ZETIA Side Effects

7020817-7 | Liver Disorder
on Sep 21, 2010 Female patient from JAPAN , 55 years of age, was diagnosed with hypercholesterolaemia and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: liver disorder. Zetia dosage: . Patient was hospitalized.

7018625-6 | Coronary Artery Disease
Patient was taking Zetia (View Usage). Patient had the following side effects: coronary artery disease (What is coronary artery disease?) on Sep 22, 2010 from AUSTRIA Additional patient health information: Male patient , 78 years of age, weighting 158.7 lb, was diagnosed with coronary artery disease (What is coronary artery disease?) and. Zetia dosage: . During the same period patient was treated with LOVASTATIN (View Lovastatin Review and Lovastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

7015611-7 | Coronary Artery Disease, Muscle Spasms, Muscular Weakness, Myalgia
Adverse event was reported on Sep 20, 2010 by a Male patient taking Zetia (View Usage) (Dosage: ) was diagnosed with arthritis (What is arthritis?) and. Location: UNITED STATES , 65 years of age, After Zetia was administered, patient had the following side effects: coronary artery disease (What is coronary artery disease?), muscle spasms, muscular weakness, myalgia. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), CELEBREX (View Celebrex Review and Celebrex Label ), PLAVIX (View Plavix Review and Plavix Label ), TRICOR (View Tricor Review and Tricor Label ), METFORMIN (View Metformin Review and Metformin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AVODART (View Avodart Review and Avodart Label ).

7015607-5 | Dizziness, Facial Bones Fracture, Fall, Loss Of Consciousness
on Sep 15, 2010 Male patient from JAPAN , 42 years of age, was diagnosed with type iia hyperlipidaemia and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), facial bones fracture, fall (What is fall?), loss of consciousness. Zetia dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), URALYT (View Uralyt Review and Uralyt Label ), ALLORIN (View Allorin Review and Allorin Label ).


7010947-8 | Insomnia, Myalgia, Pain
on Sep 22, 2010 Female patient from UNITED STATES , 73 years of age, weighting 225.0 lb, was diagnosed with blood cholesterol increased and was treated with Zetia (View Usage). Patient had the following side effects: insomnia, myalgia, pain (What is pain?). Zetia dosage: .

7008693-X | Aphasia, Choking Sensation, Dysphonia, Foreign Body, Hypoaesthesia Oral, Tablet Issue
Patient was taking Zetia (View Usage). After Zetia was administered, patient had the following side effects: aphasia (What is aphasia?), choking sensation, dysphonia, foreign body, hypoaesthesia oral, tablet issue on Sep 17, 2010 from UNITED STATES Additional patient health information: Female patient , 92 years of age, was diagnosed with blood cholesterol and. Zetia dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), CELEBREX (View Celebrex Review and Celebrex Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ).

7006456-2 | Abdominal Discomfort, Diarrhoea, Limb Discomfort, Muscle Spasms, Nausea
Adverse event was reported on Sep 17, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) was diagnosed with blood cholesterol increased and. Location: GERMANY , 86 years of age, Patient experienced the following unwanted or unexpected effects: abdominal discomfort, diarrhoea, limb discomfort, muscle spasms, nausea (What is nausea?).

7006422-7 | Atrioventricular Block Complete
on Aug 30, 2010 Male patient from JAPAN , 85 years of age, was diagnosed with hypercholesterolaemia and was treated with Zetia (View Usage). Patient had the following side effects: atrioventricular block complete. Zetia dosage: 10 Mg/daily. During the same period patient was treated with MG OXIDE (View Mg Oxide Review and Mg Oxide Label ), DONEPEZIL HYDROCHLORIDE (View Donepezil Hydrochloride Review and Donepezil Hydrochloride Label ), ETHYL ICOSAPENTATE (View Ethyl Icosapentate Review and Ethyl Icosapentate Label ), GLIMEPIRIDE (View Glimepiride Review and Glimepiride Label ), PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), SOLIFENACIN SUCCINATE (View Solifenacin Succinate Review and Solifenacin Succinate Label ), TAMSULOSIN HYDROCHLORIDE (View Tamsulosin Hydrochloride Review and Tamsulosin Hydrochloride Label ). Patient was hospitalized.

7001882-X | Amnesia, Cardiac Flutter, Dysgraphia, Fatigue, Life Expectancy Shortened, Mental Impairment, Weight Increased
on Sep 13, 2010 Female patient from AUSTRALIA , 58 years of age, was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: amnesia, cardiac flutter, dysgraphia, fatigue, life expectancy shortened, mental impairment, weight increased. Zetia dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ).

7001868-5 | Abdominal Pain, Lipase Abnormal, Pancreatitis
Patient was taking Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), lipase abnormal, pancreatitis on Sep 13, 2010 from CANADA Additional patient health information: Male patient , 78 years of age, . Zetia dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ). Patient was hospitalized.

7001867-3 | Epistaxis, Platelet Count Decreased
Adverse event was reported on Sep 13, 2010 by a Male patient taking Zetia (View Usage) (Dosage: ) . Location: CANADA , 51 years of age, weighting 121.3 lb, Patient had the following side effects: epistaxis, platelet count decreased.

6989704-4 | Dehydration, Nausea, Syncope
on Sep 07, 2010 Female patient from JAPAN , 72 years of age, was diagnosed with hypercholesterolaemia and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: dehydration, nausea (What is nausea?), syncope. Zetia dosage: . During the same period patient was treated with LIPIDIL (View Lipidil Review and Lipidil Label ), PROMAC (View Promac Review and Promac Label ), TOUGHMAC E (View Toughmac E Review and Toughmac E Label ), ALINAMIN F (FURSULTIAMINE HYDROCHLORIDE) (View Alinamin F (fursultiamine Hydrochloride) Review and Alinamin F (fursultiamine Hydrochloride) Label ), JUVELA N (View Juvela N Review and Juvela N Label ), MERISLON (View Merislon Review and Merislon Label ), ISALON (View Isalon Review and Isalon Label ), NAUZELIN (View Nauzelin Review and Nauzelin Label ).

6981107-1 | Gingival Pain, Headache, Hypertonic Bladder, Mitral Valve Disease, Toothache
on Sep 02, 2010 Female patient from UNITED STATES , 72 years of age, weighting 160.9 lb, was diagnosed with mitral valve prolapse, blood cholesterol and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: gingival pain, headache (What is headache?), hypertonic bladder, mitral valve disease, toothache. Zetia dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), FIORICET (View Fioricet Review and Fioricet Label ).

6981094-6 | Renal Impairment
Patient was taking Zetia (View Usage). Patient had the following side effects: renal impairment on Sep 02, 2010 from JAPAN Additional patient health information: Female patient , 80 years of age, was diagnosed with hypercholesterolaemia and. Zetia dosage: . Patient was hospitalized.

6979601-2 | Thrombosis In Device
Adverse event was reported on Sep 02, 2010 by a Male patient taking Zetia (View Usage) (Dosage: ) . Location: CANADA , 48 years of age, weighting 231.5 lb, After Zetia was administered, patient had the following side effects: thrombosis in device. During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), PLAVIX (View Plavix Review and Plavix Label ), ASPIRINE (View Aspirine Review and Aspirine Label ). Patient was hospitalized.

6978949-5 | Dizziness, Fatigue, Headache, Muscular Weakness, Nystagmus, Pain In Extremity
on Sep 02, 2010 Female patient from CANADA , 61 years of age, weighting 136.7 lb, was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), fatigue, headache (What is headache?), muscular weakness, nystagmus, pain in extremity. Zetia dosage: . During the same period patient was treated with APO FUROSEMIDE (View Apo Furosemide Review and Apo Furosemide Label ), TRIMIPRAMINE (View Trimipramine Review and Trimipramine Label ), ASAPHEN (View Asaphen Review and Asaphen Label ), LITHIUM CARBONATE (View Lithium Carbonate Review and Lithium Carbonate Label ), DESYREL (View Desyrel Review and Desyrel Label ), DIAMICRON MR (View Diamicron Mr Review and Diamicron Mr Label ), ESTRACE (View Estrace Review and Estrace Label ), ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ).

6973452-0 | Dehydration, Pancreatitis Acute
on Sep 02, 2010 Male patient from CANADA , 69 years of age, weighting 180.8 lb, was treated with Zetia (View Usage). Patient had the following side effects: dehydration, pancreatitis acute. Zetia dosage: . During the same period patient was treated with ALTACE (View Altace Review and Altace Label ), BISOPROLOL COMP (View Bisoprolol Comp Review and Bisoprolol Comp Label ), PMS ASA (View Pms Asa Review and Pms Asa Label ), LASIX (View Lasix Review and Lasix Label ), LOPID (View Lopid Review and Lopid Label ), METFORMIN (View Metformin Review and Metformin Label ), PARIET (View Pariet Review and Pariet Label ). Patient was hospitalized.

6971792-2 | Pain In Extremity, Pruritus
Patient was taking Zetia (View Usage). After Zetia was administered, patient had the following side effects: pain in extremity, pruritus on Sep 03, 2010 from UNITED KINGDOM Additional patient health information: Male patient , 72 years of age, weighting 169.8 lb, was diagnosed with hypercholesterolaemia, hypertension and. Zetia dosage: . During the same period patient was treated with BENDROFLUMETHIAZIDE (View Bendroflumethiazide Review and Bendroflumethiazide Label ), BETAHISTINE (View Betahistine Review and Betahistine Label ), DOXAZOSIN MESYLATE (View Doxazosin Mesylate Review and Doxazosin Mesylate Label ), RAMIPRIL (View Ramipril Review and Ramipril Label ).

6971790-9 | Gait Disturbance, Myalgia, Peripheral Sensory Neuropathy
Adverse event was reported on Aug 31, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia and. Location: FRANCE , 69 years of age, Patient experienced the following unwanted or unexpected effects: gait disturbance, myalgia, peripheral sensory neuropathy. During the same period patient was treated with FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ). Patient was hospitalized.

6969029-3 | Myalgia
on Sep 03, 2010 Female patient from UNITED STATES , weighting 200.0 lb, was diagnosed with blood cholesterol increased and was treated with Zetia (View Usage). Patient had the following side effects: myalgia. Zetia dosage: 1 Tablet Daily.

6968731-7 | Gait Disturbance, Myalgia, Peripheral Sensory Neuropathy
on Aug 31, 2010 Female patient from FRANCE , 69 years of age, was diagnosed with hypercholesterolaemia and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: gait disturbance, myalgia, peripheral sensory neuropathy. Zetia dosage: . During the same period patient was treated with FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), ATORVASTATIN CALCIUM (View Atorvastatin Calcium Review and Atorvastatin Calcium Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ). Patient was hospitalized.

6968721-4 | Blood Disorder, Pain In Extremity
Patient was taking Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: blood disorder, pain in extremity on Aug 31, 2010 from UNITED STATES Additional patient health information: Female patient , 74 years of age, was diagnosed with blood cholesterol and. Zetia dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

6963265-8 | Hypokalaemia, Renal Failure Chronic
Adverse event was reported on Aug 27, 2010 by a Male patient taking Zetia (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia, angina pectoris, hypertension, prophylaxis and. Location: KOREA, REPUBLIC OF , 64 years of age, Patient had the following side effects: hypokalaemia, renal failure chronic. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), CARVEDILOL (View Carvedilol Review and Carvedilol Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ISOSORBIDE DINITRATE (View Isosorbide Dinitrate Review and Isosorbide Dinitrate Label ), CILOSTAZOL (View Cilostazol Review and Cilostazol Label ). Patient was hospitalized.

6955942-X | Liver Disorder
on Aug 23, 2010 Female patient from JAPAN , 55 years of age, was diagnosed with hypercholesterolaemia and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: liver disorder. Zetia dosage: .

6945635-7 | Abdominal Distension, Abdominal Pain Upper, Asthenia, Back Pain, Dandruff, Dark Circles Under Eyes, Diarrhoea, Dry Mouth, Fatigue
on Aug 18, 2010 Male patient from UNITED KINGDOM , 62 years of age, weighting 141.1 lb, was diagnosed with blood cholesterol abnormal, pruritus and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal distension, abdominal pain upper, asthenia, back pain (What is back pain?), dandruff, dark circles under eyes, diarrhoea, dry mouth, fatigue. Zetia dosage: . During the same period patient was treated with BETAMETHASONE (View Betamethasone Review and Betamethasone Label ), HYDROCORTISONE (View Hydrocortisone Review and Hydrocortisone Label ).

6943009-6 | Blood Disorder, Pain In Extremity
Patient was taking Zetia (View Usage). Patient had the following side effects: blood disorder, pain in extremity on Aug 19, 2010 from UNITED STATES Additional patient health information: Female patient , 74 years of age, was diagnosed with blood cholesterol and. Zetia dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

6939061-4 | Hepatic Function Abnormal, Interstitial Lung Disease
Adverse event was reported on Aug 12, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) was diagnosed with hypercholesterolaemia and. Location: JAPAN , 68 years of age, After Zetia was administered, patient had the following side effects: hepatic function abnormal, interstitial lung disease. During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ). Patient was hospitalized.

6938461-6 | Sepsis
on Aug 12, 2010 Male patient from PHILIPPINES , 67 years of age, was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: sepsis (What is sepsis?). Zetia dosage: Po. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), CLOPIDOGREL BISULFATE (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), ISOSORBIDE MONONITRATE (View Isosorbide Mononitrate Review and Isosorbide Mononitrate Label ), PERINDOPRIL (View Perindopril Review and Perindopril Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ). Patient was hospitalized.

6932487-4 | Blood Disorder, Pain In Extremity
on Aug 09, 2010 Female patient from UNITED STATES , 74 years of age, was diagnosed with blood cholesterol and was treated with Zetia (View Usage). Patient had the following side effects: blood disorder, pain in extremity. Zetia dosage: . During the same period patient was treated with COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

6928360-8 | Back Pain, Chest Pain, Depression, Dizziness, Dyspnoea, Headache, Musculoskeletal Pain, Myalgia, Pain In Extremity
Patient was taking Zetia (View Usage). After Zetia was administered, patient had the following side effects: back pain (What is back pain?), chest pain (What is chest pain?), depression (What is depression?), dizziness (What is dizziness?), dyspnoea, headache (What is headache?), musculoskeletal pain, myalgia, pain in extremity on Aug 12, 2010 from AUSTRALIA Additional patient health information: Female patient , 51 years of age, weighting 125.7 lb, was diagnosed with ldl/hdl ratio and. Zetia dosage: .

6925589-X | Convulsion, Rhabdomyolysis
Adverse event was reported on Aug 05, 2010 by a Male patient taking Zetia (View Usage) (Dosage: ) was diagnosed with dyslipidaemia and. Location: JAPAN , 50 years of age, Patient experienced the following unwanted or unexpected effects: convulsion, rhabdomyolysis. During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), FLOPROPIONE (View Flopropione Review and Flopropione Label ), METOCLOPRAMIDE (View Metoclopramide Review and Metoclopramide Label ), CAMOSTAT MESYLATE (View Camostat Mesylate Review and Camostat Mesylate Label ). Patient was hospitalized.

6917274-5 | Pancreatitis, Rhabdomyolysis
on Aug 04, 2010 Female patient from SPAIN , 76 years of age, was diagnosed with dyslipidaemia and was treated with Zetia (View Usage). Patient had the following side effects: pancreatitis, rhabdomyolysis. Zetia dosage: . During the same period patient was treated with TORSEMIDE (View Torsemide Review and Torsemide Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), FLUVASTATIN SODIUM (View Fluvastatin Sodium Review and Fluvastatin Sodium Label ). Patient was hospitalized.

6914643-4 | Abdominal Pain, Constipation, Deep Vein Thrombosis, Diarrhoea, Pelvic Pain
on Aug 03, 2010 Male patient from UNITED STATES , 71 years of age, weighting 231.5 lb, was diagnosed with hyperlipidaemia, coronary artery disease (What is coronary artery disease?) and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), constipation (What is constipation?), deep vein thrombosis (What is deep vein thrombosis?), diarrhoea, pelvic pain (What is pelvic pain?). Zetia dosage: . During the same period patient was treated with COZAAR (View Cozaar Review and Cozaar Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).

6911146-8 | Spinal Cord Haemorrhage
Patient was taking Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: spinal cord haemorrhage on Jul 27, 2010 from JAPAN Additional patient health information: Female patient , 50 years of age, . Zetia dosage: . Patient was hospitalized.

6911144-4 | Blood Cholesterol Increased, Limb Injury, Neuralgia, Pain, Post Thrombotic Syndrome, Pyelonephritis, Vascular Insufficiency
Adverse event was reported on Aug 02, 2010 by a Male patient taking Zetia (View Usage) (Dosage: Every P. M.) was diagnosed with blood cholesterol increased and. Location: UNITED STATES , 52 years of age, weighting 306.4 lb, Patient had the following side effects: blood cholesterol increased, limb injury, neuralgia, pain (What is pain?), post thrombotic syndrome, pyelonephritis, vascular insufficiency. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), SIMVASTATIN (Every P. M.) (View Simvastatin Review and Simvastatin Label ), NIASPAN (View Niaspan Review and Niaspan Label ), METFORMIN HYDROCHLORIDE (View Metformin Hydrochloride Review and Metformin Hydrochloride Label ), BYSTOLIC (View Bystolic Review and Bystolic Label ), BENAZEPRIL HYDROCHLORIDE (View Benazepril Hydrochloride Review and Benazepril Hydrochloride Label ).

6911141-9 | Aphasia, Choking Sensation, Dysphonia, Foreign Body, Hypoaesthesia Oral, Tablet Issue
on Jul 27, 2010 Female patient from UNITED STATES , 92 years of age, was diagnosed with blood cholesterol and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: aphasia (What is aphasia?), choking sensation, dysphonia, foreign body, hypoaesthesia oral, tablet issue. Zetia dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), AMITRIPTYLINE HYDROCHLORIDE (View Amitriptyline Hydrochloride Review and Amitriptyline Hydrochloride Label ), TOPROL XL (View Toprol-xl Review and Toprol-xl Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), CELEBREX (View Celebrex Review and Celebrex Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ).

6895281-9 | Coronary Artery Disease
on Jul 27, 2010 Male patient from AUSTRIA , 78 years of age, weighting 158.7 lb, was diagnosed with coronary artery disease (What is coronary artery disease?) and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: coronary artery disease (What is coronary artery disease?). Zetia dosage: . During the same period patient was treated with LOVASTATIN (View Lovastatin Review and Lovastatin Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

6882022-4 | Foot Operation, Unevaluable Event
Patient was taking Zetia (View Usage). Patient had the following side effects: foot operation, unevaluable event on Jul 28, 2010 from UNITED STATES Additional patient health information: Female patient , 52 years of age, weighting 170.0 lb, . Zetia dosage: .

6878483-7 | Oedema Peripheral, Pain In Extremity
Adverse event was reported on Jul 23, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) was diagnosed with dyslipidaemia and. Location: UNITED KINGDOM , 30 years of age, After Zetia was administered, patient had the following side effects: oedema peripheral, pain in extremity. During the same period patient was treated with SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ).

6877913-4 | Abdominal Discomfort, Abdominal Pain, Arthralgia, Asthenia, Bone Disorder, Dizziness, Fatigue, Foot Deformity, Gastrointestinal Motility Disorder
on Jul 22, 2010 Female patient from UNITED STATES , 49 years of age, weighting 176.4 lb, was diagnosed with blood cholesterol increased, gastrooesophageal reflux disease, adrenal disorder and was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, abdominal pain (What is abdominal pain?), arthralgia, asthenia, bone disorder, dizziness (What is dizziness?), fatigue, foot deformity, gastrointestinal motility disorder. Zetia dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), NEXIUM (View Nexium Review and Nexium Label ), PREDNISONE (View Prednisone Review and Prednisone Label ), ATACAND (View Atacand Review and Atacand Label ), VERELAN PM (View Verelan Pm Review and Verelan Pm Label ), PEPCID (View Pepcid Review and Pepcid Label ).

6877910-9 | Muscle Rupture
on Jul 22, 2010 Male patient from FRANCE , 83 years of age, was diagnosed with escherichia urinary tract infection and was treated with Zetia (View Usage). Patient had the following side effects: muscle rupture. Zetia dosage: . During the same period patient was treated with OFLOXACIN (View Ofloxacin Review and Ofloxacin Label ), NEBIVOLOL HYDROCHLORIDE (View Nebivolol Hydrochloride Review and Nebivolol Hydrochloride Label ), CANDESARTAN CILEXETIL (View Candesartan Cilexetil Review and Candesartan Cilexetil Label ), ASPIRIN LYSINE (View Aspirin Lysine Review and Aspirin Lysine Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ).

6876047-2 | Interstitial Lung Disease
Patient was taking Zetia (View Usage). After Zetia was administered, patient had the following side effects: interstitial lung disease on Jul 15, 2010 from JAPAN Additional patient health information: Male patient , 60 years of age, was diagnosed with hyperlipidaemia, hypertension and. Zetia dosage: . During the same period patient was treated with RASILEZ (View Rasilez Review and Rasilez Label ), SELOKEN (View Seloken Review and Seloken Label ).

6876044-7 | Hyperglycaemia
Adverse event was reported on Jul 22, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) . Location: SPAIN , 39 years of age, Patient experienced the following unwanted or unexpected effects: hyperglycaemia. During the same period patient was treated with ALPRAZOLAM (View Alprazolam Review and Alprazolam Label ), ROSUVASTATIN CALCIUM (View Rosuvastatin Calcium Review and Rosuvastatin Calcium Label ), CLOPIDOGREL BISULFATE (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), TORSEMIDE (View Torsemide Review and Torsemide Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), ASPIRIN (View Aspirin Review and Aspirin Label ).

6871491-1 | Platelet Count Decreased, Renal Impairment
on Jul 13, 2010 Female patient from JAPAN , 40 years of age, was treated with Zetia (View Usage). Patient had the following side effects: platelet count decreased, renal impairment. Zetia dosage: .

6871490-X | Agranulocytosis
on Jul 20, 2010 Male patient from FRANCE , 57 years of age, was diagnosed with dyslipidaemia, renal transplant, hypertension and was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: agranulocytosis. Zetia dosage: . During the same period patient was treated with MYCOPHENOLATE MOFETIL (View Mycophenolate Mofetil Review and Mycophenolate Mofetil Label ), TACROLIMUS (View Tacrolimus Review and Tacrolimus Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), BROMAZEPAM (View Bromazepam Review and Bromazepam Label ).

6864242-8 | Arthralgia, Coordination Abnormal, Fatigue, Myalgia, Paraesthesia
Patient was taking Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: arthralgia, coordination abnormal, fatigue, myalgia, paraesthesia on Jul 20, 2010 from NETHERLANDS Additional patient health information: Female patient , 55 years of age, weighting 158.7 lb, was diagnosed with hypercholesterolaemia and. Zetia dosage: .

6860809-1 | Dermatitis, Glaucoma, Hypersensitivity
Adverse event was reported on Jul 16, 2010 by a Female patient taking Zetia (View Usage) (Dosage: ) . Location: UNITED STATES , 73 years of age, Patient had the following side effects: dermatitis, glaucoma (What is glaucoma?), hypersensitivity. During the same period patient was treated with TIMOPTIC IN OCUDOSE (View Timoptic In Ocudose Review and Timoptic In Ocudose Label ), PRAVASTATIN SODIUM (View Pravastatin Sodium Review and Pravastatin Sodium Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LYSINE (View Lysine Review and Lysine Label ).

6848442-9 | Anaphylactic Shock
on Jul 01, 2010 Female patient from ISRAEL , 60 years of age, was treated with Zetia (View Usage). After Zetia was administered, patient had the following side effects: anaphylactic shock. Zetia dosage: .

6848421-1 | Anaphylactic Shock
on Jul 09, 2010 Female patient from ISRAEL , 60 years of age, was treated with Zetia (View Usage). Patient experienced the following unwanted or unexpected effects: anaphylactic shock. Zetia dosage: .

6843426-9 | Haemorrhagic Cerebral Infarction
Patient was taking Zetia (View Usage). Patient had the following side effects: haemorrhagic cerebral infarction on Jul 06, 2010 from PHILIPPINES Additional patient health information: Male patient , 48 years of age, . Zetia dosage: 10 Mg/daily Po. During the same period patient was treated with HUMALOG (View Humalog Review and Humalog Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CITICOLINE (View Citicoline Review and Citicoline Label ), CLOPIDOGREL BISULFATE (View Clopidogrel Bisulfate Review and Clopidogrel Bisulfate Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ).