Who Calls For 'Immediate' Action After Cough Syrup Deaths

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World health body says more than 300 deaths in 3 countries reported incidents of contaminated cough syrups over 4 months.

The World Health Organization has called for “immediate and concerted action” to protect children from contaminated medicines after a spate of child deaths linked to cough syrups last year.

More than 300 children died from contaminated cough syrup in the Gambia, Uzbekistan and Indonesia in 2022. Many of the victims were younger than five years old.

The incidents are believed to be caused by the contamination of Indian and Indonesian-made cough syrups with dangerously high levels of diethylene glycol and ethylene glycol.

"These contaminants are toxic chemicals used as industrial solvents and antifreeze agents that can be fatal even taken in small amounts, and should never be found in medicines," the WHO said.

The UN health agency first issued an alert about the child deaths seen in The Gambia back in October, followed by one a month later focused on Indonesia and another earlier this month on Uzbekistan.

It has issued warnings against the use of cough syrups made by Indian firms Marion Biotech and Maiden Pharmaceuticals in connection with the deaths.

In its alerts, the WHO called on countries to boost efforts to detect and remove any contaminated medicines from circulation, up surveillance within supply chains and to immediately sound the alarm if any of the substandard products were found.

But on Monday, the UN agency stressed that "these are not isolated incidents", urging all parties involved in medical supply chains to take "immediate and coordinated action".

Regulators and governments, it said, should be working to spot and remove any substandard medical product identified by the WHO alerts.

They should also ensure that all medical products sold in their respective markets are approved for sale by competent authorities from authorized and licensed suppliers.

Medicine manufacturers meanwhile have a responsibility to "only purchase pharmaceutical-grade excipients from bona fide suppliers", the WHO said.

They should also keep complete records of their purchases, and carry out "comprehensive testing" of any supplies received before using them to make medicines, and should issue certificates of analysis attesting to the quality of a product.

The WHO added that suppliers and distributors of medical products should among other things "always check for signs of falsification" and only sell medicines authorized by competent authorities.