Indication

Acute myelomonocytic leukemia

Acute myelomonocytic leukemia is an aggressive subtype of acute myeloid leukemia characterized by the neoplastic proliferation of both granulocytic and monocytic precursor cells in the bone marrow and peripheral blood. Read more about Acute myelomonocytic leukemia

17 drugs 17 manufacturers

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Drugs that treat it

Common Acute myelomonocytic leukemia therapies.

Showing 10–17 of 17 drugs

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
ZYDUS PHARMACEU

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
ATHENEX PHARMAC

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
NOVADOZ PHARMAC

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
SINTETICA US LL

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
ZYDUS USA-NOVAP

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
Amneal Pharmaceuticals

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
SANDOZ

ARSENIC TRIOXIDE

ANTINEOPLASTICS - ARSENIC COMPOUNDS·ACUTE PROMYELOCYTIC LEUKEMIA·+1
Avet Pharmaceuticals
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About Acute myelomonocytic leukemia.

Acute myelomonocytic leukemia is an aggressive subtype of acute myeloid leukemia characterized by the neoplastic proliferation of both granulocytic and monocytic precursor cells in the bone marrow and peripheral blood.

Primarily affecting adults, this hematologic malignancy disrupts normal hematopoiesis, leading to severe cytopenias that clinically manifest as fatigue, susceptibility to recurrent infections, and bleeding diatheses.

Pathophysiologically, the condition is defined by elevated blast counts with significant dual differentiation, where both neutrophilic lineage cells and monocytic lineage cells each comprise at least 20% of bone marrow leukocytes.

Patients frequently demonstrate extramedullary tissue infiltration—including gingival hyperplasia, hepatosplenomegaly, and skin involvement—driven by the intrinsic tissue-migratory properties of the leukemic monocytic lineage.

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