Azulfidine and white blood cell count decreased Patient Reports February 11, 2012

Azulfidine Side Effects Report #5302760-4
Azulfidine side effect was reported by a Pharmacist from JAPAN on Apr 16, 2007. Female patient, 72 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: anorexia, eczema , white blood cell count decreased. Azulfidine dosage: unknown. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5307606-6
Azulfidine side effect was reported by a Physician from JAPAN on Apr 17, 2007. Female patient, 72 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: white blood cell count decreased. Azulfidine dosage: unknown. During the same period patient was treated with PREDNISOLONE, ALENDRONATE, SELBEX, MOBIC, OMEPRAL. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5141068-7
Azulfidine side effect was reported by a Physician from JAPAN on Oct 17, 2006. Female patient, 68 years of age, weighting 79.37 lb, was diagnosed with rheumatoid arthritis , renal failure chronic and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: abdominal distension, constipation , disseminated intravascular coagulation, gastrointestinal necrosis, large intestine perforation, pelvic mass, peritonitis, white blood cell count decreased. Azulfidine dosage: 1000 MG (500 MG, 2 IN 1 D) ORAL. During the same period patient was treated with SALAZOPYRIN, KREMEZIN, NORVASC, PERSANTIN, AZUCERENIN S, BISOLVON, URINORM, ALLOPURINOL. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5141068-7
Azulfidine side effect was reported by a Physician from JAPAN on Oct 17, 2006. Female patient, 68 years of age, weighting 79.37 lb, was diagnosed with rheumatoid arthritis , renal failure chronic and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: abdominal distension, constipation , disseminated intravascular coagulation, gastrointestinal necrosis, large intestine perforation, pelvic mass, peritonitis, white blood cell count decreased. Azulfidine dosage: 1000 MG (500 MG, 2 IN 1 D) ORAL. During the same period patient was treated with SALAZOPYRIN, KREMEZIN, NORVASC, PERSANTIN, AZUCERENIN S, BISOLVON, URINORM, ALLOPURINOL. Patient was hospitalized. Patient recovered.


Azulfidine Side Effects Report #4747922-X
Azulfidine side effect was reported by a Physician from JAPAN on Aug 11, 2005. Female patient, 47 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: hepatic function abnormal, rash , transaminases increased, white blood cell count decreased. Azulfidine dosage: 1000 MG, ORAL. During the same period patient was treated with MEDROL, MOBIC, STOMILASE, MAGNESIUM OXIDE, FAMOTIDINE. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5263099-9
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Feb 28, 2007. Female patient, weighting 99.21 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: arthralgia, joint swelling, liver function test abnormal, pyrexia, white blood cell count decreased. Azulfidine dosage: unknown. During the same period patient was treated with METHOTREXATE, BUCILLAMINE, LOXONIN, MUCOSTA. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5280787-9
Azulfidine side effect was reported by a Physician from JAPAN on Mar 19, 2007. Female patient, weighting 101.6 lb, was diagnosed with rheumatoid arthritis , hyperuricaemia and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: hepatic function abnormal, platelet count decreased, white blood cell count decreased. Azulfidine dosage: unknown. During the same period patient was treated with ALLOPURINOL, ETANERCEPT, PREDONINE. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5165074-1
Azulfidine side effect was reported by a Physician from JAPAN on Nov 13, 2006. Female patient, 75 years of age, weighting 88.18 lb, was diagnosed with arthralgia, rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: bacterial infection , decreased appetite, interstitial lung disease, nausea , white blood cell count decreased. Azulfidine dosage: 1 GRAM (500 MG, 2 IN 1 D), ORAL. During the same period patient was treated with AZULFIDINE EN, PREDNISOLONE, ACTONEL, ZANTAC, ASPARA, DEXTROMETHORPHAN HYDROBROMIDE, LOXONIN, MARZULENE. Patient was hospitalized. Patient recovered.