Sortis and aspartate aminotransferase increased Patient Reports February 13, 2012

Sortis Side Effects Report #4753641-6
Sortis side effect was reported by a Physician from SWITZERLAND on Aug 15, 2005. Male patient, 39 years of age, was diagnosed with hyperlipidaemia 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, myocardial infarction. Sortis dosage: 60 MG (1 IN 1 D), ORAL. During the same period patient was treated with ASPIRIN, PLAVIX, EZETROL, TENORMIN, PANTOPRAZOLE, ACETYLSALICYLIC ACID SRT. Patient recovered.

Sortis Side Effects Report #4895886-0
Sortis side effect was reported by a Physician from GERMANY on Jan 12, 2006. Female patient was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, cardiac failure, gamma-glutamyltransferase increased, pneumonia , rhabdomyolysis. Sortis dosage: 40 MG, ORAL. Patient was hospitalized. 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 #4609451-3
Sortis side effect was reported by a Physician from on Mar 01, 2005. Male patient, 76 years of age, weighting 152.1 lb, was diagnosed with coronary artery disease , atrial fibrillation  and was treated with Sortis. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatine increased, blood lactate dehydrogenase increased, blood potassium decreased, gamma-glutamyltransferase increased, pruritus. Sortis dosage: 40 MG (40 MG, 1 IN 1 D), ORAL. During the same period patient was treated with AMIODARONE, METOPROLOL TARTRATE, ENALAPRIL MALEATE, PHENPROCOUMON, FUROSEMIDE, ALLOPURINOL, POTASSIUM CHLORIDE, LEVOTHYROXINE. Patient recovered.