Scientific Name: Black Cohosh
Other Names: Actea racemosa, Cimicifuga racemosa

Who is this for?

Uses

Note: Black cohosh is different from both blue cohosh and white cohosh. Blue cohosh is frequently used in combination with black cohosh, but the effects of the two products are very different. White cohosh, also called white baneberry, is poisonous. It should never be taken by mouth. Individuals who have any doubts about the origin of a cohosh product should not use it.

Because premenopausal women have fewer heart problems than men of similar ages, the female hormones estrogen and progestin were thought to protect against heart disease. Therefore, hormone replacement therapy (HRT) drugs were prescribed widely for postmenopausal women. However, two recent large clinical trials--the Women's Health Initiative (WHI) and the Heart Estrogen/progestin Replacement Study (HERS)--showed that supplemental HRT is not heart protective. In fact, it increased risks of heart disease, breast cancer, and stroke for some women.

Interest has been renewed in the use of black cohosh and other "natural" alternatives for female HRT. Although black cohosh was long thought to contain chemicals that act like estrogen in the body, results of recent clinical studies have found that it not only has little or no estrogenic activity, but that it actually blocks estrogen. Still, black cohosh is used mostly to treat complaints such as premenstrual syndrome (PMS), hormone-related migraines, and menopausal symptoms. For many women, it is at least mildly effective in relieving bloating, breast soreness, cramps, emotional changes, swelling, and other menstrual or menopausal problems. However, in clinical studies, black cohosh generally has not relieved treatment-related symptoms such as hot flashes for women who previously had breast cancer.

Studies in animals suggest that black cohosh may also have other beneficial effects. It may help slow or prevent osteoporosis, for example. A few studies that were done in the 1960s and 1970s found black cohosh to have a blood-pressure lowering effect in laboratory animals. Black cohosh also seems to be a mild sedative, which may relieve anxiety or encourage sleep. However, few human studies have been conducted to verify these results. Currently, the Office of Dietary Supplements, a division of the U.S. National Institutes of Health, is sponsoring clinical trials to test the usefulness of black cohosh for treating several conditions.

When should I be careful taking it?

Sometimes, black cohosh is used by midwives to start labor in women about to give birth. However, it should never be used by a pregnant woman without the supervision of a trained healthcare provider because it may stimulate the uterus to contract--possibly causing a miscarriage.

Women with hormone-dependent conditions such as endometriosis, uterine fibroids, and cancers of the breast, ovaries, or uterus should not take black cohosh due to its possible hormonal effects.

Men with prostate cancer should also avoid taking black cohosh.

Case reports from Australia and Europe associate black cohosh with rare instances of hepatitis,or liver damage, which resulted in liver transplants for some of the affected individuals. Although a direct relationship has not been established, individuals who have liver disease or who drink large amounts of alcohol are advised to avoid taking black cohosh.

Precautions

Not enough is known about black cohosh to recommend it for use while a woman is breastfeeding an infant.

What side effects should I watch for?

Major Side Effects

Large doses of black cohosh may result in:

  • Seizures
  • Slow heartbeat
  • Vision changes

Less Serious Side Effects

Side effects that have been reported from taking black cohosh include:

  • Breast pain
  • Cramps
  • Dizziness
  • Headache
  • Nausea
  • Rash
  • Sweating
  • Upset stomach
  • Vomiting
  • Weight gain

What interactions should I watch for?

Prescription Drugs

Chemicals in black cohosh may block estrogen in the body. When it is taken at the same time as estrogen replacement therapy or oral contraceptives, black cohosh may interfere with the way the body uses estrogen. As a result, estrogens or oral contraceptives may not be as effective, some women may experience increased side effects, and the risk of anunintended pregnancy may be slightly higher.

No interactions have been reported between black cohosh and non-prescription drugs, other herbal supplements, or foods. However, because few reliable studies of black cohosh have been conducted, its possible interactions with drugs, foods, and other dietary supplements are not understood completely. Individuals interested in using black cohosh should discuss with a doctor or pharmacist all the prescription medications, non-prescription drugs, and dietary supplements they take before beginning black cohosh.

Some interactions between herbal products and medications can be more severe than others. The best way for you to avoid harmful interactions is to tell your doctor and/or pharmacist what medications you are currently taking, including any over-the-counter products, vitamins, and herbals. For specific information on how black cohosh interacts with drugs, other herbals, and foods and the severity of those interactions, please use our Drug Interactions Checker to check for possible interactions.

Should I take it?

Black cohosh grows in wooded areas as a tall perennial bush with jagged-edged leaves and long stalks of white flowers. It is named for its rough, dark roots and rhizomes--the parts used in making medicine. "Cohosh" is derived from an native North American word that means rough. Rhizomes are fleshy extensions of plant stems that run along or under the ground and often produce shoots and roots for new plants.

Black cohosh was introduced to European settlers by the native people of eastern and central North America. Native Americans used the juice of the plant to repel insects and they applied a salve of black cohosh to snake bites. They used a tea made from the dried roots for menstrual cramps and difficult childbirth. As a drink, black cohosh was also used for coughs and sore throats, as well as for upset stomach.

In 1986, the FDA concluded that not enough was known about black cohosh to include it on the list of herbal products generally recognized as safe (GRAS). Newly renewed interest in its possible effects has opened new clinical trials for the usefulness of black cohosh in treating several conditions. In Germany, it has been recognized for nearly 20 years as effective for relieving menstrual and menopausal complaints.

Dosage and Administration

The most active chemical in black cohosh is believed to be a glycoside called 27-deoxyacetin. Glycosides are chemicals that decompose into a sugar and other substances. Many glycosides have medicinal effects. The activity of black cohosh may vary greatly from individual to individual, however. Additionally, black cohosh usually needs to be taken daily for several weeks before it reaches full effectiveness.

In Europe, the use of black cohosh is fairly common as both a prescription drug and an herbal supplement. Often, it is combined with other herbals, such as dong quai and red clover, that may have similar effects in the body. Commercial preparations of black cohosh alone include tablets that may be standardized to contain one mg of glycoside per 20 mg tablet. Standardization by the manufacturer should assure the same amount of active ingredient in every batch of the commercial preparation. Standardization of herbal products is not required by the U.S. Food and Drug Administration (FDA), so not every product sold in the United States will contain the same amounts of active ingredients. Liquid extracts and tinctures of black cohosh are also available. Extracts are concentrated liquid preparations usually made by soaking chopped or mashed plant parts in a liquid such as alcohol, which is then strained to remove the solid plant parts. Tinctures are less concentrated than extracts, but they are prepared in similar ways.

A commercial black cohosh product has been introduced to the non-prescription market in the United States after years on the German market. Its manufacturer suggests that its use be limited to 6 months or less because no long-term studies have been done to evaluate longer therapy.

Dried roots or rhizomes of black cohosh can also be made into a tea that may be taken one time to three times a day. Rhizomes are fleshy extensions of plant stems that run along or under the ground and often produce shoots and roots for new plants. The tea is made by chopping or grating up to 2,000 mg (2 grams) of the dried roots or rhizomes, dropping them into boiling water, and allowing them to simmer for about 10 minutes. The tea is then strained to remove the solid particles before drinking it.

Typical doses are:
Commercially available tablets1 tablet to 4 tablets (20 mg to 80 mg) Twice a Day
Liquid extract 0.3 mL to 2 mL Daily
Tincture 2 mL to 4 mL Daily
Dried root/rhizome 300 mg to 2000 mg (0.3 gram to 2 grams)Daily


Summary

Black cohosh is used primarily by women to relieve hot flashes, mood swings, and other uncomfortable symptoms of menopause and to lessen menstrual cramps and bloating.

Risks

Individuals with liver conditions should avoid taking black cohosh, which may cause liver damage in rare cases. Because black cohosh may affect levels of the female hormone estrogen, it may cause uterine contractions; therefore, it should not be taken by pregnant women. Not much is known about how black cohosh affects children or whether it is passed to babies in breast milk, so women who are breast-feeding should not take black cohosh.

Side Effects

Large doses of black cohosh are reported to have resulted in:

  • Low heart rate
  • Seizures
  • Temporary vision changes

Side effects commonly associated with taking black cohosh in any amount include:

  • Dizziness
  • Headache
  • Sweating
  • Upset stomach
  • Weight gain

Interactions

Because it may interfere with estrogen in the body, black cohosh could lessen the effects of hormone replacement therapy or oral contraceptives.

Last Revised July 15, 2008

References

Al-Akoum M, Dodin S, Akoum A. Synergistic cytotoxic effects of tamoxifen and black cohosh on MCF-7 and MDA-MB-231 human breast cancer cells: an in vitro study. Canadian Journal of Physiology and Pharmacology. 2007;85(11):1153-1159.

Albertazzi P. A review of non-hormonal options for the relief of menopausal symptoms. Treat Endocrinol. 2006;5(2):101-113.

Amato P, Christophe S, Mellon PL. Estrogenic activity of herbs commonly used as remedies for menopausal symptoms. Menopause. 2002;9(2):145-150.

Amato P, Marcus DM. Review of alternative therapies for treatment of menopausal symptoms. Climacteric. 2003;6(4):278-284.

Anon. Cimicifuga racemosa. Monograph. Alternative Medicine Review. 2003;8(2):186-189.

Anon. The use of black cohosh to treat symptoms of menopause. Fertility and Sterility. 2004;81(Suppl 2):27-34.

Anon: Black cohosh. In: DerMarderosian A, Beutler JA, eds. Facts and Comparisons: The Review of Natural Products. St. Louis, MO, Facts and Comparisons. May 1998.

Anon: Blue cohosh. In: DerMarderosian A, Beutler JA, eds. Facts and Comparisons: The Review of Natural Products. St. Louis, MO, Facts and Comparisons. January 2003.

Blumenthal M, Gruenwald J, Hall T, Rister RS, eds. The Complete German Commission E Monographs. Austin, Texas: American Botanical Council; 1998.

Bodinet C, Freudenstein J. Influence of Cimicifuga racemosa on the proliferation of estrogen receptor-positive human breast cancer cells. Breast Cancer Research and Treatment. 2002;76(1):1-10.

Boekhout AH, Beijnen JH, Schellens JH. Symptoms and treatment in cancer therapy-induced early menopause. Oncologist. 2006;11(6):641-654.

Borrelli F, Ernst E. Black cohosh (Cimicifuga racemosa) for menopausal symptoms: A systematic review of its efficacy. Pharmacology Research. Epublished ahead of print. June 8, 2008.

Borrelli F, Izzo AA, Ernst E. Pharmacological effects of Cimicifuga racemosa. Life Sciences. 2003;73(10):1215-1229.

Briese V, Stammwitz U, Friede M, Henneicke-von Zepelin HH. Black cohosh with or without St. John's wort for symptom-specific climacteric treatment--results of a large-scale, controlled, observational study. Maturitas. 2007;57(4):405-414.

Brinker F. Herb Contraindications and Drug Interactions. Sandy, Oregon: Eclectic Institute, 1997.

Burdette JE, Liu J, Chen SN, et al. Black cohosh acts as a mixed competitive ligand and partial agonist of the serotonin receptor. Journal of Agricultural and Food Chemistry. 2003;51(19):5661-5670.

Burke BE, Olson RD, Cusack BJ. Randomized, controlled trial of phytoestrogen in the prophylactic treatment of menstrual migraine. Biomedicine and Pharmacotherapy. 2002;56(6):283-288.

Carroll DG. Nonhormonal therapies for hot flashes in menopause. American Family Physician. 2006;73(3):457-464.

Chan BY, Lau KS, Jiang B, Kennelly EJ, Kronenberg F, Kung AW. Ethanolic extract of Actaea racemosa (black cohosh) potentiates bone nodule formation in MC3T3-E1 preosteoblast cells. Bone. Epublished ahead of print. May 7, 2008.

Chow EC, Teo M, Ring JA, Chen JW. Liver failure associated with the use of black cohosh for menopausal symptoms. Medical Journal of Australia. 2008;188(7):420-422.

Chung DJ, Kim HY, Park KH, et al. Black cohosh and St. John's wort (GYNO-Plus) for climacteric symptoms. Yonsei Medical Journal. 2007;48(2):289-294.

Dog TL, Powell KL, Weisman SM. Critical evaluation of the safety of Cimicifuga racemosa in menopause symptom relief. Menopause. 2003;10(4):299-313.

Dugoua J-J, Seely D, Perri D, Koren G, Mills E. Safety and efficacy of black cohosh (cimicifuga racemosa) during pregnancy and lactation. Canadian Journal of Clinical Pharmacology. 2006;13(3):e257-e261.

Duker EM, Kopanski L, Jarry H, Wuttke W. Effects of extracts from Cimicifuga racemosa on gonadotropin release in menopausal women and ovariectomized rats. Planta Medica. 1991;57(5):420-424.

Ehrlich M, Rao J, Pabby A, Goldman MP. Improvement in the appearance of wrinkles with topical transforming growth factor beta(1) and l-ascorbic acid. Dermatologic Surgery. 2006;32(5):618-625.

Einbond LS, Shimizu M, Xiao D, et al. Growth inhibitory activity of extracts and purified components of black cohosh on human breast cancer cells. Breast Cancer Research and Treatment. 2004;83(3):221-231.

Frei-Kleiner S, Schaffner W, Rahlfs VW, Bodmer Ch, Birkhauser M. Cimicifuga racemosa dried ethanolic extract in menopausal disorders: a double-blind placebo-controlled clinical trial. Maturitas. 2005;51(4):397-404.

Garita-Hernandez M, Calzado MA, Caballero FJ, et al. The growth inhibitory activity of the Cimicifuga racemosa extract Ze 450 is mediated through estrogen and progesterone receptors-independent pathways. Planta Medica. 2006;72(4):317-323.

Gaube F, Wolfl S, Pusch L, Kroll TC, Hamburger M. Gene expression profiling reveals effects of Cimicifuga racemosa (L.) NUTT. (black cohosh) on the estrogen receptor positive human breast cancer cell line MCF-7. BMC Pharmacology. 2007 Sep;7:11.

Geller SE, Studee L. Botanical and dietary supplements for menopausal symptoms: what works, what does not. Journal of Womens Health (Larchmont). 2005;14(7):634-649.

Geller SE, Studee L. Botanical and dietary supplements for mood and anxiety in menopausal women. Menopause. 2007;14(3 Pt 1):541-549.

Geller SE, Studee L. Contemporary alternatives to plant estrogens for menopause. Maturitas. 2006;55(Suppl 1):S3-S13.

Gurley B, Hubbard MA, Williams DK, et al. 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. Journal of Clinical Pharmacology. 2006;46(2):201-213.

Gurley BJ, Barone GW, Williams DK, et al. Effect of milk thistle (Silybum marianum) and black cohosh (Cimicifuga racemosa) supplementation on digoxin pharmacokinetics in humans. Drug Metabolism Disposable. 2006;34(1):69-74.

Gurley BJ, Gardner SF, Hubbard MA, et al. In vivo effects of goldenseal, kava kava, black cohosh, and valerian on human cytochrome P450 1A2, 2D6, 2E1, and 3A4/5 phenotypes. Clinical Pharmacology and Therapeutics. 2005;77(5):415-426.

Gurley BJ, Swain A, Hubbard MA, et al. Clinical assessment of CYP2D6-mediated herb-drug interactions in humans: Effects of milk thistle, black cohosh, goldenseal, kava kava, St. John's wort, and Echinacea. Molecular Nutrition and Food Research. Epublished ahead of print. January 23, 2008.

Haimov-Kochman R, Brzezinski A, Hochner-Celnikier D. Herbal remedies for menopausal symptoms: Are we cautious enough? European Journal of Contraception and Reproductive Health Care. 2008;13(2):133-137.

Haimov-Kochman R, Hochner-Celnikier D. Hot flashes revisited: pharmacological and herbal options for hot flashes management. What does the evidence tell us? Acta Obstetrica et Gynecologica Scandinavica. 2005;84(10):972-979.

Hernandez Munoz G, Pluchino S. Cimicifuga racemosa for the treatment of hot flushes in women surviving breast cancer. Maturitas. 2004;44(Suppl 1):S59-S65.

Hostanska K, Nisslein T, Freudenstein J, Reichling J, Saller R. Cimicifuga racemosa extract inhibits proliferation of estrogen receptor-positive and negative human breast carcinoma cell lines by induction of apoptosis. Breast Cancer Research and Treatment. 2004;84(2):151-160.

Huntley A, Ernst E. A systematic review of the safety of black cohosh. Menopause. 2003;10(1):58-64.

Irikura B, Kennelly EJ. Blue Cohosh: a word of caution. Alternative Therapies in Womens Health. 1999;1(10):81-83.

Jacobson JS, Troxel AB, Evans J, Klaus L, Vahdat L, Kinne D, et al. Randomized trial of black cohosh for the treatment of hot flashes among women with a history of breast cancer. Journal of Clinical Oncology. 2001;19(10):2739-2745.

Jellin JM, Gregory P, Batz F, Hitchens K, et al, eds. Pharmacist's Letter/Prescriber's Letter. Natural Medicines Comprehensive Database, 3rd Edition. Stockton CA: Therapeutic Research Facility, 2000.

Jiang B, Kronenberg F, Balick MJ, Kennelly EJ. Analysis of formononetin from black cohosh (Actaea racemosa). Phytomedicine. 2006 Jul;13(7):477-486.

Jones TK, Lawson BM. Profound neonatal congestive heart failure caused by maternal consumption of blue cohosh herbal medication. Journal of Pediatrics. 1998;132(3 Pt 1):550-552.

Joy D, Joy J, Duane P. Black cohosh: a cause of abnormal postmenopausal liver function tests. Climacteric. 2008;11(1):84-88.

Kanadys WM, Bozena LG, Jan O. Efficacy and safety of Black cohosh (Actaea/Cimicifuga racemosa) in the treatment of vasomotor symptoms--review of clinical trials. [Article in Polish] Ginekol Pol. 2008;79(4):287-296.

Kang HJ, Ansbacher R, Hammoud MM. Use of alternative and complementary medicine in menopause. International Journal of Gynaecology [sic] and Obstetrics. 2002;79(3):195-207.

Kim CD, Lee WK, Lee MH, Cho HS, Lee YK, Roh SS. Inhibition of mast cell-dependent allergy reaction by extract of black cohosh (Cimicifuga racemosa). Immunopharmacology and Immunotoxicology. 2004;26(2):299-308.

Kim HY, Shin HS, Park H, et al. In vitro inhibition of coronavirus replications by the traditionally used medicinal herbal extracts, Cimicifuga rhizoma, Meliae cortex, Coptidis rhizoma, and Phellodendron cortex. Journal of Clinical Virology. 2008;41(2):122-128.

Kretzschmar G, Nisslein T, Zierau O, Vollmer G. No estrogen-like effects of an isopropanolic extract of Rhizoma Cimicifugae racemosae on uterus and vena cava of rats after 17 day treatment. Journal of Steroid Biochemistry and Molecular Biology. 2005;97(3):271-277.

Kronenberg F, Fugh-Berman A. Complementary and alternative medicine for menopausal symptoms: a review of randomized, controlled trials. Annals of Internal Medicine. 2002;137(10):805-813.

Li JX, Liu J, He CC, et al. Triterpenoids from Cimicifugae rhizoma, a novel class of inhibitors on bone resorption and ovariectomy-induced bone loss. Maturitas. 2007;58(1):59-69.

Lieberman S. A review of the effectiveness of Cimicifuga racemosa (black cohosh) for the symptoms of menopause. Journal of Womens Health. 1998;7(5):525-529.

Liske E, Hanggi W, Henneicke-von Zepelin HH, Boblitz N, Wustenberg P, Rahlfs VW. Physiological investigation of a unique extract of black cohosh (Cimicifugae racemosae rhizoma): a 6-month clinical study demonstrates no systemic estrogenic effect. Journal of Womens Health and Gender Based Medicine. 2002;11(2):163-174.

Liske E. Therapeutic efficacy and safety of Cimicifuga racemosa for gynecologic disorders. Advances in Therapeutics. 1998;15(1):45-53.

Lontos S, Jones RM, Angus PW, Gow PJ. Acute liver failure associated with the use of herbal preparations containing black cohosh. Medical Journal of Australia. 2003;179(7):390-391.

Loprinzi CL, Barton DL, Sloan JA, et al. Mayo Clinic and North Central Cancer Treatment Group hot flash studies: a 20-year experience. Menopause. Epublished ahead of print. April 18, 2008.

Low Dog T. Menopause: a review of botanical dietary supplements. American Journal of Medicine. 2005;118(12 Suppl 2):98-108.

Lude S, Torok M, Dieterle S, et al. Hepatic effects of Cimicifuga racemosa extract in vivo and in vitro. Cellular and Molecular Life Sciences. 2007;64(21):2848-2857.

Lupu R, Mehmi I, Atlas E, et al. Black cohosh, a menopausal remedy, does not have estrogenic activity and does not promote breast cancer cell growth. International Journal of Oncology. 2003;23(5):1407-1412.

Lynch CR, Folkers ME, Hutson WR. Fulminant hepatic failure associated with the use of black cohosh: a case report. Liver Transpl. 2006;12(6):989-992.

Mahady GB, Fabricant D, Chadwick LR, Dietz B. Black cohosh: an alternative therapy for menopause? Nutrition in Clinical Care. 2002;5(6):283-289.

Mahady GB. Is black cohosh estrogenic? Nutrition Review. 2003;61(5 Pt 1):183-186.

Mahady GB, Dog TL, Barrett ML, et al. United States Pharmacopeia review of the black cohosh case reports of hepatotoxicity. Menopause. Epublished ahead of print. May 12, 2008.

Mahady GB, Fabricant D, Chadwick LR, Dietz B. Black cohosh: an alternative therapy for menopause? Nutrition in Clinical Care. 2002;5(6):283-289.

McBane SE. Easing vasomotor symptoms: Besides HRT, what works? JAAPA. 2008;21(4):26-31.

McFarlin BL, Gibson MH, O'Rear J, Harman P. A national survey of herbal preparation use by nurse-midwives for labor stimulation. Review of the literature and recommendations for practice. Journal of Nurse Midwifery. 1999;44(3):205-216.

McKenna DJ, Jones K, Humphrey S, Hughes K. Black cohosh: efficacy, safety, and use in clinical and preclinical applications. Alternative Therapies in Health and Medicine. 2001;7(3):93-100.

Minciullo PL, Saija A, Patafi M, Marotta G, Ferlazzo B, Gangemi S. Muscle damage induced by black cohosh (Cimicifuga racemosa). Phytomedicine. 2006;13(1-2):115-118.

Moyad MA. Complementary/alternative therapies for reducing hot flashes in prostate cancer patients: reevaluating the existing indirect data from studies of breast cancer and postmenopausal women. Urology. 2002;59(4 Suppl 1):20-33.

Newton KM, Reed SD, Grothaus L, et al. The Herbal Alternatives for Menopause (HALT) Study: background and study design. Maturitas. 2005;52(2):134-146.

Nisbet BC, O'Connor RE. Black cohosh-induced hepatitis. Delaware Medical Journal. 2007;79(11):441-4444.

North American Menopause Society. Treatment of menopause-associated vasomotor symptoms: position statement of The North American Menopause Society. Menopause. 2004;11(1):11-33.

Oerter Klein K, Janfaza M, Wong JA, Chang RJ. Estrogen bioactivity in fo-ti and other herbs used for their estrogen-like effects as determined by a recombinant cell bioassay. Journal of Clinical Endocrinology and Metabolism. 2003;88(9):4077-4079.

Philp HA. Hot flashes--a review of the literature on alternative and complementary treatment approaches. Alternative Medicine Review. 2003;8(3):284-302.

Piersen CE. Phytoestrogens in botanical dietary supplements: implications for cancer. Integrated Cancer Therapy. 2003;2(2):120-138.

Pockaj BA, Gallagher JG, Loprinzi CL, et al. Phase III double-blind, randomized, placebo-controlled crossover trial of black cohosh in the management of hot flashes: NCCTG Trial N01CC1. Journal of Clinical Oncology. 2006;24(18):2836-2841.

Pockaj BA, Loprinzi CL, Sloan JA, et al. Pilot evaluation of black cohosh for the treatment of hot flashes in women. Cancer Investigation. 2004;22(4):515-521.

Qiu SX, Dan C, Ding LS, et al. A triterpene glycoside from black cohosh that inhibits osteoclastogenesis by modulating RANKL and TNFalpha signaling pathways. Chemistry and Biology. 2007;14(7):860-869.

Raus K, Brucker C, Gorkow C, Wuttke W. First-time proof of endometrial safety of the special black cohosh extract (Actaea or Cimicifuga racemosa extract) CR BNO 1055. Menopause. 2006;13(4):678-691.

Reame NE, Lukacs JL, Padmanabhan V, Eyvazzadeh AD, Smith YR, Zubieta JK. Black cohosh has central opioid activity in postmenopausal women: evidence from naloxone blockade and positron emission tomography neuroimaging. Menopause. Epublished ahead of print. May 20, 2008.

Rebbeck TR, Troxel AB, Norman S, et al. A retrospective case-control study of the use of hormone-related supplements and association with breast cancer. International Journal of Cancer. 2007;120(7):1523-1528.

Reed SD, Newton KM, LaCroix AZ, Grothaus LC, Grieco VS, Ehrlich K. Vaginal, endometrial, and reproductive hormone findings: randomized, placebo-controlled trial of black cohosh, multibotanical herbs, and dietary soy for vasomotor symptoms: the Herbal Alternatives for Menopause (HALT) Study. Menopause. 2008;15(1):51-58.

Rice S, Amon A, Whitehead SA. Ethanolic extracts of black cohosh (Actaea racemosa) inhibit growth and oestradiol [sic] synthesis from oestrone [sic] sulphate in breast cancer cells. Maturitas. 2007;56(4):359-367.

Roemheld-Hamm B, Dahl NV. Herbs, menopause, and dialysis. Seminars in Dialysis. 2002;15(1):53-59.

Russell L, Hicks GS, Low AK, Shepherd JM, Brown CA. Phytoestrogens: a viable option? American Journal of Medical Science. 2002;324(4):185-188.

Sakurai N, Wu JH, Sashida Y, et al. Anti-AIDS agents. Part 57: Actein, an anti-HIV principle from the rhizome of Cimicifuga racemosa (black cohosh), and the anti-HIV activity of related saponins. Bioorganic and Medicinal Chemistry Letter. 2004;14(5):1329-1332.

Schonberg MA, Wee CC. Menopausal symptom management and prevention counseling after the Women's Health Initiative among women seen in an internal medicine practice. Journal of Womens Health (Larchmont). 2005;14(6):507-514.

Scott GN. Black cohosh for menopausal symptoms. Detail Document #200714. Pharmacist's Letter/Prescriber's Letter. July 2004.

Seidlova-Wuttke D, Hesse O, Jarry H, Christoffel V, Spengler B, Becker T, Wuttke W. Evidence for selective estrogen receptor modulator activity in a black cohosh (Cimicifuga racemosa) extract: comparison with estradiol-17beta. European Journal of Endocrinology. 2003;149(4):351-362.

Seidlova-Wuttke D, Jarry H, Becker T, Christoffel V, Wuttke W. Pharmacology of Cimicifuga racemosa extract BNO 1055 in rats: bone, fat and uterus. Maturitas. 2003;44(Suppl 1):S39-S50.

Seidlova-Wuttke D, Jarry H, Pitzel L, Wuttke W. Effects of estradiol-17beta, testosterone and a black cohosh preparation on bone and prostate in orchidectomized rats. Maturitas. 2005;51(2):177-186.

Seidlova-Wuttke D, Thelen P, Wuttke W. Inhibitory effects of a black cohosh (Cimicifuga racemosa) extract on prostate cancer. Planta Medica. 2006;72(6):521-526.

Spangler L, Newton KM, Grothaus LC, Reed SD, Ehrlich K, LaCroix AZ. The effects of black cohosh therapies on lipids, fibrinogen, glucose and insulin. Maturitas. 2007 Jun 20;57(2):195-204.

Taylor M. Alternatives to HRT: an evidence-based review. International Journal of Fertility and Womens Medicine. 2003;48(2):64-68.

Tesch BJ. Herbs commonly used by women: an evidence-based review. Disease of the Month. 2002;48(10):671-696.

Uebelhack R, Blohmer JU, Graubaum HJ, Busch R, Gruenwald J, Wernecke KD. Black cohosh and St. John's wort for climacteric complaints: a randomized trial. Obstetrics and Gynecology. 2006;107(2 Pt 1):247-255.

Verhoeven MO, van der Mooren MJ, van de Weijer PH, et al. Effect of a combination of isoflavones and Actaea racemosa Linnaeus on climacteric symptoms in healthy symptomatic perimenopausal women: a 12-week randomized, placebo-controlled, double-blind study. Menopause. 2005;12(4):412-420.

Viereck V, Emons G, Wuttke W. Black cohosh: just another phytoestrogen? Trends in Endocrinology and Metabolism. 2005;16(5):214-221.

Viereck V, Grundker C, Friess SC, et al. Isopropanolic extract of black cohosh stimulates osteoprotegerin production by human osteoblasts. Journal of Bone Mineral Research. 2005;20(11):2036-2043.

Walji R, Boon H, Guns E, Oneschuk D, Younus J. Black cohosh (Cimicifuga racemosa [L.] Nutt.): safety and efficacy for cancer patients. Supportive Care in Cancer. 2007;15(8):913-921.

Warren BS, Devine CM. Herbal Medicines and breast cancer risk. Fact Sheet #53. Cornell University Program on Breast Cancer and Environmental Risk Factors. Revised November 2004. Available at: http://envirocancer.cornell.edu/factsheet/diet/fs53/herbal.pdf. Accessed July 14, 2005.

Whiting PW, Clouston A, Kerlin P. Black cohosh and other herbal remedies associated with acute hepatitis. Medical Journal of Australia. 2002;177:440-443.

Winterhoff H, Spengler B, Christoffel V, Butterweck V, Lohning A. Cimicifuga extract BNO 1055: reduction of hot flushes and hints on antidepressant activity. Maturitas. 2003;44(Suppl 1):S51-S58.

Woo KC, Park YS, Jun DJ, et al. Phytoestrogen cimicifugoside-mediated inhibition of catecholamine secretion by blocking nicotinic acetylcholine receptor in bovine adrenal chromaffin cells. Journal of Pharmacology and Experimental Therapeutics. 2004;309(2):641-649.

Wuttke W, Gorkow C, Seidlova-Wuttke D. Effects of black cohosh (Cimicifuga racemosa) on bone turnover, vaginal mucosa, and various blood parameters in postmenopausal women: a double-blind, placebo-controlled, and conjugated estrogens-controlled study. Menopause. 2006;13(2):185-196.

Wuttke W, Seidlova-Wuttke D, Gorkow C. The Cimicifuga preparation BNO 1055 vs. conjugated estrogens in a double-blind placebo-controlled study: effects on menopause symptoms and bone markers. Maturitas. 2003;44(Suppl 1):S67-S77.

Zierau O, Bodinet C, Kolba S, Wulf M, Vollmer G. Antiestrogenic activities of Cimicifuga racemosa extracts. Journal of Steroid Biochemistry and Molecular Biology. 2002;80(1):125-130.

Last Revised July 15, 2008


Note: The above information is not intended to replace the advice of your physician, pharmacist, or other healthcare professional. It is not meant to indicate that the use of the product is safe, appropriate, or effective for you.

In general, herbal products are not subject to review or approval by the U.S. Food and Drug Administration (FDA). They are not required to be standardized, meaning that the amounts of active ingredients or contaminants they contain may vary between brands or between different batches of the same brand. Not all of the risks, side effects, or interactions associated with the use of herbal products are known because few reliable studies of their use in humans have been done.

This information is provided for your education only. Please share this information with your healthcare provider and be sure that you talk to your doctor and pharmacist about all the prescription and non-prescription medicines you take before you begin to use any herbal product.

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