Sortis and difficulty in walking Patient Reports February 12, 2012

Sortis Side Effects Report #4708789-9
Sortis side effect was reported by a Physician from FRANCE on June 22, 2005. Female patient, 55 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: abasia, activities of daily living impaired, blood cholesterol increased, bone pain, bradykinesia, cholecystectomy, difficulty in walking, diplegia. Sortis dosage: unknown. During the same period patient was treated with STALTOR, PRAVASTATIN, DIHYDROCODEINE, LEVOCARNITINE. Patient was hospitalized and became disabled. Patient recovered.

Sortis Side Effects Report #4724946-X
Sortis side effect was reported by a Consumer or non-health professional from SWITZERLAND on July 12, 2005. Female patient was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: difficulty in walking, muscular weakness, weight decreased. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), 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 #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.