Predonine and blood urea increased Patient Reports February 12, 2012

Predonine Side Effects Report #4792407-8
Predonine side effect was reported by a Consumer or non-health professional from JAPAN on Sept 28, 2005. Male patient, 27 years of age, was diagnosed with nasopharyngitis, arthralgia and was treated with Predonine. After drug was administered, patient experienced 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. Predonine dosage: 5 MG/DAY. During the same period patient was treated with VOLTAREN. Patient was hospitalized. Patient recovered.

Predonine Side Effects Report #4865747-1
Predonine side effect was reported by a Consumer or non-health professional from JAPAN on Sept 28, 2005. Male patient, 27 years of age, was diagnosed with nasopharyngitis, arthralgia and was treated with Predonine. After drug was administered, patient experienced 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. Predonine dosage: 5 MG/DAY. During the same period patient was treated with VOLTAREN. Patient was hospitalized. Patient recovered.

Predonine Side Effects Report #5060606-6
Predonine side effect was reported by a Physician from JAPAN 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 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 #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.