Does EDARAVONE Cause Product dose omission? 20 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 20 reports of Product dose omission have been filed in association with EDARAVONE (edaravone). This represents 0.5% of all adverse event reports for EDARAVONE.
20
Reports of Product dose omission with EDARAVONE
0.5%
of all EDARAVONE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission From EDARAVONE?
Of the 20 reports, 2 (10.0%) 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 EDARAVONE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does EDARAVONE Cause?
Death (707)
Disease progression (309)
Drug ineffective (292)
Amyotrophic lateral sclerosis (199)
Fatigue (174)
Asthenia (157)
Condition aggravated (147)
Muscular weakness (138)
Dyspnoea (136)
Gait disturbance (111)
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 EDARAVONE Alternatives Have Lower Product dose omission Risk?
EDARAVONE vs EDETATE
EDARAVONE vs EDOXABAN
EDARAVONE vs EDOXABAN TOSILATE
EDARAVONE vs EFALIZUMAB
EDARAVONE vs EFANESOCTOCOG ALFA