The National Agency for Food and Drug Administration and Control (NAFDAC) is investigating suspected counterfeit Deekins Amoxycillin 500mg capsules.
This was disclosed by a statement personally signed by the agency’s Director-General, Prof. Mojisola Adeyeye.
Reports of serious adverse reactions have raised concerns over the safety of the affected lot of the medication. The statement emphasized that the investigation is critical to ensuring public safety and maintaining high regulatory standards.
The batch in question, Lot 4C639001, was reportedly linked to harmful side effects in patients across the country. Prof. Adeyeye’s statement urged immediate vigilance from the public, healthcare providers, and distributors to prevent further incidents.
Ecomed Pharma Ltd, the manufacturer, claims to have produced only 20 packets of Lot 4C639001 for registration purposes. However, 790 packs of this batch were reportedly recalled, raising suspicions of discrepancies in the company’s production claims.
NAFDAC has collected samples of the product for laboratory analysis to verify its authenticity and safety standards. The agency’s investigation is ongoing, and it is working closely with the Pharmacy Council of Nigeria to resolve the matter.
The public is urged to immediately stop using, selling, or distributing the suspected counterfeit Deekins Amoxycillin 500mg capsules. NAFDAC remains committed to ensuring the safety of the nation’s drug supply.
