SORTIS Side Effects

6633281-4 | Burning Sensation, Muscle Spasms, Peripheral Coldness
on Mar 04, 2010 Female patient from GERMANY , 72 years of age, was diagnosed with blood cholesterol increased, blood triglycerides increased and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: burning sensation, muscle spasms, peripheral coldness. Sortis dosage: Unk. During the same period patient was treated with APROVEL (Unk) (View Aprovel Review and Aprovel Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ), BISOPROLOL (Unk) (View Bisoprolol Review and Bisoprolol Label ).

6614211-8 | Blood Amylase Increased, Lipase Increased, Myalgia
Patient was taking Sortis (View Usage). Patient had the following side effects: blood amylase increased, lipase increased, myalgia on Feb 22, 2010 from GERMANY Additional patient health information: Male patient , 70 years of age, was diagnosed with lipids increased and. Sortis dosage: 40 Mg, Unk. During the same period patient was treated with ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6591277-5 | Palatal Disorder
Adverse event was reported on Feb 11, 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, After Sortis was administered, patient had the following side effects: palatal disorder.

6590829-6 | Liver Injury
on Feb 11, 2010 Female patient from SWITZERLAND , 88 years of age, was diagnosed with bronchopneumonia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: liver injury. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with LIQUAEMIN INJ (Unk) (View Liquaemin Inj Review and Liquaemin Inj Label ), TIENAM (500 Mg, 3x/day) (View Tienam Review and Tienam Label ), SINTROM (2 Mg, Unk) (View Sintrom Review and Sintrom Label ), METOPROLOL (Unk) (View Metoprolol Review and Metoprolol Label ), ZOLPIDEM (5 Mg, 1x/day) (View Zolpidem Review and Zolpidem Label ), PARACETAMOL (1 G, 1x/day) (View Paracetamol Review and Paracetamol Label ), PRIMPERAN TAB (10 Mg, 1x/day) (View Primperan Tab Review and Primperan Tab Label ), ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ). Patient was hospitalized.


6590828-4 | Pancreatitis Acute
on Feb 11, 2010 Male patient from ROMANIA , 51 years of age, weighting 205.0 lb, was diagnosed with dyslipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: pancreatitis acute. Sortis dosage: 40 Mg, 1x/day.

6590800-4 | Gamma-glutamyltransferase Increased
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: gamma-glutamyltransferase increased on Feb 09, 2010 from GERMANY Additional patient health information: Male patient , 69 years of age, weighting 154.3 lb, was diagnosed with blood cholesterol increased, hypertension and. Sortis dosage: 1/2 Of A 40 Mg Tablet/day. During the same period patient was treated with SIMVASTATIN (Unk) (View Simvastatin Review and Simvastatin Label ), RAMIPRIL (Unk) (View Ramipril Review and Ramipril Label ), METOPROLOL (Unk) (View Metoprolol Review and Metoprolol Label ).

6585102-6 | Blood Creatine Phosphokinase Mb Increased
Adverse event was reported on Feb 02, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 10 Mg/day) was diagnosed with hypercholesterolaemia and. Location: GERMANY , 62 years of age, weighting 163.1 lb, Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase mb increased. During the same period patient was treated with ASPIRIN (100) (View Aspirin Review and Aspirin Label ), FINASTERIDE (1 Mg, Unk) (View Finasteride Review and Finasteride Label ).

6582678-X | Dry Skin, Skin Exfoliation
on Feb 05, 2010 Male patient from SWITZERLAND , 72 years of age, was treated with Sortis (View Usage). Patient had the following side effects: dry skin, skin exfoliation. Sortis dosage: 40 Mg, 1x/day. During the same period patient was treated with ASPIRIN (100 Mg, 1x/day) (View Aspirin Review and Aspirin Label ), METFORMIN HYDROCHLORIDE (500 Mg, 2x/day) (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), NOCTAMID (2 Mg, 1x/day) (View Noctamid Review and Noctamid Label ), ZOLPIDEM (10 Mg, 1x/day) (View Zolpidem Review and Zolpidem Label ), COAPROVEL (300 Mg, 1x/day) (View Coaprovel Review and Coaprovel Label ).

6572710-1 | Decreased Appetite, Parosmia, Weight Decreased
on Jan 28, 2010 Female patient from GERMANY , weighting 132.0 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: decreased appetite, parosmia, weight decreased. 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 ).

6571965-7 | Musculoskeletal Discomfort, Tendonitis
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: musculoskeletal discomfort, tendonitis on Jan 27, 2010 from GERMANY Additional patient health information: Male patient , 49 years of age, weighting 196.2 lb, was diagnosed with blood cholesterol increased, type iia hyperlipidaemia and. Sortis dosage: 20 Mg, 1x/day.

6571432-0 | Blood Creatine Phosphokinase Mb Increased
Adverse event was reported on Jan 26, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 10 Mg/day) . Location: GERMANY , 61 years of age, Patient had the following side effects: blood creatine phosphokinase mb increased. During the same period patient was treated with ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ), FINASTERIDE (1 Mg, Unk) (View Finasteride Review and Finasteride Label ).

6568921-1 | Gamma-glutamyltransferase Increased
on Jan 22, 2010 Male patient from GERMANY , 69 years of age, weighting 154.3 lb, was diagnosed with blood cholesterol increased, hypertension and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: gamma-glutamyltransferase increased. Sortis dosage: 1/2 Of A 40 Mg Tablet/day. During the same period patient was treated with SIMVASTATIN (Unk) (View Simvastatin Review and Simvastatin Label ), RAMIPRIL (Unk) (View Ramipril Review and Ramipril Label ), METOPROLOL (Unk) (View Metoprolol Review and Metoprolol Label ).

6566229-1 | Gamma-glutamyltransferase Increased, Treatment Noncompliance
on Jan 22, 2010 Male patient from GERMANY , 69 years of age, weighting 154.3 lb, was diagnosed with blood cholesterol increased, hypertension and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: gamma-glutamyltransferase increased, treatment noncompliance. Sortis dosage: 1/2 Of A 40 Mg Tablet/day. During the same period patient was treated with SIMVASTATIN (Unk) (View Simvastatin Review and Simvastatin Label ), RAMIPRIL (Unk) (View Ramipril Review and Ramipril Label ), METOPROLOL (Unk) (View Metoprolol Review and Metoprolol Label ).

6558711-8 | Pancreatitis Acute
Patient was taking Sortis (View Usage). Patient had the following side effects: pancreatitis acute on Jan 21, 2010 from SWITZERLAND Additional patient health information: Female patient , 74 years of age, was diagnosed with hyperlipidaemia, prophylaxis, myocardial ischaemia and. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with ACETYLSALICYLIC ACID (100 Mg, 1x/day) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), COVERSUM (4 Mg, 1x/day) (View Coversum Review and Coversum Label ), BELOC ZOK (50 Mg, 1x/day) (View Beloc Zok Review and Beloc Zok Label ). Patient was hospitalized.

6556665-1 | Hepatitis, Inguinal Hernia Repair, Lymphadenopathy
Adverse event was reported on Jan 19, 2010 by a Male patient taking Sortis (View Usage) (Dosage: 40 Mg, 1x/day) was diagnosed with hypercholesterolaemia, mood altered, nervousness, alopecia, inguinal hernia repair and. Location: GERMANY , 60 years of age, weighting 128.0 lb, After Sortis was administered, patient had the following side effects: hepatitis (What is hepatitis?), inguinal hernia repair, lymphadenopathy. During the same period patient was treated with LAIF (600 Mg, As Needed, Irregularly, Approx. Twice Weekly) (View Laif Review and Laif Label ), PROPECIA (1.25 Mg, 1x/day) (View Propecia Review and Propecia Label ), DESFLURANE (Unk) (View Desflurane Review and Desflurane Label ), VALERIAN EXTRACT (Unk) (View Valerian Extract Review and Valerian Extract Label ). Patient was hospitalized.

6552383-4 | Blood Creatine Phosphokinase Increased, Muscle Atrophy, Myalgia, Neuritis
on Jan 19, 2010 Male patient from GERMANY , 57 years of age, weighting 176.0 lb, was diagnosed with arteriosclerosis, hyperlipidaemia, hypertension and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, muscle atrophy, myalgia, neuritis. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with KARVEA (Unk) (View Karvea Review and Karvea Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6547306-8 | Hepatitis, Jaundice Hepatocellular, Nausea
on Jan 14, 2010 Male patient from SWITZERLAND , 44 years of age, weighting 183.0 lb, was diagnosed with hyperlipidaemia, type 1 diabetes mellitus and was treated with Sortis (View Usage). Patient had the following side effects: hepatitis (What is hepatitis?), jaundice hepatocellular, nausea (What is nausea?). Sortis dosage: 80 Mg, 1x/day. During the same period patient was treated with METFORMIN HYDROCHLORIDE (1000 Mg, 3x/day) (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), DAFALGAN (1 G, 2x/day) (View Dafalgan Review and Dafalgan Label ), LANTUS (40 Iu, Unk) (View Lantus Review and Lantus Label ), NOVORAPID (8 Iu, Unk) (View Novorapid Review and Novorapid Label ). Patient was hospitalized.

6545505-2 | Musculoskeletal Discomfort, Tendonitis
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: musculoskeletal discomfort, tendonitis on Jan 13, 2010 from GERMANY Additional patient health information: Male patient , 40 years of age, was diagnosed with blood cholesterol increased, type iia hyperlipidaemia and. Sortis dosage: 20 Mg, 1x/day.

6522133-6 | Hepatocellular Injury, International Normalised Ratio Increased
Adverse event was reported on Dec 16, 2009 by a Female patient taking Sortis (View Usage) (Dosage: 20 Mg, 1x/day) was diagnosed with hypercholesterolaemia, essential hypertension, restlessness, agitation, dementia alzheimer's type and. Location: SWITZERLAND , 82 years of age, Patient experienced the following unwanted or unexpected effects: hepatocellular injury, international normalised ratio increased. During the same period patient was treated with ALDACTONE (25 Mg, 1x/day) (View Aldactone Review and Aldactone Label ), SEROQUEL (5 Mg, 1x/day) (View Seroquel Review and Seroquel Label ), PANTOPRAZOLE (40 Mg, 1x/day) (View Pantoprazole Review and Pantoprazole Label ), MEMANTINE HYDROCHLORIDE (10 Mg, 1x/day) (View Memantine Hydrochloride Review and Memantine Hydrochloride Label ), DAFALGAN (500 Mg, 3x/day) (View Dafalgan Review and Dafalgan Label ), BELOC (25 Mg, 2x/day) (View Beloc Review and Beloc Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ).

6518744-4 | Muscle Atrophy, Muscle Contractions Involuntary, Neuropathy Peripheral
on Dec 21, 2009 Male patient from GERMANY , 68 years of age, was diagnosed with type iia hyperlipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: muscle atrophy, muscle contractions involuntary, neuropathy peripheral. Sortis dosage: 20 Mg/day. During the same period patient was treated with MAGNESIUM (View Magnesium Review and Magnesium Label ), L THYROXIN (View L-thyroxin Review and L-thyroxin Label ).

6506003-5 | Pancreatitis Acute
on Dec 10, 2009 Female patient from SWITZERLAND , 74 years of age, was diagnosed with hyperlipidaemia, myocardial ischaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: pancreatitis acute. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with ACETYLSALICYLIC ACID (100 Mg, 1x/day) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ), COVERSUM (4 Mg, 1x/day) (View Coversum Review and Coversum Label ), BELOC ZOK (50 Mg, 1x/day) (View Beloc Zok Review and Beloc Zok Label ). Patient was hospitalized.

6490874-5 | Blood Creatine Phosphokinase Increased, Muscle Atrophy, Myalgia
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, muscle atrophy, myalgia on Dec 11, 2009 from GERMANY Additional patient health information: Male patient , 57 years of age, was diagnosed with carotid artery stenosis, hypertension and. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with KARVEA (Unk) (View Karvea Review and Karvea Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6477696-6 | Polyneuropathy
Adverse event was reported on Nov 25, 2009 by a Male patient taking Sortis (View Usage) (Dosage: ) . Location: SWITZERLAND , 66 years of age, Patient had the following side effects: polyneuropathy.

6475556-8 | Hepatocellular Injury, Jaundice
on Nov 26, 2009 Female patient from SWITZERLAND , 52 years of age, weighting 169.8 lb, was diagnosed with type 2 diabetes mellitus and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: hepatocellular injury, jaundice (What is jaundice?). Sortis dosage: Unk. During the same period patient was treated with GALVUS (50 Mg, 1x/day) (View Galvus Review and Galvus Label ), METOPROLOL SUCCINATE (50 Mg, 1x/day) (View Metoprolol Succinate Review and Metoprolol Succinate Label ), LISINOPRIL (10 Mg, 1x/day) (View Lisinopril Review and Lisinopril Label ), OMEPRAZOLE (20 Mg, 1x/day) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

6470395-6 | Cataract, Dementia Alzheimer's Type
on Nov 23, 2009 Female patient from AUSTRIA , 86 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: cataract (What is cataract?), dementia alzheimer's type. Sortis dosage: Unk. During the same period patient was treated with ADALAT (Unk) (View Adalat Review and Adalat Label ).

6467095-5 | Blood Creatine Phosphokinase Increased, Muscle Atrophy
Patient was taking Sortis (View Usage). Patient had the following side effects: blood creatine phosphokinase increased, muscle atrophy on Nov 30, 2009 from GERMANY Additional patient health information: Female patient , 59 years of age, was diagnosed with hypertension and. Sortis dosage: . During the same period patient was treated with MICARDIS (Unk) (View Micardis Review and Micardis Label ). Patient was hospitalized and became disabled.

6462445-8 | Asphyxia, Blister, Dyspnoea, Face Oedema, Localised Oedema, Malaise, Oedema Mouth, Oedema Peripheral, Rash
Adverse event was reported on Nov 20, 2009 by a Female patient taking Sortis (View Usage) (Dosage: Unk) was diagnosed with hyperlipidaemia and. Location: CROATIA (local name: Hrvatska) , 64 years of age, After Sortis was administered, patient had the following side effects: asphyxia, blister, dyspnoea, face oedema, localised oedema, malaise, oedema mouth, oedema peripheral, rash (What is rash?). During the same period patient was treated with NORVASC (Unk) (View Norvasc Review and Norvasc Label ), CLOPIDOGREL (Unk) (View Clopidogrel Review and Clopidogrel Label ), CONCOR (Unk) (View Concor Review and Concor Label ), IRUMED (Unk) (View Irumed Review and Irumed Label ), IRUZID (Unk) (View Iruzid Review and Iruzid Label ), FURSEMID (Unk) (View Fursemid Review and Fursemid Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ).

6452824-7 | Dysarthria
on Nov 16, 2009 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. Sortis dosage: 10 Mg Per 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 ).

6452774-6 | Asphyxia, Blister, Dyspnoea, Face Oedema, Localised Oedema, Malaise, Oedema Mouth, Oedema Peripheral, Rash
on Nov 18, 2009 Female patient from CROATIA (local name: Hrvatska) , 64 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: asphyxia, blister, dyspnoea, face oedema, localised oedema, malaise, oedema mouth, oedema peripheral, rash (What is rash?). Sortis dosage: Unk. During the same period patient was treated with NORVASC (Unk) (View Norvasc Review and Norvasc Label ), CLOPIDOGREL (Unk) (View Clopidogrel Review and Clopidogrel Label ), CONCOR (Unk) (View Concor Review and Concor Label ), IRUMED (Unk) (View Irumed Review and Irumed Label ), IRUZID (Unk) (View Iruzid Review and Iruzid Label ), FURSEMID (Unk) (View Fursemid Review and Fursemid Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ).

6448912-1 | Cataract, Dementia Alzheimer's Type
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: cataract (What is cataract?), dementia alzheimer's type on Nov 10, 2009 from AUSTRIA Additional patient health information: Female patient , 86 years of age, . Sortis dosage: Unk. During the same period patient was treated with ADALAT (Unk) (View Adalat Review and Adalat Label ).

6440051-9 | Aspartate Aminotransferase Increased, Blood Creatine Phosphokinase Increased, Blood Lactate Dehydrogenase Increased, Gamma-glutamyltransferase Increased, Haemolysis
Adverse event was reported on Nov 02, 2009 by a Female patient taking Sortis (View Usage) (Dosage: 10 Mg, 1x/day) was diagnosed with hypercholesterolaemia, coronary artery disease (What is coronary artery disease?) and. Location: GERMANY , weighting 163.1 lb, Patient experienced the following unwanted or unexpected effects: aspartate aminotransferase increased, blood creatine phosphokinase increased, blood lactate dehydrogenase increased, gamma-glutamyltransferase increased, haemolysis. During the same period patient was treated with EZETROL (Unk) (View Ezetrol Review and Ezetrol Label ), NOVODIGAL (Unk) (View Novodigal Review and Novodigal Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6437920-2 | Muscle Atrophy, Muscle Contractions Involuntary, Neuropathy Peripheral
on Nov 04, 2009 Male patient from GERMANY , 68 years of age, was diagnosed with type iia hyperlipidaemia and was treated with Sortis (View Usage). Patient had the following side effects: muscle atrophy, muscle contractions involuntary, neuropathy peripheral. Sortis dosage: 20 Mg/day. During the same period patient was treated with MAGNESIUM (View Magnesium Review and Magnesium Label ), L THYROXIN (View L-thyroxin Review and L-thyroxin Label ).

6425470-9 | Blood Creatine Phosphokinase Increased, Muscle Atrophy, Myalgia
on Oct 27, 2009 Male patient from GERMANY , 57 years of age, was diagnosed with carotid artery stenosis, hypertension and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: blood creatine phosphokinase increased, muscle atrophy, myalgia. Sortis dosage: 20 Mg, 1x/day. During the same period patient was treated with KARVEA (Unk) (View Karvea Review and Karvea Label ), ASPIRIN (Unk) (View Aspirin Review and Aspirin Label ).

6409011-8 | Blood Creatine Phosphokinase Increased, Muscle Atrophy
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine phosphokinase increased, muscle atrophy on Oct 15, 2009 from GERMANY Additional patient health information: Female patient , 59 years of age, was diagnosed with hypertension and. Sortis dosage: . During the same period patient was treated with MICARDIS (Unk) (View Micardis Review and Micardis Label ). Patient was hospitalized and became disabled.

6402036-8 | Restless Legs Syndrome, Sleep Apnoea Syndrome
Adverse event was reported on Oct 09, 2009 by a Female patient taking Sortis (View Usage) (Dosage: Unk) . Location: SWITZERLAND , 62 years of age, Patient had the following side effects: restless legs syndrome, sleep apnoea syndrome. During the same period patient was treated with LESCOL (Unk) (View Lescol Review and Lescol Label ), EZETROL (View Ezetrol Review and Ezetrol Label ).

6359953-7 | Polyneuropathy
on Sep 10, 2009 Female patient from GERMANY , 81 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: polyneuropathy. Sortis dosage: 20 Mg, Unk.

6355614-9 | Anxiety, Dyspnoea, Eyelid Oedema, Laryngeal Oedema, Lip Oedema, Oedema Peripheral
on Aug 31, 2009 Female patient from ROMANIA , 54 years of age, was diagnosed with mixed hyperlipidaemia, essential hypertension, loss of consciousness, ischaemic cardiomyopathy and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), dyspnoea, eyelid oedema, laryngeal oedema, lip oedema, oedema peripheral. Sortis dosage: 10 Mg, 1x/day. During the same period patient was treated with METOPROLOL TARTRATE (1 Df, 1x/day) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), SERMION (1 Df, 1x/day) (View Sermion Review and Sermion Label ), ACETYLSALICYLIC ACID (1 Df, 1x/day) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ).

6344182-3 | Restless Legs Syndrome, Sleep Apnoea Syndrome
Patient was taking Sortis (View Usage). Patient had the following side effects: restless legs syndrome, sleep apnoea syndrome on Aug 25, 2009 from SWITZERLAND Additional patient health information: Female patient , 62 years of age, . Sortis dosage: Unk. During the same period patient was treated with LESCOL (Unk) (View Lescol Review and Lescol Label ), EZETROL (View Ezetrol Review and Ezetrol Label ).

6343943-4 | Fall, Tendon Injury, Tendon Rupture
Adverse event was reported on Aug 27, 2009 by a Female patient taking Sortis (View Usage) (Dosage: 10 Mg/day) was diagnosed with hypercholesterolaemia and. Location: GERMANY , 64 years of age, After Sortis was administered, patient had the following side effects: fall (What is fall?), tendon injury, tendon rupture. Patient was hospitalized.

6338128-1 | Blood Test Abnormal, Gammopathy
on Aug 25, 2009 Female patient from GERMANY , 48 years of age, was diagnosed with dyslipidaemia and was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: blood test abnormal, gammopathy. Sortis dosage: 10 Mg, 1x/day.

6331470-X | Fall, Tendon Injury, Tendon Rupture
on Aug 19, 2009 Female patient from GERMANY , 64 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). Patient had the following side effects: fall (What is fall?), tendon injury, tendon rupture. Sortis dosage: 10 Mg/day. Patient was hospitalized.

6318318-4 | Meniere's Disease, Sudden Hearing Loss
Patient was taking Sortis (View Usage). After Sortis was administered, patient had the following side effects: meniere's disease (What is meniere's disease?), sudden hearing loss on Aug 12, 2009 from GERMANY Additional patient health information: Female patient , 73 years of age, was diagnosed with diabetes mellitus, prostatic disorder and. Sortis dosage: 20 Mg/day. During the same period patient was treated with PENTOXIFYLLINE (View Pentoxifylline Review and Pentoxifylline Label ), NOVONORM (View Novonorm Review and Novonorm Label ), AVANDIA (View Avandia Review and Avandia Label ), TAMSULOSIN (View Tamsulosin Review and Tamsulosin Label ).

6316457-5 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Gamma-glutamyltransferase Increased
Adverse event was reported on Aug 12, 2009 by a Female patient taking Sortis (View Usage) (Dosage: 80 Mg, 1x/day) was diagnosed with carotid arteriosclerosis and. Location: SWITZERLAND , 72 years of age, Patient experienced the following unwanted or unexpected effects: alanine aminotransferase increased, aspartate aminotransferase increased, gamma-glutamyltransferase increased.

6309854-5 | Meniere's Disease, Sudden Hearing Loss
on Aug 06, 2009 Female patient from GERMANY , 73 years of age, was treated with Sortis (View Usage). Patient had the following side effects: meniere's disease (What is meniere's disease?), sudden hearing loss. Sortis dosage: 20 Mg/day. During the same period patient was treated with PENTOXIFYLLINE (View Pentoxifylline Review and Pentoxifylline Label ).

6309819-3 | Fall, Tendon Injury, Tendon Rupture
on Aug 05, 2009 Female patient from GERMANY , 64 years of age, was diagnosed with hypercholesterolaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: fall (What is fall?), tendon injury, tendon rupture. Sortis dosage: 10 Mg/day. Patient was hospitalized.

6305982-9 | Muscle Disorder
Patient was taking Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: muscle disorder (What is muscle disorder?) on Aug 12, 2009 from AUSTRIA Additional patient health information: Female patient , 64 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: 40 Mg, Unk.

6303987-5 | Hypoacusis, Myalgia, Paraesthesia, Parosmia, Polyneuropathy, Visual Impairment
Adverse event was reported on Jul 31, 2009 by a Female patient taking Sortis (View Usage) (Dosage: 10 Mg, 1x/day) . Location: SWITZERLAND , 75 years of age, Patient had the following side effects: hypoacusis, myalgia, paraesthesia, parosmia, polyneuropathy, visual impairment. During the same period patient was treated with PANTOZOL (40 Mg, 1x/day) (View Pantozol Review and Pantozol Label ), ACETYLSALICYLIC ACID (100 Mg, 1x/day) (View Acetylsalicylic Acid Review and Acetylsalicylic Acid Label ). Patient was hospitalized and became disabled.

6300816-0 | Polyneuropathy
on Jul 27, 2009 Female patient from GERMANY , 81 years of age, was diagnosed with hyperlipidaemia and was treated with Sortis (View Usage). After Sortis was administered, patient had the following side effects: polyneuropathy. Sortis dosage: 20 Mg, Unk.

6274015-5 | Polyneuropathy
on Jul 10, 2009 Female patient from GERMANY , 81 years of age, was treated with Sortis (View Usage). Patient experienced the following unwanted or unexpected effects: polyneuropathy. Sortis dosage: 20 Mg, Unk.

6268465-0 | Acute Myocardial Infarction, High Density Lipoprotein Decreased
Patient was taking Sortis (View Usage). Patient had the following side effects: acute myocardial infarction, high density lipoprotein decreased on Jul 07, 2009 from HUNGARY Additional patient health information: Female patient , 53 years of age, was diagnosed with hypercholesterolaemia and. Sortis dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), FUROSEMID (View Furosemid Review and Furosemid Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ), PLAVIX (View Plavix Review and Plavix Label ).