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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 Drug hypersensitivity? 185 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 185 reports of Drug hypersensitivity have been filed in association with RUXOLITINIB (OPZELURA). This represents 0.3% of all adverse event reports for RUXOLITINIB.

185
Reports of Drug hypersensitivity with RUXOLITINIB
0.3%
of all RUXOLITINIB reports
7
Deaths
49
Hospitalizations

How Dangerous Is Drug hypersensitivity From RUXOLITINIB?

Of the 185 reports, 7 (3.8%) resulted in death, 49 (26.5%) required hospitalization, and 4 (2.2%) were considered life-threatening.

Is Drug hypersensitivity Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUXOLITINIB. However, 185 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 Drug hypersensitivity?

METHOTREXATE (16,677) ETANERCEPT (12,991) ADALIMUMAB (11,599) MORPHINE (11,095) RITUXIMAB (8,924) LEFLUNOMIDE (8,148) INFLIXIMAB (8,119) TOCILIZUMAB (7,883) ABATACEPT (7,808) CODEINE (7,479)

Which RUXOLITINIB Alternatives Have Lower Drug hypersensitivity 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 Drug hypersensitivity Reports All Drugs Causing Drug hypersensitivity RUXOLITINIB Demographics