ESIDRIX Side Effects

6984337-8 | Dizziness Postural, Orthostatic Hypotension
on Sep 03, 2010 Male patient from FRANCE , 61 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness postural, orthostatic hypotension. Esidrix dosage: Half A Tablet Daily. During the same period patient was treated with IRBESARTAN (50 Mg, Unk) (View Irbesartan Review and Irbesartan Label ), SOTALOL (View Sotalol Review and Sotalol Label ). Patient was hospitalized.

6643361-5 | Blood Pressure Fluctuation, Loss Of Consciousness, Malaise, Orthostatic Hypotension
Patient was taking Esidrix (View Usage). Patient had the following side effects: blood pressure fluctuation, loss of consciousness, malaise, orthostatic hypotension on Mar 09, 2010 from FRANCE Additional patient health information: Male patient , 61 years of age, . Esidrix dosage: 25 Mg, Unk. During the same period patient was treated with PRAZOSIN HCL (View Prazosin Hcl Review and Prazosin Hcl Label ), TEMERIT (5 Mg, Unk) (View Temerit Review and Temerit Label ), TRIATEC (10 Mg, Unk) (View Triatec Review and Triatec Label ), AMLOR (10 Mg, Unk) (View Amlor Review and Amlor Label ), TEGRETOL (200 Mg, Unk) (View Tegretol Review and Tegretol Label ), CRESTOR (10 Mg, Unk) (View Crestor Review and Crestor Label ), NEXIUM (20 Mg, Unk) (View Nexium Review and Nexium Label ), KARDEGIC (75 Mg, Unk) (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6446759-3 | Anuria, Blood Creatinine Increased, Blood Sodium Decreased, Diabetes Mellitus Inadequate Control, Diarrhoea, Dyspepsia, Hyperkalaemia, Renal Failure Acute
Adverse event was reported on Nov 06, 2009 by a Female patient taking Esidrix (View Usage) (Dosage: 1 Df (25 Mg ) Daily) was diagnosed with hypertension, type 2 diabetes mellitus and. Location: FRANCE , 65 years of age, After Esidrix was administered, patient had the following side effects: anuria, blood creatinine increased, blood sodium decreased, diabetes mellitus inadequate control, diarrhoea, dyspepsia, hyperkalaemia, renal failure acute. During the same period patient was treated with METFORMIN HCL (850 Mg Daily) (View Metformin Hcl Review and Metformin Hcl Label ), JANUVIA (60 Mg Daily) (View Januvia Review and Januvia Label ), COVERSYL (View Coversyl Review and Coversyl Label ), DIAMICRON (Unk) (View Diamicron Review and Diamicron Label ), TAHOR (View Tahor Review and Tahor Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), BISOPROLOL (2 Df (10 Mg ) Daily) (View Bisoprolol Review and Bisoprolol Label ). Patient was hospitalized.

6106315-3 | Blood Pressure Systolic Decreased, Diarrhoea, Erysipelas, Presyncope, Renal Failure Acute, Vomiting
on Feb 23, 2009 Female patient from FRANCE , 67 years of age, was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure systolic decreased, diarrhoea, erysipelas, presyncope, renal failure acute, vomiting. Esidrix dosage: 12.5 Mg/day. During the same period patient was treated with TRIATEC (1 Df, Qd) (View Triatec Review and Triatec Label ), METHOTREXATE (10 Mg Weekly) (View Methotrexate Review and Methotrexate Label ), AMARYL (Unk) (View Amaryl Review and Amaryl Label ), GLUCOPHAGE (Unk) (View Glucophage Review and Glucophage Label ). Patient was hospitalized.


5899606-2 | Anti-ss-a Antibody Positive, Antinuclear Antibody Positive, Blood Uric Acid Increased, C-reactive Protein Increased, Conjunctivitis, Dehydration, Dermatitis Bullous, Epidermolysis, Erythema Multiforme
on Sep 25, 2008 Female patient from FRANCE , 79 years of age, was diagnosed with depression (What is depression?), asthenia and was treated with Esidrix (View Usage). Patient had the following side effects: anti-ss-a antibody positive, antinuclear antibody positive, blood uric acid increased, c-reactive protein increased, conjunctivitis, dehydration, dermatitis bullous, epidermolysis, erythema multiforme. Esidrix dosage: Unk, Unk. During the same period patient was treated with ARCALION (Unk, Unk) (View Arcalion Review and Arcalion Label ), PRIMPERAN TAB (View Primperan Tab Review and Primperan Tab Label ), TRIFLUCAN (View Triflucan Review and Triflucan Label ), DESLORATADINE (1 Df, Qd) (View Desloratadine Review and Desloratadine Label ). Patient was hospitalized.

5745158-7 | Agitation, Alcohol Induced Persisting Dementia, Anxiety, Confusional State, Depressed Level Of Consciousness, Hyponatraemia
Patient was taking Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: agitation, alcohol induced persisting dementia, anxiety (What is anxiety?), confusional state, depressed level of consciousness, hyponatraemia on May 13, 2008 from SWEDEN Additional patient health information: Female patient , 64 years of age, was diagnosed with hypertension, blood pressure (What is blood pressure?) and. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with ATACAND (16 Mg, Qd) (View Atacand Review and Atacand Label ), PLENDIL (5 Mg, Qd) (View Plendil Review and Plendil Label ), METOPROLOL TARTRATE (50 Mg, Unk) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), ORALOVITE (View Oralovite Review and Oralovite Label ), AERIUS (View Aerius Review and Aerius Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), ALCOHOL (View Alcohol Review and Alcohol Label ). Patient was hospitalized.

5720814-5 | Blood Pressure Decreased, Circulatory Collapse, Headache
Adverse event was reported on Apr 23, 2008 by a Female patient taking Esidrix (View Usage) (Dosage: 0.5 Df/d) was diagnosed with hypertension and. Location: GERMANY , 82 years of age, Patient experienced the following unwanted or unexpected effects: blood pressure decreased, circulatory collapse, headache (What is headache?). During the same period patient was treated with VALERIAN (View Valerian Review and Valerian Label ), ACETYLSALICYLIC ACID SRT (View Acetylsalicylic Acid Srt Review and Acetylsalicylic Acid Srt Label ), CARMEN (10 Mg, Bid) (View Carmen Review and Carmen Label ), HOMEOPATHIC PREPARATIONS (View Homeopathic Preparations Review and Homeopathic Preparations Label ).

5710926-4 | Asterixis, Blood Bicarbonate Increased, Blood Ph Increased, Depressed Level Of Consciousness, Diaphragmatic Disorder, Encephalopathy, Hypercapnia, Hypoventilation, Lung Infiltration
on Apr 14, 2008 Male patient from FRANCE , 61 years of age, was treated with Esidrix (View Usage). Patient had the following side effects: asterixis, blood bicarbonate increased, blood ph increased, depressed level of consciousness, diaphragmatic disorder, encephalopathy, hypercapnia, hypoventilation, lung infiltration. Esidrix dosage: . During the same period patient was treated with LASILIX (40 Mg/day) (View Lasilix Review and Lasilix Label ), ZOCOR (20 Mg, Qd) (View Zocor Review and Zocor Label ), NEO MERCAZOLE /SCH/ (2.5 Mg, Qd) (View Neo-mercazole /sch/ Review and Neo-mercazole /sch/ Label ), XATRAL SLOW RELEASE (10 Mg, Qd) (View Xatral - Slow Release Review and Xatral - Slow Release Label ), TRIATEC (View Triatec Review and Triatec Label ), DIFFU K (View Diffu K Review and Diffu K Label ), IPRATROPIUM BROMIDE (View Ipratropium Bromide Review and Ipratropium Bromide Label ). Patient was hospitalized.

5614985-9 | Abdominal Pain Upper, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Hepatitis Acute, Vomiting
on Jan 28, 2008 Female patient from ITALY , 75 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hepatitis acute, vomiting. Esidrix dosage: 25 Mg/day. During the same period patient was treated with SELOKEN (100 Mg/day) (View Seloken Review and Seloken Label ), ASPIRIN (100 Mg/day) (View Aspirin Review and Aspirin Label ), DEPONIT (10 Mg/day) (View Deponit Review and Deponit Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ). Patient was hospitalized.

5613598-2 | Blood Pressure Decreased, Circulatory Collapse, Headache
Patient was taking Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: blood pressure decreased, circulatory collapse, headache (What is headache?) on Jan 28, 2008 from GERMANY Additional patient health information: Female patient , 82 years of age, was diagnosed with hypertension and. Esidrix dosage: 0.5 Df/d. During the same period patient was treated with VALERIAN (View Valerian Review and Valerian Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), CARMEN (10 Mg, Bid) (View Carmen Review and Carmen Label ), HOMEOPATHIC PREPARATIONS (View Homeopathic Preparations Review and Homeopathic Preparations Label ).

5507274-4 | Blood Sodium Decreased, Fatigue
Adverse event was reported on Oct 29, 2007 by a Female patient taking Esidrix (View Usage) (Dosage: 25 Mg, Qd) . Location: UNITED STATES , 78 years of age, weighting 146.0 lb, Patient had the following side effects: blood sodium decreased, fatigue. Patient was hospitalized.

5487700-X | Bedridden, Blood Creatine Phosphokinase Increased, Blood Creatinine Increased, Blood Urea Increased, Dehydration, Fall, Fluid Replacement, Hypotension
on Oct 08, 2007 Male patient from FRANCE , 98 years of age, was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: bedridden, blood creatine phosphokinase increased, blood creatinine increased, blood urea increased, dehydration, fall (What is fall?), fluid replacement, hypotension. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with LASIX (60 Mg, Qd) (View Lasix Review and Lasix Label ), PERINDOPRIL ERBUMINE (4 Mg, Qd) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), DIGOXIN (0.125 Mg, Qw4) (View Digoxin Review and Digoxin Label ), KARDEGIC (75 Mg, Qd) (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

5428788-1 | Cerebral Haemorrhage, Cerebrovascular Accident
on Aug 21, 2007 Male patient from UNITED STATES , 50 years of age, was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: cerebral haemorrhage, cerebrovascular accident. Esidrix dosage: 25 Mg, Unk. During the same period patient was treated with NORVASC (10 Mg, Unk) (View Norvasc Review and Norvasc Label ), TOPROL XL (50 Mg, Unk) (View Toprol-xl Review and Toprol-xl Label ).

5423301-7 | Bronchitis, Cough, Interstitial Lung Disease
Patient was taking Esidrix (View Usage). Patient had the following side effects: bronchitis (What is bronchitis?), cough, interstitial lung disease on Aug 20, 2007 from FRANCE Additional patient health information: Female patient , 74 years of age, . Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with CIBACENE (10 Mg, Qd) (View Cibacene Review and Cibacene Label ), CORTANCYL (5 Mg, Qod) (View Cortancyl Review and Cortancyl Label ), TAHOR (10 Mg, Qd) (View Tahor Review and Tahor Label ). Patient was hospitalized.

5421976-X | C-reactive Protein Increased, Convulsion, Epilepsy, Fluid Retention, Haemoglobin Decreased, Hypoglycaemia, Oedema, Platelet Count Decreased, Pyrexia
Adverse event was reported on Aug 20, 2007 by a Female patient taking Esidrix (View Usage) (Dosage: 25 Mg, Qd) was diagnosed with hypoglycaemia and. Location: FRANCE , 33 years of age, After Esidrix was administered, patient had the following side effects: c-reactive protein increased, convulsion, epilepsy (What is epilepsy?), fluid retention, haemoglobin decreased, hypoglycaemia, oedema, platelet count decreased, pyrexia. During the same period patient was treated with PROGLYCEM (100 Mg, Tid) (View Proglycem Review and Proglycem Label ). Patient was hospitalized.

5419069-0 | Abdominal Pain Upper, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Bilirubin Increased, Hepatitis Acute, Vomiting
on Aug 10, 2007 Female patient from ITALY , 75 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, blood bilirubin increased, hepatitis acute, vomiting. Esidrix dosage: 25 Mg/day. During the same period patient was treated with METOPROLOL TARTRATE (100 Mg/day) (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), ASPIRIN (100 Mg/day) (View Aspirin Review and Aspirin Label ), DEPONIT (10 Mg/day) (View Deponit Review and Deponit Label ), MODURETIC 5 50 (View Moduretic 5-50 Review and Moduretic 5-50 Label ). Patient was hospitalized.

5406756-3 | C-reactive Protein Increased, Convulsion, Epilepsy, Haemoglobin Decreased, Hypoglycaemia, Oedema, Platelet Count Decreased, Pyrexia, Rash
on Jul 30, 2007 Female patient from FRANCE , 33 years of age, was diagnosed with hypoglycaemia and was treated with Esidrix (View Usage). Patient had the following side effects: c-reactive protein increased, convulsion, epilepsy (What is epilepsy?), haemoglobin decreased, hypoglycaemia, oedema, platelet count decreased, pyrexia, rash (What is rash?). Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with PROGLYCEM (100 Mg, Tid) (View Proglycem Review and Proglycem Label ). Patient was hospitalized.

5301711-6 | Anorexia, Asthenia, Blood Creatinine Increased, Creatinine Renal Clearance Decreased, Dark Circles Under Eyes, Dehydration, Dizziness, Lip Dry
Patient was taking Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: anorexia, asthenia, blood creatinine increased, creatinine renal clearance decreased, dark circles under eyes, dehydration, dizziness (What is dizziness?), lip dry on Apr 06, 2007 from FRANCE Additional patient health information: Male patient , 92 years of age, weighting 154.3 lb, was diagnosed with oedema peripheral and. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), DIGOXIN (1 Df, Qd) (View Digoxin Review and Digoxin Label ), DIDRONEL (400 Mg, Qd) (View Didronel Review and Didronel Label ), PERINDOPRIL ERBUMINE (4 Mg, Bid) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), NEXIUM (20 Mg, Qd) (View Nexium Review and Nexium Label ), CORTANCYL (5 Mg, Qd) (View Cortancyl Review and Cortancyl Label ), CACIT D3 (1 Df, Qd) (View Cacit D3 Review and Cacit D3 Label ), XANAX (0.5 Mg, Qd) (View Xanax Review and Xanax Label ). Patient was hospitalized.

5268109-0 | Aphasia, Cerebral Infarction, Dizziness, Dysarthria, Hyperlipidaemia, Hypertension, Hyponatraemia, Listless, Transient Ischaemic Attack
Adverse event was reported on Mar 06, 2007 by a Female patient taking Esidrix (View Usage) (Dosage: 25mg) was diagnosed with hypertonia and. Location: SWEDEN , 71 years of age, Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), cerebral infarction, dizziness (What is dizziness?), dysarthria, hyperlipidaemia, hypertension, hyponatraemia, listless, transient ischaemic attack. During the same period patient was treated with XALATAN (50 Ug/ml) (View Xalatan Review and Xalatan Label ), ENALAPRIL MALEATE (10mg Daily) (View Enalapril Maleate Review and Enalapril Maleate Label ), SIMVASTATIN (40mg) (View Simvastatin Review and Simvastatin Label ), LEVAXIN (100ug) (View Levaxin Review and Levaxin Label ), WARAN (2.5mg) (View Waran Review and Waran Label ). Patient was hospitalized.

5149861-1 | Arthralgia, Face Injury, Fall, Limb Discomfort, Pain In Extremity, Syncope
on Oct 16, 2006 Female patient from SWITZERLAND , 69 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient had the following side effects: arthralgia, face injury, fall (What is fall?), limb discomfort, pain in extremity, syncope. Esidrix dosage: 12.5 Mg, Qd. During the same period patient was treated with VALSARTAN (View Valsartan Review and Valsartan Label ). Patient was hospitalized.

5143816-9 | Blood Potassium Decreased, Hypokalaemia, Muscle Spasms, Nausea, Palpitations, Polyuria, Thirst, Weight Decreased
on Oct 26, 2006 Male patient from FRANCE , 22 years of age, was diagnosed with nephrogenic diabetes insipidus and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: blood potassium decreased, hypokalaemia, muscle spasms, nausea (What is nausea?), palpitations, polyuria, thirst, weight decreased. Esidrix dosage: 50 Mg, Bid. During the same period patient was treated with INDOCID (50 Mg, Bid) (View Indocid Review and Indocid Label ). Patient was hospitalized.

5143814-5 | Blood Creatinine Increased, Confusional State, Hyperkalaemia, Hyponatraemia, Renal Failure
Patient was taking Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatinine increased, confusional state, hyperkalaemia, hyponatraemia, renal failure on Oct 10, 2006 from FRANCE Additional patient health information: Female patient , 90 years of age, . Esidrix dosage: . During the same period patient was treated with ATACAND (8 Mg, Qd) (View Atacand Review and Atacand Label ). Patient was hospitalized.

5141963-9 | Arthralgia, Face Injury, Fall, Limb Discomfort, Pain In Extremity, Rhinalgia, Syncope
Adverse event was reported on Oct 16, 2006 by a Female patient taking Esidrix (View Usage) (Dosage: 12.5 Mg, Qd) was diagnosed with hypertension and. Location: SWITZERLAND , 69 years of age, Patient had the following side effects: arthralgia, face injury, fall (What is fall?), limb discomfort, pain in extremity, rhinalgia, syncope. During the same period patient was treated with VALSARTAN (View Valsartan Review and Valsartan Label ). Patient was hospitalized.

5137036-1 | Aspiration Bone Marrow Abnormal, Bone Marrow Failure, Bronchitis, Cardiac Disorder, Neutropenia
on Apr 06, 2006 Female patient from ITALY , 77 years of age, was diagnosed with cardiac failure and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: aspiration bone marrow abnormal, bone marrow failure, bronchitis (What is bronchitis?), cardiac disorder, neutropenia. Esidrix dosage: 25 Mg/day. During the same period patient was treated with EUTIROX (View Eutirox Review and Eutirox Label ), SIGACORA SLOW RELEASE (View Sigacora - Slow Release Review and Sigacora - Slow Release Label ), CORDARONE (View Cordarone Review and Cordarone Label ), PANTOPAN (View Pantopan Review and Pantopan Label ), LASIX (View Lasix Review and Lasix Label ), LUVION (View Luvion Review and Luvion Label ), COUMADIN (View Coumadin Review and Coumadin Label ).

5132336-3 | Asthenia, Blood Creatinine Increased, Confusional State, Hyperkalaemia, Hyponatraemia, Renal Failure
on Oct 10, 2006 Female patient from FRANCE , 90 years of age, was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, blood creatinine increased, confusional state, hyperkalaemia, hyponatraemia, renal failure. Esidrix dosage: . During the same period patient was treated with ATACAND (8 Mg, Qd) (View Atacand Review and Atacand Label ). Patient was hospitalized.

5122568-2 | Arthralgia, Biopsy Skin Abnormal, Blood Alkaline Phosphatase Increased, C-reactive Protein Increased, Cholestasis, Creatinine Renal Clearance Decreased, Cytolytic Hepatitis, Eosinophil Count Increased, Gamma-glutamyltransferase Increased
Patient was taking Esidrix (View Usage). Patient had the following side effects: arthralgia, biopsy skin abnormal, blood alkaline phosphatase increased, c-reactive protein increased, cholestasis, creatinine renal clearance decreased, cytolytic hepatitis, eosinophil count increased, gamma-glutamyltransferase increased on Jul 27, 2006 from FRANCE Additional patient health information: Male patient , 71 years of age, weighting 167.6 lb, was diagnosed with hypertension, hyperlipidaemia and. Esidrix dosage: 12.5 Mg, Qd. During the same period patient was treated with COZAAR (100 Mg, Qd) (View Cozaar Review and Cozaar Label ), CRESTOR (5 Mg, Qd) (View Crestor Review and Crestor Label ), NEBIVOLOL HYDROCHLORIDE (2.5 Mg, Qd) (View Nebivolol Hydrochloride Review and Nebivolol Hydrochloride Label ). Patient was hospitalized.

5101063-0 | Dehydration, Hypokalaemia, Hyponatraemia
Adverse event was reported on Apr 12, 2006 by a Female patient taking Esidrix (View Usage) (Dosage: 2 Tablets Daily) was diagnosed with hypertension and. Location: FRANCE , 85 years of age, weighting 105.8 lb, After Esidrix was administered, patient had the following side effects: dehydration, hypokalaemia, hyponatraemia. During the same period patient was treated with LAXATIVES (View Laxatives Review and Laxatives Label ).

5092520-4 | Dyspnoea, Hypotension, Myocardial Infarction
on Aug 11, 2006 Female patient from UNITED STATES , 75 years of age, was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: dyspnoea, hypotension, myocardial infarction. Esidrix dosage: . During the same period patient was treated with ENBREL (10 Mg, Bid) (View Enbrel Review and Enbrel Label ), MAXZIDE (1.5 Tabs Of 50/75mg, Qd) (View Maxzide Review and Maxzide Label ).

5083520-9 | Dyspnoea, Hypotension, Myocardial Infarction
on Aug 11, 2006 Female patient from UNITED STATES , 75 years of age, was treated with Esidrix (View Usage). Patient had the following side effects: dyspnoea, hypotension, myocardial infarction. Esidrix dosage: . During the same period patient was treated with ENBREL (10 Mg, Bid) (View Enbrel Review and Enbrel Label ), MAXZIDE (1.5 Tabs Of 50/75mg, Qd) (View Maxzide Review and Maxzide Label ).

5073561-X | Coma, Escherichia Infection, Hyperthermia, Hyponatraemia, Renal Failure, Staphylococcal Bacteraemia
Patient was taking Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: coma, escherichia infection, hyperthermia, hyponatraemia, renal failure, staphylococcal bacteraemia on Jul 28, 2006 from FRANCE Additional patient health information: Female patient , 51 years of age, weighting 116.8 lb, . Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with LASILIX (1 Df, Tid) (View Lasilix Review and Lasilix Label ), OFLOCET (1 Df, Bid) (View Oflocet Review and Oflocet Label ), OMEPRAZOLE (20 Mg, Qd) (View Omeprazole Review and Omeprazole Label ), AUGMENTIN (View Augmentin Review and Augmentin Label ), TRILEPTAL (1.5 Df, Bid) (View Trileptal Review and Trileptal Label ). Patient was hospitalized.

5073305-1 | Arthralgia, Blood Alkaline Phosphatase Increased, C-reactive Protein Increased, Cholestasis, Creatinine Renal Clearance Decreased, Cytolytic Hepatitis, Eosinophil Count Increased, Gamma-glutamyltransferase Increased, Inflammation
Adverse event was reported on Jul 27, 2006 by a Male patient taking Esidrix (View Usage) (Dosage: 12.5 Mg, Qd) was diagnosed with hypertension, hyperlipidaemia and. Location: FRANCE , 71 years of age, weighting 167.6 lb, Patient experienced the following unwanted or unexpected effects: arthralgia, blood alkaline phosphatase increased, c-reactive protein increased, cholestasis, creatinine renal clearance decreased, cytolytic hepatitis, eosinophil count increased, gamma-glutamyltransferase increased, inflammation. During the same period patient was treated with COZAAR (100 Mg, Qd) (View Cozaar Review and Cozaar Label ), CRESTOR (5 Mg, Qd) (View Crestor Review and Crestor Label ), NEBIVOLOL HYDROCHLORIDE (2.5 Mg, Qd) (View Nebivolol Hydrochloride Review and Nebivolol Hydrochloride Label ). Patient was hospitalized.

5065919-X | Calculus Urinary, No Adverse Effect
on Jul 21, 2006 Female patient from FRANCE , child 1 years of age, was diagnosed with haematuria and was treated with Esidrix (View Usage). Patient had the following side effects: calculus urinary, no adverse effect. Esidrix dosage: 5 Mg, Bid. Patient was hospitalized.

5040723-7 | Blood Creatinine Increased, Dementia, Extrapyramidal Disorder, Facial Palsy, Fall, Haemoglobin Decreased, Head Injury, Hyperhidrosis
on Jun 22, 2006 Female patient from DENMARK , 90 years of age, was diagnosed with hypertension, depression (What is depression?), deep vein thrombosis (What is deep vein thrombosis?) and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: blood creatinine increased, dementia (What is dementia?), extrapyramidal disorder, facial palsy, fall (What is fall?), haemoglobin decreased, head injury, hyperhidrosis. Esidrix dosage: 12.5 Mg, Unk. During the same period patient was treated with RAMIPRIL (2.5 Mg, Qd) (View Ramipril Review and Ramipril Label ), MEPRONIZINE (View Mepronizine Review and Mepronizine Label ), TERCIAN (16 Drp, Qd) (View Tercian Review and Tercian Label ), HEPARIN (1.4 Ml (0.7)) (View Heparin Review and Heparin Label ), EFFEXOR (View Effexor Review and Effexor Label ), ANAFRANIL (View Anafranil Review and Anafranil Label ), TRANXENE (View Tranxene Review and Tranxene Label ), COUMADIN (View Coumadin Review and Coumadin Label ). Patient was hospitalized.

4964340-X | Blood Creatine Increased, Chest Pain, Hypokalaemia
Patient was taking Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: blood creatine increased, chest pain (What is chest pain?), hypokalaemia on Mar 30, 2006 from FRANCE Additional patient health information: Female patient , 68 years of age, was diagnosed with hypertension, dyslipidaemia and. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with TRIATEC (View Triatec Review and Triatec Label ), TAHOR (View Tahor Review and Tahor Label ), AMLOR (View Amlor Review and Amlor Label ), CORDARONE (View Cordarone Review and Cordarone Label ), PREVISCAN (View Previscan Review and Previscan Label ). Patient was hospitalized.

4953995-1 | Diplopia, Dry Eye, Eye Inflammation, Eye Irritation, Myasthenic Syndrome
Adverse event was reported on Mar 21, 2006 by a Male patient taking Esidrix (View Usage) (Dosage: 25 Mg, Qd) was diagnosed with hypertension and. Location: FRANCE , 47 years of age, Patient had the following side effects: diplopia, dry eye, eye inflammation, eye irritation, myasthenic syndrome. During the same period patient was treated with TEVETEN (View Teveten Review and Teveten Label ), ZANIDIP (View Zanidip Review and Zanidip Label ).

4944620-4 | Blood Creatinine Increased, Renal Failure, Urine Output Decreased
on Mar 07, 2006 Female patient from SWEDEN , 80 years of age, was diagnosed with essential hypertension and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: blood creatinine increased, renal failure, urine output decreased. Esidrix dosage: 12.5 Mg/day. During the same period patient was treated with ATACAND (1 Dfd/day) (View Atacand Review and Atacand Label ), METOPROLOL SUCCINATE (50 Mg, Unk) (View Metoprolol Succinate Review and Metoprolol Succinate Label ), ACETAMINOPHEN (500 Mg, Unk) (View Acetaminophen Review and Acetaminophen Label ), NORVASC (10 Mg, Unk) (View Norvasc Review and Norvasc Label ), IMOVANE (7.5 Mg, Unk) (View Imovane Review and Imovane Label ), ACETYLCYSTEINE (200 Mg, Unk) (View Acetylcysteine Review and Acetylcysteine Label ), KALCIPOS D (View Kalcipos-d Review and Kalcipos-d Label ).

4889535-5 | International Normalised Ratio Increased
on Jan 16, 2006 Female patient from FRANCE , 82 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: international normalised ratio increased. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ).

4865924-X | Cerebrovascular Accident, Hyponatraemia, Polydipsia
Patient was taking Esidrix (View Usage). Patient had the following side effects: cerebrovascular accident, hyponatraemia, polydipsia on Dec 13, 2005 from FRANCE Additional patient health information: Female patient , 73 years of age, . Esidrix dosage: .

4859843-2 | Aplastic Anaemia, Bone Marrow Disorder, Cerebrovascular Accident, Haemoglobin Decreased, Thrombocytopenia
Adverse event was reported on Sep 16, 2005 by a Male patient taking Esidrix (View Usage) (Dosage: 25 Mg, Qd) was diagnosed with hypertension and. Location: NORWAY , 81 years of age, After Esidrix was administered, patient had the following side effects: aplastic anaemia, bone marrow disorder, cerebrovascular accident, haemoglobin decreased, thrombocytopenia. Patient was hospitalized.

4832773-8 | Syncope
on Sep 16, 2005 Male patient from GERMANY , weighting 136.7 lb, was diagnosed with osteoporosis (What is osteoporosis?) and was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: syncope. Esidrix dosage: 25 Mg/d. During the same period patient was treated with CALCIUM GLUCONATE (View Calcium Gluconate Review and Calcium Gluconate Label ), FOSAMAX (10 Mg/d) (View Fosamax Review and Fosamax Label ), ANTIINFLAMMATORY/ANTIRHEUMATIC NON STEROIDS (Unk, Prn) (View Antiinflammatory/antirheumatic Non-steroids Review and Antiinflammatory/antirheumatic Non-steroids Label ). Patient was hospitalized.

4818450-8 | Aplastic Anaemia, Bone Marrow Disorder, Cerebrovascular Accident, Haemoglobin Decreased, Thrombocytopenia
on Sep 16, 2005 Male patient from NORWAY , 81 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient had the following side effects: aplastic anaemia, bone marrow disorder, cerebrovascular accident, haemoglobin decreased, thrombocytopenia. Esidrix dosage: 25 Mg, Qd. Patient was hospitalized.

4772131-8 | Aplastic Anaemia, Bone Marrow Disorder, Cerebrovascular Accident, Thrombocytopenia
Patient was taking Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: aplastic anaemia, bone marrow disorder, cerebrovascular accident, thrombocytopenia on Sep 16, 2005 from NORWAY Additional patient health information: Male patient , 81 years of age, was diagnosed with hypertension and. Esidrix dosage: 25 Mg, Qd.

4751647-4 | Creatinine Renal Clearance Decreased, Depressed Level Of Consciousness, Grand Mal Convulsion, Hyponatraemia, Ischaemic Stroke
Adverse event was reported on Mar 14, 2005 by a Female patient taking Esidrix (View Usage) (Dosage: 12.5 Mg/day) was diagnosed with dementia alzheimer's type and. Location: FRANCE , 85 years of age, weighting 121.3 lb, Patient experienced the following unwanted or unexpected effects: creatinine renal clearance decreased, depressed level of consciousness, grand mal convulsion, hyponatraemia, ischaemic stroke. During the same period patient was treated with STILNOX (5 Mg/day) (View Stilnox Review and Stilnox Label ), EXELON (3 Mg/day) (View Exelon Review and Exelon Label ). Patient was hospitalized.

4710714-1 | Asthenia, Cerebral Disorder, Depressed Level Of Consciousness, Encephalopathy, Hyponatraemia, Inappropriate Antidiuretic Hormone Secretion, Swelling
on Jun 29, 2005 Female patient from SWEDEN , 66 years of age, was diagnosed with hypertension and was treated with Esidrix (View Usage). Patient had the following side effects: asthenia, cerebral disorder, depressed level of consciousness, encephalopathy, hyponatraemia, inappropriate antidiuretic hormone secretion, swelling. Esidrix dosage: 12.5 Mg/day. During the same period patient was treated with TIOTROPIUM BROMIDE (View Tiotropium Bromide Review and Tiotropium Bromide Label ), BUDESONIDE W/FORMOTEROL FUMARATE (View Budesonide W/formoterol Fumarate Review and Budesonide W/formoterol Fumarate Label ). Patient was hospitalized.

4688971-X | Acute Pulmonary Oedema, Asthenia, Atrial Fibrillation, Azotaemia, Blister, Blood Alkaline Phosphatase Increased, Blood Chloride Decreased, Blood Creatinine Increased, Blood Potassium Increased
on Aug 09, 2002 Male patient from , 65 years of age, was diagnosed with cardiac failure and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: acute pulmonary oedema, asthenia, atrial fibrillation (What is atrial fibrillation?), azotaemia, blister, blood alkaline phosphatase increased, blood chloride decreased, blood creatinine increased, blood potassium increased. Esidrix dosage: . During the same period patient was treated with TAREG (40 Mg, Qd) (View Tareg Review and Tareg Label ), CORDARONE (200 Mg/day) (View Cordarone Review and Cordarone Label ), LASIX (250 Mg, Qd) (View Lasix Review and Lasix Label ), ASPEGIC 325 (250 Mg, Qd) (View Aspegic 325 Review and Aspegic 325 Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ). Patient was hospitalized.

4678612-X | Abdominal Pain Upper, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Constipation, Hepatitis, Obesity
Patient was taking Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain upper, alanine aminotransferase increased, aspartate aminotransferase increased, constipation (What is constipation?), hepatitis (What is hepatitis?), obesity (What is obesity?) on May 23, 2005 from Additional patient health information: Female patient , 59 years of age, weighting 187.4 lb, was diagnosed with hypertension, obesity (What is obesity?), systemic lupus erythematosus, constipation (What is constipation?) and. Esidrix dosage: 12.5 Mg, Qd. During the same period patient was treated with LIVIAL (Unk, Unk) (View Livial Review and Livial Label ), XENICAL (1 Df, Qd) (View Xenical Review and Xenical Label ), OMEPRAZOLE (20 Mg, Qd) (View Omeprazole Review and Omeprazole Label ), AMLOR (View Amlor Review and Amlor Label ), PLAQUENIL (View Plaquenil Review and Plaquenil Label ), FOSAMAX (View Fosamax Review and Fosamax Label ), HERBAL PREPARATION (ERNST RICHTER) (View Herbal Preparation (ernst Richter) Review and Herbal Preparation (ernst Richter) Label ). Patient was hospitalized.

4661217-4 | Blood Potassium Decreased, Electrocardiogram St Segment Depression, Hyperhidrosis, Night Sweats, Sleep Disorder, Ventricular Extrasystoles, Ventricular Hypertrophy
Adverse event was reported on Dec 22, 2004 by a Female patient taking Esidrix (View Usage) (Dosage: 1 Df, Qd) was diagnosed with hypertension and. Location: , 73 years of age, Patient had the following side effects: blood potassium decreased, electrocardiogram st segment depression, hyperhidrosis, night sweats, sleep disorder (What is sleep disorder?), ventricular extrasystoles, ventricular hypertrophy. During the same period patient was treated with PANKREOFLAT (View Pankreoflat Review and Pankreoflat Label ).

4650823-9 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Blood Creatinine Increased, Blood Urea Increased, Transaminases Increased
on Apr 26, 2005 Male patient from , 77 years of age, was diagnosed with cardiac failure, hypothyroidism and was treated with Esidrix (View Usage). After Esidrix was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, blood bilirubin increased, blood creatinine increased, blood urea increased, transaminases increased. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with PLAVIX (300 Mg, Qd) (View Plavix Review and Plavix Label ), DIURAL (40 Mg, Bid) (View Diural Review and Diural Label ), ALLOPUR (300 Mg, Qd) (View Allopur Review and Allopur Label ), EMCONCOR (2.5 Mg, Qd) (View Emconcor Review and Emconcor Label ), LEVAXIN (0.1 Mg, Qd) (View Levaxin Review and Levaxin Label ). Patient was hospitalized.

4615269-8 | Angle Closure Glaucoma, Diarrhoea Infectious, Trabeculectomy
on Mar 14, 2005 Male patient from , 67 years of age, was diagnosed with diarrhoea infectious and was treated with Esidrix (View Usage). Patient experienced the following unwanted or unexpected effects: angle closure glaucoma, diarrhoea infectious, trabeculectomy. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with IMODIUM (2 Mg, Bid) (View Imodium Review and Imodium Label ).

4603028-1 | Dizziness, Hypokalaemia, Hyponatraemia, Petit Mal Epilepsy, Subdural Haematoma, Vomiting
Patient was taking Esidrix (View Usage). Patient had the following side effects: dizziness (What is dizziness?), hypokalaemia, hyponatraemia, petit mal epilepsy, subdural haematoma, vomiting on Mar 03, 2005 from Additional patient health information: Male patient , 90 years of age, was diagnosed with hypertension and. Esidrix dosage: 25 Mg, Qd. During the same period patient was treated with MINIRIN (View Minirin Review and Minirin Label ), ZOCORD (View Zocord Review and Zocord Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), IMOVANE (View Imovane Review and Imovane Label ). Patient was hospitalized.