Gleevec and blood bilirubin increased 
Gleevec and blood bilirubin increased Patient Reports February 11, 2012
Gleevec Side Effects Report #4732995-0
Gleevec side effect was reported by a Physician from JAPAN on July 12, 2005. Male patient, 73 years of age, weighting 90.39 lb, was diagnosed with spindle cell sarcoma and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, depressed level of consciousness, hypoxia, interstitial lung disease, malignant neoplasm progression, pseudomonas infection, pulmonary oedema, pyrexia, respiratory failure. Gleevec dosage: 100 MG, BID. During the same period patient was treated with CIPROXAN. Patient died on 07/09/2005.
Gleevec Side Effects Report #4733056-7
Gleevec side effect was reported by a Physician from JAPAN on July 12, 2005. Male patient, 73 years of age, weighting 90.39 lb, was diagnosed with spindle cell sarcoma and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, depressed level of consciousness, hypoxia, interstitial lung disease, malignant neoplasm progression, pseudomonas infection, pulmonary oedema, pyrexia, respiratory failure. Gleevec dosage: 100 MG, BID. During the same period patient was treated with CIPROXAN. Patient died on 07/09/2005.
Gleevec Side Effects Report #6060812-8
Gleevec side effect was reported by a Health Professional from SPAIN on Jan 26, 2009. Female patient, 50 years of age, was diagnosed with pulmonary arterial hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, dilatation ventricular, gamma-glutamyltransferase abnormal, hepatic necrosis, hepatotoxicity, jaundice
. Gleevec dosage: 200 MG/D.. During the same period patient was treated with EPOPROSTENOL, DIURETICS, BOSENTAN, PROPYL. Patient died.Gleevec Side Effects Report #5141936-6
Gleevec side effect was reported by a Physician from UNITED STATES on July 07, 2006. Male patient, 59 years of age, weighting 172.1 lb, was diagnosed with non-small cell lung cancer and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood creatinine increased, dyspnoea, hyponatraemia, influenza like illness, oedema peripheral, sensation of heaviness, weight increased. Gleevec dosage: 600 MG, QD. During the same period patient was treated with LASIX, ACETYLCYSTEINE, TAXOTERE, ALBUTEROL, CITALOPRAM HYDROCHLORIDE, DEXAMETHASONE, ACETAMINOPHEN AND CODEINE PHOSPHATE, DOCETAXEL. Patient died on 06/28/2006.
Gleevec Side Effects Report #5712404-5
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Apr 17, 2008. Female patient, 77 years of age, weighting 141.1 lb, was diagnosed with gastrointestinal stromal tumour, constipation
, hepatitis c , insomnia, gastritis, osteoporosis and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, ammonia increased, anuria, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, eyelid oedema, gastric haemorrhage, haematochezia. Gleevec dosage: 200 MG/DAY, UNK. During the same period patient was treated with MAGNESIUM OXIDE, URSO, NITRAZEPAM, LAXOBERON, ULCERLMIN, ALFAROL, PARIET. Patient was hospitalized. Patient died on 08/12/2007.Gleevec Side Effects Report #5713075-4
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Apr 17, 2008. Female patient, 77 years of age, weighting 141.1 lb, was diagnosed with gastrointestinal stromal tumour, constipation
, hepatitis c , insomnia, gastritis, osteoporosis and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, ammonia increased, anuria, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, eyelid oedema, gastric haemorrhage, haematochezia. Gleevec dosage: 200 MG/DAY, UNK. During the same period patient was treated with MAGNESIUM OXIDE, URSO, NITRAZEPAM, LAXOBERON, ULCERLMIN, ALFAROL, PARIET. Patient was hospitalized. Patient died on 08/12/2007.Gleevec Side Effects Report #4571891-9
Gleevec side effect was reported by a Physician from on Sept 02, 2004. Female patient, 72 years of age, weighting 127.9 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood bilirubin increased, cholangitis, cholecystitis acute, memory impairment, pyrexia, white blood cell count decreased. Gleevec dosage: 300 MG, QD. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #4611405-8
Gleevec side effect was reported by a Physician from on Sept 02, 2004. Female patient, 72 years of age, weighting 127.9 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood bilirubin increased, cholangitis, cholecystitis acute, memory impairment, pyrexia, white blood cell count decreased. Gleevec dosage: 300 MG, QD. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5630072-8
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Feb 12, 2008. Male patient, 65 years of age, weighting 130.1 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, eyelid oedema, face oedema, hepatic function abnormal. Gleevec dosage: 400 MG, QD. During the same period patient was treated with LAC B. Patient died on 02/18/2006.Gleevec Side Effects Report #5653922-8
Gleevec side effect was reported by a Health Professional from JAPAN on Feb 29, 2008. Male patient, 65 years of age, weighting 130.1 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, eyelid oedema, face oedema, hepatic function abnormal. Gleevec dosage: 400 MG, QD. During the same period patient was treated with LAC B. Patient died on 02/18/2006.Gleevec Side Effects Report #4902514-4
Gleevec side effect was reported by a Physician from SPAIN on Feb 03, 2006. Male patient, 61 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased. Gleevec dosage: 400 MG/D. Patient died on 12/30/2005.Gleevec Side Effects Report #4907969-7
Gleevec side effect was reported by a Physician from PORTUGAL on Jan 04, 2006. Female patient, 61 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anti-hbc antibody positive, anti-hbs antibody positive, antinuclear antibody positive, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, chronic hepatitis. Gleevec dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #4702721-X
Gleevec side effect was reported by a Physician from on June 20, 2005. Male patient, 52 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hepatitis acute. Gleevec dosage: 200 MG/DAY. Patient recovered.
Gleevec Side Effects Report #4787070-6
Gleevec side effect was reported by a Physician from BRAZIL on June 20, 2005. Male patient, 52 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hepatitis acute. Gleevec dosage: 200 MG/DAY. Patient recovered.
Gleevec Side Effects Report #4804773-5
Gleevec side effect was reported by a Physician from BRAZIL on June 20, 2005. Male patient, 52 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure increased, diarrhoea. Gleevec dosage: 200 MG/DAY. Patient recovered.
Gleevec Side Effects Report #4813406-3
Gleevec side effect was reported by a Physician from BRAZIL on June 20, 2005. Male patient, 52 years of age, weighting 143.3 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, bilirubin conjugated increased, blood alkaline phosphatase increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood creatinine increased, blood pressure increased, blood urea increased. Gleevec dosage: 200 MG/DAY. Patient recovered.
Gleevec Side Effects Report #5370661-1
Gleevec side effect was reported by a Physician from UNITED STATES on June 06, 2006. Female patient, 47 years of age, weighting 112.0 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, bone marrow failure, fatigue, insomnia, malignant neoplasm progression, pain
. Gleevec dosage: 400 MG, QD, ORAL, NO TREATMENT. During the same period patient was treated with TYLENOL PM, VICODIN, PROTONIX, PREVACID. Patient recovered.Gleevec Side Effects Report #5281669-9
Gleevec side effect was reported by a Physician from CHINA on Jan 15, 2007. Female patient, 43 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, chest discomfort, cough, nasal oedema, pleural effusion, protein total decreased, rash
, tachycardia. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient died.Gleevec Side Effects Report #5072259-1
Gleevec side effect was reported by a Physician from UNITED STATES on Aug 22, 2005. Male patient, 41 years of age, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: adhesiolysis, blood bilirubin increased, pyrexia, small intestinal obstruction, white blood cell count decreased. Gleevec dosage: 600 MG, QD, ORAL. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5272589-4
Gleevec side effect was reported by a Physician from SLOVENIA on Mar 14, 2007. Female patient, 33 years of age, weighting 136.7 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, chest x-ray abnormal, computerised tomogram abnormal, confusional state, cough, gamma-glutamyltransferase increased. Gleevec dosage: 400 MG, QD. Patient died on 12/26/2006.
Gleevec Side Effects Report #5763611-7
Gleevec side effect was reported by a Health Professional from JAPAN on June 03, 2008. Female patient, weighting 141.1 lb, was diagnosed with gastrointestinal stromal tumour, constipation
, hepatitis c , oedema, insomnia, gastritis, osteoporosis and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, ammonia increased, anuria, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, eyelid oedema, gastric haemorrhage, haematochezia. Gleevec dosage: 200 MG/DAY, UNK. During the same period patient was treated with MAGNESIUM OXIDE, URSO, LASIX, NITRAZEPAM, LAXOBERON, ULCERLMIN, ALFAROL. Patient was hospitalized. Patient died on 08/12/2007.Gleevec Side Effects Report #5777359-6
Gleevec side effect was reported by a Physician from UNITED STATES on June 13, 2008. Female patient was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, biliary dilatation, blood bilirubin increased, hepatic failure, hepatic necrosis, international normalised ratio increased, jaundice
. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ZOCOR, ASPIRIN, PRILOSEC, TOPROL, ARICEPT, COZAAR, ALLEGRA, FERROUS SULPHATE. Patient was hospitalized. Patient died on 04/23/2008.Gleevec Side Effects Report #5816935-9
Gleevec side effect was reported by a Health Professional from JAPAN on July 09, 2008. Male patient, weighting 116.8 lb, was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, peritonitis, red blood cell count decreased, surgery . Gleevec dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5823142-2
Gleevec side effect was reported by a Health Professional from JAPAN on July 15, 2008. Male patient, weighting 116.8 lb, was diagnosed with gastrointestinal stromal tumour, metastases to liver and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, haematocrit decreased, haemoglobin decreased, intra-abdominal haemorrhage, peritonitis, red blood cell count decreased. Gleevec dosage: 400 MG/DAY. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #6099840-5
Gleevec side effect was reported by a Physician from JAPAN on Feb 24, 2009. Male patient, weighting 132.3 lb, was diagnosed with gastrointestinal stromal tumour, pleural effusion and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain
, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, fluid retention, gastrointestinal perforation, liver disorder. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with GASTER, PROMAC, LASIX. Patient was hospitalized and became disabled. Patient died on 12/07/2008.Gleevec Side Effects Report #6110474-6
Gleevec side effect was reported by a Physician from SWITZERLAND on Feb 27, 2009. Male patient was diagnosed with gastrointestinal stromal tumour and was treated with Gleevec. After drug was administered, patient experienced the following side effects: anaemia, blood bilirubin increased, emphysema, liver function test abnormal, myelodysplastic syndrome, pancytopenia, pyrexia, transaminases increased. Gleevec dosage: 600 MG/D. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #4889706-8
Gleevec side effect was reported by a Physician from FRANCE on Oct 20, 2005. Male patient, 76 years of age, weighting 216.1 lb, was diagnosed with chronic myeloid leukaemia, hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: bile duct obstruction, biliary dilatation, biliary tract operation, blood bilirubin increased, jaundice
, malignant neoplasm progression, pancreatic duct dilatation, surgery . Gleevec dosage: 400 MG PER DAY. During the same period patient was treated with ALPRESS, CHRONADALATE, COAPROVEL, EUPANTOL. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #4554447-3
Gleevec side effect was reported by a Consumer or non-health professional from on Feb 12, 2002. Female patient, 75 years of age, weighting 92.59 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blister, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, epidermolysis, erythema, hepatic function abnormal. Gleevec dosage: 400 MG/D. During the same period patient was treated with GASMOTIN, CALSLOT. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5072361-4
Gleevec side effect was reported by a Physician from UNITED STATES on Dec 21, 2005. Male patient, 73 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, chronic hepatitis, hepatic failure, international normalised ratio increased, liver disorder, liver function test abnormal, periorbital oedema. Gleevec dosage: 400 MG, QD, ORAL. During the same period patient was treated with CALCIUM W, ASCORBIC ACID, GLUCOSAMINE, CELEBREX. Patient recovered.
Gleevec Side Effects Report #5338802-X
Gleevec side effect was reported by a Physician from JAPAN on May 26, 2007. Male patient, 70 years of age, weighting 143.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, basophilia, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea decreased, blood urea increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ALLOPURINOL, ULCERMIN, SIGMART, GASTER D, EUGLUCON, GLYBURIDE. Patient died on 02/27/2005.
Gleevec Side Effects Report #5064896-5
Gleevec side effect was reported by a Physician from JAPAN on Apr 16, 2004. Male patient, 70 years of age, weighting 143.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, basophilia, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea decreased, blood urea increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ALLOPURINOL, ULCERMIN, SIGMART, GASTER D, EUGLUCON, DAONIL. Patient died on 02/27/2005.
Gleevec Side Effects Report #4745169-4
Gleevec side effect was reported by a Physician from JAPAN on Apr 16, 2004. Male patient, 70 years of age, weighting 143.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, basophilia, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea decreased, blood urea increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ALOSITOL, ULCERMIN, SIGMART, GASTER D, GLYBURIDE, DAONIL. Patient died on 02/27/2005.
Gleevec Side Effects Report #5734195-4
Gleevec side effect was reported by a Consumer or non-health professional from FRANCE on May 05, 2008. Male patient, 69 years of age, was diagnosed with chronic myeloid leukaemia, abdominal pain upper and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, c-reactive protein increased, central venous catheterisation, confusional state, cytolytic hepatitis, disorientation, dyspepsia, gastrooesophageal reflux disease. Gleevec dosage: 600 MG DAILY. During the same period patient was treated with ZOMETA, ARANESP, PANTOPRAZOLE, ARACYTINE. Patient was hospitalized. Patient died on 03/08/2008.
Gleevec Side Effects Report #4724853-2
Gleevec side effect was reported by a Physician from UNITED KINGDOM on June 02, 2005. Male patient, 65 years of age, was diagnosed with chronic myeloid leukaemia, hypertension, transient ischaemic attack and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, dysgeusia, hepatitis
, malaise. Gleevec dosage: 400 MG, QD. During the same period patient was treated with BENDROFLUAZIDE, CANDESARTAN, ASPIRIN. Patient recovered.Gleevec Side Effects Report #4736230-9
Gleevec side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on June 02, 2005. Male patient, 65 years of age, was diagnosed with chronic myeloid leukaemia, hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, dysgeusia, hepatitis
, malaise. Gleevec dosage: 400 MG, QD. During the same period patient was treated with BENDROFLUAZIDE, CANDESARTAN, ASPIRIN, HYDROXYCARBAMIDE, ALLOPURINOL. Patient recovered.Gleevec Side Effects Report #5479233-1
Gleevec side effect was reported by a Consumer or non-health professional from GERMANY on Oct 01, 2007. Male patient, 62 years of age, weighting 176.4 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain upper, antithrombin iii decreased, arteriogram coronary abnormal, biopsy, blood bilirubin increased, blood creatinine increased, blood fibrinogen increased, blood lactic acid increased, chest pain
. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with RAMIPRIL, PANTOPRAZOLE, TORSEMIDE, NEBILET, INSULIN, PROTAPHAN. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5303149-4
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Apr 06, 2007. Male patient, 61 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: arthralgia, blast crisis in myelogenous leukaemia, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, bone cancer metastatic, bone marrow failure, c-reactive protein increased, dyspnoea. Gleevec dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5332524-7
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on May 11, 2007. Male patient, 61 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: arthralgia, blast crisis in myelogenous leukaemia, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, bone cancer metastatic, bone marrow failure, c-reactive protein increased, dyspnoea. Gleevec dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #4760464-0
Gleevec side effect was reported by a Physician from FRANCE on July 07, 2005. Female patient, 61 years of age, weighting 152.1 lb, was diagnosed with chronic myeloid leukaemia, hypothyroidism and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, cytolytic hepatitis, gamma-glutamyltransferase increased, jaundice cholestatic. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with LEVOTHYROXINE, ERCEFURYL, DICETEL. Patient recovered.
Gleevec Side Effects Report #4974729-0
Gleevec side effect was reported by a Physician from UNITED STATES on Nov 22, 2005. Female patient, 60 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased. Gleevec dosage: 400 MG, QD, ORAL. Patient recovered.
Gleevec Side Effects Report #5034868-5
Gleevec side effect was reported by a Physician from UNITED STATES on Apr 10, 2006. Female patient, 60 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased. Gleevec dosage: unknown. During the same period patient was treated with STARNOC, DILANTIN, HYDREA. Patient recovered.
Gleevec Side Effects Report #5283255-3
Gleevec side effect was reported by a Physician from FRANCE on Mar 19, 2007. Male patient, 58 years of age, weighting 176.4 lb, was diagnosed with chronic myeloid leukaemia, lung disorder and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aortic stenosis, arrhythmia
, blood albumin decreased, blood bilirubin increased, blood creatinine increased, blood urea increased, c-reactive protein increased, cardiac failure, cardiac murmur. Gleevec dosage: 400 MG DAILY. During the same period patient was treated with TAVANIC, MUCOMYST, DOLIPRANE, ROCEPHIN, OFLOCET. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5664297-2
Gleevec side effect was reported by a Health Professional from JAPAN on Feb 29, 2008. Male patient, 58 years of age, weighting 127.9 lb, was diagnosed with chronic myeloid leukaemia, hypertension, hyperlipidaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hbv-dna polymerase increased, hepatitis b
, skin disorder. Gleevec dosage: 100 MG, QID. During the same period patient was treated with NORVASC, MEVALOTIN, BARACLUDE. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5664749-5
Gleevec side effect was reported by a Health Professional from JAPAN on Feb 29, 2008. Male patient, 58 years of age, weighting 127.9 lb, was diagnosed with chronic myeloid leukaemia, hypertension, hyperlipidaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hbv-dna polymerase increased, hepatitis b
, skin disorder. Gleevec dosage: 100 MG, QID. During the same period patient was treated with NORVASC, MEVALOTIN, BARACLUDE. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5690931-7
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Mar 17, 2008. Male patient, 58 years of age, weighting 127.9 lb, was diagnosed with chronic myeloid leukaemia, hypertension, hyperlipidaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hbv-dna polymerase increased, hepatitis b
, skin disorder. Gleevec dosage: 100 MG, QID. During the same period patient was treated with NORVASC, MEVALOTIN, BARACLUDE. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5691019-1
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Mar 17, 2008. Male patient, 58 years of age, weighting 127.9 lb, was diagnosed with chronic myeloid leukaemia, hypertension, hyperlipidaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hbv-dna polymerase increased, hepatitis b
, skin disorder. Gleevec dosage: 100 MG, QID. During the same period patient was treated with NORVASC, MEVALOTIN, BARACLUDE. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #4940097-3
Gleevec side effect was reported by a Physician from FRANCE on Jan 27, 2006. Male patient, 58 years of age, weighting 176.4 lb, was diagnosed with chronic myeloid leukaemia, lung disorder and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aortic valve stenosis, arrhythmia
, blood albumin decreased, blood bilirubin increased, blood creatinine increased, blood urea increased, c-reactive protein increased, cardiac failure, cardiac murmur. Gleevec dosage: 400 MG DAILY. During the same period patient was treated with TAVANIC, MUCOMYST, DOLIPRANE, ROCEPHIN, OFLOCET. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #4841780-0
Gleevec side effect was reported by a Physician from UNITED KINGDOM on Nov 02, 2005. Female patient, 57 years of age, weighting 132.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood bilirubin increased, blood lactate dehydrogenase increased, eye pain, gamma-glutamyltransferase increased, hepatic function abnormal, jaundice
, liver disorder, nausea . Gleevec dosage: 400 MG/DAY. Patient recovered.Gleevec Side Effects Report #5098882-6
Gleevec side effect was reported by a Physician from JAPAN on June 30, 2006. Male patient, 56 years of age, weighting 114.6 lb, was diagnosed with chronic myeloid leukaemia, cardiomyopathy
and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, eosinophilia, gamma-glutamyltransferase increased, hepatic function abnormal, rash . Gleevec dosage: 400 MG, QD. During the same period patient was treated with ARTIST. Patient recovered.Gleevec Side Effects Report #5103754-4
Gleevec side effect was reported by a Physician from JAPAN on June 30, 2006. Male patient, 56 years of age, weighting 114.6 lb, was diagnosed with chronic myeloid leukaemia, cardiomyopathy
and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, eosinophilia, gamma-glutamyltransferase increased, hepatic function abnormal, rash . Gleevec dosage: 400 MG, QD. During the same period patient was treated with ARTIST. Patient recovered.Gleevec Side Effects Report #5714388-2
Gleevec side effect was reported by a Consumer or non-health professional from FRANCE on Apr 11, 2008. Male patient, 55 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, cholestasis, cytolytic hepatitis, eosinophilia, gamma-glutamyltransferase increased. Gleevec dosage: unknown. During the same period patient was treated with ALLOPURINOL, HYDREA. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5405648-3
Gleevec side effect was reported by a Health Professional from JAPAN on July 30, 2007. Male patient, 54 years of age, weighting 149.9 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, coma hepatic, depressed level of consciousness, dyspepsia, fatigue, haemoglobin decreased, hepatic encephalopathy, hepatitis
, hepatitis b . Gleevec dosage: 300 MG/DAY. During the same period patient was treated with ADALAT, ALLOPURINOL. Patient was hospitalized. Patient died on 06/21/2004.Gleevec Side Effects Report #4910873-1
Gleevec side effect was reported by a Health Professional from JAPAN on June 08, 2004. Male patient, 54 years of age, weighting 149.9 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, coma hepatic, depressed level of consciousness, dyspepsia, fatigue, haemoglobin decreased, hepatic encephalopathy, hepatic necrosis, hepatitis
. Gleevec dosage: 300 MG/DAY. During the same period patient was treated with ADALAT, ZYLORIC. Patient was hospitalized. Patient died on 06/21/2004.Gleevec Side Effects Report #5491540-5
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 11, 2007. Female patient, 52 years of age, was diagnosed with chronic myeloid leukaemia, insomnia, depression
and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, arthropod bite, aspartate aminotransferase increased, autoimmune hepatitis, bilirubin conjugated increased, blood albumin decreased, blood bilirubin increased, blood bilirubin unconjugated increased, haematoma. Gleevec dosage: 300 MG, QD. During the same period patient was treated with AMBIEN, PROZAC. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5253175-9
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Feb 16, 2007. Female patient, 40 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, constipation
, diarrhoea, diastolic hypotension, dizziness , tachyarrhythmia, vomiting. Gleevec dosage: 400 MG, QD. Patient recovered.Gleevec Side Effects Report #5285116-2
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 30, 2007. Female patient, 39 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal discomfort, anaemia, ascites, aspartate aminotransferase increased, blood bilirubin increased, coma hepatic, fatigue, gallbladder disorder. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient died on 03/26/2007.
Gleevec Side Effects Report #5293423-2
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 04, 2007. Female patient, 39 years of age, weighting 187.0 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal discomfort, anaemia, ascites, aspartate aminotransferase increased, blood bilirubin increased, coma hepatic, fatigue, gallbladder disorder, hepatic failure. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient died on 03/26/2007.
Gleevec Side Effects Report #4614877-8
Gleevec side effect was reported by a Physician from on Mar 11, 2005. Female patient, 38 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, hepatitis toxic, ileus paralytic, lung infiltration, neurotoxicity, pleural effusion, pulmonary toxicity, respiratory failure. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with METHOTREXATE, CYCLOPHOSPHAMIDE, DEXAMETHASONE. Patient recovered.
Gleevec Side Effects Report #5370746-X
Gleevec side effect was reported by a Health Professional from UNITED STATES on Sept 15, 2006. Female patient, 28 years of age, weighting 155.0 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood lactate dehydrogenase increased, liver function test abnormal. Gleevec dosage: 400 MG, QD, ORAL; 300 MG, QD, ORAL; 400 MG, QD, ORAL; 300 MG, QD, ORAL. During the same period patient was treated with SYNTHROID, HYDREA, ALLOPURINOL, ACYCLOVIR. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #4774303-5
Gleevec side effect was reported by a Physician from RUSSIAN FEDERATION on July 13, 2005. Male patient, 26 years of age, weighting 185.2 lb, was diagnosed with chronic myeloid leukaemia, pyrexia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, hepatitis toxic, transaminases increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with PARACETAMOL, ANALGIN. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5371514-5
Gleevec side effect was reported by a Physician from UNITED STATES on Jan 10, 2007. Female patient, 22 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, hepatitis acute, jaundice
, liver function test abnormal. Gleevec dosage: 400 MG, QOD, ORAL; NO TREATMENT; 400 MG, QOD, ORAL. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5066728-8
Gleevec side effect was reported by a Physician from UNITED STATES on Mar 28, 2006. Female patient was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood bilirubin increased. Gleevec dosage: 100 MG, QOD, ORAL. Patient recovered.
Gleevec Side Effects Report #5106696-3
Gleevec side effect was reported by a Physician from RUSSIAN FEDERATION on Aug 14, 2006. Female patient was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, depressed level of consciousness, gastrointestinal carcinoma, hepatotoxicity, jaundice
, jaundice cholestatic, transaminases increased. Gleevec dosage: 400 MG/D. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5745150-2
Gleevec side effect was reported by a Physician from UNITED STATES on Apr 30, 2008. Female patient was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain upper, blood alkaline phosphatase increased, blood bilirubin increased, cholestasis, endoscopic retrograde cholangiopancreatography, gamma-glutamyltransferase increased, nausea
, pyrexia. Gleevec dosage: 200 MG, BID. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5758880-3
Gleevec side effect was reported by a Health Professional from SINGAPORE on May 21, 2008. Male patient was diagnosed with chronic myeloid leukaemia, prophylaxis, hepatitis b virus, herpes simplex
and was treated with Gleevec. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, acute hepatic failure, alanine aminotransferase increased, aspartate aminotransferase increased, blood albumin decreased, blood bilirubin increased, haemoglobin decreased, hbv dna increased, hepatic encephalopathy. Gleevec dosage: 400 MG, QD. During the same period patient was treated with LACTULOSE, VITAMIN K, PROTON PUMP INHIBITORS, ANTIBIOTICS, LAMIVUDINE, ACYCLOVIR. Patient was hospitalized. Patient died on 05/27/2005.Gleevec Side Effects Report #5865790-X
Gleevec side effect was reported by a Health Professional from JAPAN on Aug 27, 2008. Female patient, weighting 119.0 lb, was diagnosed with chronic myeloid leukaemia, dizziness
, hyperuricaemia, nausea and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, alpha tumour necrosis factor increased, aspartate aminotransferase increased, blood bilirubin increased, blood creatine phosphokinase increased, blood creatinine increased, blood pressure decreased, blood urea increased, c-reactive protein increased. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with VONTROL, URALYT, ZYLORIC, NOVAMIN, PANALDINE, MERISLON. Patient was hospitalized. Patient died on 10/10/2006.Gleevec Side Effects Report #5977386-X
Gleevec side effect was reported by a Health Professional from JAPAN on Nov 26, 2008. Male patient, weighting 141.1 lb, was diagnosed with chronic myeloid leukaemia, hypertension, hyperuricaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, coma hepatic, depressed level of consciousness, dyspepsia, fatigue, haemoglobin decreased, hepatic encephalopathy, hepatitis
, hepatitis b . Gleevec dosage: 400 MG/DAY. During the same period patient was treated with ADALAT, ZYLORIC. Patient was hospitalized. Patient died on 06/21/2004.Gleevec Side Effects Report #5511054-3
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Oct 30, 2007. Male patient, 66 years of age, weighting 208.8 lb, was diagnosed with adenoid cystic carcinoma, benign prostatic hyperplasia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: arrhythmia
, atrial fibrillation , biopsy intestine abnormal, blood bicarbonate increased, blood bilirubin increased, blood creatinine increased, blood phosphorus decreased, blood thyroid stimulating hormone decreased, brunner's gland hyperplasia. Gleevec dosage: 400 MG, QD. During the same period patient was treated with FLOMAX, VERAPAMIL, BENICAR. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #5527466-8
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 23, 2007. Male patient, 66 years of age, weighting 208.8 lb, was diagnosed with adenoid cystic carcinoma, benign prostatic hyperplasia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: arrhythmia
, atrial fibrillation , biopsy intestine abnormal, blood bicarbonate increased, blood bilirubin increased, blood creatinine increased, blood phosphorus decreased, blood thyroid stimulating hormone decreased, brunner's gland hyperplasia. Gleevec dosage: 400 MG, QD. During the same period patient was treated with FLOMAX, VERAPAMIL, BENICAR. Patient was hospitalized. Patient recovered.Gleevec Side Effects Report #4816923-5
Gleevec side effect was reported by a Consumer or non-health professional from FRANCE on Sept 20, 2005. Female patient, 68 years of age, weighting 138.9 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, asthenia, bilirubin conjugated increased, blood bilirubin increased, blood bilirubin unconjugated increased, blood lactate dehydrogenase increased, bone marrow failure. Gleevec dosage: 600 MG DAILY. During the same period patient was treated with PLITICAN, PURINETHOL, LEVOTHYROX. Patient was hospitalized. Patient recovered.
Gleevec Side Effects Report #5556872-0
Gleevec side effect was reported by a Physician from JAPAN on Dec 04, 2007. Female patient, 66 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, haemolytic anaemia, reticulocyte count increased. Gleevec dosage: 600MG/D. During the same period patient was treated with PREDNISOLONE, BONALON, GASTER. Patient recovered.
Gleevec Side Effects Report #5591080-9
Gleevec side effect was reported by a Physician from JAPAN on Jan 08, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena. Gleevec dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.
Gleevec Side Effects Report #5669304-9
Gleevec side effect was reported by a Physician from JAPAN on Mar 05, 2008. Female patient, 66 years of age, weighting 130.1 lb, was diagnosed with acute lymphocytic leukaemia, osteoporosis prophylaxis and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, disseminated intravascular coagulation, fibrin d dimer increased, fibrin decreased, fibrin degradation products increased, gastric haemorrhage, haemoglobin decreased, haemolytic anaemia, melaena. Gleevec dosage: 600 MG/DAY. During the same period patient was treated with PREDNISOLONE, BONALON. Patient recovered.
Gleevec Side Effects Report #5803441-0
Gleevec side effect was reported by a Physician from FRANCE on July 01, 2008. Male patient, weighting 132.3 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aplasia, arrhythmia
, atrial fibrillation , blood bilirubin increased, citrobacter infection, cough, gastrostomy, hypotonia, intracranial venous sinus thrombosis. Gleevec dosage: 800 MG, QD. Patient recovered.Gleevec Side Effects Report #5803444-6
Gleevec side effect was reported by a Physician from FRANCE on June 24, 2008. Male patient, weighting 132.3 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: aplasia, arrhythmia
, atrial fibrillation , blood bilirubin increased, citrobacter infection, cough, gastrostomy, hypotonia, intracranial venous sinus thrombosis. Gleevec dosage: 800 MG, QD. Patient recovered.Gleevec Side Effects Report #5838914-8
Gleevec side effect was reported by a Physician from on Aug 01, 2008. Male patient, weighting 143.3 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: blood bilirubin increased, blood lactate dehydrogenase increased, disseminated intravascular coagulation, haematocrit decreased, haemoglobin decreased, platelet count decreased, red blood cell count decreased, tumour lysis syndrome, white blood cell count decreased. Gleevec dosage: 400 MG, QD. Patient recovered.
Gleevec Side Effects Report #4690247-1
Gleevec side effect was reported by a Physician from on June 02, 2005. Male patient, 65 years of age, was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, dysgeusia, hepatitis
, liver function test abnormal. Gleevec dosage: 400 MG, QD. During the same period patient was treated with BENDROFLUAZIDE, CANDESARTAN. Patient recovered.Gleevec Side Effects Report #5903224-7
Gleevec side effect was reported by a Consumer or non-health professional from FRANCE on Sept 16, 2008. Male patient, weighting 205.0 lb, was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, bone marrow failure, cheilitis, cholestasis, cytolytic hepatitis. Gleevec dosage: 600 MG/DAY. During the same period patient was treated with METHOTREXATE, VINCRISTINE. Patient was hospitalized. Patient recovered.