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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 Haemoglobin increased? 332 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 332 reports of Haemoglobin increased have been filed in association with RUXOLITINIB (OPZELURA). This represents 0.5% of all adverse event reports for RUXOLITINIB.

332
Reports of Haemoglobin increased with RUXOLITINIB
0.5%
of all RUXOLITINIB reports
12
Deaths
58
Hospitalizations

How Dangerous Is Haemoglobin increased From RUXOLITINIB?

Of the 332 reports, 12 (3.6%) resulted in death, 58 (17.5%) required hospitalization, and 12 (3.6%) were considered life-threatening.

Is Haemoglobin increased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for RUXOLITINIB. However, 332 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 Haemoglobin increased?

TREPROSTINIL (245) SOTATERCEPT (151) CLOZAPINE (142) SOTATERCEPT-CSRK (100) DARBEPOETIN ALFA (99) TESTOSTERONE (96) METFORMIN (93) VOXELOTOR (86) ROSUVASTATIN (85) ADALIMUMAB (81)

Which RUXOLITINIB Alternatives Have Lower Haemoglobin increased 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 Haemoglobin increased Reports All Drugs Causing Haemoglobin increased RUXOLITINIB Demographics