Does DEUTETRABENAZINE 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 DEUTETRABENAZINE (Austedo). This represents 0.3% of all adverse event reports for DEUTETRABENAZINE.
20
Reports of Product dose omission with DEUTETRABENAZINE
0.3%
of all DEUTETRABENAZINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product dose omission From DEUTETRABENAZINE?
Of the 20 reports, 3 (15.0%) 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 DEUTETRABENAZINE. However, 20 reports have been filed with the FAERS database.
What Other Side Effects Does DEUTETRABENAZINE Cause?
Drug ineffective (865)
Depression (437)
Dyskinesia (370)
Death (355)
Tremor (287)
Product use issue (286)
Somnolence (271)
Insomnia (264)
Suicidal ideation (259)
Fatigue (257)
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 DEUTETRABENAZINE Alternatives Have Lower Product dose omission Risk?
DEUTETRABENAZINE vs DEUTIVACAFTOR\TEZACAFTOR\VANZACAFTOR
DEUTETRABENAZINE vs DEVICE
DEUTETRABENAZINE vs DEXAMETHASONE
DEUTETRABENAZINE vs DEXAMETHASONE\DEXAMETHASONE
DEUTETRABENAZINE vs DEXAMETHASONE\NEOMYCIN