Public Health Alert: NAFDAC Recalls Deekins Amoxycillin 500mg Capsules Over Adverse Reactions

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The National Agency for Food and Drug Administration and Control (NAFDAC) has issued a public health alert.

This alert concerns the recall of Deekins Amoxycillin 500mg Capsules, batch number 4C639001, following serious adverse drug reactions.

Three patients suffered severe reactions after using the affected batch, prompting immediate action by NAFDAC.

The capsules, manufactured by Ecomed Pharma Ltd and marketed by DevineKings Pharmaceutical Ltd, were identified as the source.

Healthcare professionals are advised to stop using this batch and closely monitor patients for any adverse effects.

Consumers who have purchased this batch are urged to contact their healthcare provider for guidance on next steps.

NAFDAC is actively investigating the reported adverse reactions and taking necessary steps to prevent further risks.

The agency also calls on the public to report any suspected substandard or falsified medicines immediately.

Those with concerns can contact NAFDAC at 0800-162-3322 or email sf.alert@nafdac.gov.ng for further assistance.

NAFDAC remains committed to safeguarding public health by ensuring the safety and efficacy of all marketed drugs.

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