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Imuran (Azathioprine) - Side Effect Reports to FDA

 
 



This is an index of side effect / adverse reaction reports (a.k.a. adverse event reports) related to Imuran (Azathioprine) and submitted to the FDA during the sample period of about a year. The information is not vetted and should not be considered as verified clinical evidence.

Reports by Event Outcome

All Cases (247)
Death (35)
Life Threatening Events (20)
Disability (12)

Reports by Reaction Type

Anaemia (16)Pneumonia (14)Liver Disorder (13)Diarrhoea (12)Pyrexia (11)Drug Interaction (10)Pleural Effusion (10)Pancytopenia (10)Drug Ineffective (9)Herpes Zoster (9)Hepatosplenic T-Cell Lymphoma (9)Maternal Exposure During Pregnancy (9)

Below are a few examples of reports where side effects / adverse reactions may be related to Imuran (Azathioprine). For a complete list or a specific selection of reports, please use the links above.

Possible Imuran side effects in male

Reported by a pharmacist from United States on 2012-08-21

Patient: male, weighing 74.0 kg (162.8 pounds)

Reactions: Hepatosplenic T-Cell Lymphoma, Pancytopenia, Pyrexia, Convulsion, Mucosal Inflammation, Tumour Lysis Syndrome, Small Intestinal Ulcer Haemorrhage, Haemorrhagic Diathesis, Neutropenia

Adverse event resulted in: death, life threatening event, hospitalization

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 1997-03-25
    End date: 1997-12-01

Imuran
    Administration route: Oral
    Start date: 1999-06-14
    End date: 2002-05-22

Imuran
    Administration route: Oral
    Start date: 1997-12-01
    End date: 1999-06-13

Imuran
    Administration route: Oral
    Start date: 2001-10-25

Remicade
    Start date: 2001-12-10

Remicade
    Start date: 2001-10-24
    End date: 2001-10-24

Remicade
    Start date: 2002-05-22
    End date: 2002-05-22

Remicade
    Start date: 2001-11-08

Remicade
    Indication: Crohn's Disease
    Start date: 2002-02-25
    End date: 2002-02-25

Other drugs received by patient: Prednisone TAB; Prednisone TAB; Probiotica; Mercaptopurine; Multi-Vitamin; Iron; Budesonide; Calcium; Entocort EC; Vitamin E; Entocort EC; Macrobid



Possible Imuran side effects in male

Reported by a pharmacist from United States on 2012-08-21

Patient: male

Reactions: Aqueductal Stenosis, Antiphospholipid Syndrome, Graft Versus Host Disease, Hepatosplenic T-Cell Lymphoma, Nuclear Magnetic Resonance Imaging Brain Abnormal, Pulmonary Embolism, Hydrocephalus, Hypertension

Adverse event resulted in: death, life threatening event

Drug(s) suspected as cause:
Imuran
    Indication: Colitis
    Start date: 2002-11-15

Imuran
    Start date: 2001-12-01
    End date: 2002-11-14

Lovenox
    Indication: Product Used FOR Unknown Indication

Remicade
    Dosage: single infusion
    Indication: Colitis Ulcerative
    Start date: 2001-12-22
    End date: 2001-12-22

Other drugs received by patient: Asacol; Heparin; Heparin; Steroids



Possible Imuran side effects in male

Reported by a physician from Japan on 2012-08-17

Patient: male, weighing 57.0 kg (125.4 pounds)

Reactions: Intestinal Perforation, Pleural Effusion, Tuberculosis Gastrointestinal, Computerised Tomogram Abnormal

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-06-01

Remicade
    Indication: Crohn's Disease
    Start date: 2012-05-31

Remicade
    Start date: 2012-04-11

Remicade
    Start date: 2012-04-24

Other drugs received by patient: Elental; Pentasa; Prednisolone; Epinastine Hydrochloride



Possible Imuran side effects in male

Reported by a physician from United States on 2012-08-17

Patient: male, weighing 109.3 kg (240.5 pounds)

Reactions: Pneumonia, Hepatosplenic T-Cell Lymphoma

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Start date: 2004-03-11
    End date: 2004-07-29

Imuran
    Administration route: Oral
    Indication: Crohn's Disease
    Start date: 2004-07-29
    End date: 2011-05-25

Remicade
    Indication: Crohn's Disease
    Start date: 2006-11-22

Remicade

Remicade
    End date: 2011-09-09

Other drugs received by patient: Imodium A-D; Imodium A-D; Prednisone TAB; Sulfamethoxazole and Trimethoprim; Folic Acid; Nplate; Multi-Vitamins



Possible Imuran side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-08-13

Patient: male, weighing 102.0 kg (224.4 pounds)

Reactions: Diarrhoea, Escherichia Urinary Tract Infection, Gastric Antral Vascular Ectasia, Concomitant Disease Progression, Anaemia Postoperative

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Augmentin '500'
    Dosage: 1000 mg, bid
    Indication: Urinary Tract Infection
    Start date: 2011-08-28
    End date: 2011-09-01

Certican
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-27
    End date: 2011-07-12

Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Start date: 2011-07-25
    End date: 2011-08-29

Imuran
    Dosage: 150 mg, qd
    Indication: Immunosuppression
    Start date: 2011-08-30
    End date: 2011-09-01

Nexium
    Dosage: unk

Prednisone TAB
    Dosage: 15 mg, daily
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-07-01
    End date: 2011-07-13

Prednisone TAB
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-07-14

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-28

Valcyte
    Dosage: 450 mg, qd
    Start date: 2011-06-27

Other drugs received by patient: Iron Dextran; Iron Dextran; Iron Dextran



Possible Imuran side effects in male

Reported by a physician from United States on 2012-08-10

Patient: male, weighing 102.0 kg (224.4 pounds)

Reactions: Diarrhoea, Escherichia Urinary Tract Infection, Gastric Antral Vascular Ectasia, Concomitant Disease Progression, Anaemia Postoperative

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Augmentin '500'
    Dosage: 1000 mg, bid
    Indication: Urinary Tract Infection
    Start date: 2011-08-28
    End date: 2011-09-01

Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Start date: 2011-07-25
    End date: 2011-08-29

Certican
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-27
    End date: 2011-07-12

Imuran
    Dosage: 150 mg, qd
    Indication: Immunosuppression
    Start date: 2011-08-30
    End date: 2011-09-01

Nexium
    Dosage: unk

Prednisone TAB
    Dosage: 15 mg, daily
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-07-01
    End date: 2011-07-13

Prednisone TAB
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-07-14

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-28

Valcyte
    Dosage: 450 mg, qd
    Start date: 2011-06-27

Other drugs received by patient: Iron Dextran; Iron Dextran; Iron Dextran



Possible Imuran side effects in female

Reported by a physician from United States on 2012-08-10

Patient: female, weighing 86.3 kg (189.8 pounds)

Reactions: Crohn's Disease, Abscess Intestinal

Drug(s) suspected as cause:
Humira
    Start date: 2012-07-19
    End date: 2012-07-19

Humira
    Indication: Crohn's Disease
    Start date: 2012-06-21
    End date: 2012-06-21

Humira
    Start date: 2012-07-05
    End date: 2012-07-05

Imuran
    Indication: Crohn's Disease



Possible Imuran side effects in female

Reported by a consumer/non-health professional from Turkey on 2012-08-07

Patient: female, weighing 48.0 kg (105.6 pounds)

Reactions: Haemoglobin Decreased, Haematocrit Decreased, Thalassaemia, Serum Ferritin Decreased

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Indication: Immunosuppressant Drug Therapy
    Start date: 2011-09-01
    End date: 2012-03-01

Rebif
    Indication: Multiple Sclerosis
    Start date: 2009-01-01



Possible Imuran side effects in male

Reported by a physician from United States on 2012-08-03

Patient: male, weighing 102.0 kg (224.4 pounds)

Reactions: Escherichia Urinary Tract Infection, Diarrhoea, Gastric Antral Vascular Ectasia, Concomitant Disease Progression, Anaemia Postoperative

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Augmentin '500'
    Dosage: 1000 mg, bid
    Indication: Urinary Tract Infection
    Start date: 2011-08-28
    End date: 2011-09-01

Certican
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-27
    End date: 2011-07-12

Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Start date: 2011-07-25
    End date: 2011-08-29

Imuran
    Dosage: 150 mg, qd
    Indication: Immunosuppression
    Start date: 2011-08-30
    End date: 2011-09-01

Nexium
    Dosage: unk

Prednisone
    Dosage: 15 mg, daily
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-07-01
    End date: 2011-07-13

Prednisone
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-07-14

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-28

Valcyte
    Dosage: 450 mg, qd
    Start date: 2011-06-27

Other drugs received by patient: Iron Dextran; Iron Dextran; Iron Dextran



Possible Imuran side effects in male

Reported by a physician from United States on 2012-08-03

Patient: male, weighing 102.0 kg (224.4 pounds)

Reactions: Escherichia Urinary Tract Infection, Diarrhoea, Gastric Antral Vascular Ectasia, Concomitant Disease Progression, Anaemia Postoperative

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Augmentin '500'
    Dosage: 1000 mg, bid
    Indication: Urinary Tract Infection
    Start date: 2011-08-28
    End date: 2011-09-01

Certican
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-27
    End date: 2011-07-12

Certican
    Dosage: 0.75 mg, bid
    Administration route: Oral
    Start date: 2011-07-25
    End date: 2011-08-29

Imuran
    Dosage: 150 mg, qd
    Indication: Immunosuppression
    Start date: 2011-08-30
    End date: 2011-09-01

Nexium
    Dosage: unk

Prednisone
    Dosage: 15 mg, daily
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-07-01
    End date: 2011-07-13

Prednisone
    Dosage: 5 mg, daily
    Administration route: Oral
    Start date: 2011-07-14

Prograf
    Dosage: 2 mg, bid
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2011-06-28

Valcyte
    Dosage: 450 mg, qd
    Start date: 2011-06-27

Other drugs received by patient: Iron Dextran; Iron Dextran; Iron Dextran



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:
Humira
    Dosage: start date approximately june or august
    Indication: Crohn's Disease
    Start date: 2008-01-01
    End date: 2010-02-01

Imuran
    Indication: Crohn's Disease
    Start date: 2008-01-01
    End date: 2010-02-01

Remicade
    Dosage: discontinued june or august 2008
    Start date: 2004-01-01
    End date: 2008-09-01

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 male

Reported by a health professional (non-physician/pharmacist) from Japan on 2012-08-01

Patient: male

Reactions: Neutropenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Bredinin
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2012-01-01

Bredinin
    Dosage: unk
    Administration route: Oral
    End date: 2012-01-01

Imuran
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant
    Start date: 2012-01-01

Imuran
    Dosage: unk
    Administration route: Oral
    End date: 2012-01-01

Rapaflo
    Dosage: 4 mg, daily
    Administration route: Oral
    Indication: Dysuria
    Start date: 2012-05-01

Sandimmune
    Dosage: unk
    Indication: Renal Transplant
    Start date: 2012-01-01

Sandimmune
    Dosage: unk
    End date: 2012-01-01

Other drugs received by patient: Eviprostat



Possible Imuran side effects in male

Reported by a physician from United States on 2012-08-01

Patient: male

Reactions: Hodgkin's Disease

Drug(s) suspected as cause:
Imuran
    Indication: Crohn's Disease
    Start date: 2000-01-01
    End date: 2008-01-01

Remicade
    Indication: Crohn's Disease
    Start date: 2004-01-01

Other drugs received by patient: Suboxone



Possible Imuran side effects in female

Reported by a physician from France on 2012-07-31

Patient: female, weighing 2.4 kg (5.2 pounds)

Reactions: Coloboma, Microphthalmos, Maternal Exposure Timing Unspecified, Microtia, External Auditory Canal Atresia, Atrophy

Drug(s) suspected as cause:
Cellcept
    Indication: Product Used FOR Unknown Indication
    End date: 2011-07-15

Cellcept
    Indication: Renal Failure

Imuran
    Indication: Product Used FOR Unknown Indication
    Start date: 2011-09-07
    End date: 2012-04-13

Other drugs received by patient: Aspirin; Lovenox



Possible Imuran side effects in male

Reported by a physician from Japan on 2012-07-27

Patient: male, weighing 71.0 kg (156.2 pounds)

Reactions: Abdominal Pain, Diarrhoea, Platelet Count Decreased, Lymphocytic Leukaemia, White Blood Cell Count Increased

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Gonadotropins
    Dosage: 3000 units per month
    Indication: Product Used FOR Unknown Indication
    Start date: 2010-02-12
    End date: 2012-01-16

Imuran
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication
    Start date: 2010-09-07

Imuran
    Administration route: Oral
    Start date: 2011-06-25

Pentasa
    Dosage: start date prior to 16-apr-1999
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Remicade
    Indication: Crohn's Disease
    Start date: 2012-01-06

Remicade
    Start date: 2011-01-26

Remicade
    Dosage: 12 total infusions
    Start date: 2010-06-25

Other drugs received by patient: Elental



Possible Imuran side effects in male

Reported by a physician from United States on 2012-07-24

Patient: male

Reactions: Anion GAP Increased, Chapped Lips, Blood Albumin Decreased, Burkitt's Lymphoma Stage II, White Blood Cell Count Increased, Blood Alkaline Phosphatase Decreased, Hypotension, Small Intestinal Obstruction, Blood Phosphorus Decreased, Aspartate Aminotransferase Increased, Epstein-Barr Virus Test Positive, Atelectasis, Blood Magnesium Decreased, Constipation, Electrolyte Depletion, Somnolence, Blood Calcium Decreased, Haematocrit Decreased, RED Blood Cell Count Decreased, Blood Uric Acid Increased, Pleural Effusion, Blood Sodium Decreased, Blood Glucose Increased, Intussusception, Nausea, LIP DRY, Blood Chloride Decreased, Febrile Neutropenia, Protein Total Decreased, Ascites, Immunosuppressant Drug Level Decreased, Renal Failure, Blood Potassium Decreased, Sepsis, Heart Rate Increased, Carbon Dioxide Decreased, Alanine Aminotransferase Decreased, Hypertension

Adverse event resulted in: life threatening event, hospitalization, disablity

Drug(s) suspected as cause:
Elidel
    Dosage: (df topical)
    Administration route: Topical
    Indication: Dermatitis Atopic

Imuran
    Dosage: (50 mg qd)
    Indication: Product Used FOR Unknown Indication

Prograf
    Dosage: (2 mg bid)
    Indication: Product Used FOR Unknown Indication

Singulair
    Dosage: ( 4 mg 4d)
    Indication: Multiple Allergies

Other drugs received by patient: Sodium Chloride; Izofran / 00955301 /; Ventolin HFA; Aloprim; Protonix; Valium; Hydromorphone Hydrochloride; Dilaudid; Nubain; Narcan; D-51 / 2 NS + KCL; Mefoxin



Possible Imuran side effects in male

Reported by a consumer/non-health professional from United States on 2012-07-20

Patient: male

Reactions: Myeloid Leukaemia

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Humira
    Dosage: start date approximately june or august
    Indication: Crohn's Disease
    Start date: 2008-01-01
    End date: 2010-02-01

Imuran
    Indication: Crohn's Disease
    Start date: 2008-01-01
    End date: 2010-02-01

Remicade
    Dosage: discontinued june or august 2008
    Indication: Crohn's Disease
    End date: 2008-01-01

Remicade
    Start date: 2004-01-01

Other drugs received by patient: Vitamin B-12; Ferrous Sulfate TAB; Vitamin D; Climara; Calcium; Prednisone TAB; Lovaza; Warfarin Sodium; Vitamin A; Prilosec; Amitriptyline HCL; Ascorbic Acid; Antibiotics



Possible Imuran side effects in male

Reported by a consumer/non-health professional from Japan on 2012-07-19

Patient: male

Reactions: Neutropenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Bredinin
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant

Imuran
    Dosage: unk
    Administration route: Oral
    Indication: Renal Transplant

Rapaflo
    Dosage: 4 mg, daily
    Administration route: Oral
    Indication: Dysuria
    Start date: 2012-05-01

Sandimmune
    Dosage: unk
    Indication: Renal Transplant

Other drugs received by patient: Eviprostat



Possible Imuran side effects in 66 year old female

Reported by a health professional (non-physician/pharmacist) from Sweden on 2012-07-19

Patient: 66 year old female

Reactions: Uterine Cancer

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2007-01-01
    End date: 2009-12-01

Imuran
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2009-12-01

Remicade
    Indication: Rheumatoid Arthritis
    Start date: 2002-01-01
    End date: 2007-01-01

Other drugs received by patient: Felodipine; Ketoprofen; Lasix



Possible Imuran side effects in 49 year old female

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-17

Patient: 49 year old female

Reactions: Lymphopenia, Anaemia, Neutropenia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Fluconazole
    Dosage: 100 mg, 1x/day
    Administration route: Oral
    Indication: Fungal Infection
    Start date: 2012-05-10
    End date: 2012-05-17

Imuran
    Dosage: 200 mg, 1x/day
    Administration route: Oral
    Indication: Inflammatory Bowel Disease
    Start date: 2012-04-01

Other drugs received by patient: Prednisone TAB; Ferrous Sulfate TAB



Possible Imuran side effects in male

Reported by a physician from United States on 2012-07-17

Patient: male

Reactions: Lymphoma

Drug(s) suspected as cause:
Imuran
    Indication: Product Used FOR Unknown Indication

Remicade
    Indication: Product Used FOR Unknown Indication



Possible Imuran side effects in 67 year old male

Reported by a consumer/non-health professional from France on 2012-07-11

Patient: 67 year old male

Reactions: Abdominal Wall Haematoma, Drug Interaction, Septic Shock, Allergic Granulomatous Angiitis

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Actonel
    Dosage: film-coated tablet
    Administration route: Oral
    Start date: 2012-03-02

Alfuzosin Hydrochloride
    Dosage: extended-release tablet
    Administration route: Oral
    Start date: 2012-02-17

Atorvastatin
    Dosage: film-coated tablet
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2012-02-17

Bisoprolol Fumarate
    Administration route: Oral

Imuran
    Indication: Allergic Granulomatous Angiitis
    Start date: 2012-03-02

Lasix
    Dosage: scored tablet
    Administration route: Oral
    Start date: 2012-02-17

Lyrica
    Dosage: caps
    Administration route: Oral
    Start date: 2012-02-17

Potassium Chloride
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2012-02-17

Prednisone TAB
    Dosage: dose decrease of 5 mg all 10 days to reach 10 mg daily,also received 25mg
    Administration route: Oral
    Indication: Allergic Granulomatous Angiitis
    Start date: 2012-03-02

Symbicort
    Dosage: 1 df = 2 puffs

Vitamin B1 + B6
    Administration route: Oral
    Start date: 2012-02-17

Vitamin D
    Indication: Osteoporosis

Other drugs received by patient possibly interacting with the suspect drug:
Ceftriaxone
    Dosage: powder for solution for injection
    Indication: Septic Shock
    Start date: 2012-03-12
    End date: 2012-03-16

Coumadin
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-01-01
    End date: 2012-03-14

Rovamycine
    Indication: Septic Shock

Other drugs received by patient: Cordarone



Possible Imuran side effects in 50 year old female

Reported by a physician from United States on 2012-07-10

Patient: 50 year old female, weighing 65.8 kg (144.7 pounds)

Reactions: Urinary Tract Infection

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Cimzia
    Indication: Crohn's Disease
    Start date: 2009-06-10

Imuran
    Indication: Crohn's Disease

Imuran
    Start date: 2009-01-01



Possible Imuran side effects in male

Reported by a physician from Japan on 2012-07-10

Patient: male, weighing 67.0 kg (147.4 pounds)

Reactions: Lymphoma

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Imuran
    Dosage: 50mg per day
    Administration route: Oral
    Indication: Idiopathic Thrombocytopenic Purpura
    Start date: 1998-11-27
    End date: 2011-11-19

Promacta
    Dosage: 12.5mg per day
    Administration route: Oral
    Indication: Idiopathic Thrombocytopenic Purpura
    Start date: 2011-10-24
    End date: 2011-11-26

Other drugs received by patient: Heavy Magnesium Oxide; Alendronate Sodium; Ketoprofen; Selbex; Digoxin; Prednisolone; Isodine Gargle



Possible Imuran side effects in female

Reported by a physician from Denmark on 2012-07-09

Patient: female

Reactions: Ovarian Epithelial Cancer

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Enbrel
    Indication: Rheumatoid Arthritis
    Start date: 2009-04-28
    End date: 2009-05-29

Humira
    Dosage: humira: field b.4.k.6: on a pause from 04apr2004 to 23oct2004.
    Indication: Rheumatoid Arthritis
    Start date: 2003-06-16
    End date: 2006-12-12

Imuran
    Indication: Rheumatoid Arthritis
    Start date: 2006-12-12
    End date: 2009-05-11

Methotrexate
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 1999-09-17
    End date: 2005-11-16

Other drugs received by patient: Tramadol HCL; Acetaminophen; Prednisolone; Tramadol HCL



Possible Imuran side effects in 67 year old male

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-06

Patient: 67 year old male

Reactions: Abdominal Wall Haematoma, Drug Interaction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Start date: 2012-03-02

Alfuzosin HCL
    Administration route: Oral
    Start date: 2012-02-17

Atorvastatin
    Administration route: Oral
    Start date: 2012-02-17

Bisoprolol Fumarate
    Administration route: Oral

Budesonide / Formoterol Fumarate

Calcidose Vitamine D
    Administration route: Oral
    Start date: 2012-03-02

Coumadin
    Administration route: Oral
    Start date: 2005-01-01
    End date: 2012-03-14

Imuran
    Administration route: Oral
    Start date: 2012-03-02

Lasix
    Administration route: Oral
    Start date: 2012-02-17

Lyrica
    Administration route: Oral
    Start date: 2012-02-17

Multi-Vitamins
    Administration route: Oral
    Start date: 2012-02-17

Potassium Chloride
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2012-02-17

Prednisone TAB
    Dosage: 30 mg per day with dosage decreased at 5 mg every 10 days up to 10 mg daily
    Administration route: Oral
    Start date: 2012-03-02

Other drugs received by patient possibly interacting with the suspect drug:
Ceftriaxone
    Indication: Septic Shock
    Start date: 2012-03-12

Rovamycine
    Indication: Septic Shock
    Start date: 2012-03-12
    End date: 2012-03-16



Possible Imuran side effects in female

Reported by a health professional (non-physician/pharmacist) from Canada on 2012-07-06

Patient: female, weighing 71.0 kg (156.2 pounds)

Reactions: Arthralgia, Alopecia

Drug(s) suspected as cause:
Imuran
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Imuran
    Administration route: Oral

Remicade
    Indication: Crohn's Disease
    Start date: 2012-03-21



Possible Imuran side effects in 67 year old male

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-06

Patient: 67 year old male

Reactions: Acute Pulmonary Oedema, Abdominal Wall Haematoma, Sepsis, Drug Interaction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Dosage: 35 mg, weekly
    Administration route: Oral
    Start date: 2012-03-02

Alfuzosin Hydrochloride
    Dosage: 10 mg, daily
    Administration route: Oral
    Start date: 2012-02-17

Atorvastatin
    Dosage: 40 mg, 1x/day
    Administration route: Oral
    Indication: Hypercholesterolaemia
    Start date: 2012-02-17

Bisoprolol Fumarate
    Dosage: 1.25 mg, 1x/day
    Administration route: Oral

Calcidose Vitamine D
    Dosage: 1 df, 2x/day
    Administration route: Oral
    Indication: Osteoporosis
    Start date: 2012-03-02

Coumadin
    Dosage: 3.75 mg, 1x/day
    Administration route: Oral
    Indication: Atrial Fibrillation
    Start date: 2005-01-01
    End date: 2012-03-14

Imuran
    Dosage: 75 mg, 1x/day
    Administration route: Oral
    Indication: Allergic Granulomatous Angiitis
    Start date: 2012-03-02

Lasix
    Dosage: 40 mg, 2x/day
    Administration route: Oral
    Start date: 2012-02-17

Lyrica
    Dosage: 25 mg, 2x/day
    Administration route: Oral
    Start date: 2012-02-17

Potassium Chloride
    Dosage: 1 df, 3x/day
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2012-02-17

Prednisone TAB
    Dosage: 30 mg, 1x/day
    Administration route: Oral
    Indication: Allergic Granulomatous Angiitis
    Start date: 2012-03-02

Prednisone TAB
    Dosage: unk
    Administration route: Oral

Symbicort
    Dosage: 1 df, 2x/day

Vitamin B1 and B6
    Dosage: 1 df, 2x/day
    Administration route: Oral
    Start date: 2012-02-17

Other drugs received by patient possibly interacting with the suspect drug:
Ceftriaxone Sodium
    Dosage: 1 df, 1x/day
    Indication: Septic Shock
    Start date: 2012-03-12

Rovamycine
    Dosage: 1500000 iu, 3x/day
    Indication: Septic Shock
    Start date: 2012-03-12
    End date: 2012-03-16

Other drugs received by patient: Cordarone



Possible Imuran side effects in 67 year old male

Reported by a health professional (non-physician/pharmacist) from France on 2012-07-06

Patient: 67 year old male

Reactions: Abdominal Wall Haematoma, Drug Interaction

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Actonel
    Administration route: Oral
    Start date: 2012-03-02

Alfuzosin HCL
    Administration route: Oral
    Start date: 2012-02-17

Atorvastatin
    Administration route: Oral
    Start date: 2012-02-17

Bisoprolol Fumarate
    Administration route: Oral

Budesonide / Formoterol Fumarate

Calcidose Vitamine D
    Administration route: Oral
    Start date: 2012-03-02

Coumadin
    Administration route: Oral
    Start date: 2005-01-01
    End date: 2012-03-14

Imuran
    Administration route: Oral
    Start date: 2012-03-02

Lasix
    Administration route: Oral
    Start date: 2012-02-17

Lyrica
    Administration route: Oral
    Start date: 2012-02-17

Multi-Vitamins
    Administration route: Oral
    Start date: 2012-02-17

Potassium Chloride
    Administration route: Oral
    Indication: Hypokalaemia
    Start date: 2012-02-17

Prednisone TAB
    Dosage: 30 mg per day with dosage decreased at 5 mg every 10 days up to 10 mg daily
    Administration route: Oral
    Start date: 2012-03-02

Other drugs received by patient possibly interacting with the suspect drug:
Ceftriaxone
    Indication: Septic Shock
    Start date: 2012-03-12

Rovamycine
    Indication: Septic Shock
    Start date: 2012-03-12
    End date: 2012-03-16



Possible Imuran side effects in female

Reported by a physician from Denmark on 2012-07-05

Patient: female

Reactions: Uterine Cancer

Drug(s) suspected as cause:
Humira
    Start date: 2010-05-03

Humira
    Indication: Rheumatoid Arthritis
    Start date: 2004-01-15

Humira
    Dosage: conflictingly reported as date of last adminstartion
    Start date: 2010-04-07

Imuran
    Start date: 2010-05-25

Imuran
    Indication: Rheumatoid Arthritis
    Start date: 2001-10-15

Remicade
    Indication: Rheumatoid Arthritis
    Start date: 2002-09-04

Remicade
    Start date: 2001-10-15

Other drugs received by patient: Mabthera; Hydroxychloroquine Sulfate; Cyclosporine; Leflunomide; Prednisolone; Myocrisin; Sulfasalazine; Methotrexate; Cyclophosphamide

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