KREDEX Side Effects

6945790-9 | Chest Discomfort, Eosinophilia, Renal Failure Acute, Troponin Increased
on Aug 19, 2010 Male patient from FRANCE , 69 years of age, was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: chest discomfort, eosinophilia, renal failure acute, troponin increased. Kredex dosage: 25mg Per Day. During the same period patient was treated with PRASUGREL (1u Per Day) (View Prasugrel Review and Prasugrel Label ), GLUCOR (View Glucor Review and Glucor Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), PANTOPRAZOLE (View Pantoprazole Review and Pantoprazole Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), IXPRIM (View Ixprim Review and Ixprim Label ), AMLODIPINE (View Amlodipine Review and Amlodipine Label ). Patient was hospitalized.

6634661-3 | Orthostatic Hypertension, Syncope
Patient was taking Kredex (View Usage). Patient had the following side effects: orthostatic hypertension, syncope on Mar 04, 2010 from SWEDEN Additional patient health information: Male patient , 89 years of age, . Kredex dosage: . During the same period patient was treated with ATACAND (View Atacand Review and Atacand Label ), MOVICOL (View Movicol Review and Movicol Label ), ATROVENT (View Atrovent Review and Atrovent Label ), TROMBYL (View Trombyl Review and Trombyl Label ). Patient was hospitalized.

6392000-X | Fall, Malaise, Orthostatic Hypotension
Adverse event was reported on Sep 30, 2009 by a Male patient taking Kredex (View Usage) (Dosage: 12.5mg Per Day) was diagnosed with cardiac failure, hypertension and. Location: FRANCE , 64 years of age, After Kredex was administered, patient had the following side effects: fall (What is fall?), malaise, orthostatic hypotension. During the same period patient was treated with APROVEL (75mg Per Day) (View Aprovel Review and Aprovel Label ), VITAMIN B1 TAB (View Vitamin B1 Tab Review and Vitamin B1 Tab Label ), DOLIPRANE (View Doliprane Review and Doliprane Label ), CACIT (View Cacit Review and Cacit Label ), GUTRON (View Gutron Review and Gutron Label ), ACTONEL (View Actonel Review and Actonel Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

6377254-8 | Myoclonus
on Sep 01, 2009 Female patient from NORWAY , 76 years of age, was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: myoclonus. Kredex dosage: . During the same period patient was treated with ADALAT (View Adalat Review and Adalat Label ), ARICEPT (View Aricept Review and Aricept Label ), IMOVANE (View Imovane Review and Imovane Label ), MAREVAN (View Marevan Review and Marevan Label ), PREDNISOLONE (View Prednisolone Review and Prednisolone Label ), SELOZOK (View Selozok Review and Selozok Label ), SIMVASTATIN (View Simvastatin Review and Simvastatin Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ).


6345938-3 | Blood Pressure Decreased, Overdose
on Aug 31, 2009 Male patient from FRANCE , 70 years of age, was diagnosed with cardiac failure and was treated with Kredex (View Usage). Patient had the following side effects: blood pressure decreased, overdose. Kredex dosage: 6.25mg Three Times Per Day. Patient was hospitalized.

6079209-X | Disturbance In Attention, Electrocardiogram Qrs Complex Prolonged, Electrocardiogram St Segment Elevation, Escherichia Urinary Tract Infection, Hyperkalaemia, Hypothermia
Patient was taking Kredex (View Usage). After Kredex was administered, patient had the following side effects: disturbance in attention, electrocardiogram qrs complex prolonged, electrocardiogram st segment elevation, escherichia urinary tract infection, hyperkalaemia, hypothermia (What is hypothermia?) on Feb 10, 2009 from FRANCE Additional patient health information: Female patient , 83 years of age, . Kredex dosage: 12.5mg Twice Per Day. During the same period patient was treated with COVERSYL (View Coversyl Review and Coversyl Label ), IMOVANE (View Imovane Review and Imovane Label ), DUPHALAC (View Duphalac Review and Duphalac Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ), RISPERDAL (View Risperdal Review and Risperdal Label ), TERCIAN (View Tercian Review and Tercian Label ). Patient was hospitalized.

5475834-5 | Osteonecrosis
Adverse event was reported on Oct 01, 2007 by a Female patient taking Kredex (View Usage) (Dosage: 6.25mg Twice Per Day) was diagnosed with hypertension, arteritis, hypothyroidism and. Location: FRANCE , 75 years of age, Patient experienced the following unwanted or unexpected effects: osteonecrosis (What is osteonecrosis?). During the same period patient was treated with LYRICA (150mg Twice Per Day) (View Lyrica Review and Lyrica Label ), ZOMETA (4mg Per Day) (View Zometa Review and Zometa Label ), PERINDOPRIL ERBUMINE (2mg Per Day) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), EXEMESTANE (25mg Per Day) (View Exemestane Review and Exemestane Label ), CORTANCYL (15mg Per Day) (View Cortancyl Review and Cortancyl Label ), PLAVIX (75mg Per Day) (View Plavix Review and Plavix Label ), LEVOTHYROX (100mcg Per Day) (View Levothyrox Review and Levothyrox Label ), HERCEPTIN (View Herceptin Review and Herceptin Label ).

5372219-7 | Angiopathy, Oedema Peripheral, Pain In Extremity
on Jun 20, 2007 Male patient from FRANCE , 64 years of age, was diagnosed with essential hypertension and was treated with Kredex (View Usage). Patient had the following side effects: angiopathy, oedema peripheral, pain in extremity. Kredex dosage: . During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ), PREVISCAN (View Previscan Review and Previscan Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), TENORMIN (View Tenormin Review and Tenormin Label ), ALDACTONE (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

5344106-1 | Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Blood Alkaline Phosphatase Increased, Dyspnoea At Rest, Gamma-glutamyltransferase Increased
on May 27, 2007 Female patient from FRANCE , 73 years of age, was treated with Kredex (View Usage). After Kredex was administered, patient had the following side effects: alanine aminotransferase increased, aspartate aminotransferase increased, blood alkaline phosphatase increased, dyspnoea at rest, gamma-glutamyltransferase increased. Kredex dosage: 6.25mg Per Day. During the same period patient was treated with ALDACTONE (25mg Per Day) (View Aldactone Review and Aldactone Label ), LASIX (40mg Per Day) (View Lasix Review and Lasix Label ), ATACAND (2mg Per Day) (View Atacand Review and Atacand Label ), PREVISCAN (View Previscan Review and Previscan Label ), CORDARONE (View Cordarone Review and Cordarone Label ), LEXOMIL (View Lexomil Review and Lexomil Label ). Patient was hospitalized.

5299379-0 | Breast Cancer, Demyelinating Polyneuropathy, Gait Disturbance, Hypoaesthesia, Paraesthesia, Sensory Disturbance
Patient was taking Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: breast cancer (What is breast cancer?), demyelinating polyneuropathy, gait disturbance, hypoaesthesia, paraesthesia, sensory disturbance on Apr 04, 2007 from FRANCE Additional patient health information: Female patient , 58 years of age, weighting 132.3 lb, was diagnosed with cardiac failure, thyroid disorder, hypercholesterolaemia, breast cancer (What is breast cancer?) and. Kredex dosage: . During the same period patient was treated with COVERSYL /FRA/ (4 Mg Daily) (View Coversyl /fra/ Review and Coversyl /fra/ Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SIMVASTATIN (1 Df, Qd) (View Simvastatin Review and Simvastatin Label ), FEMARA (2.5 Mg, Qd) (View Femara Review and Femara Label ), HORMONES AND RELATED AGENTS (View Hormones And Related Agents Review and Hormones And Related Agents Label ).

5262783-0 | Intermittent Claudication, Muscle Fatigue, Nervous System Disorder, Neuropathy, Polyneuropathy
Adverse event was reported on Feb 28, 2007 by a Male patient taking Kredex (View Usage) (Dosage: 12.5mg Twice Per Day) was diagnosed with cardiac failure and. Location: FRANCE , 76 years of age, Patient had the following side effects: intermittent claudication, muscle fatigue, nervous system disorder, neuropathy, polyneuropathy. During the same period patient was treated with AMLODIPINE (View Amlodipine Review and Amlodipine Label ), IRBESARTAN (View Irbesartan Review and Irbesartan Label ), FLECAINIDE ACETATE (View Flecainide Acetate Review and Flecainide Acetate Label ).

5256120-5 | Demyelinating Polyneuropathy, Gait Disturbance, Hypoaesthesia, Paraesthesia, Sensory Disturbance
on Feb 21, 2007 Female patient from FRANCE , 58 years of age, weighting 132.3 lb, was diagnosed with cardiac failure, thyroid disorder, hypercholesterolaemia, breast cancer (What is breast cancer?) and was treated with Kredex (View Usage). After Kredex was administered, patient had the following side effects: demyelinating polyneuropathy, gait disturbance, hypoaesthesia, paraesthesia, sensory disturbance. Kredex dosage: . During the same period patient was treated with COVERSYL /FRA/ (4 Mg Daily) (View Coversyl /fra/ Review and Coversyl /fra/ Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SIMVASTATIN (1 Df, Qd) (View Simvastatin Review and Simvastatin Label ), FEMARA (2.5 Mg, Qd) (View Femara Review and Femara Label ).

5247840-7 | Demyelinating Polyneuropathy, Gait Disturbance, Hypoaesthesia, Paraesthesia, Sensory Disturbance
on Feb 07, 2007 Female patient from FRANCE , 58 years of age, weighting 132.3 lb, was diagnosed with cardiac failure, thyroid disorder, hypercholesterolaemia, breast cancer (What is breast cancer?) and was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: demyelinating polyneuropathy, gait disturbance, hypoaesthesia, paraesthesia, sensory disturbance. Kredex dosage: . During the same period patient was treated with COVERSYL /FRA/ (4 Mg Daily) (View Coversyl /fra/ Review and Coversyl /fra/ Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SIMVASTATIN (1 Df, Qd) (View Simvastatin Review and Simvastatin Label ), FEMARA (2.5 Mg, Qd) (View Femara Review and Femara Label ).

5243471-3 | Demyelinating Polyneuropathy, Gait Disturbance, Hypoaesthesia, Paraesthesia, Sensory Disturbance
Patient was taking Kredex (View Usage). Patient had the following side effects: demyelinating polyneuropathy, gait disturbance, hypoaesthesia, paraesthesia, sensory disturbance on Feb 07, 2007 from FRANCE Additional patient health information: Female patient , 58 years of age, weighting 132.3 lb, was diagnosed with cardiac failure, thyroid disorder, hypercholesterolaemia, breast cancer (What is breast cancer?) and. Kredex dosage: . During the same period patient was treated with COVERSYL /FRA/ (4 Mg Daily) (View Coversyl /fra/ Review and Coversyl /fra/ Label ), LEVOTHYROXINE SODIUM (View Levothyroxine Sodium Review and Levothyroxine Sodium Label ), SIMVASTATIN (1 Df, Qd) (View Simvastatin Review and Simvastatin Label ), FEMARA (2.5 Mg, Qd) (View Femara Review and Femara Label ).

5213514-1 | Angiopathy, Nephropathy, Renal Failure Acute
Adverse event was reported on Jan 10, 2007 by a Male patient taking Kredex (View Usage) (Dosage: ) was diagnosed with ill-defined disorder, back pain (What is back pain?) and. Location: FRANCE , 58 years of age, After Kredex was administered, patient had the following side effects: angiopathy, nephropathy, renal failure acute. During the same period patient was treated with PERINDOPRIL ERBUMINE (Daily Dose: 4 Milligram(s)) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), NEXEN (View Nexen Review and Nexen Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), LASIX (Daily Dose: 20 Milligram(s)) (View Lasix Review and Lasix Label ). Patient was hospitalized.

5097322-0 | Anorexia, Asthenia, Dizziness, Fall, Gastric Cancer, Haematoma, Orthostatic Hypotension
on Apr 24, 2006 Male patient from FRANCE , 83 years of age, was diagnosed with angina pectoris and was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: anorexia, asthenia, dizziness (What is dizziness?), fall (What is fall?), gastric cancer, haematoma, orthostatic hypotension. Kredex dosage: 12.5mg Twice Per Day. During the same period patient was treated with ADANCOR (10mg Twice Per Day) (View Adancor Review and Adancor Label ), COVERSYL (2mg Per Day) (View Coversyl Review and Coversyl Label ), CORVASAL (2mg Per Day) (View Corvasal Review and Corvasal Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), MOVICOL (View Movicol Review and Movicol Label ), NEXIUM (View Nexium Review and Nexium Label ), PLAVIX (View Plavix Review and Plavix Label ). Patient was hospitalized.

5020075-9 | C-reactive Protein Increased, Eosinophilia, Gamma-glutamyltransferase Increased, Pruritus, Rash Maculo-papular
on May 26, 2006 Female patient from FRANCE , 68 years of age, was treated with Kredex (View Usage). Patient had the following side effects: c-reactive protein increased, eosinophilia, gamma-glutamyltransferase increased, pruritus, rash maculo-papular. Kredex dosage: . During the same period patient was treated with TAHOR (View Tahor Review and Tahor Label ), LOVENOX (View Lovenox Review and Lovenox Label ), COVERSYL (View Coversyl Review and Coversyl Label ), VISIPAQUE (View Visipaque Review and Visipaque Label ), PLAVIX (View Plavix Review and Plavix Label ), ASPIRIN (View Aspirin Review and Aspirin Label ), INTEGRILIN (View Integrilin Review and Integrilin Label ), VIRLIX (View Virlix Review and Virlix Label ). Patient was hospitalized.

5001848-5 | Fall, Haematoma, Orthostatic Hypotension
Patient was taking Kredex (View Usage). After Kredex was administered, patient had the following side effects: fall (What is fall?), haematoma, orthostatic hypotension on Apr 24, 2006 from FRANCE Additional patient health information: Male patient , 83 years of age, was diagnosed with angina pectoris and. Kredex dosage: 12.5mg Twice Per Day. During the same period patient was treated with ADANCOR (10mg Twice Per Day) (View Adancor Review and Adancor Label ), COVERSYL (2mg Per Day) (View Coversyl Review and Coversyl Label ), CORVASAL (2mg Per Day) (View Corvasal Review and Corvasal Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), PARACETAMOL (View Paracetamol Review and Paracetamol Label ), MOVICOL (View Movicol Review and Movicol Label ). Patient was hospitalized.

5001054-4 | Anorexia, Asthenia, Dizziness, Fall, Gastric Cancer, Haematoma, Orthostatic Hypotension
Adverse event was reported on May 02, 2006 by a Male patient taking Kredex (View Usage) (Dosage: 25mg Per Day) was diagnosed with angina pectoris and. Location: FRANCE , 82 years of age, weighting 174.2 lb, Patient experienced the following unwanted or unexpected effects: anorexia, asthenia, dizziness (What is dizziness?), fall (What is fall?), gastric cancer, haematoma, orthostatic hypotension. During the same period patient was treated with ADANCOR (View Adancor Review and Adancor Label ), COVERSYL (2mg Per Day) (View Coversyl Review and Coversyl Label ), CORVASAL (2mg Per Day) (View Corvasal Review and Corvasal Label ), PLAVIX (View Plavix Review and Plavix Label ), CORDARONE (View Cordarone Review and Cordarone Label ), NEXIUM (View Nexium Review and Nexium Label ), PERMIXON (View Permixon Review and Permixon Label ), MOVICOL (View Movicol Review and Movicol Label ). Patient was hospitalized.

4993984-4 | Fall, Haematoma, Orthostatic Hypotension
on Apr 24, 2006 Male patient from FRANCE , 83 years of age, was diagnosed with angina pectoris and was treated with Kredex (View Usage). Patient had the following side effects: fall (What is fall?), haematoma, orthostatic hypotension. Kredex dosage: 12.5mg Twice Per Day. During the same period patient was treated with ADANCOR (10mg Twice Per Day) (View Adancor Review and Adancor Label ), COVERSYL (2mg Per Day) (View Coversyl Review and Coversyl Label ), CORVASAL (2mg Per Day) (View Corvasal Review and Corvasal Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ), MOVICOL (View Movicol Review and Movicol Label ). Patient was hospitalized.

4964561-6 | Abdominal Pain, Atrial Fibrillation, Bone Marrow Failure, Normochromic Normocytic Anaemia, Tension, Thrombocytopenia
on Mar 28, 2006 Male patient from FRANCE , 74 years of age, was diagnosed with cardiac failure, staphylococcal infection (What is staphylococcal infection?) and was treated with Kredex (View Usage). After Kredex was administered, patient had the following side effects: abdominal pain (What is abdominal pain?), atrial fibrillation (What is atrial fibrillation?), bone marrow failure, normochromic normocytic anaemia, tension, thrombocytopenia. Kredex dosage: 25mg Twice Per Day. During the same period patient was treated with COLCHICINE (1mg Per Day) (View Colchicine Review and Colchicine Label ), BURINEX (1mg Twice Per Day) (View Burinex Review and Burinex Label ), TIENAM (500mg Per Day) (View Tienam Review and Tienam Label ), MOPRAL (20mg Per Day) (View Mopral Review and Mopral Label ), ZYVOXID (600mg Twice Per Day) (View Zyvoxid Review and Zyvoxid Label ), ALLOPURINOL (View Allopurinol Review and Allopurinol Label ), TAHOR (View Tahor Review and Tahor Label ), ALDACTONE (View Aldactone Review and Aldactone Label ). Patient was hospitalized.

4956721-5 | Asthenia, Cardiac Failure, Dyspnoea, Myocardial Ischaemia, Oedema Peripheral
Patient was taking Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: asthenia, cardiac failure, dyspnoea, myocardial ischaemia, oedema peripheral on Mar 22, 2006 from FRANCE Additional patient health information: Male patient , 71 years of age, . Kredex dosage: 6.25mg Per Day. During the same period patient was treated with NOVOMIX (View Novomix Review and Novomix Label ), DI ANTALVIC (View Di Antalvic Review and Di Antalvic Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), ZOCOR (View Zocor Review and Zocor Label ), TRIATEC (View Triatec Review and Triatec Label ). Patient was hospitalized.

4933423-2 | Anaemia, Sinusitis
Adverse event was reported on Sep 27, 2005 by a Male patient taking Kredex (View Usage) (Dosage: ) . Location: FRANCE , 66 years of age, Patient had the following side effects: anaemia, sinusitis (What is sinusitis?). During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), INIPOMP (View Inipomp Review and Inipomp Label ), ELISOR (View Elisor Review and Elisor Label ), TRIATEC (View Triatec Review and Triatec Label ). Patient was hospitalized.

4928977-6 | Thrombocytopenia, Thrombophlebitis, Venous Thrombosis
on Feb 21, 2006 Female patient from FRANCE , 84 years of age, was treated with Kredex (View Usage). After Kredex was administered, patient had the following side effects: thrombocytopenia, thrombophlebitis, venous thrombosis. Kredex dosage: 6.25mg Twice Per Day. During the same period patient was treated with LASILIX (40mg Per Day) (View Lasilix Review and Lasilix Label ), ELISOR (40mg Per Day) (View Elisor Review and Elisor Label ), LOVENOX (View Lovenox Review and Lovenox Label ), XANAX (View Xanax Review and Xanax Label ), INIPOMP (View Inipomp Review and Inipomp Label ), HEPARIN SODIUM (View Heparin Sodium Review and Heparin Sodium Label ). Patient was hospitalized.

4920292-X | Abdominal Pain, Anorexia, Ascites, Asthenia, Bedridden, Blood Bilirubin Increased, Chromaturia, Diarrhoea, Dry Skin
on Feb 15, 2006 Male patient from NORWAY , 78 years of age, was diagnosed with hypertension, angina pectoris, blood cholesterol increased, cardiovascular event prophylaxis and was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal pain (What is abdominal pain?), anorexia, ascites, asthenia, bedridden, blood bilirubin increased, chromaturia, diarrhoea, dry skin. Kredex dosage: 25mg Twice Per Day. During the same period patient was treated with NITROGLYCERIN (.5mg As Required) (View Nitroglycerin Review and Nitroglycerin Label ), LIPITOR (10mg Per Day) (View Lipitor Review and Lipitor Label ), ALBYL E (75mg Per Day) (View Albyl E Review and Albyl E Label ), COZAAR (50mg Per Day) (View Cozaar Review and Cozaar Label ), PANCREON (View Pancreon Review and Pancreon Label ), COMBIZYM (View Combizym Review and Combizym Label ), FLUNIPAM (.5mg At Night) (View Flunipam Review and Flunipam Label ). Patient was hospitalized and became disabled.

4895271-1 | Bradycardia, Cardiac Arrest, Hypocalcaemia, Torsade De Pointes, Ventricular Extrasystoles
Patient was taking Kredex (View Usage). Patient had the following side effects: bradycardia, cardiac arrest (What is cardiac arrest?), hypocalcaemia, torsade de pointes, ventricular extrasystoles on Jan 26, 2006 from FRANCE Additional patient health information: Male patient , 82 years of age, . Kredex dosage: . During the same period patient was treated with DIGOXIN (View Digoxin Review and Digoxin Label ), CORDARONE (View Cordarone Review and Cordarone Label ), COVERSYL (View Coversyl Review and Coversyl Label ), LASILIX (View Lasilix Review and Lasilix Label ). Patient was hospitalized.

4878852-0 | Bradycardia, Dyspnoea, Electrocardiogram Qrs Complex Prolonged
Adverse event was reported on Jan 10, 2006 by a Male patient taking Kredex (View Usage) (Dosage: 3.125mg Twice Per Day) . Location: FRANCE , 85 years of age, After Kredex was administered, patient had the following side effects: bradycardia, dyspnoea, electrocardiogram qrs complex prolonged. During the same period patient was treated with DIFFU K (View Diffu K Review and Diffu K Label ), PREVISCAN (View Previscan Review and Previscan Label ), FUROSEMIDE (View Furosemide Review and Furosemide Label ), TRIATEC (View Triatec Review and Triatec Label ). Patient was hospitalized.

4787001-9 | Anaemia, Sinusitis
on Sep 27, 2005 Male patient from FRANCE , 66 years of age, was treated with Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: anaemia, sinusitis (What is sinusitis?). Kredex dosage: . During the same period patient was treated with PLAVIX (View Plavix Review and Plavix Label ), INIPOMP (View Inipomp Review and Inipomp Label ), ELISOR (View Elisor Review and Elisor Label ), TRIATEC (View Triatec Review and Triatec Label ). Patient was hospitalized.

4632372-7 | Hypertonia, Visual Acuity Reduced
on Feb 01, 2005 Male patient from , 49 years of age, was diagnosed with ill-defined disorder and was treated with Kredex (View Usage). Patient had the following side effects: hypertonia, visual acuity reduced. Kredex dosage: . During the same period patient was treated with LASILIX (View Lasilix Review and Lasilix Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), PLAVIX (View Plavix Review and Plavix Label ), KALEORID (View Kaleorid Review and Kaleorid Label ), COVERSYL (View Coversyl Review and Coversyl Label ).

4609993-0 | Musculoskeletal Stiffness, Weight Increased
Patient was taking Kredex (View Usage). After Kredex was administered, patient had the following side effects: musculoskeletal stiffness, weight increased on Mar 10, 2005 from Additional patient health information: Male patient , 65 years of age, was diagnosed with nail tinea and. Kredex dosage: . During the same period patient was treated with LAMISIL (250 Mg/d) (View Lamisil Review and Lamisil Label ).

4603943-9 | Cerebrovascular Accident, Hemiplegia
Adverse event was reported on Nov 08, 2004 by a Female patient taking Kredex (View Usage) (Dosage: ) . Location: , 66 years of age, Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, hemiplegia. Patient was hospitalized.

4580265-6 | Eye Disorder, Hypertonia, Visual Acuity Reduced
on Feb 01, 2005 Male patient from , 49 years of age, was treated with Kredex (View Usage). Patient had the following side effects: eye disorder, hypertonia, visual acuity reduced. Kredex dosage: . During the same period patient was treated with LASILIX (View Lasilix Review and Lasilix Label ), DIGOXIN (View Digoxin Review and Digoxin Label ), GLUCOPHAGE (View Glucophage Review and Glucophage Label ), NITRODERM (View Nitroderm Review and Nitroderm Label ), LEVOTHYROX (View Levothyrox Review and Levothyrox Label ), PLAVIX (View Plavix Review and Plavix Label ), KALEORID (View Kaleorid Review and Kaleorid Label ), COVERSYL (View Coversyl Review and Coversyl Label ).

4556048-X | Asthenia, Fatigue, Malaise, Syncope, Tachyarrhythmia, Vertigo, Vomiting
on Dec 09, 2004 Male patient from , 68 years of age, was diagnosed with cardiac valve disease and was treated with Kredex (View Usage). After Kredex was administered, patient had the following side effects: asthenia, fatigue, malaise, syncope, tachyarrhythmia, vertigo, vomiting. Kredex dosage: . During the same period patient was treated with CAPTOPRIL (View Captopril Review and Captopril Label ), TAHOR (View Tahor Review and Tahor Label ), SINTROM (View Sintrom Review and Sintrom Label ). Patient was hospitalized.

4543616-4 | Bradycardia, Sick Sinus Syndrome
Patient was taking Kredex (View Usage). Patient experienced the following unwanted or unexpected effects: bradycardia, sick sinus syndrome on Dec 20, 2004 from Additional patient health information: Male patient , 82 years of age, was diagnosed with hypertension and. Kredex dosage: .