Search Results for: PositiveNaija Public Alert

Nigerian Public Alert 62: The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying healthcare professionals and the public of confirmed counterfeit batches of Avastin® 400mg/16ml (Bevacizumab) and Tecentriq® 1200mg/20ml (Atezolizumab) circulating in Nigeria. This alert is issued in response to official communications from Roche Nigeria, which have confirmed several cases of … Continue reading Nigerian Public Alert 62: NAFDAC Notifies on Confirmed Counterfeit of Avastin 400mg/ 16ml and Tecentriq 1200mg/20ml in Nigeria

Nigerian Public Alert 61: The Marketing Authorization Holder (MAH), Roche, received these complaints from Lagos University Teaching Hospital (LUTH-NSIA) reporting suspected counterfeit Phesgo® 600mg with batch numbers B2346B16 and C3809C5. The batch C3809C5 vial volume was observed to be approximately 20mL instead of the expected 10mL. Both products were reported to be brought in by patients for administration.

Nigerian Public Alert 60: The National Agency for Food and Drugs Administration and Control (NAFDAC) is informing the public that Stuff by Nainax LLC is voluntarily recalling all lots of “MR.7 SUPER 700000’’ capsules to the consumer level over safety concerns.

Nigerian Public Alert 59: The National Agency for Food and Drugs Administration and Control (NAFDAC) is informing the healthcare providers and the public of a report of confirmed counterfeit Avastin 400mg in Nigeria.

Nigerian Public Alert 58: The National Agency for Food and Drug Administration and Control (NAFDAC) is warning healthcare providers, patients, and the public about reports of counterfeit and parallel-imported unregistered versions of the VISITECT HIV Advanced Disease Test Kits circulating in Nigeria.

Nigerian Public Alert 57: The National Agency for Food and Drug Administration and Control (NAFDAC) is notifying healthcare providers, patients, and the public of the Notice of Concern (NOC) issued by the WHO Prequalification Service for some NAFDAC-registered medical devices manufactured by Meril Diagnostics Pvt. Ltd, India.

Nigerian Public Alert 56: The National Agency for Food and Drugs Administration and Control (NAFDAC) is reminding the public of the Regulatory Directive issued last year on the discontinued registration of Multi-Dose Anti-Malarial (Artemether/Lumefantrine) dry powder for Oral Suspension due to the instability of the reconstituted formulations, which results in the loss of efficacy of … Continue reading Nigerian Public Alert 56: NAFDAC Notifies on Discontinued Registration of Multi-Dose Artemether /Lumefantrine Dry Powder for Oral Suspension