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Volume 1
in Humans
Toxicological Effects of Veterinary Medicinal Products
View Online
Issues in Toxicology
Series Editors:
Professor Diana Anderson, University of Bradford, UK
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Toxicological Effects of
Veterinary Medicinal Products
Published on 31 December 2012 on http://pubs.rsc.org | doi:10.1039/9781849735483-FP001
in Humans
Volume 1
Kevin N. Woodward
TSGE, Concordia House, St James Business Park, Grimbald Crag Court,
Knaresborough, North Yorkshire, HG5 8QB, UK
Email: [email protected]
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ISBN: 978-1-84973-417-2
ISSN: 1757-7179
A catalogue record for this book is available from the British Library
Apart from fair dealing for the purposes of researchfor non-commercial purposes or for
private study, criticism or review, as permitted under the Copyright, Designs and Patents
Act 1988 and the Copyright and Related Rights Regulations 2003, this publication may not
be reproduced, stored or transmitted, in any form or by any means, without the prior
permission in writing of The Royal Society of Chemistry or the copyright owner, or in the
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appropriate Reproduction Rights Organization outside the UK. Enquiries concerning
reproduction outside the terms stated here should be sent to The Royal Society of
Chemistry at the address printed on this page.
The RSC is not responsible for individual opinions expressed in this work.
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Preface
The term ‘‘veterinary medicinal product’’ describes those medicines devel-
oped specifically for use in animals. The development of these products
involves an enormous amount of intellectual effort and physical labour as
well as a considerable amount of financial investment in order to ensure that
animals have available products that are of the appropriate quality and with
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the correct degree of effectiveness. These products also need to be safe for
the animal patient as well as for the user, for the consumer of edible animal
products and for the environment. On the other hand, the term ‘‘veterinary
drug’’ is misleading, as the majority of drugs used in veterinary medicine,
with very few exceptions, either are used in human medicine or have been
used in the past in human medicine. As a consequence, we tend to know a
considerable amount about the toxicity of veterinary drugs from their use in
human medicine. We only know a little regarding the safety of veterinary
medicinal products in humans from their use in animals.
This books attempts to bring together some of this knowledge and experi-
ence to assess the safety of veterinary medicinal products. As described in the
pages that follow, this involves user safety and safety of those who consume
products derived from animals treated with veterinary medicines, and for the
most part this means examining their toxicological and pharmacological
properties. However, some veterinary drugs are also microbiologically active,
and this presents certain hazards that also need to be taken into account.
Finally, like human drugs, these products also eventually find their way into the
environment. As a result, to examine the potential hazards arising from
veterinary medicine, we need to evaluate their toxicological and pharmacolo-
gical properties, and we need to consider their microbiological properties and
their eventual fate in the natural environment. This latter aspect is of concern
not only because organisms might encounter the remnants of veterinary
medicines as a result of environmental contamination, but also because of the
potential effects for human health from the contamination of land and drinking
v
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vi Preface
water. I have tried to reach a balance, and review the main issues that might
impact on human safety arising from the use of veterinary medicinal products.
It is not possible to cover every product or drug in a work of this nature, and I
have made no attempt to do so. Some products are used infrequently, and some
Published on 31 December 2012 on http://pubs.rsc.org | doi:10.1039/9781849735483-FP005
are only used in certain countries. Many others are human drugs that are used
off-label in animals. I have attempted to cover the major drug classes as well as
some individual drugs of interest. Some of these are now of historical interest as
many have fallen out of use or have been replaced with more effective and safer
alternatives. Nevertheless, it would be remiss to avoid discussion of these where
they may have impacted human safety in the past, so I have included them here.
I would like to thank the authors who have invested significant efforts by
providing chapters for this book – Dr Tim Marrs, Derek Renshaw and Pro-
fessor Peter Silley. I would also like to thank my family – and dogs – for their
forbearance and patience while I have been working on this project.
Kevin Woodward
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Surrey
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Contents
Volume 1
1.1 Introduction 1
1.2 Physical Injuries 2
1.2.1 Accidents and Related Incidents 2
1.2.2 Needlestick Injuries 4
1.2.3 Zoonotic Diseases 5
1.2.4 Dermatoses 5
1.2.5 Allergies 6
1.2.6 Neoplastic Diseases 6
1.2.7 Specific Risks for Women 7
1.2.8 Mental Health 7
1.3 Conclusions 8
References 8
2.1 Introduction 21
2.2 Criteria for Evaluation and Authorisation of
Veterinary Medicinal Products 22
2.3 European Union Legislation 24
2.3.1 The National Procedure 25
2.3.2 The Mutual Recognition Procedure 25
2.3.3 The Decentralised Procedure 27
2.3.4 The Centralised Procedure 27
vii
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viii Contents
2.3.5 Maximum Residue Limits 28
2.3.6 Pharmacovigilance 29
2.4 Conclusions 36
References 37
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3.1 Introduction 40
3.2 Establishment of MRLs in the EU 41
3.3 MRLs – Other Considerations 46
3.4 The Joint FAO/WHO Expert Committee on
Food Additives (JECFA) 50
3.5 Practical Uses of MRLs 51
3.6 Residues Surveillance 53
3.6.1 Residues and Residues Studies 54
3.6.2 Residues Surveillance for Veterinary Drugs in
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the UK 56
3.7 Residues Avoidance 59
3.8 Conclusions 62
References 63
4.1 Introduction 81
4.2 The Assessment Process 83
4.2.1 Hazard Identification and Assessment 83
4.2.2 Exposure Assessment 86
4.3 Biological Monitoring 92
4.4 Risk Assessment 93
4.5 Risk Management 95
4.6 Risk Communication 96
4.7 Conclusions 97
References 98
9.1 Introduction 1
9.1.1 Coccidiosis, Coccidiostats and Anticoccidial
Medicines 1
9.1.2 Human Exposure 2
9.1.3 Committees that Evaluate the Safety of
Coccidiostats 2
9.2 Approaches Taken to Ensure the Human Safety of
Coccidiostats 2
9.2.1 Consumer Safety 2
9.2.2 User Safety 3
9.2.3 Inconsistencies in the Values of ADIs 3
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10.1 Introduction 33
10.2 Anticholinesterase Activity 38
10.3 Clinical Effects 39
10.3.1 Syndromes Associated with OP
Exposure 39
10.3.2 Other Effects of OPs 44
10.3.3 Diagnostic Tests and Biomarkers 47
10.3.4 Management of OP Poisoning 49
10.4 Exposure and Regulatory Aspects 50
10.4.1 European Union 50
10.4.2 USA 51
10.4.3 Interpretation of Regulatory Studies 51
10.4.4 Pharmacovigilance 52
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xii Contents
10.5 Sheep Dips in the United Kingdom 52
10.5.1 Introduction 52
10.5.2 Treatments 53
10.5.3 Organophosphate Plunge
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Dips 53
10.6 Conclusion 54
References 54
11.1 Introduction 71
11.2 Griseofulvin 72
11.3 Amphotericin B and Other Polyenes 74
11.4 The Azoles 76
11.4.1 Steroidogenesis Inhibition 76
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11.4.2 Hepatotoxicity 79
11.4.3 Other Effects 79
11.5 Conclusions 80
References 81
12.1 Introduction 95
12.2 Individual Drugs or Groups of Drugs 95
12.2.1 The Benzimidazoles 95
12.2.2 Levamisole 98
12.2.3 Salicylanilides 99
12.2.4 Clorsulon 101
12.2.5 Tetrahydropyrimidines 102
12.2.6 Pyrazinoisoquinolones 104
12.2.7 Monepantel 107
12.2.8 Piperazine 108
12.2.9 Diethylcarbamazine 110
12.2.10 Nitroxynil 111
12.2.11 Halofuginone 112
12.2.12 Nitroimidazoles 113
12.2.13 Imidocarb 116
12.2.14 The Trypanocidal Drugs – Isometamidium
and Diminazene 118
12.2.15 Emodepside 122
12.3 Conclusions 123
References 126
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Contents xiii
Chapter 13 Some Other Pharmacologically Active Drugs 155
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CHAPTER 1
1.1 Introduction
Many people use, and are therefore potentially exposed to, veterinary medicinal
products. These include the pet-owning public, farmers, animal breeders and
keepers, and, of course, veterinarians and other veterinary staff such as veter-
inary nurses and practice receptionists. The public may be intermittently
exposed to veterinary medicinal products, apart from those with animals with
chronic conditions such as epilepsy and diabetes where exposures may be more
frequent. Farmers may be responsible for the administration of a wide variety
of drugs and, occasionally, exposures have the potential to be significant, for
example when dipping sheep and mixing or administering in-feed antimicrobial
agents. Veterinarians and veterinary nurses are potentially exposed to a wide
range of veterinary drugs including anaesthetics, euthanasia agents, anti-
neoplastic agents and non-steroidal anti-inflammatory drugs. It is thus
tempting to assume that these professionals are assailed on a daily basis by the
combined actions of a number of pharmacologically and toxicologically active
agents, and if these could be removed from veterinary practice, the world, or at
least the veterinary world, would be a better place in which to live and work.
However, just as it would be wrong to assume that the industrial workplace
is a chemophobe’s nightmare, or a toxicologists dream, it is equally incorrect to
think of the veterinary surgery or clinic as a toxicological playground.
Although industry, especially the chemical industry, has had its fair share of
chemical disasters, such as those involving asbestos, benzene, vinyl chloride
1
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2 Chapter 1
monomer and a number of halogenated hydrocarbons to name but a few, the
vast majority of mortalities and morbidities in industry arise from accidents
including those involving machinery, explosions and fires. Similarly, it would
be incorrect to assume that veterinary workers are immersed in toxic soups of
Published on 31 December 2012 on http://pubs.rsc.org | doi:10.1039/9781849735483-00001
pharmacologically active materials. Even if they were, there are numerous other
hazards, with associated risks, which may pose greater dangers than the
majority of pharmaceutical or biological agents encountered in veterinary
practice.
The main topic of this book is the potential for veterinary pharmaceutical
products to cause harm to human beings, especially through toxicological
modes of action. However, just as with industry, this must be seen in per-
spective with all other potential hazards and this chapter attempts to review this
perspective.
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