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: Cleveland Personal Injury LawyerBaxter Heparin Recall Demonstrates Limitations On FDA's Ability To Adequately Protect Patient Safety
By Rhonda Baker Debevec
On February 28, 2008, the U.S. Food and Drug Administration issued its most recent Public Health Advisory concerning a popular blood thinner, Heparin, manufactured by Baxter Healthcare Corporation. An unusually high number of severe allergic reactions have been associated with this product when it is administered in high doses over short periods of time - commonly referred to as a bolus. The FDA continues to investigate but has not yet determined the cause. In the meantime, Baxter has temporarily suspended manufacturing its multiple-dose vials of heparin sodium.
Full post as published by Cleveland Personal Injury Lawyer on March 05, 2008 (boomark / email).
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