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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 RUXOLITINIB Cause Hypercholesterolaemia? 24 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 24 reports of Hypercholesterolaemia have been filed in association with RUXOLITINIB (OPZELURA). This represents 0.0% of all adverse event reports for RUXOLITINIB.

24
Reports of Hypercholesterolaemia with RUXOLITINIB
0.0%
of all RUXOLITINIB reports
3
Deaths
11
Hospitalizations

How Dangerous Is Hypercholesterolaemia From RUXOLITINIB?

Of the 24 reports, 3 (12.5%) resulted in death, 11 (45.8%) required hospitalization, and 2 (8.3%) were considered life-threatening.

Is Hypercholesterolaemia Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUXOLITINIB. However, 24 reports have been filed with the FAERS database.

What Other Side Effects Does RUXOLITINIB Cause?

Off label use (12,492) Death (6,561) Fatigue (5,663) Anaemia (3,593) Haemoglobin decreased (3,297) Platelet count decreased (3,028) Diarrhoea (2,531) Asthenia (2,529) Dizziness (2,398) Pneumonia (2,343)

What Other Drugs Cause Hypercholesterolaemia?

ALENDRONATE (1,607) METHOTREXATE (1,547) TOCILIZUMAB (1,483) ADALIMUMAB (1,479) ABATACEPT (1,410) RITUXIMAB (1,389) PREDNISONE (1,377) INFLIXIMAB (1,338) DICLOFENAC (1,331) LEFLUNOMIDE (1,322)

Which RUXOLITINIB Alternatives Have Lower Hypercholesterolaemia Risk?

RUXOLITINIB vs SABRIL RUXOLITINIB vs SACCHAROMYCES CEREVISIAE RUXOLITINIB vs SACITUZUMAB GOVITECAN RUXOLITINIB vs SACITUZUMAB GOVITECAN-HZIY RUXOLITINIB vs SACROSIDASE

Related Pages

RUXOLITINIB Full Profile All Hypercholesterolaemia Reports All Drugs Causing Hypercholesterolaemia RUXOLITINIB Demographics