Does ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM Cause Full blood count abnormal? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Full blood count abnormal have been filed in association with ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM. This represents 0.7% of all adverse event reports for ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM.
How Dangerous Is Full blood count abnormal From ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM?
Of the 13 reports, 13 (100.0%) resulted in death, 12 (92.3%) required hospitalization, and 12 (92.3%) were considered life-threatening.
Is Full blood count abnormal Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ASCORBIC ACID\POLYETHYLENE GLYCOL 3350\POTASSIUM\SODIUM ASCORBATE\SODIUM\SODIUM. However, 13 reports have been filed with the FAERS database.