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Drug Interactions Between Linezolid and Selective Serotonin Reuptake Inhibitors: Case Report Involving Sertraline and Review of the Literature


Author(s): Deidre B. Clark | Miranda R. Andrus | Debbie C. Byrd
doi: 10.1592/phco.26.2.269
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  Pharmacotherapy
 
Print ISSN: 0277-0008
Volume: 26 | Issue: 2
Cover date: February 2006
Page(s): 269-276
 
 
  Key Words
 
linezolid, selective serotonin reuptake inhibitor, SSRI, drug interaction, serotonin syndrome, sertraline
 
  Abstract

A 47-year-old woman developed confusion, incoordination, and hypertension after she was given linezolid in addition to sertraline for 5 days. Her symptoms resolved within 4 days of discontinuing linezolid. One and a half months later, she received a second course of linezolid; sertraline was discontinued on day 1 of linezolid therapy. On day 9 of therapy, the patient developed confusion, myoclonus, and incoordination, and cardiopulmonary arrest occurred, leaving the patient in a coma. Diarrhea, hypertension, and tachycardia developed after cardiopulmonary arrest. Linezolid was discontinued on day 10, and cyproheptadine was given. Linezolid is a weak monoamine oxidase inhibitor and has been reported to interact with selective serotonin reuptake inhibitors (SSRIs). Several cases of serotonin syndrome in patients taking linezolid and SSRIs have been reported, including two reports with sertraline, one with paroxetine, four with citalopram, and two with fluoxetine. One abstract of a retrospective analysis reported that serotonin syndrome did not occur in patients who received linezolid and fluoxetine, paroxetine, or sertraline. Because of several limitations, however, no conclusions can be drawn from that retrospective analysis. A drug interaction involving escitalopram and linezolid has not been documented. Caution should be used when linezolid is used in patients receiving an SSRI. Other antibiotic options should be considered first, and linezolid should be reserved as the last resort if possible. If the infection requires linezolid, the SSRI should be discontinued, and the patient should be monitored closely for serotonin syndrome.

 
  Author(s) affiliations
 
1Department of Pharmacy, Tuscaloosa Veterans Affairs Medical Center, Tuscaloosa, Alabama.
2Department of Pharmacy Practice, Auburn University Harrison School of Pharmacy, Auburn, Alabama; Department of Family Medicine, University of Alabama School of Medicine, Huntsville, Alabama.
3Department of Pharmacy Practice, Auburn University Harrison School of Pharmacy, Auburn, Alabama.
1Address reprint requests to Deidre B. Clark, Pharm.D., BCPS, Department of Pharmacy (119), Tuscaloosa VA Medical Center, 3701 Loop Road East, Tuscaloosa, AL 35404.
 
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