Sedating child congenital heart disease

Each 100 mg Activase vial (58 million IU) is packaged with diluent for reconstitution (100 m L Sterile Water for Injection, USP), and one transfer device: NDC 50242-085-27.The product was distributed nationwide to hospitals.Serotonin syndrome is associated with increased serotonergic activity in the central nervous system.Most reports of serotonin syndrome have been associated with concomitant use of certain drugs, some commonly used during surgery, such as fenta NYL.Customers that have any of the affected medications that are being recalled should immediately quarantine the product, discontinue use and destroy per their hospital protocol.Customers with any of the affected medications can also reference Phar MEDium Services website for more information on the specific lot numbers affected and contact information:

Distributors are instructed to immediately notify their customers that have been shipped, or may have been shipped the product involved in this recall.Sub-Potency of Oxytocin by Phar MEDium - Recall Notice(posted 9/1/2017)Phar MEDium Services, LLC (Phar MEDium) is voluntarily recalling all unexpired lots of Oxytocin compounded with Lactated Ringers and all unexpired lots of Oxytocin compounded with Lactated Ringers and Dextrose products that were produced between July 6, 2017 and August 29, 2017 to the hospital/user level.The recall is being issued based on laboratory test results indicating a lower than expected potency on certain lots of Oxytocin compounded with Lactated Ringers and Oxytocin Compounded with Lactated Ringers and Dextrose which would lead to a lower dose being administered.See press release (https://gov/Safety/Recalls/ucm574980.htm) for affected lots.The use of impacted Sterile Water for Injection could result in adverse events such as fever, chills, phlebitis, and granuloma or more severe adverse events such as sepsis or invasive systemic infections.

Sedating child congenital heart disease