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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 Hypertriglyceridaemia? 18 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 18 reports of Hypertriglyceridaemia have been filed in association with PAROXETINE (Paroxetine). This represents 0.1% of all adverse event reports for PAROXETINE.

18
Reports of Hypertriglyceridaemia with PAROXETINE
0.1%
of all PAROXETINE reports
0
Deaths
7
Hospitalizations

How Dangerous Is Hypertriglyceridaemia From PAROXETINE?

Of the 18 reports, 7 (38.9%) required hospitalization, and 9 (50.0%) were considered life-threatening.

Is Hypertriglyceridaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for PAROXETINE. However, 18 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 Hypertriglyceridaemia?

PEGASPARGASE (399) VINCRISTINE (373) METHOTREXATE (372) DEXAMETHASONE (358) CYTARABINE (244) CYCLOPHOSPHAMIDE (191) QUETIAPINE (181) MERCAPTOPURINE (176) PREDNISONE (161) DAUNORUBICIN (143)

Which PAROXETINE Alternatives Have Lower Hypertriglyceridaemia 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 Hypertriglyceridaemia Reports All Drugs Causing Hypertriglyceridaemia PAROXETINE Demographics