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Inrebic Side Effects

Generic name: fedratinib

Medically reviewed by Last updated on May 3, 2023.

Note: This document contains side effect information about fedratinib. Some dosage forms listed on this page may not apply to the brand name Inrebic.

Applies to fedratinib: oral capsule.


Oral route (Capsule)

Warning: Encephalopathy including Wernicke'sSerious and fatal encephalopathy, including Wernicke’s, has occurred in patients treated with fedratinib. Wernicke’s encephalopathy is a neurologic emergency. Assess thiamine levels in all patients prior to starting fedratinib, periodically during treatment, and as clinically indicated. Do not start fedratinib in patients with thiamine deficiency; replete thiamine prior to treatment initiation. If encephalopathy is suspected, immediately discontinue fedratinib and initiate parenteral thiamine. Monitor until symptoms resolve or improve and thiamine levels normalize.

Serious side effects of Inrebic

Along with its needed effects, fedratinib (the active ingredient contained in Inrebic) may cause some unwanted effects. Although not all of these side effects may occur, if they do occur they may need medical attention.

Check with your doctor immediately if any of the following side effects occur while taking fedratinib:

More common

Less common

Incidence not known

Other side effects of Inrebic

Some side effects of fedratinib may occur that usually do not need medical attention. These side effects may go away during treatment as your body adjusts to the medicine. Also, your health care professional may be able to tell you about ways to prevent or reduce some of these side effects.

Check with your health care professional if any of the following side effects continue or are bothersome or if you have any questions about them:

More common

For Healthcare Professionals

Applies to fedratinib: oral capsule.


The most commonly reported side effects included anemia, diarrhea, nausea, and increased blood creatinine.[Ref]


Common (1% to 10%): Cardiac failure, cardiogenic shock, hypertension, myocardial ischemia

Frequency not reported: Major adverse cardiac events (MACE), thrombosis[Ref]


Very common (10% or more): Diarrhea (up to 67.5%), nausea (up to 62%), vomiting (up to 44.8%), increased lipase (up to 35%), increased amylase (up to 24%)

Common (1% to 10%): Constipation, dyspepsia

Frequency not reported: Gastrointestinal toxicity[Ref]


Common (1% to 10%): Dysuria, urinary tract infection[Ref]


Very common (10% or more): Anemia (up to 99%), thrombocytopenia (up to 68.5%), neutropenia (up to 23%)

Common (1% to 10%): Bleeding[Ref]


Very common (10% or more): Elevated ALT (up to 43%), elevated AST (up to 40%)

Frequency not reported: Liver toxicity[Ref]


Very common (10% or more): Hyponatremia (up to 26%)

Common (1% to 10%): Weight gain[Ref]


Very common (10% or more): Muscle spasms (up to 12%), extremity pain (up to 10%)

Common (1% to 10%): Bone pain[Ref]

Nervous system

Common (1% to 10%): Dizziness, headache, Wernicke's encephalopathy

Frequency not reported: Encephalopathy[Ref]


Very common (10% or more): Asthenia/fatigue (up to 19%)[Ref]


Very common (10% or more): Blood creatinine increased (up to 59%)

Frequency not reported: Cystitis[Ref]


Frequency not reported: Secondary malignancies[Ref]

Frequently asked questions


1. Product Information. Inrebic (fedratinib). Bristol-Myers Squibb. 2022.

2. Product Information. Inrebic (fedratinib). Bristol-Myers Squibb Pharmaceuticals Ltd. 2021.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Some side effects may not be reported. You may report them to the FDA.