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Imuran (Azathioprine) - Drug Ineffective - Suspected Cause - Side Effect Reports

 
 



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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