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Meds & supplements  ›  Ibrutinib

Medicine · Kinase Inhibitor

Ibrutinib

IMBRUVICA is a kinase inhibitor indicated for the treatment of

Prescribing label

Selected manufacturer label information, organised into consistent sections by Sofidex. This source is written for healthcare professionals; ask your pharmacist to explain instructions that are unclear. Read the full label at DailyMed ↗

Drug facts

Used for
  • Adult patients with chronic lymphocytic leukemia (CLL)/Small lymphocytic lymphoma (SLL) with 17p deletion.
  • Adult patients with Waldenström’s macroglobulinemia (WM).
  • Adult and pediatric patients age 1 year and older with chronic graft versus host disease (cGVHD) after failure of one or more lines of systemic therapy.

What it is used for

IMBRUVICA is a kinase inhibitor indicated for the treatment of: Adult patients with chronic lymphocytic leukemia (CLL)/Small lymphocytic lymphoma (SLL). Adult patients with chronic lymphocytic leukemia (CLL)/Small lymphocytic lymphoma (SLL) with 17p deletion. Adult patients with Waldenström’s macroglobulinemia (WM). Adult and pediatric patients age 1 year and older with chronic graft versus host disease (cGVHD) after failure of one or more lines of systemic therapy.

Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma IMBRUVICA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL). 1. Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with 17p deletion IMBRUVICA is indicated for the treatment of adult patients with chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) with 17p deletion.

1. Waldenström’s Macroglobulinemia IMBRUVICA is indicated for the treatment of adult patients with Waldenström’s macroglobulinemia (WM). 1. Chronic Graft versus Host Disease IMBRUVICA is indicated for the treatment of adult and pediatric patients age 1 year and older with chronic graft-versus-host disease (cGVHD) after failure of one or more lines of systemic therapy.

Side effects, and when to stop

The following clinically significant adverse reactions are described elsewhere in the labeling:

  • Hemorrhage
  • Infections
  • Cardiac Arrhythmias, Cardiac Failure, and Sudden Death
  • Hypertension
  • Cytopenias
  • Second Primary Malignancies
  • Hepatotoxicity, including DILI
  • Tumor Lysis Syndrome

Who should not take it

None

Cite this page

NLM

sofidex [Internet]. Daloreum; c2026. Ibrutinib; [reviewed 2026 Aug 2; cited 2026 Nov 10]. Available from: https://sofidex.com/patients/medicines/ibrutinib

APA 7th

sofidex. (2026, August 2). Ibrutinib. Daloreum. Retrieved November 10, 2026, from https://sofidex.com/patients/medicines/ibrutinib

AMA 11th

Ibrutinib. sofidex. Reviewed August 2, 2026. Accessed November 10, 2026. https://sofidex.com/patients/medicines/ibrutinib

The cited date is today’s, because a citation records when you read the page. The reviewed date is when a clinician last checked it.