The results of a study on the knowledge, perceptions and use of generic and biosimilar drugs in Latin America and the Caribbean were recently presented at an event organized by the World Bank during the workshop ‘Rethinking Pharmaceutical Policies in Latin America and the Caribbean’ held in Washington DC, USA.
Study of the use of generic and biosimilar drugs in Latin America
Home/Reports | Posted 12/05/2023 0 Post your comment
In this review, conducted by Professor Aguilera, a panoramic review of articles that have investigated the topic of knowledge, perceptions and use of generics and biosimilars in Latin America and the Caribbean was presented. To do this, 668 articles were examined, of which 22 met the inclusion criteria to be part of the review. Of these, 17 correspond to studies on generic drugs and only five to studies on biosimilar products. The majority of studies on generic drugs come from Brazil, while studies on biosimilar products are more limited.
The preliminary results of the review found that the vast majority of patients and the general population have good knowledge and a positive opinion of generic drugs, while doctors have greater concerns about their safety and efficacy. As for biosimilar products, less knowledge and use were observed among patients and doctors. In all the groups studied, it was observed that the economic factor, specifically the price, is crucial when deciding whether to prescribe or acquire generic or biosimilar drugs. There are relatively few studies in the region, and none of them were conducted in Chile.
One of the conclusions of this review is that more empirical research is needed on the topic, especially regarding biosimilars, as the use of biological drugs will continue to increase over time and have a high cost.
Professor Aguilera emphasizes that health policies targeting the enhancement of generics and biosimilars’ perception and usage must be complemented by a regulatory and institutional framework that instills trust in the healthcare professionals and the general public regarding the products' safety and efficacy compared to the reference products. Furthermore, it is crucial to have a clear understanding of the levels of knowledge, perception, and usage of alternative pharmaceutical products to facilitate the development and monitoring of health policies that promote their usage.
Another review conducted in 2020 of the biosimilars market in Latin America revealed that Argentina, Brazil and Mexico have the highest number of similar biopharmaceutical products approved, while information in other countries is more limited [1].
Related articles
Challenges for Spanish generics and biosimilars industry: sustainable profitability
Low biosimilar uptake in regions of low social and political trust
Recommendations to address challenges to biosimilars in Latin America
LATIN AMERICAN FORUM View the latest headline article: Una actualización sobre la declaración conjunta EMA-HMA sobre la intercambiabilidad de biosimilares Browse the news in the Latin American Forum! Register to receive the GaBI Latin American Forum newsletter. Inform colleagues and friends of this new initiative.
FORO LATINOAMERICANO Ver el último artículo de cabecera: Una actualización sobre la declaración conjunta EMA-HMA sobre la intercambiabilidad de biosimilares !Explore las noticias en el Foro Latinoamericano! Regístrese para recibir el boletín informativo GaBI Foro Latinoamericano. Informe a colegas y amigos sobre esta nueva iniciativa. |
Reference
1. GaBI Online - Generics and Biosimilars Initiative. The biosimilar market in Latin America: a summary [www.gabionline.net]. Mol, Belgium: Pro Pharma Communications International; [cited 2023 May 12]. Available from:
www.gabionline.net/biosimilars/research/The-biosimilars-market-in-Latin-America-a-summary
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2023 Pro Pharma Communications International. All Rights Reserved.
Source: Universidad San Sebastián
Guidelines
Regulatory update for post-registration of biological products in Brazil
New regulations in Brazil for the registration of biosimilars
Policies & Legislation
NPRA Malaysia trials new timelines for variation applications
Regulatory evolution and impact of simplified requirements for interchangeable biosimilars in the US
Comments (0)
Post your comment