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Published on: May 29, 2020
Reversible oxacillin-associated hepatitis in a 9-month-old boy
Chun-Yi Lee1, Po-Yen Chen, Fang-Liang Huang
1Paediatric Infectious Diseases Section, Paediatric Department, Taichung Veterans General Hospital, Taiwan. lee821083@gmail.com
A young boy developed acute hepatitis and rash from oxacillin treatment for bone infection. Symptoms resolved after switching to teicoplanin, marking the youngest reported case of oxacillin-induced liver injury.
Area of Science:
- Pediatric Infectious Diseases
- Hepatology
- Clinical Pharmacology
Background:
- Osteomyelitis and septic arthritis are serious pediatric infections requiring prompt antibiotic treatment.
- Oxacillin is a common antibiotic used for Staphylococcus aureus infections, including bone and joint infections.
- Drug-induced liver injury (DILI) is a potential adverse effect of various medications, though rare in infants.
Observation:
- A 9-month-old boy receiving intravenous oxacillin for femoral osteomyelitis and hip septic arthritis developed acute hepatitis and a concurrent skin rash on day six.
- Other potential causes of hepatitis and rash, including viral infections and other drug reactions, were ruled out.
- The patient's clinical condition improved significantly after discontinuation of oxacillin and initiation of teicoplanin therapy.
Findings:
- The case presents the youngest reported instance of oxacillin-associated hepatitis in medical literature.
- The adverse event was directly linked to oxacillin therapy, given the temporal relationship and resolution upon drug substitution.
- Complete recovery without sequelae was achieved following the switch to teicoplanin.
Implications:
- This case highlights the importance of considering DILI, specifically oxacillin-induced hepatitis, in pediatric patients presenting with unexplained hepatitis and rash.
- Clinicians should maintain a high index of suspicion for drug-induced liver injury in infants receiving oxacillin.
- Further investigation into the mechanisms and incidence of oxacillin-related hepatotoxicity in pediatric populations may be warranted.
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