Arixtra and vomiting Patient Reports February 11, 2012

Arixtra Side Effects Report #5661717-4
Arixtra side effect was reported by a Physician from JAPAN on Mar 07, 2008. Female patient, 88 years of age, weighting 68.34 lb, was diagnosed with thrombosis prophylaxis, cystitis, pain , procedural hypertension, infection prophylaxis, gastritis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: asphyxia, aspiration, haematemesis, oral intake reduced, respiratory arrest, stress , upper gastrointestinal haemorrhage, vomiting. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with CRAVIT, FAMOTIDINE, FENTANYL, PERDIPINE, HALOSPOR, MEIACT, SELBEX. Patient died on 02/05/2008.

Arixtra Side Effects Report #5961570-5
Arixtra side effect was reported by a Physician from JAPAN on Nov 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: abdominal pain , defaecation urgency, haematemesis, shock haemorrhagic, upper gastrointestinal haemorrhage, ventricular fibrillation, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with DEPAS, MAGNESIUM OXIDE, MARZULENE S, HERBESSER, ALMARL, ITOROL, GRAMALIL. Patient died on 09/29/2008.

Arixtra Side Effects Report #5989022-7
Arixtra side effect was reported by a Physician from JAPAN on Dec 08, 2008. Female patient, 88 years of age, weighting 72.75 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain , defaecation urgency, haematemesis, shock haemorrhagic, upper gastrointestinal haemorrhage, ventricular fibrillation, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with DEPAS, MAGNESIUM OXIDE, MARZULENE S, HERBESSER, ALMARL, ITOROL, GRAMALIL. Patient died on 09/29/2008.

Arixtra Side Effects Report #5684352-0
Arixtra side effect was reported by a Physician from JAPAN on Mar 27, 2008. Female patient, 79 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, hypertension, osteoarthritis  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dizziness , gastrointestinal ulcer, meniere's disease , nausea . Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with DIOVAN, BONALON, LORCAM. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5708154-1
Arixtra side effect was reported by a Physician from JAPAN on Apr 11, 2008. Female patient, 79 years of age, weighting 134.5 lb, was diagnosed with thrombosis prophylaxis, hypertension, osteoarthritis  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dizziness , gastrointestinal ulcer, meniere's disease , nausea . Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with DIOVAN, BONALON, LORCAM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5456551-4
Arixtra side effect was reported by a Pharmacist from JAPAN on Sept 13, 2007. Male patient, 77 years of age, weighting 163.4 lb, was diagnosed with thrombosis prophylaxis, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain , hepatic function abnormal, jaundice , vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, DIOVAN, POTACOL, SOLITA, FENTANYL, ULTIVA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5532049-X
Arixtra side effect was reported by a Pharmacist from JAPAN on Nov 30, 2007. Male patient, 77 years of age, weighting 163.4 lb, was diagnosed with thrombosis prophylaxis, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain , hepatic function abnormal, jaundice , vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, DIOVAN, POTACOL, SOLITA, FENTANYL, ULTIVA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5551109-0
Arixtra side effect was reported by a Pharmacist from JAPAN on Dec 07, 2007. Male patient, 77 years of age, weighting 163.4 lb, was diagnosed with thrombosis prophylaxis, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain , hepatic function abnormal, jaundice , vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, DIOVAN, POTACOL, SOLITA, FENTANYL, ULTIVA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5520861-2
Arixtra side effect was reported by a Physician from JAPAN on Nov 13, 2007. Female patient, 74 years of age, weighting 101.4 lb, was diagnosed with thrombosis prophylaxis, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: cerebellar haemorrhage, cheyne-stokes respiration, headache , neck pain, respiratory arrest, vision blurred, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with FLUMARIN, LOXONIN, SELBEX, SOLULACT, VOLTAREN, AMLODIN, SENNOSIDE. Patient died on 10/27/2007.


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 #5818505-5
Arixtra side effect was reported by a Physician from UNITED STATES on July 08, 2008. Female patient, 48 years of age, weighting 238.0 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: addison's disease , adrenal haemorrhage, deep vein thrombosis , diarrhoea, heparin-induced thrombocytopenia, impaired work ability, myalgia, vomiting. Arixtra dosage: 2.5 MG/ PER DAY/ SUBCUTANEOUS. During the same period patient was treated with VICODIN, SUMATRIPTAN SUCCINATE, POTASSIUM CITRATE, MAGNESIUM SALT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5711378-0
Arixtra side effect was reported by a Consumer or non-health professional from GERMANY on Apr 15, 2008. Female patient was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: angina pectoris, myalgia, nausea . Arixtra dosage: 2.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #5504205-8
Arixtra side effect was reported by a Physician from FRANCE on Oct 31, 2007. Female 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: altered state of consciousness, arthralgia, brain herniation, cerebral haematoma, joint swelling, mydriasis, vomiting. Arixtra dosage: 7.5MG PER DAY. Patient was hospitalized. Patient died on 10/23/2007.


Arixtra Side Effects Report #5664481-8
Arixtra side effect was reported by a Physician from FRANCE on Mar 07, 2008. Female patient, 73 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, arthralgia, brain herniation, cerebral haematoma, cerebral haemorrhage, joint swelling, mydriasis, vomiting. Arixtra dosage: 7.5MG PER DAY. Patient was hospitalized. Patient died on 10/23/2007.

Arixtra Side Effects Report #5700913-4
Arixtra side effect was reported by a Physician from FRANCE on Mar 31, 2008. Female patient, 73 years of age, weighting 172.0 lb, was diagnosed with pulmonary embolism  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: altered state of consciousness, arthralgia, brain herniation, cerebral haematoma, cerebral haemorrhage, joint swelling, mydriasis, vomiting. Arixtra dosage: 7.5MG PER DAY. Patient was hospitalized. Patient died on 10/23/2007.

Arixtra Side Effects Report #6064657-4
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Apr 11, 2008. Male patient, 48 years of age, was diagnosed with pulmonary embolism  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: nausea , pyrexia. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with PREDNISONE, PROTONIX. Patient recovered.

Arixtra Side Effects Report #5508783-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Oct 29, 2007. Female patient, 86 years of age, was diagnosed with phlebitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: cerebral haemorrhage, fall , headache , nausea , subdural haematoma, tinnitus . Arixtra dosage: unknown. During the same period patient was treated with GABACET, SERMION, VASTAREL, DEBRIDAT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5286626-4
Arixtra side effect 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 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.


Arixtra Side Effects Report #5901727-2
Arixtra side effect was reported by a Physician from SPAIN on Sept 26, 2008. Male patient, 69 years of age, was diagnosed with knee operation and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastrointestinal haemorrhage, haematemesis, haemodynamic instability, hypovolaemic shock, vomiting. Arixtra dosage: 2.5MG SINGLE DOSE. During the same period patient was treated with ANTIBIOTIC. Patient died on 08/02/2008.

Arixtra Side Effects Report #5733291-5
Arixtra side effect was reported by a Consumer or non-health professional from ITALY on May 06, 2008. Female patient, 76 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dehydration, haematoma, heparin-induced thrombocytopenia, renal failure, subdural haematoma, vomiting. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ANTICOAGULANT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5771863-2
Arixtra side effect was reported by a Consumer or non-health professional from ITALY on June 06, 2008. Female patient, 76 years of age, was diagnosed with heparin-induced thrombocytopenia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dehydration, haematoma, heparin-induced thrombocytopenia, renal failure, subdural haematoma, vomiting. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ANTICOAGULANT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5527802-2
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Nov 20, 2007. Female patient was diagnosed with factor v leiden mutation and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dyspnoea, haemorrhage, nausea . Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with VICODIN, ANTIBIOTIC. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5489546-5
Arixtra side effect was reported by a Physician from UNITED STATES on Oct 16, 2007. Female patient, 72 years of age, weighting 143.3 lb, was diagnosed with deep vein thrombosis  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: dehydration, vomiting. Arixtra dosage: 5MG DAILY SQ. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #6064724-5
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Sept 09, 2008. Female patient, 67 years of age, was diagnosed with deep vein thrombosis  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure increased, dyspnoea, paraesthesia, vomiting, weight decreased. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with BENADRYL. Patient recovered.

Arixtra Side Effects Report #5833891-8
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on July 31, 2008. Female patient, 35 years of age, was diagnosed with deep vein thrombosis  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: coagulation time shortened, headache , heart rate irregular, no therapeutic response, vomiting. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5211996-2
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Jan 08, 2007. Female patient, 81 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: breath sounds abnormal, cerebral haemorrhage, coma, excoriation, fall , haemorrhagic stroke, hydrocephalus , vomiting. Arixtra dosage: unknown. During the same period patient was treated with CORDARONE, DISCOTRINE, OROCAL D, FORLAX, TANAKAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5357378-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on June 08, 2007. Female patient, 76 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: epistaxis, haemoptysis, nausea . Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with AUGMENTIN, GENTAMICIN, VANCOMYCIN, ZYVOX, OMEPRAZOLE, NEXIUM, TRIATEC, PREVISCAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5227165-6
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES 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 side effects: chest pain , diarrhoea, dysarthria, kidney infection, vision blurred, vomiting. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5594791-4
Arixtra side effect was reported by a Physician from FRANCE on Jan 15, 2008. Male patient, child 4 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: anorexia, fatigue, gamma-glutamyltransferase increased, hepatitis , hepatocellular injury, transaminases increased, vomiting. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5520864-8
Arixtra side effect was reported by a Pharmacist from JAPAN on Nov 16, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain upper, fall , hepatic haemorrhage, shock, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.

Arixtra Side Effects Report #5527311-0
Arixtra side effect was reported by a Pharmacist from JAPAN on Nov 22, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain upper, fall , hepatic haemorrhage, shock, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.

Arixtra Side Effects Report #5564945-1
Arixtra side effect was reported by a Pharmacist from JAPAN on Dec 14, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain upper, fall , hepatic haemorrhage, pyrexia, shock, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.

Arixtra Side Effects Report #5571757-1
Arixtra side effect was reported by a Pharmacist from JAPAN on Dec 18, 2007. Male patient, 38 years of age, weighting 114.6 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain upper, fall , hepatic haemorrhage, pyrexia, shock, vomiting. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, KENTAN, MUCOSTA, DASEN. Patient recovered.


Arixtra Side Effects Report #5615129-X
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on June 19, 2007. Female patient, 31 years of age, weighting 240.5 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: epistaxis, headache , nausea , pyrexia. Arixtra dosage: 10MG PER DAY. During the same period patient was treated with PROAMATINE, FERROUS SULPHATE, VERAPAMIL, LEVOTHYROXINE, CALCIUM GLUCONATE, DIGOXIN, ALLOPURINOL. Patient recovered.