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Heparin In Baxter Multiple Dose Vials In FDA Alert
Allergy The US Food and Drug Administration (FDA) has advised doctors and patients to stop using Baxter's Multiple-dose vial heparin and switch to another supplier until they have found out why the product appears to be causing severe allergic reactions and low blood pressure in hundreds of patients who have been given high "bolus" doses of the blood thinning drug. Deaths have also occurred, said the agency.
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