Related Experiment Video
Updated: Jul 17, 2026

Assay Development for High-Throughput Drug Screening Against Mycobacteria
Published on: October 25, 2024
Moxifloxacin and torsade de pointes
Krista M Dale1, Kirkeith Lertsburapa, Jeffrey Kluger
1Division of Cardiology, School of Pharmacy, University of Connecticut, Hartford, CT, USA.
Moxifloxacin, an antibiotic, can cause torsade de pointes, a dangerous heart rhythm, especially in patients with existing QT interval prolongation risk factors. Careful monitoring is crucial.
Area of Science:
- Cardiology
- Pharmacology
- Infectious Diseases
Background:
- Moxifloxacin is a fluoroquinolone antibiotic commonly used for bacterial infections.
- Fluoroquinolones are known to carry a risk of QTc interval prolongation and associated arrhythmias.
- Limited data exists specifically linking moxifloxacin to torsade de pointes.
Observation:
- An 87-year-old female patient developed torsade de pointes 8-10 hours after initiating intravenous moxifloxacin for pneumonia.
- The patient exhibited significant QTc interval prolongation two hours post-moxifloxacin administration.
- The arrhythmia resolved spontaneously after a precordial thump, and the QTc interval normalized after moxifloxacin discontinuation.
Findings:
- The case suggests a probable causal relationship between intravenous moxifloxacin and the development of torsade de pointes.
- The Naranjo probability scale indicated a probable association between the event and moxifloxacin.
- Underlying risk factors for prolonged QT interval may predispose patients to this adverse event.
Implications:
- Clinicians should exercise caution when prescribing moxifloxacin to patients with risk factors for QT interval prolongation.
- Judicious administration and close monitoring for cardiac events are recommended in such patients.
- This case highlights the potential for moxifloxacin to trigger life-threatening arrhythmias in susceptible individuals.
Related Concept Videos
Antiarrhythmic Drugs: Class III Agents as Potassium Channel Blockers
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Inhibitors of Bacterial DNA Synthesis
Antiepileptic Drugs: Potassium Channel Activators
Ezogabine has gained approval as an adjunctive treatment...
Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
Antiepileptic Drugs: Calcium Channel Blockers
Calcium channel blockers exert their antiepileptic effects by targeting T-type calcium channels, which are integral to transmitting nerve signals in the central nervous system. These channels allow the passage of calcium ions, which are vital for neuronal communication. By inhibiting T-type calcium channels, calcium channel blockers effectively reduce the release of neurotransmitters and...