Does FLUOXETINE Cause Intentional product misuse? 413 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 413 reports of Intentional product misuse have been filed in association with FLUOXETINE (Fluoxetine). This represents 1.3% of all adverse event reports for FLUOXETINE.
413
Reports of Intentional product misuse with FLUOXETINE
1.3%
of all FLUOXETINE reports
91
Deaths
211
Hospitalizations
How Dangerous Is Intentional product misuse From FLUOXETINE?
Of the 413 reports, 91 (22.0%) resulted in death, 211 (51.1%) required hospitalization, and 44 (10.7%) 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 FLUOXETINE. However, 413 reports have been filed with the FAERS database.
What Other Side Effects Does FLUOXETINE Cause?
Toxicity to various agents (3,172)
Drug ineffective (2,471)
Completed suicide (2,345)
Drug interaction (2,054)
Intentional overdose (2,026)
Foetal exposure during pregnancy (1,670)
Off label use (1,472)
Serotonin syndrome (1,457)
Suicide attempt (1,441)
Anxiety (1,347)
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 FLUOXETINE Alternatives Have Lower Intentional product misuse Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE