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Azulfidine (Sulfasalazine) - Histiocytosis Haematophagic - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Histiocytosis Haematophagic (10)

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

Possible Azulfidine side effects in male

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

Patient: male, weighing 55.0 kg (121.0 pounds)

Reactions: Agranulocytosis, Histiocytosis Haematophagic, Pseudomonal Sepsis, Disseminated Intravascular Coagulation, Cytomegalovirus Infection, Deep Vein Thrombosis

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 1000 mg, 1x/day
    Administration route: Oral
    Indication: Sjogren's Syndrome
    Start date: 2012-03-29
    End date: 2012-04-17

Azulfidine
    Indication: Arthropathy

Azulfidine
    Dosage: 500 mg, 1x/day
    Administration route: Oral
    Indication: Scleroderma
    Start date: 2012-03-14
    End date: 2012-03-28

Other drugs received by patient: Actos; Rabeprazole Sodium; Lobu; Prednisolone



Possible Azulfidine side effects in 77 year old female

Reported by a physician from Japan on 2012-05-16

Patient: 77 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Histiocytosis Haematophagic, Meningitis Bacterial

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-08
    End date: 2011-07-01

Celebrex
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-07

Other drugs received by patient: Amaryl; Omeprazole; Amlodipine; Pravastatin Sodium; Basen; Gaslon



Possible Azulfidine side effects in 53 year old female

Reported by a physician from Japan on 2012-03-14

Patient: 53 year old female, weighing 50.0 kg (110.0 pounds)

Reactions: Histiocytosis Haematophagic, Acute Hepatic Failure, Drug Rash With Eosinophilia and Systemic Symptoms, Serum Ferritin Increased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Loxonin



Possible Azulfidine side effects in 54 year old female

Reported by a physician from Japan on 2012-03-02

Patient: 54 year old female

Reactions: Histiocytosis Haematophagic, Acute Hepatic Failure, Drug Rash With Eosinophilia and Systemic Symptoms, Serum Ferritin Increased

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine



Possible Azulfidine side effects in 76 year old female

Reported by a physician from Japan on 2012-02-22

Patient: 76 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Histiocytosis Haematophagic, Meningitis Bacterial

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-08
    End date: 2011-07-01

Celecoxib
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-07

Other drugs received by patient: Omeprazole; Amaryl; Amlodipine; Pravastatin Sodium; Gaslon; Basen



Possible Azulfidine side effects in 54 year old female

Reported by a physician from Japan on 2012-02-17

Patient: 54 year old female

Reactions: Histiocytosis Haematophagic, Acute Hepatic Failure, Serum Ferritin Increased, Drug Rash With Eosinophilia and Systemic Symptoms

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine



Possible Azulfidine side effects in 76 year old female

Reported by a physician from Japan on 2012-02-16

Patient: 76 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Histiocytosis Haematophagic, Meningitis Bacterial

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Celecoxib
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-07

Azulfidine
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-08
    End date: 2011-07-01

Other drugs received by patient: Amaryl; Pravastatin Sodium; Omeprazole; Amlodipine; Basen; Gaslon



Possible Azulfidine side effects in 76 year old female

Reported by a physician from Japan on 2012-02-13

Patient: 76 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Histiocytosis Haematophagic

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-08
    End date: 2011-01-01

Celecoxib
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-07

Other drugs received by patient: Pravastatin Sodium; Omeprazole; Amaryl; Basen; Amlodipine; Gaslon



Possible Azulfidine side effects in 76 year old female

Reported by a physician from Japan on 2012-02-06

Patient: 76 year old female, weighing 48.0 kg (105.6 pounds)

Reactions: Histiocytosis Haematophagic

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Celecoxib
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-07

Azulfidine
    Dosage: 250 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-07-08
    End date: 2011-01-01

Other drugs received by patient: Omeprazole; Basen; Amaryl; Pravastatin Sodium; Gaslon; Amlodipine



Possible Azulfidine side effects in 77 year old female

Reported by a physician from Japan on 2012-01-24

Patient: 77 year old female

Reactions: Histiocytosis Haematophagic

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine

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