Does ATOMOXETINE Cause Intentional product misuse? 139 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 139 reports of Intentional product misuse have been filed in association with ATOMOXETINE (Atomoxetine). This represents 1.5% of all adverse event reports for ATOMOXETINE.
139
Reports of Intentional product misuse with ATOMOXETINE
1.5%
of all ATOMOXETINE reports
14
Deaths
21
Hospitalizations
How Dangerous Is Intentional product misuse From ATOMOXETINE?
Of the 139 reports, 14 (10.1%) resulted in death, 21 (15.1%) required hospitalization, and 13 (9.4%) were considered life-threatening.
Is Intentional product misuse Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for ATOMOXETINE. However, 139 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 misuse?
ETANERCEPT (3,992)
PREGABALIN (3,731)
BUDESONIDE\FORMOTEROL (3,399)
ACETAMINOPHEN (2,924)
ESOMEPRAZOLE (2,852)
MINOXIDIL (2,418)
TOFACITINIB (2,331)
CINACALCET (2,092)
QUETIAPINE (1,855)
ALPRAZOLAM (1,709)
Which ATOMOXETINE Alternatives Have Lower Intentional product misuse Risk?
ATOMOXETINE vs ATOMOXETINE\ATOMOXETINE
ATOMOXETINE vs ATORVASTATIN
ATOMOXETINE vs ATORVASTATIN\EZETIMIBE
ATOMOXETINE vs ATOSIBAN
ATOMOXETINE vs ATOVAQUONE