Sutent and platelet count decreased Patient Reports February 11, 2012

Sutent Side Effects Report #5757655-9
Sutent side effect was reported by a Physician from INDIA on May 22, 2008. Male patient, 72 years of age, was diagnosed with renal cell carcinoma recurrent and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, conjunctival haemorrhage, headache

, jaundice

, oedema, oral candidiasis, pain

, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with AMLODIPINE. Patient recovered.

Sutent Side Effects Report #5716978-X
Sutent side effect was reported by a Physician from CHINA on Apr 15, 2008. Male patient, 76 years of age, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: anorexia, asthenia, body temperature increased, constipation

, dry mouth, feeling cold, platelet count decreased, skin discolouration, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5890153-0
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Sept 08, 2008. Male patient, 74 years of age, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: parotid gland enlargement, platelet count decreased, pyrexia. Sutent dosage: DAILY DOSE:50MG. Patient recovered.

Sutent Side Effects Report #5911404-X
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Sept 25, 2008. Male patient, 74 years of age, weighting 119.0 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: parotid gland enlargement, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with CIMETIDINE, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5934565-5
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 20, 2008. Male patient, 74 years of age, weighting 119.0 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: parotid gland enlargement, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with CIMETIDINE, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5595339-0
Sutent side effect was reported by a Health Professional from UNITED STATES on Jan 09, 2008. Female patient, weighting 112.4 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haematocrit decreased, monocyte count increased, pancytopenia, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5611426-2
Sutent side effect was reported by a Health Professional from UNITED STATES on Jan 11, 2008. Female patient, weighting 112.4 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: haematocrit decreased, monocyte count increased, pancytopenia, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. 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 #5943651-5
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 28, 2008. Male patient, weighting 145.5 lb, was diagnosed with renal cell carcinoma, pain

and was treated with Sutent. After drug was administered, patient experienced the following side effects: disseminated intravascular coagulation, intestinal perforation, peritonitis, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with MOBIC, ALOSITOL, GASLON, SELBEX, MICARDIS, MAGNESIUM OXIDE, PENTAZOCINE LACTATE. Patient died on 09/01/2008.

Sutent Side Effects Report #5945425-8
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 27, 2008. Female patient, weighting 103.6 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: anorexia, hepatic function abnormal, neutrophil count decreased, oesophagitis, platelet count decreased, pyrexia, white blood cell count decreased. Sutent dosage: DAILY DOSE:50MG. During the same period patient was treated with DEPAS, FENTANYL, VOLTAREN, NOVAMIN, MAGNESIUM OXIDE, PURSENNID, FAMOTIDINE, MORPHINE ELIXIR. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5947427-4
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 29, 2008. Male patient, weighting 101.4 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with NOVAMIN, OXYCONTIN, MICARDIS, TENORMIN, CALONAL, PANTOSIN, MAGNESIUM OXIDE, FENTANYL. Patient died on 10/27/2008.

Sutent Side Effects Report #5950929-8
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 31, 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: disseminated intravascular coagulation, hepatic function abnormal, jaundice

, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with AMLODIN, CORTRIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5969724-9
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 18, 2008. Male patient, weighting 101.4 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: disease progression, platelet count decreased, renal cell carcinoma. Sutent dosage: unknown. During the same period patient was treated with NOVAMIN, OXYCONTIN, MICARDIS, TENORMIN, CALONAL, PANTOSIN, MAGNESIUM OXIDE, FENTANYL. Patient died on 10/27/2008.

Sutent Side Effects Report #5971423-4
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 25, 2008. Male patient, weighting 116.8 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: disseminated intravascular coagulation, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with PREDONINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5974886-3
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 20, 2008. Male patient, weighting 147.7 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, hypoalbuminaemia, neutropenia, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with OXYCONTIN, NOVAMIN, LACTULOSE. Patient was hospitalized. Patient died on 11/09/2008.

Sutent Side Effects Report #5974925-X
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 27, 2008. Male patient, weighting 187.4 lb, was diagnosed with renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: hepatic function abnormal, organising pneumonia, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with OXYCONTIN, OMEPRAL, GASLON, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5148316-8
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Oct 24, 2006. Male patient, 59 years of age, weighting 231.5 lb, was diagnosed with renal cancer metastatic and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure decreased, bone pain, contusion, haematocrit decreased, platelet count decreased, red blood cell count decreased, spinal disorder, white blood cell count decreased. Sutent dosage: 50 MG. During the same period patient was treated with DICLOFENAC, BETAMETHASONE, OMEPRAZOLE. Patient recovered.

Sutent Side Effects Report #5176620-6
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Nov 24, 2006. Male patient, 59 years of age, weighting 231.5 lb, was diagnosed with renal cancer metastatic and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, blood pressure decreased, blood pressure fluctuation, haematocrit decreased, nausea

, platelet count decreased, red blood cell count decreased, white blood cell count decreased. Sutent dosage: 50 MG. During the same period patient was treated with DICLOFENAC, BETAMETHASONE, OMEPRAZOLE, MORPHINE. Patient recovered.

Sutent Side Effects Report #5930234-6
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Oct 13, 2008. Female patient, 46 years of age, was diagnosed with renal cancer metastatic and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, fatigue, gait disturbance, palmar-plantar erythrodysaesthesia syndrome, platelet count decreased, stomatitis, white blood cell count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5575113-1
Sutent side effect was reported by a Pharmacist from FRANCE on Dec 17, 2007. Male patient, weighting 209.4 lb, was diagnosed with renal cancer metastatic and was treated with Sutent. After drug was administered, patient experienced the following side effects: cerebrovascular accident, pain in extremity, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with LANSOPRAZOLE, FINASTERIDE, FLUOXETINE HYDROCHLORIDE, BROMAZEPAM, ACETAMINOPHEN, GRAPE SEED, INSULIN, VALSARTAN. Patient was hospitalized and became disabled. Patient recovered.

Sutent Side Effects Report #5950928-6
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 31, 2008. Male patient, weighting 154.3 lb, was diagnosed with renal cancer and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, blood urea increased, c-reactive protein increased, hyperuricaemia, oedema peripheral, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with VALSARTAN, HOKUNALIN, AMLODIN, HERBAL PREPARATION, LASIX, ALDACTONE, GASTER OD. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5969547-0
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 14, 2008. Male patient, weighting 154.3 lb, was diagnosed with renal cancer and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, anorexia, blood urea increased, c-reactive protein increased, hyperuricaemia, hypoalbuminaemia, oedema peripheral, platelet count decreased, thrombocytopenia. Sutent dosage: unknown. During the same period patient was treated with VALSARTAN, HOKUNALIN, AMLODIN, HERBAL PREPARATION, LASIX, ALDACTONE, GASTER OD. 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 glucose increased, haemoglobin decreased, platelet count 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 #5189538-X
Sutent side effect was reported by a Physician from UNITED STATES on Dec 05, 2006. Female patient, 86 years of age, weighting 156.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood calcium decreased, blood chloride increased, blood copper increased, blood creatinine increased, blood glucose increased, platelet count decreased. Sutent dosage: 25 MG (25 MG, 1 IN 1D). During the same period patient was treated with WARFARIN, TRICOR, CLONIDINE, COMPAZINE, LOPERAMIDE, LASIX, METOPROLOL TARTRATE, ASPIRIN. Patient died on 11/01/2006.

Sutent Side Effects Report #5763053-4
Sutent side effect was reported by a Physician from GERMANY on May 28, 2008. Male patient, 72 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 creatinine increased, confusional state, fatigue, platelet count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5797280-7
Sutent side effect was reported by a Consumer or non-health professional from FRANCE on June 20, 2008. Male patient, 70 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: asthenia, dehydration, platelet count decreased, purpura. Sutent dosage: unknown. During the same period patient was treated with CORTICOSTEROID NOS. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5026269-0
Sutent side effect was reported by a Physician from UNITED KINGDOM on May 26, 2006. Male patient, 69 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: hepatitis

, neutrophil count decreased, platelet count decreased, white blood cell count decreased. Sutent dosage: 50 MG (50 MG, CYCLIC), ORAL; 37.5 MG (37.5 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ATORVASTATIN CALCIUM, ATENOLOL, LANSOPRAZOLE, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4949992-2
Sutent side effect was reported by a Physician from ITALY on Mar 03, 2006. Male patient, 68 years of age, 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: asthenia, cerebral ischaemia, confusional state, fibrin d dimer increased, lethargy, platelet count decreased, troponin increased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with OMEPRAZOLE, LOSARTAN POTASSIUM, METFORMIN, DIAMICRON, ASPIRIN, LORAZEPAM, NADROPARIN CALCIUM, NITROGLYCERIN. Patient was hospitalized. Patient died on 02/05/2006.

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 #5243214-3
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Feb 09, 2007. Male patient, 56 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: back pain

, chest discomfort, chest pain

, fatigue, mouth ulceration, pain in extremity, platelet count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5253585-X
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Feb 19, 2007. Male patient, 56 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: back pain

, chest discomfort, chest pain

, fatigue, mouth ulceration, pain in extremity, platelet count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5370952-4
Sutent side effect was reported by a Consumer or non-health professional from INDIA on June 14, 2007. Male patient, 56 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: back pain

, chest discomfort, chest pain

, coma, fatigue, mouth ulceration, pain in extremity, platelet count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5000123-2
Sutent side effect was reported by a Health Professional from CANADA on Apr 26, 2006. Male patient, 43 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: dyspnoea, hypotension, pain

, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TYLENOL, SENOKOT, COLACE, MORPHINE, OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN, ZOFRAN. Patient was hospitalized. Patient died on 03/17/2006.

Sutent Side Effects Report #5000123-2
Sutent side effect was reported by a Health Professional from CANADA on Apr 26, 2006. Male patient, 43 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: dyspnoea, hypotension, pain

, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ACETAMINOPHEN, SENOKOT, COLACE, MORPHINE, OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN, ZOFRAN. Patient was hospitalized. Patient died on 03/17/2006.

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 #5524251-8
Sutent side effect was reported by a Pharmacist from UNITED STATES on Nov 09, 2007. Female patient, weighting 147.7 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, blood lactate dehydrogenase increased, blood uric acid increased, hepatic enzyme increased, metastases to stomach, neurological symptom, platelet count decreased, protein total increased, red blood cell schistocytes present. Sutent dosage: unknown. During the same period patient was treated with NIFEDIPINE, HYDROCHLOROTHIAZIDE, SYNTHROID. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5772836-6
Sutent side effect was reported by a Health Professional from UNITED STATES on June 04, 2008. Male patient, weighting 304.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: contusion, ecchymosis, haematuria, oedema peripheral, oropharyngeal candidiasis, performance status decreased, platelet count decreased, pyrexia, urinary incontinence

. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5809196-8
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on July 02, 2008. Female patient, weighting 125.0 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: burning mouth syndrome, haemorrhage, lethargy, nausea

, oral pain, platelet count decreased, red blood cell count decreased, somnolence, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. 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 #6070586-2
Sutent side effect was reported by a Physician from UNITED STATES on Jan 28, 2009. Female patient was diagnosed with metastases to kidney and was treated with Sutent. After drug was administered, patient experienced the following side effects: platelet count decreased, thrombotic thrombocytopenic purpura. Sutent dosage: 50 MG, 1X/DAY. Patient died.

Sutent Side Effects Report #5043289-0
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on July 03, 2006. Male patient, 55 years of age, weighting 163.1 lb, was diagnosed with hepatic neoplasm malignant and was treated with Sutent. After drug was administered, patient experienced the following side effects: neutrophil count decreased, platelet count decreased. Sutent dosage: 37.5 MG QD ORAL. Patient recovered.

Sutent Side Effects Report #5070162-4
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 02, 2006. Male patient, 55 years of age, weighting 163.1 lb, was diagnosed with hepatic neoplasm malignant and was treated with Sutent. After drug was administered, patient experienced the following side effects: neutrophil count decreased, platelet count decreased. Sutent dosage: 37.5 MG QD ORAL. During the same period patient was treated with PANZEM. Patient recovered.

Sutent Side Effects Report #5664820-8
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 04, 2008. Female patient, weighting 112.0 lb, was diagnosed with glioblastoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: blood sodium decreased, cerebral haemorrhage, fall

, loss of consciousness, neoplasm progression, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with BACTRIM DS, CALCIUM WITH VITAMIN D, COMPAZINE, LIPITOR, RITALIN, LEVOTHYROXINE. 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 #4938519-7
Sutent side effect was reported by a Physician from UNITED KINGDOM on Feb 17, 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: aspartate aminotransferase increased, blood creatinine increased, cellulitis

, dyspnoea, hyperbilirubinaemia, platelet count decreased. Sutent dosage: 50 MG (50 MG, DAILY INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with NICORANDIL, OMEPRAZOLE, ATENOLOL, SIMVASTATIN, LISINOPRIL, CLOPIDOGREL BISULPHATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4947917-7
Sutent side effect was reported by a Physician from UNITED STATES on Mar 09, 2006. Male patient, 65 years of age, weighting 160.0 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anorexia, aspartate aminotransferase increased, blood bilirubin increased, body temperature increased, glossodynia, haemolytic anaemia, memory impairment, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PANTOTHENIC ACID, VITAMIN, ZINC SULPHATE, ADVAIR DISKUS, ALBUTEROL, ZETIA, SPIRIVA. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5099698-7
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Aug 21, 2006. Male patient, 38 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: blood albumin decreased, blood pressure increased, blood sodium decreased, gingival bleeding, platelet count decreased, renal failure acute. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TRAMADOL, AMLODIPINE, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5099825-1
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Aug 21, 2006. Male patient, 38 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: blood albumin decreased, blood pressure increased, blood sodium decreased, gingival bleeding, platelet count decreased, renal failure acute. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL; SEE IMAGE. During the same period patient was treated with TRAMADOL, AMLODIPINE, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5117936-9
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Sept 13, 2006. Male patient, 38 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: blood albumin decreased, blood pressure diastolic increased, blood pressure systolic increased, blood sodium decreased, gingival bleeding, platelet count decreased, renal failure acute. Sutent dosage: 37.5 MG (37.5 MG, 1 IN 1 D), ORAL. During the same period patient was treated with TRAMADOL, AMLODIPINE, MAGNESIUM OXIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5933232-1
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 16, 2008. Male patient, weighting 92.59 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, laryngeal oedema, platelet count decreased. Sutent dosage: DAILY DOSE:50MG. During the same period patient was treated with NAIXAN, BIOFERMIN, LANSOPRAZOLE, RABEPRAZOLE, HOKUNALIN, AZUNOL, LAFUTIDINE, FLOMOX. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5943594-7
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Oct 27, 2008. Male patient, weighting 112.4 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, hyperbilirubinaemia, hypoalbuminaemia, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with FIRSTCIN, PENTCILLIN, FENTANYL, FLUMARIN, ADONA, TRANSAMIN. Patient was hospitalized. Patient died on 01/01/2008.

Sutent Side Effects Report #5967496-5
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 13, 2008. Male patient, weighting 92.59 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, cardiac failure, face oedema, laryngeal oedema, platelet count decreased. Sutent dosage: DAILY DOSE:50MG. During the same period patient was treated with NAIXAN, BIOFERMIN, TAKEPRON, RABEPRAZOLE, HOKUNALIN, AZUNOL, LAFUTIDINE, FLOMOX. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5974134-4
Sutent side effect was reported by a Consumer or non-health professional from JAPAN on Nov 19, 2008. Male patient, weighting 112.4 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, disease progression, gastrointestinal stromal tumour, hyperbilirubinaemia, hypoalbuminaemia, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with FIRSTCIN, PENTCILLIN, FENTANYL, FLUMARIN, ADONA, TRANSAMIN. Patient was hospitalized. Patient died on 01/01/2008.

Sutent Side Effects Report #5377709-9
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on June 21, 2007. Female patient, 78 years of age, weighting 167.6 lb, was diagnosed with cervix carcinoma, ill-defined disorder and was treated with Sutent. After drug was administered, patient experienced the following side effects: international normalised ratio increased, metrorrhagia, platelet count decreased, vaginal haemorrhage. Sutent dosage: unknown. During the same period patient was treated with INNOHEP. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5406548-5
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on July 25, 2007. Female patient, 78 years of age, weighting 167.6 lb, was diagnosed with cervix carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: hyponatraemia, international normalised ratio increased, platelet count decreased, vaginal haemorrhage. Sutent dosage: unknown. During the same period patient was treated with INNOHEP. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5655999-2
Sutent side effect was reported by a Physician from UNITED KINGDOM on Feb 26, 2008. Female patient, 81 years of age, was diagnosed with pyrexia and was treated with Sutent. After drug was administered, patient experienced the following side effects: disseminated intravascular coagulation, platelet count decreased, pyrexia. Sutent dosage: unknown. During the same period patient was treated with ANTIBIOTICS. Patient recovered.

Sutent Side Effects Report #5533427-5
Sutent side effect was reported by a Pharmacist from ARGENTINA on Nov 22, 2007. Male patient, 78 years of age, weighting 220.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anaemia, anorexia, dry mouth, fatigue, hepatotoxicity, mouth ulceration, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5121292-X
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2006. Male patient, 76 years of age, weighting 196.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood parathyroid hormone increased, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with PROTONIX, ZOCOR, TOPROL, NORVASC, ASPIRIN, RENAGEL, SENSIPAR. Patient recovered.

Sutent Side Effects Report #5177350-7
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Nov 24, 2006. Male patient, 67 years of age, weighting 209.4 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: ageusia, anaemia, anorexia, mediastinum neoplasm, pallor, platelet count decreased, skin discolouration, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with METHYLPREDNISOLONE, TERAZOSIN. 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 #4998411-9
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on Apr 24, 2006. Female patient, 65 years of age, weighting 148.4 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, chromaturia, gamma-glutamyltransferase increased, headache

, infection

, pharyngolaryngeal pain, platelet count decreased, red blood cell sedimentation rate increased. Sutent dosage: 50 MG (50 MG, DAILY INTERVAL: CYCLIC), ORAL. During the same period patient was treated with ATENOLOL, BENDROFLUAZIDE, LIPITOR, LACTULOSE, SENOKOT, FYBOGEL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5065480-X
Sutent side effect was reported by a Health Professional from JAPAN on July 12, 2006. Male patient, 64 years of age, weighting 152.8 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anal fistula, condition aggravated, haemorrhoidal haemorrhage, platelet count decreased. Sutent dosage: 50 MG (50 MG, DAILY - INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, FLUNITRAZEPAM, BROTIZOLAM, ZOPICLONE, DIFLUPREDNATE, SENNA LEAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5076564-4
Sutent side effect was reported by a Health Professional from JAPAN on July 25, 2006. Male patient, 64 years of age, weighting 152.8 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anal fistula, disease progression, haemorrhoidal haemorrhage, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, FLUNITRAZEPAM, BROTIZOLAM, ZOPICLONE, DIFLUPREDNATE, SENNA LEAF, POSTERISANTE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5131677-3
Sutent side effect was reported by a Physician from JAPAN on Oct 03, 2006. Male patient, 64 years of age, weighting 152.8 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: anal fistula, condition aggravated, haemorrhoidal haemorrhage, platelet count decreased. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, FLUNITRAZEPAM, BROTIZOLAM, ZOPICLONE, DIFLUPREDNATE, SENNA LEAF. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4921441-X
Sutent side effect was reported by a Physician from COLOMBIA on Feb 06, 2006. Female patient, 63 years of age, weighting 127.9 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood potassium decreased, hypocalcaemia, hyponatraemia, platelet count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5121438-3
Sutent side effect was reported by a Physician from UNITED STATES on Sept 19, 2006. Female patient, 60 years of age, weighting 131.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: hepatic function abnormal, platelet count decreased. Sutent dosage: 12.5 MG (12.5 MG, 1 IN 1 D), ORAL. 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 #5165096-0
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Nov 09, 2006. Male patient, 59 years of age, weighting 242.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal haematoma, blood pressure diastolic increased, bone lesion, implant site pain, platelet count decreased, radioisotope scan abnormal, red blood cell count decreased, scintigraphy, white blood cell count decreased. Sutent dosage: 50 MG. During the same period patient was treated with DICLOFENAC, DELTISONA B, MORPHINE, RELIVERAN. Patient recovered.

Sutent Side Effects Report #5176624-3
Sutent side effect was reported by a Physician from GERMANY on Nov 27, 2006. Female patient, 59 years of age, weighting 127.9 lb, was diagnosed with urinary tract infection

and was treated with Sutent. After drug was administered, patient experienced the following side effects: acute hepatic failure, anuria, cardiovascular disorder, diarrhoea, hypoglycaemia, hypothermia

, platelet count decreased, urinary tract infection

, vomiting. Sutent dosage: 50 MG, ORAL. During the same period patient was treated with COTRIM. Patient was hospitalized. Patient died on 01/01/2006.

Sutent Side Effects Report #5341536-9
Sutent side effect was reported by a Pharmacist from UNITED STATES on May 30, 2007. Male patient, 57 years of age, weighting 206.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood creatinine increased, dehydration, diarrhoea, nausea

, pain

, platelet count decreased. Sutent dosage: 50 MG DAILY PO. During the same period patient was treated with METFORMIN, GLIPIZIDE, ASPIRIN, ASCORBIC ACID, ATENOLOL, CLONIDINE, FOLIC ACID, LISINOPRIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5030630-8
Sutent side effect was reported by a Physician from UNITED STATES on June 02, 2006. Male patient, 55 years of age, weighting 166.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: asthenia, blood glucose increased, dehydration, hypotension, nausea

, platelet count decreased, renal failure acute, troponin i increased. Sutent dosage: 37.5 MG (37.5 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MAXZIDE, POTASSIUM CHLORIDE, METOPROLOL SUCCINATE, GEMFIBROZIL, OXYCONTIN, OXYCODONE, CELECOXIB, FLUTICASONE PROPIONATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4974388-7
Sutent side effect was reported by a Health Professional from UNITED STATES on Mar 28, 2006. Male patient, 46 years of age, weighting 231.7 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood culture positive, catheter related infection, disease progression, hyperglycaemia, hyperhidrosis, klebsiella bacteraemia, platelet count decreased, staphylococcal infection

, tachypnoea. Sutent dosage: 50 MG (50 MG, QD X 28D WITH 14 DAY REST), ORAL. During the same period patient was treated with FIBERCON, COUMADIN, DEXAMETHASONE, LIDOCAINE, TOPROL, OXYCONTIN, PANTOPRAZOLE, SENNOSIDES. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5083631-8
Sutent side effect was reported by a Physician from JAPAN on Aug 02, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, hepatic function abnormal, malaise, malignant neoplasm progression, platelet count decreased, pyrexia. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTOBACILLUE BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ASPIRIN, DICLOFENAC, LOXOPROFEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5091899-7
Sutent side effect was reported by a Physician from JAPAN on Aug 14, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, disease progression, hepatic function abnormal, malaise, platelet count decreased, pyrexia, white blood cell count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ASPIRIN, DICLOFENAC, LOXOPROFEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5104077-X
Sutent side effect was reported by a Health Professional from JAPAN on Aug 28, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, computerised tomogram abnormal, decreased appetite, disease progression, hepatic function abnormal, malaise, platelet count decreased, pyrexia. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ASPIRIN, DICLOFENAC, LOXOPROFEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5121530-3
Sutent side effect was reported by a Health Professional from JAPAN on Aug 28, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, hepatic function abnormal, malaise, platelet count decreased, pyrexia, white blood cell count decreased, yellow skin. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ASPIRIN, DICLOFENAC, LOXOPROFEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5009604-9
Sutent side effect was reported by a Physician from JAPAN on May 09, 2006. Female patient, 42 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, hepatic function abnormal, malaise, platelet count decreased, pyrexia, white blood cell count decreased, yellow skin. Sutent dosage: 50 MG (50 MG DAILY-INTERVAL: EVERY DAY) ORAL. During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE, ASPIRIN, DICLOFENAC. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5018277-0
Sutent side effect was reported by a Physician from JAPAN on May 17, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, hepatic function abnormal, malaise, platelet count decreased, pyrexia, white blood cell count decreased, yellow skin. Sutent dosage: 50 MG (50 MG, DAILY- INTERVAL: EVERYDAY), ORAL. During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ACETYLSALICYLIC ACID SRT, DICLOFENAC, LOXOPROFEN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5030115-9
Sutent side effect was reported by a Physician from JAPAN on June 01, 2006. Female patient, 42 years of age, weighting 99.87 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, decreased appetite, hepatic function abnormal, malaise, platelet count decreased, pyrexia, white blood cell count decreased, yellow skin. Sutent dosage: 50 MG (50 MG, DAILY). During the same period patient was treated with LACTOBACILLUS BIFIDUS, LOPERAMIDE HYDROCHLORIDE, ASPIRIN, DICLOFENAC, LOXOPROFEN )LOXOPROFEN SOIDUM). Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5227829-4
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Jan 22, 2007. Male patient, weighting 177.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, malaise, platelet count decreased, red blood cell count decreased, unresponsive to stimuli, vomiting, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient died on 01/15/2007.

Sutent Side Effects Report #5288950-8
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 29, 2007. Male patient, weighting 177.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, malaise, platelet count decreased, red blood cell count decreased, unresponsive to stimuli, vomiting, white blood cell count decreased. Sutent dosage: unknown. Patient was hospitalized. Patient died on 01/15/2007.

Sutent Side Effects Report #5447851-2
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Aug 28, 2007. Female patient, weighting 121.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: dyspnoea, hypertension, oedema peripheral, pain in extremity, platelet count decreased, post procedural haemorrhage, visual disturbance, white blood cell count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5467386-0
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Aug 28, 2007. Female patient, weighting 121.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: dyspnoea, hypertension, oedema peripheral, pain in extremity, platelet count decreased, post procedural haemorrhage, visual disturbance, white blood cell count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5481011-4
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Sept 27, 2007. Female patient, weighting 121.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: dyspnoea, erythema, hypertension, oedema peripheral, pain in extremity, platelet count decreased, post procedural haemorrhage, visual disturbance, white blood cell count decreased. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5484759-0
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Oct 01, 2007. Female patient, weighting 160.9 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood pressure increased, hepatitis

, platelet count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, CLONAZEPAM, METFORMIN. Patient recovered.

Sutent Side Effects Report #5503382-2
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Oct 22, 2007. Female patient, weighting 160.9 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, liver disorder, platelet count decreased, red blood cell count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, CLONAZEPAM, METFORMIN. Patient recovered.

Sutent Side Effects Report #5510378-3
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Oct 29, 2007. Female patient, weighting 160.9 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: blood pressure increased, liver disorder, platelet count decreased, red blood cell count decreased, white blood cell count decreased. Sutent dosage: unknown. During the same period patient was treated with ENALAPRIL MALEATE, CLONAZEPAM, METFORMIN. Patient recovered.

Sutent and platelet count decreased

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Sutent and platelet count decreased Patient Reports February 11, 2012

side effects of Sutent