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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 Haemoptysis? 119 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 119 reports of Haemoptysis have been filed in association with RUXOLITINIB (OPZELURA). This represents 0.2% of all adverse event reports for RUXOLITINIB.

119
Reports of Haemoptysis with RUXOLITINIB
0.2%
of all RUXOLITINIB reports
36
Deaths
77
Hospitalizations

How Dangerous Is Haemoptysis From RUXOLITINIB?

Of the 119 reports, 36 (30.3%) resulted in death, 77 (64.7%) required hospitalization, and 6 (5.0%) were considered life-threatening.

Is Haemoptysis Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUXOLITINIB. However, 119 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 Haemoptysis?

RIVAROXABAN (1,961) ASPIRIN (1,255) APIXABAN (846) TREPROSTINIL (838) ALBUTEROL (652) CLOPIDOGREL BISULFATE (643) PREDNISONE (618) WARFARIN (555) ADALIMUMAB (472) TIOTROPIUM (462)

Which RUXOLITINIB Alternatives Have Lower Haemoptysis 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 Haemoptysis Reports All Drugs Causing Haemoptysis RUXOLITINIB Demographics