Index of reports
> Cases with Pyrexia (108)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Gleevec (Imatinib) where reactions include pyrexia. The selected reports were submitted to the FDA during the sample period of about a year.
Reports 1 - 30 of 108 Next >>
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-08-23
Patient: male, weighing 74.8 kg (164.6 pounds)
Reactions: Viral Infection, Pyrexia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-08-21
Patient: female
Reactions: Blood Iron Decreased, Asthenopia, Vomiting, Nausea, Anaemia, Pyrexia, Laboratory Test Abnormal, Diarrhoea, Ocular Hyperaemia, Eye Swelling, Vision Blurred, Lacrimation Increased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Digoxin
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2011-05-17
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-08-20
Patient: male, weighing 100.0 kg (220.0 pounds)
Reactions: Weight Decreased, Asthma, Thrombosis, Wheezing, Chills, Pyrexia, Malaise, Oedema Peripheral, Sinus Congestion, Diabetes Mellitus Inadequate Control, Decreased Appetite, Back Pain, Vein Disorder, Dyspnoea, Blast Crisis in Myelogenous Leukaemia, Nasal Congestion, Chronic Myeloid Leukaemia, Rhinitis Allergic, Neoplasm Malignant, Infection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2011-05-25
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2009-09-10
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2009-09-01
Other drugs received by patient: Warfarin Sodium; Atenolol; Fexofenadine; Novolog; Uroxatral; Coumadin
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from United States on 2012-08-15
Patient: female, weighing 134.0 kg (294.8 pounds)
Reactions: Urinary Tract Infection, Sepsis, Pyrexia, Escherichia Bacteraemia, Acute Myocardial Infarction, Pyelonephritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Ferrous Sulfate TAB; Tricor; Valium; Multi-Vitamins; Fiorinal
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-08-14
Patient: female, weighing 113.4 kg (249.4 pounds)
Reactions: Asthma, Vomiting, Increased Upper Airway Secretion, Pneumonia, Dyspnoea, Nausea, Pyrexia, Pulmonary Mass, Diarrhoea, Chest Pain, Bronchitis, White Blood Cell Count Increased, Cough
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2010-06-08
End date: 2010-10-01
Gleevec
Dosage: 600mg daily
Administration route: Oral
Start date: 2010-10-25
Gleevec
Dosage: 600mg daily
Administration route: Oral
Start date: 2010-10-25
End date: 2010-12-03
Other drugs received by patient: Prednisone TAB; Allopurinol
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from South Africa on 2012-08-09
Patient: female, weighing 29.0 kg (63.8 pounds)
Reactions: Myalgia, Tuberculosis, Sepsis, Pyrexia, Neutropenia, Thrombocytopenia, Abdominal Pain Upper, Influenza
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 260 mg, unk
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2006-04-12
Gleevec
Dosage: 250 mg, unk
Administration route: Oral
Start date: 2006-05-04
End date: 2006-06-12
Gleevec
Dosage: 600 mg, unk
Administration route: Oral
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-08-07
Patient: male, weighing 78.6 kg (172.9 pounds)
Reactions: Weight Decreased, Renal Infarct, Metastases To Liver, Tachycardia, Platelet Count Increased, Pyrexia, Colon Neoplasm, Comminuted Fracture, Spinal Compression Fracture, Pathological Fracture, White Blood Cell Count Increased, Intervertebral Disc Protrusion, Back Pain, Hiatus Hernia, Loss of Control of Legs, Anaemia, Early Satiety, Lumbar Vertebral Fracture, Osteopenia, Hypoaesthesia, Cholelithiasis, Metastases To Spine, Metastases To Kidney, Hepatic Lesion, Fall, Constipation, Metastases To Lymph Nodes, Fatigue, Ileus, Metastases To Adrenals, Spinal Deformity, Blood Sodium Decreased, Metastatic Renal Cell Carcinoma, Blood Glucose Increased, Metastases To Lung, Decreased Appetite, Spinal Cord Compression, Vomiting, Excoriation, Nausea, Nerve Compression, Diarrhoea, Metastases To Bone, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Benazepril Hydrochloride; Amitiza; Promethazine; Dulcolax; Multi-Vitamins; Norco; Colace; Darvocet-N 50; Lactulose
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-07-31
Patient: male
Reactions: Pneumonia, Diarrhoea, Drug Ineffective, Nausea, Pyrexia, Leukaemia Recurrent, Muscle Spasms
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Sprycel
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-07-26
Patient: male, weighing 100.0 kg (220.0 pounds)
Reactions: Thrombosis, Weight Decreased, Asthma, Chills, Wheezing, Pyrexia, Malaise, Oedema Peripheral, Sinus Congestion, Decreased Appetite, Diabetes Mellitus Inadequate Control, Back Pain, Dyspnoea, Vein Disorder, Blast Crisis in Myelogenous Leukaemia, Nasal Congestion, Chronic Myeloid Leukaemia, Rhinitis Allergic, Neoplasm Malignant, Infection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2009-09-01
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2009-09-10
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2011-05-25
Other drugs received by patient: Uroxatral; Novolog; Fexofenadine; Coumadin; Warfarin Sodium; Atenolol
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-07-20
Patient: male
Reactions: Asthma, Thrombosis, Weight Decreased, Wheezing, Chills, Pyrexia, Malaise, Oedema Peripheral, Sinus Congestion, Decreased Appetite, Diabetes Mellitus Inadequate Control, Back Pain, Vein Disorder, Dyspnoea, Nasal Congestion, Chronic Myeloid Leukaemia, Rhinitis Allergic, Neoplasm Malignant, Infection
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2009-09-01
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2009-09-10
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Start date: 2011-05-25
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Other drugs received by patient: Atenolol; Fexofenadine; Novolog; Uroxatral; Warfarin Sodium
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-19
Patient: female
Reactions: Incision Site Abscess, Pyrexia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from United States on 2012-07-19
Patient: female, weighing 90.7 kg (199.5 pounds)
Reactions: Metabolic Acidosis, Vomiting, Nausea, Blast Crisis in Myelogenous Leukaemia, Chills, Mental Status Changes, Pyrexia, Cardiopulmonary Failure, Hypoxia, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-07-16
Patient: female, weighing 85.8 kg (188.8 pounds)
Reactions: Pyrexia, Abdominal Pain Upper, Fatigue, Upper Respiratory Tract Infection, Exostosis, Blood Creatinine Increased, Blood Glucose Increased, Cough, Fluid Overload, Pneumonia, Dyspnoea, Hypotension, Anaemia, Dysgeusia, Bronchitis, Neutropenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2010-05-01
Gleevec
Dosage: 100 mg, unk
Administration route: Oral
Gleevec
Dosage: 200 mg, unk
Administration route: Oral
Other drugs received by patient: Allegra; Omeprazole; Neurontin; Insulin; Iron; Mucinex; Allopurinol; Humulin 70 / 30; Prilosec; Keflex; Toprol-XL; Codeine Sulfate; Potassium Chloride; Omega-3 Fatty Acids; Coenzyme Q10; Fish OIL; Levaquin; Calcium; Levothyroxine Sodium; Metoprolol Tartrate; Potassium Chloride; Steroids NOS; Gabapentin; Vitamin D; Fexofenadine; Cephalexin
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-06-21
Patient: male
Reactions: Pneumonia, Drug Ineffective, Nausea, Diarrhoea, Pyrexia, Leukaemia Recurrent, Muscle Spasms
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Sprycel
Possible Gleevec side effects in 84 year old female
Reported by a consumer/non-health professional from Taiwan, Province of China on 2012-06-07
Patient: 84 year old female
Reactions: Wrong Technique in Drug Usage Process, Dysphagia, Lung Infection, Dementia, Duodenal Ulcer, Pyrexia, Fall, Haemoglobin Decreased, Choking
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a physician from Viet NAM on 2012-06-06
Patient: male, weighing 52.0 kg (114.4 pounds)
Reactions: Haemoglobin Decreased, C-Reactive Protein Increased, Hypoglycaemia, Pyrexia, White Blood Cells Urine Positive
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from Viet NAM on 2012-06-05
Patient: male, weighing 52.0 kg (114.4 pounds)
Reactions: Blood Glucose Decreased, Pyrexia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-06-01
Patient: male, weighing 76.0 kg (167.2 pounds)
Reactions: Blood Bilirubin Increased, Hepatic Function Abnormal, Oropharyngeal Pain, Pyrexia, Erythema, Genital Lesion, LIP Erosion, Liver Disorder, Haematocrit Decreased, Malaise, C-Reactive Protein Increased, Oral Candidiasis, Anorectal Disorder, Conjunctival Hyperaemia, Urinary Retention, Erythema Multiforme, Melaena, Stevens-Johnson Syndrome, Alanine Aminotransferase Increased, Dyschezia, Blood Lactate Dehydrogenase Increased, Drug Intolerance, Monocyte Count Increased, Oral Disorder, Aspartate Aminotransferase Increased, Platelet Count Decreased, Leucine Aminopeptidase Increased, Leukopenia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in 37 year old female
Reported by a consumer/non-health professional from Mexico on 2012-06-01
Patient: 37 year old female
Reactions: Gingival Bleeding, Drug Ineffective, Bone Pain, Pyrexia, Chronic Myeloid Leukaemia, Shock
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Gleevec
Dosage: 200 mg, daily
Administration route: Oral
Start date: 2012-05-24
Gleevec
Dosage: 600 mg daily
Administration route: Oral
End date: 2012-03-27
Possible Gleevec side effects in 61 year old female
Reported by a health professional (non-physician/pharmacist) from Korea, Republic of on 2012-06-01
Patient: 61 year old female
Reactions: Pneumonia, Drug Resistance, Dyspnoea, Blast Crisis in Myelogenous Leukaemia, Nausea, General Physical Health Deterioration, Pyrexia, Death, Grand MAL Convulsion, Ileus, Hypoxia, Asthenia, Azotaemia, Leukocytosis, Decreased Appetite
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a physician from Sudan on 2012-05-28
Patient: male, weighing 68.0 kg (149.6 pounds)
Reactions: Anaemia, Sepsis, Pyrexia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-05-23
Patient: female, weighing 48.0 kg (105.6 pounds)
Reactions: Dyspnoea, Normal Newborn, Nausea, Maternal Exposure During Pregnancy, Pyrexia, Malaise, Interstitial Lung Disease, Suicide Attempt, Pleural Effusion, Delivery, Cough
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 600 mg, unk
Start date: 2005-05-01
Gleevec
Dosage: 100 mg, daily
Administration route: Oral
Start date: 2004-10-21
Gleevec
Dosage: 400 mg, per day
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2004-09-30
End date: 2004-10-10
Gleevec
Dosage: 100 mg, per day
Hydrea
Dosage: 1 g, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2004-09-09
End date: 2004-09-29
Possible Gleevec side effects in 91 year old female
Reported by a physician from Japan on 2012-05-22
Patient: 91 year old female
Reactions: Pneumonia Aspiration, Pyrexia
Adverse event resulted in: death
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in 37 year old female
Reported by a consumer/non-health professional from Mexico on 2012-05-16
Patient: 37 year old female
Reactions: Gingival Bleeding, Drug Ineffective, Bone Pain, Pyrexia, Chronic Myeloid Leukaemia, Shock
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Gleevec
Dosage: 600 mg daily
Administration route: Oral
End date: 2012-03-27
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from United Kingdom on 2012-05-14
Patient: female
Reactions: Dysphagia, Drug Ineffective, Anaemia, Tonsillar Hypertrophy, Pyrexia, Chronic Myeloid Leukaemia, Thrombocytosis, Neutropenia, White Blood Cell Count Increased, Hepatosplenomegaly
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 600 mg, daily
Start date: 2011-08-03
End date: 2011-12-21
Gleevec
Indication: Chronic Myeloid Leukaemia
Start date: 2010-01-01
Gleevec
Dosage: 800 mg, daily
Start date: 2011-12-21
End date: 2012-03-12
Possible Gleevec side effects in female
Reported by a physician from United Kingdom on 2012-05-04
Patient: female
Reactions: Dysphagia, Drug Ineffective, Anaemia, Tonsillar Hypertrophy, Pyrexia, Chronic Myeloid Leukaemia, Thrombocytosis, Neutropenia, Hepatosplenomegaly, White Blood Cell Count Increased
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Gleevec
Indication: Chronic Myeloid Leukaemia
Start date: 2010-01-01
Gleevec
Dosage: 600 mg, daily
Start date: 2011-08-03
End date: 2011-12-21
Gleevec
Dosage: 800 mg, daily
Start date: 2011-12-21
End date: 2012-03-12
Possible Gleevec side effects in 84 year old female
Reported by a consumer/non-health professional from Taiwan, Province of China on 2012-04-25
Patient: 84 year old female
Reactions: Wrong Technique in Drug Usage Process, Dysphagia, Lung Infection, Dementia, Duodenal Ulcer, Pyrexia, Fall, Haemoglobin Decreased, Choking
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a physician from Mexico on 2012-04-25
Patient: male
Reactions: Death, Haemoglobin Decreased, General Physical Condition Abnormal, Blast Crisis in Myelogenous Leukaemia, Platelet Count Decreased, Pyrexia
Adverse event resulted in: death
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2011-10-25
Gleevec
Dosage: 600 mg daily
Administration route: Oral
Possible Gleevec side effects in male
Reported by a health professional (non-physician/pharmacist) from Japan on 2012-04-12
Patient: male, weighing 78.0 kg (171.6 pounds)
Reactions: Eyelid Oedema, Pruritus, Bundle Branch Block Right, Pyrexia, Pericardial Effusion, Colonic Polyp, Oedema Peripheral, Blood Creatinine Increased, Fluid Retention, Hiatus Hernia, Pneumonia, Anaemia, Skin Oedema, Renal Atrophy, Occult Blood Positive, Gastric Cancer Stage II, Dehydration, Upper Gastrointestinal Haemorrhage, Normochromic Normocytic Anaemia, Eye Oedema, Gastritis, Haematemesis, Abdominal Distension, Oedema, Bone Marrow Failure, Pleural Effusion, Renal Failure Acute, Decreased Appetite, Nephrogenic Anaemia, Atrial Fibrillation, Rash, Renal Failure Chronic, Ascites, Haemoglobin Decreased, Renal Impairment, Cardiac Failure, Neoplasm Malignant, Pigmentation Disorder, Hypothyroidism, Hypoalbuminaemia, Hypogammaglobulinaemia, Blood Pressure Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 200 mg daily
Administration route: Oral
Start date: 2011-06-21
End date: 2011-10-18
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2005-06-03
End date: 2011-04-15
Other drugs received by patient: Mucosta; Lasix; Aspirin; Candesartan Cilexetil; Lasix; RED Blood Cells, Concentrated; Amlodipine Besylate; Isosorbide Mononitrate; RED Blood Cells, Concentrated
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from Mexico on 2012-04-12
Patient: male
Reactions: Death, Haemoglobin Decreased, General Physical Condition Abnormal, Blast Crisis in Myelogenous Leukaemia, Platelet Count Decreased, Pyrexia, Chronic Myeloid Leukaemia
Adverse event resulted in: death
Drug(s) suspected as cause:
Gleevec
Dosage: 600 mg daily
Administration route: Oral
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2011-12-15
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