BLOPRESS Side Effects

7022299-8 | Interstitial Lung Disease
on Sep 21, 2010 Male patient from JAPAN , 64 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: interstitial lung disease. Blopress dosage: . During the same period patient was treated with FINIBAX (View Finibax Review and Finibax Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), GASTER (View Gaster Review and Gaster Label ), LOXONIN (View Loxonin Review and Loxonin Label ), CLARITHROMYCIN (View Clarithromycin Review and Clarithromycin Label ), METHYCOBAL (View Methycobal Review and Methycobal Label ).

7022204-4 | Overdose, Renal Artery Stenosis, Renal Failure Acute
Patient was taking Blopress (View Usage). Patient had the following side effects: overdose, renal artery stenosis, renal failure acute on Sep 21, 2010 from JAPAN Additional patient health information: Male patient , 69 years of age, was diagnosed with hypertension and. Blopress dosage: . During the same period patient was treated with VALSARTAN (View Valsartan Review and Valsartan Label ). Patient was hospitalized.

6987845-9 | Constipation, Inflammation, Liver Function Test Abnormal, Pneumonia, Urinary Retention, Ventricular Tachycardia, Weight Decreased
Adverse event was reported on Sep 07, 2010 by a Male patient taking Blopress (View Usage) (Dosage: ) . Location: JAPAN , 74 years of age, After Blopress was administered, patient had the following side effects: constipation (What is constipation?), inflammation, liver function test abnormal, pneumonia (What is pneumonia?), urinary retention, ventricular tachycardia, weight decreased. During the same period patient was treated with BLOPRESS PLUS (View Blopress Plus Review and Blopress Plus Label ). Patient was hospitalized.

6987834-4 | Depression, Renal Failure Acute, Suicide Attempt
on Feb 01, 2010 Male patient from JAPAN , 46 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: depression (What is depression?), renal failure acute, suicide attempt. Blopress dosage: . During the same period patient was treated with AMLODIPINE BESYLATE (View Amlodipine Besylate Review and Amlodipine Besylate Label ). Patient was hospitalized.


6972514-1 | Rhabdomyolysis
on Aug 31, 2010 Female patient from JAPAN , 82 years of age, weighting 101.4 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient had the following side effects: rhabdomyolysis. Blopress dosage: . Patient was hospitalized.

6967460-3 | Interstitial Lung Disease, Rhinitis
Patient was taking Blopress (View Usage). After Blopress was administered, patient had the following side effects: interstitial lung disease, rhinitis on Aug 26, 2010 from JAPAN Additional patient health information: Female patient , 61 years of age, weighting 134.5 lb, was diagnosed with hypertension, hyperlipidaemia and. Blopress dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ). Patient was hospitalized.

6942212-9 | Erythema Multiforme, Hyperthermia
Adverse event was reported on Jul 21, 2010 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 60 years of age, Patient experienced the following unwanted or unexpected effects: erythema multiforme, hyperthermia.

6922899-7 | Interstitial Lung Disease
on Aug 04, 2010 Female patient from JAPAN , 61 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient had the following side effects: interstitial lung disease. Blopress dosage: . During the same period patient was treated with ALLEGRA (View Allegra Review and Allegra Label ). Patient was hospitalized.

6913951-0 | Cough, Haemoptysis, Oropharyngeal Discomfort
on Aug 02, 2010 Female patient from JAPAN , 58 years of age, weighting 130.1 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: cough, haemoptysis, oropharyngeal discomfort. Blopress dosage: .

6907709-6 | Transient Ischaemic Attack
Patient was taking Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: transient ischaemic attack on Jul 27, 2010 from JAPAN Additional patient health information: Male patient , weighting 127.9 lb, was diagnosed with hypertension, reflux oesophagitis, cerebral infarction, constipation (What is constipation?), hyperlipidaemia, tachycardia and. Blopress dosage: . During the same period patient was treated with TAKEPRON (View Takepron Review and Takepron Label ), PANALDINE (View Panaldine Review and Panaldine Label ), PURSENNID (View Pursennid Review and Pursennid Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), ARTIST (View Artist Review and Artist Label ). Patient was hospitalized.

6894823-7 | Cough, Haemoptysis, Oropharyngeal Discomfort
Adverse event was reported on Jul 22, 2010 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 58 years of age, weighting 130.1 lb, Patient had the following side effects: cough, haemoptysis, oropharyngeal discomfort.

6887042-1 | Interstitial Lung Disease
on Jul 26, 2010 Male patient from JAPAN , weighting 138.9 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: interstitial lung disease. Blopress dosage: . During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ). Patient was hospitalized.

6882497-0 | Cerebral Haemorrhage
on Jul 23, 2010 Female patient from JAPAN , 71 years of age, weighting 112.4 lb, was diagnosed with hypertension, hyperlipidaemia and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage. Blopress dosage: . During the same period patient was treated with HMG COA REDUCTASE INHIBITORS (View Hmg Coa Reductase Inhibitors Review and Hmg Coa Reductase Inhibitors Label ).

6826072-2 | Hepatic Function Abnormal, Rhabdomyolysis
Patient was taking Blopress (View Usage). Patient had the following side effects: hepatic function abnormal, rhabdomyolysis on Jul 02, 2010 from JAPAN Additional patient health information: Male patient , 80 years of age, was diagnosed with hypertension, dyslipidaemia, hyperuricaemia and. Blopress dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), AMLODIN (View Amlodin Review and Amlodin Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GASTER (View Gaster Review and Gaster Label ). Patient was hospitalized.

6795438-1 | C-reactive Protein Increased, Loss Of Consciousness
Adverse event was reported on Jun 17, 2010 by a Male patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 74 years of age, After Blopress was administered, patient had the following side effects: c-reactive protein increased, loss of consciousness. During the same period patient was treated with GLYCORAN (View Glycoran Review and Glycoran Label ), TAIKODO NO BOUFUUTSUUSHOUSAN (View Taikodo No Boufuutsuushousan Review and Taikodo No Boufuutsuushousan Label ).

6795434-4 | Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion
on Jun 16, 2010 Male patient from JAPAN , 74 years of age, was diagnosed with arrhythmia prophylaxis and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: hyponatraemia, inappropriate antidiuretic hormone secretion. Blopress dosage: . During the same period patient was treated with TAKEPRON (View Takepron Review and Takepron Label ), SUNRYTHM (View Sunrythm Review and Sunrythm Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PRONON (View Pronon Review and Pronon Label ), URIEF (View Urief Review and Urief Label ). Patient was hospitalized.

6765786-X | Renal Aplasia
on Jun 02, 2010 Male patient from JAPAN , weighting 4.41 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient had the following side effects: renal aplasia. Blopress dosage: . During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ), ALDOMET (View Aldomet Review and Aldomet Label ), MAINTATE (View Maintate Review and Maintate Label ), FLUITRAN (View Fluitran Review and Fluitran Label ).

6632149-7 | Gastrointestinal Haemorrhage, Thrombocytopenia
Patient was taking Blopress (View Usage). After Blopress was administered, patient had the following side effects: gastrointestinal haemorrhage, thrombocytopenia on Mar 04, 2010 from SWEDEN Additional patient health information: Female patient , 77 years of age, was diagnosed with hypertension and. Blopress dosage: . During the same period patient was treated with MEXITIL (View Mexitil Review and Mexitil Label ), ACTOS (View Actos Review and Actos Label ), STARSIS (View Starsis Review and Starsis Label ), SUNRYTHM (View Sunrythm Review and Sunrythm Label ), MELBIN (View Melbin Review and Melbin Label ), GASTER (View Gaster Review and Gaster Label ), CETAPRIL (View Cetapril Review and Cetapril Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6631794-2 | Pneumonitis
Adverse event was reported on Mar 03, 2010 by a Female patient taking Blopress (View Usage) (Dosage: ) . Location: JAPAN , 82 years of age, weighting 143.3 lb, Patient experienced the following unwanted or unexpected effects: pneumonitis. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), MEVALOTIN (View Mevalotin Review and Mevalotin Label ), ALTAT (View Altat Review and Altat Label ), LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6618717-7 | Atrial Septal Defect, Congenital Renal Disorder, Hand Deformity, Hearing Impaired, Hepatomegaly, Hypoglycaemia Neonatal, Hypotonia Neonatal, Microcephaly, Pulmonary Hypoplasia
on Mar 02, 2010 Male patient from JAPAN , weighting 8.82 lb, was treated with Blopress (View Usage). Patient had the following side effects: atrial septal defect, congenital renal disorder, hand deformity, hearing impaired, hepatomegaly, hypoglycaemia neonatal, hypotonia neonatal, microcephaly, pulmonary hypoplasia. Blopress dosage: . During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), TRIAMCINOLONE (View Triamcinolone Review and Triamcinolone Label ). Patient was hospitalized and became disabled.

6611355-1 | Thalamus Haemorrhage
on Feb 23, 2010 Male patient from JAPAN , 59 years of age, weighting 167.6 lb, was diagnosed with hypertension, hyperlipidaemia and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: thalamus haemorrhage. Blopress dosage: . During the same period patient was treated with HMG COA REDUCTASE INHIBITORS (View Hmg Coa Reductase Inhibitors Review and Hmg Coa Reductase Inhibitors Label ), ANTITHROMBOTIC AGENTS (View Antithrombotic Agents Review and Antithrombotic Agents Label ). Patient was hospitalized.

6607789-1 | Erythema Multiforme
Patient was taking Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: erythema multiforme on Feb 19, 2010 from JAPAN Additional patient health information: Male patient , 61 years of age, was diagnosed with hypertension and. Blopress dosage: . During the same period patient was treated with CRESTOR (View Crestor Review and Crestor Label ), PARIET (View Pariet Review and Pariet Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), PLAVIX (View Plavix Review and Plavix Label ), GANATON (View Ganaton Review and Ganaton Label ), ZYLORIC (View Zyloric Review and Zyloric Label ), CORTICOSTEROIDS (View Corticosteroids Review and Corticosteroids Label ).

6604940-4 | Ear Discomfort, Loss Of Consciousness
Adverse event was reported on Feb 19, 2010 by a Male patient taking Blopress (View Usage) (Dosage: ) was diagnosed with essential hypertension and. Location: JAPAN , 41 years of age, Patient had the following side effects: ear discomfort, loss of consciousness. During the same period patient was treated with NATRIX (View Natrix Review and Natrix Label ). Patient was hospitalized.

6601872-2 | Liver Disorder, Malaise
on Feb 16, 2010 Male patient from JAPAN , weighting 127.9 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: liver disorder, malaise. Blopress dosage: . During the same period patient was treated with VOLTAREN SUPPO (View Voltaren Suppo Review and Voltaren Suppo Label ), CALBLOCK (View Calblock Review and Calblock Label ). Patient was hospitalized.

6600707-1 | Cerebellar Haemorrhage, Diabetes Mellitus Inadequate Control
on Feb 15, 2010 Male patient from JAPAN , 70 years of age, weighting 163.1 lb, was diagnosed with hypertension, diabetes mellitus and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: cerebellar haemorrhage, diabetes mellitus inadequate control. Blopress dosage: . During the same period patient was treated with CALCIUM CHANNEL BLOCKERS (View Calcium Channel Blockers Review and Calcium Channel Blockers Label ), DIBETOS (View Dibetos Review and Dibetos Label ). Patient was hospitalized.

6585190-7 | Ear Discomfort, Loss Of Consciousness
Patient was taking Blopress (View Usage). Patient had the following side effects: ear discomfort, loss of consciousness on Feb 09, 2010 from JAPAN Additional patient health information: Male patient , 41 years of age, was diagnosed with essential hypertension and. Blopress dosage: . During the same period patient was treated with NATRIX (View Natrix Review and Natrix Label ). Patient was hospitalized.

6582989-8 | Systemic Lupus Erythematosus
Adverse event was reported on Feb 08, 2010 by a Male patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension, basilar artery stenosis, diabetes mellitus, lipid metabolism disorder, benign prostatic hyperplasia and. Location: JAPAN , 79 years of age, weighting 105.8 lb, After Blopress was administered, patient had the following side effects: systemic lupus erythematosus. During the same period patient was treated with PANALDINE (View Panaldine Review and Panaldine Label ), MELBIN (View Melbin Review and Melbin Label ), ATELEC (View Atelec Review and Atelec Label ), NICHI E NATE (View Nichi E-nate Review and Nichi E-nate Label ), EPICALS S (View Epicals-s Review and Epicals-s Label ), ORIVATE (View Orivate Review and Orivate Label ), TAMSLON (View Tamslon Review and Tamslon Label ). Patient was hospitalized.

6577564-5 | Gastrointestinal Haemorrhage, Thrombocytopenia
on Feb 03, 2010 Female patient from JAPAN , 77 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: gastrointestinal haemorrhage, thrombocytopenia. Blopress dosage: . During the same period patient was treated with MEXITIL (View Mexitil Review and Mexitil Label ), ACTOS (View Actos Review and Actos Label ), STARSIS (View Starsis Review and Starsis Label ), SUNRYTHM (View Sunrythm Review and Sunrythm Label ), MELBIN (View Melbin Review and Melbin Label ), GASTER (View Gaster Review and Gaster Label ), CETAPRIL (View Cetapril Review and Cetapril Label ), LIPITOR (View Lipitor Review and Lipitor Label ). Patient was hospitalized.

6573594-8 | Somnolence, Transaminases Increased
on Jan 29, 2010 Female patient from JAPAN , 70 years of age, weighting 99.21 lb, was diagnosed with hypertension, prophylaxis against gastrointestinal ulcer, pain (What is pain?), restless legs syndrome, type 2 diabetes mellitus, dyslipidaemia, osteoporosis (What is osteoporosis?), hyperparathyroidism secondary and was treated with Blopress (View Usage). Patient had the following side effects: somnolence, transaminases increased. Blopress dosage: . During the same period patient was treated with OMEPRAZOLE (View Omeprazole Review and Omeprazole Label ), FENTANYL (Three Times A Week) (View Fentanyl Review and Fentanyl Label ), RESTEX (Levodopa 100 Mg Plus Benserazide 25 Mg, Daily) (View Restex Review and Restex Label ), CARVEDILOL 1 A PHARMA (View Carvedilol 1 A Pharma Review and Carvedilol 1 A Pharma Label ), NOVONORM (View Novonorm Review and Novonorm Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), ACTONEL (View Actonel Review and Actonel Label ), MIMPARA (View Mimpara Review and Mimpara Label ). Patient was hospitalized.

6571446-0 | Atrial Septal Defect, Congenital Renal Disorder, Hand Deformity, Hearing Impaired, Hepatomegaly, Hypoglycaemia Neonatal, Hypotonia Neonatal, Microcephaly, Pulmonary Hypoplasia
Patient was taking Blopress (View Usage). After Blopress was administered, patient had the following side effects: atrial septal defect, congenital renal disorder, hand deformity, hearing impaired, hepatomegaly, hypoglycaemia neonatal, hypotonia neonatal, microcephaly, pulmonary hypoplasia on Jan 28, 2010 from JAPAN Additional patient health information: Male patient , weighting 8.82 lb, . Blopress dosage: . During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), TRIAMCINOLONE (View Triamcinolone Review and Triamcinolone Label ). Patient was hospitalized and became disabled.

6567861-1 | Cerebellar Haemorrhage, Diabetes Mellitus
Adverse event was reported on Jan 26, 2010 by a Male patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 70 years of age, weighting 163.1 lb, Patient experienced the following unwanted or unexpected effects: cerebellar haemorrhage, diabetes mellitus. During the same period patient was treated with CALCIUM CHANNEL BLOCKERS (View Calcium Channel Blockers Review and Calcium Channel Blockers Label ). Patient was hospitalized.

6567785-X | Interstitial Lung Disease
on Jan 25, 2010 Male patient from JAPAN , 83 years of age, was treated with Blopress (View Usage). Patient had the following side effects: interstitial lung disease. Blopress dosage: .

6564644-3 | Systemic Lupus Erythematosus
on Jan 29, 2010 Male patient from JAPAN , 76 years of age, was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: systemic lupus erythematosus. Blopress dosage: . During the same period patient was treated with TICLOPIDINE HYDROCHLORIDE (View Ticlopidine Hydrochloride Review and Ticlopidine Hydrochloride Label ). Patient was hospitalized.

6526961-2 | Photodermatosis
Patient was taking Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: photodermatosis on Dec 29, 2009 from JAPAN Additional patient health information: Male patient , weighting 119.0 lb, was diagnosed with hypertension, cerebrovascular accident prophylaxis and. Blopress dosage: . During the same period patient was treated with CONIEL (View Coniel Review and Coniel Label ), BUFFERIN (View Bufferin Review and Bufferin Label ).

6516190-0 | Depressed Level Of Consciousness, Hyperuricaemia, Hypotension, Intentional Overdose, Renal Impairment
Adverse event was reported on Dec 14, 2009 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension, type 2 diabetes mellitus and. Location: JAPAN , weighting 121.3 lb, Patient had the following side effects: depressed level of consciousness, hyperuricaemia, hypotension, intentional overdose, renal impairment. During the same period patient was treated with AMARYL (View Amaryl Review and Amaryl Label ), METFORMIN HCL (View Metformin Hcl Review and Metformin Hcl Label ). Patient was hospitalized.

6515771-8 | Photosensitivity Reaction
on Dec 15, 2009 Male patient from SWEDEN , 75 years of age, was diagnosed with hypertension, xeroderma and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: photosensitivity reaction. Blopress dosage: . During the same period patient was treated with CONIEL (View Coniel Review and Coniel Label ), INFLUENZA HA VACCINE (View Influenza Ha Vaccine Review and Influenza Ha Vaccine Label ), HIRUDOID (View Hirudoid Review and Hirudoid Label ), LOCOID (View Locoid Review and Locoid Label ).

6515015-7 | Myocardial Infarction
on Dec 15, 2009 Female patient from JAPAN , weighting 132.3 lb, was diagnosed with hypertension, diabetes mellitus, cerebral infarction, dyslipidaemia, gastritis prophylaxis and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Blopress dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), PLAVIX (View Plavix Review and Plavix Label ), LIPITOR (View Lipitor Review and Lipitor Label ), MUCOSTA (View Mucosta Review and Mucosta Label ), NOVOLOG (View Novolog Review and Novolog Label ).

6510027-1 | Caesarean Section, Oligohydramnios
Patient was taking Blopress (View Usage). Patient had the following side effects: caesarean section, oligohydramnios on Dec 14, 2009 from JAPAN Additional patient health information: Female patient , 34 years of age, weighting 251.3 lb, was diagnosed with hypertension and. Blopress dosage: . During the same period patient was treated with LANSOPRAZOLE (View Lansoprazole Review and Lansoprazole Label ), MIRTAZAPINE (View Mirtazapine Review and Mirtazapine Label ), TRIAMCINOLONE (View Triamcinolone Review and Triamcinolone Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

6506826-2 |
Adverse event was reported on Dec 14, 2009 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 68 years of age, . During the same period patient was treated with ACTOS (View Actos Review and Actos Label ), CRESTOR (View Crestor Review and Crestor Label ), PLETAL (View Pletal Review and Pletal Label ), THYRADIN S (View Thyradin S Review and Thyradin S Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), GASTER D (View Gaster D Review and Gaster D Label ).

6500149-3 | Cerebral Haemorrhage
on Dec 07, 2009 Female patient from JAPAN , weighting 134.5 lb, was diagnosed with hypertension, diabetes mellitus, cerebral infarction, oedema and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage. Blopress dosage: . During the same period patient was treated with NORVASC (View Norvasc Review and Norvasc Label ), BASEN OD (View Basen Od Review and Basen Od Label ), ACTOS (View Actos Review and Actos Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), EUGLUCON (View Euglucon Review and Euglucon Label ), DICHLOTRIDE (View Dichlotride Review and Dichlotride Label ), ALDACTONE (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

6480505-2 | Anaemia, Angina Pectoris, Cerebral Infarction, Small Intestinal Haemorrhage
on Dec 01, 2009 Male patient from JAPAN , weighting 134.5 lb, was diagnosed with hypertension, diabetes mellitus and was treated with Blopress (View Usage). Patient had the following side effects: anaemia, angina pectoris, cerebral infarction, small intestinal haemorrhage. Blopress dosage: . During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ), PANALDINE (View Panaldine Review and Panaldine Label ), BASEN (View Basen Review and Basen Label ), VOGLIBOSE (View Voglibose Review and Voglibose Label ). Patient was hospitalized.

6479683-0 | Cerebral Haemorrhage
Patient was taking Blopress (View Usage). After Blopress was administered, patient had the following side effects: cerebral haemorrhage on Nov 30, 2009 from JAPAN Additional patient health information: Male patient , 59 years of age, weighting 167.6 lb, was diagnosed with hypertension, hyperlipidaemia and. Blopress dosage: . During the same period patient was treated with HMG COA REDUCTASE INHIBITORS (View Hmg Coa Reductase Inhibitors Review and Hmg Coa Reductase Inhibitors Label ), ANTITHROMBOTIC AGENTS (View Antithrombotic Agents Review and Antithrombotic Agents Label ). Patient was hospitalized.

6478514-2 | Cerebral Haemorrhage
Adverse event was reported on Nov 27, 2009 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension, diabetes mellitus and. Location: JAPAN , 66 years of age, weighting 136.7 lb, Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage. During the same period patient was treated with CALCIUM CHANNEL BLOCKERS (View Calcium Channel Blockers Review and Calcium Channel Blockers Label ), ANGIOTENSIN II ANTAGONISTS (View Angiotensin Ii Antagonists Review and Angiotensin Ii Antagonists Label ), ALPHA GLUCOSIDASE INHIBITORS (View Alpha Glucosidase Inhibitors Review and Alpha Glucosidase Inhibitors Label ), SULFONAMIDES, UREA DERIVATIVES (View Sulfonamides, Urea Derivatives Review and Sulfonamides, Urea Derivatives Label ), BIGUANIDES (View Biguanides Review and Biguanides Label ), ANTITHROMBOTIC AGENTS (View Antithrombotic Agents Review and Antithrombotic Agents Label ). Patient was hospitalized.

6462726-8 | Renal Failure Acute, Rhabdomyolysis
on Nov 20, 2009 Female patient from JAPAN , 80 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient had the following side effects: renal failure acute, rhabdomyolysis. Blopress dosage: .

6462374-X | Cerebral Infarction, Myocardial Ischaemia
on Nov 18, 2009 Male patient from JAPAN , weighting 143.3 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: cerebral infarction, myocardial ischaemia. Blopress dosage: . During the same period patient was treated with FLUITRAN (View Fluitran Review and Fluitran Label ), GLYCORAN (View Glycoran Review and Glycoran Label ), TANATRIL (View Tanatril Review and Tanatril Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CINALONG (View Cinalong Review and Cinalong Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

6460466-2 | Myocardial Infarction
Patient was taking Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction on Nov 19, 2009 from SWEDEN Additional patient health information: Female patient , 63 years of age, was diagnosed with hypertension and. Blopress dosage: . During the same period patient was treated with LANTUS (View Lantus Review and Lantus Label ), PLAVIX (View Plavix Review and Plavix Label ), LIPITOR (View Lipitor Review and Lipitor Label ), MUCOSTA (View Mucosta Review and Mucosta Label ).

6454147-9 | Hypoglycaemia
Adverse event was reported on Nov 11, 2009 by a Female patient taking Blopress (View Usage) (Dosage: ) was diagnosed with hypertension and. Location: JAPAN , 85 years of age, Patient had the following side effects: hypoglycaemia. Patient was hospitalized.

6450842-6 | Pancytopenia
on Nov 11, 2009 Female patient from JAPAN , weighting 108.0 lb, was diagnosed with hypertension and was treated with Blopress (View Usage). After Blopress was administered, patient had the following side effects: pancytopenia. Blopress dosage: . During the same period patient was treated with CONIEL (View Coniel Review and Coniel Label ), CARDENALIN (View Cardenalin Review and Cardenalin Label ).

6448480-4 | Fall, Hypoglycaemia
on Nov 11, 2009 Female patient from JAPAN , 85 years of age, was diagnosed with hypertension and was treated with Blopress (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), hypoglycaemia. Blopress dosage: . Patient was hospitalized.

6441723-2 | Eosinophil Count Increased, Organising Pneumonia
Patient was taking Blopress (View Usage). Patient had the following side effects: eosinophil count increased, organising pneumonia on Nov 06, 2009 from JAPAN Additional patient health information: Female patient , weighting 83.78 lb, was diagnosed with hypertension, lumbar spinal stenosis, reflux oesophagitis, osteoporosis (What is osteoporosis?) and. Blopress dosage: . During the same period patient was treated with NIFLAN (View Niflan Review and Niflan Label ), PARIET (View Pariet Review and Pariet Label ), EVISTA (View Evista Review and Evista Label ), LOXONIN (View Loxonin Review and Loxonin Label ), METHYCOBAL (View Methycobal Review and Methycobal Label ), DEPAS (View Depas Review and Depas Label ), EPADEL S (View Epadel S Review and Epadel S Label ), GANATON (View Ganaton Review and Ganaton Label ). Patient was hospitalized.