LOPRESSOR Side Effects

5727342-1 | Anaemia, Asthenia, Dizziness, Duodenal Ulcer, Haematemesis, Mallory-weiss Syndrome, Syncope
on Apr 25, 2008 Male patient from UNITED STATES , weighting 210.1 lb, was diagnosed with myocardial infarction and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, asthenia, dizziness (What is dizziness?), duodenal ulcer, haematemesis, mallory-weiss syndrome, syncope. Lopressor dosage: Unk. During the same period patient was treated with NIASPAN (Unk) (View Niaspan Review and Niaspan Label ), ZOCOR (Unk) (View Zocor Review and Zocor Label ), PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5722941-5 | Blood Pressure Decreased, Dyspnoea, Dystonia, Ill-defined Disorder
Patient was taking Lopressor (View Usage). Patient had the following side effects: blood pressure decreased, dyspnoea, dystonia (What is dystonia?), ill-defined disorder on Apr 29, 2008 from UNITED STATES Additional patient health information: Male patient , weighting 180.0 lb, . Lopressor dosage: . During the same period patient was treated with DILAUDID (View Dilaudid Review and Dilaudid Label ), PHENERGAN (View Phenergan Review and Phenergan Label ), NARCAN (View Narcan Review and Narcan Label ).

5694437-0 | Chest Discomfort, Chest Pain, Cough, Dyspnoea, Headache, Hyperhidrosis, Hypoaesthesia, Paraesthesia, Syncope
Adverse event was reported on Mar 25, 2008 by a Male patient taking Lopressor (View Usage) (Dosage: ) . Location: UNITED STATES , 59 years of age, After Lopressor was administered, patient had the following side effects: chest discomfort, chest pain (What is chest pain?), cough, dyspnoea, headache (What is headache?), hyperhidrosis, hypoaesthesia, paraesthesia, syncope. During the same period patient was treated with COREG (View Coreg Review and Coreg Label ), MIRAPEX (View Mirapex Review and Mirapex Label ), ZETIA (View Zetia Review and Zetia Label ), ZANTAC (View Zantac Review and Zantac Label ), NEXIUM (View Nexium Review and Nexium Label ), NORVASC (View Norvasc Review and Norvasc Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), AMBIEN (View Ambien Review and Ambien Label ). Patient was hospitalized.

5681036-X | Alopecia, Myocardial Infarction, Stent Placement
on Mar 19, 2008 Male patient from UNITED STATES , 51 years of age, was diagnosed with myocardial infarction and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: alopecia, myocardial infarction, stent placement. Lopressor dosage: 25 Mg, Bid. During the same period patient was treated with CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), CRESTOR (View Crestor Review and Crestor Label ), ASPIRIN (81 Mg, Unk) (View Aspirin Review and Aspirin Label ), AMBIEN (View Ambien Review and Ambien Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).


5680212-X | Alopecia, Myocardial Infarction, Stent Placement
on Mar 19, 2008 Male patient from UNITED STATES , 51 years of age, was diagnosed with myocardial infarction and was treated with Lopressor (View Usage). Patient had the following side effects: alopecia, myocardial infarction, stent placement. Lopressor dosage: 25 Mg, Bid. During the same period patient was treated with CENTRUM SILVER (View Centrum Silver Review and Centrum Silver Label ), CRESTOR (View Crestor Review and Crestor Label ), ASPIRIN (81 Mg, Unk) (View Aspirin Review and Aspirin Label ), AMBIEN (View Ambien Review and Ambien Label ), ALBUTEROL (View Albuterol Review and Albuterol Label ).

5659676-3 | Nausea
Patient was taking Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: nausea (What is nausea?) on Mar 10, 2008 from UNITED STATES Additional patient health information: Female patient , 70 years of age, weighting 198.0 lb, was diagnosed with angina pectoris, hypertension and. Lopressor dosage: 50mg Bid Po.

5635924-0 | Beta 2 Microglobulin Urine Increased, Blood Creatinine Increased, Renal Tubular Disorder
Adverse event was reported on Feb 15, 2008 by a Female patient taking Lopressor (View Usage) (Dosage: 50 Mg/day) was diagnosed with blood iron abnormal and. Location: ITALY , 17 years of age, Patient experienced the following unwanted or unexpected effects: beta 2 microglobulin urine increased, blood creatinine increased, renal tubular disorder. During the same period patient was treated with FOLINA (15 Mg/d) (View Folina Review and Folina Label ), EXJADE (1000 Mg/day) (View Exjade Review and Exjade Label ).

5613136-4 | Asthenia, Blood Pressure Decreased, Bradycardia, Hyperhidrosis, Hypotension, Loss Of Consciousness, Nervous System Disorder, Presyncope
on Feb 01, 2008 Male patient from UNITED STATES , 70 years of age, weighting 223.0 lb, was diagnosed with arterial occlusive disease, diabetes mellitus, transient ischaemic attack, hypertension, dyslipidaemia and was treated with Lopressor (View Usage). Patient had the following side effects: asthenia, blood pressure decreased, bradycardia, hyperhidrosis, hypotension, loss of consciousness, nervous system disorder, presyncope. Lopressor dosage: 25 Mg, Bid. During the same period patient was treated with GLUCOPHAGE (500 Mg, Qd) (View Glucophage Review and Glucophage Label ), PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label ), FOSINOPRIL SODIUM (40) (View Fosinopril Sodium Review and Fosinopril Sodium Label ), ZOCOR (20 Mg, Qd) (View Zocor Review and Zocor Label ), LEXAPRO (View Lexapro Review and Lexapro Label ), HYDROCHLOROTHIAZIDE (25 Mg, Qd) (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), SERTRALINE (50 Mg, Unk) (View Sertraline Review and Sertraline Label ), LISINOPRIL AND HYDROCHLOROTHIAZIDE (20/12.5 Mg Qd) (View Lisinopril And Hydrochlorothiazide Review and Lisinopril And Hydrochlorothiazide Label ). Patient was hospitalized.

5612147-2 | Blood Pressure Decreased, Bradycardia, Hyperhidrosis, Loss Of Consciousness, Presyncope
on Jan 29, 2008 Male patient from UNITED STATES , 70 years of age, weighting 229.3 lb, was diagnosed with arterial occlusive disease, transient ischaemic attack, hypertension, dyslipidaemia and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: blood pressure decreased, bradycardia, hyperhidrosis, loss of consciousness, presyncope. Lopressor dosage: 25 Mg, Bid. During the same period patient was treated with GLUCOPHAGE (View Glucophage Review and Glucophage Label ), PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label ), FOSINOPRIL W/HYDROCHLOROTHIAZIDE (20/12.5 Mg, Qd) (View Fosinopril W/hydrochlorothiazide Review and Fosinopril W/hydrochlorothiazide Label ), ZOCOR (20 Mg, Qd) (View Zocor Review and Zocor Label ), LEXAPRO (View Lexapro Review and Lexapro Label ). Patient was hospitalized.

5599561-9 | Multiple Sclerosis, Paraesthesia, Tachycardia, Underweight
Patient was taking Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: multiple sclerosis (What is multiple sclerosis?), paraesthesia, tachycardia, underweight on Jan 15, 2008 from CANADA Additional patient health information: Female patient , 48 years of age, weighting 99.98 lb, was diagnosed with tachycardia and. Lopressor dosage: 50 Mg, Bid.

5583839-9 | Acute Coronary Syndrome, Angina Pectoris, Angina Unstable, Arteriogram Coronary Abnormal, Blood Creatinine Increased, Bradycardia, Coronary Artery Bypass, Coronary Artery Disease, Dizziness
Adverse event was reported on Jan 03, 2008 by a Male patient taking Lopressor (View Usage) (Dosage: 50 Mg, Bid) was diagnosed with hypertension, acute coronary syndrome, atrial fibrillation (What is atrial fibrillation?), diabetes mellitus and. Location: UNITED STATES , 68 years of age, weighting 227.1 lb, Patient had the following side effects: acute coronary syndrome, angina pectoris, angina unstable, arteriogram coronary abnormal, blood creatinine increased, bradycardia, coronary artery bypass (What is coronary artery bypass?), coronary artery disease (What is coronary artery disease?), dizziness (What is dizziness?). During the same period patient was treated with EPTIFIBATIDE (9 Ml, Once2sdo) (View Eptifibatide Review and Eptifibatide Label ), AMIODARONE HCL (200 Mg, Qd) (View Amiodarone Hcl Review and Amiodarone Hcl Label ), METFORMIN HCL (850 Mg, Bid) (View Metformin Hcl Review and Metformin Hcl Label ), OMEPRAZOLE (Unk, Unk) (View Omeprazole Review and Omeprazole Label ), ASPIRIN (Unk, Unk) (View Aspirin Review and Aspirin Label ), HEPARIN (Unk, Unk) (View Heparin Review and Heparin Label ), CLONIDINE (Unk, Unk) (View Clonidine Review and Clonidine Label ). Patient was hospitalized.

5577658-7 | Multiple Sclerosis, Paraesthesia, Tachycardia, Underweight
on Dec 21, 2007 Female patient from CANADA , 48 years of age, weighting 99.98 lb, was diagnosed with tachycardia and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: multiple sclerosis (What is multiple sclerosis?), paraesthesia, tachycardia, underweight. Lopressor dosage: 50 Mg, Bid.

5564302-8 | Anaemia, Bacteraemia, Blood Calcium Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Decreased, Blood Phosphorus Increased, Blood Urea Increased, Confusional State, Dialysis
on Dec 12, 2007 Male patient from UNITED STATES , 72 years of age, weighting 154.0 lb, was diagnosed with hypertension and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, bacteraemia, blood calcium increased, blood creatinine increased, blood lactate dehydrogenase decreased, blood phosphorus increased, blood urea increased, confusional state, dialysis (What is dialysis?). Lopressor dosage: 25mg Bid. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), COZAAR (100mg Qd) (View Cozaar Review and Cozaar Label ), NORVASC (10mg Qd) (View Norvasc Review and Norvasc Label ), DAILY VITE (View Daily-vite Review and Daily-vite Label ), PHOSLO (View Phoslo Review and Phoslo Label ), ZEMPLAR (4mcgiv Push) (View Zemplar Review and Zemplar Label ), RENAGEL (2tabs With Snacks, Meals) (View Renagel Review and Renagel Label ).

5545290-7 | Anaemia, Bacteraemia, Blood Calcium Increased, Blood Creatinine Increased, Blood Lactate Dehydrogenase Decreased, Blood Phosphorus Increased, Blood Urea Increased, Confusional State, Dialysis
Patient was taking Lopressor (View Usage). Patient had the following side effects: anaemia, bacteraemia, blood calcium increased, blood creatinine increased, blood lactate dehydrogenase decreased, blood phosphorus increased, blood urea increased, confusional state, dialysis (What is dialysis?) on Dec 05, 2007 from UNITED STATES Additional patient health information: Male patient , 72 years of age, was diagnosed with hypertension and. Lopressor dosage: 25mg Bid. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), COZAAR (100mg Qd) (View Cozaar Review and Cozaar Label ), NORVASC (10mg Qd) (View Norvasc Review and Norvasc Label ), DAILY VITE (View Daily-vite Review and Daily-vite Label ), PHOSLO (View Phoslo Review and Phoslo Label ), ZEMPLAR (4mcgiv Push) (View Zemplar Review and Zemplar Label ), RENAGEL (2tabs With Snacks, Meals) (View Renagel Review and Renagel Label ).

5502597-7 | Obliterative Bronchiolitis, Pneumonia
Adverse event was reported on Oct 22, 2007 by a Female patient taking Lopressor (View Usage) (Dosage: 100 Mg/day) was diagnosed with supraventricular tachycardia and. Location: GERMANY , 82 years of age, After Lopressor was administered, patient had the following side effects: obliterative bronchiolitis, pneumonia (What is pneumonia?). During the same period patient was treated with AMIODARONE (View Amiodarone Review and Amiodarone Label ), TORVAST (View Torvast Review and Torvast Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.

5492778-3 | Abdominal Pain, Arthralgia, Arthritis, Collagen-vascular Disease, Decreased Appetite, Diarrhoea, Dyspepsia, Haematuria, Narcolepsy
on Oct 15, 2007 Male patient from UNITED STATES , 17 years of age, weighting 133.8 lb, was diagnosed with iron overload, sickle cell anaemia, cerebrovascular accident, convulsion and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), arthralgia, arthritis (What is arthritis?), collagen-vascular disease, decreased appetite, diarrhoea, dyspepsia, haematuria, narcolepsy. Lopressor dosage: . During the same period patient was treated with EXJADE (1500mg, Qd) (View Exjade Review and Exjade Label ), DEMEROL (View Demerol Review and Demerol Label ), BACTRIM (View Bactrim Review and Bactrim Label ), FOLIC ACID (1 Mg, Qd) (View Folic Acid Review and Folic Acid Label ), ASPIRIN (81 Mg, Qd) (View Aspirin Review and Aspirin Label ), TRILEPTAL (600 Mg, Bid) (View Trileptal Review and Trileptal Label ). Patient was hospitalized.

5488118-6 | Hallucination, Insomnia
on Sep 18, 2006 Female patient from UNITED STATES , 62 years of age, was diagnosed with hypertension, cardiac failure congestive and was treated with Lopressor (View Usage). Patient had the following side effects: hallucination, insomnia. Lopressor dosage: 25 Mg, Bid, Oral. During the same period patient was treated with PACERONE (800 Mg Qd, Oral; 200 Mg Qd) (View Pacerone Review and Pacerone Label ), PRILOSEC (View Prilosec Review and Prilosec Label ), WARFARIN SODIUM (View Warfarin Sodium Review and Warfarin Sodium Label ), ZOLOFT (View Zoloft Review and Zoloft Label ), LANTUS (View Lantus Review and Lantus Label ), HUMALOG (View Humalog Review and Humalog Label ), ALEVE (View Aleve Review and Aleve Label ).

5482919-6 | Abnormal Dreams, Amnesia, Dysstasia, Eye Disorder, Haemorrhage, Impaired Driving Ability, Incoherent, Joint Injury, Legal Problem
Patient was taking Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: abnormal dreams, amnesia, dysstasia, eye disorder, haemorrhage, impaired driving ability, incoherent, joint injury, legal problem on Oct 02, 2007 from UNITED STATES Additional patient health information: Male patient , weighting 259.9 lb, was diagnosed with insomnia and. Lopressor dosage: Unk. During the same period patient was treated with LEXAPRO (Unk) (View Lexapro Review and Lexapro Label ), DIOVAN (Unk) (View Diovan Review and Diovan Label ), AMBIEN (View Ambien Review and Ambien Label ).

5475384-6 | Myocardial Infarction, Rash Pruritic
Adverse event was reported on Sep 25, 2007 by a Male patient taking Lopressor (View Usage) (Dosage: ) was diagnosed with diabetes mellitus and. Location: UNITED STATES , 69 years of age, Patient experienced the following unwanted or unexpected effects: myocardial infarction, rash pruritic. During the same period patient was treated with SYMLIN (60 Mcg Sq Bid) (View Symlin Review and Symlin Label ), HUMALOG (View Humalog Review and Humalog Label ), PLAVIX (View Plavix Review and Plavix Label ).

5430315-X | Inflammation, Pancreatitis
on Aug 21, 2007 Male patient from UNITED STATES , 40 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). Patient had the following side effects: inflammation, pancreatitis. Lopressor dosage: . During the same period patient was treated with TEKTURNA (150 Mg, Qd) (View Tekturna Review and Tekturna Label ). Patient was hospitalized.

5429396-9 | Inflammation, Pancreatitis
on Aug 21, 2007 Male patient from UNITED STATES , 40 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: inflammation, pancreatitis. Lopressor dosage: . During the same period patient was treated with TEKTURNA (150 Mg, Qd) (View Tekturna Review and Tekturna Label ). Patient was hospitalized.

5381730-4 | Atrial Flutter, Cardiogenic Shock, Lactic Acidosis, Pulmonary Oedema, Sinus Tachycardia
Patient was taking Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: atrial flutter, cardiogenic shock, lactic acidosis, pulmonary oedema, sinus tachycardia on Jul 05, 2007 from GERMANY Additional patient health information: Female patient , 43 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Lopressor dosage: 15 Mg, Once/single. During the same period patient was treated with FLUCLOXACILLINE (2 G, Qid) (View Flucloxacilline Review and Flucloxacilline Label ), ENDOXAPARINE (40 Mg, Qd) (View Endoxaparine Review and Endoxaparine Label ), PARACETAMOL (1 G, Qid) (View Paracetamol Review and Paracetamol Label ), VITAMIN B COMPLEX CAP (View Vitamin B Complex Cap Review and Vitamin B Complex Cap Label ), RIFAMPICIN (600 Mg, Qd) (View Rifampicin Review and Rifampicin Label ), BROMAZEPAM (1.5 Mg, Qd) (View Bromazepam Review and Bromazepam Label ), POTASSIUM ACETATE (30 Mmol, Bid) (View Potassium Acetate Review and Potassium Acetate Label ), MORPHINE (25 Mg, Qid) (View Morphine Review and Morphine Label ). Patient was hospitalized.

5379732-7 | Agoraphobia, Loss Of Consciousness, Pancreatic Disorder
Adverse event was reported on Jun 28, 2007 by a Female patient taking Lopressor (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 84 years of age, Patient had the following side effects: agoraphobia, loss of consciousness, pancreatic disorder.

5356283-7 | Anorexia, Asthenia, Atrial Fibrillation, Atrial Flutter, Bundle Branch Block Right, Chest Discomfort, Chills, Cough, Electrocardiogram Abnormal
on Jun 04, 2007 Male patient from UNITED STATES , 50 years of age, was diagnosed with atrial fibrillation (What is atrial fibrillation?), non-small cell lung cancer and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: anorexia, asthenia, atrial fibrillation (What is atrial fibrillation?), atrial flutter, bundle branch block right, chest discomfort, chills, cough, electrocardiogram abnormal. Lopressor dosage: 25 Mg, Qd. During the same period patient was treated with BIBF 1120 (View Bibf 1120 Review and Bibf 1120 Label ), PACLITAXEL + CARBOPLATIN (View Paclitaxel + Carboplatin Review and Paclitaxel + Carboplatin Label ), CALCIUM CITRATE (View Calcium Citrate Review and Calcium Citrate Label ), PRENATAL VITAMINS (View Prenatal Vitamins Review and Prenatal Vitamins Label ), IRON SUPPLEMENTS (View Iron Supplements Review and Iron Supplements Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), ULTRAM (View Ultram Review and Ultram Label ). Patient was hospitalized.

5348931-2 | Lichen Planus
on May 29, 2007 Female patient from UNITED STATES , 55 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: lichen planus. Lopressor dosage: 100 Mg, Bid.

5348883-5 | Bradycardia, Sinus Arrest
Patient was taking Lopressor (View Usage). Patient had the following side effects: bradycardia, sinus arrest on May 30, 2007 from JAPAN Additional patient health information: Male patient , 72 years of age, . Lopressor dosage: 40 Mg/day. During the same period patient was treated with SILECE (View Silece Review and Silece Label ), VEGETAMIN A (View Vegetamin A Review and Vegetamin A Label ), VEGETAMIN B (View Vegetamin B Review and Vegetamin B Label ), HIRNAMIN (View Hirnamin Review and Hirnamin Label ), SEROQUEL (View Seroquel Review and Seroquel Label ).

5333237-8 | Bradycardia, Sinus Arrest
Adverse event was reported on May 14, 2007 by a Male patient taking Lopressor (View Usage) (Dosage: 40 Mg/day) . Location: JAPAN , 72 years of age, After Lopressor was administered, patient had the following side effects: bradycardia, sinus arrest. During the same period patient was treated with SILECE (View Silece Review and Silece Label ), VEGETAMIN A (View Vegetamin A Review and Vegetamin A Label ), VEGETAMIN B (View Vegetamin B Review and Vegetamin B Label ), HIRNAMIN (View Hirnamin Review and Hirnamin Label ), SEROQUEL (View Seroquel Review and Seroquel Label ).

5318248-0 | Asthenia, Blood Potassium Decreased, Heart Rate Decreased, Loss Of Consciousness
on Apr 25, 2007 Female patient from UNITED STATES , 62 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, blood potassium decreased, heart rate decreased, loss of consciousness. Lopressor dosage: Unk, Unk. During the same period patient was treated with DIOVAN (Unk, Unk) (View Diovan Review and Diovan Label ). Patient was hospitalized.

5272858-8 | Abdominal Pain, Atrioventricular Block Complete, Cardiac Arrest, Glasgow Coma Scale Abnormal, Intentional Overdose, Loss Of Consciousness, Shock, Vomiting
on Mar 09, 2007 Female patient from JAPAN , 38 years of age, was diagnosed with incorrect dose administered and was treated with Lopressor (View Usage). Patient had the following side effects: abdominal pain (What is abdominal pain?), atrioventricular block complete, cardiac arrest (What is cardiac arrest?), glasgow coma scale abnormal, intentional overdose, loss of consciousness, shock, vomiting. Lopressor dosage: 200 Mg, Once/single. During the same period patient was treated with CIBENOL (1000 Mg, Once/single) (View Cibenol Review and Cibenol Label ), TOLEDOMIN (200 Mg, Once/single) (View Toledomin Review and Toledomin Label ), SOLANAX (96 Mg, Once/single) (View Solanax Review and Solanax Label ), DOGMATYL (400 Mg, Once/single) (View Dogmatyl Review and Dogmatyl Label ). Patient was hospitalized.

5263753-9 | Psychotic Disorder
Patient was taking Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: psychotic disorder (What is psychotic disorder?) on Mar 08, 2007 from UNITED STATES Additional patient health information: Male patient , 77 years of age, was diagnosed with hypertension and. Lopressor dosage: . Patient was hospitalized.

5220593-4 | Bradycardia, Dizziness
Adverse event was reported on Jan 25, 2007 by a Female patient taking Lopressor (View Usage) (Dosage: 50mg Po Bid Prior To Admission) was diagnosed with hypertension and. Location: UNITED STATES , weighting 176.0 lb, Patient experienced the following unwanted or unexpected effects: bradycardia, dizziness (What is dizziness?). During the same period patient was treated with ZETIA (View Zetia Review and Zetia Label ), PLAVIX (View Plavix Review and Plavix Label ), ZOCOR (View Zocor Review and Zocor Label ), VASOTEC (View Vasotec Review and Vasotec Label ). Patient was hospitalized.

5214091-1 | Blood Pressure Increased, Cardiac Pacemaker Insertion, Electrocardiogram Qt Prolonged, Flushing, Sinus Arrest
on Jan 11, 2007 Male patient from UNITED STATES , 67 years of age, weighting 211.7 lb, was treated with Lopressor (View Usage). Patient had the following side effects: blood pressure increased, cardiac pacemaker insertion, electrocardiogram qt prolonged, flushing, sinus arrest. Lopressor dosage: 50 Mg, Bid. During the same period patient was treated with CLOPIDOGREL (4 Capsules) (View Clopidogrel Review and Clopidogrel Label ), SYNTHROID (0.2 Mg, Qd) (View Synthroid Review and Synthroid Label ), ALTACE (10 Mg, Qd) (View Altace Review and Altace Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label ), LIPITOR (80 Mg, Qd) (View Lipitor Review and Lipitor Label ). Patient was hospitalized and became disabled.

5201534-2 | Angina Pectoris, Blood Pressure Increased
on Feb 28, 2006 Female patient from UNITED STATES , 88 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: angina pectoris, blood pressure increased. Lopressor dosage: 50 Mg, Bid, Oral. During the same period patient was treated with PILOCARPINE (PILOCARPINE) (View Pilocarpine (pilocarpine) Review and Pilocarpine (pilocarpine) Label ).

5191107-2 | Atrioventricular Block Second Degree, Bradycardia, Dyspnoea, Echocardiogram Abnormal, Ejection Fraction Decreased, Electrocardiogram Abnormal, Hypotension, Left Ventricular Failure, Mitral Valve Incompetence
Patient was taking Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: atrioventricular block second degree, bradycardia, dyspnoea, echocardiogram abnormal, ejection fraction decreased, electrocardiogram abnormal, hypotension, left ventricular failure, mitral valve incompetence on Dec 18, 2006 from FRANCE Additional patient health information: Female patient , 81 years of age, was diagnosed with hypertension and. Lopressor dosage: 200 Mg/day. During the same period patient was treated with DILTIAZEM HCL (120 Mg, Unk) (View Diltiazem Hcl Review and Diltiazem Hcl Label ), AMIODARONE HCL (200 Mg, Unk) (View Amiodarone Hcl Review and Amiodarone Hcl Label ), FLECAINIDE ACETATE (100 Mg, Unk) (View Flecainide Acetate Review and Flecainide Acetate Label ), ASPIRIN (100 Mg, Unk) (View Aspirin Review and Aspirin Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

5190296-3 | Haemorrhoids
Adverse event was reported on Dec 20, 2006 by a Female patient taking Lopressor (View Usage) (Dosage: 95 Mg/day) . Location: GERMANY , 38 years of age, weighting 163.1 lb, Patient had the following side effects: haemorrhoids. Patient was hospitalized.

5175393-0 | Blood Pressure Decreased, Incorrect Dose Administered, Pulse Absent, Respiratory Failure
on Dec 12, 2006 Male patient from UNITED STATES , 72 years of age, was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: blood pressure decreased, incorrect dose administered, pulse absent, respiratory failure. Lopressor dosage: Tablet.

5157078-X | C-reactive Protein Increased, Hypotension, Leukocytosis, Pyrexia, Rash, Superinfection
on Nov 14, 2006 Male patient from GERMANY , 75 years of age, was diagnosed with hypertension, arthralgia and was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: c-reactive protein increased, hypotension, leukocytosis, pyrexia, rash (What is rash?), superinfection. Lopressor dosage: 200 Mg/day. During the same period patient was treated with DEBRIDAT (View Debridat Review and Debridat Label ), DIOSMINE (View Diosmine Review and Diosmine Label ), BROMAZEPAM (View Bromazepam Review and Bromazepam Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ), MICARDIS (View Micardis Review and Micardis Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ). Patient was hospitalized.

5154937-9 | Blood Pressure Decreased, Incorrect Dose Administered, Pulse Absent, Respiratory Arrest
Patient was taking Lopressor (View Usage). Patient had the following side effects: blood pressure decreased, incorrect dose administered, pulse absent, respiratory arrest on Nov 15, 2006 from UNITED STATES Additional patient health information: Male patient , 72 years of age, . Lopressor dosage: 50 Mg, Once/single.

5147762-6 | Abdominal Discomfort, Depression, Fatigue, Nausea
Adverse event was reported on Sep 28, 2006 by a Female patient taking Lopressor (View Usage) (Dosage: 1/2 A 50 Mg Tablet Bid) was diagnosed with hypertension, anxiety (What is anxiety?), cervical spinal stenosis and. Location: UNITED STATES , 73 years of age, After Lopressor was administered, patient had the following side effects: abdominal discomfort, depression (What is depression?), fatigue, nausea (What is nausea?). During the same period patient was treated with VALIUM (Unk, Prn) (View Valium Review and Valium Label ), CALCIUM (View Calcium Review and Calcium Label ).

5134173-2 | Blood Pressure Increased, Cardiac Pacemaker Insertion, Mitral Valve Incompetence, Sinus Arrest, Tricuspid Valve Incompetence
on Sep 25, 2006 Male patient from UNITED STATES , 67 years of age, weighting 211.7 lb, was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased, cardiac pacemaker insertion, mitral valve incompetence, sinus arrest, tricuspid valve incompetence. Lopressor dosage: 50 Mg, Bid. During the same period patient was treated with CLOPIDOGREL (4 Capsules) (View Clopidogrel Review and Clopidogrel Label ), SYNTHROID (0.2 Mg, Qd) (View Synthroid Review and Synthroid Label ), ALTACE (10 Mg, Qd) (View Altace Review and Altace Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PLAVIX (75 Mg, Qd) (View Plavix Review and Plavix Label ), LIPITOR (80 Mg, Qd) (View Lipitor Review and Lipitor Label ).

5127677-X | Opiates Positive
on Oct 03, 2006 Female patient from CANADA , 64 years of age, was treated with Lopressor (View Usage). Patient had the following side effects: opiates positive. Lopressor dosage: . During the same period patient was treated with OXYCODONE HCL (View Oxycodone Hcl Review and Oxycodone Hcl Label ). Patient was hospitalized.

5126831-0 | Aphasia, Confusional State, Electroencephalogram Abnormal, Memory Impairment, Transient Ischaemic Attack
Patient was taking Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: aphasia (What is aphasia?), confusional state, electroencephalogram abnormal, memory impairment, transient ischaemic attack on Sep 29, 2006 from GERMANY Additional patient health information: Male patient , 72 years of age, . Lopressor dosage: 100 Mg/day. During the same period patient was treated with DEPAKENE (750 Mg/day) (View Depakene Review and Depakene Label ), OMEPRAZOLE (20 Mg/day) (View Omeprazole Review and Omeprazole Label ). Patient was hospitalized.

5121901-5 | Cardiac Pacemaker Insertion, Sinus Arrest
Adverse event was reported on Sep 25, 2006 by a Male patient taking Lopressor (View Usage) (Dosage: 50 Mg, Bid) . Location: UNITED STATES , 67 years of age, weighting 211.7 lb, Patient experienced the following unwanted or unexpected effects: cardiac pacemaker insertion, sinus arrest. During the same period patient was treated with CLOPIDOGREL (4 Capsules) (View Clopidogrel Review and Clopidogrel Label ), SYNTHROID (View Synthroid Review and Synthroid Label ), ALTACE (View Altace Review and Altace Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PLAVIX (View Plavix Review and Plavix Label ).

5118357-5 | Transient Ischaemic Attack
on Sep 21, 2006 Male patient from UNITED STATES , 88 years of age, was diagnosed with hypertension and was treated with Lopressor (View Usage). Patient had the following side effects: transient ischaemic attack. Lopressor dosage: 50 Mg, Bid. During the same period patient was treated with LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), LISINOPRIL (View Lisinopril Review and Lisinopril Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), TERAZOSIN HCL (View Terazosin Hcl Review and Terazosin Hcl Label ). Patient was hospitalized.

5113675-9 | Atrioventricular Block Third Degree, Fall
on Sep 21, 2006 Male patient from UNITED STATES , 78 years of age, weighting 166.0 lb, was diagnosed with hypertension and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: atrioventricular block third degree, fall (What is fall?). Lopressor dosage: 50 Mg Po Bid. During the same period patient was treated with CLONIDINE (0.1-0.2 Mg Prn) (View Clonidine Review and Clonidine Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), LOSARTAN POSTASSIUM (View Losartan Postassium Review and Losartan Postassium Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), NEPHROCAP (View Nephrocap Review and Nephrocap Label ), TEMAZEPAM (View Temazepam Review and Temazepam Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

5112567-9 | Abdominal Pain, Acute Myocardial Infarction, Acute Pulmonary Oedema, Acute Respiratory Failure, Agitation, Anaemia, Anuria, Blood Alkaline Phosphatase Increased, Blood Creatinine Increased
Patient was taking Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), acute myocardial infarction, acute pulmonary oedema, acute respiratory failure, agitation, anaemia, anuria, blood alkaline phosphatase increased, blood creatinine increased on Sep 15, 2006 from UNITED STATES Additional patient health information: Female patient , 74 years of age, weighting 200.6 lb, was diagnosed with agitation and. Lopressor dosage: . During the same period patient was treated with LOVENOX (1 Mg/kg) (View Lovenox Review and Lovenox Label ), EPHEDRA (View Ephedra Review and Ephedra Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), LASIX (View Lasix Review and Lasix Label ), PROPOFOL (View Propofol Review and Propofol Label ). Patient was hospitalized.

5109976-0 | Blood Pressure Diastolic Decreased, Bradycardia, Dizziness, Nodal Rhythm, Sick Sinus Syndrome
Adverse event was reported on Sep 19, 2006 by a Female patient taking Lopressor (View Usage) (Dosage: 25 Mg Po Bid) was diagnosed with atrial fibrillation (What is atrial fibrillation?) and. Location: UNITED STATES , 69 years of age, weighting 138.9 lb, Patient had the following side effects: blood pressure diastolic decreased, bradycardia, dizziness (What is dizziness?), nodal rhythm, sick sinus syndrome. During the same period patient was treated with SOTALOL HYDROCHLORIDE (80 Mg Po Bid) (View Sotalol Hydrochloride Review and Sotalol Hydrochloride Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), FAMOTIDINE (View Famotidine Review and Famotidine Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), INSULIN ASPART (View Insulin Aspart Review and Insulin Aspart Label ), MAGNESIUM (View Magnesium Review and Magnesium Label ), NEOSPORIN (View Neosporin Review and Neosporin Label ), PANTOPRAZOLE SODIUM (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ). Patient was hospitalized.

5107595-3 | Abnormal Behaviour, Aggression, Amnesia, Confusional State, Flushing, Memory Impairment, Nausea, Physical Assault, Pruritus
on Sep 13, 2006 Male patient from UNITED STATES , 81 years of age, weighting 157.0 lb, was diagnosed with hypertension, blood cholesterol increased and was treated with Lopressor (View Usage). After Lopressor was administered, patient had the following side effects: abnormal behaviour, aggression, amnesia, confusional state, flushing, memory impairment, nausea (What is nausea?), physical assault, pruritus. Lopressor dosage: . During the same period patient was treated with ADVICOR (View Advicor Review and Advicor Label ).

5034845-4 | Biliary Tract Disorder, Cholestasis, Diarrhoea, Dysphagia, Graft Versus Host Disease, Haemoglobin Decreased, Hyperbilirubinaemia, Leukopenia, Pharyngolaryngeal Pain
on Jun 21, 2006 Male patient from UNITED STATES , 82 years of age, was treated with Lopressor (View Usage). Patient experienced the following unwanted or unexpected effects: biliary tract disorder, cholestasis, diarrhoea, dysphagia, graft versus host disease, haemoglobin decreased, hyperbilirubinaemia, leukopenia, pharyngolaryngeal pain. Lopressor dosage: . During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), LASIX (View Lasix Review and Lasix Label ), AMIODARONE HCL (View Amiodarone Hcl Review and Amiodarone Hcl Label ), NEURONTIN (View Neurontin Review and Neurontin Label ), TYLENOL (CAPLET) (View Tylenol (caplet) Review and Tylenol (caplet) Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), POTASSIUM CHLORIDE (View Potassium Chloride Review and Potassium Chloride Label ).

5026420-2 | Amnesia, Blood Glucose Increased, Convulsion, Craniotomy, Haematocrit Decreased, Haematoma, Haemoglobin Decreased, Headache, Meningioma
Patient was taking Lopressor (View Usage). Patient had the following side effects: amnesia, blood glucose increased, convulsion, craniotomy, haematocrit decreased, haematoma, haemoglobin decreased, headache (What is headache?), meningioma on May 11, 2006 from UNITED STATES Additional patient health information: Male patient , 45 years of age, was diagnosed with pain (What is pain?) and. Lopressor dosage: 50 Mg, Bid. During the same period patient was treated with ANALGESICS (View Analgesics Review and Analgesics Label ), VICODIN (5/500 Mg 1-2 Tabs Po Q6h) (View Vicodin Review and Vicodin Label ).