Azulfidine and hepatic function abnormal Patient Reports February 11, 2012

Azulfidine Side Effects Report #4896768-0
Azulfidine side effect was reported by a Physician from JAPAN on Jan 13, 2006. Male patient, 74 years of age, weighting 110.2 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: agranulocytosis, fatigue, hepatic function abnormal, pneumonia , rash . Azulfidine dosage: unknown. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #4910995-5
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Jan 27, 2006. Male patient, 74 years of age, weighting 110.2 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: agranulocytosis, fatigue, hepatic function abnormal, pneumonia , rash . Azulfidine dosage: unknown. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5899065-X
Azulfidine side effect was reported by a Physician from JAPAN on Sept 17, 2008. Female patient, 71 years of age, weighting 120.2 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: hepatic function abnormal, jaundice , lymphocyte stimulation test positive. Azulfidine dosage: unknown. During the same period patient was treated with OPALMON, CELECOXIB, MUCOSTA, LORCAM, AMARYL, BASEN, SIGMART, ANPLAG. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #4817549-X
Azulfidine side effect was reported by a Physician from JAPAN on Oct 20, 2005. Female patient, 65 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: aplastic anaemia, arthralgia, bone marrow failure, condition aggravated, hepatic function abnormal. Azulfidine dosage: unknown. Patient was hospitalized. Patient recovered.


Azulfidine Side Effects Report #4546827-7
Azulfidine side effect was reported by a Physician from on Dec 24, 2004. Female patient, 50 years of age, weighting 92.59 lb, was diagnosed with rheumatoid arthritis , exanthem and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: alpha haemolytic streptococcal infection, diarrhoea, disease recurrence, exanthem, hepatic function abnormal, immunodeficiency, pleural effusion, pruritus, pyothorax. Azulfidine dosage: 500 MG (250 MG, 1 IN 2 D), ORAL. During the same period patient was treated with ALENDRONATE, PREDNISOLONE, CALCITRIOL. 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 #4634629-2
Azulfidine side effect was reported by a Physician from on Mar 28, 2005. Female patient, 43 years of age, weighting 120.2 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: exanthem, hepatic function abnormal, infectious mononucleosis , lymphadenopathy, lymphocyte morphology abnormal, malaise, pharyngolaryngeal pain, pyrexia, splenomegaly. Azulfidine dosage: 1 GRM (500 MG, 2 IN 1 D), ORAL. During the same period patient was treated with LAFUTIDINE, PHELLOBERIN A, TIQUIZIUM BROMIDE, LOPERAMIDE HYDROCHLORIDE, VALSARTAN. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #4830601-8
Azulfidine side effect was reported by a Physician from JAPAN on Nov 04, 2005. Female patient, 36 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: bone marrow failure, hepatic function abnormal, malaise, pyrexia, stevens-johnson syndrome. Azulfidine dosage: 500 MG (500 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #4849404-3
Azulfidine side effect was reported by a Physician from JAPAN on Nov 24, 2005. Female patient, 36 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: bone marrow failure, hepatic function abnormal, malaise, pyrexia, stevens-johnson syndrome. Azulfidine dosage: 500 MG (500 MG, 1 IN 1 D), ORAL. Patient was hospitalized. Patient recovered.


Azulfidine Side Effects Report #4866935-0
Azulfidine side effect was reported by a Physician from JAPAN on Nov 04, 2005. Female patient, 36 years of age, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: bone marrow failure, erythema, hepatic function abnormal, malaise, pruritus, pyrexia. Azulfidine dosage: 500 MG (500 MG, 1 IN 1D), ORAL. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5106177-7
Azulfidine side effect was reported by a Physician from JAPAN on Sept 01, 2006. Female patient, 33 years of age, weighting 110.2 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: condition aggravated, hepatic function abnormal, liver disorder, rheumatoid arthritis . Azulfidine dosage: 1000 MG (500 MG, 2 IN 1D); ORAL. During the same period patient was treated with FOSAMAX, VOLTAREN, SHIOSOL. 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 #5391583-6
Azulfidine side effect was reported by a Physician from JAPAN on July 09, 2007. Female patient was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: hepatic function abnormal, interstitial lung disease, leukopenia. Azulfidine dosage: DAILY DOSE:500MG. Patient recovered.

Azulfidine Side Effects Report #5370984-6
Azulfidine side effect was reported by a Physician from JAPAN on June 18, 2007. Female patient, weighting 108.0 lb, was diagnosed with exostosis and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: arthralgia, chills, dyspnoea, headache , hepatic function abnormal, nausea , pyrexia. Azulfidine dosage: unknown. Patient was hospitalized. Patient recovered.


Azulfidine Side Effects Report #5400661-4
Azulfidine side effect was reported by a Physician from JAPAN on July 18, 2007. Female patient, weighting 108.0 lb, was diagnosed with exostosis and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: arthralgia, c-reactive protein increased, chills, dyspnoea, headache , hepatic function abnormal, liver disorder, nausea , pyrexia. Azulfidine dosage: unknown. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5642059-X
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Feb 18, 2008. Male patient, 69 years of age, weighting 124.1 lb, was diagnosed with arthralgia, rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: acute lymphocytic leukaemia, hepatic function abnormal, pancytopenia, pyrexia. Azulfidine dosage: unknown. During the same period patient was treated with AUROTHIOMALATE. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5660988-8
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Feb 28, 2008. Male patient, 69 years of age, weighting 124.1 lb, was diagnosed with arthralgia, rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: acute lymphocytic leukaemia, hepatic function abnormal, pancytopenia, pyrexia. Azulfidine dosage: unknown. During the same period patient was treated with AUROTHIOMALATE. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5718557-7
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Apr 17, 2008. Male patient, weighting 140.7 lb, was diagnosed with arthralgia, rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: acute lymphocytic leukaemia, hepatic function abnormal, pancytopenia, pyrexia. Azulfidine dosage: unknown. During the same period patient was treated with AZULFIDINE EN, AUROTHIOMALATE, OSTELUC, FAMOTIDINE, PANALDINE, SERMION, CEROCRAL, IMIDAPRIL. Patient was hospitalized. Patient recovered.

Azulfidine Side Effects Report #5292406-6
Azulfidine side effect was reported by a Consumer or non-health professional from JAPAN on Aug 25, 2004. Female patient, 83 years of age, was treated with Azulfidine. After drug was administered, patient experienced the following side effects: acute respiratory failure, bone marrow failure, diffuse large b-cell lymphoma, disseminated intravascular coagulation, hepatic function abnormal, leukoerythroblastosis, lumbar spinal stenosis, metastases to bone marrow. Azulfidine dosage: unknown. During the same period patient was treated with METHOTREXATE, BUCILLAMINE, PREDNISOLONE, NSAID. Patient was hospitalized. Patient died on 08/04/2002.