ARIXTRA Side Effects

7022733-3 | Deep Vein Thrombosis, Oedema Peripheral
on Sep 27, 2010 Male patient from UNITED STATES , 44 years of age, weighting 271.2 lb, was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: deep vein thrombosis (What is deep vein thrombosis?), oedema peripheral. Arixtra dosage: 10mg Per Day. During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ), ESOMEPRAZOLE (View Esomeprazole Review and Esomeprazole Label ).

7016607-1 |
Patient was taking Arixtra (View Usage). on Sep 20, 2010 from UNITED STATES Additional patient health information: Female patient , 80 years of age, . Arixtra dosage: .

7014612-2 | Injection Site Haematoma, Skin Nodule
Adverse event was reported on Sep 24, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: 0.6ml 2 Times/day Sq) was diagnosed with pulmonary embolism (What is pulmonary embolism?) and. Location: UNITED STATES , 51 years of age, weighting 140.0 lb, After Arixtra was administered, patient had the following side effects: injection site haematoma, skin nodule.

7014354-3 | Haematocrit Decreased, Haemoglobin Decreased
on Sep 24, 2010 Male patient from UNITED STATES , 45 years of age, was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: haematocrit decreased, haemoglobin decreased. Arixtra dosage: Arixtra 7.5 Daily Iv. Patient was hospitalized.


7012838-5 | Cerebral Haemorrhage, Convulsion
on Sep 16, 2010 Male patient from KENYA , 74 years of age, was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and was treated with Arixtra (View Usage). Patient had the following side effects: cerebral haemorrhage, convulsion. Arixtra dosage: . During the same period patient was treated with WARFARIN (View Warfarin Review and Warfarin Label ). Patient was hospitalized.

7008403-6 | Foreign Body, Incision Site Haematoma, Off Label Use, Product Quality Issue
Patient was taking Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: foreign body, incision site haematoma, off label use, product quality issue on Sep 13, 2010 from FRANCE Additional patient health information: Female patient , weighting 132.3 lb, was diagnosed with thrombosis prophylaxis and. Arixtra dosage: 2.5mg Per Day.

7008397-3 | Haemorrhage, International Normalised Ratio Increased
Adverse event was reported on Sep 13, 2010 by a Male patient taking Arixtra (View Usage) (Dosage: 2.5mg Per Day) . Location: EGYPT , 72 years of age, weighting 216.1 lb, Patient experienced the following unwanted or unexpected effects: haemorrhage, international normalised ratio increased.

7005665-6 | Melaena, Rectal Haemorrhage
on Sep 10, 2010 Male patient from FRANCE , 88 years of age, was treated with Arixtra (View Usage). Patient had the following side effects: melaena, rectal haemorrhage. Arixtra dosage: . During the same period patient was treated with PERINDOPRIL ERBUMINE (1unit Per Day) (View Perindopril Erbumine Review and Perindopril Erbumine Label ), DIGOXIN (1unit Per Day) (View Digoxin Review and Digoxin Label ), NEXIUM (1unit Per Day) (View Nexium Review and Nexium Label ), OXYCONTIN (View Oxycontin Review and Oxycontin Label ), NITROGLYCERIN (View Nitroglycerin Review and Nitroglycerin Label ), SOLUPRED (View Solupred Review and Solupred Label ), LASIX (1unit Per Day) (View Lasix Review and Lasix Label ). Patient was hospitalized.

6994569-0 | Haemoglobin Decreased, Muscle Haemorrhage
on Sep 16, 2010 Female patient from UNITED STATES , 64 years of age, weighting 388.0 lb, was diagnosed with pulmonary embolism (What is pulmonary embolism?) and was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: haemoglobin decreased, muscle haemorrhage. Arixtra dosage: 10mg Qd Sq. During the same period patient was treated with FOLIC ACID (View Folic Acid Review and Folic Acid Label ), GABAPENTIN (View Gabapentin Review and Gabapentin Label ), LIDODERM (View Lidoderm Review and Lidoderm Label ), METHOTREXATE (View Methotrexate Review and Methotrexate Label ), METOPROLOL TARTRATE (View Metoprolol Tartrate Review and Metoprolol Tartrate Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), NEXIUM (View Nexium Review and Nexium Label ), PREDNISONE TAB (View Prednisone Tab Review and Prednisone Tab Label ).

6988124-6 | Gastric Haemorrhage, Haematemesis
Patient was taking Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: gastric haemorrhage, haematemesis on Sep 08, 2010 from EGYPT Additional patient health information: Male patient , 68 years of age, weighting 176.4 lb, . Arixtra dosage: 7.5mg Per Day. During the same period patient was treated with ASPIRIN (View Aspirin Review and Aspirin Label ).

6985493-8 | Off Label Use, Thrombocytosis
Adverse event was reported on Sep 07, 2010 by a Male patient taking Arixtra (View Usage) (Dosage: 2.5mg Per Day) was diagnosed with thrombosis prophylaxis and. Location: FRANCE , 56 years of age, Patient had the following side effects: off label use, thrombocytosis.

6985459-8 | Deep Vein Thrombosis
on Sep 09, 2010 Female patient from UNITED STATES , 61 years of age, was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: deep vein thrombosis (What is deep vein thrombosis?). Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with VITAMIN B 12 (View Vitamin B-12 Review and Vitamin B-12 Label ), FOLIC ACID (View Folic Acid Review and Folic Acid Label ), IRON (View Iron Review and Iron Label ).

6985458-6 | Deep Vein Thrombosis, Oedema Peripheral
on Sep 09, 2010 Male patient from UNITED STATES , 44 years of age, was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: deep vein thrombosis (What is deep vein thrombosis?), oedema peripheral. Arixtra dosage: 10mg Per Day. During the same period patient was treated with VICODIN (View Vicodin Review and Vicodin Label ), ESOMEPRAZOLE MAGNESIUM (View Esomeprazole Magnesium Review and Esomeprazole Magnesium Label ).

6981002-8 | Gastric Haemorrhage, Haematemesis
Patient was taking Arixtra (View Usage). Patient had the following side effects: gastric haemorrhage, haematemesis on Sep 05, 2010 from EGYPT Additional patient health information: Male patient , 68 years of age, . Arixtra dosage: 7.5mg Per Day.

6976876-0 | Asthenia, Erythema Multiforme, Hypersensitivity, Injection Site Pruritus, Rash Maculo-papular, Toxic Skin Eruption
Adverse event was reported on Sep 01, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: ) was diagnosed with deep vein thrombosis (What is deep vein thrombosis?) and. Location: FRANCE , 48 years of age, After Arixtra was administered, patient had the following side effects: asthenia, erythema multiforme, hypersensitivity, injection site pruritus, rash maculo-papular, toxic skin eruption. During the same period patient was treated with PREVISCAN (View Previscan Review and Previscan Label ).

6976875-9 | Cholestasis, Hepatocellular Injury
on Sep 01, 2010 Male patient from FRANCE , 84 years of age, weighting 154.3 lb, was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: cholestasis, hepatocellular injury. Arixtra dosage: . During the same period patient was treated with XANAX (.25mg Twice Per Day) (View Xanax Review and Xanax Label ), LASIX (View Lasix Review and Lasix Label ), DIGITALINE NATIVELLE (View Digitaline Nativelle Review and Digitaline Nativelle Label ), LOVENOX (View Lovenox Review and Lovenox Label ), TRIATEC (View Triatec Review and Triatec Label ), FORLAX (View Forlax Review and Forlax Label ), CRESTOR (View Crestor Review and Crestor Label ), BRICANYL (View Bricanyl Review and Bricanyl Label ).

6976874-7 | Ascites, Cerebral Ischaemia, Haemoglobin Decreased, Hemiparesis, Hypovolaemic Shock, Malaise, Overdose, Pain, Renal Disorder
on Sep 01, 2010 Male patient from FRANCE , weighting 119.9 lb, was diagnosed with thrombosis prophylaxis, depression (What is depression?) and was treated with Arixtra (View Usage). Patient had the following side effects: ascites, cerebral ischaemia, haemoglobin decreased, hemiparesis, hypovolaemic shock, malaise, overdose, pain (What is pain?), renal disorder. Arixtra dosage: 7.5mg Per Day. During the same period patient was treated with ATACAND (16mg Per Day) (View Atacand Review and Atacand Label ), SEROPLEX (.5unit Per Day) (View Seroplex Review and Seroplex Label ), SPECIAFOLDINE (3unit Per Day) (View Speciafoldine Review and Speciafoldine Label ), FUMAFER (2unit Per Day) (View Fumafer Review and Fumafer Label ), ACETAMINOPHEN (1g Four Times Per Day) (View Acetaminophen Review and Acetaminophen Label ), UVEDOSE (1unit Monthly) (View Uvedose Review and Uvedose Label ), PENICILLIN G (View Penicillin G Review and Penicillin G Label ), BACTRIM (View Bactrim Review and Bactrim Label ). Patient was hospitalized.

6973861-X | Anaemia, Contraindication To Medical Treatment, Haemorrhage, Overdose
Patient was taking Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: anaemia, contraindication to medical treatment, haemorrhage, overdose on Sep 01, 2010 from FRANCE Additional patient health information: Female patient , weighting 70.55 lb, was diagnosed with thrombosis prophylaxis, depression (What is depression?), anxiety (What is anxiety?), osteoporosis (What is osteoporosis?) and. Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with SEROPLEX (10mg Per Day) (View Seroplex Review and Seroplex Label ), LASIX (20mg Per Day) (View Lasix Review and Lasix Label ), ALDACTONE (12.5mg Per Day) (View Aldactone Review and Aldactone Label ), RIVOTRIL (3drop As Required) (View Rivotril Review and Rivotril Label ), BISOPROLOL FUMARATE (1.25mg Per Day) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), FOSAVANCE (70mg Weekly) (View Fosavance Review and Fosavance Label ), PERINDOPRIL ERBUMINE (2mg Single Dose) (View Perindopril Erbumine Review and Perindopril Erbumine Label ). Patient was hospitalized.

6968138-2 | Abdominal Wall Haematoma, Haemoglobin Decreased, Shock Haemorrhagic
Adverse event was reported on Aug 27, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: 7.5mg Per Day) was diagnosed with pulmonary embolism (What is pulmonary embolism?) and. Location: FRANCE , 70 years of age, weighting 218.3 lb, Patient experienced the following unwanted or unexpected effects: abdominal wall haematoma, haemoglobin decreased, shock haemorrhagic. During the same period patient was treated with LOVENOX (.4ml Single Dose) (View Lovenox Review and Lovenox Label ). Patient was hospitalized.

6968136-9 | Feeling Abnormal, Headache, Hyperhidrosis, Nausea, Off Label Use, Suicidal Ideation
on Aug 27, 2010 Male patient from FRANCE , 20 years of age, was diagnosed with thrombosis prophylaxis, pain (What is pain?) and was treated with Arixtra (View Usage). Patient had the following side effects: feeling abnormal, headache (What is headache?), hyperhidrosis, nausea (What is nausea?), off label use, suicidal ideation. Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with MORPHINE (2inj Per Day) (View Morphine Review and Morphine Label ).

6965473-9 | Haematoma, Normochromic Normocytic Anaemia, Overdose, Thrombocytopenia
on Sep 01, 2010 Female patient from FRANCE , weighting 152.1 lb, was diagnosed with phlebitis, mediastinitis, clostridium difficile colitis and was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: haematoma, normochromic normocytic anaemia, overdose, thrombocytopenia. Arixtra dosage: 7.5mg Twice Per Day. During the same period patient was treated with VANCOMYCIN HCL (View Vancomycin Hcl Review and Vancomycin Hcl Label ), NEXIUM (40mg Per Day) (View Nexium Review and Nexium Label ), FLAGYL (View Flagyl Review and Flagyl Label ). Patient was hospitalized.

6963447-5 | Haematoma, Haemoglobin Decreased, Platelet Count Increased
Patient was taking Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: haematoma, haemoglobin decreased, platelet count increased on Sep 01, 2010 from FRANCE Additional patient health information: Female patient , weighting 132.3 lb, was diagnosed with thrombosis prophylaxis, pain (What is pain?), constipation (What is constipation?), anxiety (What is anxiety?), insomnia and. Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with PROFENID (View Profenid Review and Profenid Label ), FORLAX (View Forlax Review and Forlax Label ), EUPHYTOSE (3tab Per Day) (View Euphytose Review and Euphytose Label ), VASTEN (10mg Per Day) (View Vasten Review and Vasten Label ), PARIET (20mg Per Day) (View Pariet Review and Pariet Label ), ACETAMINOPHEN (3g Per Day) (View Acetaminophen Review and Acetaminophen Label ), STILNOX (10mg Per Day) (View Stilnox Review and Stilnox Label ). Patient was hospitalized.

6963446-3 | Anaemia, Contraindication To Medical Treatment, Haemorrhage
Adverse event was reported on Aug 23, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: 2.5mg Per Day) was diagnosed with thrombosis prophylaxis, depression (What is depression?), anxiety (What is anxiety?), osteoporosis (What is osteoporosis?) and. Location: FRANCE , weighting 70.55 lb, Patient had the following side effects: anaemia, contraindication to medical treatment, haemorrhage. During the same period patient was treated with SEROPLEX (10mg Per Day) (View Seroplex Review and Seroplex Label ), LASIX (20mg Per Day) (View Lasix Review and Lasix Label ), ALDACTONE (12.5mg Per Day) (View Aldactone Review and Aldactone Label ), RIVOTRIL (3drop As Required) (View Rivotril Review and Rivotril Label ), BISOPROLOL FUMARATE (1.25mg Per Day) (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), FOSAVANCE (70mg Weekly) (View Fosavance Review and Fosavance Label ), PERINDOPRIL ERBUMINE (2mg Single Dose) (View Perindopril Erbumine Review and Perindopril Erbumine Label ). Patient was hospitalized.

6961362-4 | Extradural Haematoma
on Aug 24, 2010 Female patient from JAPAN , 72 years of age, was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: extradural haematoma. Arixtra dosage: 2.5mg Per Day. Patient was hospitalized and became disabled.

6956988-8 | Abdominal Wall Haematoma
on Aug 27, 2010 Male patient from UNITED STATES , 75 years of age, weighting 216.1 lb, was diagnosed with pulmonary embolism (What is pulmonary embolism?) and was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal wall haematoma. Arixtra dosage: 7.5mg Daily Sq. Patient was hospitalized.

6956377-6 | Catheter Placement, Coma, Platelet Count Decreased, Pneumothorax, Respiratory Arrest
Patient was taking Arixtra (View Usage). Patient had the following side effects: catheter placement, coma, platelet count decreased, pneumothorax, respiratory arrest on Aug 18, 2010 from UNITED STATES Additional patient health information: Female patient , 52 years of age, . Arixtra dosage: . During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), MULTI VITAMIN (View Multi-vitamin Review and Multi-vitamin Label ), ASCORBIC ACID (View Ascorbic Acid Review and Ascorbic Acid Label ), OSCAL D (View Oscal-d Review and Oscal-d Label ), HYDROCHLOROTHIAZIDE (View Hydrochlorothiazide Review and Hydrochlorothiazide Label ), KDUR (View Kdur Review and Kdur Label ), MAALOX (View Maalox Review and Maalox Label ). Patient was hospitalized.

6945786-7 | Arterial Thrombosis Limb, Thrombosis In Device
Adverse event was reported on Aug 19, 2010 by a Male patient taking Arixtra (View Usage) (Dosage: 2.5mg Per Day) was diagnosed with thrombosis prophylaxis and. Location: FRANCE , 61 years of age, weighting 196.2 lb, After Arixtra was administered, patient had the following side effects: arterial thrombosis limb, thrombosis in device. During the same period patient was treated with COMPRESSION STOCKINGS (View Compression Stockings Review and Compression Stockings Label ).

6943925-5 | Abdominal Compartment Syndrome, Anaemia, Extrinsic Vascular Compression, Fistula, Haematoma
on Aug 19, 2010 Female patient from FRANCE , child 10 years of age, was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: abdominal compartment syndrome, anaemia, extrinsic vascular compression, fistula (What is fistula?), haematoma. Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with LASIX (View Lasix Review and Lasix Label ). Patient was hospitalized.

6943911-5 | Hospitalisation
on Aug 19, 2010 Female patient from UNITED STATES , 39 years of age, was treated with Arixtra (View Usage). Patient had the following side effects: hospitalisation. Arixtra dosage: . Patient was hospitalized.

6943901-2 | Hip Surgery
Patient was taking Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: hip surgery on Aug 19, 2010 from UNITED STATES Additional patient health information: Male patient , 49 years of age, . Arixtra dosage: . Patient was hospitalized.

6943896-1 |
Adverse event was reported on Aug 18, 2010 by a Male patient taking Arixtra (View Usage) (Dosage: ) . Location: UNITED STATES , 79 years of age, .

6940974-8 | Fall, Oedema Peripheral, Skin Laceration, Staphylococcal Infection
on Aug 17, 2010 Female patient from UNITED STATES , 50 years of age, was treated with Arixtra (View Usage). Patient had the following side effects: fall (What is fall?), oedema peripheral, skin laceration, staphylococcal infection (What is staphylococcal infection?). Arixtra dosage: . Patient was hospitalized.

6937282-8 | Haematoma, Post Procedural Haematoma, Skin Disorder
on Aug 13, 2010 Female patient from FRANCE , weighting 286.6 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: haematoma, post procedural haematoma, skin disorder. Arixtra dosage: 2.5mg Per Day. Patient was hospitalized.

6934341-0 | Cerebrovascular Accident, Fall, Speech Disorder
Patient was taking Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: cerebrovascular accident, fall (What is fall?), speech disorder on Aug 13, 2010 from UNITED STATES Additional patient health information: Male patient , 40 years of age, . Arixtra dosage: 7.5mg Per Day.

6932168-7 | Pulmonary Embolism
Adverse event was reported on Aug 10, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: 1.5mg Per Day) was diagnosed with thrombosis prophylaxis and. Location: JAPAN , 63 years of age, Patient had the following side effects: pulmonary embolism (What is pulmonary embolism?).

6932153-5 | Ear Haemorrhage
on Aug 11, 2010 Female patient from FRANCE , 81 years of age, weighting 132.3 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: ear haemorrhage. Arixtra dosage: 2.5mg Per Day.

6930542-6 |
on Aug 09, 2010 Female patient from UNITED STATES , 61 years of age, was treated with Arixtra (View Usage). . Arixtra dosage: .

6928727-8 | Abdominal Symptom, Gamma-glutamyltransferase Increased, Oesophageal Candidiasis, Transaminases Increased
Patient was taking Arixtra (View Usage). Patient had the following side effects: abdominal symptom, gamma-glutamyltransferase increased, oesophageal candidiasis, transaminases increased on Aug 12, 2010 from GERMANY Additional patient health information: Male patient , 51 years of age, was diagnosed with pulmonary embolism (What is pulmonary embolism?), hypertension, brain neoplasm and. Arixtra dosage: . During the same period patient was treated with BISOPROLOL (View Bisoprolol Review and Bisoprolol Label ), PANTOPRAZOLE (View Pantoprazole Review and Pantoprazole Label ), TORSEMIDE (View Torsemide Review and Torsemide Label ), FORTECORTIN (View Fortecortin Review and Fortecortin Label ). Patient was hospitalized.

6919368-7 | Hospitalisation
Adverse event was reported on Aug 04, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: ) . Location: UNITED STATES , 83 years of age, After Arixtra was administered, patient had the following side effects: hospitalisation. Patient was hospitalized.

6917090-4 | Haemoglobin Decreased, Platelet Count Increased, Post Procedural Haemorrhage
on Jul 30, 2010 Female patient from JAPAN , weighting 132.3 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: haemoglobin decreased, platelet count increased, post procedural haemorrhage. Arixtra dosage: 2.5mg Per Day. During the same period patient was treated with ROPION (250mg Per Day) (View Ropion Review and Ropion Label ), LORCAM (100mg Per Day) (View Lorcam Review and Lorcam Label ), VOLTAREN (100mg Per Day) (View Voltaren Review and Voltaren Label ). Patient was hospitalized.

6917050-3 | Disease Complication, Lung Disorder, Lung Neoplasm Malignant
on Aug 02, 2010 Male patient from UNITED STATES , 57 years of age, was treated with Arixtra (View Usage). Patient had the following side effects: disease complication, lung disorder, lung neoplasm malignant. Arixtra dosage: .

6917039-4 |
Patient was taking Arixtra (View Usage). on Aug 04, 2010 from UNITED STATES Additional patient health information: Female patient , 80 years of age, was diagnosed with thrombosis prophylaxis and. Arixtra dosage: . During the same period patient was treated with TARCEVA (View Tarceva Review and Tarceva Label ).

6917019-9 | Urticaria
Adverse event was reported on Aug 06, 2010 by a Male patient taking Arixtra (View Usage) (Dosage: ) was diagnosed with embolism arterial and. Location: UNITED STATES , 49 years of age, Patient experienced the following unwanted or unexpected effects: urticaria. During the same period patient was treated with LOVENOX (View Lovenox Review and Lovenox Label ), OXYCODONE (View Oxycodone Review and Oxycodone Label ), COUMADIN (View Coumadin Review and Coumadin Label ), ACETAMINOPHEN (View Acetaminophen Review and Acetaminophen Label ). Patient was hospitalized.

6916996-X | Bladder Cancer, Disease Progression
on Aug 03, 2010 Male patient from UNITED STATES , 60 years of age, weighting 190.5 lb, was treated with Arixtra (View Usage). Patient had the following side effects: bladder cancer (What is bladder cancer?), disease progression. Arixtra dosage: .

6916936-3 | Body Temperature Decreased, Dizziness, Dyspnoea, Headache, Myocardial Infarction, Pain
on Aug 04, 2010 Female patient from UNITED STATES , 49 years of age, was diagnosed with antiphospholipid syndrome, inflammation and was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: body temperature decreased, dizziness (What is dizziness?), dyspnoea, headache (What is headache?), myocardial infarction, pain (What is pain?). Arixtra dosage: 7.5mg Per Day. During the same period patient was treated with PANCREATIN (View Pancreatin Review and Pancreatin Label ), TUMERIC (View Tumeric Review and Tumeric Label ), FISH OIL (View Fish Oil Review and Fish Oil Label ), VITAMIN E (View Vitamin E Review and Vitamin E Label ).

6914296-5 | Liver Function Test Abnormal, Platelet Count Increased
Patient was taking Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: liver function test abnormal, platelet count increased on Jul 30, 2010 from JAPAN Additional patient health information: Male patient , 55 years of age, . Arixtra dosage: .

6911042-6 | Anaemia, Haemorrhage, Pain, Swelling
Adverse event was reported on Jul 29, 2010 by a Female patient taking Arixtra (View Usage) (Dosage: 2.5mg Per Day) was diagnosed with thrombosis prophylaxis and. Location: JAPAN , weighting 94.80 lb, Patient had the following side effects: anaemia, haemorrhage, pain (What is pain?), swelling. During the same period patient was treated with LOXONIN (180mg Per Day) (View Loxonin Review and Loxonin Label ), GASTER (20mg Per Day) (View Gaster Review and Gaster Label ), ARICEPT (5mg Per Day) (View Aricept Review and Aricept Label ). Patient was hospitalized.

6911007-4 | Acute Myocardial Infarction, Cardiac Failure
on Jul 29, 2010 Female patient from UNITED STATES , 84 years of age, was treated with Arixtra (View Usage). After Arixtra was administered, patient had the following side effects: acute myocardial infarction, cardiac failure. Arixtra dosage: .

6910971-7 | Pulmonary Embolism
on Jul 27, 2010 Male patient from UNITED STATES , 77 years of age, was diagnosed with bone operation and was treated with Arixtra (View Usage). Patient experienced the following unwanted or unexpected effects: pulmonary embolism (What is pulmonary embolism?). Arixtra dosage: . During the same period patient was treated with ASPIRIN (325mg Per Day) (View Aspirin Review and Aspirin Label ).

6908854-1 | Abdominal Wall Haematoma, Haemoglobin Decreased
Patient was taking Arixtra (View Usage). Patient had the following side effects: abdominal wall haematoma, haemoglobin decreased on Aug 03, 2010 from FRANCE Additional patient health information: Female patient , 80 years of age, weighting 163.1 lb, was diagnosed with thrombophlebitis and. Arixtra dosage: 7.5mg Per Day. During the same period patient was treated with PREVISCAN (20mg Per Day) (View Previscan Review and Previscan Label ), PLAVIX (View Plavix Review and Plavix Label ), INDAPAMIDE (View Indapamide Review and Indapamide Label ), AMLOR (View Amlor Review and Amlor Label ), BISOPROLOL FUMARATE (View Bisoprolol Fumarate Review and Bisoprolol Fumarate Label ), NEXIUM (View Nexium Review and Nexium Label ), CACIT D3 (View Cacit D3 Review and Cacit D3 Label ), LYRICA (25mg Twice Per Day) (View Lyrica Review and Lyrica Label ). Patient was hospitalized.