Drug interactions between dofetilide and Inderide

Results for the following 2 drugs:
dofetilide
Inderide (hydrochlorothiazide/propranolol)

Interactions between your selected drugs

hydrochlorothiazide ↔ dofetilide

Applies to:Inderide (hydrochlorothiazide/propranolol) and dofetilide

CONTRAINDICATED: Coadministration with hydrochlorothiazide (HCTZ) may increase the plasma concentrations and pharmacodynamic effects of dofetilide. The mechanism of interaction has not been described. Concurrent administration of HCTZ (50 mg once a day) and dofetilide (500 mcg twice a day) for 5 days (following 2 days of diuretic use at half dose) has been shown to increase dofetilide peak plasma concentration (Cmax) by 21% and systemic exposure (AUC) by 27%. However, the QTc increase over time and the maximum QTc increase values went up by 197% and 95%, respectively. In patients who received HCTZ-triamterene (50 mg-100 mg once a day) with dofetilide for 5 days, dofetilide Cmax was increased by 16% and AUC by 30%, while the QTc increase over time and maximum QTc increase values went up by 190% and 84%, respectively. The increased QT prolongation effects can be explained by a combination of the increase in dofetilide exposure and the HCTZ-induced reductions in serum potassium.

MANAGEMENT: Because QT interval prolongation may be associated with serious ventricular arrhythmias such as torsade de pointes tachycardia, use of dofetilide in combination with hydrochlorothiazide is considered contraindicated.

See also...

Drug Interaction Classification

The classifications below are a guideline only. The relevance of a particular drug interaction to a specific patient is difficult to determine using this tool alone given the large number of variables that may apply.

Major Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit.
Moderate Moderately clinically significant. Usually avoid combinations; use it only under special circumstances.
Minor Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan.

Do not stop taking any medications without consulting your healthcare provider.


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