Arixtra and haemoglobin decreased Patient Reports February 10, 2012

Arixtra Side Effects Report #5411211-0
Arixtra side effect was reported by a Physician from FRANCE on Aug 02, 2007. Female patient, 74 years of age, weighting 198.4 lb, was diagnosed with venous thrombosis limb, hypercholesterolaemia, arrhythmia

, gastritis, anxiety

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematoma, haemoglobin decreased, shock, traumatic haematoma. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with LIPANTHYL, SECTRAL, FLECAINIDE ACETATE, OMEPRAZOLE, SERESTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5486473-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 10, 2007. Male patient, 63 years of age, was diagnosed with venous thrombosis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, back pain

, haemoglobin decreased, hypercapnia, hypotension, melaena, renal failure acute, renal haemorrhage, retroperitoneal haematoma. Arixtra dosage: unknown. During the same period patient was treated with PREVISCAN, ESBERIVENT, KALEORID, VIAGRA, STABLON, EUPRESSYL, IRBESARTAN, CELIPROLOL. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5523368-1
Arixtra side effect was reported by a Physician from JAPAN on Nov 19, 2007. Male patient, 91 years of age, weighting 132.3 lb, was diagnosed with thrombosis prophylaxis, atrial fibrillation

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, gastric ulcer haemorrhage, gastrointestinal haemorrhage, haemoglobin decreased, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN. Patient recovered.

Arixtra Side Effects Report #5535824-0
Arixtra side effect was reported by a Physician from JAPAN on Nov 30, 2007. Male patient, 91 years of age, weighting 132.3 lb, was diagnosed with thrombosis prophylaxis, atrial fibrillation

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, gastric ulcer haemorrhage, gastrointestinal haemorrhage, haemoglobin decreased, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN. Patient recovered.

Arixtra Side Effects Report #5642987-5
Arixtra side effect was reported by a Pharmacist from JAPAN on Feb 22, 2008. Female patient, 91 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer, haemoglobin decreased, melaena. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, THYRADIN. Patient recovered.

Arixtra Side Effects Report #5707069-2
Arixtra side effect was reported by a Physician from FRANCE on Apr 09, 2008. Female patient, 91 years of age, weighting 121.3 lb, was diagnosed with thrombosis prophylaxis, phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematoma, haemoglobin decreased, incision site haemorrhage, phlebitis, pyrexia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ANTIVITAMINS K. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5602518-2
Arixtra side effect was reported by a Physician from JAPAN on Jan 18, 2008. Female patient, 88 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: diverticulum intestinal, gastrointestinal haemorrhage, haemoglobin decreased, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with FUROSEMIDE, ALDACTONE, TAKEPRON, NEUTROPIN, MUCOSTA, MARZULENE, BERIZYM, LAC B. Patient recovered.

Arixtra Side Effects Report #5612601-3
Arixtra side effect was reported by a Physician from JAPAN on Feb 01, 2008. Female patient, 88 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: diverticulum intestinal, gastrointestinal haemorrhage, haemoglobin decreased, melaena, shock. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with FUROSEMIDE, ALDACTONE, TAKEPRON, NEUTROPIN, MUCOSTA, MARZULENE, BERIZYM, LAC B. Patient recovered.

Arixtra Side Effects Report #6128349-5
Arixtra side effect was reported by a Physician from JAPAN on Mar 16, 2009. Female patient, 87 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, blood pressure decreased, haematocrit decreased, haemoglobin decreased, pallor. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with GASTER D, MICARDIS, AMLODIN. Patient recovered.

Arixtra Side Effects Report #5479660-2
Arixtra side effect was reported by a Pharmacist from JAPAN on Oct 02, 2007. Male patient, 86 years of age, weighting 220.5 lb, was diagnosed with thrombosis prophylaxis, gastritis, constipation

, insomnia, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal tenderness, anorexia, blood bilirubin increased, blood creatine increased, faeces discoloured, gastric ulcer haemorrhage, haematocrit decreased, haemoglobin decreased, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, DASEN, KELNAC, VOLTAREN, MAGLAX, EVAMYL, CEFZON. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5778675-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on June 09, 2008. Male patient, 86 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, muscle haemorrhage, oedema peripheral. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PAROXETINE, PLAVIX, AMLODIPINE, NEXIUM, XANAX. Patient recovered.

Arixtra Side Effects Report #5912257-6
Arixtra side effect was reported by a Physician from JAPAN on Oct 03, 2008. Female patient, 86 years of age, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, basophil count decreased, binocular eye movement disorder, blood cholesterol increased, blood glucose increased, cerebral haemorrhage, haematocrit decreased, haemoglobin decreased, hemiplegia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, DASEN, MARZULENE, MEIACT. Patient recovered.

Arixtra Side Effects Report #5929526-6
Arixtra side effect was reported by a Physician from JAPAN on Oct 20, 2008. Female patient, 86 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, basophil count decreased, binocular eye movement disorder, blood cholesterol increased, blood glucose increased, cerebral haemorrhage, haematocrit decreased, haemoglobin decreased, hemiplegia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, DASEN, MARZULENE, MEIACT. Patient recovered.

Arixtra Side Effects Report #5989018-5
Arixtra side effect was reported by a Physician from JAPAN on Dec 08, 2008. Female patient, 86 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis, analgesia, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, basophil count decreased, binocular eye movement disorder, blood cholesterol increased, blood glucose increased, cerebral haemorrhage, haematocrit decreased, haemoglobin decreased, hemiplegia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, DASEN, MARZULENE, MEIACT. Patient recovered.

Arixtra Side Effects Report #5684371-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 21, 2008. Male patient, 85 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood creatinine increased, haemoglobin decreased, haemorrhage subcutaneous, mobility decreased, pain in extremity, subcutaneous haematoma. Arixtra dosage: unknown. During the same period patient was treated with PLAVIX, ZYLORIC, ACETAMINOPHEN, XATRAL, SIMVASTATIN, ENALAPRIL MALEATE, LASIX, FORLAX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5390111-9
Arixtra side effect was reported by a Pharmacist from JAPAN on July 13, 2007. Female patient, 83 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis, gout

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, post procedural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with WARFARIN POTASSIUM, FUROSEMIDE, ALDACTONE, ALLOPURINOL, MEVARICH, PURSENNID, LENDORMIN, HERBESSER. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5427566-7
Arixtra side effect was reported by a Pharmacist from JAPAN on Aug 24, 2007. Female patient, 83 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis, mitral valve replacement, gout

, constipation

, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, post procedural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with WARFARIN POTASSIUM, FUROSEMIDE, ALDACTONE, ALLOPURINOL, MEVARICH, PURSENNID, LENDORMIN, DILTIAZEM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5778674-2
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on June 09, 2008. Male patient, 80 years of age, weighting 174.2 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gingival bleeding, gout

, haemoglobin decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AUGMENTIN, OFLOCET, ASPIRIN, HEMIGOXINE NATIVELLE, PERINDOPRIL ERBUMINE, ALDACTONE, LASIX, CORTICOIDS. Patient recovered.

Arixtra Side Effects Report #5471019-7
Arixtra side effect was reported by a Physician from JAPAN on Sept 21, 2007. Female patient, 79 years of age, weighting 77.16 lb, was diagnosed with thrombosis prophylaxis, pain

, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: decreased appetite, gastric ulcer, haemoglobin decreased, melaena, post procedural haemorrhage, upper gastrointestinal haemorrhage. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with RINGEREAZE, PURSENNID, LENDORMIN, DIOVAN, ULGUT, MAXIPIME, ADONA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5805991-X
Arixtra side effect was reported by a Physician from JAPAN on July 07, 2008. Male patient, 79 years of age, weighting 110.2 lb, was diagnosed with thrombosis prophylaxis, cerebral infarction and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, oedema peripheral, post procedural haemorrhage. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with ASPIRIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6135505-9
Arixtra side effect was reported by a Physician from JAPAN on Mar 19, 2009. Female patient, 79 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, post procedural haematoma, red blood cell count decreased, white blood cell count increased. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with ASPIRIN, IFENPRODIL, TARTRATE, PRAVASTATIN, SPIRONOLACTONE, FAMOTIDINE, IMIPRAMINE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5737733-0
Arixtra side effect was reported by a Physician from JAPAN on May 12, 2008. Male patient, 77 years of age, weighting 125.7 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: eosinophil count decreased, haematocrit decreased, haemoglobin decreased, interstitial lung disease, lymphocyte count decreased, neutrophil count increased, pulmonary alveolar haemorrhage, red blood cell count decreased, white blood cell count increased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with SULPERAZON, LOXONIN, MUCOSTA, CEFAMEZIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5759783-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on May 29, 2008. Female patient, 77 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, hernial eventration, subcutaneous haematoma, subileus, thrombosis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN, SEROPLEX, PROPYL, NEXIUM, ALPRAZOLAM, TRIFLUCAN, ALDALIX, COZAAR. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5775208-3
Arixtra side effect was reported by a Physician from JAPAN on June 12, 2008. Male patient, 77 years of age, weighting 125.7 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: eosinophil count decreased, haematocrit decreased, haemoglobin decreased, interstitial lung disease, lymphocyte count decreased, neutrophil count increased, pulmonary alveolar haemorrhage, red blood cell count decreased, respiratory disorder. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with SULPERAZON, LOXONIN, MUCOSTA, CEFAMEZIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6037276-3
Arixtra side effect was reported by a Physician from JAPAN on Jan 13, 2009. Female patient, 76 years of age, was diagnosed with thrombosis prophylaxis, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage subcutaneous, oedema peripheral, pain in extremity, platelet count decreased, platelet count increased, red blood cell count decreased. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with PANSPORIN, LOXONIN, MUCOSTA, DASEN, BENET. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6013744-5
Arixtra side effect was reported by a Physician from JAPAN on Dec 15, 2008. Female patient, 75 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, angina pectoris, gastric haemorrhage, haemoglobin decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN. Patient recovered.

Arixtra Side Effects Report #5478383-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 03, 2007. Male patient, 74 years of age, weighting 191.8 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: activated partial thromboplastin time prolonged, haematoma, haemoglobin decreased, induration, penis disorder

, prothrombin time ratio abnormal, testicular disorder

. Arixtra dosage: unknown. During the same period patient was treated with MUCOMYST, CORDARONE, TANAKAN, TRIVASTAL, PNEUMOREL, PREDNISOLONE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5502939-2
Arixtra side effect was reported by a Physician from JAPAN on Oct 23, 2007. Male patient, 74 years of age, weighting 156.5 lb, was diagnosed with thrombosis prophylaxis, cerebral infarction, infection

, hypertension, pain

, gastric ulcer, constipation

, hypertension, pain

, gastric ulcer, constipation

, hypertension, pain

, gastric ulcer, constipation

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, feeling hot, gastric ulcer haemorrhage, haematemesis, haemoglobin decreased, haemorrhage subcutaneous, post procedural haematoma, pyrexia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PLETAL, PENTCILLIN, TIENAM, MINOMYCIN, AMLODIN, LOXONIN, GASTER, PANTOSIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5707043-6
Arixtra side effect was reported by a Pharmacist from JAPAN on Apr 11, 2008. Female patient, 74 years of age, was diagnosed with thrombosis prophylaxis, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, bleeding time prolonged, cerebral haemorrhage, cerebrovascular accident, haemoglobin decreased, haemorrhagic diathesis, hemiplegia, heparin-induced thrombocytopenia, platelet count decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with FRAGMIN, HEPARIN, PANSPORIN, FLOMOX, URSO, RANITAC, MICARDIS, HYPEN. Patient died on 03/02/2008.

Arixtra Side Effects Report #5401373-3
Arixtra side effect was reported by a Physician from JAPAN on July 31, 2007. Female patient, 73 years of age, weighting 121.3 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, haemoglobin decreased, haemorrhage, shock haemorrhagic, urine output decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAZOLIN, SOLDEM, GLUCOSE, HUMULIN, SULBACTAM, SEISHOKU. Patient recovered.

Arixtra Side Effects Report #5931541-3
Arixtra side effect was reported by a Physician from JAPAN on Oct 21, 2008. Female patient, 73 years of age, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, haematochezia, haemoglobin decreased, red blood cell count decreased, upper gastrointestinal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with OSTELUC, VOLTAREN, ROPION, NITRODERM. Patient recovered.

Arixtra Side Effects Report #5946506-5
Arixtra side effect was reported by a Physician from JAPAN on Oct 31, 2008. Female patient, 73 years of age, weighting 143.3 lb, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, haematochezia, haemoglobin decreased, red blood cell count decreased, upper gastrointestinal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with OSTELUC, VOLTAREN, ROPION, NITRODERM. Patient recovered.

Arixtra Side Effects Report #5917425-5
Arixtra side effect was reported by a Physician from JAPAN on Oct 09, 2008. Female patient, 72 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematochezia, haemoglobin decreased, haemorrhage. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5819178-8
Arixtra side effect was reported by a Physician from JAPAN on July 17, 2008. Female patient, 71 years of age, weighting 158.7 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer, haemoglobin decreased, upper gastrointestinal haemorrhage. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5840101-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Aug 04, 2008. Male patient, 69 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: atrioventricular block, haematuria, haemoglobin decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPERIUM, LOXEN, FUROSEMIDE, ATACAND, DIFFU K, INIPOMP, EFFEXOR, DANTRIUM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5557616-9
Arixtra side effect was reported by a Physician from FRANCE on Dec 05, 2007. Female patient, 67 years of age, weighting 110.2 lb, was diagnosed with thrombosis prophylaxis, rheumatoid arthritis

, cardiac failure and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dyspnoea, haematoma, haemoglobin decreased, hyperkalaemia, muscle haemorrhage, postoperative renal failure, renal failure acute, shock haemorrhagic. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOVENOX, NIVAQUINE, CONTRAMAL, INDOCIN, COVERSYL, LASIX, SINGULAIR. Patient was hospitalized. Patient died on 10/15/2007.

Arixtra Side Effects Report #5499406-1
Arixtra side effect was reported by a Physician from JAPAN on Oct 22, 2007. Male patient, 65 years of age, weighting 112.4 lb, was diagnosed with thrombosis prophylaxis, osteonecrosis

, gastritis, anxiety

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, arthralgia, haemoglobin decreased, induration, platelet count decreased, post procedural haematoma, wound complication. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ALLOPURINOL, FERROMIA, LOXONIN, SELBEX, DEPAS, FLUMARIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5483788-0
Arixtra side effect was reported by a Physician from JAPAN on Oct 10, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Arixtra Side Effects Report #5499395-X
Arixtra side effect was reported by a Physician from JAPAN on Oct 23, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Arixtra Side Effects Report #5506527-3
Arixtra side effect was reported by a Physician from JAPAN on Oct 30, 2007. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, ZOLPIDEM, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Arixtra Side Effects Report #5913889-1
Arixtra side effect was reported by a Physician from JAPAN on Oct 06, 2008. Female patient, 64 years of age, weighting 160.9 lb, was diagnosed with thrombosis prophylaxis, osteoporosis

, pain

, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, haematocrit decreased, haemoglobin decreased, platelet count increased, red blood cell count decreased, white blood cell count increased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with MUCOSTA, GANATON, FLOMOX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5956509-2
Arixtra side effect was reported by a Physician from JAPAN on Nov 14, 2008. Female patient, 64 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: fibrin d dimer increased, haematocrit decreased, haemoglobin decreased, platelet count increased, post procedural haemorrhage, protein total decreased, red blood cell count decreased, vision blurred, vitreous haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, FERROMIA, MYSLEE, LENDORMIN, ADONA, HYALEIN. Patient recovered.

Arixtra Side Effects Report #5757085-X
Arixtra side effect was reported by a Physician from JAPAN on May 29, 2008. Male patient, 63 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, gastritis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, gamma-glutamyltransferase increased, haemoglobin decreased, hepatic function abnormal. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPEN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5771873-5
Arixtra side effect was reported by a Physician from JAPAN on June 03, 2008. Male patient, 63 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, gastritis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, gamma-glutamyltransferase increased, haemoglobin decreased, hepatic function abnormal. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPEN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5793357-0
Arixtra side effect was reported by a Physician from JAPAN on June 26, 2008. Male patient, 63 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, gastritis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, gamma-glutamyltransferase increased, haemoglobin decreased, hepatic function abnormal. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPEN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5813658-7
Arixtra side effect was reported by a Physician from JAPAN on July 11, 2008. Female patient, 63 years of age, weighting 176.4 lb, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis, haematocrit decreased, haemoglobin decreased, platelet count increased, red blood cell count decreased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, NORVASC, OLMETEC, THYRADIN, URSO, DASEN, SELBEX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5830222-4
Arixtra side effect was reported by a Physician from JAPAN on July 28, 2008. Female patient, 63 years of age, weighting 176.4 lb, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis, haematocrit decreased, haemoglobin decreased, platelet count increased, red blood cell count decreased, small intestinal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, NORVASC, OLMESARTAN MEDOXOMIL, THYRADIN, URSO, DASEN, SELBEX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6004046-1
Arixtra side effect was reported by a Physician from JAPAN on Dec 15, 2008. Male patient, 63 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, femoral neck fracture, gastritis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: alanine aminotransferase increased, anaemia, aspartate aminotransferase increased, gamma-glutamyltransferase increased, haemoglobin decreased, hepatic function abnormal. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPEN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5661256-0
Arixtra side effect was reported by a Physician from JAPAN on Mar 07, 2008. Male patient, 59 years of age, weighting 130.1 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage subcutaneous, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage subcutaneous, pain

, platelet count increased, red blood cell count decreased, white blood cell count increased. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with RHEUMATREX, AZULFIDINE EN, PROGRAF, PREDONINE, HEPARIN. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #6121158-2
Arixtra side effect was reported by a Physician from JAPAN on Mar 13, 2009. Male patient, 59 years of age, was diagnosed with thrombosis prophylaxis, procedural pain, swelling, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, joint swelling, post procedural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with HYPEN, DASEN, RINLAXER, MARZULENE, PANSPORIN, FLUMARIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5400393-2
Arixtra side effect was reported by a Physician from JAPAN on July 20, 2007. Female patient, 58 years of age, weighting 92.59 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, diabetes mellitus and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia postoperative, diabetic nephropathy, haemoglobin decreased, muscle haemorrhage, post procedural swelling, renal impairment. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PANSPORIN, INSULIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5409733-1
Arixtra side effect was reported by a Physician from JAPAN on Aug 06, 2007. Female patient, 58 years of age, weighting 92.59 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, diabetes mellitus and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia postoperative, diabetic nephropathy, haemoglobin decreased, muscle haemorrhage, post procedural haemorrhage, post procedural swelling, renal impairment. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PANSPORIN, INSULIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5423674-5
Arixtra side effect was reported by a Physician from JAPAN on Aug 20, 2007. Female patient, 58 years of age, weighting 92.59 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, diabetes mellitus and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia postoperative, diabetic nephropathy, haemoglobin decreased, muscle haemorrhage, post procedural haemorrhage, post procedural swelling, renal impairment. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PANSPORIN, INSULIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5426201-1
Arixtra side effect was reported by a Physician from JAPAN on Aug 20, 2007. Male patient, 55 years of age, weighting 180.8 lb, was diagnosed with thrombosis prophylaxis, schizophrenia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, c-reactive protein increased, haemoglobin decreased, post procedural haemorrhage, postoperative wound complication, traumatic haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LITHIUM CARBONATE, VEGETAMIN A, NEULEPTIL, PROMETHAZINE, RISPERDAL, PENTCILLIN, FERROMIA, SULPERAZON. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5452900-1
Arixtra side effect was reported by a Physician from JAPAN on Sept 11, 2007. Male patient, 55 years of age, weighting 180.8 lb, was diagnosed with thrombosis prophylaxis, schizophrenia, infection

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, c-reactive protein increased, haemoglobin decreased, post procedural haemorrhage, postoperative wound complication, postoperative wound infection, traumatic haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LITHIUM CARBONATE, VEGETAMIN A, NEULEPTIL, PROMETHAZINE, RISPERDAL, PENTCILLIN, FERROMIA, SULPERAZON. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5564958-X
Arixtra side effect was reported by a Pharmacist from JAPAN on Dec 14, 2007. Female patient, 54 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, shock haemorrhagic. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEPHALOSPORIN. Patient recovered.

Arixtra Side Effects Report #5579199-X
Arixtra side effect was reported by a Pharmacist from JAPAN on Dec 21, 2007. Female patient, 54 years of age, weighting 119.0 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, pain

, gastritis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, haemoglobin decreased, nausea

, shock haemorrhagic, swelling, tachycardia, wound complication. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEPHALOSPORIN, LOXONIN. Patient recovered.

Arixtra Side Effects Report #5589707-0
Arixtra side effect was reported by a Pharmacist from JAPAN on Jan 11, 2008. Female patient, 54 years of age, weighting 119.0 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, pain

, gastritis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, haemoglobin decreased, nausea

, post procedural haemorrhage, shock haemorrhagic, tachycardia, wound complication. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEPHALOSPORIN, LOXONIN. Patient recovered.

Arixtra Side Effects Report #5684353-2
Arixtra side effect was reported by a Physician from JAPAN on Mar 25, 2008. Male patient, 51 years of age, weighting 141.1 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, bone pain, conjunctival discolouration, haemoglobin decreased, malaise, pain in extremity, pallor, post procedural haematoma, post procedural haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFMETAZON, HEPARIN LOCK, LACTEC, MORPHINE ELIXIR, ALPRAZOLAM, MAGLAX, GLYSENNID. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #4970371-6
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Mar 06, 2006. Male patient, 50 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: catheter site discharge, haematocrit decreased, haemoglobin decreased, incisional drainage, unevaluable event. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LIPITOR, SINGULAIR, NASONEX, PERCOCET, REGLAN, IBUPROFEN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5490728-7
Arixtra side effect was reported by a Physician from JAPAN on Oct 12, 2007. Female patient, 42 years of age, weighting 123.5 lb, was diagnosed with thrombosis prophylaxis, application site pain and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastrointestinal haemorrhage, gastrointestinal ulcer, haemoglobin decreased, post procedural haematoma, subcutaneous haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LORCAM, LIVALO, OLMETEC, THEOPHYLLINE, ZYLORIC, LORAZEPAM, DIGOXIN SEMI, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5499397-3
Arixtra side effect was reported by a Physician from JAPAN on Oct 24, 2007. Female patient, 42 years of age, weighting 123.5 lb, was diagnosed with thrombosis prophylaxis, application site pain and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastrointestinal haemorrhage, gastrointestinal ulcer, haemoglobin decreased, post procedural haematoma, subcutaneous haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LORCAM, LIVALO, OLMETEC, THEOPHYLLINE, ZYLORIC, LORAZEPAM, DIGOXIN SEMI, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5939104-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 23, 2008. Male patient, 60 years of age, was diagnosed with thrombophlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: aspartate aminotransferase increased, asterixis, blood bilirubin increased, chromaturia, feeling hot, gamma-glutamyltransferase increased, haematoma, haemoglobin decreased, hepatosplenomegaly. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5305830-X
Arixtra side effect was reported by a Pharmacist from UNITED STATES on Apr 20, 2007. Male patient, 55 years of age, was diagnosed with surgery

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric haemorrhage, haemoglobin decreased, refusal of treatment by patient. Arixtra dosage: 2.5MG EVERY DAY SQ. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5316775-3
Arixtra side effect was reported by a Pharmacist from UNITED STATES on May 01, 2007. Male patient, 55 years of age, was diagnosed with surgery

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure systolic decreased, convulsion, fall

, gastric haemorrhage, haematochezia, haemoglobin decreased, hip fracture, pallor. Arixtra dosage: 2.5MG EVERY DAY SQ. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5366259-1
Arixtra side effect was reported by a Pharmacist from UNITED STATES on June 19, 2007. Male patient, 55 years of age, was diagnosed with surgery

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure systolic decreased, convulsion, fall

, gastric haemorrhage, haematochezia, haemoglobin decreased, hip fracture, pallor, refusal of treatment by patient. Arixtra dosage: 2.5MG EVERY DAY SQ. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5597605-1
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Jan 10, 2008. Male patient, 86 years of age, was diagnosed with pulmonary embolism

, asthma

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: circulatory collapse, haemoglobin decreased, muscle haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with SERETIDE, TEGRETOL, SPIRIVA, ASPEGIC, TRIATEC, TAREG, ELISOR, LYRICA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5623138-X
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Feb 04, 2008. Male patient, 73 years of age, was diagnosed with pulmonary embolism

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer, gastrointestinal haemorrhage, haematocrit decreased, haemoglobin decreased, melaena, platelet count decreased. Arixtra dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5237150-6
Arixtra side effect 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 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.

Arixtra Side Effects Report #5946514-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 28, 2008. Female patient, 64 years of age, was diagnosed with pulmonary embolism

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain upper, duodenitis, haematemesis, haemoglobin decreased, ill-defined disorder, melaena, pallor, ulcer

. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5767379-X
Arixtra side effect was reported by a Pharmacist from FRANCE on June 02, 2008. Male patient, 36 years of age, was diagnosed with pulmonary embolism

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, muscle haemorrhage, muscular weakness, pain in extremity, thrombosis. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN, METHADONE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6124635-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 11, 2009. Female patient, 76 years of age, was diagnosed with prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain

, constipation

, haematoma, haemoglobin decreased, hyperlactacidaemia, hypotension, nausea

, retroperitoneal haematoma, shock haemorrhagic. Arixtra dosage: unknown. During the same period patient was treated with SKENAN, BISOPROLOL, CORTANCYL, LEVOTHYROXINE, FORTZAAR, PYOSTACINE, DOLIPRANE. Patient recovered.

Arixtra Side Effects Report #5537418-X
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Nov 28, 2007. Male patient, 71 years of age, was diagnosed with prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: deep vein thrombosis

, haemoglobin decreased, overdose, peritoneal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with LASIX, CALCIPARINE. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6015901-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Dec 12, 2008. Female patient, 70 years of age, was diagnosed with prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: c-reactive protein increased, cytomegalovirus test positive, haemoglobin decreased, neutrophil count increased, platelet count increased, rash maculo-papular, skin disorder, skin exfoliation, white blood cell count increased. Arixtra dosage: unknown. During the same period patient was treated with TARGOCID, CEFTRIAXONE, FUMAFER, RIFADIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6107818-8
Arixtra side effect was reported by a Physician from ITALY on Mar 04, 2009. Male patient, 55 years of age, was diagnosed with prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, melaena. Arixtra dosage: 2.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #6122862-2
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 12, 2009. Female patient, 51 years of age, was diagnosed with prophylaxis, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: diarrhoea, gastric ulcer haemorrhage, haemoglobin decreased, melaena, pyrexia, rash

, rash maculo-papular, rash pustular. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with CLAMOXYL, AUGMENTIN, PENICILLIN G, GENTALLINE, MOPRAL, DALACINE, TOPALGIC, ACUPAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #4867786-3
Arixtra side effect was reported by a Pharmacist from UNITED STATES on Dec 27, 2005. Female patient, weighting 130.1 lb, was diagnosed with prophylaxis, pulmonary embolism

, thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematocrit decreased, haemoglobin decreased, haemoptysis, lung neoplasm, post procedural haemorrhage, procedural complication. Arixtra dosage: 2.5 MG Q DAY SUBCUT. During the same period patient was treated with WARFARIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5214380-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Jan 12, 2007. Male patient, 78 years of age, was diagnosed with phlebitis superficial, essential hypertension, prophylaxis, arteritis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: angina pectoris, haemoglobin decreased, rectal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with APROVEL, LERCAN, PLAVIX, FONZYLANE, INSULATARD NPH, MYOLASTAN, ZAMUDOL. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5240495-7
Arixtra side effect 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 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.

Arixtra Side Effects Report #5363610-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on June 12, 2007. Female patient, 87 years of age, was diagnosed with phlebitis, essential hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal haematoma, aphasia

, haemoglobin decreased, hemiplegia, intra-abdominal haemorrhage, myocardial ischaemia, renal failure acute. Arixtra dosage: unknown. During the same period patient was treated with LASIX, VASTAREL, ATHYMIL, LEXOMIL, DESLORATADINE. Patient recovered.

Arixtra Side Effects Report #5593306-4
Arixtra side effect was reported by a Physician from FRANCE on Jan 09, 2008. Female patient, 87 years of age, weighting 154.3 lb, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, skin disorder, skin necrosis, subcutaneous haematoma. Arixtra dosage: unknown. During the same period patient was treated with LOVENOX, EFFEXOR, NITRODERM, FUROSEMIDE, LEVOTHYROX, KARDEGIC, FORLAX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5530655-X
Arixtra side effect was reported by a Physician from FRANCE on Nov 21, 2007. Female patient, 86 years of age, weighting 154.3 lb, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, skin necrosis, subcutaneous haematoma. Arixtra dosage: unknown. During the same period patient was treated with LOVENOX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5879406-X
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Sept 10, 2008. Female patient, 83 years of age, weighting 189.6 lb, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, injection site haematoma, platelet count decreased, red blood cell count decreased, shock haemorrhagic. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ALLOPURINOL, ASPIRIN, GLUCOPHAGE, GLIBENESE, CRESTOR. Patient recovered.

Arixtra Side Effects Report #5908729-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Sept 25, 2008. Female patient, 83 years of age, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, intra-abdominal haematoma, leukocytosis. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ZYLORIC, PROTHIADEN, LEXOMIL, STILNOX, TARDYFERON, FORLAX, NEXIUM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5953623-2
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 15, 2008. Female patient, 83 years of age, weighting 132.3 lb, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, intra-abdominal haematoma, leukocytosis. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ZYLORIC, PROTHIADEN, LEXOMIL, ZOLPIDEM, TARDYFERON, FORLAX, NEXIUM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5245309-7
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE 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 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 Side Effects Report #5642997-8
Arixtra side effect was reported by a Physician from JAPAN on Feb 25, 2008. Female patient, 84 years of age, weighting 110.2 lb, was diagnosed with osteosynthesis, diabetes mellitus, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, haemoglobin decreased, melaena. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with ASPIRIN, ITOROL, CELECOXIB, ACTOS, BLOPRESS. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #4988542-1
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 28, 2006. Female patient, 77 years of age, weighting 137.3 lb, was diagnosed with heparin-induced thrombocytopenia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage, renal failure. Arixtra dosage: 5MG PER DAY. During the same period patient was treated with COUMADIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5759766-0
Arixtra side effect was reported by a Physician from FRANCE on May 29, 2008. Female patient, 85 years of age, weighting 121.3 lb, was diagnosed with deep vein thrombosis

, venous thrombosis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: fistula

, haematoma, haemoglobin decreased, skin necrosis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PREVISCAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5653433-X
Arixtra side effect was reported by a Physician from JAPAN on Mar 03, 2008. Female patient, 84 years of age, weighting 110.2 lb, was diagnosed with deep vein thrombosis

, angina pectoris, pain

, hypertension, diabetes mellitus and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bleeding time prolonged, blood pressure decreased, blood urea increased, gastrointestinal haemorrhage, haemoglobin decreased, melaena, protein total decreased, red blood cell count decreased. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with ASPIRIN, CELECOXIB, ITOROL, ACTOS, BLOPRESS, NOVOLIN R. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5672975-4
Arixtra side effect was reported by a Physician from JAPAN on Mar 14, 2008. Female patient, 84 years of age, weighting 110.2 lb, was diagnosed with deep vein thrombosis

, angina pectoris, pain

, hypertension, diabetes mellitus and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bleeding time prolonged, blood pressure decreased, blood urea increased, gastrointestinal haemorrhage, haemoglobin decreased, melaena, protein total decreased, red blood cell count decreased. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with ASPIRIN, CELECOXIB, ITOROL, ACTOS, BLOPRESS, NOVOLIN R. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5753905-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on May 21, 2008. Male patient, 80 years of age, was diagnosed with deep vein thrombosis

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain

, anuria, haemoglobin decreased, renal failure, retroperitoneal haematoma, shock haemorrhagic. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with TAHOR, EXFORGE, ASPIRIN, PANTOPRAZOLE, FLUDEX, ART, FORADIL, AIROMIR. Patient died on 04/15/2008.

Arixtra Side Effects Report #5213344-0
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on June 05, 2006. Female patient, 46 years of age, was diagnosed with deep vein thrombosis

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, platelet count decreased. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with FLUOROURACIL, OXALIPLATIN, IRINOTECAN, AVASTIN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5213372-5
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 14, 2006. Female patient was diagnosed with deep vein thrombosis

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, haemorrhage. Arixtra dosage: 2.5MG AS REQUIRED. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5780363-5
Arixtra side effect was reported by a Physician from FRANCE on June 12, 2008. Female patient, 90 years of age, was diagnosed with ankle fracture and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemoglobin decreased, incorrect dose administered, retroperitoneal haematoma. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.

Arixtra and haemoglobin decreased

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Arixtra and haemoglobin decreased Patient Reports February 10, 2012

side effects of Arixtra