Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture

Roger Bate,1 Lorraine Mooney,2 Kimberly Hess,3 Julissa Milligan,1 Amir Attaran41American Enterprise Institute, Washington DC, USA; 2Africa Fighting Malaria, London, UK; 3Africa Fighting Malaria, Washington DC, USA; 4Faculty of Law and Medicine, University of Ottawa, Ottawa, CanadaBackground: Some me...

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Main Authors: Bate R, Mooney L, Hess K, Milligan J, Attaran A
Format: Article
Language:English
Published: Dove Medical Press 2012-07-01
Series:Research and Reports in Tropical Medicine
Online Access:http://www.dovepress.com/anti-infective-medicine-quality-analysis-of-basic-product-quality-by-a-a10412
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spelling doaj-68cd12bfe5064d3399006081bd8b9e752020-11-24T21:29:09ZengDove Medical PressResearch and Reports in Tropical Medicine1179-72822012-07-012012default5761Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufactureBate RMooney LHess KMilligan JAttaran ARoger Bate,1 Lorraine Mooney,2 Kimberly Hess,3 Julissa Milligan,1 Amir Attaran41American Enterprise Institute, Washington DC, USA; 2Africa Fighting Malaria, London, UK; 3Africa Fighting Malaria, Washington DC, USA; 4Faculty of Law and Medicine, University of Ottawa, Ottawa, CanadaBackground: Some medicines for sale in developing countries are approved by a stringent regulatory authority (SRA) or the World Health Organization (WHO) prequalification program; many of these are global brands. This study ascertains whether medicines approved by SRAs or the WHO perform better in simple quality tests than those that have not been approved by either.Methods: Over the past 4 years, 2652 essential drugs (products to treat malaria, tuberculosis, and bacterial infections) were procured by covert shoppers from eleven African cities and eight cities in a variety of mid-income nations. All samples were assessed using the Global Pharma Health Fund eV Minilab® protocol to identify whether they were substandard, degraded, or counterfeit.Results: The failure rate among SRA-approved products was 1.01%, among WHO-approved products was 6.80%, and 13.01% among products that were not approved by either. African cities had a greater proportion of SRA- or WHO-approved products (31.50%) than Indian cities (26.57%), but they also experienced a higher failure rate (14.21%) than Indian cities (7.83%). The remainder of cities tested had both the highest proportion of approved products at 34.46% and the lowest failure rate at 2.70%. Products made in Africa had the highest failure rate at 25.77%, followed by Chinese products at 15.74%, Indian products at 3.70%, and European/US products, which failed least often, at 1.70%. Most worrying is that 17.65% of Chinese products approved by the WHO failed.Conclusion: The results strongly indicate that approval by either an SRA or the WHO is correlated with higher medicine quality at a statistically significant level. The comparatively high failure rates among WHO-approved products suggest there may be some weakness in post-marketing surveillance of these products, especially of Chinese-made WHO-approved products. The discrepancy between the failure rate of WHO-approved products from India (2.39%) and China (17.65%) is cause for concern. It is possible that more of the failures originating in China are counterfeit products, but this cannot be ascertained without greater help from the manufacturers themselves.Keywords: stringent regulatory authority, World Health Organization prequalification program, product approval, counterfeit, India, Chinahttp://www.dovepress.com/anti-infective-medicine-quality-analysis-of-basic-product-quality-by-a-a10412
collection DOAJ
language English
format Article
sources DOAJ
author Bate R
Mooney L
Hess K
Milligan J
Attaran A
spellingShingle Bate R
Mooney L
Hess K
Milligan J
Attaran A
Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
Research and Reports in Tropical Medicine
author_facet Bate R
Mooney L
Hess K
Milligan J
Attaran A
author_sort Bate R
title Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
title_short Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
title_full Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
title_fullStr Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
title_full_unstemmed Anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
title_sort anti-infective medicine quality: analysis of basic product quality by approval status and country of manufacture
publisher Dove Medical Press
series Research and Reports in Tropical Medicine
issn 1179-7282
publishDate 2012-07-01
description Roger Bate,1 Lorraine Mooney,2 Kimberly Hess,3 Julissa Milligan,1 Amir Attaran41American Enterprise Institute, Washington DC, USA; 2Africa Fighting Malaria, London, UK; 3Africa Fighting Malaria, Washington DC, USA; 4Faculty of Law and Medicine, University of Ottawa, Ottawa, CanadaBackground: Some medicines for sale in developing countries are approved by a stringent regulatory authority (SRA) or the World Health Organization (WHO) prequalification program; many of these are global brands. This study ascertains whether medicines approved by SRAs or the WHO perform better in simple quality tests than those that have not been approved by either.Methods: Over the past 4 years, 2652 essential drugs (products to treat malaria, tuberculosis, and bacterial infections) were procured by covert shoppers from eleven African cities and eight cities in a variety of mid-income nations. All samples were assessed using the Global Pharma Health Fund eV Minilab® protocol to identify whether they were substandard, degraded, or counterfeit.Results: The failure rate among SRA-approved products was 1.01%, among WHO-approved products was 6.80%, and 13.01% among products that were not approved by either. African cities had a greater proportion of SRA- or WHO-approved products (31.50%) than Indian cities (26.57%), but they also experienced a higher failure rate (14.21%) than Indian cities (7.83%). The remainder of cities tested had both the highest proportion of approved products at 34.46% and the lowest failure rate at 2.70%. Products made in Africa had the highest failure rate at 25.77%, followed by Chinese products at 15.74%, Indian products at 3.70%, and European/US products, which failed least often, at 1.70%. Most worrying is that 17.65% of Chinese products approved by the WHO failed.Conclusion: The results strongly indicate that approval by either an SRA or the WHO is correlated with higher medicine quality at a statistically significant level. The comparatively high failure rates among WHO-approved products suggest there may be some weakness in post-marketing surveillance of these products, especially of Chinese-made WHO-approved products. The discrepancy between the failure rate of WHO-approved products from India (2.39%) and China (17.65%) is cause for concern. It is possible that more of the failures originating in China are counterfeit products, but this cannot be ascertained without greater help from the manufacturers themselves.Keywords: stringent regulatory authority, World Health Organization prequalification program, product approval, counterfeit, India, China
url http://www.dovepress.com/anti-infective-medicine-quality-analysis-of-basic-product-quality-by-a-a10412
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