Does FLUOXETINE Cause Product prescribing error? 118 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 118 reports of Product prescribing error have been filed in association with FLUOXETINE (Fluoxetine). This represents 0.4% of all adverse event reports for FLUOXETINE.
118
Reports of Product prescribing error with FLUOXETINE
0.4%
of all FLUOXETINE reports
4
Deaths
100
Hospitalizations
How Dangerous Is Product prescribing error From FLUOXETINE?
Of the 118 reports, 4 (3.4%) resulted in death, 100 (84.7%) required hospitalization, and 3 (2.5%) were considered life-threatening.
Is Product prescribing error Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOXETINE. However, 118 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 Product prescribing error?
SOMATROPIN (1,123)
SACUBITRIL\VALSARTAN (1,023)
SECUKINUMAB (821)
TOFACITINIB (805)
DUPILUMAB (725)
NIRMATRELVIR\RITONAVIR (611)
PREGABALIN (476)
METHOTREXATE (434)
TORSEMIDE (352)
METOPROLOL (325)
Which FLUOXETINE Alternatives Have Lower Product prescribing error Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE