Clinically Significant Adverse Events from a Drug Interaction Between Quetiapine and Atazanavir-Ritonavir in Two Patients

被引:28
|
作者
Pollack, Todd M. [1 ]
McCoy, Christopher [2 ]
Stead, Wendy [1 ]
机构
[1] Beth Israel Deaconess Med Ctr, Dept Med, Div Infect Dis, Boston, MA 02215 USA
[2] Beth Israel Deaconess Med Ctr, Dept Pharm Serv, Boston, MA 02215 USA
来源
PHARMACOTHERAPY | 2009年 / 29卷 / 11期
关键词
quetiapine; ritonavir; atazanavir; drug interaction; antipsychotic agents; HIV protease inhibitors; HEALTHY-VOLUNTEERS; UNITED-STATES; PHARMACOKINETICS; ANTIPSYCHOTICS; RISPERIDONE; SCHIZOPHRENIA; CARBAMAZEPINE; METHADONE; THERAPY;
D O I
10.1592/phco.29.11.1386
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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 ritonavir-boosted atazanavir. The first patient was a 57-year-old man with HIV and bipolar disease who developed rapid and severe weight gain when quetiapine was added to a stable atazanavir-ritonavir-based antiretroviral regimen. After the patient discontinued both quetiapine and ritonavir, his weight returned to its baseline value. The second patient was a 32-year-old woman with HIV, anxiety disorder, and a history of intravenous drug abuse who developed increased sedation and mental confusion when an atazanavir-ritonavir-based antiretroviral regimen was added to her stable antianxiety drug regimen, which included quetiapine. Her symptoms resolved promptly after discontinuation of the quetiapine. Use of the Naranjo adverse drug reaction probability scale indicated that the adverse effects experienced by the two patients were possibly related and probably related, respectively, to an interaction between quetiapine and atazanavir-ritonavir. Quetiapine is primarily metabolized by cytochrome P450 (CYP) 3A4, and ritonavir is a potent inhibitor of CYP3A4. Thus, it is reasonable to theorize that quetiapine concentrations will increase when these drugs are used concurrently, which would be the likely cause of the toxicities in these two patients. To our knowledge, these are the first published reports of a clinically significant interaction between atazanavir-ritonavir and quetiapine. Clinicians should be aware of the potential for this interaction, and extreme caution should be used when prescribing quetiapine and other atypical antipsychotic agents in HIV-positive patients who are receiving antiretroviral therapy.
引用
收藏
页码:1386 / 1391
页数:6
相关论文
共 50 条
  • [1] Interactions between atazanavir-ritonavir and tenofovir in heavily pretreated human immunodeficiency virus-infected patients
    Taburet, AM
    Piketty, C
    Chazallon, C
    Vincent, I
    Gérard, L
    Calvez, V
    Clavel, F
    Aboulker, JP
    Girard, PM
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) : 2091 - 2096
  • [2] Clinically Significant Pharmacokinetic Interaction Between Colchicine and Ritonavir in Healthy Volunteers
    Wason, Suman
    DiGiacinto, Jennifer L.
    Davis, Matthew W.
    CLINICAL MEDICINE INSIGHTS-THERAPEUTICS, 2013, 5 : 25 - 32
  • [3] Clinically significant drug interaction between tipranavir-ritonavir and phenobarbital in an HIV-infected subject
    Bonora, Stefano
    Calcagno, Andrea
    Fontana, Silvia
    D'Avolio, Antonio
    Siccardi, Marco
    Gobbi, Federico
    Di Perri, Giovanni
    CLINICAL INFECTIOUS DISEASES, 2007, 45 (12) : 1654 - 1655
  • [4] Aprepitant quetiapine: a clinically significant drug interaction in a patient treated for head and neck cancer
    Verwimp-Hoeks, M. P. A.
    van Herpen, C. M. L.
    Burger, D. M.
    ANNALS OF ONCOLOGY, 2012, 23 (03)
  • [5] Clinically Significant Drug-Drug Interaction Between Methadone and Cannabidiol
    Madden, Kevin
    Tanco, Kimberson
    Bruera, Eduardo
    PEDIATRICS, 2020, 145 (06)
  • [6] Dual treatment with atazanavir-ritonavir plus lamivudine versus triple treatment with atazanavir-ritonavir plus two nucleos(t)ides in virologically stable patients with HIV-1 (SALT): 48 week results from a randomised, open-label, non-inferiority trial
    Perez-Molina, Jose A.
    Rubio, Rafael
    Rivero, Antonio
    Pasquau, Juan
    Suarez-Lozano, Ignacio
    Riera, Melcior
    Estebanez, Miriam
    Santos, Jesus
    Sanz-Moreno, Jose
    Troya, Jesus
    Marino, Ana
    Antela, Antonio
    Navarro, Jose
    Esteban, Herminia
    Moreno, Santiago
    LANCET INFECTIOUS DISEASES, 2015, 15 (07): : 775 - 784
  • [7] Identifying clinically significant preventable adverse drug events through a hospital's database of adverse drug reaction reports
    Winterstein, AG
    Hatton, RC
    Gonzalez-Rothi, R
    Johns, TE
    Segal, R
    AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY, 2002, 59 (18) : 1742 - 1749
  • [8] Prediction of clinically relevant adverse drug events in surgical patients
    Bos, Jacqueline M.
    Kalkman, Gerard A.
    Groenewoud, Hans
    van den Bemt, Patricia M. L. A.
    De Smet, Peter A. G. M.
    Nagtegaal, J. Elsbeth
    Wieringa, Andre
    van der Wilt, Gert Jan
    Kramers, Cornelis
    PLOS ONE, 2018, 13 (08):
  • [9] Evidence of a clinically significant drug-drug interaction between cannabidiol and tacrolimus
    Leino, Abbie D.
    Emoto, Chie
    Fukuda, Tsuyoshi
    Privitera, Michael
    Vinks, Alexander A.
    Alloway, Rita R.
    AMERICAN JOURNAL OF TRANSPLANTATION, 2019, 19 (10) : 2944 - 2948
  • [10] Lack of interaction between atazanavir and proton pump inhibitors in HIV-infected patients treated with ritonavir-boosted atazanavir
    Meynard, JL
    Poirier, JM
    Bonnard, P
    Meynard, JL
    JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2006, 41 (03) : 393 - 394