Does PAROXETINE Cause Extra dose administered? 30 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 30 reports of Extra dose administered have been filed in association with PAROXETINE (Paroxetine). This represents 0.1% of all adverse event reports for PAROXETINE.
30
Reports of Extra dose administered with PAROXETINE
0.1%
of all PAROXETINE reports
1
Deaths
20
Hospitalizations
How Dangerous Is Extra dose administered From PAROXETINE?
Of the 30 reports, 1 (3.3%) resulted in death, 20 (66.7%) required hospitalization, and 9 (30.0%) were considered life-threatening.
Is Extra dose administered Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 30 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 Extra dose administered?
TIRZEPATIDE (6,774)
DULAGLUTIDE (3,047)
LORATADINE (1,556)
DUPILUMAB (1,422)
FEXOFENADINE (1,413)
NAPROXEN (908)
POLYETHYLENE GLYCOL 3350 (589)
ACETAMINOPHEN (552)
DALFAMPRIDINE (519)
FLUTICASONE\SALMETEROL (499)
Which PAROXETINE Alternatives Have Lower Extra dose administered Risk?
PAROXETINE vs PAROXETINE\PAROXETINE
PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS
PAROXETINE vs PASIREOTIDE
PAROXETINE vs PASIREOTIDE DIASPARTATE
PAROXETINE vs PATIROMER