2009
DOI: 10.1592/phco.29.11.1386
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Clinically Significant Adverse Events from a Drug Interaction Between Quetiapine and Atazanavir‐Ritonavir in Two Patients

Abstract: Clinicians caring for patients infected with the human immunodeficiency virus (HIV) and diagnosed with psychiatric comorbidities must be aware of potential drug-drug interactions, particularly with protease inhibitor-based antiretroviral therapy. Although possible interactions can be predicted based on a drug's pharmacokinetic parameters, the clinical significance is often unknown. We describe two patients who experienced serious quetiapine adverse effects potentially mediated through an interaction with riton… Show more

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Cited by 34 publications
(17 citation statements)
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References 28 publications
(24 reference statements)
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“…The potential for interactions between psychotropic and HIV drugs requires expertise in both areas for effective clinical management. 62,63 Transitioning youth with PHIV to adult care providers is fraught with many clinical concerns as mental health issues are often chronic. 64,65 For example, many (41%) of our youth with PHIV who met Symptom Cutoff criteria at study entry also met criteria during follow-up.…”
Section: Discussionmentioning
confidence: 99%
“…The potential for interactions between psychotropic and HIV drugs requires expertise in both areas for effective clinical management. 62,63 Transitioning youth with PHIV to adult care providers is fraught with many clinical concerns as mental health issues are often chronic. 64,65 For example, many (41%) of our youth with PHIV who met Symptom Cutoff criteria at study entry also met criteria during follow-up.…”
Section: Discussionmentioning
confidence: 99%
“…42 Reports of increased adverse effects due to quetiapine 43,44 and aripiprazole 45 in patients receiving protease inhibitors have been published.…”
Section: Psychotropic Agentsmentioning
confidence: 99%
“…Human oral pharmacokinetic parameters were obtained following a single dose of 240 mg per person. combination therapies (Pollack et al 2009) and therefore, it is preferable to use a drug, like BI 201335, with an intrinsically longer t 1/2 , which can be administered less frequently without the need for PK boosting agents.…”
Section: Discussionmentioning
confidence: 99%