Index of reports
> Cases with Drug Ineffective (9)
Below is the selection of side effect reports (a.k.a. adverse event reports) related to Imuran (Azathioprine) where reactions include drug ineffective. The selected reports were submitted to the FDA during the sample period of about a year.
Possible Imuran side effects in male
Reported by a lawyer from United States on 2012-08-03
Patient: male, weighing 78.9 kg (173.6 pounds)
Reactions: Gastrointestinal Haemorrhage, Drug Ineffective, Crohn's Disease, Anaemia, Myeloid Leukaemia
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Remicade
Dosage: discontinued june or august 2008
Start date: 2004-01-01
End date: 2008-09-01
Imuran
Indication: Crohn's Disease
Start date: 2008-01-01
End date: 2010-02-01
Humira
Dosage: start date approximately june or august
Indication: Crohn's Disease
Start date: 2008-01-01
End date: 2010-02-01
Remicade
Indication: Crohn's Disease
Start date: 2004-01-01
Other drugs received by patient: Climara; Prednisone; Ferrous Sulfate TAB; Vitamin D; Amitriptyline HCL; Vitamin B-12; Antibiotics; Flagyl; Warfarin Sodium; Lovaza; Calcium; Prilosec; Vitamin A; Ascorbic Acid; Norco
Possible Imuran side effects in 38 year old male
Reported by a health professional (non-physician/pharmacist) from France on 2012-07-05
Patient: 38 year old male
Reactions: Colon Cancer, Drug Ineffective
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Prograf
Administration route: Oral
Indication: Crohn's Disease
Start date: 2001-01-01
Remicade
Dosage: received 5 infusions
Indication: Crohn's Disease
Start date: 2005-09-06
End date: 2006-03-01
Imuran
Administration route: Oral
Indication: Crohn's Disease
Start date: 2001-01-01
End date: 2004-01-01
Remicade
Dosage: received 5 infusions
Start date: 2001-01-01
End date: 2001-01-01
Possible Imuran side effects in 38 year old male
Reported by a health professional (non-physician/pharmacist) from France on 2012-06-29
Patient: 38 year old male
Reactions: Colon Cancer, Drug Ineffective
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Prograf
Administration route: Oral
Indication: Crohn's Disease
Start date: 2001-01-01
Remicade
Dosage: received 5 infusions
Indication: Crohn's Disease
Start date: 2005-09-01
End date: 2006-03-01
Remicade
Dosage: received 5 infusions
Start date: 2001-01-01
End date: 2001-01-01
Imuran
Administration route: Oral
Indication: Crohn's Disease
Start date: 2001-01-01
End date: 2004-01-01
Possible Imuran side effects in female
Reported by a consumer/non-health professional from United States on 2012-05-30
Patient: female, weighing 59.0 kg (129.7 pounds)
Reactions: Drug Ineffective, Maternal Exposure During Pregnancy, Nephrolithiasis, Cholelithiasis, Body Height Decreased, Food Allergy, Tendon Disorder, Abnormal Loss of Weight, Lipoma, Juvenile Arthritis
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Morphine
Indication: Product Used FOR Unknown Indication
Solu-Medrol
Indication: Premedication
Benadryl
Indication: Premedication
Benadryl
Administration route: Oral
Indication: Multiple Allergies
Start date: 2009-07-10
End date: 2012-04-10
Remicade
Start date: 2007-01-01
Epipen
Indication: Multiple Allergies
Start date: 2008-03-24
End date: 2012-04-10
Remicade
Start date: 2009-01-13
End date: 2012-04-10
Imuran
Indication: Rheumatoid Arthritis
Start date: 2011-09-01
End date: 2012-04-10
Remicade
Dosage: also reported as every 6 weeks
Indication: Juvenile Arthritis
Fexofenadine
Administration route: Oral
Indication: Multiple Allergies
Start date: 2008-03-24
End date: 2012-04-10
Other drugs received by patient: Calcium with Vitamin D
Possible Imuran side effects in female
Reported by a consumer/non-health professional from United States on 2012-01-18
Patient: female, weighing 59.0 kg (129.7 pounds)
Reactions: Drug Ineffective, Atrial Fibrillation, Rash, Cerebrovascular Accident, Flushing, Multi-Organ Failure, Gastrointestinal Infection, Renal Failure, Urosepsis, Arthritis, Myocardial Infarction, Cardiac Failure Congestive, Infusion Related Reaction
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Remicade
Start date: 2004-01-01
End date: 2004-08-11
Remicade
Start date: 2002-07-01
Remicade
Indication: Rheumatoid Arthritis
Start date: 2004-08-11
Remicade
Start date: 2004-04-01
Imuran
Indication: Inflammation
End date: 2004-09-02
Imuran
Indication: Rheumatoid Arthritis
End date: 2004-09-02
Remicade
Start date: 2002-07-01
End date: 2004-04-01
Other drugs received by patient: Hydrochlorothiazide; Fosamax; Prednisone TAB; Prednisone TAB; Potassium Chloride
Possible Imuran side effects in female
Reported by a consumer/non-health professional from United States on 2012-01-05
Patient: female, weighing 59.0 kg (129.7 pounds)
Reactions: Drug Ineffective, Atrial Fibrillation, Rash, Cerebrovascular Accident, Gastrointestinal Infection, Multi-Organ Failure, Flushing, Renal Failure, Urosepsis, Myocardial Infarction, Arthritis, Cardiac Failure Congestive, Infusion Related Reaction
Adverse event resulted in: death, life threatening event, hospitalization
Drug(s) suspected as cause:
Remicade
Indication: Rheumatoid Arthritis
Start date: 2004-08-11
Remicade
Start date: 2002-07-01
Remicade
Start date: 2002-07-01
End date: 2004-04-01
Remicade
Start date: 2004-01-01
End date: 2004-08-11
Imuran
Indication: Rheumatoid Arthritis
End date: 2004-09-02
Imuran
Indication: Inflammation
End date: 2004-09-02
Remicade
Start date: 2004-04-01
Other drugs received by patient: Hydrochlorothiazide; Prednisone TAB; Potassium Chloride; Fosamax; Prednisone TAB
Possible Imuran side effects in male
Reported by a physician from Japan on 2011-10-17
Patient: male, weighing 52.0 kg (114.4 pounds)
Reactions: Gingivitis, Drug Ineffective, Acute Myelomonocytic Leukaemia
Adverse event resulted in: hospitalization
Drug(s) suspected as cause:
Remicade
Start date: 2010-02-01
Imuran
Administration route: Oral
Indication: Crohn's Disease
Start date: 2003-03-01
End date: 2005-07-01
Remicade
Start date: 2005-07-01
Remicade
Dosage: 60th infusion
Start date: 2010-03-03
Remicade
Indication: Crohn's Disease
Start date: 2008-06-01
Remicade
Start date: 2003-04-01
Imuran
Administration route: Oral
Start date: 2005-07-01
Other drugs received by patient: Ferrous Citrate; Lendormin D; Loperamide HCL; Halcion; Phelloberin; Miya BM; Nizatidine; Sulfasalazine
Possible Imuran side effects in 37 year old female
Reported by a individual with unspecified qualification from France on 2011-10-06
Patient: 37 year old female
Reactions: Pneumonia Aspiration, Drug Ineffective, Progressive Multifocal Leukoencephalopathy
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Mabthera
Indication: Polymyositis
Methotrexate
Indication: Polymyositis
Start date: 2001-12-01
End date: 2002-11-01
Mabthera
Mycophenolate Mofetil
Indication: Polymyositis
Cyclosporine
Indication: Polymyositis
Mabthera
Imuran
Indication: Polymyositis
Start date: 2002-11-01
End date: 2005-02-01
Mabthera
Mabthera
Dosage: form: infusion
Other drugs received by patient: Prednisone; Prednisone; Prednisone; Prednisone; Prednisone; Immune Globulin NOS; Prednisone; Prednisone
Possible Imuran side effects in 39 year old female
Reported by a health professional (non-physician/pharmacist) from France on 2011-10-03
Patient: 39 year old female
Reactions: Pneumonia Aspiration, Drug Ineffective, Progressive Multifocal Leukoencephalopathy
Adverse event resulted in: death, hospitalization
Drug(s) suspected as cause:
Mycophenolate Mofetil
Indication: Polymyositis
Imuran
Indication: Polymyositis
Start date: 2002-11-01
End date: 2005-02-01
Cyclosporine
Indication: Polymyositis
Methotrexate
Indication: Polymyositis
Start date: 2001-12-01
End date: 2002-11-01
Mabthera
Indication: Polymyositis
Mabthera
Dosage: form: infusion
Mabthera
Mabthera
Mabthera
Other drugs received by patient: Prednisone; Prednisone; Prednisone; Prednisone; Prednisone; Prednisone; Prednisone
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