Quality of amoxicillin/clavulanic acid oral formulations for intended veterinary use in the UK, Malaysia, Serbia and Thailand

Author:

Pelligand L.1ORCID,Baker D.2,Sivagurunathan A.3,Kovačević Z.4,Suemanotham N.5,Stair J. L.2,Scott M.2,Liu F.2,Page S. W.6,Guardabassi L.7,Steagall P. V.89ORCID,

Affiliation:

1. Department of Clinical Services and Sciences and Department of Comparative Biomedical Sciences Royal Veterinary College Hatfield UK

2. Department of Clinical, Pharmaceutical & Biological Sciences, School of Life and Medical Sciences University of Hertfordshire Hatfield UK

3. Animal Medical Centre Kuala Lumpur Malaysia

4. Department for Veterinary Medicine, Faculty of Agriculture University of Novi Sad Novi Sad Serbia

5. Department of Pathology, Faculty of Veterinary Science Chulalongkorn University Bangkok Thailand

6. Veterinary Clinical Pharmacology and Toxicology, Advanced Veterinary Therapeutics Newtown NSW 2042 Australia

7. Department of Veterinary and Animal Sciences, Faculty of Health and Medical Sciences University of Copenhagen Frederiksberg Denmark

8. Department of Clinical Sciences, Faculty of Veterinary Medicine Université de Montréal Saint‐Hyacinthe QC J2S 2M2 Canada

9. Department of Veterinary Clinical Sciences, Centre for Animal Health and Welfare, Jockey Club College of Veterinary Medicine and Life Sciences City University of Hong Kong Hong Kong China

Abstract

ObjectivesAmoxicillin/clavulanate is the most commonly used oral antimicrobial drug in companion animals. The objective of the study was to detect types and frequency of deficits in the quality of veterinary oral formulations of amoxicillin/clavulanate in various countries.Materials and MethodsIn a prospective study with purposive sampling, amoxicillin/clavulanate tablet formulations for canine use were collected in four countries (wholesalers or veterinary practice) and shipped to a central bioanalytical laboratory. Twenty‐four samples were collected from the UK (nine), Malaysia (nine), Serbia (four) and Thailand (two), yielding 18 different formulations (10 veterinary). Packaging inspection, tablet disintegration and content assay were conducted (validated high‐performance liquid chromatography with ultra‐violet detection); content was acceptable when within the 90% to 120% pre‐specified range (US Pharmacopeia).ResultsSecondary packaging was present for 13 of 24 samples and primary packaging integrity was verified for all but one sample. Amoxicillin trihydrate/potassium clavulanate label ratio was 4:1, except for three formulations (2:1). Tablet dose strength ranged from 250 to 625 mg. All formulations contained both analytes. For amoxicillin, two of 24 samples were out of specification with 72.8% (Malaysia) and 82.3% (Thailand) of labelled content. For clavulanate, four of 24 samples were out of specification with 46.9% (Serbia), 79.0% (UK), 84.3% (Serbia) and 86.5% (Thailand) of labelled content. One formulation (Thailand) failed for both analytes.Clinical SignificanceAntimicrobial formulations of substandard quality have negative consequences for efficacy in patients and potentially promote antimicrobial resistance. There was evidence of substandard formulations in all countries, not only for amoxicillin but especially for clavulanate; this could compromise equitable access to acceptable quality essential veterinary medicines worldwide.

Publisher

Wiley

Subject

Small Animals

Reference20 articles.

1. European Medicines Agency(2019)20 years of sampling and testing of centrally Authorised products 1998–2017 https://www.ema.europa.eu/en/documents/report/20‐years‐sampling‐testing‐centrally‐authorised‐products‐1998‐2017_en.pdf. Accessed November 5 2022

2. Evaluation of Amoxicillin Content in Commonly Used Multisource Injectable Brands in Veterinary Practice

3. Lot quality assurance sampling: single‐ and double‐sampling plans/Stanley Lemeshow & Scott Taber;Lemeshow S.;World Health Statistics Quarterly,1991

4. Guidelines for Field Surveys of the Quality of Medicines: A Proposal

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