Does FLUOXETINE Cause Wrong technique in product usage process? 103 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 103 reports of Wrong technique in product usage process have been filed in association with FLUOXETINE (Fluoxetine). This represents 0.3% of all adverse event reports for FLUOXETINE.
103
Reports of Wrong technique in product usage process with FLUOXETINE
0.3%
of all FLUOXETINE reports
1
Deaths
19
Hospitalizations
How Dangerous Is Wrong technique in product usage process From FLUOXETINE?
Of the 103 reports, 1 (1.0%) resulted in death, 19 (18.4%) required hospitalization, and 1 (1.0%) were considered life-threatening.
Is Wrong technique in product usage process Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for FLUOXETINE. However, 103 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 technique in product usage process?
EVOLOCUMAB (21,664)
ALBUTEROL (17,114)
ADALIMUMAB (11,766)
PEGFILGRASTIM (10,217)
ETANERCEPT (9,835)
ERENUMAB-AOOE (9,359)
SACUBITRIL\VALSARTAN (8,022)
LEUPROLIDE (5,062)
FENTANYL (2,812)
SEMAGLUTIDE (2,538)
Which FLUOXETINE Alternatives Have Lower Wrong technique in product usage process Risk?
FLUOXETINE vs FLUOXETINE\FLUOXETINE
FLUOXETINE vs FLUOXETINE\OLANZAPINE
FLUOXETINE vs FLUPENTIXOL
FLUOXETINE vs FLUPENTIXOL DECANOATE
FLUOXETINE vs FLUPHENAZINE