Maturitas
Volume 66, Issue 4 , Pages 355-362, August 2010

Assessing safety of herbal products for menopausal complaints: An international perspective

  • Tieraona Low Dog

      Affiliations

    • Arizona Center for Integrative Medicine, Tucson, AZ, USA
    • Corresponding Author InformationCorresponding author at: Arizona Center for Integrative Medicine, University of Arizona, 3055 N. Campbell Avenue, Suite 113, Tucson, AZ 85719, USA. Tel.: +1 520 626 3503; fax: +1 520 760 1009.
  • ,
  • Robin Marles

      Affiliations

    • Natural Health Products Directorate, Health Canada, Ontario, Canada
  • ,
  • Gail Mahady

      Affiliations

    • University of Illinois, Chicago, IL, USA
  • ,
  • Paula Gardiner

      Affiliations

    • Boston University Medical Center, Boston, MA, USA
  • ,
  • Richard Ko

      Affiliations

    • Herbal Synergy, Oakland, CA, USA
  • ,
  • Jo Barnes

      Affiliations

    • University of Auckland, Auckland, New Zealand
  • ,
  • Mary L. Chavez

      Affiliations

    • Texas A&M Health Science Center, Kingsville, TX, USA
  • ,
  • James Griffiths

      Affiliations

    • United States Pharmacopeial Convention, Rockville, MD, USA
  • ,
  • Gabriel Giancaspro

      Affiliations

    • United States Pharmacopeial Convention, Rockville, MD, USA
  • ,
  • Nandakumara D. Sarma

      Affiliations

    • United States Pharmacopeial Convention, Rockville, MD, USA

Received 22 February 2010; accepted 18 March 2010. published online 05 April 2010.

Abstract 

Future research of herbal products for menopausal women should include long-term safety assessments because women may use these products for prolonged periods of time. Growing numbers of women take prescription medications and concurrently use herbal products for alleviation of menopausal symptoms. Because of possible herb–drug interactions, both drug and supplement manufacturers should provide basic pharmacokinetic data to reduce the risk of adverse interactions. In addition, herbal products produced to high quality standards are essential for ensuring consumer safety. Regulatory frameworks must be in place to ensure that herbal ingredients’ identities have been verified, that they have been properly quantified per unit dose, that the product is within tolerance limits for contaminants, that the product's safety and effectiveness under the recommended conditions of use have been assessed before sale to the public, and that a system is in place to detect and deal with adverse reactions when they arise. This article explores these and related concerns.

Keywords: Herbal medicine, Safety, Regulatory, Toxicology

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PII: S0378-5122(10)00117-9

doi:10.1016/j.maturitas.2010.03.008

Maturitas
Volume 66, Issue 4 , Pages 355-362, August 2010