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Abstract
Annual Review of Pharmacology and Toxicology
Vol. 45: 203-226 (Volume publication date February 2005)
(doi:10.1146/annurev.pharmtox.45.120403.095950)
First published online as a Review in Advance on September 07, 2004
NATURAL HEALTH PRODUCTS AND DRUG DISPOSITION*

Brian C. Foster,1,2­ J. Thor Arnason,2 and ­ Colin J. Briggs3­
1Therapeutic Products Directorate, Health Canada, Holland Cross 3102C3, Ottawa, Ontario, Canada, K1A 1B6; email:
2Center for Research in Biopharmaceuticals and Biotechnology, University of Ottawa, Ottawa, Ontario, Canada, K1N 6N5; email:
3Faculty of Pharmacy, University of Manitoba, Winnipeg, Manitoba, Canada, R3T 2N2; email:

▪ Abstract  Botanicals such as herbal products (HPs) and nutraceuticals (NCs) are often regarded as low risk because of their long history of human use. Anecdotal and literature reports of adverse drug events (ADEs) and clinical studies with HPs are increasing, but many of the reports are incomplete and contradictory. These reports need to identify confounding factors and explain contradictory findings if they are to help health care professionals or patients understand what risks are involved. HPs are complex botanicals, not single-active ingredient (SAI) products. Studies can be confounded by different manufacturing processes and formulations, including cosmetics and food supplements; environment; chemotypes; misidentification or adulteration; and factors associated with the patient or user population such as use, total drug load, and genetics. Future studies need to be conducted with characterized product that includes all commercially available related products. Clinical trials should be relevant to the user population and take into account the confounding factors that may influence the interpretation of the findings.

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Authors:
Brian C. Foster
J. Thor Arnason
Colin J. Briggs
Keywords:
herbal
metabolism
transport
cytochrome P450

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