Oroken and aspartate aminotransferase increased Patient Reports February 13, 2012

Oroken Side Effects Report #5721516-1
Oroken side effect was reported by a Health Professional from JAPAN on Apr 18, 2008. Female patient, 30 years of age, was treated with Oroken. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, cholestasis. Oroken dosage: unknown. During the same period patient was treated with TARDYFERON. Patient was hospitalized. Patient recovered.

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.