Boldo (Peumus boldus)

Peumus boldus
Evidence Level
Preliminary
6 Clinical Trials
4 Documented Benefits
1/5 Evidence Score

Boldo is the dried leaf of Peumus boldus, an evergreen tree native to Chile, used as a digestive tea in South America and Europe. Its safety record matters more than its research. The leaf oil is rich in ascaridole, a compound regulators call highly toxic, so the European Medicines Agency accepts only boldo teas and water extracts for short use, at most 2 weeks, and advises against use in pregnancy, breastfeeding, anyone under 18, and people with liver or bile duct problems or gallstones. Case reports describe liver injury, mostly in older adults who recovered after stopping, plus one fatal case in a conference abstract, an allergic reaction and two possible drug interactions. The only human dosing study is a 12-person trial in which a boldo extract slowed gut transit. Claims about bile flow and liver protection rest on animal and lab work, much of it on boldine, the main alkaloid.

Studied Dose One human dosing study: 2.5 g/day of a dry ethanol extract for 4 days. EU traditional use: 1 to 2 g leaf as tea 2 to 3 times daily, or 200 to 400 mg water extract twice daily, for no more than 2 weeks.
Active Compound Isoquinoline alkaloids (0.25 to 0.7%, mainly boldine) and 2 to 4% volatile oil rich in ascaridole.

Benefits

Traditional use as a digestive tea

The European Medicines Agency accepts boldo leaf tea and water extract as a traditional herbal medicine for indigestion (dyspepsia) and mild gut cramping, based only on long-standing use. Its assessors found no clinical trials of boldo-only products and say efficacy is only plausible, not shown. Use is limited to short courses of up to 2 weeks.

Gut transit time in healthy volunteers

In a crossover study in 12 healthy volunteers, 4 days of a dry boldo extract lengthened the time for a test sugar to reach the large bowel (about 113 vs 87 minutes with placebo). In a separate test in 43 healthy adults, a sip of bitter boldo tea did not change how quickly liquid moved through the mouth, throat or esophagus.

Bile flow in animal studies of boldine

Boldo is sold for bile flow, but this has not been measured in people. In rats, boldine, the main alkaloid, increased bile flow when infused and after 28 days of oral dosing. A hydroalcoholic boldo leaf extract did not increase bile flow in rats, so the whole-leaf effect is unconfirmed.

Liver cell responses in lab and animal studies

A hydroalcoholic boldo extract protected isolated rat liver cells and mouse livers from chemical injury in lab models, and boldine acts as an antioxidant in many lab tests. No human trial has tested liver outcomes, and published case reports link boldo tea and supplements to liver injury in people.

Mechanism of action

1

Boldine and bile secretion

In rats, boldine raised bile flow by an osmotic effect when infused, and 28 days of oral dosing gave a slight lasting rise in bile flow alongside more of the Bsep transporter that pumps bile acids into bile; boldine also stimulated FXR, the receptor that controls Bsep. These findings are for isolated boldine in animals; the amount reaching the liver from boldo tea in people is unknown.

2

Smooth muscle relaxation

In isolated rat intestine, boldine relaxed muscle contractions triggered by acetylcholine by competing at the same receptor, a possible basis for the traditional use against mild gut cramping. A 12-person human study found slower gut transit with a boldo extract, which fits but does not prove this action.

3

Ascaridole and why water preparations are preferred

Ascaridole is a peroxide-containing compound that makes up 16 to 38% of boldo leaf oil and is classed as highly toxic. It dissolves poorly in water, so regulators accept teas and water extracts but not powdered leaf as such or alcohol extracts. One analysis found ascaridole in all 10 commercial boldo leaf samples it tested (sold in tea bags or loose).

Clinical trials

1
Dry boldo extract and gut transit: 12-volunteer crossover
PubMed

Placebo-controlled crossover study, indexed as randomized: 2.5 g of a dry boldo extract (60% ethanol, 0.12% boldine per the EMA) or glucose placebo for 4 days each, with a lactulose hydrogen breath test on day 4. (Gotteland et al. 1995, Rev Med Chil)

12 healthy volunteers in Chile.

Oro-cecal transit time was longer with boldo than with placebo (112.5 vs 87 minutes, P < 0.05). Only transit time was measured; there were no symptom or digestion outcomes, the study was tiny and short, and the extract was an alcohol extract, a type the EU monograph does not accept for traditional herbal medicines.

2
Bitter boldo tea and swallowing transit in 43 adults
PubMed

Scintigraphy study comparing 5 mL of bitter boldo tea (2 g leaves boiled in 50 mL water) with 5 mL of a sweet sucrose drink, swallowed in random order. (Alves et al. 2013, Arq Gastroenterol)

43 healthy adults aged 23 to 71 without swallowing, digestive, heart or nerve problems.

No difference between the bitter boldo bolus and the sweet bolus in mouth, throat or esophageal transit, clearance or residue. The study used boldo as a bitter taste, not as a supplement dose.

3
Case report: liver enzyme rise after boldo was added to a laxative
PubMed

Single case report of suspected herb-induced liver injury. (Piscaglia et al. 2005, Scand J Gastroenterol)

An elderly man with fatty liver who had used a herbal laxative mixture for years.

Transaminases and GGT rose several-fold within months after the maker added boldo leaf extract to the mixture; transaminases returned to normal promptly after he stopped it. One case cannot prove cause.

4
Case report: jaundice after 2 weeks of boldo tea
PubMed

Single case report of suspected herb-induced liver injury. (Ribeiro et al. 2017, J Diet Suppl)

A 72-year-old woman who drank boldo leaf infusion repeatedly for 2 weeks.

She developed jaundice and raised liver enzymes; after common causes were excluded, boldo was judged the probable cause, and she recovered after stopping. The EMA notes no formal causality score was reported.

5
Case report: jaundice after a month of boldo tea
PubMed

Single case report of suspected herb-induced liver injury. (Oliveira Sá et al. 2020, Eur J Case Rep Intern Med)

An 87-year-old man who had repeatedly drunk boldo leaf infusions over the previous month.

He was admitted with 2 weeks of weakness, poor appetite and jaundice. Other causes were excluded, boldo was judged the probable cause, and he recovered fully within a week of stopping. The EMA notes no formal causality score was reported.

6
Case report: raised INR on warfarin with boldo and fenugreek
PubMed

Single case report of a suspected herb-drug interaction, with rechallenge. (Lambert et al. 2001, Pharmacotherapy)

A woman taking warfarin for atrial fibrillation who also took several natural products, including boldo and fenugreek.

Her INR rose, returned to normal a week after she stopped the products, and rose again when both were restarted. The authors rated the link to the two products together as probable; the EMA notes it cannot be concluded whether one or both contributed. The patient reported no adverse reaction.

Side effects and drug interactions

Common Potential side effects

Liver injury: published case reports describe jaundice or a several-fold rise in liver enzymes in older adults (a woman of 72, a man of 87 and an elderly man) after boldo tea or a boldo-containing laxative, which cleared after stopping. A conference abstract (not PubMed-indexed) reports a 48-year-old woman who died of liver injury that began after 15 days of a boldo-based supplement. No case had a formal causality score, and the EMA plans to look for new cases at its next review.
Ascaridole: boldo leaf oil is classed as highly toxic and should not be taken internally. The EU accepts only teas and water extracts because ascaridole dissolves poorly in water; it does not accept powdered leaf as such or alcohol extracts, and sets no numeric ascaridole limit, only that levels be measured.
Do not use with bile duct blockage, cholangitis, liver disease, gallstones or other bile disorders that need medical care (EU monograph).
Not recommended in pregnancy or breastfeeding: in rats, high doses (800 mg/kg) of a boldo extract or boldine caused fetal malformations and some miscarriages.
Not recommended under 18. A 12-year-old girl developed behavior changes and hallucinations after drinking boldo infusions.
Allergic reactions: one case of anaphylaxis (hives, facial swelling, trouble swallowing and breathing) after a boldo leaf infusion was confirmed by oral challenge (Monzón 2004, as summarized in the EMA assessment report).
EU guidance limits use to 2 weeks; see a doctor if symptoms persist or worsen.

Important Drug interactions

Warfarin: in one case, INR rose with boldo plus fenugreek and rose again on restarting both; check INR if you take an anticoagulant.
Tacrolimus: one kidney transplant recipient had low tacrolimus levels on boldo that recovered after stopping it.
The EU monograph lists no confirmed interactions, but no formal interaction studies have been done.

Frequently asked questions about Boldo (Peumus boldus)

What is ascaridole, and why does it matter for boldo?

Ascaridole is a toxic compound in boldo leaf oil; it makes up 16 to 38% of the oil. EU regulators say boldo oil should not be taken at all and accept only boldo teas and water extracts, because little ascaridole dissolves in water. One analysis found ascaridole in all 10 commercial boldo leaf samples it tested (sold in tea bags or loose); it did not report how much reaches the brewed tea.

Is boldo tea different from boldo capsules or tinctures?

The EU monograph covers only cut leaf brewed as tea and a water-based dry extract. Powdered leaf taken as such and alcohol extracts, such as tinctures, are not accepted because they may carry more ascaridole. Product labels rarely state ascaridole content.

Can boldo affect liver tests?

Several case reports describe jaundice or high liver enzymes in older adults after boldo tea or boldo-containing products, which cleared after stopping, and one conference report describes a death. A doctor should know about any boldo use if liver tests are abnormal, and people with liver or gallbladder problems should not use it.

Does boldo increase bile flow in people?

This has not been measured in people. Boldine, boldo's main alkaloid, increased bile flow in rats, but a boldo leaf extract did not in another rat study. The only human study measured gut transit time, which was slower with boldo.

What is Boldo?

Boldo is the dried leaf of Peumus boldus, an evergreen tree native to Chile, used as a digestive tea in South America and Europe. Its safety record matters more than its research.

What is Boldo used for?

NutraSmarts does not list Boldo under a health category. What the research covers: The European Medicines Agency accepts boldo leaf tea and water extract as a traditional herbal medicine for indigestion (dyspepsia) and mild gut cramping, based only on long-standing use.

What is the recommended dosage of Boldo?

The clinically studied dose is One human dosing study: 2.5 g/day of a dry ethanol extract for 4 days. EU traditional use: 1 to 2 g leaf as tea 2 to 3 times daily, or 200 to 400 mg water extract twice daily, for no more than 2 weeks. Always follow the product label and check with a healthcare provider for personal advice.

Is Boldo safe, and does it have side effects?

Side effects and cautions reported for Boldo include: Liver injury: published case reports describe jaundice or a several-fold rise in liver enzymes in older adults (a woman of 72, a man of 87 and an elderly man) after boldo tea or a boldo-containing laxative, which cleared after stopping. It may also interact with some medications. Boldo is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Boldo interact with any medications?

Possible interactions include: Warfarin: in one case, INR rose with boldo plus fenugreek and rose again on restarting both; check INR if you take an anticoagulant. Tacrolimus: one kidney transplant recipient had low tacrolimus levels on boldo that recovered after stopping it. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Boldo?

NutraSmarts rates the evidence for Boldo as Preliminary (1 out of 5). It is backed by 6 study summaries and 16 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(16 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Committee on Herbal Medicinal Products (HMPC), European Medicines Agency. European Union herbal monograph on Peumus boldus Molina, folium (EMA/HMPC/453725/2016). European Medicines Agency. 2016;Final monograph adopted 22 November 2016, published 12 January 2017 (not PubMed-indexed)..SourceUsed to support: Not PubMed-indexed: EU regulatory monograph. Traditional use only, for symptomatic relief of dyspepsia and mild spasmodic disorders of the gastrointestinal tract, based exclusively on long-standing use. Covers only cut leaf as a herbal tea (1 to 2 g in 150 ml boiling water, 2 to 3 times daily) and a water-based dry extract (5:1; 200 to 400 mg twice daily, 400 to 800 mg a day). See a doctor if symptoms last more than 2 weeks. Contraindications: hypersensitivity, bile duct obstruction, cholangitis, liver disease, gallstones and other biliary disorders needing medical supervision. Not recommended under 18 or in pregnancy and lactation. Interactions: none reported. Undesirable effects: hypersensitivity (anaphylaxis), frequency not known. No genotoxicity or carcinogenicity tests. Ascaridole levels in preparations and products should be determined; no numeric limit is set.
  2. Committee on Herbal Medicinal Products (HMPC), European Medicines Agency. Assessment report on Peumus boldus Molina, folium (EMA/HMPC/453726/2016). European Medicines Agency. 2016;Final assessment report dated 22 November 2016, published 12 January 2017 (not PubMed-indexed)..SourceUsed to support: Not PubMed-indexed: EU regulatory assessment. Leaf contains 0.25 to 0.7% isoquinoline alkaloids (boldine usually the main one) and 2 to 4% volatile oil, in which ascaridole makes up 16 to 38%. Calls ascaridole highly toxic and boldo oil one of the most toxic oils (rat oral LD50 0.13 g/kg); the oil should not be used internally or externally. Because ascaridole dissolves poorly in water, only teas and water extracts are accepted; powdered leaf as such and alcohol extracts are not. No clinical studies of boldo-only products were found; efficacy is only plausible from long-standing use. Duration should be limited to 2 weeks. Summarizes a 2004 anaphylaxis case confirmed by oral challenge, the warfarin and tacrolimus case reports, rat reproductive toxicity, and a rat study in which boldine relaxed isolated gut muscle. Not included in the EU list because Ames mutagenicity data are missing.
  3. Committee on Herbal Medicinal Products (HMPC), European Medicines Agency. Addendum to Assessment report on Peumus boldus Molina, folium (EMA/HMPC/329351/2024). European Medicines Agency. 2024;Periodic review adopted 25 September 2024, published 11 February 2025 (not PubMed-indexed)..SourceUsed to support: Not PubMed-indexed: EU periodic review (2016 to 2024). Found no new clinical studies. A EudraVigilance search found nine reports naming boldo: four involved multi-herb products taken with three or more other medicines, three gave no relevant information and one involved misuse of three herbal products; none was judged directly related to boldo leaf. A separate interaction search found one case reported three times (vaginal bleeding, raised INR). Notes the published liver injury cases in elderly patients but says they lacked a formal causality score. Concluded the reported reactions "cannot be attributed" to boldo leaf and found no new safety concern, so no revision was needed, while flagging new liver case reports as relevant for the next review.
  4. Piscaglia F, Leoni S, Venturi A, Graziella F, Donati G, Bolondi L. Caution in the use of boldo in herbal laxatives: a case of hepatotoxicity. Scand J Gastroenterol. 2005;40(2):236-9. doi: 10.1080/00365520410009537.PubMedUsed to support: Case report: an elderly man with fatty liver who had taken a herbal laxative mixture for years developed a several-fold rise in transaminases and GGT within months after the maker added boldo leaf extract to it. Transaminases promptly returned to normal after he stopped the product. The authors suggest boldo leaf extract might be hepatotoxic, at least in elderly people with fatty liver.
  5. Ribeiro RJ, Silvestre C, Duarte C. Hidden Risks of Alternative Medicines: A Case of Boldo-Induced Hepatotoxicity. J Diet Suppl. 2017;14(2):186-190. doi: 10.1080/19390211.2016.1207123.PubMedUsed to support: Case report: a 72-year-old woman developed jaundice and raised liver enzymes after drinking boldo leaf infusion repeatedly for 2 weeks. Other common causes were excluded, boldo-induced liver injury was judged probable, and she recovered after stopping.
  6. Oliveira Sá A, Pimentel T, Oliveira N. Boldo-Induced Hepatotoxicity: A Case of Unexplained Jaundice. Eur J Case Rep Intern Med. 2020;7(12):002116. doi: 10.12890/2020_002116.PubMedUsed to support: Case report: an 87-year-old man admitted with 2 weeks of weakness, poor appetite and jaundice had been drinking boldo leaf infusions for the previous month. After other causes were excluded, boldo-induced liver injury was judged probable; he recovered fully within a week of stopping.
  7. Reyes-Ferreira E, González-Chávez HE, Arrazola-Mendoza KS, De la Peña-Camacho F, Vargas-Torrescano LH, Castrejón-Mora JL. Liver Injury Induced by Peumus boldus with Fatal Outcome. Case Report. Annals of Hepatology. 2025;30(Suppl 1):101878. doi: 10.1016/j.aohep.2025.101878 (conference abstract, not PubMed-indexed)..SourceUsed to support: Not PubMed-indexed: conference abstract from the Mexican Association of Hepatology 2024 meeting. A 48-year-old woman with type 2 diabetes on insulin, gallbladder removed years earlier, took a herbal supplement based on Peumus boldus (other ingredients not stated) in the previous 15 days and developed jaundice with a cholestatic pattern that kept progressing after she stopped. Infectious and autoimmune causes were ruled out; biopsy showed steatohepatitis with features of toxic injury. She died 65 days after symptoms began. Dose and a formal causality score were not reported.
  8. Lambert JP, Cormier J. Potential interaction between warfarin and boldo-fenugreek. Pharmacotherapy. 2001;21(4):509-12. doi: 10.1592/phco.21.5.509.34492.PubMedUsed to support: Case report: a woman on warfarin for atrial fibrillation had a rise in INR while taking several natural products including boldo and fenugreek. INR returned to normal a week after she stopped them and rose again when both were restarted. The authors rated the link to boldo and fenugreek together as probable (Naranjo algorithm); the EMA assessment notes it cannot be concluded whether one or both contributed.
  9. Carbajal R, Yisfalem A, Pradhan N, Baumstein D, Chaudhari A. Case report: boldo (Peumus boldus) and tacrolimus interaction in a renal transplant patient. Transplant Proc. 2014;46(7):2400-2. doi: 10.1016/j.transproceed.2014.01.021.PubMedUsed to support: Case report: a 78-year-old kidney transplant recipient taking boldo 300 mg twice daily for the last few weeks had tacrolimus levels below 3 ng/mL; one week after stopping boldo, levels reached 6.1 ng/mL on the same tacrolimus dose. A single case suggesting a possible interaction.
  10. Chaboussant PJ, Gagez AL, Graber M, Zhao JM, Chavant F, Perault-Pochat MC, Graber D. [Behavioural impairments and hallucinations after consumption of boldo leaf infusions]. Therapie. 2014;69(5):465-7. doi: 10.2515/therapie/2014052.PubMedUsed to support: Case report (letter, in French): a 12-year-old girl developed behavioral problems and hallucinations after drinking boldo leaf infusions; the authors suspect boldine and say children should avoid boldo infusions.
  11. Almeida ER, Melo AM, Xavier H. Toxicological evaluation of the hydro-alcohol extract of the dry leaves of Peumus boldus and boldine in rats. Phytother Res. 2000;14(2):99-102. doi: 10.1002/(sici)1099-1573(200003)14:2<99::aid-ptr600>3.0.co;2-4.PubMedUsed to support: Rat study: a hydroalcoholic boldo leaf extract and boldine given to pregnant rats showed abortive and teratogenic effects and changed blood bilirubin, cholesterol, glucose, ALT, AST and urea; 90 days of dosing caused no tissue changes on histology per the abstract, although the EMA summary of the paper notes steatosis in two animals at 800 mg/kg. The EMA reports the effects occurred at 800 mg/kg, a high dose.
  12. de Souza WFM, Mariano XM, Isnard JL, de Souza GS, de Souza Gomes AL, de Carvalho RJT, Rocha CB, Junior CLS, Moreira RFA. Evaluation of the volatile composition, toxicological and antioxidant potentials of the essential oils and teas of commercial Chilean boldo samples. Food Res Int. 2019;124:27-33. doi: 10.1016/j.foodres.2018.12.059.PubMedUsed to support: Lab analysis of 10 commercial Chilean boldo samples sold in Brazil: ascaridole, boldine, p-cymene and 1,8-cineole were found in all samples; the essential oils were highly cytotoxic in a lab assay (estimated LD50 values below 200 ppm), and the teas held most of the antioxidant activity. No human testing.
  13. Gotteland M, Espinoza J, Cassels B, Speisky H. [Effect of a dry boldo extract on oro-cecal intestinal transit in healthy volunteers]. Rev Med Chil. 1995;123(8):955-60..PubMedUsed to support: Placebo-controlled crossover study (in Spanish) in 12 healthy volunteers: 2.5 g of a dry boldo extract or glucose placebo for 4 days each. Oro-cecal transit time, measured by lactulose breath hydrogen, was longer with boldo (112.5 vs 87 minutes, P < 0.05). The EMA describes the extract as made with 60% ethanol and containing 0.12% boldine.
  14. Alves LM, Secaf M, Dantas RO. Effect of a bitter bolus on oral, pharyngeal and esophageal transit of healthy subjects. Arq Gastroenterol. 2013;50(1):31-4. doi: 10.1590/s0004-28032013000100007.PubMedUsed to support: Scintigraphy study in 43 healthy adults: 5 mL of a bitter boldo leaf tea (2 g leaves boiled in 50 mL water) and 5 mL of a sweet sucrose drink were each swallowed in random order. Mouth, throat and esophageal transit and clearance did not differ between the two.
  15. Lanhers MC, Joyeux M, Soulimani R, Fleurentin J, Sayag M, Mortier F, Younos C, Pelt JM. Hepatoprotective and anti-inflammatory effects of a traditional medicinal plant of Chile, Peumus boldus. Planta Med. 1991;57(2):110-5. doi: 10.1055/s-2006-960043.PubMedUsed to support: Animal and cell study: a dried hydroalcoholic boldo extract protected isolated rat liver cells and mouse livers from chemical injury in lab models, with boldine apparently involved, and reduced paw swelling in rats. The bile-increasing (choleretic) effect claimed in traditional use was not confirmed in rats.
  16. Cermanova J, Kadova Z, Zagorova M, Hroch M, Tomsik P, Nachtigal P, Kudlackova Z, Pavek P, Dubecka M, Ceckova M, Staud F, Laho T, Micuda S. Boldine enhances bile production in rats via osmotic and farnesoid X receptor dependent mechanisms. Toxicol Appl Pharmacol. 2015;285(1):12-22. doi: 10.1016/j.taap.2015.03.004.PubMedUsed to support: Rat study: intravenous boldine raised bile flow 1.4-fold through an osmotic effect, and 28 days of oral boldine produced a mild lasting rise in bile formation linked to activation of the FXR receptor and the Bsep bile acid transporter. Boldine alone, in animals; not tested with boldo products in people.