Does ARMODAFINIL Cause Product use issue? 90 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 90 reports of Product use issue have been filed in association with ARMODAFINIL (Armodafinil). This represents 3.6% of all adverse event reports for ARMODAFINIL.
90
Reports of Product use issue with ARMODAFINIL
3.6%
of all ARMODAFINIL reports
1
Deaths
6
Hospitalizations
How Dangerous Is Product use issue From ARMODAFINIL?
Of the 90 reports, 1 (1.1%) resulted in death, 6 (6.7%) required hospitalization, and 1 (1.1%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARMODAFINIL. However, 90 reports have been filed with the FAERS database.
What Other Side Effects Does ARMODAFINIL Cause?
Drug ineffective (451)
Somnolence (262)
Headache (253)
Fatigue (248)
Anxiety (194)
Nausea (188)
Feeling abnormal (180)
Insomnia (154)
Dizziness (125)
Product substitution issue (120)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ARMODAFINIL Alternatives Have Lower Product use issue Risk?
ARMODAFINIL vs AROMASIN
ARMODAFINIL vs ARSENIC TRIOXIDE
ARMODAFINIL vs ARTEMETHER\LUMEFANTRINE
ARMODAFINIL vs ARTESUNATE
ARMODAFINIL vs ARTICAINE\EPINEPHRINE