Does FLUOXETINE Cause Product quality issue? 70 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 70 reports of Product quality issue have been filed in association with FLUOXETINE (Fluoxetine). This represents 0.2% of all adverse event reports for FLUOXETINE.
70
Reports of Product quality issue with FLUOXETINE
0.2%
of all FLUOXETINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product quality issue From FLUOXETINE?
Of the 70 reports, 3 (4.3%) required hospitalization, and 3 (4.3%) were considered life-threatening.
Is Product quality issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOXETINE. However, 70 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 quality issue?
ETONOGESTREL (4,651)
ALBUTEROL (4,466)
TIOTROPIUM (3,821)
MOMETASONE FUROATE (3,406)
LIDOCAINE (3,126)
FLUTICASONE\SALMETEROL (2,986)
FORMOTEROL\MOMETASONE FUROATE (2,458)
FENTANYL (2,450)
NICOTINE (1,987)
EXENATIDE (1,839)
Which FLUOXETINE Alternatives Have Lower Product quality issue Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE