Does ATOMOXETINE Cause Intentional product use issue? 489 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 489 reports of Intentional product use issue have been filed in association with ATOMOXETINE (Atomoxetine). This represents 5.3% of all adverse event reports for ATOMOXETINE.
489
Reports of Intentional product use issue with ATOMOXETINE
5.3%
of all ATOMOXETINE reports
480
Deaths
419
Hospitalizations
How Dangerous Is Intentional product use issue From ATOMOXETINE?
Of the 489 reports, 480 (98.2%) resulted in death, 419 (85.7%) required hospitalization, and 425 (86.9%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 489 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 Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which ATOMOXETINE Alternatives Have Lower Intentional product use issue Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE