GLOBALKRATOM.ORG · Evidence-based policy resources

Hepatotoxicity & Liver Injury

Published case reports, systematic reviews, and forensic literature documenting kratom‑associated cholestatic hepatitis, liver failure, and transplantation.

Key Findings

Systematic Reviews & Overviews
Liver Injury Associated with Kratom: A Systematic Review (32 cases)

Systematic review of 32 published cases: predominantly cholestatic injury, 4 progressed to liver transplantation. Kratom causes severe, sometimes irreversible liver damage.

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Kratom‑Induced Hepatotoxicity: Systematic Review of Case Reports

Review of 20 cases; majority cholestatic, some requiring liver transplant. Highlights unpredictable hepatotoxicity even at low doses.

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Mitragyna speciosa Korth toxicity: Experimental findings & future prospects

Comprehensive review of in vitro, in vivo, and case study toxicities including hepatotoxicity, nephrotoxicity, and cardiotoxicity.

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Case Reports – Cholestatic & Mixed Injury
Severe jaundice with life‑threatening liver failure reversed by plasma exchange

Total bilirubin 70.6 mg/dL – highest reported. Plasma exchange saved the patient. Kratom can cause catastrophic liver failure.

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Kratom‑induced acute liver injury (J Hepatol, 2023)

Patient with jaundice and total bilirubin 10.7 mg/dL after 3 weeks of kratom. Injury resolved only after cessation.

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Kratom (Mitragyna speciosa)‑Induced Hepatitis

High‑dose kratom (30 g/day) caused bilirubin 34.3 mg/dL and perivenular necrosis on biopsy. RUCAM score 6 (probable).

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Kratom‑Associated Mixed Cholestatic‑Hepatocellular Injury in Long COVID patient

ALT 1635, AST 642, bilirubin 10.6 mg/dL after 2 weeks of kratom cocktail. RUCAM score 7 (probable).

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Kratom induced severe cholestatic injury mimicking primary biliary cholangitis

Low‑dose kratom (3 g total) produced jaundice and severe cholestasis. Even small amounts can trigger injury.

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Kratom‑Induced Cholestatic Liver Injury – Conservative Management

Peak bilirubin 28.9 mg/dL after 2 months of kratom use. Severe cholestatic hepatitis confirmed by biopsy.

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Acute liver injury following short‑term use of kratom

30‑year‑old with ALT 1057, AST 332, total bilirubin 6.7 mg/dL after 2 weeks kratom. Normalized after discontinuation.

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Drug‑Induced Liver Injury Caused by Kratom as Alternative Pain Treatment

47‑year‑old with mixed liver injury after 3 weeks kratom. Positive rechallenge with shorter latency. RUCAM score +9 (highly probable).

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Kratom‑Induced Liver Injury – Case Report (Cureus)

Case report of kratom‑induced seizures and elevated liver enzymes, highlighting hepatotoxicity.

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Histologic Characterization of Kratom Use‑Associated Liver Injury

Liver biopsy showing cholestatic injury and bile duct damage.

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Recurrent Kratom‑Induced Hepatotoxicity with Rechallenge

Patient re‑challenged after recovery and developed liver injury again – confirming causality.

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Severe Outcomes – Liver Failure & Transplantation
Multiorgan Dysfunction Related to Kratom Ingestion

Mixed liver injury, kidney failure requiring dialysis, colitis. Required liver transplantation and remains on dialysis.

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Kratom: a dangerous player in the opioid crisis

32‑year‑old developed severe cholestatic liver injury (CIOMS 8, highly probable). Authors conclude kratom has “potentially lethal side effects”.

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Kratom‑induced transaminitis with precipitated opioid withdrawal

38‑year‑old with AST 173, ALT 586 after chronic kratom use. Highlights need for liver monitoring.

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Legally Lethal Kratom – Overdose with Hepatorenal Injury

36‑year‑old consumed >500g kratom; AST 1347, ALT 3717, renal injury. Required 14 days ICU.

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Clinical Summary

Kratom‑associated liver injury typically presents as cholestatic or mixed hepatocellular‑cholestatic hepatitis. Common symptoms include jaundice, pruritus, dark urine, abdominal pain, nausea, and fatigue. Laboratory abnormalities include elevated bilirubin (often >10 mg/dL), alkaline phosphatase, and transaminases (AST/ALT). Latency from kratom initiation to injury ranges from days to months; rechallenge can produce rapid recurrence. Severe cases have progressed to acute liver failure, requiring intensive care, plasma exchange, or liver transplantation. The FDA has issued multiple warnings regarding hepatotoxicity, and poison center surveillance continues to identify liver injury cases.

Clinicians should consider kratom exposure in the differential diagnosis of unexplained cholestatic or mixed liver injury, especially in patients who use herbal supplements. Routine toxicology screens do not detect kratom alkaloids – directed history is essential.