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  • FDA Date: 03/28/2012

    Celexa FDA Drug Safety Communication

    Revised recommendations for Celexa (citalopram hydrobromide) related to a potential risk of abnormal heart rhythms with high doses

    This information reflects FDA's current analysis of data available to FDA concerning this drug. FDA intends to update this sheet when additional information or analyses become available.

    The FDA is clarifying dosing and warning recommendations for the antidepressant Celexa (citalopram hydrobromide; also available in generic form). In August 2011, FDA issued a Drug Safety Communication (DSC) stating that citalopram should no longer be used at doses greater than 40 mg per day because it could cause potentially dangerous abnormalities in the electrical activity of the heart.

    Citalopram use at any dose is discouraged in patients with certain conditions because of the risk of QT prolongation; however, because it may be important for some of those patients to use citalopram, the drug label has been changed to describe the particular caution that needs to be taken when citalopram is used in such patients. The revised drug label also describes lower doses that should be used in patients over 60 years of age.

    Changes in the electrical activity of the heart (specifically, prolongation of the QT interval of the electrocardiogram [ECG]) can lead to a risk of an abnormal heart rhythm called torsade de pointes, which can be fatal. Patients at particular risk for developing prolongation of the QT interval include those with underlying heart conditions and those who are predisposed to having low levels of potassium and magnesium in the blood.

    The citalopram drug label was revised on August 12, 2011 and again on March 27, 2012, to include new warnings about the potential for QT interval prolongation and torsade de pointes, as well as new drug dosage and usage recommendations.

    The following changes have been made to the citalopram drug label as of 3/27/12:

    - Recognition that although citalopram use should be avoided, if possible, in patients with certain conditions because of the risk of QT prolongation, ECG monitoring and/or electrolyte monitoring should be performed if citalopram must be used in such patients.

    - Patients with congenital long QT syndrome are at particular risk of torsade de pointes, ventricular tachycardia, and sudden death when given drugs that prolong the QT interval. Nevertheless, the labeling recommendation for patients with congenital long QT syndrome has been changed from "contraindicated" to "not recommended" because it is recognized that there may be some patients with this condition who could benefit from a low dose of citalopram and who lack viable alternatives.

    - The maximum recommended dose of citalopram is 20 mg per day for patients older than 60 years of age.

    - Citalopram should be discontinued in patients who are found to have persistent QTc measurements greater than 500 ms.

    View the full FDA Drug Safety Communication on FDA.gov