Does MODAFINIL Cause Product administration interrupted? 52 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 52 reports of Product administration interrupted have been filed in association with MODAFINIL (Modafinil). This represents 1.5% of all adverse event reports for MODAFINIL.
52
Reports of Product administration interrupted with MODAFINIL
1.5%
of all MODAFINIL reports
0
Deaths
13
Hospitalizations
How Dangerous Is Product administration interrupted From MODAFINIL?
Of the 52 reports, 13 (25.0%) required hospitalization.
Is Product administration interrupted Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for MODAFINIL. However, 52 reports have been filed with the FAERS database.
What Other Side Effects Does MODAFINIL Cause?
Drug ineffective (636)
Fatigue (330)
Somnolence (273)
Headache (252)
Anxiety (213)
Nausea (209)
Off label use (200)
Product substitution issue (158)
Insomnia (150)
Feeling abnormal (146)
What Other Drugs Cause Product administration interrupted?
CALCIUM OXYBATE\MAGNESIUM OXYBATE\POTASSIUM OXYBATE\SODIUM OXYBATE (1,446)
SODIUM OXYBATE (1,272)
CANNABIDIOL (511)
ISOTRETINOIN (503)
APREMILAST (314)
TREPROSTINIL (295)
EPOPROSTENOL (205)
LENALIDOMIDE (146)
ETANERCEPT (142)
INTERFERON BETA-1A (115)
Which MODAFINIL Alternatives Have Lower Product administration interrupted Risk?
MODAFINIL vs MOGAMULIZUMAB
MODAFINIL vs MOGAMULIZUMAB-KPKC
MODAFINIL vs MOLNUPIRAVIR
MODAFINIL vs MOLSIDOMINE
MODAFINIL vs MOMELOTINIB