PROCRIT Side Effects

7023618-9 | Erythema, Inflammation, Pain In Extremity, Skin Irritation
on Sep 30, 2010 Female patient from UNITED STATES , weighting 135.0 lb, was diagnosed with nephrogenic anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, inflammation, pain in extremity, skin irritation. Procrit dosage: 30,000 U/ml Every 2 Weeks Sq.

7018240-4 | Venous Insufficiency
Patient was taking Procrit (View Usage). Patient had the following side effects: venous insufficiency on Sep 27, 2010 from UNITED STATES Additional patient health information: Female patient , 78 years of age, weighting 250.0 lb, was diagnosed with renal failure and. Procrit dosage: 10,000 Units As Needed Im.

7016872-0 | Abdominal Pain Upper, Amnesia, Depression, Diarrhoea, Dyspnoea, Headache, Migraine, Pyrexia
Adverse event was reported on Sep 14, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with anaemia and. Location: UNITED STATES , weighting 145.1 lb, After Procrit was administered, patient had the following side effects: abdominal pain upper, amnesia, depression (What is depression?), diarrhoea, dyspnoea, headache (What is headache?), migraine (What is migraine?), pyrexia. During the same period patient was treated with ACETAMINOPHEN/DEXTROMETHORPHAN HBR/PSEUDOEPHEDRINE HCL (View Acetaminophen/dextromethorphan Hbr/pseudoephedrine Hcl Review and Acetaminophen/dextromethorphan Hbr/pseudoephedrine Hcl Label ), RIBAVIRIN (View Ribavirin Review and Ribavirin Label ), AMITRIPTYLINE HCL (View Amitriptyline Hcl Review and Amitriptyline Hcl Label ), PEG INTRON (View Peg-intron Review and Peg-intron Label ), ZANTAC (View Zantac Review and Zantac Label ), PREVACID (View Prevacid Review and Prevacid Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), TRAZODONE HCL (View Trazodone Hcl Review and Trazodone Hcl Label ).

7009457-3 | Convulsion, Hip Fracture
on Sep 13, 2010 Male patient from UNITED STATES , 65 years of age, weighting 139.1 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: convulsion, hip fracture. Procrit dosage: . During the same period patient was treated with TUMS (View Tums Review and Tums Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ). Patient was hospitalized.


7007170-X | Cold Type Haemolytic Anaemia, Haemoglobin Decreased
on Sep 14, 2010 Male patient from UNITED STATES , weighting 159.2 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient had the following side effects: cold type haemolytic anaemia, haemoglobin decreased. Procrit dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ).

6994362-9 | Haematocrit Decreased
Patient was taking Procrit (View Usage). After Procrit was administered, patient had the following side effects: haematocrit decreased on Sep 08, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 149.0 lb, was diagnosed with renal failure chronic and. Procrit dosage: . During the same period patient was treated with MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), CARDURA (View Cardura Review and Cardura Label ), NORVASC (View Norvasc Review and Norvasc Label ), COREG (View Coreg Review and Coreg Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), IRON (View Iron Review and Iron Label ).

6989327-7 | Asthenia, Central Venous Catheterisation, Diarrhoea, Hospitalisation, Nausea
Adverse event was reported on Sep 08, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with anaemia of malignant disease and. Location: UNITED STATES , weighting 183.2 lb, Patient experienced the following unwanted or unexpected effects: asthenia, central venous catheterisation, diarrhoea, hospitalisation, nausea (What is nausea?). During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ANTINEOPLASTIC AGENTS (View Antineoplastic Agents Review and Antineoplastic Agents Label ). Patient was hospitalized.

6988460-3 | Aplasia Pure Red Cell, Blood Product Transfusion Dependent
on Sep 07, 2010 Male patient from UNITED STATES , weighting 180.3 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). Patient had the following side effects: aplasia pure red cell, blood product transfusion dependent. Procrit dosage: . During the same period patient was treated with ARANESP (View Aranesp Review and Aranesp Label ), TYLENOL (View Tylenol Review and Tylenol Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), COLCHICINE (View Colchicine Review and Colchicine Label ).

6978448-0 | Aplasia Pure Red Cell
on Sep 03, 2010 Female patient from UNITED STATES , 39 years of age, weighting 88.18 lb, was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: aplasia pure red cell. Procrit dosage: .

6973703-2 | Dyspnoea, Pharyngeal Oedema, Pruritus, Urticaria
Patient was taking Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, pharyngeal oedema, pruritus, urticaria on Sep 01, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 201.3 lb, was diagnosed with anaemia and. Procrit dosage: . During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ), COPEGUS (View Copegus Review and Copegus Label ), ALBUTEROL SULATE (View Albuterol Sulate Review and Albuterol Sulate Label ), PROPRANOLOL (View Propranolol Review and Propranolol Label ), DARVOCET N 100 (View Darvocet-n 100 Review and Darvocet-n 100 Label ), LYRICA (View Lyrica Review and Lyrica Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), VITAMIN B 12 (View Vitamin B-12 Review and Vitamin B-12 Label ).

6956510-6 | Epistaxis, Flatulence, Sinus Headache
Adverse event was reported on Jul 29, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with anaemia of malignant disease and. Location: UNITED STATES , 61 years of age, weighting 220.2 lb, Patient had the following side effects: epistaxis, flatulence, sinus headache. During the same period patient was treated with NEUPOGEN (View Neupogen Review and Neupogen Label ), ZANTAC (View Zantac Review and Zantac Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), VITAMIN B1 TAB (View Vitamin B1 Tab Review and Vitamin B1 Tab Label ), ADVIL LIQUI GELS (View Advil Liqui-gels Review and Advil Liqui-gels Label ).

6934503-2 | Burning Sensation, Cold Sweat, Eating Disorder, Hyperhidrosis, Impaired Gastric Emptying, Insomnia, Malaise, Nausea, Nightmare
on Aug 12, 2010 Female patient from UNITED STATES , weighting 117.1 lb, was diagnosed with myelodysplastic syndrome and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: burning sensation, cold sweat, eating disorder (What is eating disorder?), hyperhidrosis, impaired gastric emptying, insomnia, malaise, nausea (What is nausea?), nightmare. Procrit dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ).

6926137-0 | Haemoglobin Decreased
on Aug 06, 2010 Female patient from UNITED STATES , weighting 139.1 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased. Procrit dosage: . During the same period patient was treated with METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ).

6926134-5 | Aplasia Pure Red Cell
Patient was taking Procrit (View Usage). Patient had the following side effects: aplasia pure red cell on Aug 06, 2010 from UNITED STATES Additional patient health information: Male patient , 87 years of age, weighting 175.3 lb, was diagnosed with renal failure chronic and. Procrit dosage: . During the same period patient was treated with ARANESP (View Aranesp Review and Aranesp Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), COLCHICINE (View Colchicine Review and Colchicine Label ).

6924169-X | Memory Impairment, Neuropathy Peripheral, Thinking Abnormal
Adverse event was reported on Aug 05, 2010 by a Male patient taking Procrit (View Usage) (Dosage: ) . Location: UNITED STATES , weighting 250.2 lb, After Procrit was administered, patient had the following side effects: memory impairment, neuropathy peripheral, thinking abnormal. During the same period patient was treated with INTERFERON (View Interferon Review and Interferon Label ).

6911072-4 | Aplasia Pure Red Cell
on Jul 30, 2010 Male patient from UNITED STATES , 87 years of age, weighting 175.3 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: aplasia pure red cell. Procrit dosage: . During the same period patient was treated with ARANESP (View Aranesp Review and Aranesp Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), COLCHICINE (View Colchicine Review and Colchicine Label ).

6901587-7 | Myelodysplastic Syndrome
on Jul 26, 2010 Female patient from UNITED STATES , weighting 140.2 lb, was diagnosed with myelodysplastic syndrome and was treated with Procrit (View Usage). Patient had the following side effects: myelodysplastic syndrome. Procrit dosage: . During the same period patient was treated with FOSAMAX (View Fosamax Review and Fosamax Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), VITAMIN B 12 (View Vitamin B-12 Review and Vitamin B-12 Label ).

6877193-X | Aplasia Pure Red Cell
Patient was taking Procrit (View Usage). After Procrit was administered, patient had the following side effects: aplasia pure red cell on Jul 19, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 140.2 lb, was diagnosed with myelodysplastic syndrome and. Procrit dosage: . During the same period patient was treated with FOSAMAX (View Fosamax Review and Fosamax Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6875239-6 | Anaemia
Adverse event was reported on Jul 16, 2010 by a Male patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , 87 years of age, weighting 175.3 lb, Patient experienced the following unwanted or unexpected effects: anaemia. During the same period patient was treated with ARANESP (View Aranesp Review and Aranesp Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ), COLCHICINE (View Colchicine Review and Colchicine Label ). Patient was hospitalized.

6875207-4 | Cardiogenic Shock, Myocardial Infarction
on Jul 16, 2010 Male patient from UNITED STATES , 49 years of age, was treated with Procrit (View Usage). Patient had the following side effects: cardiogenic shock, myocardial infarction. Procrit dosage: .

6872198-7 | Haematocrit Decreased, Renal Failure
on Jul 15, 2010 Female patient from UNITED STATES , weighting 168.2 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: haematocrit decreased, renal failure. Procrit dosage: . During the same period patient was treated with SERTRALINE HCL (View Sertraline Hcl Review and Sertraline Hcl Label ), ARICEPT (View Aricept Review and Aricept Label ), JANUVIA (View Januvia Review and Januvia Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), NORVASC (View Norvasc Review and Norvasc Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ). Patient was hospitalized.

6863281-0 | Aplasia Pure Red Cell, Arteriovenous Fistula Aneurysm, Complications Of Transplanted Kidney, Diarrhoea, Dyspepsia, Helicobacter Test Positive, Hepatosplenomegaly, Kidney Fibrosis, Parathyroidectomy
Patient was taking Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: aplasia pure red cell, arteriovenous fistula aneurysm, complications of transplanted kidney, diarrhoea, dyspepsia, helicobacter test positive, hepatosplenomegaly, kidney fibrosis, parathyroidectomy on Jul 13, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 210.1 lb, was diagnosed with dialysis (What is dialysis?), renal transplant and. Procrit dosage: . During the same period patient was treated with ARANESP (View Aranesp Review and Aranesp Label ), BACTRIM (View Bactrim Review and Bactrim Label ), CAMPATH (View Campath Review and Campath Label ), DECADRON (View Decadron Review and Decadron Label ), THYMOGLOBULIN (View Thymoglobulin Review and Thymoglobulin Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ), CYCLOSPORINE (View Cyclosporine Review and Cyclosporine Label ). Patient was hospitalized.

6860090-3 | Acinetobacter Infection, Anaemia, Anti-erythropoietin Antibody Positive, Aplasia Pure Red Cell, Bronchitis, Haemosiderosis, Leukocytosis, Lymphopenia, Myelodysplastic Syndrome
Adverse event was reported on Jul 09, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , weighting 146.2 lb, Patient had the following side effects: acinetobacter infection, anaemia, anti-erythropoietin antibody positive, aplasia pure red cell, bronchitis (What is bronchitis?), haemosiderosis, leukocytosis, lymphopenia, myelodysplastic syndrome. During the same period patient was treated with COLCHICINE (View Colchicine Review and Colchicine Label ), PHOSLO (View Phoslo Review and Phoslo Label ), TRAMADOL (View Tramadol Review and Tramadol Label ), CARTIA XT (View Cartia Xt Review and Cartia Xt Label ), DIOVAN (View Diovan Review and Diovan Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ). Patient was hospitalized.

6850655-7 | Pneumonia, Red Blood Cell Count Decreased, Renal Disorder
on Jul 08, 2010 Female patient from UNITED STATES , 46 years of age, was diagnosed with hiv infection (What is hiv infection?) and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: pneumonia (What is pneumonia?), red blood cell count decreased, renal disorder. Procrit dosage: . During the same period patient was treated with NORVIR (View Norvir Review and Norvir Label ), PREZISTA (View Prezista Review and Prezista Label ), ZIDOVUDINE (View Zidovudine Review and Zidovudine Label ), CLONIDINE (View Clonidine Review and Clonidine Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ), LEVEMIR (View Levemir Review and Levemir Label ). Patient was hospitalized.

6849263-3 | Haemoglobin Decreased
on Jul 06, 2010 Female patient from UNITED STATES , weighting 142.2 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased. Procrit dosage: . Patient was hospitalized.

6840184-9 | Anti-erythropoietin Antibody Positive, Aplasia Pure Red Cell, Blood Erythropoietin Decreased, Bone Marrow Failure, Haemochromatosis, Hepatic Cirrhosis, Hepatitis C, Myelodysplastic Syndrome, Neutralising Antibodies Positive
Patient was taking Procrit (View Usage). Patient had the following side effects: anti-erythropoietin antibody positive, aplasia pure red cell, blood erythropoietin decreased, bone marrow failure, haemochromatosis, hepatic cirrhosis, hepatitis c (What is hepatitis c?), myelodysplastic syndrome, neutralising antibodies positive on Jul 06, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 162.0 lb, was diagnosed with anaemia and. Procrit dosage: . During the same period patient was treated with EXJADE (View Exjade Review and Exjade Label ), PREMARIN (View Premarin Review and Premarin Label ), INTERFERON (View Interferon Review and Interferon Label ), RIBAVIRIN (View Ribavirin Review and Ribavirin Label ), ALLEGRA (View Allegra Review and Allegra Label ), COMBIVENT (View Combivent Review and Combivent Label ), PEGINTERFERON ALFA 2A (View Peginterferon Alfa-2a Review and Peginterferon Alfa-2a Label ).

6821788-6 | Anaemia, Weight Decreased
Adverse event was reported on Sep 01, 2009 by a Male patient taking Procrit (View Usage) (Dosage: ) was diagnosed with anaemia and. Location: UNITED STATES , weighting 153.2 lb, After Procrit was administered, patient had the following side effects: anaemia, weight decreased. During the same period patient was treated with CATAPRES (View Catapres Review and Catapres Label ), LOPRESSOR (View Lopressor Review and Lopressor Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), HYDRALAZINE HCL (View Hydralazine Hcl Review and Hydralazine Hcl Label ), VICODIN (View Vicodin Review and Vicodin Label ), ZOCOR (View Zocor Review and Zocor Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ).

6818571-4 | Asthenia, Cardiac Failure Congestive, Clostridial Infection, Fall, Haemoglobin Decreased, Hypertension, Oedema, Oedema Peripheral, Pneumonia
on Jun 28, 2010 Female patient from UNITED STATES , weighting 127.2 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, cardiac failure congestive, clostridial infection, fall (What is fall?), haemoglobin decreased, hypertension, oedema, oedema peripheral, pneumonia (What is pneumonia?). Procrit dosage: . During the same period patient was treated with IRON (View Iron Review and Iron Label ), MULTIVITAMINS AND IRON (View Multivitamins And Iron Review and Multivitamins And Iron Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), HEMATIDE (View Hematide Review and Hematide Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ASA (View Asa Review and Asa Label ), GLUCOSAMINE (View Glucosamine Review and Glucosamine Label ). Patient was hospitalized.

6817974-1 | Amnesia, Dehydration, Hepatic Encephalopathy
on Jun 25, 2010 Male patient from UNITED STATES , weighting 300.3 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient had the following side effects: amnesia, dehydration, hepatic encephalopathy. Procrit dosage: . During the same period patient was treated with CLONIDINE (View Clonidine Review and Clonidine Label ), VITRON C (View Vitron-c Review and Vitron-c Label ), DITROPAN (View Ditropan Review and Ditropan Label ), CORGARD (View Corgard Review and Corgard Label ), ALDACTONE (View Aldactone Review and Aldactone Label ), FINASTERIDE (View Finasteride Review and Finasteride Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), LOSARTAN POSTASSIUM (View Losartan Postassium Review and Losartan Postassium Label ). Patient was hospitalized.

6815684-8 | Arthralgia, Atrial Fibrillation, Bile Duct Stone, Gallbladder Operation, Headache, Myalgia, Weight Decreased
Patient was taking Procrit (View Usage). After Procrit was administered, patient had the following side effects: arthralgia, atrial fibrillation (What is atrial fibrillation?), bile duct stone, gallbladder operation, headache (What is headache?), myalgia, weight decreased on Jun 24, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 81.13 lb, . Procrit dosage: . During the same period patient was treated with SYNTHROID (View Synthroid Review and Synthroid Label ), PROMETRIUM (View Prometrium Review and Prometrium Label ), ESTRADIOL (View Estradiol Review and Estradiol Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ), TYLENOL (View Tylenol Review and Tylenol Label ). Patient was hospitalized.

6811424-7 | Skin Atrophy, Skin Laceration
Adverse event was reported on Apr 22, 2010 by a Male patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , 84 years of age, weighting 163.1 lb, Patient experienced the following unwanted or unexpected effects: skin atrophy, skin laceration. During the same period patient was treated with PROCARDIA XL (View Procardia Xl Review and Procardia Xl Label ), TOPOLOL (View Topolol Review and Topolol Label ), MONOCORDIL (View Monocordil Review and Monocordil Label ), LASIX (View Lasix Review and Lasix Label ), POTASSIUM (View Potassium Review and Potassium Label ), ARICEPT (View Aricept Review and Aricept Label ).

6811423-5 | Fatigue, Haemoglobin Abnormal, Occult Blood Positive, Oedema Peripheral
on Apr 20, 2010 Female patient from UNITED STATES , weighting 108.0 lb, was diagnosed with myelodysplastic syndrome and was treated with Procrit (View Usage). Patient had the following side effects: fatigue, haemoglobin abnormal, occult blood positive, oedema peripheral. Procrit dosage: . During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), VITAMIN B6 (View Vitamin B6 Review and Vitamin B6 Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), CENTRUM (View Centrum Review and Centrum Label ), VITAMIN B 12 (View Vitamin B-12 Review and Vitamin B-12 Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), PLAVIX (View Plavix Review and Plavix Label ), VITAMIN C (View Vitamin C Review and Vitamin C Label ).

6811411-9 | Therapeutic Response Decreased
on Apr 19, 2010 Female patient from UNITED STATES , weighting 242.3 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: therapeutic response decreased. Procrit dosage: . During the same period patient was treated with INDERAL (View Inderal Review and Inderal Label ), BLOOD CELLS, PACKED HUMAN (View Blood Cells, Packed Human Review and Blood Cells, Packed Human Label ), PHOSLO (View Phoslo Review and Phoslo Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), SODIUM BICARBONATE (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), TRILIPIX (View Trilipix Review and Trilipix Label ), TRAZODONE HYDROCHLORIDE (View Trazodone Hydrochloride Review and Trazodone Hydrochloride Label ), NORVASC (View Norvasc Review and Norvasc Label ).

6811410-7 | Anaemia, Blood Count Abnormal, Injection Site Haematoma, Vitamin D Deficiency
Patient was taking Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, blood count abnormal, injection site haematoma, vitamin d deficiency on Apr 12, 2010 from UNITED STATES Additional patient health information: Male patient , weighting 270.3 lb, . Procrit dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ), INSULIN (View Insulin Review and Insulin Label ), INVIRASE (View Invirase Review and Invirase Label ), ABACAVIR (View Abacavir Review and Abacavir Label ).

6811405-3 | Night Sweats
Adverse event was reported on May 04, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , weighting 120.2 lb, Patient had the following side effects: night sweats. During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ), RIBAVIRIN (View Ribavirin Review and Ribavirin Label ), DOXAZOSIN MESYLATE (View Doxazosin Mesylate Review and Doxazosin Mesylate Label ), BENICAR (View Benicar Review and Benicar Label ), PREMARIN (View Premarin Review and Premarin Label ), POTASSIUM (View Potassium Review and Potassium Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), INSPRA (View Inspra Review and Inspra Label ).

6811401-6 | Asthenia, Decreased Appetite, Nausea, Rash
on May 10, 2010 Female patient from UNITED STATES , weighting 111.1 lb, was diagnosed with anaemia of malignant disease and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: asthenia, decreased appetite, nausea (What is nausea?), rash (What is rash?). Procrit dosage: . During the same period patient was treated with EVISTA (View Evista Review and Evista Label ), LYRICA (View Lyrica Review and Lyrica Label ), DETROL (View Detrol Review and Detrol Label ), BLOOD CELLS, PACKED HUMAN (View Blood Cells, Packed Human Review and Blood Cells, Packed Human Label ).

6811400-4 | Haemoglobin Decreased, Weight Decreased
on May 07, 2010 Male patient from UNITED STATES , weighting 200.2 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased, weight decreased. Procrit dosage: .

6811399-0 | Anaemia, Dysphagia, Fatigue, Feeling Cold, Oesophageal Disorder, Pruritus, Rash
Patient was taking Procrit (View Usage). Patient had the following side effects: anaemia, dysphagia, fatigue, feeling cold, oesophageal disorder, pruritus, rash (What is rash?) on May 17, 2010 from UNITED STATES Additional patient health information: Male patient , 87 years of age, . Procrit dosage: . During the same period patient was treated with LISINOPRIL (View Lisinopril Review and Lisinopril Label ), VITAMINS (View Vitamins Review and Vitamins Label ), PRAZOSIN HCL (View Prazosin Hcl Review and Prazosin Hcl Label ), HYDROCODONE (View Hydrocodone Review and Hydrocodone Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ).

6811398-9 | Accidental Exposure, Eye Pain
Adverse event was reported on May 18, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) . Location: UNITED STATES , 40 years of age, After Procrit was administered, patient had the following side effects: accidental exposure, eye pain.

6811393-X | Haematocrit Decreased
on Mar 31, 2010 Female patient from UNITED STATES , weighting 145.1 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: haematocrit decreased. Procrit dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), VERAPAMIL (View Verapamil Review and Verapamil Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), VITAMIN D (View Vitamin D Review and Vitamin D Label ), CALCITRIOL (View Calcitriol Review and Calcitriol Label ), GEMFIBROZIL (View Gemfibrozil Review and Gemfibrozil Label ), NICOTINE (View Nicotine Review and Nicotine Label ).

6811391-6 | Activities Of Daily Living Impaired, Fatigue
on Mar 29, 2010 Male patient from UNITED STATES , weighting 171.1 lb, was treated with Procrit (View Usage). Patient had the following side effects: activities of daily living impaired, fatigue. Procrit dosage: . During the same period patient was treated with PROGRAF (View Prograf Review and Prograf Label ), MYFORTIC (View Myfortic Review and Myfortic Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LIPITOR (View Lipitor Review and Lipitor Label ), NIACIN (View Niacin Review and Niacin Label ), VITAMIN C (View Vitamin C Review and Vitamin C Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ).

6811390-4 | Malaise
Patient was taking Procrit (View Usage). After Procrit was administered, patient had the following side effects: malaise on Apr 08, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 143.1 lb, was diagnosed with renal failure chronic and. Procrit dosage: .

6811389-8 | Ageusia, Dysgeusia, Paraesthesia Oral, Tongue Disorder
Adverse event was reported on Apr 08, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , weighting 69.00 lb, Patient experienced the following unwanted or unexpected effects: ageusia, dysgeusia, paraesthesia oral, tongue disorder. During the same period patient was treated with NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), CRESTOR (View Crestor Review and Crestor Label ), LASIX (View Lasix Review and Lasix Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), ACTOS (View Actos Review and Actos Label ), MULTI VITAMINS (View Multi-vitamins Review and Multi-vitamins Label ), CLARITIN (View Claritin Review and Claritin Label ).

6811388-6 | Abdominal Pain Upper, Acne, Blister, Diarrhoea, Headache, Joint Destruction, Oropharyngeal Blistering, Polyarthritis, Rash
on Apr 08, 2010 Female patient from UNITED STATES , weighting 120.2 lb, was diagnosed with preoperative care and was treated with Procrit (View Usage). Patient had the following side effects: abdominal pain upper, acne (What is acne?), blister, diarrhoea, headache (What is headache?), joint destruction, oropharyngeal blistering, polyarthritis, rash (What is rash?). Procrit dosage: . During the same period patient was treated with ETODOLAC (View Etodolac Review and Etodolac Label ), TYLENOL (View Tylenol Review and Tylenol Label ), VICODIN (View Vicodin Review and Vicodin Label ).

6811385-0 | Haematochezia, Haemoglobin Decreased
on Mar 25, 2010 Male patient from UNITED STATES , weighting 205.3 lb, was diagnosed with renal failure chronic and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: haematochezia, haemoglobin decreased. Procrit dosage: . During the same period patient was treated with INSULIN (View Insulin Review and Insulin Label ), BYETTA (View Byetta Review and Byetta Label ), LASIX (View Lasix Review and Lasix Label ).

6811381-3 | Haemoglobin Increased
Patient was taking Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin increased on Mar 18, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 137.1 lb, was diagnosed with anaemia and. Procrit dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), AMLODIPINE BESYLATE AND ATORVASTATIN CALIUM (View Amlodipine Besylate And Atorvastatin Calium Review and Amlodipine Besylate And Atorvastatin Calium Label ), LIPITOR (View Lipitor Review and Lipitor Label ), PAXIL (View Paxil Review and Paxil Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), JANUVIA (View Januvia Review and Januvia Label ), GLYBURIDE (View Glyburide Review and Glyburide Label ).

6811378-3 | Vision Blurred
Adverse event was reported on Mar 04, 2010 by a Female patient taking Procrit (View Usage) (Dosage: ) was diagnosed with renal failure chronic and. Location: UNITED STATES , 79 years of age, weighting 210.1 lb, Patient had the following side effects: vision blurred.

6811366-7 | Back Pain
on Jan 14, 2010 Male patient from UNITED STATES , weighting 167.1 lb, was diagnosed with myelodysplastic syndrome and was treated with Procrit (View Usage). After Procrit was administered, patient had the following side effects: back pain (What is back pain?). Procrit dosage: . During the same period patient was treated with ACTOS (View Actos Review and Actos Label ), GLIPIZIDE (View Glipizide Review and Glipizide Label ), INSULIN (View Insulin Review and Insulin Label ).

6811361-8 | Blister, Erythema, Rash
on Jan 20, 2010 Female patient from UNITED STATES , weighting 135.1 lb, was diagnosed with anaemia and was treated with Procrit (View Usage). Patient experienced the following unwanted or unexpected effects: blister, erythema, rash (What is rash?). Procrit dosage: . During the same period patient was treated with TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), DETROL (View Detrol Review and Detrol Label ), VICTAN (View Victan Review and Victan Label ), VICODIN (View Vicodin Review and Vicodin Label ), IRON (View Iron Review and Iron Label ).

6811358-8 | Injection Site Haemorrhage
Patient was taking Procrit (View Usage). Patient had the following side effects: injection site haemorrhage on Feb 01, 2010 from UNITED STATES Additional patient health information: Female patient , weighting 163.1 lb, . Procrit dosage: . During the same period patient was treated with PEGASYS (View Pegasys Review and Pegasys Label ), NEUPOGEN (View Neupogen Review and Neupogen Label ).