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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 Adverse event? 42 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 42 reports of Adverse event have been filed in association with ENASIDENIB (Idhifa). This represents 1.1% of all adverse event reports for ENASIDENIB.

42
Reports of Adverse event with ENASIDENIB
1.1%
of all ENASIDENIB reports
1
Deaths
14
Hospitalizations

How Dangerous Is Adverse event From ENASIDENIB?

Of the 42 reports, 1 (2.4%) resulted in death, 14 (33.3%) required hospitalization, and 2 (4.8%) were considered life-threatening.

Is Adverse event Listed in the Official Label?

Yes, Adverse event is listed as a known adverse reaction in the official FDA drug label for ENASIDENIB.

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 Adverse event?

ABATACEPT (4,028) APIXABAN (3,871) ETANERCEPT (3,096) LENALIDOMIDE (2,426) INFLIXIMAB (2,269) ADALIMUMAB (2,121) METHOTREXATE (1,846) LEFLUNOMIDE (1,476) RIVAROXABAN (1,465) ALENDRONATE (1,462)

Which ENASIDENIB Alternatives Have Lower Adverse event Risk?

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

Related Pages

ENASIDENIB Full Profile All Adverse event Reports All Drugs Causing Adverse event ENASIDENIB Demographics