w/ acetazolamide, barbiturates, corticosteroids, diazoxide, diuretics, epinephrine (adrenaline) & other sympathomimetics, glucagon, laxatives (after protracted use), nicotinic acid (high dose), oestrogens & progestogens, phenothiazines, phenytoin, rifampicin, thyroid hormones. Either potentiated or weakened blood sugar-lowering effect w/ H
2 receptor antagonist, clonidine & reserpine, acute & chronic alcohol intake. Decreased glucose tolerance & increased hypoglycemia tendency w/ β-blockers. Reduced or absence of adrenergic counter-regulation signs w/ β-blockers, clonidine, guanethidine & reserpine. Potentiated or weakened effect of coumarin derivatives. Reduced absorption from GI tract w/ colesevelam.