AMLOR Side Effects

6910581-1 | Lung Disorder, Lymphopenia
on Jul 29, 2010 Female patient from FRANCE , 70 years of age, was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: lung disorder, lymphopenia. Amlor dosage: Unk. During the same period patient was treated with SOTALEX (Unk) (View Sotalex Review and Sotalex Label ), MABTHERA (1 G, Unk) (View Mabthera Review and Mabthera Label ), ARAVA (20 Mg, Per Day) (View Arava Review and Arava Label ), CORTANCYL (5 Mg, Per Day) (View Cortancyl Review and Cortancyl Label ), NEXIUM (View Nexium Review and Nexium Label ), ISOPTIN (View Isoptin Review and Isoptin Label ), SINGULAIR ^DIECKMANN^ (View Singulair ^dieckmann^ Review and Singulair ^dieckmann^ Label ), ZOLPIDEM (View Zolpidem Review and Zolpidem Label ). Patient was hospitalized.

6894016-3 | Diarrhoea, Renal Failure Acute
Patient was taking Amlor (View Usage). Patient had the following side effects: diarrhoea, renal failure acute on Jul 13, 2010 from FRANCE Additional patient health information: Male patient , 14 years of age, was diagnosed with hypertension and. Amlor dosage: 10 Mg, Unk. During the same period patient was treated with PROGRAF (0.1 Mg/kg, Unk) (View Prograf Review and Prograf Label ), AZATHIOPRINE (2 Mg/kg, Unk) (View Azathioprine Review and Azathioprine Label ). Patient was hospitalized.

6887142-6 | Psoriasis, Toxic Skin Eruption
Adverse event was reported on Jul 22, 2010 by a Male patient taking Amlor (View Usage) (Dosage: Unk) . Location: FRANCE , 60 years of age, After Amlor was administered, patient had the following side effects: psoriasis, toxic skin eruption. Patient was hospitalized.

6881998-9 | Iron Binding Capacity Total Decreased, Restless Legs Syndrome, Serum Ferritin Decreased
on Jul 20, 2010 Male patient from FRANCE , 81 years of age, weighting 158.7 lb, was diagnosed with hypertension, cardiac failure and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: iron binding capacity total decreased, restless legs syndrome, serum ferritin decreased. Amlor dosage: 10 Mg, 1x/day.


6878339-X | Pyrexia, Toxic Skin Eruption
on Jul 19, 2010 Male patient from FRANCE , 74 years of age, was diagnosed with coagulopathy and was treated with Amlor (View Usage). Patient had the following side effects: pyrexia, toxic skin eruption. Amlor dosage: Unk. During the same period patient was treated with PREVISCAN (Unk) (View Previscan Review and Previscan Label ), LASIX (Unk) (View Lasix Review and Lasix Label ), PANTOPRAZOLE SODIUM (Unk) (View Pantoprazole Sodium Review and Pantoprazole Sodium Label ), RABEPRAZOLE SODIUM (Unk) (View Rabeprazole Sodium Review and Rabeprazole Sodium Label ). Patient was hospitalized.

6847469-0 | Iron Binding Capacity Total Decreased, Restless Legs Syndrome, Serum Ferritin Decreased
Patient was taking Amlor (View Usage). After Amlor was administered, patient had the following side effects: iron binding capacity total decreased, restless legs syndrome, serum ferritin decreased on Jul 07, 2010 from FRANCE Additional patient health information: Male patient , 81 years of age, was diagnosed with hypertension and. Amlor dosage: 10 Mg, Unk.

6817699-2 | Hyperkalaemia, Renal Failure Acute
Adverse event was reported on Jun 28, 2010 by a Male patient taking Amlor (View Usage) (Dosage: 5 Mg, 2x/day) was diagnosed with hypertension and. Location: FRANCE , 51 years of age, Patient experienced the following unwanted or unexpected effects: hyperkalaemia, renal failure acute. During the same period patient was treated with APROVEL (300 Mg, 1x/day) (View Aprovel Review and Aprovel Label ), ALLOPURINOL (300 Mg, 1x/day) (View Allopurinol Review and Allopurinol Label ), SPECIAFOLDINE (5 Mg, 1x/day) (View Speciafoldine Review and Speciafoldine Label ), DAFALGAN (Unk) (View Dafalgan Review and Dafalgan Label ), DI ANTALVIC (Unk) (View Di-antalvic Review and Di-antalvic Label ). Patient was hospitalized.

6789867-X | Staphylococcal Infection
on Jun 15, 2010 Female patient from FRANCE , 59 years of age, was diagnosed with hypertension and was treated with Amlor (View Usage). Patient had the following side effects: staphylococcal infection (What is staphylococcal infection?). Amlor dosage: 5 Mg, Unk.

6715026-2 | Toxic Skin Eruption
on Apr 29, 2010 Female patient from FRANCE , 84 years of age, was diagnosed with hypertension and was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: toxic skin eruption. Amlor dosage: 10 Mg, 1x/day. During the same period patient was treated with NEXIUM (1 Df, 1x/day) (View Nexium Review and Nexium Label ), VASTAREL (View Vastarel Review and Vastarel Label ), PRAXILENE (View Praxilene Review and Praxilene Label ), RIVOTRIL (View Rivotril Review and Rivotril Label ), LORAZEPAM (View Lorazepam Review and Lorazepam Label ). Patient was hospitalized.

6712116-5 | Dizziness, Fall, Ischaemic Cerebral Infarction, Orthostatic Hypotension, Urinary Tract Infection, Wrist Fracture
Patient was taking Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: dizziness (What is dizziness?), fall (What is fall?), ischaemic cerebral infarction, orthostatic hypotension, urinary tract infection (What is urinary tract infection?), wrist fracture on Apr 06, 2010 from FRANCE Additional patient health information: Female patient , 73 years of age, weighting 119.3 lb, was diagnosed with renal transplant and. Amlor dosage: . During the same period patient was treated with TENORMIN (Unk) (View Tenormin Review and Tenormin Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), LASIX (Unk) (View Lasix Review and Lasix Label ), EVEROLIMUS (0.5 Mg, 2x/day) (View Everolimus Review and Everolimus Label ), NEORAL (Unk) (View Neoral Review and Neoral Label ), NEXIUM (View Nexium Review and Nexium Label ), OROCAL VITAMIN D (View Orocal Vitamin D Review and Orocal Vitamin D Label ), IMOVANE (View Imovane Review and Imovane Label ). Patient was hospitalized.

6703949-X | Pancreatitis Necrotising
Adverse event was reported on Apr 22, 2010 by a Male patient taking Amlor (View Usage) (Dosage: 5 Mg, 2x/day) . Location: FRANCE , 21 years of age, Patient had the following side effects: pancreatitis necrotising. During the same period patient was treated with MINOCYCLINE (100 Mg, 2x/day) (View Minocycline Review and Minocycline Label ), RIFADIN (600 Mg, 2x/day) (View Rifadin Review and Rifadin Label ), MYFORTIC (540 Mg, 2x/day) (View Myfortic Review and Myfortic Label ), PROGRAF (10 Mg, 2x/day) (View Prograf Review and Prograf Label ), MOPRAL (20 Mg, 1x/day) (View Mopral Review and Mopral Label ), SECTRAL (View Sectral Review and Sectral Label ), FUNGIZONE (1 G, 2x/day) (View Fungizone Review and Fungizone Label ).

6703807-0 | Systemic Lupus Erythematosus
on Apr 21, 2010 Female patient from FRANCE , 97 years of age, was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: systemic lupus erythematosus. Amlor dosage: 5 Mg, 1x/day. During the same period patient was treated with CARDENSIEL (1 Df, 1x/day) (View Cardensiel Review and Cardensiel Label ), ODRIK (2 Mg, 1x/day) (View Odrik Review and Odrik Label ), FUROSEMIDE (0.5 Tablet Daily) (View Furosemide Review and Furosemide Label ), KARDEGIC (1 Sachet Daily) (View Kardegic Review and Kardegic Label ), BUFLOMEDIL (2 Tablets Daily) (View Buflomedil Review and Buflomedil Label ), ZOPICLONE (0.5 Tablet Daily) (View Zopiclone Review and Zopiclone Label ), PAROXETINE (0.5 Tablet Daily) (View Paroxetine Review and Paroxetine Label ), ALPRAZOLAM (1.5 Tablets Daily) (View Alprazolam Review and Alprazolam Label ). Patient was hospitalized.

6693934-9 | Cutaneous Lupus Erythematosus, Rash Macular
on Apr 14, 2010 Female patient from FRANCE , 85 years of age, was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: cutaneous lupus erythematosus, rash macular. Amlor dosage: 5 Mg, 1x/day. Patient was hospitalized.

6688142-1 | Fall, Orthostatic Hypotension
Patient was taking Amlor (View Usage). Patient had the following side effects: fall (What is fall?), orthostatic hypotension on Apr 09, 2010 from FRANCE Additional patient health information: Male patient , 72 years of age, was diagnosed with hypertension and. Amlor dosage: 10 Mg, 1x/day. During the same period patient was treated with PRAZOSIN HCL (5 Mg, Unk) (View Prazosin Hcl Review and Prazosin Hcl Label ), BISOPROLOL FUMARATE (10 Mg, 1x/day) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), LASIX (40 Mg, 1x/day) (View Lasix Review and Lasix Label ), HYPERIUM (1 Mg, Unk) (View Hyperium Review and Hyperium Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), PRAVASTATIN (View Pravastatin Review and Pravastatin Label ), KAYEXALATE (View Kayexalate Review and Kayexalate Label ), ARANESP (View Aranesp Review and Aranesp Label ). Patient was hospitalized.

6683948-7 | Agranulocytosis, Hepatitis, Thrombocytopenia
Adverse event was reported on Apr 08, 2010 by a Male patient taking Amlor (View Usage) (Dosage: Unk) was diagnosed with acute myeloid leukaemia, sinusitis (What is sinusitis?) and. Location: FRANCE , 52 years of age, After Amlor was administered, patient had the following side effects: agranulocytosis, hepatitis (What is hepatitis?), thrombocytopenia. During the same period patient was treated with METHOTREXATE SODIUM (Unk) (View Methotrexate Sodium Review and Methotrexate Sodium Label ), PURINETHOL (Unk) (View Purinethol Review and Purinethol Label ), BACTRIM DS (3 Df, Weekly) (View Bactrim Ds Review and Bactrim Ds Label ), ZELITREX (500 Mg, 2x/day) (View Zelitrex Review and Zelitrex Label ), AUGMENTIN '125' (2 G Daily) (View Augmentin '125' Review and Augmentin '125' Label ), SOLUPRED (40 Mg Daily) (View Solupred Review and Solupred Label ), NASONEX (Unk) (View Nasonex Review and Nasonex Label ), NEXIUM (Unk) (View Nexium Review and Nexium Label ). Patient was hospitalized.

6682346-X | Erythema, Eye Irritation, Malaise
on Apr 06, 2010 Female patient from FRANCE , 73 years of age, was diagnosed with hypertension and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: erythema, eye irritation, malaise. Amlor dosage: 10 Mg, 1x/day. Patient was hospitalized.

6663452-2 | Systemic Lupus Erythematosus
on Mar 22, 2010 Female patient from FRANCE , 97 years of age, was treated with Amlor (View Usage). Patient had the following side effects: systemic lupus erythematosus. Amlor dosage: 5 Mg, 1x/day. During the same period patient was treated with CARDENSIEL (1 Df, 1x/day) (View Cardensiel Review and Cardensiel Label ), ODRIK (2 Mg, 1x/day) (View Odrik Review and Odrik Label ), FUROSEMIDE (0.5 Tablet Daily) (View Furosemide Review and Furosemide Label ), KARDEGIC (1 Sachet Daily) (View Kardegic Review and Kardegic Label ), BUFLOMEDIL (2 Tablets Daily) (View Buflomedil Review and Buflomedil Label ), ZOPICLONE (0.5 Tablet Daily) (View Zopiclone Review and Zopiclone Label ), PAROXETINE (0.5 Tablet Daily) (View Paroxetine Review and Paroxetine Label ), ALPRAZOLAM (1.5 Tablets Daily) (View Alprazolam Review and Alprazolam Label ). Patient was hospitalized.

6642430-3 | Aplastic Anaemia
Patient was taking Amlor (View Usage). After Amlor was administered, patient had the following side effects: aplastic anaemia on Mar 08, 2010 from FRANCE Additional patient health information: Male patient , 32 years of age, . Amlor dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), TAMOXIFEN CITRATE (20 Mg, Daily) (View Tamoxifen Citrate Review and Tamoxifen Citrate Label ), TRIATEC (View Triatec Review and Triatec Label ), OFLOCET (View Oflocet Review and Oflocet Label ), VANCOMYCIN (View Vancomycin Review and Vancomycin Label ), TIENAM (View Tienam Review and Tienam Label ), EPOETIN BETA (View Epoetin Beta Review and Epoetin Beta Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ). Patient was hospitalized.

6634815-6 | Loss Of Consciousness, Malaise, Orthostatic Hypotension
Adverse event was reported on Mar 05, 2010 by a Male patient taking Amlor (View Usage) (Dosage: 10 Mg, Unk) . Location: FRANCE , 61 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness, malaise, orthostatic hypotension. 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 ), ESIDRIX (25 Mg, Unk) (View Esidrix Review and Esidrix Label ), NEXIUM (20 Mg, Unk) (View Nexium Review and Nexium Label ), INSULIN (View Insulin Review and Insulin Label ), TEGRETOL (200 Mg, Unk) (View Tegretol Review and Tegretol Label ), KARDEGIC (75 Mg, Unk) (View Kardegic Review and Kardegic Label ). Patient was hospitalized.

6634787-4 | Aplastic Anaemia
on Mar 05, 2010 Male patient from FRANCE , 32 years of age, was treated with Amlor (View Usage). Patient had the following side effects: aplastic anaemia. Amlor dosage: Unk. During the same period patient was treated with TAMOXIFEN CITRATE (Unk) (View Tamoxifen Citrate Review and Tamoxifen Citrate Label ), TENORMIN (Unk) (View Tenormin Review and Tenormin Label ), TRIATEC (Unk) (View Triatec Review and Triatec Label ), OFLOCET (Unk) (View Oflocet Review and Oflocet Label ), VANCOMYCIN (Unk) (View Vancomycin Review and Vancomycin Label ), TIENAM (Unk) (View Tienam Review and Tienam Label ), NEORECORMON ^BOEHRINGER MANNHEIM^ (Unk) (View Neorecormon ^boehringer Mannheim^ Review and Neorecormon ^boehringer Mannheim^ Label ), SPECIAFOLDINE (View Speciafoldine Review and Speciafoldine Label ). Patient was hospitalized.

6608842-9 | Haematoma, International Normalised Ratio Increased
on Feb 19, 2010 Male patient from FRANCE , 76 years of age, was diagnosed with hypertension, hypercholesterolaemia, depression (What is depression?), renal failure chronic, hypersensitivity and was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: haematoma, international normalised ratio increased. Amlor dosage: 10 Mg, Daily. During the same period patient was treated with TAHOR (10 Mg, Daily) (View Tahor Review and Tahor Label ), PREVISCAN (Unk) (View Previscan Review and Previscan Label ), CORDARONE (200 Mg, Daily) (View Cordarone Review and Cordarone Label ), PARIET (10 Mg, Daily) (View Pariet Review and Pariet Label ), FLUOXETINE (20 Mg, Daily) (View Fluoxetine Review and Fluoxetine Label ), ALFACALCIDOL (0.25 Ug, Unk) (View Alfacalcidol Review and Alfacalcidol Label ), AERIUS (5 Mg, Unk) (View Aerius Review and Aerius Label ). Patient was hospitalized.

6578121-7 | Hallucination, Auditory, Memory Impairment
Patient was taking Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: hallucination, auditory, memory impairment on Feb 01, 2010 from FRANCE Additional patient health information: Male patient , 37 years of age, . Amlor dosage: 5 Mg, 2x/day. During the same period patient was treated with ATENOLOL (Unk) (View Atenolol Review and Atenolol Label ), SODIUM BICARBONATE (Unk) (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), NEORAL (60 Mg, 2x/day) (View Neoral Review and Neoral Label ), CELLCEPT (1 G, 2x/day) (View Cellcept Review and Cellcept Label ), SOLUPRED (Unk) (View Solupred Review and Solupred Label ), EZETROL (10 Mg, 1x/day) (View Ezetrol Review and Ezetrol Label ), VASTEN (20 Mg, 1x/day) (View Vasten Review and Vasten Label ), MIRCERA (75 Ug, Monthly) (View Mircera Review and Mircera Label ). Patient was hospitalized.

6576703-X | Hallucination, Auditory, Memory Impairment
Adverse event was reported on Feb 01, 2010 by a Male patient taking Amlor (View Usage) (Dosage: 5 Mg, 2x/day) . Location: FRANCE , 37 years of age, Patient had the following side effects: hallucination, auditory, memory impairment. During the same period patient was treated with SODIUM BICARBONATE (Unk) (View Sodium Bicarbonate Review and Sodium Bicarbonate Label ), NEORAL (60 Mg, 2x/day) (View Neoral Review and Neoral Label ), CELLCEPT (1 G, 2x/day) (View Cellcept Review and Cellcept Label ), TENORMIN (Unk) (View Tenormin Review and Tenormin Label ), SOLUPRED (Unk) (View Solupred Review and Solupred Label ), EZETROL (10 Mg, 1x/day) (View Ezetrol Review and Ezetrol Label ), VASTEN (20 Mg, 1x/day) (View Vasten Review and Vasten Label ), MIRCERA (75 Ug, Monthly) (View Mircera Review and Mircera Label ). Patient was hospitalized.

6575466-1 | Haematoma, International Normalised Ratio Increased
on Jan 29, 2010 Male patient from FRANCE , 76 years of age, was diagnosed with hypertension, hypercholesterolaemia, depression (What is depression?), renal failure chronic, hypersensitivity and was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: haematoma, international normalised ratio increased. Amlor dosage: 10 Mg, Daily. During the same period patient was treated with TAHOR (10 Mg, Daily) (View Tahor Review and Tahor Label ), PREVISCAN (Unk) (View Previscan Review and Previscan Label ), CORDARONE (200 Mg, Daily) (View Cordarone Review and Cordarone Label ), PARIET (10 Mg, Daily) (View Pariet Review and Pariet Label ), FLUOXETINE (20 Mg, Daily) (View Fluoxetine Review and Fluoxetine Label ), ALFACALCIDOL (0.25 Ug, Unk) (View Alfacalcidol Review and Alfacalcidol Label ), AERIUS (5 Mg, Unk) (View Aerius Review and Aerius Label ). Patient was hospitalized.

6572022-6 | Haematoma
on Jan 28, 2010 Male patient from FRANCE , 76 years of age, was diagnosed with hypertension, hypercholesterolaemia, depression (What is depression?), renal failure chronic, hypersensitivity and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: haematoma. Amlor dosage: 10 Mg, Daily. During the same period patient was treated with TAHOR (10 Mg, Daily) (View Tahor Review and Tahor Label ), PREVISCAN (Unk) (View Previscan Review and Previscan Label ), CORDARONE (200 Mg, Daily) (View Cordarone Review and Cordarone Label ), PARIET (10 Mg, Daily) (View Pariet Review and Pariet Label ), FLUOXETINE (20 Mg, Daily) (View Fluoxetine Review and Fluoxetine Label ), ALFACALCIDOL (0.25 Ug, Unk) (View Alfacalcidol Review and Alfacalcidol Label ), AERIUS (5 Mg, Unk) (View Aerius Review and Aerius Label ). Patient was hospitalized.

6564857-0 | Thrombocytopenia
Patient was taking Amlor (View Usage). Patient had the following side effects: thrombocytopenia on Jan 22, 2010 from FRANCE Additional patient health information: Female patient , 73 years of age, was diagnosed with hypertension and. Amlor dosage: 5 Mg, 1x/day. During the same period patient was treated with RIFADIN (300 Mg, 2x/day) (View Rifadin Review and Rifadin Label ), OFLOCET (200 Mg, 1x/day) (View Oflocet Review and Oflocet Label ). Patient was hospitalized.

6456186-0 | Blood Creatine Phosphokinase Increased, Haematoma, Hypotension, Musculoskeletal Stiffness, Myalgia, Myoglobin Blood Increased
Adverse event was reported on Nov 17, 2009 by a Female patient taking Amlor (View Usage) (Dosage: 5 Mg, Unk) was diagnosed with hypertension and. Location: FRANCE , 71 years of age, After Amlor was administered, patient had the following side effects: blood creatine phosphokinase increased, haematoma, hypotension, musculoskeletal stiffness, myalgia, myoglobin blood increased. During the same period patient was treated with ABILIFY (40 Mg, Daily) (View Abilify Review and Abilify Label ), TEGRETOL (400 Mg, 1x/day) (View Tegretol Review and Tegretol Label ), KEPPRA (500 Mg, 1x/day) (View Keppra Review and Keppra Label ). Patient was hospitalized.

6448667-0 | Aphasia, Extrapyramidal Disorder
on Nov 12, 2009 Female patient from FRANCE , 70 years of age, was diagnosed with hypertension and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: aphasia (What is aphasia?), extrapyramidal disorder. Amlor dosage: Unk. During the same period patient was treated with RISPERDAL (Unk) (View Risperdal Review and Risperdal Label ), MEMANTINE (Unk) (View Memantine Review and Memantine Label ). Patient was hospitalized.

6447027-6 | Nosocomial Infection, Proteus Infection, Pulmonary Oedema, Urinary Tract Infection Bacterial
on Nov 10, 2009 Female patient from FRANCE , 84 years of age, was diagnosed with urinary tract infection (What is urinary tract infection?) and was treated with Amlor (View Usage). Patient had the following side effects: nosocomial infection, proteus infection, pulmonary oedema, urinary tract infection bacterial. Amlor dosage: 10 Mg, 2x/day. During the same period patient was treated with COLOPEG (1 Df, 2x/day) (View Colopeg Review and Colopeg Label ), BACTRIM DS (1 Df, 1x/day) (View Bactrim Ds Review and Bactrim Ds Label ), COZAAR (50 Mg, 1x/day) (View Cozaar Review and Cozaar Label ), SECTRAL (200 Mg, 2x/day) (View Sectral Review and Sectral Label ), SPECIAFOLDINE (5 Mg, 2x/day) (View Speciafoldine Review and Speciafoldine Label ), HYPERIUM (1 Mg, Unk) (View Hyperium Review and Hyperium Label ). Patient was hospitalized.

6439260-4 | Blood Creatine Phosphokinase Increased, Hypotension, Musculoskeletal Stiffness, Myalgia, Myoglobin Blood Increased
Patient was taking Amlor (View Usage). After Amlor was administered, patient had the following side effects: blood creatine phosphokinase increased, hypotension, musculoskeletal stiffness, myalgia, myoglobin blood increased on Nov 05, 2009 from FRANCE Additional patient health information: Female patient , 71 years of age, was diagnosed with hypertension and. Amlor dosage: 5 Mg, Unk. During the same period patient was treated with ABILIFY (Unk) (View Abilify Review and Abilify Label ), TEGRETOL (200 Mg, Unk) (View Tegretol Review and Tegretol Label ), KEPPRA (500 Mg, Unk) (View Keppra Review and Keppra Label ). Patient was hospitalized.

6437835-X | Loss Of Consciousness, Malaise
Adverse event was reported on Nov 03, 2009 by a Male patient taking Amlor (View Usage) (Dosage: 10 Mg, 1x/day) was diagnosed with hypertension, glaucoma (What is glaucoma?) and. Location: FRANCE , 85 years of age, Patient experienced the following unwanted or unexpected effects: loss of consciousness, malaise. During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), NOVONORM (80 Unk, Unk) (View Novonorm Review and Novonorm Label ), FENOFIBRATE (View Fenofibrate Review and Fenofibrate Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), GANFORT (View Ganfort Review and Ganfort Label ), NISIS (View Nisis Review and Nisis Label ). Patient was hospitalized.

6428612-4 | Dermatitis Exfoliative, Eosinophilia
on Oct 27, 2009 Male patient from FRANCE , 81 years of age, was treated with Amlor (View Usage). Patient had the following side effects: dermatitis exfoliative, eosinophilia. Amlor dosage: Unk. During the same period patient was treated with ALLOPURINOL (Unk) (View Allopurinol Review and Allopurinol Label ), OXYGEN (View Oxygen Review and Oxygen Label ), SPIRIVA (View Spiriva Review and Spiriva Label ), SYMBICORT (View Symbicort Review and Symbicort Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), CRESTOR (View Crestor Review and Crestor Label ), LASILIX (View Lasilix Review and Lasilix Label ), DIFFU K (View Diffu K Review and Diffu K Label ). Patient was hospitalized.

6404086-4 | Malaise, Petit Mal Epilepsy
on Oct 08, 2009 Female patient from FRANCE , 87 years of age, was diagnosed with hypertension, urinary tract infection (What is urinary tract infection?) and was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: malaise, petit mal epilepsy. Amlor dosage: 5 Mg, Unk. During the same period patient was treated with NORFLOXACIN (400 Mg, 2x/day) (View Norfloxacin Review and Norfloxacin Label ), RAMIPRIL (1 Df, 1x/day) (View Ramipril Review and Ramipril Label ), KARDEGIC (1 Df, 1x/day) (View Kardegic Review and Kardegic Label ), DEROXAT (1 Df, 1x/day) (View Deroxat Review and Deroxat Label ). Patient was hospitalized.

6394120-2 | Cytolytic Hepatitis, Renal Failure
Patient was taking Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: cytolytic hepatitis, renal failure on Sep 28, 2009 from FRANCE Additional patient health information: Female patient , 76 years of age, . Amlor dosage: 10 Mg, 1x/day. During the same period patient was treated with PREVISCAN (20 Mg, 1x/day) (View Previscan Review and Previscan Label ), BISOPROLOL FUMARATE (1 Df, 1x/day) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ).

6388302-3 | Fall, Orthostatic Hypotension
Adverse event was reported on Sep 24, 2009 by a Female patient taking Amlor (View Usage) (Dosage: 10 Mg, 1x/day) was diagnosed with hypertension and. Location: FRANCE , 72 years of age, Patient had the following side effects: fall (What is fall?), orthostatic hypotension. During the same period patient was treated with PRAZOSIN HCL (5 Mg, Unk) (View Prazosin Hcl Review and Prazosin Hcl Label ), DETENSIEL (10 Mg, 1x/day) (View Detensiel Review and Detensiel Label ), LASILIX (40 Mg, 1x/day) (View Lasilix Review and Lasilix Label ), HYPERIUM (1 Mg, Unk) (View Hyperium Review and Hyperium Label ), KARDEGIC (View Kardegic Review and Kardegic Label ), VASTEN (View Vasten Review and Vasten Label ), KAYEXALATE (View Kayexalate Review and Kayexalate Label ), ARANESP (View Aranesp Review and Aranesp Label ). Patient was hospitalized.

6384251-5 | Dizziness, Fall, Ischaemic Cerebral Infarction, Orthostatic Hypotension, Urinary Tract Infection, Wrist Fracture
on Aug 21, 2009 Female patient from FRANCE , 73 years of age, was diagnosed with renal transplant and was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: dizziness (What is dizziness?), fall (What is fall?), ischaemic cerebral infarction, orthostatic hypotension, urinary tract infection (What is urinary tract infection?), wrist fracture. Amlor dosage: . During the same period patient was treated with TENORMIN (Unk) (View Tenormin Review and Tenormin Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), EVEROLIMUS (0.5 Mg, 2x/day) (View Everolimus Review and Everolimus Label ), LASILIX (Unk) (View Lasilix Review and Lasilix Label ), NEORAL (Unk) (View Neoral Review and Neoral Label ), NEXIUM (View Nexium Review and Nexium Label ), OROCAL VITAMIN D (View Orocal Vitamin D Review and Orocal Vitamin D Label ), IMOVANE (View Imovane Review and Imovane Label ). Patient was hospitalized.

6376584-3 |
on Sep 15, 2009 Female patient from FRANCE , 34 years of age, was treated with Amlor (View Usage). . Amlor dosage: 5 Mg, 1x/day. During the same period patient was treated with ATARAX (25 Mg, 1x/day) (View Atarax Review and Atarax Label ), PIVALONE (2 Gtt, 2x/day) (View Pivalone Review and Pivalone Label ), IMUREL (1.5 Df, 2x/day) (View Imurel Review and Imurel Label ), NEORAL (100 Mg, 2x/day) (View Neoral Review and Neoral Label ).

6317992-6 | Dizziness, Fall, Ischaemic Cerebral Infarction, Orthostatic Hypotension, Urinary Tract Infection, Wrist Fracture
Patient was taking Amlor (View Usage). Patient had the following side effects: dizziness (What is dizziness?), fall (What is fall?), ischaemic cerebral infarction, orthostatic hypotension, urinary tract infection (What is urinary tract infection?), wrist fracture on Aug 13, 2009 from FRANCE Additional patient health information: Female patient , 73 years of age, . Amlor dosage: . During the same period patient was treated with TENORMIN (View Tenormin Review and Tenormin Label ), AMIODARONE (View Amiodarone Review and Amiodarone Label ), NEORAL (Unk) (View Neoral Review and Neoral Label ). Patient was hospitalized.

6306842-X | Toxic Skin Eruption
Adverse event was reported on Aug 03, 2009 by a Female patient taking Amlor (View Usage) (Dosage: 5 Mg, 1x/day) was diagnosed with hypertension, dyslipidaemia, pain (What is pain?) and. Location: FRANCE , 72 years of age, After Amlor was administered, patient had the following side effects: toxic skin eruption. During the same period patient was treated with TAHOR (20 Mg, 1x/day) (View Tahor Review and Tahor Label ), ATACAND (8 Mg, 1x/day) (View Atacand Review and Atacand Label ), NEXIUM (40 Mg, 1x/day) (View Nexium Review and Nexium Label ), DAFALGAN (1 G, 4x/day) (View Dafalgan Review and Dafalgan Label ), CALCIPARINE ^DIFREX^ (View Calciparine ^difrex^ Review and Calciparine ^difrex^ Label ), TOPALGIC (View Topalgic Review and Topalgic Label ), DROLEPTAN (View Droleptan Review and Droleptan Label ). Patient was hospitalized.

6299309-9 | Myocardial Infarction
on Jul 29, 2009 Female patient from FRANCE , 70 years of age, was diagnosed with hypertension, acute myeloid leukaemia, dyslipidaemia and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: myocardial infarction. Amlor dosage: 1 Df, Unk. During the same period patient was treated with ARACYTINE (200 Mg, 1x/day) (View Aracytine Review and Aracytine Label ), TAHOR (1 Df, 1x/day) (View Tahor Review and Tahor Label ), ATARAX (Unk) (View Atarax Review and Atarax Label ), BELUSTINE (400 Mg, 1x/day) (View Belustine Review and Belustine Label ), CIFLOX (Unk) (View Ciflox Review and Ciflox Label ), ONDANSETRON HCL (8mg/4ml) (View Ondansetron Hcl Review and Ondansetron Hcl Label ), DEXAMETHASONE (8 Mg, Unk) (View Dexamethasone Review and Dexamethasone Label ), LASIX (Unk) (View Lasix Review and Lasix Label ). Patient was hospitalized.

6298910-6 | Hypotension, Overdose, Renal Failure Acute
on Jul 29, 2009 Female patient from FRANCE , 61 years of age, was treated with Amlor (View Usage). Patient had the following side effects: hypotension, overdose, renal failure acute. Amlor dosage: 150 Mg, Single. During the same period patient was treated with COTAREG (30 Df, Single) (View Cotareg Review and Cotareg Label ), SIMVASTATIN (40 Mg, 1x/day (in The Evening)) (View Simvastatin Review and Simvastatin Label ), OMEPRAZOLE (20 Mg, 1x/day (in The Evening)) (View Omeprazole Review and Omeprazole Label ), PARACETAMOL (1 G Every 6 Hours, As Needed) (View Paracetamol Review and Paracetamol Label ), TRAMADOL (1 Df, 2x/day (in The Morning And In The Evening)) (View Tramadol Review and Tramadol Label ), NOVOMIX (14 U In The Morning And 18 U In The Evening) (View Novomix Review and Novomix Label ). Patient was hospitalized.

6295990-9 | Myocardial Infarction
Patient was taking Amlor (View Usage). After Amlor was administered, patient had the following side effects: myocardial infarction on Jul 29, 2009 from FRANCE Additional patient health information: Female patient , 70 years of age, was diagnosed with hypertension, acute myeloid leukaemia, dyslipidaemia and. Amlor dosage: 1 Df, Unk. During the same period patient was treated with ARACYTINE (200 Mg, 1x/day) (View Aracytine Review and Aracytine Label ), TAHOR (1 Df, 1x/day) (View Tahor Review and Tahor Label ), ATARAX (Unk) (View Atarax Review and Atarax Label ), BELUSTINE (400 Mg, 1x/day) (View Belustine Review and Belustine Label ), CIFLOX (Unk) (View Ciflox Review and Ciflox Label ), ONDANSETRON HCL (8mg/4ml) (View Ondansetron Hcl Review and Ondansetron Hcl Label ), DEXAMETHASONE (8 Mg, Unk) (View Dexamethasone Review and Dexamethasone Label ), LASIX (Unk) (View Lasix Review and Lasix Label ). Patient was hospitalized.

6280415-X | Intentional Overdose
Adverse event was reported on Jun 29, 2009 by a Female patient taking Amlor (View Usage) (Dosage: ) . Location: FRANCE , 30 years of age, Patient experienced the following unwanted or unexpected effects: intentional overdose.

6279479-9 | Cardiogenic Shock, Intentional Overdose
on Jul 15, 2009 Female patient from FRANCE , 24 years of age, was treated with Amlor (View Usage). Patient had the following side effects: cardiogenic shock, intentional overdose. Amlor dosage: 26 Df, Single. During the same period patient was treated with ATENOLOL (32 Df, Single) (View Atenolol Review and Atenolol Label ), CORVASAL (7 Df, Single) (View Corvasal Review and Corvasal Label ), COVERSYL (30 Df, Single) (View Coversyl Review and Coversyl Label ), LEXOMIL (30 Df, Single) (View Lexomil Review and Lexomil Label ).

6232830-8 |
on Jun 12, 2009 Female patient from FRANCE , 34 years of age, was treated with Amlor (View Usage). . Amlor dosage: 5 Mg, 1x/day. During the same period patient was treated with ATARAX (25 Mg, 1x/day) (View Atarax Review and Atarax Label ), PIVALONE (2 Gtt, 2x/day) (View Pivalone Review and Pivalone Label ), IMUREL (1.5 Df, 2x/day) (View Imurel Review and Imurel Label ), NEORAL (100 Mg, 2x/day) (View Neoral Review and Neoral Label ).

6214640-0 | Agranulocytosis, Lymphopenia
Patient was taking Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: agranulocytosis, lymphopenia on May 25, 2009 from FRANCE Additional patient health information: Female patient , 81 years of age, was diagnosed with hypertension, atrial fibrillation (What is atrial fibrillation?), bronchitis (What is bronchitis?), obstructive airways disorder and. Amlor dosage: Unk. During the same period patient was treated with PREVISCAN (20 Mg, Unk) (View Previscan Review and Previscan Label ), TAVANIC (500 Mg, 1x/day) (View Tavanic Review and Tavanic Label ), TAZOCILLINE (4 G, 3x/day) (View Tazocilline Review and Tazocilline Label ), AMIKLIN (900 Mg, 1x/day) (View Amiklin Review and Amiklin Label ), TIENAM (1 G, 3x/day) (View Tienam Review and Tienam Label ), SYMBICORT (Unk) (View Symbicort Review and Symbicort Label ), BRICANYL (Unk) (View Bricanyl Review and Bricanyl Label ), ATROVENT (Unk) (View Atrovent Review and Atrovent Label ). Patient was hospitalized.

5817826-X | Acute Respiratory Distress Syndrome, Haemoptysis, Melaena
Adverse event was reported on Jul 16, 2008 by a Male patient taking Amlor (View Usage) (Dosage: Unk) was diagnosed with aortic valve incompetence and. Location: FRANCE , weighting 147.7 lb, Patient had the following side effects: acute respiratory distress syndrome, haemoptysis, melaena. During the same period patient was treated with CORDARONE (Unk) (View Cordarone Review and Cordarone Label ), DETENSIEL (Unk) (View Detensiel Review and Detensiel Label ), NEXIUM (Unk) (View Nexium Review and Nexium Label ), ZOLPIDEM TARTRATE (Unk) (View Zolpidem Tartrate Review and Zolpidem Tartrate Label ), DOLIPRANE (Unk) (View Doliprane Review and Doliprane Label ), PLAVIX (Unk) (View Plavix Review and Plavix Label ). Patient was hospitalized.

5774407-4 | Congenital Skin Disorder, Melanocytic Naevus
on Jun 06, 2008 Female patient from FRANCE , weighting 3.69 lb, was treated with Amlor (View Usage). After Amlor was administered, patient had the following side effects: congenital skin disorder, melanocytic naevus. Amlor dosage: . During the same period patient was treated with KARDEGIC (View Kardegic Review and Kardegic Label ), TRANDATE (View Trandate Review and Trandate Label ), ALDOMET (View Aldomet Review and Aldomet Label ).

5754751-7 | Fall, Orthostatic Hypotension
on May 23, 2008 Female patient from FRANCE , 90 years of age, was diagnosed with myocardial ischaemia and was treated with Amlor (View Usage). Patient experienced the following unwanted or unexpected effects: fall (What is fall?), orthostatic hypotension. Amlor dosage: . During the same period patient was treated with TRIATEC (View Triatec Review and Triatec Label ), NITRODERM (Text:10 Mg/24h-freq:every Day) (View Nitroderm Review and Nitroderm Label ), XANAX (View Xanax Review and Xanax Label ), LASILIX (View Lasilix Review and Lasilix Label ), TARDYFERON (View Tardyferon Review and Tardyferon Label ), IMOVANE (View Imovane Review and Imovane Label ). Patient was hospitalized.

5732366-4 | Fall, Hypotension, Loss Of Consciousness, Malaise
Patient was taking Amlor (View Usage). Patient had the following side effects: fall (What is fall?), hypotension, loss of consciousness, malaise on Apr 28, 2008 from FRANCE Additional patient health information: Male patient , 74 years of age, was diagnosed with hypertension, myocardial infarction and. Amlor dosage: . During the same period patient was treated with ATENOLOL (View Atenolol Review and Atenolol Label ), PERINDOPRIL ERBUMINE (View Perindopril Erbumine Review and Perindopril Erbumine Label ), MOLSIDOMINE (View Molsidomine Review and Molsidomine Label ), TAHOR (View Tahor Review and Tahor Label ), NEXIUM (View Nexium Review and Nexium Label ), VASTAREL (View Vastarel Review and Vastarel Label ), ASPIRIN (View Aspirin Review and Aspirin Label ). Patient was hospitalized.