Indication
Zidovudine-induced anemia
Zidovudine-induced anemia is an acquired hematologic toxicity occurring in individuals undergoing antiretroviral therapy with the nucleoside reverse transcriptase inhibitor zidovudine, most commonly in the context of human immunodeficiency virus (HIV) infection. Read more about Zidovudine-induced anemia
5 drugs 5 manufacturers
Drugs that treat it
Common Zidovudine-induced anemia therapies.
EPOGEN (epoetin alfa)
PROCRIT (epoetin alfa)
RETACRIT (epoetin alfa-epbx)
RETACRIT (epoetin alfa-epbx)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonZidovudine-induced anemia is an acquired hematologic toxicity occurring in individuals undergoing antiretroviral therapy with the nucleoside reverse transcriptase inhibitor zidovudine, most commonly in the context of human immunodeficiency virus (HIV) infection.
It is characterized by dose- and duration-dependent bone marrow suppression, wherein the drug inhibits hematopoietic progenitor cells and impairs erythroid differentiation.
Clinically, affected patients present with a progressive decline in hemoglobin concentrations and red blood cell counts, typically accompanied by marked macrocytosis.
In severe cases, this condition leads to profound symptomatic fatigue, pallor, and a reliance on red blood cell transfusions, serving as a specific indication for intervention with erythropoiesis-stimulating agents.
- fda.gov
Zidovudine-induced anemia is an acquired hematologic toxicity occurring in individuals undergoing antiretroviral therapy with the nucleoside reverse transcriptase inhibitor zidovudine, most commonly in the context of human immunodeficiency virus (HIV) infection
- nih.gov
Zidovudine-induced anemia is an acquired hematologic toxicity occurring in individuals undergoing antiretroviral therapy with the nucleoside reverse transcriptase inhibitor zidovudine, most commonly in the context of human immunodeficiency virus (HIV) infection It is characterized by dose- and duration-dependent bone marrow suppression, wherein the drug inhibits hematopoietic progenitor cells and impairs erythroid differentiation
- procrit.com
It is characterized by dose- and duration-dependent bone marrow suppression, wherein the drug inhibits hematopoietic progenitor cells and impairs erythroid differentiation Clinically, affected patients present with a progressive decline in hemoglobin concentrations and red blood cell counts, typically accompanied by marked macrocytosis In severe cases, this condition leads to profound symptomatic fatigue, pallor, and a reliance on red blood cell transfusions, serving as a specific indication for...
- nih.gov
Clinically, affected patients present with a progressive decline in hemoglobin concentrations and red blood cell counts, typically accompanied by marked macrocytosis In severe cases, this condition leads to profound symptomatic fatigue, pallor, and a reliance on red blood cell transfusions, serving as a specific indication for intervention with erythropoiesis-stimulating agents
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