DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more

Azulfidine (Sulfasalazine) - Hepatic Function Abnormal - Suspected Cause - Side Effect Reports

 
 



Index of reports > Cases with Hepatic Function Abnormal (10)

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

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 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 46 year old female

Reported by a physician from Japan on 2012-01-06

Patient: 46 year old female, weighing 51.0 kg (112.2 pounds)

Reactions: Hepatic Function Abnormal

Drug(s) suspected as cause:
Azulfidine
    Dosage: 500 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-11-29

Enbrel
    Dosage: 50 mg, weekly
    Start date: 2011-12-09

Methotrexate Sodium
    Dosage: 5 mg, 2x/day
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    End date: 2011-11-29

Methotrexate Sodium
    Dosage: 7.5 mg, weekly (5 mg in the morning, 2.5 mg in the evening)
    Administration route: Oral
    Start date: 2011-12-16

Enbrel
    Dosage: 50 mg, weekly
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-04
    End date: 2011-11-25

Other drugs received by patient: Folic Acid



Possible Azulfidine side effects in

Reported by a physician from Japan on 2012-01-02

Patient:

Reactions: Hepatic Function Abnormal

Drug(s) suspected as cause:
Methotrexate Sodium
    Dosage: 10 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-01

Azulfidine
    Dosage: 2 tablets, daily
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-01
    End date: 2011-12-02

Enbrel
    Dosage: 50 mg, weekly
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-04
    End date: 2011-12-02

Methotrexate Sodium
    Dosage: 7.5 mg, weekly
    Administration route: Oral

Other drugs received by patient: Folic Acid



Possible Azulfidine side effects in

Reported by a physician from Japan on 2011-12-16

Patient:

Reactions: Hepatic Function Abnormal

Drug(s) suspected as cause:
Methotrexate Sodium
    Dosage: 7.5 mg, weekly
    Administration route: Oral

Azulfidine
    Dosage: 2 tablets, daily
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-01
    End date: 2011-11-25

Enbrel
    Dosage: 50 mg, weekly
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-04
    End date: 2011-11-25

Methotrexate Sodium
    Dosage: 10 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-01

Other drugs received by patient: Folic Acid



Possible Azulfidine side effects in

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

Patient:

Reactions: Hepatic Function Abnormal

Drug(s) suspected as cause:
Azulfidine
    Dosage: unk
    Indication: Rheumatoid Arthritis
    End date: 2011-11-25

Enbrel
    Dosage: 50 mg, weekly
    Indication: Rheumatoid Arthritis
    Start date: 2011-11-04
    End date: 2011-11-25

Methotrexate Sodium
    Dosage: 10 mg, weekly
    Administration route: Oral
    Indication: Rheumatoid Arthritis



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

-- advertisement -- The American Red Cross
 
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2017