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Expert Opinion on Drug Safety Volume 16, 2017 - Issue 12
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Original Research

Filling quality of the reports of adverse drug reactions received at the Pharmacovigilance Centre of São Paulo (Brazil): missing information hinders the analysis of suspected associations

Adalton RibeiroNúcleo de Farmacovigilância, Centro de Vigilância Sanitária de São Paulo, São Paulo, BrazilView further author information
,
Silvana LimaNúcleo de Farmacovigilância, Centro de Vigilância Sanitária de São Paulo, São Paulo, BrazilView further author information
,
Maria-Elisa ZampieriNúcleo de Farmacovigilância, Centro de Vigilância Sanitária de São Paulo, São Paulo, BrazilView further author information
,
Mirtes PeinadoNúcleo Técnico de Planejamento e Informação, Centro de Vigilância Sanitária de São Paulo, São Paulo, BrazilView further author information
&
Albert FiguerasFundació Institut Català de Farmacologia, Barcelona, Spain;Departament de Farmacologia, de Terapèutica i de Toxicologia, Universitat Autònoma de Barcelona, Barcelona, SpainCorrespondence[email protected]
ORCID Iconhttp://orcid.org/0000-0002-2740-2013View further author information
ORCID Icon
Pages 1329-1334 | Received 26 Apr 2017, Accepted 09 Aug 2017, Published online: 23 Aug 2017

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Raymond Li, Kate Curtis, Syed Tabish Zaidi, Connie Van & Ronald Castelino. (2022) A new paradigm in adverse drug reaction reporting: consolidating the evidence for an intervention to improve reporting. Expert Opinion on Drug Safety 21:9, pages 1193-1204.
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Raymond Li, Kate Curtis, Syed Tabish Razi Zaidi, Connie Van, Amy Thomson & Ronald Castelino. (2021) Prevalence, characteristics, and reporting of adverse drug reactions in an Australian hospital: a retrospective review of hospital admissions due to adverse drug reactions. Expert Opinion on Drug Safety 20:10, pages 1267-1274.
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Raymond Li, Kate Curtis, Syed Tabish Razi Zaidi, Connie Van & Ronald Castelino. (2020) Effect of the black triangle scheme and its online educational campaign on the quantity and quality of adverse drug event reporting in Australia: a time series analysis. Expert Opinion on Drug Safety 19:6, pages 747-753.
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Rui Niu, Yufang Xiang, Tingting Wu, Zhi Zhang, Yue Chen & Bianling Feng. (2019) The quality of spontaneous adverse drug reaction reports from the pharmacovigilance centre in western China. Expert Opinion on Drug Safety 18:1, pages 51-58.
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Alemayehu Lelisa Duga, Francesco Salvo, Alexander Kay & Albert Figueras. (2023) Safety Profile of Medicines Used for the Treatment of Drug-Resistant Tuberculosis: A Descriptive Study Based on the WHO Database (VigiBase®). Antibiotics 12:5, pages 811.
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Antonela Simunovic, Krunoslav Kranjcec, Marija Pekas & Siniša Tomic. (2023) Quality analysis of manufacturer's incident reports regarding medical devices. Journal of Pharmaceutical Policy and Practice 16:1.
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Jingchao Yan, Xiaomei Xiong, Jianwen Shen & Taomin Huang. (2022) Adverse drug reaction reporting quality among different health professionals and the contribution of clinical pharmacists: A pilot study. Journal of Clinical Pharmacy and Therapeutics 47:11, pages 1768-1774.
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Raymond Li, Kate Curtis, Connie Van, Syed Tabish Razi Zaidi, Chin Yen Yeo, Christina Arun Kali, Mithila Zaheen, Grace Therese Moujalli & Ronald Castelino. (2022) Why hospital-based healthcare professionals do not report adverse drug reactions: a mixed methods study using the Theoretical Domains Framework. European Journal of Clinical Pharmacology 78:7, pages 1165-1175.
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Ar Kar Aung, Steven Walker, Yin Li Khu, Mei Jie Tang, Jennifer I. Lee & Linda Velta Graudins. (2022) Adverse drug reaction management in hospital settings: review on practice variations, quality indicators and education focus. European Journal of Clinical Pharmacology 78:5, pages 781-791.
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Mário Rui Salvador, Cristina Monteiro, Luísa Pereira & Ana Paula Duarte. (2022) Quality of Spontaneous Reports of Adverse Drug Reactions Sent to a Regional Pharmacovigilance Unit. International Journal of Environmental Research and Public Health 19:7, pages 3754.
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Inyoung Lee, Jeremy D. Jokinen, Stephanie Y. Crawford, Gregory S. Calip, Ryan D. Kilpatrick & Todd A. Lee. (2020) Exploring Completeness of Adverse Event Reports as a Tool for Signal Detection in Pharmacovigilance. Therapeutic Innovation & Regulatory Science 55:1, pages 142-151.
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Vera Lúcia Edais Pepe & Hillegonda Maria Dutilh Novaes. (2020) Sistema Nacional de Farmacovigilância no Brasil e em Portugal: semelhanças, diferenças e desafios. Cadernos de Saúde Pública 36:7.
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Paulo Henrique Santos Andrade, Amanda Carvalho Barreiros de Almeida, Ana Keilla Santana dos Santos, Iza Maria Fraga Lobo, Francilene Amaral da Silva & Wellington Barros da Silva. (2020) Challenges to the consolidation of pharmacovigilance practices in Brazil: limitations of the hospital pharmacist. Therapeutic Advances in Drug Safety 11, pages 204209862093374.
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Raymond Li, Syed Tabish Razi Zaidi, Timothy Chen & Ronald Castelino. (2019) Effectiveness of interventions to improve adverse drug reaction reporting by healthcare professionals over the last decade: A systematic review. Pharmacoepidemiology and Drug Safety 29:1, pages 1-8.
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