Arixtra and subdural haematoma Patient Reports February 10, 2012

Arixtra Side Effects Report #5963384-9
Arixtra side effect was reported by a Physician from JAPAN on Nov 20, 2008. Female patient, 95 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, depressed level of consciousness, fall , subdural haematoma, urinary incontinence . Arixtra dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5299989-0
Arixtra side effect was reported by a Physician from FRANCE on Mar 29, 2007. Female patient, 83 years of age, weighting 176.0 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: subdural haematoma. Arixtra dosage: 2.5 MG/PER DAY/SUBCUTANEOUS. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5661716-2
Arixtra side effect was reported by a Physician from JAPAN on Mar 10, 2008. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bone pain, fall , muscular weakness, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5700920-1
Arixtra side effect was reported by a Physician from JAPAN on Apr 08, 2008. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bone pain, fall , muscular weakness, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5746445-9
Arixtra side effect was reported by a Physician from JAPAN on May 19, 2008. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bone pain, fall , muscular weakness, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5798198-6
Arixtra side effect was reported by a Physician from JAPAN on June 30, 2008. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: bone pain, fall , muscular weakness, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5841826-7
Arixtra side effect was reported by a Physician from JAPAN on Aug 07, 2008. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: arthropathy, bone pain, fall , muscular weakness, peroneal nerve palsy, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6077305-4
Arixtra side effect was reported by a Physician from JAPAN on Feb 09, 2009. Female patient, 80 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: arthropathy, bone pain, fall , muscular weakness, peroneal nerve palsy, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5537414-2
Arixtra side effect was reported by a Physician from JAPAN on Dec 05, 2007. 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: subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.


Arixtra Side Effects Report #5571770-4
Arixtra side effect was reported by a Physician from JAPAN on Dec 17, 2007. Female patient, 79 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: hypokinesia, monoplegia, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PETHILORFAN. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5614171-2
Arixtra side effect was reported by a Physician from JAPAN on Feb 01, 2008. Female patient, 79 years of age, weighting 97.00 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: hypokinesia, monoplegia, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PETHILORFAN. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5972556-9
Arixtra side effect was reported by a Physician from JAPAN on Nov 26, 2008. Female patient, 73 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: aphasia , cerebral haemorrhage, hemiplegia, nausea , subdural haematoma. Arixtra dosage: 1.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #5987019-4
Arixtra side effect was reported by a Physician from JAPAN on Dec 02, 2008. Female patient, 73 years of age, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: aphasia , cerebral haemorrhage, hemiplegia, nausea , subdural haematoma. Arixtra dosage: 1.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #6023159-1
Arixtra side effect was reported by a Physician from JAPAN on Dec 22, 2008. Female patient, 73 years of age, weighting 48.50 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, insomnia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: aphasia , cerebral haemorrhage, hemiplegia, movement disorder , nausea , subdural haematoma. Arixtra dosage: 1.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, LENDORMIN. Patient recovered.


Arixtra Side Effects Report #4855919-4
Arixtra side effect was reported by a Physician from FRANCE on Nov 25, 2005. Female patient, 73 years of age, weighting 165.3 lb, was diagnosed with thrombosis prophylaxis and was treated with Arixtra. After drug was administered, patient experienced the following side effects: anaemia, brain herniation, cerebral haemorrhage, coma, confusional state, incision site haemorrhage, post procedural haematoma, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with PERFALGAN, PROFENID, ALLOPURINOL, ISOBAR, PROPRANOLOL, OMEPRAZOLE, TEMESTA, RELVENE. Patient died on 10/29/2005.

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 #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 #5179004-X
Arixtra side effect was reported by a Pharmacist from UNITED STATES on Dec 15, 2006. Female patient, 59 years of age, weighting 244.7 lb, was diagnosed with deep vein thrombosis , heparin-induced thrombocytopenia and was treated with Arixtra. After drug was administered, patient experienced the following side effects: haemorrhage intracranial, post procedural complication, subdural haematoma. Arixtra dosage: 7.5 MG DAILY PO SQ. During the same period patient was treated with WARFARIN. Patient died on 11/01/2006.


Arixtra Side Effects Report #5272771-6
Arixtra side effect was reported by a Physician from FRANCE on Mar 13, 2007. Female patient, 90 years of age, weighting 88.18 lb, was diagnosed with atrial fibrillation  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, malaise, off label use, subdural haematoma. Arixtra dosage: unknown. During the same period patient was treated with CORDARONE, TRIATEC, LASIX, VADILEX, KARDEGIC. Patient was hospitalized. Patient died on 02/26/2007.

Arixtra Side Effects Report #5337251-8
Arixtra side effect was reported by a Physician from FRANCE on May 18, 2007. Female patient, 87 years of age, weighting 88.18 lb, was diagnosed with atrial fibrillation , myocardial ischaemia, arterial disorder and was treated with Arixtra. After drug was administered, patient experienced the following side effects: brain herniation, coma, hypotonia, malaise, mydriasis, off label use, subdural haematoma. Arixtra dosage: unknown. During the same period patient was treated with CORDARONE, TRIATEC, LASIX, VADILEX, KARDEGIC, CARDENSIEL. Patient was hospitalized. Patient died on 02/28/2007.

Arixtra Side Effects Report #5267312-3
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 06, 2007. Female patient, 75 years of age, was diagnosed with atrial fibrillation  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: off label use, subdural haematoma. Arixtra dosage: unknown. Patient died on 03/04/2007.

Arixtra Side Effects Report #5702739-4
Arixtra side effect was reported by a Physician from FRANCE on Apr 07, 2008. Female patient, 75 years of age, weighting 191.8 lb, was diagnosed with atrial fibrillation  and was treated with Arixtra. After drug was administered, patient experienced the following side effects: abdominal pain , back pain , extradural haematoma, off label use, paraplegia, spinal haematoma, subdural haematoma. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN, ATORVASTATIN CALCIUM, SOTALOL, PERFALGAN, SPASFON. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5745241-6
Arixtra side effect was reported by a Physician from FRANCE on May 15, 2008. Female patient, 95 years of age, weighting 92.59 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: cerebral haematoma, fall , haemoglobin decreased, ischaemic stroke, subdural haematoma, traumatic brain injury . Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with IMOVANE, DOLIPRANE, ASPIRIN, LOVENOX, CORDARONE, MEDIATENSYL, MORPHINE. Patient died on 02/17/2006.


Arixtra Side Effects Report #6042919-4
Arixtra side effect was reported by a Physician from JAPAN on Jan 13, 2009. Female patient, 95 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, depressed level of consciousness, fall , subdural haematoma, urinary incontinence . Arixtra dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #6111364-5
Arixtra side effect was reported by a Physician from JAPAN on Mar 06, 2009. Female patient, 95 years of age, weighting 81.57 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, depressed level of consciousness, fall , hydrocephalus , subdural haematoma, urinary incontinence . Arixtra dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5469533-3
Arixtra side effect was reported by a Physician from JAPAN on Sept 25, 2007. Female patient, 92 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized and became disabled. Patient recovered.

Arixtra Side Effects Report #5480453-0
Arixtra side effect was reported by a Physician from JAPAN on Oct 05, 2007. Female patient, 92 years of age, weighting 85.98 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: monoparesis, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient recovered.

Arixtra Side Effects Report #5480569-9
Arixtra side effect was reported by a Physician from JAPAN on Oct 05, 2007. Female patient, 92 years of age, weighting 85.98 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: monoparesis, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient recovered.


Arixtra Side Effects Report #5317919-X
Arixtra side effect was reported by a Physician from FRANCE on May 04, 2007. Male patient, 91 years of age, weighting 132.3 lb, was diagnosed with essential hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: cerebral haemorrhage, coma, confusional state, subdural haematoma, thrombocytopenia. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with ATARAX, XATRAL, PARACETAMOL, AMLOR, FOZITEC. Patient was hospitalized. Patient died on 03/15/2007.

Arixtra Side Effects Report #6122858-0
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on Mar 09, 2009. Male patient, 86 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, subcutaneous haematoma, subdural haematoma. Arixtra dosage: 2.5MG PER DAY. During the same period patient was treated with KARDEGIC. Patient recovered.

Arixtra Side Effects Report #5385556-7
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on July 02, 2007. Female patient, 80 years of age, was diagnosed with asthma , essential hypertension and was treated with Arixtra. After drug was administered, patient experienced the following side effects: cerebrovascular accident, confusional state, dysphasia, hemiparesis, injection site oedema, motor dysfunction, subdural haematoma. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN, FORADIL, EURELIX. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5747823-4
Arixtra side effect was reported by a Consumer or non-health professional from FRANCE on May 16, 2008. Female patient, 76 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: coma, fall , glasgow coma scale abnormal, head injury, neurological symptom, pupils unequal, subdural haematoma. Arixtra dosage: unknown. During the same period patient was treated with ASPIRIN, MICARDIS, ZANIDIP, DIAMICRON, PANTOPRAZOLE, FENOFIBRATE, BROMAZEPAM, BUFLOMEDIL. Patient was hospitalized. Patient recovered.

Arixtra Side Effects Report #5281751-6
Arixtra side effect was reported by a Physician from FRANCE on Mar 22, 2007. Male patient, 75 years of age, weighting 176.4 lb, was treated with Arixtra. After drug was administered, patient experienced the following side effects: fall , off label use, subdural haematoma, syncope. Arixtra dosage: 7.5MG PER DAY. Patient died on 03/04/2007.


Arixtra Side Effects Report #5311517-X
Arixtra side effect was reported by a Physician from FRANCE on Apr 18, 2007. Male patient, 75 years of age, weighting 176.4 lb, was diagnosed with prostatism and was treated with Arixtra. After drug was administered, patient experienced the following side effects: brain herniation, convulsion, disturbance in attention, fall , off label use, subdural haematoma, syncope. Arixtra dosage: 7.5MG PER DAY. During the same period patient was treated with TAREG, PERMIXON, LASIX, DIFFU K. Patient died on 03/02/2007.

Arixtra Side Effects Report #6126196-1
Arixtra side effect was reported by a Physician from FRANCE on Mar 11, 2009. Male patient, 75 years of age, was treated with Arixtra. After drug was administered, patient experienced the following side effects: fall , subdural haematoma. Arixtra dosage: 2.5MG PER DAY. Patient was hospitalized. Patient recovered.