Sortis and myalgia Patient Reports February 12, 2012

Sortis Side Effects Report #5511930-1
Sortis side effect was reported by a Physician from GERMANY on Oct 29, 2007. Female patient, 59 years of age, was diagnosed with prophylaxis and was treated with Sortis. After drug was administered, patient experienced the following side effects: myalgia, osteoarthritis . Sortis dosage: DAILY DOSE:20MG. During the same period patient was treated with LEVOTHYROXINE, HARPAGOPHYTUM PROCUMBENS. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5522552-0
Sortis side effect was reported by a Physician from GERMANY on Nov 12, 2007. Female patient, weighting 187.4 lb, was diagnosed with prophylaxis, hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: myalgia, osteoarthritis , sciatica . Sortis dosage: unknown. During the same period patient was treated with HARPAGOPHYTUM PROCUMBENS. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5772829-9
Sortis side effect was reported by a Pharmacist from GERMANY on June 04, 2008. Male patient was diagnosed with prophylaxis and was treated with Sortis. After drug was administered, patient experienced the following side effects: muscle spasms, myalgia, myocardial infarction. Sortis dosage: DAILY DOSE:10MG. During the same period patient was treated with NORVASC, FOSINOPRIL. Patient recovered.

Sortis Side Effects Report #4751169-0
Sortis side effect was reported by a Physician from GERMANY on Aug 15, 2005. Male patient, 61 years of age, weighting 176.4 lb, was diagnosed with lipid metabolism disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: fatigue, muscle disorder , myalgia, myopathy, pain in extremity, tendon rupture, treatment noncompliance. Sortis dosage: 20 MG (20 MG, DAILY), ORAL. During the same period patient was treated with CERIVASTATIN. Patient recovered.


Sortis Side Effects Report #4556904-2
Sortis side effect was reported by a Physician from on Jan 11, 2005. Male patient, 41 years of age, was diagnosed with lipid metabolism disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: abdominal pain , c-reactive protein increased, gastrointestinal infection, joint effusion, liver disorder, liver function test abnormal, myalgia. Sortis dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. Patient recovered.

Sortis Side Effects Report #4607752-6
Sortis side effect was reported by a Physician from on Mar 01, 2005. Male patient, 41 years of age, was diagnosed with lipid metabolism disorder and was treated with Sortis. After drug was administered, patient experienced the following side effects: abdominal pain , c-reactive protein increased, gastrointestinal infection, joint effusion, liver function test abnormal, myalgia. Sortis dosage: 10 MG (10 MG, 1 IN 1 D), ORAL. 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 #5588013-8
Sortis side effect was reported by a Pharmacist from POLAND on Jan 03, 2008. Male patient, weighting 202.8 lb, was diagnosed with hypertension, myocardial infarction and was treated with Sortis. After drug was administered, patient experienced the following side effects: myalgia. Sortis dosage: DAILY DOSE:40MG. During the same period patient was treated with LIPANTHYL, SERTRALINE, ACARD, PLAVIX, BISOCARD. Patient recovered.

Sortis Side Effects Report #5853392-0
Sortis side effect was reported by a Physician from GERMANY on Aug 12, 2008. Male patient, weighting 180.8 lb, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: eyelid oedema, food intolerance, gastric disorder, laryngospasm, muscle spasms, myalgia, nephrotic syndrome. Sortis dosage: DAILY DOSE:20MG. Patient was hospitalized. Patient recovered.


Sortis Side Effects Report #5958590-3
Sortis side effect was reported by a Physician from GERMANY on Nov 10, 2008. Male patient, weighting 180.8 lb, was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: eyelid oedema, food intolerance, gastric disorder, laryngospasm, muscle spasms, myalgia, nephrotic syndrome. Sortis dosage: DAILY DOSE:20MG. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #6070756-3
Sortis side effect was reported by a Physician from ROMANIA on Jan 30, 2009. Female patient was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, lipids increased, low density lipoprotein increased, myalgia, overdose. Sortis dosage: 40 MG, 1X/DAY. During the same period patient was treated with HERBAL PREPARATION. Patient recovered.

Sortis Side Effects Report #6083789-8
Sortis side effect was reported by a Physician from ROMANIA on Feb 12, 2009. Female patient was diagnosed with hyperlipidaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: blood cholesterol increased, blood triglycerides increased, lipids increased, low density lipoprotein increased, myalgia, overdose. Sortis dosage: 40 MG, 1X/DAY. During the same period patient was treated with HERBAL PREPARATION. Patient recovered.

Sortis Side Effects Report #4692420-5
Sortis side effect was reported by a Consumer or non-health professional from on June 02, 2005. Male patient, 68 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: myalgia, sensation of heaviness. Sortis dosage: 20 MG ORAL. During the same period patient was treated with TENORMIN, PANTOPRAZOLE, ACERBON, MARCUMAR, PROSTA FINK. 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 #4701632-3
Sortis side effect was reported by a Health Professional from on June 15, 2005. Male patient, 66 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: angina pectoris, myalgia, sensation of heaviness, stress . Sortis dosage: 20 MG, ORAL. During the same period patient was treated with TENORMIN, PANTOPRAZOLE, ACERBON, MARCUMAR, PROSTA FINK. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5603095-2
Sortis side effect was reported by a Physician from SWITZERLAND on Jan 15, 2008. Female patient, 60 years of age, was diagnosed with hypercholesterolaemia, gastric ulcer and was treated with Sortis. After drug was administered, patient experienced the following side effects: haematuria, liver injury, myalgia. Sortis dosage: unknown. During the same period patient was treated with KLACID, AMOXI, NEXIUM. Patient recovered.

Sortis Side Effects Report #4746517-1
Sortis side effect was reported by a Consumer or non-health professional from GERMANY on Aug 08, 2005. Male patient, 59 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: myalgia. Sortis dosage: unknown. During the same period patient was treated with BISOPROLOL FUMARATE, ASPIRIN, COVERSUM. Patient recovered.

Sortis Side Effects Report #5471611-X
Sortis side effect was reported by a Physician from GERMANY on Sept 20, 2007. Male patient, weighting 160.9 lb, was diagnosed with hypercholesterolaemia, parkinson's disease  and was treated with Sortis. After drug was administered, patient experienced the following side effects: dysphagia, hordeolum, muscle spasms, myalgia, parkinson's disease . Sortis dosage: DAILY DOSE:20MG. During the same period patient was treated with SIFROL, GODAMED. Patient recovered.


Sortis Side Effects Report #5757556-6
Sortis side effect was reported by a Consumer or non-health professional from GERMANY on May 27, 2008. Male patient, weighting 160.9 lb, was diagnosed with hypercholesterolaemia, parkinson's disease  and was treated with Sortis. After drug was administered, patient experienced the following side effects: amyotrophic lateral sclerosis , dysphagia, hordeolum, muscle spasms, myalgia, parkinson's disease . Sortis dosage: DAILY DOSE:10MG. During the same period patient was treated with SIFROL, GODAMED. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #6124760-7
Sortis side effect was reported by a Consumer or non-health professional from GERMANY on Mar 09, 2009. Female patient was diagnosed with hypercholesterolaemia and was treated with Sortis. After drug was administered, patient experienced the following side effects: hyperhidrosis, myalgia, type 2 diabetes mellitus. Sortis dosage: 10 MG, 1X/DAY. During the same period patient was treated with MARCUMAR. 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 #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.

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 #5846963-9
Sortis side effect was reported by a Physician from GERMANY on Aug 08, 2008. Male patient, 48 years of age, was treated with Sortis. After drug was administered, patient experienced the following side effects: muscle spasms, myalgia, nephrotic syndrome, oedema. Sortis dosage: DAILY DOSE:40MG. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5732119-7
Sortis side effect was reported by a Pharmacist from GERMANY on Apr 28, 2008. Male patient, 38 years of age, was treated with Sortis. After drug was administered, patient experienced the following side effects: borrelia burgdorferi serology positive, dizziness , myalgia, paraesthesia, somatisation disorder, tension headache. Sortis dosage: DAILY DOSE:10MG. During the same period patient was treated with ERYTHROMYCIN, ROCEPHIN. Patient was hospitalized. Patient recovered.

Sortis Side Effects Report #5806416-0
Sortis side effect was reported by a Pharmacist from GERMANY on July 01, 2008. Male patient, 38 years of age, was treated with Sortis. After drug was administered, patient experienced the following side effects: borrelia burgdorferi serology positive, diarrhoea, dizziness , myalgia, paraesthesia, somatisation disorder, tension headache. Sortis dosage: DAILY DOSE:10MG. During the same period patient was treated with ERYTHROMYCIN, ROCEPHIN. Patient was hospitalized. Patient recovered.