Does ATOMOXETINE Cause Product dose omission in error? 5 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 5 reports of Product dose omission in error have been filed in association with ATOMOXETINE (Atomoxetine). This represents 0.1% of all adverse event reports for ATOMOXETINE.
5
Reports of Product dose omission in error with ATOMOXETINE
0.1%
of all ATOMOXETINE reports
0
Deaths
2
Hospitalizations
How Dangerous Is Product dose omission in error From ATOMOXETINE?
Of the 5 reports, 2 (40.0%) 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 ATOMOXETINE. However, 5 reports have been filed with the FAERS database.
What Other Side Effects Does ATOMOXETINE Cause?
Drug ineffective (1,352)
Off label use (1,132)
Nausea (889)
Vomiting (820)
Fatigue (786)
Abdominal pain upper (755)
Headache (741)
Dizziness (720)
Pain (705)
Insomnia (695)
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 ATOMOXETINE Alternatives Have Lower Product dose omission in error Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE