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Procrit Safety Reports

Total Procrit reports: 878.
Procrit FDA safety alerts: 2002 2003 2004 2005 2006 2007 2008 .
Reported deaths: 36    Reported hospitalizations: 112.
Take Procrit Side Effects Survey or Share Your Procrit Story.
Reported Procrit Side Effects: therapeutic response decreased, condition aggravated, fatigue, asthenia, oedema peripheral, headache, aplasia pure red cell, injection site pain, pain in extremity, nausea, blood glucose increased.
More About Procrit.

< Previous  Showing 101-150 of 878 Next >

Procrit Side Effects Report #5054878-1
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Oct 03, 2005. Female patient, weighting 293.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: diarrhoea, oedema, ovarian cancer, paraesthesia, pulmonary embolism. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5054880-X
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 06, 2005. Female patient, 74 years of age, weighting 138.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased appetite. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5054914-2
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Mar 13, 2006. Female patient, 41 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: chest pain. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5054916-6
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2006. Male patient, weighting 184.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: condition aggravated, headache. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055088-4
Physician from UNITED STATES reported PROCRIT problem on Nov 11, 2004. Female patient, weighting 279.3 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: balance disorder, condition aggravated, decreased appetite, dry mouth, dysgeusia, fatigue, hypertension, vertigo. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055089-6
PROCRIT problem was reported by a Physician from UNITED STATES on Nov 17, 2004. Female patient, weighting 163.1 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: arthralgia, condition aggravated, hypoglycaemia, oedema peripheral, weight increased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055092-6
Physician from UNITED STATES reported PROCRIT problem on Mar 07, 2005. Female patient, 42 years of age, was diagnosed with pre-existing disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin increased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055093-8
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 02, 2005. Male patient, 78 years of age, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: injection site bruising, injection site pain. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055095-1
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Mar 03, 2005. Female patient, 83 years of age, weighting 116.2 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: pruritus. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055098-7
PROCRIT problem was reported by a Physician from UNITED STATES on Mar 01, 2005. Male patient, 95 years of age, weighting 130.1 lb, was diagnosed with pre-existing disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: injection site pain. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055099-9
Physician from UNITED STATES reported PROCRIT problem on Mar 01, 2005. Female patient, weighting 264.3 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: fatigue, lethargy, myalgia. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055102-6
PROCRIT problem was reported by a Physician from UNITED STATES on Dec 10, 2004. Female patient, weighting 146.2 lb, was diagnosed with pre-existing disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: asthenia, blood bilirubin increased, chills, fatigue, feeling abnormal, hot flush, night sweats, pseudomonas infection, urinary tract infection. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055104-X
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Mar 02, 2005. Female patient, 29 years of age, weighting 80.03 lb, was diagnosed with hiv infection and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: hypoaesthesia, infection. PROCRIT dosage: unknown. During the same period patient was treated with NEULASTA, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055114-2
PROCRIT problem was reported by a Health Professional from UNITED STATES on Mar 08, 2006. Female patient, weighting 148.2 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: headache. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055266-4
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Dec 27, 2004. Female patient, 73 years of age, weighting 128.1 lb, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: decreased appetite, gastritis, injection site pain, nausea, vomiting, weight decreased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055267-6
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 30, 2006. Female patient, weighting 145.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: musculoskeletal pain, pain in extremity. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055275-5
Physician from UNITED STATES reported PROCRIT problem on May 16, 2006. Female patient, weighting 147.0 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: pulmonary embolism. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5055280-9
PROCRIT problem was reported by a Health Professional from UNITED STATES on May 11, 2006. Male patient, child 5 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: condition aggravated, essential tremor. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055285-8
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Apr 21, 2006. Male patient, 86 years of age, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: asthenia, chest pain, dyspnoea, insomnia, pollakiuria. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055287-1
PROCRIT problem was reported by a Health Professional from UNITED STATES on Apr 21, 2006. Female patient, weighting 140.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: oedema peripheral. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055290-1
Health Professional from UNITED STATES reported PROCRIT problem on Apr 25, 2006. Female patient, weighting 197.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055291-3
PROCRIT problem was reported by a Health Professional from UNITED STATES on Apr 26, 2006. Male patient, weighting 300.3 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: diarrhoea. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055293-7
Pharmacist from UNITED STATES reported PROCRIT problem on Dec 01, 2005. Male patient, weighting 135.1 lb, was diagnosed with hiv infection and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: asthenia, incorrect dose administered. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055295-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on May 03, 2006. Female patient, weighting 160.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: skin exfoliation. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055542-5
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on May 01, 2006. Female patient, weighting 113.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, diarrhoea, muscle spasms. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055543-7
PROCRIT problem was reported by a Pharmacist from UNITED STATES on Feb 16, 2006. Male patient, weighting 266.3 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: hypoglycaemia, loss of consciousness. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055549-8
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on May 05, 2006. Female patient, 50 years of age, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: bone pain, injection site pain, insomnia. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055550-4
PROCRIT problem was reported by a Health Professional from UNITED STATES on May 05, 2006. Female patient, 60 years of age, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: vaginal haemorrhage. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055553-X
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Apr 18, 2006. Female patient, weighting 170.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: oedema peripheral. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055581-4
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 31, 2006. Male patient, weighting 170.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: agitation, anger, asthenia, balance disorder, blood glucose increased, chills, confusional state, cough, insomnia. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055586-3
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Apr 06, 2006. Male patient, 79 years of age, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: anorexia, asthma, bronchitis, diarrhoea, vomiting, weight decreased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055593-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Apr 10, 2006. Male patient, weighting 190.3 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: blood glucose increased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055607-8
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Apr 13, 2006. Female patient, weighting 155.2 lb, was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: bedridden, malaise. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055608-X
PROCRIT problem was reported by a Pharmacist from UNITED STATES on Apr 10, 2006. Female patient, 63 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: blood glucose increased. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055620-0
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Mar 23, 2006. Female patient, weighting 160.1 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: oedema peripheral. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055621-2
PROCRIT problem was reported by a Health Professional from UNITED STATES on Mar 07, 2006. Female patient, weighting 155.2 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: therapeutic response delayed. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055628-5
Pharmacist from UNITED STATES reported PROCRIT problem on Mar 09, 2006. Female patient, 92 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: haemoglobin decreased. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055632-7
PROCRIT problem was reported by a Pharmacist from UNITED STATES on Mar 09, 2006. Male patient, 77 years of age, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: glomerular filtration rate decreased. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055633-9
Physician from UNITED STATES reported PROCRIT problem on Mar 08, 2006. Male patient, weighting 185.2 lb, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, malaise, myalgia. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055638-8
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 21, 2006. Female patient, weighting 163.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: blood creatine increased, blood glucose increased, paraesthesia. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055640-6
Consumer or non-health professional from UNITED STATES reported PROCRIT problem on Mar 02, 2006. Female patient, weighting 160.1 lb, was diagnosed with anaemia and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: anorexia, epistaxis, malaise, pain in extremity, skin discolouration. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055654-6
PROCRIT problem was reported by a Physician from UNITED STATES on Sept 29, 2004. Male patient, weighting 172.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: thrombosis. PROCRIT dosage: unknown. During the same period patient was treated with ARANESP. Patient was hospitalized. Patient recovered.

Procrit Side Effects Report #5055655-8
Health Professional from UNITED STATES reported PROCRIT problem on Mar 21, 2005. Male patient, 67 years of age, weighting 146.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: blood potassium decreased, diarrhoea. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055657-1
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 15, 2005. Female patient, 66 years of age, weighting 200.2 lb, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: rectal haemorrhage. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055660-1
Physician from UNITED STATES reported PROCRIT problem on Jan 19, 2005. Female patient, 66 years of age, was diagnosed with renal failure chronic and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: leukocytoclastic vasculitis, rash pruritic. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055661-3
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 23, 2005. Female patient, weighting 120.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: hypersensitivity, pruritus, rash. PROCRIT dosage: unknown. Patient recovered.

Procrit Side Effects Report #5055663-7
Physician from UNITED STATES reported PROCRIT problem on Oct 18, 2004. Male patient, weighting 224.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: arthropod sting, condition aggravated, psoriasis, rash papular, testicular swelling. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055676-5
PROCRIT problem was reported by a Physician from UNITED STATES on Sept 27, 2005. Male patient, 77 years of age, weighting 224.2 lb, was diagnosed with myelodysplastic syndrome and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: asthenia, hypokinesia. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER, MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055678-9
Physician from UNITED STATES reported PROCRIT problem on Feb 24, 2006. Female patient, 76 years of age, weighting 120.2 lb, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: pulmonary oedema. PROCRIT dosage: unknown. During the same period patient was treated with MEDICINALPRODUCT NOT SPECIFIED BY SENDER. Patient recovered.

Procrit Side Effects Report #5055679-0
PROCRIT problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 24, 2006. Male patient, 75 years of age, was diagnosed with anaemia of malignant disease and was treated with PROCRIT. After drug was administered, patient experienced the following problems/side effects: bone pain. PROCRIT dosage: unknown. Patient recovered.

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Drug Information: Epoetin Alfa Injection

URL of this page: http://www.nlm.nih.gov/medlineplus/druginfo/medmaster/a692034.html

(e poe' e tin)

IMPORTANT WARNING:

All patients:Epoetin alfa increases the risk of blood clots forming in or moving to the legs, lungs, or brain. Call your doctor immediately if you experience any of the following symptoms: pain, tenderness, redness, warmth, and/or swelling in the legs; shortness of breath; cough that won't go away or that brings up blood; chest pain; sudden trouble seeing in one or both eyes; sudden trouble speaking or understanding speech; sudden confusion; sudden weakness or numbness of an arm or leg (especially on one side of the body), or of the face; sudden trouble walking or loss of balance or coordination; sudden severe headache; or seizures.Using epoetin alfa increases the risk that you will develop a blood clot during or after surgery. Before you have surgery, tell your doctor that you are using epoetin alfa. Your doctor may prescribe an anticoagulant ('blood thinner') to help prevent blood clots from forming during or after surgery.Keep all appointments with your doctor and the laboratory. Your doctor will order certain lab tests to check your body's response to epoetin alfa. Your doctor may decrease your dose if the tests show that you are at high risk of experiencing serious side effects of epoetin alfa.Talk to your doctor about the risks of using epoetin alfa.Patients with chronic renal failure:Your doctor will adjust your dose of epoetin alfa so that your hemoglobin level (amount of a protein found in red blood cells) is between 10-12 g/dL. If your hemoglobin level is higher than this, there is a greater risk that you will develop serious side effects including heart attack, stroke, heart failure, blood clots, and death. Call your doctor immediately if you experience any of the following symptoms: chest pain, squeezing pressure, or tightness; shortness of breath; nausea, lightheadedness, sweating, and other early signs of heart attack; discomfort or pain in the arms, shoulder, neck, jaw, or back; fast or irregular heartbeat; swelling of the hands, feet, or ankles; blue-grey coloring or darkening around mouth or nails; extreme tiredness or weakness; or fainting or loss of consciousness.If you are receiving hemodialysis (treatment in which the blood is passed through a filter to remove wastes that would normally be removed by the kidneys), you may develop a blood clot in your vascular access (place on your body where your blood is removed and returned during dialysis). Call your doctor right away if you think you have a blood clot in your vascular access.Cancer patients:In clinical studies, people with certain cancers who received epoetin alfa died sooner or experienced tumor growth or cancer that spread sooner than people who did not receive the medication. If you have cancer, there is a risk that your tumor will grow faster or you will die sooner if you receive epoetin alfa, even if your hemoglobin level is kept lower than 12 g/dL. To decrease these risks, you should receive the lowest possible dose of epoetin alfa and you should only receive epoetin alfa while you are receiving chemotherapy. Treatment with epoetin alfa should be stopped when your course of chemotherapy ends.

Why is this medication prescribed?

Epoetin alfa is used to treat anemia (a lower than normal number of red blood cells) in people with chronic kidney failure (condition in which the kidneys slowly and permanently stop working over a period of time). Epoetin alfa is also used to treat anemia caused by chemotherapy (medications to treat cancer) or zidovudine (AZT, Retrovir, in Trizivir, in Combivir), a medication used to treat human immunodeficiency virus (HIV). Epoetin alfa is also used before and after certain types of surgery to decrease the number of blood transfusions (transfer of one person's blood to another person's body) needed for expected or actual blood loss during surgery. Epoetin alfa is in a class of medications called erythropoiesis-stimulating agents (ESAs). It works by causing the bone marrow (soft tissue inside the bones where blood is made) to make more red blood cells.

How should this medicine be used?

Epoetin alfa comes as a solution (liquid) to inject subcutaneously (just under the skin) or intravenously (into a vein). It is usually injected one to three times weekly. When epoetin alfa is used to prevent and treat anemia due to surgery, it is sometimes injected once daily for 10 days before surgery, on the day of surgery and for 4 days after surgery. Alternatively, epoetin alfa is sometimes injected once weekly, beginning 3 weeks before surgery, with a dose also on the day of surgery. To help you remember to use epoetin alfa, mark a calendar to keep track of when you are to receive a dose. Follow the directions on your prescription label carefully, and ask your doctor or pharmacist to explain any part you do not understand. Use epoetin alfa exactly as directed. Do not use more or less of it or use it more often than prescribed by your doctor.

Your doctor may start you on the lowest possible dose of epoetin alfa and gradually increase or decrease your dose, usually not more than once every month. Your doctor may also tell you to stop using epoetin alfa for a time. Follow these instructions carefully. If your doctor tells you to stop using epoetin alfa, do not begin using it again until your doctor tells you that you should. It is likely that your doctor will restart your treatment with a lower dose of epoetin alfa than you were using.

Epoetin alfa is used to reduce the need for red blood cell transfusions. It does not cure anemia. It may take up to 2 to 6 weeks of treatment before there is an increase in the number of red blood cells. Do not stop using epoetin alfa without talking to your doctor. If you do not respond to treatment with epoetin alfa, your doctor may check to see if there is another cause for your anemia.

Epoetin alfa injections are usually given by a doctor or nurse. Your doctor may decide that you can inject epoetin alfa yourself or that you may have a friend or relative give the injections. Your doctor will make sure the person who will be injecting the medication can give the injection correctly. Always follow the instructions of your doctor concerning the dose, how to give the medication, and how often to give the medication. Be sure that you and the person who will be giving the injections read the manufacturer's information for the patient that comes with epoetin alfa before you use it for the first time at home.

If you are using epoetin alfa at home, you will need to use disposable syringes and needles to inject your medication. Your doctor or pharmacist will tell you what type of syringe you should use. Do not use any other type of syringe because you may not get the right amount of medication. Always keep a spare syringe and needle on hand.

Use a disposable syringe or needle only one time. Throw away used syringes in a puncture-resistant container, out of the reach of children. Talk to your doctor or pharmacist about how to throw away the puncture-resistant container. Do not throw the container in your household trash. There may be special state and local laws for throwing away used needles and syringes.

If your doctor has prescribed epoetin alfa in a single use vial, the vial can be used only one time. Do not put a needle through the rubber stopper of the vial more than once. Throw away the vial after you have used it for one dose, even if it is not empty.

Always inject epoetin alfa in its own syringe; never mix it with any other medication.

If you are injecting epoetin alfa subcutaneously, you can inject it just under the skin anywhere on the outer area of your upper arms, middle of the front thighs, stomach (except for a 2-inch area around the navel), or outer area of the buttocks. Do not inject epoetin alfa into a spot that is tender, red, bruised, hard, or has scars or stretch marks. Choose a new spot each time you inject epoetin alfa, as directed by your doctor. Write down the date, time, dose of epoetin alfa, and the spot where you injected your dose in a record book.

Ask your pharmacist or doctor for a copy of the manufacturer's information for the patient.

Other uses for this medicine

This medication may be prescribed for other uses. Talk to your doctor about the risks of using this medication for your condition.

What special precautions should I follow?

Before using epoetin alfa,

  • tell your doctor and pharmacist if you are allergic to epoetin alfa, darbepoetin alfa (Aranesp), medications made from animal cells, albumin, any other medications or benzyl alcohol. Ask your doctor or pharmacist if you don't know if a medication you are allergic to is made from animal cells.
  • tell your doctor and pharmacist what other prescription and nonprescription medications, vitamins, nutritional supplements, and herbal products you are taking or plan to take. Your doctor may need to change the doses of your medications or monitor you carefully for side effects.
  • tell your doctor if you have or have had high blood pressure. Your doctor may tell you not to use epoetin alfa.
  • tell your doctor if you have or have ever had bleeding or blood clotting problems; cancer; diseases that affect your blood such as leukemia, myelodysplastic syndrome (condition in which the bone marrow can not produce enough blood cells), sickle cell disease (an inherited blood disease that causes pain, anemia, and organ damage), thalassemia (an inherited blood disease that causes abnormal development and other problems), or porphyria (an inherited blood disease that may cause skin or nervous system problems); blood clots in your heart, legs, or lungs; a heart attack; an infection; stroke or mini-stroke (TIA); tumors; heart disease, or any disease that affects your brain or nervous system.
  • tell your doctor if you have used epoetin alfa or another erythropoiesis-stimulating agent such as darbepoetin alfa (Aranesp) in the past. Be sure to tell your doctor if your anemia worsened during your treatment with one of these medications, or if you were ever told to stop using one of these medications.
  • tell your doctor if you are pregnant, plan to become pregnant, or are breast-feeding. If you become pregnant while using epoetin alfa, call your doctor. If you stopped menstruating (getting your period) because of your anemia, you may begin to menstruate again while you are using epoetin alfa. This may increase the chance that you will become pregnant. Talk to your doctor about the type of birth control that is right for you.
  • if you are having surgery, including dental surgery, tell the doctor or dentist that you are using epoetin alfa.
  • you should know that epoetin alfa may cause seizures, usually during the first 3 months of treatment. Talk to your doctor about driving a car, operating machinery, or participating in dangerous activities during this time.
  • you should know that your blood pressure may increase while you are using epoetin alfa. Your doctor may ask you to monitor your blood pressure frequently. Be sure to check your blood pressure as often as your doctor tells you that you should, to call your doctor if your blood pressure is higher than your doctor says it should be, and to take any medications your doctor prescribes to control your blood pressure exactly as directed.
  • you should call your doctor if you are planning to travel or if your activity becomes limited, such as spending more time sitting or in bed.

What special dietary instructions should I follow?

If you are following a prescribed special diet because you have kidney disease or high blood pressure, follow it carefully, even if you feel better while using epoetin alfa. Epoetin alfa will not work unless your body has enough iron. Your doctor or dietician will probably tell you to eat foods that are rich in iron. If you cannot get enough iron from your diet, your doctor may prescribe an iron supplement. Take this supplement exactly as directed.

What should I do if I forget a dose?

Call your doctor to ask what to do if you miss a dose of epoetin alfa. Do not use a double dose to make up for a missed one.

What side effects can this medication cause?

Epoetin alfa may cause side effects. Tell your doctor if any of these symptoms are severe or do not go away:

  • headache
  • joint or muscle aches, pain, or soreness
  • nausea
  • vomiting
  • indigestion
  • stomach pain
  • diarrhea
  • constipation
  • difficulty falling asleep or staying asleep
  • rash
  • itching
  • pain, burning, numbness, or tingling in the hands or feet

Some side effects can be serious. If you experience any of the following symptoms, or those listed in the IMPORTANT WARNING section, call your doctor immediately.

  • fever, sore throat, chills, cough, and other signs of infection
  • redness, swelling, pain, or itching at the injection spot
  • spreading rash over the whole body
  • hives
  • swelling of the face, throat, tongue, lips, eyes
  • wheezing
  • difficulty breathing or swallowing
  • hoarseness
  • lack of energy
  • feeling cold most of the time

Epoetin alfa may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

If you experience a serious side effect, you or your doctor may send a report to the Food and Drug Administration's (FDA) MedWatch Adverse Event Reporting program online [at http://www.fda.gov/MedWatch/index.html] or by phone [1-800-332-1088].

What storage conditions are needed for this medicine?

Keep this medication in the container it came in, tightly closed, and out of reach of children. Store it in the refrigerator, but do not freeze it. Keep epoetin alfa away from excess heat and moisture (not in the bathroom) and sunlight. Throw away any medication that is outdated or no longer needed. Throw away a multidose vial of epoetin alfa 21 days after you first use it. Talk to your pharmacist about the proper disposal of your medication.

When traveling, place epoetin alfa in its original box in an insulated cooler with coolant such as blue ice. Do not place epoetin alfa vials directly on ice or coolants, and do not allow them to freeze. If a vial does freeze, do not use it. Once you arrive, place the medication in a refrigerator as soon as possible.

In case of emergency/overdose

In case of overdose, call your local poison control center at 1-800-222-1222. If the victim has collapsed or is not breathing, call local emergency services at 911.

Symptoms of overdose may include:

  • pain, tenderness, redness, warmth, and/or swelling in the legs
  • chest pain, squeezing pressure, or tightness
  • discomfort or pain in the arms, shoulder, neck, jaw, or back
  • fast or irregular heartbeat
  • shortness of breath
  • cough that won't go away or coughing up blood
  • swelling of the hands, feet, or ankles
  • blue-grey color or darkening around mouth or nails
  • excessive sweating
  • dizziness or lightheadedness
  • fainting or loss of consciousness
  • sudden trouble seeing in one or both eyes
  • sudden confusion
  • sudden trouble speaking or understanding speech
  • sudden weakness or numbness of an arm or leg, (especially on one side of the body) or face
  • sudden trouble walking or loss of balance or coordination
  • sudden severe headache
  • extreme tiredness or weakness
  • seizure
  • increased blood pressure
  • blood clot in hemodialysis port

What other information should I know?

Before having any laboratory test, tell your doctor and the laboratory personnel that you are using epoetin alfa.

Do not let anyone else use your medication. Ask your pharmacist any questions you have about refilling your prescription.

It is important for you to keep a written list of all of the prescription and nonprescription (over-the-counter) medicines you are taking, as well as any products such as vitamins, minerals, or other dietary supplements. You should bring this list with you each time you visit a doctor or if you are admitted to a hospital. It is also important information to carry with you in case of emergencies.

Brand name(s):

  • Epogen®
  • Procrit®

Other name(s):

  • EPO
  • Erythropoietin Human Glycoform alpha (Recombinant)
  • rHuEPO-alpha

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PatientsVille.com does not provide medical advice, diagnosis or treatment. The information contained on PatientsVille.com site has not been scientifically or otherwise verified as to a cause and effect relationship and cannot be used to estimate the incidence of adverse drug reactions or for establishing or changing of patient treatments.


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