Azathioprine and haemoglobin decreased Patient Reports February 10, 2010

Azathioprine Side Effects Report #5972017-7
Azathioprine side effect was reported by a Physician from ITALY on Nov 10, 2008. Male patient, 53 years of age, was diagnosed with systemic lupus erythematosus and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: c-reactive protein increased, fatigue, haemoglobin decreased, hypergammaglobulinaemia, nausea , platelet count decreased, pyrexia, transaminases increased, visceral leishmaniasis. Azathioprine dosage: 100 MG; QD. During the same period patient was treated with STEROIDS, ENALAPRIL, HYDROXYCHLOROQUINE, LYSINE ACETYLSALICYLATE, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5594327-8
Azathioprine side effect was reported by a Health Professional from IRAN (ISLAMIC REPUBLIC OF) on Jan 09, 2008. Male patient, 36 years of age, was diagnosed with renal transplant and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: biopsy lung, blood creatinine increased, breath sounds abnormal, chest x-ray abnormal, computerised tomogram abnormal, diffuse alveolar damage, dyspnoea, haemoglobin decreased, haemoptysis. Azathioprine dosage: 4 MG/KG/D. During the same period patient was treated with PREDNISONE, MYCOPHENOLATE MOFETIL, CYCLOSPORINE, PREDNISOLONE. Patient died.

Azathioprine Side Effects Report #5640685-5
Azathioprine side effect was reported by a Physician from TURKEY on Feb 08, 2008. Female patient, 52 years of age, was diagnosed with proteinuria and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood pressure diastolic increased, haematocrit decreased, haemoglobin decreased, kaposi's sarcoma , white blood cell count decreased. Azathioprine dosage: 125 MG; QD; PO. During the same period patient was treated with CYCLOSPORINE, MYCOPHENOLATE MOFETIL, PREDNISOLONE, LOSARTAN POTASSIUM, ASPIRIN, HYDROCHLOROTHIAZIDE, RAMIPRIL, SIMVASTATIN. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5884476-9
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Aug 28, 2008. Male patient was diagnosed with myasthenia gravis, non-small cell lung cancer and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: haematuria, haemoglobin decreased, haemoptysis, prothrombin time shortened, white blood cell count decreased. Azathioprine dosage: 100 MG;TWICE A DAY ORAL. During the same period patient was treated with ERLOTINIB, ITRACONAZOLE, PYRIDOSTIGMINE, VALPROATE. Patient died.


Azathioprine Side Effects Report #4991543-0
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 17, 2006. Female patient, 18 years of age, was diagnosed with multiple sclerosis  and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: disease progression, fatigue, haematoma, haemoglobin decreased, headache , platelet count decreased, pyrexia, vertigo, white blood cell count decreased. Azathioprine dosage: 50 MG DAILY. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5729861-0
Azathioprine side effect was reported by a Health Professional from UNITED STATES on Apr 18, 2008. Female patient, 85 years of age, was diagnosed with immunosuppression and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, hypoxia, platelet count decreased, urosepsis. Azathioprine dosage: unknown. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5988390-X
Azathioprine side effect was reported by a Health Professional from UNITED KINGDOM on Nov 19, 2008. Male patient, 42 years of age, was diagnosed with henoch-schonlein purpura and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, cerebral haemorrhage, convulsion, haemodialysis, haemoglobin decreased, hypertension, prothrombin time prolonged, renal impairment. Azathioprine dosage: 100 MG. During the same period patient was treated with RAMIPRIL. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5093256-6
Azathioprine side effect was reported by a Pharmacist from UNITED STATES on Aug 29, 2006. Male patient, 57 years of age, weighting 146.6 lb, was diagnosed with crohn's disease  and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: haemoglobin decreased, reticulocyte count increased, white blood cell count decreased. Azathioprine dosage: 50 MG TID PO. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5747238-9
Azathioprine side effect was reported by a Physician from JAPAN on May 01, 2008. Female patient, 57 years of age, was diagnosed with crohn's disease  and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: abdominal tenderness, blood beta-d-glucan increased, cough, dyspnoea, haematochezia, haemoglobin decreased, hypoxia, leukopenia. Azathioprine dosage: 50 MG; PO. During the same period patient was treated with INFLIXIMAB, MESALAMINE, PREDNISOLONE. Patient was hospitalized. Patient recovered.


Azathioprine Side Effects Report #4879802-3
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED STATES on Dec 28, 2005. Male patient, 46 years of age, was diagnosed with crohn's disease  and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: cholestasis, haemoglobin decreased, hepatic fibrosis, hepatic steatosis, hepatotoxicity, peliosis hepatis, platelet count decreased, varices oesophageal. Azathioprine dosage: 200 MG (NR), NR. Patient recovered.

Azathioprine Side Effects Report #5586131-1
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Oct 12, 2007. Female patient, 36 years of age, was diagnosed with crohn's disease  and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: disseminated intravascular coagulation, gallbladder disorder, haemoglobin decreased, heart rate increased, peritonitis, salmonellosis, white blood cell count increased. Azathioprine dosage: unknown. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5223878-0
Azathioprine side effect was reported by a Consumer or non-health professional from JAPAN on Jan 18, 2007. Female patient, 14 years of age, was diagnosed with congenital aplastic anaemia and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: anaemia, blood product transfusion dependent, depressive symptom, disease progression, haemoglobin decreased, menorrhagia, mental disorder. Azathioprine dosage: unknown. During the same period patient was treated with NEORAL, STEROIDS NOS, STEROIDS NOS, PREDONINE. Patient recovered.

Azathioprine Side Effects Report #5163560-1
Azathioprine side effect was reported by a Consumer or non-health professional from JAPAN on Nov 22, 2006. Female patient, 14 years of age, was diagnosed with congenital aplastic anaemia and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: disease progression, haemoglobin decreased, mental disorder, polymenorrhagia. Azathioprine dosage: unknown. During the same period patient was treated with CYCLOSPORINE. Patient recovered.

Azathioprine Side Effects Report #5175857-X
Azathioprine side effect was reported by a Consumer or non-health professional from JAPAN on Nov 22, 2006. Female patient, 14 years of age, was diagnosed with congenital aplastic anaemia and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: anaemia, blood product transfusion dependent, disease progression, haemoglobin decreased, menorrhagia, mental disorder. Azathioprine dosage: unknown. During the same period patient was treated with CYCLOSPORINE, STEROIDS NOS, STEROIDS NOS. Patient recovered.


Azathioprine Side Effects Report #4673995-9
Azathioprine side effect was reported by a Physician from on May 06, 2005. Male patient, 29 years of age, was diagnosed with colitis ulcerative and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: haemoglobin decreased, hypoxia, leukopenia, pneumocystis jiroveci pneumonia, pyrexia, thrombocytopenia. Azathioprine dosage: 100 MG QD. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5934849-0
Azathioprine side effect was reported by a Physician from GERMANY on Oct 08, 2008. Male patient, 15 years of age, was diagnosed with colitis ulcerative and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: blood lactate dehydrogenase increased, blood uric acid increased, central nervous system lymphoma, cerebral artery embolism, epstein-barr virus infection, fatigue, haemoglobin decreased, hepatosplenic t-cell lymphoma, histiocytosis haematophagic. Azathioprine dosage: 1 MG/KG;. During the same period patient was treated with BOSWELLIA ACID. Patient was hospitalized. Patient died.

Azathioprine Side Effects Report #5025453-X
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED STATES on May 22, 2006. Female patient, 18 years of age, was diagnosed with central nervous system inflammation, demyelination and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: enzyme abnormality, fatigue, haemoglobin decreased, headache , platelet count decreased, pyrexia, spontaneous haematoma, vertigo, white blood cell count decreased. Azathioprine dosage: 50 MG QDAY PO. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #6072910-3
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Jan 20, 2009. Female patient, 60 years of age, was treated with Azathioprine. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, blood alkaline phosphatase increased, c-reactive protein increased, chills, cough, cytomegalovirus infection , dyspnoea, haemoglobin decreased, malaise. Azathioprine dosage: 125 MG. During the same period patient was treated with TACROLIMUS, GANCICLOVIR, TAZOCIN. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #4950259-7
Azathioprine side effect was reported by a Consumer or non-health professional from CANADA on Mar 03, 2006. Female patient, 47 years of age, was treated with Azathioprine. After drug was administered, patient experienced the following side effects: haemodialysis, haemoglobin decreased, heart rate increased, kidney fibrosis, nephritis interstitial, pleural effusion, pyrexia, renal abscess, renal failure acute. Azathioprine dosage: 100 MG. During the same period patient was treated with RAMIPRIL, OMEPRAZOLE, SULFAMETHOXAZOLE, ZOPICLONE. Patient was hospitalized. Patient recovered.


Azathioprine Side Effects Report #5001546-8
Azathioprine side effect was reported by a Physician from CANADA on Apr 24, 2006. Female patient, 47 years of age, was treated with Azathioprine. After drug was administered, patient experienced the following side effects: abdominal pain , back pain , haemodialysis, haemoglobin decreased, heart rate decreased, nephritis interstitial, pleural effusion, red blood cell sedimentation rate increased, renal failure chronic. Azathioprine dosage: 100 MG QDAY. During the same period patient was treated with PREDNISONE, RAMIPRIL, OMEPRAZOLE, SULFAMETHOXAZOLE, ZOPICLONE. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #5727104-5
Azathioprine side effect was reported by a Consumer or non-health professional from UNITED KINGDOM on Apr 15, 2008. Male patient, 45 years of age, was treated with Azathioprine. After drug was administered, patient experienced the following side effects: chills, condition aggravated, haemoglobin decreased, hypotension, neutrophilia, renal failure, tubulointerstitial nephritis, white blood cell count increased, white blood cells urine positive. Azathioprine dosage: 150 MG; DAILY. During the same period patient was treated with PREDNISOLONE. Patient was hospitalized. Patient recovered.

Azathioprine Side Effects Report #4723832-9
Azathioprine side effect was reported by a Physician from UNITED STATES on July 05, 2005. Male patient, 42 years of age, weighting 124.0 lb, was diagnosed with nephrogenic anaemia and was treated with Azathioprine. After drug was administered, patient experienced the following side effects: blood immunoglobulin g increased, blood immunoglobulin m decreased, bone marrow depression, gout , haemoglobin decreased, red blood cell count decreased, reticulocyte count decreased. Azathioprine dosage: 25 MG QDAY. During the same period patient was treated with PROCRIT. Patient was hospitalized. Patient recovered.