Does DEXTROAMPHETAMINE Cause Suspected product quality issue? 14 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 14 reports of Suspected product quality issue have been filed in association with DEXTROAMPHETAMINE (Zenzedi). This represents 0.7% of all adverse event reports for DEXTROAMPHETAMINE.
14
Reports of Suspected product quality issue with DEXTROAMPHETAMINE
0.7%
of all DEXTROAMPHETAMINE reports
0
Deaths
0
Hospitalizations
How Dangerous Is Suspected product quality issue From DEXTROAMPHETAMINE?
Of the 14 reports.
Is Suspected product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for DEXTROAMPHETAMINE. However, 14 reports have been filed with the FAERS database.
What Other Side Effects Does DEXTROAMPHETAMINE Cause?
Drug ineffective (513)
Fatigue (170)
Anxiety (169)
Product substitution issue (163)
Headache (145)
Nausea (130)
Off label use (121)
Somnolence (110)
Feeling abnormal (108)
Product availability issue (106)
What Other Drugs Cause Suspected product quality issue?
AMPHETAMINE ASPARTATE\AMPHETAMINE\DEXTROAMPHETAMINE SACCHARATE\DEXTROAMPHETAMINE (64)
LEVOTHYROXINE (37)
HUMAN IMMUNOGLOBULIN G (32)
ESTRADIOL (30)
ONABOTULINUMTOXINA (30)
SODIUM (30)
CLONAZEPAM (29)
AFLIBERCEPT (27)
INSULIN GLARGINE (27)
IOPROMIDE (25)
Which DEXTROAMPHETAMINE Alternatives Have Lower Suspected product quality issue Risk?
DEXTROAMPHETAMINE vs DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE AND AMPHETAMINE
DEXTROAMPHETAMINE vs DEXTROMETHORPHAN
DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE
DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN
DEXTROAMPHETAMINE vs DEXTROMETHORPHAN HYDROBROMIDE\GUAIFENESIN\PHENYLEPHRINE