Drug-induced liver injury secondary to tirzepatide

Tirzepatide is a dual gastric inhibitory polypeptide and glucagon-like peptide-1 receptor agonist, used for the treatment of type 2 diabetes mellitus and obesity. While gastrointestinal side effects are well described in the literature, hepatotoxicity is not a recognised complication. Recent case reports have emerged describing drug-induced liver injury associated with tirzepatide. We present a case of a woman aged in her 20s who developed acute hepatocellular injury within four weeks of commencing tirzepatide. Extensive investigations did not reveal an alternative cause of liver injury. Following the cessation of tirzepatide, the patient demonstrated clinical and biochemical recovery over the following four weeks.

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Publication Details

Journal
BMJ Case Reports
Published
2026-04-01
DOI
https://doi.org/10.1136/bcr-2025-269172
Citations
1
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
27.99
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article

Drug-induced liver injury secondary to tirzepatide

Adam Haig, Deloshaan Subhaharan, Peter Mikhail-Gouda, Chester Yixuan Cao
1 citations
BMJ Case Reports
Drug-Induced Hepatotoxicity and Protection
27.99
article

Drug-induced liver injury secondary to tirzepatide

Adam Haig, Deloshaan Subhaharan, Peter Mikhail-Gouda, Chester Yixuan Cao
article en
1 citations

Abstract

Tirzepatide is a dual gastric inhibitory polypeptide and glucagon-like peptide-1 receptor agonist, used for the treatment of type 2 diabetes mellitus and obesity. While gastrointestinal side effects are well described in the literature, hepatotoxicity is not a recognised complication. Recent case reports have emerged describing drug-induced liver injury associated with tirzepatide. We present a case of a woman aged in her 20s who developed acute hepatocellular injury within four weeks of commencing tirzepatide. Extensive investigations did not reveal an alternative cause of liver injury. Following the cessation of tirzepatide, the patient demonstrated clinical and biochemical recovery over the following four weeks.

BMJ Case ReportsVol. 19(4)
Griffith University (AU), Bond University (AU), Gold Coast Hospital (AU)
Good health and well-being
Openalex Percentile: Top 0%
Drug-Induced Hepatotoxicity and Protection
27.99
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