Most representative drugs in different cholestatic phenotypes of liver damage
Acute cholestasis | Chronic cholestasis | |||||
---|---|---|---|---|---|---|
Bland cholestasis | Cholestatic hepatitis | Autoimmune features | Vanishing bile duct syndrome | Secondary sclerosing cholestasis | Autoimmune features | Fibrosis/cirrhosis |
AAS Herbs (tribulus) Warfarin Thiabendazole Oral contraceptives SARS-CoV-2 vaccines | NSAIDs Antiinfectives (amoxicillin-clavulanate, penicillins, macrolides, TMP-SMX, etc.) Statins Tricyclic antidepressants Selective serotonin reuptake inhibitors Azathioprine Eculizumab Cisplatin Herbs (Kratom, Ashwagandha) | Statins (atorvastatin) Nitrofurantoin SARS-CoV-2 vaccines | Antibiotics (amoxicillin/clavulanate, azithromycin, flucloxacillin, quinolones, etc.) NSAIDs (ibuprofen, diclofenac) Psychotropes (chlorpromazine, imipramine, carbamazepine, etc.) | Immunotherapy (nivolumab, pembrolizumab, durvalumab, etc.) Docetaxel Ketamine Atorvastatin | Nitrofurantoin | Chlorpromazine Nitrofurantoin |
JMPB and JPTO equally contributed to: Conceptualization and Writing—original draft. RJA: Conceptualization, Writing—original draft, and Writing—review & editing. MGC: Writing—review & editing. All authors have read and agreed to the published version of the manuscript.
The authors declare that they have no conflicts of interest.
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