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darbepoetin alfa (Aranesp)
Hematinics

How it is administered

Darbepoetin alfa is administered as an injection, either under the skin (subcutaneous) or into a vein (intravenous). It is available as a sterile, colorless, preservative-free solution in vials or prefilled syringes. The medication is typically given once a week, every two weeks, or every three weeks, depending on the indication and patient needs. Patients or caregivers may be trained to give the injections at home if appropriate.

How it works

Darbepoetin alfa is a man-made protein that stimulates the production of red blood cells in the body, similar to the natural hormone erythropoietin. It works by signaling the bone marrow to make more red blood cells, which helps to treat anemia (a low red blood cell count). This is especially important in patients who have anemia due to chronic kidney disease or as a result of chemotherapy for cancer.

By increasing red blood cell production, darbepoetin alfa helps improve oxygen delivery throughout the body, which can reduce symptoms of anemia such as fatigue and weakness. However, the effects are not immediate; it may take 2 to 6 weeks to see an increase in hemoglobin levels after starting treatment.

Common side effects

  • Hypertension (high blood pressure)
  • Dyspnea (shortness of breath)
  • Peripheral edema (swelling in the limbs)
  • Cough
  • Procedural hypotension (low blood pressure during procedures)
  • Abdominal pain
  • Edema (general swelling)
  • Thromboembolic events (blood clots)

Serious but less common side effects include seizures, pure red cell aplasia, serious allergic reactions, and severe skin reactions.

Who Should take it

Darbepoetin alfa is indicated for patients with anemia due to chronic kidney disease (CKD), whether or not they are on dialysis. It is also used to treat anemia in patients with non-myeloid cancers who are receiving myelosuppressive chemotherapy, provided there are at least two more months of planned chemotherapy.

For patients with blood cancers like myelofibrosis, darbepoetin alfa may be considered if anemia is present and is due to the effects of chemotherapy. It is not meant to be used in patients whose anemia can be managed with transfusions or in those receiving only hormonal, biologic, or radiotherapy for cancer.

Who should not take it

Darbepoetin alfa should not be used in patients with uncontrolled high blood pressure, a history of pure red cell aplasia (PRCA) after treatment with darbepoetin alfa or other erythropoietin protein drugs, or those who have had serious allergic reactions to darbepoetin alfa.

It is also not indicated for patients with cancer who are not receiving chemotherapy, or whose anticipated outcome is cure, or whose anemia can be managed by transfusion. It should not be used as a substitute for red blood cell transfusions in patients who need immediate correction of anemia.

Commonly used with

Darbepoetin alfa is often used alongside iron supplements, as adequate iron levels are necessary for the medication to work effectively. In patients with blood cancers or those undergoing chemotherapy, it may be used with other supportive care medications such as anti-nausea drugs, antibiotics, or growth factors for white blood cells.

It is not typically combined with other erythropoiesis-stimulating agents.

Commonly tested with

Darbepoetin alfa has been tested in combination with chemotherapy regimens in patients with non-myeloid cancers. It has also been compared to epoetin alfa in studies for anemia management in chronic kidney disease and cancer patients. In clinical trials, it is often evaluated alongside iron supplementation and standard supportive care.

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