Does ARMODAFINIL Cause Product dose omission? 7 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Product dose omission have been filed in association with ARMODAFINIL (Armodafinil). This represents 0.3% of all adverse event reports for ARMODAFINIL.
7
Reports of Product dose omission with ARMODAFINIL
0.3%
of all ARMODAFINIL reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission From ARMODAFINIL?
Of the 7 reports, 1 (14.3%) required hospitalization.
Is Product dose omission Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ARMODAFINIL. However, 7 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 dose omission?
APREMILAST (4,567)
DUPILUMAB (2,729)
ALBUTEROL (1,742)
USTEKINUMAB (1,653)
INSULIN GLARGINE (1,500)
ETANERCEPT (1,400)
LENALIDOMIDE (1,400)
RUXOLITINIB (1,376)
ALIROCUMAB (1,354)
DIMETHYL (1,248)
Which ARMODAFINIL Alternatives Have Lower Product dose omission Risk?
ARMODAFINIL vs AROMASIN
ARMODAFINIL vs ARSENIC TRIOXIDE
ARMODAFINIL vs ARTEMETHER\LUMEFANTRINE
ARMODAFINIL vs ARTESUNATE
ARMODAFINIL vs ARTICAINE\EPINEPHRINE