Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância

Bibliographic Details
Main Author: Mendes, Diogo
Publication Date: 2019
Other Authors: Alves, Carlos, Batel Marques, Francisco
Format: Article
Language: por
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: https://doi.org/10.25756/rpf.v11i2-3.217
Summary: Introduction: Our objective was to investigate associations between oral antidiabetics and adverse drug reactions through disproportionality analysis in the Portuguese Pharmacovigilance System database. Methods: Spontaneous reports of adverse drug reactions reported for oral antidiabetics (2008–2017) were considered. Adverse drug reactions were coded according to MedDRA (preferred term), and oral antidiabetics according to Anatomical Therapeutic Chemical classification (4th level). Associations between oral antidiabetics and adverse drug reactions were assessed through a case/non-case methodology, using reporting odds ratio (ROR) with 95% confidence interval (CI) to identify signals of disproportionate reporting. Results: A total of 413 cases (262 serious; 63.4%) containing 1047 adverse drug reactions were included. Signals of disproportionate reporting were found: i) alpha-glucosidase inhibitors – abdominal pain (ROR: 9.7 [2.5-37.7]) and flatulence (ROR: 76.1[13.0-444.4]); ii) Dipeptidyl peptidase-4 inhibitors – upper abdominal pain (ROR: 5.5[1.5-20.7]), headache (ROR: 5.5[1.5-20.7]) and acute pancreatitis (ROR: 22.0[2.6-189.9]); iii) Glucagon-like peptide-1 agonists – vomiting (ROR: 3.4[1.4-8.4]; iv) metformin – abdominal pain (ROR: 3.6[1.1-11.6]), diarrhea (ROR: 5.6[2.4-13.2]) and lactic acidosis (ROR: 76.9[4.7-1269.0]); v) SGLT2 inhibitors – candida infection (ROR: 51.5[2.8-950.1], diabetic ketoacidosis(ROR: 84.8[4.8-1487.8]), pollakiuria (ROR: 15.2[1.6-147.1]), somnolence (ROR:30.4[1.5-610.3] and urinary tract infection (ROR: 15.2[1.6-147.1]); vi) sulfonylureas – hypoglycemia (ROR: 44.8[14.4-139.8]). Conclusion: The results are in line with previous knowledge on the safety profiles of the different classes of oral antidiabetics, reinforcing the need to monitoring closely certain adverse drug reactions in clinical practice depending on the therapy prescribed to diabetic patients.
id RCAP_3bc57a0ec97342f9092cdf9f815885ab
oai_identifier_str oai:ojs.farmacoterapia.pt:article/216
network_acronym_str RCAP
network_name_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository_id_str https://opendoar.ac.uk/repository/7160
spelling Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de FarmacovigilânciaSafety of Oral Antidiabetics: A Disproportionality Analysis in the Portuguese Pharmacovigilance SystemIntroduction: Our objective was to investigate associations between oral antidiabetics and adverse drug reactions through disproportionality analysis in the Portuguese Pharmacovigilance System database. Methods: Spontaneous reports of adverse drug reactions reported for oral antidiabetics (2008–2017) were considered. Adverse drug reactions were coded according to MedDRA (preferred term), and oral antidiabetics according to Anatomical Therapeutic Chemical classification (4th level). Associations between oral antidiabetics and adverse drug reactions were assessed through a case/non-case methodology, using reporting odds ratio (ROR) with 95% confidence interval (CI) to identify signals of disproportionate reporting. Results: A total of 413 cases (262 serious; 63.4%) containing 1047 adverse drug reactions were included. Signals of disproportionate reporting were found: i) alpha-glucosidase inhibitors – abdominal pain (ROR: 9.7 [2.5-37.7]) and flatulence (ROR: 76.1[13.0-444.4]); ii) Dipeptidyl peptidase-4 inhibitors – upper abdominal pain (ROR: 5.5[1.5-20.7]), headache (ROR: 5.5[1.5-20.7]) and acute pancreatitis (ROR: 22.0[2.6-189.9]); iii) Glucagon-like peptide-1 agonists – vomiting (ROR: 3.4[1.4-8.4]; iv) metformin – abdominal pain (ROR: 3.6[1.1-11.6]), diarrhea (ROR: 5.6[2.4-13.2]) and lactic acidosis (ROR: 76.9[4.7-1269.0]); v) SGLT2 inhibitors – candida infection (ROR: 51.5[2.8-950.1], diabetic ketoacidosis(ROR: 84.8[4.8-1487.8]), pollakiuria (ROR: 15.2[1.6-147.1]), somnolence (ROR:30.4[1.5-610.3] and urinary tract infection (ROR: 15.2[1.6-147.1]); vi) sulfonylureas – hypoglycemia (ROR: 44.8[14.4-139.8]). Conclusion: The results are in line with previous knowledge on the safety profiles of the different classes of oral antidiabetics, reinforcing the need to monitoring closely certain adverse drug reactions in clinical practice depending on the therapy prescribed to diabetic patients.Introdução: O nosso objetivo foi investigar associações entre antidiabéticos orais e reações adversas a medicamentos com base em análises de desproporcionalidade na base de dados do Sistema Português de Farmacovigilância. Métodos: Foram consideradas as notificações espontâneas de reações adversas a medicamentos a antidiabéticos orais recebidas entre 2008 e 2017. As RAMs foram codificadas de acordo com a terminologia MedDRA (termo preferido) e os antidiabéticos orais de acordo com a classificação Anatomical Therapeutic Chemical (4º nível). Aplicou-se a metodologia de tirar espaços caso/não-caso e calcularam-se reporting odds ratios (RORs) e respetivos intervalos de confiança (ICs) a 95% para se identificarem sinais de desproporcionalidade. Resultados: Foram incluídas 413 notificações espontâneas (262 graves; 63,4%), que continham 1047 reações adversas a medicamentos. Foram identificados os seguintes sinais de desproporcionalidade: i) Inibidores da alfa-glucosidase – dor abdominal (ROR: 9,7 [2,5-37,7]) e flatulência (ROR: 76,1 [13,0-444,4]); ii) Inibidores da dipeptidil peptidase-4 – dor abdominal superior (ROR: 5,5 [1,5-20,7]), cefaleia (ROR: 5,5 [1,5-20,7]) e pancreatite aguda (ROR: 22,0 [2,6-189,9]); iii) Agonistas de glucagon-like peptide-1 – vómitos (ROR: 3,4 [1,4-8,4]; iv) Metformina – dor abdominal (ROR: 3,6 [1,1-11,6]), diarreia (ROR: 5,6 [2,4-13,2]) e acidose lática (ROR: 76,9 [4,7-1269,0]); v) Inibidores do co-transportador de sódio e glucose 2 – infeção por cândida (ROR: 51,5 [2,8-950,1], cetoacidose diabética (ROR: 84,8 [4,8-1487,8]), polaquiúria (ROR: 15,2 [1,6-147,1]), sonolência (ROR: 30,4 [1,5- 610,3] e infeção do trato urinário (ROR: 15,2 [1,6-147,1]); vi) sulfonilureias – hipoglicemia (ROR: 44,8 [14,4-139,8]). Conclusão: Os resultados estão em linha com o conhecimento prévio existente acerca dos perfis de segurança dos diferentes antidiabéticos orais, reforçando a necessidade de monitorizar na prática clínica os diferentes tipos de reações adversas a medicamentos em função das terapêuticas prescritas para os doentes diabéticos.Formifarma2019-10-14info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://doi.org/10.25756/rpf.v11i2-3.217https://doi.org/10.25756/rpf.v11i2-3.217Revista Portuguesa de Farmacoterapia / Portuguese Journal of Pharmacotherapy; Vol 11 No 2-3 (2019): Abril / Julho; 20-30Revista Portuguesa de Farmacoterapia; v. 11 n. 2-3 (2019): Abril / Julho; 20-302183-73411647-354Xreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAPporhttp://revista.farmacoterapia.pt/index.php/rpf/article/view/216http://revista.farmacoterapia.pt/index.php/rpf/article/view/216/194Direitos de Autor (c) 2019 Revista Portuguesa de Farmacoterapiainfo:eu-repo/semantics/openAccessMendes, DiogoAlves, CarlosBatel Marques, Francisco2025-02-28T04:33:46Zoai:ojs.farmacoterapia.pt:article/216Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T00:06:02.564496Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
Safety of Oral Antidiabetics: A Disproportionality Analysis in the Portuguese Pharmacovigilance System
title Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
spellingShingle Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
Mendes, Diogo
title_short Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
title_full Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
title_fullStr Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
title_full_unstemmed Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
title_sort Segurança de Antidiabéticos Orais: Análise de Desproporcionalidade no Sistema Português de Farmacovigilância
author Mendes, Diogo
author_facet Mendes, Diogo
Alves, Carlos
Batel Marques, Francisco
author_role author
author2 Alves, Carlos
Batel Marques, Francisco
author2_role author
author
dc.contributor.author.fl_str_mv Mendes, Diogo
Alves, Carlos
Batel Marques, Francisco
description Introduction: Our objective was to investigate associations between oral antidiabetics and adverse drug reactions through disproportionality analysis in the Portuguese Pharmacovigilance System database. Methods: Spontaneous reports of adverse drug reactions reported for oral antidiabetics (2008–2017) were considered. Adverse drug reactions were coded according to MedDRA (preferred term), and oral antidiabetics according to Anatomical Therapeutic Chemical classification (4th level). Associations between oral antidiabetics and adverse drug reactions were assessed through a case/non-case methodology, using reporting odds ratio (ROR) with 95% confidence interval (CI) to identify signals of disproportionate reporting. Results: A total of 413 cases (262 serious; 63.4%) containing 1047 adverse drug reactions were included. Signals of disproportionate reporting were found: i) alpha-glucosidase inhibitors – abdominal pain (ROR: 9.7 [2.5-37.7]) and flatulence (ROR: 76.1[13.0-444.4]); ii) Dipeptidyl peptidase-4 inhibitors – upper abdominal pain (ROR: 5.5[1.5-20.7]), headache (ROR: 5.5[1.5-20.7]) and acute pancreatitis (ROR: 22.0[2.6-189.9]); iii) Glucagon-like peptide-1 agonists – vomiting (ROR: 3.4[1.4-8.4]; iv) metformin – abdominal pain (ROR: 3.6[1.1-11.6]), diarrhea (ROR: 5.6[2.4-13.2]) and lactic acidosis (ROR: 76.9[4.7-1269.0]); v) SGLT2 inhibitors – candida infection (ROR: 51.5[2.8-950.1], diabetic ketoacidosis(ROR: 84.8[4.8-1487.8]), pollakiuria (ROR: 15.2[1.6-147.1]), somnolence (ROR:30.4[1.5-610.3] and urinary tract infection (ROR: 15.2[1.6-147.1]); vi) sulfonylureas – hypoglycemia (ROR: 44.8[14.4-139.8]). Conclusion: The results are in line with previous knowledge on the safety profiles of the different classes of oral antidiabetics, reinforcing the need to monitoring closely certain adverse drug reactions in clinical practice depending on the therapy prescribed to diabetic patients.
publishDate 2019
dc.date.none.fl_str_mv 2019-10-14
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.25756/rpf.v11i2-3.217
https://doi.org/10.25756/rpf.v11i2-3.217
url https://doi.org/10.25756/rpf.v11i2-3.217
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv http://revista.farmacoterapia.pt/index.php/rpf/article/view/216
http://revista.farmacoterapia.pt/index.php/rpf/article/view/216/194
dc.rights.driver.fl_str_mv Direitos de Autor (c) 2019 Revista Portuguesa de Farmacoterapia
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Direitos de Autor (c) 2019 Revista Portuguesa de Farmacoterapia
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Formifarma
publisher.none.fl_str_mv Formifarma
dc.source.none.fl_str_mv Revista Portuguesa de Farmacoterapia / Portuguese Journal of Pharmacotherapy; Vol 11 No 2-3 (2019): Abril / Julho; 20-30
Revista Portuguesa de Farmacoterapia; v. 11 n. 2-3 (2019): Abril / Julho; 20-30
2183-7341
1647-354X
reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron:RCAAP
instname_str FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
instacron_str RCAAP
institution RCAAP
reponame_str Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
repository.name.fl_str_mv Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologia
repository.mail.fl_str_mv info@rcaap.pt
_version_ 1833600397228376064