Evidence map›Paper›PMID 41377793›Full record

ArticleEuropean journal of case reports in internal medicine2025

Empagliflozin-Induced Liver Injury.

Hélder Diogo Gonçalves, Inês Parreira, Sara Vasconcelos-Teixeira, Ana Melício, Mariana Dias, João Madeira Lopes, Leila Duarte

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Article in European journal of case reports in internal medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Hélder Diogo GonçalvesServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Inês ParreiraServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Sara Vasconcelos-TeixeiraServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Ana MelícioServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Mariana DiasServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
João Madeira LopesServiço de Medicina Interna, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.
Leila DuarteServiço de Urgência Central, Unidade Local de Saúde Santa Maria, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Drug-induced liver injury is an uncommon, idiosyncratic adverse reaction with heterogeneous clinical presentations, ranging from asymptomatic transaminase elevations to acute liver failure. Sodium-glucose cotransporter 2 inhibitors, widely prescribed for type 2 diabetes due to their glycaemic, cardiovascular, and renal benefits, are generally considered safe to the liver. Nonetheless, rare cases of cholestatic and hepatocellular drug-induced liver injury have been reported, highlighting the need for vigilance and systematic evaluation when liver dysfunction occurs in patients receiving these agents. Case report: We describe a 56-year-old man with type 2 diabetes and chronic schizophrenia who developed cholestatic liver injury 36 days after initiating empagliflozin 10 mg od. The patient presented with jaundice, dark urine, and pale stools, with laboratory findings revealing elevated bilirubin, gamma-glutamyl transferase, and alkaline phosphatase disproportionate to alanine aminotransferase. Comprehensive work-up excluded viral, autoimmune, metabolic, and obstructive causes. Imaging confirmed intrahepatic cholestasis without biliary obstruction. Causality assessment using the Roussel Uclaf Causality Assessment Method, Maria and Victorino and Naranjo scores indicated probable adverse drug reaction. Liver biopsy demonstrated acute cholestatic injury with portal inflammatory infiltrates and ductular reaction, consistent with drug-related pathology. Empagliflozin withdrawal led to gradual clinical and biochemical recovery. Conclusion: Empagliflozin can, in rare cases, trigger idiosyncratic cholestatic drug-induced liver injury, even in patients with cirrhosis. Early recognition, prompt drug withdrawal, and systematic evaluation are essential. This case adds to the limited literature on sodium-glucose cotransporter 2 inhibitor-associated hepatotoxicity. LEARNING POINTS: Drug-induced liver injury is a diagnosis of exclusion. Clinicians must rule out other causes, especially biliary obstruction, and use structured causality assessment tools to identify the offending drug.Empagliflozin and other sodium-glucose cotransporter 2 inhibitors can, in rare cases, cause liver injury. Monitoring liver function after initiating these drugs is advisable, particularly in patients with pre-existing liver disease.There is no specific treatment for idiosyncratic drug-induced liver injury. Prompt withdrawal of the offending and supportive care are usually sufficient for recovery.

Indexed as

cholestatic hepatitisDrug-induced liver injuryempagliflozinidiosyncratic hepatotoxicitysodium-glucose cotransporter 2 inhibitor

Identifiers

PMID41377793
PMCPMC12688582

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.