Oroken and blood bilirubin increased Patient Reports February 10, 2010

Oroken Side Effects Report #4920958-1
Oroken side effect was reported by a Health Professional from FRANCE on Feb 13, 2006. Male patient, child 11 years of age, was treated with Oroken. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, bradycardia, c-reactive protein increased, coagulation factor decreased, ecchymosis, gastrointestinal haemorrhage, haemoglobin decreased. Oroken dosage: 160 MG DAILY ORAL. During the same period patient was treated with ALDACTONE, JOSACINE, PREVISCAN, DIGOXIN, LOPRIL, FUROSEMIDE. Patient was hospitalized. Patient died.