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Are we doing enough to prevent poor-quality antimalarial medicines in the developing world?
Erin J Walker1,2, Gregory M Peterson3, James Grech1,2
1Faculty of Health, University of Canberra, Building 12, Room D36, Kirinari Street, Bruce, Canberra, ACT 2601, Australia.
BMC Public Health
|May 17, 2018
Summary
Poor-quality antimalarial medicines cause significant deaths, especially in children. Enhancing drug regulation and developing new detection technologies are crucial to combat this global health threat.
Area of Science:
- Global Health
- Pharmaceutical Quality Control
- Parasitic Diseases
Background:
- Malaria is a deadly parasitic disease affecting over 3 billion people, predominantly in resource-poor nations.
- Poor-quality antimalarial medicines contribute to substantial preventable deaths, particularly among children under five in sub-Saharan Africa.
- An estimated 122,000 child deaths in sub-Saharan Africa in 2013 were linked to substandard antimalarials.
Purpose of the Study:
- To highlight the critical issue of poor-quality antimalarial medicines.
- To discuss the risks and contributing factors associated with substandard antimalarials.
- To emphasize the need for collective action and technological advancements in combating counterfeit drugs.
Main Methods:
- Review of existing studies on antimalarial drug quality.
- Analysis of factors contributing to the circulation of poor-quality medicines.
- Examination of current strategies and future needs for quality assurance.
Main Results:
- The prevalence of poor-quality antimalarials varies widely, with studies reporting 4-92% of tested products being substandard.
- Substandard antimalarials lead to severe illness, increased healthcare costs, and reduced patient confidence.
- Key factors include weak regulatory systems, insufficient funding, poor regulatory coordination, and ineffective import/export controls.
Conclusions:
- Significant progress has been made in delivering high-quality antimalarials, but challenges remain.
- An urgent, collective international response is required, involving political commitment and increased R&D funding.
- Strengthening and harmonizing drug regulation practices globally, alongside developing innovative field detection technologies, is essential.
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