How can we assess the safety of antimalarials? from ACT Consortium on Vimeo.
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Phase II and III clinical trials are aimed at identifying common adverse effects of drugs in carefully selected patients, but their sample size means that they are not suitable for identifying rare but potentially serious adverse effects or defining safety in high risk populations.
Setting up and maintaining systems capable of collecting and collating data on adverse events will be challenging in most countries, but particularly so in Africa where it is anticipated the bulk of antimalarials will be used, and where the potentially most vulnerable populations reside.
During the lifetime of the ACT Consortium, there was a particular concern about efficacy and safety in those co-infected with HIV/AIDs, who constitute a significant proportion of those requiring ACTs. There were similar concerns about safety of antimalarials in infants and the malnourished.
Research questions addressed by the consortium
Learn about our projects and resources on assessing the safety of ACTs or download a summary of our research findings.