Does PAROXETINE Cause Product complaint? 13 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 13 reports of Product complaint have been filed in association with PAROXETINE (Paroxetine). This represents 0.1% of all adverse event reports for PAROXETINE.
13
Reports of Product complaint with PAROXETINE
0.1%
of all PAROXETINE reports
0
Deaths
3
Hospitalizations
How Dangerous Is Product complaint From PAROXETINE?
Of the 13 reports, 3 (23.1%) required hospitalization, and 1 (7.7%) were considered life-threatening.
Is Product complaint Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 13 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 Product complaint?
FLUTICASONE FUROATE\UMECLIDINIUM\VILANTEROL TRIFENATATE (2,417)
ALBUTEROL (2,291)
FLUTICASONE FUROATE\VILANTEROL TRIFENATATE (1,826)
FLUTICASONE\SALMETEROL (1,601)
MEPOLIZUMAB (1,296)
FLUTICASONE (1,112)
UMECLIDINIUM\VILANTEROL TRIFENATATE (1,108)
BELIMUMAB (1,079)
SUMATRIPTAN (718)
NICOTINE (700)
Which PAROXETINE Alternatives Have Lower Product complaint Risk?
PAROXETINE vs PAROXETINE\PAROXETINE
PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS
PAROXETINE vs PASIREOTIDE
PAROXETINE vs PASIREOTIDE DIASPARTATE
PAROXETINE vs PATIROMER