Sutent and haemoglobin decreased Patient Reports February 11, 2012

Sutent Side Effects Report #5596533-5
Sutent side effect was reported by a Consumer or non-health professional from on Jan 07, 2008. Male patient, weighting 252.0 lb, was diagnosed with transitional cell carcinoma, tumour pain and was treated with Sutent. After drug was administered, patient experienced the following side effects: asthenia, confusional state, fatigue, haemoglobin decreased, hallucination. Sutent dosage: unknown. During the same period patient was treated with MS CONTIN, OMEPRAZOLE, LIPITOR, COMPAZINE, ALLOPURINOL, NIFEDIPINE, VICODIN, ASACOL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5745604-9
Sutent side effect was reported by a Health Professional from UNITED STATES on May 09, 2008. Female patient, weighting 113.1 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with NYSTATIN. Patient recovered.

Sutent Side Effects Report #5890227-4
Sutent side effect was reported by a Health Professional from UNITED STATES on Sept 09, 2008. Male patient, weighting 167.6 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: ascites, haemoglobin decreased, white blood cell count increased. Sutent dosage: unknown. During the same period patient was treated with LISINOPRIL, LIPITOR, DEFERASIROX. Patient recovered.

Sutent Side Effects Report #6018840-4
Sutent side effect was reported by a Health Professional from UNITED STATES on Dec 22, 2008. Male patient, weighting 205.0 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: electrocardiogram st segment depression, haemoglobin decreased, infection

, pneumonia

, pyrexia. Sutent dosage: 37.5 MG, 1X/DAY. During the same period patient was treated with GEMCITABINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6044933-1
Sutent side effect was reported by a Health Professional from UNITED STATES on Dec 11, 2008. Male patient, weighting 205.0 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, infection

, left ventricular dysfunction, pyrexia, troponin increased. Sutent dosage: 37.5 MG, 1X/DAY. During the same period patient was treated with GEMCITABINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5118554-9
Sutent side effect was reported by a Physician from FRANCE on Sept 14, 2006. Female patient, 70 years of age, weighting 130.1 lb, was diagnosed with renal cancer metastatic and was treated with Sutent. After drug was administered, patient experienced the following side effects: asthenia, cholecystitis, constipation

, gastric ulcer haemorrhage, haemoglobin decreased, muscular weakness, peritonitis, thrombocytopenia, vertigo. Sutent dosage: 50 MG (50 MG, DAILY FOR 4 WEEKS OF A 6 WEEKS CYCLE), ORAL. During the same period patient was treated with METOPROLOL, AMLODIPINE, BENAZEPRIL, ALLOPURINOL, GEMFIBROZIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5149846-5
Sutent side effect was reported by a Health Professional from UNITED STATES on Oct 26, 2006. Male patient, 78 years of age, weighting 169.0 lb, was diagnosed with prostate cancer

and was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood phosphorus increased, haemoglobin decreased, syncope. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with DILTIAZEM, ZOCOR, ALTACE, ASPIRIN, PROSCAR. Patient recovered.

Sutent Side Effects Report #5107758-7
Sutent side effect was reported by a Physician from GERMANY on Sept 01, 2006. Female patient, 75 years of age, weighting 187.4 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: diarrhoea, haemoglobin decreased, haemolysis, hepatitis toxic. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with FERRO SANOL DUODENAL, ALLOPURINOL, LOPERAMIDE, BELOC, LEVOTHYROXINE, NORVASC, DIMENHYDRINATE, NOVALGIN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5121565-0
Sutent side effect was reported by a Physician from GERMANY on Sept 20, 2006. Female patient, 75 years of age, weighting 187.4 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, diarrhoea, gamma-glutamyltransferase increased, haemoglobin decreased, haemolysis, hepatitis toxic, jaundice

, vomiting. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with FERRO SANOL DUODENAL, ALLOPURINOL, LOPERAMIDE, METOPROLOL SUCCINATE, LEVOTHYROXINE, NORVASC, DIMENHYDRINATE, NOVALGIN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5906283-0
Sutent side effect was reported by a Physician from MALAYSIA on Sept 23, 2008. Male patient, 65 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, haemoglobin decreased, renal mass. Sutent dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5919836-0
Sutent side effect was reported by a Physician from MALAYSIA on Oct 06, 2008. Male patient, 65 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, haemoglobin decreased, renal mass. Sutent dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5949026-7
Sutent side effect was reported by a Physician from MALAYSIA on Oct 30, 2008. Male patient, 65 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, haemoglobin decreased, renal mass. Sutent dosage: unknown. During the same period patient was treated with METOPROLOL TARTRATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4988059-4
Sutent side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Apr 10, 2006. Male patient, 63 years of age, weighting 152.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: bone pain, haemoglobin decreased, pleural effusion, pneumonia

. Sutent dosage: 50 MG (50 MG, EVERY DAY), ORAL. During the same period patient was treated with NAPROXEN, MORPHINE, DOMPERIDONE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5002684-6
Sutent side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on Apr 27, 2006. Male patient, 63 years of age, weighting 152.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: bone pain, dyspnoea, haemoglobin decreased, pleural effusion, pneumonia

. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NAPROXEN, MORPHINE, DOMPERIDONE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5018357-X
Sutent side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on May 16, 2006. Male patient, 63 years of age, weighting 152.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: bone pain, femur fracture, haemoglobin decreased, pleural effusion, pneumonia

, respiratory failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NAPROXEN, MORPHINE, DOMPERIDONE. Patient was hospitalized. Patient died on 05/15/2006.

Sutent Side Effects Report #5123577-X
Sutent side effect was reported by a Physician from PORTUGAL on Sept 23, 2006. Female patient, 62 years of age, weighting 83.78 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain upper, gastrointestinal mucosal disorder, haematochezia, haemoglobin decreased, hiatus hernia, metastasis, oedema, petechiae, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL; SEE IMAGE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5128257-2
Sutent side effect was reported by a Physician from PORTUGAL on Sept 28, 2006. Female patient, 62 years of age, weighting 83.78 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: disease progression, gastrointestinal haemorrhage, haemoglobin decreased, hiatus hernia, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5760407-7
Sutent side effect was reported by a Physician from PORTUGAL on May 26, 2008. Female patient, 62 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, cerebral haemorrhage, haemoglobin decreased, thrombocytopenia. Sutent dosage: unknown. During the same period patient was treated with ACETAMINOPHEN, FERROUS SULPHATE, METOCLOPRAMIDE, AIRTAL. Patient died on 05/15/2008.

Sutent Side Effects Report #5792607-4
Sutent side effect was reported by a Physician from CHINA on June 17, 2008. Male patient, 62 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abnormal behaviour, depressed level of consciousness, haemoglobin decreased, speech disorder. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5823697-8
Sutent side effect was reported by a Physician from CHINA on July 16, 2008. Male patient, 62 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abnormal behaviour, depressed level of consciousness, haemoglobin decreased, speech disorder. Sutent dosage: unknown. During the same period patient was treated with ENDOSTATIN. Patient recovered.

Sutent Side Effects Report #5088500-5
Sutent side effect was reported by a Physician from LEBANON on Aug 09, 2006. Male patient, 60 years of age, weighting 154.3 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: cardio-respiratory arrest, disseminated intravascular coagulation, fatigue, haematocrit decreased, haemoglobin decreased, haemolysis, jaundice

, leukocytosis, lung infection. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with AMLODIPINE, FOSINOPRIL, NOVONORM, CORTICOSTEROID NOS, LANTUS. Patient was hospitalized. Patient died on 08/06/2006.

Sutent Side Effects Report #5117079-4
Sutent side effect was reported by a Physician from TURKEY on Sept 11, 2006. Male patient, 60 years of age, weighting 136.7 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: diarrhoea, haematocrit decreased, haemoglobin decreased, leukopenia, necrotising fasciitis, neutropenia, red blood cell count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TRAMADOL, FOSINOPRIL, CODEINE SUL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5146618-2
Sutent side effect was reported by a Physician from TURKEY on Oct 19, 2006. Male patient, 60 years of age, weighting 134.5 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: anal infection, diarrhoea, haematocrit decreased, haemoglobin decreased, leukopenia, necrotising fasciitis, neutropenia, pneumonia

, red blood cell count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TRAMADOL, FOSINOPRIL, CODEINE SUL. Patient was hospitalized. Patient died on 09/29/2006.

Sutent Side Effects Report #5018216-2
Sutent side effect was reported by a Physician from TAIWAN, PROVINCE OF CHINA on May 16, 2006. Male patient, 56 years of age, weighting 105.8 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: chills, disease progression, disseminated intravascular coagulation, haemoglobin decreased, jaundice

, neutropenia, respiratory failure, thrombocytopenia. Sutent dosage: unknown. During the same period patient was treated with METOCLOPRAMIDE, DEXAMETHASONE, MEDICON A. Patient died on 05/19/2006.

Sutent Side Effects Report #5150319-4
Sutent side effect was reported by a Physician from GERMANY on Oct 27, 2006. Male patient, 53 years of age, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood alkaline phosphatase increased, blood creatinine increased, blood potassium increased, gamma-glutamyltransferase increased, glomerular filtration rate decreased, haemoglobin decreased, loss of consciousness, sepsis

. Sutent dosage: 50 MG (50 MG, 1 IN 1 D); ORAL. During the same period patient was treated with MORPHINE, DIMETICONE, ENOXAPARIN, RABEPRAZOLE, FUROSEMIDE, LERCANIDIPINE, LEVOTHYROXINE. Patient was hospitalized. Patient died on 07/13/2006.

Sutent Side Effects Report #4974551-5
Sutent side effect was reported by a Physician from POLAND on Mar 28, 2006. Male patient, 53 years of age, weighting 138.9 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood albumin decreased, blood calcium decreased, gastrointestinal haemorrhage, haemoglobin decreased, ileus, prothrombin time prolonged, red blood cell count decreased, retroperitoneal abscess. Sutent dosage: 50 MG (50 MG, 1IN 1 D), ORAL. During the same period patient was treated with RED BLOOD CELLS, CYCLONAMINE, EXACYL, RANITIDINE, MORPHINE, PLASMA, HYOSCINE HYT, HYDROCORTISONE. Patient was hospitalized. Patient died on 03/25/2006.

Sutent Side Effects Report #4974537-0
Sutent side effect was reported by a Physician from SINGAPORE on Mar 28, 2006. Female patient, 36 years of age, weighting 87.74 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: gastritis, haemoglobin decreased, refusal of treatment by patient, vomiting. Sutent dosage: 50 MG (50 MG, OM INTERVAL: DAILY), ORAL. During the same period patient was treated with MORPHINE, OMEPRAZOLE, MYLANTA, PYRIDOXINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4978929-5
Sutent side effect was reported by a Health Professional from SINGAPORE on Apr 03, 2006. Female patient, 36 years of age, weighting 87.74 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: body temperature increased, gastritis, haemoglobin decreased, refusal of treatment by patient. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MORPHINE, OMEPRAZOLE, MYLANTA, PYRIDOXINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5091323-4
Sutent side effect was reported by a Health Professional from BRAZIL on Aug 11, 2006. Male patient, 26 years of age, weighting 143.3 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: disease progression, haemoglobin decreased, neutropenia, pneumomediastinum, purulence, scar

, subcutaneous emphysema, wound dehiscence. Sutent dosage: unknown. During the same period patient was treated with OMEPRAZOLE, BROMOPRIDE, CODEINE, SPARTEINE, HOMATROPINE. Patient was hospitalized. Patient died on 05/05/2006.

Sutent Side Effects Report #4960401-X
Sutent side effect was reported by a Health Professional from BRAZIL on Mar 13, 2006. Male patient, 26 years of age, weighting 154.3 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, infection

, neutropenia, pneumomediastinum, postoperative wound complication, skin necrosis, subcutaneous emphysema, wound dehiscence. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with OMEPRAZOLE, BROMOPRIDE, CODEINE, SPARTEINE, HOMATROPINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5007604-6
Sutent side effect was reported by a Health Professional from BRAZIL on May 08, 2006. Male patient, 26 years of age, weighting 143.3 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: disease progression, haemoglobin decreased, necrosis, neutropenia, pneumomediastinum, postoperative thoracic procedure complication, purulent discharge, subcutaneous emphysema, wound dehiscence. Sutent dosage: 50 MG (50 MG DAILY INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with OMEPRAZOLE, BROMOPRIDE, CODEINE, SPARTEINE, HOMATROPINE. Patient was hospitalized. Patient died on 05/05/2006.

Sutent Side Effects Report #5261247-8
Sutent side effect was reported by a Physician from UNITED STATES on Feb 27, 2007. Male patient, weighting 250.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, papilloedema, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with AVANDIA, ZOCOR, GLIMEPIRIDE, AMBIEN, TRAMADOL, DILANTIN, PRILOSEC, AVODART. Patient recovered.

Sutent Side Effects Report #5306719-2
Sutent side effect was reported by a Health Professional from UNITED STATES on Apr 13, 2007. Female patient, weighting 257.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal abscess, haemoglobin decreased, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with LISINOPRIL, VITAMIN CAP, CENESTIN, BYETTA, ZETIA. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5356145-5
Sutent side effect was reported by a Health Professional from UNITED STATES on June 01, 2007. Female patient, weighting 257.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal abscess, haemoglobin decreased, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with LISINOPRIL, VITAMIN CAP, CENESTIN, BYETTA, ZETIA. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5599335-9
Sutent side effect was reported by a Consumer or non-health professional from NETHERLANDS on Jan 13, 2008. Female patient, weighting 134.5 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: fatigue, haemoglobin decreased, intestinal perforation, musculoskeletal discomfort, weight decreased. Sutent dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, NIFEDIPINE, OXAZEPAM. Patient was hospitalized. Patient died on 01/13/2008.

Sutent Side Effects Report #5744768-0
Sutent side effect was reported by a Health Professional from UNITED STATES on May 12, 2008. Male patient, weighting 280.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, blood creatinine increased, blood urea increased, colon injury, diverticulitis, haematocrit decreased, haemoglobin decreased, intestinal functional disorder, mean cell volume. Sutent dosage: unknown. During the same period patient was treated with PERCOCET, LORAZEPAM, LOVASTATIN, LISINOPRIL AND HYDROCHLOROTHIAZIDE, NOVOLOG, LANTUS. Patient recovered.

Sutent Side Effects Report #5772827-5
Sutent side effect was reported by a Health Professional from UNITED STATES on June 04, 2008. Male patient, weighting 280.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, adhesion

, blood creatinine increased, blood urea increased, colon injury, diverticulitis, haematocrit decreased, haemoglobin decreased, intestinal functional disorder. Sutent dosage: unknown. During the same period patient was treated with ALDESLEUKIN, PERCOCET, LORAZEPAM, LOVASTATIN, LISINOPRIL AND HYDROCHLOROTHIAZIDE, NOVOLOG, LANTUS. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5911353-7
Sutent side effect was reported by a Physician from UNITED STATES on Sept 25, 2008. Male patient, weighting 172.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, angioedema, aspartate aminotransferase increased, blood albumin decreased, haematocrit decreased, haemoglobin decreased. Sutent dosage: unknown. During the same period patient was treated with LISINOPRIL. Patient recovered.

Sutent Side Effects Report #5953828-0
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 04, 2008. Female patient, weighting 134.5 lb, was diagnosed with metastatic renal cell carcinoma, vitamin supplementation, cardiac disorder, nausea

and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, hypocalcaemia, hypoglycaemia, hypokalaemia, syncope. Sutent dosage: unknown. During the same period patient was treated with INTERFERON ALFA, FERROUS SULPHATE, ACETYLSALICYLIC ACID SRT, STOOL SOFTENER, COMPAZINE, LOVAZA, CALTRATE, COENZYME Q. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5958559-9
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 07, 2008. Male patient, weighting 172.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood pressure increased, haematocrit decreased, haemoglobin decreased. Sutent dosage: unknown. During the same period patient was treated with LISINOPRIL. Patient recovered.

Sutent Side Effects Report #6000170-8
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Dec 03, 2008. Male patient was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage urinary tract, urinary retention. Sutent dosage: 50 MG, UNK. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6065049-4
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Jan 24, 2009. Female patient was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage urinary tract, urinary retention. Sutent dosage: 50 MG, UNK. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6065453-4
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Jan 24, 2009. Male patient was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage urinary tract, urinary retention. Sutent dosage: 50 MG, UNK. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6087155-0
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Feb 11, 2009. Female patient was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage urinary tract, urinary retention. Sutent dosage: 50 MG, UNK. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6136544-4
Sutent side effect was reported by a Physician from SOUTH AFRICA on Mar 19, 2009. Female patient was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, duodenal ulcer, haemoglobin decreased, haemorrhage, platelet count decreased. Sutent dosage: 25 MG, UNK. Patient was hospitalized. Patient died on 03/01/2009.

Sutent Side Effects Report #5587158-6
Sutent side effect was reported by a Physician from UNITED KINGDOM on Jan 02, 2008. Female patient, weighting 154.3 lb, was diagnosed with metastatic neoplasm and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood calcium abnormal, cerebral ischaemia, dissociation, grand mal convulsion, haemoglobin decreased, hallucination, visual, headache

, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5440978-0
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient, weighting 134.0 lb, was diagnosed with malignant melanoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haemoglobin decreased, pneumonia

. Sutent dosage: unknown. During the same period patient was treated with TEMOZOLOMIDE, PENTOXIFYLLINE, VITAMIN CAP, CALCIUM CARBONATE, VITAMIN D, TYLENOL, AMBIEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5030667-9
Sutent side effect was reported by a Physician from FRANCE on June 02, 2006. Female patient, 43 years of age, weighting 119.0 lb, was diagnosed with hepatic neoplasm malignant non-resectable and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, haemoglobin decreased, pelvic pain

, peritoneal effusion, peritoneal haemorrhage. Sutent dosage: 50 MG (50 MG, 4 WEEKS INTERVAL: 2 WEEKS), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5165061-3
Sutent side effect was reported by a Physician from FRANCE on Nov 10, 2006. Female patient, 77 years of age, weighting 145.5 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood albumin decreased, blood bilirubin increased, blood lactate dehydrogenase increased, haemoglobin decreased, neoplasm progression, phlebitis, protein total decreased, renal disorder, urinary tract infection

. Sutent dosage: 50 MG, ORAL. During the same period patient was treated with ACEBUTOLOL, LEVOTHYROXINE, DOMPERIDONE, LEUCOVORIN CALCIUM, OMEPRAZOLE. Patient died on 08/12/2006.

Sutent Side Effects Report #4947313-2
Sutent side effect was reported by a Health Professional from UNITED STATES on Mar 01, 2006. Male patient, 77 years of age, weighting 147.7 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anal fistula, anal haemorrhage, haematocrit decreased, haemoglobin decreased, international normalised ratio increased, prothrombin time prolonged, red blood cell count decreased. Sutent dosage: 50 MG (50 MG, ONCE IN MORNING (AM)), ORAL. During the same period patient was treated with DURAGESIC, WELLBUTRIN, XALATAN, LOMOTIL, NORCO, NEXIUM, WARFARIN, COSOPT. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5103991-9
Sutent side effect was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on Aug 29, 2006. Male patient, 76 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, ammonia decreased, dysphagia, fatigue, haemoglobin decreased, lobar pneumonia, septic shock, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5115356-4
Sutent side effect was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on Sept 11, 2006. Male patient, 76 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, ammonia increased, dysphagia, fatigue, haemoglobin decreased, hypotension, lobar pneumonia, pyrexia, septic shock. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5127477-0
Sutent side effect was reported by a Health Professional from TAIWAN, PROVINCE OF CHINA on Sept 25, 2006. Male patient, 76 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, ammonia increased, blood pressure decreased, dysphagia, haemoglobin decreased, platelet count decreased, platelet count increased, pneumonia

, septic shock. Sutent dosage: 50 MG (50 MG, 1 IN 1 D) ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5127519-2
Sutent side effect was reported by a Physician from FRANCE on Sept 27, 2006. Male patient, 76 years of age, was diagnosed with gastrointestinal stromal tumour, pain

and was treated with Sutent. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, blood calcium decreased, blood chloride increased, blood iron decreased, blood uric acid increased, haematocrit decreased, haemoglobin decreased, hepatic failure. Sutent dosage: 37.5 MG (1 IN 1 D) ORAL. During the same period patient was treated with MORPHINE SULPHATE, MORPHINE SULPHATE. Patient was hospitalized. Patient died on 09/08/2006.

Sutent Side Effects Report #5164784-X
Sutent side effect was reported by a Physician from UNITED KINGDOM on Nov 13, 2006. Male patient, 71 years of age, weighting 138.9 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood amylase decreased, blood creatinine increased, blood urea increased, cardiac failure congestive, cough, dizziness

, haemoglobin decreased, hypotension, liver disorder. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with SIMVASTATIN, CARVEDILOL, MORPHINE SULPHATE, LANSOPRAZOLE, LISINOPRIL, FUROSEMIDE, NICORANDIL, CLOPIDOGREL. Patient was hospitalized. Patient died on 03/22/2006.

Sutent Side Effects Report #5009092-2
Sutent side effect was reported by a Physician from UNITED KINGDOM on May 04, 2006. Male patient, 71 years of age, weighting 138.9 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, cardiac failure congestive, cough, dizziness

, haemoglobin decreased, hypotension, liver disorder. Sutent dosage: 50 MG (50 MG, CYCLIC), ORAL. During the same period patient was treated with SIMVASTATIN, CARVEDILOL, MORPHINE SULPHATE, LANSOPRAZOLE, LISINOPRIL, FUROSEMIDE, NICORANDIL, CLOPIDOGREL. Patient was hospitalized. Patient died on 03/22/2006.

Sutent Side Effects Report #5009607-4
Sutent side effect was reported by a Physician from UNITED KINGDOM on May 09, 2006. Male patient, 71 years of age, weighting 138.9 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood creatinine increased, blood urea increased, cardiac failure congestive, dizziness

, haemoglobin decreased, hypertension, hypotension, liver disorder. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with SIMVASTATIN, CARVEDILOL, MORPHINE SULPHATE, LANSOPRAZOLE, LISINOPRIL, FUROSEMIDE, NICORANDIL, CLOPIDOGREL. Patient was hospitalized. Patient died on 03/22/2006.

Sutent Side Effects Report #5156859-6
Sutent side effect was reported by a Physician from UNITED KINGDOM on Nov 02, 2006. Male patient, 66 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood albumin decreased, blood potassium increased, blood sodium decreased, gastrointestinal haemorrhage, gastrointestinal stromal tumour, haemodynamic instability, haemoglobin decreased, hepatic encephalopathy, hepatic failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient died on 11/08/2006.

Sutent Side Effects Report #5167221-4
Sutent side effect was reported by a Physician from UNITED KINGDOM on Nov 17, 2006. Male patient, 66 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood albumin decreased, blood creatinine increased, blood potassium increased, disease progression, fatigue, gastrointestinal haemorrhage, haemoglobin decreased, hepatic encephalopathy, hepatic failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NYSTATIN, DOMPERIDONE, DEXAMETHASONE, LANSOPRAZOLE. Patient was hospitalized. Patient died on 11/08/2006.

Sutent Side Effects Report #4969244-4
Sutent side effect was reported by a Health Professional from UNITED STATES on Mar 23, 2006. Female patient, 66 years of age, weighting 174.0 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: duodenal ulcer, fatigue, haemoglobin decreased, hypothyroidism, thrombosis. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5090849-7
Sutent side effect was reported by a Physician from JAPAN on Aug 10, 2006. Male patient, 59 years of age, weighting 94.80 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: aspiration, blood albumin decreased, choking

, collapse of lung, depressed level of consciousness, emphysema, haemoglobin decreased, hypoxia, neutrophil count decreased. Sutent dosage: 50 MG (50 MG, DAILY EVERYDAY), ORAL. During the same period patient was treated with FERRIC CITRATE, UREA, BETAMETHASONE, AZULENE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4930803-6
Sutent side effect was reported by a Physician from FRANCE on Feb 14, 2006. Male patient, 59 years of age, weighting 65.00 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood pressure diastolic decreased, dyspnoea, haemoglobin decreased, hepatic encephalopathy, hepatic failure, hepatic haemorrhage, hepatomegaly, jaundice

. Sutent dosage: (50 MG, EVERY DAY), ORAL. During the same period patient was treated with MORPHINE SULPHATE, AMARYL, OMEPRAZOLE, ERYTHROPOIETIN, TOTAL PARENTERAL NUTRITION. Patient was hospitalized. Patient died on 03/29/2005.

Sutent Side Effects Report #5177728-1
Sutent side effect was reported by a Health Professional from UNITED STATES on Nov 28, 2006. Female patient, 58 years of age, weighting 106.0 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: ascites, blood creatine increased, blood ph decreased, blood urea increased, dehydration, disseminated intravascular coagulation, fibrin d dimer increased, haemoglobin decreased, hepatic failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with SYNTHROID, PREVACID, MONTELUKAST, ZYRTEC, ALBUTEROL, MOTRIN, TYLENOL PM, ZANTAC. Patient was hospitalized. Patient died on 07/09/2005.

Sutent Side Effects Report #5113791-1
Sutent side effect was reported by a Physician from AUSTRIA on Sept 07, 2006. Male patient, 57 years of age, weighting 132.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: body temperature decreased, disease progression, electroencephalogram abnormal, grand mal convulsion, haemoglobin decreased, hypertension, hypoglycaemia, leukoencephalopathy, nuclear magnetic resonance imaging brain abnormal. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with DURAGESIC, LISINOPRIL, ARANSEP, LASILACTON, ACECOMB. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5020502-7
Sutent side effect was reported by a Physician from AUSTRIA on May 22, 2006. Male patient, 57 years of age, weighting 132.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: aphasia

, areflexia, electroencephalogram abnormal, epilepsy

, grand mal convulsion, haemoglobin decreased, hypertension, hypoglycaemia, leukoencephalopathy. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with DURAGESIC, LISINOPRIL, ARANESP, LASILACTON, ACECOMB. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5386878-6
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on July 03, 2007. Male patient, weighting 171.1 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: asthenia, fatigue, haematocrit decreased, haemoglobin decreased, stent placement, swelling. Sutent dosage: unknown. During the same period patient was treated with UROXATRAL, SIMVASTATIN, PREVACID, GLIMEPIRIDE, HYDROCHLOROTHIAZIDE, LISINOPRIL, DOCUSATE, VITAMIN. Patient recovered.

Sutent Side Effects Report #5394673-7
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on July 11, 2007. Female patient, weighting 173.9 lb, was diagnosed with gastrointestinal stromal tumour, hypertension, depression

, hyperlipidaemia and was treated with Sutent. After drug was administered, patient experienced the following side effects: duodenal ulcer, haemoglobin decreased, hypothyroidism. Sutent dosage: unknown. During the same period patient was treated with ADALAT, MOTRIN, OXYCODONE, HYDROCHLOROTHIAZIDE, POTASSIUM CHLORIDE, ZOLOFT, LIPITOR. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5148097-8
Sutent side effect was reported by a Physician from ITALY on Oct 23, 2006. Male patient, 78 years of age, weighting 141.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abnormal faeces, epistaxis, haemoglobin decreased, syncope, vomiting. Sutent dosage: 50 MG (50 MG, FREQUENCY: DAILY), ORAL. During the same period patient was treated with CLONIDINE, MODURETIC. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5047045-9
Sutent side effect was reported by a Health Professional from UNITED STATES on June 20, 2006. Male patient, 74 years of age, weighting 175.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood albumin decreased, blood fibrinogen abnormal, blood thyroid stimulating hormone increased, coagulopathy, fibrin d dimer increased, haemoglobin decreased, international normalised ratio increased, mental status changes, pneumonia

. Sutent dosage: 50 MG (50 MG, FREQUENCY: QD, INTERVAL: EVERY 28 DAYS), ORAL. During the same period patient was treated with LIPITOR, HUMULIN N, HUMULIN R. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5146442-0
Sutent side effect was reported by a Health Professional from UNITED STATES on Oct 20, 2006. Male patient, 74 years of age, weighting 175.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: bacteraemia, blood albumin decreased, blood thyroid stimulating hormone increased, brain mass, coagulopathy, disease progression, haemoglobin decreased, hypotension, hypothyroidism. Sutent dosage: 50 MG (50 MG, ONC DAILY FOR 28 DAYS), ORAL. During the same period patient was treated with LIPITOR, HUMULIN N, HUMULIN R, CIPROFLOXACIN, FLUCONAZOLE, VANCOMYCIN, SYNTHROID, DAPTOMYCIN. Patient was hospitalized. Patient died on 06/16/2006.

Sutent Side Effects Report #5155713-3
Sutent side effect was reported by a Health Professional from UNITED STATES on Oct 31, 2006. Male patient, 74 years of age, weighting 175.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: bacteraemia, brain mass, coagulopathy, disease progression, fibrin d dimer increased, fibrin degradation products increased, haemoglobin decreased, hypotension, hypothyroidism. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LIPITOR, HUMULIN N, HUMULIN R. Patient was hospitalized. Patient died on 06/16/2006.

Sutent Side Effects Report #5298333-2
Sutent side effect was reported by a Consumer or non-health professional from CANADA on Apr 04, 2007. Female patient, 70 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: asthenia, body temperature decreased, fatigue, haematuria, haemoglobin decreased, kidney infection. Sutent dosage: unknown. During the same period patient was treated with HEPARIN, LOSEC. Patient recovered.

Sutent Side Effects Report #5047442-1
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on June 20, 2006. Male patient, 67 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: fatigue, haemoglobin decreased, pyrexia, white blood cell count decreased. Sutent dosage: 25 MG (25 MG, CYCLIC), ORAL. During the same period patient was treated with TINZAPARIN, MORPHINE, ORAMORPH, ALLOPURINOL, METOCLOPRAMIDE, ENSURE, DICLOFENAC, PROCHLORPERAZINE MALEATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5108942-9
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on Sept 04, 2006. Male patient, 67 years of age, weighting 169.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, c-reactive protein increased, fall

, gamma-glutamyltransferase increased, haemoglobin decreased, loss of consciousness, syncope. Sutent dosage: 50 MG (50 MG, DAILY - INTERVAL: CYCLIC), ORAL. During the same period patient was treated with METFORMIN, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5117931-X
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on Sept 13, 2006. Male patient, 67 years of age, weighting 169.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, fall

, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, loss of consciousness, syncope. Sutent dosage: 50 MG (50 MG, DAILY - INTERVAL: CYCLIC), ORAL. During the same period patient was treated with METFORMIN, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5531775-6
Sutent side effect was reported by a Pharmacist from UNITED STATES on Nov 28, 2007. Female patient, 65 years of age, weighting 147.7 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, condition aggravated, haemodialysis, haemoglobin decreased, multiple sclerosis

, myocardial infarction, nausea

, platelet count decreased, red blood cell schistocytes present. Sutent dosage: 50 MG PO QHS. During the same period patient was treated with SYNTHROID, CLONIDINE, LABETALOL. Patient recovered.

Sutent Side Effects Report #5188355-4
Sutent side effect was reported by a Health Professional from UNITED STATES on Dec 01, 2006. Male patient, 64 years of age, weighting 132.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, atelectasis, bacterial infection

, blood culture positive, disease recurrence, enterobacter bacteraemia, haemoglobin decreased, leukopenia, musculoskeletal pain. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with OXYCODONE, SIMVASTATIN, DOCUSATE, MAGNESIUM OXIDE, MILK OF MAGNESIA, LACTULOSE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5146320-7
Sutent side effect was reported by a Physician from MEXICO on Oct 19, 2006. Female patient, 61 years of age, weighting 123.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: enterocutaneous fistula, haemoglobin decreased. Sutent dosage: unknown. During the same period patient was treated with GLYBURIDE, CHLORTALIDONE, RANITIDINE, AMIKACIN, DIPIRONE, CEFOTAXIME. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5158057-9
Sutent side effect was reported by a Physician from MEXICO on Nov 06, 2006. Female patient, 61 years of age, weighting 123.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: disease recurrence, enterocutaneous fistula, gastrointestinal disorder, haemoglobin decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with GLYBURIDE, CHLORTALIDONE, LOPERAMIDE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5140854-7
Sutent side effect was reported by a Physician from UNITED STATES on Oct 13, 2006. Male patient, 60 years of age, weighting 131.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, hepatic function abnormal, hepatic steatosis, hyperbilirubinaemia, laboratory test abnormal, platelet count decreased, red cell distribution width increased. Sutent dosage: 12.5 MG (12.5 MG, I IN 1 D), ORAL. Patient recovered.

Sutent Side Effects Report #5133246-8
Sutent side effect was reported by a Physician from JAPAN on Oct 05, 2006. Male patient, 58 years of age, weighting 154.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, anal ulcer, aphagia, bacterial infection

, haemoglobin decreased, infected skin ulcer, malaise. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, REBAMIPIDE, MAGNESIUM OXIDE, RANITIDINE HYDROCHLORIDE, POSTERISANTE, LOXOPROFEN, TRIAMCINOLONE ACETONIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5154538-2
Sutent side effect was reported by a Physician from FRANCE on Oct 31, 2006. Male patient, 58 years of age, weighting 132.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood chloride decreased, blood urea decreased, cholangitis, haematocrit decreased, haemoglobin decreased, red blood cell count decreased, shunt stenosis, white blood cell count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient recovered.

Sutent Side Effects Report #5082501-9
Sutent side effect was reported by a Health Professional from UNITED STATES on July 31, 2006. Female patient, 54 years of age, weighting 210.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: diarrhoea, dyspnoea, haemoglobin decreased, malignant neoplasm progression, metastases to bone, nausea

, rash

. Sutent dosage: 50 MG (50 MG, 1 IN 1 D). During the same period patient was treated with OXYCONTIN, OXYCODONE, DILAUDID, VITAMINS. Patient was hospitalized. Patient died on 07/24/2006.

Sutent Side Effects Report #5105019-3
Sutent side effect was reported by a Physician from UNITED STATES on Aug 29, 2006. Female patient, 54 years of age, weighting 210.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: diarrhoea, disease progression, haemoglobin decreased, lung neoplasm malignant, metastases to bone, metastases to central nervous system, nausea

, rash

, respiratory failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D). During the same period patient was treated with OXYCONTIN, OXYCODONE, DILAUDID, VITAMINS. Patient was hospitalized. Patient died on 07/24/2006.

Sutent Side Effects Report #5131719-5
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on Oct 03, 2006. Female patient, 54 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, ascites, blood albumin decreased, blood chloride decreased, blood potassium decreased, carbon dioxide increased, dyspnoea, haemoglobin decreased, mass. Sutent dosage: 37.5 MG (37.5 MG, 1 IN1 D); ORAL. During the same period patient was treated with ZOLPIDEM TARTRATE, IBANDRONIC ACID. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5453127-X
Sutent side effect was reported by a Health Professional from FRANCE on Sept 04, 2007. Female patient, 45 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: diarrhoea, haemoglobin decreased, metrorrhagia, tongue disorder. Sutent dosage: DAILY DOSE:50MG. Patient recovered.

Sutent Side Effects Report #5457561-3
Sutent side effect was reported by a Health Professional from FRANCE on Sept 06, 2007. Female patient, 45 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: ageusia, anaemia, diarrhoea, dry eye, dysphagia, haemoglobin decreased, metrorrhagia, skin discolouration, tinnitus

. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5049200-0
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on June 23, 2006. Female patient, 19 years of age, weighting 82.45 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alopecia, blood albumin decreased, blood bicarbonate decreased, blood calcium decreased, blood sodium decreased, fatigue, haematocrit decreased, haemoglobin decreased, lower respiratory tract infection. Sutent dosage: 50 MG (50 MG, CYCLIC), ORAL. During the same period patient was treated with DEXAMETHASONE, LYRICA, FENTANYL TRANSDERMAL SYSTEM. Patient was hospitalized. Patient died on 06/22/2006.

Sutent Side Effects Report #5302695-7
Sutent side effect was reported by a Physician from UNITED STATES on Apr 09, 2007. Male patient, weighting 145.9 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: contusion, haemoglobin decreased, joint swelling, oedema peripheral, petechiae, pleural effusion. Sutent dosage: unknown. During the same period patient was treated with ANTIEMETICS AND ANTINAUSEANTS, APPETITE STIMULANTS, SYNTHROID. Patient recovered.

Sutent Side Effects Report #5425361-6
Sutent side effect was reported by a Physician from CANADA on Aug 10, 2007. Male patient, weighting 253.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood thyroid stimulating hormone abnormal, dyslipidaemia, dyspnoea, fatigue, haematocrit decreased, haemoglobin decreased, hyperglycaemia, left atrial dilatation. Sutent dosage: unknown. During the same period patient was treated with CHOLESTEROL, INSULIN, NORVASC, HYDROCHLOROTHIAZIDE, METOPROLOL SUCCINATE, AVANDIA, DIAMICRON, EFFEXOR. Patient was hospitalized and became disabled. Patient recovered.

Sutent and haemoglobin decreased

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Sutent and haemoglobin decreased Patient Reports February 11, 2012

side effects of Sutent