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Review Blood Safety Reports submitted to FDA

Total Blood reports: 3.
Blood FDA safety alerts: 2001 2002 2003 2004 2005 2006 2007 2008 .
Reported deaths: 1    .
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FDA Reported Blood Side Effects: unevaluable event, multi-organ failure, jugular vein thrombosis, visual acuity reduced, retinal detachment, maculopathy, renal failure acute, pulmonary oedema, pneumonia, lung hyperinflation, visual field defect.
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Blood Side Effects Report #5486738-6
Consumer or non-health professional from UNITED STATES reported BLOOD problem on Oct 12, 2007. Male patient, weighting 8.38 lb, was treated with BLOOD. After drug was administered, patient experienced the following problems/side effects: septic shock, transfusion reaction. BLOOD dosage: unknown. Patient died on 09/30/2007.

Blood Side Effects Report #5393382-8
BLOOD problem was reported by a Health Professional from UNITED STATES on July 10, 2007. Female patient, 65 years of age, was treated with BLOOD. After drug was administered, patient experienced the following problems/side effects: maculopathy, retinal detachment, visual acuity reduced. BLOOD dosage: unknown. During the same period patient was treated with DEFEROXAMINE MESYLATE. Patient recovered.

Blood Side Effects Report #5393382-8
Health Professional from UNITED STATES reported BLOOD problem on July 10, 2007. Female patient, 65 years of age, was treated with BLOOD. After drug was administered, patient experienced the following problems/side effects: maculopathy, retinal detachment, visual acuity reduced. BLOOD dosage: unknown. During the same period patient was treated with DEFEROXAMINE MESYLATE. Patient recovered.


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septic shock, transfusion reaction, maculopathy, retinal detachment, visual acuity reduced, maculopathy, retinal detachment, visual acuity reduced, ,