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Azulfidine (Sulfasalazine) - Pyrexia - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Pyrexia (9)

Below is the selection of side effect reports (a.k.a. adverse event reports) related to Azulfidine (Sulfasalazine) where reactions include pyrexia. The selected reports were submitted to the FDA during the sample period of about a year.

Possible Azulfidine side effects in

Reported by a physician from Japan on 2012-08-07

Patient:

Reactions: Malaise, Pyrexia, Rash

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine



Possible Azulfidine side effects in

Reported by a physician from Japan on 2012-07-18

Patient:

Reactions: Malaise, Rash, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine



Possible Azulfidine side effects in 50 year old female

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

Patient: 50 year old female

Reactions: Weight Decreased, Biliary Cirrhosis Primary, Steatorrhoea, Wrist Fracture, Ganglioneuroma, Cholestasis, Pyrexia, Multiple Fractures, Hepatic Steatosis, Chest Pain, Sjogren's Syndrome, RIB Fracture

Adverse event resulted in: hospitalization

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

Alendronate Sodium
    Indication: Rheumatoid Arthritis
    Start date: 2003-01-01

Azathioprine
    Dosage: frequency: everyday (qd)
    Indication: Rheumatoid Arthritis
    Start date: 1997-12-01
    End date: 2004-06-01

Azulfidine
    Dosage: frequency: everyday (qd)
    Indication: Rheumatoid Arthritis

Etanercept
    Indication: Rheumatoid Arthritis

Methotrexate

Methotrexate
    Indication: Rheumatoid Arthritis
    Start date: 1995-09-01
    End date: 1997-09-01

Methotrexate

Methotrexate
    Start date: 1996-11-01
    End date: 1997-01-01

Prednisolone
    Dosage: frequency: everyday (qd). dose reported: 5 mg qd} 10 mg qd
    Indication: Rheumatoid Arthritis

Prednisolone
    Dosage: frequency: everyday (qd)

Rituximab
    Indication: Rheumatoid Arthritis

Rituximab

Other drugs received by patient: Hydroxychloroquine Sulfate; Hydroxychloroquine Sulfate



Possible Azulfidine side effects in 50 year old female

Reported by a physician from Portugal on 2012-06-20

Patient: 50 year old female

Reactions: Weight Decreased, Steatorrhoea, Biliary Cirrhosis Primary, Wrist Fracture, Ganglioneuroma, Cholestasis, Multiple Fractures, Pyrexia, Hepatic Steatosis, Chest Pain, Sjogren's Syndrome, RIB Fracture

Adverse event resulted in: hospitalization

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

Alendronate Sodium
    Indication: Rheumatoid Arthritis
    Start date: 2003-01-01

Azathioprine
    Dosage: frequency: everyday (qd)
    Indication: Rheumatoid Arthritis
    Start date: 1997-12-01
    End date: 2004-06-01

Azulfidine
    Dosage: frequency: everyday (qd)
    Indication: Rheumatoid Arthritis

Etanercept
    Indication: Rheumatoid Arthritis

Methotrexate
    Indication: Rheumatoid Arthritis
    Start date: 1995-09-01
    End date: 1997-09-01

Methotrexate
    Start date: 1996-11-01
    End date: 1997-01-01

Methotrexate

Methotrexate

Prednisolone
    Dosage: frequency: everyday (qd)

Prednisolone
    Dosage: frequency: everyday (qd). dose reported: 5 mg qd} 10 mg qd
    Indication: Rheumatoid Arthritis

Rituximab
    Indication: Rheumatoid Arthritis

Rituximab

Other drugs received by patient: Hydroxychloroquine Sulfate; Hydroxychloroquine Sulfate



Possible Azulfidine side effects in 70 year old female

Reported by a physician from Japan on 2011-11-18

Patient: 70 year old female

Reactions: Organising Pneumonia, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 1 g daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Prograf
    Dosage: 1 mg daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Rheumatrex
    Dosage: 4 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Other drugs received by patient: Prednisolone; Prednisolone; Remicade



Possible Azulfidine side effects in 70 year old female

Reported by a physician from Japan on 2011-11-03

Patient: 70 year old female

Reactions: Organising Pneumonia, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 1 g daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Prograf
    Dosage: 1 mg daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Rheumatrex
    Dosage: 4 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-08-26

Other drugs received by patient: Remicade; Prednisolone; Prednisolone



Possible Azulfidine side effects in 42 year old female

Reported by a physician from Japan on 2011-10-25

Patient: 42 year old female, weighing 45.0 kg (99.0 pounds)

Reactions: Hepatic Function Abnormal, Listless, Urticaria, Pyrexia

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Loxonin; Zantac



Possible Azulfidine side effects in 78 year old male

Reported by a physician from Japan on 2011-10-11

Patient: 78 year old male, weighing 60.2 kg (132.4 pounds)

Reactions: Disseminated Intravascular Coagulation, Oropharyngeal Pain, Pyrexia, Chest X-RAY Abnormal, Agranulocytosis, Corynebacterium Test Positive, Sepsis, Septic Shock, Leukopenia

Adverse event resulted in: death

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2010-03-04

Azulfidine
    Dosage: 500 mg, 2x/day
    Start date: 2010-03-11
    End date: 2010-04-19

Other drugs received by patient: Olmesartan Medoxomil; Calblock; Insulin Detemir; Aspirin; Lansoprazole; Glufast; Montelukast Sodium; Alendronate Sodium; Prednisolone



Possible Azulfidine side effects in 62 year old male

Reported by a physician from Japan on 2011-10-05

Patient: 62 year old male

Reactions: General Physical Condition Abnormal, Vomiting, Pyrexia, Erythema, Drug Rash With Eosinophilia and Systemic Symptoms, Skin Irritation, Multi-Organ Failure, Haematochezia, Renal Failure, Diarrhoea

Adverse event resulted in: death, hospitalization

Drug(s) suspected as cause:
Azulfidine

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