COZAAR Side Effects

6902162-0 | Cardiac Disorder, Heart Rate Decreased, Hypertension, Pruritus, Rash
on Jul 26, 2010 Female patient from UNITED STATES , 73 years of age, was diagnosed with hypertension and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: cardiac disorder, heart rate decreased, hypertension, pruritus, rash (What is rash?). Cozaar dosage: . During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), PREMARIN (View Premarin Review and Premarin Label ). Patient was hospitalized.

6898634-8 | Abscess Bacterial, Aphthous Stomatitis, Gingival Abscess, Nausea, Oral Bacterial Infection, Oropharyngeal Pain
Patient was taking Cozaar (View Usage). Patient had the following side effects: abscess bacterial, aphthous stomatitis, gingival abscess, nausea (What is nausea?), oral bacterial infection, oropharyngeal pain on Jul 16, 2010 from UNITED STATES Additional patient health information: Female patient , 60 years of age, weighting 182.0 lb, was diagnosed with hypertension and. Cozaar dosage: 50 Mg/daily/po. During the same period patient was treated with KENALOG (View Kenalog Review and Kenalog Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), ATENOLOL AND CHLORTHALIDONE (View Atenolol And Chlorthalidone Review and Atenolol And Chlorthalidone Label ). Patient was hospitalized.

6896430-9 | Oedema Peripheral, Overdose, Skin Lesion, Wound Secretion
Adverse event was reported on Jul 21, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: FRANCE , 87 years of age, After Cozaar was administered, patient had the following side effects: oedema peripheral, overdose, skin lesion, wound secretion. During the same period patient was treated with ACENOCOUMAROL (View Acenocoumarol Review and Acenocoumarol Label ), BUMETANIDE (View Bumetanide Review and Bumetanide Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), AMIODARONE HYDROCHLORIDE (View Amiodarone Hydrochloride Review and Amiodarone Hydrochloride Label ). Patient was hospitalized.

6895284-4 | Anxiety, Hypertension, Nervousness, Pruritus
on Jul 28, 2010 Female patient from UNITED STATES , 75 years of age, weighting 158.7 lb, was diagnosed with hypertension and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), hypertension, nervousness, pruritus. Cozaar dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ). Patient was hospitalized and became disabled.


6888919-3 | Acute Phosphate Nephropathy
on Jul 21, 2010 Male patient from JAPAN , 65 years of age, was diagnosed with endoscopy large bowel and was treated with Cozaar (View Usage). Patient had the following side effects: acute phosphate nephropathy. Cozaar dosage: . During the same period patient was treated with VISICLEAR (View Visiclear Review and Visiclear Label ). Patient was hospitalized.

6878445-X | Atrioventricular Block, Hyperkalaemia
Patient was taking Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: atrioventricular block, hyperkalaemia on Jul 22, 2010 from SPAIN Additional patient health information: Male patient , 79 years of age, was diagnosed with hypertension, atrial fibrillation (What is atrial fibrillation?) and. Cozaar dosage: . During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), EPLERENONE (View Eplerenone Review and Eplerenone Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), ACENOCOUMAROL (View Acenocoumarol Review and Acenocoumarol Label ). Patient was hospitalized.

6877922-5 | Erythema Multiforme
Adverse event was reported on Jul 15, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) . Location: JAPAN , 70 years of age, Patient experienced the following unwanted or unexpected effects: erythema multiforme.

6877113-8 | Diarrhoea, Myocardial Infarction, Renal Failure Acute, Transaminases Increased, Vomiting
on Jul 22, 2010 Female patient from SWEDEN , 91 years of age, was diagnosed with essential hypertension, immunisation and was treated with Cozaar (View Usage). Patient had the following side effects: diarrhoea, myocardial infarction, renal failure acute, transaminases increased, vomiting. Cozaar dosage: . During the same period patient was treated with INFLUENZA VIRUS A SPLIT VIRION VACCINE INACTIVATED (H1N1) (View Influenza Virus A Split Virion Vaccine Inactivated (h1n1) Review and Influenza Virus A Split Virion Vaccine Inactivated (h1n1) Label ). Patient was hospitalized.

6877111-4 | Asthenia, Asthma, Back Pain, Balance Disorder, Disorientation, Dizziness, Oedema Peripheral, Pleural Effusion, Polyuria
on Jul 21, 2010 Female patient from UNITED STATES , 84 years of age, was diagnosed with hypertension and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: asthenia, asthma (What is asthma?), back pain (What is back pain?), balance disorder, disorientation, dizziness (What is dizziness?), oedema peripheral, pleural effusion, polyuria. Cozaar dosage: . During the same period patient was treated with ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), SINGULAIR (View Singulair Review and Singulair Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ), NASACORT (View Nasacort Review and Nasacort Label ).

6875914-3 | Bradycardia, Torsade De Pointes
Patient was taking Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, torsade de pointes on Jul 14, 2010 from SWEDEN Additional patient health information: Male patient , 66 years of age, was diagnosed with acute coronary syndrome and. Cozaar dosage: 100 Mg/daily, Po. During the same period patient was treated with BISOPROLOL (20 Mg/daily, Po) (View Bisoprolol Review and Bisoprolol Label ), ATROVENT (View Atrovent Review and Atrovent Label ), BRICANYL (View Bricanyl Review and Bricanyl Label ), FURIX (View Furix Review and Furix Label ). Patient was hospitalized.

6867315-9 | Blood Pressure Increased
Adverse event was reported on Jul 19, 2010 by a Male patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 66 years of age, Patient had the following side effects: blood pressure increased. Patient was hospitalized.

6863528-0 | Cystitis Radiation, Hyponatraemia, Peripheral Sensorimotor Neuropathy, Somnolence, Urinary Incontinence, Urinary Retention, Urinary Tract Infection
on Jul 12, 2010 Female patient from INDIA , 82 years of age, was diagnosed with thrombosis prophylaxis and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: cystitis radiation, hyponatraemia, peripheral sensorimotor neuropathy, somnolence, urinary incontinence (What is urinary incontinence?), urinary retention, urinary tract infection (What is urinary tract infection?). Cozaar dosage: Po. During the same period patient was treated with HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), CIPRALEX (View Cipralex Review and Cipralex Label ), NOVOLET (View Novolet Review and Novolet Label ), CLONAZEPAM (View Clonazepam Review and Clonazepam Label ), AMILORIDE HYDROCHLORIDE (View Amiloride Hydrochloride Review and Amiloride Hydrochloride Label ), CALCITRIOL + CALCIUM CARBONATE + ZIN (View Calcitriol + Calcium Carbonate + Zin Review and Calcitriol + Calcium Carbonate + Zin Label ). Patient was hospitalized.

6861509-4 | Formication, Middle Insomnia, Photopsia, Pruritus
on Jul 20, 2010 Female patient from UNITED STATES , 62 years of age, weighting 207.0 lb, was diagnosed with diabetes mellitus, prophylaxis, renal disorder and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: formication, middle insomnia, photopsia, pruritus. Cozaar dosage: 1/2 Tablet Daily Po.

6860456-1 | Bladder Cancer, Gastrointestinal Carcinoma, Mesenteric Artery Embolism, Pancreatic Carcinoma, Skin Cancer
Patient was taking Cozaar (View Usage). Patient had the following side effects: bladder cancer (What is bladder cancer?), gastrointestinal carcinoma, mesenteric artery embolism, pancreatic carcinoma, skin cancer (What is skin cancer?) on Jul 19, 2010 from UNITED STATES Additional patient health information: Male patient , 84 years of age, weighting 192.0 lb, was diagnosed with cardiac failure congestive, hypertension and. Cozaar dosage: Many Years.

6859937-6 | Blood Pressure Increased, Product Colour Issue, Product Formulation Issue, Product Substitution Issue
Adverse event was reported on Jul 19, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: 1 Tablet Every Day Merck + Co. France) was diagnosed with hypertension and. Location: UNITED STATES , 72 years of age, weighting 134.0 lb, After Cozaar was administered, patient had the following side effects: blood pressure increased, product colour issue, product formulation issue, product substitution issue.

6858472-9 | Blood Pressure Decreased, Bradycardia, Hypoglycaemia, Marasmus, Respiratory Arrest
on Jul 14, 2010 Female patient from JAPAN , 93 years of age, was diagnosed with hypertension, cardiac failure and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, bradycardia, hypoglycaemia, marasmus, respiratory arrest. Cozaar dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), LASIX (View Lasix Review and Lasix Label ), PANTOSIN (View Pantosin Review and Pantosin Label ).

6850768-X | Heart Rate Irregular, Malaise
on Jul 13, 2010 Female patient from UNITED STATES , 58 years of age, was diagnosed with hypertension and was treated with Cozaar (View Usage). Patient had the following side effects: heart rate irregular, malaise. Cozaar dosage: . During the same period patient was treated with PROPRANOLOL HYDROCHLORIDE (View Propranolol Hydrochloride Review and Propranolol Hydrochloride Label ), PROTONIX (View Protonix Review and Protonix Label ), LORATADINE (View Loratadine Review and Loratadine Label ), TYLENOL (View Tylenol Review and Tylenol Label ), LOSARTAN POTASSIUM (View Losartan Potassium Review and Losartan Potassium Label ). Patient was hospitalized.

6848433-8 | Muscular Weakness, Product Substitution Issue, Salivary Gland Enlargement
Patient was taking Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: muscular weakness, product substitution issue, salivary gland enlargement on Jul 12, 2010 from UNITED STATES Additional patient health information: Female patient , 72 years of age, was diagnosed with hypertension and. Cozaar dosage: . During the same period patient was treated with NEXIUM (View Nexium Review and Nexium Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ). Patient was hospitalized.

6840291-0 | Abdominal Discomfort, Chest Discomfort, Diarrhoea, Nausea, Throat Tightness
Adverse event was reported on Jul 08, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with blood pressure (What is blood pressure?) and. Location: UNITED STATES , 62 years of age, Patient experienced the following unwanted or unexpected effects: abdominal discomfort, chest discomfort, diarrhoea, nausea (What is nausea?), throat tightness. During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), CRESTOR (View Crestor Review and Crestor Label ), FLONASE (View Flonase Review and Flonase Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ). Patient was hospitalized.

6831298-8 | Alopecia, Insomnia, Pruritus
on Jul 09, 2010 Male patient from UNITED STATES , 75 years of age, weighting 230.0 lb, was diagnosed with hypertension and was treated with Cozaar (View Usage). Patient had the following side effects: alopecia, insomnia, pruritus. Cozaar dosage: One Twice Daily Po.

6827063-8 | Hypoglycaemia
on Jul 02, 2010 Male patient from JAPAN , 79 years of age, weighting 121.3 lb, was diagnosed with hypertension, diabetes mellitus, cerebral infarction, myasthenia gravis, gastric ulcer, osteoporosis (What is osteoporosis?) and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: hypoglycaemia. Cozaar dosage: . During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PREDONINE (View Predonine Review and Predonine Label ), GLUCOBAY (View Glucobay Review and Glucobay Label ), GAMOFA (View Gamofa Review and Gamofa Label ), ONEALFA (View Onealfa Review and Onealfa Label ). Patient was hospitalized.

6817823-1 | Anxiety, Hypertension, Pruritus
Patient was taking Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: anxiety (What is anxiety?), hypertension, pruritus on Jul 01, 2010 from UNITED STATES Additional patient health information: Female patient , 75 years of age, was diagnosed with hypertension and. Cozaar dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ). Patient was hospitalized.

6813743-7 | Confusional State
Adverse event was reported on Jun 25, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with cardiac disorder and. Location: UNITED STATES , 73 years of age, Patient had the following side effects: confusional state. Patient was hospitalized and became disabled.

6813742-5 | Asthma, Back Pain, Balance Disorder, Disorientation, Pleural Effusion, Polyuria, Sensation Of Heaviness
on Jun 22, 2010 Female patient from UNITED STATES , 84 years of age, was diagnosed with hypertension and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: asthma (What is asthma?), back pain (What is back pain?), balance disorder, disorientation, pleural effusion, polyuria, sensation of heaviness. Cozaar dosage: . During the same period patient was treated with LOSARTAN POTASSIUM (View Losartan Potassium Review and Losartan Potassium Label ), ADVAIR DISKUS 100/50 (View Advair Diskus 100/50 Review and Advair Diskus 100/50 Label ), SINGULAIR (View Singulair Review and Singulair Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ), NASACORT (View Nasacort Review and Nasacort Label ).

6810187-9 | Abdominal Discomfort, Adverse Event, Blood Pressure Abnormal, Cholelithiasis, Headache
on Jun 25, 2010 Male patient from UNITED STATES , 92 years of age, was diagnosed with blood pressure (What is blood pressure?) and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, adverse event, blood pressure abnormal, cholelithiasis, headache (What is headache?). Cozaar dosage: . Patient was hospitalized.

6810186-7 | Blood Pressure Increased
Patient was taking Cozaar (View Usage). Patient had the following side effects: blood pressure increased on Jun 25, 2010 from UNITED STATES Additional patient health information: Male patient , 66 years of age, was diagnosed with hypertension and. Cozaar dosage: . Patient was hospitalized.

6810184-3 | Pancreatitis
Adverse event was reported on Jun 25, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) . Location: NETHERLANDS , 87 years of age, weighting 132.3 lb, After Cozaar was administered, patient had the following side effects: pancreatitis. During the same period patient was treated with GLIMEPIRIDE (View Glimepiride Review and Glimepiride Label ), ASPIRIN CALCIUM (View Aspirin Calcium Review and Aspirin Calcium Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ). Patient was hospitalized.

6810180-6 | Blood Pressure Increased
on Jun 24, 2010 Female patient from UNITED STATES , 80 years of age, was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure increased. Cozaar dosage: .

6810179-X | Blood Pressure Decreased, Bradycardia, Hypoglycaemia, Marasmus, Respiratory Arrest
on Jun 23, 2010 Female patient from JAPAN , 93 years of age, was diagnosed with hypertension, cardiac failure and was treated with Cozaar (View Usage). Patient had the following side effects: blood pressure decreased, bradycardia, hypoglycaemia, marasmus, respiratory arrest. Cozaar dosage: . During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), LASIX (View Lasix Review and Lasix Label ), PANTOSIN (View Pantosin Review and Pantosin Label ).

6803542-4 | Hypertension
Patient was taking Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: hypertension on Jun 22, 2010 from UNITED STATES Additional patient health information: Female patient , 75 years of age, was diagnosed with hypertension and. Cozaar dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ). Patient was hospitalized.

6797339-1 | Acute Lymphocytic Leukaemia, Anaemia, Aphasia, Arthralgia, Disseminated Intravascular Coagulation, Glomerulonephritis Membranous, Haemodialysis, Hepatic Failure, Hyperlipidaemia
Adverse event was reported on Jun 15, 2010 by a Male patient taking Cozaar (View Usage) (Dosage: 50 Mg/daily/po; 25 Mg/daily/po) was diagnosed with proteinuria and. Location: PERU , 14 years of age, weighting 108.0 lb, Patient experienced the following unwanted or unexpected effects: acute lymphocytic leukaemia, anaemia, aphasia (What is aphasia?), arthralgia, disseminated intravascular coagulation, glomerulonephritis membranous, haemodialysis, hepatic failure, hyperlipidaemia. Patient was hospitalized.

6795649-5 | Abdominal Discomfort, Chest Discomfort, Diarrhoea, Nausea, Throat Tightness
on Jun 14, 2010 Female patient from UNITED STATES , 62 years of age, was diagnosed with blood pressure (What is blood pressure?) and was treated with Cozaar (View Usage). Patient had the following side effects: abdominal discomfort, chest discomfort, diarrhoea, nausea (What is nausea?), throat tightness. Cozaar dosage: . During the same period patient was treated with PROTONIX (View Protonix Review and Protonix Label ), CRESTOR (View Crestor Review and Crestor Label ), FLONASE (View Flonase Review and Flonase Label ), ZYRTEC (View Zyrtec Review and Zyrtec Label ). Patient was hospitalized.

6795640-9 | Blood Pressure Increased, Chest Discomfort, Dyspnoea, Neck Pain, Nervousness, Oedema, Skin Disorder
on Jun 18, 2010 Female patient from UNITED STATES , 72 years of age, weighting 172.0 lb, was diagnosed with hypertension and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: blood pressure increased, chest discomfort, dyspnoea, neck pain, nervousness, oedema, skin disorder. Cozaar dosage: . During the same period patient was treated with LIPITOR (View Lipitor Review and Lipitor Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ). Patient was hospitalized.

6784353-5 | Hepatitis Fulminant
Patient was taking Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: hepatitis fulminant on Jun 16, 2010 from FRANCE Additional patient health information: Female patient , 55 years of age, was diagnosed with hypertension, hiv infection (What is hiv infection?) and. Cozaar dosage: . During the same period patient was treated with SUSTIVA (View Sustiva Review and Sustiva Label ), EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE (View Emtricitabine And Tenofovir Disoproxil Fumarate Review and Emtricitabine And Tenofovir Disoproxil Fumarate Label ), EFAVIRENZ AND EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE (View Efavirenz And Emtricitabine And Tenofovir Disoproxil Fumarate Review and Efavirenz And Emtricitabine And Tenofovir Disoproxil Fumarate Label ).

6784343-2 | Cardiac Disorder, Dizziness, Fatigue
Adverse event was reported on Jun 11, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with blood pressure (What is blood pressure?) and. Location: UNITED STATES , 86 years of age, Patient had the following side effects: cardiac disorder, dizziness (What is dizziness?), fatigue. During the same period patient was treated with VIOXX (View Vioxx Review and Vioxx Label ). Patient was hospitalized.

6782781-5 | Myocardial Infarction, Spider Naevus
on Jun 09, 2010 Male patient from FRANCE , 65 years of age, was diagnosed with hypertension, myocardial infarction and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: myocardial infarction, spider naevus. Cozaar dosage: . During the same period patient was treated with RANITIDINE (View Ranitidine Review and Ranitidine Label ), DILTIAZEM HYDROCHLORIDE (View Diltiazem Hydrochloride Review and Diltiazem Hydrochloride Label ). Patient was hospitalized.

6779914-3 | Abdominal Discomfort, Adverse Event, Blood Pressure Abnormal, Cholelithiasis, Headache
on Jun 10, 2010 Male patient from UNITED STATES , 92 years of age, was diagnosed with blood pressure (What is blood pressure?) and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal discomfort, adverse event, blood pressure abnormal, cholelithiasis, headache (What is headache?). Cozaar dosage: . Patient was hospitalized.

6776040-4 | Blood Pressure Increased, Cerebral Haemorrhage, Cerebrovascular Accident, Thyroid Disorder, Vascular Rupture, Visual Impairment
Patient was taking Cozaar (View Usage). Patient had the following side effects: blood pressure increased, cerebral haemorrhage, cerebrovascular accident, thyroid disorder, vascular rupture, visual impairment on Jun 14, 2010 from UNITED KINGDOM Additional patient health information: Female patient , 63 years of age, weighting 191.8 lb, was diagnosed with hypertension, diabetes mellitus and. Cozaar dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), INDAPAMIDE (View Indapamide Review and Indapamide Label ). Patient was hospitalized.

6772448-1 | Blood Pressure Decreased, Bradycardia, Hypoglycaemia, Marasmus, Respiratory Arrest
Adverse event was reported on Jun 03, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with hypertension, cardiac failure and. Location: JAPAN , 93 years of age, After Cozaar was administered, patient had the following side effects: blood pressure decreased, bradycardia, hypoglycaemia, marasmus, respiratory arrest. During the same period patient was treated with ALDACTONE (View Aldactone Review and Aldactone Label ), LASIX (View Lasix Review and Lasix Label ), PANTOSIN (View Pantosin Review and Pantosin Label ).

6772440-7 | Lactic Acidosis, Renal Failure Acute
on Jun 10, 2010 Male patient from SWEDEN , 71 years of age, was diagnosed with essential hypertension, diabetes mellitus and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: lactic acidosis, renal failure acute. Cozaar dosage: . During the same period patient was treated with METFORMIN (View Metformin Review and Metformin Label ), PERSANTINE (View Persantine Review and Persantine Label ), INSULATARD (INSULIN HUMAN, ISOPHANE) (View Insulatard (insulin Human, Isophane) Review and Insulatard (insulin Human, Isophane) Label ), PAMOL (View Pamol Review and Pamol Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), TROMBYL (View Trombyl Review and Trombyl Label ), LOGIMAX (View Logimax Review and Logimax Label ). Patient was hospitalized.

6772437-7 | Anaemia, Asthenia, Renal Failure Acute, Thrombocytopenia, Thrombotic Microangiopathy
on Jun 11, 2010 Male patient from FRANCE , 82 years of age, was diagnosed with hypertension, prostate cancer (What is prostate cancer?) and was treated with Cozaar (View Usage). Patient had the following side effects: anaemia, asthenia, renal failure acute, thrombocytopenia, thrombotic microangiopathy. Cozaar dosage: . During the same period patient was treated with FLUTAMIDE (View Flutamide Review and Flutamide Label ), ASPIRIN LYSINE (View Aspirin Lysine Review and Aspirin Lysine Label ), NIFEDIPINE (View Nifedipine Review and Nifedipine Label ), GOSERELIN ACETATE (View Goserelin Acetate Review and Goserelin Acetate Label ), CYPROTERONE ACETATE (View Cyproterone Acetate Review and Cyproterone Acetate Label ). Patient was hospitalized.

6768205-2 | Hepatitis Fulminant
Patient was taking Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: hepatitis fulminant on Jun 04, 2010 from JAPAN Additional patient health information: Male patient , 70 years of age, . Cozaar dosage: . Patient was hospitalized.

6766543-0 | Hypertension
Adverse event was reported on Jun 08, 2010 by a Female patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: UNITED STATES , 31 years of age, Patient experienced the following unwanted or unexpected effects: hypertension.

6766542-9 | Chest Discomfort, Dyspnoea, Neck Pain, Skin Disorder
on Jun 02, 2010 Female patient from UNITED STATES , 72 years of age, was diagnosed with hypertension and was treated with Cozaar (View Usage). Patient had the following side effects: chest discomfort, dyspnoea, neck pain, skin disorder. Cozaar dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), ATENOLOL (View Atenolol Review and Atenolol Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6766522-3 | Bradycardia, Hypoglycaemia, Marasmus, Respiratory Arrest
on Jun 03, 2010 Female patient from JAPAN , 93 years of age, was diagnosed with hypertension, cardiac failure and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: bradycardia, hypoglycaemia, marasmus, respiratory arrest. Cozaar dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), PANTOSIN (View Pantosin Review and Pantosin Label ), ALDACTONE (View Aldactone Review and Aldactone Label ).

6765033-9 | Fall, Humerus Fracture, Malaise
Patient was taking Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), humerus fracture, malaise on Jun 09, 2010 from FRANCE Additional patient health information: Female patient , 86 years of age, . Cozaar dosage: . During the same period patient was treated with ACETAMINOPHEN AND CAFFEINE AND OPIUM (View Acetaminophen And Caffeine And Opium Review and Acetaminophen And Caffeine And Opium Label ), DONEPEZIL HYDROCHLORIDE (View Donepezil Hydrochloride Review and Donepezil Hydrochloride Label ), MILNACIPRAN HYDROCHLORIDE (View Milnacipran Hydrochloride Review and Milnacipran Hydrochloride Label ), GINKGO (View Ginkgo Review and Ginkgo Label ). Patient was hospitalized.

6764289-6 | Lactic Acidosis, Renal Failure Acute
Adverse event was reported on May 31, 2010 by a Male patient taking Cozaar (View Usage) (Dosage: ) was diagnosed with essential hypertension, diabetes mellitus and. Location: SWEDEN , 71 years of age, Patient had the following side effects: lactic acidosis, renal failure acute. During the same period patient was treated with PAMOL (View Pamol Review and Pamol Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), TROMBYL (View Trombyl Review and Trombyl Label ), METFORMIN (View Metformin Review and Metformin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), PERSANTINE (View Persantine Review and Persantine Label ), LOGIMAX (View Logimax Review and Logimax Label ), INSULATARD (INSULIN HUMAN, ISOPHANE) (View Insulatard (insulin Human, Isophane) Review and Insulatard (insulin Human, Isophane) Label ). Patient was hospitalized.

6758730-2 | Loss Of Consciousness
on Jun 02, 2010 Female patient from UNITED STATES , 73 years of age, was diagnosed with cardiac disorder and was treated with Cozaar (View Usage). After Cozaar was administered, patient had the following side effects: loss of consciousness. Cozaar dosage: . Patient was hospitalized.

6756719-0 | Diarrhoea, Heart Rate Irregular, Product Formulation Issue, Product Odour Abnormal, Product Substitution Issue
on Jun 03, 2010 Male patient from UNITED STATES , 66 years of age, weighting 182.0 lb, was diagnosed with malaise and was treated with Cozaar (View Usage). Patient experienced the following unwanted or unexpected effects: diarrhoea, heart rate irregular, product formulation issue, product odour abnormal, product substitution issue. Cozaar dosage: . During the same period patient was treated with LOSARTAN POTASSIUM (View Losartan Potassium Review and Losartan Potassium Label ).

6754848-9 | Lactic Acidosis, Renal Failure Acute
Patient was taking Cozaar (View Usage). Patient had the following side effects: lactic acidosis, renal failure acute on May 31, 2010 from SWEDEN Additional patient health information: Male patient , 71 years of age, was diagnosed with essential hypertension, diabetes mellitus and. Cozaar dosage: . During the same period patient was treated with PAMOL (View Pamol Review and Pamol Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ), TROMBYL (View Trombyl Review and Trombyl Label ), METFORMIN (View Metformin Review and Metformin Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), PERSANTINE (View Persantine Review and Persantine Label ), LOGIMAX (View Logimax Review and Logimax Label ), INSULATARD (INSULIN HUMAN, ISOPHANE) (View Insulatard (insulin Human, Isophane) Review and Insulatard (insulin Human, Isophane) Label ). Patient was hospitalized.