dc.contributor.author | Ambooken, Betsy | |
dc.contributor.author | George, Sandhya | |
dc.contributor.author | Azeez, Neema | |
dc.contributor.author | Asokan, N | |
dc.contributor.author | Xavier, TD | |
dc.date.accessioned | 2025-01-15T06:07:18Z | |
dc.date.available | 2025-01-15T06:07:18Z | |
dc.date.issued | 2017-06-01 | |
dc.identifier.citation | Leprosy Review Volume 88 Issue 2 | en_US |
dc.identifier.issn | 2162-8807 | |
dc.identifier.uri | 10.47276/lr.88.2.197 | |
dc.identifier.uri | http://starc.stthomas.ac.in:8080/xmlui/xmlui/handle/123456789/370 | |
dc.description.abstract | Objective: To assess the frequency and type of adverse drug reactions (ADR) that necessitated modification of multi-drug therapy (MDT) in Hansen’s disease, with emphasis to find out the interval between initiation of MDT and the occurrence of ADR. Design: A retrospective analysis of case records of patients diagnosed with Hansen’s disease (HD) and registered for MDT in a tertiary care institution between 2010 and 2015. Clinical details and laboratory data were collected using a proforma. Results: One hundred and ninety-six patients were registered for treatment during the study period. We analysed 150 records that met the inclusion criteria. Thirty-six among them (24%) had ADR that needed modification of MDT. The most common ADR was haemolytic anemia (19 patients; 12.7%) followed by hepatitis (14 patients; 9.3%). The most serious ADR was agranulocytosis (three patients; 2%). Adverse effects were more common (72%) during the initial 2 months of MDT compared to later months. (P = 0.004). | en_US |
dc.language.iso | en | en_US |
dc.publisher | Lepra | en_US |
dc.title | Adverse Drug Reactions (ADR) necessitating modification of multi-drug therapy (MDT) in Hansens disease: a retrospective study from Kerala, India | en_US |
dc.type | Article | en_US |