Does AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE Cause Wrong technique in product usage process? 210 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 210 reports of Wrong technique in product usage process have been filed in association with AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE. This represents 1.3% of all adverse event reports for AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE.
How Dangerous Is Wrong technique in product usage process From AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE?
Of the 210 reports, 2 (1.0%) resulted in death, 11 (5.2%) required hospitalization.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE. However, 210 reports have been filed with the FAERS database.