Sortis and blood creatine phosphokinase increased Patient Reports February 13, 2012

Sortis Side Effects Report #5595248-7
Sortis side effect was reported by a Consumer or non-health professional from GERMANY on Jan 07, 2008. Female patient, 59 years of age, was diagnosed with type iia hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, heart valve operation, paraesthesia. Sortis dosage: unknown. During the same period patient was treated with EZETROL. Patient was hospitalized. Patient recovered.

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 #5960555-2
Sortis side effect was reported by a Physician from SWITZERLAND on Nov 13, 2008. Female patient, 57 years of age, weighting 110.2 lb, was diagnosed with myocardial infarction and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, pain , paraesthesia. Sortis dosage: unknown. During the same period patient was treated with ASPIRIN, PLAVIX, BISOPROLOL FUMARATE, TRIATEC. Patient recovered.

Sortis Side Effects Report #5611637-6
Sortis side effect was reported by a Physician from GERMANY on Jan 24, 2008. Female patient, 55 years of age, was diagnosed with low density lipoprotein increased, cardiovascular evaluation and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, muscle disorder , myocardial infarction. Sortis dosage: DAILY DOSE:20MG. During the same period patient was treated with SIMVASTATIN, ASPIRIN, PLAVIX, METOPROLOL TARTRATE, RAMIPRIL. Patient was hospitalized. Patient recovered.


Sortis Side Effects Report #4596618-6
Sortis side effect was reported by a Physician from on Feb 21, 2005. Male patient, 80 years of age, was diagnosed with ill-defined disorder 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. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with XIPAMIDE, TORSEMIDE, RAMIPRIL, ASPIRIN. 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 #4770984-0
Sortis side effect was reported by a Physician from GERMANY on Sept 06, 2005. Male patient, 60 years of age, was diagnosed with ill-defined disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, calculus ureteric, erectile dysfunction , nephrolithiasis. Sortis dosage: 40 MG (40 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 #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 #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 #4795093-6
Sortis side effect was reported by a Physician from GERMANY on Sept 27, 2005. Male patient, 48 years of age, weighting 264.6 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, decreased activity, muscle spasms. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. During the same period patient was treated with LEVOTHYROXINE, METOPROLOL TARTRATE, RAMIPRIL, ASS. Patient was hospitalized. 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.

Sortis Side Effects Report #5620787-X
Sortis side effect was reported by a Physician from GERMANY on Jan 31, 2008. Male patient, weighting 264.6 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, muscle spasms. Sortis dosage: unknown. During the same period patient was treated with EUTHYROX, METOPROLOL TARTRATE, DELIX, ASPIRIN. Patient was hospitalized. Patient recovered.


Sortis Side Effects Report #5760313-8
Sortis side effect was reported by a Physician from GERMANY on May 29, 2008. Male patient, weighting 264.6 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, muscle spasms. Sortis dosage: unknown. During the same period patient was treated with EUTHYROX, METOPROLOL TARTRATE, DELIX, ASPIRIN. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5799261-6
Sortis side effect was reported by a Physician from GERMANY on June 25, 2008. Male patient, weighting 205.0 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: arthropathy, blood creatine phosphokinase increased, blood creatine phosphokinase mb increased, muscle disorder . Sortis dosage: DAILY DOSE:20MG. 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 #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.

Sortis Side Effects Report #4489385-8
Sortis side effect was reported by a Physician from on Oct 13, 2004. Male patient, 58 years of age, weighting 222.7 lb, was diagnosed with coronary artery disease  and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, polymyositis. Sortis dosage: 20 MG (20 MG, 1 IN 1 D), ORAL. Patient recovered.


Sortis Side Effects Report #5572145-4
Sortis side effect was reported by a Physician from ROMANIA on Dec 12, 2007. Female patient, weighting 169.8 lb, was diagnosed with cardiovascular event prophylaxis, dyslipidaemia, hypertension and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, blood creatine phosphokinase mb increased, myalgia, rhabdomyolysis, transaminases increased. Sortis dosage: unknown. During the same period patient was treated with INDAPAMIDE, AMLODIPINE, PERINDOPRIL, DIOSMIN, ACETYLSALICYLIC ACID SRT, AUGMENTIN. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5708550-2
Sortis side effect was reported by a Consumer or non-health professional from GERMANY on Apr 07, 2008. Male patient was diagnosed with blood cholesterol increased and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased, muscle disorder , muscle spasms. Sortis dosage: DAILY DOSE:20MG. During the same period patient was treated with EZETROL. Patient recovered.

Sortis Side Effects Report #5863489-7
Sortis side effect was reported by a Physician from SWITZERLAND on Aug 25, 2008. Male patient, 67 years of age, weighting 216.1 lb, was diagnosed with acute myocardial infarction, pneumonia  and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood creatine phosphokinase increased. Sortis dosage: unknown. During the same period patient was treated with KLACID, TAVANIC, CEDUR, ADALAT, ASPIRIN, COVERSUM, LASIX, LORASIFAR. Patient died on 07/17/2008.