Sortis and asthenia Patient Reports February 12, 2012

Sortis Side Effects Report #4903759-X
Sortis side effect was reported by a Physician from GERMANY on Jan 23, 2006. Male patient, 62 years of age, weighting 132.3 lb, was diagnosed with myocardial infarction and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, fall , haematoma, oedema peripheral, tendon rupture. Sortis dosage: 80MG TO 120MG (DAILY), ORAL. During the same period patient was treated with EZETROL, PIRETANIDE, ASPIRIN. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4691119-9
Sortis side effect was reported by a Physician from on June 03, 2005. Male patient, 70 years of age, was diagnosed with lipid metabolism disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, escherichia urinary tract infection, inflammation, myositis , neutrophil percentage increased, pyrexia, red blood cell sedimentation rate increased, respiratory tract infection, rhabdomyolysis. Sortis dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PANTOPRAZOLE, SPASMOLYT, ANTIINFLAMMATORY. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4773107-7
Sortis side effect was reported by a Physician from SWITZERLAND on Sept 05, 2005. Male patient, 75 years of age, weighting 176.4 lb, was diagnosed with ill-defined disorder, hyperthyroidism and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, night sweats, pain in extremity, polymyositis, rhabdomyolysis, troponin t increased, weight decreased. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with NEO MERCAZOLE, MARCUMAR, NEXIUM, LAXOBERON, KONAKION, TOREM, BISOPROLOL FUMARATE, RYTMONORM. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4716797-7
Sortis side effect was reported by a Physician from GERMANY on July 05, 2005. Female patient, 68 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, cardiovascular disorder, dysstasia, myalgia, refusal of treatment by patient, transient ischaemic attack. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MARCUMAR, ENALAPRIL MALEATE, NIFEDIPINE. Patient recovered.


Sortis Side Effects Report #4546349-3
Sortis side effect was reported by a Physician from on Dec 20, 2004. Male patient, 59 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, c-reactive protein increased, muscle atrophy, myositis , paraneoplastic syndrome, paresis. Sortis dosage: 10 MG (10 MG, 1 IN 1 D) ORAL. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4613352-4
Sortis side effect was reported by a Physician from on Mar 04, 2005. Male patient, 75 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: anaemia, asthenia, blood creatine phosphokinase increased, dialysis , hyperkalaemia, myoglobin blood increased, nausea , pyelonephritis chronic, renal disorder. Sortis dosage: 20 MG, ORAL. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4767079-9
Sortis side effect was reported by a Physician from GERMANY on Aug 29, 2005. Male patient, 75 years of age, weighting 167.6 lb, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: anaemia, asthenia, biopsy kidney abnormal, bone marrow disorder, bone marrow tumour cell infiltration, clear cell carcinoma of the kidney, dialysis , hyperkalaemia, myoglobin blood increased. Sortis dosage: 20 MG (1 IN 1 D), ORAL. Patient was hospitalized. Patient died on 03/27/2005.

Sortis Side Effects Report #4765640-9
Sortis side effect was reported by a Physician from GERMANY on Aug 24, 2005. Male patient, 65 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, insomnia, loss of control of legs, paraesthesia, visual disturbance. Sortis dosage: 20 MG (1 IN 1 D), ORAL. During the same period patient was treated with REPAGLINIDE. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #4776513-X
Sortis side effect was reported by a Physician from GERMANY on Sept 08, 2005. Female patient, 68 years of age, weighting 110.2 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, cardiovascular disorder, diplegia, myalgia, refusal of treatment by patient, syncope, transient ischaemic attack. Sortis dosage: unknown. During the same period patient was treated with MARCUMAR, ENALAPRIL MALEATE, NIFEDIPINE. Patient recovered.


Sortis Side Effects Report #4891888-9
Sortis side effect was reported by a Physician from GERMANY on Jan 09, 2006. Female patient, 68 years of age, weighting 112.4 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, diplegia, myalgia, transient ischaemic attack. Sortis dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. During the same period patient was treated with MARCUMAR, ENALAPRIL MALEATE, NIFEDIPINE. Patient recovered.

Sortis Side Effects Report #4597105-1
Sortis side effect was reported by a Physician from on Feb 18, 2005. Male patient, 42 years of age, weighting 174.2 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: asthenia, blood creatine phosphokinase increased, pain , performance status decreased. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with PRAVASTATIN, LOVASTATIN, LIPOREDUCT. Patient recovered.