Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Pharmacokinetics: Drug–Food and Drug–Viral Interactions01:26

Pharmacokinetics: Drug–Food and Drug–Viral Interactions

A drug interaction occurs when the concurrent use of another drug, food, or an external substance alters the pharmacological activity of a drug. This interaction can modify the action of the original drug, affecting its effectiveness and safety.Drug–food interactions are significant as they impact drug absorption, metabolism, and excretion. For example, grapefruit juice is a well-known disruptor of drug metabolism. It inhibits the cytochrome P450 3A4 enzyme, crucial for the metabolism of many...
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants01:18

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants

Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
Drug toxicity: Drug–Drug Interaction01:30

Drug toxicity: Drug–Drug Interaction

Drug–drug interactions can precipitate toxicity through multiple mechanisms. Absorption interactions alter how drugs enter the body, exemplified when ranitidine increases the absorption of basic drugs, while cholestyramine decreases the levels of propranolol. Protein binding interactions occur when drugs share the same binding sites on plasma proteins. Drugs like aspirin and warfarin, when bound in excess, can lead to increased free drug concentrations, enhancing the potential for...
Factors Affecting Protein-Drug Binding: Drug Interactions01:23

Factors Affecting Protein-Drug Binding: Drug Interactions

Drug interactions are a critical aspect of pharmacology and can occur when two or more drugs compete for the same binding site. This competition can result in one drug displacing another, altering the effect of the displaced drug. Drug interactions are complex processes that rely heavily on how much of the displacer drug is present and how strongly it can bind to the same sites as the displaced drug.
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The Medication Possession Ratio as a Predictor of Longitudinal HIV-1 Viral Suppression.

The Annals of pharmacotherapy·2023
Same author

Evaluation of human immunodeficiency virus curricular content in schools of pharmacy in the United States.

Currents in pharmacy teaching & learning·2020
Same author

National estimates of case-mix, mortality, and economic outcomes among inpatient HIV/AIDS mono-infection and hepatitis C co-infection cases in the US.

Journal of evaluation in clinical practice·2018
Same author

Sustained Virologic Response and Costs Associated with Direct-Acting Antivirals for Chronic Hepatitis C Infection in Oklahoma Medicaid.

Journal of managed care & specialty pharmacy·2018
Same author

Evaluation of the concurrent use of dolutegravir and metformin in human immunodeficiency virus-infected patients.

International journal of STD & AIDS·2017
Same author

Acute Care Management of the HIV-Infected Patient: A Report from the HIV Practice and Research Network of the American College of Clinical Pharmacy.

Pharmacotherapy·2017

Related Experiment Video

Updated: Jun 25, 2026

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors
05:46

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors

Published on: April 9, 2014

Warfarin-antiretroviral interactions.

Michelle D Liedtke1, R Chris Rathbun

  • 1Department of Pharmacy, College of Pharmacy, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73117, USA. michelle-liedtke@ouhsc.edu

The Annals of Pharmacotherapy
|February 7, 2009
PubMed
Summary
This summary is machine-generated.

Warfarin drug interactions with antiretrovirals, particularly protease inhibitors (PIs) and nonnucleoside reverse transcriptase inhibitors (NNRTIs), can alter warfarin metabolism. Close international normalized ratio (INR) monitoring is crucial when these medications are used together.

More Related Videos

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
10:29

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors

Published on: May 9, 2025

Related Experiment Videos

Last Updated: Jun 25, 2026

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors
05:46

Rapid Screening of HIV Reverse Transcriptase and Integrase Inhibitors

Published on: April 9, 2014

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
10:29

Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors

Published on: May 9, 2025

Area of Science:

  • Pharmacology
  • Drug Interactions
  • HIV Therapeutics

Background:

  • Warfarin is a widely used anticoagulant.
  • Antiretroviral agents are crucial for HIV management.
  • Potential drug interactions between these classes require careful evaluation.

Purpose of the Study:

  • To review and evaluate literature on interactions between warfarin and antiretroviral agents.
  • To assess the clinical significance of these drug interactions.

Main Methods:

  • Comprehensive literature search of MEDLINE and International Pharmaceutical Abstracts.
  • Inclusion of conference abstracts and manufacturer information.
  • Evaluation of case reports and studies on CYP2C9 metabolism and interactions.

Main Results:

  • Twelve case reports identified interactions primarily with protease inhibitors (PIs) and nonnucleoside reverse transcriptase inhibitors (NNRTIs).
  • Interactions are mediated via CYP2C9 metabolism, leading to either over-anticoagulation (e.g., with efavirenz, saquinavir) or subtherapeutic anticoagulation (e.g., with lopinavir/ritonavir, nevirapine).
  • Interactions with other antiretroviral classes are not anticipated.

Conclusions:

  • Drug interactions between warfarin and antiretrovirals are probable, especially with PIs and NNRTIs.
  • Specific antiretroviral agents can induce or inhibit warfarin metabolism.
  • Close international normalized ratio (INR) monitoring is recommended over empiric dose adjustments due to limited evidence.