SORTIS Side Effects

7009670-5 | Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Myalgia, Rhabdomyolysis, Transaminases Increased
on Sep 16, 2010 Female patient from CROATIA (local name: Hrvatska) , 65 years of age, was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, myalgia, rhabdomyolysis, transaminases increased. Sortis dosage: Unk. During the same period patient was treated with ATORVASTATIN (Unk) (View Atorvastatin Review and Atorvastatin Label ), TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN (View Tramadol Hydrochloride And Acetaminophen Review and Tramadol Hydrochloride And Acetaminophen Label ), IBRUPROFEN (Unk) (View Ibruprofen Review and Ibruprofen Label ).

7009585-2 | Arthralgia, Blood Cholesterol Increased, Bronchitis, Contusion, Dyspnoea, Haemorrhage, Maculopathy, Myalgia
Patient was taking Sortis (View Usage). Patient had the following side effects: arthralgia, blood cholesterol increased, bronchitis (What is bronchitis?), contusion, dyspnoea, haemorrhage, maculopathy, myalgia on Sep 14, 2010 from GERMANY Additional patient health information: Female patient , 68 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: 1/2 40 Mg Tablet In The Evening. During the same period patient was treated with LIPITOR (20 Mg, Unk) (View Lipitor Review and Lipitor Label ), TENORMIN (1/2 50 Mg Tablet Twice Daily) (View Tenormin Review and Tenormin Label ), ASPIRIN (100, 1/2 Of Tablet At Noon) (View Aspirin Review and Aspirin Label ), BLOPRESS (8 Mg, 1x/day) (View Blopress Review and Blopress Label ).

7007684-2 | Arthritis, Blood Creatine Phosphokinase Increased, Bone Density Decreased, Cubital Tunnel Syndrome, Paresis
Adverse event was reported on Sep 13, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 20 Mg, 1x/day) was diagnosed with hypercholesterolaemia and. Location: GERMANY , 75 years of age, weighting 152.1 lb, After Sortis was administered, patient had the following side effects: arthritis (What is arthritis?), blood creatine phosphokinase increased, bone density decreased, cubital tunnel syndrome, paresis.

7007625-8 | Mixed Liver Injury
on Sep 14, 2010 Male patient from SWITZERLAND , 88 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: mixed liver injury. Sortis dosage: 10-20mg, 1x/day. During the same period patient was treated with NORVASC (5 Mg, Unk) (View Norvasc Review and Norvasc Label ), PERINDOPRIL ARGININE (2.5 Mg, 1x/day) (View Perindopril Arginine Review and Perindopril Arginine Label ), PRADIF (400 Ug, 1x/day) (View Pradif Review and Pradif Label ), ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), PLAVIX (75 Mg, 1x/day) (View Plavix Review and Plavix Label ), PHYSIOTENS (0.2 Mg, 2x/day) (View Physiotens Review and Physiotens Label ), NITRODERM (5 Mg, 1x/day) (View Nitroderm Review and Nitroderm Label ). Patient was hospitalized.


6987179-2 | Arthralgia, Arthritis, Myalgia, Red Blood Cell Sedimentation Rate Increased
on Sep 08, 2010 Male patient from GERMANY , 40 years of age, was diagnosed with type iia hyperlipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: arthralgia, arthritis (What is arthritis?), myalgia, red blood cell sedimentation rate increased. Sortis dosage: 40 Mg, Unk. During the same period patient was treated with EZETROL (Unk) (View Ezetrol Review and Ezetrol Label ).

6984845-X | Arthralgia, Blood Cholesterol Increased, Bronchitis, Dyspnoea, Maculopathy, Myalgia
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: arthralgia, blood cholesterol increased, bronchitis (What is bronchitis?), dyspnoea, maculopathy, myalgia on Sep 07, 2010 from GERMANY Additional patient health information: Female patient , 68 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: 1/2 40 Mg Tablet In The Evening. During the same period patient was treated with TENORMIN (1/2 50 Mg Tablet Twice Daily) (View Tenormin Review and Tenormin Label ), ASPIRIN (100, 1/2 Of Tablet At Noon) (View Aspirin Review and Aspirin Label ), BLOPRESS (8 Mg, 1x/day) (View Blopress Review and Blopress Label ).

6972655-9 | Arthralgia, Musculoskeletal Stiffness, Myalgia
Adverse event was reported on Aug 31, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 40 Mg, 1x/day) was diagnosed with hyperlipidaemia and. Location: SWITZERLAND , 63 years of age, Patient experienced the following unwanted or unexpected effects: arthralgia, musculoskeletal stiffness, myalgia. During the same period patient was treated with METOPROLOL SUCCINATE (Unk) (View Metoprolol Succinate Review and Metoprolol Succinate Label ).

6970403-X | Fracture, Muscle Spasms
on Aug 30, 2010 Female patient from SWITZERLAND , 44 years of age, was treated with Sortis (View Usage). Patient had the following side effects: fracture (What is fracture?), muscle spasms. Sortis dosage: 40 Mg, 1x/day.

6933971-X | Arthritis, Blood Creatine Phosphokinase Increased, Bone Density Decreased, Cubital Tunnel Syndrome
on Aug 11, 2010 Female patient from GERMANY , 75 years of age, weighting 152.1 lb, was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: arthritis (What is arthritis?), blood creatine phosphokinase increased, bone density decreased, cubital tunnel syndrome. Sortis dosage: 20 Mg, 1x/day.

6925961-8 | Haemoglobin Decreased, Malaise, Musculoskeletal Stiffness
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased, malaise, musculoskeletal stiffness on Aug 06, 2010 from GERMANY Additional patient health information: Female patient , 75 years of age, . Sortis dosage: 20 Mg, Unk.

6921819-9 | Arthritis, Blood Creatine Phosphokinase Increased, Bone Density Decreased, Cubital Tunnel Syndrome
Adverse event was reported on Aug 02, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 20 Mg, 1x/day) . Location: GERMANY , 75 years of age, Patient had the following side effects: arthritis (What is arthritis?), blood creatine phosphokinase increased, bone density decreased, cubital tunnel syndrome.

6910460-X | Acarodermatitis, Dermatitis Bullous, Hypoacusis
on Aug 04, 2010 Female patient from ESTONIA , 87 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: acarodermatitis, dermatitis bullous, hypoacusis. Sortis dosage: 10 Mg, 1x/day.

6908921-2 | Dysarthria, Motor Neurone Disease, Quadriparesis
on Jul 29, 2010 Female patient from GERMANY , 81 years of age, weighting 127.0 lb, was diagnosed with hypercholesterolaemia, hypertension, dizziness (What is dizziness?) and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: dysarthria, motor neurone disease, quadriparesis. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with BLOPRESS PLUS (Daily Dose 1 Df = 16 Mg Candesartan Cilexetil/ 12.5 Mg Hydrochlorothiazide) (View Blopress Plus Review and Blopress Plus Label ), AMLODIPINE MESILATE (5 Mg Per Day) (View Amlodipine Mesilate Review and Amlodipine Mesilate Label ), TEBONIN (80 Mg Per Day) (View Tebonin Review and Tebonin Label ), ASPIRIN (100 Unk, 1x/day) (View Aspirin Review and Aspirin Label ), NEBIVOLOL HCL (1/2 5 Mg, 1x/day) (View Nebivolol Hcl Review and Nebivolol Hcl Label ), SCOPODERM (Every 3 Days) (View Scopoderm Review and Scopoderm Label ). Patient was hospitalized.

6906660-5 | Blood Test Abnormal
Patient was taking Sortis (View Usage). Patient had the following side effects: blood test abnormal on Jul 26, 2010 from GERMANY Additional patient health information: Female patient , 65 years of age, . Sortis dosage: 40 Mg/day.

6886794-4 | Asthenia, Back Pain, Gait Disturbance, Hypoaesthesia, Muscle Spasms, Myalgia, Pain In Extremity
Adverse event was reported on Jul 20, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 20 Mg, Unk) was diagnosed with hypercholesterolaemia and. Location: GERMANY , 60 years of age, weighting 143.3 lb, After Sortis was administered, patient had the following side effects: asthenia, back pain (What is back pain?), gait disturbance, hypoaesthesia, muscle spasms, myalgia, pain in extremity. During the same period patient was treated with PROVAS COMP (80 Mg, Unk) (View Provas Comp Review and Provas Comp Label ), ASCO TOP (5 Mg, As Needed) (View Asco Top Review and Asco Top Label ), DICLOFENAC RESINATE (Unk) (View Diclofenac Resinate Review and Diclofenac Resinate Label ).

6878247-4 | Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Myalgia, Renal Pain
on Jul 19, 2010 Male patient from GERMANY , 66 years of age, weighting 156.5 lb, was diagnosed with carotid artery stenosis, hypercholesterolaemia, colitis ulcerative and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, blood lactate dehydrogenase increased, myalgia, renal pain. Sortis dosage: 10 Mg, Unk. During the same period patient was treated with ASPIRIN (100 Mg/day) (View Aspirin Review and Aspirin Label ), MESALAZINE (500 Mg/day) (View Mesalazine Review and Mesalazine Label ).

6871314-0 | Acarodermatitis, Dermatitis Bullous, Hypoacusis
on Jul 15, 2010 Female patient from ESTONIA , 87 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient had the following side effects: acarodermatitis, dermatitis bullous, hypoacusis. Sortis dosage: 10 Mg, 1x/day.

6847480-X | Blood Creatine Phosphokinase Increased, Depression, Gait Disturbance, Muscular Weakness, Myalgia
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: blood creatine phosphokinase increased, depression (What is depression?), gait disturbance, muscular weakness, myalgia on Jul 08, 2010 from GERMANY Additional patient health information: Male patient , 73 years of age, weighting 165.3 lb, was diagnosed with blood cholesterol abnormal, coronary artery disease (What is coronary artery disease?) and. Sortis dosage: 60 - 80 Mg, 1x/day In The Evening. During the same period patient was treated with MARCUMAR (Unk) (View Marcumar Review and Marcumar Label ), EZETROL (Unk) (View Ezetrol Review and Ezetrol Label ). Patient was hospitalized.

6844814-7 | Dermatitis Bullous, Hypoacusis
Adverse event was reported on Jul 05, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 10 Mg, 1x/day) was diagnosed with hypercholesterolaemia and. Location: ESTONIA , 87 years of age, Patient experienced the following unwanted or unexpected effects: dermatitis bullous, hypoacusis.

6843972-8 | Asthenia, Back Pain, Gait Disturbance, Hypoaesthesia, Muscle Spasms, Myalgia, Pain In Extremity
on Jul 07, 2010 Female patient from GERMANY , 60 years of age, weighting 143.3 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient had the following side effects: asthenia, back pain (What is back pain?), gait disturbance, hypoaesthesia, muscle spasms, myalgia, pain in extremity. Sortis dosage: 20 Mg, Unk. During the same period patient was treated with PROVAS COMP (80 Mg, Unk) (View Provas Comp Review and Provas Comp Label ), ASCO TOP (5 Mg, As Needed) (View Asco Top Review and Asco Top Label ), DICLOFENAC RESINATE (Unk) (View Diclofenac Resinate Review and Diclofenac Resinate Label ).

6839771-3 | Amyotrophic Lateral Sclerosis
on Jul 07, 2010 Male patient from GERMANY , 68 years of age, weighting 167.6 lb, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: amyotrophic lateral sclerosis (What is amyotrophic lateral sclerosis?). Sortis dosage: 20 Mg, Daily.

6812541-8 | Bursitis, Hyperhidrosis, Myalgia, Type 2 Diabetes Mellitus
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: bursitis (What is bursitis?), hyperhidrosis, myalgia, type 2 diabetes mellitus on Jun 22, 2010 from GERMANY Additional patient health information: Female patient , 75 years of age, weighting 156.5 lb, was diagnosed with hypercholesterolaemia and. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with MARCUMAR (Unk) (View Marcumar Review and Marcumar Label ).

6809639-7 | Amyotrophic Lateral Sclerosis
Adverse event was reported on Jun 24, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 20 Mg, Daily) was diagnosed with hyperlipidaemia and. Location: GERMANY , 68 years of age, weighting 167.6 lb, Patient had the following side effects: amyotrophic lateral sclerosis (What is amyotrophic lateral sclerosis?).

6784710-7 | Adenomatous Polyposis Coli, Autonomic Nervous System Imbalance, Aversion, Barrett's Oesophagus, Breast Cancer Female, Decreased Appetite, Diverticulum Intestinal, Gastritis, Haemorrhoids
on Jun 14, 2010 Female patient from AUSTRIA , 68 years of age, weighting 134.5 lb, was diagnosed with blood cholesterol increased, alpha-1 anti-trypsin deficiency and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: adenomatous polyposis coli, autonomic nervous system imbalance, aversion, barrett's oesophagus, breast cancer female, decreased appetite, diverticulum intestinal, gastritis, haemorrhoids. Sortis dosage: 10 Mg, Unk. During the same period patient was treated with CORTISONE (Unk) (View Cortisone Review and Cortisone Label ), BERODUAL (Unk) (View Berodual Review and Berodual Label ). Patient was hospitalized.

6779003-8 | Hepatocellular Injury
on Jun 09, 2010 Male patient from SWITZERLAND , 69 years of age, weighting 198.4 lb, was diagnosed with cardiac disorder, type 2 diabetes mellitus and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: hepatocellular injury. Sortis dosage: 40 Mg, Unk. During the same period patient was treated with THROMBACE (100 Mg, Unk) (View Thrombace Review and Thrombace Label ), METFORMIN (1000 Mg, Unk) (View Metformin Review and Metformin Label ).

6778998-6 | Abdominal Pain, Arthralgia, Bursitis, Myalgia, Tendon Disorder
Patient was taking Sortis (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), arthralgia, bursitis (What is bursitis?), myalgia, tendon disorder on Jun 09, 2010 from SWITZERLAND Additional patient health information: Male patient , 57 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: 20 Mg, 1x/day.

6775469-8 | Gait Disturbance, Muscle Spasms, Pain In Extremity
Adverse event was reported on Jun 08, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 20 Mg, Unk) . Location: GERMANY , 60 years of age, After Sortis was administered, patient had the following side effects: gait disturbance, muscle spasms, pain in extremity.

6770449-0 | Adenomatous Polyposis Coli, Autonomic Nervous System Imbalance, Aversion, Barrett's Oesophagus, Decreased Appetite, Diverticulum Intestinal, Gastritis, Haemorrhoids, Hiatus Hernia
on Jun 07, 2010 Female patient from AUSTRIA , 68 years of age, weighting 134.5 lb, was diagnosed with blood cholesterol increased, alpha-1 anti-trypsin deficiency and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: adenomatous polyposis coli, autonomic nervous system imbalance, aversion, barrett's oesophagus, decreased appetite, diverticulum intestinal, gastritis, haemorrhoids, hiatus hernia. Sortis dosage: 10 Mg, Unk. During the same period patient was treated with CORTISONE (Unk) (View Cortisone Review and Cortisone Label ), BERODUAL (Unk) (View Berodual Review and Berodual Label ). Patient was hospitalized.

6768513-5 | Blood Pressure Increased
on Jun 04, 2010 Male patient from GERMANY , 65 years of age, was treated with Sortis (View Usage). Patient had the following side effects: blood pressure increased. Sortis dosage: Unk.

6742479-6 | Epistaxis, Hepatocellular Injury, Jaundice
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: epistaxis, hepatocellular injury, jaundice (What is jaundice?) on May 18, 2010 from SWITZERLAND Additional patient health information: Male patient , 72 years of age, was diagnosed with cerebral infarction and. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with MARCUMAR (3 Mg, As Needed) (View Marcumar Review and Marcumar Label ), COVERSUM (4 Mg, 1x/day) (View Coversum Review and Coversum Label ), BENERVA (View Benerva Review and Benerva Label ), BECOZYME FORTE (View Becozyme Forte Review and Becozyme Forte Label ). Patient was hospitalized.

6738605-5 | Tendon Disorder
Adverse event was reported on May 14, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 20 Mg, 1x/day) was diagnosed with hyperlipidaemia and. Location: GERMANY , 55 years of age, weighting 229.0 lb, Patient experienced the following unwanted or unexpected effects: tendon disorder.

6736074-2 | Blood Creatinine Increased, Blood Urea Increased, Eczema, Erythema, Glomerular Filtration Rate Decreased, Haemoglobin Decreased, Myalgia, Pruritus, Red Blood Cell Count Decreased
on May 12, 2010 Male patient from GERMANY , 83 years of age, weighting 191.8 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient had the following side effects: blood creatinine increased, blood urea increased, eczema (What is eczema?), erythema, glomerular filtration rate decreased, haemoglobin decreased, myalgia, pruritus, red blood cell count decreased. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with CONCOR (10 Mg, Unk) (View Concor Review and Concor Label ), ACETYLSALICYLIC ACID (100 Mg, Unk) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), PROSCAR (Unk) (View Proscar Review and Proscar Label ).

6733307-3 | Polyneuropathy, Tarsal Tunnel Syndrome
on May 11, 2010 Male patient from GERMANY , 66 years of age, weighting 205.0 lb, was diagnosed with hyperlipidaemia, metabolic syndrome (What is metabolic syndrome?) and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: polyneuropathy, tarsal tunnel syndrome. Sortis dosage: 20 Mg, 1x/day.

6718206-5 | Neuropathy Peripheral, Paraesthesia
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: neuropathy peripheral, paraesthesia on May 01, 2010 from GERMANY Additional patient health information: Male patient , 66 years of age, weighting 167.6 lb, was diagnosed with type iia hyperlipidaemia and. Sortis dosage: 10 Mg, Alternate Day.

6717710-3 | Autonomic Nervous System Imbalance, Aversion, Decreased Appetite, Gastritis, Hernia, Nausea, Parosmia, Weight Decreased
Adverse event was reported on Apr 30, 2010 by a Female patient taking Sortis (View Usage) (Dosage: 10 Mg, Unk) was diagnosed with blood cholesterol increased, alpha-1 anti-trypsin deficiency and. Location: GERMANY , 68 years of age, weighting 134.5 lb, Patient had the following side effects: autonomic nervous system imbalance, aversion, decreased appetite, gastritis, hernia (What is hernia?), nausea (What is nausea?), parosmia, weight decreased. During the same period patient was treated with CORTISONE (Unk) (View Cortisone Review and Cortisone Label ), BERODUAL (Unk) (View Berodual Review and Berodual Label ).

6715043-2 | Haematoma, Myositis
on Apr 29, 2010 Male patient from GERMANY , 89 years of age, weighting 165.3 lb, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: haematoma, myositis (What is myositis?). Sortis dosage: 40 Mg, Unk.

6706912-8 | Retinal Detachment, Retinal Oedema, Visual Acuity Reduced
on Apr 23, 2010 Male patient from GERMANY , 60 years of age, weighting 185.2 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: retinal detachment, retinal oedema, visual acuity reduced. Sortis dosage: Unk. During the same period patient was treated with AMLODIPINE (Unk) (View Amlodipine Review and Amlodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6703835-5 | Back Pain, Intervertebral Disc Disorder
Patient was taking Sortis (View Usage). Patient had the following side effects: back pain (What is back pain?), intervertebral disc disorder on Apr 21, 2010 from GERMANY Additional patient health information: Male patient , 72 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: 20 Mg, Unk. During the same period patient was treated with ATACAND (Unk) (View Atacand Review and Atacand Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ).

6702600-2 | Blood Triglycerides Increased
Adverse event was reported on Apr 20, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 20 Mg/day) was diagnosed with hypercholesterolaemia, hypertension and. Location: GERMANY , 67 years of age, After Sortis was administered, patient had the following side effects: blood triglycerides increased. During the same period patient was treated with DELIX (View Delix Review and Delix Label ).

6688195-0 | Erectile Dysfunction
on Apr 11, 2010 Male patient from SWITZERLAND , 57 years of age, was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: erectile dysfunction (What is erectile dysfunction?). Sortis dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), TRIATEC (View Triatec Review and Triatec Label ), ISOPTIN (View Isoptin Review and Isoptin Label ).

6687190-5 | Bursitis, Hyperhidrosis, Myalgia, Type 2 Diabetes Mellitus
on Apr 09, 2010 Female patient from GERMANY , 75 years of age, weighting 156.5 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient had the following side effects: bursitis (What is bursitis?), hyperhidrosis, myalgia, type 2 diabetes mellitus. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with MARCUMAR (Unk) (View Marcumar Review and Marcumar Label ).

6687058-4 | Autonomic Nervous System Imbalance, Aversion, Decreased Appetite, Nausea, Parosmia, Weight Decreased
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: autonomic nervous system imbalance, aversion, decreased appetite, nausea (What is nausea?), parosmia, weight decreased on Apr 09, 2010 from GERMANY Additional patient health information: Female patient , 68 years of age, weighting 134.5 lb, was diagnosed with blood cholesterol increased, alpha-1 anti-trypsin deficiency and. Sortis dosage: 10 Mg, Unk. During the same period patient was treated with CORTISONE (Unk) (View Cortisone Review and Cortisone Label ), BERODUAL (Unk) (View Berodual Review and Berodual Label ).

6685153-7 | Muscle Atrophy, Muscle Contractions Involuntary, Muscle Spasms, Polyneuropathy
Adverse event was reported on Apr 08, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 40 Mg/day) was diagnosed with type iia hyperlipidaemia and. Location: GERMANY , 68 years of age, weighting 185.2 lb, Patient experienced the following unwanted or unexpected effects: muscle atrophy, muscle contractions involuntary, muscle spasms, polyneuropathy. During the same period patient was treated with MAGNESIUM (Unk) (View Magnesium Review and Magnesium Label ), LEVOTHYROXINE SODIUM (Unk) (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), ATACAND (Unk) (View Atacand Review and Atacand Label ).

6683913-X | Muscle Spasms, Withdrawal Syndrome
on Apr 06, 2010 Female patient from GERMANY , 43 years of age, weighting 169.8 lb, was diagnosed with hypercholesterolaemia, dyslipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: muscle spasms, withdrawal syndrome. Sortis dosage: 10 Mg/day.

6680024-4 | Lipoprotein (a) Increased
on Apr 08, 2010 Male patient from GERMANY , 48 years of age, was diagnosed with hypercholesterolaemia, vascular calcification and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: lipoprotein (a) increased. Sortis dosage: Unk.

6675148-1 | Intraocular Pressure Increased
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: intraocular pressure increased on Mar 31, 2010 from GERMANY Additional patient health information: Male patient , 75 years of age, was diagnosed with blood cholesterol increased, intraocular pressure increased, hypertension and. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with XALATAN (1 Gtt Bilaterally) (View Xalatan Review and Xalatan Label ), OLMESARTAN MEDOXOMIL (Unk) (View Olmesartan Medoxomil Review and Olmesartan Medoxomil Label ), CONCOR (View Concor Review and Concor Label ).

6675133-X | Blood Amylase Increased, C-reactive Protein Increased, Lipase Increased, Polymyalgia Rheumatica
Adverse event was reported on Mar 30, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 40 Mg, Unk) was diagnosed with hyperlipidaemia, osteoarthritis (What is osteoarthritis?), coronary artery disease (What is coronary artery disease?) and. Location: GERMANY , 69 years of age, weighting 163.1 lb, Patient had the following side effects: blood amylase increased, c-reactive protein increased, lipase increased, polymyalgia rheumatica (What is polymyalgia rheumatica?). During the same period patient was treated with IBUPROFEN TABLETS (600 Mg, Unk) (View Ibuprofen Tablets Review and Ibuprofen Tablets Label ), CONCOR (5 Mg Daily) (View Concor Review and Concor Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ).

6662238-2 | Blood Amylase Increased, C-reactive Protein Increased, Lipase Increased, Polymyalgia Rheumatica
on Mar 05, 2010 Male patient from GERMANY , 69 years of age, weighting 163.1 lb, was diagnosed with hyperlipidaemia, osteoarthritis (What is osteoarthritis?), coronary artery disease (What is coronary artery disease?) and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: blood amylase increased, c-reactive protein increased, lipase increased, polymyalgia rheumatica (What is polymyalgia rheumatica?). Sortis dosage: 40 Mg, Unk. During the same period patient was treated with IBUPROFEN (600 Mg, Unk) (View Ibuprofen Review and Ibuprofen Label ), CONCOR (5 Mg Daily) (View Concor Review and Concor Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ).

6636989-X | Retinal Detachment, Retinal Oedema, Visual Acuity Reduced
on Mar 08, 2010 Male patient from GERMANY , 60 years of age, weighting 185.2 lb, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: retinal detachment, retinal oedema, visual acuity reduced. Sortis dosage: Unk. During the same period patient was treated with AMLODIPINE (Unk) (View Amlodipine Review and Amlodipine Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6635204-0 | Blood Amylase Increased, C-reactive Protein Increased, Lipase Increased, Myalgia
Patient was taking Sortis (View Usage). Patient had the following side effects: blood amylase increased, c-reactive protein increased, lipase increased, myalgia on Mar 05, 2010 from GERMANY Additional patient health information: Male patient , 69 years of age, weighting 163.1 lb, was diagnosed with hyperlipidaemia, osteoarthritis (What is osteoarthritis?), coronary artery disease (What is coronary artery disease?) and. Sortis dosage: 40 Mg, Unk. During the same period patient was treated with IBUPROFEN (600 Mg, Unk) (View Ibuprofen Review and Ibuprofen Label ), CONCOR (5 Mg Daily) (View Concor Review and Concor Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ).