Does FLUOXETINE Cause Wrong product administered? 19 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 19 reports of Wrong product administered have been filed in association with FLUOXETINE (Fluoxetine). This represents 0.1% of all adverse event reports for FLUOXETINE.
19
Reports of Wrong product administered with FLUOXETINE
0.1%
of all FLUOXETINE reports
0
Deaths
11
Hospitalizations
How Dangerous Is Wrong product administered From FLUOXETINE?
Of the 19 reports, 11 (57.9%) required hospitalization, and 3 (15.8%) were considered life-threatening.
Is Wrong product administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOXETINE. However, 19 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 Wrong product administered?
INSULIN LISPRO (337)
INSULIN GLARGINE (226)
RISPERIDONE (141)
QUETIAPINE (137)
ACETAMINOPHEN (133)
INSULIN ASPART (112)
CLOZAPINE (106)
INSULIN HUMAN (104)
TUBERCULIN PURIFIED PROTEIN DERIVATIVE (104)
IBUPROFEN (102)
Which FLUOXETINE Alternatives Have Lower Wrong product administered Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE