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ARIXTRA Safety Reports
Total ARIXTRA reports: 479.ARIXTRA FDA safety alerts: No.
Reported deaths: 86 Reported hospitalizations: 289.
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Physician from FRANCE reported ARIXTRA problem on Jan 18, 2007. Female patient, 40 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cerebral haemorrhage, coma, depressed level of consciousness, haematoma, speech disorder. ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient died on 10/18/2006.ARIXTRA problem was reported by a Physician from FRANCE on Jan 19, 2007. Female patient, weighting 110.2 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: muscle haemorrhage, renal disorder, retroperitoneal haemorrhage, shock. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CELLCEPT, CORTICOID, PLASMAPHERESIS. Patient died.
Physician from AUSTRIA reported ARIXTRA problem on Jan 29, 2007. Female patient, 74 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: pulmonary embolism. ARIXTRA dosage: unknown. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from AUSTRIA on Jan 31, 2007. Female patient, 77 years of age, was diagnosed with prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: circulatory collapse, dyspnoea, pulmonary embolism. ARIXTRA dosage: .4ML SEE TEXT. Patient recovered.
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Feb 01, 2007. Female patient, 59 years of age, weighting 290.0 lb, was diagnosed with knee arthroplasty and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: chest pain, diarrhoea, dysarthria, kidney infection, vision blurred, vomiting. ARIXTRA dosage: unknown. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 23, 2007. Female patient, 75 years of age, weighting 198.4 lb, was diagnosed with venous thrombosis, cardiac failure, hypertension, arteritis coronary, osteoarthritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anaemia, aortic aneurysm rupture, hypotension, intra-abdominal haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with KLIPAL, PERINDOPRIL ERBUMINE, VASODILATOR, LASIX, POTASSIUM ACETATE, NITRODERM, ACETAMINOPHEN. Patient was hospitalized. Patient died on 09/22/2006.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Jan 23, 2007. Female patient, 92 years of age, weighting 99.21 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma. ARIXTRA dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 24, 2007. Female patient, 78 years of age, weighting 154.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: neurological symptom, overdose, pain in extremity, retroperitoneal haematoma, sciatica. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with HEPARIN. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Jan 24, 2007. Female patient, 84 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma, nerve compression. ARIXTRA dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 25, 2007. Female patient, 75 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal distension, abdominal pain, diabetes mellitus, gastrointestinal haemorrhage, injection site haematoma. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with INSULINE, VALSARTAN AND HYDROCHLOROTHIAZIDE, CARDENSIEL, LASIX, KALEORID, PLAVIX. Patient was hospitalized. Patient died on 01/14/2007.
Physician from FRANCE reported ARIXTRA problem on Jan 25, 2007. Female patient, 81 years of age, weighting 154.3 lb, was diagnosed with deep vein thrombosis, asthma, infection and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, anaemia, anuria, circulatory collapse, intra-abdominal haemorrhage, muscle haemorrhage, pallor, renal tubular necrosis, shock. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with ASPIRIN, THEOSTAT, PYOSTACINE, PULMICORT, BURINEX, EUPRESSYL, ZADITEN, DAFLON. Patient was hospitalized. Patient died on 02/18/2006.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 24, 2007. Male patient, 85 years of age, weighting 132.3 lb, was diagnosed with atrial fibrillation and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blister, blood blister, off label use. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Jan 26, 2007. Female patient, 24 years of age, weighting 114.6 lb, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN, CONTRACEPTIVE. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Jan 29, 2007. Female patient, 70 years of age, weighting 216.1 lb, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, dyspnoea, haematoma, malaise, tachycardia. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Feb 06, 2007. Female patient, weighting 290.0 lb, was diagnosed with knee arthroplasty and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cardiac arrest, thrombosis. ARIXTRA dosage: unknown. Patient died on 02/01/2007.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 30, 2007. Female patient, 21 years of age, weighting 187.4 lb, was diagnosed with periphlebitis, contraception and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: dizziness, hyperhidrosis, malaise, off label use, syncope. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with MICROVAL. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Feb 07, 2007. Male patient, 81 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal haematoma, abdominal pain, anaemia, injection site induration, retroperitoneal haemorrhage, urinary tract disorder. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN, ASPIRIN, LOGIRENE. Patient was hospitalized. Patient died on 01/04/2007.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 05, 2007. Male patient, 83 years of age, weighting 105.8 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, duodenal ulcer perforation, hypovolaemia, peritonitis, renal failure, sepsis. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with NON STEROIDAL ANTI, LASIX, FUMAFER, TOPALGIC, OMEPRAZOLE, MYOLASTAN, DAFALGAN. Patient died on 04/27/2006.
Physician from FRANCE reported ARIXTRA problem on Feb 01, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: thrombocythaemia. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Jan 22, 2007. Female patient, 79 years of age, weighting 136.7 lb, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma, nerve compression. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Pharmacist from UNITED STATES reported ARIXTRA problem on Feb 08, 2007. Female patient, weighting 132.3 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: deep vein thrombosis. ARIXTRA dosage: 2.5 MG DAILY SQ. Patient recovered.
ARIXTRA problem was reported by a Physician from GERMANY on Feb 07, 2007. Female patient, 30 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: eosinophilia, leukopenia. ARIXTRA dosage: unknown. During the same period patient was treated with PHENHYDAN, SALOFALK, AZATHIOPRINE. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 06, 2007. Female patient, 83 years of age, weighting 141.1 lb, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blister, haematoma, pulmonary embolism. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with GINKORT, ATACAND, SYMBICORT, CATAPRES, TETRAZEPAM, SIMVASTATIN. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 06, 2007. Male patient, 72 years of age, weighting 143.3 lb, was diagnosed with pulmonary embolism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cardiac failure, haematuria, haemoglobin decreased, heart rate increased, oedema peripheral, overdose, purulent discharge, urinary retention. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with OMEPRAZOLE, FUROSEMIDE, AMIODARONE. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Feb 07, 2007. Female patient, 48 years of age, weighting 238.5 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, adrenal haemorrhage, back pain, deep vein thrombosis, heparin-induced thrombocytopenia. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with VICODIN, IMITREX, UROCIT, MAGNESIUM. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 06, 2007. Female patient, 87 years of age, weighting 136.7 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma, paralysis. ARIXTRA dosage: unknown. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 07, 2007. Male patient, 82 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: activated partial thromboplastin time prolonged, anaemia, muscle haemorrhage, prothrombin level decreased, subcutaneous haematoma. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with KARDEGIC, TAHOR, NEXIUM, PLAVIX, HYDREA, DETENSIEL, LASIX, SPECIAFOLDINE. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 07, 2007. Male patient, 78 years of age, was diagnosed with phlebitis superficial, prophylaxis, essential hypertension, arteritis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: angina pectoris, haemoglobin decreased, rectal haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with PLAVIX, APROVEL, LERCAN, FONZYLANE, INSULATARD, MYOLASTAN, ZAMUDOL. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 07, 2007. Female patient, 76 years of age, was diagnosed with deep vein thrombosis, angina pectoris, arthropathy and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: muscle haemorrhage, pain in extremity. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with INNOHEP, VERAPAMIL, ACETAMINOPHEN, VASTAREL, CHONDROSULF. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 09, 2007. Female patient, 55 years of age, weighting 240.3 lb, was diagnosed with thrombophlebitis superficial and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, muscle haemorrhage, off label use. ARIXTRA dosage: 10MG PER DAY. During the same period patient was treated with NICOTINE SUBSTITUTE, NICOTINE SUBSTITUTE, COMPRESSION STOCKINGS. Patient was hospitalized. Patient recovered.
Physician from GERMANY reported ARIXTRA problem on Feb 14, 2007. Male patient, 27 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ecchymosis, gingival bleeding, injection site haematoma, petechiae, thrombocytopenia. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with EMBOLEX, MARCUMAR. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 16, 2007. Female patient, 79 years of age, weighting 130.1 lb, was diagnosed with phlebitis, erysipelas, hypertension and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bradycardia, cerebral haematoma, cerebral haemorrhage, coma, depressed level of consciousness, haemodynamic instability, respiratory arrest, suicide attempt, ventricular extrasystoles. ARIXTRA dosage: unknown. During the same period patient was treated with PREVISCAN, AMOXICILLIN TRIHYDRATE, PYOSTACINE, LEXOMIL, KERLONE, LOXEN, DAFLON, PHYSIOTENS. Patient was hospitalized. Patient died on 06/27/2006.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 16, 2007. Female patient, 79 years of age, weighting 130.1 lb, was diagnosed with phlebitis, erysipelas, essential hypertension and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bradycardia, cerebral haematoma, cerebral haemorrhage, coma, depressed level of consciousness, haemodynamic instability, haemoglobin decreased, respiratory arrest, suicide attempt. ARIXTRA dosage: unknown. During the same period patient was treated with PREVISCAN, PYOSTACINE, LEXOMIL, KERLONE, LOXEN, DAFLON, PHYSIOTENS, AMOXICILLIN TRIHYDRATE. Patient was hospitalized. Patient died on 06/27/2006.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 16, 2007. Female patient, 70 years of age, weighting 216.1 lb, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain, dyspnoea, haematoma, malaise, tachycardia. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Feb 12, 2007. Male patient, 86 years of age, weighting 198.4 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, ecchymosis, off label use, renal failure acute. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 20, 2007. Female patient, 69 years of age, weighting 160.9 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: off label use, purpura non-thrombocytopenic. ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Feb 19, 2007. Male patient, 69 years of age, was diagnosed with cardiac valve prosthesis user and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bronchial haemorrhage, haemoptysis, overdose, renal impairment. ARIXTRA dosage: 7.5MG SEE TEXT. During the same period patient was treated with CALCIPARINE, ACUPAN. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 20, 2007. Female patient, 84 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma, joint swelling, nerve compression, spinal cord disorder. ARIXTRA dosage: unknown. Patient was hospitalized and became disabled. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Feb 20, 2007. Male patient, 75 years of age, weighting 154.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bundle branch block left, bundle branch block right, cardiomegaly, colitis, colonic haematoma, gastrointestinal necrosis, hypocalcaemia, hypokalaemia, rectal ulcer. ARIXTRA dosage: unknown. During the same period patient was treated with OMEPRAZOLE, SOLUPRED, SPASFON, IMOVANE, ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE, DOLIPRANE, DIFFU K, EFFERALGAN CODEINE. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Feb 21, 2007. Female patient, 25 years of age, weighting 132.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: thrombocythaemia, thrombosis. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOVENOX. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Feb 26, 2007. Female patient, 84 years of age, weighting 123.5 lb, was diagnosed with phlebitis, iron deficiency and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, haematoma, hypoaesthesia, hypokalaemia, leukocytosis, mobility decreased, nerve compression, overdose, paralysis. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with INDAPAMIDE, LASIX, ZOLPIDEM TARTRATE, TRIVASTAL, LIORESAL, FRACTAL, MAXEPA, FUMAFER. Patient was hospitalized and became disabled. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 21, 2007. Female patient, 87 years of age, weighting 136.7 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haematoma, nerve compression, paralysis. ARIXTRA dosage: unknown. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Mar 08, 2007. Male patient, 87 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, haematuria, haemorrhage, off label use, oliguria, renal failure, shock, shock haemorrhagic. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with SYMBICORT, LASIX, CORDARONE, DIGOXIN, ATACAND, FLUINDIONE. Patient was hospitalized. Patient died on 12/31/2006.
ARIXTRA problem was reported by a Physician from AUSTRIA on Mar 01, 2007. Female patient, 77 years of age, weighting 160.9 lb, was diagnosed with thrombosis prophylaxis, blood pressure, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: circulatory collapse, dyspnoea, pulmonary embolism. ARIXTRA dosage: unknown. During the same period patient was treated with FRAXIPARIN, BLOPRESS, EUTHYROX, NEXIUM, HALCION. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Mar 05, 2007. Male patient, 75 years of age, weighting 154.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bundle branch block left, bundle branch block right, cardiomegaly, colitis, colonic haematoma, gastrointestinal necrosis, hypocalcaemia, hypokalaemia, rectal ulcer. ARIXTRA dosage: unknown. During the same period patient was treated with MOPRAL, SOLUPRED, SPASFON, IMOVANE, ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE, DOLIPRANE, DIFFU K, EFFERALGAN CODEINE. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2007. Male patient, 85 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cerebral haematoma. ARIXTRA dosage: unknown. During the same period patient was treated with PLAVIX, KARDEGIC, MOXIFLOXACIN HYDROCHLORIDE, ZOCOR, TAREG, SECTRAL, RIVOTRIL, INIPOMP. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Feb 27, 2007. Male patient, 61 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: thrombocythaemia. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 02, 2007. Female patient, 61 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage, hypovolaemia. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 08, 2007. Male patient, 67 years of age, weighting 220.5 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, deep vein thrombosis, haematoma, oedema peripheral, renal disorder. ARIXTRA dosage: unknown. During the same period patient was treated with KARDEGIC. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Mar 07, 2007. Female patient, 29 years of age, was diagnosed with portal vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: breast feeding. ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.
Physician from AUSTRIA reported ARIXTRA problem on Mar 01, 2007. Female patient, 74 years of age, weighting 160.9 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: pulmonary embolism. ARIXTRA dosage: unknown. During the same period patient was treated with BEZALIP, GINKO BILOBA, CALCIUM, FOSAMAX, BLOPRESS. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2007. Female patient, 81 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: gastric ulcer, gastrointestinal haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with XELODA. Patient died on 01/20/2007.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 02, 2007. Female patient, 45 years of age, weighting 143.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: diarrhoea, faecal incontinence. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
ARIXTRA problem was reported by a Physician from GERMANY on Mar 06, 2007. Female patient, 30 years of age, weighting 127.9 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: eosinophilia, leukopenia. ARIXTRA dosage: unknown. During the same period patient was treated with PHENYTOIN, SALOFALK, AZATHIOPRINE. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Mar 05, 2007. Male patient, 69 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: off label use, rectal haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. Patient died on 03/01/2007.
ARIXTRA problem was reported by a Physician from FRANCE on Mar 05, 2007. Female patient was treated with ARIXTRA. ARIXTRA dosage: 7.5MG PER DAY. Patient died.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 05, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemothorax, lung neoplasm malignant. ARIXTRA dosage: 7.5MG PER DAY. Patient died.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 05, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemoptysis. ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 06, 2007. Female patient, 75 years of age, was diagnosed with atrial fibrillation and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: off label use, subdural haematoma. ARIXTRA dosage: unknown. Patient died on 03/04/2007.
ARIXTRA problem was reported by a Physician from FRANCE on Mar 13, 2007. Female patient, 90 years of age, weighting 88.18 lb, was diagnosed with atrial fibrillation and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: coma, malaise, off label use, subdural haematoma. ARIXTRA dosage: unknown. During the same period patient was treated with CORDARONE, TRIATEC, LASIX, VADILEX, KARDEGIC. Patient was hospitalized. Patient died on 02/26/2007.
Physician from FRANCE reported ARIXTRA problem on Mar 13, 2007. Male patient, 83 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. Patient died on 01/01/2007.
ARIXTRA problem was reported by a Physician from FRANCE on Mar 22, 2007. Male patient, 75 years of age, weighting 176.4 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: fall, off label use, subdural haematoma, syncope. ARIXTRA dosage: 7.5MG PER DAY. Patient died on 03/04/2007.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 22, 2007. Female patient, 72 years of age, weighting 147.7 lb, was diagnosed with pulmonary embolism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, haematoma, muscle haemorrhage. ARIXTRA dosage: unknown. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Pharmacist from GERMANY on Mar 28, 2007. Male patient, 70 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anorexia, dizziness, haemorrhage, movement disorder, nausea. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with MARCUMAR. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Mar 21, 2007. Male patient, 75 years of age, weighting 154.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: bundle branch block left, bundle branch block right, cardiomegaly, colitis, colonic haematoma, gastrointestinal necrosis, haematoma infection, hypocalcaemia, hypokalaemia. ARIXTRA dosage: unknown. During the same period patient was treated with OMEPRAZOLE, SOLUPRED, SPASFON, IMOVANE, ALUMINUM HYDROXIDE AND MAGNESIUM TRISILICATE, DOLIPRANE, DIFFU K, EFFERALGAN CODEINE. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 22, 2007. Male patient, 85 years of age, was diagnosed with cardiac failure and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cardiac failure acute, cerebral haemorrhage, confusional state, haemorrhagic stroke, off label use, pneumonia aspiration, quadriparesis, septic shock, somnolence. ARIXTRA dosage: unknown. During the same period patient was treated with TAHOR, LASIX, DIGOXIN, OMEPRAZOLE, XATRAL. Patient was hospitalized. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Mar 22, 2007. Female patient, 89 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, haematoma, pain in extremity. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized and became disabled. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Mar 26, 2007. Female patient, 81 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anuria, gastric ulcer, gastrointestinal haemorrhage, hyperaesthesia, intestinal obstruction, vomiting. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with XELODA. Patient died on 01/29/2007.
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Apr 03, 2007. Female patient, 48 years of age, weighting 238.5 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal pain upper, adrenal haemorrhage, back pain, deep vein thrombosis, heparin-induced thrombocytopenia. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with VICODIN, IMITREX, UROCIT, MAGNESIUM. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Apr 05, 2007. Male patient, 53 years of age, was diagnosed with angina pectoris and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: angioedema. ARIXTRA dosage: unknown. Patient recovered.
Consumer or non-health professional from FRANCE reported ARIXTRA problem on Apr 05, 2007. Female patient, 86 years of age, was diagnosed with phlebitis, bipolar i disorder and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: abdominal haematoma, anaemia, renal failure acute, somnolence. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with KARDEGIC. Patient was hospitalized. Patient recovered.
ARIXTRA problem was reported by a Physician from FRANCE on Apr 05, 2007. Female patient was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: melaena. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Pharmacist from FRANCE reported ARIXTRA problem on Apr 06, 2007. Male patient, 58 years of age, was diagnosed with cerebral thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: hepatocellular damage, transaminases increased. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with NEURONTIN, FLUANXOL, CORTICOIDS. Patient recovered.
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Apr 05, 2007. Female patient, 89 years of age, weighting 136.7 lb, was diagnosed with chronic obstructive pulmonary disease, essential hypertension and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anaemia, haematoma, renal failure acute. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with VENTOLIN, ASPEGIC, HEMIGOXINE NATIVELLE, LASIX, PERINDOPRIL ERBUMINE, AMARYL, DIFFU K, OMEPRAZOLE. Patient was hospitalized. Patient recovered.
Physician from FRANCE reported ARIXTRA problem on Mar 29, 2007. Female patient, 83 years of age, weighting 176.0 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: subdural haematoma. ARIXTRA dosage: 2.5 MG/PER DAY/SUBCUTANEOUS. Patient was hospitalized. Patient recovered.
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