Preliminary safety assessment of sulphadoxine-pyrimethamine during intermittent presumptive treatment of pregnant women in a region with high prevalence of G6PD deficiency
dc.contributor.author | Dodoo, A.N.O. | |
dc.contributor.author | Gyansa-Lutterodt, M. | |
dc.contributor.author | Frempong, N. | |
dc.contributor.author | Thompson, H. | |
dc.contributor.author | Amofa, G. | |
dc.contributor.author | Bart-Plange, C. | |
dc.contributor.author | Allotey, N.K. | |
dc.contributor.author | Eghan, K.E. | |
dc.date.accessioned | 2019-03-21T09:18:04Z | |
dc.date.available | 2019-03-21T09:18:04Z | |
dc.date.issued | 2005-01 | |
dc.description.abstract | Pregnant women in 20 administrative districts of Ghana are being monitored intensively for adverse events following intermittent presumptive treatment with sulphadoxine-pyrimethamine. Preliminary results indicate a low level of adverse events (0.16%) suggesting good tolerability of the drug, despite the relatively high G6PD deficiency prevalence of more than 20%. Since the real possibility of under-reporting cannot be overlooked, the focused surveillance approach being used in the study is being complemented with in-depth interviews following home visits and focus group discussions with patients and healthcare workers. © 2005 - IOS Press and the authors. All rights reserved. | en_US |
dc.identifier.other | Vol. 17, pp 13-18 | |
dc.identifier.uri | http://ugspace.ug.edu.gh/handle/123456789/28755 | |
dc.language.iso | en | en_US |
dc.publisher | International Journal of Risk and Safety in Medicine | en_US |
dc.subject | G6PD deficiency | en_US |
dc.subject | Intermittent presumptive therapy | en_US |
dc.subject | Sulfadoxine-pyrimethamine | en_US |
dc.title | Preliminary safety assessment of sulphadoxine-pyrimethamine during intermittent presumptive treatment of pregnant women in a region with high prevalence of G6PD deficiency | en_US |
dc.type | Article | en_US |
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