Epoetin alfa (Injection)
Generic name: epoetin alfa [ e-POE-e-tin-AL-fa ]
Brand names: Epogen, Procrit
Drug class: Recombinant human erythropoietins
Medically reviewed by Drugs.com. Last updated on Jan 1, 2024.
Erythropoiesis-stimulating agents (ESAs) increase the risks for death, myocardial infarction, stroke, and other serious cardiovascular events. In patients with chronic kidney disease (CKD), patients are at a greater risk for death, serious adverse cardiovascular reactions, and stroke when administered ESAs to target Hb levels of 11 g/dL and above. No clinical trial has identified an Hb target level, ESA dose, or dosing strategy that does not increase these risks; use at lowest sufficient dose is recommended. In cancer patients with certain tumor types (ie, breast, non-small cell lung, head and neck, lymphoid, cervical), ESAs shortened overall survival and/or increased the risk of tumor progression or recurrence in some clinical studies. In patients with cancer, use the lowest ESA dose needed to avoid RBC transfusions and serious cardiovascular and thromboembolic reactions. Use ESAs only for treatment of anemia due to concomitant myelosuppressive chemotherapy, and discontinue following the completion of a chemotherapy course. Patients receiving myelosuppressive chemotherapy should not be treated with ESAs when the anticipated outcome is cure. Deep venous thrombosis prophylaxis should be considered when epoetin alfa is used preoperatively .
Uses for epoetin alfa
Epoetin injection is a man-made version of human erythropoietin (EPO). EPO is produced naturally in the body, mostly by the kidneys. It stimulates the bone marrow to produce red blood cells. If the body does not produce enough EPO, severe anemia can occur. This often occurs in patients with chronic kidney disease whose kidneys are not working properly. Epoetin is used to treat severe anemia in patients on kidney dialysis or for those not on dialysis.
Epoetin may also be used to prevent or treat anemia that is caused by surgery or medicines (eg, zidovudine) that are used for other conditions, such as HIV or cancer.
This medicine is available only with your doctor's prescription.
Before using epoetin alfa
In deciding to use a medicine, the risks of taking the medicine must be weighed against the good it will do. This is a decision you and your doctor will make. For this medicine, the following should be considered:
Allergies
Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines. Also tell your health care professional if you have any other types of allergies, such as to foods, dyes, preservatives, or animals. For non-prescription products, read the label or package ingredients carefully.
Pediatric
Appropriate studies performed to date have not demonstrated pediatric-specific problems that would limit the usefulness of epoetin injection in children 1 month of age and older. Safety and efficacy have not been established in children younger than 1 month of age with chronic kidney disease undergoing dialysis, children younger than 5 years of age with cancer, children with chronic kidney disease not undergoing dialysis, or children with HIV infection.
Geriatric
Appropriate studies performed to date have not demonstrated geriatric-specific problems that would limit the usefulness of epoetin injection in the elderly.
Breast Feeding
There are no adequate studies in women for determining infant risk when using this medication during breastfeeding. Weigh the potential benefits against the potential risks before taking this medication while breastfeeding.
Interactions with Medicines
Although certain medicines should not be used together at all, in other cases two different medicines may be used together even if an interaction might occur. In these cases, your doctor may want to change the dose, or other precautions may be necessary. Tell your healthcare professional if you are taking any other prescription or nonprescription (over-the-counter [OTC]) medicine.
Interactions with Food/Tobacco/Alcohol
Certain medicines should not be used at or around the time of eating food or eating certain types of food since interactions may occur. Using alcohol or tobacco with certain medicines may also cause interactions to occur. Discuss with your healthcare professional the use of your medicine with food, alcohol, or tobacco.
Other Medical Problems
The presence of other medical problems may affect the use of this medicine. Make sure you tell your doctor if you have any other medical problems, especially:
- Aluminum poisoning, severe or
- Bleeding, severe or
- Blood disorders (eg, thalassemia, myelodysplastic syndrome) or
- Bone problems or
- Folic acid, iron, or vitamin B12 deficiencies or
- Infection, inflammation, or cancer or
- Porphyrin (red blood cell pigment) metabolism disorder or
- Sickle cell anemia—Epoetin may not work properly.
- Blood clots (history of) or other problems with the blood or
- Cancer, active or
- Congestive heart failure or
- Heart attack, history of or
- Heart bypass surgery or
- Heart or blood vessel disease or
- Seizures, history of or
- Stroke, history of or
- Thrombosis, at risk for—The chance of side effects may be increased.
- Cancer, history of—May cause some tumors to progress or come back.
- Hypertension (high blood pressure), uncontrolled or
- Pure red cell aplasia (rare bone marrow disease)—Should not be used in patients with these conditions.
Proper use of epoetin alfa
Epoetin injection is usually given by a doctor after a kidney dialysis treatment in a hospital or clinic. However, medicines given by injection are sometimes used at home. If you will be using epoetin at home, your doctor will teach you how the injections are to be given. Be sure that you understand exactly how the medicine is to be injected.
It may be given as a shot under your skin or into a vein. If your doctor tells you to inject it in a certain way, follow your doctor's instructions.
This medicine comes with a Medication Guide. Read and follow these instructions carefully. Ask your doctor if you have any questions.
If you are using this medicine at home:
- Use a new needle and syringe each time you inject your medicine.
- Do not use more medicine or use it more often than your doctor tells you to.
- You will be shown the body areas where this shot can be given.
- If you use the vials that have one dose, you might not use all of the medicine in each vial. Use each vial only once and throw any extra medicine away. Do not save an opened vial.
- If you use the vial that has enough medicine for more than one dose, put it back in the refrigerator after use. Write the date on the vial that you first used it and throw away any unused medicine after 21 days.
Do not shake the vial before using it. Do not use this medicine if it has been frozen.
If the medicine in the vial has changed color, or if you see particles in it, do not use it.
Carefully follow your doctor's instructions about any special diet. You may need to eat foods that contain iron, folic acid, or vitamin B12 such as eggs, certain cereals, meats, and vegetables, or you may take an iron, folic acid, or vitamin B12 supplement while you are using this medicine.
Dosing
The dose of this medicine will be different for different patients. Follow your doctor's orders or the directions on the label. The following information includes only the average doses of this medicine. If your dose is different, do not change it unless your doctor tells you to do so.
The amount of medicine that you take depends on the strength of the medicine. Also, the number of doses you take each day, the time allowed between doses, and the length of time you take the medicine depend on the medical problem for which you are using the medicine.
- For injection dosage form:
- For anemia from chemotherapy:
- Adults—Dose is based on body weight and must be determined by your doctor. The starting dose is 150 units per kilogram (kg) injected under the skin three times a week or 40,000 units injected under the skin once a week. Your doctor may adjust the dose as needed.
- Children 5 years of age and older—Dose is based on body weight and must be determined by your doctor. The starting dose is 600 units per kg injected into a vein once a week. Your doctor may adjust the dose as needed.
- Children younger than 5 years of age—Use and dose must be determined by your doctor.
- For anemia from chronic kidney failure on dialysis:
- Adults—Dose is based on body weight and must be determined by your doctor. The starting dose is 50 to 100 units per kilogram (kg) injected into a vein or under the skin three times a week. Your doctor may adjust the dose as needed.
- Children 1 month to 16 years of age—Dose is based on body weight and must be determined by your doctor. The starting dose is 50 units per kg injected into a vein or under the skin three times a week. Your doctor may adjust the dose as needed.
- Children younger than 1 month of age—Use and dose must be determined by your doctor.
- For anemia from chronic kidney failure not on dialysis:
- Adults—Dose is based on body weight and must be determined by your doctor. The starting dose is 50 to 100 units per kilogram (kg) injected into a vein or under the skin three times a week. Your doctor may adjust the dose as needed.
- Children—Use and dose must be determined by your doctor.
- For anemia from HIV therapy:
- Adults—Dose is based on body weight and must be determined by your doctor. The starting dose is 100 units per kilogram (kg) injected into a vein or under the skin three times a week for 8 weeks. Your doctor may adjust the dose as needed.
- Children—Use and dose must be determined by your doctor.
- For anemia from surgery:
- Adults—Dose is based on body weight and must be determined by your doctor. The starting dose is 300 units per kilogram (kg) injected under the skin for 10 days before the surgery, on the day of the surgery, and for 4 days after surgery.
- Children—Use and dose must be determined by your doctor.
- For anemia from chemotherapy:
Missed Dose
If you miss a dose of this medicine, take it as soon as possible. However, if it is almost time for your next dose, skip the missed dose and go back to your regular dosing schedule. Do not double doses.
Storage
Keep out of the reach of children.
Do not keep outdated medicine or medicine no longer needed.
Ask your healthcare professional how you should dispose of any medicine you do not use.
Store in the refrigerator. Do not freeze.
Protect the medicine from bright light. Keep your medicine in the original package until you are ready to use it.
Throw away used needles in a hard, closed container that the needles cannot poke through (puncture-resistant). Keep this container away from children and pets.
Related/similar drugs
ferrous sulfate, pyridoxine, Revlimid, FeroSul, Aranesp, lenalidomide, ferrous gluconate, Vitamin B6, Epogen, Procrit
Precautions while using epoetin alfa
It is very important that your doctor check the blood of you or your child on a regular basis while you are using this medicine. You may also need to monitor your blood pressure at home. If you notice any changes to your recommended blood pressure, call your doctor right away. .
Do not use this medicine if you or your child have had an allergic reaction to albumin or products derived from human or animal cells.
This medicine contains benzyl alcohol which may cause serious reactions to newborn or premature infants. Discuss this with your doctor if you are concerned.
Epoetin sometimes causes seizures, especially during the first 90 days of treatment. During this time, it is best to avoid driving, using heavy machinery, or doing other activities that could cause serious injury if a seizure occurs while you are performing them.
People with severe anemia usually feel very tired and sick. When epoetin begins to work, usually in about 6 weeks, most people start to feel better. Some people are able to be more active. However, epoetin only corrects anemia. It has no effect on kidney disease, cancer, or any other medical problem that needs regular medical attention. Even if you or your child are feeling much better, it is very important that you do not miss any appointments with your doctor or any dialysis treatments. .
This medicine may increase your risk of having serious heart and blood vessel problems, such as congestive heart failure, heart attacks, or stroke. Check with your doctor right away if you or your child start having dizziness, fainting spells, severe tiredness, chest pain, trouble with breathing, sudden or severe headache, or problems with vision, speech, or walking. .
This medicine may increase your risk of having blood clots. This is more likely in patients who use high doses of this medicine, or who use this medicine before a major surgery. Call your doctor right away if you have chest pain, trouble breathing, or pain, redness, or swelling in your arms or legs while using this medicine. If you are getting dialysis treatments, tell your doctor right away if you notice blood clots at the injection site. Your doctor may give you a blood thinner before surgery to help prevent blood clots.
This medicine may cause blood clots to form in the access port (A-V shunt) for patients with chronic kidney disease who receive dialysis treatments. This would cause the access port to stop working. Tell your doctor right away if you or your child see blood clots forming in the access port.
When used in patients with certain types of cancer (eg, breast, cervix, lymphoid, lung, head, or neck cancer), this medicine has shortened survival time and worsened the tumor or cancer in some patients. If you or your child are concerned about this, talk with your doctor.
This medicine may cause serious allergic reactions, including anaphylaxis and angioedema. These can be life-threatening and require immediate medical attention. Tell your doctor right away if you have a rash, itching, hoarseness, trouble breathing, trouble swallowing, or any swelling of your hands, face, or mouth after using this medicine.
Serious skin reactions can occur with this medicine. Check with your doctor right away if you have blistering, peeling, or loosening of the skin, red skin lesions, severe acne or a skin rash, sores or ulcers on the skin, or fever or chills with this medicine.
Epoetin is made from donated human blood. Some human blood products have transmitted certain viruses to people who have received them, although the risk is low. Human donors and donated blood are both tested for viruses to keep the transmission risk low. Talk with your doctor if you have concerns.
Many people with kidney problems need to be on a special diet. Also, people with high blood pressure (which may be caused by kidney disease or by epoetin treatment) may need to be on a special diet or to take medicine to keep their blood pressure under control. After their anemia has been corrected, some people feel so much better that they want to eat more than before. To keep your kidney disease or your high blood pressure from getting worse, it is very important that you or your child follow your special diet and take your medicines regularly, even if you are feeling better.
In addition to epoetin, your body needs iron and vitamins to make red blood cells. Your doctor may direct you or your child to take iron or vitamin supplements. Be sure to follow your doctor's orders carefully. Epoetin will not work properly if there is not enough iron or vitamins in your body.
Side Effects of epoetin alfa
Along with its needed effects, a medicine 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:
More common
- Chest pain
- fever
- headache
- increased blood pressure
- swelling of the face, fingers, ankles, feet, or lower legs
- weight gain
Less common
- Anxiety
- blurred vision
- change in skin color
- change in vision
- cough
- dizziness or lightheadedness
- double vision
- fainting
- fast heartbeat
- migraine headache
- nausea
- pain or discomfort in the arms, jaw, back, or neck
- pain, tenderness, or swelling of the foot or leg
- pain in the chest, groin, or legs, especially calves of the legs
- pale skin
- partial or complete loss of vision in the eye
- seizures
- severe headache of sudden onset
- skin rash or hives
- slurred speech
- sore throat
- sudden and severe inability to speak
- sudden loss of coordination
- sweating
- temporary blindness
- tenderness, pain, swelling, warmth, or skin discoloration at the injection site
- unusual bleeding or bruising
- unusual tiredness or weakness
- vision problems
- vomiting
- weakness in the arm or leg on one side of the body, sudden and severe
Incidence not known
- Blistering, peeling, or loosening of the skin
- chills
- diarrhea
- itching
- joint or muscle pain
- red, irritated eyes
- red skin lesions, often with a purple center
- sore throat
- sores, ulcers, or white spots in the mouth or on the lips
Some side effects 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
- Bone or joint pain
- constipation
- general feeling of tiredness or weakness
- heartburn or belching
- itching or stinging at the injection site
- loss of strength or energy
- muscle aches or weakness
- shivering
- skin pain
- stomach discomfort, upset, pain, or swelling
- weight loss
Other side effects not listed may also occur in some patients. If you notice any other effects, check with your healthcare professional.
Call your doctor for medical advice about side effects. You may report side effects to the FDA at 1-800-FDA-1088.
Commonly used brand name(s)
In the U.S.
- Epogen
- Procrit
Available Dosage Forms:
- Solution
Therapeutic Class: Hematopoietic
Pharmacologic Class: Erythropoietin
Biological Products Related to epoetin alfa
Find detailed information on biosimilars for this medication.
Frequently asked questions
More about epoetin alfa
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- During pregnancy
- Drug class: recombinant human erythropoietins
- Breastfeeding
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