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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 Electrocardiogram qt prolonged? 260 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 260 reports of Electrocardiogram qt prolonged have been filed in association with PAROXETINE (Paroxetine). This represents 1.2% of all adverse event reports for PAROXETINE.

260
Reports of Electrocardiogram qt prolonged with PAROXETINE
1.2%
of all PAROXETINE reports
5
Deaths
126
Hospitalizations

How Dangerous Is Electrocardiogram qt prolonged From PAROXETINE?

Of the 260 reports, 5 (1.9%) resulted in death, 126 (48.5%) required hospitalization, and 74 (28.5%) were considered life-threatening.

Is Electrocardiogram qt prolonged Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 260 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 Electrocardiogram qt prolonged?

QUETIAPINE (1,869) OLANZAPINE (1,325) RIBOCICLIB (1,020) AMIODARONE (1,000) HYDROXYCHLOROQUINE (992) CLOZAPINE (958) CITALOPRAM HYDROBROMIDE (917) ESCITALOPRAM OXALATE (899) ONDANSETRON (881) BUPROPION (853)

Which PAROXETINE Alternatives Have Lower Electrocardiogram qt prolonged 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 Electrocardiogram qt prolonged Reports All Drugs Causing Electrocardiogram qt prolonged PAROXETINE Demographics