Arixtra Side Effects
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Arixtra Side Effects summary
Total Arixtra reports: 972.Arixtra FDA safety alerts: No.
Reported deaths: 164 Reported hospitalizations: 561.
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Arixtra Side Effects: haematoma infection, anaemia, pain in extremity, pulmonary embolism, muscle haemorrhage, haemoglobin decreased, deep vein thrombosis, off label use, oedema peripheral, anaemia postoperative, malaise,
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Arixtra Side Effects reported to FDA
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Arixtra Side Effects Report #5615146-XConsumer or non-health professional from UNITED STATES reported ARIXTRA problem on Oct 31, 2007. Male patient, 56 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: application site dryness, injection site pain. ARIXTRA dosage: unknown. During the same period patient was treated with DIGOXIN, REGLAN, ZOFRAN, HYDROMORPHONE. Patient recovered.
Arixtra Side Effects Report #5615147-1
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 20, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site rash. ARIXTRA dosage: 2.5MG TWICE PER DAY. Patient recovered.
Arixtra Side Effects Report #5615148-3
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Aug 23, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: incision site haemorrhage, post procedural haematoma. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5615149-5
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 09, 2007. Female patient, 39 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site haemorrhage, skin laceration. ARIXTRA dosage: unknown. During the same period patient was treated with HEPARIN. Patient recovered.
Arixtra Side Effects Report #5615152-5
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Aug 27, 2007. Male patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site pain. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with INSULIN. Patient recovered.
Arixtra Side Effects Report #5615155-0
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Aug 31, 2007. Male patient was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blood glucose increased. ARIXTRA dosage: 10MG PER DAY. During the same period patient was treated with ACIPHEX, METFORMIN, ATACAND, FLEXERIL, CELEBREX, ZYRTEC, FUROSEMIDE. Patient recovered.
Arixtra Side Effects Report #5615156-2
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Sept 06, 2007. Male patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with PLAQUENIL. Patient recovered.
Arixtra Side Effects Report #5615157-4
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 05, 2007. Female patient, 43 years of age, was diagnosed with white blood cell count and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site pain. ARIXTRA dosage: 5MG PER DAY. During the same period patient was treated with ZOFRAN, PHENERGAN, CARAFATE, DARVON, NEXIUM. Patient recovered.
Arixtra Side Effects Report #5615158-6
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Sept 11, 2007. Male patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: blood blister. ARIXTRA dosage: 5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5615159-8
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 14, 2007. Female patient, 48 years of age, was diagnosed with deep vein thrombosis, colon cancer and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: diarrhoea. ARIXTRA dosage: unknown. During the same period patient was treated with IRINOTECAN. Patient recovered.
Arixtra Side Effects Report #5615160-4
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Sept 18, 2007. Female patient, 49 years of age, was diagnosed with catheter thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site swelling. ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5615161-6
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Sept 20, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: international normalised ratio increased. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with WARFARIN. Patient recovered.
Arixtra Side Effects Report #5615162-8
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Sept 24, 2007. Male patient, 69 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: headache, vision blurred. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with KEPPRA, TOPROL, AVAPRO, ERYTHROMYCIN, OMEGA, ESTER. Patient recovered.
Arixtra Side Effects Report #5615165-3
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 09, 2007. Female patient, 62 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: pruritus, swelling face, urticaria. ARIXTRA dosage: unknown. During the same period patient was treated with GABAPENTIN, NORVASC, ARTHROTEC, THYROID. Patient recovered.
Arixtra Side Effects Report #5615166-5
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Oct 10, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage. ARIXTRA dosage: 7.5MG PER DAY. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5615167-7
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Oct 11, 2007. Male patient, 58 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site bruising. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with AMANTADINE, AMBIEN, CARBOLEVURE, REQUIP, COMTAN, ARTANE, ZYRTEC. Patient recovered.
Arixtra Side Effects Report #5615169-0
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Oct 29, 2007. Male patient, 58 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: contusion. ARIXTRA dosage: unknown. Patient recovered.
Arixtra Side Effects Report #5615170-7
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 01, 2007. Female patient, 62 years of age, weighting 130.3 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: rash. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with PREMARIN. Patient recovered.
Arixtra Side Effects Report #5615171-9
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Oct 25, 2007. Female patient, 57 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: burning sensation, dry eye, dysphonia, dyspnoea, eye irritation, oral discomfort. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with COUMADIN, WARFARIN, BUPROPION, HYDROCODONE BITARTRATE, TRICOR. Patient recovered.
Arixtra Side Effects Report #5615173-2
ARIXTRA problem was reported by a Health Professional from UNITED STATES on Nov 13, 2007. Female patient, 31 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: injection site pain. ARIXTRA dosage: unknown. During the same period patient was treated with VITAMIN AND MINERAL PRENATAL SUPPLEMENT W, THYROID. Patient recovered.
Arixtra Side Effects Report #5615174-4
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Nov 13, 2007. Male patient, 72 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: faeces discoloured. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with GLIPIZIDE, METFORMIN, ACID REFLUX MED, THYROID. Patient recovered.
Arixtra Side Effects Report #5615176-8
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 12, 2007. Female patient was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: haemorrhage. ARIXTRA dosage: 2.5MG AS REQUIRED. During the same period patient was treated with ASPIRIN. Patient was hospitalized and became disabled. Patient recovered.
Arixtra Side Effects Report #5615177-X
Health Professional from UNITED STATES reported ARIXTRA problem on Nov 12, 2007. Female patient, 21 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: international normalised ratio decreased. ARIXTRA dosage: 5MG PER DAY. During the same period patient was treated with COUMADIN. Patient recovered.
Arixtra Side Effects Report #5615178-1
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Nov 14, 2007. Female patient, 69 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: prothrombin time prolonged. ARIXTRA dosage: unknown. Patient recovered.
Arixtra Side Effects Report #5615179-3
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Nov 14, 2007. Female patient, 64 years of age, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: diplopia, dizziness, lethargy, malaise. ARIXTRA dosage: unknown. During the same period patient was treated with ATIVAN, ACIPHEX, ULTRAM, TYLENOL. Patient recovered.
Arixtra Side Effects Report #5615182-3
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Dec 04, 2007. Female patient, 76 years of age, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: malaise, nausea. ARIXTRA dosage: unknown. Patient recovered.
Arixtra Side Effects Report #5615323-8
Physician from JAPAN reported ARIXTRA problem on Feb 01, 2008. Female patient was diagnosed with fracture and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: ascites, pleural effusion. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5615628-0
ARIXTRA problem was reported by a Physician from JAPAN on Feb 01, 2008. Female patient, 75 years of age, weighting 138.9 lb, was diagnosed with thrombosis prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: anuria, renal amyloidosis, renal failure, renal tubular necrosis, tubulointerstitial nephritis, urinary tract infection. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with LOXONIN, ROPION, CEFMETAZON, GLYSENNID, TEGRETOL, SIGMART, MUCOSTA, JUVELA N. Patient recovered.
Arixtra Side Effects Report #5615647-4
Physician from INDIA reported ARIXTRA problem on Jan 31, 2008. Female patient, 55 years of age, was diagnosed with prophylaxis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: cerebral infarction. ARIXTRA dosage: 2.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5618479-6
ARIXTRA problem was reported by a Physician from FRANCE on Feb 01, 2008. Male patient, 91 years of age, weighting 123.5 lb, was diagnosed with parkinsonism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: faecaloma, gastrointestinal haemorrhage, gastrointestinal obstruction, lung infection, oxygen saturation decreased, rales, renal failure, respiratory failure, sputum purulent. ARIXTRA dosage: 1.5MG PER DAY. During the same period patient was treated with MODOPAR, VERAPAMIL, DUPHALAC. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5618481-4
Physician from FRANCE reported ARIXTRA problem on Feb 01, 2008. Female patient, 81 years of age, weighting 110.2 lb, was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: dyspnoea, pneumothorax. ARIXTRA dosage: 1.5MG PER DAY. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5620244-0
ARIXTRA problem was reported by a Physician from JAPAN on Feb 05, 2008. Female patient, 72 years of age, weighting 112.4 lb, was diagnosed with thrombosis prophylaxis, pain, insomnia, postoperative care and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: c-reactive protein increased, inflammation, post procedural haematoma, postoperative wound complication, subcutaneous haematoma. ARIXTRA dosage: 1.5MG PER DAY. During the same period patient was treated with LOXONIN, MUCOSTA, DASEN, VOLTAREN, LENDORMIN, PENTCILLIN, ROPION. Patient was hospitalized. Patient recovered.
Arixtra Side Effects Report #5620269-5
Physician from FRANCE reported ARIXTRA problem on Feb 01, 2008. Male patient was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: atrial thrombosis, pulmonary embolism. ARIXTRA dosage: 7.5MG PER DAY. Patient recovered.
Arixtra Side Effects Report #5621974-7
ARIXTRA problem was reported by a Physician from FRANCE on Feb 06, 2008. Female patient, 92 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: burning sensation, cerebral haemorrhage, hemiplegia. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with PREVISCAN. Patient was hospitalized. Patient died.
Arixtra Side Effects Report #5623138-X
Consumer or non-health professional from FRANCE reported ARIXTRA problem 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 problems/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 #5623139-1
ARIXTRA problem was reported by a Consumer or non-health professional from FRANCE on Feb 04, 2008. Male patient, 56 years of age, was diagnosed with phlebitis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: agitation, coma, delirium, haemorrhagic stroke, intracranial haematoma, septic shock. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with DIAMICRON, GLUCOR, GLUCOPHAGE, INDAPAMIDE, AMLOR, ATACAND, INNOHEP, AUGMENTIN. Patient was hospitalized. Patient died on 12/10/2007.
Arixtra Side Effects Report #5624673-0
Consumer or non-health professional from UNITED STATES reported ARIXTRA problem on Feb 07, 2008. Female patient, 50 years of age, was diagnosed with pulmonary embolism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: fear, haemorrhagic disorder, injection site bruising. ARIXTRA dosage: 7.5MG PER DAY. During the same period patient was treated with NORCO, METFORMIN, CIMETIDINE, CLONIDINE, LEVOTHYROXINE, XANAX, HYZAAR. Patient recovered.
Arixtra Side Effects Report #5624678-X
ARIXTRA problem was reported by a Consumer or non-health professional from UNITED STATES on Feb 11, 2008. Male patient, 62 years of age, was diagnosed with deep vein thrombosis and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: balance disorder, epistaxis, feeling abnormal, neuropathy peripheral, paraesthesia, penile ulceration, renal haemorrhage, skin discolouration, skin haemorrhage. ARIXTRA dosage: 10MG PER DAY. During the same period patient was treated with COUMADIN. Patient recovered.
Arixtra Side Effects Report #5624688-2
Pharmacist from JAPAN reported ARIXTRA problem on Feb 07, 2008. Female patient, 70 years of age, weighting 143.3 lb, was diagnosed with thrombosis prophylaxis, infection prophylaxis, analgesia, insomnia and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: delirium, haemorrhage subcutaneous, injection site bruising, insomnia, restlessness, speech disorder. ARIXTRA dosage: 2.5MG PER DAY. During the same period patient was treated with CEFAMEZIN, SEISHOKU, PENTAZOCINE LACTATE, MYSLEE, LENDORMIN. Patient recovered.
Arixtra Side Effects Report #5624692-4
ARIXTRA problem was reported by a Physician from FRANCE on Feb 08, 2008. Male patient, 91 years of age, weighting 123.5 lb, was diagnosed with parkinsonism and was treated with ARIXTRA. After drug was administered, patient experienced the following problems/side effects: acute coronary syndrome, anaemia, arrhythmia, atrial fibrillation, faecaloma, gastrointestinal haemorrhage, gastrointestinal obstruction, hypoxia, lung infection. ARIXTRA dosage: 1.5MG PER DAY. During the same period patient was treated with MODOPAR, VERAPAMIL, DUPHALAC. Patient was hospitalized. Patient died on 01/28/2008.
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