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Evidence collection2 February 2021

Veterinary medicines and the environment

Evidence-based veterinary medicineSmall animalsMedicine

Published 2 February 2021 | Updated 18 November 2024

Introduction

A paper recently published in Science of the Total Environment has received coverage in both the national and veterinary press, raising concern about the extent to which commonly used parasiticides for companion animals may contaminate the environment.  A summary of the paper is available.

Press coverage

References

Other relevant resources

This paper aimed to assess the contribution of dog swimming to the detection of selected pet ectoparasiticides in aquatic habitats in protected urban green spaces, and to understand dog owners’ knowledge and perceptions of the use of flea and tick treatments and their potential environmental risks.

This paper aimed to estimate the contribution of ‘down the drain’ contamination from washing dogs and their bedding as well as from handwashing following treatment with Fipronil and Imidacloprid.

European Legislation

European legislation requires that all veterinary medicines undergo an environmental risk assessment (ERA) based on their expected use. The ERA is an evaluation of the possible hazards to the environment posed by a veterinary medicine.

The purpose of the ERA is to:

There are two phases to the ERA. Phase 1 is an environmental impact assessment which considers the medicine’s active substance and excipients, its method of administration, target species and proposed pattern of use.

Phase 2 is an ecotoxicological assessment, which is tier-based and structured around the risk quotient (RQ) which provides an indication of the likelihood of adverse effects on the environment. Medicines whose phase 1 assessment concludes that their environmental exposure is not negligible (e.g. PECsoil value higher than 100 µg/kg) have to undergo the phase 2 ecotoxicological assessment. This generally applies to veterinary medicines used for aquaculture, intensively reared terrestrial animals, or pasture animals.

Currently the assessment for veterinary products used in companion animals is limited to phase 1, as exposure from veterinary medicinal products used in companion animals has been considered negligible in the scope of the current environmental risk assessment framework.

However, a recent concept paper, published by the European Medicines Agency (EMA) challenges the conclusion that environmental risk associated with these products is always negligible, and calls for a review of the current blanket exclusion of a higher-tier risk assessment for all these products. The concept paper recommends the development of a more detailed reflection paper, on whether the current approach for the environmental risk assessment of Veterinary Medicinal Products containing parasiticides, that are used in companion animals, remains scientifically justified and the need and feasibility of mitigation measures for such products.

Other publications from the EMA indicate that the effect of veterinary medicines on the broader environment is a subject of interest.

VMD strategy

It should also be noted that the recently published Regulatory Science Strategy from the Veterinary Medicines Directorate (VMD) includes, as part of their goal of ‘Strengthening a life cycle approach to benefit-risk assessment’, the proposal to ‘Improve the evaluation of environmental and residues adverse events’ (2.4.3).

The strategy document notes that there is growing concern regarding the impact of pharmaceuticals in the environment, both in relation to their potential effects on ecosystems and effects on human safety.

The strategy goes on to list the steps that the VMD will look to undertake in order to improve the evaluation of environmental and residues adverse events. These will include:

Reference

VMD Regulatory Science Strategy (2020) [VMD] [online] Available from: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/936195/PCDOCS-_1853658-v8-Regulatory_Science_Strategy_17.11.20.pdf [accessed 29/1/2021]

Further reading

While there is already a wide literature base available regarding the impact of pharmaceuticals on the environment these papers are mostly published in journals that cover toxicology and environmental science. For those who would like to read more about this subject the following may be of interest.

About evidence collections

Evidence collections bring together collections of published papers on topics of interest and importance to the veterinary professions. Papers are chosen for relevance and accessibility, with the full text of articles either being available through the RCVS Knowledge library, on open access or from other publications to which a significant number of veterinary professionals are likely to have access. This means that there may be relevant evidence that is not included.

If you would like assistance in searching for further evidence on this topic you may find the following helpful EBVM Toolkit 2: Finding the best available evidence.

If you would like to suggest a paper for inclusion in one of our published evidence collections, or a topic for a future collection, please email library@rcvsknowledge.org

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