Literature DB >> 22111680

Establishing pharmacovigilance programs in resource-limited settings: the example of treating malaria.

Ushma Mehta1, Elizabeth Allen, Karen I Barnes.   

Abstract

The unprecedented levels of political, technical and financial support for improved malaria control, and particularly for changes in the malaria treatment policy, have heralded a renewed appreciation of the role of pharmacovigilance, its relationship with other areas of public health and the development of novel approaches to addressing the pharmacovigilance priorities in malaria-endemic countries. In order to become a valuable public health activity in these resource-limited settings, pharmacovigilance needs to be viewed within its broadest definition of detecting, understanding and preventing adverse drug reactions and drug-related problems. Pharmacovigilance in resource-limited settings provides an opportunity to identify and address health system failures that significantly impact on patient morbidity and mortality, particularly those that are drug related. Countries need to establish a national strategy that identifies realistic and relevant objectives that meet the most pressing pharmacovigilance needs, taking into consideration the conditions under which these systems are likely to develop.

Entities:  

Year:  2010        PMID: 22111680     DOI: 10.1586/ecp.10.37

Source DB:  PubMed          Journal:  Expert Rev Clin Pharmacol        ISSN: 1751-2433            Impact factor:   5.045


  6 in total

1.  Global patterns of adverse drug reactions over a decade: analyses of spontaneous reports to VigiBase™.

Authors:  Lise Aagaard; Johanna Strandell; Lars Melskens; Paw S G Petersen; Ebba Holme Hansen
Journal:  Drug Saf       Date:  2012-12-01       Impact factor: 5.606

2.  Designing adverse event forms for real-world reporting: participatory research in Uganda.

Authors:  Emma C Davies; Clare I R Chandler; Simeon H S Innocent; Charles Kalumuna; Dianne J Terlouw; David G Lalloo; Sarah G Staedke; Ane Haaland
Journal:  PLoS One       Date:  2012-03-29       Impact factor: 3.240

3.  Influences on participant reporting in the World Health Organisation drugs exposure pregnancy registry; a qualitative study.

Authors:  Elizabeth N Allen; Melba Gomes; Lucy Yevoo; Omar Egesah; Christine Clerk; Josaphat Byamugisha; Anthony Mbonye; Edwin Were; Ushma Mehta; Lynn M Atuyambe
Journal:  BMC Health Serv Res       Date:  2014-10-31       Impact factor: 2.655

4.  Intermittent preventive treatment for malaria among children in a refugee camp in Northern Uganda: lessons learned.

Authors:  Matthew E Coldiron; Estrella Lasry; Malika Bouhenia; Debashish Das; Peter Okui; Dan Nyehangane; Juliet Mwanga; Celine Langendorf; Greg Elder; Léon Salumu; Rebecca F Grais
Journal:  Malar J       Date:  2017-05-23       Impact factor: 2.979

5.  EDCTP regional networks of excellence: initial merits for planned clinical trials in Africa.

Authors:  George M Miiro; Odile Ouwe Missi Oukem-Boyer; Ousmane Sarr; Maerangis Rahmani; Francine Ntoumi; Keertan Dheda; Alexander Pym; Souleymane Mboup; Pontiano Kaleebu
Journal:  BMC Public Health       Date:  2013-03-22       Impact factor: 3.295

6.  Evaluating harm associated with anti-malarial drugs: a survey of methods used by clinical researchers to elicit, assess and record participant-reported adverse events and related data.

Authors:  Elizabeth N Allen; Clare I R Chandler; Nyaradzo Mandimika; Cheryl Pace; Ushma Mehta; Karen I Barnes
Journal:  Malar J       Date:  2013-09-16       Impact factor: 2.979

  6 in total

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