Review Article
Clinically relevant drug interactions in anxiety disorders
Article first published online: 7 FEB 2012
DOI: 10.1002/hup.2217
Copyright © 2012 John Wiley & Sons, Ltd.
Issue

Human Psychopharmacology: Clinical and Experimental
Volume 27, Issue 3, pages 239–253, May 2012
Additional Information
How to Cite
Muscatello, M. R., Spina, E., Bandelow, B. and Baldwin, D. S. (2012), Clinically relevant drug interactions in anxiety disorders. Hum. Psychopharmacol. Clin. Exp., 27: 239–253. doi: 10.1002/hup.2217
Publication History
- Issue published online: 15 MAY 2012
- Article first published online: 7 FEB 2012
- Manuscript Accepted: 6 JAN 2012
- Manuscript Received: 12 JUL 2011
- Abstract
- Article
- References
- Cited By
Keywords:
- anxiety disorders;
- drug interactions;
- selective serotonin reuptake inhibitors;
- serotonin–noradrenaline reuptake inhibitors;
- benzodiazepines;
- pregabalin
Objective
Certain drugs used in the treatment of patients with anxiety disorders can interact with other psychotropic drugs and with pharmacological treatments for physical illnesses. There is a need for an updated comparative review of clinically relevant drug interactions in this area.
Design
Relevant literature on drug interactions with medications used in the treatment of anxiety disorders was identified through a search in MEDLINE and EMBASE.
Results
Drug interactions involving medications used to treat anxiety disorders may be pharmacokinetic, such as enzyme inhibition or induction in the cytochrome P450 system and transporter-mediated drug interactions, or pharmacodynamic, such as additive effects in causing drowsiness or additive effects at neurotransmitter receptors. Certain selective serotonin reuptake inhibitors (fluoxetine, fluvoxamine, and paroxetine) are particularly liable to be potentially involved in untoward pharmacokinetic interactions.
Conclusions
The potential for drug interactions with medications used in anxiety disorders should be the cause of clinical concern, particularly in elderly individuals. However, the liability for harmful drug interactions may be anticipated, and the risk reduced. Although not all interactions are clinically relevant, careful monitoring of clinical response and possible interactions is essential. Copyright © 2012 John Wiley & Sons, Ltd.

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