The warning underscores the critical risk posed by monotherapies that undermine the global standard of combination-based malaria treatment.
According to a recent media report in LiveMint, DCGI Dr Rajeev Singh Raghuvanshi noted that despite a nationwide prohibition issued in 2009, certain manufacturers are still suspected of producing and distributing oral single-ingredient artemisinin formulations. These medicines, although capable of killing malaria parasites quickly, fail to remain in the bloodstream long enough to eliminate the infection completely, leaving behind stronger parasites that may lead to resistance.
International health guidelines have long discouraged the use of artemisinin monotherapy. The World Health Organization (WHO) advises that artemisinin must always be administered alongside another antimalarial to ensure full parasite clearance and prevent resistance from spreading. This resulted in the adoption of artemisinin-based combination therapies (ACTs) as the global gold standard. ACTs work through a two-step mechanism that reduces the likelihood of parasites surviving and developing resistance pathways.
Medical experts have warned that even isolated pockets of reduced drug sensitivity - particularly in some regions near India’s borders—could threaten the long-term success of ACTs. The DCGI’s directive reflects growing caution within the public health community that unregulated monotherapies, if allowed to circulate, could weaken the country’s malaria control strategies.
State drug authorities have been instructed to intensify surveillance, carry out targeted inspections, and remove any illegal single-drug artemisinin stocks found in the market. The manufacturing or sale of such products is a punishable offence under Section 26A of the Drugs and Cosmetics Act, 1940, inviting legal consequences including fines, imprisonment and license cancellation, reports LiveMint.
Industry observers note that while major pharmaceutical players dominate India’s $30-million antimalarial segment, officials did not disclose names of any companies suspected in the ongoing probe, stating that enforcement action remains underway.
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