Azulfidine and bone marrow failure Patient Reports February 12, 2012

Azulfidine Side Effects Report #5019393-X
Azulfidine side effect was reported by a Physician from JAPAN on May 18, 2006. Female patient, 75 years of age, weighting 94.80 lb, was diagnosed with rheumatoid arthritis  and was treated with Azulfidine. After drug was administered, patient experienced the following side effects: anorexia, aplastic anaemia, bone marrow failure, fall , haemorrhage subcutaneous, malaise, nausea , pleurisy, pyrexia. Azulfidine dosage: 1000 MG (TWICE DAILY), ORAL. During the same period patient was treated with LOXONIN, MARZULENE, ALFACALCIDOL, OSTEN, NORVASC, ASPIRIN. 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 #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 #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.