Increased serum levels & potential toxicity of theophylline. Elevated serum levels of digoxin. Increased effects of oral anticoagulants. Acute ergot toxicity w/ ergotamine or dihydroergotamine. Decreased clearance of triazolam & midazolam, which may increase pharmacologic effect of these benzodiazepines. Significantly altered metabolism of nonsedating antihistamines terfenadine & astemizole; rare cases of serious CV adverse events, including electrocardiographic QT/QTc interval prolongation, cardiac arrest, torsades de pointes, & other ventricular arrhythmias have been observed. Post-marketing reports of drug interactions w/ cisapride, resulting in QT prolongation, cardiac arrhythmias, ventricular tachycardia, ventricular fibrillation, & torsades de pointes.
Ilosone 200 Risk of colchicine toxicity w/ colchicine; rhabdomyolysis w/ simvastatin, lovastatin, & atorvastatin; hypotension w/ Ca channel blockers metabolized by CYP3A4 (eg, verapamil, amlodipine, diltiazem). Decreased serum conc w/ theophylline. Hypotension, bradyarrhythmias, & lactic acidosis w/ verapamil. Co-administration w/ drugs primarily metabolized by CYP3A may be associated w/ elevations in drug conc that could increase or prolong both the therapeutic & adverse effects of the concomitant drug. Increased conc of HMG-CoA reductase inhibitors (eg, lovastatin & simvastatin). Increased systemic exposure of sildenafil. Reports of interactions w/ cyclosporine, carbamazepine, tacrolimus, alfentanil, disopyramide, rifabutin, quinidine, methylprednisolone, cilostazol, vinblastine, & bromocriptine; hexobarbital, phenytoin, & valproate.
Ilosone DS Maintenance of plasma levels may be prolonged w/ probenecid. Avoid lincomycin or clindamycin therapy in treatment of infections due to erythromycin-resistant organisms. Elevated serum conc of carbamazepine, cyclosporine, hexobarbital, phenytoin, alfentanil, disopyramide, quinidine, HMG-CoA reductase inhibitors (eg, simvastatin & lovastatin), bromocriptine, PDE5 inhibitors (eg, sildenafil, tadalafil, & vardenafil). May interfere w/ AST determinations if zone-fast violet B or diphenylhydrazine colorimetric determinations are used. Interferes w/ fluorometric determination of urinary catecholamine.