Sortis and fatigue Patient Reports February 12, 2012

Sortis Side Effects Report #4680967-7
Sortis side effect was reported by a Consumer or non-health professional from on May 19, 2005. Male patient, 83 years of age, weighting 132.3 lb, was diagnosed with mixed hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: anorexia, faeces discoloured, fatigue, hepatic encephalopathy, hepatitis cholestatic, hepatocellular damage, hepatorenal syndrome, jaundice , leukocytosis. Sortis dosage: 20 MG (DAILY), ORAL. During the same period patient was treated with SORBIDILAT, ASPIRIN, BECLOFORTE, FORADIL, OXAZEPAM. Patient was hospitalized. Patient died on 01/01/2002.

Sortis Side Effects Report #4751169-0
Sortis side effect was reported by a Physician from GERMANY on Aug 15, 2005. Male patient, 61 years of age, weighting 176.4 lb, was diagnosed with lipid metabolism disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: fatigue, muscle disorder , myalgia, myopathy, pain in extremity, tendon rupture, treatment noncompliance. Sortis dosage: 20 MG (20 MG, DAILY), ORAL. During the same period patient was treated with CERIVASTATIN. Patient recovered.

Sortis Side Effects Report #4765821-4
Sortis side effect was reported by a Physician from SWITZERLAND on Aug 29, 2005. Female patient, 69 years of age, was diagnosed with dyslipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, difficulty in walking, fatigue, muscular weakness, myalgia, myopathy. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with APROVEL, ELTROXIN. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4852357-5
Sortis side effect was reported by a Physician from SWITZERLAND on Nov 30, 2005. Female patient, 69 years of age, was diagnosed with dyslipidaemia, ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, apathy, aspartate aminotransferase increased, blood lactate dehydrogenase increased, difficulty in walking, fatigue, fear, mood altered, myopathy. Sortis dosage: 20 MG (20 MG, 1 IN 1 D); ORAL. During the same period patient was treated with PREDNISONE, AZATHIOPRINE, APROVEL, LEVOTHYROXINE. Patient was hospitalized. Patient recovered.


Sortis Side Effects Report #4889557-4
Sortis side effect was reported by a Physician from SWITZERLAND on Jan 12, 2006. Female patient, 69 years of age, was diagnosed with dyslipidaemia, ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: apathy, difficulty in walking, fatigue, fear, mood altered, movement disorder , muscular weakness, myalgia, myopathy. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PREDNISONE, APROVEL, LEVOTHYROXINE, AZATHIOPRINE. Patient was hospitalized. Patient recovered.