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Azulfidine (Sulfasalazine) - Drug Eruption - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Drug Eruption (12)

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

Possible Azulfidine side effects in 68 year old male

Reported by a physician from Japan on 2012-08-03

Patient: 68 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Drug Eruption, Asthma, Respiratory Failure, Drug Hypersensitivity, Platelet Count Decreased, Liver Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Lansoprazole; Acetaminophen; Loxonin



Possible Azulfidine side effects in 68 year old male

Reported by a physician from Japan on 2012-07-30

Patient: 68 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Asthma, Drug Eruption, Respiratory Failure, Platelet Count Decreased, Liver Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Loxonin; Lansoprazole; Acetaminophen



Possible Azulfidine side effects in 68 year old male

Reported by a physician from Japan on 2012-07-25

Patient: 68 year old male, weighing 60.0 kg (132.0 pounds)

Reactions: Asthma, Drug Eruption, Respiratory Failure, Platelet Count Decreased, Liver Disorder

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Acetaminophen; Lansoprazole; Loxonin



Possible Azulfidine side effects in 67 year old male

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

Patient: 67 year old male

Reactions: Drug Eruption

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg, 1x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2012-04-23
    End date: 2012-05-06

Azulfidine
    Dosage: 500mg tabs, 2 tabs/day
    Administration route: Oral
    Start date: 2012-05-07
    End date: 2012-05-08

Other drugs received by patient: Cytotec; Uralyt-U; Prednisolone; Celebrex; Urinorm; Rimatil



Possible Azulfidine side effects in 59 year old female

Reported by a pharmacist from Japan on 2012-07-16

Patient: 59 year old female, weighing 64.8 kg (142.6 pounds)

Reactions: Drug Eruption, Hepatic Function Abnormal, Oesophagitis Ulcerative, Febrile Neutropenia, Agranulocytosis, RED Blood Cell Count Decreased, Arthralgia, Oral Candidiasis, Herpes Oesophagitis, Abscess Limb

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-05

Celebrex
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-04

Other drugs received by patient: Prednisolone; Prednisolone



Possible Azulfidine side effects in 59 year old female

Reported by a pharmacist from Japan on 2012-07-05

Patient: 59 year old female, weighing 64.8 kg (142.6 pounds)

Reactions: Drug Eruption, Hepatic Function Abnormal, Febrile Neutropenia, Oesophagitis Ulcerative, Agranulocytosis, Oral Candidiasis, RED Blood Cell Count Decreased, Arthralgia, Herpes Oesophagitis, Abscess Limb

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-05

Celebrex
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-04

Other drugs received by patient: Prednisolone Sodium Succinate INJ; Prednisolone Sodium Succinate INJ



Possible Azulfidine side effects in 59 year old female

Reported by a physician from Japan on 2012-06-04

Patient: 59 year old female, weighing 64.8 kg (142.6 pounds)

Reactions: Drug Eruption, Hepatic Function Abnormal, Febrile Neutropenia, Oesophagitis Ulcerative, Agranulocytosis, Oral Candidiasis, Arthralgia, RED Blood Cell Count Decreased, Herpes Oesophagitis, Abscess Limb

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-05

Celebrex
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-04

Other drugs received by patient: Prednisolone; Prednisolone



Possible Azulfidine side effects in 59 year old female

Reported by a pharmacist from Japan on 2012-05-25

Patient: 59 year old female, weighing 64.8 kg (142.6 pounds)

Reactions: Drug Eruption, Hepatic Function Abnormal, Effusion, Oesophagitis Ulcerative, Oropharyngeal Pain, Malaise, RED Blood Cell Count Decreased, Gamma-Glutamyltransferase Increased, Oral Candidiasis, Abscess Limb, Blood Alkaline Phosphatase Increased, Blood Lactate Dehydrogenase Increased, Alanine Aminotransferase Increased, Febrile Neutropenia, Agranulocytosis, Arthralgia, Aspartate Aminotransferase Increased, Herpes Oesophagitis

Adverse event resulted in: life threatening event, hospitalization

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-05

Celebrex
    Dosage: 200 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-10-01
    End date: 2011-11-04

Other drugs received by patient: Prednisolone; Prednisolone



Possible Azulfidine side effects in 69 year old female

Reported by a physician from Japan on 2012-05-14

Patient: 69 year old female

Reactions: Drug Eruption

Drug(s) suspected as cause:
Rimatil
    Dosage: 200 mg daily
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2009-01-01
    End date: 2012-05-01

Azulfidine
    Dosage: 1000 mg/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2009-01-01
    End date: 2012-05-01

Other drugs received by patient: Risedronate Sodium; Mucosta



Possible Azulfidine side effects in 58 year old female

Reported by a consumer/non-health professional from Japan on 2012-04-20

Patient: 58 year old female

Reactions: Drug Eruption, Thrombocytopenia, Leukopenia

Drug(s) suspected as cause:
Azulfidine



Possible Azulfidine side effects in 68 year old female

Reported by a pharmacist from Japan on 2012-03-30

Patient: 68 year old female

Reactions: Drug Eruption, Hepatic Function Abnormal, Malaise, Nasopharyngitis, Pruritus, Pain in Extremity, Erythema

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

Other drugs received by patient: Rheumatrex; Rimatil; Prednisolone; Folic Acid; Celebrex



Possible Azulfidine side effects in

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

Patient:

Reactions: Drug Eruption

Adverse event resulted in: hospitalization

Drug(s) suspected as cause:
Azulfidine

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