NAFDAC Alerts Nigerians On Suspected Falsified Augmentin

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NAFDAC claims that the product fell short of meeting the labeling criteria.

The alert was found on the NAFDAC website, which was signed by the organization’s management and was captioned “NAFDAC Alert And Sensitization Of The Public On Suspected Falsified Augmentin 625mg.”

The suspected counterfeit Augmentin, which was produced in April 2021, will expire in April 2024, according to NAFDAC.

It further mentioned that the forged drug’s batch number is 562626 and that it has the NAFDAC registration number 04-1928.

It said “The product failed short of the labeling requirements. No inscription “manufactured by” is written on the label -only the address.

“Manufacturing and Expiry dates do not meet the acceptable format. No MAS scratch number for verification.

The logo “gsk” is not properly positioned as on the original. The listed information indicates the product is falsified and counterfeited.

“In view of the above, NAFDAC has notified all its formations in the zones and 36 states of the federation including the FCT to carry out surveillance and mop up the falsified Augmentin tablets.”

It added, “Please note that the genuine Augmentin 625mg has legible product labeling information including date markings – expiration and manufactured dates, batch number and NAFDAC registration number.

“NAFDAC advise to wholesalers, distributors, and pharmacies is that medicines should be obtained from authorized/licensed suppliers, increased vigilance is hereby encouraged within the supply chain to avoid infiltration of the falsified product. The products’ authenticity, physical condition and labels should be carefully checked.

“NAFDAC implores healthcare providers to ensure vigilance to prevent the administration of falsified products to unsuspecting patients. Members of the public in possession of the above suspected counterfeit product are advised to discontinue sale or use and submit stock to the nearest NAFDAC office.

“Healthcare providers and the public should notify the nearest NAFDAC office of any information concerning the distribution, sale, and use of the falsified version of the Augmentin product. Report any suspicion of adverse drug reaction and substandard and falsified medicines to NAFDAC on 0800-162-3322 or email: sf.alert@nafdac.gov.ng.”

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