Trial reportAntimicrobial agents and chemotherapy1998
Effect of fluoxetine on pharmacokinetics of ritonavir.
Trial report in Antimicrobial agents and chemotherapy, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
18 citing papers in PubMed, 42 citations in OpenAlex.
- Interaction study of the combined use of paroxetine and fosamprenavir-ritonavir in healthy subjects.Antimicrobial agents and chemotherapy · 2007Trial
- Development of a physiologically-based pharmacokinetic model for Ritonavir characterizing exposure and drug interaction potential at both acute and steady-state conditions.CPT: pharmacometrics & systems pharmacology · 2025Article
- Clinically Significant Drug Interactions Between Psychotropic Agents and Repurposed COVID-19 Therapies.CNS drugs · 2021Review
- HIV Infection and Related Mental Disorders.Brain sciences · 2021Review
- A Review of the Toxicity of HIV Medications II: Interactions with Drugs and Complementary and Alternative Medicine Products.Journal of medical toxicology : official journal of the American College of Medical Toxicology · 2015Review
- Investigating the contribution of CYP2J2 to ritonavir metabolism in vitro and in vivo.Biochemical pharmacology · 2014Article
- Safety considerations in drug treatment of depression in HIV-positive patients: an updated review.Drug safety · 2011Review
- Psychopharmacologic treatment of patients with HIV/AIDS.Current psychiatry reports · 2009Article
- Choosing Antidepressants for HIV and AIDS Patients: Insights on Safety and Side Effects.Psychiatry (Edgmont (Pa. : Township)) · 2008Article
- Integration and co-location of HIV/AIDS, tuberculosis and drug treatment services.The International journal on drug policy · 2007Article
- Evaluation of pharmacokinetic interaction between cetirizine and ritonavir, an HIV-1 protease inhibitor, in healthy male volunteers.European journal of clinical pharmacology · 2005Article
- Review
- Pharmacokinetics of ritonavir and delavirdine in human immunodeficiency virus-infected patients.Antimicrobial agents and chemotherapy · 2003Article
- Drug interactions between antiretroviral drugs and comedicated agents.Clinical pharmacokinetics · 2003Review
- Review
- Ritonavir-fluoxetine interaction.Antimicrobial agents and chemotherapy · 1999Article
- Ritonavir. Clinical pharmacokinetics and interactions with other anti-HIV agents.Clinical pharmacokinetics · 1998Review
- Drug Interactions of Psychiatric and COVID-19 Medications.Basic and clinical neuroscienceReview
Corrections and comments
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Authors and funding
7 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The potential interaction between fluoxetine, a known inhibitor of cytochrome P-450 isoform 2D6 (CYP2D6), and ritonavir, a human immunodeficiency virus type 1 protease inhibitor, was evaluated in this open-label study. Sixteen male and female subjects ranging in age from 18 to 40 years completed the study. Subjects received single doses of 600 mg of ritonavir on days 1 and 10. On study days 3 to 10, all subjects received 30 mg of fluoxetine every 12 h for a total of 16 consecutive doses. Serial blood samples for determination of ritonavir concentrations in plasma were collected after the administration of ritonavir on days 1 and 10. A limited number of blood samples for determination of fluoxetine and norfluoxetine concentrations were collected after administration of the morning dose on day 10. A statistically significant increase (19%) in the ritonavir area under the concentration-time curve (AUC) was observed with concomitant fluoxetine administration, with individual changes ranging from -12 to +56%. The change in the ritonavir AUC with concomitant fluoxetine administration was positively correlated with the norfluoxetine 24-h AUC (AUC24) (r2 = 0.42), the norfluoxetine/fluoxetine AUC24 ratio (r2 = 0.53), and the fluoxetine elimination rate constant (r2 = 0.65), with larger increases in the ritonavir AUC tending to occur with higher norfluoxetine concentrations and higher fluoxetine elimination rate constants. The effect of fluoxetine appeared to be larger in subjects with the CYP2D6 wt/wt genotype. There was little or no effect on the time to maximum drug concentration (Cmax) in serum, Cmax, and the elimination rate constant of ritonavir with concomitant fluoxetine administration. Considering the magnitude of the change observed, no ritonavir dose adjustment is recommended during concomitant fluoxetine administration.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.