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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 Extra dose administered? 72 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 72 reports of Extra dose administered have been filed in association with RUXOLITINIB (OPZELURA). This represents 0.1% of all adverse event reports for RUXOLITINIB.

72
Reports of Extra dose administered with RUXOLITINIB
0.1%
of all RUXOLITINIB reports
6
Deaths
7
Hospitalizations

How Dangerous Is Extra dose administered From RUXOLITINIB?

Of the 72 reports, 6 (8.3%) resulted in death, 7 (9.7%) required hospitalization, and 1 (1.4%) were considered life-threatening.

Is Extra dose administered Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUXOLITINIB. However, 72 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 Extra dose administered?

TIRZEPATIDE (6,774) DULAGLUTIDE (3,047) LORATADINE (1,556) DUPILUMAB (1,422) FEXOFENADINE (1,413) NAPROXEN (908) POLYETHYLENE GLYCOL 3350 (589) ACETAMINOPHEN (552) DALFAMPRIDINE (519) FLUTICASONE\SALMETEROL (499)

Which RUXOLITINIB Alternatives Have Lower Extra dose administered 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 Extra dose administered Reports All Drugs Causing Extra dose administered RUXOLITINIB Demographics