Latest Baxter International Inc. Stories
Twice-Weekly Prophylactic Regimen Resulted in 95% Reduction in Median Annualized Bleed Rate Compared to On-Demand Treatment SAN FRANCISCO, Dec.
On November 21, the US FDA announced that one lot of Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter International Inc., is recalled due to mislabeled overpouch.
MISSISSAUGA, ON, Nov.
DALLAS, October 30, 2014 /PRNewswire/ -- ReportsnReports.com adds The Global Pre-Filled Syringe Market to 2024 and Market Research Report on Global and Chinese Digital
On September 17, the FDA announced that Baxter International Inc. recalls one lot of Potassium Chloride Injection 10mEq per 100mL due to a labeling error on the shipping cartons.
Top executives to be honored at Chicago United's annual Bridge Awards Gala CHICAGO, Sept. 15, 2014 /PRNewswire/ -- On November 18, Chicago United will honor Robert L.
On August 15, the FDA announced that two lots of Dianeal Low Calcium (2.5mEq/L) Peritoneal Dialysis Solution with 2.5% Dextrose 5000mL (Ambu-Flex II), by Baxter International Inc., are recalled
Twice-Weekly Prophylactic Regimen Resulted in 95% Reduction in Median Annualized Bleed Rate Compared to On-Demand DEERFIELD, Ill., Aug.
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