Does PAROXETINE Cause Condition aggravated? 599 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), 599 reports of Condition aggravated have been filed in association with PAROXETINE (Paroxetine). This represents 2.8% of all adverse event reports for PAROXETINE.
599
Reports of Condition aggravated with PAROXETINE
2.8%
of all PAROXETINE reports
50
Deaths
275
Hospitalizations
How Dangerous Is Condition aggravated From PAROXETINE?
Of the 599 reports, 50 (8.3%) resulted in death, 275 (45.9%) required hospitalization, and 31 (5.2%) were considered life-threatening.
Is Condition aggravated Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 599 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 Condition aggravated?
TOFACITINIB (16,925)
INFLIXIMAB (16,616)
DUPILUMAB (16,459)
ETANERCEPT (15,897)
METHOTREXATE (14,938)
ADALIMUMAB (13,527)
PREDNISONE (10,751)
INFLIXIMAB-DYYB (10,275)
HYDROXYCHLOROQUINE (8,848)
RITUXIMAB (8,627)
Which PAROXETINE Alternatives Have Lower Condition aggravated Risk?
PAROXETINE vs PAROXETINE\PAROXETINE
PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS
PAROXETINE vs PASIREOTIDE
PAROXETINE vs PASIREOTIDE DIASPARTATE
PAROXETINE vs PATIROMER