Posted on: Fri 19-01-2024

The National Agency for Food and Drug Administration (NAFDAC) has said there is no evidence that low-quality Paracetamol tablets currently exist in Nigeria.

A statement signed by NAFDAC’s Resident Media Consultant, Sayo Akintola, said the agency was aware of a recent report on social media alleging that nearly all paracetamol tablets sold in Nigeria are “under-dosed”.

However, he said that the outcome of investigations on the matter proved the allegations wrong and misleading.

” We have received a copy of the publication of the research finding of the subject and we wish to state categorically that the report is misleading, and the science is questionable,” it said.

The statement stated that as the quality culture of NAFDAC demanded, as soon as the agency became aware of the news, the Director General had meetings with the respective directors and gave a directive that a survey of the market should be done to sample and test.

It said the director general of the agency had also met with the leadership of the Pharmaceutical Manufacturing Group of the Manufacturing Association of Nigeria to inform them of the agency’s intent.

“NAFDAC’s laboratories are ISO 17025-certified every year to ensure that the procedures used for testing are based on international standards and the equipment or instruments used are qualified similarly.

“We do a yearly post-marketing survey of medicines to ensure that the quality and safety are maintained.  Where there is a deviation from this, i.e., whenever we find any regulated product to be substandard or falsified, NAFDAC regularly issues public alerts or do recalls,” it said.

NAFDAC said that in the last two years, it had issued 88 public alerts and ordered 32 recalls for medicines and foods.

“We are using this medium to assure the public that NAFDAC is using international standards and scientific methods to survey the paracetamol product where samples are collected from different parts of the country in the right amount and will be tested using well calibrated, and qualified state-of-the-art equipment or instruments.

“This is part of our routine regulatory post-marketing surveillance among others throughout the life cycle of a medicine.

We want to reiterate that NAFDAC has five ISO-17025 laboratories across the country, and a World Health Organization (WHO) prequalified laboratory at Yaba Lagos where medicines are tested for quality and safety.

“The laboratories test medicines using official monographs of British Pharmacopoeia, United States Pharmacopoeia, and International Pharmacopoeia. As soon as we finish the laboratory testing, we will update the public.

“NAFDAC wishes to reassure the public that the agency is very vigilant in its responsibilities in safeguarding the health of the nation.

‘It is on this basis that NAFDAC has been recognized by WHO as a stable, well-functioning agency, and by other international partners as an organization that places a premium on the quality, safety and efficacy of medicines, food, and other regulated products,” it said.

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