Does FLUOXETINE Cause Incorrect product administration duration? 7 Reports in FDA Database
Sharpen Your Memory & Focus Naturally
NeuroZoom — 35 clinically studied ingredients. No stimulants. Pure brain support.
According to the FDA Adverse Event Reporting System (FAERS), 7 reports of Incorrect product administration duration have been filed in association with FLUOXETINE (Fluoxetine). This represents 0.0% of all adverse event reports for FLUOXETINE.
7
Reports of Incorrect product administration duration with FLUOXETINE
0.0%
of all FLUOXETINE reports
0
Deaths
6
Hospitalizations
How Dangerous Is Incorrect product administration duration From FLUOXETINE?
Of the 7 reports, 6 (85.7%) required hospitalization.
Is Incorrect product administration duration Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOXETINE. However, 7 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 Incorrect product administration duration?
ETONOGESTREL (3,974)
POLYETHYLENE GLYCOL 3350 (2,129)
NIRMATRELVIR\RITONAVIR (744)
DOCOSANOL (634)
LANSOPRAZOLE (564)
LOPERAMIDE (543)
NAPROXEN (499)
INSULIN LISPRO (479)
DICLOFENAC (362)
OMEPRAZOLE (302)
Which FLUOXETINE Alternatives Have Lower Incorrect product administration duration Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE