Does VILOXAZINE Cause Product dose omission in error? 8 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product dose omission in error have been filed in association with VILOXAZINE (QELBREE). This represents 0.9% of all adverse event reports for VILOXAZINE.
8
Reports of Product dose omission in error with VILOXAZINE
0.9%
of all VILOXAZINE reports
0
Deaths
1
Hospitalizations
How Dangerous Is Product dose omission in error From VILOXAZINE?
Of the 8 reports, 1 (12.5%) required hospitalization.
Is Product dose omission in error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for VILOXAZINE. However, 8 reports have been filed with the FAERS database.
What Other Side Effects Does VILOXAZINE Cause?
Headache (108)
Vomiting (95)
Nausea (92)
Migraine (82)
Fatigue (81)
Insomnia (75)
Somnolence (70)
Suicidal ideation (64)
Withdrawal syndrome (46)
Anxiety (44)
What Other Drugs Cause Product dose omission in error?
DUPILUMAB (7,586)
TOFACITINIB (2,461)
LENALIDOMIDE (618)
PALBOCICLIB (592)
DIROXIMEL (481)
ABALOPARATIDE (457)
NIRAPARIB (428)
RUXOLITINIB (425)
TERIFLUNOMIDE (371)
DIMETHYL (308)
Which VILOXAZINE Alternatives Have Lower Product dose omission in error Risk?
VILOXAZINE vs VIMPAT
VILOXAZINE vs VIMSELTINIB
VILOXAZINE vs VINBLASTINE
VILOXAZINE vs VINCRISTINE
VILOXAZINE vs VINDESINE