Adapting regulatory drug‐drug interaction guidance to design clinical pharmacokinetic natural product‐drug interaction studies: A NaPDI Center recommended approach-Reference-Cited by-同舟云学术

Adapting regulatory drug‐drug interaction guidance to design clinical pharmacokinetic natural product‐drug interaction studies: A NaPDI Center recommended approach

Published:2021-10-26 Issue: Volume: Page:
ISSN:1752-8054
Container-title:Clinical and Translational Science
language:en
Short-container-title:Clin Transl Sci

Author:

Cox Emily J.¹,Rettie Allan E.²³,Unadkat Jashvant D.³⁴,Thummel Kenneth E.³⁴,McCune Jeannine S.³⁴,Paine Mary F.¹³

Affiliation:

1. Department of Pharmaceutical Sciences College of Pharmacy and Pharmaceutical Sciences Washington State University Spokane Washington USA

2. Department of Medicinal Chemistry School of Pharmacy University of Washington Seattle Washington USA

3. Center of Excellence for Natural Product Drug Interaction Research Spokane Washington USA

4. Department of Pharmaceutics School of Pharmacy University of Washington Seattle Washington USA

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cts.13172

Reference26 articles.

1. Prevalence and Predictors of Herbal Medicine Use Among Adults in the United States

2. Potential of chemotherapy?herb interactions in adult cancer patients

3. Use of Natural Health Products

4. Understanding the role of scientific evidence in consumer evaluation of natural health products for osteoarthritis an application of the means end chain approach

5. Clinical relevance of St. John's wort drug interactions revisited

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