PREDONINE Side Effects

5699663-2 | Abscess, Abscess Jaw, C-reactive Protein Increased, Computerised Tomogram Abnormal, Condition Aggravated, Impaired Healing, Malnutrition, Multiple Myeloma, Osteitis
on Mar 27, 2008 Female patient from JAPAN , 64 years of age, weighting 85.98 lb, was diagnosed with bone lesion and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: abscess (What is abscess?), abscess jaw, c-reactive protein increased, computerised tomogram abnormal, condition aggravated, impaired healing, malnutrition, multiple myeloma (What is multiple myeloma?), osteitis. Predonine dosage: 5 Mg/day. During the same period patient was treated with ZOMETA (4 Mg) (View Zometa Review and Zometa Label ). Patient was hospitalized.

5677601-6 | Anaemia, Cytomegalovirus Enterocolitis, Gastrointestinal Ulcer Haemorrhage, Haematochezia, Melaena, Shock Haemorrhagic
Patient was taking Predonine (View Usage). Patient had the following side effects: anaemia, cytomegalovirus enterocolitis, gastrointestinal ulcer haemorrhage, haematochezia, melaena, shock haemorrhagic on Mar 14, 2008 from JAPAN Additional patient health information: Male patient , 56 years of age, was diagnosed with nephritis and. Predonine dosage: 60 Mg/day. During the same period patient was treated with NEORAL (150 Mg/day) (View Neoral Review and Neoral Label ), PARIET (10 Mg/day) (View Pariet Review and Pariet Label ), BAKTAR (1 G/day) (View Baktar Review and Baktar Label ).

5657539-0 | Abscess, Abscess Jaw, C-reactive Protein Increased, Computerised Tomogram Abnormal, Impaired Healing, Malnutrition, Multiple Myeloma, Osteitis, Osteomyelitis
Adverse event was reported on Feb 27, 2008 by a Female patient taking Predonine (View Usage) (Dosage: 5 Mg/day) was diagnosed with bone lesion and. Location: JAPAN , 64 years of age, weighting 85.98 lb, After Predonine was administered, patient had the following side effects: abscess (What is abscess?), abscess jaw, c-reactive protein increased, computerised tomogram abnormal, impaired healing, malnutrition, multiple myeloma (What is multiple myeloma?), osteitis, osteomyelitis. During the same period patient was treated with ZOMETA (4 Mg) (View Zometa Review and Zometa Label ). Patient was hospitalized.

5633563-9 | Blood Creatinine Increased, Cells In Urine, Chronic Allograft Nephropathy, Kidney Transplant Rejection, Polyomavirus-associated Nephropathy, Renal Impairment
on Feb 15, 2008 Male patient from , 38 years of age, was diagnosed with renal transplant and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, cells in urine, chronic allograft nephropathy, kidney transplant rejection, polyomavirus-associated nephropathy, renal impairment. Predonine dosage: . During the same period patient was treated with SIMULECT (20 Mg, Unk) (View Simulect Review and Simulect Label ), DEOXYSPERGUALIN (DSG) (View Deoxyspergualin (dsg) Review and Deoxyspergualin (dsg) Label ), PROGRAF (Unk, Unk) (View Prograf Review and Prograf Label ), CELLCEPT (Unk, Unk) (View Cellcept Review and Cellcept Label ), METHYLPREDNISOLONE (Unk, Unk) (View Methylprednisolone Review and Methylprednisolone Label ).


5611950-2 | Cerebral Infarction
on Jan 28, 2008 Male patient from JAPAN , 78 years of age, was diagnosed with skin disorder, parkinson's disease (What is parkinson's disease?) and was treated with Predonine (View Usage). Patient had the following side effects: cerebral infarction. Predonine dosage: . During the same period patient was treated with COMTAN (100 Mg, Bid) (View Comtan Review and Comtan Label ). Patient was hospitalized.

5525832-8 | Lung Disorder, Neutropenia, Pneumonia Aspiration, Sepsis
Patient was taking Predonine (View Usage). After Predonine was administered, patient had the following side effects: lung disorder, neutropenia, pneumonia aspiration, sepsis (What is sepsis?) on Nov 22, 2007 from JAPAN Additional patient health information: Male patient , 20 years of age, was diagnosed with acute lymphocytic leukaemia and. Predonine dosage: . During the same period patient was treated with DAUNOMYCIN (View Daunomycin Review and Daunomycin Label ), ONCOVIN (View Oncovin Review and Oncovin Label ), CYCLOPHOSPHAMIDE (View Cyclophosphamide Review and Cyclophosphamide Label ), GLEEVEC (600 Mg, Qd) (View Gleevec Review and Gleevec Label ).

5491506-5 | Failure To Thrive, Headache, Hypogammaglobulinaemia, Rash, Vomiting
Adverse event was reported on Oct 11, 2007 by a Female patient taking Predonine (View Usage) (Dosage: 7.5 Mg/d) was diagnosed with rash (What is rash?), chronic myeloid leukaemia and. Location: JAPAN , child 6 years of age, weighting 37.48 lb, Patient experienced the following unwanted or unexpected effects: failure to thrive, headache (What is headache?), hypogammaglobulinaemia, rash (What is rash?), vomiting. During the same period patient was treated with FAMOTIDINE (10 Mg/d) (View Famotidine Review and Famotidine Label ), GLEEVEC (300 Mg/d) (View Gleevec Review and Gleevec Label ).

5487706-0 | Anaemia, Cytomegalovirus Enterocolitis, Gastrointestinal Ulcer Haemorrhage, Haematochezia, Shock Haemorrhagic
on Oct 09, 2007 Male patient from JAPAN , 55 years of age, was diagnosed with nephritis and was treated with Predonine (View Usage). Patient had the following side effects: anaemia, cytomegalovirus enterocolitis, gastrointestinal ulcer haemorrhage, haematochezia, shock haemorrhagic. Predonine dosage: 40 Mg/day. During the same period patient was treated with CICLOSPORIN (150 Mg/day) (View Ciclosporin Review and Ciclosporin Label ).

5482298-4 | Lung Disorder, Neutropenia, Pneumonia Aspiration, Sepsis
on Oct 05, 2007 Male patient from JAPAN , 20 years of age, was diagnosed with acute lymphocytic leukaemia and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: lung disorder, neutropenia, pneumonia aspiration, sepsis (What is sepsis?). Predonine dosage: . During the same period patient was treated with DAUNOMYCIN (View Daunomycin Review and Daunomycin Label ), ONCOVIN (View Oncovin Review and Oncovin Label ), ENDOXAN (View Endoxan Review and Endoxan Label ), GLEEVEC (600 Mg, Qd) (View Gleevec Review and Gleevec Label ).

5481172-7 | Failure To Thrive, Headache, Hypogammaglobulinaemia, Rash, Vomiting
Patient was taking Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: failure to thrive, headache (What is headache?), hypogammaglobulinaemia, rash (What is rash?), vomiting on Oct 03, 2007 from JAPAN Additional patient health information: Female patient , child 6 years of age, weighting 37.48 lb, was diagnosed with rash (What is rash?), chronic myeloid leukaemia and. Predonine dosage: 7.5 Mg/d. During the same period patient was treated with FAMOTIDINE (10 Mg/d) (View Famotidine Review and Famotidine Label ), GLEEVEC (300 Mg/d) (View Gleevec Review and Gleevec Label ).

5479309-9 | Ascites, Blood Alkaline Phosphatase Increased, Blood Glucose Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, C-reactive Protein Increased, Cardiac Failure
Adverse event was reported on Oct 01, 2007 by a Female patient taking Predonine (View Usage) (Dosage: 20 Mg, Unk) . Location: JAPAN , 68 years of age, Patient had the following side effects: ascites, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, c-reactive protein increased, cardiac failure. During the same period patient was treated with DEPAKENE (800 Mg, Unk) (View Depakene Review and Depakene Label ), PREDNISOLONE (40 Mg, Unk) (View Prednisolone Review and Prednisolone Label ), TAGAMET (800 Mg, Unk) (View Tagamet Review and Tagamet Label ), ALLELOCK (10 Mg, Unk) (View Allelock Review and Allelock Label ), BIOFERMIN (3 G, Unk) (View Biofermin Review and Biofermin Label ), GASMOTIN (15 Mg, Unk) (View Gasmotin Review and Gasmotin Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ). Patient was hospitalized.

5479148-9 | Cytomegalovirus Enterocolitis
on Oct 03, 2007 Male patient from JAPAN , 55 years of age, was diagnosed with nephritis and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: cytomegalovirus enterocolitis. Predonine dosage: 40 Mg/day. During the same period patient was treated with CYCLOSPORINE (150 Mg/day) (View Cyclosporine Review and Cyclosporine Label ).

5474450-9 | Ascites, Blood Alkaline Phosphatase Increased, Blood Glucose Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, C-reactive Protein Increased, Cardiac Failure
on Sep 27, 2007 Female patient from JAPAN , 69 years of age, was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: ascites, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, c-reactive protein increased, cardiac failure. Predonine dosage: 20 Mg, Unk. During the same period patient was treated with DEPAKENE (800 Mg, Unk) (View Depakene Review and Depakene Label ), PREDNISOLONE (40 Mg, Unk) (View Prednisolone Review and Prednisolone Label ), TAGAMET (800 Mg, Unk) (View Tagamet Review and Tagamet Label ), ALLELOCK (10 Mg, Unk) (View Allelock Review and Allelock Label ), BIOFERMIN (3 G, Unk) (View Biofermin Review and Biofermin Label ), GASMOTIN (15 Mg, Unk) (View Gasmotin Review and Gasmotin Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ). Patient was hospitalized.

5465857-4 | Ascites, Blood Alkaline Phosphatase Increased, Blood Glucose Increased, Blood Lactate Dehydrogenase Increased, Blood Urea Increased, C-reactive Protein Increased, Cardiac Failure
Patient was taking Predonine (View Usage). Patient had the following side effects: ascites, blood alkaline phosphatase increased, blood glucose increased, blood lactate dehydrogenase increased, blood urea increased, c-reactive protein increased, cardiac failure on Sep 19, 2007 from JAPAN Additional patient health information: Female patient , 69 years of age, . Predonine dosage: 20 Mg, Unk. During the same period patient was treated with DEPAKENE (800 Mg, Unk) (View Depakene Review and Depakene Label ), PREDNISOLONE (40 Mg, Unk) (View Prednisolone Review and Prednisolone Label ), TAGAMET (800 Mg, Unk) (View Tagamet Review and Tagamet Label ), ALLELOCK (10 Mg, Unk) (View Allelock Review and Allelock Label ), BIOFERMIN (3 G, Unk) (View Biofermin Review and Biofermin Label ), GASMOTIN (15 Mg, Unk) (View Gasmotin Review and Gasmotin Label ), VALPROATE SODIUM (View Valproate Sodium Review and Valproate Sodium Label ).

5325917-5 | Haemorrhage, Local Swelling, Osteonecrosis, Pain In Jaw, Primary Sequestrum, Purulent Discharge, Tooth Extraction
Adverse event was reported on May 10, 2007 by a Male patient taking Predonine (View Usage) (Dosage: ) was diagnosed with hypercalcaemia and. Location: JAPAN , 68 years of age, weighting 154.3 lb, After Predonine was administered, patient had the following side effects: haemorrhage, local swelling, osteonecrosis (What is osteonecrosis?), pain in jaw, primary sequestrum, purulent discharge, tooth extraction. During the same period patient was treated with SUCRALFATE (View Sucralfate Review and Sucralfate Label ), ZOMETA (4 Mg, Unk) (View Zometa Review and Zometa Label ), BISPHONAL (10 Mg, Unk) (View Bisphonal Review and Bisphonal Label ).

5304229-X | Pancytopenia, Platelet Count Decreased, White Blood Cell Count Decreased
on Apr 12, 2007 Female patient from JAPAN , 21 years of age, was diagnosed with histiocytosis haematophagic and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: pancytopenia, platelet count decreased, white blood cell count decreased. Predonine dosage: Unk, Unk. During the same period patient was treated with ANTIBIOTICS (View Antibiotics Review and Antibiotics Label ), NEORAL (Unk, Unk) (View Neoral Review and Neoral Label ), CARBENIN (View Carbenin Review and Carbenin Label ), MINOCYCLINE HCL (View Minocycline Hcl Review and Minocycline Hcl Label ), FIRSTCIN (View Firstcin Review and Firstcin Label ).

5208672-9 | Osteonecrosis, Pain
on Jan 05, 2007 Male patient from JAPAN , 68 years of age, was diagnosed with multiple myeloma (What is multiple myeloma?) and was treated with Predonine (View Usage). Patient had the following side effects: osteonecrosis (What is osteonecrosis?), pain (What is pain?). Predonine dosage: . During the same period patient was treated with SUCRALFATE (View Sucralfate Review and Sucralfate Label ), ZOMETA (View Zometa Review and Zometa Label ).

5142153-6 | Aphasia, Blood Creatinine Increased, Cerebral Infarction, Convulsion, Dysarthria, Grip Strength Decreased, Hemiparesis, Jc Virus Infection, Leukoaraiosis
Patient was taking Predonine (View Usage). After Predonine was administered, patient had the following side effects: aphasia (What is aphasia?), blood creatinine increased, cerebral infarction, convulsion, dysarthria, grip strength decreased, hemiparesis, jc virus infection, leukoaraiosis on Oct 26, 2005 from JAPAN Additional patient health information: Male patient , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

5124777-5 | Blood Pressure Increased, Depression, Herpes Simplex, Herpes Zoster, Necrotising Retinitis, Reactive Psychosis
Adverse event was reported on Apr 14, 2004 by a Female patient taking Predonine (View Usage) (Dosage: Unk, Unk) was diagnosed with interstitial lung disease and. Location: JAPAN , 59 years of age, Patient experienced the following unwanted or unexpected effects: blood pressure increased, depression (What is depression?), herpes simplex (What is herpes simplex?), herpes zoster, necrotising retinitis, reactive psychosis. During the same period patient was treated with NEORAL (50 Mg/d) (View Neoral Review and Neoral Label ).

5118511-2 | Blood Pressure Increased, Cd4/cd8 Ratio Increased, Depression, Diabetes Mellitus, Herpes Simplex, Herpes Zoster
on Apr 14, 2004 Female patient from JAPAN , 59 years of age, was diagnosed with interstitial lung disease and was treated with Predonine (View Usage). Patient had the following side effects: blood pressure increased, cd4/cd8 ratio increased, depression (What is depression?), diabetes mellitus, herpes simplex (What is herpes simplex?), herpes zoster. Predonine dosage: Unk, Unk. During the same period patient was treated with NEORAL (50 Mg/d) (View Neoral Review and Neoral Label ).

5089833-9 | Aphasia, Blood Creatinine Increased, Cerebral Infarction, Convulsion, Dysarthria, Grip Strength Decreased, Hemiparesis, Jc Virus Infection, Leukoaraiosis
on Oct 26, 2005 Male patient from JAPAN , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: aphasia (What is aphasia?), blood creatinine increased, cerebral infarction, convulsion, dysarthria, grip strength decreased, hemiparesis, jc virus infection, leukoaraiosis. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

5084604-1 | Aphasia, Blood Creatinine Increased, Cerebral Infarction, Convulsion, Dysarthria, Grip Strength Decreased, Hemiparesis, Jc Virus Infection, Leukoaraiosis
Patient was taking Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), blood creatinine increased, cerebral infarction, convulsion, dysarthria, grip strength decreased, hemiparesis, jc virus infection, leukoaraiosis on Oct 26, 2005 from JAPAN Additional patient health information: Male patient , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

5066352-7 | Aphasia, Blood Creatinine Increased, Cerebral Infarction, Convulsion, Depressed Level Of Consciousness, Dysarthria, Grip Strength Decreased, Hemiparesis, Immunosuppression
Adverse event was reported on Oct 26, 2005 by a Male patient taking Predonine (View Usage) (Dosage: 10 Mg/d) was diagnosed with nephrotic syndrome, hypertension and. Location: JAPAN , 50 years of age, weighting 141.1 lb, Patient had the following side effects: aphasia (What is aphasia?), blood creatinine increased, cerebral infarction, convulsion, depressed level of consciousness, dysarthria, grip strength decreased, hemiparesis, immunosuppression. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

5060793-X | Blood Creatinine Increased, Cerebral Infarction, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Progressive Multifocal Leukoencephalopathy
on Oct 26, 2005 Male patient from JAPAN , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: blood creatinine increased, cerebral infarction, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, progressive multifocal leukoencephalopathy. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

5060606-6 | Aplastic Anaemia, Blood Urea Increased, Haematocrit Decreased, Haemoglobin Decreased, Neutrophil Count Decreased, Pancytopenia, Platelet Count Decreased, Pneumonia, Protein Urine Present
on May 08, 2006 Male patient from JAPAN , 76 years of age, weighting 132.3 lb, was diagnosed with glomerulonephritis, pain in extremity, gastritis and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: aplastic anaemia, blood urea increased, haematocrit decreased, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet count decreased, pneumonia (What is pneumonia?), protein urine present. Predonine dosage: 10 Mg/day. During the same period patient was treated with SOLU MEDROL (500 Mg/day) (View Solu-medrol Review and Solu-medrol Label ), SOLU MEDROL (60 Mg/day) (View Solu-medrol Review and Solu-medrol Label ), TEGRETOL (400 Mg/day) (View Tegretol Review and Tegretol Label ), GASTER (20 Mg/day) (View Gaster Review and Gaster Label ), ADRENAL HORMONE PREPARATIONS (View Adrenal Hormone Preparations Review and Adrenal Hormone Preparations Label ).

5052521-9 | Abdominal Pain, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Increased, Blood Pressure Decreased, C-reactive Protein Increased, Diarrhoea
Patient was taking Predonine (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), alanine aminotransferase increased, aspartate aminotransferase increased, blood creatine phosphokinase increased, blood creatinine increased, blood lactate dehydrogenase increased, blood pressure decreased, c-reactive protein increased, diarrhoea on Feb 20, 2006 from JAPAN Additional patient health information: Male patient , 68 years of age, weighting 143.3 lb, was diagnosed with eosinophilia, hypertension and. Predonine dosage: 5 Mg/d. During the same period patient was treated with NEORAL (300 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (50 Mg/d) (View Nu Lotan Review and Nu Lotan Label ), BONALON (5 Mg/d) (View Bonalon Review and Bonalon Label ), TAKEPRON (15 Mg/d) (View Takepron Review and Takepron Label ), ALESION (40 Mg/d) (View Alesion Review and Alesion Label ). Patient was hospitalized.

5034400-6 | Retinal Detachment, Surgery
Adverse event was reported on Mar 29, 2006 by a Male patient taking Predonine (View Usage) (Dosage: 5 Mg/d) was diagnosed with aplastic anaemia and. Location: JAPAN , 62 years of age, After Predonine was administered, patient had the following side effects: retinal detachment, surgery (What is surgery?). During the same period patient was treated with MUCOSTA (300 Mg/d) (View Mucosta Review and Mucosta Label ), NEORAL (200 Mg/d) (View Neoral Review and Neoral Label ).

5034245-7 | Aplastic Anaemia, Haematocrit Decreased, Pancytopenia, Platelet Count Decreased, Pneumonia, Respiratory Failure, White Blood Cell Count Decreased
on May 08, 2006 Male patient from JAPAN , 76 years of age, weighting 132.3 lb, was diagnosed with glomerulonephritis, pain in extremity, gastritis and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: aplastic anaemia, haematocrit decreased, pancytopenia, platelet count decreased, pneumonia (What is pneumonia?), respiratory failure, white blood cell count decreased. Predonine dosage: 10 Mg/day. During the same period patient was treated with SOLU MEDROL (500 Mg/day) (View Solu-medrol Review and Solu-medrol Label ), SOLU MEDROL (60 Mg/day) (View Solu-medrol Review and Solu-medrol Label ), TEGRETOL (400 Mg/day) (View Tegretol Review and Tegretol Label ), GASTER (20 Mg/day) (View Gaster Review and Gaster Label ), ADRENAL HORMONE PREPARATIONS (View Adrenal Hormone Preparations Review and Adrenal Hormone Preparations Label ).

4967328-8 | Retinal Detachment, Surgery
on Mar 29, 2006 Male patient from JAPAN , 62 years of age, was diagnosed with aplastic anaemia and was treated with Predonine (View Usage). Patient had the following side effects: retinal detachment, surgery (What is surgery?). Predonine dosage: 5 Mg/d. During the same period patient was treated with MUCOSTA (300 Mg/d) (View Mucosta Review and Mucosta Label ), NEORAL (200 Mg/d) (View Neoral Review and Neoral Label ).

4961722-7 | Blood Creatinine Increased, Cerebral Infarction, Condition Aggravated, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Nephrotic Syndrome, Progressive Multifocal Leukoencephalopathy
Patient was taking Predonine (View Usage). After Predonine was administered, patient had the following side effects: blood creatinine increased, cerebral infarction, condition aggravated, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, nephrotic syndrome, progressive multifocal leukoencephalopathy on Oct 26, 2005 from JAPAN Additional patient health information: Male patient , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

4911975-6 | Blood Creatinine Increased, Cerebral Infarction, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Progressive Multifocal Leukoencephalopathy
Adverse event was reported on Oct 26, 2005 by a Male patient taking Predonine (View Usage) (Dosage: 10 Mg/d) was diagnosed with nephrotic syndrome, hypertension and. Location: JAPAN , 50 years of age, weighting 141.1 lb, Patient experienced the following unwanted or unexpected effects: blood creatinine increased, cerebral infarction, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, progressive multifocal leukoencephalopathy. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

4896386-4 | Hypoxia, Pneumocystis Jiroveci Pneumonia, Pyrexia, Respiratory Failure
on Dec 27, 2005 Female patient from JAPAN , 75 years of age, was diagnosed with nephrotic syndrome and was treated with Predonine (View Usage). Patient had the following side effects: hypoxia, pneumocystis jiroveci pneumonia, pyrexia, respiratory failure. Predonine dosage: 40 Mg/day. During the same period patient was treated with NEORAL (150 Mg/day) (View Neoral Review and Neoral Label ).

4888241-0 | Blood Glucagon Decreased, Blood Pressure Increased, Depression, Herpes Simplex, Herpes Zoster, Herpes Zoster Infection Neurological, Lung Infection, Necrotising Retinitis
on Apr 14, 2004 Female patient from JAPAN , 59 years of age, was diagnosed with interstitial lung disease and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: blood glucagon decreased, blood pressure increased, depression (What is depression?), herpes simplex (What is herpes simplex?), herpes zoster, herpes zoster infection neurological, lung infection, necrotising retinitis. Predonine dosage: Unk, Unk. During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ).

4865753-7 | Blood Creatinine Increased, Cerebral Infarction, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Progressive Multifocal Leukoencephalopathy
Patient was taking Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, cerebral infarction, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, progressive multifocal leukoencephalopathy on Oct 26, 2005 from JAPAN Additional patient health information: Male patient , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

4865747-1 | Blood Albumin Increased, Blood Creatinine Increased, Blood Urea Increased, Nephrotic Syndrome, Oedema Peripheral, Post Streptococcal Glomerulonephritis, Protein Urine Present, Renal Impairment, Streptococcal Serology Positive
Adverse event was reported on Sep 28, 2005 by a Male patient taking Predonine (View Usage) (Dosage: 5 Mg/day) was diagnosed with nasopharyngitis, arthralgia and. Location: JAPAN , 27 years of age, Patient had the following side effects: blood albumin increased, blood creatinine increased, blood urea increased, nephrotic syndrome, oedema peripheral, post streptococcal glomerulonephritis, protein urine present, renal impairment, streptococcal serology positive. During the same period patient was treated with VOLTAREN (Unk, Unk) (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

4846824-8 | Blood Creatinine Increased, Cerebral Infarction, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Progressive Multifocal Leukoencephalopathy
on Oct 26, 2005 Male patient from JAPAN , 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: blood creatinine increased, cerebral infarction, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, progressive multifocal leukoencephalopathy. Predonine dosage: 10 Mg/d. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ). Patient was hospitalized and became disabled.

4845518-2 | Deep Vein Thrombosis, Dyspnoea Exertional, Hypoxia, Pulmonary Embolism
on Nov 07, 2005 Female patient from JAPAN , 57 years of age, was diagnosed with dermatomyositis and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: deep vein thrombosis (What is deep vein thrombosis?), dyspnoea exertional, hypoxia, pulmonary embolism (What is pulmonary embolism?). Predonine dosage: 15 Mg/d. During the same period patient was treated with NEORAL (Unk, Unk) (View Neoral Review and Neoral Label ). Patient was hospitalized.

4828573-5 | Deep Vein Thrombosis, Pulmonary Embolism
Patient was taking Predonine (View Usage). Patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?), pulmonary embolism (What is pulmonary embolism?) on Nov 07, 2005 from JAPAN Additional patient health information: Female patient , 55 years of age, was diagnosed with dermatomyositis and. Predonine dosage: . During the same period patient was treated with NEORAL (View Neoral Review and Neoral Label ).

4828038-0 | Cerebral Infarction, Dysarthria, Grip Strength Decreased, Jc Virus Infection, Leukoaraiosis, Progressive Multifocal Leukoencephalopathy, Renal Disorder
Adverse event was reported on Oct 26, 2005 by a Male patient taking Predonine (View Usage) (Dosage: 10 Mg/d) was diagnosed with nephrotic syndrome, hypertension and. Location: JAPAN , 50 years of age, weighting 141.1 lb, After Predonine was administered, patient had the following side effects: cerebral infarction, dysarthria, grip strength decreased, jc virus infection, leukoaraiosis, progressive multifocal leukoencephalopathy, renal disorder. During the same period patient was treated with BREDININ (75 Mg/d) (View Bredinin Review and Bredinin Label ), NEORAL (100 Mg/d) (View Neoral Review and Neoral Label ), NU LOTAN (25 Mg/d) (View Nu Lotan Review and Nu Lotan Label ), TENORMIN (25 Mg/d) (View Tenormin Review and Tenormin Label ). Patient was hospitalized and became disabled.

4827529-6 | Cerebral Haemorrhage, Completed Suicide, Decreased Appetite, Dizziness, Fall, Fatigue, Head Injury, Interstitial Lung Disease, Nausea
on Jul 09, 2003 Male patient from JAPAN , 81 years of age, was diagnosed with blast crisis in myelogenous leukaemia and was treated with Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage, completed suicide, decreased appetite, dizziness (What is dizziness?), fall (What is fall?), fatigue, head injury, interstitial lung disease, nausea (What is nausea?). Predonine dosage: 10 Mg/day. During the same period patient was treated with PRIMPERAN INJ (View Primperan Inj Review and Primperan Inj Label ), FENTANYL (2.5 Mg/d) (View Fentanyl Review and Fentanyl Label ), OMEPRAL (View Omepral Review and Omepral Label ), MOBIC (10 Mg/d) (View Mobic Review and Mobic Label ), GLEEVEC (100-400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

4816526-2 | Cerebral Haemorrhage, Completed Suicide, Decreased Appetite, Dizziness, Fall, Fatigue, Haemoglobin Decreased, Head Injury, Interstitial Lung Disease
on Jul 09, 2003 Male patient from JAPAN , 81 years of age, was diagnosed with blast crisis in myelogenous leukaemia and was treated with Predonine (View Usage). Patient had the following side effects: cerebral haemorrhage, completed suicide, decreased appetite, dizziness (What is dizziness?), fall (What is fall?), fatigue, haemoglobin decreased, head injury, interstitial lung disease. Predonine dosage: 10 Mg/day. During the same period patient was treated with PRIMPERAN INJ (View Primperan Inj Review and Primperan Inj Label ), FENTANYL (2.5 Mg/d) (View Fentanyl Review and Fentanyl Label ), OMEPRAL (View Omepral Review and Omepral Label ), MOBIC (10 Mg/d) (View Mobic Review and Mobic Label ), GLEEVEC (100-400 Mg/day) (View Gleevec Review and Gleevec Label ). Patient was hospitalized.

4792407-8 | Blood Albumin Increased, Blood Creatinine Increased, Blood Urea Increased, Nephrotic Syndrome, Oedema Peripheral, Post Streptococcal Glomerulonephritis, Protein Urine Present, Renal Impairment, Streptococcal Serology Positive
Patient was taking Predonine (View Usage). After Predonine was administered, patient had the following side effects: blood albumin increased, blood creatinine increased, blood urea increased, nephrotic syndrome, oedema peripheral, post streptococcal glomerulonephritis, protein urine present, renal impairment, streptococcal serology positive on Sep 28, 2005 from JAPAN Additional patient health information: Male patient , 27 years of age, was diagnosed with nasopharyngitis, arthralgia and. Predonine dosage: 5 Mg/day. During the same period patient was treated with VOLTAREN (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

4736233-4 | Anuria, Bronchopulmonary Aspergillosis, Disseminated Tuberculosis, Dyspnoea, Gastrointestinal Haemorrhage, Hepatic Function Abnormal, Histiocytosis Haematophagic, Metabolic Acidosis, Pancytopenia
Adverse event was reported on May 18, 2005 by a Female patient taking Predonine (View Usage) (Dosage: 25 Mg/d) was diagnosed with lupus nephritis and. Location: JAPAN , 63 years of age, weighting 94.80 lb, Patient experienced the following unwanted or unexpected effects: anuria, bronchopulmonary aspergillosis, disseminated tuberculosis, dyspnoea, gastrointestinal haemorrhage, hepatic function abnormal, histiocytosis haematophagic, metabolic acidosis, pancytopenia. During the same period patient was treated with NEORAL (140 Mg/d) (View Neoral Review and Neoral Label ), LASIX (20 Mg/d) (View Lasix Review and Lasix Label ), ALFAROL (1 Ug/d) (View Alfarol Review and Alfarol Label ), THYRADIN S (50 Mg/d) (View Thyradin S Review and Thyradin S Label ), BAKTAR (480 Mg/d) (View Baktar Review and Baktar Label ), CYANOCOBALAMIN (1500 Ug/d) (View Cyanocobalamin Review and Cyanocobalamin Label ), MEVALOTIN (20 Mg/d) (View Mevalotin Review and Mevalotin Label ), NITOROL (60 Mg/d) (View Nitorol Review and Nitorol Label ).

4717072-7 | Anuria, Bronchopulmonary Aspergillosis, Disseminated Tuberculosis, Dyspnoea, Gastrointestinal Haemorrhage, Hepatic Function Abnormal, Histiocytosis Haematophagic, Metabolic Acidosis, Pancytopenia
on May 18, 2005 Female patient from JAPAN , 63 years of age, weighting 94.80 lb, was diagnosed with lupus nephritis and was treated with Predonine (View Usage). Patient had the following side effects: anuria, bronchopulmonary aspergillosis, disseminated tuberculosis, dyspnoea, gastrointestinal haemorrhage, hepatic function abnormal, histiocytosis haematophagic, metabolic acidosis, pancytopenia. Predonine dosage: 25 Mg/d. During the same period patient was treated with NEORAL (140 Mg/d) (View Neoral Review and Neoral Label ), LASIX (20 Mg/d) (View Lasix Review and Lasix Label ), ALFAROL (1 Ug/d) (View Alfarol Review and Alfarol Label ), THYRADIN S (50 Mg/d) (View Thyradin S Review and Thyradin S Label ), BAKTAR (480 Mg/d) (View Baktar Review and Baktar Label ), CYANOCOBALAMIN (1500 Ug/d) (View Cyanocobalamin Review and Cyanocobalamin Label ), MEVALOTIN (20 Mg/d) (View Mevalotin Review and Mevalotin Label ), NITOROL (60 Mg/d) (View Nitorol Review and Nitorol Label ).

4688752-7 | Cytomegalovirus Antigen Positive, Cytomegalovirus Infection, Lung Transplant Rejection, Osteoporotic Fracture, White Blood Cell Count Decreased
on Feb 15, 2005 Female patient from , 45 years of age, weighting 97.00 lb, was diagnosed with lung transplant (What is lung transplant?) and was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: cytomegalovirus antigen positive, cytomegalovirus infection (What is cytomegalovirus infection?), lung transplant rejection, osteoporotic fracture, white blood cell count decreased. Predonine dosage: 25mg Daily. During the same period patient was treated with IMURAN (50mg Daily) (View Imuran Review and Imuran Label ), CELLCEPT (1.5 G Daily Dose) (View Cellcept Review and Cellcept Label ), BAKTAR (View Baktar Review and Baktar Label ), DIFLUCAN (View Diflucan Review and Diflucan Label ), GASTER (View Gaster Review and Gaster Label ), NEORAL (300mg Daily Dose) (View Neoral Review and Neoral Label ).

4627983-9 | Acute Respiratory Distress Syndrome, Akinesia, Amnesia, Blood Pressure Increased, Blood Urine Present, Depressed Level Of Consciousness, Dyskinesia, Encephalitis Viral, Epilepsy
Patient was taking Predonine (View Usage). Patient experienced the following unwanted or unexpected effects: acute respiratory distress syndrome, akinesia, amnesia, blood pressure increased, blood urine present, depressed level of consciousness, dyskinesia, encephalitis viral, epilepsy (What is epilepsy?) on Dec 22, 2004 from Additional patient health information: Male patient , child 8 years of age, weighting 37.48 lb, . Predonine dosage: 20 Mg/day. During the same period patient was treated with MABLIN (10 G/day) (View Mablin Review and Mablin Label ), ALKERAN (65 Mg/day) (View Alkeran Review and Alkeran Label ), ZOVIRAX (View Zovirax Review and Zovirax Label ), SANDIMMUNE (60 Mg/day) (View Sandimmune Review and Sandimmune Label ).

4591105-3 | Cytomegalovirus Antigen Positive, Lung Transplant Rejection, Osteoporotic Fracture, White Blood Cell Count Decreased
Adverse event was reported on Feb 15, 2005 by a Female patient taking Predonine (View Usage) (Dosage: 25mg Daily) was diagnosed with lung transplant (What is lung transplant?) and. Location: , 45 years of age, weighting 97.00 lb, Patient had the following side effects: cytomegalovirus antigen positive, lung transplant rejection, osteoporotic fracture, white blood cell count decreased. During the same period patient was treated with IMURAN (50mg Daily) (View Imuran Review and Imuran Label ), CELLCEPT (1.5 G Daily Dose) (View Cellcept Review and Cellcept Label ), BAKTAR (View Baktar Review and Baktar Label ), DIFLUCAN (View Diflucan Review and Diflucan Label ), GASTER (View Gaster Review and Gaster Label ), NEORAL (300mg Daily Dose) (View Neoral Review and Neoral Label ).

4588778-8 | Acute Respiratory Distress Syndrome, Akinesia, Amnesia, Blood Pressure Increased, Blood Urine Present, Depressed Level Of Consciousness, Dyskinesia, Encephalitis Viral, Epilepsy
on Dec 22, 2004 Male patient from , child 8 years of age, weighting 37.48 lb, was treated with Predonine (View Usage). After Predonine was administered, patient had the following side effects: acute respiratory distress syndrome, akinesia, amnesia, blood pressure increased, blood urine present, depressed level of consciousness, dyskinesia, encephalitis viral, epilepsy (What is epilepsy?). Predonine dosage: 20 Mg/day. During the same period patient was treated with MABLIN (10 G/day) (View Mablin Review and Mablin Label ), ALKERAN (65 Mg/day) (View Alkeran Review and Alkeran Label ), ZOVIRAX (View Zovirax Review and Zovirax Label ), SANDIMMUNE (60 Mg/day) (View Sandimmune Review and Sandimmune Label ).