BY : DARI KWABENA MATHEW (+233555395925)
The World Health Organisation, WHO, has appealed to countries to take action to prevent, detect and respond to incidents of substandard and falsified medical products.
WHO cites recent incidents where over-the-counter cough syrups for children had confirmed traces or suspected amount of contamination in them and this resulted in more than 300 fatalities in three of the seven countries (at least) affected.
WHO said most affected are young children under the age of five.
“Over the past four months, countries have reported on several incidents of over-the-counter cough syrups for children with confirmed or suspected contamination with high levels of diethylene glycol (DEG) and ethylene glycol (EG)” the world health body said.
According to WHO, the contaminants are toxic chemicals used as industrial solvents and antifreeze agents that can be fatal, even taken in small amounts.
It warns that the contaminants should never be found in medicines.
The Gambia, Indonesia, and Uzbekistan were among countries cited.
To raise awareness, medical product alerts were rapidly disseminated to national health authorities of all 194 WHO Member States.
The 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, and immediate notification to WHO if these substandard products are discovered in-country; and inform the public of the dangers and toxic effects of the substandard medicines at issue.
As these incidents are not isolated, WHO is urging stakeholders engaged in the medical supply chain to take “immediate and coordinated action.”
WHO calls on regulators and governments to:
detect and remove from circulation in their respective markets any substandard medical products that have been identified in the WHO medical alerts referred to as potential causes of deaths and disease;
ensure that all medical products in their respective markets are approved for sale by competent authorities and obtainable from authorized/licensed suppliers;
assign appropriate resources to improve and increase risk-based inspections of manufacturing sites within their jurisdiction in accordance with international norms and standards;
increase market surveillance including risk-based targeted testing for medical products released in their respective markets including informal markets; and
enact and enforce, where relevant and as appropriate, laws and other relevant legal measures to help combat the manufacture, distribution and/or use of substandard and falsified medicines.
WHO calls 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 manufacture of finished products;”
“provide assurance of product quality including through certificates of analyses based on appropriate testing results;” and
“keep accurate, complete and proper records of purchase of materials, testing, manufacture, and distribution to facilitate traceability during investigations in case of incidents.”
WHO urges all suppliers and distributors of medical products to:
“always check for signs of falsification and physical condition of medicines and other health products they distribute and/or sell;”
“only distribute and/or sell medicines authorized by, and from sources approved by, competent authorities;”
“keep accurate, complete and proper records relating to the medicines and their distribution and/or sale;” and
“engage competent personnel to handle medicines and provide advice to the public on appropriate use of the medicines.”
To save lives, WHO says “it will continue to work with the Member State Mechanism on substandard and falsified medical products in implementing its mandate to promote effective collaboration in the prevention, detection and response to substandard and falsified medical products.”
