Adverse reactions to meglumine antimoniate in Brazilian inpatients with visceral leishmaniases: A case series.

What is known and objectives: Adverse drug reactions (ADR) related to the treatment of visceral leishmaniasis (VL) can cause severe clinical complications. We report a case series of ADR in hospitalized VL patients on meglumine antimoniate (MA). Case description: Seven cases of patients taking MA ha...

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Detalles Bibliográficos
Publicado en:Journal of Clinical Pharmacy & Therapeutics Vol. 45; no. 3; pp. 573 - 577
Autores principales: Serbate Borges Portela, Áquila, Margotto Bertollo, Caryne, Silva Praxedes, Marcus Fernando, Silva Brasileiro, Sandro Aurélio, Moreira Reis, Adriano Max, Parreiras Martins, Maria Auxiliadora
Formato: research tables/charts Journal Article
Publicado: Wiley-Blackwell Jun2020
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:What is known and objectives: Adverse drug reactions (ADR) related to the treatment of visceral leishmaniasis (VL) can cause severe clinical complications. We report a case series of ADR in hospitalized VL patients on meglumine antimoniate (MA). Case description: Seven cases of patients taking MA had at least one objective evidence for suspected ADR, including electrocardiographic, laboratory or clinical alteration. What is new and conclusion: Meglumine antimoniate is highly toxic. Adherence to treatment guidelines is important. Pharmacists working in multidisciplinary teams may contribute to early detection and management of MA therapy‐related ADR.