WHO calls for action to protect children from contaminated medicines after cough syrups deaths

In the wake of fatalities among children linked to cough syrups and medicines made by manufacturers based in India and Indonesia the WHO has issued an urgent call to action to countries to detect and respond to incidents of falsified medical products and protect children from contaminated medicinesThe World Health Organisation WHO said that over the past four months countries reported several incidents of overthecounter cough syrups for children with confirmed or suspected contamination with high levels of diethylene glycol DEG and ethylene glycol EGThe cases are from at least seven countries associated with more than 300 fatalities in three of these countries with most young children under the age of fiveThe WHO said the contaminants are toxic chemicals used as industrial solvents and antifreeze agents that can be fatal even in small amounts and should never be found in medicinesWHO is releasing an urgent call to action to countries to prevent detect and respond to incidents of substandard and falsified medical products the global health agency saidSince October last year the WHO has issued three global medical alerts over substandard paediatric medicines and syrupsIn October 2022 it issued an alert over Promethazine Oral Solution Kofexmalin Baby Cough Syrup Makoff Baby Cough Syrup and Magrip N Cold Syrup manufactured by Maiden Pharmaceuticals Limited Haryana IndiaAlso Read Cough syrup linked deaths in Uzbekistan Drugs Standard Control Organisation initiates probeThe four substandard products were identified in the Gambia and reported to the WHO in September 2022In November an alert was issued by the WHO over eight products including Unibebi Cough Syrup Unibebi Demam Paracetamol Drops and Unibebi Demam Paracetamol Syrup identified in Indonesia and manufactured by PT Afi FarmaEarlier this month the WHO issued an alert to warn against the use of two substandard cough syrups manufactured by Marion Biotech India that have been linked to the deaths of 18 children in UzbekistanAmbronol syrup and DOK1 Max syrup were manufactured by Marion Biotech based in Noida Uttar PradeshThe global health organisation issued the alert saying the syrups fail to meet quality standards and contain contaminants that can prove fatalThe WHOs medical product alerts were rapidly disseminated to the national health authorities of all 194 WHO Member StatesThese medical product alerts requested the detection and removal of contaminated medicines from circulation in the markets increased surveillance and diligence within the supply chains of countries and regions likely to be affected immediate notification to WHO if these substandard products are discovered incountry and otherwise inform the public of the dangers and toxic effects of the substandard medicines at issueIt noted that since these are not isolated incidents the WHO called on regulators and governments to detect and remove from circulation in their respective markets any substandard medical products that have been identified in the alerts as potential causes of death and disease ensure that all medical products in their respective markets are approved for sale by competent authorities and obtainable from authorisedlicensed suppliersIt also urged authorities to assign appropriate resources to improve and increase riskbased inspections of manufacturing sites within their jurisdiction in accordance with international norms and standards and enact and enforce laws and other relevant legal measures to help combat the manufacture distribution andor use of substandard and falsified medicinesThe WHO called on manufacturers of medicines to only purchase pharmaceutical grade excipients from qualified and bona fide suppliers conduct comprehensive testing upon receipt of supplies and before use in the manufacture of finished products and provide assurance of product quality including through certificates of analyses based on appropriate testing resultsIt also urged suppliers and distributors of medical products to always check for signs of falsification and physical condition of medicines and other health products they distribute andor sell and only distribute andor sell medicines authorised by and from sources approved by competent authorities among other measuresIn December Indias drug regulator told the WHO that the global health body drew a premature link between the deaths of children in Gambia and the four Indiamade cough syrups which adversely impacted the image of the countrys pharmaceutical products across the globeIn a letter to Dr Rogerio Gaspar Director Regulation and Prequalification at WHO DCGI Dr V G Somani said a statement issued by the global health body in October in the wake of the deaths was unfortunately amplified by the global media which led to a narrative being built internationally targeting the quality of Indian pharmaceutical productsThis story has been sourced from a third party syndicated feed agencies Midday accepts no responsibility or liability for its 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