Rapid Alerts - Pharmacy and Poisons Board To protect the health of the public by regulating the Profession of Pharmacy and ensuring quality, safety and efficacy of Medical Products and Health Techonologies. Wed, 26 Jun 2024 10:53:22 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.2 /wp-content/uploads/2021/11/cropped-logo-1-150x150.png Rapid Alerts - Pharmacy and Poisons Board 32 32 PUBLIC NOTICE ON FALSIFIED BATCH OF HERCEPTIN 440MG (TRASTUZUMAB 440MG) /download/public-notice-on-falsified-batch-of-herceptin-440mg-trastuzumab-440mg/?utm_source=rss&utm_medium=rss&utm_campaign=public-notice-on-falsified-batch-of-herceptin-440mg-trastuzumab-440mg /download/public-notice-on-falsified-batch-of-herceptin-440mg-trastuzumab-440mg/#respond Wed, 26 Jun 2024 10:53:22 +0000 /?post_type=wpdmpro&p=9675 The Pharmacy and Poisons Board (PPB) wishes to alert the public about a suspicious batch of falsified Herceptin 440mg (Trastuzumab 440mg) product that has been detected in the market. The product batch is CLAIMED to be manufactured in Germany by: Roche Products Ltd, bearing the Batch number C5830083, Mfg. Date: 12/2021, Exp. Date: 11/2024. The […]

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The Pharmacy and Poisons Board (PPB) wishes to alert the public about a suspicious batch of falsified Herceptin 440mg (Trastuzumab 440mg) product that has been detected in the market. The product batch is CLAIMED to be manufactured in Germany by: Roche Products Ltd, bearing the Batch number C5830083, Mfg. Date: 12/2021, Exp. Date: 11/2024.
The public is notified that this specific product batch number C5830083 is a confirmed counterfeit. It is not authorized to be in the market and is a falsified product in view of the falsified contents, packaging and labelling aspects which have been confirmed by the brand owner.
Consequently, the PPB cautions the public against the use, supply, sale or distribution of the product batch number C5830083 as their safety, quality and efficacy CANNOT be assured.
Further, the PPB in collaboration with government investigative agencies has instituted legal and regulatory actions against individuals suspected to be perpetrating the illegal activities in contravention of the Pharmacy and Poisons Act (Cap. 244).
The PPB has initiated a rapid response and heightened surveillance of the market to ensure that safety and public health is protected. We would like to assure the public that PPB has established robust market surveillance and control system that continuously monitor the quality and safety of medical products in the Kenyan market.

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PUBLIC ALERT ON BENYLIN PAEDIATRIC 1OOMLs COUGH SYRUP, BATCH NO. 329304 /download/public-alert-on-benylin-paediatric-1oomls-cough-syrup/?utm_source=rss&utm_medium=rss&utm_campaign=public-alert-on-benylin-paediatric-1oomls-cough-syrup /download/public-alert-on-benylin-paediatric-1oomls-cough-syrup/#respond Wed, 26 Jun 2024 10:13:58 +0000 /?post_type=wpdmpro&p=9667 The Pharmacy and Poisons Board (PPB) wishes to inform the public that it has received information regarding a medical product alert and recall of Benylin pediatric 100mls cough syrup Batch No 329304, by the National Agency for Food and Drug Administration and Control (NAFDAC) of Nigeria. This cough syrup manufactured by Johnson & Johnson (Pty), […]

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The Pharmacy and Poisons Board (PPB) wishes to inform the public that it has received information regarding a medical product alert and recall of Benylin pediatric 100mls cough syrup Batch No 329304, by the National Agency for Food and Drug Administration and Control (NAFDAC) of Nigeria. This cough syrup manufactured by Johnson & Johnson (Pty), South Africa, is being recalled due to quality concerns arising from an unacceptable high level of diethylene glycol detected through laboratory analysis conducted by NAFDAC. Diethylene glycol is a contaminant which is toxic to humans when consumed and can prove fatal. Toxic effects can include abdominal pain, vomiting, diarrhoea, inability to pass urine, headache, altered mental state, and acute kidney injury which may lead to death.

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