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Delese Mimi Darko – FDA Boss
The Food and Drug Authority (FDA) has issued a warning to health professionals that they stop using a diagnostic kit Rapid Malaria (SDT) called SD Bio Line Malaria. A statement issued in Accra and signed by FDA chief executive, Delese A. Darko, said that although the kit was registered by the authority, its investigations showed that the product had been "relabeled"
According to the FDA, people using the kit may suffer from an inaccurate diagnosis, which can have serious health implications.
"The Food and Drug Authority wants to alert the general public An expired malaria rapid diagnostic test kit (TDR) is being offered for sale on the Ghanaian market." The FDA has investigated a complaint and has established the fact that people have tampered with information about this expired product, "the statement said.
"It is therefore dangerous to have a malaria test using the RDT kit, which would certainly produce a false result and could lead to an inaccurate diagnosis," he added.
The FDA also asked the public to provide information if they ever saw the product on the Ghanaian market
The 2012 Auditor General's Report to the Parliament's Public Accounts Committee (PAC) revealed that many unregistered drugs were imported into Ghana without the prior approval of the FDA.
Among the non-registered drugs that entered the Ghanaian market between 2012 and 2013 According to the Auditor General's report, we find the popular anti-malarial drug Coartem and the vermifuge Zentel.
Others include Tres-Orix, Procold, Lofnac-50 tablets, Atenolol, Lofnac Eyedrops, Quine Syrup, among others
In total, 72 me unregistered drugs were imported during this period. The report also revealed that seven drugs were introduced into the country "before importers seek FDA clearance."
Ms. Darko later badured that her equipment was at the top of the problems to ensure the safety of citizens.
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