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CONTINUOUS HAEMODIAFILTRATION side effect

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Bisoprolol Side Effects Report #5679866-3
Consumer or non-health professional from JAPAN reported BISOPROLOL FUMARATE problem on Mar 19, 2008. Male patient, 39 years of age, was treated with BISOPROLOL FUMARATE. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, pleural effusion, pulmonary congestion, renal failure, shock, . BISOPROLOL FUMARATE dosage: 150 MG (150 MG, 1 IN 1 D) ORAL. During the same period patient was treated with AMLODIPINE. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5633941-8
METFORMIN problem was reported by a Consumer or non-health professional from GERMANY on Feb 03, 2008. Female patient, 74 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, diabetic nephropathy, haemodialysis, lactic acidosis, renal failure acute, shock, . METFORMIN dosage: unknown. Patient was hospitalized. Patient died.

Metformin Side Effects Report #5635757-5
Consumer or non-health professional from GERMANY reported METFORMIN problem on Feb 03, 2008. Male patient, 74 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, lactic acidosis, multi-organ failure, renal failure acute, shock, . METFORMIN dosage: unknown. Patient was hospitalized. Patient died.

Mabthera Side Effects Report #5582967-1
MABTHERA problem was reported by a Physician from UNITED KINGDOM on Dec 05, 2007. Male patient, 65 years of age, was diagnosed with non-hodgkin's lymphoma and was treated with MABTHERA. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, encephalopathy, hepatitis b, . MABTHERA dosage: unknown. During the same period patient was treated with CYCLOPHOSPHAMIDE, DOXORUBICIN, VINCRISTINE, PREDNISOLONE. Patient was hospitalized. Patient died on 05/05/2007.


Dactinomycin Side Effects Report #5485297-1
Pharmacist from UNITED STATES reported DACTINOMYCIN problem on Oct 10, 2007. Male patient, weighting 30.42 lb, was diagnosed with nephroblastoma and was treated with DACTINOMYCIN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, venoocclusive liver disease, . DACTINOMYCIN dosage: 0.6 MG - 0.045 MG/KG EVERY 3 WEEKS IV. During the same period patient was treated with VINCRISTINE, ONDANSETRON, MIRALAX, BACTRIM, NIFEREX, CEPHALEXIN. Patient recovered.

Renagel Side Effects Report #5416508-6
RENAGEL problem was reported by a Physician from JAPAN on July 31, 2007. Female patient, 72 years of age, weighting 78.26 lb, was diagnosed with hyperphosphataemia, hyperkalaemia and was treated with RENAGEL. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, diverticulum, haemodialysis, large intestine perforation, . RENAGEL dosage: unknown. During the same period patient was treated with CALCIUM POLYSTYRENE SULFONATE, AMLODIPINE BESYLATE, ENALAPRIL MALEATE, CARVEDILOL, BLOPRESS, SPIRONOLACTONE, ASPIRIN, ALLOPURINOL. Patient recovered.

Pepcid Side Effects Report #5440821-X
Physician from JAPAN reported PEPCID RPD problem on Aug 29, 2007. Male patient, 56 years of age, was treated with PEPCID RPD. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, hepatic atrophy, hepatic encephalopathy, hepatitis fulminant, liver transplant, no therapeutic response, . PEPCID RPD dosage: unknown. During the same period patient was treated with PERSANTINE, RYTHMODAN, CANDESARTAN CILEXETIL, WARFARIN. Patient was hospitalized. Patient recovered.

Clarithromycin Side Effects Report #5772538-6
CLARITHROMYCIN problem was reported by a Consumer or non-health professional from JAPAN on June 06, 2008. Female patient, 16 years of age, was diagnosed with nervous system disorder and was treated with CLARITHROMYCIN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, infection, multi-organ failure, neuroleptic malignant syndrome, rhabdomyolysis, ventricular extrasystoles, . CLARITHROMYCIN dosage: unknown. During the same period patient was treated with PRANLUKAST, PHENOBARBITAL, CLONAZEPAM, VALPROATE. Patient was hospitalized. Patient recovered.

Ibuprofen Side Effects Report #5731160-8
Consumer or non-health professional from UNITED KINGDOM reported IBUPROFEN problem on Apr 23, 2008. Female patient, child 12 years of age, weighting 105.8 lb, was diagnosed with pyrexia and was treated with IBUPROFEN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, renal failure acute, . IBUPROFEN dosage: 300 MG/BID/ORAL. During the same period patient was treated with CHLORPHENAMINE, ACETAMINOPHEN. Patient was hospitalized. Patient recovered.


Nifedipine Side Effects Report #5741350-6
NIFEDIPINE problem was reported by a Consumer or non-health professional from ITALY on Apr 28, 2008. Female patient, 45 years of age, was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, multi-organ failure, renal failure, . NIFEDIPINE dosage: unknown. During the same period patient was treated with ATENOLOL. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5720971-0
Health Professional from UNITED STATES reported METFORMIN problem on Apr 14, 2008. Male patient, 71 years of age, weighting 114.6 lb, was diagnosed with diabetes mellitus and was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, lactic acidosis, renal failure acute, . METFORMIN dosage: unknown. Patient recovered.

Metformin Side Effects Report #5368309-5
METFORMIN HYDROCHLORIDE problem was reported by a Consumer or non-health professional from on June 05, 2007. Female patient, 70 years of age, was diagnosed with diabetes mellitus and was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, hypotension, lactic acidosis, renal failure acute, . METFORMIN HYDROCHLORIDE dosage: unknown. During the same period patient was treated with ACE INHIBITOR, NSAID. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5300362-7
Physician from JAPAN reported PROGRAF problem on Mar 26, 2007. Male patient, 41 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: continuous haemodiafiltration, graft thrombosis, pleural haemorrhage, renal impairment, systemic mycosis, thrombotic microangiopathy, . PROGRAF dosage: unknown. Patient died.

Methotrexate Side Effects Report #5677604-1
METHOTREXATE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 04, 2008. Female patient, 60 years of age, weighting 176.4 lb, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: beta haemolytic streptococcal infection, continuous haemodiafiltration, multi-organ failure, sepsis, . METHOTREXATE dosage: 7.5 MG WEEKLY. During the same period patient was treated with ENBREL, PREDNISOLONE, ASPIRIN, ATENOLOL, FUROSEMIDE, GLICLAZIDE, MELOXICAM, OMEPRAZOLE. Patient recovered.


Simulect Side Effects Report #5624212-4
Consumer or non-health professional from JAPAN reported SIMULECT problem on Feb 06, 2008. Male patient, 56 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, continuous haemodiafiltration, hypersensitivity, hypotension, kidney transplant rejection, respiratory disorder, urine output decreased, . SIMULECT dosage: 20 MG, ONCE/SINGLE. During the same period patient was treated with CELLCEPT, NEORAL, SANDIMMUNE, PROPOFOL, FENTANYL, VECURONIUM BROMIDE, SEVOFLURANE. Patient was hospitalized. Patient recovered.

Tacrolimus Side Effects Report #5646324-1
TACROLIMUS problem was reported by a Physician from AUSTRALIA on Feb 11, 2008. Male patient, 47 years of age, was diagnosed with liver transplant and was treated with TACROLIMUS. After drug was administered, patient experienced the following problems/side effects: biliary anastomosis complication, continuous haemodiafiltration, metabolic acidosis, nephrogenic systemic fibrosis, portal vein thrombosis, post procedural complication, renal failure acute, . TACROLIMUS dosage: 7 MG, BID, ORAL. During the same period patient was treated with PREDNISOLONE, CYCLOSPORINE, MYCOPHENOLATE MOFETIL, OMNISCAN. Patient recovered.

Zonisamide Side Effects Report #5572353-2
Physician from JAPAN reported ZONISAMIDE problem on Dec 07, 2007. Male patient, 30 years of age, was diagnosed with epilepsy and was treated with ZONISAMIDE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, continuous haemodiafiltration, disseminated intravascular coagulation, faecal incontinence, feeding disorder, heat stroke, malaise, multi-organ failure, renal failure, . ZONISAMIDE dosage: 400 MG, ORAL. Patient was hospitalized and became disabled. Patient recovered.

Simulect Side Effects Report #5506157-3
SIMULECT problem was reported by a Consumer or non-health professional from JAPAN on Oct 29, 2007. Male patient, 56 years of age, was diagnosed with renal transplant, induction of anaesthesia and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, continuous haemodiafiltration, hypersensitivity, hypotension, respiratory disorder, . SIMULECT dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, VECURONIUM BROMIDE, SEVOFLURANE, OXYGEN, ANESTHETICS NOS. Patient was hospitalized. Patient recovered.

Simulect Side Effects Report #5518962-8
Consumer or non-health professional from JAPAN reported SIMULECT problem on Nov 08, 2007. Male patient, 56 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, continuous haemodiafiltration, hypersensitivity, hypotension, kidney transplant rejection, respiratory disorder, urine output decreased, . SIMULECT dosage: 20 MG, ONCE/SINGLE. During the same period patient was treated with CELLCEPT, NEORAL, SANDIMMUNE, PROPOFOL, FENTANYL, VECURONIUM BROMIDE, SEVOFLURANE. Patient was hospitalized. Patient recovered.


Simulect Side Effects Report #5519038-6
SIMULECT problem was reported by a Consumer or non-health professional from JAPAN on Nov 08, 2007. Male patient, 56 years of age, was diagnosed with renal transplant, induction of anaesthesia and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, continuous haemodiafiltration, hypersensitivity, hypotension, respiratory disorder, . SIMULECT dosage: unknown. During the same period patient was treated with PROPOFOL, FENTANYL, VECURONIUM BROMIDE, SEVOFLURANE, OXYGEN, ANESTHETICS NOS. Patient was hospitalized. Patient recovered.

Simulect Side Effects Report #5524832-1
Physician from JAPAN reported SIMULECT problem on Nov 19, 2007. Male patient, 56 years of age, was diagnosed with renal transplant and was treated with SIMULECT. After drug was administered, patient experienced the following problems/side effects: anaphylactic shock, continuous haemodiafiltration, hypersensitivity, hypotension, kidney transplant rejection, respiratory disorder, urine output decreased, . SIMULECT dosage: 20 MG, ONCE/SINGLE. During the same period patient was treated with CELLCEPT, NEORAL, SANDIMMUNE, PROPOFOL, FENTANYL, VECURONIUM BROMIDE, SEVOFLURANE. Patient was hospitalized. Patient recovered.

Busulfan Side Effects Report #5528069-1
BUSULFAN problem was reported by a Health Professional from JAPAN on Nov 09, 2007. Female patient, child .7 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: ascites, continuous haemodiafiltration, dyspnoea, gallbladder enlargement, haematemesis, hepatic failure, hepatomegaly, hypopnoea, multi-organ failure, . BUSULFAN dosage: 6.6 MG;QID;IV. Patient recovered.

Prednisolone Side Effects Report #5413356-8
Consumer or non-health professional from UNITED KINGDOM reported PREDNISOLONE problem on July 25, 2007. Male patient, 42 years of age, was diagnosed with crohn's disease, hepatic haematoma and was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: acute abdomen, continuous haemodiafiltration, device migration, haemodynamic instability, hepatic haematoma, intra-abdominal haematoma, oliguria, procedural complication, thrombosis in device, . PREDNISOLONE dosage: unknown. During the same period patient was treated with HAEMOFILTRATION, WARFARIN. Patient recovered.

Cytarabine Side Effects Report #5419187-7
CYTARABINE problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 15, 2007. Female patient, weighting 196.2 lb, was treated with CYTARABINE. After drug was administered, patient experienced the following problems/side effects: blood bilirubin increased, continuous haemodiafiltration, hypotension, multi-organ failure, pneumonia, renal tubular necrosis, respiratory distress, respiratory failure, sepsis, . CYTARABINE dosage: 1013.55 MG. During the same period patient was treated with DAUNORUBICIN, ETOPOSIDE. Patient was hospitalized. Patient recovered.

Gemzar Side Effects Report #5430548-2
Physician from JAPAN reported GEMZAR problem on Aug 27, 2007. Female patient, 53 years of age, was diagnosed with lung adenocarcinoma stage ii and was treated with GEMZAR. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, continuous haemodiafiltration, diffuse alveolar damage, gastrointestinal haemorrhage, hepatic failure, interstitial lung disease, lung infiltration, multi-organ failure, . GEMZAR dosage: unknown. Patient was hospitalized. Patient died on 08/23/2006.

Metformin Side Effects Report #5776585-X
METFORMIN problem was reported by a Health Professional from NETHERLANDS on June 04, 2008. Female patient, 45 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: abdominal discomfort, continuous haemodiafiltration, diarrhoea, haemodynamic instability, lactic acidosis, loss of consciousness, nausea, renal failure acute, respiratory distress, . METFORMIN dosage: 500 MG, TID. During the same period patient was treated with FLUPENTIXOL. Patient was hospitalized. Patient recovered.

Rebif Side Effects Report #5728422-7
Physician from UNITED STATES reported REBIF problem on May 02, 2008. Female patient, 33 years of age, was treated with REBIF. After drug was administered, patient experienced the following problems/side effects: cholestasis, continuous haemodiafiltration, haemodynamic instability, hepatic failure, hepatic necrosis, hepatitis acute, hepatotoxicity, hypotension, . REBIF dosage: unknown. Patient recovered.

Tracleer Side Effects Report #5738399-6
TRACLEER problem was reported by a Physician from UNITED STATES on Apr 29, 2008. Male patient, 28 years of age, was diagnosed with pulmonary hypertension and was treated with TRACLEER. After drug was administered, patient experienced the following problems/side effects: coagulopathy, continuous haemodiafiltration, disease progression, heart and lung transplant, hepatic congestion, hepatic function abnormal, hepatic ischaemia, international normalised ratio increased, intestinal ischaemia, . TRACLEER dosage: unknown. During the same period patient was treated with COUMADIN. Patient was hospitalized. Patient died on 04/12/2008.

Nifedipine Side Effects Report #5739634-0
Consumer or non-health professional from ITALY reported NIFEDIPINE problem on Apr 28, 2008. Female patient, 45 years of age, was treated with NIFEDIPINE. After drug was administered, patient experienced the following problems/side effects: blood pressure abnormal, continuous haemodiafiltration, heart rate abnormal, multi-organ failure, no therapeutic response, renal failure, . NIFEDIPINE dosage: unknown. During the same period patient was treated with ATENOLOL. Patient was hospitalized. Patient recovered.

Prednisolone Side Effects Report #5702332-3
PREDNISOLONE problem was reported by a Consumer or non-health professional from UNITED KINGDOM on Mar 28, 2008. Female patient, 72 years of age, weighting 176.4 lb, was treated with PREDNISOLONE. After drug was administered, patient experienced the following problems/side effects: beta haemolytic streptococcal infection, continuous haemodiafiltration, multi-organ failure, sepsis, . PREDNISOLONE dosage: unknown. During the same period patient was treated with METHOTREXATE, ENBREL, ASPIRIN, ATENOL, FUROSEMIDE, GLICLAZIDE, MELOXICAM, OMEPRAZOLE. Patient was hospitalized. Patient recovered.

Methotrexate Side Effects Report #5704202-3
Health Professional from UNITED KINGDOM reported METHOTREXATE problem on Mar 28, 2008. Female patient, 72 years of age, weighting 176.4 lb, was treated with METHOTREXATE. After drug was administered, patient experienced the following problems/side effects: beta haemolytic streptococcal infection, continuous haemodiafiltration, multi-organ failure, streptococcal sepsis, . METHOTREXATE dosage: 7.5 MG WEEKLY;. During the same period patient was treated with ENBREL, PREDNISOLONE, ASPIRIN, ATENOLOL, FUROSEMIDE, GLICLAZIDE, MELOXICAM, OMEPRAZOLE. Patient recovered.

Maintate Side Effects Report #5713844-0
MAINTATE problem was reported by a Consumer or non-health professional from JAPAN on Apr 07, 2008. Male patient, 39 years of age, was treated with MAINTATE. After drug was administered, patient experienced the following problems/side effects: blood creatinine increased, continuous haemodiafiltration, oliguria, pleural effusion, pulmonary congestion, renal failure, shock, somnolence, . MAINTATE dosage: 150 MG (150 MG, 1 IN 1 D). During the same period patient was treated with AMLODIPINE. Patient was hospitalized. Patient recovered.

Prednisone Side Effects Report #5347115-1
Consumer or non-health professional from UNITED STATES reported PREDNISONE problem on May 22, 2007. Female patient, 56 years of age, was diagnosed with immunosuppression and was treated with PREDNISONE. After drug was administered, patient experienced the following problems/side effects: cardiac failure, continuous haemodiafiltration, hypotension, jugular vein distension, pulmonary hypertension, renal failure acute, scleroderma renal crisis, . PREDNISONE dosage: 2.5 MG. During the same period patient was treated with TACROLIMUS. Patient was hospitalized. Patient recovered.

Rocephin Side Effects Report #5355722-5
ROCEPHIN problem was reported by a Physician from JAPAN on June 01, 2007. Male patient, 59 years of age, weighting 160.9 lb, was diagnosed with infection, hepatic failure, cardiac failure acute, coagulopathy and was treated with ROCEPHIN. After drug was administered, patient experienced the following problems/side effects: cardiac failure, continuous haemodiafiltration, erythema multiforme, ischaemic hepatitis, renal failure, ventricular fibrillation, ventricular tachycardia, viral myocarditis, . ROCEPHIN dosage: unknown. During the same period patient was treated with LASIX, DOBUTREX, FRESH FROZEN PLASMA, NEO MINOPHAGEN C, KAYTWO, ZITHROMAC. Patient was hospitalized. Patient recovered.

Prograf Side Effects Report #5363087-8
Physician from JAPAN reported PROGRAF problem on June 05, 2007. Male patient, 54 years of age, weighting 156.5 lb, was diagnosed with bone marrow transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: cerebral infarction, continuous haemodiafiltration, diabetic hyperglycaemic coma, encephalitis herpes, haemoglobin decreased, histiocytosis haematophagic, no therapeutic response, platelet count decreased, . PROGRAF dosage: unknown. During the same period patient was treated with METHOTREXATE, CORTICOSTEROIDS, GANCICLOVIR, FOSCARNET, IMMUNE GLOBULIN INTRAVENOUS, MAXIPIME, MEROPEN, DIFLUCAN. Patient was hospitalized and became disabled. Patient died on 10/14/2006.

Acetaminophen Side Effects Report #5364342-8
ACETAMINOPHEN problem was reported by a Health Professional from UNITED KINGDOM on June 05, 2007. Male patient, 21 years of age, was treated with ACETAMINOPHEN. After drug was administered, patient experienced the following problems/side effects: acute hepatic failure, continuous haemodiafiltration, hepatic encephalopathy, overdose, renal failure acute, . ACETAMINOPHEN dosage: unknown. During the same period patient was treated with ALCOHOL. Patient was hospitalized. Patient died on 06/14/2007.

Busulfan Side Effects Report #5324444-9
Consumer or non-health professional from JAPAN reported BUSULFAN problem on Apr 24, 2007. Male patient, 23 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: acute graft versus host disease, continuous haemodiafiltration, convulsion, diarrhoea, encephalitis viral, engraftment syndrome, haemorrhage, human herpesvirus 6 infection, liver disorder, . BUSULFAN dosage: 9.4 ML; QID; IV. During the same period patient was treated with VALPROATE, FLUDARABINE PHOSPHATE, CYCLOPHOSPHAMIDE. Patient recovered.

Prograf Side Effects Report #5300359-7
PROGRAF problem was reported by a Physician from JAPAN on Mar 26, 2007. Male patient, 33 years of age, was diagnosed with liver transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: acidosis, continuous haemodiafiltration, graft thrombosis, hepatic artery thrombosis, renal failure, thrombotic microangiopathy, . PROGRAF dosage: unknown. Patient died.

Valtrex Side Effects Report #5266223-7
Physician from JAPAN reported VALTREX problem on Mar 08, 2007. Female patient, 76 years of age, weighting 114.6 lb, was diagnosed with herpes zoster, cardiac failure, gastric ulcer, hypertension, hyperkalaemia, angina pectoris and was treated with VALTREX. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, continuous haemodiafiltration, depressed level of consciousness, dyslalia, headache, hemiplegia, vomiting, . VALTREX dosage: 1000MG PER DAY. During the same period patient was treated with FUROSEMIDE, PARIET, PROMAC, ARTIST, ADALAT, ARGAMATE, ASPIRIN, GASMOTIN. Patient was hospitalized. Patient recovered.

Metformin Side Effects Report #5679749-9
METFORMIN HYDROCHLORIDE problem was reported by a Consumer or non-health professional from GERMANY on Mar 10, 2008. Male patient, 74 years of age, was treated with METFORMIN HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: cardiogenic shock, concomitant disease aggravated, continuous haemodiafiltration, diabetic nephropathy, dyspnoea, lactic acidosis, multi-organ failure, renal failure acute, . METFORMIN HYDROCHLORIDE dosage: unknown. Patient was hospitalized. Patient died.

Metformin Side Effects Report #5635761-7
Consumer or non-health professional from GERMANY reported METFORMIN problem on Feb 03, 2008. Female patient, 74 years of age, was treated with METFORMIN. After drug was administered, patient experienced the following problems/side effects: anuria, condition aggravated, continuous haemodiafiltration, diabetic nephropathy, lactic acidosis, renal failure acute, shock, . METFORMIN dosage: unknown. Patient was hospitalized. Patient died.

Byetta Side Effects Report #5581487-8
BYETTA problem was reported by a Pharmacist from UNITED STATES on Jan 03, 2008. Female patient, 55 years of age, weighting 218.3 lb, was diagnosed with type 2 diabetes mellitus and was treated with BYETTA. After drug was administered, patient experienced the following problems/side effects: bradycardia, cardiac arrest, continuous haemodiafiltration, dyspnoea, fat necrosis, fatigue, hypotension, metabolic acidosis, multi-organ failure, . BYETTA dosage: unknown. During the same period patient was treated with METFORMIN, GLIPIZIDE, LISINOPRIL. Patient was hospitalized. Patient died on 10/31/2007.

Glyburide Side Effects Report #5590857-3
Consumer or non-health professional from SPAIN reported GLYBURIDE problem on Dec 26, 2007. Female patient, 61 years of age, was diagnosed with diabetes mellitus and was treated with GLYBURIDE. After drug was administered, patient experienced the following problems/side effects: acute prerenal failure, blood glucose increased, continuous haemodiafiltration, dehydration, food intolerance, haemodialysis, hypotension, kussmaul respiration, lactic acidosis, . GLYBURIDE dosage: 5 MG TWICE DAILY. During the same period patient was treated with METFORMIN, LOVASTATIN, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.

Busulfan Side Effects Report #5608393-4
BUSULFAN problem was reported by a Consumer or non-health professional from JAPAN on Jan 11, 2008. Male patient, child 7 years of age, was diagnosed with stem cell transplant and was treated with BUSULFAN. After drug was administered, patient experienced the following problems/side effects: anorexia, coagulopathy, continuous haemodiafiltration, febrile neutropenia, gastritis, haemosiderosis, hepatic function abnormal, hyperbilirubinaemia, hypoproteinaemia, . BUSULFAN dosage: 6 ML; IV. Patient was hospitalized. Patient died on 11/29/2007.

Prograf Side Effects Report #5535082-7
Physician from JAPAN reported PROGRAF problem on Nov 15, 2007. Male patient, 67 years of age, was diagnosed with renal transplant and was treated with PROGRAF. After drug was administered, patient experienced the following problems/side effects: back pain, biliary tract disorder, continuous haemodiafiltration, hepatic fibrosis, hepatitis b, hepatitis cholestatic, hyperplasia, pancreatitis acute, . PROGRAF dosage: unknown. During the same period patient was treated with STEROIDMULATION. Patient died.

Clofarabine Side Effects Report #5527535-2
CLOFARABINE problem was reported by a Health Professional from UNITED STATES on Nov 08, 2007. Female patient, 15 years of age, weighting 207.9 lb, was diagnosed with acute lymphocytic leukaemia and was treated with CLOFARABINE. After drug was administered, patient experienced the following problems/side effects: acidosis, capillary leak syndrome, continuous haemodiafiltration, febrile neutropenia, haematocrit decreased, haemoglobin decreased, hepatosplenomegaly, hypotension, hypoxia, . CLOFARABINE dosage: 80 MG QD IV. During the same period patient was treated with ETOPOSIDE, CYCLOPHOSPHAMIDE, ACETAMINOPHEN, ACYCLOVIR, ALLOPURINOL, AMIKACIN, CALCITRIOL, CHLOROTHIAZIDE. Patient was hospitalized. Patient recovered.

Zonisamide Side Effects Report #5531699-4
Physician from JAPAN reported ZONISAMIDE problem on Nov 14, 2007. Male patient, 30 years of age, was diagnosed with epilepsy and was treated with ZONISAMIDE. After drug was administered, patient experienced the following problems/side effects: acute respiratory distress syndrome, brain stem syndrome, continuous haemodiafiltration, disseminated intravascular coagulation, faecal incontinence, feeding disorder, heat stroke, malaise, multi-organ failure, . ZONISAMIDE dosage: 400 MG, ORAL. Patient was hospitalized and became disabled. Patient recovered.

Verapamil Side Effects Report #5491436-9
VERAPAMIL HYDROCHLORIDE problem was reported by a Health Professional from FRANCE on Oct 05, 2007. Male patient, 51 years of age, was diagnosed with hypertensive cardiomyopathy and was treated with VERAPAMIL HYDROCHLORIDE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, atrioventricular block complete, continuous haemodiafiltration, metabolic acidosis, multi-organ failure, renal failure, shock, . VERAPAMIL HYDROCHLORIDE dosage: 7200 MG;X1. Patient died.

Lansoprazole Side Effects Report #5450974-5
Consumer or non-health professional from JAPAN reported LANSOPRAZOLE problem on Sept 04, 2007. Male patient, 71 years of age, was diagnosed with gastric ulcer, reflux oesophagitis and was treated with LANSOPRAZOLE. After drug was administered, patient experienced the following problems/side effects: altered state of consciousness, condition aggravated, continuous haemodiafiltration, electroencephalogram abnormal, hepatic encephalopathy, hepatic failure, hyperammonaemia, hypoglycaemia, renal failure, . LANSOPRAZOLE dosage: 15 MG (15 MG, 1 IN 1 D) PER ORAL. During the same period patient was treated with ITOROL, CARVEDILOL, MUCOSTA, FOIPAN, SIGMART, ALLOPURINOL, LASIX. Patient was hospitalized. Patient recovered.

Fluconazole Side Effects Report #5420599-6
FLUCONAZOLE problem was reported by a Consumer or non-health professional from FINLAND on July 20, 2007. Male patient, 76 years of age, was diagnosed with graft infection, hyperlipidaemia and was treated with FLUCONAZOLE. After drug was administered, patient experienced the following problems/side effects: anuria, cardiomegaly, continuous haemodiafiltration, dyspnoea, haemoglobin decreased, hypotension, international normalised ratio increased, multi-organ failure, . FLUCONAZOLE dosage: 150 MG (150 MG, 1 IN 1 D). During the same period patient was treated with ATORVASTATIN CALCIUM, ESOMEPRAZOLE, FUSIDIC ACID, DOXYCYCLINE, PREDNISOLONE, WARFARIN, DIGOXIN, BISOPROLOL FUMARATE. Patient was hospitalized. Patient died.

Velcade Side Effects Report #5391777-X
Physician from GERMANY reported VELCADE problem on July 06, 2007. Male patient, 53 years of age, weighting 220.5 lb, was diagnosed with plasmacytoma and was treated with VELCADE. After drug was administered, patient experienced the following problems/side effects: blood pressure decreased, cardiac failure, continuous haemodiafiltration, disseminated intravascular coagulation, heart rate increased, hepatic failure, multi-organ failure, pulmonary embolism, renal failure acute, . VELCADE dosage: 2.60 MG, INTRAVENOUS. During the same period patient was treated with CYCLOPHOSPHAMIDE, DEXAMETHASONE, DIPYRONE, BUPRENORPHINE HYDROCHLORIDE, PANTOPRAZOLE. Patient was hospitalized. Patient recovered.