Sortis and blood lactate dehydrogenase increased Patient Reports February 13, 2012

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.

Sortis Side Effects Report #4608905-3
Sortis side effect was reported by a Physician from on Mar 01, 2005. Male patient, 65 years of age, weighting 200.6 lb, was diagnosed with coronary artery disease , diabetes mellitus, hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, blood creatine phosphokinase mb increased, blood creatinine increased, blood lactate dehydrogenase increased, blood urea increased, concomitant disease aggravated. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with CLAVULIN. Patient was hospitalized. Patient recovered.