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Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
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In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess the...
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Drug Toxicity: Risk factors

Adverse Drug Reactions (ADRs) are potential complications that arise during pharmacotherapy, influenced by multiple risk factors. Age plays a significant role; both neonates and the elderly are at heightened risk due to their respective immature and diminished metabolic and elimination processes. Gender also impacts ADRs, with females experiencing a 1.5 to 1.7-fold greater risk than males, which may be linked to pharmacokinetic, pharmacodynamic, and hormonal differences. Notably, neonates, the...
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Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug binding...
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Drug-related allergies are immune-mediated responses triggered by the administration of pharmacological agents. These hypersensitivity reactions are classified based on the immune mechanisms involved. The four primary types—Type I, II, III, and IV—are mediated by different immunological pathways and exhibit distinct clinical manifestations.Type I Hypersensitivity/ IgE-Mediated Reactions: Immunoglobulin E (IgE) immediately mediates Type I hypersensitivity reactions. Upon initial exposure to a...
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Updated: Jun 13, 2026

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
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Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro

Published on: January 31, 2022

Azithromycin-induced liver injury.

Alissa M Lockwood1, Sabrina Cole, Marina Rabinovich

  • 1Department of Pharmacy and Drug Information, Parkland Health and Hospital System, Dallas, TX 75235, USA. alissalockwood@yahoo.com

American Journal of Health-System Pharmacy : AJHP : Official Journal of the American Society of Health-System Pharmacists
|May 19, 2010
PubMed
Summary

This case report details azithromycin-induced liver injury in a 69-year-old woman. High-dose azithromycin for bronchitis led to cholestatic hepatitis, highlighting potential drug toxicity.

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Area of Science:

  • Hepatology
  • Pharmacology
  • Internal Medicine

Background:

  • Azithromycin is a widely prescribed macrolide antibiotic.
  • Drug-induced liver injury (DILI) is a significant clinical concern.
  • Cholestatic hepatitis is a specific pattern of liver damage.

Observation:

  • A 69-year-old woman presented with jaundice, pruritus, nausea, vomiting, and diarrhea.
  • Elevated liver enzymes (transaminitis) and an elevated International Normalized Ratio were noted.
  • Medical history included hypertension, hypothyroidism, depression, dyslipidemia, and COPD, with no prior liver disease.

Findings:

  • Liver injury was temporally associated with high-dose azithromycin therapy for suspected bronchitis.
  • Other causes of liver injury, including viral, metabolic, autoimmune, and ischemic hepatitis, were excluded.
  • Diagnostic scales indicated a probable azithromycin-associated drug-induced liver disease, specifically cholestatic hepatitis.

Implications:

  • This case underscores the potential for azithromycin to cause hepatotoxicity, even in patients without pre-existing liver conditions.
  • Clinicians should consider azithromycin as a potential cause of liver injury in patients presenting with compatible symptoms.
  • Further vigilance and investigation into antibiotic-associated liver injury are warranted.