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Imuran (Azathioprine) - Pneumonia - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Pneumonia (14)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Imuran (Azathioprine) where reactions include pneumonia. 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 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 47 year old male

Reported by a physician from Japan on 2012-06-29

Patient: 47 year old male, weighing 69.7 kg (153.3 pounds)

Reactions: Drug Eruption, White Blood Cell Count Decreased, Pneumonia, Anaemia, Bronchitis, Liver Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Prednisolone Sodium Succinate INJ
    Dosage: unk
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-08-21
    End date: 2010-11-30

Imuran
    Dosage: unk
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-10-18
    End date: 2010-11-16

Tacrolimus
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-09-03
    End date: 2010-09-13

Tacrolimus
    Dosage: 1 mg, bid
    Administration route: Oral
    Start date: 2010-09-14
    End date: 2010-11-10

Cefotiam Hydrochloride
    Dosage: 2000 mg, unknown/d
    Indication: Pneumonia
    Start date: 2010-11-18
    End date: 2010-11-23

Other drugs received by patient: Sulfasalazine; Zithromax; Cravit; Pentasa; Betamethasone; Famotidine; Acetaminophen; Miya BM; Lansoprazole



Possible Imuran side effects in 47 year old male

Reported by a physician from Japan on 2012-06-18

Patient: 47 year old male, weighing 69.7 kg (153.3 pounds)

Reactions: Drug Eruption, White Blood Cell Count Decreased, Pneumonia, Anaemia, Bronchitis, Liver Disorder

Drug(s) suspected as cause:
Tacrolimus
    Dosage: 1 mg, bid
    Administration route: Oral
    Start date: 2010-09-14
    End date: 2010-11-10

Cefotiam Hydrochloride
    Dosage: 2000 mg, unknown/d
    Indication: Pneumonia
    Start date: 2010-11-18
    End date: 2010-11-23

Imuran
    Dosage: unk
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-10-18
    End date: 2010-11-16

Tacrolimus
    Dosage: 1.5 mg, bid
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-09-03
    End date: 2010-09-13

Prednisolone
    Dosage: unk
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2010-08-21
    End date: 2010-11-30

Other drugs received by patient: Pentasa; Acetaminophen; Miya BM; Sulfasalazine; Betamethasone; Lansoprazole; Famotidine; Levofloxacin; Zithromax



Possible Imuran side effects in female

Reported by a physician from United States on 2012-06-12

Patient: female

Reactions: Rheumatoid Arthritis, Pneumonia, Vomiting, Pain, Pleural Effusion, Bronchitis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Oxycontin
    Dosage: 80 mg, q12h
    Administration route: Oral
    Indication: Product Used FOR Unknown Indication

Imuran
    Dosage: unk
    Indication: Product Used FOR Unknown Indication
    Start date: 2012-05-01



Possible Imuran side effects in female

Reported by a consumer/non-health professional from United States on 2012-05-15

Patient: female

Reactions: Pneumonia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Letairis
    Indication: Rheumatoid Arthritis

Letairis
    Dosage: 5 mg, unk
    Administration route: Oral
    Indication: Pulmonary Hypertension
    Start date: 2011-09-23

Letairis
    Indication: Interstitial Lung Disease

Imuran



Possible Imuran side effects in male

Reported by a physician from Japan on 2012-03-16

Patient: male, weighing 58.0 kg (127.6 pounds)

Reactions: Pneumonia, Neutrophil Count Decreased

Drug(s) suspected as cause:
Remicade
    Dosage: 5 mg/kg.
    Indication: Colitis Ulcerative
    Start date: 2011-10-06

Tacrolimus
    Indication: Product Used FOR Unknown Indication

Imuran
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2008-01-04
    End date: 2011-10-24

Other drugs received by patient: Tamsulosin HCL; Alfarol; Famotidine; Dutasteride; Levemir; Humalog; Pentasa; Prograf



Possible Imuran side effects in male

Reported by a physician from Japan on 2012-03-01

Patient: male, weighing 58.0 kg (127.6 pounds)

Reactions: Pneumonia, Haemorrhage, Neutrophil Count Decreased

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

Imuran
    Administration route: Oral
    Indication: Colitis Ulcerative
    Start date: 2008-01-04
    End date: 2011-10-24

Remicade
    Dosage: 5 mg/kg.
    Indication: Colitis Ulcerative
    Start date: 2011-10-06

Other drugs received by patient: Pentasa; Levemir; Famotidine; Humalog; Dutasteride; Tamsulosin HCL; Prograf; Alfarol



Possible Imuran side effects in male

Reported by a physician from United States on 2012-02-16

Patient: male

Reactions: Pneumonia, Effusion, Pancytopenia, Atrial Fibrillation, Empyema, Histoplasmosis Disseminated, Hydropneumothorax, Respiratory Failure, Systemic Inflammatory Response Syndrome, Deep Vein Thrombosis, Renal Failure Acute

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2011-01-31

Remicade
    Start date: 2011-02-03

Remicade
    Start date: 2010-02-22

Remicade
    Start date: 2009-07-15

Remicade
    Indication: Crohn's Disease
    Start date: 2010-06-14

Remicade
    Start date: 2010-04-19

Remicade
    Start date: 2009-12-28

Remicade
    Start date: 2010-08-24

Remicade
    Start date: 2010-10-12

Remicade
    Start date: 2011-07-15

Remicade
    Start date: 2009-02-11

Remicade
    Start date: 2010-12-06

Remicade
    Start date: 2011-04-11

Remicade
    Start date: 2011-06-16

Remicade
    Start date: 2009-09-14

Remicade
    Start date: 2011-10-26

Remicade
    Start date: 2011-03-28

Remicade
    Start date: 2011-05-20

Remicade
    Start date: 2009-01-27

Remicade
    Start date: 2011-09-09

Imuran
    Administration route: Oral
    Indication: Crohn's Disease

Remicade
    Start date: 2009-11-09

Prednisone TAB
    Dosage: tapering dose
    Administration route: Oral
    Indication: Crohn's Disease

Remicade
    Start date: 2010-08-09

Remicade
    Start date: 2009-05-20

Remicade
    Dosage: frequency:every 4-8 weeks
    Start date: 2000-12-06

Other drugs received by patient: Zofran; Phenergan; Klor-CON; Coumadin; Lortab; Omeprazole; Paxil; Welchol; Metoprolol Tartrate



Possible Imuran side effects in male

Reported by a physician from United States on 2012-02-14

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

Remicade

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

Remicade
    End date: 2011-09-09

Imuran
    Administration route: Oral
    Start date: 2004-03-11
    End date: 2004-07-29

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



Possible Imuran side effects in male

Reported by a health professional (non-physician/pharmacist) from United States on 2012-02-03

Patient: male

Reactions: Pneumonia, Effusion, Atrial Fibrillation, Pancytopenia, Empyema, Histoplasmosis Disseminated, Hydropneumothorax, Respiratory Failure, Systemic Inflammatory Response Syndrome, Renal Failure Acute, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2011-04-11

Remicade
    Start date: 2011-07-15

Remicade
    Dosage: frequency:every 4-8 weeks
    Start date: 2000-12-06

Remicade
    Start date: 2009-11-09

Remicade
    Start date: 2009-05-20

Remicade
    Start date: 2011-09-09

Remicade
    Start date: 2009-09-14

Remicade
    Start date: 2010-10-12

Remicade
    Start date: 2011-05-20

Remicade
    Start date: 2010-02-22

Remicade
    Start date: 2009-12-28

Remicade
    Start date: 2009-07-15

Remicade
    Indication: Crohn's Disease
    Start date: 2010-06-14

Prednisone TAB
    Dosage: tapering dose
    Administration route: Oral
    Indication: Crohn's Disease

Remicade
    Start date: 2011-03-28

Remicade
    Start date: 2010-08-09

Remicade
    Start date: 2010-08-24

Remicade
    Start date: 2010-12-06

Remicade
    Start date: 2011-01-31

Remicade
    Start date: 2011-02-03

Remicade
    Start date: 2010-04-19

Remicade
    Start date: 2009-02-11

Remicade
    Start date: 2009-01-27

Remicade
    Start date: 2011-10-26

Remicade
    Start date: 2011-06-16

Imuran
    Administration route: Oral
    Indication: Crohn's Disease

Other drugs received by patient: Welchol; Lortab; Omeprazole; Klor-CON; Paxil; Phenergan; Metoprolol; Coumadin; Ondansetron HCL



Possible Imuran side effects in male

Reported by a physician from United States on 2012-01-09

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
    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

Imuran
    Administration route: Oral
    Start date: 2004-03-11
    End date: 2004-07-29

Remicade
    End date: 2011-09-09

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



Possible Imuran side effects in male

Reported by a physician from Japan on 2011-12-28

Patient: male, weighing 48.0 kg (105.6 pounds)

Reactions: Pneumonia, Cytomegalovirus Test Positive, Meningitis Cryptococcal

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Indication: Behcet's Syndrome
    Start date: 2011-01-11

Remicade
    Start date: 2010-02-24

Remicade
    Start date: 2010-12-15

Prednisolone
    Administration route: Oral
    Indication: Behcet's Syndrome
    Start date: 2010-12-28

Imuran
    Administration route: Oral
    Indication: Behcet's Syndrome
    End date: 2011-02-09

Remicade
    Start date: 2010-03-05

Remicade
    Start date: 2010-11-30

Other drugs received by patient: Pentasa; Bactar



Possible Imuran side effects in male

Reported by a physician from Japan on 2011-11-07

Patient: male, weighing 48.0 kg (105.6 pounds)

Reactions: Pneumonia, Cytomegalovirus Test Positive, Meningitis Cryptococcal

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2010-02-24

Remicade
    Start date: 2010-03-05

Remicade
    Start date: 2010-11-30

Prednisolone
    Administration route: Oral
    Indication: Behcet's Syndrome
    Start date: 2010-12-28

Remicade
    Indication: Behcet's Syndrome
    Start date: 2011-01-11

Remicade
    Start date: 2010-12-15

Imuran
    Administration route: Oral
    Indication: Behcet's Syndrome
    End date: 2011-02-09

Other drugs received by patient: Pentasa; Bactar



Possible Imuran side effects in male

Reported by a physician from Japan on 2011-10-03

Patient: male, weighing 48.0 kg (105.6 pounds)

Reactions: Pneumonia, Cytomegalovirus Test Positive, Meningitis Cryptococcal

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Remicade
    Start date: 2011-01-11

Remicade
    Indication: Behcet's Syndrome
    Start date: 2010-02-24

Remicade
    Start date: 2010-11-30

Remicade
    Start date: 2010-12-15

Imuran
    Administration route: Oral
    Indication: Behcet's Syndrome
    End date: 2011-02-09

Remicade
    Start date: 2010-03-05

Prednisolone
    Administration route: Oral
    Indication: Behcet's Syndrome
    Start date: 2010-12-28

Other drugs received by patient: Pentasa; Bactar

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