Related Experiment Video
Updated: Jul 6, 2025

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
Published on: January 31, 2022
Fifth-Generation Cephalosporins Is Not Spared From Drug-Induced Liver Injury
1Internal Medicine, Baylor College of Medicine, Temple, USA.
Abstract:
Ceftaroline fosamil is a fairly new parenteral cephalosporin antibacterial approved by the US Food and Drug Administration (FDA) for use in the treatment of acute bacterial skin and skin structure infections (ABSSSI). Drug-induced liver injury (DILI) is an important side effect profile to consider with antibiotic use. This case reports DILI in a previously healthy individual associated with a widely used antibiotic, ceftaroline, after only two doses. Discontinuation of the ceftaroline resulted in a resolution of DILI in a three-week period. Ceftaroline-induced liver injury is highlighted in this case report, along with a discussion of how we excluded other potential factors that can cause liver injury with the use of the Roussel Uclaf Causality Assessment Method (RUCAM) score. We also explained why other causes like hemochromatosis, Wilson's disease, celiac disease, and thyroid disease were unlikely.
Insights
Ceftaroline, an antibiotic for skin infections, can cause liver injury (DILI) even after two doses. Stopping the drug resolved the injury, highlighting ceftaroline-induced liver injury as a potential concern.
Area of Science:
- Pharmacology
- Hepatology
- Infectious Diseases
Background:
- Ceftaroline fosamil is an FDA-approved cephalosporin antibiotic for acute bacterial skin and skin structure infections (ABSSSI).
- Drug-induced liver injury (DILI) is a critical consideration for antibiotic safety profiles.
- Early identification and management of DILI are essential for patient outcomes.
Observation:
- A previously healthy individual developed DILI after receiving only two doses of ceftaroline.
- The patient exhibited signs and symptoms consistent with liver injury shortly after antibiotic initiation.
- Causality was assessed using the Roussel Uclaf Causality Assessment Method (RUCAM) score.
Findings:
- Ceftaroline was identified as the causative agent for DILI in this case.
- Discontinuation of ceftaroline led to a complete resolution of liver injury within three weeks.
- Other potential causes of liver injury, including hemochromatosis, Wilson's disease, celiac disease, and thyroid disease, were systematically excluded.
Implications:
- This case underscores the potential for ceftaroline to cause DILI, even with short-term use.
- Clinicians should maintain a high index of suspicion for DILI in patients treated with ceftaroline.
- Prompt recognition and drug withdrawal are crucial for managing ceftaroline-induced liver injury.
Related Concept Videos
Combined Effects of Drugs: Synergism
Such synergistic combinations...
Hepatic Drug Excretion: Enterohepatic Cycling
Post-release drugs and metabolites can be reabsorbed into the body from the intestine. For conjugated metabolites like glucuronides, reabsorption requires enzymatic hydrolysis by intestinal microflora. This...
Hepatic Drug Clearance: Role of Transporters
Pharmacovigilance
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
Inflammatory Bowel Disease I: Ulcerative Colitis
Inflammatory bowel disease, or IBD, encompasses a group of disorders characterized by chronic inflammation or ulceration of the gastrointestinal tract.
Risk Factors
The exact cause of IBD remains unclear, although it is believed to be due to a mix of genetic, environmental, microbial, and immune factors. Genetic factors are significant in determining susceptibility to IBD, with family history being a critical risk factor. Individuals with a first-degree relative who has IBD are at...
Hepatic Drug Clearance: Effect of Protein Binding
For low-extraction-ratio drugs that are less than 80% protein-bound, minor changes in protein binding...

