US/Silver Spring:
Bristol-Myers Squibb updates its existing recall for one (1) batch/lots of Eliquis (apixaban) 5 mg Tablets due to suspected incorrect dosage packaging and consequential failure to protect against serious and life-changing cardiovascular events and/or Death, all serious health hazards. FDA: http://ht.ly/CpHA30cGw9G
Direct link: https://www.fda.gov/Safety/Recalls/ucm563547.htm
Additional information:
The US Food and Drug Administration (“FDA”) reports the following Drugs are subject to this recall:
Filed under: apixaban, Drugs, Labeling or regulatory issues, Medical / Veterinary, US FDA | Tagged: apixaban, Atrial Fibrillation, Bristol-Myers Squibb, drug, Eliquis, FDA, packaging error hazard, Recalls Direct RIN: 8824-2017, US Food and Drug Administration | Leave a comment »