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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 ENASIDENIB Cause Haemoglobin abnormal? 23 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 23 reports of Haemoglobin abnormal have been filed in association with ENASIDENIB (Idhifa). This represents 0.6% of all adverse event reports for ENASIDENIB.

23
Reports of Haemoglobin abnormal with ENASIDENIB
0.6%
of all ENASIDENIB reports
2
Deaths
1
Hospitalizations

How Dangerous Is Haemoglobin abnormal From ENASIDENIB?

Of the 23 reports, 2 (8.7%) resulted in death, 1 (4.3%) required hospitalization.

Is Haemoglobin abnormal Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ENASIDENIB. However, 23 reports have been filed with the FAERS database.

What Other Side Effects Does ENASIDENIB Cause?

Death (650) Off label use (213) Fatigue (202) Nausea (197) Acute myeloid leukaemia (163) Hospitalisation (149) Diarrhoea (144) Decreased appetite (122) Platelet count decreased (113) Drug ineffective (108)

What Other Drugs Cause Haemoglobin abnormal?

RUXOLITINIB (500) ECULIZUMAB (466) VENETOCLAX (248) DARBEPOETIN ALFA (213) ADALIMUMAB (207) LENALIDOMIDE (172) RITUXIMAB (157) ERYTHROPOIETIN (154) IBRUTINIB (148) DEXAMETHASONE (147)

Which ENASIDENIB Alternatives Have Lower Haemoglobin abnormal Risk?

ENASIDENIB vs ENBREL ENASIDENIB vs ENCORAFENIB ENASIDENIB vs ENDOXAN ENASIDENIB vs ENDOXAN BAXTER ENASIDENIB vs ENDOXAN INJ

Related Pages

ENASIDENIB Full Profile All Haemoglobin abnormal Reports All Drugs Causing Haemoglobin abnormal ENASIDENIB Demographics