Related Experiment Video
Updated: May 11, 2026

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors
Published on: April 9, 2014
Psychiatric treatment considerations with direct acting antivirals in hepatitis C
Sanjeev Sockalingam1, Alice Tseng, Pierre Giguere
1University Health Network, Program in Medical Psychiatry, Toronto General Hospital, 200 Elizabeth Street 8EN-228, Toronto, ON M5G 2C4, Canada. sanjeev.sockalingam@uhn.ca
Insights
Direct acting antivirals (DAAs) for hepatitis C (HCV) show minimal neuropsychiatric risk but pose a high potential for drug-drug interactions (DDIs) with psychiatric medications. Careful consideration of DDIs is crucial for safe and effective HCV treatment.
Area of Science:
- Hepatology
- Psychiatry
- Pharmacology
Background:
- Pegylated interferon-alpha is central to hepatitis C (HCV) therapy, despite advances with direct acting antivirals (DAAs).
- Neuropsychiatric effects and drug interactions of DAAs with psychiatric drugs are a concern during HCV treatment.
Purpose of the Study:
- To review neuropsychiatric adverse effects of DAAs.
- To examine drug-drug interactions (DDIs) between DAAs and psychiatric medications.
Main Methods:
- Literature search of Pubmed and conference abstracts.
- Hand-searched reference lists of review articles.
- Contacted pharmaceutical companies for additional data.
Main Results:
- DAAs demonstrate minimal neuropsychiatric risk in clinical trials.
- DAAs can interact with psychotropic agents via cytochrome P450 and p-glycoprotein pathways.
- Contraindicated drugs include triazolam, midazolam, St. John's Wort, carbamazepine, and pimozide.
Conclusions:
- DAAs do not significantly increase neuropsychiatric risk.
- High potential for DDIs between DAAs and psychiatric drugs necessitates careful management.
- Managing DDIs is essential for medication adherence and mitigating adverse effects in HCV therapy.
Background:
Despite recent advances in hepatitis C (HCV) treatment, specifically the addition of direct acting antivirals (DAAs), pegylated interferon-alpha remains the backbone of HCV therapy. Therefore, the impact of DAAs on the management of co-morbid psychiatric illness and neuropsychiatric sequalae remains an ongoing concern during HCV therapy. This paper provides a review of the neuropsychiatric adverse effects of DAAs and drug-drug interactions (DDIs) between DAAs and psychiatric medications.
Methods:
We conducted a Pubmed search using relevant search terms and hand searched reference lists of related review articles. In addition, we searched abstracts for major hepatology conferences and contacted respective pharmaceutical companies for additional studies.
Results:
Limited data is available on the neuropsychiatric adverse effects of DAAs; however, data from major clinical trials suggest that DAAs have minimal neuropsychiatric risk. DAAs can potentially interact with a variety of psychotropic agents via cytochrome P450 and p-glycoprotein interactions. Triazolam, oral midazolam, St. John's Wort, carbamazepine and pimozide, are contraindicated with DAAs. DDIs between DAAs and antidepressants, anxiolytics, hypnotics, mood stabilizers, antipsychotics and treatments for opioid dependence are summarized.
Conclusions:
Although DAAs do not add significant neuropsychiatric risk, the potential for DDIs is high. Consideration of DDIs is paramount to improving medication adherence and mitigating adverse effects during HCV therapy.
More Related Videos
Related Concept Videos
Hepatitis
Psychosis: Goals of Pharmacotherapy
Retrovirus Life Cycles
Drug Therapy
Antianxiety Medications
Inhibitors of Viral Protein Synthesis
Psychosis and Antipsychotic Drugs: Overview

