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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 REVUMENIB Cause Haemoglobin decreased? 16 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Haemoglobin decreased have been filed in association with REVUMENIB (Revuforj). This represents 4.3% of all adverse event reports for REVUMENIB.

16
Reports of Haemoglobin decreased with REVUMENIB
4.3%
of all REVUMENIB reports
2
Deaths
8
Hospitalizations

How Dangerous Is Haemoglobin decreased From REVUMENIB?

Of the 16 reports, 2 (12.5%) resulted in death, 8 (50.0%) required hospitalization.

Is Haemoglobin decreased Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for REVUMENIB. However, 16 reports have been filed with the FAERS database.

What Other Side Effects Does REVUMENIB Cause?

Off label use (57) Platelet count decreased (50) Nausea (49) Product dose omission issue (40) Death (38) Vomiting (26) Fatigue (24) Pyrexia (22) Differentiation syndrome (16) White blood cell count decreased (16)

What Other Drugs Cause Haemoglobin decreased?

LENALIDOMIDE (4,031) RUXOLITINIB (3,297) ECULIZUMAB (3,028) ADALIMUMAB (2,459) CLOZAPINE (2,396) RITUXIMAB (1,803) APIXABAN (1,779) NIRAPARIB (1,759) METHOTREXATE (1,754) RIBAVIRIN (1,753)

Which REVUMENIB Alternatives Have Lower Haemoglobin decreased Risk?

REVUMENIB vs REYATAZ REVUMENIB vs REZAFUNGIN REVUMENIB vs RIBASPHERE REVUMENIB vs RIBAVIRIN REVUMENIB vs RIBOCICLIB

Related Pages

REVUMENIB Full Profile All Haemoglobin decreased Reports All Drugs Causing Haemoglobin decreased REVUMENIB Demographics