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J Clin Pharm Ther ; 45(3): 573-576, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31793023

ABSTRACT

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.


Subject(s)
Antiprotozoal Agents/therapeutic use , Leishmaniasis, Visceral/drug therapy , Meglumine Antimoniate/therapeutic use , Adolescent , Adult , Brazil , Female , Humans , Inpatients , Male , Middle Aged , Treatment Outcome , Young Adult
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