Pharmacovigilance in resource-limited countries

dc.contributor.authorOlsson, S.
dc.contributor.authorPal, S.N.
dc.contributor.authorDodoo, A.
dc.date.accessioned2018-09-14T16:51:13Z
dc.date.available2018-09-14T16:51:13Z
dc.date.issued2015-06
dc.description.abstractIn the past 20 years, many low- and middle-income countries have created national pharmacovigilance (PV) systems and joined the WHO’s global PV network. However, very few of them have fully functional systems. Scientific evidence on the local burden of medicine-related harm and their preventability is missing. Legislation and regulatory framework as well as financial support to build sustainable PV systems are needed. Public health programs need to integrate PV to monitor new vaccines and medicines introduced through these programs. Signal analysis should focus on high-burden preventable adverse drug problems. Increased involvement of healthcare professionals from public and private sectors, pharmaceutical companies, academic institutions and the public at large is necessary to assure a safe environment for drug therapy. WHO has a major role in supporting and coordinating these developments. (PDF) Pharmacovigilance in resource-limited countries. Available from: https://www.researchgate.net/publication/277724256_Pharmacovigilance_in_resource-limited_countries [accessed Sep 14 2018].en_US
dc.identifier.otherVolume 8,Issue 4
dc.identifier.otherhttps://doi.org/10.1586/17512433.2015.1053391
dc.identifier.urihttp://ugspace.ug.edu.gh/handle/123456789/24190
dc.language.isoenen_US
dc.publisherExpert Review of Clinical Pharmacologyen_US
dc.subjectPharmacovigilanceen_US
dc.subjectadverse drug reactionsen_US
dc.subjectconsumer involvementen_US
dc.subjectdrug regulationen_US
dc.subjectharmen_US
dc.subjectlow and middle income countriesen_US
dc.subjectmedicinesen_US
dc.subjectpatient safetyen_US
dc.subjectpublic health programsen_US
dc.titlePharmacovigilance in resource-limited countriesen_US
dc.typeArticleen_US

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