Sutent and aspartate aminotransferase increased Patient Reports February 11, 2012

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 #4970916-6
Sutent side effect was reported by a Pharmacist from UNITED STATES on Apr 11, 2006. Female patient, 75 years of age, weighting 114.2 lb, was diagnosed with neoplasm malignant and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5339072-9
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on May 18, 2007. Male patient, 13 years of age, weighting 73.19 lb, was diagnosed with neoplasm and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, dehydration, hypokalaemia, hypophosphataemia, hypotension, hypothyroidism, weight decreased. Sutent dosage: unknown. During the same period patient was treated with POTASSIUM IODIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5353000-1
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on May 31, 2007. Male patient, 13 years of age, weighting 73.19 lb, was diagnosed with neoplasm and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, dehydration, fatigue, hypokalaemia, hypophosphataemia, hypotension, hypothyroidism. Sutent dosage: unknown. During the same period patient was treated with POTASSIUM IODIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5073152-0
Sutent side effect was reported by a Physician from BELGIUM on July 26, 2006. Male patient, 72 years of age, weighting 169.8 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 lactate dehydrogenase increased, disseminated intravascular coagulation, dyspnoea, faecaloma, haemolytic uraemic syndrome, rectal haemorrhage. Sutent dosage: 37.5 MG (37.5 MG, DAILY, INTERVAL: 4 WKS ON, 2 WKS OFF), ORAL. During the same period patient was treated with ALDACTAZINE, AMIODARONE, LOSARTAN POSTASSIUM, DICLOFENAC, ALLOPURINOL, LORMETAZEPAM, ACETAMINOPHEN W. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5083098-X
Sutent side effect was reported by a Physician from BELGIUM on July 31, 2006. Male patient, 72 years of age, weighting 169.8 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, anorexia, aspartate aminotransferase increased, blood lactate dehydrogenase increased, constipation

, disseminated intravascular coagulation, dyspnoea, faecaloma, haemolytic uraemic syndrome. Sutent dosage: 37.5 MG (37.5 MG, DIALY, INTERVAL: 4 WKS ON, 2 WKS OFF), ORAL. During the same period patient was treated with ALDACTAZINE, AMIODARONE, LOSARTAN POSTASSIUM, DICLOFENAC, ALLOPURINOL, LORMETAZEPAM, ACETAMINOPHEN W. Patient was hospitalized. Patient died on 07/29/2006.

Sutent Side Effects Report #5301172-7
Sutent side effect was reported by a Physician from FRANCE on Apr 06, 2007. 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: alanine aminotransferase increased, anaemia, anorexia, aspartate aminotransferase increased, asthenia, blood creatine phosphokinase increased, mucosal inflammation, muscular weakness. Sutent dosage: DAILY DOSE:50MG. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5641963-6
Sutent side effect was reported by a Consumer or non-health professional from INDIA on Feb 15, 2008. Male patient, 63 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: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, blood bilirubin increased, epistaxis, lung infection, oropharyngeal blistering, pyrexia. Sutent dosage: unknown. Patient was hospitalized. Patient died.

Sutent Side Effects Report #5700346-0
Sutent side effect was reported by a Physician from INDIA on Mar 28, 2008. Male patient, 63 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: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, blood bilirubin increased, disease progression, epistaxis, lung infection, metastatic renal cell carcinoma, oropharyngeal blistering. Sutent dosage: unknown. Patient was hospitalized. Patient died on 02/05/2008.

Sutent Side Effects Report #5053964-X
Sutent side effect was reported by a Physician from BRAZIL on June 29, 2006. Male patient, 61 years of age, weighting 148.2 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, cachexia, confusional state, dialysis

, dyspnoea, endotracheal intubation complication, hemiparesis, hepatotoxicity. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with GLYBURIDE, ATENOLOL, MINOXIDIL, CALCIUM ACETATE, METFORMIN, ENALAPRIL MALEATE, FUROSEMIDE, IRBESARTAN. Patient was hospitalized. Patient died on 06/21/2006.

Sutent Side Effects Report #5159263-X
Sutent side effect was reported by a Physician from BRAZIL on Nov 08, 2006. Male patient, 61 years of age, weighting 148.2 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, cachexia, confusional state, delirium, dialysis

, dyspnoea, hepatotoxicity, opportunistic infection, renal failure acute, respiratory tract infection, tumour lysis syndrome. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with GLIBENCLAMIDE, ATENOLOL, MINOXIDIL, CALCIUM ACETATE, METFORMIN, ENALAPRIL, FUROSEMIDE, IRBESARTAN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5030117-2
Sutent side effect was reported by a Health Professional from BRAZIL on June 01, 2006. Male patient, 61 years of age, weighting 148.2 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, confusional state, dialysis

, dyspnoea, hemiparesis, hepatotoxicity, metabolic disorder

, metastases to central nervous system. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with GLYBURIDE, ATENOLOL, MINOXIDIL, CALCIUM ACETATE, METFORMIN, ENALAPRIL MALEATE, FUROSEMIDE, IRBESARTAN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5042580-1
Sutent side effect was reported by a Physician from BRAZIL on June 14, 2006. Male patient, 61 years of age, weighting 148.2 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, cachexia, confusional state, device related infection, dialysis

, dyspnoea, hemiparesis, hepatotoxicity. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with GLYBURIDE, ATENOLOL, MINOXIDIL, CALCIUM ACETATE, METFORMIN, ENALAPRIL MALEATE, FUROSEMIDE, IRBESARTAN. Patient was hospitalized and became disabled. Patient recovered.

Sutent Side Effects Report #5113638-3
Sutent side effect was reported by a Physician from MALAYSIA on Sept 07, 2006. Male patient, 57 years of age, weighting 107.1 lb, was diagnosed with metastatic renal cell carcinoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, dehydration, hyperbilirubinaemia, renal impairment, vomiting. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ALLOPURINOL, MORPHINE, COLCHICUM JTL LIQ, RANITIDINE, BENZYDAMINE, XYLOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5320681-8
Sutent side effect was reported by a Physician from FRANCE on Apr 27, 2007. Male patient, weighting 132.3 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, anaemia, anorexia, aspartate aminotransferase increased, asthenia, blood creatine phosphokinase increased, mucosal inflammation, muscular weakness, rhabdomyolysis. Sutent dosage: unknown. During the same period patient was treated with NITRENDIPINE, FUROSEMIDE, ALLOPURINOL, ROSUVASTATIN, ASPIRIN, TRIMETAZIDINE DIHYDROCHLORIDE, FLECAINIDE ACETATE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5160595-X
Sutent side effect was reported by a Physician from UNITED STATES on Nov 08, 2006. Female patient 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. Sutent dosage: 50 MG (50 MG, QD). Patient recovered.

Sutent Side Effects Report #5588612-3
Sutent side effect was reported by a Physician from GERMANY on Jan 03, 2008. Male patient, weighting 156.5 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 alkaline phosphatase increased, chills, cough, dyspepsia, gamma-glutamyltransferase increased, hyperhidrosis, pyrexia. Sutent dosage: unknown. During the same period patient was treated with CONTRAST MEDIA, ALLOPURINOL, TORSEMIDE. 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 #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 #5322819-5
Sutent side effect was reported by a Consumer or non-health professional from on Apr 30, 2007. Female patient, 58 years of age, weighting 152.7 lb, was diagnosed with leiomyosarcoma and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, aspartate aminotransferase increased, international normalised ratio increased. Sutent dosage: unknown. During the same period patient was treated with WARFARIN, ATENOLOL, OXYCODONE, PROMETHAZINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5022181-1
Sutent side effect was reported by a Physician from FRANCE on May 23, 2006. Male patient, 65 years of age, weighting 198.4 lb, was diagnosed with hepatic neoplasm malignant and was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, confusional state, gamma-glutamyltransferase increased, hyperbilirubinaemia, somnolence, thrombocytopenia. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PROPRANOLOL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5000079-2
Sutent side effect was reported by a Pharmacist from SPAIN on Apr 20, 2006. Male patient, 74 years of age, weighting 121.3 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, aspartate aminotransferase increased, back pain

, blood lactate dehydrogenase increased, chest pain

, discomfort, hyperuricaemia, renal impairment, tumour lysis syndrome. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5103799-4
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Aug 29, 2006. Male patient, 71 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 pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, azotaemia, blood albumin decreased, blood creatinine increased, mental status changes, protein total decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MEGESTROL ACETATE, DOMPERIDONE. 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 #4954288-9
Sutent side effect was reported by a Physician from UNITED KINGDOM on Mar 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: aspartate aminotransferase increased, bacteria sputum identified, blood creatinine increased, blood urea increased, candidiasis, cardiac failure congestive, cellulitis

, chest pain

, condition aggravated. Sutent dosage: 50 MG (50 MG, CYCLIC), 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 #4968701-4
Sutent side effect was reported by a Physician from UNITED KINGDOM on Mar 22, 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, cardiac failure congestive, cellulitis

, condition aggravated, haemophilus infection, jaundice

, liver disorder, lower respiratory tract infection. Sutent dosage: 50 MG (50 MG, CYCLIC), ORAL. During the same period patient was treated with NICORANDIL, OMEPRAZOLE, ATENOLOL, SIMVASTATIN, LISINOPRIL, CLOPIDOGREL. 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 #4967209-X
Sutent side effect was reported by a Physician from UNITED STATES on Mar 21, 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, glossodynia, haemolytic anaemia, memory impairment, myocardial infarction, pulmonary oedema, thrombocytopenia. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PATHOTHENIC ACID, VITAMIN, ZINC SULPHATE, ADVIR, ALBUTEROL, ZETIA, SPIRIVA. Patient was hospitalized. Patient died on 03/14/2006.

Sutent Side Effects Report #5086133-8
Sutent side effect was reported by a Physician from JAPAN on Aug 07, 2006. Male patient, 61 years of age, weighting 126.5 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood amylase increased, discomfort, disease progression, gamma-glutamyltransferase increased, gastritis, hypoproteinaemia. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with INSULIN, DIMETICONE, AZULENE, GLUTAMINE, ALBUMIN, ASPARTATE CALCIUM. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4961109-7
Sutent side effect was reported by a Physician from JAPAN on Mar 15, 2006. Male patient, 61 years of age, weighting 126.5 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 albumin decreased, eyelid oedema, gastritis, hypoproteinaemia, nephrotic syndrome, oedema peripheral, protein urine present. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with INSULIN, DIMETICONE, AZULENE, GLUTAMINE, ALBUMIN, ASPARTATE CALCIUM. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5045929-9
Sutent side effect was reported by a Physician from JAPAN on June 21, 2006. Male patient, 61 years of age, weighting 126.5 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, aspartate aminotransferase increased, blood alkaline phosphatase increased, creatinine renal clearance decreased, discomfort, gamma-glutamyltransferase increased, gastritis, nephrotic syndrome. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with INSULIN, DIMETICONE, AZULENE, GLUTAMINE, ALBUMIN, ASPARTATE CALCIUM. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5114867-5
Sutent side effect was reported by a Physician from GERMANY on Sept 08, 2006. Male patient, 58 years of age, weighting 185.2 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, hypertension, hypotension, syncope, transaminases increased. Sutent dosage: 50 MG (50 MG, DAILY INTERVAL: 28 DAYS ON/14 DAYS OFF), ORAL. During the same period patient was treated with DOXORUBICIN, LIPIODOL, METOCLOPRAMIDE, PANTOZOL, NORVASC, COSOPT, FOSINORM, LACTULOSE. Patient recovered.

Sutent Side Effects Report #5053655-5
Sutent side effect was reported by a Health Professional from NETHERLANDS on June 28, 2006. Female patient, 57 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal pain

, alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, blood pressure diastolic increased. Sutent dosage: unknown. During the same period patient was treated with DURAGESIC, AMILORIDE, ARANESP. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5030950-7
Sutent side effect was reported by a Health Professional from NETHERLANDS on June 02, 2006. Female patient, 57 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal mass, alanine aminotransferase increased, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, cachexia. Sutent dosage: 50 MG (50 MG, DAILY INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with DURAGESIC, AMILORIDE, ARANESP. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4974557-6
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Mar 28, 2006. Female patient, 56 years of age, weighting 88.18 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, asthenia, azotaemia, blood amylase increased, blood bilirubin increased, blood phosphorus increased, dehydration, fatigue. Sutent dosage: 50 MG (50 MG, EVERYDAY), ORAL. During the same period patient was treated with MAGNESIUM OXIDE, ALPRAZOLAM, MORPHINE SULPHATE, TRANEXAMIC ACID, CALCIUM POLYSTYENE SULFONATE, LACTULOSE, TRAMADOL, FUROSEMIDE. Patient recovered.

Sutent Side Effects Report #4983275-X
Sutent side effect was reported by a Physician from KOREA, REPUBLIC OF on Apr 06, 2006. Female patient, 56 years of age, weighting 88.18 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, asthenia, blood amylase increased, blood bilirubin increased, dehydration, fatigue, hypertension, lipase increased. Sutent dosage: 50 MG (50 MG, EVERYDAY), ORAL. During the same period patient was treated with MAGNESIUM OXIDE, ALPRAZOLAM, MORPHINE SULPHATE, TRANEXAMIC ACID, CALCIUM POLYSTYRENE SULFONATE, LACTULOSE, TRAMADOL, FUROSEMIDE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5186347-2
Sutent side effect was reported by a Health Professional from AUSTRALIA on Nov 30, 2006. Male patient, 51 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: aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, coagulopathy, diarrhoea, gastrointestinal disorder, haematemesis, haemoglobin decreased. Sutent dosage: (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5065720-7
Sutent side effect was reported by a Physician from FRANCE on July 12, 2006. Female patient, 50 years of age, 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: alanine aminotransferase increased, aspartate aminotransferase increased, escherichia bacteraemia, mucosal inflammation, myositis

, oral mucosal disorder, petechiae, purpura. Sutent dosage: 50 MG (50 MG, FREQUENCY: DAILY INTERVAL: EVERY DAY), ORAL. During the same period patient was treated with CEFTRIAXONE, CIPROFLOXACIN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #6108101-7
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 05, 2009. Female patient, 44 years of age, weighting 150.8 lb, was diagnosed with gastrointestinal stromal tumour, ill-defined disorder and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, aspartate aminotransferase increased, blood bilirubin increased, blood calcium increased, cardiac failure congestive, cardiomyopathy

, chest x-ray abnormal, dehydration, diarrhoea. Sutent dosage: 50 MG (50MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTULOSE, MIRALAX. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4959808-6
Sutent side effect was reported by a Physician from UNITED STATES on Mar 14, 2006. Female patient, 44 years of age, weighting 150.8 lb, was diagnosed with gastrointestinal stromal tumour, ill-defined disorder and was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal pain

, aspartate aminotransferase increased, blood bilirubin increased, blood calcium increased, carbon dioxide decreased, cardiac failure congestive, dehydration, hypertension. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LACTULOSE, MIRALAX. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5133066-4
Sutent side effect was reported by a Pharmacist from JAPAN on Oct 04, 2006. Male patient, 78 years of age, weighting 114.6 lb, was diagnosed with gastric cancer and was treated with Sutent. After drug was administered, patient experienced the following side effects: anorexia, aspartate aminotransferase increased, bedridden, blood albumin decreased, blood bilirubin increased, blood urea increased, blood uric acid increased, body temperature decreased, bone marrow failure. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with HERBAL PREPARATION, MAGNESIUM OXIDE, UREA, BROTIZOLAM. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5169155-8
Sutent side effect was reported by a Physician from UNITED STATES on Nov 22, 2006. Female patient, 69 years of age, weighting 176.4 lb, was diagnosed with breast cancer

and was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, aspiration pleural cavity, blood bilirubin increased, blood lactate dehydrogenase increased, breast cancer

, depressed level of consciousness, disorientation, hepatic enzyme increased. Sutent dosage: 37.5 MG (12.5 MG, 3 IN 1 D), ORAL. During the same period patient was treated with VICODIN, XANAX. Patient was hospitalized. Patient died on 11/21/2006.

Sutent Side Effects Report #5466259-7
Sutent side effect was reported by a Consumer or non-health professional from on Sept 12, 2007. Male patient, 76 years of age, weighting 184.1 lb, was diagnosed with adenocarcinoma pancreas and was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood culture positive, confusional state, cystitis, hyperbilirubinaemia, hyponatraemia, klebsiella infection, liver function test abnormal. Sutent dosage: unknown. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5053664-6
Sutent side effect was reported by a Physician from JAPAN on June 29, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood gases abnormal, blood glucose increased, blood potassium decreased, body temperature decreased, hyperamylasaemia. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5056353-7
Sutent side effect was reported by a Physician from JAPAN on June 29, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood gases abnormal, blood glucose increased, blood potassium decreased, blood sodium decreased, blood urine present, body temperature decreased, hepatic function abnormal. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5090764-9
Sutent side effect was reported by a Physician from JAPAN on Aug 10, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood amylase increased, blood bilirubin increased, blood creatinine increased, blood glucose increased, blood potassium decreased, blood sodium decreased. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5109497-5
Sutent side effect was reported by a Physician from VENEZUELA on Sept 05, 2006. Female patient, 78 years of age, weighting 123.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, activated partial thromboplastin time prolonged, acute respiratory failure, anaemia, aspartate aminotransferase increased, blood albumin decreased, blood calcium decreased, blood glucose decreased, blood lactate dehydrogenase increased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ENALAPRIL MALEATE, NIFEDIPINE, DICLOFENAC, CODEINE SUL, NIMODIPINE, AMIODARONE. Patient was hospitalized. Patient died on 09/06/2006.

Sutent Side Effects Report #5115367-9
Sutent side effect was reported by a Physician from JAPAN on Sept 08, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood amylase increased, blood bilirubin increased, blood glucose increased, blood potassium decreased, blood sodium decreased. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5120071-7
Sutent side effect was reported by a Physician from VENEZUELA on Sept 14, 2006. Female patient, 78 years of age, weighting 123.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal distension, abdominal pain

, anaemia, aspartate aminotransferase increased, blood albumin decreased, blood calcium decreased, blood glucose decreased, blood lactate dehydrogenase increased, blood pressure diastolic decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with ENALAPRIL MALEATE, NIFEDIPINE, DICLOFENAC, CODEINE SUL, NIMODIPINE, AMIODARONE, ZOLEDRONIC ACID. Patient was hospitalized. Patient died on 09/06/2006.

Sutent Side Effects Report #5121540-6
Sutent side effect was reported by a Physician from JAPAN on Sept 21, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, beta 2 microglobulin increased, beta-n-acetyl-d-glucosaminidase increased, blood albumin decreased, blood bilirubin increased, blood creatinine increased, blood glucose increased, blood potassium decreased. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4960275-7
Sutent side effect was reported by a Physician from JAPAN on Mar 15, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood urine present, dehydration, hepatic function abnormal, hyperamylasaemia, hyperbilirubinaemia, hypertension, protein urine present. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4965920-8
Sutent side effect was reported by a Physician from JAPAN on Mar 20, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, beta 2 microglobulin increased, beta-n-acetyl-d-glucosaminidase increased, blood glucose increased, blood urine present, dehydration, hepatic function abnormal. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4975484-0
Sutent side effect was reported by a Physician from JAPAN on Mar 30, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood amylase increased, blood bilirubin, blood bilirubin increased, blood pressure increased, blood urine present, dehydration, hepatic function abnormal. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4983269-4
Sutent side effect was reported by a Physician from JAPAN on Apr 06, 2006. Male patient, 78 years of age, weighting 163.1 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, beta 2 microglobulin increased, blood albumin decreased, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood potassium decreased, blood sodium decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #4998516-2
Sutent side effect was reported by a Physician from JAPAN on Apr 24, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, beta 2 microglobulin increased, beta-n-acetyl-d-glucosaminidase increased, blood albumin decreased, blood glucose increased, blood pressure increased, dehydration. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, BLOOD AND RELATED PRODUCTS, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5002680-9
Sutent side effect was reported by a Physician from JAPAN on Apr 27, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anuria, aspartate aminotransferase increased, blood albumin decreased, blood calcitonin increased, blood glucose increased, blood potassium decreased, blood sodium decreased, blood urine present. Sutent dosage: unknown. During the same period patient was treated with CANDESARTAN CILEXETIL, BLOOD AND RELATED PRODUCTS, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5013895-8
Sutent side effect was reported by a Physician from JAPAN on May 12, 2006. Male patient, 78 years of age, weighting 157.2 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, beta 2 microglobulin increased, beta-n-acetyl-d-glucosaminidase increased, blood albumin decreased, blood alkaline phosphatase increased, blood glucose increased, blood potassium decreased, blood sodium decreased. Sutent dosage: 50 + 37.5 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CANDESARTAN CILEXETIL, GLUCOSE, FAMOTIDINE, ACETAMINOPHEN, DIFLUCORTOLONE VALERATE, LIDOCAINE. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5593223-X
Sutent side effect was reported by a Health Professional from UNITED STATES on Jan 15, 2008. Female patient, 77 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, brain oedema, oral candidiasis, thrombocytopenia. Sutent dosage: unknown. Patient recovered.

Sutent Side Effects Report #5073008-3
Sutent side effect was reported by a Health Professional from BELGIUM on July 20, 2006. Female patient, 73 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, cholestasis. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5160565-1
Sutent side effect was reported by a Physician from UNITED STATES on Nov 08, 2006. Female patient, 70 years of age, weighting 278.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood magnesium decreased, cardio-respiratory arrest. Sutent dosage: 50 MG (50 MG, FREQUENCY: 1Q.D INTERVAL: DAILY). During the same period patient was treated with LORATADINE, TOPROL, LIPITOR, LOTREL. Patient died on 08/20/2006.

Sutent Side Effects Report #5080761-1
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on July 27, 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, 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 #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 #5165547-1
Sutent side effect was reported by a Physician from FRANCE on Nov 08, 2006. Male patient, 67 years of age, weighting 194.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, international normalised ratio increased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PREVISCAN. Patient was hospitalized. Patient died.

Sutent Side Effects Report #5073003-4
Sutent side effect was reported by a Physician from JAPAN on July 20, 2006. Male patient, 66 years of age, weighting 167.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood amylase increased, hepatic function abnormal, lipase increased, lymphocyte count decreased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D) ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5018234-4
Sutent side effect was reported by a Physician from JAPAN on May 16, 2006. Male patient, 66 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood amylase increased, hepatic function abnormal, lipase increased, lymphocyte count decreased. Sutent dosage: 50 MG (50 MG,DAILY - INTERVAL: EVERYDAY), ORAL. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5121290-6
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 18, 2006. Female patient, 65 years of age, weighting 122.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, aspartate aminotransferase increased, blood chloride decreased, blood pressure decreased, blood sodium decreased, constipation

, contusion, diarrhoea. Sutent dosage: 50 MG (50 MG, 1 IN 1 D),ORAL. During the same period patient was treated with ACETAMINOPHEN, ADVIL, ASPIRIN. Patient recovered.

Sutent Side Effects Report #5192425-4
Sutent side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 07, 2006. Female patient, 65 years of age, weighting 121.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, aspartate aminotransferase increased, blood chloride decreased, blood pressure decreased, blood pressure increased, blood sodium decreased, constipation

, contusion. Sutent dosage: 50 MG (50 MG, QD: EVERY DAY), ORAL. During the same period patient was treated with TYLENOL, ADVIL, ASPIRIN. Patient recovered.

Sutent Side Effects Report #5476363-5
Sutent side effect was reported by a Consumer or non-health professional from ARGENTINA on Sept 21, 2007. Male patient, 60 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, dyspepsia, hypertension, jaundice

. Sutent dosage: unknown. During the same period patient was treated with ANTIHYPERTENSIVES. Patient recovered.

Sutent Side Effects Report #5000104-9
Sutent side effect was reported by a Physician from FRANCE on Apr 27, 2006. Female patient, 54 years of age, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, chest pain

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

Sutent Side Effects Report #5120031-6
Sutent side effect was reported by a Health Professional from UNITED KINGDOM on Sept 19, 2006. Male patient, 45 years of age, weighting 185.4 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood albumin decreased, blood alkaline phosphatase increased, blood bilirubin increased, blood calcium decreased, fasciitis, lower gastrointestinal haemorrhage, lymphocyte count decreased, perianal abscess. Sutent dosage: 50 MG (50 MG, CYCLIC QD: 4 WEEKS ON, 2 WEEKS OFF), ORAL. During the same period patient was treated with ATENOLOL. 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 #5102460-X
Sutent side effect was reported by a Physician from FRANCE on Aug 25, 2006. Male patient, 37 years of age, weighting 156.5 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood albumin increased, blood alkaline phosphatase increased, blood amylase increased, blood bicarbonate abnormal, blood bilirubin increased. Sutent dosage: 50 MG (50 MG, 1 IN 1 D), ORAL. During the same period patient was treated with SPASFON, TRIMEBUTINE MALEATE, TRAMADOL, SOLUPRED, EPOETIN BETA, IBUPROFEN, ACETAMINOPHEN W, FERROUS SULPHATE. Patient died on 08/22/2006.

Sutent Side Effects Report #5236209-7
Sutent side effect was reported by a Physician from FRANCE on Jan 31, 2007. Male patient, weighting 183.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, aspartate aminotransferase increased, bacillus infection, bacterial infection

, bile duct obstruction, biliary tract disorder, blood alkaline phosphatase increased, blood calcium increased. Sutent dosage: unknown. During the same period patient was treated with ALLOPURINOL, METFORMIN, ASPIRIN. Patient was hospitalized. Patient recovered.

Sutent Side Effects Report #5333923-X
Sutent side effect was reported by a Pharmacist from UNITED STATES on May 12, 2007. Female patient, weighting 110.0 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aphasia

, aspartate aminotransferase increased, blood alkaline phosphatase increased, confusional state, hepatitis

, pruritus, rash

, rash erythematous. Sutent dosage: unknown. During the same period patient was treated with NEXIUM, LIPITOR, TYLOX, STOOL SOFTENER, VITAMIN CAP. Patient recovered.

Sutent Side Effects Report #5074959-6
Sutent side effect was reported by a Physician from UNITED STATES on July 22, 2006. Female patient was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, febrile neutropenia, hepatotoxicity. Sutent dosage: 50 M G (50 MG, FREQUENCY: QD INTERVAL EVERY DAY), ORAL. Patient recovered.

Sutent Side Effects Report #5133482-0
Sutent side effect was reported by a Physician from UNITED STATES on Oct 05, 2006. Female patient, weighting 165.3 lb, was treated with Sutent. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, fatigue, infection

, lymphocyte count decreased, oral candidiasis, pain

, platelet count decreased. Sutent dosage: 4X12.5 MG QD X 4 WEEKS, 2 WEEKS OFF, ORAL. During the same period patient was treated with BAY, DYAZIDE, INDERAL, MONOPRIL, NIACIN, NORVASC, PROZAC. Patient was hospitalized. Patient recovered.

Sutent and aspartate aminotransferase increased

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Sutent and aspartate aminotransferase increased Patient Reports February 11, 2012

side effects of Sutent