Evaluation of the FDA warning against prescribing citalopram at doses exceeding 40 mg

Kara Zivin, Paul N. Pfeiffer, Amy S B Bohnert, Dara Ganoczy, Frederic C. Blow, Brahmajee K. Nallamothu, Helen C. Kales

Research output: Contribution to journalArticle

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Abstract

Objective: A recent Food and Drug Administration (FDA) warning cautioned that citalopram dosages exceeding 40mg/daymay cause abnormal heart rhythms, including torsade de pointes. The authors assessed relationships between citalopram use and ventricular arrhythmias and mortality. Method: A cohort study was conducted using Veterans Health Administration data between 2004 and 2009 from depressed patients who received a prescription for citalopram (N=618,450) or for sertraline (N=365,898), a comparison medication with no FDA warning. Cox regression models, adjusted for demographic and clinical characteristics, were used to examine associations of antidepressant dosing with ventricular arrhythmia and cardiac, noncardiac, and all-cause mortality. Results: Citalopram daily doses >40 mg were associated with lower risks of ventricular arrhythmia (adjusted hazard ratio= 0.68, 95% CI=0.61-0.76), all-cause mortality (adjusted hazard ratio=0.94, 95% CI=0.90-0.99), and noncardiac mortality (adjusted hazard ratio=0.90, 95% CI=0.86-0.96) compared with daily doses of 1-20 mg. No increased risks of cardiac mortality were found. Citalopram daily doses of 21-40 mg were associated with lower risks of ventricular arrhythmia (adjusted hazard ratio=0.80, 95% CI=0.74-0.86) compared with dosages of 1-20 mg/day but did not have significantly different risks of any cause of mortality. The sertraline cohort revealed similar findings, except there were no significant associations between daily dose and either all-cause or noncardiac mortality. Conclusions: This large study found no elevated risks of ventricular arrhythmia or all-cause, cardiac, or noncardiac mortality associated with citalopram dosages >40 mg/day. Higher dosages were associated with fewer adverse outcomes, and similar findings were observed for a comparison medication, sertraline, not subject to the FDA warning. These results raise questions regarding the continued merit of the FDA warning.

Original languageEnglish (US)
Pages (from-to)642-650
Number of pages9
JournalAmerican Journal of Psychiatry
Volume170
Issue number6
DOIs
StatePublished - Jun 1 2013
Externally publishedYes

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Citalopram
United States Food and Drug Administration
Mortality
Cardiac Arrhythmias
Sertraline
Veterans Health
Torsades de Pointes
United States Department of Veterans Affairs
Proportional Hazards Models
Antidepressive Agents
Prescriptions
Cohort Studies
Demography

ASJC Scopus subject areas

  • Psychiatry and Mental health
  • Medicine(all)

Cite this

Zivin, K., Pfeiffer, P. N., Bohnert, A. S. B., Ganoczy, D., Blow, F. C., Nallamothu, B. K., & Kales, H. C. (2013). Evaluation of the FDA warning against prescribing citalopram at doses exceeding 40 mg. American Journal of Psychiatry, 170(6), 642-650. https://doi.org/10.1176/appi.ajp.2013.12030408

Evaluation of the FDA warning against prescribing citalopram at doses exceeding 40 mg. / Zivin, Kara; Pfeiffer, Paul N.; Bohnert, Amy S B; Ganoczy, Dara; Blow, Frederic C.; Nallamothu, Brahmajee K.; Kales, Helen C.

In: American Journal of Psychiatry, Vol. 170, No. 6, 01.06.2013, p. 642-650.

Research output: Contribution to journalArticle

Zivin, K, Pfeiffer, PN, Bohnert, ASB, Ganoczy, D, Blow, FC, Nallamothu, BK & Kales, HC 2013, 'Evaluation of the FDA warning against prescribing citalopram at doses exceeding 40 mg', American Journal of Psychiatry, vol. 170, no. 6, pp. 642-650. https://doi.org/10.1176/appi.ajp.2013.12030408
Zivin, Kara ; Pfeiffer, Paul N. ; Bohnert, Amy S B ; Ganoczy, Dara ; Blow, Frederic C. ; Nallamothu, Brahmajee K. ; Kales, Helen C. / Evaluation of the FDA warning against prescribing citalopram at doses exceeding 40 mg. In: American Journal of Psychiatry. 2013 ; Vol. 170, No. 6. pp. 642-650.
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