Predonine and blood glucose increased Patient Reports February 12, 2012

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 #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.