Does ATOMOXETINE Cause Product use issue? 349 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 349 reports of Product use issue have been filed in association with ATOMOXETINE (Atomoxetine). This represents 3.8% of all adverse event reports for ATOMOXETINE.
349
Reports of Product use issue with ATOMOXETINE
3.8%
of all ATOMOXETINE reports
321
Deaths
300
Hospitalizations
How Dangerous Is Product use issue From ATOMOXETINE?
Of the 349 reports, 321 (92.0%) resulted in death, 300 (86.0%) required hospitalization, and 296 (84.8%) were considered life-threatening.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 349 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 use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)
Which ATOMOXETINE Alternatives Have Lower Product use issue Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE