Does PAROXETINE Cause Intentional product use issue? 65 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 65 reports of Intentional product use issue have been filed in association with PAROXETINE (Paroxetine). This represents 0.3% of all adverse event reports for PAROXETINE.
65
Reports of Intentional product use issue with PAROXETINE
0.3%
of all PAROXETINE reports
17
Deaths
34
Hospitalizations
How Dangerous Is Intentional product use issue From PAROXETINE?
Of the 65 reports, 17 (26.2%) resulted in death, 34 (52.3%) required hospitalization, and 18 (27.7%) were considered life-threatening.
Is Intentional product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 65 reports have been filed with the FAERS database.
What Other Side Effects Does PAROXETINE Cause?
Foetal exposure during pregnancy (1,894)
Drug ineffective (1,457)
Toxicity to various agents (1,407)
Drug abuse (1,214)
Anxiety (1,201)
Nausea (1,063)
Suicidal ideation (999)
Drug interaction (991)
Confusional state (975)
Dizziness (937)
What Other Drugs Cause Intentional product use issue?
INFLIXIMAB (11,028)
RITUXIMAB (9,602)
INFLIXIMAB-DYYB (7,549)
TOCILIZUMAB (5,078)
METHOTREXATE (4,087)
PREDNISONE (3,961)
ABATACEPT (3,693)
ADALIMUMAB (3,557)
NIVOLUMAB (3,297)
LEFLUNOMIDE (3,280)
Which PAROXETINE Alternatives Have Lower Intentional product use issue Risk?
PAROXETINE vs PAROXETINE\PAROXETINE
PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS
PAROXETINE vs PASIREOTIDE
PAROXETINE vs PASIREOTIDE DIASPARTATE
PAROXETINE vs PATIROMER