Gleevec and alanine aminotransferase increased Patient Reports February 11, 2012

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 #6013543-4
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 16, 2008. Male patient, weighting 176.4 lb, was diagnosed with metastatic malignant melanoma, metastases to lung, malignant melanoma of sites other than skin and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, albumin urine present, alcohol poisoning, anion gap increased, anxiety

, apnoea, aspartate aminotransferase increased, blood creatinine increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ACETAMINOPHEN, DUONEB, ALLOPURINOL, ALPRAZOLAM, MYLANTA, ATENOLOL. Patient was hospitalized. Patient died on 07/16/2008.

Gleevec Side Effects Report #5669805-3
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 14, 2008. Female patient, 64 years of age, weighting 145.5 lb, was diagnosed with glioblastoma multiforme and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, faecal incontinence, haemoglobin decreased, hepatic enzyme increased, hyperglycaemia, mucosal inflammation, muscular weakness, myopathy, oesophageal candidiasis. Gleevec dosage: 400MG QD PO. During the same period patient was treated with HYDROXYUREA, ZACTIMA, ZOLPIDEM, FUROSEMIDE, GLIPIZIDE, CYMBALTA, DECADRON. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5230992-2
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Jan 25, 2007. Female patient, 86 years of age, weighting 103.6 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, gastrectomy, hepatic function abnormal, nausea

, platelet count decreased, white blood cell count decreased. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with FAMOTIDINE. Patient was hospitalized. Patient recovered.

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

, 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 #5157329-1
Gleevec side effect was reported by a Pharmacist from JAPAN on Nov 02, 2006. Female patient, 73 years of age, weighting 125.7 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, alopecia, anorexia, aspartate aminotransferase increased, asthenia, blood alkaline phosphatase increased, cardio-respiratory arrest, eyelid oedema, face oedema. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient died on 11/06/2006.

Gleevec Side Effects Report #5158493-0
Gleevec side effect was reported by a Physician from JAPAN on Dec 14, 2005. Male patient, 73 years of age, weighting 108.0 lb, was diagnosed with gastrointestinal stromal tumour, hypertrophic cardiomyopathy, hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, amyloidosis, aspartate aminotransferase increased, blood creatinine increased, cardiac arrest

, cardiac failure, cardiomyopathy

, concomitant disease progression, face oedema. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ASPIRIN, OLMETEC, MAGLAX, LASIX, LAXOBERON, DIASTASE. Patient was hospitalized. Patient died on 04/05/2006.

Gleevec Side Effects Report #5164500-1
Gleevec side effect was reported by a Pharmacist from JAPAN on Nov 02, 2006. Female patient, 73 years of age, weighting 125.7 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, alopecia, anorexia, aspartate aminotransferase increased, asthenia, blood alkaline phosphatase increased, cardio-respiratory arrest, eyelid oedema, face oedema. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient died on 11/06/2006.

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 #4646342-6
Gleevec side effect was reported by a Physician from on Nov 17, 2004. Female patient, 63 years of age, weighting 110.2 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, eosinophilia, platelet count decreased, rash

, white blood cell count decreased. Gleevec dosage: unknown. Patient recovered.

Gleevec Side Effects Report #4690888-1
Gleevec side effect was reported by a Physician from on Nov 17, 2004. Female patient, 63 years of age, weighting 110.2 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, duodenal ulcer, eosinophilia, platelet count decreased, rash

, white blood cell count decreased. Gleevec dosage: unknown. Patient recovered.

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 #5482296-0
Gleevec side effect was reported by a Physician from JAPAN on Oct 04, 2007. Female patient, 58 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, aspartate aminotransferase increased, hepatic function abnormal, hepatitis viral, rash

. Gleevec dosage: 400 MG/D. Patient recovered.

Gleevec Side Effects Report #5521728-6
Gleevec side effect was reported by a Physician from JAPAN on Nov 12, 2007. Female patient, 58 years of age, weighting 99.21 lb, was diagnosed with gastrointestinal stromal tumour, abdominal pain upper, nausea

, insomnia 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 lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic function abnormal, leukopenia. Gleevec dosage: 100 MG/DAY. During the same period patient was treated with ACINON, PRIMPERAN, MYSLEE. 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 #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

. 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 #6005057-2
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 08, 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, autoimmune hepatitis, therapeutic response unexpected. Gleevec dosage: unknown. Patient recovered.

Gleevec Side Effects Report #6015016-1
Gleevec side effect was reported by a Health Professional from FRANCE on Dec 17, 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, blood amylase increased, gamma-glutamyltransferase increased, lipase increased, pancreatitis necrotising, peritoneal effusion. 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 #4553937-7
Gleevec side effect was reported by a Consumer or non-health professional from on Jan 03, 2005. Female patient, 33 years of age, weighting 216.1 lb, was diagnosed with eosinophilia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aldolase increased, arthralgia, back pain

, blood creatine phosphokinase increased, inflammation, leukocytosis, myalgia, myoglobinaemia. Gleevec dosage: 100 MG DAILY. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5195710-5
Gleevec side effect was reported by a Physician from JAPAN on Dec 27, 2006. Male patient, 79 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, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, bronchitis

, eosinophil count increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with NORVASC, FIRSTCIN, AMINOFLUID, GLUCOSE, VASOLAN, PHYSIO. Patient was hospitalized. Patient died.

Gleevec Side Effects Report #5075700-3
Gleevec side effect was reported by a Physician from JAPAN on Aug 03, 2006. Male patient, 79 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, anorexia, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, bronchitis

, eosinophil count increased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with NORVASC, FIRSTCIN, AMINOFLUID, GLUCOSE, VASOLAN, PHYSIO. Patient was hospitalized. Patient died.

Gleevec Side Effects Report #5073221-5
Gleevec side effect was reported by a Physician from UNITED STATES on July 27, 2005. Male patient, 76 years of age, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, alanine aminotransferase increased, aspartate aminotransferase increased, blood creatinine increased, blood glucose increased, blood urea increased, cardiac failure congestive, fall

, haematocrit decreased. Gleevec dosage: 400 MG, QD, ORAL. During the same period patient was treated with COUMADIN, HEPARIN, ASPIRIN. 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 #4839931-7
Gleevec side effect was reported by a Physician from FRANCE on Oct 03, 2005. Male patient, 75 years of age, weighting 154.3 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, anorexia, aspartate aminotransferase increased, asthenia, gamma-glutamyltransferase increased, hepatitis

. Gleevec dosage: 400 MG DAILY. During the same period patient was treated with FLECAINIDE ACETATE, DILTIAZEM HYDROCHLORIDE, PLAVIX, VASTEN, PERMIXON. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5611252-4
Gleevec side effect was reported by a Physician from JAPAN on Jan 10, 2008. Male patient, 74 years of age, was diagnosed with chronic myeloid leukaemia, malnutrition, respiratory failure, pyelonephritis, pleural effusion and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, aspiration, bladder disorder, bladder irrigation, blood creatinine increased, blood lactate dehydrogenase increased, dysuria. Gleevec dosage: 400MG DAILY. During the same period patient was treated with MINERALIN, NEOPHYLLIN, CIPROFLOXACIN, LASIX, ALBUMIN. Patient was hospitalized. Patient died on 04/15/2006.

Gleevec Side Effects Report #5612711-0
Gleevec side effect was reported by a Physician from JAPAN on Jan 25, 2008. Male patient, 74 years of age, was diagnosed with chronic myeloid leukaemia, malnutrition, respiratory failure, pyelonephritis, pleural effusion and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, aspiration, bladder disorder, bladder irrigation, blood creatinine increased, blood lactate dehydrogenase increased, dysuria. Gleevec dosage: 400MG DAILY. During the same period patient was treated with MINERALIN, NEOPHYLLIN, CIPROFLOXACIN, LASIX, ALBUMIN. Patient was hospitalized. Patient died on 04/15/2006.

Gleevec Side Effects Report #5283266-8
Gleevec side effect was reported by a Physician from DENMARK on Mar 20, 2007. Female patient, 72 years of age, was diagnosed with chronic myeloid leukaemia, hypercholesterolaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood creatine phosphokinase increased, cardiotoxicity, gait disturbance, hepatic enzyme abnormal, muscle enzyme increased, muscular weakness, myoglobin blood increased. Gleevec dosage: 200 MG/DAY. During the same period patient was treated with SIMVASTATIN, NEXIUM, CENTYL, TRIATEC, HJERTEMAGNYL, ZOLPIDEM TARTRATE. Patient was hospitalized. 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 #5931142-7
Gleevec side effect was reported by a Physician from JAPAN on Oct 16, 2008. Male patient, 68 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 amylase increased, lipase increased. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with PREDNISOLONE, THYRADIN, FAMOTIDINE, AMARYL, HUMALOG, CAMOSTAT MESILATE, EPADEL. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5937138-3
Gleevec side effect was reported by a Physician from JAPAN on Oct 24, 2008. Male patient, 68 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 amylase increased, hepatic enzyme increased, lipase increased, pancreatic enzymes increased. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with PREDNISOLONE, THYRADIN, FAMOTIDINE, AMARYL, HUMALOG, CAMOSTAT MESILATE, EPADEL. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5100055-5
Gleevec side effect was reported by a Physician from UNITED STATES on May 05, 2006. Male patient, 67 years of age, was diagnosed with chronic myeloid leukaemia, non-hodgkin's lymphoma 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, bronchitis

, cellulitis

, chronic myeloid leukaemia, feeling abnormal, pancytopenia, red blood cell count decreased. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ATIVAN, PROTONIX, IMIPRAMINE, REGLAN, VITAMINS, GEMZAR. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5240371-X
Gleevec side effect was reported by a Consumer or non-health professional from GERMANY on Feb 05, 2007. Female patient, 66 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, cholecystectomy, gamma-glutamyltransferase increased, lipase increased, transaminases increased. Gleevec dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5364666-4
Gleevec side effect was reported by a Consumer or non-health professional from GERMANY on June 11, 2007. Female patient, 66 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, cholecystectomy, gamma-glutamyltransferase increased, lipase increased, transaminases increased. Gleevec dosage: 300 MG/DAY. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5066663-5
Gleevec side effect was reported by a Physician from UNITED STATES on Feb 08, 2006. Male patient, 65 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, blood albumin decreased, blood alkaline phosphatase increased, blood creatinine increased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, headache

, hypoaesthesia. Gleevec dosage: unknown. During the same period patient was treated with HYDREA, LEVOXYL, NEURONTIN, DURAGESIC, PRILOSEC, METFORMIN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5680193-9
Gleevec side effect was reported by a Pharmacist from UNITED STATES on Mar 17, 2008. Female patient, 65 years of age, weighting 181.0 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, bile duct obstruction, blood alkaline phosphatase increased, chromaturia, computerised tomogram abnormal, gastritis, jaundice

, pancreatic enlargement. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5727696-6
Gleevec side effect was reported by a Pharmacist from UNITED STATES on Apr 22, 2008. Female patient, 65 years of age, weighting 181.0 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, bile duct obstruction, blood alkaline phosphatase increased, chromaturia, computerised tomogram abnormal, gastritis, haemoglobin decreased, jaundice

. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.

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 #4794477-X
Gleevec side effect was reported by a Physician from FRANCE on Oct 03, 2005. Male patient, 65 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, asthenia, gamma-glutamyltransferase increased, hepatitis

. Gleevec dosage: 400 MG DAILY. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #4591277-0
Gleevec side effect was reported by a Physician from on Feb 21, 2005. Female patient, 64 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, hepatitis cholestatic. Gleevec dosage: 400 MG/DAY. Patient recovered.

Gleevec Side Effects Report #5162792-6
Gleevec side effect was reported by a Physician from GERMANY on Oct 27, 2006. Male patient, 63 years of age, weighting 224.9 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, ascites, aspartate aminotransferase increased, blood alkaline phosphatase increased, condition aggravated, gamma-glutamyltransferase increased, hepatic cirrhosis, metastatic malignant melanoma, oedema peripheral. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient died on 11/21/2006.

Gleevec Side Effects Report #4617217-3
Gleevec side effect was reported by a Consumer or non-health professional from on Mar 14, 2005. Female patient, 63 years of age, was diagnosed with chronic myeloid leukaemia, hepatitis

and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, autoimmune hepatitis, blood alkaline phosphatase increased, dyspepsia, gamma-glutamyltransferase increased, hepatic necrosis. Gleevec dosage: 400 MG DAILY. During the same period patient was treated with CORTICOSTEROID NOS. 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 #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 #4617211-2
Gleevec side effect was reported by a Physician from on Mar 16, 2005. Female patient, 59 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, anaemia, aspartate aminotransferase increased, autoimmune hepatitis, blood lactate dehydrogenase increased, haematocrit decreased, nausea

. Gleevec dosage: 400 MG/D. Patient recovered.

Gleevec Side Effects Report #4630409-2
Gleevec side effect was reported by a Physician from on Sept 17, 2004. Female patient, 59 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, blood creatinine increased, blood uric acid increased, dialysis

, diarrhoea, dysuria, malaise. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ASPIRIN, COENZA Q, OTC ANTIDIARRHEALS. Patient was hospitalized and became disabled. 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

, arrhythmia

, nausea

, prothrombin level decreased, pyrexia. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with ACETAMINOPHEN, CORTANCYL, PLAQUENIL, AMIODARONE, RYTHMOL, RAMIPRIL, PREVISCAN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #4771959-8
Gleevec side effect was reported by a Physician from FRANCE on July 05, 2005. Male patient, 57 years of age, weighting 185.2 lb, was diagnosed with chronic myeloid leukaemia, pyrexia, vasculitis

, arrhythmia

, hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, asthenia, blood iron increased, c-reactive protein increased, chills, cholelithiasis, cytolytic hepatitis. Gleevec dosage: 400 MG/DAY. During the same period patient was treated with PARACETAMOL, CORTANCYL, PLAQUENIL, AMIODARONE, RYTHMOL, TRIATEC, PREVISCAN. Patient was hospitalized. 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

. 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

. Gleevec dosage: 400 MG, QD. During the same period patient was treated with ARTIST. Patient recovered.

Gleevec Side Effects Report #5464242-9
Gleevec side effect was reported by a Physician from UNITED STATES on Sept 13, 2007. Male patient, 56 years of age, weighting 184.0 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, aldolase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, muscle disorder

, myalgia, myositis

, neuropathy, synovial cyst. Gleevec dosage: 400 MG, QD. Patient recovered.

Gleevec Side Effects Report #4885282-4
Gleevec side effect was reported by a Physician from JAPAN on Apr 08, 2004. Female patient, 56 years of age, weighting 99.21 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, arthralgia, aspartate aminotransferase increased, difficulty in walking, malignant neoplasm progression, myalgia, pain in extremity, platelet count increased. Gleevec dosage: 800 MG, QD. During the same period patient was treated with ZANTAC, VOLTAREN, MAGNESIUM OXIDE, PENTAZOCINE LACTATE. Patient was hospitalized. Patient died on 10/09/2005.

Gleevec Side Effects Report #5024414-4
Gleevec side effect was reported by a Physician from JAPAN on Apr 08, 2004. Female patient, 56 years of age, weighting 99.21 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, arthralgia, aspartate aminotransferase increased, difficulty in walking, malignant neoplasm progression, myalgia, pain in extremity, platelet count increased. Gleevec dosage: 800 MG, QD. During the same period patient was treated with ZANTAC, VOLTAREN, MAGNESIUM OXIDE, PENTAZOCINE LACTATE. Patient was hospitalized. Patient died on 10/09/2005.

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 #5105683-9
Gleevec side effect was reported by a Physician from UNITED KINGDOM on Aug 22, 2006. Male patient, 52 years of age, weighting 154.3 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, retroviral infection. Gleevec dosage: 400MG DAILY. Patient recovered.

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 #4962927-1
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 23, 2006. Female patient, 51 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, pyrexia, rash

, rash macular. Gleevec dosage: 400 MG, QD. During the same period patient was treated with FORTAZ. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #4707067-1
Gleevec side effect was reported by a Physician from SWITZERLAND on June 22, 2005. Female patient, 50 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, hepatic necrosis, hepatitis

. Gleevec dosage: 400 MG/D. Patient recovered.

Gleevec Side Effects Report #4707069-5
Gleevec side effect was reported by a Physician from SWITZERLAND on June 22, 2005. Female patient, 50 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, hepatic necrosis, hepatitis

. Gleevec dosage: 400 MG/D. Patient recovered.

Gleevec Side Effects Report #5371043-9
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 13, 2007. Female patient, 46 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, bone pain, nausea

, oral pain, periorbital oedema, rash

. Gleevec dosage: 400 MG, QD, ORAL. Patient recovered.

Gleevec Side Effects Report #4916688-2
Gleevec side effect was reported by a Pharmacist from CANADA on Feb 06, 2006. Male 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: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, gamma-glutamyltransferase increased, tuberculosis

. Gleevec dosage: 600 MG/D. During the same period patient was treated with FUROSEMIDE. Patient recovered.

Gleevec Side Effects Report #5610718-0
Gleevec side effect was reported by a Physician from UNITED KINGDOM on Jan 23, 2008. Male patient, 37 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 lactate dehydrogenase increased, gamma-glutamyltransferase increased, hepatic necrosis, liver function test abnormal. Gleevec dosage: unknown. Patient recovered.

Gleevec Side Effects Report #4765889-5
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 17, 2005. Female patient, 35 years of age, weighting 246.9 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, aspiration pleural cavity, atelectasis, blood alkaline phosphatase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood sodium decreased, blood uric acid increased. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5581322-8
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Dec 26, 2007. Female patient, 33 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: abortion induced, alanine aminotransferase increased, basophil count increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased. Gleevec dosage: 400 MG, QD. Patient recovered.

Gleevec Side Effects Report #4994914-1
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Jan 27, 2006. Female patient, 33 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: abortion induced, alanine aminotransferase increased, basophil count increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haematocrit decreased, haemoglobin decreased, lymphocyte count decreased. Gleevec dosage: 400 MG, QD. Patient recovered.

Gleevec Side Effects Report #5159935-7
Gleevec side effect was reported by a Physician from POLAND on Nov 16, 2006. Male patient, 29 years of age, weighting 158.7 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, hepatic enzyme abnormal, hepatitis b

. Gleevec dosage: 400 MG, QD. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5370620-9
Gleevec side effect was reported by a Physician from UNITED STATES on May 02, 2006. Female patient 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, hypoaesthesia, paraesthesia. Gleevec dosage: 400 MG, QD, ORAL. During the same period patient was treated with ANTIBIOTICS, ATENOLOL, HYDROCHLOROTHIAZIDE, ALLOPURINOL, IBUPROFEN, PHENERGAN. Patient recovered.

Gleevec Side Effects Report #5371523-6
Gleevec side effect was reported by a Pharmacist from UNITED STATES on Feb 07, 2007. Female patient 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. Gleevec dosage: unknown. 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 #5906117-4
Gleevec side effect was reported by a Pharmacist from UNITED STATES on Sept 25, 2008. Female patient, weighting 162.3 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal pain

, alanine aminotransferase increased, aspartate aminotransferase increased, bile duct obstruction, blood alkaline phosphatase increased, carbohydrate antigen 19-9 increased, cholecystectomy, fatigue, haemoglobin decreased. Gleevec dosage: 400 MG, UNK. During the same period patient was treated with ASPIRIN, LASIX, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5916292-3
Gleevec side effect was reported by a Health Professional from JAPAN on Oct 07, 2008. Male patient, weighting 187.4 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: acute myeloid leukaemia recurrent, alanine aminotransferase increased, aspartate aminotransferase increased, blast crisis in myelogenous leukaemia, blood lactate dehydrogenase increased, bone marrow transplant

, platelet count decreased, thrombocytopenia, white blood cell count decreased. Gleevec dosage: 400 MG/D. Patient died.

Gleevec Side Effects Report #5935822-9
Gleevec side effect was reported by a Health Professional from JAPAN on Oct 21, 2008. Male patient, weighting 187.4 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: acute myeloid leukaemia recurrent, alanine aminotransferase increased, aspartate aminotransferase increased, blast crisis in myelogenous leukaemia, blood lactate dehydrogenase increased, bone marrow transplant

, platelet count decreased, thrombocytopenia, white blood cell count decreased. Gleevec dosage: 400 MG/D. Patient died.

Gleevec Side Effects Report #5949517-9
Gleevec side effect was reported by a Health Professional from JAPAN on Nov 05, 2008. Male patient, weighting 187.4 lb, was diagnosed with chronic myeloid leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: acute myeloid leukaemia recurrent, alanine aminotransferase increased, aspartate aminotransferase increased, blast crisis in myelogenous leukaemia, blood lactate dehydrogenase increased, bone marrow transplant

, platelet count decreased, thrombocytopenia, white blood cell count decreased. Gleevec dosage: 400 MG/D. Patient died.

Gleevec Side Effects Report #6032011-7
Gleevec side effect was reported by a Physician from AUSTRIA on Dec 30, 2008. Male patient, weighting 260.1 lb, was diagnosed with chronic myeloid leukaemia, thrombocythaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, biopsy bone marrow abnormal, chronic myeloid leukaemia, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet disorder. Gleevec dosage: 400 MG, UNK. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #6036841-7
Gleevec side effect was reported by a Physician from AUSTRIA on Jan 08, 2009. Male patient, weighting 260.1 lb, was diagnosed with chronic myeloid leukaemia, thrombocythaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, biopsy bone marrow abnormal, chronic myeloid leukaemia, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet disorder. Gleevec dosage: 400 MG, UNK. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #6080432-9
Gleevec side effect was reported by a Health Professional from UNITED STATES on Feb 09, 2009. Male patient, weighting 200.6 lb, was diagnosed with chronic myeloid leukaemia, pain

and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aldolase increased, aspartate aminotransferase increased, back pain

, blood creatine phosphokinase increased, muscle spasms, myositis

, pain in extremity. Gleevec dosage: 400 MG, QD. During the same period patient was treated with IBUPROFEN, VITAMIN D. Patient recovered.

Gleevec Side Effects Report #6127020-3
Gleevec side effect was reported by a Physician from FINLAND on Mar 10, 2009. Female patient was diagnosed with chronic myeloid leukaemia, hypertonia, muscle spasms, pain

and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, gingival infection, influenza, muscular weakness, myalgia, myositis

, red blood cell sedimentation rate abnormal. Gleevec dosage: 400 MG DAILY. During the same period patient was treated with RENITEC COMP, EMGESAN, BURANA, PARACETAMOL. Patient recovered.

Gleevec Side Effects Report #5034898-3
Gleevec side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 03, 2006. Female patient 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, hypoaesthesia, paraesthesia. Gleevec dosage: 400 MG, QD, ORAL. During the same period patient was treated with ATENOLOL, HYDROCHLOROTHIAZIDE, ALLOPURINOL, IBUPROFEN, PHENERGAN. Patient recovered.

Gleevec Side Effects Report #5317677-9
Gleevec side effect was reported by a Physician from JAPAN on Apr 26, 2007. Male patient, 25 years of age, was diagnosed with acute lymphocytic leukaemia recurrent, infection

, disseminated intravascular coagulation, hypertension and was treated with Gleevec. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood creatine phosphokinase increased, disseminated intravascular coagulation, encephalitis

, hypertension, rhabdomyolysis. Gleevec dosage: 600 MG/DAY. During the same period patient was treated with DORMICUM, DIPRIVAN, BAKTAR, ANCOTIL, PROBITOR, CLARUTE, ACIROVEC. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5355941-8
Gleevec side effect was reported by a Physician from JAPAN on May 31, 2007. Male patient, 25 years of age, was diagnosed with acute lymphocytic leukaemia recurrent, infection

, hypertension, rhabdomyolysis. Gleevec dosage: 600 MG/DAY. During the same period patient was treated with DORMICUM, BAKTAR, ANCOTIL, PROBITOR, CLARUTE, ACIROVEC. Patient was hospitalized. Patient recovered.

Gleevec Side Effects Report #5700131-X
Gleevec side effect was reported by a Physician from JAPAN on Apr 04, 2008. Female patient, 69 years of age, weighting 119.0 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal distension, acute lymphocytic leukaemia, alanine aminotransferase increased, aspartate aminotransferase increased, b-cell lymphoma, bone marrow failure, chromosomal mutation, dyspnoea. Gleevec dosage: unknown. Patient was hospitalized. Patient died on 10/06/2007.

Gleevec Side Effects Report #5723148-8
Gleevec side effect was reported by a Consumer or non-health professional from JAPAN on Apr 25, 2008. Female patient, 69 years of age, weighting 119.0 lb, was diagnosed with acute lymphocytic leukaemia and was treated with Gleevec. After drug was administered, patient experienced the following side effects: abdominal distension, acute lymphocytic leukaemia recurrent, alanine aminotransferase increased, aspartate aminotransferase increased, bone marrow failure, chromosomal mutation, dyspnoea, leukaemic infiltration extramedullary. Gleevec dosage: unknown. During the same period patient was treated with PREDONINE. Patient was hospitalized. Patient died on 10/06/2007.

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 and alanine aminotransferase increased

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Gleevec and alanine aminotransferase increased Patient Reports February 11, 2012

side effects of Gleevec