Sortis and hepatic failure Patient Reports February 13, 2012

Sortis Side Effects Report #4617969-2
Sortis side effect was reported by a Physician from on Mar 14, 2005. Male patient, 69 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: chromaturia, hepatic failure, nuclear magnetic resonance imaging abnormal, pancreatitis. Sortis dosage: 20 MG (1 D), ORAL. During the same period patient was treated with EZETIMIBE, CLOPIDOGREL BISULPHATE, CANDESARTAN CILEXETIL, PHENPROCOUMON. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4551802-2
Sortis side effect was reported by a Pharmacist from on Jan 03, 2005. Female patient, 51 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: hepatic failure. Sortis dosage: 80 MG, ORAL. Patient died.

Sortis Side Effects Report #4576457-2
Sortis side effect was reported by a Pharmacist from on Jan 26, 2005. Female patient, 51 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: gallbladder disorder, hepatic failure. Sortis dosage: (80 MG), ORAL. Patient was hospitalized. Patient died.

Sortis Side Effects Report #4783693-9
Sortis side effect was reported by a Physician from GERMANY on Sept 15, 2005. Male patient, 60 years of age, weighting 149.9 lb, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: abasia, dialysis , haematuria, haemodialysis, hepatic failure, hepatocellular damage, immobile, renal failure acute, rhabdomyolysis. Sortis dosage: 20 MG, ORAL. During the same period patient was treated with AVELOX. Patient was hospitalized. Patient recovered.