Roidipedia.Compound reference & reporting
05 AUG 2026
CompoundsOther TUDCA (Tauroursodeoxycholic Acid)
OtherSupplementBile acidHepatoprotective

TUDCA (Tauroursodeoxycholic Acid)

Also known as Tauroursodeoxycholic acid · TUDCA · Tauroursodiol

TUDCA is the taurine conjugate of ursodeoxycholic acid, a hydrophilic bile acid marketed as a liver-support supplement. PED users take it primarily on oral 17-alpha-alkylated steroid cycles to relieve cholestasis — the bile-flow impairment that drives raised bilirubin, jaundice and itching. Human evidence for its use in AAS-induced cholestasis is largely anecdotal and extrapolated from cholestatic-liver-disease trials of its parent compound UDCA.

01 Overview

TUDCA works as a choleretic: it expands the hydrophilic bile-acid pool, displacing more toxic hydrophobic bile acids, stabilising hepatocyte membranes and stimulating bile flow. This is the same mechanistic basis on which UDCA (ursodiol) is licensed for primary biliary cholangitis and gallstone dissolution. TUDCA additionally has documented ER-stress-reducing (chemical chaperone) activity in preclinical models.

Among PED users it is taken during methylated oral cycles to counter the intrahepatic cholestasis those compounds cause, and to lower elevated bilirubin. It does not meaningfully protect against the transaminase elevations or the rare peliosis/adenoma risk of oral AAS, and its dosing in this population is derived from anecdote rather than trials. It is generally very well tolerated, with loose stools the main complaint.

02 Mechanism

Hydrophilic bile acid that enriches the bile-acid pool with less cytotoxic species, stabilises hepatocyte and mitochondrial membranes, promotes bile flow (choleresis) and acts as a chemical chaperone reducing endoplasmic-reticulum stress.

03 Dosing

TierDoseRouteNotes
Parent UDCA cholestasis dosing (reference)13–15 mg/kg/dayOralLicensed ursodiol dose for primary biliary cholangitis, for context only.
General liver support250–500 mg/dayOralCommon maintenance range used alongside non-methylated cycles.
On methylated orals500–1000 mg/dayOralAnecdotal dosing to counter cholestasis from 17aa oral steroids; split through the day.

04 Effects

EffectMagnitudeEvidence
Improved bile flow / lower bilirubinRelieves cholestasis and can lower elevated bilirubin; strongest evidence is for the parent UDCA in cholestatic liver disease.variableObservational
Relief of cholestatic itchUsers report reduced pruritus and jaundice on methylated orals, consistent with restored bile flow.subjectiveAnecdotal

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Diarrhoea / loose stoolsThe most frequent complaint; dose-related loosening of stool.MildCommonObservational
False sense of hepatic safetyTUDCA addresses cholestasis but not transaminase-marked hepatocellular stress or structural lesions from oral AAS, so users may run harsh orals longer than is safe.ModerateSituationalAnecdotal

07 References

Tauroursodeoxycholic acid: a bile acid with therapeutic potentialWorld J Gastroenterol, 2017
Ursodeoxycholic acid in cholestatic liver diseaseHepatology (review)

08 Discussion0 comments

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This page is reference information, not medical advice. Doses and protocols are documented as they appear in the clinical literature and in practice — describing them is not a recommendation to use them. Countermeasures listed here are not a substitute for a physician. Legal status varies by jurisdiction and changes.