Abstract

BackgroundIn 2011 there was a strengthening of European Union (EU) legislation on the licencing of herbal products which, in the UK, resulted in the introduction of the Traditional Herbal Registration (THR) scheme. This scheme sets out standards for the safety and quality of herbal medicines and includes the provision of information to the customer on the safe use of the product.The aim of this study is to replicate a survey undertaken in 2011, prior to the implementation of the THR scheme, and evaluate the impact of this scheme on the information provided with herbal products bought over-the-counter.MethodsWe undertook a survey on 5 herbal products commonly available over-the-counter (St John’s wort, echinacea, Ginkgo biloba, Asian ginseng, garlic). The information was searched for key safety messages identified by the National Center for Complementary and Integrative Health (NCCIH). We also explored the presence of risk of harm information.ResultsWe recorded a rise in the number of products registered with the THR scheme (37% in 2016 compared to 7% in 2011). We also identified a reduction in the number of products that did not contain key safety information (75% in 2011 compared to 20% of products obtained in 2016). Risk of harm information was only communicated in products containing a PIL. We identified more products containing frequency of risk of harm information but this was not statistically significant.ConclusionThe introduction of the THR scheme appears to be associated with an increase in the provision of information about key safety messages on the safe use of herbal products. However, it is important to note that at least half of the products on the market that are not included in the THR scheme do not contain any information about their safe use; this includes information about precautions, interactions and side effects.The use of NCCIH herbal monographs replicated the methods used in the previous study; we recognise that the use of a different resource might effect the appraisal of the information provided. We also acknowledge that surveying presence of information does not assure that the latter is effectively communicated to patients, for which a close textual analysis would be required. While it is promising that more information is available after the introduction of the THR scheme, the public needs to be informed about ways to optimise safe use of all herbal products.

Highlights

  • In 2011 there was a strengthening of European Union (EU) legislation on the licencing of herbal products which, in the UK, resulted in the introduction of the Traditional Herbal Registration (THR) scheme

  • In the previous study we identified there was no ‘gold standard’, authoritative source on herbal medicines and so we opted to use the US National Centre for Complementary and Alternative Medicines (NCCAM) herbal monographs as these covered all of the herbal products we had purchased

  • Regulatory category 39.7% (n = 25) of the products were THR registered, this demonstrates a large increase in the number of licenced products available on the market, from the situation in 2011 when just 7% of the herbal products (n = 5) were licensed (Chi2 = 19.4; df = 1; p = 0.000011)

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Summary

Introduction

In 2011 there was a strengthening of European Union (EU) legislation on the licencing of herbal products which, in the UK, resulted in the introduction of the Traditional Herbal Registration (THR) scheme This scheme sets out standards for the safety and quality of herbal medicines and includes the provision of information to the customer on the safe use of the product. For optimal use of herbal medicines it is important that patients have access to information about their safe and effective use, as the public can perceive herbal medicines as safe despite documented evidence of precautions, interactions and side effects associated with some products [4, 5] Knowledge of these issues is important for consumers to allow them to make informed decisions about herbal medicines. An ethnographic study of herbal products retailers in the USA suggested there can be variable verbal information provided to consumers at the point of purchase, with the quality of information provided being unreliable and dependent on staff training and expertise [7]

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