Fludara and ascites Patient Reports February 12, 2012

Fludara Side Effects Report #6050418-9
Fludara side effect was reported by a Pharmacist from UNITED STATES on Jan 19, 2009. Female patient, 74 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites. Fludara dosage: unknown. During the same period patient was treated with RITUXAN, CYCLOPHOSPHAMIDE. Patient recovered.

Fludara Side Effects Report #4914308-4
Fludara side effect was reported by a Consumer or non-health professional from CANADA on Jan 31, 2006. Male patient, 15 years of age, was diagnosed with congenital dyskeratosis, prophylaxis against transplant rejection and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, blood bilirubin increased, brain herniation, brain oedema, cerebral haemorrhage, diarrhoea, gastritis, gastrointestinal disorder. Fludara dosage: 30 MG/M2, 1X/DAY, INTRAVENOUS. During the same period patient was treated with CYCLOPHOSPHAMIDE, ANTITHYMOCYTE IMMUNOGLOBULIN, ANTITHYMOCYTE IMMUNOGLOBULIN, CYCLOSPORINE. Patient died.

Fludara Side Effects Report #5110899-1
Fludara side effect was reported by a Physician from FRANCE on Sept 07, 2006. Female patient, 70 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with Fludara. After drug was administered, patient experienced the following side effects: acute respiratory distress syndrome, ascites, oedema peripheral, pleural effusion, pulmonary hypertension . Fludara dosage: unknown. Patient recovered.

Fludara Side Effects Report #5145569-7
Fludara side effect was reported by a Consumer or non-health professional from TURKEY on Oct 17, 2006. Male patient, 59 years of age, was diagnosed with chronic lymphocytic leukaemia and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, hepatitis b , splenomegaly, subacute hepatic failure, treatment noncompliance. Fludara dosage: unknown. Patient died.


Fludara Side Effects Report #4941543-1
Fludara side effect was reported by a Physician from JAPAN on Feb 22, 2006. Male patient, 56 years of age, weighting 138.9 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, bone marrow failure, chronic lymphocytic leukaemia transformation, colon cancer, disease progression, ileus, infection , intestinal adenocarcinoma, pneumonia . Fludara dosage: 33.2 MG, CYCLE X 5D, INTRAVENOUS. During the same period patient was treated with PREDONINELET, MEROPEN, EXACIN, CEFTAZIDIME, MINOCYCLINE, SULPERAZON. Patient recovered.

Fludara Side Effects Report #5044243-5
Fludara side effect was reported by a Physician from JAPAN on June 15, 2006. Male patient, 56 years of age, weighting 138.9 lb, was diagnosed with chronic lymphocytic leukaemia and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, bone marrow failure, disease progression, ileus, intestinal adenocarcinoma, neutrophil count decreased, spinal cord compression. Fludara dosage: 33.2 MG, CYCLE X 5D, INTRAVENOUS. During the same period patient was treated with PREDONINELET, MEROPEN, EXACIN, CEFTAZIDIME, MINOCYCLINE, SULPERAZON. Patient recovered.

Fludara Side Effects Report #5346419-6
Fludara side effect was reported by a Health Professional from UNITED KINGDOM on May 22, 2007. Male patient, weighting 192.9 lb, was diagnosed with b-cell lymphoma and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, constipation , deep vein thrombosis , febrile neutropenia, intestinal obstruction, white blood cell count decreased. Fludara dosage: unknown. During the same period patient was treated with NOVANTRONE, ALLOPURINOL, DEXAMETHASONE, PARACETAMOL, SPIRONOLACTONE, SULFAMETHOXAZOLE. Patient recovered.

Fludara Side Effects Report #4557117-0
Fludara side effect was reported by a Physician from on Jan 04, 2005. Female patient, 41 years of age, weighting 123.5 lb, was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, asterixis, bk virus infection, blood lactate dehydrogenase increased, bone marrow transplant , catheter related infection, cholangitis, cystitis haemorrhagic, diarrhoea. Fludara dosage: 48 MG, 1X/DAY FOR BMT , INTRAVENOUS : 50 MG, 1X/DAY FOR PBSCT, INTRAVENOUS. During the same period patient was treated with CYTARABINE, ETOPOSIDE, CYCLOPHOSPHAMIDE, MYCOPHENOLATE MOFETIL, METHOTREXATE, METHYLPREDNISOLONE. Patient died on 11/10/2004.

Fludara Side Effects Report #4690126-X
Fludara side effect was reported by a Physician from on June 03, 2005. Female patient, 41 years of age, weighting 123.5 lb, was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, asterixis, back pain , biliary ischaemia, bk virus infection, bone marrow transplant , cholangitis, complications of transplant surgery, condition aggravated. Fludara dosage: unknown. During the same period patient was treated with CYTARABINE, ETOPOSIDE, CYCLOPHOSPHAMIDE, MYCOPHENOLATE MOFETIL, METHOTREXATE, METHYLPREDNISOLONE. Patient was hospitalized. Patient died on 11/10/2004.


Fludara Side Effects Report #4711012-2
Fludara side effect was reported by a Physician from JAPAN on June 27, 2005. Female patient, 41 years of age, weighting 123.5 lb, was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, asterixis, bk virus infection, catheter related infection, cholangitis, condition aggravated, diarrhoea, gastrointestinal hypomotility, graft versus host disease. Fludara dosage: unknown. During the same period patient was treated with CYTARABINE, ETOPOSIDE. Patient was hospitalized. Patient died on 11/10/2004.

Fludara Side Effects Report #5420085-3
Fludara side effect was reported by a Health Professional from JAPAN on Aug 09, 2007. Female patient, 13 years of age, was diagnosed with prophylaxis against graft versus host disease and was treated with Fludara. After drug was administered, patient experienced the following side effects: ascites, bone sarcoma, malignant neoplasm progression, malignant pleural effusion, pleural haemorrhage, pulmonary oedema, respiratory failure. Fludara dosage: 30 MG/M2, 1X/DAY. During the same period patient was treated with BUSULFAN, CYCLOSPORINE, METHOTREXATE. Patient died on 05/25/2003.