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Index of reports
> Cases with Haemoglobin Decreased ()
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Gleevec (Imatinib) where reactions include haemoglobin decreased. The selected reports were submitted to the FDA during the sample period of about a year. Reports 1 - 30 of Next >>
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-08-13
Patient: male
Reactions: Drug Ineffective, Pain, Sensory Loss, Neoplasm Progression, Fatigue, Measles, Adverse Event, Rash Morbilliform, Muscle Spasms, Product Quality Issue, Dyspnoea, Rash, Tremor, Haemoglobin Decreased, Neoplasm Malignant, Diarrhoea, Heart Rate Increased, Asthenia, Influenza Like Illness
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Start date: 2011-07-13
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chordoma
Start date: 2011-06-14
Gleevec
Dosage: 800 mg, daily
Administration route: Oral
Other drugs received by patient: Cisplatin
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-08-13
Patient: male
Reactions: Haemoglobin Decreased, Lung Disorder, Blast Crisis in Myelogenous Leukaemia, RED Blood Cell Count Decreased
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 600 mg, qd
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2012-04-07
Gleevec
Dosage: 400mg daily
Administration route: Oral
Start date: 2012-04-07
Other drugs received by patient: Blood Transfusion, Auxiliary Products
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-08-06
Patient: male
Reactions: Blood Iron Decreased, Blood Chloride Decreased, Glomerular Filtration Rate Decreased, Incorrect Dose Administered, Alanine Aminotransferase Increased, Drug Prescribing Error, Transferrin Saturation Decreased, Haemoglobin Decreased, Renal Impairment, Aspartate Aminotransferase Increased, Oedema, Blood Sodium Decreased, Blood Creatinine Increased, Lethargy
Adverse event resulted in: life threatening event
Drug(s) suspected as cause:
Gleevec
Dosage: 600 mg, 100 mg 6 tablets daily
Administration route: Oral
Start date: 2012-02-16
End date: 2012-06-19
Gleevec
Dosage: 2400 mg, qd (three days)
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2012-06-01
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-07-27
Patient: female, weighing 65.8 kg (144.7 pounds)
Reactions: Blood Bilirubin Increased, Lymphadenopathy, Stomach Mass, Nephrolithiasis, Fatigue, Haematocrit Decreased, Malaise, Pleural Effusion, Blood Creatinine Increased, Retroperitoneal Mass, Metastatic Neoplasm, Vomiting, Hydronephrosis, Blood Pressure Systolic Increased, Nausea, Varices Oesophageal, Ascites, Haemoglobin Decreased, Lung Disorder, Platelet Count Decreased, Asthenia
Drug(s) suspected as cause:
Gleevec
Dosage: 200 mg, daily
Administration route: Oral
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Gastrointestinal Stromal Tumour
Start date: 2011-08-31
Gleevec
Dosage: 100 mg, bid
Administration route: Oral
Gleevec
Dosage: 100 mg, qd
Administration route: Oral
Indication: Gastric Cancer
Start date: 2011-09-01
Other drugs received by patient: Zofran; Fluid / Electrolyte Replacement Therapy; Omeprazole; Vytorin; Aspirin; Plavix; Ranexa; Metformin Hydrochloride; Lopressor
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-07-05
Patient: male
Reactions: Haemoglobin Decreased, Renal Impairment, Atrioventricular Block, Gastroenteritis, Aortic Valve Disease
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Pepcid; Epogen; Iron
Possible Gleevec side effects in male
Reported by a physician from United States on 2012-06-25
Patient: male
Reactions: Haemoglobin Decreased, Renal Impairment, Atrioventricular Block, Gastroenteritis, Aortic Valve Incompetence
Drug(s) suspected as cause:
Gleevec
Other drugs received by patient: Pepcid; Iron; Epogen
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-06-22
Patient: female, weighing 79.0 kg (173.8 pounds)
Reactions: Haemoglobin Decreased, Haematocrit Decreased, Dementia
Drug(s) suspected as cause:
Diphenhydramine HCL
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2008-01-14
Possible Gleevec side effects in female
Reported by a pharmacist from United States on 2012-06-22
Patient: female, weighing 79.0 kg (173.8 pounds)
Reactions: Haemoglobin Decreased, Haematocrit Decreased, Dementia
Drug(s) suspected as cause:
Diphenhydramine HCL
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2008-01-14
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from EL Salvador on 2012-06-07
Patient: female
Reactions: Haemoglobin Decreased, Lymphocyte Count Increased, White Blood Cell Count Decreased, Pneumonia, Blast Crisis in Myelogenous Leukaemia, Thrombocytosis, Platelet Count Increased, Status Epilepticus, Respiratory Tract Infection, Terminal State
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 800 mg, unk
End date: 2012-04-01
Gleevec
Dosage: 300 mg, daily
Gleevec
Dosage: 400 mg, unk
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2010-07-01
Gleevec
Dosage: 400 mg, unk
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 female
Reported by a physician from Sudan on 2012-06-05
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Haemoglobin Decreased, Vomiting, Diarrhoea, White Blood Cell Count Increased
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from United States on 2012-06-05
Patient: female, weighing 73.6 kg (161.8 pounds)
Reactions: Body Temperature Increased, Visual Acuity Reduced, Blood Albumin Decreased, Mean Cell Volume Decreased, Headache, Constipation, Hyperhidrosis, Herpes Zoster, Hot Flush, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Sodium Decreased, Blood Glucose Increased, Back Pain, Spinal Cord Compression, White Blood Cell Count Decreased, Bowel Movement Irregularity, Vomiting, Nausea, Rash, Mean Cell Volume Increased, Nasal Congestion, Radicular Pain, Muscle Twitching, Burning Sensation, Haemoglobin Decreased, Arthralgia, Gait Disturbance
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Gleevec
Dosage: 400 mg every other day
Administration route: Oral
Start date: 2012-02-16
Gleevec
Dosage: 800 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2005-12-20
Other drugs received by patient: Metformin HCL; Hydrea; Aspirin; Aranesp; Vitamin D; Lotrel; Clonazepam; Miraphen; Mirtazapine; Hydrochlorothiazide; Multi-Vitamins
Possible Gleevec side effects in female
Reported by a physician from Sudan on 2012-06-05
Patient: female, weighing 89.0 kg (195.8 pounds)
Reactions: Haemoglobin Decreased, White Blood Cell Count Decreased, Vomiting
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from Sudan on 2012-05-28
Patient: male, weighing 71.0 kg (156.2 pounds)
Reactions: Death, Haemoglobin Decreased, Renal Failure, White Blood Cell Count Increased
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2005-10-13
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Start date: 2005-10-20
End date: 2011-11-01
Possible Gleevec side effects in female
Reported by a physician from Sudan on 2012-05-28
Patient: female, weighing 89.0 kg (195.8 pounds)
Reactions: White Blood Cell Count Decreased, Haemoglobin Decreased, Death, Vomiting
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from Sudan on 2012-05-28
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Death, Haemoglobin Decreased, Vomiting, Diarrhoea, White Blood Cell Count Increased
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from Sudan on 2012-05-28
Patient: male, weighing 68.0 kg (149.6 pounds)
Reactions: Haemoglobin Decreased, Cardiac Failure, Anaemia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from Sudan on 2012-05-28
Patient: female, weighing 49.0 kg (107.8 pounds)
Reactions: Haemoglobin Decreased, Death, Platelet Count Decreased, White Blood Cell Count Increased, Ascites, Epistaxis
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from Sudan on 2012-05-25
Patient: male, weighing 60.0 kg (132.0 pounds)
Reactions: Haemoglobin Decreased, Pancytopenia
Adverse event resulted in: disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a physician from Sudan on 2012-05-24
Patient: female, weighing 68.0 kg (149.6 pounds)
Reactions: Haemoglobin Decreased, Haemorrhage, White Blood Cell Count Increased
Adverse event resulted in: death, disablity
Drug(s) suspected as cause:
Gleevec
Possible Gleevec side effects in female
Reported by a health professional (non-physician/pharmacist) from United States on 2012-05-22
Patient: female, weighing 73.6 kg (161.8 pounds)
Reactions: Body Temperature Increased, Blood Albumin Decreased, Visual Acuity Reduced, Mean Cell Volume Decreased, Headache, Constipation, Hyperhidrosis, Herpes Zoster, Hot Flush, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Sodium Decreased, Blood Glucose Increased, Spinal Cord Compression, Bowel Movement Irregularity, White Blood Cell Count Decreased, Vomiting, Nausea, Nasal Congestion, Rash, Mean Cell Volume Increased, Radicular Pain, Muscle Twitching, Burning Sensation, Haemoglobin Decreased, Arthralgia, Gait Disturbance
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Gleevec
Dosage: 800 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2005-12-20
Gleevec
Dosage: 400 mg every other day
Administration route: Oral
Start date: 2012-02-16
Other drugs received by patient: Multi-Vitamins; Metformin HCL; Aranesp; Mirtazapine; Miraphen; Clonazepam; Hydrea; Hydrochlorothiazide; Lotrel; Vitamin D; Aspirin
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 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 Australia on 2012-04-23
Patient: male, weighing 85.4 kg (187.9 pounds)
Reactions: Haemoglobin Decreased, Arthralgia, Bone Pain, Platelet Count Decreased
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2009-12-05
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Start date: 2011-12-03
Other drugs received by patient: Usana; Inflavanoid; Tamsulosin HCL
Possible Gleevec side effects in female
Reported by a consumer/non-health professional from United States on 2012-04-18
Patient: female
Reactions: Weight Decreased, Labyrinthitis, Pruritus, Pain, Abdominal Discomfort, Fatigue, Dyspepsia, Chest Pain, Otorrhoea, Dizziness, Oedema, Vomiting, Nausea, Acne, Rash, Full Blood Count Decreased, Haemoglobin Decreased, Diarrhoea, Vertigo
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg, daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2008-06-23
Gleevec
Dosage: 400 mg, qd
Administration route: Oral
Start date: 2011-04-08
Gleevec
Dosage: 1 df, daily
Administration route: Oral
Start date: 2011-04-08
Other drugs received by patient: Boniva
Possible Gleevec side effects in male
Reported by a consumer/non-health professional from United States on 2012-04-16
Patient: male
Reactions: Gastrointestinal Haemorrhage, Pruritus, Aortic Stenosis, Angina Unstable, Tricuspid Valve Incompetence, Device Occlusion, Pulmonary Arterial Pressure Increased, Iron Deficiency Anaemia, Blood Pressure Inadequately Controlled, Radiation Proctopathy, Blood Creatinine Increased, Hiatus Hernia, Coronary Artery Disease, Duodenal Ulcer, Helicobacter Infection, Troponin Increased, Cardiomyopathy, Anaemia Macrocytic, Periorbital Oedema, Heart Rate Decreased, Diverticulum, Normochromic Normocytic Anaemia, Venous Occlusion, Gastric Ulcer, Pallor, Sinus Bradycardia, Chest Pain, Bone Marrow Failure, Acute Myocardial Infarction, Gastrooesophageal Reflux Disease, Blood Glucose Increased, Blood Urea Increased, Rash, Renal Failure Chronic, Full Blood Count Decreased, Osteoarthritis, Haemoglobin Decreased, Mitral Valve Incompetence, Ventricular Fibrillation, Hypertension
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Gleevec
Dosage: 100 mg, tid
Administration route: Oral
Start date: 2010-12-06
Gleevec
Dosage: 400 mg, qd
Indication: Chronic Myeloid Leukaemia
Start date: 2001-06-01
Gleevec
Dosage: 100 mg, qid
Administration route: Oral
Start date: 2008-06-16
Other drugs received by patient: Ziac; Nitroglycerin; Epipen; Aspirin; Osteo BI-Flex; Magnesium Oxide; Ferrous Sulfate TAB; Carafate; RED Blood Cells, Concentrated; Valturna; Ascorbic Acid; Heparin; Plavix
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
Possible Gleevec side effects in male
Reported by a physician from Mexico on 2012-04-09
Patient: male
Reactions: Haemoglobin Decreased, Death, General Physical Condition Abnormal, Platelet Count Decreased, Pyrexia, Chronic Myeloid Leukaemia
Adverse event resulted in: death
Drug(s) suspected as cause:
Gleevec
Dosage: 400 mg daily
Administration route: Oral
Indication: Chronic Myeloid Leukaemia
Start date: 2011-12-15
Gleevec
Dosage: 600 mg daily
Administration route: Oral
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