Zantac (ranitidine): Safety Information - NDMA Found in Samples of Some Ranitidine Medicines
FDA has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain NDMA.
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FDA has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain NDMA.
FDA is warning that Ibrance (palbociclib), Kisqali (ribociclib), and Verzenio (abemaciclib) used to treat some patients with advanced breast cancers may cause rare but severe inflammation of the lungs.
FDA is warning that Ibrance (palbociclib), Kisqali (ribociclib), and Verzenio (abemaciclib) used to treat some patients with advanced breast cancers may cause rare but severe inflammation of the lungs.
Fri, 13 Sep 2019 00:00:00 -0400
FDA has learned that some ranitidine medicines, including some products commonly known as the brand-name drug Zantac, contain NDMA.
Allergan Recalls Natrelle Biocell Textured Breast Implants Due to Risk of BIA-ALCL Cancer
Darmerica LLC is voluntarily recalling two lots, DR4654A and DL4654A, of Quinacrine Dihydrochloride, bulk API powder packaged in Amber HDPE Bottles to the consumer level. This product is being recalled due to a label mix-up. Product intended for further compounding use by pharmacies labeled as Quin
KRS Global Biotechnology, Inc. is voluntarily recalling all lots of unexpired human and animal drugs intended to be sterile to the consumer level. The products are being recalled due to lack of assurance of sterility.
Patients with diabetes using these models should switch their insulin pump to models that are better equipped to protect against these potential risks.
Consumers are likely aware of the recent reports of respiratory illnesses – including some resulting in deaths – following the use of vaping products.The FDA is working closely with the CDC, as well as state and local public health partners to investigate them as quickly as possible.
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