Predonine Side Effects
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Predonine Safety Reports reported to FDA
Total Predonine reports: 13.Predonine FDA safety alerts: No.
Reported deaths: 7 Reported hospitalizations: 6.
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Reported Predonine Side Effects: blood creatinine increased, grip strength decreased, dysarthria, cerebral infarction, hemiparesis, convulsion, aphasia, leukoaraiosis, jc virus infection, herpes zoster, herpes simplex.
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Predonine Side Effects Report #5208672-9
Physician from JAPAN reported PREDONINE problem on Jan 05, 2007. Male patient, 68 years of age, was diagnosed with multiple myeloma and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: osteonecrosis, pain. PREDONINE dosage: unknown. During the same period patient was treated with SUCRALFATE, ZOMETA. Patient recovered.
Predonine Side Effects Report #5304229-X
PREDONINE problem was reported by a Physician from JAPAN on Apr 12, 2007. Female patient, 21 years of age, was diagnosed with histiocytosis haematophagic and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: pancytopenia, platelet count decreased, white blood cell count decreased. PREDONINE dosage: unknown. During the same period patient was treated with ANTIBIOTICS, NEORAL, CARBENIN, MINOCYCLINE, FIRSTCIN. Patient recovered.
Predonine Side Effects Report #5325917-5
Physician from JAPAN reported PREDONINE problem on May 10, 2007. Male patient, 68 years of age, weighting 154.3 lb, was diagnosed with hypercalcaemia and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: haemorrhage, local swelling, osteonecrosis, pain in jaw, primary sequestrum, purulent discharge, tooth extraction. PREDONINE dosage: unknown. During the same period patient was treated with SUCRALFATE, ZOMETA, BISPHONAL. Patient recovered.
Predonine Side Effects Report #5052521-9
PREDONINE problem was reported by a Pharmacist from JAPAN on Feb 20, 2006. Male patient, 68 years of age, weighting 143.3 lb, was diagnosed with eosinophilia, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: 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. PREDONINE dosage: 5 MG/D. During the same period patient was treated with NEORAL, NU LOTAN, BONALON, TAKEPRON, ALESION. Patient was hospitalized. Patient recovered.
Predonine Side Effects Report #5060606-6
Physician from JAPAN reported PREDONINE problem on May 08, 2006. Male patient, 76 years of age, weighting 132.3 lb, was diagnosed with glomerulonephritis, pain in extremity, gastritis and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: aplastic anaemia, blood urea increased, haematocrit decreased, haemoglobin decreased, neutrophil count decreased, pancytopenia, platelet count decreased, pneumonia, protein urine present. PREDONINE dosage: 10 MG/DAY. During the same period patient was treated with TEGRETOL, GASTER, ADRENAL HORMONE PREPARATIONS. Patient died on 04/17/2006.
Predonine Side Effects Report #5060793-X
PREDONINE problem was reported by a Consumer or non-health professional from JAPAN on Oct 26, 2005. Male patient, 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/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, NEORAL, NU LOTAN. Patient was hospitalized and became disabled. Patient died.
Predonine Side Effects Report #5066352-7
Consumer or non-health professional from JAPAN reported PREDONINE problem on Oct 26, 2005. Male patient, 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: aphasia, blood creatinine increased, cerebral infarction, convulsion, depressed level of consciousness, dysarthria, grip strength decreased, hemiparesis, immunosuppression. PREDONINE dosage: 10 MG/D. During the same period patient was treated with BREDININ, NEORAL, NU LOTAN. Patient was hospitalized and became disabled. Patient died.
Predonine Side Effects Report #5084604-1
PREDONINE problem was reported by a Consumer or non-health professional from JAPAN on Oct 26, 2005. Male patient, 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: 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, NEORAL, NU LOTAN. Patient was hospitalized and became disabled. Patient died on 04/05/2006.
Predonine Side Effects Report #5089833-9
Consumer or non-health professional from JAPAN reported PREDONINE problem on Oct 26, 2005. Male patient, 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: 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, NEORAL, NU LOTAN. Patient was hospitalized and became disabled. Patient died on 04/05/2006.
Predonine Side Effects Report #5118511-2
PREDONINE problem was reported by a Consumer or non-health professional from JAPAN on Apr 14, 2004. Female patient, 59 years of age, was diagnosed with interstitial lung disease and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, cd4/cd8 ratio increased, depression, diabetes mellitus, herpes simplex, herpes zoster. PREDONINE dosage: unknown. During the same period patient was treated with NEORAL. Patient recovered.
Predonine Side Effects Report #5124777-5
Consumer or non-health professional from JAPAN reported PREDONINE problem on Apr 14, 2004. Female patient, 59 years of age, was diagnosed with interstitial lung disease and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: blood pressure increased, depression, herpes simplex, herpes zoster, necrotising retinitis, reactive psychosis. PREDONINE dosage: unknown. During the same period patient was treated with NEORAL. Patient recovered.
Predonine Side Effects Report #5142153-6
PREDONINE problem was reported by a Consumer or non-health professional from JAPAN on Oct 26, 2005. Male patient, 50 years of age, weighting 141.1 lb, was diagnosed with nephrotic syndrome, hypertension and was treated with PREDONINE. After drug was administered, patient experienced the following problems/side effects: 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, NEORAL, NU LOTAN. Patient was hospitalized and became disabled. Patient died on 04/08/2006.
Predonine Side Effects Report #5465857-4
Pharmacist from JAPAN reported PREDONINE problem on Sept 19, 2007. Female patient, 69 years of age, was treated with PREDONINE. After drug was administered, patient experienced the following problems/side 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, PREDNISOLONE, TAGAMET, ALLELOCK, BIOFERMIN, GASMOTIN, VALPROATE. Patient died on 09/01/2007.