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Substandard, falsified and unregistered medicines in Latin America, 2017-2018
OBJECTIVE. To assess all the incidents of substandard, falsified and unregistered medicines in 2017 and 2018 in Latin America, determining the types of products affected, stages of the supply chain in which incidents were detected, quality deviations identified in tested samples, and regulatory meas...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Organización Panamericana de la Salud
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537817/ https://www.ncbi.nlm.nih.gov/pubmed/33033498 http://dx.doi.org/10.26633/RPSP.2020.125 |
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author | Rojas-Cortés, Robin |
author_facet | Rojas-Cortés, Robin |
author_sort | Rojas-Cortés, Robin |
collection | PubMed |
description | OBJECTIVE. To assess all the incidents of substandard, falsified and unregistered medicines in 2017 and 2018 in Latin America, determining the types of products affected, stages of the supply chain in which incidents were detected, quality deviations identified in tested samples, and regulatory measures taken by authorities. METHODS. A comprehensive search of the websites of the Latin American national regulatory authorities was conducted, identifying all eligible incidents during 2017-2018. Standardized values were collected from each incident for pre-determined variables: country, year, type of incident, therapeutic group, supply chain, regulatory measures and laboratory data. RESULTS. A total of 596 incidents in 13 countries were included (236 substandard, 239 falsified, 116 unregistered and 5 stolen). The therapeutic categories with the highest incidents were: anti-infectives, medicines for pain/palliative care, hormones/contraceptives, medicines for the respiratory tract, and medicines for mental/behavioural disorders. The most common places where incidents were detected were commercial establishments, pharmacies, health services and manufacturers. The most recurrent quality deviations were failure in parameters (appearance or physicochemical), incorrect labelling, different quantity of active pharmaceutical ingredient, presence of unknown particles, and microbiological contamination. The most frequent regulatory measures identified were alerts, withdrawals, seizures, and prohibition of marketing/distribution/use. CONCLUSIONS. In Latin America, substandard, falsified and unregistered medicines persist as a highly prevalent problem. An advanced degree of regulatory development in countries is associated with higher incident detection/reporting rates and a more comprehensive set of measures. The pharmaceutical supply chain is more vulnerable in its final node. Quality deviations identified in tested samples pose serious risks to public health. |
format | Online Article Text |
id | pubmed-7537817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Organización Panamericana de la Salud |
record_format | MEDLINE/PubMed |
spelling | pubmed-75378172020-10-07 Substandard, falsified and unregistered medicines in Latin America, 2017-2018 Rojas-Cortés, Robin Rev Panam Salud Publica Original Research OBJECTIVE. To assess all the incidents of substandard, falsified and unregistered medicines in 2017 and 2018 in Latin America, determining the types of products affected, stages of the supply chain in which incidents were detected, quality deviations identified in tested samples, and regulatory measures taken by authorities. METHODS. A comprehensive search of the websites of the Latin American national regulatory authorities was conducted, identifying all eligible incidents during 2017-2018. Standardized values were collected from each incident for pre-determined variables: country, year, type of incident, therapeutic group, supply chain, regulatory measures and laboratory data. RESULTS. A total of 596 incidents in 13 countries were included (236 substandard, 239 falsified, 116 unregistered and 5 stolen). The therapeutic categories with the highest incidents were: anti-infectives, medicines for pain/palliative care, hormones/contraceptives, medicines for the respiratory tract, and medicines for mental/behavioural disorders. The most common places where incidents were detected were commercial establishments, pharmacies, health services and manufacturers. The most recurrent quality deviations were failure in parameters (appearance or physicochemical), incorrect labelling, different quantity of active pharmaceutical ingredient, presence of unknown particles, and microbiological contamination. The most frequent regulatory measures identified were alerts, withdrawals, seizures, and prohibition of marketing/distribution/use. CONCLUSIONS. In Latin America, substandard, falsified and unregistered medicines persist as a highly prevalent problem. An advanced degree of regulatory development in countries is associated with higher incident detection/reporting rates and a more comprehensive set of measures. The pharmaceutical supply chain is more vulnerable in its final node. Quality deviations identified in tested samples pose serious risks to public health. Organización Panamericana de la Salud 2020-10-06 /pmc/articles/PMC7537817/ /pubmed/33033498 http://dx.doi.org/10.26633/RPSP.2020.125 Text en https://creativecommons.org/licenses/by-nc-nd/3.0/igo/legalcode This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 IGO License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited. No modifications or commercial use of this article are permitted. In any reproduction of this article there should not be any suggestion that PAHO or this article endorse any specific organization or products. The use of the PAHO logo is not permitted. This notice should be preserved along with the article’s original URL. |
spellingShingle | Original Research Rojas-Cortés, Robin Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title | Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title_full | Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title_fullStr | Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title_full_unstemmed | Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title_short | Substandard, falsified and unregistered medicines in Latin America, 2017-2018 |
title_sort | substandard, falsified and unregistered medicines in latin america, 2017-2018 |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7537817/ https://www.ncbi.nlm.nih.gov/pubmed/33033498 http://dx.doi.org/10.26633/RPSP.2020.125 |
work_keys_str_mv | AT rojascortesrobin substandardfalsifiedandunregisteredmedicinesinlatinamerica20172018 |