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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does PAROXETINE Cause Adverse event? 168 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 168 reports of Adverse event have been filed in association with PAROXETINE (Paroxetine). This represents 0.8% of all adverse event reports for PAROXETINE.

168
Reports of Adverse event with PAROXETINE
0.8%
of all PAROXETINE reports
6
Deaths
19
Hospitalizations

How Dangerous Is Adverse event From PAROXETINE?

Of the 168 reports, 6 (3.6%) resulted in death, 19 (11.3%) required hospitalization, and 7 (4.2%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 168 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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which PAROXETINE Alternatives Have Lower Adverse event Risk?

PAROXETINE vs PAROXETINE\PAROXETINE PAROXETINE vs PAROXETINE\PAROXETINE ANHYDROUS PAROXETINE vs PASIREOTIDE PAROXETINE vs PASIREOTIDE DIASPARTATE PAROXETINE vs PATIROMER

Related Pages

PAROXETINE Full Profile All Adverse event Reports All Drugs Causing Adverse event PAROXETINE Demographics