Botanical

Terminalia arjuna

Also called arjuna, arjun, arjuna bark, arjun chal, E-OJ-01

By Kymata Labs EditorialMedical review pendingLast reviewed October 13, 2026 · What changed

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Summary

Terminalia arjuna bark has small, mostly Indian trials in heart disease. A 2026 meta-analysis of 9 heart-failure trials (537 patients) found less left-ventricular mass but no significant change in ejection fraction, and the largest single trial (100 patients) found no ejection-fraction benefit. Angina evidence was judged insufficient. All trials used it alongside standard heart medicines.

Top graded outcomes:B evidence grade Ejection fraction in chronic heart failureC evidence grade Left-ventricular mass, ejection fraction, lipids and blood pressure in heart failureD evidence grade Angina frequency and treadmill performance in stable angina

Key facts

What it is
Bark of the arjuna tree, used in Ayurveda as a cardiotonic; extracts contain triterpenoids (arjunic acid), glycosides, flavonoids and tannins[3][1]
Heart failure
9 trials, 537 patients: left-ventricular mass fell, HDL rose, ejection fraction did not change significantly[1]
Largest trial
100 heart-failure patients, 750 mg twice daily for 12 weeks: no change in ejection fraction[4]
Angina
A 2014 systematic review found poor-quality studies and no significant pooled differences[2]
Typical trial dose
500 mg every 8 hours (1,500 mg/day) of bark extract or powder[3][5]
Evidence base
6 graded human outcomes on this page
Last reviewed
October 13, 2026

How it works

ProposedArjuna bark contains triterpenoids, glycosides and antioxidant flavonoids, tannins and proanthocyanidins, and is described as having anti-ischaemic and anti-failure effects. In people, it lowered lipid peroxidation and LDL in one trial and preserved red-cell antioxidant enzymes in another; how it might act on the heart is proposed.[3][4][6]

What the human research says

Human trials only, one row per outcome. The form column shows what each trial actually tested. Grades follow our evidence-grading policy.

At a glance: strongest evidence per outcome

Evidence at a glance: strongest human evidence per outcome
OutcomeGradeEffectStrongest evidenceRows
Heart failureGrade BNo effectRCT · n = 100 · 2016Form tested: Standardised water extract of arjuna stem bark3 rows
CholesterolGrade DMixedRCT · n = 105 · 2001Form tested: Arjuna bark powder1 row
AnginaGrade DImprovedCrossover RCT · n = 58 · 2002Form tested: Arjuna bark extract (IPC-53)1 row
EnduranceGrade DImprovedRCT · n = 32 · 2017Form tested: Proprietary arjuna extract (E-OJ-01)1 row

Every graded row

Outcome
Grade
Form tested
Sort

Showing 6 of 6 outcomes. Human trials only.

OutcomeEffectGradeBest evidencePMID
Ejection fraction in chronic heart failureNo effectGrade B

RCT · n = 100 · 2016

Patients with NYHA class II heart failure and ejection fraction 40% or less on standard drugs

Form: Standardised water extract of arjuna stem bark · Dose: 750 mg twice daily · Duration: 12 weeks

No change in ejection fraction versus placebo (24.3% vs 25.5%, p=0.4) or in secondary outcomes except red-cell catalase; post-hoc subgroup gains in walk distance and symptoms.

26988798 (opens PubMed)Source [4]
Left-ventricular mass, ejection fraction, lipids and blood pressure in heart failureMixedGrade C

Meta-analysis · n = 537 · 2026

Adults with heart failure in 9 trials

Form: Terminalia arjuna preparations, added to usual treatment · Dose: Varied · Duration: Varied

Left-ventricular mass fell (mean difference −44.3) and HDL rose (+3.5), but ejection fraction improved only non-significantly (+1.85, p=0.1) and blood pressure, triglycerides and LDL did not change.

42389976 (opens PubMed)Source [1]
Cholesterol and lipid peroxidation in coronary heart diseaseMixedGrade D

RCT · n = 105 · 2001

Patients with coronary heart disease not on lipid-lowering drugs

Form: Arjuna bark powder · Dose: 500 mg/day · Duration: 30 days

Total cholesterol fell 9.7% and LDL 15.8% within the arjuna group; lipid peroxides fell 29.3% (vitamin E: 36.4%).

11225136 (opens PubMed)Source [6]
Angina frequency and treadmill performance in stable anginaImprovedGrade D

Crossover RCT · n = 58 · 2002

Men with chronic stable angina

Form: Arjuna bark extract (IPC-53) · Dose: 500 mg every 8 hours · Duration: 1 week per treatment

Angina episodes and rescue nitrate use fell (5.7 vs 18.2 mg/week isosorbide dinitrate) and treadmill exercise time rose (6.1 vs 4.8 min) versus placebo.

12086380 (opens PubMed)Source [3]
Ejection fraction and exertion in exercising young menImprovedGrade D

RCT · n = 32 · 2017

Healthy men aged 18–40 doing regular endurance exercise

Form: Proprietary arjuna extract (E-OJ-01) · Dose: 400 mg/day · Duration: 56 days

Ejection fraction rose and right-ventricular performance index and perceived exertion fell versus placebo; CK-MB and troponin did not change.

27930383 (opens PubMed)Source [7]
Symptoms and echocardiography in refractory heart failureImprovedGrade D

Crossover RCT · n = 12 · 1995

Patients with NYHA class IV heart failure, mostly dilated cardiomyopathy

Form: Arjuna bark extract · Dose: 500 mg every 8 hours · Duration: 2 weeks per treatment

Ejection fraction rose (35% vs 30%) and NYHA class, ventricular volumes and stroke volume improved versus placebo.

7649665 (opens PubMed)Source [5]

Forms

FormElemental %Absorption (human data)GI toleranceStudied for
Arjuna bark extract (standardised)Varies[3][4][5][7]Not applicable (whole compound or extract; no elemental fraction)No human absorption data.[3][4]Well tolerated in a 12-week trial of 750 mg twice daily.[4]Heart failure, angina and athlete trials (400–1,500 mg/day)
Arjuna bark powderVaries[6]Not applicable (whole compound or extract; no elemental fraction)No human absorption data.[6]No adverse effects reported in the abstract of the 30-day trial.[6]Cholesterol trial in coronary heart disease (500 mg/day)

Studied doses

Doses studied in human trials ranged from 400 mg/day of an extract (8 weeks) and 500 mg/day of bark powder (30 days) to 1,500 mg/day given as 750 mg twice daily (12 weeks) or 500 mg every 8 hours (1–2 week crossover periods).[3][4][5][6][7]

These are amounts used in research, not personal advice. Your clinician or pharmacist can say what fits you.

Interactions

Published interactions only: each row cites a source. No row means none was found in our sources, not that a combination is safe.

Medicines

  • Heart medicinesRCTe.g. Digoxin, anticoagulants such as warfarin, nitrates, beta-blockersEvery trial gave arjuna on top of standard heart drugs, but no human interaction studies have been published, including with digoxin or anticoagulants; in angina it reduced rescue nitrate use.[3][4][5]
  • Drugs cleared by CYP3A4, CYP2D6 or CYP2C9PK studye.g. Warfarin (CYP2C9), metoprolol (CYP2D6), many statins and calcium-channel blockers (CYP3A4)Alcoholic and water extracts of arjuna bark strongly inhibited all three enzymes in human liver microsomes, which could raise levels of these drugs; not yet tested in people.[8]

Who should be careful

Heart failure and angina
Arjuna was studied only as an add-on to prescribed heart medicines under specialist care; the largest heart-failure trial found no ejection-fraction benefit. Lab tests show it blocks enzymes that clear warfarin and several heart drugs, so prescribers should know about it.[4][1][8]
Pregnancy, breastfeeding and children
The trials enrolled adults only, so there are no safety data for these groups.[3][4][7]

Talk to your pharmacist or clinician before starting a supplement, especially if you take prescription medicines.

How to read the label

  1. Studied dose is higher than many labelsMost heart trials used 1,500 mg/day of bark extract, split into two or three doses.[3][4][5]
  2. Extract vs bark powderTrials used standardised water extracts, a branded extract (E-OJ-01) or plain bark powder; results from one do not automatically apply to another.[4][6][7]

Cost per studied dose, without the sales pitch

Compare any product you already have by the amount it delivers, not by capsule count or front-of-pack weight.

Cost per studied dose

Enter the price, servings and the amount per serving from your label.

Formula: price ÷ (servings × amount per serving) × reference amount. Use the amount printed on the Supplement Facts panel, not the front-of-pack compound weight. Reference amounts are what trials studied or official limits, not advice for you. We don't rank or link products on this page.

Frequently asked questions

Does Terminalia arjuna help heart failure?

Unclear. A meta-analysis of 9 trials found lower left-ventricular mass but no significant ejection-fraction change, and the largest single trial (100 patients) found no ejection-fraction benefit.[1][4]

Does arjuna help angina?

One 58-person crossover trial reported fewer angina episodes, but a systematic review judged the angina evidence poor and insufficient.[2][3]

Does arjuna lower cholesterol?

One 30-day study found total and LDL cholesterol fell within the arjuna group; the heart-failure meta-analysis found HDL rose but LDL did not change.[6][1]

Can it replace heart medicines?

No trial tested that. Arjuna was always given in addition to standard heart drugs.[3][4][5]

What dose was studied?

Mostly 500 mg every 8 hours or 750 mg twice daily of bark extract (1,500 mg/day).[3][4][5]

Sources

  1. [1]Evaluation of the Therapeutic Potential and Safety of Terminalia arjuna in Heart Failure Management: A Systematic Review and Meta-analysis of Randomized Controlled Trials.. Ann Afr Med, 2026. meta-analysis PMID 42389976
  2. [2]Terminalia arjuna in Chronic Stable Angina: Systematic Review and Meta-Analysis.. Cardiol Res Pract, 2014. systematic-review PMID 24600529
  3. [3]Efficacy of Terminalia arjuna in chronic stable angina: a double-blind, placebo-controlled, crossover study comparing Terminalia arjuna with isosorbide mononitrate.. Indian Heart J, 2002. crossover-RCT PMID 12086380
  4. [4]Clinical efficacy of water extract of stem bark of Terminalia arjuna (Roxb. ex DC.) Wight & Arn. in patients of chronic heart failure: a double-blind, randomized controlled trial.. Phytomedicine, 2016. RCT PMID 26988798
  5. [5]Salutary effect of Terminalia Arjuna in patients with severe refractory heart failure.. Int J Cardiol, 1995. crossover-RCT PMID 7649665
  6. [6]Antioxidant and hypocholesterolaemic effects of Terminalia arjuna tree-bark powder: a randomised placebo-controlled trial.. J Assoc Physicians India, 2001. RCT PMID 11225136
  7. [7]Effect of E-OJ-01 on Cardiac Conditioning in Young Exercising Adults: A Randomized Controlled Trial.. Am J Ther, 2017. RCT PMID 27930383
  8. [8]In vitro modulatory effects of Terminalia arjuna, arjunic acid, arjunetin and arjungenin on CYP3A4, CYP2D6 and CYP2C9 enzyme activity in human liver microsomes.. Toxicol Rep, 2015. animal-study PMID 28962416

What changed

  1. October 13, 2026 · evidence, safety · reviewIndependent adversarial review: added in-vitro CYP3A4/CYP2D6/CYP2C9 inhibition (human liver microsomes) as an interaction caution, named digoxin and anticoagulants as unstudied combinations, and added industry and erratum notes. All PMIDs re-verified; evidence figures match abstracts.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  2. October 13, 2026 · all · reviewAdversarial second pass: every PMID re-checked against NCBI esummary (title, year, no retraction, erratum or expression-of-concern flags) and every number in each evidence row re-read against its PubMed abstract (PMC full text where the abstract lacked dose or duration). Countries and funding notes kept only where the abstract or full text states them; interactions listed only where a source supports them, otherwise stated as unstudied.Writer: Kymata Labs Editorial · No credentialed reviewer yet
  3. October 13, 2026 · all · new pageFirst draft. Every PMID checked against NCBI E-utilities esummary (title and year taken from the record) and abstracts read for the cited rows.Writer: Kymata Labs Editorial · No credentialed reviewer yet

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