Herb
    Moderate Evidence

    Black Cohosh

    Actaea racemosa / Cimicifuga racemosa

    TL;DR

    Black cohosh is a root extract used at 20–40 mg twice daily for hot flushes. Evidence is mixed but favourable; rare liver injury reports warrant monitoring.

    Ideal For

    • Women with hot flushes and night sweats who cannot or prefer not to use hormone therapy
    • Breast cancer survivors on tamoxifen, with oncology awareness
    • Women with perimenopausal mood and sleep disruption

    Avoid If

    • You have liver disease or raised liver enzymes
    • You are pregnant or breastfeeding
    • You take hepatotoxic medications
    • You have unexplained abdominal pain, dark urine or jaundice

    Frequently Asked Questions

    Is black cohosh a phytoestrogen?
    No. Modern receptor work finds no meaningful oestrogenic binding. Its effect appears to be serotonergic, which is why it has been studied in breast cancer survivors.
    How long until it helps hot flushes?
    Trials typically measured at 8-12 weeks. Give it a full 12 weeks before deciding.
    Is the liver risk real?
    Cases are rare and causality is often uncertain, but they are numerous enough that regulators added warnings. Avoid it with liver disease and stop at the first sign of jaundice or abdominal pain.
    Can it be used with tamoxifen?
    Studies in breast cancer survivors on tamoxifen have not shown interference, but this should be an oncologist-informed decision.

    Overview

    Black cohosh (Actaea racemosa) is a North American woodland plant used traditionally by Indigenous peoples and now among the most widely used botanicals for menopausal symptoms in Europe, where the standardised extracts iCR and BNO 1055 have been studied most.

    Its mechanism is not oestrogenic, despite decades of assumption. Modern work indicates serotonergic activity at 5-HT7 receptors and possible dopaminergic effects, which fits the thermoregulatory nature of hot flushes better than an oestrogen model does. That matters clinically, because it means black cohosh does not stimulate breast or endometrial tissue in the way phytoestrogens might, and it has been studied in breast cancer survivors on tamoxifen.

    Efficacy evidence is genuinely mixed. A Cochrane review found insufficient evidence overall, while several individual trials and later meta-analyses of standardised extracts report meaningful reductions in hot flush frequency and Kupperman index scores versus placebo. The pragmatic reading is that it helps some women modestly and is worth a 12-week trial. Rare cases of hepatotoxicity have been reported; causality is often unclear, but liver function should be checked if symptoms appear.

    How It Works

    • Acts on 5-HT7 serotonin receptors involved in central thermoregulation
    • Possible dopaminergic activity affecting hypothalamic temperature set point
    • Not oestrogen receptor binding — modern assays find no significant oestrogenic activity
    • Triterpene glycosides including actein are considered the active constituents
    • May modulate hypothalamic-pituitary signalling without changing FSH or LH

    Quick Facts

    • Reduces hot flashes
    • Alleviates night sweats
    • Improves sleep in menopause
    • Mood support during menopause
    • Non-estrogenic mechanism

    Supporting Research
    18 studies

    Safety and Efficacy of Black Cohosh and Red Clover for the Management of Vasomotor Symptoms: A Randomized Controlled Trial

    Score: 8/10
    2009
    rct
    n=89

    Geller SE, Shulman LP, van Breemen RB +10 more

    Neither red clover nor black cohosh reduced vasomotor symptoms significantly more than placebo over 12 months, while hormone therapy did.

    View source

    In vivo effects of goldenseal, kava kava, black cohosh, and valerian on human cytochrome P450 1A2, 2D6, 2E1, and 3A4 phenotypes

    Score: 8/10
    2005
    rct
    n=12

    Gurley BJ, Gardner SF, Hubbard MA +4 more

    Goldenseal produced strong inhibition of both CYP2D6 (approximately 40%) and CYP3A4/5 (approximately 40%); the other botanicals had minimal effect.

    View source

    Phase III double-blind, randomized, placebo-controlled crossover trial of black cohosh in the management of hot flashes: NCCTG Trial N01CC1

    Score: 8/10
    2006
    crossover
    n=132

    Pockaj BA, Gallagher JG, Loprinzi CL +4 more

    failed to provide any evidence that black cohosh reduced hot flashes more than the placebo

    View source

    Complementary therapies for management of menopausal symptoms: a systematic review to inform the update of the International Menopause Society recommendations on women's midlife health

    Score: 8/10
    2026
    systematic_review

    Maunder A, Mardon AK, Rao V +4 more

    moderate-certainty evidence supports black cohosh (vasomotor/menopausal symptoms)

    View source

    Randomized trial of black cohosh for the treatment of hot flashes among women with a history of breast cancer

    Score: 7/10
    2001
    rct
    n=85

    Jacobson JS, Troxel AB, Evans J +4 more

    Black cohosh was not significantly more efficacious than placebo against most menopausal symptoms

    View source

    Efficacy and safety of isopropanolic black cohosh extract for climacteric symptoms

    Score: 7/10
    2005
    rct
    n=304

    Osmers R, Friede M, Liske E +3 more

    effective in relieving climacteric symptoms, especially in early climacteric women

    View source

    Cimicifuga racemosa dried ethanolic extract in menopausal disorders: a double-blind placebo-controlled clinical trial

    Score: 6/10
    2005
    rct
    n=122

    Frei-Kleiner S, Schaffner W, Rahlfs VW +2 more

    showed no superiority of the tested black cohosh extract compared to placebo

    View source

    Black cohosh and breast cancer: a systematic review

    Score: 7/10
    2014
    systematic_review

    Fritz H, Seely D, McGowan J +4 more

    Current evidence does not support an association between black cohosh and increased risk of breast cancer

    View source

    Review & meta-analysis: isopropanolic black cohosh extract iCR for menopausal symptoms - an update on the evidence

    Score: 6/10
    2021
    meta_analysis
    n=13096

    Castelo-Branco C, Gambacciani M, Cano A +4 more

    iCR was significantly superior for treating neurovegetative and psychological menopausal symptoms

    View source

    Vasomotor symptoms resulting from natural menopause: a systematic review and network meta-analysis of treatment effects from the National Institute for Health and Care Excellence guideline on menopause

    Score: 8/10
    2017
    meta_analysis
    n=8326

    Sarri G, Pedder H, Dias S +2 more

    Isoflavones and black cohosh were more effective than placebo

    View source

    Black cohosh (Cimicifuga spp.) for menopausal symptoms

    Score: 9/10
    2012
    meta_analysis
    n=2027

    Leach MJ, Moore V

    There was no significant difference between black cohosh and placebo in the frequency of hot flushes or in menopausal symptom scores across the pooled trials.

    View source

    Effects of herbal preparations on symptom clusters during the menopausal transition

    Score: 6/10
    2015
    systematic_review

    Ismail R, et al.

    Black cohosh mixed with other herbals, Rheum rhaponticum, and French maritime pine bark had significant effects on hot flushes and at least one other symptom.

    View source

    Black cohosh extracts in women with menopausal symptoms: an updated pairwise meta-analysis

    Score: 7/10
    2023
    meta_analysis
    n=2310

    Sadahiro R, Matsuoka LN, Zeng BS +1 more

    Black cohosh extracts were associated with significant improvements in overall menopausal symptoms (Hedges' g = 0.575, 95% CI = 0.283 to 0.867, P < 0.001), as well as in hot flashes (Hedges' g = 0.315, 95% CIs = 0.107 to 0.524, P = 0.003)

    View source

    Assessing the clinical significance of botanical supplementation on human cytochrome P450 3A activity: comparison of a milk thistle and black cohosh product to rifampin and clarithromycin

    Score: 8/10
    2006
    rct

    Gurley B, Hubbard MA, Williams DK +1 more

    Milk thistle and black cohosh appear to have no clinically relevant effect on CYP3A activity in vivo.

    View source

    Black cohosh (Cimicifuga racemosa) for menopausal symptoms

    Score: 8/10
    2012
    systematic_review
    n=1164

    Leach MJ, Moore V

    There was insufficient evidence that black cohosh reduced hot flushes or night sweats compared with placebo

    View source

    Treatment of vasomotor symptoms of menopause with black cohosh, multibotanicals, soy, hormone therapy, or placebo: a randomized trial

    Score: 9/10
    2006
    rct
    n=351

    Newton KM, Reed SD, LaCroix AZ +3 more

    Black cohosh, multibotanical preparations and soy did not reduce vasomotor symptom frequency or intensity more than placebo at any timepoint, whereas hormone therapy did.

    View source

    Efficacy of black cohosh extracts for improving low estrogen status induced by postoperative GnRHa treatment in patients with endometriosis: a systematic review

    Score: 6/10
    2020
    systematic_review
    n=745

    Peng J, Xu W, Li X +1 more

    The addition of BCE did not alter hormone levels of patients, including serum estradiol levels [MD=1.24, 95% CI(-4.58, 7.08), P>0.05] and luteinizing hormone levels.

    View source

    Suspected black cohosh hepatotoxicity: no evidence by meta-analysis of randomized controlled clinical trials for isopropanolic black cohosh extract

    Score: 6/10
    2011
    meta_analysis
    n=1117

    Naser B, Schnitker J, Minkin MJ +3 more

    Pooled liver function data from randomized trials of isopropanolic black cohosh extract showed no signal of hepatotoxicity compared with placebo.

    View source

    Safety Information

    Potential Side Effects

    Usually mild: stomach upset, headache, rash and occasional weight gain. The important rare risk is idiosyncratic liver injury, reported in case series across Europe and the US, which prompted labelling warnings in several countries.

    Contraindications

    Do not use with existing liver disease. Discontinue immediately and seek medical review if jaundice, dark urine, upper abdominal pain or unusual fatigue develops. Not for use in pregnancy — it has been used traditionally to induce labour.

    Drug Interactions

    • Hepatotoxic drugs including methotrexate and high-dose paracetamol — additive liver risk
    • Tamoxifen — studied together with no evidence of interference, but discuss with oncology
    • CYP2D6 substrates — weak inhibition reported in vitro
    • Sedatives — possible additive drowsiness

    Pregnancy & Breastfeeding

    Pregnancy: Unsafe

    Breastfeeding: Not enough evidence to judge

    Dosage Guidelines

    Dosage Used in Studies

    20-40 mg

    Best Time to Take

    Morning and evening, split doses

    Best Form

    A standardised extract such as iCR or BNO 1055 from a supplier that verifies species identity

    Bioavailability

    Used for menopausal symptoms. Mechanism unclear - does not appear to be estrogenic. Rare cases of liver toxicity reported. Discontinue if liver symptoms develop. Effects may take 4-8 weeks.

    Dosing by Goal

    GoalDoseNotes
    Standard20 mg twice daily of standardised extract
    Range20-80 mg/day
    Trials40 mg/day for 12 weeks is the most common regimen
    NotesAssess at 12 weeks; most guidance advises against continuous use beyond 6-12 months without review

    Forms Compared

    iCR (Remifemin) standardised extract

    The most studied preparation, 20 mg twice daily

    BNO 1055 extract

    European standardised extract with its own trial base

    Crude root powder

    Not standardised; potency and identity vary and adulteration with Asian Actaea species is documented

    Food & Timing

    With food to reduce stomach upset

    Medical Disclaimer

    The information provided on this website is for educational and informational purposes only and is not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition or before starting any supplement regimen.

    Individual results may vary. The statements on this website have not been evaluated by the Food and Drug Administration. Products and information are not intended to diagnose, treat, cure, or prevent any disease.