Predonine and c-reactive protein increased Patient Reports February 10, 2010

Predonine Side Effects Report #5465857-4
Predonine side effect was reported by a Pharmacist from JAPAN on Sept 19, 2007. Female patient, 69 years of age, was treated with Predonine. After drug was administered, patient experienced 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. 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.

Predonine Side Effects Report #5474450-9
Predonine side effect was reported by a Pharmacist from JAPAN on Sept 27, 2007. Female patient, 69 years of age, was treated with Predonine. After drug was administered, patient experienced 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. Predonine dosage: 20 MG, UNK. During the same period patient was treated with DEPAKENE, PREDNISOLONE, TAGAMET, ALLELOCK, BIOFERMIN, GASMOTIN, VALPROATE. Patient was hospitalized. Patient died on 09/01/2007.

Predonine Side Effects Report #5052521-9
Predonine side effect 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 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 #5479309-9
Predonine side effect was reported by a Consumer or non-health professional from JAPAN on Oct 01, 2007. Female patient, 68 years of age, was treated with Predonine. After drug was administered, patient experienced 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. Predonine dosage: 20 MG, UNK. During the same period patient was treated with DEPAKENE, PREDNISOLONE, TAGAMET, ALLELOCK, BIOFERMIN, GASMOTIN, VALPROATE. Patient was hospitalized. Patient died on 09/01/2007.


Predonine Side Effects Report #5657539-0
Predonine side effect was reported by a Physician from JAPAN on Feb 27, 2008. Female patient, 64 years of age, weighting 85.98 lb, was diagnosed with bone lesion and was treated with Predonine. After drug was administered, patient experienced the following side effects: abscess , abscess jaw, c-reactive protein increased, computerised tomogram abnormal, impaired healing, malnutrition, multiple myeloma , osteitis, osteomyelitis. Predonine dosage: 5 MG/DAY. During the same period patient was treated with ZOMETA. Patient was hospitalized. Patient recovered.

Predonine Side Effects Report #5699663-2
Predonine side effect was reported by a Physician from JAPAN on Mar 27, 2008. Female patient, 64 years of age, weighting 85.98 lb, was diagnosed with bone lesion and was treated with Predonine. After drug was administered, patient experienced the following side effects: abscess , abscess jaw, c-reactive protein increased, computerised tomogram abnormal, condition aggravated, impaired healing, malnutrition, multiple myeloma , osteitis. Predonine dosage: 5 MG/DAY. During the same period patient was treated with ZOMETA. Patient was hospitalized. Patient recovered.