Arixtra and haematemesis Patient Reports February 09, 2010

Arixtra Side Effects Report #5789040-8
Arixtra side effect was reported by a Physician from JAPAN on June 24, 2008. Female patient, 97 years of age, weighting 88.18 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric haemorrhage, gastric ulcer, haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with FERROMIA, DIOVAN, EVISTA, HYPEN, AMLODIPINE, SELECTOL, ALOSENN, MUCOSTA. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6045550-X
Arixtra side effect was reported by a Physician from JAPAN on Jan 20, 2009. Female patient, 91 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6074106-8
Arixtra side effect was reported by a Physician from JAPAN on Feb 06, 2009. Female patient, 91 years of age, was diagnosed with thrombosis prophylaxis, analgesia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, gastric cancer, gastric ulcer, haematemesis. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with THREENOFEN, ADEFURONIC, ISALON. Patient recovered.

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 #5958093-6
Arixtra side effect was reported by a Physician from JAPAN on Nov 14, 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: haematemesis, shock haemorrhagic. Arixtra dosage: 1.5MG PER DAY. Patient died on 09/29/2008.

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 #5517127-3
Arixtra side effect was reported by a Pharmacist from JAPAN on Nov 08, 2007. Female patient, 87 years of age, weighting 99.21 lb, was diagnosed with thrombosis prophylaxis, constipation

, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with BAYASPIRIN, LOXONIN, SELBEX, MAGMITT, ARICEPT, ADALAT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5589691-X
Arixtra side effect was reported by a Pharmacist from JAPAN on Jan 11, 2008. Female patient, 87 years of age, weighting 99.21 lb, was diagnosed with thrombosis prophylaxis, gastritis, constipation

, hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ASPIRIN, LOXONIN, SELBEX, MAGMITT, ARICEPT, ADALAT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5806000-9
Arixtra side effect was reported by a Physician from JAPAN on July 07, 2008. Male 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: disseminated intravascular coagulation, gastrointestinal necrosis, haematemesis, hepatic failure, multi-organ failure, renal failure acute, shock, shock haemorrhagic, upper gastrointestinal haemorrhage. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with BLOPRESS, LANDEL, LENDORMIN, KARY UNI, BAYCARON. Patient died on 05/06/2008.

Arixtra Side Effects Report #5830229-7
Arixtra side effect was reported by a Physician from JAPAN on July 28, 2008. Male patient, 87 years of age, weighting 110.2 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: disseminated intravascular coagulation, gastrointestinal necrosis, haematemesis, haematochezia, hepatic failure, lower gastrointestinal haemorrhage, melaena, multi-organ failure, renal failure acute. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with CANDESARTAN CILEXETIL, LANDEL, LENDORMIN, KARY UNI, BAYCARON. Patient died on 05/06/2008.

Arixtra Side Effects Report #5506524-8
Arixtra side effect was reported by a Physician from JAPAN on Oct 30, 2007. Female patient, 84 years of age, weighting 92.59 lb, was diagnosed with thrombosis prophylaxis, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer haemorrhage, haematemesis. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, NORVASC, BLOPRESS, PRAVASTATIN, MAGLAX, PLETAL. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5514569-7
Arixtra side effect was reported by a Pharmacist from JAPAN on Nov 08, 2007. Male patient, 84 years of age, weighting 110.2 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with NORVASC, LOXONIN, MICARDIS, SELBEX, NEUROTROPIN, FLUMARIN, ALTAT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5579191-5
Arixtra side effect was reported by a Physician from JAPAN on Dec 21, 2007. Female patient, 84 years of age, weighting 94.80 lb, was diagnosed with thrombosis prophylaxis, pain

, preoperative care, hypertension, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, eating disorder

, gastric ulcer, gastric ulcer haemorrhage, haematemesis, melaena, metaplasia, restlessness, stomach discomfort. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with VOLTAREN, MOHRUS TAPE, GLYCERIN, MYSLEE, ADJUST A, AMLODIN, CEFAMEZIN, RHYTHMY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5594792-6
Arixtra side effect was reported by a Pharmacist from JAPAN on Jan 11, 2008. Male patient, 84 years of age, weighting 110.2 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with NORVASC, LOXONIN, MICARDIS, SELBEX, NEUROTROPIN, FLUMARIN, ALTAT. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5606517-6
Arixtra side effect was reported by a Physician from JAPAN on Jan 25, 2008. Female patient, 84 years of age, weighting 94.80 lb, was diagnosed with thrombosis prophylaxis, pain

, preoperative care, hypertension, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, eating disorder

, gastric haemorrhage, gastric ulcer, haematemesis, melaena, metaplasia, restlessness, stomach discomfort. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with VOLTAREN, MOHRUS TAPE, GLYCERIN, MYSLEE, ADJUST A, AMLODIPINE BESYLATE, CEFAMEZIN, RHYTHMY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5453875-1
Arixtra side effect was reported by a Physician from JAPAN on Sept 12, 2007. 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: abdominal discomfort, duodenal ulcer haemorrhage, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with MUCOSTA. Patient died on 09/06/2007.

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 #5525576-2
Arixtra side effect was reported by a Physician from JAPAN on Nov 22, 2007. Female patient, 63 years of age, weighting 176.4 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with NORVASC, OLMETEC, THYRADIN, URSO, LOXONIN, DASEN, SELBEX. 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 #5443430-1
Arixtra side effect was reported by a Health Professional from JAPAN on Aug 31, 2007. Male patient, 58 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AMLODIPINE, URSO. Patient recovered.

Arixtra Side Effects Report #5447510-6
Arixtra side effect was reported by a Health Professional from JAPAN on Sept 06, 2007. Male patient, 58 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: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AMLODIPINE, URSO. Patient recovered.

Arixtra Side Effects Report #5456552-6
Arixtra side effect was reported by a Health Professional from JAPAN on Sept 14, 2007. Male patient, 58 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: haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AMLODIPINE, URSO, CEFMETAZON. Patient recovered.

Arixtra Side Effects Report #5477198-X
Arixtra side effect was reported by a Health Professional from JAPAN on Oct 01, 2007. Male patient, 58 years of age, weighting 121.3 lb, was diagnosed with thrombosis prophylaxis, hypertension, chronic hepatitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, upper gastrointestinal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AMLODIPINE, URSO, CEFMETAZON. Patient recovered.

Arixtra Side Effects Report #5583049-5
Arixtra side effect was reported by a Health Professional from JAPAN on Dec 28, 2007. Male patient, 58 years of age, weighting 121.3 lb, was diagnosed with thrombosis prophylaxis, hypertension, chronic hepatitis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer, haematemesis, upper gastrointestinal haemorrhage. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with AMLODIN, URSO, CEFMETAZON. Patient recovered.

Arixtra Side Effects Report #5752432-7
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on May 19, 2008. Male patient, 75 years of age, was diagnosed with pulmonary embolism

, prostate cancer metastatic, epilepsy

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, duodenal ulcer haemorrhage, haematemesis, melaena, syncope, thrombosis. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with TEGRETOL, FELODIPINE. 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 #5702769-2
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Apr 04, 2008. Male patient, 72 years of age, was diagnosed with portal vein thrombosis, back pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: biliary tract disorder, feeling abnormal, gastrointestinal haemorrhage, haematemesis, melaena, varices oesophageal. Arixtra dosage: unknown. During the same period patient was treated with NAPROXEN, NOLVADEX, ELISOR, LASILIX, BISOPROLOL FUMARATE AND HYDROCHLOROTHIAZIDE, AVLOCARDYL, SPIRONOLACTONE, GLUCOPHAGE. Patient was hospitalized. Patient recovered.

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 #5382993-1
Arixtra side effect was reported by a Physician from JAPAN on July 06, 2007. Female patient, 84 years of age, was diagnosed with femur fracture and was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, NORVASC, BLOPRESS, MEVALOTIN, MAGLAX, PLETAL. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5390112-0
Arixtra side effect was reported by a Physician from JAPAN on July 13, 2007. Female patient, 84 years of age, weighting 92.59 lb, was diagnosed with femur fracture and was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, NORVASC, BLOPRESS, PRAVASTATIN, MAGLAX, PLETAL. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5411228-6
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Aug 08, 2007. Male patient, 61 years of age, was diagnosed with deep vein thrombosis

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, haematemesis, hyperhidrosis, oesophageal ulcer, pallor. Arixtra dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5532050-6
Arixtra side effect was reported by a Physician from FRANCE on Nov 27, 2007. Female patient, 61 years of age, weighting 132.3 lb, was diagnosed with acute coronary syndrome, hypothyroidism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, oesophageal haemorrhage, off label use. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, RISORDAN, LEVOTHYROX, LANSOPRAZOLE, MOTILIUM. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5653420-1
Arixtra side effect was reported by a Physician from FRANCE on Feb 25, 2008. Female patient, 61 years of age, weighting 132.3 lb, was diagnosed with acute coronary syndrome, hypothyroidism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, incorrect dose administered, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LEVOTHYROX, LANZOR, MOTILIUM, RISORDAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5664478-8
Arixtra side effect was reported by a Physician from FRANCE on Mar 07, 2008. Female patient, 61 years of age, weighting 132.3 lb, was diagnosed with acute coronary syndrome, hypothyroidism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: acute coronary syndrome, chest pain

, haematemesis, haemoglobin decreased, incorrect dose administered, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LEVOTHYROX, LANZOR, MOTILIUM, RISORDAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5670928-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 07, 2008. Female patient, 61 years of age, weighting 145.5 lb, was diagnosed with acute coronary syndrome, gastric ulcer, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, helicobacter gastritis, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LOVENOX, RISORDAN, NEXIUM, PERFALGAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5696072-7
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 26, 2008. Female patient, 61 years of age, weighting 145.5 lb, was diagnosed with acute coronary syndrome, gastric ulcer, pain

, hypothyroidism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, helicobacter gastritis, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LOVENOX, RISORDAN, NEXIUM, PERFALGAN, LEVOTHYROXINE, LANZOR. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5865191-4
Arixtra side effect was reported by a Physician from FRANCE on Aug 08, 2008. Female patient, 61 years of age, weighting 145.5 lb, was diagnosed with acute coronary syndrome, hypothyroidism, gastric ulcer, pain

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, helicobacter gastritis, incorrect dose administered, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LEVOTHYROX, LANZOR, MOTILIUM, LOVENOX, RISORDAN, NEXIUM, PERFALGAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5865193-8
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Aug 08, 2008. Female patient, 61 years of age, weighting 145.5 lb, was diagnosed with acute coronary syndrome, gastric ulcer, pain

, hypothyroidism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, haemoglobin decreased, helicobacter gastritis, oesophageal haemorrhage. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with ASPEGIC, LOVENOX, RISORDAN, NEXIUM, PERFALGAN, LEVOTHYROX, LANZOR. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5939107-6
Arixtra side effect was reported by a Physician from FRANCE on Oct 22, 2008. Female patient, 83 years of age, weighting 121.3 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain lower, fall

, haematemesis, immobile, malaise, muscle haemorrhage, renal failure, rhabdomyolysis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with KARDEGIC. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5849534-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Aug 14, 2008. Female patient, 81 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, gastric ulcer haemorrhage, haematemesis, hypotension, melaena. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ATENOLOL, PYOSTACINE, AMLOR, LASILIX RETARD, DAFALGAN. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5488358-6
Arixtra side effect was reported by a Physician from JAPAN on Oct 15, 2007. Male patient, 78 years of age, weighting 121.3 lb, was diagnosed with dementia

, constipation

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric ulcer haemorrhage, haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with SERMION, MAGMITT, RISPERDAL, ARICEPT, THROMBIN LOCAL SOLUTION. Patient recovered.

Arixtra Side Effects Report #5511506-6
Arixtra side effect was reported by a Physician from JAPAN on Nov 05, 2007. Male patient, 78 years of age, weighting 121.3 lb, was diagnosed with dementia

, constipation

and was treated with Arixtra. After drug was administered, patient experienced the following side effects: gastric haemorrhage, haematemesis. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with SERMION, MAGMITT, RISPERDAL, ARICEPT, THROMBIN LOCAL SOLUTION. Patient recovered.

Arixtra Side Effects Report #4900193-3
Arixtra side effect was reported by a Consumer or non-health professional from UNITED STATES on Aug 11, 2005. Male patient, 75 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure decreased, dyspepsia, gastrointestinal haemorrhage, haematemesis, haematocrit decreased. Arixtra dosage: unknown. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6000067-3
Arixtra side effect was reported by a Physician from JAPAN on Dec 12, 2008. Female patient, 70 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #5807212-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on July 04, 2008. Female patient, 66 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, haematemesis, hypothermia

. Arixtra dosage: 2.5MG TWICE PER DAY. Patient died on 06/22/2008.

Arixtra Side Effects Report #5744098-7
Arixtra side effect was reported by a Physician from FRANCE on May 16, 2008. Female patient, 64 years of age, weighting 110.2 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5749468-9
Arixtra side effect was reported by a Physician from FRANCE on May 20, 2008. Female patient, 64 years of age, weighting 110.2 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5749519-1
Arixtra side effect was reported by a Physician from FRANCE on May 16, 2008. Female patient, 64 years of age, weighting 110.2 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: duodenal ulcer, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5824432-X
Arixtra side effect was reported by a Physician from FRANCE on July 16, 2008. Female patient, 64 years of age, weighting 110.2 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, duodenal ulcer, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5951818-5
Arixtra side effect was reported by a Physician from FRANCE on Nov 07, 2008. Female patient, 64 years of age, weighting 110.2 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, duodenal ulcer, haematemesis, melaena. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6055546-X
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Jan 19, 2009. Male patient, 54 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure immeasurable, gastrointestinal haemorrhage, gaze palsy, haematemesis, skin discolouration. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6097209-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Feb 16, 2009. Male patient, 54 years of age, weighting 176.4 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: blood pressure immeasurable, gastrointestinal haemorrhage, gaze palsy, haematemesis, skin discolouration. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5512911-4
Arixtra side effect was reported by a Physician from FRANCE on Nov 06, 2007. Female patient, child 10 years of age, weighting 116.8 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: acute abdomen, haematemesis, intestinal ischaemia, melaena, renal failure acute. Arixtra dosage: 1.5MG PER DAY. Patient died on 11/03/2007.

Arixtra Side Effects Report #5525562-2
Arixtra side effect was reported by a Physician from FRANCE on Nov 16, 2007. Female patient, child 10 years of age, weighting 116.8 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain

, acute abdomen, diarrhoea haemorrhagic, haematemesis, intestinal ischaemia, leukocytosis, melaena, renal failure acute. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with PERFALGAN, CONTRAMAL, MONOTILDIEM, VASTAREL. Patient died on 11/03/2007.

Arixtra Side Effects Report #5472927-3
Arixtra side effect was reported by a Physician from JAPAN on Sept 28, 2007. Male patient was treated with Arixtra. After drug was administered, patient experienced the following side effects: haematemesis. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra and haematemesis

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Arixtra and haematemesis Patient Reports February 09, 2010

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